diff --git a/src/ontology/Makefile b/src/ontology/Makefile index 4dba74b44a..d07c6fb3a7 100644 --- a/src/ontology/Makefile +++ b/src/ontology/Makefile @@ -85,7 +85,7 @@ all_imports: $(IMPORT_FILES) COMPONENTS = mondo-tags COMPONENT_FILES = $(foreach n, $(COMPONENTS), components/$(n).owl) -SUBSETS = mondo-rare +SUBSETS = mondo-rare mondo-clingen SUBSET_ROOTS = $(patsubst %, subsets/%, $(SUBSETS)) SUBSET_FILES = $(foreach n,$(SUBSET_ROOTS), $(n).owl $(n).obo $(n).json $(n)_nodes.tsv $(n)_edges.tsv) @@ -400,6 +400,15 @@ subsets/mondo-rare.owl: $(ONT)-base.owl $(TMPDIR)/hgnc_import.owl tmp/rare-seed $(ROBOT) annotate --input $@ --ontology-iri $(ONTBASE)/$@ $(ANNOTATE_ONTOLOGY_VERSION) -o $@.tmp.owl && mv $@.tmp.owl $@ .PRECIOUS: $(SUBSETDIR)/mondo-rare.owl +tmp/clingen-seed.txt: $(SRC) + $(ROBOT) merge -i $< query --query ../sparql/signature/clingen-subset.sparql $@ +.PRECIOUS: tmp/rare-seed-entities.txt + +subsets/mondo-clingen.owl: $(ONT)-base.owl tmp/clingen-seed.txt | $(SUBSETDIR) + $(ROBOT) merge -i $< query --update ../sparql/update/clingen-labels.ru extract --method subset -T tmp/clingen-seed.txt --copy-ontology-annotations true --output $@ &&\ + $(ROBOT) annotate --input $@ --ontology-iri $(ONTBASE)/$@ $(ANNOTATE_ONTOLOGY_VERSION) -o $@.tmp.owl && mv $@.tmp.owl $@ +.PRECIOUS: $(SUBSETDIR)/mondo-rare.owl + subsets/%.json: subsets/%.owl $(ROBOT) convert -i $< -o $@ diff --git a/src/ontology/metadata/mondo.sssom.config.yml b/src/ontology/metadata/mondo.sssom.config.yml index 44bc0b55ef..a4c74dfe6f 100644 --- a/src/ontology/metadata/mondo.sssom.config.yml +++ b/src/ontology/metadata/mondo.sssom.config.yml @@ -70,7 +70,7 @@ curie_map: # ICD10: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/ICD10/" ICD10EXP: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/ICD10EXP/" DERMO: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/DERMO/" - GARD: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/GARD/" + GARD: "https://rarediseases.info.nih.gov/diseases/" # SNOMEDCT_US: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/SNOMEDCT_US/" # MSH: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/MSH/" GC_ID: "http://purl.obolibrary.org/obo/mondo/mappings/unknown_prefix/GC_ID/" diff --git a/src/ontology/mondo-edit.obo b/src/ontology/mondo-edit.obo index 827ab4ddb2..c597e707de 100644 --- a/src/ontology/mondo-edit.obo +++ b/src/ontology/mondo-edit.obo @@ -45,6 +45,7 @@ synonymtypedef: DUBIOUS "dubious synonym" synonymtypedef: EXCLUDE "Synonym to be removed from public release but maintained in edit version as record of external usage" synonymtypedef: MISSPELLING "A synonym that is recorded for consistency with another source but is a misspelling" synonymtypedef: NON_HUMAN "A synonym that is used for non-human animal variants of a disease" +synonymtypedef: NORD_PREFERRED "NORD preferred" synonymtypedef: OMO:0003005 "UK spelling synonym" import: http://purl.obolibrary.org/obo/mondo/components/mondo-tags.owl import: http://purl.obolibrary.org/obo/mondo/imports/axioms.owl diff --git a/src/ontology/mondo.Makefile b/src/ontology/mondo.Makefile index 6fb3410043..365d27fcbd 100644 --- a/src/ontology/mondo.Makefile +++ b/src/ontology/mondo.Makefile @@ -183,6 +183,9 @@ reports/mondo_analysis.md: $(QC_REPORTS) # This is a hack to get rid of \n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
subject_idsubject_labelpredicate_idobject_idobject_labelmapping_justificationconfidence
0MONDO:0000001diseaseskos:exactMatchDOID:4diseasesemapv:UnspecifiedMatching0.95
1MONDO:0000001diseaseskos:exactMatchMEDGEN:4347semapv:UnspecifiedMatching0.95
2MONDO:0000001diseaseskos:exactMatchNCIT:C2991Disease or Disordersemapv:UnspecifiedMatching0.95
3MONDO:0000001diseaseskos:exactMatchOrphanet:377788Diseasesemapv:UnspecifiedMatching0.95
4MONDO:0000001diseaseskos:exactMatchSCTID:64572001semapv:UnspecifiedMatching0.95
........................
98855MONDO:8000030obsolete morphological anomalyskos:exactMatchOrphanet:377791Morphological anomalysemapv:UnspecifiedMatching0.95
98856MONDO:8000031obsolete subtype of a disorderskos:exactMatchOrphanet:557494subtype of a disordersemapv:UnspecifiedMatching0.95
98857MONDO:8000032obsolete malformation syndromeskos:exactMatchOrphanet:377789Malformation syndromesemapv:UnspecifiedMatching0.95
98858MONDO:8000033obsolete group of disordersskos:exactMatchOrphanet:557492group of disorderssemapv:UnspecifiedMatching0.95
98859MONDO:8000034obsolete disorderskos:exactMatchOrphanet:557493disordersemapv:UnspecifiedMatching0.95
\n", + "

98783 rows × 7 columns

\n", + "" + ], + "text/plain": [ + " subject_id subject_label predicate_id \\\n", + "0 MONDO:0000001 disease skos:exactMatch \n", + "1 MONDO:0000001 disease skos:exactMatch \n", + "2 MONDO:0000001 disease skos:exactMatch \n", + "3 MONDO:0000001 disease skos:exactMatch \n", + "4 MONDO:0000001 disease skos:exactMatch \n", + "... ... ... ... \n", + "98855 MONDO:8000030 obsolete morphological anomaly skos:exactMatch \n", + "98856 MONDO:8000031 obsolete subtype of a disorder skos:exactMatch \n", + "98857 MONDO:8000032 obsolete malformation syndrome skos:exactMatch \n", + "98858 MONDO:8000033 obsolete group of disorders skos:exactMatch \n", + "98859 MONDO:8000034 obsolete disorder skos:exactMatch \n", + "\n", + " object_id object_label mapping_justification \\\n", + "0 DOID:4 disease semapv:UnspecifiedMatching \n", + "1 MEDGEN:4347 semapv:UnspecifiedMatching \n", + "2 NCIT:C2991 Disease or Disorder semapv:UnspecifiedMatching \n", + "3 Orphanet:377788 Disease semapv:UnspecifiedMatching \n", + "4 SCTID:64572001 semapv:UnspecifiedMatching \n", + "... ... ... ... \n", + "98855 Orphanet:377791 Morphological anomaly semapv:UnspecifiedMatching \n", + "98856 Orphanet:557494 subtype of a disorder semapv:UnspecifiedMatching \n", + "98857 Orphanet:377789 Malformation syndrome semapv:UnspecifiedMatching \n", + "98858 Orphanet:557492 group of disorders semapv:UnspecifiedMatching \n", + "98859 Orphanet:557493 disorder semapv:UnspecifiedMatching \n", + "\n", + " confidence \n", + "0 0.95 \n", + "1 0.95 \n", + "2 0.95 \n", + "3 0.95 \n", + "4 0.95 \n", + "... ... \n", + "98855 0.95 \n", + "98856 0.95 \n", + "98857 0.95 \n", + "98858 0.95 \n", + "98859 0.95 \n", + "\n", + "[98783 rows x 7 columns]" + ] + }, + "execution_count": 44, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "def sanitize_table(df, mondo, source, default_value=0.5):\n", + " \"\"\"\n", + " Ensure the confidence column exists, and all values are valid floats between 0 and 1.\n", + " Replace invalid or missing values with the default value.\n", + " \"\"\"\n", + " if 'confidence' not in df.columns:\n", + " df['confidence'] = default_value\n", + " else:\n", + " df['confidence'] = pd.to_numeric(df['confidence'], errors='coerce') # Convert to numeric, invalid parsing will be NaN\n", + " df['confidence'] = df['confidence'].apply(lambda x: x if 0 <= x <= 1 else default_value) # Replace out of range values with default\n", + " df['confidence'].fillna(default_value, inplace=True) # Replace NaN with default value\n", + " \n", + " df['subject_label'] = df.apply(\n", + " lambda row: mondo.label(row['subject_id']) if pd.notnull(mondo.label(row['subject_id'])) \n", + " else source.label(row['subject_id']) if pd.notnull(source.label(row['subject_id'])) \n", + " else row['subject_label'] if 'subject_label' in row and pd.notnull(row['subject_label'])\n", + " else '', axis=1\n", + " )\n", + " df['object_label'] = df.apply(\n", + " lambda row: mondo.label(row['object_id']) if pd.notnull(mondo.label(row['object_id'])) \n", + " else source.label(row['object_id']) if pd.notnull(source.label(row['object_id'])) \n", + " else row['object_label'] if 'object_label' in row and pd.notnull(row['object_label'])\n", + " else '', axis=1\n", + " )\n", + " return df\n", + "\n", + "df_mondo_mappings = mondo_mappings.df.copy()\n", + "df_mondo_mappings_exact = sanitize_table(df_mondo_mappings[df_mondo_mappings['predicate_id'] == 'skos:exactMatch'], mondo, source, 0.95)\n", + "df_source_mappings = sanitize_table(source_mappings.df.copy(), mondo, source)\n", + "df_lexmatch_matches = lexmatch_matches.df.copy()\n", + "df_negative_matches = negative_matches.df.copy()\n", + "#negative_matches.df = negative_matches.df.astype(str)\n", + "\n", + "df_mondo_mappings_exact" + ] + }, + { + "cell_type": "code", + "execution_count": 45, + "id": "74ef510a", + "metadata": {}, + "outputs": [ + { + "data": { + "text/plain": [ + "False" + ] + }, + "execution_count": 45, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "pd.notnull(mondo.label(\"kkk\"))" + ] + }, + { + "cell_type": "code", + "execution_count": 46, + "id": "a88986a5", + "metadata": {}, + "outputs": [ + { + "name": "stderr", + "output_type": "stream", + "text": [ + "/var/folders/vj/ks1_0k8x3t9ftrwcr0t9vjwr0000gn/T/ipykernel_59403/133923016.py:11: ChainedAssignmentError: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "When using the Copy-on-Write mode, such inplace method never works to update the original DataFrame or Series, because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " df['confidence'].fillna(default_value, inplace=True) # Replace NaN with default value\n" + ] + }, + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
subject_idsubject_labelpredicate_idobject_idobject_labelmapping_justificationmapping_toolconfidencesubject_match_fieldobject_match_fieldmatch_stringcomment
0MONDO:0000001diseaseskos:exactMatchNCIT:C156809Medical Conditionsemapv:LexicalMatchingoaklib0.800000oio:hasExactSynonymrdfs:labelmedical conditionNaN
1MONDO:0000001diseaseskos:exactMatchNCIT:C25457Conditionsemapv:LexicalMatchingoaklib0.800000oio:hasExactSynonymrdfs:labelconditionNaN
2MONDO:0000004adrenocortical insufficiencyskos:exactMatchNCIT:C113211Hypocortisolemiasemapv:LexicalMatchingoaklib0.800000oio:hasExactSynonymrdfs:labelhypocortisolemiaNaN
3MONDO:0000328hyperphosphatemiaskos:exactMatchNCIT:C113750Hyperphosphatemiasemapv:LexicalMatchingoaklib0.800000oio:hasExactSynonymrdfs:labelhyperphosphatemiaNaN
4MONDO:0000328hyperphosphatemiaskos:exactMatchNCIT:C113750Hyperphosphatemiasemapv:LexicalMatchingoaklib0.849779rdfs:labelrdfs:labelhyperphosphatemiaNaN
.......................................
2598MONDO:0956990supratentorial ependymoma, ZFTA fusion–positiveskos:exactMatchNCIT:C186350Supratentorial Ependymoma ZFTA Fusion-Positivesemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
2599MONDO:0956991supratentorial ependymoma, YAP1 fusion–positiveskos:exactMatchNCIT:C186351Supratentorial Ependymoma YAP1 Fusion-Positivesemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
2600MONDO:0956992posterior fossa group A ependymomaskos:exactMatchNCIT:C186450Posterior Fossa Ependymoma, Group A (PFA)semapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
2601MONDO:0956993posterior fossa group B ependymomaskos:exactMatchNCIT:C186451Posterior Fossa Ependymoma, Group B (PFB)semapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
2602MONDO:0957197diffuse glioma, H3 G34 mutantskos:exactMatchNCIT:C185371Diffuse Hemispheric Glioma, H3 G34-Mutantsemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
\n", + "

2351 rows × 12 columns

\n", + "
" + ], + "text/plain": [ + " subject_id subject_label \\\n", + "0 MONDO:0000001 disease \n", + "1 MONDO:0000001 disease \n", + "2 MONDO:0000004 adrenocortical insufficiency \n", + "3 MONDO:0000328 hyperphosphatemia \n", + "4 MONDO:0000328 hyperphosphatemia \n", + "... ... ... \n", + "2598 MONDO:0956990 supratentorial ependymoma, ZFTA fusion–positive \n", + "2599 MONDO:0956991 supratentorial ependymoma, YAP1 fusion–positive \n", + "2600 MONDO:0956992 posterior fossa group A ependymoma \n", + "2601 MONDO:0956993 posterior fossa group B ependymoma \n", + "2602 MONDO:0957197 diffuse glioma, H3 G34 mutant \n", + "\n", + " predicate_id object_id \\\n", + "0 skos:exactMatch NCIT:C156809 \n", + "1 skos:exactMatch NCIT:C25457 \n", + "2 skos:exactMatch NCIT:C113211 \n", + "3 skos:exactMatch NCIT:C113750 \n", + "4 skos:exactMatch NCIT:C113750 \n", + "... ... ... \n", + "2598 skos:exactMatch NCIT:C186350 \n", + "2599 skos:exactMatch NCIT:C186351 \n", + "2600 skos:exactMatch NCIT:C186450 \n", + "2601 skos:exactMatch NCIT:C186451 \n", + "2602 skos:exactMatch NCIT:C185371 \n", + "\n", + " object_label mapping_justification \\\n", + "0 Medical Condition semapv:LexicalMatching \n", + "1 Condition semapv:LexicalMatching \n", + "2 Hypocortisolemia semapv:LexicalMatching \n", + "3 Hyperphosphatemia semapv:LexicalMatching \n", + "4 Hyperphosphatemia semapv:LexicalMatching \n", + "... ... ... \n", + "2598 Supratentorial Ependymoma ZFTA Fusion-Positive semapv:MappingChaining \n", + "2599 Supratentorial Ependymoma YAP1 Fusion-Positive semapv:MappingChaining \n", + "2600 Posterior Fossa Ependymoma, Group A (PFA) semapv:MappingChaining \n", + "2601 Posterior Fossa Ependymoma, Group B (PFB) semapv:MappingChaining \n", + "2602 Diffuse Hemispheric Glioma, H3 G34-Mutant semapv:MappingChaining \n", + "\n", + " mapping_tool confidence subject_match_field object_match_field \\\n", + "0 oaklib 0.800000 oio:hasExactSynonym rdfs:label \n", + "1 oaklib 0.800000 oio:hasExactSynonym rdfs:label \n", + "2 oaklib 0.800000 oio:hasExactSynonym rdfs:label \n", + "3 oaklib 0.800000 oio:hasExactSynonym rdfs:label \n", + "4 oaklib 0.849779 rdfs:label rdfs:label \n", + "... ... ... ... ... \n", + "2598 NaN 0.475000 NaN NaN \n", + "2599 NaN 0.475000 NaN NaN \n", + "2600 NaN 0.475000 NaN NaN \n", + "2601 NaN 0.475000 NaN NaN \n", + "2602 NaN 0.475000 NaN NaN \n", + "\n", + " match_string \\\n", + "0 medical condition \n", + "1 condition \n", + "2 hypocortisolemia \n", + "3 hyperphosphatemia \n", + "4 hyperphosphatemia \n", + "... ... \n", + "2598 NaN \n", + "2599 NaN \n", + "2600 NaN \n", + "2601 NaN \n", + "2602 NaN \n", + "\n", + " comment \n", + "0 NaN \n", + "1 NaN \n", + "2 NaN \n", + "3 NaN \n", + "4 NaN \n", + "... ... \n", + "2598 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "2599 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "2600 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "2601 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "2602 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "\n", + "[2351 rows x 12 columns]" + ] + }, + "execution_count": 46, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "def get_one_hop_mappings(df_mondo_mappings, df_source_mappings):\n", + " # Get all mappings that are one hop away from Mondo\n", + " merged_df = pd.merge(\n", + " df_mondo_mappings,\n", + " df_source_mappings,\n", + " on=[\"object_id\", \"predicate_id\"],\n", + " suffixes=(\"_mondo\", \"_source\")\n", + " )\n", + " \n", + " # Create the new mappings\n", + " one_hop_mappings = pd.DataFrame({\n", + " \"subject_id\": merged_df[\"subject_id_mondo\"],\n", + " \"object_id\": merged_df[\"subject_id_source\"],\n", + " \"predicate_id\": merged_df[\"predicate_id\"],\n", + " \"mapping_justification\": \"semapv:MappingChaining\",\n", + " \"confidence\": merged_df[\"confidence_mondo\"] * merged_df[\"confidence_source\"],\n", + " \"comment\": \"Generated by matching the object of a Mondo mapping to the object of a source mapping.\"\n", + " })\n", + " \n", + " return one_hop_mappings\n", + "\n", + "def prepare_mapping_candidates(df_mondo_mappings, df_source_mappings, df_lexmatch_matches, df_negative_matches):\n", + " \n", + " # 1. Take all lexical matches found\n", + " candidate_mappings = df_lexmatch_matches.copy()\n", + " \n", + " # 2. Add all simple one hop mappings\n", + " one_hop_mappings = get_one_hop_mappings(df_mondo_mappings, df_source_mappings)\n", + " one_hop_mappings = one_hop_mappings.merge(\n", + " candidate_mappings[['subject_id', 'predicate_id', 'object_id']],\n", + " on=['subject_id', 'predicate_id', 'object_id'],\n", + " how='left',\n", + " indicator=True\n", + " )\n", + " one_hop_mappings = one_hop_mappings[one_hop_mappings['_merge'] == 'left_only']\n", + " one_hop_mappings.drop(columns=['_merge'], inplace=True)\n", + " candidate_mappings = pd.concat([candidate_mappings, one_hop_mappings], ignore_index=True)\n", + "\n", + " # 3. Remove all mappings that are already in Mondo\n", + " candidate_mappings = candidate_mappings[~candidate_mappings['object_id'].isin(df_mondo_mappings['object_id'])]\n", + "\n", + " # 4. Remove all mappings that are already in the source\n", + " candidate_mappings = candidate_mappings.merge(\n", + " df_negative_matches[['subject_id', 'predicate_id', 'object_id']],\n", + " on=['subject_id', 'predicate_id', 'object_id'],\n", + " how='left',\n", + " indicator=True\n", + " )\n", + " candidate_mappings = candidate_mappings[candidate_mappings['_merge'] == 'left_only']\n", + " candidate_mappings.drop(columns=['_merge'], inplace=True)\n", + " \n", + " # 5. Remove all mappings that are not between the source and Mondo\n", + " candidate_mappings = candidate_mappings[\n", + " candidate_mappings['subject_id'].str.startswith('MONDO') & \n", + " candidate_mappings['object_id'].str.startswith(source_id_space)\n", + " ]\n", + " \n", + " return candidate_mappings\n", + "\n", + "candidate_mappings = prepare_mapping_candidates(df_mondo_mappings_exact, df_source_mappings, df_lexmatch_matches, df_negative_matches)\n", + "candidate_mappings = sanitize_table(candidate_mappings, mondo, source)\n", + "candidate_mappings.to_csv(\"candidate_mappings.tsv\", sep=\"\\t\", index=False)\n", + "candidate_mappings" + ] + }, + { + "cell_type": "markdown", + "id": "808268d0", + "metadata": {}, + "source": [ + "[Back](#overview)\n", + "\n", + "---\n", + "\n", + "### Load Mondo using OAK pronto adapter\n" + ] + }, + { + "cell_type": "code", + "execution_count": 47, + "id": "05c0d034", + "metadata": {}, + "outputs": [], + "source": [ + "from oaklib.datamodels.vocabulary import IS_A\n", + "\n", + "def get_unmapped_disease_list(source_diseases_to_align, mondo_mappings):\n", + " unmapped_source_diseases = []\n", + "\n", + " # Iterate through all source diseases, and find those that are not yet mapped exactly to Mondo\n", + " for source_disease in source_diseases_to_align:\n", + " matches = mondo_mappings[mondo_mappings[\"object_id\"] == source_disease]['subject_id'].tolist()\n", + " if not matches:\n", + " unmapped_source_diseases.append(source_disease)\n", + " \n", + " return unmapped_source_diseases\n", + "\n", + "def create_matches_index_for_unmapped_disease(unmapped_source_diseases, candidate_mappings):\n", + " matches_list = {}\n", + " for disease in unmapped_source_diseases:\n", + " matches = candidate_mappings[candidate_mappings[\"object_id\"] == disease]\n", + " matches_list[disease] = matches\n", + " return matches_list\n", + "\n", + "# Get all the descendants of the source roots. The goal is to align all diseases under these roots.\n", + "source_diseases_to_align = list(set(source.descendants(source_roots, predicates=[IS_A])))\n", + "\n", + "# Get all the diseases that are not yet mapped to Mondo\n", + "unmapped_source_diseases = get_unmapped_disease_list(source_diseases_to_align, df_mondo_mappings_exact)\n", + "\n", + "# Generate a dictionary that maps each unmapped source disease to its candidate mappings\n", + "matches_index = create_matches_index_for_unmapped_disease(unmapped_source_diseases, candidate_mappings)\n" + ] + }, + { + "cell_type": "code", + "execution_count": 48, + "id": "b358c92b", + "metadata": {}, + "outputs": [], + "source": [ + "import getpass\n", + "import os\n", + "from langchain_openai import ChatOpenAI\n", + "from langchain_core.output_parsers import StrOutputParser\n", + "from langchain_core.output_parsers import JsonOutputParser\n", + "from langchain_core.prompts import ChatPromptTemplate\n", + "\n", + "#os.environ[\"OPENAI_API_KEY\"] = getpass.getpass()\n", + "\n", + "model = ChatOpenAI(model=\"gpt-4o\")" + ] + }, + { + "cell_type": "code", + "execution_count": 49, + "id": "2e05096b", + "metadata": {}, + "outputs": [], + "source": [ + "from pydantic import BaseModel, Field\n", + "from typing import List, Optional\n", + "from datetime import date\n", + "#from sssom_pydantic import Mapping\n", + "\n", + "# Assuming PredicateModifierEnum, EntityTypeEnum, MappingCardinalityEnum are defined elsewhere\n", + "\n", + "class Mapping(BaseModel):\n", + " \"\"\"\n", + " Represents an individual mapping between a pair of entities.\n", + " \"\"\"\n", + " subject_id: str = Field(..., description=\"The ID of the subject of the mapping.\")\n", + " subject_label: Optional[str] = Field(None, description=\"The label of subject of the mapping.\")\n", + " subject_category: Optional[str] = Field(None, description=\"The conceptual category to which the subject belongs to. This can be a string denoting the category or a term from a controlled vocabulary. This slot is deliberately underspecified. Conceptual categories can range from those that are found in general upper ontologies such as BFO (e.g. process, temporal region, etc) to those that serve as upper ontologies in specific domains, such as COB or BioLink (e.g. gene, disease, chemical entity). The purpose of this optional field is documentation for human reviewers - when a category is known and documented clearly, the cost of interpreting and evaluating the mapping decreases.\")\n", + " predicate_id: str = Field(..., description=\"The ID of the predicate or relation that relates the subject and object of this match.\")\n", + " predicate_label: Optional[str] = Field(None, description=\"The label of the predicate/relation of the mapping.\")\n", + " predicate_modifier: Optional[str] = Field(None, description=\"A modifier for negating the predicate. See https://github.com/mapping-commons/sssom/issues/40 for discussion.\")\n", + " object_id: str = Field(..., description=\"The ID of the object of the mapping.\")\n", + " object_label: Optional[str] = Field(None, description=\"The label of object of the mapping.\")\n", + " object_category: Optional[str] = Field(None, description=\"The conceptual category to which the subject belongs to. This can be a string denoting the category or a term from a controlled vocabulary. This slot is deliberately underspecified. Conceptual categories can range from those that are found in general upper ontologies such as BFO (e.g. process, temporal region, etc) to those that serve as upper ontologies in specific domains, such as COB or BioLink (e.g. gene, disease, chemical entity). The purpose of this optional field is documentation for human reviewers - when a category is known and documented clearly, the cost of interpreting and evaluating the mapping decreases.\")\n", + " mapping_justification: str = Field(..., description=\"A mapping justification is an action (or the written representation of that action) of showing a mapping to be right or reasonable.\")\n", + " author_id: Optional[List[str]] = Field(default_factory=list, description=\"Identifies the persons or groups responsible for asserting the mappings. Recommended to be a list of ORCIDs or otherwise identifying URIs.\")\n", + " author_label: Optional[List[str]] = Field(default_factory=list, description=\"A string identifying the author of this mapping. In the spirit of provenance, consider using author_id instead.\")\n", + " reviewer_id: Optional[List[str]] = Field(default_factory=list, description=\"Identifies the persons or groups that reviewed and confirmed the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.\")\n", + " reviewer_label: Optional[List[str]] = Field(default_factory=list, description=\"A string identifying the reviewer of this mapping. In the spirit of provenance, consider using reviewer_id instead.\")\n", + " creator_id: Optional[List[str]] = Field(default_factory=list, description=\"Identifies the persons or groups responsible for the creation of the mapping. The creator is the agent that put the mapping in its published form, which may be different from the author, which is a person that was actively involved in the assertion of the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.\")\n", + " creator_label: Optional[List[str]] = Field(default_factory=list, description=\"A string identifying the creator of this mapping. In the spirit of provenance, consider using creator_id instead.\")\n", + " license: Optional[str] = Field(None, description=\"A url to the license of the mapping. In absence of a license we assume no license.\")\n", + " subject_type: Optional[str] = Field(None, description=\"The type of entity that is being mapped.\")\n", + " subject_source: Optional[str] = Field(None, description=\"URI of vocabulary or identifier source for the subject.\")\n", + " subject_source_version: Optional[str] = Field(None, description=\"Version IRI or version string of the source of the subject term.\")\n", + " object_type: Optional[str] = Field(None, description=\"The type of entity that is being mapped.\")\n", + " object_source: Optional[str] = Field(None, description=\"URI of vocabulary or identifier source for the object.\")\n", + " object_source_version: Optional[str] = Field(None, description=\"Version IRI or version string of the source of the object term.\")\n", + " mapping_provider: Optional[str] = Field(None, description=\"URL pointing to the source that provided the mapping, for example an ontology that already contains the mappings, or a database from which it was derived.\")\n", + " mapping_source: Optional[str] = Field(None, description=\"The mapping set this mapping was originally defined in. mapping_source is used for example when merging multiple mapping sets or deriving one mapping set from another.\")\n", + " mapping_cardinality: Optional[str] = Field(None, description=\"A string indicating whether this mapping is from a 1:1 (the subject_id maps to a single object_id), 1:n (the subject maps to more than one object_id), n:1, 1:0, 0:1 or n:n group. Note that this is a convenience field that should be derivable from the mapping set.\")\n", + " mapping_tool: Optional[str] = Field(None, description=\"A reference to the tool or algorithm that was used to generate the mapping. Should be a URL pointing to more info about it, but can be free text.\")\n", + " mapping_tool_version: Optional[str] = Field(None, description=\"Version string that denotes the version of the mapping tool used.\")\n", + " mapping_date: Optional[date] = Field(None, description=\"The date the mapping was asserted. This is different from the date the mapping was published or compiled in a SSSOM file.\")\n", + " publication_date: Optional[date] = Field(None, description=\"The date the mapping was published. This is different from the date the mapping was asserted.\")\n", + " confidence: Optional[float] = Field(None, description=\"A score between 0 and 1 to denote the confidence or probability that the match is correct, where 1 denotes total confidence.\")\n", + " curation_rule: Optional[List[str]] = Field(default_factory=list, description=\"A curation rule is a (potentially) complex condition executed by an agent that led to the establishment of a mapping. Curation rules often involve complex domain-specific considerations, which are hard to capture in an automated fashion. The curation rule is captured as a resource rather than a string, which enables higher levels of transparency and sharing across mapping sets. The URI representation of the curation rule is expected to be a resolvable identifier which provides details about the nature of the curation rule.\")\n", + " curation_rule_text: Optional[List[str]] = Field(default_factory=list, description=\"A curation rule is a (potentially) complex condition executed by an agent that led to the establishment of a mapping. Curation rules often involve complex domain-specific considerations, which are hard to capture in an automated fashion. The curation rule should be captured as a resource (entity reference) rather than a string (see curation_rule element), which enables higher levels of transparency and sharing across mapping sets. The textual representation of curation rule is intended to be used in cases where (1) the creation of a resource is not practical from the perspective of the mapping_provider and (2) as an additional piece of metadata to augment the curation_rule element with a human readable text.\")\n", + " subject_match_field: Optional[List[str]] = Field(default_factory=list, description=\"A list of properties (term annotations on the subject) that was used for the match.\")\n", + " object_match_field: Optional[List[str]] = Field(default_factory=list, description=\"A list of properties (term annotations on the object) that was used for the match.\")\n", + " match_string: Optional[List[str]] = Field(default_factory=list, description=\"String that is shared by subj/obj. It is recommended to indicate the fields for the match using the object and subject_match_field slots.\")\n", + " subject_preprocessing: Optional[List[str]] = Field(default_factory=list, description=\"Method of preprocessing applied to the fields of the subject. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.\")\n", + " object_preprocessing: Optional[List[str]] = Field(default_factory=list, description=\"Method of preprocessing applied to the fields of the object. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.\")\n", + " semantic_similarity_score: Optional[float] = Field(None, description=\"A score between 0 and 1 to denote the semantic similarity, where 1 denotes equivalence.\")\n", + " semantic_similarity_measure: Optional[str] = Field(None, description=\"The measure used for computing the the semantic similarity score. To make processing this field as unambiguous as possible, we recommend using wikidata identifiers, but wikipedia pages could also be acceptable.\")\n", + " see_also: Optional[List[str]] = Field(default_factory=list, description=\"\"\"A URL specific for the mapping instance. E.g. for kboom we have a per-mapping image that shows surrounding axioms that drive probability. Could also be a github issue URL that discussed a complicated alignment\"\"\")\n", + " issue_tracker_item: Optional[str] = Field(None, description=\"\"\"The issue tracker item discussing this mapping.\"\"\")\n", + " other: Optional[str] = Field(None, description=\"\"\"Pipe separated list of key value pairs for properties not part of the SSSOM spec. Can be used to encode additional provenance data.\"\"\")\n", + " comment: Optional[str] = Field(None, description=\"\"\"Free text field containing either curator notes or text generated by tool providing additional informative information.\"\"\")\n", + "\n", + "class MappingList(BaseModel):\n", + " mappings: List[Mapping]" + ] + }, + { + "cell_type": "code", + "execution_count": 52, + "id": "96e03fde", + "metadata": {}, + "outputs": [], + "source": [ + "from langchain_core.output_parsers import JsonOutputParser\n", + "from langchain_core.prompts import PromptTemplate\n", + "\n", + "output_parser = JsonOutputParser(pydantic_object=MappingList)\n", + "\n", + "prompt = PromptTemplate(\n", + " template=\"\"\"\n", + " You are a medical terminology specialist. \n", + " \n", + " Your task is to find an appropriate match for the disease \"{disease}\" \n", + " in the Mondo Ontology from a set of candidate mappings.\n", + " \n", + " {disease} has has the following definition in the source ontology: {definition}.\n", + " \n", + " You will evaluate set of candidate mappings in SSSOM format. If you believe a mapping is wrong,\n", + " set the predicate_modifier to \"not\" and provide a comment explaining why you believe the mapping is incorrect.\n", + " \n", + " Do not duplicate rows, the number of reviewed mappings should be equal to the number of candidate mappings.\n", + " \n", + " Candidate mappings:\n", + " {mappings}\n", + " \n", + " {format_instructions}\n", + " \"\"\",\n", + " input_variables=[\"disease\", \"definition\", \"mappings\"],\n", + " partial_variables={\"format_instructions\": output_parser.get_format_instructions()},\n", + ")\n", + "\n", + "chain = prompt | model | output_parser" + ] + }, + { + "cell_type": "code", + "execution_count": 53, + "id": "85ea1d47", + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
subject_idsubject_labelpredicate_idpredicate_modifierobject_idobject_labelmapping_justificationmapping_toolconfidencesubject_match_fieldobject_match_fieldmatch_stringcomment
0MONDO:0016733gangliogliomaskos:closeMatchnotNCIT:C27362Childhood Gangliogliomasemapv:LexicalMatchingoaklib0.500000oio:hasNarrowSynonymrdfs:labelchildhood gangliogliomaThe term 'ganglioglioma' is a broader category that includes both childhood and adult cases, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is not appropriate to consider them as close matches.
1MONDO:0016733gangliogliomaskos:exactMatchnotNCIT:C27362Childhood Gangliogliomasemapv:MappingChainingNaN0.475000NaNNaNNaNThe term 'ganglioglioma' encompasses both childhood and adult forms of the disease, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is incorrect to consider them as exact matches.
2MONDO:0022096pyogenic granulomaskos:closeMatchnotNCIT:C3480Lobular Capillary Hemangiomasemapv:LexicalMatchingoaklib0.500000[oio:hasRelatedSynonym][rdfs:label]lobular capillary hemangiomaPyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true.
3MONDO:0022096pyogenic granulomaskos:closeMatchnotNCIT:C3480Lobular Capillary Hemangiomasemapv:LexicalMatchingoaklib0.500000[oio:hasRelatedSynonym][rdfs:label]lobular capillary hemangiomaPyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true.
4MONDO:0006292malignant mesotheliomaskos:closeMatchNaNNCIT:C8420Diffuse Malignant Mesotheliomasemapv:LexicalMatchingoaklib0.500000oio:hasNarrowSynonymrdfs:labeldiffuse malignant mesotheliomaNone
5MONDO:0006292malignant mesotheliomaskos:exactMatchnotNCIT:C8420Diffuse Malignant Mesotheliomasemapv:MappingChainingNone0.475000NoneNoneNoneThe term 'malignant mesothelioma' is broader and not an exact match for 'Diffuse Malignant Mesothelioma'.
6MONDO:0007959medulloblastomaskos:closeMatchnotNCIT:C27294Localized Primitive Neuroectodermal Tumorsemapv:LexicalMatchingoaklib0.500000[oio:hasRelatedSynonym][rdfs:label]localized primitive neuroectodermal tumorMedulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor.
7MONDO:0007959medulloblastomaskos:exactMatchnotNCIT:C27294Localized Primitive Neuroectodermal Tumorsemapv:MappingChainingNaN0.475000NaNNaNNaNMedulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor.
8MONDO:0006292malignant mesotheliomaskos:closeMatchnotNCIT:C27926Asbestos-Related Malignant Mesotheliomasemapv:LexicalMatchingoaklib0.500000[oio:hasNarrowSynonym][rdfs:label][asbestos-related malignant mesothelioma]Malignant mesothelioma is a broader category that includes asbestos-related malignant mesothelioma as a subset. Therefore, this should not be a 'closeMatch'.
9MONDO:0006292malignant mesotheliomaskos:exactMatchnotNCIT:C27926Asbestos-Related Malignant Mesotheliomasemapv:MappingChainingNaN0.475000NaNNaNNaNMalignant mesothelioma is a more general term than asbestos-related malignant mesothelioma. Therefore, they are not exact matches.
10MONDO:0006312myofibromaskos:closeMatchnotNCIT:C27498Infantile Hemangiopericytomasemapv:LexicalMatchingoaklib0.500000[oio:hasRelatedSynonym][rdfs:label][infantile hemangiopericytoma]Myofibroma and Infantile Hemangiopericytoma are distinct entities. Myofibroma is a benign neoplasm of myofibroblasts, whereas Infantile Hemangiopericytoma is a vascular tumor. The lexical match is misleading.
11MONDO:0016824infantile myofibromatosisskos:exactMatchNaNNCIT:C27498Infantile Hemangiopericytomasemapv:LexicalMatchingoaklib0.800000[oio:hasExactSynonym][rdfs:label][infantile hemangiopericytoma]Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease.
12MONDO:0004520intratubular embryonal carcinomaskos:exactMatchNaNNCIT:C192096Intratubular Embryonal Carcinomasemapv:LexicalMatchingoaklib0.800000[oio:hasExactSynonym][rdfs:label][intratubular embryonal carcinoma]None
13MONDO:0004520intratubular embryonal carcinomaskos:exactMatchNaNNCIT:C192096Intratubular Embryonal Carcinomasemapv:LexicalMatchingoaklib0.849779[rdfs:label][rdfs:label][intratubular embryonal carcinoma]None
14MONDO:0018177glioblastomaskos:exactMatchnotNCIT:C39750Glioblastoma, IDH-Wildtypesemapv:MappingChainingNaN0.475000NaNNaNNaNThe subject label 'glioblastoma' is too general to be an exact match for 'Glioblastoma, IDH-Wildtype', as the latter specifies a particular genetic subtype.
15MONDO:0850335IDH-wildtype glioblastomaskos:exactMatchNoneNCIT:C39750Glioblastoma, IDH-Wildtypesemapv:MappingChainingNaN0.475000NaNNaNNaNThis mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'.
16MONDO:0003766thalamic cancerskos:closeMatchnotNCIT:C6221Thalamic Neoplasmsemapv:LexicalMatchingoaklib0.500000[oio:hasRelatedSynonym][rdfs:label]thalamic neoplasmThalamic cancer and thalamic neoplasm are not exact matches; cancer is a type of neoplasm, but a neoplasm does not necessarily imply malignancy.
17MONDO:0003766thalamic cancerskos:exactMatchnotNCIT:C6221Thalamic Neoplasmsemapv:MappingChainingNone0.475000NoneNoneNoneThalamic cancer is a specific type of thalamic neoplasm. An exact match is not appropriate due to the broader scope of 'neoplasm' compared to 'cancer'.
18MONDO:0016733gangliogliomaskos:closeMatchnotNCIT:C27363Adult Gangliogliomasemapv:LexicalMatchingoaklib0.500000oio:hasNarrowSynonymrdfs:labeladult gangliogliomaGanglioglioma is a broad category, whereas Adult Ganglioglioma specifically refers to a subset of gangliogliomas occurring in adults. A close match is not appropriate; it should be a narrower match.
19MONDO:0016733gangliogliomaskos:exactMatchnotNCIT:C27363Adult Gangliogliomasemapv:MappingChainingNaN0.475000NaNNaNNaNGanglioglioma is a general term that includes various subtypes, including those in adults and children. An exact match is not appropriate because Adult Ganglioglioma is a more specific condition.
20MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
21MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
22MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
23MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
24MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
25MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
26MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
27MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
28MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
29MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
30MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][oio:hasDbXref-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
31MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
32MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
33MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
34MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
35MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
36MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
37MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
38MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
39MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapv:LexicalMatchingoaklib0.500000[rdf:ID][skos:relatedMatch-INVERSE][mondo:0000503]Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma.
40MONDO:0000503lung adenocarcinoma in situskos:closeMatchnotNCIT:C8748Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7semapNaNNaNNaNNaNNaNNaN
41MONDO:0015686primary peritoneal carcinomaskos:exactMatchnotNCIT:C4182Serous Surface Papillary Carcinomasemapv:LexicalMatchingoaklib0.800000oio:hasExactSynonymrdfs:labelserous surface papillary carcinomaThe term 'primary peritoneal carcinoma' is broader than 'Serous Surface Papillary Carcinoma' and not specific enough to consider an exact match.
42MONDO:0002368papillary serous cystadenocarcinomaskos:exactMatchNaNNCIT:C4182Serous Surface Papillary Carcinomasemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
43MONDO:0006055sex cord-stromal tumorskos:closeMatchnotNCIT:C39948Malignant Testicular Sex Cord-Stromal Tumorsemapv:LexicalMatchingoaklib0.500000[oio:hasNarrowSynonym][rdfs:label]malignant testicular sex cord-stromal tumorThe subject 'sex cord-stromal tumor' is a broader term and does not specifically refer to 'malignant testicular sex cord-stromal tumor'.
44MONDO:0003125testicular sex cord-stromal neoplasmskos:exactMatchNaNNCIT:C39948Malignant Testicular Sex Cord-Stromal Tumorsemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
45MONDO:0016642meningiomaskos:closeMatchnotNCIT:C7048Supratentorial Meningiomasemapv:LexicalMatchingoaklib0.500000oio:hasRelatedSynonymrdfs:labelsupratentorial meningiomaThe subject label 'meningioma' is too broad compared to the specific term 'Supratentorial Meningioma'. Hence, this is not a close match.
46MONDO:0850303supratentorial meningiomaskos:exactMatchNaNNCIT:C7048Supratentorial Meningiomasemapv:LexicalMatchingoaklib0.849779rdfs:labelrdfs:labelsupratentorial meningiomaNone
47MONDO:0011655alveolar soft part sarcomaskos:closeMatchNoneNCIT:C8092Childhood Alveolar Soft Part Sarcomasemapv:LexicalMatchingoaklib0.500000[oio:hasNarrowSynonym][rdfs:label][childhood alveolar soft part sarcoma]None
48MONDO:0011655alveolar soft part sarcomaskos:exactMatchnotNCIT:C8092Childhood Alveolar Soft Part Sarcomasemapv:MappingChainingNone0.475000NoneNoneNoneGenerated by matching the object of a Mondo mapping to the object of a source mapping. Alveolar soft part sarcoma is a broader term and not an exact match for Childhood Alveolar Soft Part Sarcoma.
\n", + "
" + ], + "text/plain": [ + " subject_id subject_label predicate_id \\\n", + "0 MONDO:0016733 ganglioglioma skos:closeMatch \n", + "1 MONDO:0016733 ganglioglioma skos:exactMatch \n", + "2 MONDO:0022096 pyogenic granuloma skos:closeMatch \n", + "3 MONDO:0022096 pyogenic granuloma skos:closeMatch \n", + "4 MONDO:0006292 malignant mesothelioma skos:closeMatch \n", + "5 MONDO:0006292 malignant mesothelioma skos:exactMatch \n", + "6 MONDO:0007959 medulloblastoma skos:closeMatch \n", + "7 MONDO:0007959 medulloblastoma skos:exactMatch \n", + "8 MONDO:0006292 malignant mesothelioma skos:closeMatch \n", + "9 MONDO:0006292 malignant mesothelioma skos:exactMatch \n", + "10 MONDO:0006312 myofibroma skos:closeMatch \n", + "11 MONDO:0016824 infantile myofibromatosis skos:exactMatch \n", + "12 MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch \n", + "13 MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch \n", + "14 MONDO:0018177 glioblastoma skos:exactMatch \n", + "15 MONDO:0850335 IDH-wildtype glioblastoma skos:exactMatch \n", + "16 MONDO:0003766 thalamic cancer skos:closeMatch \n", + "17 MONDO:0003766 thalamic cancer skos:exactMatch \n", + "18 MONDO:0016733 ganglioglioma skos:closeMatch \n", + "19 MONDO:0016733 ganglioglioma skos:exactMatch \n", + "20 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "21 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "22 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "23 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "24 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "25 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "26 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "27 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "28 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "29 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "30 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "31 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "32 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "33 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "34 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "35 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "36 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "37 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "38 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "39 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "40 MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch \n", + "41 MONDO:0015686 primary peritoneal carcinoma skos:exactMatch \n", + "42 MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch \n", + "43 MONDO:0006055 sex cord-stromal tumor skos:closeMatch \n", + "44 MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch \n", + "45 MONDO:0016642 meningioma skos:closeMatch \n", + "46 MONDO:0850303 supratentorial meningioma skos:exactMatch \n", + "47 MONDO:0011655 alveolar soft part sarcoma skos:closeMatch \n", + "48 MONDO:0011655 alveolar soft part sarcoma skos:exactMatch \n", + "\n", + " predicate_modifier object_id \\\n", + "0 not NCIT:C27362 \n", + "1 not NCIT:C27362 \n", + "2 not NCIT:C3480 \n", + "3 not NCIT:C3480 \n", + "4 NaN NCIT:C8420 \n", + "5 not NCIT:C8420 \n", + "6 not NCIT:C27294 \n", + "7 not NCIT:C27294 \n", + "8 not NCIT:C27926 \n", + "9 not NCIT:C27926 \n", + "10 not NCIT:C27498 \n", + "11 NaN NCIT:C27498 \n", + "12 NaN NCIT:C192096 \n", + "13 NaN NCIT:C192096 \n", + "14 not NCIT:C39750 \n", + "15 None NCIT:C39750 \n", + "16 not NCIT:C6221 \n", + "17 not NCIT:C6221 \n", + "18 not NCIT:C27363 \n", + "19 not NCIT:C27363 \n", + "20 not NCIT:C8748 \n", + "21 not NCIT:C8748 \n", + "22 not NCIT:C8748 \n", + "23 not NCIT:C8748 \n", + "24 not NCIT:C8748 \n", + "25 not NCIT:C8748 \n", + "26 not NCIT:C8748 \n", + "27 not NCIT:C8748 \n", + "28 not NCIT:C8748 \n", + "29 not NCIT:C8748 \n", + "30 not NCIT:C8748 \n", + "31 not NCIT:C8748 \n", + "32 not NCIT:C8748 \n", + "33 not NCIT:C8748 \n", + "34 not NCIT:C8748 \n", + "35 not NCIT:C8748 \n", + "36 not NCIT:C8748 \n", + "37 not NCIT:C8748 \n", + "38 not NCIT:C8748 \n", + "39 not NCIT:C8748 \n", + "40 not NCIT:C8748 \n", + "41 not NCIT:C4182 \n", + "42 NaN NCIT:C4182 \n", + "43 not NCIT:C39948 \n", + "44 NaN NCIT:C39948 \n", + "45 not NCIT:C7048 \n", + "46 NaN NCIT:C7048 \n", + "47 None NCIT:C8092 \n", + "48 not NCIT:C8092 \n", + "\n", + " object_label \\\n", + "0 Childhood Ganglioglioma \n", + "1 Childhood Ganglioglioma \n", + "2 Lobular Capillary Hemangioma \n", + "3 Lobular Capillary Hemangioma \n", + "4 Diffuse Malignant Mesothelioma \n", + "5 Diffuse Malignant Mesothelioma \n", + "6 Localized Primitive Neuroectodermal Tumor \n", + "7 Localized Primitive Neuroectodermal Tumor \n", + "8 Asbestos-Related Malignant Mesothelioma \n", + "9 Asbestos-Related Malignant Mesothelioma \n", + "10 Infantile Hemangiopericytoma \n", + "11 Infantile Hemangiopericytoma \n", + "12 Intratubular Embryonal Carcinoma \n", + "13 Intratubular Embryonal Carcinoma \n", + "14 Glioblastoma, IDH-Wildtype \n", + "15 Glioblastoma, IDH-Wildtype \n", + "16 Thalamic Neoplasm \n", + "17 Thalamic Neoplasm \n", + "18 Adult Ganglioglioma \n", + "19 Adult Ganglioglioma \n", + "20 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "21 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "22 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "23 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "24 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "25 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "26 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "27 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "28 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "29 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "30 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "31 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "32 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "33 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "34 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "35 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "36 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "37 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "38 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "39 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "40 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 \n", + "41 Serous Surface Papillary Carcinoma \n", + "42 Serous Surface Papillary Carcinoma \n", + "43 Malignant Testicular Sex Cord-Stromal Tumor \n", + "44 Malignant Testicular Sex Cord-Stromal Tumor \n", + "45 Supratentorial Meningioma \n", + "46 Supratentorial Meningioma \n", + "47 Childhood Alveolar Soft Part Sarcoma \n", + "48 Childhood Alveolar Soft Part Sarcoma \n", + "\n", + " mapping_justification mapping_tool confidence subject_match_field \\\n", + "0 semapv:LexicalMatching oaklib 0.500000 oio:hasNarrowSynonym \n", + "1 semapv:MappingChaining NaN 0.475000 NaN \n", + "2 semapv:LexicalMatching oaklib 0.500000 [oio:hasRelatedSynonym] \n", + "3 semapv:LexicalMatching oaklib 0.500000 [oio:hasRelatedSynonym] \n", + "4 semapv:LexicalMatching oaklib 0.500000 oio:hasNarrowSynonym \n", + "5 semapv:MappingChaining None 0.475000 None \n", + "6 semapv:LexicalMatching oaklib 0.500000 [oio:hasRelatedSynonym] \n", + "7 semapv:MappingChaining NaN 0.475000 NaN \n", + "8 semapv:LexicalMatching oaklib 0.500000 [oio:hasNarrowSynonym] \n", + "9 semapv:MappingChaining NaN 0.475000 NaN \n", + "10 semapv:LexicalMatching oaklib 0.500000 [oio:hasRelatedSynonym] \n", + "11 semapv:LexicalMatching oaklib 0.800000 [oio:hasExactSynonym] \n", + "12 semapv:LexicalMatching oaklib 0.800000 [oio:hasExactSynonym] \n", + "13 semapv:LexicalMatching oaklib 0.849779 [rdfs:label] \n", + "14 semapv:MappingChaining NaN 0.475000 NaN \n", + "15 semapv:MappingChaining NaN 0.475000 NaN \n", + "16 semapv:LexicalMatching oaklib 0.500000 [oio:hasRelatedSynonym] \n", + "17 semapv:MappingChaining None 0.475000 None \n", + "18 semapv:LexicalMatching oaklib 0.500000 oio:hasNarrowSynonym \n", + "19 semapv:MappingChaining NaN 0.475000 NaN \n", + "20 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "21 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "22 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "23 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "24 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "25 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "26 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "27 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "28 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "29 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "30 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "31 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "32 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "33 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "34 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "35 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "36 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "37 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "38 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "39 semapv:LexicalMatching oaklib 0.500000 [rdf:ID] \n", + "40 semap NaN NaN NaN \n", + "41 semapv:LexicalMatching oaklib 0.800000 oio:hasExactSynonym \n", + "42 semapv:MappingChaining NaN 0.475000 NaN \n", + "43 semapv:LexicalMatching oaklib 0.500000 [oio:hasNarrowSynonym] \n", + "44 semapv:MappingChaining NaN 0.475000 NaN \n", + "45 semapv:LexicalMatching oaklib 0.500000 oio:hasRelatedSynonym \n", + "46 semapv:LexicalMatching oaklib 0.849779 rdfs:label \n", + "47 semapv:LexicalMatching oaklib 0.500000 [oio:hasNarrowSynonym] \n", + "48 semapv:MappingChaining None 0.475000 None \n", + "\n", + " object_match_field match_string \\\n", + "0 rdfs:label childhood ganglioglioma \n", + "1 NaN NaN \n", + "2 [rdfs:label] lobular capillary hemangioma \n", + "3 [rdfs:label] lobular capillary hemangioma \n", + "4 rdfs:label diffuse malignant mesothelioma \n", + "5 None None \n", + "6 [rdfs:label] localized primitive neuroectodermal tumor \n", + "7 NaN NaN \n", + "8 [rdfs:label] [asbestos-related malignant mesothelioma] \n", + "9 NaN NaN \n", + "10 [rdfs:label] [infantile hemangiopericytoma] \n", + "11 [rdfs:label] [infantile hemangiopericytoma] \n", + "12 [rdfs:label] [intratubular embryonal carcinoma] \n", + "13 [rdfs:label] [intratubular embryonal carcinoma] \n", + "14 NaN NaN \n", + "15 NaN NaN \n", + "16 [rdfs:label] thalamic neoplasm \n", + "17 None None \n", + "18 rdfs:label adult ganglioglioma \n", + "19 NaN NaN \n", + "20 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "21 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "22 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "23 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "24 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "25 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "26 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "27 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "28 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "29 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "30 [oio:hasDbXref-INVERSE] [mondo:0000503] \n", + "31 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "32 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "33 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "34 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "35 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "36 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "37 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "38 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "39 [skos:relatedMatch-INVERSE] [mondo:0000503] \n", + "40 NaN NaN \n", + "41 rdfs:label serous surface papillary carcinoma \n", + "42 NaN NaN \n", + "43 [rdfs:label] malignant testicular sex cord-stromal tumor \n", + "44 NaN NaN \n", + "45 rdfs:label supratentorial meningioma \n", + "46 rdfs:label supratentorial meningioma \n", + "47 [rdfs:label] [childhood alveolar soft part sarcoma] \n", + "48 None None \n", + "\n", + " comment \n", + "0 The term 'ganglioglioma' is a broader category that includes both childhood and adult cases, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is not appropriate to consider them as close matches. \n", + "1 The term 'ganglioglioma' encompasses both childhood and adult forms of the disease, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is incorrect to consider them as exact matches. \n", + "2 Pyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true. \n", + "3 Pyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true. \n", + "4 None \n", + "5 The term 'malignant mesothelioma' is broader and not an exact match for 'Diffuse Malignant Mesothelioma'. \n", + "6 Medulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor. \n", + "7 Medulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor. \n", + "8 Malignant mesothelioma is a broader category that includes asbestos-related malignant mesothelioma as a subset. Therefore, this should not be a 'closeMatch'. \n", + "9 Malignant mesothelioma is a more general term than asbestos-related malignant mesothelioma. Therefore, they are not exact matches. \n", + "10 Myofibroma and Infantile Hemangiopericytoma are distinct entities. Myofibroma is a benign neoplasm of myofibroblasts, whereas Infantile Hemangiopericytoma is a vascular tumor. The lexical match is misleading. \n", + "11 Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease. \n", + "12 None \n", + "13 None \n", + "14 The subject label 'glioblastoma' is too general to be an exact match for 'Glioblastoma, IDH-Wildtype', as the latter specifies a particular genetic subtype. \n", + "15 This mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'. \n", + "16 Thalamic cancer and thalamic neoplasm are not exact matches; cancer is a type of neoplasm, but a neoplasm does not necessarily imply malignancy. \n", + "17 Thalamic cancer is a specific type of thalamic neoplasm. An exact match is not appropriate due to the broader scope of 'neoplasm' compared to 'cancer'. \n", + "18 Ganglioglioma is a broad category, whereas Adult Ganglioglioma specifically refers to a subset of gangliogliomas occurring in adults. A close match is not appropriate; it should be a narrower match. \n", + "19 Ganglioglioma is a general term that includes various subtypes, including those in adults and children. An exact match is not appropriate because Adult Ganglioglioma is a more specific condition. \n", + "20 Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "21 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "22 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "23 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "24 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "25 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "26 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "27 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "28 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "29 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "30 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "31 Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "32 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "33 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "34 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "35 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "36 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "37 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "38 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "39 Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. \n", + "40 NaN \n", + "41 The term 'primary peritoneal carcinoma' is broader than 'Serous Surface Papillary Carcinoma' and not specific enough to consider an exact match. \n", + "42 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "43 The subject 'sex cord-stromal tumor' is a broader term and does not specifically refer to 'malignant testicular sex cord-stromal tumor'. \n", + "44 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "45 The subject label 'meningioma' is too broad compared to the specific term 'Supratentorial Meningioma'. Hence, this is not a close match. \n", + "46 None \n", + "47 None \n", + "48 Generated by matching the object of a Mondo mapping to the object of a source mapping. Alveolar soft part sarcoma is a broader term and not an exact match for Childhood Alveolar Soft Part Sarcoma. " + ] + }, + "execution_count": 53, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "def review_mappings(matches_index, chain, source, count):\n", + " reviewed_mappings = [] \n", + " for disease, matches in matches_index.items():\n", + " label = source.label(disease)\n", + " definition = source.definition(disease)\n", + " if len(matches)>1:\n", + " result = chain.invoke({\n", + " \"mappings\": matches.to_markdown(index=False),\n", + " \"disease\": label,\n", + " \"definition\": definition\n", + " })\n", + " reviewed_mappings.extend(result['mappings'])\n", + " count -= 1\n", + " if count <= 0:\n", + " break\n", + " df_reviewed_mappings = pd.DataFrame(reviewed_mappings)\n", + " return df_reviewed_mappings\n", + "\n", + "count = 15\n", + "df_reviewed_mappings = review_mappings(matches_index, chain, source, count)\n", + "df_reviewed_mappings.to_csv(\"reviewed_mappings.tsv\", sep=\"\\t\", index=False)\n", + "df_reviewed_mappings" + ] + }, + { + "cell_type": "code", + "execution_count": 57, + "id": "d238278c", + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
subject_idsubject_labelpredicate_idpredicate_modifierobject_idobject_labelmapping_justificationmapping_toolconfidencesubject_match_fieldobject_match_fieldmatch_stringcomment
11MONDO:0016824infantile myofibromatosisskos:exactMatchNaNNCIT:C27498Infantile Hemangiopericytomasemapv:LexicalMatchingoaklib0.800000[oio:hasExactSynonym][rdfs:label][infantile hemangiopericytoma]Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease.
12MONDO:0004520intratubular embryonal carcinomaskos:exactMatchNaNNCIT:C192096Intratubular Embryonal Carcinomasemapv:LexicalMatchingoaklib0.800000[oio:hasExactSynonym][rdfs:label][intratubular embryonal carcinoma]None
13MONDO:0004520intratubular embryonal carcinomaskos:exactMatchNaNNCIT:C192096Intratubular Embryonal Carcinomasemapv:LexicalMatchingoaklib0.849779[rdfs:label][rdfs:label][intratubular embryonal carcinoma]None
15MONDO:0850335IDH-wildtype glioblastomaskos:exactMatchNoneNCIT:C39750Glioblastoma, IDH-Wildtypesemapv:MappingChainingNaN0.475000NaNNaNNaNThis mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'.
42MONDO:0002368papillary serous cystadenocarcinomaskos:exactMatchNaNNCIT:C4182Serous Surface Papillary Carcinomasemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
44MONDO:0003125testicular sex cord-stromal neoplasmskos:exactMatchNaNNCIT:C39948Malignant Testicular Sex Cord-Stromal Tumorsemapv:MappingChainingNaN0.475000NaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
46MONDO:0850303supratentorial meningiomaskos:exactMatchNaNNCIT:C7048Supratentorial Meningiomasemapv:LexicalMatchingoaklib0.849779rdfs:labelrdfs:labelsupratentorial meningiomaNone
\n", + "
" + ], + "text/plain": [ + " subject_id subject_label predicate_id \\\n", + "11 MONDO:0016824 infantile myofibromatosis skos:exactMatch \n", + "12 MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch \n", + "13 MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch \n", + "15 MONDO:0850335 IDH-wildtype glioblastoma skos:exactMatch \n", + "42 MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch \n", + "44 MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch \n", + "46 MONDO:0850303 supratentorial meningioma skos:exactMatch \n", + "\n", + " predicate_modifier object_id \\\n", + "11 NaN NCIT:C27498 \n", + "12 NaN NCIT:C192096 \n", + "13 NaN NCIT:C192096 \n", + "15 None NCIT:C39750 \n", + "42 NaN NCIT:C4182 \n", + "44 NaN NCIT:C39948 \n", + "46 NaN NCIT:C7048 \n", + "\n", + " object_label mapping_justification \\\n", + "11 Infantile Hemangiopericytoma semapv:LexicalMatching \n", + "12 Intratubular Embryonal Carcinoma semapv:LexicalMatching \n", + "13 Intratubular Embryonal Carcinoma semapv:LexicalMatching \n", + "15 Glioblastoma, IDH-Wildtype semapv:MappingChaining \n", + "42 Serous Surface Papillary Carcinoma semapv:MappingChaining \n", + "44 Malignant Testicular Sex Cord-Stromal Tumor semapv:MappingChaining \n", + "46 Supratentorial Meningioma semapv:LexicalMatching \n", + "\n", + " mapping_tool confidence subject_match_field object_match_field \\\n", + "11 oaklib 0.800000 [oio:hasExactSynonym] [rdfs:label] \n", + "12 oaklib 0.800000 [oio:hasExactSynonym] [rdfs:label] \n", + "13 oaklib 0.849779 [rdfs:label] [rdfs:label] \n", + "15 NaN 0.475000 NaN NaN \n", + "42 NaN 0.475000 NaN NaN \n", + "44 NaN 0.475000 NaN NaN \n", + "46 oaklib 0.849779 rdfs:label rdfs:label \n", + "\n", + " match_string \\\n", + "11 [infantile hemangiopericytoma] \n", + "12 [intratubular embryonal carcinoma] \n", + "13 [intratubular embryonal carcinoma] \n", + "15 NaN \n", + "42 NaN \n", + "44 NaN \n", + "46 supratentorial meningioma \n", + "\n", + " comment \n", + "11 Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease. \n", + "12 None \n", + "13 None \n", + "15 This mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'. \n", + "42 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "44 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "46 None " + ] + }, + "execution_count": 57, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "df_reviewed_mappings_exact = df_reviewed_mappings[df_reviewed_mappings['predicate_id']==\"skos:exactMatch\"]\n", + "df_reviewed_mappings_exact_correct = df_reviewed_mappings_exact[df_reviewed_mappings_exact['predicate_modifier']!=\"not\"]\n", + "df_reviewed_mappings_exact_not = df_reviewed_mappings_exact[df_reviewed_mappings_exact['predicate_modifier']==\"not\"]\n", + "df_reviewed_mappings_exact_correct" + ] + }, + { + "cell_type": "code", + "execution_count": 62, + "id": "a3871250", + "metadata": {}, + "outputs": [ + { + "name": "stdout", + "output_type": "stream", + "text": [ + "MONDO:0001147 has multiple mappings: ['NCIT:C101209', 'NCIT:C105595']\n", + "MONDO:0001748 has multiple mappings: ['NCIT:C3540', 'NCIT:C9332']\n", + "MONDO:0002119 has multiple mappings: ['NCIT:C173820', 'NCIT:C8422']\n", + "MONDO:0002142 has multiple mappings: ['NCIT:C114541', 'NCIT:C4247']\n", + "MONDO:0002277 has multiple mappings: ['NCIT:C34398', 'NCIT:C34403']\n", + "MONDO:0002368 has multiple mappings: ['NCIT:C8377', 'NCIT:C4182']\n", + "MONDO:0003125 has multiple mappings: ['NCIT:C6358', 'NCIT:C39948']\n", + "MONDO:0003143 has multiple mappings: ['NCIT:C2874', 'NCIT:C4488']\n", + "MONDO:0003947 has multiple mappings: ['NCIT:C3990', 'NCIT:C84783']\n", + "MONDO:0004473 has multiple mappings: ['NCIT:C35697', 'NCIT:C4836']\n", + "MONDO:0004520 has multiple mappings: ['NCIT:C7325', 'NCIT:C192096', 'NCIT:C192096']\n", + "MONDO:0004795 has multiple mappings: ['NCIT:C3299', 'NCIT:C79601']\n", + "MONDO:0005244 has multiple mappings: ['NCIT:C119734', 'NCIT:C4731']\n", + "MONDO:0005272 has multiple mappings: ['NCIT:C2872', 'NCIT:C82591']\n", + "MONDO:0005283 has multiple mappings: ['NCIT:C26875', 'NCIT:C62601']\n", + "MONDO:0005311 has multiple mappings: ['NCIT:C35768', 'NCIT:C35771']\n", + "MONDO:0005380 has multiple mappings: ['NCIT:C34880', 'NCIT:C35476']\n", + "MONDO:0005446 has multiple mappings: ['NCIT:C34768', 'NCIT:C34770']\n", + "MONDO:0005672 has multiple mappings: ['NCIT:C34428', 'NCIT:C34429']\n", + "MONDO:0005988 has multiple mappings: ['NCIT:C34758', 'NCIT:C85194']\n", + "MONDO:0006490 has multiple mappings: ['NCIT:C180915', 'NCIT:C7736']\n", + "MONDO:0006969 has multiple mappings: ['NCIT:C115165', 'NCIT:C26882']\n", + "MONDO:0006982 has multiple mappings: ['NCIT:C35071', 'NCIT:C35828']\n", + "MONDO:0007308 has multiple mappings: ['NCIT:C134952', 'NCIT:C150609']\n", + "MONDO:0008855 has multiple mappings: ['NCIT:C176823', 'NCIT:C3895']\n", + "MONDO:0009025 has multiple mappings: ['NCIT:C123231', 'NCIT:C131083']\n", + "MONDO:0011655 has multiple mappings: ['NCIT:C3750', 'NCIT:C7943']\n", + "MONDO:0012105 has multiple mappings: ['NCIT:C123111', 'NCIT:C3444']\n", + "MONDO:0013171 has multiple mappings: ['NCIT:C176817', 'NCIT:C3963']\n", + "MONDO:0015540 has multiple mappings: ['NCIT:C34792', 'NCIT:C35439']\n", + "MONDO:0015912 has multiple mappings: ['NCIT:C131646', 'NCIT:C158788']\n", + "MONDO:0016824 has multiple mappings: ['NCIT:C3742', 'NCIT:C27498']\n", + "MONDO:0017278 has multiple mappings: ['NCIT:C129726', 'NCIT:C84576']\n", + "MONDO:0017991 has multiple mappings: ['NCIT:C34391', 'NCIT:C35062']\n", + "MONDO:0019118 has multiple mappings: ['NCIT:C35194', 'NCIT:C35625']\n", + "MONDO:0019234 has multiple mappings: ['NCIT:C146639', 'NCIT:C155747']\n", + "MONDO:0019384 has multiple mappings: ['NCIT:C26761', 'NCIT:C34576']\n", + "MONDO:0019991 has multiple mappings: ['NCIT:C158968', 'NCIT:C96182']\n", + "MONDO:0020804 has multiple mappings: ['NCIT:C156767', 'NCIT:C7586']\n", + "MONDO:0021632 has multiple mappings: ['NCIT:C170814', 'NCIT:C4952']\n", + "MONDO:0024477 has multiple mappings: ['NCIT:C7103', 'NCIT:C7106']\n", + "MONDO:0044792 has multiple mappings: ['NCIT:C3944', 'NCIT:C4234']\n", + "MONDO:0700092 has multiple mappings: ['NCIT:C1535926', 'NCIT:C89338']\n" + ] + }, + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
subject_idsubject_labelpredicate_idobject_idobject_labelmapping_justificationconfidencereview_idpredicate_modifiermapping_toolsubject_match_fieldobject_match_fieldmatch_stringcomment
2MONDO:0000001diseaseskos:exactMatchNCIT:C2991Disease or Disordersemapv:UnspecifiedMatching0.950000MONDO:MONDONaNNaNNaNNaNNaNNaN
9MONDO:0000004adrenocortical insufficiencyskos:exactMatchNCIT:C26691Adrenocortical Insufficiencysemapv:UnspecifiedMatching0.950000MONDO:MONDONaNNaNNaNNaNNaNNaN
22MONDO:0000022nocturnal enuresisskos:exactMatchNCIT:C118172Nocturnal Enuresissemapv:UnspecifiedMatching0.950000MONDO:MONDONaNNaNNaNNaNNaNNaN
61MONDO:0000087polymicrogyriaskos:exactMatchNCIT:C116936Polymicrogyriasemapv:UnspecifiedMatching0.950000MONDO:MONDONaNNaNNaNNaNNaNNaN
68MONDO:0000088precocious pubertyskos:exactMatchNCIT:C79704Precocious Pubertysemapv:UnspecifiedMatching0.950000MONDO:MONDONaNNaNNaNNaNNaNNaN
.............................................
13MONDO:0004520intratubular embryonal carcinomaskos:exactMatchNCIT:C192096Intratubular Embryonal Carcinomasemapv:LexicalMatching0.849779NaNNaNoaklib[rdfs:label][rdfs:label][intratubular embryonal carcinoma]None
15MONDO:0850335IDH-wildtype glioblastomaskos:exactMatchNCIT:C39750Glioblastoma, IDH-Wildtypesemapv:MappingChaining0.475000NaNNaNNaNNaNNaNNaNThis mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'.
42MONDO:0002368papillary serous cystadenocarcinomaskos:exactMatchNCIT:C4182Serous Surface Papillary Carcinomasemapv:MappingChaining0.475000NaNNaNNaNNaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
44MONDO:0003125testicular sex cord-stromal neoplasmskos:exactMatchNCIT:C39948Malignant Testicular Sex Cord-Stromal Tumorsemapv:MappingChaining0.475000NaNNaNNaNNaNNaNNaNGenerated by matching the object of a Mondo mapping to the object of a source mapping.
46MONDO:0850303supratentorial meningiomaskos:exactMatchNCIT:C7048Supratentorial Meningiomasemapv:LexicalMatching0.849779NaNNaNoaklibrdfs:labelrdfs:labelsupratentorial meningiomaNone
\n", + "

7182 rows × 14 columns

\n", + "
" + ], + "text/plain": [ + " subject_id subject_label predicate_id \\\n", + "2 MONDO:0000001 disease skos:exactMatch \n", + "9 MONDO:0000004 adrenocortical insufficiency skos:exactMatch \n", + "22 MONDO:0000022 nocturnal enuresis skos:exactMatch \n", + "61 MONDO:0000087 polymicrogyria skos:exactMatch \n", + "68 MONDO:0000088 precocious puberty skos:exactMatch \n", + ".. ... ... ... \n", + "13 MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch \n", + "15 MONDO:0850335 IDH-wildtype glioblastoma skos:exactMatch \n", + "42 MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch \n", + "44 MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch \n", + "46 MONDO:0850303 supratentorial meningioma skos:exactMatch \n", + "\n", + " object_id object_label \\\n", + "2 NCIT:C2991 Disease or Disorder \n", + "9 NCIT:C26691 Adrenocortical Insufficiency \n", + "22 NCIT:C118172 Nocturnal Enuresis \n", + "61 NCIT:C116936 Polymicrogyria \n", + "68 NCIT:C79704 Precocious Puberty \n", + ".. ... ... \n", + "13 NCIT:C192096 Intratubular Embryonal Carcinoma \n", + "15 NCIT:C39750 Glioblastoma, IDH-Wildtype \n", + "42 NCIT:C4182 Serous Surface Papillary Carcinoma \n", + "44 NCIT:C39948 Malignant Testicular Sex Cord-Stromal Tumor \n", + "46 NCIT:C7048 Supratentorial Meningioma \n", + "\n", + " mapping_justification confidence review_id predicate_modifier \\\n", + "2 semapv:UnspecifiedMatching 0.950000 MONDO:MONDO NaN \n", + "9 semapv:UnspecifiedMatching 0.950000 MONDO:MONDO NaN \n", + "22 semapv:UnspecifiedMatching 0.950000 MONDO:MONDO NaN \n", + "61 semapv:UnspecifiedMatching 0.950000 MONDO:MONDO NaN \n", + "68 semapv:UnspecifiedMatching 0.950000 MONDO:MONDO NaN \n", + ".. ... ... ... ... \n", + "13 semapv:LexicalMatching 0.849779 NaN NaN \n", + "15 semapv:MappingChaining 0.475000 NaN NaN \n", + "42 semapv:MappingChaining 0.475000 NaN NaN \n", + "44 semapv:MappingChaining 0.475000 NaN NaN \n", + "46 semapv:LexicalMatching 0.849779 NaN NaN \n", + "\n", + " mapping_tool subject_match_field object_match_field \\\n", + "2 NaN NaN NaN \n", + "9 NaN NaN NaN \n", + "22 NaN NaN NaN \n", + "61 NaN NaN NaN \n", + "68 NaN NaN NaN \n", + ".. ... ... ... \n", + "13 oaklib [rdfs:label] [rdfs:label] \n", + "15 NaN NaN NaN \n", + "42 NaN NaN NaN \n", + "44 NaN NaN NaN \n", + "46 oaklib rdfs:label rdfs:label \n", + "\n", + " match_string \\\n", + "2 NaN \n", + "9 NaN \n", + "22 NaN \n", + "61 NaN \n", + "68 NaN \n", + ".. ... \n", + "13 [intratubular embryonal carcinoma] \n", + "15 NaN \n", + "42 NaN \n", + "44 NaN \n", + "46 supratentorial meningioma \n", + "\n", + " comment \n", + "2 NaN \n", + "9 NaN \n", + "22 NaN \n", + "61 NaN \n", + "68 NaN \n", + ".. ... \n", + "13 None \n", + "15 This mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'. \n", + "42 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "44 Generated by matching the object of a Mondo mapping to the object of a source mapping. \n", + "46 None \n", + "\n", + "[7182 rows x 14 columns]" + ] + }, + "execution_count": 62, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "df_mondo_mappings_exact_source = df_mondo_mappings_exact[df_mondo_mappings_exact['object_id'].str.startswith(source_id_space)]\n", + "df_mondo_mappings_exact_source['review_id']=\"MONDO:MONDO\"\n", + "\n", + "df_mondo_mappings_exact_source_with_matches = pd.concat(\n", + " [df_mondo_mappings_exact_source,\n", + " df_reviewed_mappings_exact_correct]\n", + ")\n", + "\n", + "for mondo_id in df_mondo_mappings_exact_source_with_matches['subject_id'].unique():\n", + " all_mappings = df_mondo_mappings_exact_source_with_matches[df_mondo_mappings_exact_source_with_matches['subject_id']==mondo_id]\n", + " if len(all_mappings) > 1:\n", + " print(f\"{mondo_id} has multiple mappings: {all_mappings['object_id'].tolist()}\")\n", + "\n", + "df_mondo_mappings_exact_source_with_matches.to_csv(\"mondo_mappings_exact_source_with_matches.tsv\", sep=\"\\t\", index=False)\n", + "df_mondo_mappings_exact_source_with_matches" + ] + } + ], + "metadata": { + "kernelspec": { + "display_name": "Python 3 (ipykernel)", + "language": "python", + "name": "python3" + }, + "language_info": { + "codemirror_mode": { + "name": "ipython", + "version": 3 + }, + "file_extension": ".py", + "mimetype": "text/x-python", + "name": "python", + "nbconvert_exporter": "python", + "pygments_lexer": "ipython3", + "version": "3.11.7" + } + }, + "nbformat": 4, + "nbformat_minor": 5 +} diff --git a/src/scripts/notebooks/mondo_mappings_exact_source_with_matches.tsv b/src/scripts/notebooks/mondo_mappings_exact_source_with_matches.tsv new file mode 100644 index 0000000000..13273fe90e --- /dev/null +++ b/src/scripts/notebooks/mondo_mappings_exact_source_with_matches.tsv @@ -0,0 +1,7183 @@ +subject_id subject_label predicate_id object_id object_label mapping_justification confidence review_id predicate_modifier mapping_tool subject_match_field object_match_field match_string comment +MONDO:0000001 disease skos:exactMatch NCIT:C2991 Disease or Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000004 adrenocortical insufficiency skos:exactMatch NCIT:C26691 Adrenocortical Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000022 nocturnal enuresis skos:exactMatch NCIT:C118172 Nocturnal Enuresis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000087 polymicrogyria skos:exactMatch NCIT:C116936 Polymicrogyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000088 precocious puberty skos:exactMatch NCIT:C79704 Precocious Puberty semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000115 Chiari malformation skos:exactMatch NCIT:C84570 Arnold-Chiari Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000128 giant axonal neuropathy skos:exactMatch NCIT:C84728 Giant Axonal Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000141 mosaic variegated aneuploidy syndrome skos:exactMatch NCIT:C128192 Mosaic Variegated Aneuploidy Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000147 polyposis skos:exactMatch NCIT:C4089 Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000153 transposition of the great arteries skos:exactMatch NCIT:C84742 Transposition of Great Vessels semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000159 bone marrow failure syndrome skos:exactMatch NCIT:C165614 Bone Marrow Failure Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000171 muscular dystrophy-dystroglycanopathy, type A skos:exactMatch NCIT:C99109 Walker-Warburg Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000179 Neu-Laxova syndrome skos:exactMatch NCIT:C14089 Nuclear Localization Signal semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000190 ventricular fibrillation skos:exactMatch NCIT:C50799 Ventricular Fibrillation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000212 hypercalcemia, infantile skos:exactMatch NCIT:C129734 Autosomal Recessive Infantile Hypercalcemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000297 baylisascariasis skos:exactMatch NCIT:C128397 Baylisascariasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000313 hypophosphatemia skos:exactMatch NCIT:C37977 Hypophosphatemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000327 Buruli ulcer disease skos:exactMatch NCIT:C84604 Buruli Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000330 endemic typhus skos:exactMatch NCIT:C84688 Endemic Typhus Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000334 multinodular goiter skos:exactMatch NCIT:C131438 Multinodular Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000337 exanthema subitum skos:exactMatch NCIT:C128420 Roseola Infantum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000355 Ullrich congenital muscular dystrophy skos:exactMatch NCIT:C123438 Ullrich Congenital Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000359 spondylocostal dysostosis skos:exactMatch NCIT:C125598 Spondylocostal Dysostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000365 primary congenital glaucoma skos:exactMatch NCIT:C150251 Primary Congenital Glaucoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000367 taeniasis skos:exactMatch NCIT:C85180 Taeniasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000371 oral cavity carcinoma in situ skos:exactMatch NCIT:C4587 Stage 0 Oral Cavity Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000372 pharynx carcinoma in situ skos:exactMatch NCIT:C4942 Stage 0 Pharyngeal Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000377 malignant Leydig cell tumor skos:exactMatch NCIT:C4213 Malignant Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000378 malignant Sertoli cell tumor skos:exactMatch NCIT:C67006 Malignant Sertoli Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000380 paranasal sinus carcinoma skos:exactMatch NCIT:C6014 Paranasal Sinus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000383 benign reproductive system neoplasm skos:exactMatch NCIT:C7617 Benign Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000384 bladder benign neoplasm skos:exactMatch NCIT:C3618 Benign Bladder Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000385 benign digestive system neoplasm skos:exactMatch NCIT:C4787 Benign Digestive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000386 digestive system neuroendocrine tumor, grade 1/2 skos:exactMatch NCIT:C95404 Digestive System Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000390 vitelliform macular dystrophy skos:exactMatch NCIT:C118788 Vitelliform Macular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000395 alcohol-related birth defect skos:exactMatch NCIT:C92727 Alcohol Related Birth Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000396 spastic cerebral palsy skos:exactMatch NCIT:C116903 Spastic Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000397 ataxic cerebral palsy skos:exactMatch NCIT:C97168 Ataxic Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000400 mixed cerebral palsy skos:exactMatch NCIT:C97177 Mixed Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000402 small cell carcinoma skos:exactMatch NCIT:C3915 Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000408 fetal alcohol spectrum disorder skos:exactMatch NCIT:C92780 Fetal Alcohol Spectrum Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000409 chorioamnionitis skos:exactMatch NCIT:C26720 Chorioamnionitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000410 funisitis skos:exactMatch NCIT:C97077 Funisitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000425 X-linked disease skos:exactMatch NCIT:C85865 X-Linked Inherited Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000430 mature T-cell and NK-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C3468 Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000432 lymphoplasmacytic lymphoma skos:exactMatch NCIT:C3212 Lymphoplasmacytic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000437 cerebellar ataxia skos:exactMatch NCIT:C82341 Spinocerebellar Ataxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000447 autosomal dominant polycystic liver disease skos:exactMatch NCIT:C82833 Polycystic Liver Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000448 paraganglioma skos:exactMatch NCIT:C3308 Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000453 short QT syndrome skos:exactMatch NCIT:C71060 Short QT Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000457 classical glioblastoma skos:exactMatch NCIT:C111694 Classical Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000458 proneural glioblastoma skos:exactMatch NCIT:C111692 Proneural Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000459 mesenchymal glioblastoma skos:exactMatch NCIT:C111695 Mesenchymal Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000460 neural glioblastoma skos:exactMatch NCIT:C111693 Neural Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000466 first-degree atrioventricular block skos:exactMatch NCIT:C62015 AV Block First Degree semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000467 second-degree atrioventricular block skos:exactMatch NCIT:C111119 AV Block Second Degree semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000468 third-degree atrioventricular block skos:exactMatch NCIT:C50501 Complete Atrioventricular Block semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000471 tricuspid valve disorder skos:exactMatch NCIT:C78649 Tricuspid Valve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000473 arterial disorder skos:exactMatch NCIT:C35317 Arterial Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000481 cervical dystonia skos:exactMatch NCIT:C85072 Spasmodic Torticollis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000490 glomerulosclerosis skos:exactMatch NCIT:C120888 Glomerulosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000495 oppositional defiant disorder skos:exactMatch NCIT:C92565 Oppositional Defiant Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000496 hemorrhagic cystitis skos:exactMatch NCIT:C114666 Hemorrhagic Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000497 pyometritis skos:exactMatch NCIT:C121207 Pyometra semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000500 tongue squamous cell carcinoma skos:exactMatch NCIT:C4648 Tongue Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000502 villous adenoma skos:exactMatch NCIT:C7399 Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000503 lung adenocarcinoma in situ skos:exactMatch NCIT:C136486 Lung Adenocarcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000520 parietal lobe ependymal tumor skos:exactMatch NCIT:C131575 Parietal Lobe Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000521 salivary gland carcinoma skos:exactMatch NCIT:C9272 Salivary Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000525 cecum villous adenoma skos:exactMatch NCIT:C5520 Cecum Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000527 colon adenoma skos:exactMatch NCIT:C3864 Colon Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000530 rectum adenoma skos:exactMatch NCIT:C5546 Rectal Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000536 pharyngeal squamous cell carcinoma skos:exactMatch NCIT:C102872 Pharyngeal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000540 small intestinal neuroendocrine tumor G1 skos:exactMatch NCIT:C4638 Small Intestinal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000541 jejunal adenocarcinoma skos:exactMatch NCIT:C181158 Jejunal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000543 ovarian melanoma skos:exactMatch NCIT:C178441 Ovarian Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000544 mucosal melanoma skos:exactMatch NCIT:C114828 Mucosal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000548 ovarian clear cell cancer skos:exactMatch NCIT:C40077 Malignant Ovarian Clear Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000550 extra-adrenal sympathetic paraganglioma skos:exactMatch NCIT:C48576 Extra-Adrenal Sympathetic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000552 breast lobular carcinoma skos:exactMatch NCIT:C3771 Breast Lobular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000554 endocervical adenocarcinoma skos:exactMatch NCIT:C127907 Endocervical Adenocarcinoma, Usual-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000565 infective endocarditis skos:exactMatch NCIT:C78265 Infective Endocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000577 congenital anemia skos:exactMatch NCIT:C35228 Congenital Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000594 pervasive developmental disorder skos:exactMatch NCIT:C97179 Pervasive Developmental Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000595 sexual and gender identity disorders skos:exactMatch NCIT:C92202 Sexual and Gender Identity Disorders semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000605 hypersensitivity reaction disease skos:exactMatch NCIT:C3114 Hypersensitivity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000607 primary cutaneous T-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C3467 Primary Cutaneous T-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000618 Her2-receptor negative breast cancer skos:exactMatch NCIT:C168519 HER2-Negative Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000620 breast benign neoplasm skos:exactMatch NCIT:C4505 Benign Breast Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000624 benign female reproductive system neoplasm skos:exactMatch NCIT:C4934 Benign Female Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000625 benign male reproductive system neoplasm skos:exactMatch NCIT:C4777 Benign Male Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000627 benign endocrine neoplasm skos:exactMatch NCIT:C4621 Benign Endocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000631 bone benign neoplasm skos:exactMatch NCIT:C4880 Benign Bone Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000632 uterine benign neoplasm skos:exactMatch NCIT:C3609 Benign Uterine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000634 thoracic benign neoplasm skos:exactMatch NCIT:C4565 Benign Thoracic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000640 central nervous system primitive neuroectodermal neoplasm skos:exactMatch NCIT:C5398 Central Nervous System Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000643 vulvar benign neoplasm skos:exactMatch NCIT:C3611 Benign Vulvar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000644 cervical benign neoplasm skos:exactMatch NCIT:C3607 Benign Cervical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000645 fallopian tube benign neoplasm skos:exactMatch NCIT:C4517 Benign Fallopian Tube Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000646 ovarian benign neoplasm skos:exactMatch NCIT:C2895 Benign Ovarian Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000647 benign vaginal neoplasm skos:exactMatch NCIT:C3610 Benign Vaginal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000648 nervous system benign neoplasm skos:exactMatch NCIT:C4789 Benign Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000650 peritoneal benign neoplasm skos:exactMatch NCIT:C8612 Benign Peritoneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000651 obsolete thoracic disorder skos:exactMatch NCIT:C35742 Thoracic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000654 benign connective and soft tissue neoplasm skos:exactMatch NCIT:C53684 Benign Connective and Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000665 apraxia skos:exactMatch NCIT:C180557 Apraxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000675 pain agnosia skos:exactMatch NCIT:C125664 Pain Agnosia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000685 visual agnosia skos:exactMatch NCIT:C35276 Visual Agnosia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000688 inborn organic aciduria skos:exactMatch NCIT:C101334 Organic Acid Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000700 familial hemiplegic migraine skos:exactMatch NCIT:C117009 Familial Hemiplegic Migraine semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000702 microscopic colitis skos:exactMatch NCIT:C38504 Microscopic Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000703 collagenous colitis skos:exactMatch NCIT:C27021 Collagenous Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000704 lymphocytic colitis skos:exactMatch NCIT:C27147 Lymphocytic Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000705 Clostridium difficile colitis skos:exactMatch NCIT:C35286 Clostridium difficile Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000709 Crohn ileitis skos:exactMatch NCIT:C35329 Crohn Ileitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000723 stutter disorder skos:exactMatch NCIT:C35043 Stutter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000728 ptosis skos:exactMatch NCIT:C27298 Ptosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000736 dyschromatosis universalis hereditaria skos:exactMatch NCIT:C173131 Dyschromatosis Universalis Hereditaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000739 uvulitis skos:exactMatch NCIT:C128385 Uvulitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000741 angular cheilitis skos:exactMatch NCIT:C112198 Angular Cheilitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000743 oral hairy leukoplakia skos:exactMatch NCIT:C3722 Oral Cavity Hairy Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000744 lung abscess skos:exactMatch NCIT:C99090 Lung Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000746 obsolete inguinal hernia skos:exactMatch NCIT:C34690 Inguinal Hernia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000747 obsolete umbilical hernia skos:exactMatch NCIT:C118375 Umbilical Hernia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000748 mastoiditis skos:exactMatch NCIT:C128368 Mastoiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000751 cervical polyp skos:exactMatch NCIT:C2939 Cervical Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000754 anal fistula skos:exactMatch NCIT:C60785 Anorectal Fistula semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000755 ectopic pregnancy skos:exactMatch NCIT:C34945 Ectopic Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000758 bacillary angiomatosis skos:exactMatch NCIT:C3477 Bacillary Angiomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000770 obsolete shellfish allergy skos:exactMatch NCIT:C172320 Shellfish Allergy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000778 obsolete fruit allergy skos:exactMatch NCIT:C172316 Fruit Allergy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000795 obsolete penicillin allergy skos:exactMatch NCIT:C34911 Penicillin Allergy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000814 B-cell adult acute lymphocytic leukemia skos:exactMatch NCIT:C9143 Adult B Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000816 abdominal obesity-metabolic syndrome skos:exactMatch NCIT:C84442 Metabolic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000819 anencephaly skos:exactMatch NCIT:C84560 Anencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000820 cerebral cavernous malformation skos:exactMatch NCIT:C84626 Cerebral Cavernous Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000827 salmonellosis skos:exactMatch NCIT:C157974 Salmonellosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000831 thrombotic disease skos:exactMatch NCIT:C26891 Thrombosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000839 obsolete congenital abnormality skos:exactMatch NCIT:C2849 Congenital Abnormality semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000845 fibrous dysplasia skos:exactMatch NCIT:C34609 Fibrous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000859 spina bifida occulta skos:exactMatch NCIT:C101044 Spina Bifida Occulta semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000866 hereditary myoglobinuria skos:exactMatch NCIT:C114705 Myoglobinuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000870 childhood acute lymphoblastic leukemia skos:exactMatch NCIT:C3168 Childhood Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000871 T-cell childhood acute lymphocytic leukemia skos:exactMatch NCIT:C7953 Childhood T Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000872 B-cell childhood acute lymphoblastic leukemia skos:exactMatch NCIT:C9140 Childhood B Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000873 lymphoblastic lymphoma skos:exactMatch NCIT:C9360 Lymphoblastic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000874 T-cell childhood lymphoblastic lymphoma skos:exactMatch NCIT:C7210 Childhood T Lymphoblastic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000875 adult acute monocytic leukemia skos:exactMatch NCIT:C8263 Adult Acute Monocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000878 cytomegalovirus retinitis skos:exactMatch NCIT:C50521 Cytomegaloviral Retinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000888 gastrointestinal mucositis skos:exactMatch NCIT:C3853 Gastrointestinal Mucositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000892 colon medullary carcinoma skos:exactMatch NCIT:C60641 Colon Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000893 mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma skos:exactMatch NCIT:C7270 Minimally Invasive Lung Mixed Non-Mucinous and Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000914 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 skos:exactMatch NCIT:C84606 CADASIL Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000918 endometritis skos:exactMatch NCIT:C26764 Endometritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000919 ampulla of vater cancer skos:exactMatch NCIT:C3536 Malignant Ampulla of Vater Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000920 duodenum cancer skos:exactMatch NCIT:C9328 Malignant Duodenal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000921 ampulla of vater neoplasm skos:exactMatch NCIT:C4443 Ampulla of Vater Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000922 pelvic inflammatory disease skos:exactMatch NCIT:C3889 Pelvic Inflammatory Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000923 interstitial emphysema skos:exactMatch NCIT:C34571 Pulmonary Interstitial Emphysema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000928 eyelid melanoma skos:exactMatch NCIT:C4358 Eyelid Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000929 balloon cell malignant melanoma skos:exactMatch NCIT:C4227 Balloon Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000930 nodular malignant melanoma skos:exactMatch NCIT:C4225 Cutaneous Nodular Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000931 endometrial disorder skos:exactMatch NCIT:C3504 Endometrial Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000933 subglottis neoplasm skos:exactMatch NCIT:C4426 Subglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000934 laryngeal leiomyoma skos:exactMatch NCIT:C6027 Laryngeal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000935 larynx squamous papilloma skos:exactMatch NCIT:C7742 Laryngeal Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000938 gastric leiomyoma skos:exactMatch NCIT:C3876 Gastric Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000939 intracranial abscess skos:exactMatch NCIT:C34734 Intracranial Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000942 corneal disorder skos:exactMatch NCIT:C26731 Corneal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000948 xerophthalmia skos:exactMatch NCIT:C34503 Xerophthalmia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000951 thymus lymphoma skos:exactMatch NCIT:C6451 Thymic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000956 small intestine cancer skos:exactMatch NCIT:C7523 Malignant Small Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000960 diabetic peripheral angiopathy skos:exactMatch NCIT:C35610 Diabetic Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000961 endobronchial lipoma skos:exactMatch NCIT:C5063 Endobronchial Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000962 spindle cell lipoma skos:exactMatch NCIT:C4254 Spindle Cell Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000963 esophageal lipoma skos:exactMatch NCIT:C5701 Esophageal Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000964 skin lipoma skos:exactMatch NCIT:C4616 Skin Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000965 liver lipoma skos:exactMatch NCIT:C5750 Liver Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000966 pleomorphic lipoma skos:exactMatch NCIT:C3703 Pleomorphic Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000967 conventional lipoma skos:exactMatch NCIT:C27530 Conventional Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000968 kidney lipoma skos:exactMatch NCIT:C5101 Kidney Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000969 pleural lipoma skos:exactMatch NCIT:C6644 Pleural Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000970 breast lipoma skos:exactMatch NCIT:C4647 Breast Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000971 chest wall lipoma skos:exactMatch NCIT:C6719 Chest Wall Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000972 gallbladder lipoma skos:exactMatch NCIT:C5835 Gallbladder Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000973 external ear lipoma skos:exactMatch NCIT:C4618 External Ear Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000974 axillary lipoma skos:exactMatch NCIT:C35419 Axillary Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000975 lipoma of spermatic cord skos:exactMatch NCIT:C3606 Spermatic Cord Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000976 paratesticular lipoma skos:exactMatch NCIT:C6384 Paratesticular Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000977 chondroid lipoma skos:exactMatch NCIT:C6503 Chondroid Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000978 extrahepatic bile duct lipoma skos:exactMatch NCIT:C5854 Extrahepatic Bile Duct Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000979 pinta disease skos:exactMatch NCIT:C85011 Pinta semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000983 exhibitionism skos:exactMatch NCIT:C94352 Exhibitionism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000984 thalassemia skos:exactMatch NCIT:C35069 Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000986 pleurisy skos:exactMatch NCIT:C26860 Pleuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000989 mumps infectious disease skos:exactMatch NCIT:C29888 Mumps semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000993 prostate squamous cell carcinoma skos:exactMatch NCIT:C5536 Prostate Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000994 malignant prostate phyllodes tumor skos:exactMatch NCIT:C5531 Malignant Prostate Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000995 familial periodic paralysis skos:exactMatch NCIT:C84709 Familial Periodic Paralysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0000996 prostate lymphoma skos:exactMatch NCIT:C5533 Prostate Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001000 mixed mineral dust pneumoconiosis skos:exactMatch NCIT:C27559 Mixed Mineral Dust Pneumoconiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001001 baritosis skos:exactMatch NCIT:C34410 Baritosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001003 pneumoconiosis due to talc skos:exactMatch NCIT:C27026 Talc Pneumoconiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001004 slate pneumoconiosis skos:exactMatch NCIT:C35397 Slate Pneumoconiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001005 kaolin pneumoconiosis skos:exactMatch NCIT:C35315 Kaolin Pneumoconiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001014 chronic leukemia skos:exactMatch NCIT:C3483 Chronic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001015 eosinophilic meningitis skos:exactMatch NCIT:C128374 Eosinophilic Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001016 epididymis cancer skos:exactMatch NCIT:C3558 Malignant Epididymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001017 epididymal adenocarcinoma skos:exactMatch NCIT:C39957 Epididymal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001020 amblyopia skos:exactMatch NCIT:C118764 Amblyopia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001023 prolymphocytic leukemia skos:exactMatch NCIT:C3181 Prolymphocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001028 acute pericementitis skos:exactMatch NCIT:C34354 Acute Periodontitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001029 Klippel-Feil syndrome skos:exactMatch NCIT:C98967 Klippel-Feil Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001036 hypopyon skos:exactMatch NCIT:C50593 Hypopyon semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001039 tonsillitis skos:exactMatch NCIT:C116006 Tonsillitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001040 nasopharyngitis skos:exactMatch NCIT:C34837 Nasopharyngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001044 esophageal atresia skos:exactMatch NCIT:C87072 Esophageal Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001045 intestinal atresia skos:exactMatch NCIT:C84790 Intestinal Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001046 imperforate anus skos:exactMatch NCIT:C84784 Imperforate Anus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001056 gastric cancer skos:exactMatch NCIT:C9331 Malignant Gastric Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001057 malignant gastric granular cell tumor skos:exactMatch NCIT:C5484 Malignant Gastric Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001059 gastric lymphoma skos:exactMatch NCIT:C4636 Gastric Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001060 microinvasive gastric cancer skos:exactMatch NCIT:C27131 Early Gastric Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001061 pylorus cancer skos:exactMatch NCIT:C188051 Malignant Pylorus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001066 late yaws skos:exactMatch NCIT:C41354 Late Yaws semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001067 early yaws skos:exactMatch NCIT:C41352 Early Yaws semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001068 osteomalacia skos:exactMatch NCIT:C26838 Osteomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001071 intellectual disability skos:exactMatch NCIT:C97250 Intellectual Disability semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001074 chronic tic disorder skos:exactMatch NCIT:C116768 Chronic Tic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001075 steatorrhea skos:exactMatch NCIT:C86917 Steatorrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001076 glucose intolerance skos:exactMatch NCIT:C34646 Glucose Intolerance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001078 tropical sprue skos:exactMatch NCIT:C45428 Tropical Sprue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001081 acute cervicitis skos:exactMatch NCIT:C27056 Acute Cervicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001082 lymph node cancer skos:exactMatch NCIT:C35812 Malignant Lymph Node Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001083 Fanconi renotubular syndrome skos:exactMatch NCIT:C3034 Fanconi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001085 interstitial nephritis skos:exactMatch NCIT:C26834 Interstitial Nephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001087 schizotypal personality disorder skos:exactMatch NCIT:C92632 Schizotypal Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001091 lipoma of colon skos:exactMatch NCIT:C5493 Colon Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001092 colon leiomyoma skos:exactMatch NCIT:C5492 Colon Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001093 colonic lymphangioma skos:exactMatch NCIT:C5500 Colon Lymphangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001095 mediastinum neuroblastoma skos:exactMatch NCIT:C6628 Mediastinal Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001096 mediastinum ganglioneuroblastoma skos:exactMatch NCIT:C6627 Mediastinal Ganglioneuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001098 separation anxiety disorder skos:exactMatch NCIT:C35014 Separation Anxiety Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001099 lactocele skos:exactMatch NCIT:C3515 Galactocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001100 hypertrophy of breast skos:exactMatch NCIT:C3125 Breast Hypertrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001101 fat necrosis of breast skos:exactMatch NCIT:C3661 Breast Fat Necrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001106 kidney failure skos:exactMatch NCIT:C4376 Renal Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001110 chronic pyelonephritis skos:exactMatch NCIT:C123216 Chronic Pyelonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001114 bacterial myocarditis skos:exactMatch NCIT:C128380 Bacterial Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001115 familial polycythemia skos:exactMatch NCIT:C26955 Familial Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001116 mesenteric lymphadenitis skos:exactMatch NCIT:C26830 Mesenteric Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001117 methemoglobinemia skos:exactMatch NCIT:C34817 Methemoglobinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001119 premature menopause skos:exactMatch NCIT:C80099 Premature Menopause semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001120 chronic frontal sinusitis skos:exactMatch NCIT:C34473 Chronic Frontal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001121 frontal sinusitis skos:exactMatch NCIT:C34626 Frontal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001122 chronic maxillary sinusitis skos:exactMatch NCIT:C34477 Chronic Maxillary Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001123 chronic sphenoidal sinusitis skos:exactMatch NCIT:C34480 Chronic Sphenoidal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001126 gastric ulcer skos:exactMatch NCIT:C3388 Gastric Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001128 nasal cavity cancer skos:exactMatch NCIT:C4918 Malignant Nasal Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001129 nasal cavity olfactory neuroblastoma skos:exactMatch NCIT:C7604 Nasal Cavity Olfactory Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001130 nasal cavity lymphoma skos:exactMatch NCIT:C6074 Nasal Cavity Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001132 sexual sadism disorder skos:exactMatch NCIT:C94358 Sexual Sadism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001133 malignant essential hypertension skos:exactMatch NCIT:C34802 Malignant Essential Hypertension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001135 voyeurism skos:exactMatch NCIT:C94360 Voyeurism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001139 sexual masochism disorder skos:exactMatch NCIT:C94356 Sexual Masochism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001142 salivary gland disorder skos:exactMatch NCIT:C26879 Salivary Gland Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001147 meningocele skos:exactMatch NCIT:C101209 Spinal Meningocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001147 meningocele skos:exactMatch NCIT:C105595 Meningocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001149 microcephaly skos:exactMatch NCIT:C85874 Microcephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001150 hydrocephalus skos:exactMatch NCIT:C3111 Hydrocephalus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001156 borderline personality disorder skos:exactMatch NCIT:C92633 Borderline Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001157 dependent personality disorder skos:exactMatch NCIT:C92637 Dependent Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001158 obsessive-compulsive personality disorder skos:exactMatch NCIT:C92638 Obsessive-Compulsive Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001159 multiple personality disorder skos:exactMatch NCIT:C94330 Dissociative Identity Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001160 dissociative disorder skos:exactMatch NCIT:C92197 Dissociative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001161 schizoid personality disorder skos:exactMatch NCIT:C92631 Schizoid Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001162 impulse control disorder skos:exactMatch NCIT:C34723 Impulse-Control Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001163 paranoid personality disorder skos:exactMatch NCIT:C92630 Paranoid Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001164 antisocial personality disorder skos:exactMatch NCIT:C88413 Antisocial Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001165 tongue disorder skos:exactMatch NCIT:C173793 Tongue Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001166 nephritis skos:exactMatch NCIT:C26833 Nephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001167 spastic diplegia skos:exactMatch NCIT:C34781 Spastic Diplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001168 spastic hemiplegia skos:exactMatch NCIT:C116905 Spastic Hemiplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001172 salpingo-oophoritis skos:exactMatch NCIT:C171201 Salpingo-Oophoritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001173 acute salpingitis skos:exactMatch NCIT:C40120 Acute Salpingitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001174 conjunctival vascular disorder skos:exactMatch NCIT:C35116 Conjunctival Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001176 lens disorder skos:exactMatch NCIT:C26812 Lens Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001180 bullous keratopathy skos:exactMatch NCIT:C26970 Bullous Keratopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001185 dissociative amnesia skos:exactMatch NCIT:C94328 Dissociative Amnesia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001186 depersonalization disorder skos:exactMatch NCIT:C94331 Depersonalization Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001187 urinary bladder cancer skos:exactMatch NCIT:C9334 Malignant Bladder Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001188 esophagus lymphoma skos:exactMatch NCIT:C5687 Esophageal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001192 esophageal melanoma skos:exactMatch NCIT:C5707 Esophageal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001204 esophagus sarcoma skos:exactMatch NCIT:C5341 Esophageal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001208 acute respiratory failure skos:exactMatch NCIT:C27043 Acute Respiratory Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001209 common wart skos:exactMatch NCIT:C27087 Verruca Vulgaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001214 acute conjunctivitis skos:exactMatch NCIT:C35195 Acute Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001217 pseudomembranous conjunctivitis skos:exactMatch NCIT:C35196 Pseudomembranous Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001220 hypoparathyroidism skos:exactMatch NCIT:C78350 Hypoparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001221 esophageal varices skos:exactMatch NCIT:C53506 Esophageal Varices semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001222 congenital T-cell immunodeficiency skos:exactMatch NCIT:C27872 Congenital T-Cell Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001223 parathyroid gland disorder skos:exactMatch NCIT:C26844 Parathyroid Gland Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001224 Angelucci syndrome skos:exactMatch NCIT:C34353 Acute Atopic Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001226 acute contagious conjunctivitis skos:exactMatch NCIT:C35704 Acute Contagious Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001235 appendix cancer skos:exactMatch NCIT:C9333 Malignant Appendix Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001236 appendiceal neoplasm skos:exactMatch NCIT:C4434 Appendix Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001237 appendix lymphoma skos:exactMatch NCIT:C5513 Appendix Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001238 polycythemia neonatorum skos:exactMatch NCIT:C27069 Polycythemia Neonatorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001239 anemia of prematurity skos:exactMatch NCIT:C97167 Anemia of Prematurity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001242 disseminated intravascular coagulation in newborn skos:exactMatch NCIT:C111856 Disseminated Intravascular Coagulation in Newborn semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001243 disseminated intravascular coagulation skos:exactMatch NCIT:C2992 Disseminated Intravascular Coagulation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001244 vitamin K deficiency hemorrhagic disease skos:exactMatch NCIT:C99108 Vitamin K Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001245 microcytic anemia skos:exactMatch NCIT:C35141 Microcytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001247 social phobia skos:exactMatch NCIT:C34927 Social Anxiety Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001252 Plummer disease skos:exactMatch NCIT:C35171 Toxic Nodular Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001256 arteriovenous hemangioma/malformation skos:exactMatch NCIT:C2882 Arteriovenous Malformation/Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001259 pituitary gland infarction skos:exactMatch NCIT:C27117 Pituitary Gland Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001260 cercarial dermatitis skos:exactMatch NCIT:C128349 Cercarial Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001261 Mobitz type II atrioventricular block skos:exactMatch NCIT:C62018 AV Block Second Degree Mobitz Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001265 schizophreniform disorder skos:exactMatch NCIT:C94376 Schizophreniform Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001269 scleral disorder skos:exactMatch NCIT:C79717 Sclera Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001271 lens subluxation skos:exactMatch NCIT:C34772 Lens Subluxation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001273 megacolon skos:exactMatch NCIT:C34810 Megacolon semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001275 spinal meningioma skos:exactMatch NCIT:C6935 Spinal Cord Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001276 expressive language disorder skos:exactMatch NCIT:C92562 Expressive Language Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001279 intraspinal meningioma skos:exactMatch NCIT:C5134 Spinal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001280 choroiditis skos:exactMatch NCIT:C35111 Posterior Uveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001282 fallopian tube endometriosis skos:exactMatch NCIT:C26763 Fallopian Tube Endometriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001283 endosalpingiosis skos:exactMatch NCIT:C40121 Peritoneal Endosalpingiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001286 exotropia skos:exactMatch NCIT:C34601 Divergent Strabismus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001288 endometriosis of rectovaginal septum and vagina skos:exactMatch NCIT:C128064 Vaginal Endometriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001290 allergic cutaneous vasculitis skos:exactMatch NCIT:C35119 Allergic Cutaneous Angiitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001293 subglottis cancer skos:exactMatch NCIT:C3546 Malignant Subglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001294 Horner syndrome skos:exactMatch NCIT:C28155 Horner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001297 cardiac tamponade skos:exactMatch NCIT:C50481 Cardiac Tamponade semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001298 congenital mitral valve insufficiency skos:exactMatch NCIT:C50888 Mitral Valve Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001299 diabetic autonomic neuropathy skos:exactMatch NCIT:C27068 Diabetic Autonomic Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001300 autonomic neuropathy skos:exactMatch NCIT:C27033 Autonomic Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001301 rumination disorder skos:exactMatch NCIT:C92567 Rumination Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001302 hypertensive heart disease skos:exactMatch NCIT:C4907 Hypertensive Cardiomegaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001307 corneal abscess skos:exactMatch NCIT:C26969 Corneal Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001309 oculomotor nerve paralysis skos:exactMatch NCIT:C27597 Cranial Nerve III Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001314 chondrocalcinosis skos:exactMatch NCIT:C34955 Pseudogout semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001322 pericardium cancer skos:exactMatch NCIT:C4567 Malignant Pericardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001325 penile cancer skos:exactMatch NCIT:C7547 Malignant Penile Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001339 portal vein thrombosis skos:exactMatch NCIT:C78565 Portal Vein Thrombosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001340 heart cancer skos:exactMatch NCIT:C3548 Malignant Cardiac Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001341 selective IgA deficiency disease skos:exactMatch NCIT:C26964 Selective IgA Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001347 facioscapulohumeral muscular dystrophy skos:exactMatch NCIT:C84704 Facioscapulohumeral Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001356 iron deficiency anemia skos:exactMatch NCIT:C84484 Iron-Deficiency Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001357 hypochromic anemia skos:exactMatch NCIT:C34380 Hypochromic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001358 bronchial disorder skos:exactMatch NCIT:C34439 Bronchospasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001369 chronic laryngitis skos:exactMatch NCIT:C26975 Chronic Laryngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001370 pericardial effusion skos:exactMatch NCIT:C3319 Pericardial Effusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001371 protein-energy malnutrition skos:exactMatch NCIT:C34952 Protein Energy Malnutrition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001374 bladder sarcoma skos:exactMatch NCIT:C4669 Bladder Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001381 bladder lymphoma skos:exactMatch NCIT:C6164 Bladder Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001382 hepatorenal syndrome skos:exactMatch NCIT:C113400 Hepatorenal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001385 cortical blindness skos:exactMatch NCIT:C118707 Cortical Blindness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001386 visual epilepsy skos:exactMatch NCIT:C3980 Visual Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001387 penile sarcoma skos:exactMatch NCIT:C7730 Penile Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001398 ureter benign neoplasm skos:exactMatch NCIT:C3617 Benign Ureter Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001399 ureter leiomyoma skos:exactMatch NCIT:C6161 Ureter Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001400 schwannoma of ureter skos:exactMatch NCIT:C6162 Ureter Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001402 vaginal cancer skos:exactMatch NCIT:C7410 Malignant Vaginal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001403 labium majus cancer skos:exactMatch NCIT:C7638 Malignant Labia Majora Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001405 dermatophytosis of groin and perianal area skos:exactMatch NCIT:C34535 Dermatophytosis of Groin and Perianal Area semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001406 peripheral nervous system neoplasm skos:exactMatch NCIT:C3321 Peripheral Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001407 tracheal cancer skos:exactMatch NCIT:C9346 Malignant Tracheal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001408 ischemic neuropathy skos:exactMatch NCIT:C27025 Ischemic Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001409 esophagitis skos:exactMatch NCIT:C9224 Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001414 osteopoikilosis skos:exactMatch NCIT:C84985 Osteopoikilosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001415 atrophy of testis skos:exactMatch NCIT:C123259 Testicular Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001416 female reproductive organ cancer skos:exactMatch NCIT:C4913 Malignant Female Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001417 tracheal lymphoma skos:exactMatch NCIT:C6248 Tracheal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001418 trachea sarcoma skos:exactMatch NCIT:C6050 Tracheal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001419 trachea squamous cell carcinoma skos:exactMatch NCIT:C4448 Tracheal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001420 trigeminal nerve neoplasm skos:exactMatch NCIT:C5122 Trigeminal Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001421 frontal lobe neoplasm skos:exactMatch NCIT:C5572 Frontal Lobe Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001422 primary aldosteronism skos:exactMatch NCIT:C34510 Conn Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001426 mediastinum neurofibroma skos:exactMatch NCIT:C6631 Mediastinal Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001429 transient arthropathy skos:exactMatch NCIT:C35761 Transient Arthropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001433 vaginal disorder skos:exactMatch NCIT:C26910 Vaginal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001436 hemosiderosis skos:exactMatch NCIT:C82892 Hemochromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001437 pulmonary alveolar proteinosis skos:exactMatch NCIT:C85037 Pulmonary Alveolar Proteinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001441 pica disease skos:exactMatch NCIT:C92566 Pica Eating Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001442 dysthymic disorder skos:exactMatch NCIT:C34562 Dysthymic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001444 Chagas disease skos:exactMatch NCIT:C84629 Chagas Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001451 peripheral retinal degeneration skos:exactMatch NCIT:C34919 Peripheral Retinal Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001470 anal margin squamous cell carcinoma skos:exactMatch NCIT:C6925 Anal Margin Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001472 testicular lymphoma skos:exactMatch NCIT:C6810 Testicular Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001476 coloboma skos:exactMatch NCIT:C98877 Coloboma of the Eye semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001479 cutaneous diphtheria skos:exactMatch NCIT:C34544 Cutaneous Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001482 testicular leukemia skos:exactMatch NCIT:C9277 Testicular Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001484 paranoid schizophrenia skos:exactMatch NCIT:C35006 Paranoid Type Schizophrenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001490 corneal granular dystrophy skos:exactMatch NCIT:C34651 Granular Corneal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001493 chronic pulmonary heart disease skos:exactMatch NCIT:C34478 Cor Pulmonale semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001494 obsolete transvestism skos:exactMatch NCIT:C94359 Transvestic Fetishism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001499 retroperitoneal lymphoma skos:exactMatch NCIT:C7353 Retroperitoneal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001500 obsolete gender identity disorder skos:exactMatch NCIT:C94362 Gender Identity Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001501 retroperitoneal sarcoma skos:exactMatch NCIT:C4832 Retroperitoneal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001502 retroperitoneum carcinoma skos:exactMatch NCIT:C7352 Retroperitoneal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001504 fetishistic disorder skos:exactMatch NCIT:C94353 Fetishism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001505 alcoholic hepatitis skos:exactMatch NCIT:C34684 Alcoholic Hepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001516 spinal muscular atrophy skos:exactMatch NCIT:C85075 Spinal Muscular Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001520 kleptomania skos:exactMatch NCIT:C94333 Kleptomania semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001521 intermittent explosive disorder skos:exactMatch NCIT:C94332 Intermittent Explosive Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001522 pyromania skos:exactMatch NCIT:C94334 Pyromania semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001526 labia minora cancer skos:exactMatch NCIT:C7637 Malignant Labia Minora Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001528 vulva cancer skos:exactMatch NCIT:C7502 Malignant Vulvar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001529 pancytopenia skos:exactMatch NCIT:C34889 Pancytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001531 blood coagulation disease skos:exactMatch NCIT:C2902 Coagulation Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001535 vagus nerve disorder skos:exactMatch NCIT:C27591 Vagus Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001536 vaginal leiomyoma skos:exactMatch NCIT:C6373 Vaginal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001540 bagassosis skos:exactMatch NCIT:C34409 Bagassosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001549 hemolytic-uremic syndrome skos:exactMatch NCIT:C75545 Hemolytic Uremic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001552 dyscalculia skos:exactMatch NCIT:C97165 Dyscalculia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001555 neonatal thyrotoxicosis skos:exactMatch NCIT:C114906 Neonatal Thyrotoxicosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001558 Potter sequence skos:exactMatch NCIT:C40435 Potter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001560 hypertrophic pyloric stenosis skos:exactMatch NCIT:C98952 Hypertrophic Pyloric Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001561 pyloric stenosis skos:exactMatch NCIT:C34966 Pyloric Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001563 vestibulocochlear nerve disorder skos:exactMatch NCIT:C27207 Vestibulocochlear Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001564 binocular vision disease skos:exactMatch NCIT:C34422 Binocular Vision Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001566 hypercalcemia disease skos:exactMatch NCIT:C3112 Hypercalcemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001567 nephrocalcinosis skos:exactMatch NCIT:C84918 Nephrocalcinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001568 mixed receptive-expressive language disorder skos:exactMatch NCIT:C92563 Mixed Receptive-Expressive Language Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001569 acoustic neuroma skos:exactMatch NCIT:C3276 Vestibular Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001571 gynecomastia disorder skos:exactMatch NCIT:C3073 Gynecomastia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001572 leiomyoma skos:exactMatch NCIT:C3157 Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001576 telangiectasis skos:exactMatch NCIT:C28194 Telangiectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001577 respiratory syncytial virus infectious disease skos:exactMatch NCIT:C3354 Respiratory Syncytial Virus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001580 lacrimal duct cancer skos:exactMatch NCIT:C3567 Malignant Nasolacrimal Duct Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001586 mucopolysaccharidosis type 1 skos:exactMatch NCIT:C85053 Mucopolysaccharidosis Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001590 quadriplegia skos:exactMatch NCIT:C50721 Quadriplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001595 choreatic disease skos:exactMatch NCIT:C84633 Chorea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001598 benign lymphoepithelial lesion of salivary gland skos:exactMatch NCIT:C3949 Benign Lymphoepithelial Lesion of the Salivary Gland semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001602 labia minora carcinoma skos:exactMatch NCIT:C9364 Labia Minora Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001606 central nervous system leukemia skos:exactMatch NCIT:C5440 Central Nervous System Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001608 vagus nerve neoplasm skos:exactMatch NCIT:C5831 Vagus Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001609 agranulocytosis skos:exactMatch NCIT:C2863 Granulocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001612 carotid stenosis skos:exactMatch NCIT:C95804 Carotid Artery Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001615 epidemic keratoconjunctivitis skos:exactMatch NCIT:C34590 Epidemic Keratoconjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001617 transient global amnesia skos:exactMatch NCIT:C85198 Transient Global Amnesia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001620 louse-borne relapsing fever skos:exactMatch NCIT:C128426 Louse-Borne Relapsing Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001621 tick-borne relapsing fever skos:exactMatch NCIT:C34976 Tick-Borne Relapsing Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001627 dementia skos:exactMatch NCIT:C4786 Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001628 tinea unguium skos:exactMatch NCIT:C112214 Onychomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001630 branch retinal artery occlusion skos:exactMatch NCIT:C34436 Retinal Arterial Branch Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001631 vertebral artery insufficiency skos:exactMatch NCIT:C35123 Vertebral Artery Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001633 central retinal artery occlusion skos:exactMatch NCIT:C34456 Central Retinal Artery Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001634 bladder leiomyoma skos:exactMatch NCIT:C6178 Bladder Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001635 bladder squamous papilloma skos:exactMatch NCIT:C39834 Bladder Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001641 severe pre-eclampsia skos:exactMatch NCIT:C112843 Severe Preeclampsia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001644 acute proliferative glomerulonephritis skos:exactMatch NCIT:C35443 Post-Streptococcal Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001645 crescentic glomerulonephritis skos:exactMatch NCIT:C35444 Crescentic Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001648 esophageal candidiasis skos:exactMatch NCIT:C27027 Candida Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001649 fungal esophagitis skos:exactMatch NCIT:C27107 Fungal Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001650 acute cystitis skos:exactMatch NCIT:C26934 Acute Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001651 scrotum squamous cell carcinoma skos:exactMatch NCIT:C4643 Scrotal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001652 scrotum melanoma skos:exactMatch NCIT:C7361 Scrotal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001654 spermatic cord cancer skos:exactMatch NCIT:C3559 Malignant Spermatic Cord Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001656 megaesophagus skos:exactMatch NCIT:C34811 Megaesophagus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001657 brain cancer skos:exactMatch NCIT:C3568 Malignant Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001658 nontoxic goiter skos:exactMatch NCIT:C35271 Nontoxic Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001660 proliferative diabetic retinopathy skos:exactMatch NCIT:C84457 Proliferative Diabetic Retinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001661 background diabetic retinopathy skos:exactMatch NCIT:C35668 Non-Proliferative Diabetic Retinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001671 mucocele of appendix skos:exactMatch NCIT:C3241 Mucocele of the Appendix semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001673 diarrheal disease skos:exactMatch NCIT:C2987 Diarrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001680 vaginal mullerian papilloma skos:exactMatch NCIT:C40255 Vaginal Mullerian Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001683 pancreatic mucinous ductal ectasia skos:exactMatch NCIT:C5717 Pancreatic Mucinous Ductal Ectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001684 exocrine pancreatic insufficiency skos:exactMatch NCIT:C84316 Pancreatic Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001692 pedophilia skos:exactMatch NCIT:C94355 Pedophilia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001700 megaloblastic anemia skos:exactMatch NCIT:C34382 Megaloblastic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001702 labia majora carcinoma skos:exactMatch NCIT:C9363 Labia Majora Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001703 color vision disorder skos:exactMatch NCIT:C3891 Color Blindness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001704 vaginal glandular neoplasm skos:exactMatch NCIT:C40250 Vaginal Glandular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001705 pure red-cell aplasia skos:exactMatch NCIT:C34974 Pure Red Cell Aplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001706 cerebral sarcoidosis skos:exactMatch NCIT:C35441 Cerebral Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001707 cardiac sarcoidosis skos:exactMatch NCIT:C35589 Cardiac Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001708 pulmonary sarcoidosis skos:exactMatch NCIT:C34997 Pulmonary Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001709 hypercalcemic sarcoidosis skos:exactMatch NCIT:C35807 Hypercalcemic Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001711 hepatic encephalopathy skos:exactMatch NCIT:C79596 Hepatic Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001718 scleritis skos:exactMatch NCIT:C119046 Scleritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001724 supraglottis cancer skos:exactMatch NCIT:C3545 Malignant Supraglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001725 balanitis xerotica obliterans skos:exactMatch NCIT:C3523 Balanitis Xerotica Obliterans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001731 benign vaginal mixed epithelial and mesenchymal neoplasm skos:exactMatch NCIT:C40275 Benign Vaginal Mixed Epithelial and Mesenchymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001732 trigonitis skos:exactMatch NCIT:C123175 Trigonitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001734 tuberous sclerosis skos:exactMatch NCIT:C3424 Tuberous Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001735 paranasal sinus disorder skos:exactMatch NCIT:C26843 Paranasal Sinus Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001737 tetanus neonatorum skos:exactMatch NCIT:C116814 Tetanus Neonatorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001740 cornea squamous cell carcinoma skos:exactMatch NCIT:C4552 Corneal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001741 hyperparathyroidism skos:exactMatch NCIT:C48259 Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001743 paranasal sinus lymphoma skos:exactMatch NCIT:C6068 Paranasal Sinus Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001748 maxillary sinus carcinoma skos:exactMatch NCIT:C3540 Malignant Maxillary Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001748 maxillary sinus carcinoma skos:exactMatch NCIT:C9332 Maxillary Sinus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001754 eclampsia skos:exactMatch NCIT:C87167 Eclampsia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001756 frontal sinus cancer skos:exactMatch NCIT:C3542 Malignant Frontal Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001757 frontal sinus neoplasm skos:exactMatch NCIT:C4419 Frontal Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001758 paranasal sinus sarcoma skos:exactMatch NCIT:C6849 Paranasal Sinus Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001760 photokeratitis skos:exactMatch NCIT:C118750 Photokeratitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001761 favism skos:exactMatch NCIT:C34607 Favism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001763 ethmoid sinus cancer skos:exactMatch NCIT:C3541 Malignant Ethmoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001764 ethmoidal sinus neoplasm skos:exactMatch NCIT:C4416 Ethmoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001778 dermoid cyst of skin skos:exactMatch NCIT:C4632 Skin Dermoid Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001779 vaginal squamous papilloma skos:exactMatch NCIT:C6374 Vaginal Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001780 premature ejaculation skos:exactMatch NCIT:C94349 Premature Ejaculation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001781 uterine corpus adenomatoid tumor skos:exactMatch NCIT:C27250 Uterine Corpus Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001783 endometrial stromal nodule skos:exactMatch NCIT:C4262 Endometrial Stromal Nodule semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001789 neurofibroma of spinal cord skos:exactMatch NCIT:C5145 Spinal Cord Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001790 spinal cord lipoma skos:exactMatch NCIT:C4619 Spinal Cord Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001794 Pthirus pubis infestation skos:exactMatch NCIT:C35777 Pediculosis Pubis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001795 plantar wart skos:exactMatch NCIT:C26913 Verruca Plantaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001806 vaginal squamous tumor skos:exactMatch NCIT:C40242 Vaginal Squamous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001810 hypoglossal nerve disorder skos:exactMatch NCIT:C26954 Hypoglossal Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001811 tetanic cataract skos:exactMatch NCIT:C35068 Tetanic Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001821 hypoactive sexual desire disorder skos:exactMatch NCIT:C94337 Hypoactive Sexual Desire Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001823 sick sinus syndrome skos:exactMatch NCIT:C62244 Sick Sinus Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001824 polyneuropathy skos:exactMatch NCIT:C26951 Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001825 squamous papilloma skos:exactMatch NCIT:C3712 Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001828 acquired color blindness skos:exactMatch NCIT:C118712 Acquired Color Blindness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001832 bacterial esophagitis skos:exactMatch NCIT:C27106 Bacterial Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001834 visual pathway disorder skos:exactMatch NCIT:C35342 Visual Pathway Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001836 amenorrhea skos:exactMatch NCIT:C61443 Amenorrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001841 uterine corpus epithelioid leiomyoma skos:exactMatch NCIT:C40164 Uterine Corpus Epithelioid Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001842 uterine corpus dissecting leiomyoma skos:exactMatch NCIT:C40172 Uterine Corpus Dissecting Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001844 uterine corpus myxoid leiomyoma skos:exactMatch NCIT:C40166 Uterine Corpus Myxoid Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001845 uterine corpus lipoleiomyoma skos:exactMatch NCIT:C40168 Uterine Corpus Lipoleiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001846 uterine corpus bizarre leiomyoma skos:exactMatch NCIT:C40167 Uterine Corpus Bizarre Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001852 small intestine lymphoma skos:exactMatch NCIT:C4007 Small Intestinal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001854 lacrimal apparatus disorder skos:exactMatch NCIT:C26809 Lacrimal System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001858 Tietze syndrome skos:exactMatch NCIT:C168333 Musculoskeletal Chest Pain due to Costochondral Junction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001871 acute diffuse glomerulonephritis skos:exactMatch NCIT:C35587 Acute Diffuse Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001875 epicondylitis skos:exactMatch NCIT:C34589 Epicondylitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001879 anus cancer skos:exactMatch NCIT:C7379 Malignant Anal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001881 toxic shock syndrome skos:exactMatch NCIT:C35498 Toxic Shock Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001884 abducens nerve neoplasm skos:exactMatch NCIT:C5826 Abducens Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001888 anus lymphoma skos:exactMatch NCIT:C5601 Anal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001889 ovarian dysfunction skos:exactMatch NCIT:C113351 Ovarian Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001892 spinal cord lymphoma skos:exactMatch NCIT:C5157 Spinal Cord Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001893 spinal cord melanoma skos:exactMatch NCIT:C5158 Spinal Cord Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001894 spinal cord sarcoma skos:exactMatch NCIT:C5152 Spinal Cord Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001896 obstructive hydrocephalus skos:exactMatch NCIT:C116347 Non-Communicating Hydrocephalus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001898 optic choroid disorder skos:exactMatch NCIT:C34468 Choroid Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001901 selective IgG subclass deficiency skos:exactMatch NCIT:C27024 Selective Immunoglobulin G Subclass Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001907 adult dermatomyositis skos:exactMatch NCIT:C27313 Adult Dermatomyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001910 ochronosis disorder skos:exactMatch NCIT:C84938 Ochronosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001920 chronic purulent otitis media skos:exactMatch NCIT:C128386 Chronic Suppurative Otitis Media semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001922 pyoureter skos:exactMatch NCIT:C35666 Ureter Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001926 ureteral disorder skos:exactMatch NCIT:C27148 Ureter Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001927 pulmonary valve insufficiency skos:exactMatch NCIT:C50848 Pulmonary Valvular Regurgitation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001928 suppurative cholangitis skos:exactMatch NCIT:C35336 Suppurative Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001929 ascending cholangitis skos:exactMatch NCIT:C35372 Ascending Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001930 acute cholangitis skos:exactMatch NCIT:C35334 Acute Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001931 pericholangitis skos:exactMatch NCIT:C34916 Pericholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001933 endocrine pancreas disorder skos:exactMatch NCIT:C27067 Endocrine Pancreas Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001938 vulvar dystrophy skos:exactMatch NCIT:C34565 Vulvar Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001939 skin epithelioid hemangioma skos:exactMatch NCIT:C7393 Skin Epithelioid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001941 blindness (disorder) skos:exactMatch NCIT:C97109 Blindness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001942 generalized anxiety disorder skos:exactMatch NCIT:C92622 Generalized Anxiety Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001943 Plasmodium malariae malaria skos:exactMatch NCIT:C34799 Quartan Malaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001945 postencephalitic Parkinson disease skos:exactMatch NCIT:C34898 Postencephalitic Parkinsonism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001947 suppurative thyroiditis skos:exactMatch NCIT:C129724 Acute Suppurative Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001951 Norwegian scabies skos:exactMatch NCIT:C34855 Norwegian Scabies semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001956 capillary leak syndrome skos:exactMatch NCIT:C62578 Capillary Leak Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001967 gonadal dysgenesis skos:exactMatch NCIT:C61420 Gonadal Dysgenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001971 farmer's lung disease skos:exactMatch NCIT:C34605 Farmer's Lung semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001974 hemangioma of orbit skos:exactMatch NCIT:C6245 Orbit Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001975 cavernous hemangioma of orbit skos:exactMatch NCIT:C4546 Orbit Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001977 ureteral lymphoma skos:exactMatch NCIT:C6175 Ureter Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001978 regional ureteric cancer skos:exactMatch NCIT:C9356 Locally Advanced Ureter Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001979 dumping syndrome skos:exactMatch NCIT:C2994 Dumping Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001982 Niemann-Pick disease skos:exactMatch NCIT:C61269 Niemann-Pick Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001985 partial arterial retinal occlusion skos:exactMatch NCIT:C35192 Partial Retinal Arterial Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001990 malignant cardiac peripheral nerve sheath neoplasm skos:exactMatch NCIT:C5367 Cardiac Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001991 malignant cardiac germ cell tumor skos:exactMatch NCIT:C5371 Malignant Cardiac Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001992 rete testis adenocarcinoma skos:exactMatch NCIT:C8955 Rete Testis Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001993 seminal vesicle adenocarcinoma skos:exactMatch NCIT:C39906 Seminal Vesicle Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001994 sphenoidal sinus cancer skos:exactMatch NCIT:C3543 Malignant Sphenoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0001995 sphenoid sinus squamous cell carcinoma skos:exactMatch NCIT:C6066 Sphenoid Sinus Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002008 labyrinthitis skos:exactMatch NCIT:C128369 Labyrinthitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002009 major depressive disorder skos:exactMatch NCIT:C35094 Unipolar Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002012 methylmalonic acidemia skos:exactMatch NCIT:C98986 Methylmalonic Acidemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002013 lymphangioma skos:exactMatch NCIT:C8965 Lymphangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002017 olivopontocerebellar atrophy skos:exactMatch NCIT:C84947 Olivopontocerebellar Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002021 gingival disorder skos:exactMatch NCIT:C173795 Gingival Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002025 psychiatric disorder skos:exactMatch NCIT:C2893 Psychiatric Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002026 candidiasis skos:exactMatch NCIT:C26711 Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002027 avoidant personality disorder skos:exactMatch NCIT:C92636 Avoidant Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002028 personality disorder skos:exactMatch NCIT:C34922 Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002030 chronic cervicitis skos:exactMatch NCIT:C27057 Chronic Cervicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002032 colon carcinoma skos:exactMatch NCIT:C4910 Colon Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002033 cecum cancer skos:exactMatch NCIT:C9329 Malignant Cecum Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002034 cecum lymphoma skos:exactMatch NCIT:C5515 Cecum Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002035 colon lymphoma skos:exactMatch NCIT:C4793 Colon Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002036 penile disorder skos:exactMatch NCIT:C26846 Penile Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002037 pleural disorder skos:exactMatch NCIT:C26859 Pleural Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002038 head and neck carcinoma skos:exactMatch NCIT:C35850 Head and Neck Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002039 cognitive disorder skos:exactMatch NCIT:C92196 Cognitive Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002041 fungal infectious disease skos:exactMatch NCIT:C3245 Fungal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002045 communicating hydrocephalus skos:exactMatch NCIT:C34501 Communicating Hydrocephalus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002048 thrombocytopenia due to immune destruction skos:exactMatch NCIT:C3991 Thrombocytopenia Due to Immune Destruction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002049 thrombocytopenia skos:exactMatch NCIT:C3408 Thrombocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002050 depressive disorder skos:exactMatch NCIT:C2982 Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002052 lymphadenitis skos:exactMatch NCIT:C26821 Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002055 benign eccrine breast spiradenoma skos:exactMatch NCIT:C5193 Breast Spiradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002056 breast fibroadenoma skos:exactMatch NCIT:C3744 Breast Fibroadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002057 breast leiomyoma skos:exactMatch NCIT:C40399 Breast Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002058 breast adenoma skos:exactMatch NCIT:C40382 Breast Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002060 intraductal papilloma skos:exactMatch NCIT:C3785 Intraductal Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002061 intraductal papillary breast neoplasm skos:exactMatch NCIT:C36090 Breast Intraductal Papillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002062 breast myofibroblastoma skos:exactMatch NCIT:C40397 Breast Myofibroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002063 obsolete breast papillomatosis skos:exactMatch NCIT:C6977 Breast Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002064 breast angiomatosis skos:exactMatch NCIT:C40381 Breast Angiomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002065 benign breast adenomyoepithelioma skos:exactMatch NCIT:C5144 Benign Breast Adenomyoepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002066 breast adenomyoepithelioma skos:exactMatch NCIT:C6899 Breast Adenomyoepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002070 ventricular septal defect skos:exactMatch NCIT:C84506 Ventricular Septal Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002071 supratentorial cancer skos:exactMatch NCIT:C4964 Malignant Supratentorial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002072 melanotic neuroectodermal tumor skos:exactMatch NCIT:C3717 Melanotic Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002073 malignant pineal area germ cell neoplasm skos:exactMatch NCIT:C6767 Malignant Pineal Region Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002074 Behcet syndrome arthropathy skos:exactMatch NCIT:C35225 Arthropathy in Behcet's Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002076 pneumothorax skos:exactMatch NCIT:C38006 Pneumothorax semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002078 heart septal defect skos:exactMatch NCIT:C84482 Congenital Septal Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002081 musculoskeletal system disorder skos:exactMatch NCIT:C107377 Musculoskeletal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002082 endocrine gland neoplasm skos:exactMatch NCIT:C3010 Endocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002083 Richter syndrome skos:exactMatch NCIT:C35424 Richter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002086 clear cell acanthoma skos:exactMatch NCIT:C97041 Clear Cell Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002087 peritoneum cancer skos:exactMatch NCIT:C3538 Malignant Peritoneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002088 partial retinal vein occlusion skos:exactMatch NCIT:C35341 Partial Retinal Vein Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002089 retinal vascular occlusion skos:exactMatch NCIT:C34980 Retinal Vascular Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002090 eccrine sweat gland neoplasm skos:exactMatch NCIT:C6796 Eccrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002092 small intestine leiomyoma skos:exactMatch NCIT:C7725 Small Intestinal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002093 acanthoma skos:exactMatch NCIT:C7419 Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002095 vascular cancer skos:exactMatch NCIT:C8538 Malignant Blood Vessel Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002096 malignant conjunctival melanoma skos:exactMatch NCIT:C4550 Conjunctival Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002098 facial nerve disorder skos:exactMatch NCIT:C27594 Facial Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002100 cardiovascular cancer skos:exactMatch NCIT:C114940 Malignant Cardiovascular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002101 facial nerve neoplasm skos:exactMatch NCIT:C5827 Facial Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002102 cheilitis skos:exactMatch NCIT:C79545 Cheilitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002103 factitious disorder skos:exactMatch NCIT:C92198 Factitious Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002108 thyroid cancer skos:exactMatch NCIT:C7510 Malignant Thyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002109 pituitary cancer skos:exactMatch NCIT:C4769 Malignant Pituitary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002110 adrenal rest tumor skos:exactMatch NCIT:C2860 Adrenal Rest Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002112 benign peritoneal mesothelioma skos:exactMatch NCIT:C7354 Peritoneal Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002114 pancreas lymphoma skos:exactMatch NCIT:C5714 Pancreatic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002116 malignant exocrine pancreas neoplasm skos:exactMatch NCIT:C7430 Malignant Exocrine Pancreas Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002117 pancreas sarcoma skos:exactMatch NCIT:C5715 Pancreatic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002118 urinary system disorder skos:exactMatch NCIT:C3430 Urinary System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002119 ossifying fibroma skos:exactMatch NCIT:C173820 Ossifying Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002119 ossifying fibroma skos:exactMatch NCIT:C8422 Cemento-Ossifying Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002120 neuroendocrine carcinoma skos:exactMatch NCIT:C3773 Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002122 neuritis skos:exactMatch NCIT:C116381 Neuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002123 calcinosis skos:exactMatch NCIT:C3672 Calcification semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002125 status epilepticus skos:exactMatch NCIT:C85079 Status Epilepticus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002127 urethral stricture skos:exactMatch NCIT:C79821 Urethral Stricture semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002128 mononeuritis multiplex skos:exactMatch NCIT:C70938 Mononeuritis Multiplex semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002129 bone cancer skos:exactMatch NCIT:C4016 Malignant Bone Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002132 skull cancer skos:exactMatch NCIT:C155790 Malignant Skull Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002135 optic nerve disorder skos:exactMatch NCIT:C79698 Optic Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002140 vagina sarcoma skos:exactMatch NCIT:C7737 Vaginal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002141 cutaneous undifferentiated pleomorphic sarcoma skos:exactMatch NCIT:C5576 Skin Undifferentiated Pleomorphic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002142 undifferentiated pleomorphic sarcoma skos:exactMatch NCIT:C114541 Adult Undifferentiated Pleomorphic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002142 undifferentiated pleomorphic sarcoma skos:exactMatch NCIT:C4247 Undifferentiated Pleomorphic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002143 vaginal yolk sac tumor skos:exactMatch NCIT:C6379 Vaginal Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002145 disorder of sexual differentiation skos:exactMatch NCIT:C103186 Sexual Differentiation Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002146 hypogonadism skos:exactMatch NCIT:C9227 Hypogonadism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002149 reproductive system cancer skos:exactMatch NCIT:C36076 Malignant Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002153 telogen effluvium skos:exactMatch NCIT:C112200 Telogen Effluvium semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002154 trichomoniasis skos:exactMatch NCIT:C35720 Trichomonas Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002155 cholecystitis skos:exactMatch NCIT:C34465 Cholecystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002156 fallopian tube disorder skos:exactMatch NCIT:C26771 Fallopian Tube Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002158 fallopian tube cancer skos:exactMatch NCIT:C7480 Malignant Fallopian Tube Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002159 fallopian tube leiomyosarcoma skos:exactMatch NCIT:C40128 Fallopian Tube Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002162 fallopian tube adenosarcoma skos:exactMatch NCIT:C40125 Fallopian Tube Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002163 thymus lipoma skos:exactMatch NCIT:C6452 Thymolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002165 rectal neoplasm skos:exactMatch NCIT:C3350 Rectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002166 rectum lymphoma skos:exactMatch NCIT:C5553 Rectal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002167 rectum malignant melanoma skos:exactMatch NCIT:C4640 Rectal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002168 rectum sarcoma skos:exactMatch NCIT:C5548 Rectal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002169 rectum adenocarcinoma skos:exactMatch NCIT:C9383 Rectal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002171 giant cell tumor skos:exactMatch NCIT:C3055 Giant Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002173 neuroma skos:exactMatch NCIT:C3275 Neuroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002178 placenta cancer skos:exactMatch NCIT:C3555 Malignant Placental Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002181 exostosis skos:exactMatch NCIT:C3029 Exostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002182 communication disorder skos:exactMatch NCIT:C2958 Communication Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002185 hyperostosis skos:exactMatch NCIT:C34712 Hyperostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002187 vulvar disease skos:exactMatch NCIT:C27631 Vulvar Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002188 vulvar nodular hidradenoma skos:exactMatch NCIT:C40312 Vulvar Nodular Hidradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002189 nodular hidradenoma skos:exactMatch NCIT:C7568 Nodular Hidradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002190 vulvar syringoma skos:exactMatch NCIT:C40311 Vulvar Syringoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002191 syringoma skos:exactMatch NCIT:C3761 Syringoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002192 vulvar angiokeratoma skos:exactMatch NCIT:C8596 Vulvar Angiokeratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002194 vestibular papilloma skos:exactMatch NCIT:C6376 Vulvar Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002195 vulvar squamous neoplasm skos:exactMatch NCIT:C40283 Vulvar Squamous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002197 minor vestibular glands adenoma skos:exactMatch NCIT:C40301 Adenoma of Minor Vestibular Glands semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002198 vulvar glandular neoplasm skos:exactMatch NCIT:C40292 Vulvar Glandular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002199 benign mixed tumor of the vulva skos:exactMatch NCIT:C40302 Benign Mixed Tumor of the Vulva semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002200 eccrine mixed tumor of skin skos:exactMatch NCIT:C4474 Benign Mixed Tumor of the Skin semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002201 vulvar trichoepithelioma skos:exactMatch NCIT:C40314 Vulvar Trichoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002203 constipation disorder skos:exactMatch NCIT:C37930 Constipation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002205 vulvar melanoma skos:exactMatch NCIT:C40329 Vulvar Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002206 sweat gland cancer skos:exactMatch NCIT:C4810 Malignant Sweat Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002207 vulval Paget disease skos:exactMatch NCIT:C4027 Vulvar Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002211 B cell deficiency skos:exactMatch NCIT:C4799 Deficiency of Humoral Immunity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002214 brain germinoma skos:exactMatch NCIT:C6284 Brain Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002216 brain sarcoma skos:exactMatch NCIT:C5154 Brain Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002217 central nervous system sarcoma skos:exactMatch NCIT:C5153 Central Nervous System Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002221 urethral urothelial papilloma skos:exactMatch NCIT:C5061 Urethral Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002222 urethra leiomyoma skos:exactMatch NCIT:C6171 Urethral Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002223 ovarian malignant mesothelioma skos:exactMatch NCIT:C40444 Ovarian Malignant Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002224 malignant ovarian cyst skos:exactMatch NCIT:C3843 Malignant Ovarian Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002225 ovarian sarcoma skos:exactMatch NCIT:C8267 Ovarian Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002227 ovarian lymphoma skos:exactMatch NCIT:C40021 Ovarian Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002229 ovarian epithelial tumor skos:exactMatch NCIT:C4381 Ovarian Epithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002230 ovarian Wilms tumor skos:exactMatch NCIT:C40443 Ovarian Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002232 nasal cavity disorder skos:exactMatch NCIT:C27102 Nasal Cavity Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002234 vaginitis skos:exactMatch NCIT:C26911 Vaginitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002235 eyelid neoplasm skos:exactMatch NCIT:C3031 Eyelid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002236 ocular cancer skos:exactMatch NCIT:C4767 Malignant Eye Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002242 coagulation protein disease skos:exactMatch NCIT:C27215 Coagulation Factor Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002243 hemorrhagic disease skos:exactMatch NCIT:C115221 Bleeding Diathesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002245 blood platelet disease skos:exactMatch NCIT:C131634 Platelet Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002247 factor X deficiency skos:exactMatch NCIT:C131632 Factor X Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002249 thrombocytosis disease skos:exactMatch NCIT:C35530 Thrombocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002250 basilar artery insufficiency skos:exactMatch NCIT:C34413 Basilar Artery Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002251 hepatitis skos:exactMatch NCIT:C3095 Hepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002252 granulomatous hepatitis skos:exactMatch NCIT:C27015 Granulomatous Hepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002254 syndromic disease skos:exactMatch NCIT:C28193 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002256 cervix disorder skos:exactMatch NCIT:C40241 Cervical Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002258 pharyngitis skos:exactMatch NCIT:C26851 Pharyngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002259 gonadal disorder skos:exactMatch NCIT:C26786 Gonadal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002260 hidradenitis skos:exactMatch NCIT:C32132 Apocrine Sweat Gland semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002261 keratopathy skos:exactMatch NCIT:C27012 Keratopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002263 female reproductive system disorder skos:exactMatch NCIT:C27020 Female Reproductive System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002268 dyspepsia skos:exactMatch NCIT:C26756 Dyspepsia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002269 gastroenteritis skos:exactMatch NCIT:C34632 Gastroenteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002270 viral gastritis skos:exactMatch NCIT:C27184 Viral Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002271 colon adenocarcinoma skos:exactMatch NCIT:C4349 Colon Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002272 polyclonal hypergammaglobulinemia skos:exactMatch NCIT:C35885 Polyclonal Hypergammaglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002275 generalized atherosclerosis skos:exactMatch NCIT:C35767 Generalized Atherosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002277 arteriosclerosis disorder skos:exactMatch NCIT:C34398 Arteriosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002277 arteriosclerosis disorder skos:exactMatch NCIT:C34403 Arteriosclerotic Cardiovascular Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002278 benign colon neoplasm skos:exactMatch NCIT:C2894 Benign Colon Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002280 anemia skos:exactMatch NCIT:C2869 Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002281 macrocytic anemia skos:exactMatch NCIT:C34381 Macrocytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002283 neuroaxonal dystrophy skos:exactMatch NCIT:C161542 Neuroaxonal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002286 renal artery disease skos:exactMatch NCIT:C101254 Renal Artery Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002287 glandular cystitis skos:exactMatch NCIT:C39860 Cystitis Glandularis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002289 iris disorder skos:exactMatch NCIT:C34737 Iris Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002290 clitoris cancer skos:exactMatch NCIT:C3557 Malignant Clitoral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002291 cutaneous granular cell tumor skos:exactMatch NCIT:C5617 Cutaneous Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002293 cutaneous ganglioneuroma skos:exactMatch NCIT:C4481 Cutaneous Ganglioneuroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002295 skin glomus tumor skos:exactMatch NCIT:C4491 Skin Glomus Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002297 epidermal appendage tumor skos:exactMatch NCIT:C4463 Skin Appendage Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002298 cutaneous glomangioma skos:exactMatch NCIT:C6750 Skin Glomangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002299 glomangioma skos:exactMatch NCIT:C4222 Glomangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002300 dermis tumor skos:exactMatch NCIT:C4475 Dermal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002301 frontal sinus squamous cell carcinoma skos:exactMatch NCIT:C6067 Frontal Sinus Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002303 central retinal vein occlusion skos:exactMatch NCIT:C118859 Central Retinal Vein Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002304 protein S deficiency skos:exactMatch NCIT:C99026 Protein S Deficiency Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002305 thrombophilia skos:exactMatch NCIT:C84479 Thrombophilia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002307 blepharoconjunctivitis skos:exactMatch NCIT:C34430 Blepharoconjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002308 giant papillary conjunctivitis skos:exactMatch NCIT:C34507 Giant Papillary Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002309 papillary conjunctivitis skos:exactMatch NCIT:C35616 Papillary Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002311 retinal vascular disorder skos:exactMatch NCIT:C35170 Retinal Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002313 vernal conjunctivitis skos:exactMatch NCIT:C34508 Vernal Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002314 chronic conjunctivitis skos:exactMatch NCIT:C35197 Chronic Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002316 motor peripheral neuropathy skos:exactMatch NCIT:C3500 Peripheral Motor Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002318 trachea leiomyoma skos:exactMatch NCIT:C6049 Tracheal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002319 phosphorus metabolism disease skos:exactMatch NCIT:C97095 Phosphorus Metabolic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002320 congenital nervous system disorder skos:exactMatch NCIT:C97172 Congenital Nervous System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002321 sensory peripheral neuropathy skos:exactMatch NCIT:C3501 Peripheral Sensory Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002323 cherry hemangioma skos:exactMatch NCIT:C4390 Cherry Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002327 intracranial cavernous angioma skos:exactMatch NCIT:C5432 Intracranial Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002328 intracranial hemangioma skos:exactMatch NCIT:C3633 Intracranial Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002329 testicular disorder skos:exactMatch NCIT:C26890 Testicular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002332 splenic disorder skos:exactMatch NCIT:C35823 Splenic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002333 splenic abscess skos:exactMatch NCIT:C35347 Splenic Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002334 hematopoietic and lymphoid system neoplasm skos:exactMatch NCIT:C35813 Hematopoietic and Lymphatic System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002337 intra-abdominal hemangioma skos:exactMatch NCIT:C3635 Intra-Abdominal Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002338 extratemporal epilepsy skos:exactMatch NCIT:C7760 Extratemporal Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002340 tactile epilepsy skos:exactMatch NCIT:C4687 Tactile Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002341 granulomatous angiitis skos:exactMatch NCIT:C34653 Granulomatous Arteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002343 splenic hemangioma skos:exactMatch NCIT:C8541 Splenic Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002345 cervicitis skos:exactMatch NCIT:C26716 Cervicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002350 familial nephrotic syndrome skos:exactMatch NCIT:C35337 Congenital Nephrotic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002351 glottis cancer skos:exactMatch NCIT:C3544 Malignant Glottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002352 larynx cancer skos:exactMatch NCIT:C7484 Malignant Laryngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002353 glottis neoplasm skos:exactMatch NCIT:C4425 Glottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002354 benign laryngeal neoplasm skos:exactMatch NCIT:C3601 Benign Laryngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002355 glottis carcinoma skos:exactMatch NCIT:C4923 Glottis Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002356 pancreas disorder skos:exactMatch NCIT:C26842 Pancreatic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002358 laryngeal carcinoma skos:exactMatch NCIT:C4855 Laryngeal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002359 periosteal chondroma skos:exactMatch NCIT:C4302 Periosteal Chondroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002360 chondroma skos:exactMatch NCIT:C53459 Chondroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002362 serous surface papilloma skos:exactMatch NCIT:C4181 Serous Surface Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002363 papilloma skos:exactMatch NCIT:C7440 Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002365 kidney hemangiopericytoma skos:exactMatch NCIT:C4527 Kidney Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002366 autonomic nervous system neoplasm skos:exactMatch NCIT:C5112 Autonomic Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002367 kidney cancer skos:exactMatch NCIT:C7548 Malignant Kidney Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch NCIT:C8377 Papillary Serous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002369 cystadenoma skos:exactMatch NCIT:C2972 Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002370 ovarian Brenner tumor skos:exactMatch NCIT:C3872 Ovarian Brenner Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002371 breast pericanalicular fibroadenoma skos:exactMatch NCIT:C4272 Breast Pericanalicular Fibroadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002372 ovarian monodermal and highly specialized teratoma skos:exactMatch NCIT:C8113 Ovarian Monodermal and Highly Specialized Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002375 sebaceous adenoma skos:exactMatch NCIT:C4174 Sebaceous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002376 spleen angiosarcoma skos:exactMatch NCIT:C4564 Splenic Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002377 breast intracanalicular fibroadenoma skos:exactMatch NCIT:C4271 Breast Intracanalicular Fibroadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002378 dermoid cyst skos:exactMatch NCIT:C9011 Dermoid Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002379 cystic teratoma skos:exactMatch NCIT:C9014 Cystic Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002380 myoepithelial tumor skos:exactMatch NCIT:C40392 Myoepithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002381 sweat gland neoplasm skos:exactMatch NCIT:C3398 Sweat Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002382 benign mesenchymoma skos:exactMatch NCIT:C4267 Benign Mesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002383 Pacinian tumor skos:exactMatch NCIT:C4328 Pacinian Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002385 benign cystic nephroma skos:exactMatch NCIT:C7504 Adult Cystic Nephroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002386 mixed epithelial stromal tumor of the kidney skos:exactMatch NCIT:C37263 Kidney Mixed Epithelial and Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002387 liver angiosarcoma skos:exactMatch NCIT:C4438 Liver Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002395 renal adenoma skos:exactMatch NCIT:C8383 Kidney Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002396 nephrogenic adenofibroma skos:exactMatch NCIT:C39812 Metanephric Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002397 liver sarcoma skos:exactMatch NCIT:C4437 Liver Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002398 mucinous adenofibroma skos:exactMatch NCIT:C8978 Mucinous Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002399 tenosynovial giant cell tumor, localized type skos:exactMatch NCIT:C6532 Tenosynovial Giant Cell Tumor, Localized Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002400 synovitis skos:exactMatch NCIT:C50766 Synovitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002401 malignant tenosynovial giant cell tumor skos:exactMatch NCIT:C6535 Malignant Tenosynovial Giant Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002402 malignant giant cell tumor skos:exactMatch NCIT:C4090 Malignant Giant Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002403 synovium cancer skos:exactMatch NCIT:C6531 Malignant Synovial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002404 liver hemangioma skos:exactMatch NCIT:C3869 Liver Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002405 hepatic vascular disorder skos:exactMatch NCIT:C35442 Liver Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002406 dermatitis skos:exactMatch NCIT:C2983 Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002407 capillary hemangioma skos:exactMatch NCIT:C7457 Capillary Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002408 hereditary hyperbilirubinemia skos:exactMatch NCIT:C84761 Hereditary Hyperbilirubinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002411 narcissistic personality disorder skos:exactMatch NCIT:C92635 Narcissistic Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002412 disorder of glycogen metabolism skos:exactMatch NCIT:C61272 Glycogen Storage Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002413 glycogen storage disease I skos:exactMatch NCIT:C84733 Glycogen Storage Disease Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002414 gastric hemangioma skos:exactMatch NCIT:C5481 Gastric Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002416 ethmoid sinus squamous cell carcinoma skos:exactMatch NCIT:C6065 Ethmoid Sinus Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002418 ethmoid sinus adenocarcinoma skos:exactMatch NCIT:C6237 Ethmoid Sinus Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002419 transient tic disorder skos:exactMatch NCIT:C116767 Transient Tic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002422 adamantinoma skos:exactMatch NCIT:C7644 Adamantinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002423 rectosigmoid junction neoplasm skos:exactMatch NCIT:C4877 Rectosigmoid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002424 rectosigmoid carcinoma skos:exactMatch NCIT:C7421 Rectosigmoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002425 rectosigmoid junction cancer skos:exactMatch NCIT:C7420 Malignant Rectosigmoid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002426 lung sarcoma skos:exactMatch NCIT:C4860 Lung Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002428 protozoa infectious disease skos:exactMatch NCIT:C34953 Protozoal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002429 idiopathic interstitial pneumonia skos:exactMatch NCIT:C35714 Idiopathic Interstitial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002432 malignant neoplasm of acoustic nerve skos:exactMatch NCIT:C4539 Malignant Vestibulocochlear Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002433 malignant cranial nerve neoplasm skos:exactMatch NCIT:C3571 Malignant Cranial Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002434 oculomotor nerve cancer skos:exactMatch NCIT:C6995 Malignant Oculomotor Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002435 oculomotor nerve neoplasm skos:exactMatch NCIT:C6994 Oculomotor Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002437 dehydration polycythemia skos:exactMatch NCIT:C27310 Dehydration Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002440 erythropoietin polycythemia skos:exactMatch NCIT:C35434 Polycythaemia due to Excess Erythropoetin Production semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002441 Jervell and Lange-Nielsen syndrome skos:exactMatch NCIT:C84793 Jervell and Lange Nielsen Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002442 long QT syndrome skos:exactMatch NCIT:C34786 Long QT Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002444 melancholia skos:exactMatch NCIT:C34812 Melancholic Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002447 endometrial carcinoma skos:exactMatch NCIT:C7558 Endometrial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002448 laryngeal sarcoma skos:exactMatch NCIT:C6020 Laryngeal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002450 prostatic adenoma skos:exactMatch NCIT:C4795 Prostate Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002451 benign prostate phyllodes tumor skos:exactMatch NCIT:C5532 Benign Prostate Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002452 prostate leiomyoma skos:exactMatch NCIT:C5544 Prostate Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002455 exocervical carcinoma skos:exactMatch NCIT:C7453 Exocervical Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002457 Treacher-Collins syndrome skos:exactMatch NCIT:C75018 Treacher Collins Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002459 type IV hypersensitivity disease skos:exactMatch NCIT:C3115 Type IV Hypersensitivity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002460 lacrimal system cancer skos:exactMatch NCIT:C5102 Lacrimal System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002461 membranoproliferative glomerulonephritis skos:exactMatch NCIT:C34644 Membranoproliferative Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002462 glomerulonephritis skos:exactMatch NCIT:C26784 Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002463 lacrimal gland carcinoma skos:exactMatch NCIT:C6129 Lacrimal Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002464 lacrimal gland cancer skos:exactMatch NCIT:C3563 Malignant Lacrimal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002465 bronchiolitis skos:exactMatch NCIT:C39658 Bronchiolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002466 eye carcinoma skos:exactMatch NCIT:C6079 Eye Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002467 inner ear disorder skos:exactMatch NCIT:C27166 Inner Ear Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002468 hyperimmunoglobulin syndrome skos:exactMatch NCIT:C27579 Hyperimmunoglobulin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002469 lacrimal gland carcinoma ex pleomorphic adenoma skos:exactMatch NCIT:C6804 Lacrimal Gland Carcinoma ex Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002471 bursitis skos:exactMatch NCIT:C94407 Bursitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002472 carcinoma ex pleomorphic adenoma skos:exactMatch NCIT:C4397 Carcinoma ex Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002473 cystic kidney disease skos:exactMatch NCIT:C34750 Cystic Kidney Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002474 primary hyperoxaluria skos:exactMatch NCIT:C123158 Primary Hyperoxaluria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002475 lacrimal gland adenocarcinoma skos:exactMatch NCIT:C4541 Lacrimal Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002477 prostate neuroendocrine neoplasm skos:exactMatch NCIT:C5545 Prostate Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002478 mixed germ cell-sex cord-stromal tumor skos:exactMatch NCIT:C5241 Mixed Germ Cell-Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002480 endometrioid tumor skos:exactMatch NCIT:C7113 Endometrioid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002481 ovarian neuroendocrine neoplasm skos:exactMatch NCIT:C5237 Ovarian Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002482 nipple neoplasm skos:exactMatch NCIT:C5212 Nipple Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002483 breast myoepithelial tumor skos:exactMatch NCIT:C40389 Breast Myoepithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002485 breast neuroendocrine neoplasm skos:exactMatch NCIT:C5169 Breast Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002486 lobular neoplasia skos:exactMatch NCIT:C27939 Breast Lobular Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002487 breast granular cell tumor skos:exactMatch NCIT:C40400 Breast Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002488 intraductal breast neoplasm skos:exactMatch NCIT:C36083 Breast Intraductal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002489 malignant breast phyllodes tumor skos:exactMatch NCIT:C4504 Malignant Breast Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002490 breast sarcoma skos:exactMatch NCIT:C4670 Breast Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002492 acute kidney failure skos:exactMatch NCIT:C26808 Acute Renal Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002493 prostatic acinar adenocarcinoma skos:exactMatch NCIT:C5596 Prostate Acinar Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002494 substance-related disorder skos:exactMatch NCIT:C92203 Substance-Related Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002495 colon signet ring cell adenocarcinoma skos:exactMatch NCIT:C7967 Colon Signet Ring Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002496 submucosal invasive colon adenocarcinoma skos:exactMatch NCIT:C38760 Submucosal Invasive Colon Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002501 brain glioblastoma skos:exactMatch NCIT:C4642 Brain Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002503 adult astrocytic tumor skos:exactMatch NCIT:C7049 Adult Astrocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002505 childhood astrocytic tumor skos:exactMatch NCIT:C9022 Childhood Astrocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002508 gingivitis skos:exactMatch NCIT:C34636 Gingivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002509 non-specific granulomatous orchitis skos:exactMatch NCIT:C27162 Non-Specific Granulomatous Orchitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002512 papillary adenocarcinoma skos:exactMatch NCIT:C2853 Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002513 kidney benign neoplasm skos:exactMatch NCIT:C4778 Benign Kidney Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002514 hepatobiliary neoplasm skos:exactMatch NCIT:C8614 Hepatobiliary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002515 hepatobiliary disorder skos:exactMatch NCIT:C3959 Hepatobiliary Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002516 digestive system cancer skos:exactMatch NCIT:C4890 Malignant Digestive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002518 gallbladder papillary neoplasm skos:exactMatch NCIT:C7130 Gallbladder Intracholecystic Papillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002519 anus disorder skos:exactMatch NCIT:C26695 Anal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002522 tenosynovial giant cell tumor skos:exactMatch NCIT:C3402 Tenosynovial Giant Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002525 inherited lipid metabolism disorder skos:exactMatch NCIT:C97092 Lipid Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002527 keratoacanthoma skos:exactMatch NCIT:C3146 Keratoacanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002528 synovium neoplasm skos:exactMatch NCIT:C8964 Synovial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002529 skin squamous cell carcinoma skos:exactMatch NCIT:C4819 Skin Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002531 skin neoplasm skos:exactMatch NCIT:C3372 Skin Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002532 squamous cell neoplasm skos:exactMatch NCIT:C3792 Squamous Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002533 papillary adenoma skos:exactMatch NCIT:C79951 Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002534 fallopian tube papilloma skos:exactMatch NCIT:C40112 Fallopian Tube Serous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002535 verrucous papilloma skos:exactMatch NCIT:C4101 Verrucous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002536 skin papilloma skos:exactMatch NCIT:C4614 Skin Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002537 inverted papilloma skos:exactMatch NCIT:C3793 Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002540 childhood oligodendroglioma skos:exactMatch NCIT:C4045 Childhood Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002541 spinal cord oligodendroglioma skos:exactMatch NCIT:C4535 Spinal Cord Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002542 spinal cord glioma skos:exactMatch NCIT:C4534 Spinal Cord Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002543 adult oligodendroglioma skos:exactMatch NCIT:C4014 Adult Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002544 brain oligodendroglioma skos:exactMatch NCIT:C9377 Brain Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002545 spinal cord disorder skos:exactMatch NCIT:C97110 Spinal Cord Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002546 schwannoma skos:exactMatch NCIT:C3269 Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002547 nerve sheath neoplasm skos:exactMatch NCIT:C4972 Nerve Sheath Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002548 cellular schwannoma skos:exactMatch NCIT:C4724 Cellular Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002549 schwannoma of twelfth cranial nerve skos:exactMatch NCIT:C5434 Schwannoma of the Twelfth Cranial Nerve semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002550 hypoglossal nerve neoplasm skos:exactMatch NCIT:C5830 Hypoglossal Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002551 c-P angle neurinoma skos:exactMatch NCIT:C5413 Cerebellopontine Angle Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002553 cerebellopontine angle tumor skos:exactMatch NCIT:C5414 Cerebellopontine Angle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002554 sympathetic neurilemmoma skos:exactMatch NCIT:C5421 Sympathetic Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002555 trigeminal schwannoma skos:exactMatch NCIT:C4655 Trigeminal Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002556 microcystic/reticular schwannoma skos:exactMatch NCIT:C5321 Microcystic/Reticular Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002558 melanotic neurilemmoma skos:exactMatch NCIT:C6970 Melanotic Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002559 plexiform schwannoma skos:exactMatch NCIT:C6969 Plexiform Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002561 lysosomal storage disease skos:exactMatch NCIT:C61250 Lysosomal Storage Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002562 demyelinating disease skos:exactMatch NCIT:C34527 Demyelinating Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002563 jejunal somatostatinoma skos:exactMatch NCIT:C5787 Jejunal Somatostatin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002564 jejunal neoplasm skos:exactMatch NCIT:C8401 Jejunal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002565 myelitis skos:exactMatch NCIT:C26832 Myelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002567 tracheal disorder skos:exactMatch NCIT:C35079 Tracheal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002568 tracheal stenosis skos:exactMatch NCIT:C78646 Tracheal Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002571 primary central nervous system lymphoma skos:exactMatch NCIT:C9301 Central Nervous System Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002572 aspiration pneumonitis skos:exactMatch NCIT:C34932 Aspiration Pneumonitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002574 prostate embryonal rhabdomyosarcoma skos:exactMatch NCIT:C5525 Prostate Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002576 embryonal extrahepatic bile duct rhabdomyosarcoma skos:exactMatch NCIT:C5847 Extrahepatic Bile Duct Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002577 extrahepatic bile duct rhabdomyosarcoma skos:exactMatch NCIT:C5860 Extrahepatic Bile Duct Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002578 botryoid rhabdomyosarcoma skos:exactMatch NCIT:C9150 Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002579 orbit embryonal rhabdomyosarcoma skos:exactMatch NCIT:C6246 Orbit Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002580 orbit rhabdomyosarcoma skos:exactMatch NCIT:C4543 Orbit Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002581 spindle cell rhabdomyosarcoma skos:exactMatch NCIT:C6519 Spindle Cell Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002583 mucinous ovarian cystadenoma skos:exactMatch NCIT:C4512 Ovarian Mucinous Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002585 breast fibrocystic change, proliferative type skos:exactMatch NCIT:C6940 Breast Fibrocystic Change, Proliferative Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002586 thymus cancer skos:exactMatch NCIT:C4962 Malignant Thymus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002587 encapsulated thymoma skos:exactMatch NCIT:C7386 Encapsulated Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002588 thymoma type A skos:exactMatch NCIT:C6454 Thymoma Type A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002592 invasive malignant thymoma skos:exactMatch NCIT:C7904 Invasive Malignant Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002594 monkeypox skos:exactMatch NCIT:C128421 Monkeypox semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002597 notochordal tumor skos:exactMatch NCIT:C7063 Notochordal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002599 teratocarcinoma skos:exactMatch NCIT:C3756 Mixed Embryonal Carcinoma and Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002601 teratoma skos:exactMatch NCIT:C3403 Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002602 central nervous system disorder skos:exactMatch NCIT:C2934 Central Nervous System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002603 angiomyolipoma skos:exactMatch NCIT:C3734 Angiomyolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002604 pericytic neoplasm skos:exactMatch NCIT:C6528 Pericytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002605 hepatic angiomyolipoma skos:exactMatch NCIT:C27485 Liver Angiomyolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002606 epithelioid type angiomyolipoma skos:exactMatch NCIT:C38151 Epithelioid Angiomyolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002613 histrionic personality disorder skos:exactMatch NCIT:C92634 Histrionic Personality Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002616 mesenchymal cell neoplasm skos:exactMatch NCIT:C7059 Mesenchymal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002617 bone angiosarcoma skos:exactMatch NCIT:C6479 Bone Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002618 undifferentiated high grade pleomorphic sarcoma of bone skos:exactMatch NCIT:C8563 Undifferentiated High Grade Pleomorphic Sarcoma of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002619 bone fibrosarcoma skos:exactMatch NCIT:C6604 Bone Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002620 localized osteosarcoma skos:exactMatch NCIT:C7780 Localized Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002621 extraosseous osteosarcoma skos:exactMatch NCIT:C8810 Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002622 multifocal osteogenic sarcoma skos:exactMatch NCIT:C6470 Multifocal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002623 pediatric osteosarcoma skos:exactMatch NCIT:C6585 Childhood Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002624 bone leiomyosarcoma skos:exactMatch NCIT:C7154 Bone Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002625 Ewing sarcoma of bone skos:exactMatch NCIT:C4835 Ewing Sarcoma of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002626 spinal accessory nerve neoplasm skos:exactMatch NCIT:C5829 Accessory Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002627 chondroblastic osteosarcoma skos:exactMatch NCIT:C4021 Chondroblastic Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002628 peripheral osteosarcoma skos:exactMatch NCIT:C7134 Bone Surface (Peripheral) Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002629 bone osteosarcoma skos:exactMatch NCIT:C53707 Bone Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002630 small cell osteogenic sarcoma skos:exactMatch NCIT:C4023 Small Cell Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002631 conventional osteosarcoma skos:exactMatch NCIT:C35870 Conventional Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002632 metachronous osteosarcoma of the bone skos:exactMatch NCIT:C38157 Metachronous Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002633 cranial nerve neoplasm skos:exactMatch NCIT:C2963 Cranial Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002634 liposarcoma of bone skos:exactMatch NCIT:C7598 Bone Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002635 periodontal disorder skos:exactMatch NCIT:C63743 Periodontal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002636 accessory nerve disorder skos:exactMatch NCIT:C26953 Accessory Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002637 histiocytosis skos:exactMatch NCIT:C3106 Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002638 glossopharyngeal nerve neoplasm skos:exactMatch NCIT:C5828 Glossopharyngeal Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002639 glossopharyngeal nerve disorder skos:exactMatch NCIT:C27211 Glossopharyngeal Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002640 optic nerve neoplasm skos:exactMatch NCIT:C4801 Optic Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002642 trochlear nerve neoplasm skos:exactMatch NCIT:C5825 Trochlear Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002644 idiopathic granulomatous myositis skos:exactMatch NCIT:C27575 Idiopathic Granulomatous Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002645 cerebritis skos:exactMatch NCIT:C27199 Cerebritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002646 viral laryngitis skos:exactMatch NCIT:C27305 Viral Laryngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002647 laryngitis skos:exactMatch NCIT:C26811 Laryngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002648 mammary Paget disease skos:exactMatch NCIT:C47857 Breast Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002649 scrotum Paget disease skos:exactMatch NCIT:C7728 Scrotal Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002650 scrotal carcinoma skos:exactMatch NCIT:C6389 Scrotal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002651 anal Paget disease skos:exactMatch NCIT:C5598 Anal Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002652 anus adenocarcinoma skos:exactMatch NCIT:C5600 Anal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002653 Paget disease of the penis skos:exactMatch NCIT:C27817 Penile Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002654 uterine disorder skos:exactMatch NCIT:C26907 Uterine Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002656 skin carcinoma skos:exactMatch NCIT:C4914 Skin Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002657 breast disorder skos:exactMatch NCIT:C26709 Breast Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002658 iris cancer skos:exactMatch NCIT:C4554 Malignant Iris Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002659 uveal cancer skos:exactMatch NCIT:C6105 Malignant Uveal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002661 uveal disorder skos:exactMatch NCIT:C26908 Uveal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002664 extrahepatic bile duct signet ring cell carcinoma skos:exactMatch NCIT:C5776 Extrahepatic Bile Duct Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002665 extrahepatic bile duct adenocarcinoma skos:exactMatch NCIT:C7975 Extrahepatic Bile Duct Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002666 pancreatic signet ring cell adenocarcinoma skos:exactMatch NCIT:C5720 Pancreatic Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002667 gallbladder signet ring cell adenocarcinoma skos:exactMatch NCIT:C5745 Gallbladder Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002669 ampullary signet ring cell adenocarcinoma skos:exactMatch NCIT:C6656 Ampulla of Vater Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002670 ampulla of vater adenocarcinoma skos:exactMatch NCIT:C6650 Ampulla of Vater Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002671 signet ring cell breast carcinoma skos:exactMatch NCIT:C5175 Breast Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002672 acinar prostate adenocarcinoma, signet ring variant skos:exactMatch NCIT:C5535 Prostate Acinar Signet Ring Cell-Like Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002676 adult fibrosarcoma skos:exactMatch NCIT:C7809 Adult Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002677 conventional fibrosarcoma skos:exactMatch NCIT:C9429 Conventional Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002678 pediatric fibrosarcoma skos:exactMatch NCIT:C8088 Childhood Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002679 cerebral infarction skos:exactMatch NCIT:C50486 Cerebral Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002681 choroid plexus cancer skos:exactMatch NCIT:C4533 Malignant Choroid Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002682 cerebral ventricle cancer skos:exactMatch NCIT:C2937 Intraventricular Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002683 adult choroid plexus neoplasm skos:exactMatch NCIT:C8568 Adult Choroid Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002684 atypical choroid plexus papilloma skos:exactMatch NCIT:C53686 Atypical Choroid Plexus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002685 childhood choroid plexus carcinoma skos:exactMatch NCIT:C124292 Childhood Choroid Plexus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002687 superior mesenteric artery syndrome skos:exactMatch NCIT:C85175 Superior Mesenteric Artery Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002691 liver cancer skos:exactMatch NCIT:C34803 Primary Malignant Liver Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002696 Sertoli cell tumor skos:exactMatch NCIT:C39976 Sertoli Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002697 ovarian gonadoblastoma skos:exactMatch NCIT:C39985 Ovarian Gonadoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002698 testicular gonadoblastoma skos:exactMatch NCIT:C39911 Testicular Gonadoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002701 ovarian mucinous cystadenocarcinoma skos:exactMatch NCIT:C4026 Ovarian Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002702 ovarian cystadenocarcinoma skos:exactMatch NCIT:C5228 Ovarian Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002703 appendix mucinous cystadenocarcinoma skos:exactMatch NCIT:C5511 Appendix Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002705 breast mucinous cystadenocarcinoma skos:exactMatch NCIT:C40354 Breast Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002706 cervix endometriosis skos:exactMatch NCIT:C27623 Cervical Endometriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002707 breast mucinous carcinoma skos:exactMatch NCIT:C9131 Breast Mucinous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002708 retinitis skos:exactMatch NCIT:C115993 Retinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002710 infiltrating angiolipoma skos:exactMatch NCIT:C7449 Infiltrating Angiolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002712 epidural spinal canal angiolipoma skos:exactMatch NCIT:C5424 Epidural Spinal Canal Angiolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002713 epidural spinal canal neoplasm skos:exactMatch NCIT:C3019 Epidural Spinal Canal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002714 central nervous system cancer skos:exactMatch NCIT:C4627 Malignant Central Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002715 uterine cancer skos:exactMatch NCIT:C3552 Malignant Uterine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002716 childhood spinal cord tumor skos:exactMatch NCIT:C9234 Childhood Spinal Cord Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002717 spinal cord intramedullary teratoma skos:exactMatch NCIT:C5428 Intramedullary Spinal Cord Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002718 central nervous system teratoma skos:exactMatch NCIT:C5441 Central Nervous System Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002719 conus medullaris neoplasm skos:exactMatch NCIT:C5443 Conus Medullaris Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002720 sella turcica neoplasm skos:exactMatch NCIT:C4944 Sellar Region Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002721 necrosis of pituitary skos:exactMatch NCIT:C27066 Pituitary Gland Necrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002722 olfactory nerve neoplasm skos:exactMatch NCIT:C5121 Olfactory Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002724 mast cell neoplasm skos:exactMatch NCIT:C9295 Mast Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002726 cutaneous solitary mastocytoma skos:exactMatch NCIT:C7138 Solitary Mastocytoma of the Skin semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002727 olfactory nerve disorder skos:exactMatch NCIT:C27210 Olfactory Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002728 rhabdoid tumor skos:exactMatch NCIT:C3808 Rhabdoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002729 rhabdoid tumor of the kidney skos:exactMatch NCIT:C8715 Rhabdoid Tumor of the Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002730 childhood kidney neoplasm skos:exactMatch NCIT:C6563 Childhood Kidney Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002731 cerebral hemisphere cancer skos:exactMatch NCIT:C4577 Malignant Cerebral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002732 lung benign neoplasm skos:exactMatch NCIT:C4454 Benign Lung Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002734 anal mucinous adenocarcinoma skos:exactMatch NCIT:C5606 Anal Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002735 anal canal adenocarcinoma skos:exactMatch NCIT:C7471 Anal Canal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002736 ampulla of vater mucinous adenocarcinoma skos:exactMatch NCIT:C27416 Ampulla of Vater Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002739 extrahepatic bile duct mucinous adenocarcinoma skos:exactMatch NCIT:C5846 Extrahepatic Bile Duct Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002740 uterine ligament mucinous adenocarcinoma skos:exactMatch NCIT:C40137 Broad Ligament Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002741 uterine ligament adenocarcinoma skos:exactMatch NCIT:C40135 Broad Ligament Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002742 cervical mucinous adenocarcinoma skos:exactMatch NCIT:C36095 Cervical Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002744 fallopian tube mucinous adenocarcinoma skos:exactMatch NCIT:C40103 Fallopian Tube Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002745 fallopian tube mucinous tumor skos:exactMatch NCIT:C40109 Fallopian Tube Mucinous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002746 fallopian tube adenocarcinoma skos:exactMatch NCIT:C6265 Fallopian Tube Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002747 endometrial mucinous adenocarcinoma skos:exactMatch NCIT:C40144 Endometrial Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002748 rectum mucinous adenocarcinoma skos:exactMatch NCIT:C7973 Rectal Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002749 extracranial neuroblastoma skos:exactMatch NCIT:C5437 Extracranial Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002750 bladder colloid adenocarcinoma skos:exactMatch NCIT:C39837 Bladder Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002751 bladder adenocarcinoma skos:exactMatch NCIT:C4032 Bladder Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002752 ovarian adenocarcinoma skos:exactMatch NCIT:C7700 Ovarian Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002754 extramedullary plasmacytoma skos:exactMatch NCIT:C4002 Extraosseous Plasmacytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002755 solitary osseous plasmacytoma skos:exactMatch NCIT:C7812 Solitary Plasmacytoma of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002756 solitary plasmacytoma of chest wall skos:exactMatch NCIT:C6711 Chest Wall Solitary Plasmacytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002758 vulva verrucous carcinoma skos:exactMatch NCIT:C6383 Vulvar Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002759 bladder verrucous carcinoma skos:exactMatch NCIT:C39832 Bladder Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002760 bladder squamous cell carcinoma skos:exactMatch NCIT:C4031 Bladder Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002761 cervical verrucous carcinoma skos:exactMatch NCIT:C40190 Cervical Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002762 esophagus verrucous carcinoma skos:exactMatch NCIT:C27420 Esophageal Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002763 urethral verrucous carcinoma skos:exactMatch NCIT:C39874 Urethral Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002764 urethra squamous cell carcinoma skos:exactMatch NCIT:C6165 Urethral Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002765 plantar verrucous skin carcinoma skos:exactMatch NCIT:C6811 Plantar Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002766 larynx verrucous carcinoma skos:exactMatch NCIT:C8188 Laryngeal Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002768 true hermaphroditism skos:exactMatch NCIT:C85207 True Hermaphroditism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002770 vaginal discharge skos:exactMatch NCIT:C50795 Abnormal Vaginal Discharge semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002771 pulmonary fibrosis skos:exactMatch NCIT:C26869 Pulmonary Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002772 intraventricular meningioma skos:exactMatch NCIT:C5273 Intraventricular Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002776 external ear disorder skos:exactMatch NCIT:C26972 External Ear Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002778 epidural spinal canal meningioma skos:exactMatch NCIT:C5310 Epidural Spinal Canal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002779 central nervous system chondroma skos:exactMatch NCIT:C7001 Central Nervous System Chondroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002781 glossopharyngeal nerve paralysis skos:exactMatch NCIT:C27335 Cranial Nerve IX Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002782 cranial nerve palsy skos:exactMatch NCIT:C26941 Cranial Nerve Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002785 skull base neoplasm skos:exactMatch NCIT:C4676 Skull Base Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002786 diencephalic cancer skos:exactMatch NCIT:C5126 Malignant Diencephalic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002787 adamantinous craniopharyngioma skos:exactMatch NCIT:C4726 Adamantinomatous Craniopharyngioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002788 papillary craniopharyngioma skos:exactMatch NCIT:C4725 Papillary Craniopharyngioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002789 hemangiopericytic tumor skos:exactMatch NCIT:C7076 Hemangiopericytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002790 seminal vesicle tumor skos:exactMatch NCIT:C39908 Seminal Vesicle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002791 large cell medulloblastoma skos:exactMatch NCIT:C6904 Large Cell Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002792 cerebellar vermis medulloblastoma skos:exactMatch NCIT:C5401 Cerebellar Vermis Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002794 adult medulloblastoma skos:exactMatch NCIT:C4011 Adult Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002795 adult central nervous system primitive neuroectodermal neoplasm skos:exactMatch NCIT:C5411 Adult Central Nervous System Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002796 melanotic medulloblastoma skos:exactMatch NCIT:C9497 Melanocytic Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002797 childhood medulloblastoma skos:exactMatch NCIT:C3997 Childhood Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002798 childhood central nervous system primitive neuroectodermal neoplasm skos:exactMatch NCIT:C5961 Childhood Central Nervous System Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002800 thrombophlebitis skos:exactMatch NCIT:C3410 Thrombophlebitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002803 intestinal pseudo-obstruction skos:exactMatch NCIT:C34733 Intestinal Pseudo-Obstruction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002804 apocrine adenoma skos:exactMatch NCIT:C4168 Apocrine Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002805 hidradenoma skos:exactMatch NCIT:C7563 Hidradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002806 bronchogenic carcinoma skos:exactMatch NCIT:C35875 Bronchogenic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002808 pancreatic serous cystadenoma skos:exactMatch NCIT:C5712 Pancreatic Serous Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002809 pancreatic cystadenoma skos:exactMatch NCIT:C4374 Pancreatic Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002810 pancreatic serous cystic neoplasm skos:exactMatch NCIT:C41248 Pancreatic Serous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002815 acute myocarditis skos:exactMatch NCIT:C35206 Acute Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002817 adrenal gland cancer skos:exactMatch NCIT:C9338 Malignant Adrenal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002822 trabecular adenocarcinoma skos:exactMatch NCIT:C4068 Trabecular Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002828 Bartholin gland transitional cell carcinoma skos:exactMatch NCIT:C40297 Bartholin Gland Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002829 bartholin gland carcinoma skos:exactMatch NCIT:C9055 Bartholin Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002831 non-keratinizing sinonasal squamous cell carcinoma skos:exactMatch NCIT:C54287 Sinonasal Non-Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002832 endometrial transitional cell carcinoma skos:exactMatch NCIT:C40154 Endometrial Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002833 fallopian tube transitional cell carcinoma skos:exactMatch NCIT:C40104 Fallopian Tube Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002834 primary prostate urothelial carcinoma skos:exactMatch NCIT:C39898 Primary Prostate Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002836 urethra transitional cell carcinoma skos:exactMatch NCIT:C6166 Urethral Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002837 sarcomatoid transitional cell carcinoma skos:exactMatch NCIT:C4120 Sarcomatoid Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002840 eosinophilic gastritis skos:exactMatch NCIT:C27052 Eosinophilic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002842 bacterial gastritis skos:exactMatch NCIT:C27340 Bacterial Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002843 fungal gastritis skos:exactMatch NCIT:C27342 Fungal Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002844 lymphocytic gastritis skos:exactMatch NCIT:C27051 Lymphocytic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002845 necrotizing gastritis skos:exactMatch NCIT:C27329 Necrotizing Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002846 granulomatous gastritis skos:exactMatch NCIT:C27348 Granulomatous Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002847 skeletal muscle cancer skos:exactMatch NCIT:C6516 Malignant Skeletal Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002848 skeletal muscle neoplasm skos:exactMatch NCIT:C6514 Skeletal Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002849 liver rhabdomyosarcoma skos:exactMatch NCIT:C5834 Liver Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002850 central nervous system rhabdomyosarcoma skos:exactMatch NCIT:C5464 Central Nervous System Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002851 mediastinum rhabdomyosarcoma skos:exactMatch NCIT:C6617 Mediastinal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002852 mediastinum sarcoma skos:exactMatch NCIT:C6606 Mediastinal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002853 rectum rhabdomyosarcoma skos:exactMatch NCIT:C5627 Rectal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002854 prostate sarcoma skos:exactMatch NCIT:C7731 Prostate Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002855 ectomesenchymoma skos:exactMatch NCIT:C4716 Ectomesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002856 gallbladder rhabdomyosarcoma skos:exactMatch NCIT:C5839 Gallbladder Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002857 gallbladder sarcoma skos:exactMatch NCIT:C5736 Gallbladder Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002858 ovary rhabdomyosarcoma skos:exactMatch NCIT:C5236 Ovarian Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002859 breast rhabdomyosarcoma skos:exactMatch NCIT:C5190 Breast Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002860 testis rhabdomyosarcoma skos:exactMatch NCIT:C6378 Testicular Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002861 testis sarcoma skos:exactMatch NCIT:C6359 Testicular Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002863 rhabdomyosarcoma with mixed embryonal and alveolar features skos:exactMatch NCIT:C4259 Rhabdomyosarcoma with Mixed Embryonal and Alveolar Features semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002864 anus rhabdomyosarcoma skos:exactMatch NCIT:C5610 Anal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002865 anus sarcoma skos:exactMatch NCIT:C5611 Anal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002867 pancreatic cystadenocarcinoma skos:exactMatch NCIT:C3874 Pancreatic Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002868 bile duct mucinous cystic neoplasm with an associated invasive carcinoma skos:exactMatch NCIT:C4130 Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002869 heart valve disorder skos:exactMatch NCIT:C45525 Valvular Heart Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002870 tricuspid valve insufficiency skos:exactMatch NCIT:C50842 Tricuspid Valve Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002871 testicular trophoblastic tumor skos:exactMatch NCIT:C39934 Testicular Trophoblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002872 trophoblastic neoplasm skos:exactMatch NCIT:C3422 Trophoblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002874 testicular pure germ cell tumor skos:exactMatch NCIT:C39915 Testicular Pure Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002876 cervical adenosarcoma skos:exactMatch NCIT:C40229 Cervical Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002877 cervical carcinosarcoma skos:exactMatch NCIT:C36097 Cervical Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002878 uterine corpus adenosarcoma skos:exactMatch NCIT:C6336 Uterine Corpus Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002879 uterine body mixed cancer skos:exactMatch NCIT:C6311 Malignant Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002880 ovarian adenosarcoma skos:exactMatch NCIT:C7317 Ovarian Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002881 vaginal adenosarcoma skos:exactMatch NCIT:C40277 Vaginal Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002882 colon neuroendocrine neoplasm skos:exactMatch NCIT:C5697 Colon Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002883 intestinal neuroendocrine neoplasm skos:exactMatch NCIT:C5695 Intestinal Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002887 bile duct disorder skos:exactMatch NCIT:C96716 Bile Duct Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002888 intraorbital meningioma skos:exactMatch NCIT:C6778 Intraorbital Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002889 orbital cancer skos:exactMatch NCIT:C3562 Malignant Orbit Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002892 skull base chordoma skos:exactMatch NCIT:C5453 Skull Base Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002894 spinal chordoma skos:exactMatch NCIT:C5156 Spinal Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002896 primary syphilis skos:exactMatch NCIT:C128412 Primary Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002897 secondary syphilis skos:exactMatch NCIT:C128413 Secondary Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002898 skin cancer skos:exactMatch NCIT:C2920 Malignant Skin Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002899 differentiating neuroblastoma skos:exactMatch NCIT:C42048 Differentiating Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002900 cerebral neuroblastoma skos:exactMatch NCIT:C4826 Central Nervous System Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002903 articulation disorder skos:exactMatch NCIT:C92564 Phonological Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002908 glucose metabolism disease skos:exactMatch NCIT:C53655 Glucose Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002910 peroneal neuropathy skos:exactMatch NCIT:C27596 Peroneal Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002911 brain stem glioma skos:exactMatch NCIT:C8501 Brain Stem Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002912 brainstem cancer skos:exactMatch NCIT:C3570 Malignant Brain Stem Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002913 cerebellar neoplasm skos:exactMatch NCIT:C2935 Cerebellar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002914 childhood brain stem neoplasm skos:exactMatch NCIT:C5969 Childhood Brain Stem Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002915 childhood infratentorial neoplasm skos:exactMatch NCIT:C5802 Childhood Infratentorial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002916 brainstem intraparenchymal clear cell meningioma skos:exactMatch NCIT:C5295 Brain Stem Intraparenchymal Clear Cell Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002917 disorder of pilosebaceous unit skos:exactMatch NCIT:C34656 Hair Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002918 clear cell meningioma skos:exactMatch NCIT:C4722 Clear Cell Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002919 posterior cranial fossa meningioma skos:exactMatch NCIT:C6775 Posterior Fossa Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002920 malignant ovarian Brenner tumor skos:exactMatch NCIT:C4270 Malignant Ovarian Brenner Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002921 congenital structural myopathy skos:exactMatch NCIT:C84648 Congenital Structural Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002923 uterine corpus endometrial stromal sarcoma skos:exactMatch NCIT:C40219 Uterine Corpus Endometrial Stromal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002924 smooth muscle cancer skos:exactMatch NCIT:C6511 Malignant Smooth Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002926 clear cell sarcoma skos:exactMatch NCIT:C3745 Clear Cell Sarcoma of Soft Tissue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002927 spindle cell sarcoma skos:exactMatch NCIT:C27005 Spindle Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002928 carcinosarcoma skos:exactMatch NCIT:C34448 Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002930 kidney sarcoma skos:exactMatch NCIT:C4525 Kidney Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002933 osteosclerosis skos:exactMatch NCIT:C41236 Osteosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002934 intravascular angioleiomyoma skos:exactMatch NCIT:C5355 Intravascular Angioleiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002935 penis basal cell carcinoma skos:exactMatch NCIT:C39961 Penile Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002936 scrotum basal cell carcinoma skos:exactMatch NCIT:C6386 Scrotal Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002937 nodular basal cell carcinoma skos:exactMatch NCIT:C5568 Skin Nodulo-Ulcerative Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002938 metatypical basal cell carcinoma skos:exactMatch NCIT:C66903 Skin Metatypical Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002939 skin pigmented basal cell carcinoma skos:exactMatch NCIT:C9359 Skin Pigmented Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002940 anal margin basal cell carcinoma skos:exactMatch NCIT:C7473 Anal Margin Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002941 anal margin carcinoma skos:exactMatch NCIT:C7472 Anal Margin Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002943 external ear basal cell carcinoma skos:exactMatch NCIT:C6082 External Ear Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002944 external ear carcinoma skos:exactMatch NCIT:C6081 External Ear Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002945 micronodular basal cell carcinoma skos:exactMatch NCIT:C27541 Skin Micronodular Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002946 gynatresia skos:exactMatch NCIT:C84743 Gynatresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002947 adamantinoid basal cell epithelioma skos:exactMatch NCIT:C7585 Skin Adamantinoid Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002948 skin fibroepithelial basal cell carcinoma skos:exactMatch NCIT:C4109 Skin Fibroepithelial Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002949 morpheaform basal cell carcinoma skos:exactMatch NCIT:C27182 Skin Sclerosing/Morphoeic Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002950 skin clear cell basal cell carcinoma skos:exactMatch NCIT:C27536 Skin Clear Cell Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002951 skin adenoid basal cell carcinoma skos:exactMatch NCIT:C27535 Skin Adenoid Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002952 follicular basal cell carcinoma skos:exactMatch NCIT:C27538 Skin Follicular Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002953 skin infiltrative basal cell carcinoma skos:exactMatch NCIT:C27539 Skin Infiltrating Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002954 superficial multifocal basal cell carcinoma skos:exactMatch NCIT:C4108 Superficial Multifocal Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002955 vulva basal cell carcinoma skos:exactMatch NCIT:C6381 Vulvar Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002956 skin cystic basal cell carcinoma skos:exactMatch NCIT:C27537 Skin Cystic Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002957 sarcomatoid basal cell carcinoma skos:exactMatch NCIT:C38111 Skin Basal Cell Carcinoma with Sarcomatoid Differentiation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002958 signet ring basal cell carcinoma skos:exactMatch NCIT:C38110 Skin Signet Ring Cell Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002960 polyradiculopathy skos:exactMatch NCIT:C34934 Polyradiculopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002961 large cell acanthoma skos:exactMatch NCIT:C27518 Large Cell Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002962 epidermolytic acanthoma skos:exactMatch NCIT:C27516 Epidermolytic Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002963 acantholytic acanthoma skos:exactMatch NCIT:C27517 Acantholytic Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002966 splenic manifestation of prolymphocytic leukemia skos:exactMatch NCIT:C7297 Splenic Manifestation of Prolymphocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002967 dermatophytosis of scalp or beard skos:exactMatch NCIT:C34536 Dermatophytosis of Scalp and Beard semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002969 ciliary body cancer skos:exactMatch NCIT:C4766 Malignant Ciliary Body Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002970 ciliary body disorder skos:exactMatch NCIT:C35775 Ciliary Body Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002971 amelanotic melanoma skos:exactMatch NCIT:C3802 Amelanotic Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002973 epithelioid cell melanoma skos:exactMatch NCIT:C4236 Epithelioid Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002974 cervical cancer skos:exactMatch NCIT:C9311 Malignant Cervical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002975 malignant breast melanoma skos:exactMatch NCIT:C8410 Breast Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002977 autoimmune disorder of the nervous system skos:exactMatch NCIT:C99383 Autoimmune Nervous System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002978 orbit alveolar rhabdomyosarcoma skos:exactMatch NCIT:C6247 Orbit Alveolar Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002979 papillary squamous carcinoma skos:exactMatch NCIT:C4102 Papillary Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002981 peripheral primitive neuroectodermal tumor of bone skos:exactMatch NCIT:C8776 Peripheral Primitive Neuroectodermal Tumor of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002982 peripheral primitive neuroectodermal tumor of soft tissues skos:exactMatch NCIT:C27471 Peripheral Primitive Neuroectodermal Tumor of Soft Tissues semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002984 reticulohistiocytic granuloma skos:exactMatch NCIT:C3356 Solitary Reticulohistiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002987 spongiotic dermatitis skos:exactMatch NCIT:C27037 Spongiotic Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002988 cervix melanoma skos:exactMatch NCIT:C40239 Cervical Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002989 benign fibrous histiocytoma skos:exactMatch NCIT:C3739 Fibrous Histiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002990 benign deep fibrous histiocytoma skos:exactMatch NCIT:C6492 Deep Fibrous Histiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002991 adenocarcinofibroma skos:exactMatch NCIT:C40035 Adenocarcinofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002993 pancreatic somatostatinoma skos:exactMatch NCIT:C95595 Pancreatic Somatostatinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002994 pancreatic delta cell neuroendocrine tumor skos:exactMatch NCIT:C28396 Pancreatic Delta Cell Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002995 small intestine neuroendocrine tumor, well differentiated, low or intermediate grade skos:exactMatch NCIT:C96061 Small Intestinal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002996 cavernous sinus meningioma skos:exactMatch NCIT:C5268 Cavernous Sinus Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002997 anterior cranial fossa meningioma skos:exactMatch NCIT:C5286 Anterior Cranial Fossa Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002998 skull base meningioma skos:exactMatch NCIT:C5272 Skull Base Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0002999 central nervous system germinoma skos:exactMatch NCIT:C7009 Central Nervous System Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003000 central nervous system germ cell tumor skos:exactMatch NCIT:C5461 Central Nervous System Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003001 seminoma skos:exactMatch NCIT:C9309 Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003003 cervical alveolar soft part sarcoma skos:exactMatch NCIT:C40225 Cervical Alveolar Soft Part Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003004 macular degeneration skos:exactMatch NCIT:C123330 Macular Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003005 macular retinal edema skos:exactMatch NCIT:C35468 Macular Edema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003007 childhood kidney cell carcinoma skos:exactMatch NCIT:C6568 Childhood Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003008 hereditary renal cell carcinoma skos:exactMatch NCIT:C39789 Hereditary Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003010 multilocular clear cell renal cell carcinoma skos:exactMatch NCIT:C4524 Multilocular Cystic Renal Neoplasm of Low Malignant Potential semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003011 mucinous tubular and spindle renal cell carcinoma skos:exactMatch NCIT:C39807 Mucinous Tubular and Spindle Cell Carcinoma of the Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003012 sarcomatoid renal cell carcinoma skos:exactMatch NCIT:C27893 Sarcomatoid Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003014 rhinitis skos:exactMatch NCIT:C34986 Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003019 potassium deficiency disease skos:exactMatch NCIT:C34939 Potassium Deficiency Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003021 central nervous system angiosarcoma skos:exactMatch NCIT:C5450 Central Nervous System Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003022 pediatric angiosarcoma skos:exactMatch NCIT:C9174 Childhood Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003023 aorta angiosarcoma skos:exactMatch NCIT:C5376 Aortic Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003024 breast angiosarcoma skos:exactMatch NCIT:C5184 Breast Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003025 conventional angiosarcoma skos:exactMatch NCIT:C9426 Conventional Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003026 gallbladder angiosarcoma skos:exactMatch NCIT:C5840 Gallbladder Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003027 thyroid gland angiosarcoma skos:exactMatch NCIT:C6043 Thyroid Gland Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003028 thyroid sarcoma skos:exactMatch NCIT:C6041 Thyroid Gland Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003029 skin angiosarcoma skos:exactMatch NCIT:C4489 Skin Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003030 endometrioid stromal sarcoma of the cervix skos:exactMatch NCIT:C40220 Endometrioid Stromal Sarcoma of the Cervix semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003031 endometrioid stromal and related neoplasms of the cervix skos:exactMatch NCIT:C40218 Cervical Endometrioid Stromal and Related Neoplasms semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003032 superior vena cava angiosarcoma skos:exactMatch NCIT:C5378 Superior Vena Cava Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003033 prostate angiosarcoma skos:exactMatch NCIT:C5528 Prostate Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003034 mediastinum angiosarcoma skos:exactMatch NCIT:C6613 Mediastinal Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003035 ovarian angiosarcoma skos:exactMatch NCIT:C5232 Ovarian Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003036 mucoepidermoid carcinoma skos:exactMatch NCIT:C3772 Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003037 hypotrichosis skos:exactMatch NCIT:C34720 Hypotrichosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003038 dysgraphia skos:exactMatch NCIT:C182452 Dysgraphia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003041 pediatric mesenchymal chondrosarcoma skos:exactMatch NCIT:C27374 Childhood Mesenchymal Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003042 adult mesenchymal chondrosarcoma skos:exactMatch NCIT:C27375 Adult Mesenchymal Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003043 obsolete extraskeletal mesenchymal chondrosarcoma skos:exactMatch NCIT:C27481 Mesenchymal Extraskeletal Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003046 anus neoplasm skos:exactMatch NCIT:C2877 Anal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003047 thymic large cell neuroendocrine carcinoma skos:exactMatch NCIT:C6461 Thymic Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003049 ovarian large-cell neuroendocrine carcinoma skos:exactMatch NCIT:C5238 Ovarian Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003050 lung large cell carcinoma skos:exactMatch NCIT:C4450 Lung Large Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003051 non specific chronic endometritis skos:exactMatch NCIT:C27625 Non Specific Chronic Endometritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003052 granulomatous endometritis skos:exactMatch NCIT:C27626 Granulomatous Endometritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003053 choroid plexus meningioma skos:exactMatch NCIT:C4719 Choroid Plexus Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003054 benign meningioma skos:exactMatch NCIT:C4055 Benign Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003055 secretory meningioma skos:exactMatch NCIT:C4718 Secretory Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003056 lymphoplasmacyte-rich meningioma skos:exactMatch NCIT:C4720 Lymphoplasmacyte-Rich Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003057 pediatric meningioma skos:exactMatch NCIT:C8264 Childhood Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003058 microcystic meningioma skos:exactMatch NCIT:C4721 Microcystic Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003061 benign muscle neoplasm skos:exactMatch NCIT:C4882 Benign Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003062 intestinal benign neoplasm skos:exactMatch NCIT:C4609 Benign Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003064 inverted transitional cell papilloma skos:exactMatch NCIT:C4118 Inverted Transitional Cell Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003065 nasal cavity inverting papilloma skos:exactMatch NCIT:C8194 Nasal Cavity Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003066 submandibular adenitis skos:exactMatch NCIT:C27016 Submandibular Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003067 cervical lymphadenitis skos:exactMatch NCIT:C26937 Cervical Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003068 postauricular lymphadenitis skos:exactMatch NCIT:C27332 Postauricular Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003069 suppurative lymphadenitis skos:exactMatch NCIT:C27135 Suppurative Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003070 axillary lymphadenitis skos:exactMatch NCIT:C27333 Axillary Lymphadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003072 retinal cancer skos:exactMatch NCIT:C3216 Malignant Retinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003073 trilateral retinoblastoma skos:exactMatch NCIT:C7019 Trilateral Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003075 bilateral retinoblastoma skos:exactMatch NCIT:C8713 Bilateral Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003076 unilateral retinoblastoma skos:exactMatch NCIT:C8714 Unilateral Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003077 intraocular retinoblastoma skos:exactMatch NCIT:C7846 Intraocular Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003078 extraocular retinoblastoma skos:exactMatch NCIT:C7848 Extraocular Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003079 mastocytoma skos:exactMatch NCIT:C9303 Mastocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003081 thalamic disorder skos:exactMatch NCIT:C85186 Thalamic Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003083 venous hemangioma skos:exactMatch NCIT:C4296 Venous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003084 uremic neuropathy skos:exactMatch NCIT:C27055 Uremic Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003085 keratitis skos:exactMatch NCIT:C26805 Keratitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003086 thymic mucoepidermoid carcinoma skos:exactMatch NCIT:C6457 Thymic Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003087 mucoepidermoid breast carcinoma skos:exactMatch NCIT:C5166 Breast Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003088 intramuscular hemangioma skos:exactMatch NCIT:C3699 Intramuscular Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003089 extrahepatic bile duct mucoepidermoid carcinoma skos:exactMatch NCIT:C5862 Extrahepatic Bile Duct Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003090 extrahepatic bile duct carcinoma skos:exactMatch NCIT:C3860 Extrahepatic Bile Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003091 cutaneous mucoepidermoid carcinoma skos:exactMatch NCIT:C4472 Skin Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003092 lacrimal gland mucoepidermoid carcinoma skos:exactMatch NCIT:C6091 Lacrimal Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003093 mucoepidermoid esophageal carcinoma skos:exactMatch NCIT:C5343 Esophageal Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003095 laryngeal mucoepidermoid carcinoma skos:exactMatch NCIT:C9463 Laryngeal Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003096 deep hemangioma skos:exactMatch NCIT:C6555 Deep Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003097 childhood mediastinal neurogenic neoplasm skos:exactMatch NCIT:C5429 Childhood Mediastinal Neurogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003098 mediastinal neural neoplasm skos:exactMatch NCIT:C6624 Mediastinal Neurogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003100 nerve plexus neoplasm skos:exactMatch NCIT:C5822 Nerve Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003103 nerve root neoplasm skos:exactMatch NCIT:C5119 Nerve Root Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003104 epicardium cancer skos:exactMatch NCIT:C4568 Malignant Epicardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003105 prostate disorder skos:exactMatch NCIT:C26865 Prostate Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003107 infratentorial cancer skos:exactMatch NCIT:C4966 Malignant Infratentorial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003108 cervicomedullary junction neoplasm skos:exactMatch NCIT:C5423 Cervicomedullary Junction Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003109 foramen magnum meningioma skos:exactMatch NCIT:C5280 Foramen Magnum Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003110 skin hemangioma skos:exactMatch NCIT:C4905 Skin Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003111 gastric neuroendocrine neoplasm skos:exactMatch NCIT:C5696 Gastric Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003112 malignant gastric germ cell tumor skos:exactMatch NCIT:C5486 Malignant Gastric Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003113 extragonadal germ cell cancer skos:exactMatch NCIT:C8881 Malignant Extragonadal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003115 subglottic hemangioma skos:exactMatch NCIT:C6026 Subglottic Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003117 somatoform disorder skos:exactMatch NCIT:C34956 Somatoform Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003118 testicular Brenner tumor skos:exactMatch NCIT:C39953 Paratesticular Brenner Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003120 mixed testicular germ cell cancer skos:exactMatch NCIT:C6347 Testicular Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003121 middle cranial fossa meningioma skos:exactMatch NCIT:C5586 Middle Cranial Fossa Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003122 striatonigral degeneration skos:exactMatch NCIT:C125695 Striatonigral Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003124 testicular Leydig cell tumor skos:exactMatch NCIT:C6356 Testicular Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch NCIT:C6358 Testicular Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003126 breast hemangioma skos:exactMatch NCIT:C5353 Breast Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003128 classic pulmonary blastoma skos:exactMatch NCIT:C36054 Biphasic Pulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003129 epithelial predominant pulmonary blastoma skos:exactMatch NCIT:C36053 Epithelial Predominant Pulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003133 exudative glomerulonephritis skos:exactMatch NCIT:C35706 Exudative Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003134 proliferative glomerulonephritis skos:exactMatch NCIT:C35281 Proliferative Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003135 focal embolic glomerulonephritis skos:exactMatch NCIT:C35707 Focal Embolic Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003136 anti-basement membrane glomerulonephritis skos:exactMatch NCIT:C35798 Anti-Basement Membrane Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003137 diffuse glomerulonephritis skos:exactMatch NCIT:C35799 Diffuse Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003138 subacute glomerulonephritis skos:exactMatch NCIT:C35801 Subacute Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003139 mesangial proliferative glomerulonephritis skos:exactMatch NCIT:C35445 Mesangial Proliferative Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003140 immune-complex glomerulonephritis skos:exactMatch NCIT:C35800 Immune Complex Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003141 cerebellopontine angle embryonal tumor skos:exactMatch NCIT:C5436 Cerebellopontine Angle Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003142 intracranial primitive neuroectodermal tumor skos:exactMatch NCIT:C5817 Intracranial Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003143 angiokeratoma skos:exactMatch NCIT:C2874 Angiokeratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003143 angiokeratoma skos:exactMatch NCIT:C4488 Skin Angiokeratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003144 medulloepithelioma skos:exactMatch NCIT:C4327 Central Nervous System Medulloepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003145 supratentorial primitive neuroectodermal tumor skos:exactMatch NCIT:C6968 Supratentorial Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003150 male reproductive system disorder skos:exactMatch NCIT:C27019 Male Reproductive System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003152 adult brainstem gliosarcoma skos:exactMatch NCIT:C9370 Adult Brain Stem Gliosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003153 adult brainstem glioma skos:exactMatch NCIT:C9091 Adult Brain Stem Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003154 hemangioma of peripheral nerve skos:exactMatch NCIT:C27507 Hemangioma of Peripheral Nerve semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003155 cavernous hemangioma skos:exactMatch NCIT:C3086 Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003158 malignant myoepithelioma skos:exactMatch NCIT:C7596 Malignant Myoepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003163 cauda equina intradural extramedullary astrocytoma skos:exactMatch NCIT:C5408 Intradural Extramedullary Cauda Equina Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003164 cauda equina neoplasm skos:exactMatch NCIT:C5479 Cauda Equina Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003165 cerebellar astrocytoma skos:exactMatch NCIT:C9475 Cerebellar Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003168 cerebellar pilocytic astrocytoma skos:exactMatch NCIT:C6809 Cerebellar Pilocytic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003169 diencephalic astrocytomas skos:exactMatch NCIT:C5128 Diencephalic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003170 gliofibroma skos:exactMatch NCIT:C5419 Gliofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003171 pineal gland astrocytoma skos:exactMatch NCIT:C8274 Pineal Gland Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003172 glomeruloid hemangioma skos:exactMatch NCIT:C27505 Glomeruloid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003173 brain stem astrocytic neoplasm skos:exactMatch NCIT:C7445 Brain Stem Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003174 spinal cord astrocytoma skos:exactMatch NCIT:C4641 Spinal Cord Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003175 salivary gland adenoid cystic carcinoma skos:exactMatch NCIT:C8026 Salivary Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003177 prostate adenoid cystic carcinoma skos:exactMatch NCIT:C5539 Prostate Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003180 cutaneous adenocystic carcinoma skos:exactMatch NCIT:C4471 Adenoid Cystic Skin Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003181 lung adenoid cystic carcinoma skos:exactMatch NCIT:C5666 Lung Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003184 trachea carcinoma skos:exactMatch NCIT:C9347 Tracheal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003185 adenoid cystic breast carcinoma skos:exactMatch NCIT:C5130 Breast Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003186 esophageal adenoid cystic carcinoma skos:exactMatch NCIT:C5342 Esophageal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003187 Bartholin gland adenoid cystic carcinoma skos:exactMatch NCIT:C40295 Bartholin Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003189 middle ear adenocarcinoma skos:exactMatch NCIT:C6848 Middle Ear Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003190 middle ear carcinoma skos:exactMatch NCIT:C6089 Middle Ear Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003191 rete ovarii adenocarcinoma skos:exactMatch NCIT:C40017 Rete Ovarii Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003192 rete ovarii neoplasm skos:exactMatch NCIT:C40016 Rete Ovarii Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003193 bile duct adenocarcinoma skos:exactMatch NCIT:C27813 Bile Duct Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003196 appendix carcinoma skos:exactMatch NCIT:C9330 Appendix Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003197 granular cell carcinoma skos:exactMatch NCIT:C3681 Granular Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003198 small intestine adenocarcinoma skos:exactMatch NCIT:C7888 Small Intestinal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003199 anal carcinoma skos:exactMatch NCIT:C9291 Anal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003200 urethra adenocarcinoma skos:exactMatch NCIT:C6167 Urethral Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003202 pituitary gland basophilic carcinoma skos:exactMatch NCIT:C27392 Pituitary Gland Basophil Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003204 villous adenocarcinoma skos:exactMatch NCIT:C4142 Villous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003205 renal pelvis adenocarcinoma skos:exactMatch NCIT:C6143 Renal Pelvis Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003206 acquired hemangioma skos:exactMatch NCIT:C27018 Acquired Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003208 breast secretory carcinoma skos:exactMatch NCIT:C4189 Breast Secretory Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003209 thymus gland adenocarcinoma skos:exactMatch NCIT:C6459 Thymic Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003210 intrahepatic cholangiocarcinoma skos:exactMatch NCIT:C35417 Intrahepatic Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003211 nasal cavity adenocarcinoma skos:exactMatch NCIT:C6015 Nasal Cavity Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003212 nasal cavity carcinoma skos:exactMatch NCIT:C9336 Nasal Cavity Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003214 apocrine adenocarcinoma skos:exactMatch NCIT:C4169 Apocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003215 apocrine sweat gland cancer skos:exactMatch NCIT:C6800 Malignant Apocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003216 ureter adenocarcinoma skos:exactMatch NCIT:C6155 Ureter Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003218 adenocarcinoma in situ skos:exactMatch NCIT:C4123 Adenocarcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003219 gastroesophageal junction adenocarcinoma skos:exactMatch NCIT:C9296 Gastroesophageal Junction Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003220 gallbladder carcinoma skos:exactMatch NCIT:C3844 Gallbladder Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003222 central nervous system melanocytic neoplasm skos:exactMatch NCIT:C5504 Central Nervous System Melanocytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003223 meninges hemangiopericytoma skos:exactMatch NCIT:C4660 Meningeal Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003225 bone marrow disorder skos:exactMatch NCIT:C34433 Bone Marrow Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003227 prosopagnosia skos:exactMatch NCIT:C85031 Prosopagnosia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003234 optic nerve astrocytoma skos:exactMatch NCIT:C6769 Optic Nerve Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003235 optic nerve glioma skos:exactMatch NCIT:C4537 Optic Nerve Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003236 atypical polypoid adenomyoma skos:exactMatch NCIT:C6895 Atypical Polypoid Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003237 adenomyoma of uterine corpus skos:exactMatch NCIT:C6338 Uterine Corpus Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003238 cervical adenomyoma skos:exactMatch NCIT:C40231 Cervical Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003240 thyroid gland disorder skos:exactMatch NCIT:C26893 Thyroid Gland Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003241 central nervous system hemangioma skos:exactMatch NCIT:C7004 Central Nervous System Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003243 hepatocellular clear cell carcinoma skos:exactMatch NCIT:C5754 Clear Cell Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003244 central nervous system mesenchymal non-meningothelial tumor skos:exactMatch NCIT:C5449 Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003245 aflatoxin-related hepatocellular carcinoma skos:exactMatch NCIT:C27922 Aflatoxins-Related Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003246 sclerosing hepatic carcinoma skos:exactMatch NCIT:C27388 Scirrhous Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003248 adult pineal parenchymal tumor skos:exactMatch NCIT:C8273 Adult Pineal Parenchymal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003249 pineal gland cancer skos:exactMatch NCIT:C3573 Malignant Pineal Region Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003250 benign granular cell tumor skos:exactMatch NCIT:C3252 Benign Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003251 esophageal granular cell tumor skos:exactMatch NCIT:C5700 Esophageal Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003252 granular cell cancer skos:exactMatch NCIT:C4336 Malignant Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003253 vulvar granular cell tumor skos:exactMatch NCIT:C40328 Vulvar Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003254 cardiac granular cell neoplasm skos:exactMatch NCIT:C5360 Cardiac Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003255 mediastinal granular cell myoblastoma skos:exactMatch NCIT:C6601 Mediastinal Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003256 neurohypophysis granular cell tumor skos:exactMatch NCIT:C7017 Granular Cell Tumor of the Sellar Region semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003257 posterior pituitary gland neoplasm skos:exactMatch NCIT:C7157 Posterior Pituitary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003258 hobnail hemangioma skos:exactMatch NCIT:C27506 Hobnail Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003260 adult cerebellar neoplasm skos:exactMatch NCIT:C5968 Adult Cerebellar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003261 papillary meningioma of the cerebellum skos:exactMatch NCIT:C5270 Cerebellar Papillary Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003262 rhabdoid meningioma skos:exactMatch NCIT:C6909 Rhabdoid Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003263 childhood cerebellar neoplasm skos:exactMatch NCIT:C5970 Childhood Cerebellar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003264 basosquamous carcinoma skos:exactMatch NCIT:C2922 Skin Basosquamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003265 adjustment disorder skos:exactMatch NCIT:C92191 Adjustment Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003266 ependymal tumor skos:exactMatch NCIT:C6770 Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003268 mixed glioma skos:exactMatch NCIT:C3903 Mixed Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003273 sternum cancer skos:exactMatch NCIT:C8408 Malignant Sternal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003274 thoracic cancer skos:exactMatch NCIT:C3576 Malignant Thoracic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003275 middle ear cancer skos:exactMatch NCIT:C4765 Malignant Middle Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003276 middle ear disorder skos:exactMatch NCIT:C27065 Middle Ear Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003277 malignant ear neoplasm skos:exactMatch NCIT:C9337 Malignant Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003279 testicular infarct skos:exactMatch NCIT:C27617 Testicular Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003281 ovarian cystic teratoma skos:exactMatch NCIT:C7283 Ovarian Cystic Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003283 epididymal neoplasm skos:exactMatch NCIT:C39958 Epididymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003284 mediastinum leiomyoma skos:exactMatch NCIT:C6598 Mediastinal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003285 fallopian tube leiomyoma skos:exactMatch NCIT:C40127 Fallopian Tube Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003286 extrahepatic bile duct leiomyoma skos:exactMatch NCIT:C5855 Extrahepatic Bile Duct Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003287 central nervous system leiomyoma skos:exactMatch NCIT:C6998 Central Nervous System Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003288 bizarre leiomyoma skos:exactMatch NCIT:C4257 Bizarre Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003289 deep leiomyoma skos:exactMatch NCIT:C6512 Deep Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003291 leiomyoma cutis skos:exactMatch NCIT:C4482 Skin Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003292 anus leiomyoma skos:exactMatch NCIT:C5608 Anal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003293 lung leiomyoma skos:exactMatch NCIT:C5660 Lung Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003294 pericardium leiomyoma skos:exactMatch NCIT:C6743 Pericardial Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003295 leiomyomatosis skos:exactMatch NCIT:C3748 Leiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003296 cellular leiomyoma skos:exactMatch NCIT:C4256 Cellular Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003297 gallbladder leiomyoma skos:exactMatch NCIT:C5747 Gallbladder Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003298 vulvar leiomyoma skos:exactMatch NCIT:C40326 Vulvar Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003299 colorectal leiomyoma skos:exactMatch NCIT:C5677 Colorectal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003300 appendix leiomyoma skos:exactMatch NCIT:C5514 Appendix Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003301 dartoic leiomyoma skos:exactMatch NCIT:C4483 Dartoic Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003302 epithelioid neurofibroma skos:exactMatch NCIT:C6558 Epithelioid Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003303 neurofibroma of gallbladder skos:exactMatch NCIT:C5746 Gallbladder Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003304 plexiform neurofibroma skos:exactMatch NCIT:C3797 Plexiform Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003305 cellular neurofibroma skos:exactMatch NCIT:C41427 Cellular Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003306 atypical neurofibroma skos:exactMatch NCIT:C41426 Neurofibroma with Atypia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003307 multiple mucosal neuroma skos:exactMatch NCIT:C6559 Multiple Mucosal Neuromas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003308 pleural mesothelioma skos:exactMatch NCIT:C9351 Pleural Mesothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003310 Monckeberg arteriosclerosis skos:exactMatch NCIT:C35770 Monckeberg Arteriosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003312 ovarian endometrioid stromal and related neoplasms skos:exactMatch NCIT:C40065 Ovarian Endometrioid Stromal and Related Neoplasms semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003313 endometrioid stromal sarcoma of the vagina skos:exactMatch NCIT:C40270 Endometrioid Stromal Sarcoma of the Vagina semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003314 endometrioid stromal and related neoplasms of the vagina skos:exactMatch NCIT:C40269 Vaginal Endometrioid Stromal and Related Neoplasms semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003316 nonanaplastic kidney Wilms tumor skos:exactMatch NCIT:C6951 Nonanaplastic Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003317 metachronous kidney Wilms' tumor skos:exactMatch NCIT:C38158 Metachronous Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003318 mixed cell type kidney Wilms' tumor skos:exactMatch NCIT:C9149 Mixed Cell Type Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003319 scrotum neoplasm skos:exactMatch NCIT:C4380 Scrotal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003320 blastema predominant kidney Wilms tumor skos:exactMatch NCIT:C9147 Blastema Predominant Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003321 hereditary Wilms tumor skos:exactMatch NCIT:C8496 Hereditary Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003322 epithelial predominant Wilms' tumor skos:exactMatch NCIT:C9146 Epithelial Predominant Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003325 nodular ganglioneuroblastoma skos:exactMatch NCIT:C42058 Ganglioneuroblastoma, Nodular semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003326 intermixed schwannian stroma-rich ganglioneuroblastoma skos:exactMatch NCIT:C42057 Ganglioneuroblastoma, Intermixed semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003327 peripheral ganglioneuroblastoma skos:exactMatch NCIT:C6594 Peripheral Ganglioneuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003328 fallopian tube adenomatoid tumor skos:exactMatch NCIT:C40129 Fallopian Tube Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003330 urinary tract obstruction skos:exactMatch NCIT:C3675 Obstructive Uropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003331 ovarian monodermal teratoma skos:exactMatch NCIT:C7286 Ovarian Monodermal Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003332 malignant struma ovarii skos:exactMatch NCIT:C4291 Thyroid Carcinoma Arising in Struma Ovarii semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003334 demyelinating polyneuropathy skos:exactMatch NCIT:C27062 Demyelinating Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003335 chronic polyneuropathy skos:exactMatch NCIT:C36071 Chronic Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003336 acute necrotizing encephalitis skos:exactMatch NCIT:C35383 Acute Necrotizing Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003337 acute hemorrhagic encephalitis skos:exactMatch NCIT:C35796 Acute Hemorrhagic Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003340 malignant glomus tumor skos:exactMatch NCIT:C4221 Malignant Glomus Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003341 subungual glomus tumor skos:exactMatch NCIT:C36079 Subungual Glomus Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003342 benign perivascular tumor skos:exactMatch NCIT:C6529 Benign Pericytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003343 retinal hemangioblastoma skos:exactMatch NCIT:C39783 Retinal Hemangioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003345 hilar cholangiocarcinoma skos:exactMatch NCIT:C36077 Hilar Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003346 central nervous system vasculitis skos:exactMatch NCIT:C84622 Central Nervous System Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003347 inflammatory leiomyosarcoma skos:exactMatch NCIT:C27495 Inflammatory Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003348 conventional leiomyosarcoma skos:exactMatch NCIT:C9428 Conventional Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003349 central nervous system leiomyosarcoma skos:exactMatch NCIT:C6999 Central Nervous System Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003350 granular cell leiomyosarcoma skos:exactMatch NCIT:C27494 Granular Cell Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003351 colon leiomyosarcoma skos:exactMatch NCIT:C5494 Colon Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003352 colon sarcoma skos:exactMatch NCIT:C5495 Colon Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003353 heart leiomyosarcoma skos:exactMatch NCIT:C5364 Cardiac Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003354 heart sarcoma skos:exactMatch NCIT:C7723 Cardiac Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003355 ovary leiomyosarcoma skos:exactMatch NCIT:C5234 Ovarian Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003356 epithelioid leiomyosarcoma skos:exactMatch NCIT:C3700 Epithelioid Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003357 lung leiomyosarcoma skos:exactMatch NCIT:C5667 Lung Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003358 anus leiomyosarcoma skos:exactMatch NCIT:C5599 Anal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003359 myxoid leiomyosarcoma skos:exactMatch NCIT:C3701 Myxoid Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003360 small intestine leiomyosarcoma skos:exactMatch NCIT:C7085 Small Intestinal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003361 small intestinal sarcoma skos:exactMatch NCIT:C5335 Small Intestinal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003362 cutaneous leiomyosarcoma skos:exactMatch NCIT:C4484 Atypical Intradermal Smooth Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003363 malignant dermis tumor skos:exactMatch NCIT:C4574 Malignant Dermal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003364 gallbladder leiomyosarcoma skos:exactMatch NCIT:C5841 Gallbladder Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003365 esophagus leiomyosarcoma skos:exactMatch NCIT:C5334 Esophageal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003367 gastric leiomyosarcoma skos:exactMatch NCIT:C27200 Gastric Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003368 prostate leiomyosarcoma skos:exactMatch NCIT:C5526 Prostate Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003369 vagina leiomyosarcoma skos:exactMatch NCIT:C6326 Vaginal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003370 retroperitoneal leiomyosarcoma skos:exactMatch NCIT:C27904 Retroperitoneal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003371 breast leiomyosarcoma skos:exactMatch NCIT:C5186 Breast Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003372 vulvar leiomyosarcoma skos:exactMatch NCIT:C40318 Vulvar Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003373 kidney leiomyosarcoma skos:exactMatch NCIT:C6183 Kidney Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003374 laryngeal leiomyosarcoma skos:exactMatch NCIT:C6022 Laryngeal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003376 mediastinum leiomyosarcoma skos:exactMatch NCIT:C6619 Mediastinal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003377 extrahepatic bile duct leiomyosarcoma skos:exactMatch NCIT:C5848 Extrahepatic Bile Duct Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003378 liver leiomyosarcoma skos:exactMatch NCIT:C5756 Liver Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003379 rectum leiomyosarcoma skos:exactMatch NCIT:C5549 Rectal Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003381 pituitary gland disorder skos:exactMatch NCIT:C26854 Pituitary Gland Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003382 eyelid disorder skos:exactMatch NCIT:C26768 Eyelid Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003383 fallopian tube clear cell adenocarcinoma skos:exactMatch NCIT:C6280 Fallopian Tube Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003384 uterine ligament clear cell adenocarcinoma skos:exactMatch NCIT:C40139 Broad Ligament Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003386 bladder clear cell adenocarcinoma skos:exactMatch NCIT:C6179 Bladder Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003387 urethra clear cell adenocarcinoma skos:exactMatch NCIT:C6172 Urethral Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003388 ampulla of vater clear cell adenocarcinoma skos:exactMatch NCIT:C27414 Ampulla of Vater Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003389 epithelial-myoepithelial carcinoma skos:exactMatch NCIT:C4199 Epithelial-Myoepithelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003390 glycogen-rich clear cell breast carcinoma skos:exactMatch NCIT:C40368 Glycogen-Rich, Clear Cell Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003391 vulvar alveolar soft part sarcoma skos:exactMatch NCIT:C40320 Vulvar Alveolar Soft Part Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003392 fallopian tube germ cell tumor skos:exactMatch NCIT:C40130 Fallopian Tube Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003393 thymus gland disorder skos:exactMatch NCIT:C26962 Thymus Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003394 dental pulp disorder skos:exactMatch NCIT:C34530 Dental Pulp Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003395 testicular granulosa cell tumor skos:exactMatch NCIT:C6357 Testicular Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003396 epulis skos:exactMatch NCIT:C3948 Gingival Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003399 pineal region yolk sac tumor skos:exactMatch NCIT:C6752 Pineal Region Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003400 childhood endodermal sinus tumor skos:exactMatch NCIT:C27364 Childhood Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003401 central nervous system endodermal sinus tumor skos:exactMatch NCIT:C6209 Childhood Central Nervous System Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003402 testicular yolk sac tumor skos:exactMatch NCIT:C8000 Testicular Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003403 testicular non-seminomatous germ cell cancer skos:exactMatch NCIT:C5027 Malignant Testicular Non-Seminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003404 adult yolk sac tumor skos:exactMatch NCIT:C27241 Adult Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003405 adult central nervous system germ cell tumor skos:exactMatch NCIT:C6285 Adult Central Nervous System Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003408 ovarian primitive germ cell tumor skos:exactMatch NCIT:C39986 Ovarian Primitive Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003410 Wolffian duct adenocarcinoma skos:exactMatch NCIT:C40254 Cervical Mesonephric Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003411 breast hemangiopericytoma skos:exactMatch NCIT:C40396 Breast Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003412 retroperitoneal hemangiopericytoma skos:exactMatch NCIT:C5386 Retroperitoneal Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003413 hair follicle neoplasm skos:exactMatch NCIT:C7367 Hair Follicle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003414 skin pilomatrix carcinoma skos:exactMatch NCIT:C4114 Pilomatrical Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003419 Bartholin gland adenoma skos:exactMatch NCIT:C40299 Bartholin Gland Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003420 bile duct cystadenoma skos:exactMatch NCIT:C4129 Bile Duct Mucinous Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003421 mixed cell adenoma skos:exactMatch NCIT:C4157 Mixed Cell Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003422 lung adenoma skos:exactMatch NCIT:C4455 Lung Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003423 middle ear adenoma skos:exactMatch NCIT:C6834 Middle Ear Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003424 oncocytic adenoma skos:exactMatch NCIT:C3759 Oncocytic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003426 clear cell adenoma skos:exactMatch NCIT:C4151 Clear Cell Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003427 bronchus adenoma skos:exactMatch NCIT:C3494 Lung Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003428 brain hemangioma skos:exactMatch NCIT:C7739 Brain Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003429 functioning pituitary gland adenoma skos:exactMatch NCIT:C8388 Functioning Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003431 lipoadenoma skos:exactMatch NCIT:C4159 Lipoadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003432 strabismus skos:exactMatch NCIT:C35040 Strabismus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003433 water-clear cell adenoma skos:exactMatch NCIT:C4155 Parathyroid Gland Water-Clear Cell Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003434 vaginal adenoma skos:exactMatch NCIT:C40256 Vaginal Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003435 microcystic adenoma skos:exactMatch NCIT:C3685 Microcystic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003437 occult small cell lung carcinoma skos:exactMatch NCIT:C6683 Occult Lung Small Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003438 combined small cell lung carcinoma skos:exactMatch NCIT:C9137 Combined Lung Small Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003439 urinary bladder villous adenoma skos:exactMatch NCIT:C7414 Bladder Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003441 dystonic disorder skos:exactMatch NCIT:C34563 Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003442 bladder papillary urothelial neoplasm skos:exactMatch NCIT:C39857 Bladder Papillary Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003443 papillary urothelial neoplasm skos:exactMatch NCIT:C27883 Papillary Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003444 intrahepatic bile duct adenoma skos:exactMatch NCIT:C7126 Intrahepatic Bile Duct Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003445 extrahepatic bile duct adenoma skos:exactMatch NCIT:C5857 Extrahepatic Bile Duct Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003446 papillary hidradenoma skos:exactMatch NCIT:C4171 Hidradenoma Papilliferum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003447 clear cell hidradenoma skos:exactMatch NCIT:C7567 Clear Cell Hidradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003448 benign spiradenoma skos:exactMatch NCIT:C4170 Spiradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003450 eccrine papillary adenoma skos:exactMatch NCIT:C4173 Papillary Eccrine Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003453 conjunctival intraepithelial neoplasm skos:exactMatch NCIT:C6120 Conjunctival Squamous Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003454 conjunctival cancer skos:exactMatch NCIT:C3564 Malignant Conjunctival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003455 bile duct papillary neoplasm skos:exactMatch NCIT:C6881 Bile Duct Intraductal Papillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003458 uterine corpus adenofibroma skos:exactMatch NCIT:C6337 Uterine Corpus Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003459 cervical adenofibroma skos:exactMatch NCIT:C40230 Cervical Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003460 clear cell adenofibroma skos:exactMatch NCIT:C8987 Clear Cell Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003461 fallopian tube serous adenofibroma skos:exactMatch NCIT:C40113 Fallopian Tube Serous Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003462 papillary adenofibroma skos:exactMatch NCIT:C8986 Papillary Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003463 ovarian endometrioid adenofibroma skos:exactMatch NCIT:C27287 Ovarian Endometrioid Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003464 cystadenofibroma skos:exactMatch NCIT:C8985 Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003465 fibrous synovial sarcoma skos:exactMatch NCIT:C6533 Fibrous Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003466 spindle cell synovial sarcoma skos:exactMatch NCIT:C4277 Spindle Cell Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003467 mediastinum synovial sarcoma skos:exactMatch NCIT:C6618 Mediastinal Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003468 biphasic synovial sarcoma skos:exactMatch NCIT:C4279 Biphasic Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003469 epithelioid cell synovial sarcoma skos:exactMatch NCIT:C4278 Epithelial Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003470 cellular ependymoma skos:exactMatch NCIT:C4713 Cellular Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003472 lice infestation skos:exactMatch NCIT:C128401 Pediculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003473 spinal cord ependymoma skos:exactMatch NCIT:C3875 Spinal Cord Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003474 tanycytic ependymoma skos:exactMatch NCIT:C6903 Tanycytic Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003475 papillary ependymoma skos:exactMatch NCIT:C4319 Papillary Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003476 clear cell ependymoma skos:exactMatch NCIT:C4714 Clear Cell Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003477 brain stem ependymoma skos:exactMatch NCIT:C5098 Brain Stem Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003478 childhood ependymoma skos:exactMatch NCIT:C8578 Childhood Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003480 pineal region dysgerminoma skos:exactMatch NCIT:C7169 Pineal Region Dysgerminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003481 dysgerminoma of ovary skos:exactMatch NCIT:C8106 Ovarian Dysgerminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003486 basaloid squamous cell carcinoma skos:exactMatch NCIT:C54244 Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003487 pseudoglandular squamous cell carcinoma skos:exactMatch NCIT:C4106 Pseudoglandular Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003490 ampulla of vater squamous cell carcinoma skos:exactMatch NCIT:C27417 Ampulla of Vater Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003492 lacrimal gland squamous cell carcinoma skos:exactMatch NCIT:C6092 Lacrimal Drainage System Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003493 thymus squamous cell carcinoma skos:exactMatch NCIT:C6455 Thymic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003494 ovarian squamous cell carcinoma skos:exactMatch NCIT:C40093 Ovarian Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003497 renal pelvis squamous cell carcinoma skos:exactMatch NCIT:C7732 Renal Pelvis Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003499 sarcomatoid squamous cell skin carcinoma skos:exactMatch NCIT:C4666 Skin Spindle Cell Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003501 external ear squamous cell carcinoma skos:exactMatch NCIT:C6083 External Ear Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003502 ureter squamous cell carcinoma skos:exactMatch NCIT:C6154 Ureter Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003503 fallopian tube squamous cell carcinoma skos:exactMatch NCIT:C6282 Fallopian Tube Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003504 anal canal neuroendocrine neoplasm skos:exactMatch NCIT:C5603 Anal Canal Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003506 pulmonary artery choriocarcinoma skos:exactMatch NCIT:C5381 Pulmonary Artery Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003507 choriocarcinoma of ovary skos:exactMatch NCIT:C4515 Ovarian Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003508 choriocarcinoma of testis skos:exactMatch NCIT:C7733 Testicular Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003509 pineal region choriocarcinoma skos:exactMatch NCIT:C6759 Pineal Region Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003510 malignant testicular germ cell tumor skos:exactMatch NCIT:C9063 Malignant Testicular Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003512 mediastinal mesenchymal tumor skos:exactMatch NCIT:C6637 Mediastinal Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003513 gastric teratoma skos:exactMatch NCIT:C5259 Gastric Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003514 malignant teratoma skos:exactMatch NCIT:C4287 Malignant Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003515 fallopian tube teratoma skos:exactMatch NCIT:C40131 Fallopian Tube Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003516 adult teratoma skos:exactMatch NCIT:C9013 Adult Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003517 mature teratoma skos:exactMatch NCIT:C9015 Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003518 mediastinum teratoma skos:exactMatch NCIT:C6438 Mediastinal Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003519 malignant syringoma skos:exactMatch NCIT:C7581 Microcystic Adnexal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003522 male orgasm disorder skos:exactMatch NCIT:C34959 Male Orgasmic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003523 gastrin-producing neuroendocrine tumor skos:exactMatch NCIT:C3050 Gastrin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003524 gastric gastrin-producing neuroendocrine tumor skos:exactMatch NCIT:C27444 Gastric Gastrin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003525 pancreatic gastrin-producing neuroendocrine tumor skos:exactMatch NCIT:C9069 Pancreatic Gastrin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003528 Volkmann contracture skos:exactMatch NCIT:C35130 Volkmann's Ischemic Contracture semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003529 acute pyelonephritis skos:exactMatch NCIT:C123215 Acute Pyelonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003531 papillary eccrine carcinoma skos:exactMatch NCIT:C27254 Papillary Eccrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003532 breast papillary carcinoma skos:exactMatch NCIT:C9134 Breast Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003534 papillary thymic adenocarcinoma skos:exactMatch NCIT:C27937 Thymic Low Grade Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003535 fallopian tube papillary adenocarcinoma skos:exactMatch NCIT:C6267 Fallopian Tube Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003537 precursor T-lymphoblastic lymphoma/leukemia skos:exactMatch NCIT:C8694 T Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003538 precursor lymphoblastic lymphoma/leukemia skos:exactMatch NCIT:C7055 Precursor Lymphoid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003539 T-cell adult acute lymphocytic leukemia skos:exactMatch NCIT:C9142 Adult T Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003541 adult acute lymphoblastic leukemia skos:exactMatch NCIT:C4967 Adult Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003543 trigeminal nerve disorder skos:exactMatch NCIT:C26952 Trigeminal Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003544 spinal cord cancer skos:exactMatch NCIT:C3572 Malignant Spinal Cord Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003545 intradural extramedullary spinal canal neoplasm skos:exactMatch NCIT:C5135 Intradural Extramedullary Spinal Canal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003546 third cranial nerve disorder skos:exactMatch NCIT:C27598 Oculomotor Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003548 adenosquamous breast carcinoma skos:exactMatch NCIT:C40361 Breast Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003550 esophageal adenosquamous carcinoma skos:exactMatch NCIT:C27421 Esophageal Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003551 thymic adenosquamous carcinoma skos:exactMatch NCIT:C6458 Thymic Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003553 ampulla of vater adenosquamous carcinoma skos:exactMatch NCIT:C27418 Ampulla of Vater Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003554 adenosquamous colon carcinoma skos:exactMatch NCIT:C5491 Colon Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003555 Bartholin gland adenosquamous carcinoma skos:exactMatch NCIT:C40296 Bartholin Gland Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003556 endometrial adenosquamous carcinoma skos:exactMatch NCIT:C114656 Endometrial Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003557 optic nerve sheath meningioma skos:exactMatch NCIT:C4538 Optic Nerve Sheath Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003558 adenosquamous prostate carcinoma skos:exactMatch NCIT:C5538 Prostate Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003561 malignant giant cell tumor of soft parts skos:exactMatch NCIT:C8380 Undifferentiated Pleomorphic Sarcoma with Osteoclast-Like Giant Cells semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003562 rete testis neoplasm skos:exactMatch NCIT:C39955 Rete Testis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003563 diffuse pulmonary fibrosis skos:exactMatch NCIT:C27216 Diffuse Pulmonary Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003564 localized pulmonary fibrosis skos:exactMatch NCIT:C27103 Localized Pulmonary Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003565 urethral villous adenoma skos:exactMatch NCIT:C39872 Urethral Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003569 cranial nerve neuropathy skos:exactMatch NCIT:C26733 Cranial Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003570 lipid-rich carcinoma skos:exactMatch NCIT:C4152 Lipid-Rich Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003572 nasopharyngeal type undifferentiated carcinoma skos:exactMatch NCIT:C4107 Nasopharyngeal-Type Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003573 pleomorphic carcinoma skos:exactMatch NCIT:C4094 Pleomorphic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003574 external ear cancer skos:exactMatch NCIT:C4653 Malignant External Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003575 comedocarcinoma skos:exactMatch NCIT:C4188 Comedo-Type Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003578 extragonadal nonseminomatous germ cell tumor skos:exactMatch NCIT:C8885 Malignant Extragonadal Nongerminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003581 ovarian embryonal carcinoma skos:exactMatch NCIT:C8108 Ovarian Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003582 hereditary breast ovarian cancer syndrome skos:exactMatch NCIT:C8493 BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003585 adult liposarcoma skos:exactMatch NCIT:C7811 Adult Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003586 esophagus liposarcoma skos:exactMatch NCIT:C5705 Esophageal Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003587 pediatric liposarcoma skos:exactMatch NCIT:C8091 Childhood Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003588 larynx liposarcoma skos:exactMatch NCIT:C6021 Laryngeal Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003589 liposarcoma of the ovary skos:exactMatch NCIT:C6419 Ovarian Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003590 fibroblastic liposarcoma skos:exactMatch NCIT:C6509 Fibroblastic Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003591 kidney liposarcoma skos:exactMatch NCIT:C6185 Kidney Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003592 gastric liposarcoma skos:exactMatch NCIT:C5488 Gastric Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003593 breast liposarcoma skos:exactMatch NCIT:C5187 Breast Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003594 mixed liposarcoma skos:exactMatch NCIT:C4253 Mixed Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003595 sclerosing liposarcoma skos:exactMatch NCIT:C6507 Sclerosing Atypical Lipomatous Tumor/Well Differentiated Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003596 spindle cell liposarcoma skos:exactMatch NCIT:C27489 Atypical Spindle Cell/Pleomorphic Lipomatous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003599 vulvar liposarcoma skos:exactMatch NCIT:C40321 Vulvar Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003600 cutaneous liposarcoma skos:exactMatch NCIT:C5615 Skin Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003601 mediastinum liposarcoma skos:exactMatch NCIT:C6614 Mediastinal Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003602 intracranial liposarcoma skos:exactMatch NCIT:C6973 Brain Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003606 adrenal medulla cancer skos:exactMatch NCIT:C4396 Malignant Adrenal Medulla Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003608 optic atrophy skos:exactMatch NCIT:C34863 Optic Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003609 seminal vesicle cystadenoma skos:exactMatch NCIT:C39907 Seminal Vesicle Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003610 rete ovarii cystadenoma skos:exactMatch NCIT:C40019 Rete Ovarii Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003611 uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease skos:exactMatch NCIT:C40142 Uterine Ligament Papillary Cystadenoma Associated with von Hippel-Lindau Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003612 uterine ligament cancer skos:exactMatch NCIT:C126498 Malignant Uterine Ligament Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003614 intravenous leiomyomatosis skos:exactMatch NCIT:C4518 Intravenous Leiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003615 nerve compression syndrome skos:exactMatch NCIT:C27221 Entrapment Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003616 salpingitis isthmica nodosa skos:exactMatch NCIT:C40119 Salpingitis Isthmica Nodosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003617 chronic salpingitis skos:exactMatch NCIT:C40118 Chronic Salpingitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003618 pyosalpinx skos:exactMatch NCIT:C34968 Pyosalpinx semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003619 salpingitis skos:exactMatch NCIT:C26880 Salpingitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003620 peripheral nervous system disorder skos:exactMatch NCIT:C27580 Peripheral Nervous System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003621 small intestinal vasoactive intestinal peptide producing tumor skos:exactMatch NCIT:C27455 Small Intestinal VIP-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003622 pancreatic vasoactive intestinal peptide producing tumor skos:exactMatch NCIT:C27454 Pancreatic VIP-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003624 acinic cell breast carcinoma skos:exactMatch NCIT:C40367 Breast Acinic Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003626 uterine ligament serous adenocarcinoma skos:exactMatch NCIT:C40136 Uterine Ligament Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003628 pulmonary valve disorder skos:exactMatch NCIT:C78579 Pulmonary Valve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003630 pancreatic serous cystadenocarcinoma skos:exactMatch NCIT:C5724 Pancreatic Serous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003631 cervical serous adenocarcinoma skos:exactMatch NCIT:C40201 Cervical Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003632 endocervicitis skos:exactMatch NCIT:C26762 Endocervicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003633 malignant mesenchymoma skos:exactMatch NCIT:C4268 Malignant Mesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003635 sebaceous breast carcinoma skos:exactMatch NCIT:C40369 Breast Sebaceous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003636 vulvar sebaceous carcinoma skos:exactMatch NCIT:C40309 Vulvar Sebaceous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003637 clear cell-sugar-tumor of the lung skos:exactMatch NCIT:C38152 Lung Clear Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003638 lung meningioma skos:exactMatch NCIT:C5668 Lung Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003639 lung hilum neoplasm skos:exactMatch NCIT:C5671 Lung Hilum Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003640 verruciform xanthoma of skin skos:exactMatch NCIT:C4478 Cutaneous Verruciform Xanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003641 central nervous system hematopoietic neoplasm skos:exactMatch NCIT:C5503 Central Nervous System Hematopoietic and Lymphoid Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003643 giant hemangioma skos:exactMatch NCIT:C27777 Giant Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003644 cavernous hemangioma of colon skos:exactMatch NCIT:C5395 Colon Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003645 cavernous hemangioma of face skos:exactMatch NCIT:C7053 Cavernous Hemangioma of the Face semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003646 rectum neuroendocrine neoplasm skos:exactMatch NCIT:C5698 Rectal Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003649 esophageal neuroendocrine tumor skos:exactMatch NCIT:C95616 Esophageal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003650 mixed hepatoblastoma skos:exactMatch NCIT:C7097 Mixed Epithelial and Mesenchymal Hepatoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003651 macrotrabecular hepatoblastoma skos:exactMatch NCIT:C7095 Macrotrabecular Hepatoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003652 acute urate nephropathy skos:exactMatch NCIT:C123037 Uric Acid Nephrolithiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003654 childhood parosteal osteosarcoma skos:exactMatch NCIT:C6589 Childhood Parosteal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003655 cerebral lymphoma skos:exactMatch NCIT:C7611 Cerebral Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003658 B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma skos:exactMatch NCIT:C37869 Gray-Zone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003659 pediatric lymphoma skos:exactMatch NCIT:C5165 Childhood Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003660 adult lymphoma skos:exactMatch NCIT:C7587 Adult Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003661 breast lymphoma skos:exactMatch NCIT:C4671 Breast Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003663 uterine ligament endometrioid adenocarcinoma skos:exactMatch NCIT:C40138 Broad Ligament Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003664 hemolytic anemia skos:exactMatch NCIT:C34376 Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003665 cervical endometrioid adenocarcinoma skos:exactMatch NCIT:C6343 Cervical Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003666 fallopian tube endometrioid adenocarcinoma skos:exactMatch NCIT:C6279 Fallopian Tube Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003668 extragonadal seminoma skos:exactMatch NCIT:C7327 Extragonadal Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003669 testicular seminoma skos:exactMatch NCIT:C7328 Testicular Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003678 silent myocardial infarction skos:exactMatch NCIT:C35400 Silent Myocardial Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003680 periosteal chondrosarcoma skos:exactMatch NCIT:C7357 Periosteal Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003682 localized chondrosarcoma skos:exactMatch NCIT:C8778 Localized Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003684 clear cell chondrosarcoma skos:exactMatch NCIT:C6475 Clear Cell Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003685 retroperitoneal germ cell neoplasm skos:exactMatch NCIT:C6447 Retroperitoneal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003686 apocrine sweat gland neoplasm skos:exactMatch NCIT:C6798 Apocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003687 endocardium cancer skos:exactMatch NCIT:C4570 Malignant Endocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003688 well differentiated papillary mesothelioma skos:exactMatch NCIT:C7635 Well Differentiated Papillary Mesothelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003689 familial hemolytic anemia skos:exactMatch NCIT:C34379 Hereditary Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003690 adult anaplastic ependymoma skos:exactMatch NCIT:C8269 Adult Anaplastic Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003691 childhood malignant mesenchymoma skos:exactMatch NCIT:C8097 Childhood Malignant Mesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003692 adult malignant mesenchymoma skos:exactMatch NCIT:C7947 Adult Malignant Mesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003693 clear cell cystadenofibroma skos:exactMatch NCIT:C8988 Clear Cell Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003694 ovarian clear cell cystadenofibroma skos:exactMatch NCIT:C40086 Ovarian Clear Cell Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003695 ovarian clear cell adenofibroma skos:exactMatch NCIT:C40085 Ovarian Clear Cell Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003697 non-invasive verrucous carcinoma of the penis skos:exactMatch NCIT:C27791 Non-Invasive Verrucous Carcinoma of the Penis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003698 penis verrucous carcinoma skos:exactMatch NCIT:C6982 Penile Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003699 phobic disorder skos:exactMatch NCIT:C35420 Phobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003700 brachial plexus neoplasm skos:exactMatch NCIT:C5823 Brachial Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003701 thyroid gland diffuse sclerosing papillary carcinoma skos:exactMatch NCIT:C7427 Diffuse Sclerosing Variant Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003702 uterus intravascular leiomyomatosis skos:exactMatch NCIT:C5356 Uterine Corpus Intravenous Leiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003704 uterine corpus diffuse leiomyomatosis skos:exactMatch NCIT:C40170 Uterine Corpus Diffuse Leiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003705 adult brainstem mixed glioma skos:exactMatch NCIT:C9371 Adult Brain Stem Mixed Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003706 adult brainstem astrocytoma skos:exactMatch NCIT:C6954 Adult Brain Stem Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003707 distal biliary tract carcinoma skos:exactMatch NCIT:C7109 Distal Bile Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003708 extrahepatic bile duct small cell adenocarcinoma skos:exactMatch NCIT:C5845 Extrahepatic Bile Duct Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003709 agoraphobia skos:exactMatch NCIT:C34362 Agoraphobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003710 ovarian mixed germ cell neoplasm skos:exactMatch NCIT:C8114 Ovarian Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003712 angiokeratoma of mibelli skos:exactMatch NCIT:C3927 Angiokeratoma of Mibelli semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003713 angiokeratoma circumscriptum skos:exactMatch NCIT:C7751 Angiokeratoma Circumscriptum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003714 bladder urachal squamous cell carcinoma skos:exactMatch NCIT:C39845 Urachal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003715 bladder urachal carcinoma skos:exactMatch NCIT:C39842 Urachal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003716 renal pelvis papillary urothelial carcinoma skos:exactMatch NCIT:C6148 Renal Pelvis Papillary Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003717 renal pelvis papillary tumor skos:exactMatch NCIT:C8603 Renal Pelvis Papillary Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003719 renal pelvis neoplasm skos:exactMatch NCIT:C8404 Renal Pelvis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003720 kidney fibrosarcoma skos:exactMatch NCIT:C7726 Kidney Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003721 kidney osteogenic sarcoma skos:exactMatch NCIT:C6181 Kidney Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003722 internal auditory canal meningioma skos:exactMatch NCIT:C5307 Internal Auditory Canal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003724 non-proliferative fibrocystic change of the breast skos:exactMatch NCIT:C6943 Breast Fibrocystic Change, Non-Proliferative Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003725 breast adenosis skos:exactMatch NCIT:C3484 Breast Adenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003726 apocrine adenosis of breast skos:exactMatch NCIT:C5198 Breast Apocrine Adenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003727 animal phobia skos:exactMatch NCIT:C35273 Animal Phobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003728 breast fibrosarcoma skos:exactMatch NCIT:C5185 Breast Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003729 aleukemic leukemia cutis skos:exactMatch NCIT:C4983 Aleukemic Leukemia Cutis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003730 aleukemic leukemia skos:exactMatch NCIT:C4982 Aleukemic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003731 adult central nervous system teratoma skos:exactMatch NCIT:C5794 Adult Central Nervous System Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003732 adult central nervous system mature teratoma skos:exactMatch NCIT:C27400 Adult Central Nervous System Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003733 central nervous system mature teratoma skos:exactMatch NCIT:C7013 Central Nervous System Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003734 adult central nervous system immature teratoma skos:exactMatch NCIT:C27401 Adult Central Nervous System Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003735 central nervous system immature teratoma skos:exactMatch NCIT:C7014 Central Nervous System Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003736 cancerophobia skos:exactMatch NCIT:C35492 Cancerphobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003737 malignant testicular Leydig cell tumor skos:exactMatch NCIT:C39942 Malignant Testicular Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003738 selective IgE deficiency disease skos:exactMatch NCIT:C27143 Selective IgE Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003739 selective immunoglobulin deficiency disease skos:exactMatch NCIT:C27870 Selective Immunoglobulin Isotype Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003740 AIDS phobia skos:exactMatch NCIT:C35614 AIDS Phobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003741 juvenile type testicular granulosa cell tumor skos:exactMatch NCIT:C39947 Juvenile Testicular Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003742 heart fibrosarcoma skos:exactMatch NCIT:C5361 Cardiac Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003743 heart malignant hemangiopericytoma skos:exactMatch NCIT:C5365 Malignant Cardiac Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003744 spindle cell intraocular melanoma skos:exactMatch NCIT:C7986 Uveal Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003745 choroid spindle cell melanoma skos:exactMatch NCIT:C6099 Choroid Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003746 ciliary body spindle cell melanoma skos:exactMatch NCIT:C6117 Ciliary Body Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003747 telangiectatic glomangioma skos:exactMatch NCIT:C5345 Telangiectatic Glomangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003748 flying phobia skos:exactMatch NCIT:C35413 Flying Phobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003749 esophageal disorder skos:exactMatch NCIT:C3027 Esophageal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003750 childhood central nervous system germ cell tumor skos:exactMatch NCIT:C6205 Childhood Central Nervous System Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003751 childhood germ cell tumor skos:exactMatch NCIT:C7928 Childhood Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003752 frontal sinus Schneiderian papilloma skos:exactMatch NCIT:C6837 Frontal Sinus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003753 nasal vestibule squamous papilloma skos:exactMatch NCIT:C4369 Nasal Vestibule Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003754 Brown-Sequard syndrome skos:exactMatch NCIT:C84601 Brown-Sequard Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003755 urinary tract non-invasive transitional cell neoplasm skos:exactMatch NCIT:C39854 Non-Invasive Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003756 ovarian mucinous neoplasm skos:exactMatch NCIT:C5242 Ovarian Mucinous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003757 paraplegia skos:exactMatch NCIT:C50687 Paraplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003758 childhood testicular germ cell tumor skos:exactMatch NCIT:C6552 Childhood Testicular Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003759 childhood ovarian yolk sac tumor skos:exactMatch NCIT:C6551 Childhood Ovarian Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003760 pediatric ovarian germ cell tumor skos:exactMatch NCIT:C8588 Childhood Ovarian Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003761 leptomeningeal melanoma skos:exactMatch NCIT:C5317 Meningeal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003762 malignant leptomeningeal tumor skos:exactMatch NCIT:C8506 Malignant Leptomeningeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003763 acute stress disorder skos:exactMatch NCIT:C92621 Acute Stress Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003764 pediatric leptomeningeal melanoma skos:exactMatch NCIT:C5318 Childhood Meningeal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003765 adult leptomeningeal melanoma skos:exactMatch NCIT:C5319 Adult Meningeal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003766 thalamic cancer skos:exactMatch NCIT:C4576 Malignant Thalamic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003767 mitral valve disorder skos:exactMatch NCIT:C78446 Mitral Valve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003768 signet ring cell variant cervical mucinous adenocarcinoma skos:exactMatch NCIT:C40205 Cervical Mucinous Adenocarcinoma, Signet Ring Cell-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003769 herpetic gastritis skos:exactMatch NCIT:C27341 Herpetic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003770 thoracic spinal canal and spinal cord meningioma skos:exactMatch NCIT:C5297 Thoracic Intraspinal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003771 jugular foramen meningioma skos:exactMatch NCIT:C5293 Jugular Foramen Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003772 cerebral meningioma skos:exactMatch NCIT:C4807 Cerebral Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003773 intracerebral cystic meningioma skos:exactMatch NCIT:C5269 Intracerebral Cystic Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003774 cerebral convexity meningioma skos:exactMatch NCIT:C4959 Cerebral Convexity Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003775 lateral ventricle meningioma skos:exactMatch NCIT:C5302 Lateral Ventricle Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003776 renal pelvis inverted papilloma skos:exactMatch NCIT:C6187 Renal Pelvis Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003777 renal pelvis urothelial papilloma skos:exactMatch NCIT:C4528 Renal Pelvis Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003780 T-cell immunodeficiency skos:exactMatch NCIT:C27145 T-Cell Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003781 bronchitis skos:exactMatch NCIT:C2911 Bronchitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003782 uterine corpus epithelioid leiomyosarcoma skos:exactMatch NCIT:C40174 Uterine Corpus Epithelioid Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003784 nasal cavity carcinoma in situ skos:exactMatch NCIT:C4589 Stage 0 Nasal Cavity Cancer AJCC v6, v7, and v8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003785 leukopenia skos:exactMatch NCIT:C26816 Leukopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003786 childhood testicular choriocarcinoma skos:exactMatch NCIT:C6544 Childhood Testicular Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003787 childhood testicular mixed germ cell cancer skos:exactMatch NCIT:C6542 Childhood Testicular Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003788 childhood embryonal testis carcinoma skos:exactMatch NCIT:C6545 Childhood Testicular Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003789 hereditary papillary renal cell carcinoma skos:exactMatch NCIT:C9222 Hereditary Papillary Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003790 prostatic urethra urothelial carcinoma skos:exactMatch NCIT:C39900 Prostatic Urethra Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003791 prostatic urethral cancer skos:exactMatch NCIT:C39870 Prostatic Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003792 ovarian carcinosarcoma skos:exactMatch NCIT:C9192 Ovarian Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003795 ovarian small cell carcinoma skos:exactMatch NCIT:C27390 Ovarian Small Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003796 rectum Kaposi sarcoma skos:exactMatch NCIT:C5550 Rectal Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003799 conjunctivitis skos:exactMatch NCIT:C34504 Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003800 conventional malignant hemangiopericytoma skos:exactMatch NCIT:C9425 Conventional Malignant Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003801 corneal intraepithelial neoplasm skos:exactMatch NCIT:C6093 Corneal Squamous Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003802 cornea cancer skos:exactMatch NCIT:C3565 Malignant Corneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003803 aortic valve disorder skos:exactMatch NCIT:C78650 Aortic Valve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003805 malignant pericardial mesothelioma skos:exactMatch NCIT:C7631 Pericardial Malignant Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003806 thyroid hyalinizing trabecular adenoma skos:exactMatch NCIT:C6846 Thyroid Gland Hyalinizing Trabecular Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003808 mediastinal extraskeletal osteosarcoma skos:exactMatch NCIT:C6615 Mediastinal Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003809 malignant mediastinum hemangiopericytoma skos:exactMatch NCIT:C6608 Malignant Mediastinal Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003810 bladder diffuse clear cell adenocarcinoma skos:exactMatch NCIT:C39849 Bladder Diffuse Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003811 ovarian seromucinous tumor skos:exactMatch NCIT:C4508 Ovarian Seromucinous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003812 ovarian endometrial cancer skos:exactMatch NCIT:C40051 Malignant Ovarian Endometrioid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003813 ovarian papillary tumor skos:exactMatch NCIT:C8430 Ovarian Papillary Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003818 childhood mature teratoma of the ovary skos:exactMatch NCIT:C6548 Childhood Ovarian Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003819 childhood teratoma of the ovary skos:exactMatch NCIT:C6554 Childhood Ovarian Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003820 mature ovarian teratoma skos:exactMatch NCIT:C8112 Mature Ovarian Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003821 ovarian biphasic or triphasic teratoma skos:exactMatch NCIT:C39992 Ovarian Biphasic or Triphasic Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003822 non-invasive bladder papillary urothelial neoplasm skos:exactMatch NCIT:C39831 Bladder Non-Invasive Papillary Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003824 hereditary kidney oncocytoma skos:exactMatch NCIT:C8960 Hereditary Kidney Oncocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003825 kidney oncocytoma skos:exactMatch NCIT:C4526 Kidney Oncocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003826 mediastinum seminoma skos:exactMatch NCIT:C6812 Mediastinal Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003827 transient hypogammaglobulinemia skos:exactMatch NCIT:C27319 Transient Hypogammaglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003828 growth hormone-producing pituitary gland carcinoma skos:exactMatch NCIT:C5963 Metastatic Somatotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003829 chromophil adenoma of the kidney skos:exactMatch NCIT:C3687 Renal Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003830 type 1 papillary adenoma of the kidney skos:exactMatch NCIT:C39809 Type 1 Renal Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003831 type 2 papillary adenoma of the kidney skos:exactMatch NCIT:C39810 Type 2 Renal Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003832 complement deficiency skos:exactMatch NCIT:C4691 Complement Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003834 gastric cardia carcinoma skos:exactMatch NCIT:C6794 Gastric Cardia Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003835 gastric cardia adenocarcinoma skos:exactMatch NCIT:C5247 Gastric Cardia Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003836 malignant thyroid stimulating hormone producing neoplasm of pituitary gland skos:exactMatch NCIT:C5965 Metastatic Thyrotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003837 TSH producing pituitary tumor skos:exactMatch NCIT:C7915 Thyrotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003839 ovarian mucinous adenocarcinofibroma skos:exactMatch NCIT:C40034 Ovarian Mucinous Adenocarcinofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003840 epicardium lipoma skos:exactMatch NCIT:C6742 Epicardial Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003841 heart lipoma skos:exactMatch NCIT:C6741 Cardiac Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003842 childhood cerebellar astrocytic neoplasm skos:exactMatch NCIT:C6286 Childhood Cerebellar Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003843 cerebral hemisphere lipoma skos:exactMatch NCIT:C6220 Cerebral Hemisphere Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003844 central nervous system lipoma skos:exactMatch NCIT:C5451 Central Nervous System Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003845 corpus callosum lipoma skos:exactMatch NCIT:C5438 Corpus Callosum Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003846 viral esophagitis skos:exactMatch NCIT:C27108 Viral Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003847 hereditary disease skos:exactMatch NCIT:C3101 Genetic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003848 ectopic thymus skos:exactMatch NCIT:C27804 Ectopic Thymus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003849 clivus chordoma skos:exactMatch NCIT:C5412 Clivus Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003850 clivus chondroid chordoma skos:exactMatch NCIT:C5426 Clivus Chondroid Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003851 ovarian fetiform teratoma skos:exactMatch NCIT:C39996 Ovarian Fetiform Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003852 ovarian solid teratoma skos:exactMatch NCIT:C7285 Ovarian Solid Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003853 Bartholin gland adenocarcinoma skos:exactMatch NCIT:C7719 Bartholin Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003856 adult malignant hemangiopericytoma skos:exactMatch NCIT:C7946 Malignant Adult Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003857 adult intracranial malignant hemangiopericytoma skos:exactMatch NCIT:C9183 Adult Central Nervous System Solitary Fibrous Tumor, Grade 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003858 anterior optic tract meningioma skos:exactMatch NCIT:C7538 Anterior Visual Pathway Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003859 bilateral meningioma of optic nerve skos:exactMatch NCIT:C5304 Bilateral Optic Nerve Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003860 cerebellopontine angle meningioma skos:exactMatch NCIT:C5300 Cerebellopontine Angle Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003861 vulvar eccrine adenocarcinoma skos:exactMatch NCIT:C40305 Vulvar Eccrine Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003862 melanotic psammomatous malignant peripheral nerve sheath tumor skos:exactMatch NCIT:C6910 Malignant Melanotic Psammomatous Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003863 malignant melanocytic neoplasm of the peripheral nerve sheath skos:exactMatch NCIT:C4748 Malignant Melanotic Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003864 chronic lymphocytic leukemia/small lymphocytic lymphoma skos:exactMatch NCIT:C27911 Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003865 acral lentiginous melanoma skos:exactMatch NCIT:C4022 Acral Lentiginous Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003866 liver extraskeletal osteosarcoma skos:exactMatch NCIT:C5833 Liver Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003867 diffuse meningeal melanocytosis skos:exactMatch NCIT:C6890 Meningeal Melanocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003868 anterior foramen magnum meningioma skos:exactMatch NCIT:C5281 Anterior Foramen Magnum Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003869 childhood brain stem glioma skos:exactMatch NCIT:C9042 Childhood Brain Stem Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003870 childhood brainstem astrocytoma skos:exactMatch NCIT:C6216 Childhood Brain Stem Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003872 ovarian papillary cystadenoma skos:exactMatch NCIT:C7278 Ovarian Papillary Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003873 ovarian surface papilloma skos:exactMatch NCIT:C7279 Ovarian Surface Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003874 ovarian serous surface papillary adenocarcinoma skos:exactMatch NCIT:C6256 Ovarian Serous Surface Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003875 childhood central nervous system mature teratoma skos:exactMatch NCIT:C27404 Childhood Central Nervous System Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003876 eyelid carcinoma skos:exactMatch NCIT:C6078 Eyelid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003878 malignant choroid melanoma skos:exactMatch NCIT:C4561 Choroid Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003879 ovarian endometrioid adenocarcinofibroma skos:exactMatch NCIT:C40060 Ovarian Endometrioid Adenocarcinofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003880 ceruminous carcinoma skos:exactMatch NCIT:C4176 Ceruminous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003881 vulvar apocrine adenocarcinoma skos:exactMatch NCIT:C40308 Vulvar Apocrine Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003882 central nervous system fibrosarcoma skos:exactMatch NCIT:C5465 Central Nervous System Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003884 lipoma of the rectum skos:exactMatch NCIT:C5551 Rectal Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003885 colorectal lipoma skos:exactMatch NCIT:C5678 Colorectal Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003886 mucinous cystadenofibroma skos:exactMatch NCIT:C8979 Mucinous Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003887 ovarian mucinous adenofibroma skos:exactMatch NCIT:C40040 Ovarian Mucinous Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003888 childhood testicular mixed embryonal carcinoma and teratoma skos:exactMatch NCIT:C6539 Childhood Testicular Mixed Embryonal Carcinoma and Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003889 infiltrating bladder urothelial carcinoma, clear cell variant skos:exactMatch NCIT:C39827 Invasive Bladder Clear Cell (Glycogen-Rich) Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003890 infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C27885 Invasive Bladder Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003891 bladder signet ring cell adenocarcinoma skos:exactMatch NCIT:C6163 Bladder Signet Ring Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003892 acinar lung adenocarcinoma skos:exactMatch NCIT:C5649 Lung Acinar Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003893 rete testis adenoma skos:exactMatch NCIT:C39956 Rete Testis Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003894 mediastinal melanocytic neurilemmoma skos:exactMatch NCIT:C6635 Mediastinal Melanotic Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003895 periosteal osteogenic sarcoma skos:exactMatch NCIT:C8970 Periosteal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003896 breast capillary hemangioma skos:exactMatch NCIT:C5210 Breast Capillary Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003897 breast epithelioid hemangioma skos:exactMatch NCIT:C5211 Breast Epithelioid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003898 pediatric myxoid chondrosarcoma skos:exactMatch NCIT:C27377 Childhood Extraskeletal Myxoid Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003900 connective tissue disorder skos:exactMatch NCIT:C26729 Connective Tissue Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003901 cerebellar hemangioblastoma skos:exactMatch NCIT:C5146 Cerebellar Hemangioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003902 brain stem hemangioblastoma skos:exactMatch NCIT:C5147 Brain Stem Hemangioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003903 benign vaginal mixed tumor skos:exactMatch NCIT:C40280 Benign Vaginal Mixed Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003904 lung occult squamous cell carcinoma skos:exactMatch NCIT:C6686 Occult Lung Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003905 ovarian yolk sac tumor, glandular pattern skos:exactMatch NCIT:C39988 Ovarian Yolk Sac Tumor, Glandular Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003906 ovarian yolk sac tumor, hepatoid pattern skos:exactMatch NCIT:C39989 Ovarian Yolk Sac Tumor, Hepatoid Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003907 ovarian yolk sac tumor, polyvesicular vitelline pattern skos:exactMatch NCIT:C39987 Ovarian Yolk Sac Tumor, Polyvesicular Vitelline Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003908 clivus meningioma skos:exactMatch NCIT:C5289 Clivus Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003909 Bartholin gland adenomyoma skos:exactMatch NCIT:C40300 Bartholin Gland Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003910 mixed cell uveal melanoma skos:exactMatch NCIT:C35781 Uveal Mixed Epithelioid and Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003911 ciliary body mixed cell melanoma skos:exactMatch NCIT:C35783 Ciliary Body Mixed Epithelioid and Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003912 malignant ciliary body melanoma skos:exactMatch NCIT:C4558 Ciliary Body Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003913 choroid mixed cell melanoma skos:exactMatch NCIT:C35782 Choroid Mixed Epithelioid and Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003915 cortical thymoma skos:exactMatch NCIT:C6888 Thymoma Type B2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003917 heart lymphoma skos:exactMatch NCIT:C5368 Cardiac Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003918 angiomatous meningioma skos:exactMatch NCIT:C4332 Angiomatous Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003921 posterior foramen magnum meningioma skos:exactMatch NCIT:C5282 Posterior Foramen Magnum Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003922 ovarian clear cell malignant adenofibroma skos:exactMatch NCIT:C40079 Ovarian Clear Cell Adenocarcinofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003923 ethmoid sinus Schneiderian papilloma skos:exactMatch NCIT:C6836 Ethmoid Sinus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003924 adrenal cortex adenoma skos:exactMatch NCIT:C9003 Adrenal Cortical Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003925 ethmoid sinus inverted papilloma skos:exactMatch NCIT:C6843 Ethmoid Sinus Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003926 neurilemmoma of the pleura skos:exactMatch NCIT:C5418 Pleural Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003928 uterine corpus myxoid leiomyosarcoma skos:exactMatch NCIT:C40175 Uterine Corpus Myxoid Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003929 vestibular micropapillomatosis skos:exactMatch NCIT:C40290 Vulvar Squamous Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003930 non-invasive bladder urothelial carcinoma skos:exactMatch NCIT:C6188 Stage 0 Bladder Urothelial Carcinoma AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003931 childhood optic tract astrocytoma skos:exactMatch NCIT:C7534 Childhood Visual Pathway Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003932 childhood optic nerve glioma skos:exactMatch NCIT:C7535 Childhood Visual Pathway Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003933 chest wall bone cancer skos:exactMatch NCIT:C6724 Malignant Chest Wall Bone Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003934 breast apocrine carcinoma skos:exactMatch NCIT:C5141 Breast Apocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003935 oncocytic breast carcinoma skos:exactMatch NCIT:C40366 Breast Oncocytic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003936 invasive tubular breast carcinoma skos:exactMatch NCIT:C9135 Breast Tubular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003938 bladder colonic type adenocarcinoma skos:exactMatch NCIT:C39835 Bladder Enteric Type Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003941 classic variant of chromophobe renal cell carcinoma skos:exactMatch NCIT:C27888 Classic Variant of Chromophobe Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003942 eosinophilic variant of chromophobe renal cell carcinoma skos:exactMatch NCIT:C27889 Eosinophilic Variant of Chromophobe Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003943 central nervous system hibernoma skos:exactMatch NCIT:C6997 Central Nervous System Hibernoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003944 endobronchial leiomyoma skos:exactMatch NCIT:C5661 Endobronchial Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003945 bone epithelioid hemangioma skos:exactMatch NCIT:C5396 Bone Epithelioid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003946 vaginal villous adenoma skos:exactMatch NCIT:C40259 Vaginal Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003947 hyper-IgM syndrome skos:exactMatch NCIT:C3990 Hyperimmunoglobulin M Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003947 hyper-IgM syndrome skos:exactMatch NCIT:C84783 Immunodeficiency with Hyper-IgM semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003948 cerebral hemangioma skos:exactMatch NCIT:C5433 Cerebral Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003950 nipple carcinoma skos:exactMatch NCIT:C28432 Nipple Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003951 scrotal hemangioma skos:exactMatch NCIT:C6387 Scrotal Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003952 adult central nervous system choriocarcinoma skos:exactMatch NCIT:C5793 Adult Central Nervous System Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003953 pediatric CNS choriocarcinoma skos:exactMatch NCIT:C6206 Childhood Central Nervous System Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003955 juvenile breast papillomatosis skos:exactMatch NCIT:C9503 Juvenile Breast Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003957 adult pineoblastoma skos:exactMatch NCIT:C8292 Adult Pineoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003958 childhood central nervous system immature teratoma skos:exactMatch NCIT:C27405 Childhood Central Nervous System Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003959 breast large cell neuroendocrine carcinoma skos:exactMatch NCIT:C40356 Breast Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003960 pulmonary large cell neuroendocrine carcinoma skos:exactMatch NCIT:C5672 Lung Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003962 Froelich syndrome skos:exactMatch NCIT:C34625 Frohlich Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003963 diffuse infiltrative lymphocytosis syndrome skos:exactMatch NCIT:C35699 Diffuse Infiltrative Lymphocytosis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003964 myositis ossificans skos:exactMatch NCIT:C3253 Myositis Ossificans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003965 Capgras syndrome skos:exactMatch NCIT:C34446 Capgras Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003966 testicular monophasic choriocarcinoma skos:exactMatch NCIT:C39935 Testicular Monophasic Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003967 synchronous multifocal osteogenic sarcoma skos:exactMatch NCIT:C6471 Synchronous Multifocal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003968 asynchronous multifocal osteogenic sarcoma skos:exactMatch NCIT:C6472 Asynchronous Multifocal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003970 gastric fundus carcinoma skos:exactMatch NCIT:C8398 Gastric Fundus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003971 gastric pylorus carcinoma skos:exactMatch NCIT:C6795 Gastric Pylorus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003972 gastric body carcinoma skos:exactMatch NCIT:C8399 Gastric Body Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003973 tubular variant testicular seminoma skos:exactMatch NCIT:C40959 Testicular Seminoma, Tubular Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003975 Littre gland carcinoma skos:exactMatch NCIT:C39865 Littre Gland Adenocarcinoma of the Urethra semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003976 malignant type AB thymoma skos:exactMatch NCIT:C6886 Malignant Type AB Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003978 colon small cell neuroendocrine carcinoma skos:exactMatch NCIT:C6761 Colon Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003979 intrahepatic bile duct cystadenoma skos:exactMatch NCIT:C96835 Intrahepatic Bile Duct Mucinous Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003980 schwannoma of jugular foramen skos:exactMatch NCIT:C5323 Jugular Foramen Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003982 bilateral breast carcinoma skos:exactMatch NCIT:C8287 Bilateral Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003983 synchronous bilateral breast carcinoma skos:exactMatch NCIT:C40370 Synchronous Bilateral Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003984 internal auditory canal lipoma skos:exactMatch NCIT:C5452 Inner Ear Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003985 chest wall lymphoma skos:exactMatch NCIT:C6712 Chest Wall Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003987 lung lymphoma skos:exactMatch NCIT:C4794 Lung Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003988 sternum lymphoma skos:exactMatch NCIT:C6716 Sternal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003989 polyembryoma of the ovary skos:exactMatch NCIT:C39990 Ovarian Polyembryoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003990 malignant breast myoepithelioma skos:exactMatch NCIT:C40395 Breast Malignant Myoepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003991 villoglandular endometrial endometrioid adenocarcinoma skos:exactMatch NCIT:C27846 Villoglandular Endometrial Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003992 childhood botryoid rhabdomyosarcoma skos:exactMatch NCIT:C35574 Childhood Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003993 childhood vagina botryoid rhabdomyosarcoma skos:exactMatch NCIT:C35556 Childhood Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003994 botryoid-type embryonal rhabdomyosarcoma of the vagina skos:exactMatch NCIT:C40268 Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003995 vulvar childhood botryoid-type embryonal rhabdomyosarcoma skos:exactMatch NCIT:C36098 Childhood Vulvar Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003997 colon Kaposi sarcoma skos:exactMatch NCIT:C5516 Colon Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003998 obsolete vaginal tubular adenoma skos:exactMatch NCIT:C40257 Vaginal Tubular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0003999 juvenile pilocytic astrocytoma skos:exactMatch NCIT:C27081 Juvenile Pilocytic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004000 childhood pilocytic astrocytoma skos:exactMatch NCIT:C4048 Childhood Pilocytic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004001 compartment syndrome skos:exactMatch NCIT:C118422 Compartment Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004005 rete ovarii adenoma skos:exactMatch NCIT:C40018 Rete Ovarii Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004006 rete ovarii cystadenofibroma skos:exactMatch NCIT:C40020 Rete Ovarii Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004007 breast intraductal proliferative lesion skos:exactMatch NCIT:C27942 Breast Intraductal Proliferative Lesion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004008 flat ductal epithelial atypia skos:exactMatch NCIT:C36086 Breast Flat Ductal Epithelial Atypia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004009 kidney pelvis sarcomatoid transitional cell carcinoma skos:exactMatch NCIT:C6186 Invasive Renal Pelvis Sarcomatoid Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004010 infiltrating renal pelvis/ureter urothelial carcinoma skos:exactMatch NCIT:C39879 Invasive Renal Pelvis and Ureter Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004012 adult botryoid rhabdomyosarcoma skos:exactMatch NCIT:C36099 Adult Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004013 adult vagina botryoid embryonal rhabdomyosarcoma skos:exactMatch NCIT:C40267 Adult Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004014 ethmoid sinus ectopic meningioma skos:exactMatch NCIT:C5309 Ethmoid Sinus Primary Ectopic Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004015 pineal region teratoma skos:exactMatch NCIT:C6753 Pineal Region Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004016 pineal region mature teratoma skos:exactMatch NCIT:C6754 Pineal Region Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004017 pineal region immature teratoma skos:exactMatch NCIT:C6755 Pineal Region Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004019 oxyphilic endometrial endometrioid adenocarcinoma skos:exactMatch NCIT:C27849 Oxyphilic Endometrial Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004020 mediastinal gray zone lymphoma skos:exactMatch NCIT:C37870 Mediastinal Gray-Zone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004021 mediastinal malignant lymphoma skos:exactMatch NCIT:C6633 Mediastinal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004022 parasagittal meningioma skos:exactMatch NCIT:C4960 Parasagittal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004024 spinal cord neuroblastoma skos:exactMatch NCIT:C5155 Spinal Cord Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004026 skin tag skos:exactMatch NCIT:C3374 Skin Tag semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004028 small intestinal fibrosarcoma skos:exactMatch NCIT:C5336 Small Intestinal Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004030 ureter transitional cell carcinoma skos:exactMatch NCIT:C4830 Ureter Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004032 ovarian seromucinous carcinoma skos:exactMatch NCIT:C40090 Ovarian Seromucinous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004034 eye lymphoma skos:exactMatch NCIT:C35690 Eye Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004035 glomangiomatosis skos:exactMatch NCIT:C27496 Glomangiomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004038 dental enamel hypoplasia skos:exactMatch NCIT:C34529 Enamel Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004040 urinary bladder inverted papilloma skos:exactMatch NCIT:C39859 Bladder Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004041 urothelial papilloma skos:exactMatch NCIT:C3842 Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004042 urethra inverted papilloma skos:exactMatch NCIT:C6173 Urethral Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004043 ureter inverted papilloma skos:exactMatch NCIT:C6174 Ureter Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004044 ureter urothelial papilloma skos:exactMatch NCIT:C6160 Ureter Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004045 pediatric intraocular retinoblastoma skos:exactMatch NCIT:C9047 Childhood Intraocular Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004046 childhood brain meningioma skos:exactMatch NCIT:C6253 Childhood Intracranial Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004047 sphenoidal sinus neoplasm skos:exactMatch NCIT:C6792 Sphenoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004048 immature gastric teratoma skos:exactMatch NCIT:C5256 Gastric Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004050 telangiectatic osteogenic sarcoma skos:exactMatch NCIT:C3902 Telangiectatic Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004051 aleukemic monocytic leukemia cutis skos:exactMatch NCIT:C5630 Aleukemic Monocytic Leukemia Cutis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004052 rectal cloacogenic carcinoma skos:exactMatch NCIT:C5555 Rectal Cloacogenic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004053 bartholin gland squamous cell carcinoma skos:exactMatch NCIT:C40293 Bartholin Gland Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004056 bladder papillary urothelial carcinoma skos:exactMatch NCIT:C7383 Bladder Papillary Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004057 micropapillary variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C27202 Invasive Bladder Micropapillary Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004058 pancreatic cholera skos:exactMatch NCIT:C3488 WDHA Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004060 peripheral epithelioid sarcoma skos:exactMatch NCIT:C27473 Distal-Type Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004062 intermediate cell type uveal melanoma skos:exactMatch NCIT:C7989 Uveal Intermediate Cell Type Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004063 intermediate cell type iris melanoma skos:exactMatch NCIT:C6101 Iris Intermediate Cell Type Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004064 iris melanoma skos:exactMatch NCIT:C9088 Iris Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004065 intermediate cell type choroid melanoma skos:exactMatch NCIT:C6100 Choroid Intermediate Cell Type Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004066 intermediate cell type ciliary body melanoma skos:exactMatch NCIT:C6118 Ciliary Body Intermediate Cell Type Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004067 gallbladder mucinous adenocarcinoma skos:exactMatch NCIT:C5744 Gallbladder Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004071 childhood cerebral astrocytoma skos:exactMatch NCIT:C4347 Childhood Cerebral Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004074 ovarian mucinous cystadenofibroma skos:exactMatch NCIT:C40041 Ovarian Mucinous Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004075 infiltrating lipoma skos:exactMatch NCIT:C7451 Infiltrating Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004076 tendon sheath lipoma skos:exactMatch NCIT:C6499 Tendon Sheath Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004077 lumbosacral lipoma skos:exactMatch NCIT:C6500 Lumbosacral Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004078 mucinous intrahepatic cholangiocarcinoma skos:exactMatch NCIT:C41618 Mucin-Producing Intrahepatic Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004079 lung mucous gland adenoma skos:exactMatch NCIT:C5664 Lung Mucous Gland Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004080 glottis squamous cell carcinoma skos:exactMatch NCIT:C8186 Glottic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004081 extrahepatic bile duct clear cell adenocarcinoma skos:exactMatch NCIT:C5775 Extrahepatic Bile Duct Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004082 childhood immature teratoma of ovary skos:exactMatch NCIT:C6547 Childhood Ovarian Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004083 Borst-Jadassohn intraepidermal carcinoma skos:exactMatch NCIT:C4110 Intraepidermal Epithelioma of Jadassohn semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004085 choroid epithelioid cell melanoma skos:exactMatch NCIT:C6102 Choroid Epithelioid Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004086 ciliary body epithelioid cell melanoma skos:exactMatch NCIT:C6119 Ciliary Body Epithelioid Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004087 basaloid large cell lung carcinoma skos:exactMatch NCIT:C7266 Lung Basaloid Large Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004088 cervical basaloid carcinoma skos:exactMatch NCIT:C40189 Cervical Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004089 basaloid carcinoma of the penis skos:exactMatch NCIT:C6980 Penile Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004090 vulvar basaloid squamous cell carcinoma skos:exactMatch NCIT:C40286 Vulvar Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004091 skin basaloid carcinoma skos:exactMatch NCIT:C27543 Skin Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004092 thymic basaloid carcinoma skos:exactMatch NCIT:C6456 Thymic Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004093 esophageal basaloid carcinoma skos:exactMatch NCIT:C7032 Esophageal Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004094 multiple skull base meningioma skos:exactMatch NCIT:C5279 Multiple Skull Base Meningiomas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004095 B-cell neoplasm skos:exactMatch NCIT:C27907 B-Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004096 spinal cord dermoid cyst skos:exactMatch NCIT:C6808 Dermoid Cyst of the Spinal Cord semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004098 malignant melanocytic peripheral nerve sheath tumor of mediastinum skos:exactMatch NCIT:C6630 Malignant Melanotic Peripheral Nerve Sheath Tumor of the Mediastinum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004099 adult cystic teratoma skos:exactMatch NCIT:C9012 Adult Cystic Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004100 lung mixed small cell and squamous cell carcinoma skos:exactMatch NCIT:C9423 Combined Lung Small Cell and Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004101 multicentric papillary thyroid carcinoma skos:exactMatch NCIT:C37304 Multicentric Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004102 columnar cell variant thyroid gland papillary carcinoma skos:exactMatch NCIT:C35830 Columnar Cell Variant Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004103 tall cell variant thyroid gland papillary carcinoma skos:exactMatch NCIT:C35558 Tall Cell Variant Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004104 splenic manifestation of hairy cell leukemia skos:exactMatch NCIT:C7301 Splenic Manifestation of Hairy Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004105 childhood epithelioid sarcoma skos:exactMatch NCIT:C8095 Childhood Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004106 testicular yolk sac tumor, macrocystic pattern skos:exactMatch NCIT:C39924 Testicular Yolk Sac Tumor, Macrocystic Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004107 splenic manifestation of leukemia skos:exactMatch NCIT:C7296 Splenic Manifestation of Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004108 diaphragma sellae meningioma skos:exactMatch NCIT:C5283 Diaphragma Sellae Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004109 epiglottis neoplasm skos:exactMatch NCIT:C4933 Epiglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004110 refractory hairy cell leukemia skos:exactMatch NCIT:C8030 Refractory Hairy Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004111 refractory hematologic cancer skos:exactMatch NCIT:C27357 Refractory Hematologic Malignancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004112 radiation cystitis skos:exactMatch NCIT:C123174 Radiation Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004114 urinary bladder small cell neuroendocrine carcinoma skos:exactMatch NCIT:C9461 Bladder Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004116 esophageal small cell neuroendocrine carcinoma skos:exactMatch NCIT:C6762 Esophageal Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004117 ampulla of vater small cell neuroendocrine carcinoma skos:exactMatch NCIT:C6655 Ampulla of Vater Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004118 cystitis cystica skos:exactMatch NCIT:C96230 Cystitis Cystica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004120 Bartholin gland small cell carcinoma skos:exactMatch NCIT:C40298 Bartholin Gland Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004122 thymus small cell carcinoma skos:exactMatch NCIT:C6460 Thymic Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004124 prostate stromal sarcoma skos:exactMatch NCIT:C5524 Prostate Stromal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004125 rectum leiomyoma skos:exactMatch NCIT:C5552 Rectal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004126 thyroiditis skos:exactMatch NCIT:C26894 Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004127 lung occult adenocarcinoma skos:exactMatch NCIT:C6699 Occult Lung Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004128 lung occult large cell carcinoma skos:exactMatch NCIT:C6685 Occult Lung Large Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004129 cloacogenic carcinoma skos:exactMatch NCIT:C8255 Anal Canal Cloacogenic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004130 anus basaloid carcinoma skos:exactMatch NCIT:C8256 Anal Basaloid Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004131 anal verrucous carcinoma skos:exactMatch NCIT:C7470 Anal Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004132 anal canal squamous cell carcinoma skos:exactMatch NCIT:C7469 Anal Canal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004133 pituitary gland mixed eosinophil-basophil adenoma skos:exactMatch NCIT:C4148 Pituitary Gland Mixed Acidophil-Basophil Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004134 benign dermal neurilemmoma skos:exactMatch NCIT:C5569 Cutaneous Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004135 subacute lymphocytic thyroiditis skos:exactMatch NCIT:C35829 Subacute Lymphocytic Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004136 ovarian endometrioid cystadenoma skos:exactMatch NCIT:C40075 Ovarian Endometrioid Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004139 normocytic anemia skos:exactMatch NCIT:C35142 Normocytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004140 intermediate malignant teratoma skos:exactMatch NCIT:C4288 Intermediate Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004141 melanomatosis skos:exactMatch NCIT:C9499 Melanomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004142 lung combined large cell neuroendocrine carcinoma skos:exactMatch NCIT:C7267 Combined Lung Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004143 psammomatous meningioma skos:exactMatch NCIT:C4331 Psammomatous Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004144 fibrous meningioma skos:exactMatch NCIT:C4330 Fibrous Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004145 meningothelial meningioma skos:exactMatch NCIT:C4329 Meningothelial Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004146 transitional meningioma skos:exactMatch NCIT:C4333 Transitional Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004147 noninvasive malignant thymoma skos:exactMatch NCIT:C9080 Noninvasive Malignant Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004148 gallbladder papillary neoplasm with an associated invasive carcinoma skos:exactMatch NCIT:C5743 Gallbladder Intracholecystic Papillary Neoplasm with an Associated Invasive Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004150 breast giant fibroadenoma skos:exactMatch NCIT:C4273 Breast Giant Fibroadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004152 chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation skos:exactMatch NCIT:C37201 Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004153 childhood central nervous system embryonal carcinoma skos:exactMatch NCIT:C6208 Childhood Central Nervous System Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004155 adult central nervous system embryonal carcinoma skos:exactMatch NCIT:C5790 Adult Central Nervous System Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004156 pancreatic mucinous cystadenocarcinoma skos:exactMatch NCIT:C5713 Pancreatic Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004158 pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma skos:exactMatch NCIT:C41246 Pancreatic Mucinous-Cystic Neoplasm with an Associated Invasive Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004159 pancreatic non-invasive mucinous cystadenocarcinoma skos:exactMatch NCIT:C41245 Pancreatic Non-Invasive Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004160 female stress incontinence skos:exactMatch NCIT:C35042 Female Stress Incontinence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004161 uterine corpus apoplectic leiomyoma skos:exactMatch NCIT:C40165 Uterine Corpus Apoplectic Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004162 uterine corpus cellular leiomyoma skos:exactMatch NCIT:C40163 Uterine Corpus Cellular Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004163 bladder urachal urothelial carcinoma skos:exactMatch NCIT:C39844 Urachal Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004164 lymphoepithelioma-like acinar prostate adenocarcinoma skos:exactMatch NCIT:C39885 Prostate Acinar Lymphoepithelioma-Like Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004165 selective IgD deficiency disease skos:exactMatch NCIT:C27144 Selective IgD Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004166 hereditary fallopian tube carcinoma skos:exactMatch NCIT:C40455 Hereditary Fallopian Tube Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004168 cribriform variant testicular seminoma skos:exactMatch NCIT:C40957 Testicular Seminoma, Cribriform Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004173 adenocarcinoma of skene gland origin skos:exactMatch NCIT:C39863 Adenocarcinoma of Skene Gland Origin semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004174 secretory uterine corpus endometrioid adenocarcinoma skos:exactMatch NCIT:C27839 Endometrial Endometrioid Adenocarcinoma, Secretory Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004175 mucin-rich endometrial endometrioid adenocarcinoma skos:exactMatch NCIT:C8717 Mucin-Rich Endometrial Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004176 childhood extraosseous osteosarcoma skos:exactMatch NCIT:C27376 Childhood Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004177 benign urethral neoplasm skos:exactMatch NCIT:C3619 Benign Urethral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004178 testicular yolk sac tumor, endodermal sinus pattern skos:exactMatch NCIT:C39927 Testicular Yolk Sac Tumor, Endodermal Sinus/Perivascular Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004180 benign urinary system neoplasm skos:exactMatch NCIT:C4893 Benign Urinary System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004181 breast adenomyoepithelial adenosis skos:exactMatch NCIT:C40391 Breast Adenomyoepithelial Adenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004182 stage IVb bladder cancer skos:exactMatch NCIT:C9368 Stage IVB Bladder Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004183 axonal neuropathy skos:exactMatch NCIT:C27301 Axonal Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004184 urethral disorder skos:exactMatch NCIT:C26903 Urethra Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004185 ovarian serous cystadenofibroma skos:exactMatch NCIT:C40032 Ovarian Serous Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004186 cranial nodular fasciitis skos:exactMatch NCIT:C27248 Cranial Nodular Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004187 nodular fasciitis skos:exactMatch NCIT:C3827 Nodular Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004188 iris spindle cell melanoma skos:exactMatch NCIT:C6098 Iris Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004190 nephrogenic adenoma of urinary bladder skos:exactMatch NCIT:C7415 Bladder Nephrogenic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004191 nephrogenic adenoma skos:exactMatch NCIT:C7413 Nephrogenic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004192 urethra cancer skos:exactMatch NCIT:C7507 Malignant Urethral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004193 pediatric ovarian dysgerminoma skos:exactMatch NCIT:C6550 Childhood Ovarian Dysgerminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004194 ovarian stromal hyperthecosis skos:exactMatch NCIT:C40446 Ovarian Stromal Hyperthecosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004195 thymic dysplasia skos:exactMatch NCIT:C27802 Thymic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004196 rectal sarcomatoid carcinoma skos:exactMatch NCIT:C5556 Rectal Sarcomatoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004197 male urethral cancer skos:exactMatch NCIT:C39867 Male Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004198 testicular yolk sac tumor, solid pattern skos:exactMatch NCIT:C39925 Testicular Yolk Sac Tumor, Solid Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004199 vulvar keratinizing squamous cell carcinoma skos:exactMatch NCIT:C40284 Vulvar Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004200 superficial urinary bladder carcinoma skos:exactMatch NCIT:C27474 Non-Muscle Invasive Bladder Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004201 pituitary hypoplasia skos:exactMatch NCIT:C27343 Pituitary Gland Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004203 female urethral cancer skos:exactMatch NCIT:C39866 Female Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004204 squamous cell skin papilloma skos:exactMatch NCIT:C4462 Skin Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004205 lymphohistiocytoid mesothelioma skos:exactMatch NCIT:C27779 Lymphohistiocytoid Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004206 pulmonary vein leiomyosarcoma skos:exactMatch NCIT:C5374 Pulmonary Vein Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004207 pulmonary artery leiomyosarcoma skos:exactMatch NCIT:C5373 Pulmonary Artery Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004208 superior vena cava leiomyosarcoma skos:exactMatch NCIT:C6745 Superior Vena Cava Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004209 cerebral primitive neuroectodermal tumor skos:exactMatch NCIT:C4970 Cerebral Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004210 colonic L-cell glucagon-like peptide producing tumor skos:exactMatch NCIT:C27447 Colon L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004211 L-cell glucagon-like peptide-producing neuroendocrine tumor skos:exactMatch NCIT:C27448 L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004213 vulvar non-keratinizing squamous cell carcinoma skos:exactMatch NCIT:C40285 Vulvar Non-Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004214 ovarian endometrioid cystadenofibroma skos:exactMatch NCIT:C27288 Ovarian Endometrioid Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004216 pineal region germinoma skos:exactMatch NCIT:C8712 Pineal Region Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004217 childhood brain germinoma skos:exactMatch NCIT:C6207 Childhood Brain Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004218 childhood germ cell brain tumor skos:exactMatch NCIT:C5795 Childhood Brain Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004219 polyvesicular vitelline pattern testicular yolk sac tumor skos:exactMatch NCIT:C39930 Testicular Yolk Sac Tumor, Polyvesicular Vitelline Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004220 endometrial endometrioid adenocarcinoma with spindled epithelial cells skos:exactMatch NCIT:C27850 Endometrial Endometrioid Adenocarcinoma with Spindled Epithelial Cells semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004221 uterine corpus perivascular epithelioid cell tumor skos:exactMatch NCIT:C40180 Uterine Corpus PEComa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004222 ovarian clear cell cystadenocarcinoma skos:exactMatch NCIT:C7980 Ovarian Clear Cell Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004223 polyp of middle ear skos:exactMatch NCIT:C6933 Middle Ear Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004224 chronic metabolic polyneuropathy skos:exactMatch NCIT:C35602 Chronic Metabolic Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004225 monoclonal gammopathy of uncertain significance skos:exactMatch NCIT:C3996 Monoclonal Gammopathy of Undetermined Significance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004226 diffuse intraductal papillomatosis skos:exactMatch NCIT:C7364 Diffuse Intraductal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004227 epididymal adenomatoid tumor skos:exactMatch NCIT:C6382 Epididymal Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004229 acantholytic variant squamous cell breast carcinoma skos:exactMatch NCIT:C40359 Breast Squamous Cell Carcinoma, Acantholytic Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004230 adenomatoid tumor skos:exactMatch NCIT:C3762 Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004231 spindle cell variant squamous cell breast carcinoma skos:exactMatch NCIT:C40358 Breast Squamous Cell Carcinoma, Spindle Cell Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004232 large cell keratinizing variant squamous cell breast carcinoma skos:exactMatch NCIT:C40357 Breast Squamous Cell Carcinoma, Large Cell Keratinizing Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004233 childhood pleomorphic rhabdomyosarcoma skos:exactMatch NCIT:C7959 Childhood Pleomorphic Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004234 chronic lymphoproliferative disorder of NK-cells skos:exactMatch NCIT:C39591 Chronic Lymphoproliferative Disorder of NK-Cells semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004235 diverticulitis skos:exactMatch NCIT:C26752 Diverticulitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004236 duodenal somatostatinoma skos:exactMatch NCIT:C27407 Duodenal Somatostatin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004237 large cell carcinoma with rhabdoid phenotype skos:exactMatch NCIT:C6876 Lung Large Cell Carcinoma with Rhabdoid Phenotype semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004238 petrous apex meningioma skos:exactMatch NCIT:C5271 Petrous Apex Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004239 cervical keratinizing squamous cell carcinoma skos:exactMatch NCIT:C40187 Cervical Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004240 posterior urethra cancer skos:exactMatch NCIT:C7640 Posterior Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004241 Osgood-Schlatter disease skos:exactMatch NCIT:C34874 Osgood-Schlatter's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004243 vulvar proximal-type epithelioid sarcoma skos:exactMatch NCIT:C40319 Vulvar Proximal-Type Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004244 proximal-type epithelioid sarcoma skos:exactMatch NCIT:C27472 Proximal-Type Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004245 ependymal tumor of brain skos:exactMatch NCIT:C3861 Brain Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004247 peptic ulcer disease skos:exactMatch NCIT:C3318 Peptic Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004248 pediatric infratentorial ependymoma skos:exactMatch NCIT:C9041 Childhood Infratentorial Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004249 pediatric supratentorial ependymoma skos:exactMatch NCIT:C9043 Childhood Supratentorial Ependymoma, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004250 extrahepatic bile duct papillary adenoma skos:exactMatch NCIT:C5849 Extrahepatic Bile Duct Papillary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004251 small intestine neoplasm skos:exactMatch NCIT:C4432 Small Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004252 small intestinal L-cell glucagon-like peptide producing tumor skos:exactMatch NCIT:C27452 Small Intestinal L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004253 intraductal breast papillomatosis skos:exactMatch NCIT:C5201 Breast Intraductal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004254 focal intraductal papillomatosis skos:exactMatch NCIT:C7365 Focal Intraductal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004255 Wolffian adnexal tumor skos:exactMatch NCIT:C40141 Wolffian Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004256 lumbar spinal canal and spinal cord meningioma skos:exactMatch NCIT:C5298 Lumbar Intraspinal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004257 childhood central nervous system mixed germ cell tumor skos:exactMatch NCIT:C27403 Childhood Central Nervous System Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004258 female orgasmic disorder skos:exactMatch NCIT:C34958 Female Orgasmic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004261 periductal breast myoepitheliosis skos:exactMatch NCIT:C40388 Breast Periductal Myoepitheliosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004262 breast myoepitheliosis skos:exactMatch NCIT:C40385 Breast Myoepitheliosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004263 pediatric infratentorial ependymoblastoma skos:exactMatch NCIT:C6773 Childhood Infratentorial Embryonal Tumor with Multilayered Rosettes, C19MC-Altered semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004265 acute endometritis skos:exactMatch NCIT:C27022 Acute Endometritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004266 anal gland adenocarcinoma skos:exactMatch NCIT:C5609 Anal Glands Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004267 squamous papillomatosis skos:exactMatch NCIT:C9009 Squamous Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004270 breast ductal adenoma skos:exactMatch NCIT:C40384 Breast Ductal Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004271 pregnancy adenoma skos:exactMatch NCIT:C9473 Lactating Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004273 breast apocrine adenoma skos:exactMatch NCIT:C40383 Breast Apocrine Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004274 mixed epithelial/mesenchymal metaplastic breast carcinoma skos:exactMatch NCIT:C40364 Breast Mixed Epithelial/Mesenchymal Metaplastic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004275 osteosarcoma arising in bone Paget disease skos:exactMatch NCIT:C6469 Osteosarcoma Arising in Paget Disease of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004276 ceruminoma skos:exactMatch NCIT:C6088 Ceruminous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004277 gonorrhea skos:exactMatch NCIT:C92950 Gonorrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004278 infiltrating bladder urothelial carcinoma sarcomatoid variant skos:exactMatch NCIT:C39824 Invasive Bladder Sarcomatoid Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004279 glossopharyngeal motor neuropathy skos:exactMatch NCIT:C27212 Glossopharyngeal Motor Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004280 asymmetric motor neuropathy skos:exactMatch NCIT:C27953 Asymmetric Motor Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004281 vulvar eccrine porocarcinoma skos:exactMatch NCIT:C40306 Vulvar Porocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004283 vulvar clear cell hidradenocarcinoma skos:exactMatch NCIT:C40307 Vulvar Clear Cell Hidradenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004285 pancreatic intraductal papillary-mucinous carcinoma skos:exactMatch NCIT:C5725 Pancreatic Intraductal Papillary-Mucinous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004286 pancreatic intraductal papillary-mucinous neoplasm skos:exactMatch NCIT:C38342 Pancreatic Intraductal Papillary-Mucinous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004287 pancreatic foamy gland adenocarcinoma skos:exactMatch NCIT:C37256 Pancreatic Foamy Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004288 scirrhous breast carcinoma skos:exactMatch NCIT:C7362 Breast Scirrhous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004289 glottis verrucous carcinoma skos:exactMatch NCIT:C8189 Glottis Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004290 subglottis verrucous carcinoma skos:exactMatch NCIT:C8190 Subglottic Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004291 subglottis squamous cell carcinoma skos:exactMatch NCIT:C8187 Subglottic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004292 supraglottis verrucous carcinoma skos:exactMatch NCIT:C8191 Supraglottic Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004293 supraglottis squamous cell carcinoma skos:exactMatch NCIT:C4945 Supraglottic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004294 gestational ovarian choriocarcinoma skos:exactMatch NCIT:C40442 Ovarian Gestational Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004295 asbestos-related lung carcinoma skos:exactMatch NCIT:C27925 Asbestos-Related Lung Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004296 cervical lymphoepithelioma-like carcinoma skos:exactMatch NCIT:C40193 Cervical Lymphoepithelioma-Like Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004297 lymphoepithelioma-like thymic carcinoma skos:exactMatch NCIT:C7998 Thymic Lymphoepithelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004298 stomach disorder skos:exactMatch NCIT:C26886 Stomach Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004299 infiltrating bladder lymphoepithelioma-like carcinoma skos:exactMatch NCIT:C39821 Invasive Bladder Lymphoepithelioma-Like Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004301 fibrosarcomatous osteosarcoma skos:exactMatch NCIT:C4020 Fibroblastic Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004302 chief cell adenoma skos:exactMatch NCIT:C4154 Parathyroid Gland Chief Cell Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004303 parathyroid gland clear cell adenoma skos:exactMatch NCIT:C7993 Parathyroid Gland Clear Cell Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004304 mixed cell type adenoma of parathyroid skos:exactMatch NCIT:C7994 Parathyroid Gland Mixed Cell Type Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004305 parathyroid oncocytic adenoma skos:exactMatch NCIT:C27393 Parathyroid Gland Oncocytic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004306 childhood intracortical osteosarcoma skos:exactMatch NCIT:C6590 Childhood Conventional Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004307 sarcomatosis of the meninges skos:exactMatch NCIT:C4334 Meningeal Sarcomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004308 meningeal sarcoma skos:exactMatch NCIT:C4073 Meningeal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004309 sarcomatosis skos:exactMatch NCIT:C4243 Sarcomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004310 adult embryonal tumor with multilayered rosettes, c19mc-altered skos:exactMatch NCIT:C8290 Adult Embryonal Tumor with Multilayered Rosettes, C19MC-Altered semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004311 carcinoma of Cowper glands skos:exactMatch NCIT:C39864 Cowper Gland Adenocarcinoma of the Urethra semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004312 suprasellar meningioma skos:exactMatch NCIT:C6776 Suprasellar Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004313 gasserian ganglion meningioma skos:exactMatch NCIT:C6779 Gasserian Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004314 malignant cutaneous granular cell skin tumor skos:exactMatch NCIT:C5614 Malignant Cutaneous Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004315 cholangiolocellular carcinoma skos:exactMatch NCIT:C41617 Cholangiolocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004316 acantholytic squamous cell skin carcinoma skos:exactMatch NCIT:C4460 Skin Acantholytic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004317 multiple spinal canal and spinal cord meningioma skos:exactMatch NCIT:C5275 Multiple Intraspinal Meningiomas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004318 pulmonary type ovarian small cell carcinoma skos:exactMatch NCIT:C40440 Ovarian Small Cell Carcinoma, Pulmonary-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004319 hypercalcemic type ovarian small cell carcinoma skos:exactMatch NCIT:C40439 Ovarian Small Cell Carcinoma, Hypercalcemic Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004320 adult infiltrating astrocytic neoplasm skos:exactMatch NCIT:C8289 Adult Infiltrating Astrocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004321 endometrial mixed adenocarcinoma skos:exactMatch NCIT:C40153 Endometrial Mixed Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004322 non-gestational ovarian choriocarcinoma skos:exactMatch NCIT:C39991 Non-Gestational Ovarian Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004324 testicular fibroma skos:exactMatch NCIT:C39951 Testicular Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004325 testicular thecoma skos:exactMatch NCIT:C39952 Testicular Thecoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004326 sphenoid sinus inverted papilloma skos:exactMatch NCIT:C6841 Sphenoid Sinus Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004327 sphenoid sinus Schneiderian papilloma skos:exactMatch NCIT:C6838 Sphenoid Sinus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004328 maxillary sinus adenocarcinoma skos:exactMatch NCIT:C6240 Maxillary Sinus Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004329 pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia skos:exactMatch NCIT:C41251 Pancreatic Intraductal Papillary-Mucinous Neoplasm, High Grade semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004330 leptomeningeal sarcoma skos:exactMatch NCIT:C8312 Leptomeningeal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004331 bladder urachal adenocarcinoma skos:exactMatch NCIT:C39843 Urachal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004332 lung hilum cancer skos:exactMatch NCIT:C4566 Malignant Lung Hilum Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004333 pancreatic ACTH-producing neuroendocrine tumor skos:exactMatch NCIT:C27466 Pancreatic ACTH-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004334 non-functional pancreatic neuroendocrine tumor skos:exactMatch NCIT:C45837 Non-Functioning Pancreatic Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004335 digestive system disorder skos:exactMatch NCIT:C2990 Digestive System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004336 rectal signet ring cell adenocarcinoma skos:exactMatch NCIT:C9168 Rectal Signet Ring Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004337 perianal skin Paget disease skos:exactMatch NCIT:C7476 Anal Margin Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004339 tuberculum sellae meningioma skos:exactMatch NCIT:C5284 Tuberculum Sellae Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004340 mixed ductal-endocrine carcinoma of pancreas skos:exactMatch NCIT:C6879 Pancreatic Mixed Ductal Adenocarcinoma-Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004341 colloid carcinoma of the pancreas skos:exactMatch NCIT:C37214 Pancreatic Colloid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004343 pancreatic acinar cell cystadenocarcinoma skos:exactMatch NCIT:C5727 Pancreatic Acinar Cell Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004344 childhood malignant hemangiopericytoma skos:exactMatch NCIT:C8090 Malignant Childhood Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004345 childhood malignant schwannoma skos:exactMatch NCIT:C8094 Childhood Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004346 signet ring cell intrahepatic cholangiocarcinoma skos:exactMatch NCIT:C41619 Signet Ring Cell Intrahepatic Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004349 retina lymphoma skos:exactMatch NCIT:C4365 Primary Retinal Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004350 pediatric extraocular retinoblastoma skos:exactMatch NCIT:C9048 Childhood Extraocular Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004351 intraocular lymphoma skos:exactMatch NCIT:C9184 Primary Intraocular Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004352 adult brain ependymoma skos:exactMatch NCIT:C9372 Adult Brain Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004353 extrahepatic biliary papillomatosis skos:exactMatch NCIT:C7124 Extrahepatic Bile Duct Intraductal Papillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004354 neonatal leukemia skos:exactMatch NCIT:C3845 Neonatal Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004355 childhood leukemia skos:exactMatch NCIT:C4989 Childhood Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004356 childhood multilocular cystic kidney neoplasm skos:exactMatch NCIT:C6566 Childhood Multilocular Cystic Renal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004357 carcinoma of supraglottis skos:exactMatch NCIT:C5973 Supraglottic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004358 subglottis carcinoma skos:exactMatch NCIT:C5972 Subglottic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004359 delusional disorder skos:exactMatch NCIT:C94379 Delusional Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004360 breast extraskeletal osteosarcoma skos:exactMatch NCIT:C5189 Breast Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004361 adult spinal cord ependymoma skos:exactMatch NCIT:C27399 Adult Spinal Cord Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004363 adult spinal cord glioblastoma skos:exactMatch NCIT:C27183 Adult Spinal Cord Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004364 choroid necrotic melanoma skos:exactMatch NCIT:C6865 Choroid Necrotic Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004365 necrotic uveal melanoma skos:exactMatch NCIT:C7990 Uveal Necrotic Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004366 mixed astrocytoma-ependymoma-oligodendroglioma skos:exactMatch NCIT:C8272 Mixed Astrocytoma-Ependymoma-Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004367 petroclival meningioma skos:exactMatch NCIT:C5278 Petroclival Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004368 sphenoorbital meningioma skos:exactMatch NCIT:C5285 Sphenoorbital Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004370 sphenocavernous meningioma skos:exactMatch NCIT:C5313 Sphenocavernous Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004371 spinal multifocal clear cell meningioma skos:exactMatch NCIT:C5287 Spinal Multifocal Clear Cell Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004372 chronic toxic polyneuropathy skos:exactMatch NCIT:C35603 Chronic Toxic Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004373 adult papillary meningioma skos:exactMatch NCIT:C8293 Adult Papillary Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004374 adult extraskeletal osteosarcoma skos:exactMatch NCIT:C7925 Adult Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004375 end stage renal failure skos:exactMatch NCIT:C9439 Chronic Kidney Disease, Stage 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004376 infiltrating nipple syringomatous adenoma skos:exactMatch NCIT:C40363 Nipple Syringomatous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004377 pancreatic non-functioning delta cell tumor skos:exactMatch NCIT:C28333 Non-Functioning Pancreatic Delta Cell Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004378 pediatric cerebral ependymoblastoma skos:exactMatch NCIT:C6957 Childhood Cerebral Embryonal Tumor with Multilayered Rosettes, C19MC-Altered semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004379 female breast carcinoma skos:exactMatch NCIT:C2918 Female Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004380 dendritic cell sarcoma skos:exactMatch NCIT:C27260 Dendritic Cell Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004381 pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia skos:exactMatch NCIT:C41249 Pancreatic Intraductal Papillary-Mucinous Neoplasm, Low Grade semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004382 laryngeal disorder skos:exactMatch NCIT:C26810 Laryngeal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004383 adult central nervous system germinoma skos:exactMatch NCIT:C5792 Adult Central Nervous System Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004384 maxillary sinus inverted papilloma skos:exactMatch NCIT:C6840 Maxillary Sinus Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004385 adult xanthogranuloma skos:exactMatch NCIT:C27514 Cutaneous Adult Xanthogranuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004386 uterine corpus atypical polypoid adenomyoma skos:exactMatch NCIT:C40235 Uterine Corpus Atypical Polypoid Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004387 luteoma of pregnancy skos:exactMatch NCIT:C40445 Leuteoma of Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004392 intracranial extraskeletal myxoid chondrosarcoma skos:exactMatch NCIT:C5462 Brain Extraskeletal Myxoid Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004393 mixed astrocytoma-ependymoma skos:exactMatch NCIT:C8271 Mixed Astrocytoma-Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004394 maxillary sinus squamous cell carcinoma skos:exactMatch NCIT:C6064 Maxillary Sinus Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004396 cervical spinal canal and spinal cord meningioma skos:exactMatch NCIT:C5296 Cervical Intraspinal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004397 benign mediastinal psammomatous neurilemmoma skos:exactMatch NCIT:C6636 Mediastinal Psammomatous Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004398 mediastinal schwannoma skos:exactMatch NCIT:C6643 Mediastinal Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004400 malignant type A thymoma skos:exactMatch NCIT:C7999 Malignant Type A Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004401 testis refractory cancer skos:exactMatch NCIT:C9077 Refractory Malignant Testicular Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004402 testicular yolk sac tumor, glandular-alveolar pattern skos:exactMatch NCIT:C39926 Testicular Yolk Sac Tumor, Glandular-Alveolar Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004403 childhood precursor T-lymphoblastic lymphoma/leukemia skos:exactMatch NCIT:C5640 Childhood T Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004404 refractory precursor T-lymphoblastic lymphoma/leukemia skos:exactMatch NCIT:C8696 Refractory T Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004405 Barrett adenocarcinoma skos:exactMatch NCIT:C7027 Barrett Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004406 adult central nervous system mixed germ cell tumor skos:exactMatch NCIT:C27402 Adult Central Nervous System Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004407 stroma-dominant and stroma-poor composite ganglioneuroblastoma skos:exactMatch NCIT:C42060 Composite Ganglioneuroblastoma, Stroma-Dominant and Stroma-Poor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004408 schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma skos:exactMatch NCIT:C42059 Composite Ganglioneuroblastoma, Schwannian Stroma-Rich and Stroma-Poor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004409 nipple duct carcinoma skos:exactMatch NCIT:C27234 Nipple Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004410 sarcomatoid penile squamous cell carcinoma skos:exactMatch NCIT:C6984 Penile Sarcomatoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004411 duodenal gastrin-producing neuroendocrine tumor skos:exactMatch NCIT:C5731 Duodenal Gastrin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004412 malignant spiradenoma skos:exactMatch NCIT:C5117 Spiradenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004413 cervical non-keratinizing squamous cell carcinoma skos:exactMatch NCIT:C40188 Cervical Non-Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004414 tamoxifen-related endometrial lesion skos:exactMatch NCIT:C40159 Tamoxifen-Related Endometrial Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004415 lipid-cell variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39828 Invasive Bladder Lipid-Rich Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004416 plasmacytoid variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39823 Invasive Bladder Plasmacytoid Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004417 nested variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39819 Invasive Bladder Nested Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004418 microcystic variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39820 Invasive Bladder Microcystic Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004419 lymphoma-like variant infiltrating bladder urothelial carcinoma skos:exactMatch NCIT:C39822 Infiltrating Bladder Urothelial Carcinoma, Lymphoma-Like Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004420 breast malignant eccrine spiradenoma skos:exactMatch NCIT:C5180 Malignant Breast Spiradenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004421 sclerosing breast papilloma skos:exactMatch NCIT:C27944 Breast Sclerosing Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004422 cerebral falx meningioma skos:exactMatch NCIT:C5267 Falx Cerebri Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004423 central nervous system extraskeletal osteosarcoma skos:exactMatch NCIT:C7002 Central Nervous System Extraskeletal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004425 hyperthyroidism skos:exactMatch NCIT:C3123 Hyperthyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004426 frontal convexity meningioma skos:exactMatch NCIT:C5292 Frontal Convexity Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004427 supraglottis neoplasm skos:exactMatch NCIT:C6793 Supraglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004428 alveoli adenoma skos:exactMatch NCIT:C4140 Alveolar Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004430 penis mixed squamous cell carcinoma skos:exactMatch NCIT:C39959 Penile Mixed Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004432 mature pericardial teratoma skos:exactMatch NCIT:C6744 Pericardial Mature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004433 papillary carcinoma of the penis skos:exactMatch NCIT:C6983 Penile Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004435 liver fibrosarcoma skos:exactMatch NCIT:C5832 Liver Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004436 ovarian myxoid liposarcoma skos:exactMatch NCIT:C5235 Ovarian Myxoid Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004438 sporadic breast cancer skos:exactMatch NCIT:C7566 Sporadic Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004439 periocular meningioma skos:exactMatch NCIT:C6777 Periocular Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004440 pineal region meningioma skos:exactMatch NCIT:C6756 Pineal Region Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004441 childhood ovarian embryonal carcinoma skos:exactMatch NCIT:C6546 Childhood Ovarian Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004442 testis polyembryoma skos:exactMatch NCIT:C40962 Testicular Polyembryoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004443 chest wall parachordoma skos:exactMatch NCIT:C6720 Chest Wall Parachordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004444 bladder tubulo-cystic clear cell adenocarcinoma skos:exactMatch NCIT:C39847 Bladder Tubulo-Cystic Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004445 bladder papillary clear cell adenocarcinoma skos:exactMatch NCIT:C39848 Bladder Papillary Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004446 olfactory groove meningioma skos:exactMatch NCIT:C6771 Olfactory Groove Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004447 pituitary stalk meningioma skos:exactMatch NCIT:C5311 Pituitary Stalk Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004448 frontal sinus inverted papilloma skos:exactMatch NCIT:C6842 Frontal Sinus Inverted Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004449 intraductal breast myoepitheliosis skos:exactMatch NCIT:C40387 Breast Intraductal Myoepitheliosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004451 sarcomatous intrahepatic cholangiocarcinoma skos:exactMatch NCIT:C41620 Sarcomatoid Intrahepatic Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004452 childhood central nervous system germinoma skos:exactMatch NCIT:C27406 Childhood Central Nervous System Germinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004453 testicular yolk sac tumor, myxomatous pattern skos:exactMatch NCIT:C39929 Testicular Yolk Sac Tumor, Myxomatous Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004454 cellular congenital mesoblastic nephroma skos:exactMatch NCIT:C39815 Cellular Congenital Mesoblastic Nephroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004455 classic congenital mesoblastic nephroma skos:exactMatch NCIT:C39814 Classic Congenital Mesoblastic Nephroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004457 maxillary sinus Schneiderian papilloma skos:exactMatch NCIT:C6839 Maxillary Sinus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004458 bladder mixed adenocarcinoma skos:exactMatch NCIT:C39839 Bladder Mixed Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004459 bladder hepatoid adenocarcinoma skos:exactMatch NCIT:C39838 Bladder Hepatoid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004460 thyroid gland fetal adenoma skos:exactMatch NCIT:C4160 Thyroid Gland Microfollicular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004461 vaginal tubulovillous adenoma skos:exactMatch NCIT:C40258 Vaginal Tubulovillous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004462 extrahepatic bile duct cystadenoma skos:exactMatch NCIT:C5851 Extrahepatic Bile Duct Mucinous Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004463 cellular phase chronic idiopathic myelofibrosis skos:exactMatch NCIT:C41237 Early/Prefibrotic Primary Myelofibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004464 nephrogenic adenoma of the urethra skos:exactMatch NCIT:C7416 Urethral Nephrogenic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004465 periampullary adenocarcinoma skos:exactMatch NCIT:C27322 Periampullary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004466 neuronitis skos:exactMatch NCIT:C34847 Neuronitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004467 mature gastric teratoma skos:exactMatch NCIT:C5260 Mature Gastric Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004468 anal canal Paget disease skos:exactMatch NCIT:C7477 Anal Canal Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004469 pseudovascular skin squamous cell carcinoma skos:exactMatch NCIT:C27542 Skin Pseudovascular Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004471 bacterial arthritis skos:exactMatch NCIT:C26699 Bacterial Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004472 breast columnar cell mucinous carcinoma skos:exactMatch NCIT:C40355 Breast Columnar Cell Mucinous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004473 epiglottis cancer skos:exactMatch NCIT:C35697 Epiglottic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004473 epiglottis cancer skos:exactMatch NCIT:C4836 Malignant Epiglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004474 gallbladder lymphoma skos:exactMatch NCIT:C5734 Gallbladder Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004475 thymus clear cell carcinoma skos:exactMatch NCIT:C6462 Thymic Clear Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004477 adrenal gland ganglioneuroblastoma skos:exactMatch NCIT:C7646 Adrenal Gland Ganglioneuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004478 pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma skos:exactMatch NCIT:C37204 Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004479 malignant childhood germ cell neoplasm skos:exactMatch NCIT:C6541 Childhood Malignant Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004481 pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma skos:exactMatch NCIT:C5726 Pancreatic Intraductal Papillary-Mucinous Neoplasm with an Associated Invasive Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004482 fibroosseous pseudotumor of the digits skos:exactMatch NCIT:C6573 Fibroosseous Pseudotumor of Digits semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004483 thyroid gland oncocytic adenoma skos:exactMatch NCIT:C6042 Thyroid Gland Oncocytic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004484 gallbladder melanoma skos:exactMatch NCIT:C5735 Gallbladder Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004485 interstitial myocarditis skos:exactMatch NCIT:C35786 Interstitial Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004486 endocervical type cervical adenomyoma skos:exactMatch NCIT:C40232 Cervical Adenomyoma, Endocervical-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004487 endometrial type cervical adenomyoma skos:exactMatch NCIT:C40233 Cervical Adenomyoma, Mesonephric-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004488 cervical atypical polypoid adenomyoma skos:exactMatch NCIT:C40234 Cervical Atypical Polypoid Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004489 fallopian tube gestational choriocarcinoma skos:exactMatch NCIT:C6278 Fallopian Tube Gestational Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004491 uterine corpus choriocarcinoma skos:exactMatch NCIT:C27246 Uterine Corpus Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004492 mediastinitis skos:exactMatch NCIT:C26827 Mediastinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004493 testicular yolk sac tumor, papillary pattern skos:exactMatch NCIT:C39928 Testicular Yolk Sac Tumor, Papillary Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004494 testicular yolk sac tumor, hepatoid pattern skos:exactMatch NCIT:C39931 Testicular Yolk Sac Tumor, Hepatoid Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004495 myotonic cataract skos:exactMatch NCIT:C34833 Myotonic Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004496 myocarditis skos:exactMatch NCIT:C34831 Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004497 tertiary syphilis skos:exactMatch NCIT:C128414 Tertiary Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004498 sacral spinal canal and spinal cord meningioma skos:exactMatch NCIT:C5299 Sacral Intraspinal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004499 lung hilum carcinoma skos:exactMatch NCIT:C7454 Lung Hilum Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004500 lung superior sulcus carcinoma skos:exactMatch NCIT:C7779 Superior Sulcus Lung Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004501 fallopian tube cystadenofibroma skos:exactMatch NCIT:C40114 Fallopian Tube Serous Cystadenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004502 parapharyngeal meningioma skos:exactMatch NCIT:C5303 Primary Parapharyngeal Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004503 upper clivus meningioma skos:exactMatch NCIT:C5290 Upper Clivus Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004504 penile urethral cancer skos:exactMatch NCIT:C39868 Penile Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004505 central breast papilloma skos:exactMatch NCIT:C36087 Breast Central Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004506 microscopic breast papilloma skos:exactMatch NCIT:C36088 Breast Peripheral Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004507 atypical breast papilloma skos:exactMatch NCIT:C36089 Breast Atypical Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004509 intrahepatic biliary papillomatosis skos:exactMatch NCIT:C7125 Intrahepatic Bile Duct Intraductal Papillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004510 inflammatory liposarcoma skos:exactMatch NCIT:C6508 Inflammatory Atypical Lipomatous Tumor/Well Differentiated Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004511 lower clivus meningioma skos:exactMatch NCIT:C5288 Lower Clivus Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004512 meningeal melanomatosis skos:exactMatch NCIT:C6891 Meningeal Melanomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004513 adult pleomorphic rhabdomyosarcoma skos:exactMatch NCIT:C27369 Adult Pleomorphic Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004514 chronic rhinitis skos:exactMatch NCIT:C34479 Chronic Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004516 bulbomembranous urethral cancer skos:exactMatch NCIT:C39869 Bulbomembranous Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004518 anterior urethra cancer skos:exactMatch NCIT:C7641 Anterior Urethral Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004519 synovial angioma skos:exactMatch NCIT:C6525 Synovial Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch NCIT:C7325 Intratubular Non-Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004521 adult epithelioid sarcoma skos:exactMatch NCIT:C7944 Adult Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004522 peritonitis skos:exactMatch NCIT:C26849 Peritonitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004523 clear cell squamous cell skin carcinoma skos:exactMatch NCIT:C4459 Skin Clear Cell Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004524 thyroid gland atypical follicular adenoma skos:exactMatch NCIT:C27729 Thyroid Gland Well-Differentiated Tumor of Uncertain Malignant Potential semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004525 scabies skos:exactMatch NCIT:C34998 Scabies semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004526 mixed endometrial stromal and smooth muscle tumor skos:exactMatch NCIT:C40178 Mixed Endometrial Stromal and Smooth Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004528 lymph node palisaded myofibroblastoma skos:exactMatch NCIT:C6584 Intranodal Palisaded Myofibroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004529 non-ossifying fibromyxoid tumor skos:exactMatch NCIT:C6583 Nonossifying Fibromyxoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004530 early invasive cervical adenocarcinoma skos:exactMatch NCIT:C36096 Early Invasive Cervical Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004531 sclerosing adenosis of breast skos:exactMatch NCIT:C5205 Breast Sclerosing Adenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004533 perineural angioma skos:exactMatch NCIT:C6526 Perineural Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004534 microglandular adenosis of breast skos:exactMatch NCIT:C5199 Breast Microglandular Adenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004535 childhood choriocarcinoma of the ovary skos:exactMatch NCIT:C6549 Childhood Ovarian Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004537 intestinal variant cervical mucinous adenocarcinoma skos:exactMatch NCIT:C40203 Cervical Mucinous Adenocarcinoma, Intestinal-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004539 aortic malignant tumor skos:exactMatch NCIT:C5375 Malignant Aortic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004540 epithelioid malignant peripheral nerve sheath tumor skos:exactMatch NCIT:C6561 Epithelioid Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004541 pseudoglandular variant testicular seminoma skos:exactMatch NCIT:C40958 Testicular Seminoma, Pseudoglandular Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004542 cervical adenosquamous carcinoma, glassy cell variant skos:exactMatch NCIT:C40212 Cervical Poorly Differentiated Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004543 enteric pattern testicular yolk sac tumor skos:exactMatch NCIT:C39932 Testicular Yolk Sac Tumor, Enteric Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004544 chordoid meningioma skos:exactMatch NCIT:C6908 Chordoid Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004545 adult malignant schwannoma skos:exactMatch NCIT:C7814 Adult Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004546 lumbar plexus neoplasm skos:exactMatch NCIT:C5824 Lumbar Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004547 reticular pattern testicular yolk sac tumor skos:exactMatch NCIT:C39923 Testicular Yolk Sac Tumor, Microcystic Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004548 adult type testicular granulosa cell tumor skos:exactMatch NCIT:C39946 Adult Testicular Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004550 malignant cornea melanoma skos:exactMatch NCIT:C4553 Corneal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004551 Meckel diverticulitis skos:exactMatch NCIT:C27300 Meckel Diverticulitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004552 microinvasive cervical squamous cell carcinoma skos:exactMatch NCIT:C36094 Early Invasive Cervical Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004554 childhood kidney angiomyolipoma skos:exactMatch NCIT:C6565 Childhood Kidney Angiomyolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004555 kidney angiomyolipoma skos:exactMatch NCIT:C3888 Kidney Angiomyolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004556 carcinoma arising in nasal papillomatosis skos:exactMatch NCIT:C27389 Carcinoma Arising in Nasal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004557 congenital fibrosarcoma skos:exactMatch NCIT:C4244 Infantile Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004558 thyroid gland macrofollicular adenoma skos:exactMatch NCIT:C4161 Thyroid Gland Macrofollicular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004559 malignant glandular tumor of peripheral nerve sheath skos:exactMatch NCIT:C6560 Glandular Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004560 follicular infundibulum tumor skos:exactMatch NCIT:C4469 Tumor of the Follicular Infundibulum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004561 retinal melanoma skos:exactMatch NCIT:C8601 Retinal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004562 breast apocrine carcinoma in situ skos:exactMatch NCIT:C5140 Breast Apocrine Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004563 physiological polycythemia skos:exactMatch NCIT:C27311 Physiological Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004564 thyroid malformation skos:exactMatch NCIT:C27331 Thyroid Gland Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004565 intestinal obstruction skos:exactMatch NCIT:C9175 Bowel Obstruction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004567 ileus skos:exactMatch NCIT:C37979 Ileus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004568 paralytic ileus skos:exactMatch NCIT:C93045 Paralytic Ileus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004574 pyridoxine deficiency anemia skos:exactMatch NCIT:C85221 Vitamin B6 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004577 corneal ulcer skos:exactMatch NCIT:C50515 Corneal Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004579 retinoschisis skos:exactMatch NCIT:C85046 Retinoschisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004580 retinal degeneration skos:exactMatch NCIT:C34979 Retinal Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004582 rheumatic myocarditis skos:exactMatch NCIT:C35202 Acute Rheumatic Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004583 transient retinal arterial occlusion skos:exactMatch NCIT:C35193 Transient Retinal Arterial Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004588 night blindness skos:exactMatch NCIT:C34850 Night Blindness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004592 impetigo skos:exactMatch NCIT:C99088 Impetigo semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004597 pulmonary embolism and infarction skos:exactMatch NCIT:C50714 Pulmonary Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004604 Hodgkin's lymphoma, lymphocytic-histiocytic predominance skos:exactMatch NCIT:C6913 Lymphocyte-Rich Classic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004608 oropharynx cancer skos:exactMatch NCIT:C7398 Malignant Oropharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004611 soft palate cancer skos:exactMatch NCIT:C3529 Malignant Soft Palate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004612 malignant histiocytosis skos:exactMatch NCIT:C7202 Malignant Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004613 acute intestinal ischemia skos:exactMatch NCIT:C34356 Acute Intestinal Ischemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004614 chronic monocytic leukemia skos:exactMatch NCIT:C34774 Chronic Monocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004616 herpetic whitlow skos:exactMatch NCIT:C128402 Herpetic Whitlow semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004619 measles skos:exactMatch NCIT:C96406 Measles semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004620 Hodgkin's lymphoma, lymphocytic depletion skos:exactMatch NCIT:C9125 Adult Lymphocyte-Depleted Classic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004624 uvula cancer skos:exactMatch NCIT:C35177 Malignant Uvula Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004625 phlebitis skos:exactMatch NCIT:C38003 Phlebitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004626 obsolete Hodgkin's paragranuloma skos:exactMatch NCIT:C26956 Hodgkin's Paragranuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004627 duodenitis skos:exactMatch NCIT:C94409 Duodenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004631 tongue cancer skos:exactMatch NCIT:C9345 Malignant Tongue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004632 obsolete Hodgkin's granuloma skos:exactMatch NCIT:C6914 Hodgkin's Granuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004633 Hodgkin's lymphoma, mixed cellularity skos:exactMatch NCIT:C3517 Mixed Cellularity Classic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004634 vein disorder skos:exactMatch NCIT:C35279 Vein Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004635 postcricoid region cancer skos:exactMatch NCIT:C9323 Malignant Postcricoid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004636 lip carcinoma in situ skos:exactMatch NCIT:C4588 Stage 0 Lip Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004638 lymphosarcoma skos:exactMatch NCIT:C26919 Lymphosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004640 alcoholic gastritis skos:exactMatch NCIT:C26977 Alcoholic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004641 skin carcinoma in situ skos:exactMatch NCIT:C3640 Stage 0 Skin Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004643 myeloid leukemia skos:exactMatch NCIT:C3172 Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004645 cheek mucosa cancer skos:exactMatch NCIT:C9320 Malignant Buccal Mucosa Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004647 in situ carcinoma skos:exactMatch NCIT:C2917 Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004648 vascular dementia skos:exactMatch NCIT:C34525 Vascular Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004650 malignant carotid body paraganglioma skos:exactMatch NCIT:C3574 Metastatic Carotid Body Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004651 smallpox skos:exactMatch NCIT:C35027 Smallpox semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004652 bacterial pneumonia skos:exactMatch NCIT:C26704 Bacterial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004653 atypical chronic myeloid leukemia, BCR-ABL1 negative skos:exactMatch NCIT:C3519 Atypical Chronic Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004656 rubella skos:exactMatch NCIT:C85051 Rubella Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004658 breast carcinoma in situ skos:exactMatch NCIT:C3641 Stage 0 Breast Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004660 lung carcinoma in situ skos:exactMatch NCIT:C27467 Stage 0 Lung Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004661 trachea carcinoma in situ skos:exactMatch NCIT:C3639 Tracheal Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004662 heterophyiasis skos:exactMatch NCIT:C128389 Heterophyiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004663 colon carcinoma in situ skos:exactMatch NCIT:C3638 Stage 0 Colon Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004664 helminthiasis skos:exactMatch NCIT:C84751 Helminthiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004665 nodular sclerosis classical Hodgkin lymphoma skos:exactMatch NCIT:C3518 Nodular Sclerosis Classic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004666 metagonimiasis skos:exactMatch NCIT:C128390 Metagonimiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004667 sublingual gland cancer skos:exactMatch NCIT:C3527 Malignant Sublingual Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004668 fascioliasis skos:exactMatch NCIT:C128387 Fasciolosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004669 salivary gland cancer skos:exactMatch NCIT:C3811 Malignant Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004670 lupus erythematosus skos:exactMatch NCIT:C27153 Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004671 penis carcinoma in situ skos:exactMatch NCIT:C27790 Penile Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004672 fasciolopsiasis skos:exactMatch NCIT:C128388 Fasciolopsiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004674 chorioretinitis skos:exactMatch NCIT:C110923 Chorioretinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004678 dermatophytosis skos:exactMatch NCIT:C26745 Dermatophytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004679 leukoplakia of vagina skos:exactMatch NCIT:C3663 Vaginal Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004681 learning disability skos:exactMatch NCIT:C89334 Learning Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004684 plantar fibromatosis skos:exactMatch NCIT:C4680 Plantar Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004691 autosomal dominant polycystic kidney disease skos:exactMatch NCIT:C84578 Autosomal Dominant Polycystic Kidney Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004693 squamous carcinoma in situ skos:exactMatch NCIT:C27093 Stage 0 Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004695 liver lymphoma skos:exactMatch NCIT:C4949 Liver Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004696 larynx carcinoma in situ skos:exactMatch NCIT:C9100 Stage 0 Laryngeal Cancer AJCC v6, v7, and V8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004697 esophageal leukoplakia skos:exactMatch NCIT:C3953 Esophageal Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004699 gastrointestinal lymphoma skos:exactMatch NCIT:C38162 Digestive System Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004700 parotid gland cancer skos:exactMatch NCIT:C3525 Malignant Parotid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004701 uterine polyp skos:exactMatch NCIT:C3662 Uterine Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004702 uterine cervix leukoplakia skos:exactMatch NCIT:C3976 Cervical Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004703 bladder carcinoma in situ skos:exactMatch NCIT:C3644 Stage 0is Bladder Urothelial Carcinoma AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004705 liver solitary fibrous tumor skos:exactMatch NCIT:C5752 Liver Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004707 anal canal carcinoma in situ skos:exactMatch NCIT:C7794 Stage 0 Anal Canal Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004708 esophagus carcinoma in situ skos:exactMatch NCIT:C89771 Stage 0 Esophageal Cancer AJCC v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004709 occipital lobe neoplasm skos:exactMatch NCIT:C5574 Occipital Lobe Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004712 herpes simplex dermatitis skos:exactMatch NCIT:C35620 Herpes Simplex Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004714 atrophic muscular disease skos:exactMatch NCIT:C84574 Atrophic Muscular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004716 stomach carcinoma in situ skos:exactMatch NCIT:C7788 Stage 0 Gastric Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004719 hard palate cancer skos:exactMatch NCIT:C3528 Malignant Hard Palate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004720 variola minor infection skos:exactMatch NCIT:C34365 Alastrim semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004723 liver leiomyoma skos:exactMatch NCIT:C5753 Liver Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004724 submandibular gland cancer skos:exactMatch NCIT:C8396 Submandibular Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004725 rectum carcinoma in situ skos:exactMatch NCIT:C4853 Stage 0 Rectal Cancer AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004726 liver inflammatory myofibroblastic tumor skos:exactMatch NCIT:C5858 Liver Inflammatory Myofibroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004730 speech disorder skos:exactMatch NCIT:C5041 Speech Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004731 central sleep apnea syndrome skos:exactMatch NCIT:C27169 Central Sleep Apnea Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004733 pyriform sinus cancer skos:exactMatch NCIT:C3531 Malignant Pyriform Fossa Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004736 inborn disorder of amino acid metabolism skos:exactMatch NCIT:C97090 Amino Acid Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004737 homocystinuria skos:exactMatch NCIT:C84765 Homocystinuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004739 urea cycle disorder skos:exactMatch NCIT:C84785 Urea Cycle Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004741 tyrosinemia skos:exactMatch NCIT:C98640 Tyrosinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004743 hyperhomocysteinemia skos:exactMatch NCIT:C84770 Hyperhomocysteinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004747 cleft lip skos:exactMatch NCIT:C87175 Cleft Lip semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004748 lip disorder skos:exactMatch NCIT:C26818 Lip Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004749 myocardium cancer skos:exactMatch NCIT:C4569 Malignant Myocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004750 language disorder skos:exactMatch NCIT:C97155 Language Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004752 neurofibroma of the heart skos:exactMatch NCIT:C5359 Cardiac Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004754 rectal prolapse skos:exactMatch NCIT:C34973 Rectal Prolapse semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004756 nasal cavity neoplasm skos:exactMatch NCIT:C4413 Nasal Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004757 chronic ethmoidal sinusitis skos:exactMatch NCIT:C34472 Chronic Ethmoidal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004763 carotid artery dissection skos:exactMatch NCIT:C125662 Carotid Artery Dissection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004766 status asthmaticus skos:exactMatch NCIT:C122577 Status Asthmaticus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004767 vesiculitis skos:exactMatch NCIT:C12787 Seminal Vesicle semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004768 keratoconjunctivitis skos:exactMatch NCIT:C34744 Keratoconjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004770 exophthalmos skos:exactMatch NCIT:C118763 Exophthalmos semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004773 iridocyclitis skos:exactMatch NCIT:C34736 Iridocyclitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004777 acute laryngitis skos:exactMatch NCIT:C26688 Acute Laryngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004779 epididymitis skos:exactMatch NCIT:C12328 Epididymis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004781 acute myocardial infarction skos:exactMatch NCIT:C35204 Acute Myocardial Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004782 diabetes insipidus skos:exactMatch NCIT:C43263 Diabetes Insipidus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004785 blepharitis skos:exactMatch NCIT:C112183 Blepharitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004786 chronic cholangitis skos:exactMatch NCIT:C35335 Chronic Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004787 cervical mullerian papilloma skos:exactMatch NCIT:C40215 Cervical Mullerian Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004788 cervix squamous papilloma skos:exactMatch NCIT:C6342 Cervical Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004789 cholangitis skos:exactMatch NCIT:C26718 Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004795 otitis externa skos:exactMatch NCIT:C3299 Infectious Otitis Externa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004795 otitis externa skos:exactMatch NCIT:C79601 Otitis Externa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004796 infectious meningitis skos:exactMatch NCIT:C79598 Infectious Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004804 dacryoadenitis skos:exactMatch NCIT:C26971 Dacryoadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004806 chronic eosinophilic pneumonia skos:exactMatch NCIT:C34471 Chronic Eosinophilic Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004815 osteosclerotic plasma cell myeloma skos:exactMatch NCIT:C7765 Osteosclerotic Multiple Myeloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004816 refractory plasma cell neoplasm skos:exactMatch NCIT:C7813 Refractory Plasma Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004817 non-secretory plasma cell myeloma skos:exactMatch NCIT:C4734 Non-Secretory Multiple Myeloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004819 indolent plasma cell myeloma skos:exactMatch NCIT:C7150 Indolent Multiple Myeloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004820 peripheral nerve schwannoma skos:exactMatch NCIT:C41430 Peripheral Nerve Schwannoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004821 nasopharyngeal disorder skos:exactMatch NCIT:C35723 Nasopharyngeal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004822 bronchiectasis skos:exactMatch NCIT:C84475 Bronchiectasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004824 neonatal candidiasis skos:exactMatch NCIT:C116810 Neonatal Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004827 esophagus squamous cell papilloma skos:exactMatch NCIT:C5344 Esophageal Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004829 Krukenberg carcinoma skos:exactMatch NCIT:C3153 Krukenberg Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004830 fasciitis skos:exactMatch NCIT:C50559 Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004831 proliferative fasciitis skos:exactMatch NCIT:C4728 Proliferative Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004832 esophagus leiomyoma skos:exactMatch NCIT:C3866 Esophageal Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004834 ischemic fasciitis skos:exactMatch NCIT:C6483 Ischemic Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004835 necrotizing fasciitis skos:exactMatch NCIT:C84916 Necrotizing Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004836 intravascular fasciitis skos:exactMatch NCIT:C4729 Intravascular Nodular Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004837 neurofibroma of the esophagus skos:exactMatch NCIT:C5704 Esophageal Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004841 kidney hypertrophy skos:exactMatch NCIT:C122991 Renal Hypertrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004842 stomatitis skos:exactMatch NCIT:C26887 Stomatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004844 oral mucosa leukoplakia skos:exactMatch NCIT:C3187 Oral Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004846 placental abruption skos:exactMatch NCIT:C26685 Placental Abruption semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004847 senile cataract skos:exactMatch NCIT:C35012 Senile Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004848 ulcerative stomatitis skos:exactMatch NCIT:C35039 Ulcerative Stomatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004849 pulmonary emphysema skos:exactMatch NCIT:C3348 Pulmonary Emphysema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004854 ophthalmia neonatorum skos:exactMatch NCIT:C116815 Ophthalmia Neonatorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004857 tendinitis skos:exactMatch NCIT:C97141 Tendonitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004872 hemorrhoid skos:exactMatch NCIT:C26792 Hemorrhoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004873 internal hemorrhoid skos:exactMatch NCIT:C35319 Internal Hemorrhoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004875 xanthogranulomatous cholecystitis skos:exactMatch NCIT:C35792 Xanthogranulomatous Cholecystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004881 myositis fibrosa skos:exactMatch NCIT:C26985 Interstitial Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004893 hypertropia skos:exactMatch NCIT:C34716 Hypertropia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004896 esotropia skos:exactMatch NCIT:C34596 Internal Strabismus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004897 hypotropia skos:exactMatch NCIT:C42086 Downward Ocular Deviation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004905 intestinal disaccharidase deficiency skos:exactMatch NCIT:C34731 Intestinal Disaccharidase Deficiency and Disaccharide Malabsorption semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004907 alopecia skos:exactMatch NCIT:C50575 Alopecia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004910 mitral valve prolapse skos:exactMatch NCIT:C50655 Mitral Valve Prolapse semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004922 developmental coordination disorder skos:exactMatch NCIT:C92561 Developmental Coordination Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004926 dacryocystitis skos:exactMatch NCIT:C34521 Dacryocystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004928 lymph node disorder skos:exactMatch NCIT:C35346 Lymph Node Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004933 hypoplastic left heart syndrome skos:exactMatch NCIT:C98894 Hypoplastic Left Heart Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004934 periostitis skos:exactMatch NCIT:C13184 Periosteum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004938 substance dependence skos:exactMatch NCIT:C35458 Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004939 hallucinogen dependence skos:exactMatch NCIT:C34657 Hallucinogen Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004942 orbit lymphoma skos:exactMatch NCIT:C6244 Orbit Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004943 orbit sarcoma skos:exactMatch NCIT:C6095 Orbit Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004944 neurosyphilis skos:exactMatch NCIT:C84935 Neurosyphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004946 hypoglycemia skos:exactMatch NCIT:C3126 Hypoglycemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004947 B-cell acute lymphoblastic leukemia skos:exactMatch NCIT:C8936 B Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004948 B-cell chronic lymphocytic leukemia skos:exactMatch NCIT:C3163 Chronic Lymphocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004949 neoplasm of mature B-cells skos:exactMatch NCIT:C27910 Mature B-Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004950 gastric carcinoma skos:exactMatch NCIT:C4911 Gastric Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004952 Hodgkins lymphoma skos:exactMatch NCIT:C9357 Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004953 invasive ductal breast carcinoma skos:exactMatch NCIT:C4194 Invasive Breast Carcinoma of No Special Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004956 metastatic prostate carcinoma skos:exactMatch NCIT:C8946 Metastatic Prostate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004957 mucinous adenocarcinoma skos:exactMatch NCIT:C26712 Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004958 oral cavity squamous cell carcinoma skos:exactMatch NCIT:C4833 Oral Cavity Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004959 plasma cell neoplasm skos:exactMatch NCIT:C4665 Plasma Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004960 monoclonal gammopathy skos:exactMatch NCIT:C35548 Monoclonal Gammopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004963 T-cell acute lymphoblastic leukemia skos:exactMatch NCIT:C3183 T Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004964 peripheral T-cell lymphoma, not otherwise specified skos:exactMatch NCIT:C4340 Peripheral T-Cell Lymphoma, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004965 acinar cell carcinoma skos:exactMatch NCIT:C3768 Acinar Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004966 gastritis skos:exactMatch NCIT:C26780 Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004967 acute lymphoblastic leukemia skos:exactMatch NCIT:C3167 Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004970 adenocarcinoma skos:exactMatch NCIT:C2852 Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004971 adenoid cystic carcinoma skos:exactMatch NCIT:C2970 Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004972 adenoma skos:exactMatch NCIT:C2855 Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004973 adenosquamous lung carcinoma skos:exactMatch NCIT:C9133 Lung Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004974 adrenal gland pheochromocytoma skos:exactMatch NCIT:C3326 Adrenal Gland Pheochromocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004975 Alzheimer disease skos:exactMatch NCIT:C2866 Alzheimer's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004976 amyotrophic lateral sclerosis skos:exactMatch NCIT:C34373 Amyotrophic Lateral Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004977 angioimmunoblastic T-cell lymphoma skos:exactMatch NCIT:C7528 Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004979 asthma skos:exactMatch NCIT:C28397 Asthma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004980 atopic eczema skos:exactMatch NCIT:C3001 Eczema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004981 atrial fibrillation skos:exactMatch NCIT:C50466 Atrial Fibrillation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004982 pancreatitis skos:exactMatch NCIT:C3306 Pancreatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004984 basal-like breast carcinoma skos:exactMatch NCIT:C53558 Basal-Like Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004985 bipolar disorder skos:exactMatch NCIT:C34423 Bipolar Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004986 urinary bladder carcinoma skos:exactMatch NCIT:C4912 Bladder Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004987 urinary bladder neoplasm skos:exactMatch NCIT:C2901 Bladder Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004988 breast adenocarcinoma skos:exactMatch NCIT:C5214 Breast Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004989 breast carcinoma skos:exactMatch NCIT:C4872 Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004991 minimally invasive lung adenocarcinoma skos:exactMatch NCIT:C2923 Minimally Invasive Lung Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004992 cancer skos:exactMatch NCIT:C9305 Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004993 carcinoma skos:exactMatch NCIT:C2916 Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004994 cardiomyopathy skos:exactMatch NCIT:C34830 Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004995 cardiovascular disorder skos:exactMatch NCIT:C2931 Cardiovascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004996 childhood acute myeloid leukemia skos:exactMatch NCIT:C9160 Childhood Acute Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0004997 chondroblastoma skos:exactMatch NCIT:C2945 Chondroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005001 chronic gastritis skos:exactMatch NCIT:C26929 Chronic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005002 chronic obstructive pulmonary disease skos:exactMatch NCIT:C3199 Chronic Obstructive Pulmonary Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005003 chronic pancreatitis skos:exactMatch NCIT:C84637 Chronic Pancreatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005004 clear cell adenocarcinoma skos:exactMatch NCIT:C3766 Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005005 clear cell renal carcinoma skos:exactMatch NCIT:C4033 Clear Cell Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005006 clear cell sarcoma of kidney skos:exactMatch NCIT:C4264 Clear Cell Sarcoma of the Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005007 colon mucinous adenocarcinoma skos:exactMatch NCIT:C7966 Colon Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005008 colorectal adenocarcinoma skos:exactMatch NCIT:C5105 Colorectal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005009 congestive heart failure skos:exactMatch NCIT:C3080 Congestive Heart Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005010 coronary artery disorder skos:exactMatch NCIT:C26732 Coronary Artery Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005011 Crohn disease skos:exactMatch NCIT:C2965 Crohn Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005012 cutaneous melanoma skos:exactMatch NCIT:C3510 Cutaneous Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005013 dedifferentiated chondrosarcoma skos:exactMatch NCIT:C6476 Dedifferentiated Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005015 diabetes mellitus skos:exactMatch NCIT:C2985 Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005016 diabetic kidney disease skos:exactMatch NCIT:C84417 Diabetic Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005017 diffuse gastric adenocarcinoma skos:exactMatch NCIT:C9159 Gastric Diffuse Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005020 intestinal disorder skos:exactMatch NCIT:C26801 Intestinal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005021 dilated cardiomyopathy skos:exactMatch NCIT:C84673 Dilated Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005023 ductal breast carcinoma in situ skos:exactMatch NCIT:C2924 Breast Ductal Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005025 endocarditis skos:exactMatch NCIT:C34582 Endocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005026 endometrioid adenocarcinoma skos:exactMatch NCIT:C3769 Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005027 epilepsy skos:exactMatch NCIT:C3020 Seizure Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005028 esophageal adenocarcinoma skos:exactMatch NCIT:C4025 Esophageal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005029 essential thrombocythemia skos:exactMatch NCIT:C3407 Essential Thrombocythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005030 fetal growth restriction skos:exactMatch NCIT:C114875 Fetus Small for Gestational Age semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005031 fibromatosis skos:exactMatch NCIT:C3042 Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005032 follicular thyroid adenoma skos:exactMatch NCIT:C3502 Thyroid Gland Follicular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005033 ganglioneuroma skos:exactMatch NCIT:C3049 Ganglioneuroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005034 thyroid gland follicular carcinoma skos:exactMatch NCIT:C8054 Thyroid Gland Follicular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005035 ganglioneuroblastoma skos:exactMatch NCIT:C3790 Ganglioneuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005036 gastric adenocarcinoma skos:exactMatch NCIT:C4004 Gastric Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005037 gastric intestinal type adenocarcinoma skos:exactMatch NCIT:C9157 Gastric Intestinal-Type Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005039 reproductive system disorder skos:exactMatch NCIT:C4875 Reproductive System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005040 germ cell tumor skos:exactMatch NCIT:C3708 Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005041 glaucoma skos:exactMatch NCIT:C26782 Glaucoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005043 hyperplasia skos:exactMatch NCIT:C3113 Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005044 hypertensive disorder skos:exactMatch NCIT:C3117 Hypertension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005045 hypertrophic cardiomyopathy skos:exactMatch NCIT:C34449 Hypertrophic Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005046 immune system disorder skos:exactMatch NCIT:C3507 Immune System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005047 infertility disorder skos:exactMatch NCIT:C3836 Infertility semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005048 pancreatic insulin-producing neuroendocrine tumor skos:exactMatch NCIT:C3140 Pancreatic Insulin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005050 invasive ductal and lobular carcinoma skos:exactMatch NCIT:C7688 Invasive Breast Ductal Carcinoma and Lobular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005051 invasive lobular breast carcinoma skos:exactMatch NCIT:C7950 Invasive Breast Lobular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005052 irritable bowel syndrome skos:exactMatch NCIT:C82343 Irritable Bowel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005053 ischemic disease skos:exactMatch NCIT:C34738 Ischemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005055 Kaposi's sarcoma skos:exactMatch NCIT:C9087 Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005056 keratinizing squamous cell carcinoma skos:exactMatch NCIT:C4105 Keratinizing Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005057 large cell neuroendocrine carcinoma skos:exactMatch NCIT:C6875 Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005058 leiomyosarcoma skos:exactMatch NCIT:C3158 Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005059 leukemia skos:exactMatch NCIT:C3161 Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005060 liposarcoma skos:exactMatch NCIT:C3194 Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005061 lung adenocarcinoma skos:exactMatch NCIT:C3512 Lung Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005062 lymphoma skos:exactMatch NCIT:C3208 Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005063 medullary breast carcinoma skos:exactMatch NCIT:C9119 Breast Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005065 mesothelioma skos:exactMatch NCIT:C3234 Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005066 metabolic disease skos:exactMatch NCIT:C3235 Metabolic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005067 monophasic synovial sarcoma skos:exactMatch NCIT:C6534 Monophasic Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005068 myocardial infarction skos:exactMatch NCIT:C27996 Myocardial Infarction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005070 neoplasm skos:exactMatch NCIT:C3262 Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005071 nervous system disorder skos:exactMatch NCIT:C26835 Nervous System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005072 neuroblastoma skos:exactMatch NCIT:C3270 Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005073 melanocytic nevus skos:exactMatch NCIT:C7570 Melanocytic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005074 papillary cystadenocarcinoma skos:exactMatch NCIT:C3777 Papillary Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005075 thyroid gland papillary carcinoma skos:exactMatch NCIT:C4035 Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005076 periodontitis skos:exactMatch NCIT:C34918 Periodontitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005077 pertussis skos:exactMatch NCIT:C85231 Whooping Cough semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005078 phyllodes tumor skos:exactMatch NCIT:C2977 Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005079 polyp skos:exactMatch NCIT:C3340 Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005080 portal hypertension skos:exactMatch NCIT:C3119 Portal Hypertension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005081 preeclampsia skos:exactMatch NCIT:C85021 Preeclampsia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005082 prostate adenocarcinoma skos:exactMatch NCIT:C2919 Prostate Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005083 psoriasis skos:exactMatch NCIT:C3346 Psoriasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005085 pterygium skos:exactMatch NCIT:C133744 Pterygium semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005087 respiratory system disorder skos:exactMatch NCIT:C26871 Respiratory System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005089 sarcoma skos:exactMatch NCIT:C9118 Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005090 schizophrenia skos:exactMatch NCIT:C3362 Schizophrenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005091 severe acute respiratory syndrome skos:exactMatch NCIT:C85064 Severe Acute Respiratory Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005092 signet ring cell carcinoma skos:exactMatch NCIT:C3774 Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005093 skin disorder skos:exactMatch NCIT:C3371 Skin Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005094 hemangiopericytoma skos:exactMatch NCIT:C3087 Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005095 spondyloarthropathy skos:exactMatch NCIT:C116778 Spondyloarthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005096 squamous cell carcinoma skos:exactMatch NCIT:C2929 Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005097 squamous cell lung carcinoma skos:exactMatch NCIT:C3493 Lung Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005098 stroke disorder skos:exactMatch NCIT:C3390 Stroke semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005100 systemic sclerosis skos:exactMatch NCIT:C72070 Systemic Scleroderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005101 ulcerative colitis skos:exactMatch NCIT:C2952 Ulcerative Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005102 undifferentiated (embryonal) sarcoma skos:exactMatch NCIT:C27096 Liver Embryonal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005104 aJCC grade 1 sarcoma skos:exactMatch NCIT:C9419 AJCC Grade 1 Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005105 melanoma skos:exactMatch NCIT:C3224 Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005106 lipoma skos:exactMatch NCIT:C3192 Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005108 viral infectious disease skos:exactMatch NCIT:C3439 Viral Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005109 HIV infectious disease skos:exactMatch NCIT:C3108 HIV Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005110 idiopathic cardiomyopathy skos:exactMatch NCIT:C53654 Idiopathic Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005111 Epstein-Barr virus infection skos:exactMatch NCIT:C38759 EBV Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005112 malignant pleural mesothelioma skos:exactMatch NCIT:C7376 Pleural Malignant Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005113 bacterial infectious disease skos:exactMatch NCIT:C2890 Bacterial Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005115 temporal lobe epilepsy skos:exactMatch NCIT:C177244 Temporal Lobe Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005116 Whipple disease skos:exactMatch NCIT:C85228 Whipple Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005119 anthrax infection skos:exactMatch NCIT:C84565 Anthrax semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005124 leprosy skos:exactMatch NCIT:C84824 Leprosy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005129 cataract skos:exactMatch NCIT:C26713 Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005130 celiac disease skos:exactMatch NCIT:C26714 Celiac Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005131 cervical carcinoma skos:exactMatch NCIT:C9039 Cervical Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005132 cytomegalovirus infection skos:exactMatch NCIT:C53649 Cytomegaloviral Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005133 endometriosis skos:exactMatch NCIT:C3014 Endometriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005135 parasitic infectious disease skos:exactMatch NCIT:C27864 Parasitic Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005136 malaria skos:exactMatch NCIT:C34797 Malaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005137 nutritional disorder skos:exactMatch NCIT:C26836 Nutritional Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005138 lung carcinoma skos:exactMatch NCIT:C4878 Lung Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005140 ovarian carcinoma skos:exactMatch NCIT:C4908 Ovarian Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005146 post-traumatic stress disorder skos:exactMatch NCIT:C3389 Post-Traumatic Stress Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005147 type 1 diabetes mellitus skos:exactMatch NCIT:C2986 Type 1 Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005148 type 2 diabetes mellitus skos:exactMatch NCIT:C26747 Type 2 Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005150 age-related macular degeneration skos:exactMatch NCIT:C84391 Age-Related Macular Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005151 endocrine system disorder skos:exactMatch NCIT:C3009 Endocrine System Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005152 hypopituitarism skos:exactMatch NCIT:C62591 Hypopituitarism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005153 cervical adenocarcinoma skos:exactMatch NCIT:C4029 Cervical Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005154 liver disorder skos:exactMatch NCIT:C3196 Liver and Intrahepatic Bile Duct Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005155 cirrhosis of liver skos:exactMatch NCIT:C2951 Cirrhosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005156 encephalomyelitis skos:exactMatch NCIT:C34580 Encephalomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005157 lymphoid neoplasm skos:exactMatch NCIT:C7065 Lymphocytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005159 prostate carcinoma skos:exactMatch NCIT:C4863 Prostate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005161 human papilloma virus infection skos:exactMatch NCIT:C27851 Human Papillomavirus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005164 fibrosarcoma skos:exactMatch NCIT:C3043 Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005165 benign neoplasm skos:exactMatch NCIT:C3677 Benign Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005166 osteoma skos:exactMatch NCIT:C3296 Osteoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005167 fibroma skos:exactMatch NCIT:C3041 Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005169 neoplasm of mature T-cells or NK-cells skos:exactMatch NCIT:C27909 Mature T-Cell and NK-Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005170 myeloid neoplasm skos:exactMatch NCIT:C9290 Myeloid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005173 actinic keratosis skos:exactMatch NCIT:C3148 Actinic Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005177 serous cystadenoma skos:exactMatch NCIT:C3783 Serous Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005178 osteoarthritis skos:exactMatch NCIT:C3293 Osteoarthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005180 Parkinson disease skos:exactMatch NCIT:C26845 Parkinson Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005183 ovarian cystadenoma skos:exactMatch NCIT:C4060 Ovarian Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005184 pancreatic ductal adenocarcinoma skos:exactMatch NCIT:C9120 Pancreatic Ductal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005185 chronic childhood arthritis skos:exactMatch NCIT:C27179 Juvenile Rheumatoid Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005186 cocaine dependence skos:exactMatch NCIT:C34492 Cocaine Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005187 human herpesvirus 8 infection skos:exactMatch NCIT:C39291 HHV8 Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005188 iatrogenic Kaposi's sarcoma skos:exactMatch NCIT:C35873 Iatrogenic Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005191 metastatic melanoma skos:exactMatch NCIT:C8925 Metastatic Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005192 exocrine pancreatic carcinoma skos:exactMatch NCIT:C3850 Pancreatic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005193 prostate intraepithelial neoplasia skos:exactMatch NCIT:C4064 Prostatic Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005197 thymus neoplasm skos:exactMatch NCIT:C3412 Thymus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005198 vulvar intraepithelial neoplasia skos:exactMatch NCIT:C4756 Vulvar Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005201 restrictive cardiomyopathy skos:exactMatch NCIT:C62798 Restrictive Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005206 renal carcinoma skos:exactMatch NCIT:C9384 Kidney Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005207 choriocarcinoma skos:exactMatch NCIT:C2948 Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005208 amelanotic skin melanoma skos:exactMatch NCIT:C4633 Amelanotic Cutaneous Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005210 uterine corpus sarcoma skos:exactMatch NCIT:C6339 Uterine Corpus Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005211 ovarian serous adenocarcinoma skos:exactMatch NCIT:C7550 Ovarian Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005212 rhabdomyosarcoma skos:exactMatch NCIT:C3359 Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005214 vulva sarcoma skos:exactMatch NCIT:C40317 Vulvar Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005215 vulvar carcinoma skos:exactMatch NCIT:C4866 Vulvar Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005216 hypopharyngeal carcinoma skos:exactMatch NCIT:C9465 Hypopharyngeal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005219 breast fibrocystic disease skos:exactMatch NCIT:C3039 Breast Fibrocystic Change semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005220 collecting duct carcinoma skos:exactMatch NCIT:C6194 Collecting Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005221 renal pelvis urothelial carcinoma skos:exactMatch NCIT:C7355 Renal Pelvis Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005223 acute myeloid leukemia with minimal differentiation skos:exactMatch NCIT:C8460 Acute Myeloid Leukemia with Minimal Differentiation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005224 acute myeloblastic leukemia without maturation skos:exactMatch NCIT:C3249 Acute Myeloid Leukemia without Maturation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005227 abscess skos:exactMatch NCIT:C26686 Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005230 cellulitis skos:exactMatch NCIT:C26715 Cellulitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005231 hepatitis C virus infection skos:exactMatch NCIT:C3098 Hepatitis C Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005232 large cell carcinoma skos:exactMatch NCIT:C3780 Large Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005233 non-small cell lung carcinoma skos:exactMatch NCIT:C2926 Lung Non-Small Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005235 smoldering plasma cell myeloma skos:exactMatch NCIT:C7149 Smoldering Multiple Myeloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005236 xanthoma skos:exactMatch NCIT:C4071 Xanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005238 round cell liposarcoma skos:exactMatch NCIT:C4252 Round Cell Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005240 kidney disorder skos:exactMatch NCIT:C3149 Kidney Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005242 empyema skos:exactMatch NCIT:C34572 Empyema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005244 peripheral neuropathy skos:exactMatch NCIT:C119734 Peripheral Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005244 peripheral neuropathy skos:exactMatch NCIT:C4731 Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005246 osteomyelitis skos:exactMatch NCIT:C27577 Osteomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005247 bacterial urinary tract infection skos:exactMatch NCIT:C50791 Urinary Tract Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005249 pneumonia skos:exactMatch NCIT:C3333 Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005252 heart failure skos:exactMatch NCIT:C50577 Heart Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005258 autism spectrum disorder skos:exactMatch NCIT:C88412 Autism Spectrum Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005259 Asperger syndrome skos:exactMatch NCIT:C97159 Asperger Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005260 autism skos:exactMatch NCIT:C97161 Autism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005262 central nervous system cyst skos:exactMatch NCIT:C4657 Central Nervous System Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005264 transient ischemic attack skos:exactMatch NCIT:C50781 Transient Ischemic Attack semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005265 inflammatory bowel disease skos:exactMatch NCIT:C3138 Inflammatory Bowel Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005266 diabetic retinopathy skos:exactMatch NCIT:C34538 Diabetic Retinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005267 heart disorder skos:exactMatch NCIT:C3079 Heart Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005269 carotid artery disorder skos:exactMatch NCIT:C84476 Carotid Artery Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005271 allergic disease skos:exactMatch NCIT:C114476 Allergic Reaction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005272 myelodysplastic syndrome with single lineage dysplasia skos:exactMatch NCIT:C2872 Refractory Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005272 myelodysplastic syndrome with single lineage dysplasia skos:exactMatch NCIT:C82591 Myelodysplastic Syndrome, Not Otherwise Specified with Single Lineage Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005275 lung disorder skos:exactMatch NCIT:C3198 Lung Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005277 migraine disorder skos:exactMatch NCIT:C89715 Migraine semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005278 serous adenocarcinoma skos:exactMatch NCIT:C40101 Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005279 pulmonary embolism skos:exactMatch NCIT:C50713 Pulmonary Embolism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005280 prostatitis skos:exactMatch NCIT:C26866 Prostatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005281 gallbladder disorder skos:exactMatch NCIT:C34631 Gallbladder Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005282 cutaneous lupus erythematosus skos:exactMatch NCIT:C26819 Cutaneous Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005283 retinal disorder skos:exactMatch NCIT:C26875 Retinal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005283 retinal disorder skos:exactMatch NCIT:C62601 Retinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005286 palatal neoplasm skos:exactMatch NCIT:C4402 Palate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005289 paranasal sinus neoplasm skos:exactMatch NCIT:C7488 Paranasal Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005290 obsolete rhabdomyolysis skos:exactMatch NCIT:C118318 Rhabdomyolysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005292 colitis skos:exactMatch NCIT:C26723 Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005293 flatfoot skos:exactMatch NCIT:C34616 Flat Foot semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005294 peripheral vascular disease skos:exactMatch NCIT:C35136 Peripheral Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005296 sleep apnea syndrome skos:exactMatch NCIT:C148023 Sleep-Disordered Breathing semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005297 urethritis skos:exactMatch NCIT:C26904 Urethritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005298 osteoporosis skos:exactMatch NCIT:C3298 Osteoporosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005299 brain ischemia skos:exactMatch NCIT:C78394 Cerebrovascular Ischemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005300 chronic kidney disease skos:exactMatch NCIT:C80078 Chronic Kidney Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005301 multiple sclerosis skos:exactMatch NCIT:C3243 Multiple Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005302 attention deficit hyperactivity disorder, inattentive type skos:exactMatch NCIT:C35092 Attention Deficit Hyperactivity Disorder, Inattentive Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005303 drug dependence skos:exactMatch NCIT:C3894 Drug Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005306 ankylosing spondylitis skos:exactMatch NCIT:C84564 Ankylosing Spondylitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005310 atrial flutter skos:exactMatch NCIT:C51224 Atrial Flutter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005311 atherosclerosis skos:exactMatch NCIT:C35768 Atherosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005311 atherosclerosis skos:exactMatch NCIT:C35771 Atherosclerotic Cardiovascular Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005313 necrotizing enterocolitis skos:exactMatch NCIT:C84915 Necrotizing Enterocolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005314 relapsing-remitting multiple sclerosis skos:exactMatch NCIT:C165675 Relapsing-Remitting Multiple Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005315 bone fracture skos:exactMatch NCIT:C3046 Fracture semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005316 bacterial vaginosis skos:exactMatch NCIT:C116973 Bacterial Vaginosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005318 canker sore skos:exactMatch NCIT:C62546 Canker Sore semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005321 Fuchs' endothelial dystrophy skos:exactMatch NCIT:C84721 Fuchs Endothelial Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005324 seasonal allergic rhinitis skos:exactMatch NCIT:C92188 Seasonal Allergic Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005328 eye disorder skos:exactMatch NCIT:C26767 Eye Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005335 colorectal neoplasm skos:exactMatch NCIT:C2956 Colorectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005336 myopathy skos:exactMatch NCIT:C101216 Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005338 open-angle glaucoma skos:exactMatch NCIT:C34641 Open Angle Glaucoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005341 skin basal cell carcinoma skos:exactMatch NCIT:C2921 Skin Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005342 IgA glomerulonephritis skos:exactMatch NCIT:C34643 IgA Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005344 hepatitis B virus infection skos:exactMatch NCIT:C3097 Hepatitis B Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005345 hypospadias skos:exactMatch NCIT:C40341 Hypospadias semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005348 keloid skos:exactMatch NCIT:C3145 Keloid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005349 otosclerosis skos:exactMatch NCIT:C185242 Otosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005351 anorexia nervosa skos:exactMatch NCIT:C34387 Anorexia Nervosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005352 conduct disorder skos:exactMatch NCIT:C89329 Conduct Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005357 Creutzfeldt Jacob disease skos:exactMatch NCIT:C26802 Creutzfeldt-Jakob Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005358 Dengue hemorrhagic fever skos:exactMatch NCIT:C34683 Dengue Hemorrhagic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005361 eosinophilic esophagitis skos:exactMatch NCIT:C27105 Eosinophilic Esophagitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005362 erectile dysfunction skos:exactMatch NCIT:C34801 Male Erectile Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005364 Graves disease skos:exactMatch NCIT:C3071 Graves Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005365 hearing loss disorder skos:exactMatch NCIT:C35731 Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005367 heroin dependence skos:exactMatch NCIT:C34694 Heroin Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005369 carcinoid tumor skos:exactMatch NCIT:C2915 Carcinoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005371 mood disorder skos:exactMatch NCIT:C92200 Mood Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005374 bone marrow neoplasm skos:exactMatch NCIT:C35370 Bone Marrow Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005375 nasopharyngeal neoplasm skos:exactMatch NCIT:C3257 Nasopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005376 membranous glomerulonephritis skos:exactMatch NCIT:C34645 Membranous Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005377 nephrotic syndrome skos:exactMatch NCIT:C34845 Nephrotic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005379 neurotic disorder skos:exactMatch NCIT:C34848 Neurosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005380 osteonecrosis skos:exactMatch NCIT:C34880 Bone Necrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005380 osteonecrosis skos:exactMatch NCIT:C35476 Aseptic Necrosis of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005382 bone Paget disease skos:exactMatch NCIT:C3292 Bone Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005383 panic disorder skos:exactMatch NCIT:C34890 Panic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005384 focal epilepsy skos:exactMatch NCIT:C122812 Partial Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005385 vascular disorder skos:exactMatch NCIT:C35117 Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005386 peripheral arterial disease skos:exactMatch NCIT:C84496 Peripheral Artery Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005387 primary ovarian failure skos:exactMatch NCIT:C113352 Primary Ovarian Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005388 primary biliary cholangitis skos:exactMatch NCIT:C27167 Primary Biliary Cirrhosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005391 restless legs syndrome skos:exactMatch NCIT:C84501 Restless Leg Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005392 scoliosis skos:exactMatch NCIT:C78603 Scoliosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005393 gout skos:exactMatch NCIT:C34650 Gout semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005395 movement disorder skos:exactMatch NCIT:C116757 Movement Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005397 goiter skos:exactMatch NCIT:C26785 Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005399 venous thromboembolism skos:exactMatch NCIT:C99537 Venous Thromboembolism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005401 colonic neoplasm skos:exactMatch NCIT:C2953 Colon Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005402 lymphoid leukemia skos:exactMatch NCIT:C7539 Lymphoid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005404 myalgic encephalomeyelitis/chronic fatigue syndrome skos:exactMatch NCIT:C3037 Chronic Fatigue Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005406 gestational diabetes skos:exactMatch NCIT:C34942 Gestational Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005411 gallbladder cancer skos:exactMatch NCIT:C7481 Gallbladder Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005412 duodenal ulcer skos:exactMatch NCIT:C26755 Duodenal Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005420 hypothyroidism skos:exactMatch NCIT:C26800 Hypothyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005429 prion disease skos:exactMatch NCIT:C128346 Transmissible Spongiform Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005438 metastatic malignant neoplasm in the lymph nodes skos:exactMatch NCIT:C4904 Metastatic Malignant Neoplasm in the Lymph Nodes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005439 familial hypercholesterolemia skos:exactMatch NCIT:C34704 Hyperlipoproteinemia, Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005440 embryonal carcinoma skos:exactMatch NCIT:C3752 Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005441 otitis media skos:exactMatch NCIT:C34885 Otitis Media semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005445 visceral leishmaniasis skos:exactMatch NCIT:C34771 Kala-Azar semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005446 cutaneous leishmaniasis skos:exactMatch NCIT:C34768 Cutaneous Leishmaniasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005446 cutaneous leishmaniasis skos:exactMatch NCIT:C34770 Asian Desert Cutaneous Leishmaniasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005447 testicular cancer skos:exactMatch NCIT:C7251 Malignant Testicular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005451 eating disorder skos:exactMatch NCIT:C89332 Eating Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005452 bulimia nervosa skos:exactMatch NCIT:C34440 Bulimia Nervosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005453 congenital heart disease skos:exactMatch NCIT:C95834 Congenital Heart Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005454 lung neuroendocrine neoplasm skos:exactMatch NCIT:C5670 Lung Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005459 human African trypanosomiasis skos:exactMatch NCIT:C84541 African Trypanosomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005460 swine influenza skos:exactMatch NCIT:C80444 H1N1 Influenza semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005461 endometrium adenocarcinoma skos:exactMatch NCIT:C7359 Endometrial Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005462 primitive neuroectodermal tumor skos:exactMatch NCIT:C3716 Primitive Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005464 rhegmatogenous retinal detachment skos:exactMatch NCIT:C118755 Rhegmatogenous Retinal Detachment semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005466 hypersomnia skos:exactMatch NCIT:C78346 Hypersomnia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005473 temporomandibular joint disorder skos:exactMatch NCIT:C63709 Temporomandibular Joint Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005475 migraine with aura skos:exactMatch NCIT:C117005 Migraine With Aura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005477 ventricular tachycardia skos:exactMatch NCIT:C50802 Ventricular Tachycardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005479 atrial tachycardia skos:exactMatch NCIT:C35481 Atrial Tachycardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005480 contact dermatitis skos:exactMatch NCIT:C26743 Contact Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005483 chemotherapy-induced alopecia skos:exactMatch NCIT:C164162 Chemotherapy-Induced Alopecia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005484 colorectal adenoma skos:exactMatch NCIT:C5673 Colorectal Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005485 psychotic disorder skos:exactMatch NCIT:C78576 Psychosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005487 schizoaffective disorder skos:exactMatch NCIT:C94378 Schizoaffective Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005489 dyslexia skos:exactMatch NCIT:C96410 Dyslexia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005492 urticaria skos:exactMatch NCIT:C3432 Urticaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005494 triple-negative breast carcinoma skos:exactMatch NCIT:C71732 Triple-Negative Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005495 adrenal gland disorder skos:exactMatch NCIT:C26690 Adrenal Gland Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005496 bile duct carcinoma skos:exactMatch NCIT:C27814 Bile Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005498 botulism skos:exactMatch NCIT:C84599 Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005502 dengue disease skos:exactMatch NCIT:C34528 Dengue Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005504 diphtheria skos:exactMatch NCIT:C34541 Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005505 dysembryoplastic neuroepithelial tumor skos:exactMatch NCIT:C9505 Dysembryoplastic Neuroepithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005506 eccrine sweat gland cancer skos:exactMatch NCIT:C5559 Malignant Eccrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005507 gingival cancer skos:exactMatch NCIT:C9317 Malignant Gingival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005508 hereditary multiple osteochondromas skos:exactMatch NCIT:C5183 Hereditary Multiple Exostoses semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005509 histiocytoma skos:exactMatch NCIT:C35765 Histiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005510 hydronephrosis skos:exactMatch NCIT:C26796 Hydronephrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005512 malignant peritoneal mesothelioma skos:exactMatch NCIT:C8704 Advanced Peritoneal Malignant Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005515 oral cavity cancer skos:exactMatch NCIT:C9314 Malignant Oral Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005516 osteochondrodysplasia skos:exactMatch NCIT:C84978 Osteochondrodysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005517 pharynx cancer skos:exactMatch NCIT:C7545 Malignant Pharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005518 pseudohermaphroditism skos:exactMatch NCIT:C124575 Pseudohermaphroditism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005519 renal pelvis carcinoma skos:exactMatch NCIT:C6142 Renal Pelvis Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005520 rickets skos:exactMatch NCIT:C26878 Rickets semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005522 small intestine carcinoma skos:exactMatch NCIT:C7724 Small Intestinal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005524 sweat gland carcinoma skos:exactMatch NCIT:C6938 Sweat Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005526 tetanus skos:exactMatch NCIT:C85185 Tetanus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005527 toxic encephalopathy skos:exactMatch NCIT:C27961 Neurotoxicity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005532 Crohn's colitis skos:exactMatch NCIT:C35211 Crohn Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005538 proctitis skos:exactMatch NCIT:C38011 Proctitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005541 spondylolysis skos:exactMatch NCIT:C35034 Spondylolysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005542 acute coronary syndrome skos:exactMatch NCIT:C53652 Acute Coronary Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005545 staphylococcus aureus infection skos:exactMatch NCIT:C122576 Staphylococcus aureus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005546 fibromyalgia skos:exactMatch NCIT:C87497 Fibromyalgia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005549 renal cell adenocarcinoma skos:exactMatch NCIT:C9385 Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005550 infectious disease skos:exactMatch NCIT:C26726 Infectious Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005552 ocular vascular disorder skos:exactMatch NCIT:C35664 Ocular Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005554 rheumatic disorder skos:exactMatch NCIT:C27204 Rheumatologic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005556 lupus nephritis skos:exactMatch NCIT:C34789 Lupus Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005558 ovarian disorder skos:exactMatch NCIT:C26841 Ovarian Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005559 neurodegenerative disease skos:exactMatch NCIT:C4802 Central Nervous System Degenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005560 brain disorder skos:exactMatch NCIT:C96413 Brain Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005561 aortic disorder skos:exactMatch NCIT:C101253 Aorta Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005563 nut midline carcinoma skos:exactMatch NCIT:C45716 NUT Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005564 embryonal neoplasm skos:exactMatch NCIT:C3264 Embryonal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005565 blastoma skos:exactMatch NCIT:C8997 Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005566 neonatal abstinence syndrome skos:exactMatch NCIT:C87101 Neonatal Abstinence Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005567 substance withdrawal syndrome skos:exactMatch NCIT:C35046 Substance Withdrawal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005570 hematologic disorder skos:exactMatch NCIT:C26323 Hematopoietic and Lymphoid Cell Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005571 polycythemia skos:exactMatch NCIT:C26863 Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005572 polycythemia due to hypoxia skos:exactMatch NCIT:C27312 Polycythemia due to Hypoxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005575 colorectal cancer skos:exactMatch NCIT:C4978 Malignant Colorectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005576 cryoglobulinemia skos:exactMatch NCIT:C26736 Cryoglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005578 arthritic joint disease skos:exactMatch NCIT:C2883 Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005579 epilepsy, idiopathic generalized skos:exactMatch NCIT:C3021 Generalized Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005580 esophageal squamous cell carcinoma skos:exactMatch NCIT:C4024 Esophageal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005582 binge eating disorder skos:exactMatch NCIT:C97162 Binge Eating semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005586 head and neck neoplasm skos:exactMatch NCIT:C3077 Head and Neck Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005590 breast ductal adenocarcinoma skos:exactMatch NCIT:C4017 Breast Ductal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005593 chronic periodontitis skos:exactMatch NCIT:C35326 Chronic Periodontitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005595 laryngeal squamous cell carcinoma skos:exactMatch NCIT:C4044 Laryngeal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005596 cystadenocarcinoma skos:exactMatch NCIT:C2971 Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005599 malignant epithelioid mesothelioma skos:exactMatch NCIT:C7985 Epithelioid Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005601 ovarian mucinous adenocarcinoma skos:exactMatch NCIT:C5243 Ovarian Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005602 ovarian teratoma skos:exactMatch NCIT:C8110 Ovarian Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005605 transitional cell papilloma skos:exactMatch NCIT:C4115 Transitional Cell Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005606 tubular adenocarcinoma skos:exactMatch NCIT:C65192 Tubular Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005607 chronic bronchitis skos:exactMatch NCIT:C26722 Chronic Bronchitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005608 varicella zoster infection skos:exactMatch NCIT:C96407 Varicella Zoster Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005609 herpes zoster skos:exactMatch NCIT:C71079 Herpes Zoster semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005611 bladder transitional cell carcinoma skos:exactMatch NCIT:C39851 Bladder Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005613 mesonephric adenocarcinoma skos:exactMatch NCIT:C4072 Mesonephric Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005614 pancreatic adenosquamous carcinoma skos:exactMatch NCIT:C5721 Pancreatic Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005615 plasmacytoma skos:exactMatch NCIT:C9349 Plasmacytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005616 pulmonary mucoepidermoid carcinoma skos:exactMatch NCIT:C45544 Lung Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005617 undifferentiated carcinoma skos:exactMatch NCIT:C3692 Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005618 anxiety disorder skos:exactMatch NCIT:C2878 Anxiety Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005619 typhoid fever skos:exactMatch NCIT:C35089 Typhoid Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005620 cerebral amyloid angiopathy skos:exactMatch NCIT:C84625 Cerebral Amyloid Angiopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005625 cerebral malaria skos:exactMatch NCIT:C128373 Cerebral Malaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005626 epithelial neoplasm skos:exactMatch NCIT:C3709 Epithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005627 head and neck cancer skos:exactMatch NCIT:C4013 Malignant Head and Neck Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005628 male breast carcinoma skos:exactMatch NCIT:C3862 Male Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005629 Acanthamoeba keratitis skos:exactMatch NCIT:C50450 Acanthamoeba Keratitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005631 actinomycosis skos:exactMatch NCIT:C34350 Actinomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005632 acute chest syndrome skos:exactMatch NCIT:C138179 Acute Chest Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005634 acute hemorrhagic conjunctivitis skos:exactMatch NCIT:C34505 Acute Hemorrhagic Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005635 adenomyoma skos:exactMatch NCIT:C3726 Adenomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005636 adenosarcoma skos:exactMatch NCIT:C9474 Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005638 agnosia skos:exactMatch NCIT:C84542 Agnosia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005642 atopic conjunctivitis skos:exactMatch NCIT:C34506 Atopic Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005644 amebiasis skos:exactMatch NCIT:C84551 Amebiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005645 ancylostomiasis skos:exactMatch NCIT:C35805 Ancylostomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005647 anogenital human papillomavirus infection skos:exactMatch NCIT:C4820 Anogenital Human Papillomavirus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005648 aortic valve insufficiency skos:exactMatch NCIT:C51223 Aortic Valve Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005649 appendicitis skos:exactMatch NCIT:C35145 Appendicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005654 ascariasis skos:exactMatch NCIT:C128392 Ascariasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005657 aspergillosis skos:exactMatch NCIT:C2886 Aspergillosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005661 babesiosis skos:exactMatch NCIT:C84581 Babesiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005662 balantidiasis skos:exactMatch NCIT:C84583 Balantidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005663 Barre-Lieou syndrome skos:exactMatch NCIT:C34411 Cervicocranial Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005664 bartonellosis skos:exactMatch NCIT:C84586 Bartonella Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005665 Bell's palsy skos:exactMatch NCIT:C26769 Cranial Nerve VII Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005668 bird fancier's lung skos:exactMatch NCIT:C34425 Bird Fancier's Lung semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005670 blackwater fever skos:exactMatch NCIT:C34426 Blackwater Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005672 blastomycosis skos:exactMatch NCIT:C34428 Blastomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005672 blastomycosis skos:exactMatch NCIT:C34429 North American Blastomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005673 blind loop syndrome skos:exactMatch NCIT:C34431 Blind Loop Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005674 bone giant cell tumor skos:exactMatch NCIT:C121932 Giant Cell Tumor of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005682 bronchopneumonia skos:exactMatch NCIT:C26710 Bronchopneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005683 brucellosis skos:exactMatch NCIT:C84602 Brucellosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005689 cannabis dependence skos:exactMatch NCIT:C34445 Cannabis Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005692 cat-scratch disease skos:exactMatch NCIT:C84620 Cat-Scratch Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005693 cauda equina syndrome skos:exactMatch NCIT:C35436 Cauda Equina Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005694 cecal neoplasm skos:exactMatch NCIT:C4433 Cecum Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005699 cervicofacial actinomycosis skos:exactMatch NCIT:C34351 Cervicofacial Actinomycotic Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005700 chickenpox skos:exactMatch NCIT:C97132 Chicken Pox semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005701 chlamydia trachomatis infectious disease skos:exactMatch NCIT:C34463 Chlamydial Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005706 coccidioidomycosis skos:exactMatch NCIT:C84642 Coccidioidomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005707 coccidiosis skos:exactMatch NCIT:C34493 Coccidiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005709 common cold skos:exactMatch NCIT:C34500 Acute Nasopharyngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005710 composite lymphoma skos:exactMatch NCIT:C38661 Composite Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005711 congenital diaphragmatic hernia skos:exactMatch NCIT:C98893 Congenital Diaphragmatic Hernia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005714 congenital syphilis skos:exactMatch NCIT:C84649 Congenital Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005715 congenital toxoplasmosis skos:exactMatch NCIT:C50503 Congenital Toxoplasmosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005722 croup skos:exactMatch NCIT:C26735 Croup semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005723 Cryptococcal meningitis skos:exactMatch NCIT:C174113 Cryptococcal Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005724 cryptococcosis skos:exactMatch NCIT:C2967 Cryptococcosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005725 cyclosporiasis skos:exactMatch NCIT:C128409 Cyclosporiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005731 dipetalonemiasis skos:exactMatch NCIT:C34540 Dipetalonemiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005737 Ebola hemorrhagic fever skos:exactMatch NCIT:C36171 Ebola Hemorrhagic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005738 echinococcosis skos:exactMatch NCIT:C84682 Echinococcosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005742 emphysematous cholecystitis skos:exactMatch NCIT:C35592 Emphysematous Cholecystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005744 yolk sac tumor skos:exactMatch NCIT:C3011 Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005746 enterobiasis skos:exactMatch NCIT:C128396 Enterobiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005749 eosinophilic pneumonia skos:exactMatch NCIT:C35150 Eosinophilic Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005753 epiglottitis skos:exactMatch NCIT:C116007 Epiglottitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005754 epilepsy with generalized tonic-clonic seizures skos:exactMatch NCIT:C3022 Tonic-Clonic Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005755 equine infectious anemia skos:exactMatch NCIT:C84694 Equine Infectious Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005756 ethmoid sinusitis skos:exactMatch NCIT:C34597 Ethmoidal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005758 eunuchism skos:exactMatch NCIT:C131195 Primary Testicular Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005761 filarial elephantiasis skos:exactMatch NCIT:C128360 Lymphatic Filariasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005764 follicular dendritic cell sarcoma skos:exactMatch NCIT:C9281 Follicular Dendritic Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005769 geniculate herpes zoster skos:exactMatch NCIT:C84763 Herpes Zoster Oticus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005770 genital herpes skos:exactMatch NCIT:C14364 Genital Herpes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005771 geographic tongue skos:exactMatch NCIT:C84588 Benign Migratory Glossitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005774 glanders skos:exactMatch NCIT:C34638 Glanders semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005775 G6PD deficiency skos:exactMatch NCIT:C98933 Glucose-6-Phosphate Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005776 gnathomiasis skos:exactMatch NCIT:C128395 Gnathostomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005777 granuloma inguinale skos:exactMatch NCIT:C3065 Granuloma Inguinale semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005779 hand, foot and mouth disease skos:exactMatch NCIT:C128439 Hand Foot and Mouth Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005780 hantavirus infectious disease skos:exactMatch NCIT:C3899 Hantavirus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005784 hantavirus hemorrhagic fever with renal syndrome skos:exactMatch NCIT:C84753 Hemorrhagic Fever with Renal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005790 hepatitis A virus infection skos:exactMatch NCIT:C3096 Hepatitis A Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005798 HIV-associated nephropathy skos:exactMatch NCIT:C26918 HIV-Associated Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005800 hordeolum skos:exactMatch NCIT:C118722 Stye semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005802 hymenolepiasis skos:exactMatch NCIT:C84768 Hymenolepiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005806 hypopharynx cancer skos:exactMatch NCIT:C7190 Malignant Hypopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005807 idiopathic CD4-positive T-lymphocytopenia skos:exactMatch NCIT:C84780 Idiopathic CD4-Positive T-Lymphocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005808 inclusion conjunctivitis skos:exactMatch NCIT:C116817 Neonatal Chlamydia Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005810 infectious mononucleosis skos:exactMatch NCIT:C34726 Infectious Mononucleosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005812 influenza skos:exactMatch NCIT:C53482 Influenza semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005813 interdigitating dendritic cell sarcoma skos:exactMatch NCIT:C9282 Interdigitating Dendritic Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005814 intestinal cancer skos:exactMatch NCIT:C4572 Malignant Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005815 pancreatic neuroendocrine neoplasm skos:exactMatch NCIT:C27031 Pancreatic Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005817 Kluver-Bucy syndrome skos:exactMatch NCIT:C84802 Kluver-Bucy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005819 laryngeal tuberculosis skos:exactMatch NCIT:C26895 Tuberculous Laryngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005820 Lassa fever skos:exactMatch NCIT:C128418 Lassa Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005822 latent syphilis skos:exactMatch NCIT:C35056 Latent Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005823 legionellosis skos:exactMatch NCIT:C128334 Legionellosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005824 Legionnaires' disease skos:exactMatch NCIT:C128339 Legionella Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005825 leptospirosis skos:exactMatch NCIT:C84825 Leptospirosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005827 lipoatrophic diabetes skos:exactMatch NCIT:C34537 Lipoatrophic Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005828 listeriosis skos:exactMatch NCIT:C82994 Listeriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005831 lymph node tuberculosis skos:exactMatch NCIT:C26896 Lymph Node Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005832 lymphangitis skos:exactMatch NCIT:C34790 Lymphangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005833 lymphatic system disorder skos:exactMatch NCIT:C50764 Lymphadenopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005834 lymphogranuloma venereum skos:exactMatch NCIT:C26822 Lymphogranuloma Venereum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005835 Lynch syndrome skos:exactMatch NCIT:C8494 Lynch Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005836 male reproductive organ cancer skos:exactMatch NCIT:C8561 Malignant Male Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005837 mandibular cancer skos:exactMatch NCIT:C35178 Malignant Neoplasm of Mandible semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005838 mansonelliasis skos:exactMatch NCIT:C84882 Mansonelliasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005842 maxillary sinusitis skos:exactMatch NCIT:C34809 Maxillary Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005843 mediastinal cancer skos:exactMatch NCIT:C3549 Malignant Mediastinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005844 chalazion skos:exactMatch NCIT:C26717 Chalazion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005845 meningoencephalitis skos:exactMatch NCIT:C34813 Meningoencephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005846 microsporidiosis skos:exactMatch NCIT:C84891 Microsporidiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005848 miliary tuberculosis skos:exactMatch NCIT:C35086 Miliary Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005851 Miller Fisher syndrome skos:exactMatch NCIT:C116958 Miller Fisher Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005852 mitral valve stenosis skos:exactMatch NCIT:C50654 Mitral Valve Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005853 malignant mixed neoplasm skos:exactMatch NCIT:C3729 Malignant Mixed Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005854 mixed connective tissue disease skos:exactMatch NCIT:C84892 Mixed Connective Tissue Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005858 mucinous cystadenocarcinoma skos:exactMatch NCIT:C3776 Mucinous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005859 mucocutaneous leishmaniasis skos:exactMatch NCIT:C34769 American Cutaneous Leishmaniasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005861 multidrug-resistant tuberculosis skos:exactMatch NCIT:C128415 Multidrug-Resistant Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005864 muscle cancer skos:exactMatch NCIT:C4883 Malignant Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005866 Mycobacterium avium complex disease skos:exactMatch NCIT:C36197 Mycobacterium Avium Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005867 Mycoplasma pneumoniae pneumonia skos:exactMatch NCIT:C122526 Mycoplasmal Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005868 myelophthisic anemia skos:exactMatch NCIT:C36218 Leukoerythroblastic Reaction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005870 necatoriasis skos:exactMatch NCIT:C34838 Necatoriasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005872 nervous system cancer skos:exactMatch NCIT:C4788 Malignant Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005875 Newcastle disease skos:exactMatch NCIT:C34849 Newcastle Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005878 ocular onchocerciasis skos:exactMatch NCIT:C34862 Ocular Onchocerciasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005885 optic neuritis skos:exactMatch NCIT:C84950 Optic Neuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005886 oral candidiasis skos:exactMatch NCIT:C28137 Oral Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005888 ornithosis skos:exactMatch NCIT:C34873 Ornithosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005890 osteitis fibrosa skos:exactMatch NCIT:C34875 Osteitis Fibrosa Cystica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005892 otitis media with effusion skos:exactMatch NCIT:C34886 Secretory Otitis Media semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005893 pancreatic endocrine carcinoma skos:exactMatch NCIT:C3770 Pancreatic Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005894 paracoccidioidomycosis skos:exactMatch NCIT:C34891 Paracoccidioidomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005895 paragonimiasis skos:exactMatch NCIT:C84995 Paragonimiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005898 paronychia skos:exactMatch NCIT:C79702 Paronychia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005900 parotitis skos:exactMatch NCIT:C114281 Parotitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005904 pericarditis skos:exactMatch NCIT:C34915 Pericarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005906 peritonsillar abscess skos:exactMatch NCIT:C128322 Peritonsillar Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005911 pharyngoconjunctival fever skos:exactMatch NCIT:C34924 Pharyngoconjunctival Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005915 pityriasis versicolor skos:exactMatch NCIT:C82981 Malassezia furfur Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005916 placenta accreta skos:exactMatch NCIT:C26856 Placenta Accreta semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005917 placenta disorder skos:exactMatch NCIT:C26857 Placenta Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005918 placenta praevia skos:exactMatch NCIT:C26858 Placenta Previa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005920 Plasmodium falciparum malaria skos:exactMatch NCIT:C34798 Falciparum Malaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005921 Plasmodium vivax malaria skos:exactMatch NCIT:C34800 Vivax Malaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005922 pleural tuberculosis skos:exactMatch NCIT:C26898 Tuberculous Pleuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005929 postpartum depression skos:exactMatch NCIT:C92852 Postpartum Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005933 pulmonary blastoma skos:exactMatch NCIT:C3732 Pulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005938 renal tuberculosis skos:exactMatch NCIT:C123020 Renal Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005941 retroperitoneal cancer skos:exactMatch NCIT:C3537 Malignant Retroperitoneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005942 Reye syndrome skos:exactMatch NCIT:C34983 Reye Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005952 scarlet fever skos:exactMatch NCIT:C94575 Scarlet Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005953 scirrhous adenocarcinoma skos:exactMatch NCIT:C2928 Scirrhous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005960 silicosis skos:exactMatch NCIT:C3369 Silicosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005961 sinusitis skos:exactMatch NCIT:C35024 Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005963 sparganosis skos:exactMatch NCIT:C35030 Sparganosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005964 sphenoid sinusitis skos:exactMatch NCIT:C35031 Sphenoidal Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005965 spinal stenosis skos:exactMatch NCIT:C177444 Spinal Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005966 spleen cancer skos:exactMatch NCIT:C3539 Malignant Splenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005971 staphyloenterotoxemia skos:exactMatch NCIT:C35037 Staphylococcal Food Poisoning semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005974 strongyloidiasis skos:exactMatch NCIT:C128398 Strongyloidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005976 syphilis skos:exactMatch NCIT:C35055 Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005977 tabes dorsalis skos:exactMatch NCIT:C35057 Tabes Dorsalis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005979 thoracic outlet syndrome skos:exactMatch NCIT:C85188 Thoracic Outlet Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005982 tinea infection skos:exactMatch NCIT:C112181 Tinea Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005983 tinea favosa skos:exactMatch NCIT:C35072 Favus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005988 toxocariasis skos:exactMatch NCIT:C34758 Visceral Larva Migrans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005988 toxocariasis skos:exactMatch NCIT:C85194 Toxocariasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005989 toxoplasmosis skos:exactMatch NCIT:C3418 Toxoplasmosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005990 tracheitis skos:exactMatch NCIT:C78643 Tracheitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005993 Trichomonas vaginitis urogenital infection skos:exactMatch NCIT:C35083 Trichomonas Vaginitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005996 trichuriasis skos:exactMatch NCIT:C128399 Trichuriasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005997 tricuspid valve stenosis skos:exactMatch NCIT:C50783 Tricuspid Valve Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0005999 tuberculous empyema skos:exactMatch NCIT:C34575 Tuberculous Empyema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006001 urinary schistosomiasis skos:exactMatch NCIT:C39294 Schistosoma Hematobium Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006003 uterine corpus cancer skos:exactMatch NCIT:C61574 Uterine Corpus Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006004 vasomotor rhinitis skos:exactMatch NCIT:C34988 Vasomotor Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006005 Venezuelan equine encephalitis skos:exactMatch NCIT:C35121 Venezuelan Equine Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006006 verrucous carcinoma skos:exactMatch NCIT:C3781 Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006009 viral encephalitis skos:exactMatch NCIT:C35302 Viral Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006011 viral hepatitis skos:exactMatch NCIT:C35124 Viral Hepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006014 vulvovaginal candidiasis skos:exactMatch NCIT:C2914 Vulvovaginal Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006015 Waterhouse-Friderichsen syndrome skos:exactMatch NCIT:C85225 Waterhouse-Friderichsen Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006019 yaws skos:exactMatch NCIT:C41353 Yaws semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006026 urinary bladder disorder skos:exactMatch NCIT:C2900 Bladder Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006028 cecum adenocarcinoma skos:exactMatch NCIT:C5543 Cecum Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006029 cecum carcinoma skos:exactMatch NCIT:C3491 Cecum Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006030 chronic cystitis skos:exactMatch NCIT:C27008 Chronic Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006031 chronic rhinosinusitis skos:exactMatch NCIT:C35151 Chronic Sinusitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006032 cystitis skos:exactMatch NCIT:C26738 Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006033 diffuse intrinsic pontine glioma skos:exactMatch NCIT:C94764 Diffuse Intrinsic Pontine Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006034 gastric adenosquamous carcinoma skos:exactMatch NCIT:C5474 Gastric Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006035 gastric tubular adenocarcinoma skos:exactMatch NCIT:C5473 Gastric Tubular Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006036 granulosa cell tumor skos:exactMatch NCIT:C3070 Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006038 indeterminate colitis skos:exactMatch NCIT:C27110 Colitis of Indeterminate Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006039 infectious colitis skos:exactMatch NCIT:C78359 Infectious Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006041 lung carcinoid tumor skos:exactMatch NCIT:C4038 Lung Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006042 meningeal tuberculosis skos:exactMatch NCIT:C84888 Meningeal Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006043 metaplastic breast carcinoma skos:exactMatch NCIT:C5164 Breast Metaplastic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006045 ovarian clear cell adenocarcinoma skos:exactMatch NCIT:C40078 Ovarian Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006046 ovarian serous cystadenocarcinoma skos:exactMatch NCIT:C7978 Ovarian Serous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006047 pancreatic adenocarcinoma skos:exactMatch NCIT:C8294 Pancreatic Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006049 papillary lung adenocarcinoma skos:exactMatch NCIT:C5650 Lung Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006050 pleomorphic breast carcinoma skos:exactMatch NCIT:C5161 Breast Pleomorphic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006052 pulmonary tuberculosis skos:exactMatch NCIT:C26899 Pulmonary Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006053 renal leiomyoma skos:exactMatch NCIT:C159209 Kidney Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006054 reproductive system neoplasm skos:exactMatch NCIT:C3674 Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006055 sex cord-stromal tumor skos:exactMatch NCIT:C3794 Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006056 squamous cell breast carcinoma skos:exactMatch NCIT:C5177 Breast Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006058 Wilms tumor skos:exactMatch NCIT:C3267 Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006059 nasal cavity squamous cell carcinoma skos:exactMatch NCIT:C8192 Nasal Cavity Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006060 nasopharyngeal squamous cell carcinoma skos:exactMatch NCIT:C167265 Nasopharyngeal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006066 acinar prostate adenocarcinoma, foamy gland variant skos:exactMatch NCIT:C39882 Prostate Acinar Foamy Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006067 acinar prostate mucinous adenocarcinoma skos:exactMatch NCIT:C5537 Prostate Acinar Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006068 ACTH-producing pituitary gland adenoma skos:exactMatch NCIT:C7462 Corticotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006069 ACTH-producing pituitary gland carcinoma skos:exactMatch NCIT:C5964 Metastatic Corticotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006071 adenofibroma skos:exactMatch NCIT:C8984 Female Reproductive System Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006073 adenomatoid odontogenic tumor skos:exactMatch NCIT:C4310 Adenomatoid Odontogenic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006074 adenosquamous carcinoma skos:exactMatch NCIT:C3727 Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006075 adrenal gland myelolipoma skos:exactMatch NCIT:C3736 Adrenal Gland Myelolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006076 adrenal gland neuroblastoma skos:exactMatch NCIT:C4827 Adrenal Gland Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006077 adrenal medullary hyperplasia skos:exactMatch NCIT:C35838 Adrenal Medullary Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006078 AIDS-related primary central nervous system lymphoma skos:exactMatch NCIT:C8284 AIDS-Related Primary Central Nervous System Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006079 ameloblastic carcinoma skos:exactMatch NCIT:C7492 Ameloblastic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006081 anal melanoma skos:exactMatch NCIT:C4639 Anal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006082 anal squamous cell carcinoma skos:exactMatch NCIT:C9161 Anal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006085 angiolipoma skos:exactMatch NCIT:C3733 Angiolipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006086 angiomyxoma skos:exactMatch NCIT:C3254 Angiomyxoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006087 appendix adenocarcinoma skos:exactMatch NCIT:C7718 Appendix Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006088 appendix adenoma skos:exactMatch NCIT:C43550 Appendix Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006090 appendix hyperplastic polyp skos:exactMatch NCIT:C96416 Appendix Hyperplastic Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006091 appendix neuroendocrine tumor G1 skos:exactMatch NCIT:C4138 Appendix Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006092 appendix villous adenoma skos:exactMatch NCIT:C5512 Appendix Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006093 ascending colon neuroendocrine tumor G1 skos:exactMatch NCIT:C6427 Ascending Colon Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006094 Askin tumor skos:exactMatch NCIT:C7542 Askin Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006095 atypical carcinoid tumor skos:exactMatch NCIT:C72074 Neuroendocrine Tumor G2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006097 atypical lipomatous tumor skos:exactMatch NCIT:C6505 Atypical Lipomatous Tumor/Well Differentiated Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006098 atypical lobular breast hyperplasia skos:exactMatch NCIT:C4730 Breast Atypical Lobular Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006102 basaloid carcinoma skos:exactMatch NCIT:C4121 Basaloid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006103 benign adrenal gland pheochromocytoma skos:exactMatch NCIT:C48305 Non-Metastatic Adrenal Gland Pheochromocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006104 benign carotid body paraganglioma skos:exactMatch NCIT:C79950 Non-Metastatic Carotid Body Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006105 benign conjunctival neoplasm skos:exactMatch NCIT:C3622 Benign Conjunctival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006106 benign smooth muscle neoplasm skos:exactMatch NCIT:C6510 Benign Smooth Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006107 benign thyroid gland neoplasm skos:exactMatch NCIT:C3628 Benign Thyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006108 bile duct adenoma skos:exactMatch NCIT:C2942 Bile Duct Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006109 malignant biphasic mesothelioma skos:exactMatch NCIT:C4282 Biphasic Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006111 bladder flat intraepithelial lesion skos:exactMatch NCIT:C37266 Bladder Urothelial Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006112 bladder inflammatory myofibroblastic tumor skos:exactMatch NCIT:C6177 Bladder Inflammatory Myofibroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006115 blast phase chronic myelogenous leukemia, BCR-ABL1 positive skos:exactMatch NCIT:C9110 Blast Phase Chronic Myeloid Leukemia, BCR-ABL1 Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006116 breast carcinoma by gene expression profile skos:exactMatch NCIT:C53553 Breast Carcinoma by Gene Expression Profile semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006117 breast diffuse large B-cell lymphoma skos:exactMatch NCIT:C40375 Breast Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006118 breast fibrosis skos:exactMatch NCIT:C3660 Breast Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006119 breast mucosa-associated lymphoid tissue lymphoma skos:exactMatch NCIT:C35688 Breast Mucosa-Associated Lymphoid Tissue Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006120 C-cell hyperplasia skos:exactMatch NCIT:C46100 C-Cell Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006121 calcifying fibrous tumor skos:exactMatch NCIT:C6488 Calcifying Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006122 calcifying nested epithelial stromal tumor of the liver skos:exactMatch NCIT:C96830 Calcifying Nested Stromal-Epithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006123 cardiac rhabdomyoma skos:exactMatch NCIT:C6739 Cardiac Rhabdomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006126 cecum neuroendocrine tumor G1 skos:exactMatch NCIT:C5501 Cecum Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006128 central nervous system anaplastic large cell lymphoma skos:exactMatch NCIT:C5322 Central Nervous System Anaplastic Large Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006130 central nervous system neoplasm skos:exactMatch NCIT:C9293 Central Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006131 cerebellar liponeurocytoma skos:exactMatch NCIT:C6905 Cerebellar Liponeurocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006132 cervical adenoid basal carcinoma skos:exactMatch NCIT:C40213 Cervical Adenoid Basal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006133 cervical adenoid cystic carcinoma skos:exactMatch NCIT:C6346 Cervical Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006134 cervical adenosquamous carcinoma skos:exactMatch NCIT:C4519 Cervical Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006135 cervical clear cell adenocarcinoma skos:exactMatch NCIT:C6344 Human Papillomavirus-Independent Cervical Adenocarcinoma, Clear Cell-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006137 cervical intraepithelial neoplasia grade 2/3 skos:exactMatch NCIT:C94676 Cervical Intraepithelial Neoplasia Grade 2/3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006138 cervical large cell neuroendocrine carcinoma skos:exactMatch NCIT:C40214 Cervical Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006140 cervical mucinous adenocarcinoma, minimal deviation variant skos:exactMatch NCIT:C40206 Human Papillomavirus-Independent Cervical Adenocarcinoma, Gastric-Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006141 cervical villoglandular adenocarcinoma skos:exactMatch NCIT:C40208 Cervical Villoglandular Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006142 cervical small cell carcinoma skos:exactMatch NCIT:C7982 Cervical Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006143 cervical squamous cell carcinoma skos:exactMatch NCIT:C4028 Cervical Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006144 cervical Wilms tumor skos:exactMatch NCIT:C40236 Cervical Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006145 chondroid chordoma skos:exactMatch NCIT:C6902 Chondroid Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006146 chondroid hamartoma skos:exactMatch NCIT:C42589 Chondroid Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006149 clear cell papillary cystadenoma skos:exactMatch NCIT:C65203 Clear Cell Papillary Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006150 colon Burkitt lymphoma skos:exactMatch NCIT:C27465 Colon Burkitt Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006151 colon dysplasia skos:exactMatch NCIT:C4847 Colon Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006152 colon inflammatory polyp skos:exactMatch NCIT:C5517 Colon Inflammatory Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006153 colon juvenile polyp skos:exactMatch NCIT:C5518 Colon Juvenile Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006154 colon mucosa-associated lymphoid tissue lymphoma skos:exactMatch NCIT:C5498 Colon Mucosa-Associated Lymphoid Tissue Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006155 colon neuroendocrine tumor G1 skos:exactMatch NCIT:C5497 Colon Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006156 colon sessile serrated adenoma/polyp skos:exactMatch NCIT:C96464 Colon Serrated Lesions and Polyps semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006157 colorectal adenosquamous carcinoma skos:exactMatch NCIT:C43589 Colorectal Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006158 colorectal diffuse large B-cell lymphoma skos:exactMatch NCIT:C96503 Colorectal Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006159 colorectal gastrointestinal stromal tumor skos:exactMatch NCIT:C27735 Colorectal Gastrointestinal Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006160 colorectal hamartoma skos:exactMatch NCIT:C96474 Colorectal Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006161 colorectal juvenile polyp skos:exactMatch NCIT:C5681 Colorectal Juvenile Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006162 colorectal neuroendocrine tumor G1 skos:exactMatch NCIT:C96160 Colorectal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006163 colorectal serrated adenocarcinoma skos:exactMatch NCIT:C96485 Colorectal Serrated Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006164 colorectal sessile serrated adenoma/polyp skos:exactMatch NCIT:C83176 Colorectal Serrated Lesions and Polyps semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006165 colorectal squamous cell carcinoma skos:exactMatch NCIT:C43588 Colorectal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006166 columnar cell hyperplasia of the breast skos:exactMatch NCIT:C54183 Breast Columnar Cell Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006167 combined lung carcinoma skos:exactMatch NCIT:C7591 Combined Lung Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006169 complex endometrial hyperplasia skos:exactMatch NCIT:C35423 Complex Endometrial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006170 conjunctival disorder skos:exactMatch NCIT:C27605 Conjunctival Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006172 conjunctival nevus skos:exactMatch NCIT:C4551 Conjunctival Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006173 conjunctival squamous cell carcinoma skos:exactMatch NCIT:C4549 Conjunctival Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006174 cortisol-producing adrenal cortex adenoma skos:exactMatch NCIT:C48449 Cortisol-Producing Adrenal Cortical Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006176 cribriform carcinoma skos:exactMatch NCIT:C3680 Cribriform Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006178 dedifferentiated solitary fibrous tumor skos:exactMatch NCIT:C79948 Dedifferentiated Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006179 desmoplastic ameloblastoma skos:exactMatch NCIT:C39758 Desmoplastic Ameloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006180 digestive system adenoma skos:exactMatch NCIT:C36207 Digestive System Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006181 digestive system carcinoma skos:exactMatch NCIT:C96963 Digestive System Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006182 digestive system mixed adenoneuroendocrine carcinoma skos:exactMatch NCIT:C95406 Digestive System Mixed Adenoneuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006183 disseminated peritoneal leiomyomatosis skos:exactMatch NCIT:C3958 Disseminated Peritoneal Leiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006184 ductal breast carcinoma in situ and lobular carcinoma in situ skos:exactMatch NCIT:C4195 Breast Ductal Carcinoma In Situ and Lobular Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006186 duodenal adenocarcinoma skos:exactMatch NCIT:C7889 Duodenal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006187 duodenal villous adenoma skos:exactMatch NCIT:C5338 Duodenal Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006188 EBV-positive T-cell lymphoproliferative disorder of childhood skos:exactMatch NCIT:C80373 EBV-Positive T-Cell/NK-Cell Lymphoproliferative Disorder of Childhood semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006189 eccrine porocarcinoma skos:exactMatch NCIT:C5560 Porocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006190 endolymphatic sac tumor skos:exactMatch NCIT:C67560 Endolymphatic Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006191 endometrial clear cell adenocarcinoma skos:exactMatch NCIT:C8028 Endometrial Clear Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006192 endometrial endometrioid adenocarcinoma skos:exactMatch NCIT:C6287 Endometrial Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006193 endometrial hyperplasia without atypia skos:exactMatch NCIT:C40157 Endometrial Hyperplasia without Atypia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006195 endometrial polyp skos:exactMatch NCIT:C6433 Endometrial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006196 endometrial serous adenocarcinoma skos:exactMatch NCIT:C27838 Endometrial Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006197 endometrial small cell carcinoma skos:exactMatch NCIT:C40155 Endometrial Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006198 endometrial squamous cell carcinoma skos:exactMatch NCIT:C8719 Endometrial Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006199 endometrial undifferentiated carcinoma skos:exactMatch NCIT:C40156 Endometrial Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006200 epithelioid cell uveal melanoma skos:exactMatch NCIT:C35780 Uveal Epithelioid Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006201 ethmoid sinus adenoid cystic carcinoma skos:exactMatch NCIT:C6238 Ethmoid Sinus Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006202 extrahepatic bile duct adenosquamous carcinoma skos:exactMatch NCIT:C5778 Extrahepatic Bile Duct Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006203 extrahepatic bile duct squamous cell carcinoma skos:exactMatch NCIT:C5777 Extrahepatic Bile Duct Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006206 fallopian tube carcinoma skos:exactMatch NCIT:C3867 Fallopian Tube Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006207 fallopian tube carcinosarcoma skos:exactMatch NCIT:C40124 Fallopian Tube Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006208 fallopian tube serous adenocarcinoma skos:exactMatch NCIT:C40099 Fallopian Tube Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006209 fibroblastic neoplasm skos:exactMatch NCIT:C7075 Fibroblastic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006210 fibrolamellar hepatocellular carcinoma skos:exactMatch NCIT:C4131 Fibrolamellar Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006211 fibrous hamartoma of infancy skos:exactMatch NCIT:C3942 Fibrous Hamartoma of Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006212 flat urothelial hyperplasia skos:exactMatch NCIT:C27878 Flat Urothelial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006213 floor of mouth mucoepidermoid carcinoma skos:exactMatch NCIT:C8178 Floor of Mouth Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006214 follicular variant thyroid gland papillary carcinoma skos:exactMatch NCIT:C126594 Follicular Variant Thyroid Gland Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006215 gallbladder adenocarcinoma skos:exactMatch NCIT:C9166 Gallbladder Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006216 gallbladder adenoma skos:exactMatch NCIT:C7720 Gallbladder Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006217 gallbladder adenosquamous carcinoma skos:exactMatch NCIT:C7356 Gallbladder Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006218 gallbladder biliary intraepithelial neoplasia skos:exactMatch NCIT:C43606 Gallbladder Biliary Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006219 gallbladder small cell neuroendocrine carcinoma skos:exactMatch NCIT:C6763 Gallbladder Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006220 gallbladder squamous cell carcinoma skos:exactMatch NCIT:C9170 Gallbladder Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006221 gastric adenoma skos:exactMatch NCIT:C7699 Gastric Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006222 gastric choriocarcinoma skos:exactMatch NCIT:C95749 Gastric Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006223 gastric diffuse large B-cell lymphoma skos:exactMatch NCIT:C5253 Gastric Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006224 gastric hamartomatous polyp skos:exactMatch NCIT:C4373 Gastric Hamartomatous Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006225 gastric mantle cell lymphoma skos:exactMatch NCIT:C27440 Gastric Mantle Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006226 gastric mucosa-associated lymphoid tissue lymphoma skos:exactMatch NCIT:C5266 Gastric Mucosa-Associated Lymphoid Tissue Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006227 gastric neuroendocrine tumor G1 skos:exactMatch NCIT:C4635 Gastric Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006228 gastric papillary adenocarcinoma skos:exactMatch NCIT:C5472 Gastric Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006229 gastric small cell neuroendocrine carcinoma skos:exactMatch NCIT:C6764 Gastric Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006230 gastric squamous cell carcinoma skos:exactMatch NCIT:C5475 Gastric Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006231 gastrointestinal hamartoma skos:exactMatch NCIT:C96475 Gastrointestinal Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006232 giant cell tumor of soft tissue skos:exactMatch NCIT:C49107 Giant Cell Tumor of Soft Tissue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006233 gonadal teratoma skos:exactMatch NCIT:C98291 Gonadal Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006234 grade III prostatic intraepithelial neoplasia skos:exactMatch NCIT:C3642 Grade III Prostatic Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006235 granular cell tumor skos:exactMatch NCIT:C3474 Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006237 granulocytic sarcoma skos:exactMatch NCIT:C35815 Granulocytic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006238 growth hormone-producing pituitary gland adenoma skos:exactMatch NCIT:C7461 Somatotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006239 head and neck paraganglioma skos:exactMatch NCIT:C5327 Head and Neck Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006243 hepatoid adenocarcinoma skos:exactMatch NCIT:C66950 Hepatoid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006244 HER2 positive breast carcinoma skos:exactMatch NCIT:C53556 HER2-Positive Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006245 hidradenocarcinoma skos:exactMatch NCIT:C54664 Hidradenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006246 high grade surface osteosarcoma skos:exactMatch NCIT:C53958 High Grade Surface Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006247 histiocytic and dendritic cell neoplasm skos:exactMatch NCIT:C9294 Histiocytic and Dendritic Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006248 hydatidiform mole skos:exactMatch NCIT:C3110 Hydatidiform Mole semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006249 hyperplastic polyp skos:exactMatch NCIT:C4083 Hyperplastic Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006250 ileal neuroendocrine tumor G1 skos:exactMatch NCIT:C4935 Ileal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006254 intestinal type adenocarcinoma skos:exactMatch NCIT:C4126 Intestinal-Type Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006255 intimal sarcoma skos:exactMatch NCIT:C53677 Intimal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006256 invasive breast carcinoma skos:exactMatch NCIT:C9245 Invasive Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006257 jejunal neuroendocrine tumor G1 skos:exactMatch NCIT:C6429 Jejunal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006258 juvenile polyp skos:exactMatch NCIT:C3826 Juvenile Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006260 kidney medullary carcinoma skos:exactMatch NCIT:C7572 Kidney Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006262 lacrimal gland adenoid cystic carcinoma skos:exactMatch NCIT:C4540 Lacrimal Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006264 laryngeal adenoid cystic carcinoma skos:exactMatch NCIT:C9462 Laryngeal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006265 laryngeal small cell carcinoma skos:exactMatch NCIT:C6025 Laryngeal Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006266 Leydig cell tumor skos:exactMatch NCIT:C3188 Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006267 liver cavernous hemangioma skos:exactMatch NCIT:C96839 Liver Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006268 liver diffuse large B-cell lymphoma skos:exactMatch NCIT:C96843 Liver Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006270 lobular breast carcinoma in situ skos:exactMatch NCIT:C4018 Breast Lobular Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006271 low grade central osteosarcoma skos:exactMatch NCIT:C6474 Low Grade Central Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006272 low grade fibromyxoid sarcoma skos:exactMatch NCIT:C45202 Low Grade Fibromyxoid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006273 low grade fibromyxoid sarcoma with giant collagen rosettes skos:exactMatch NCIT:C45203 Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006274 low grade vulvar intraepithelial neoplasia skos:exactMatch NCIT:C4760 Low Grade Vulvar Squamous Intraepithelial Lesion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006275 lung giant cell carcinoma skos:exactMatch NCIT:C4452 Lung Giant Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006276 lung inflammatory myofibroblastic tumor skos:exactMatch NCIT:C39740 Lung Inflammatory Myofibroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006277 lung lymphangioleiomyomatosis skos:exactMatch NCIT:C38153 Lung Lymphangioleiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006278 lung papilloma skos:exactMatch NCIT:C8295 Bronchial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006279 lung sarcomatoid carcinoma skos:exactMatch NCIT:C45540 Lung Sarcomatoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006280 lung sclerosing hemangioma skos:exactMatch NCIT:C5656 Sclerosing Pneumocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006281 lung signet ring cell carcinoma skos:exactMatch NCIT:C45514 Lung Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006282 lymphangiosarcoma skos:exactMatch NCIT:C3205 Lymphangiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006283 lymphoepithelioma-like lung carcinoma skos:exactMatch NCIT:C45519 Lung Lymphoepithelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006284 major salivary gland carcinoma skos:exactMatch NCIT:C5907 Major Salivary Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006285 major salivary gland carcinoma ex pleomorphic adenoma skos:exactMatch NCIT:C5975 Major Salivary Gland Carcinoma ex Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006286 major salivary gland mucoepidermoid carcinoma skos:exactMatch NCIT:C5906 Major Salivary Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006287 malignancy in giant cell tumor of bone skos:exactMatch NCIT:C4304 Malignancy in Giant Cell Tumor of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006288 malignant adrenal gland pheochromocytoma skos:exactMatch NCIT:C4220 Metastatic Adrenal Gland Pheochromocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006290 malignant germ cell tumor skos:exactMatch NCIT:C4925 Malignant Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006291 malignant jugulotympanic paraganglioma skos:exactMatch NCIT:C4623 Metastatic Jugulotympanic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006292 malignant mesothelioma skos:exactMatch NCIT:C4456 Malignant Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006294 pleural cancer skos:exactMatch NCIT:C3547 Malignant Pleural Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006295 malignant urinary system neoplasm skos:exactMatch NCIT:C9297 Malignant Urinary System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006297 maxillary sinus adenoid cystic carcinoma skos:exactMatch NCIT:C6239 Maxillary Sinus Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006298 mediastinal malignant germ cell tumor skos:exactMatch NCIT:C6446 Malignant Mediastinal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006300 medullomyoblastoma with myogenic differentiation skos:exactMatch NCIT:C3706 Medullomyoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006301 metanephric adenoma skos:exactMatch NCIT:C27253 Metanephric Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006302 micropapillary serous carcinoma skos:exactMatch NCIT:C6882 Micropapillary Serous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006303 middle ear squamous cell carcinoma skos:exactMatch NCIT:C6086 Middle Ear Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006304 minor salivary gland adenocarcinoma skos:exactMatch NCIT:C5948 Minor Salivary Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006306 mixed lobular and ductal breast carcinoma skos:exactMatch NCIT:C5160 Breast Mixed Ductal and Lobular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006307 mixed somatotroph-lactotroph pituitary gland adenoma skos:exactMatch NCIT:C45927 Mixed Somatotroph and Lactotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006309 mucinous gastric adenocarcinoma skos:exactMatch NCIT:C5248 Gastric Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006311 myelodysplastic/myeloproliferative neoplasm skos:exactMatch NCIT:C27262 Myelodysplastic/Myeloproliferative Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006312 myofibroma skos:exactMatch NCIT:C7052 Myofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006313 nabothian cyst skos:exactMatch NCIT:C34835 Nabothian Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006314 nasal cavity polyp skos:exactMatch NCIT:C3256 Nasal Cavity Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006315 obsolete neoplastic medium-sized B-lymphocyte with basophilic cytoplasm skos:exactMatch NCIT:C37005 Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006316 neuroblastic tumor skos:exactMatch NCIT:C6963 Neuroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006317 neurothekeoma skos:exactMatch NCIT:C7018 Nerve Sheath Myxoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006320 non-cutaneous melanoma skos:exactMatch NCIT:C8711 Non-Cutaneous Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006321 non-functioning adrenal cortex adenoma skos:exactMatch NCIT:C48458 Non-Functioning Adrenal Cortical Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006322 non-neoplastic bile duct disorder skos:exactMatch NCIT:C35774 Non-Neoplastic Bile Duct Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006324 normal breast-like subtype of breast carcinoma skos:exactMatch NCIT:C53557 Normal Breast-Like Subtype of Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006325 ocular melanoma skos:exactMatch NCIT:C8562 Ocular Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006326 ocular melanoma with extraocular extension skos:exactMatch NCIT:C7913 Ocular Melanoma with Extraocular Extension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006327 ocular sebaceous carcinoma skos:exactMatch NCIT:C43340 Eye Sebaceous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006328 odontogenic cyst skos:exactMatch NCIT:C54220 Odontogenic Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006329 olfactory neuroblastoma skos:exactMatch NCIT:C3789 Olfactory Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006330 ossifying fibromyxoid tumor skos:exactMatch NCIT:C6582 Ossifying Fibromyxoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006335 ovarian endometrioid adenocarcinoma skos:exactMatch NCIT:C7979 Ovarian Endometrioid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006336 ovarian endometrioid adenocarcinoma with squamous differentiation skos:exactMatch NCIT:C40061 Ovarian Endometrioid Adenocarcinoma with Squamous Differentiation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006337 ovarian endometriosis skos:exactMatch NCIT:C27628 Ovarian Endometriosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006339 ovarian microcystic stromal tumor skos:exactMatch NCIT:C121953 Ovarian Microcystic Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006340 ovarian serous adenofibroma skos:exactMatch NCIT:C40031 Ovarian Serous Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006343 ovarian transitional cell carcinoma skos:exactMatch NCIT:C5240 Ovarian Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006344 ovarian yolk sac tumor skos:exactMatch NCIT:C8107 Ovarian Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006345 palmar fibromatosis skos:exactMatch NCIT:C3469 Palmar Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006346 pancreatic acinar cell carcinoma skos:exactMatch NCIT:C7977 Pancreatic Acinar Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006347 pancreatic large cell neuroendocrine carcinoma skos:exactMatch NCIT:C95582 Pancreatic Large Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006348 pancreatic small cell neuroendocrine carcinoma skos:exactMatch NCIT:C95583 Pancreatic Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006349 papillary cystic neoplasm skos:exactMatch NCIT:C4179 Papillary Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006350 papillary transitional cell carcinoma skos:exactMatch NCIT:C4122 Papillary Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006351 parachordoma skos:exactMatch NCIT:C6581 Parachordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006352 paranasal sinus adenoid cystic carcinoma skos:exactMatch NCIT:C6019 Paranasal Sinus Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006353 paranasal sinus Schneiderian papilloma skos:exactMatch NCIT:C6835 Paranasal Sinus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006354 parathyroid hyperplasia skos:exactMatch NCIT:C3989 Parathyroid Gland Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006355 parotid gland acinic cell carcinoma skos:exactMatch NCIT:C5933 Parotid Gland Acinic Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006356 parotid gland adenoid cystic carcinoma skos:exactMatch NCIT:C5937 Parotid Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006357 parotid gland carcinoma ex pleomorphic adenoma skos:exactMatch NCIT:C5974 Parotid Gland Carcinoma ex Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006358 parotid gland squamous cell carcinoma skos:exactMatch NCIT:C5942 Parotid Gland Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006359 neoplasm with perivascular epithelioid cell differentiation skos:exactMatch NCIT:C38150 PEComa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006360 penile carcinoma skos:exactMatch NCIT:C9061 Penile Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006362 peritoneal mesothelioma skos:exactMatch NCIT:C7633 Peritoneal Mesothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006363 peritoneal multicystic mesothelioma skos:exactMatch NCIT:C6536 Peritoneal Multicystic Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006364 peritoneal well differentiated papillary mesothelioma skos:exactMatch NCIT:C45661 Peritoneal Well Differentiated Papillary Mesothelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006365 Peutz-Jeghers polyp skos:exactMatch NCIT:C4733 Peutz-Jeghers Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006366 Peutz-Jeghers polyp of the stomach skos:exactMatch NCIT:C36205 Peutz-Jeghers Polyp of the Stomach semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006367 pharyngeal adenoid cystic carcinoma skos:exactMatch NCIT:C5818 Pharyngeal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006368 phosphaturic mesenchymal tumor skos:exactMatch NCIT:C67237 Phosphaturic Mesenchymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006369 pineal parenchymal tumor of intermediate differentiation skos:exactMatch NCIT:C6967 Pineal Parenchymal Tumor of Intermediate Differentiation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006372 pituicytoma skos:exactMatch NCIT:C94524 Pituicytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006373 pituitary gland adenoma skos:exactMatch NCIT:C3329 Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006374 placental choriocarcinoma skos:exactMatch NCIT:C8893 Placental Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006375 placental hemangioma skos:exactMatch NCIT:C4868 Placental Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006377 pleural biphasic mesothelioma skos:exactMatch NCIT:C45665 Pleural Biphasic Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006378 pleural epithelioid mesothelioma skos:exactMatch NCIT:C45662 Pleural Epithelioid Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006380 pleural sarcomatoid mesothelioma skos:exactMatch NCIT:C45663 Pleural Sarcomatoid Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006381 plexiform ameloblastoma skos:exactMatch NCIT:C39753 Plexiform Ameloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006382 poorly differentiated thyroid gland carcinoma skos:exactMatch NCIT:C6040 Poorly Differentiated Thyroid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006383 primary cutaneous diffuse large B-cell lymphoma, Leg type skos:exactMatch NCIT:C45194 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006385 primary intraosseous squamous cell carcinoma skos:exactMatch NCIT:C54295 Primary Intraosseous Carcinoma, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006386 primary peritoneal serous adenocarcinoma skos:exactMatch NCIT:C40023 Primary Peritoneal Serous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006387 primary pulmonary diffuse large B-cell lymphoma skos:exactMatch NCIT:C45605 Lung Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006388 prolactin-producing pituitary gland carcinoma skos:exactMatch NCIT:C5962 Metastatic Lactotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006389 prostate rhabdomyosarcoma skos:exactMatch NCIT:C5522 Prostate Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006390 prostate small cell carcinoma skos:exactMatch NCIT:C6766 Prostate Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006391 pyloric gland adenoma skos:exactMatch NCIT:C43526 Gastric Pyloric Gland Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006392 rectal hyperplastic polyp skos:exactMatch NCIT:C5619 Rectal Hyperplastic Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006393 rectal traditional serrated adenoma skos:exactMatch NCIT:C96463 Rectal Traditional Serrated Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006394 rectal tubular adenoma skos:exactMatch NCIT:C96477 Rectal Tubular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006395 rectal tubulovillous adenoma skos:exactMatch NCIT:C5620 Rectal Tubulovillous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006396 rectal villous adenoma skos:exactMatch NCIT:C4919 Rectal Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006397 renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions skos:exactMatch NCIT:C27891 TFE3-Rearranged Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006398 retroperitoneal inflammatory myofibroblastic tumor skos:exactMatch NCIT:C39741 Retroperitoneal Inflammatory Myofibroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006400 salivary gland acinic cell carcinoma skos:exactMatch NCIT:C8013 Salivary Gland Acinic Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006401 salivary gland adenosquamous carcinoma skos:exactMatch NCIT:C35737 Salivary Gland Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006402 salivary gland basal cell adenocarcinoma skos:exactMatch NCIT:C3678 Salivary Gland Basal Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006403 salivary gland carcinoma ex pleomorphic adenoma skos:exactMatch NCIT:C40410 Salivary Gland Carcinoma ex Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006404 salivary gland large cell carcinoma skos:exactMatch NCIT:C35735 Salivary Gland Large Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006405 salivary gland small cell carcinoma skos:exactMatch NCIT:C35703 Salivary Gland Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006406 sarcomatoid carcinoma skos:exactMatch NCIT:C27004 Sarcomatoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006407 sarcomatoid mesothelioma skos:exactMatch NCIT:C45655 Sarcomatoid Mesothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006408 sex hormone-producing adrenal cortex adenoma skos:exactMatch NCIT:C48452 Sex Hormone-Producing Adrenal Cortical Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006409 signet ring cell gastric adenocarcinoma skos:exactMatch NCIT:C5250 Gastric Signet Ring Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006410 simple endometrial hyperplasia skos:exactMatch NCIT:C35463 Simple Endometrial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006411 sinonasal undifferentiated carcinoma skos:exactMatch NCIT:C54294 Sinonasal Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006412 sinus histiocytosis with massive lymphadenopathy skos:exactMatch NCIT:C36075 Rosai-Dorfman-Destombes Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006414 skin sarcoma skos:exactMatch NCIT:C5585 Skin Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006416 small intestinal Burkitt lymphoma skos:exactMatch NCIT:C27409 Small Intestinal Burkitt Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006417 small intestinal diffuse large B-cell lymphoma skos:exactMatch NCIT:C96055 Small Intestinal Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006418 small intestinal enteropathy-associated T-cell lymphoma skos:exactMatch NCIT:C39610 Small Intestinal Enteropathy-Associated T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006419 small intestinal intraepithelial neoplasia skos:exactMatch NCIT:C27462 Small Intestinal Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006420 small intestinal mucosa-associated lymphoid tissue lymphoma skos:exactMatch NCIT:C5635 Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006421 small intestinal tubular adenoma skos:exactMatch NCIT:C43552 Small Intestinal Tubular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006422 small intestinal tubulovillous adenoma skos:exactMatch NCIT:C43553 Small Intestinal Tubulovillous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006423 soft tissue chondroma skos:exactMatch NCIT:C9482 Soft Tissue Chondroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006424 soft tissue neoplasm skos:exactMatch NCIT:C3377 Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006426 spinal cord primitive neuroectodermal tumor skos:exactMatch NCIT:C5406 Spinal Cord Embryonal Tumor, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006427 spindle cell melanoma skos:exactMatch NCIT:C4237 Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006428 splenic diffuse large B-cell lymphoma skos:exactMatch NCIT:C7308 Splenic Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006429 splenic hodgkin lymphoma skos:exactMatch NCIT:C7295 Splenic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006430 splenic mantle cell lymphoma skos:exactMatch NCIT:C7306 Splenic Mantle Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006432 stromal predominant kidney Wilms tumor skos:exactMatch NCIT:C9148 Stromal Predominant Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006435 submandibular gland adenocarcinoma skos:exactMatch NCIT:C5940 Submandibular Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006436 submandibular gland adenoid cystic carcinoma skos:exactMatch NCIT:C5935 Submandibular Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006438 synovial chondromatosis skos:exactMatch NCIT:C34467 Synovial Chondromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006442 tendon sheath fibroma skos:exactMatch NCIT:C6485 Tendon Sheath Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006444 teratoma with malignant transformation skos:exactMatch NCIT:C4289 Teratoma with Somatic-Type Malignancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006446 testicular embryonal carcinoma skos:exactMatch NCIT:C6341 Testicular Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006447 testicular non-seminomatous germ cell tumor skos:exactMatch NCIT:C9313 Testicular Non-Seminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006450 therapy-related myeloid neoplasm skos:exactMatch NCIT:C27912 Myeloid Neoplasm Post Cytotoxic Therapy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006451 thymic carcinoma skos:exactMatch NCIT:C7569 Thymic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006452 thymic sarcomatoid carcinoma skos:exactMatch NCIT:C6463 Thymic Sarcomatoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006455 thymic undifferentiated carcinoma skos:exactMatch NCIT:C35718 Thymic Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006456 thymoma skos:exactMatch NCIT:C3411 Thymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006458 thymoma type B3 skos:exactMatch NCIT:C7997 Thymoma Type B3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006459 thymoma type B1 skos:exactMatch NCIT:C6887 Thymoma Type B1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006462 thyroid gland diffuse large B-cell lymphoma skos:exactMatch NCIT:C6046 Thyroid Gland Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006463 thyroid gland mucoepidermoid carcinoma skos:exactMatch NCIT:C38762 Thyroid Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006464 thyroid gland mucosa-associated lymphoid tissue lymphoma skos:exactMatch NCIT:C7601 Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006465 thyroid gland oncocytic follicular carcinoma skos:exactMatch NCIT:C4946 Thyroid Gland Oncocytic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006466 thyroid gland spindle cell tumor with thymus-like differentiation skos:exactMatch NCIT:C46105 Thyroid Gland Spindle Epithelial Tumor with Thymus-Like Elements semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006467 thyroid gland squamous cell carcinoma skos:exactMatch NCIT:C46008 Thyroid Gland Anaplastic Carcinoma, Squamous Cell Carcinoma Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006468 thyroid gland undifferentiated (anaplastic) carcinoma skos:exactMatch NCIT:C3878 Thyroid Gland Anaplastic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006469 tibial adamantinoma skos:exactMatch NCIT:C8461 Tibial Adamantinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006470 tonsillar squamous cell carcinoma skos:exactMatch NCIT:C8183 Tonsillar Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006471 tracheal adenoid cystic carcinoma skos:exactMatch NCIT:C6051 Tracheal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006474 transitional cell carcinoma skos:exactMatch NCIT:C2930 Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006475 obsolete unclassified renal cell carcinoma skos:exactMatch NCIT:C27892 Unclassified Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006476 undifferentiated gallbladder carcinoma skos:exactMatch NCIT:C9167 Gallbladder Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006477 undifferentiated ovarian carcinoma skos:exactMatch NCIT:C4509 Ovarian Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006478 undifferentiated pancreatic carcinoma skos:exactMatch NCIT:C5722 Pancreatic Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006479 undifferentiated pancreatic carcinoma with osteoclast-like giant cells skos:exactMatch NCIT:C5723 Pancreatic Undifferentiated Carcinoma with Osteoclast-Like Giant Cells semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006480 undifferentiated pleomorphic sarcoma, inflammatory variant skos:exactMatch NCIT:C6497 Undifferentiated Pleomorphic Sarcoma, Inflammatory Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006481 ureter carcinoma skos:exactMatch NCIT:C8993 Ureter Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006482 ureter small cell carcinoma skos:exactMatch NCIT:C6176 Ureter Small Cell Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006483 urothelial dysplasia skos:exactMatch NCIT:C39856 Urothelial Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006484 usual ductal breast hyperplasia skos:exactMatch NCIT:C27941 Breast Usual Ductal Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006485 uterine carcinosarcoma skos:exactMatch NCIT:C42700 Uterine Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006486 uveal melanoma skos:exactMatch NCIT:C7712 Uveal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006487 vaginal adenoid cystic carcinoma skos:exactMatch NCIT:C40261 Vaginal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006488 vaginal carcinosarcoma skos:exactMatch NCIT:C40278 Vaginal Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006489 vaginal melanoma skos:exactMatch NCIT:C27394 Vaginal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006490 vaginal squamous cell carcinoma skos:exactMatch NCIT:C180915 Vaginal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006490 vaginal squamous cell carcinoma skos:exactMatch NCIT:C7736 Vaginal Squamous Cell Carcinoma, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006491 vulvar lichen sclerosus skos:exactMatch NCIT:C27723 Vulvar Lichen Sclerosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006493 Warthin tumor skos:exactMatch NCIT:C2854 Warthin Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006497 cerebral palsy skos:exactMatch NCIT:C34460 Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006498 adenomatous colon polyp skos:exactMatch NCIT:C96479 Colon Adenomatous Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006499 hamartoma skos:exactMatch NCIT:C3075 Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006500 hemangioma skos:exactMatch NCIT:C3085 Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006502 acute respiratory distress syndrome skos:exactMatch NCIT:C3353 Acute Respiratory Distress Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006507 hereditary hemochromatosis skos:exactMatch NCIT:C84481 Hereditary Hemochromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006509 papillary carcinoma skos:exactMatch NCIT:C2927 Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006515 acute pancreatitis skos:exactMatch NCIT:C95437 Acute Pancreatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006517 childhood malignant neoplasm skos:exactMatch NCIT:C4005 Childhood Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006519 rectal cancer skos:exactMatch NCIT:C7418 Malignant Rectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006520 Achenbach syndrome skos:exactMatch NCIT:C35467 Achenbach Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006521 acneiform dermatitis skos:exactMatch NCIT:C35277 Acneiform Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006522 acquired keratosis skos:exactMatch NCIT:C34746 Acquired Keratoderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006523 acrodermatitis skos:exactMatch NCIT:C84532 Acrodermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006525 allergic contact dermatitis skos:exactMatch NCIT:C26998 Allergic Contact Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006530 cholesteatoma skos:exactMatch NCIT:C2944 Cholesteatoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006533 cholesteatoma of middle ear skos:exactMatch NCIT:C3654 Middle Ear Cholesteatoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006539 diffuse lipomatosis skos:exactMatch NCIT:C6504 Diffuse Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006541 epidermolysis bullosa skos:exactMatch NCIT:C67383 Epidermolysis Bullosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006543 epidermolysis bullosa dystrophica skos:exactMatch NCIT:C84691 Epidermolysis Bullosa Dystrophica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006544 erythema infectiosum skos:exactMatch NCIT:C84695 Erythema Infectiosum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006545 erythema multiforme skos:exactMatch NCIT:C3024 Erythema Multiforme semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006546 erythematosquamous dermatosis skos:exactMatch NCIT:C34591 Erythematosquamous Dermatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006547 exanthem skos:exactMatch NCIT:C39594 Skin Rash semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006549 fibroepithelial polyp of the anus skos:exactMatch NCIT:C4435 Anal Fibroepithelial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006550 fibroepithelial polyp of urethra skos:exactMatch NCIT:C6170 Urethra Fibroepithelial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006551 alopecia mucinosa skos:exactMatch NCIT:C82859 Alopecia Mucinosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006552 folliculitis skos:exactMatch NCIT:C94408 Folliculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006553 Fox-Fordyce disease skos:exactMatch NCIT:C84716 Fox-Fordyce Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006554 granuloma annulare skos:exactMatch NCIT:C3470 Granuloma Annulare semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006555 granulomatous dermatitis skos:exactMatch NCIT:C3505 Granulomatous Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006557 hemangioma of subcutaneous tissue skos:exactMatch NCIT:C8540 Subcutaneous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006558 pemphigoid gestationis skos:exactMatch NCIT:C85003 Pemphigoid Gestationis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006563 inverted follicular keratosis skos:exactMatch NCIT:C9007 Inverted Follicular Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006564 irritant dermatitis skos:exactMatch NCIT:C27151 Irritant Contact Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006566 keratosis skos:exactMatch NCIT:C34745 Keratoderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006567 kernicterus due to isoimmunization skos:exactMatch NCIT:C101270 Kernicterus Related to Isoimmunization semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006572 lichen planus skos:exactMatch NCIT:C3189 Lichen Planus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006573 lipodystrophy skos:exactMatch NCIT:C97093 Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006574 lipomatosis skos:exactMatch NCIT:C3193 Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006577 maxillary sinus cholesteatoma skos:exactMatch NCIT:C35868 Maxillary Sinus Cholesteatoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006578 mediastinal lipomatosis skos:exactMatch NCIT:C27488 Mediastinal Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006579 melanoacanthoma skos:exactMatch NCIT:C27548 Melanoacanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006580 miliaria skos:exactMatch NCIT:C34820 Miliaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006582 mongolian spot skos:exactMatch NCIT:C3945 Congenital Dermal Melanocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006583 necrobiosis lipoidica skos:exactMatch NCIT:C34840 Necrobiosis Lipoidica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006585 neurodermatitis skos:exactMatch NCIT:C111963 Neurodermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006589 occupational dermatitis skos:exactMatch NCIT:C34859 Occupational Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006590 palmoplantar keratosis skos:exactMatch NCIT:C34748 Palmoplantar Keratoderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006591 panniculitis skos:exactMatch NCIT:C33645 Subcutis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006592 parapsoriasis skos:exactMatch NCIT:C3312 Parapsoriasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006593 pelvic lipomatosis skos:exactMatch NCIT:C27486 Pelvic Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006594 pemphigus skos:exactMatch NCIT:C34909 Pemphigus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006598 phototoxic dermatitis skos:exactMatch NCIT:C4816 Photosensitive Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006601 pityriasis rosea skos:exactMatch NCIT:C26855 Pityriasis Rosea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006602 porokeratosis skos:exactMatch NCIT:C85019 Porokeratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006603 reactive cutaneous fibrous lesion skos:exactMatch NCIT:C27549 Reactive Cutaneous Fibrous Lesion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006604 rosacea skos:exactMatch NCIT:C97136 Rosacea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006606 scleredema adultorum skos:exactMatch NCIT:C85057 Scleredema Adultorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006608 seborrheic dermatitis skos:exactMatch NCIT:C111888 Seborrheic Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006610 skin atrophy skos:exactMatch NCIT:C35163 Skin Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006611 skin sarcoidosis skos:exactMatch NCIT:C34996 Cutaneous Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006612 steroid lipomatosis skos:exactMatch NCIT:C27487 Steroid Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006620 vulva fibroepithelial polyp skos:exactMatch NCIT:C6857 Vulvar Fibroepithelial Stromal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006621 vulvar inverted follicular keratosis skos:exactMatch NCIT:C40291 Vulvar Inverted Follicular Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006622 vulvar seborrheic keratosis skos:exactMatch NCIT:C6375 Vulvar Seborrheic Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006626 diabetic neuropathy skos:exactMatch NCIT:C26748 Diabetic Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006629 osteoarthritis, hip skos:exactMatch NCIT:C34876 Hip Osteoarthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006633 acalculous cholecystitis skos:exactMatch NCIT:C35578 Acalculous Cholecystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006634 pituitary gland acidophil adenoma skos:exactMatch NCIT:C6780 Pituitary Gland Acidophil Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006637 acute kidney tubular necrosis skos:exactMatch NCIT:C34749 Acute Tubular Necrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006639 adrenal cortex carcinoma skos:exactMatch NCIT:C9325 Adrenal Cortical Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006643 alcoholic cardiomyopathy skos:exactMatch NCIT:C53653 Alcoholic Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006644 alcoholic liver cirrhosis skos:exactMatch NCIT:C34782 Alcoholic Cirrhosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006645 alcoholic polyneuropathy skos:exactMatch NCIT:C26926 Alcoholic Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006646 angioleiomyoma skos:exactMatch NCIT:C3747 Angioleiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006651 anterior uveitis skos:exactMatch NCIT:C35109 Anterior Uveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006653 anthracosilicosis skos:exactMatch NCIT:C34389 Anthracosilicosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006654 anthracosis skos:exactMatch NCIT:C34390 Anthracosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006656 aortitis skos:exactMatch NCIT:C97085 Aortitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006658 arteriolosclerosis skos:exactMatch NCIT:C35543 Arteriolosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006660 arthus reaction skos:exactMatch NCIT:C34400 Arthus Reaction semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006662 aseptic meningitis skos:exactMatch NCIT:C118299 Aseptic Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006663 perinatal asphyxia skos:exactMatch NCIT:C116313 Perinatal Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006664 atrial septal defect skos:exactMatch NCIT:C84473 Atrial Septal Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006665 chronic atrophic gastritis skos:exactMatch NCIT:C7405 Chronic Atrophic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006666 atrophy of thyroid skos:exactMatch NCIT:C26942 Thyroid Gland Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006668 bacterial conjunctivitis skos:exactMatch NCIT:C53656 Bacterial Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006669 bacterial endocarditis skos:exactMatch NCIT:C128359 Bacterial Endocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006670 bacterial meningitis skos:exactMatch NCIT:C118297 Bacterial Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006672 balanitis skos:exactMatch NCIT:C26705 Balanitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006673 pituitary gland basophil adenoma skos:exactMatch NCIT:C2856 Pituitary Gland Basophil Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006676 beriberi skos:exactMatch NCIT:C34418 Vitamin B1 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006680 blue nevus skos:exactMatch NCIT:C3803 Blue Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006682 brachial plexus neuritis skos:exactMatch NCIT:C84600 Brachial Plexus Neuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006683 brachial plexus neuropathy skos:exactMatch NCIT:C27194 Brachial Plexopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006687 burning mouth syndrome skos:exactMatch NCIT:C62545 Burning Mouth Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006688 byssinosis skos:exactMatch NCIT:C84605 Byssinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006692 central pontine myelinolysis skos:exactMatch NCIT:C84623 Central Pontine Myelinolysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006694 cerebral atherosclerosis skos:exactMatch NCIT:C34459 Cerebral Atherosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006700 choroid cancer skos:exactMatch NCIT:C3566 Malignant Choroid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006701 chromophobe adenoma skos:exactMatch NCIT:C2857 Pituitary Gland Chromophobe Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy skos:exactMatch NCIT:C84636 Chronic Inflammatory Demyelinating Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006711 constrictive pericarditis skos:exactMatch NCIT:C78246 Constrictive Pericarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006717 cutaneous fibrous histiocytoma skos:exactMatch NCIT:C6801 Skin Fibrous Histiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006722 dental fluorosis skos:exactMatch NCIT:C85059 Dental Fluorosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006726 diaphragmatic eventration skos:exactMatch NCIT:C98912 Diaphragmatic Eventration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006733 dry eye syndrome skos:exactMatch NCIT:C34553 Dry Eye Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006734 benign duodenal neoplasm skos:exactMatch NCIT:C4775 Benign Duodenal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006738 eccrine acrospiroma skos:exactMatch NCIT:C27273 Poroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006740 empty sella syndrome skos:exactMatch NCIT:C84686 Empty Sella Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006741 encephalomalacia skos:exactMatch NCIT:C98920 Encephalomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006742 endemic goiter skos:exactMatch NCIT:C35023 Endemic Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006745 endometrioid stromal sarcoma skos:exactMatch NCIT:C8973 Endometrioid Stromal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006746 endomyocardial fibrosis skos:exactMatch NCIT:C34585 Endomyocardial Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006749 mixed epithelioid and spindle cell melanoma skos:exactMatch NCIT:C66756 Mixed Epithelioid and Spindle Cell Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006755 euthyroid sick syndrome skos:exactMatch NCIT:C113170 Sick Euthyroid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006759 femoral neuropathy skos:exactMatch NCIT:C27595 Femoral Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006760 fetal erythroblastosis skos:exactMatch NCIT:C101304 Hemolytic Disease of the Newborn semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006761 fibromuscular dysplasia skos:exactMatch NCIT:C84714 Fibromuscular Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006767 gastric antral vascular ectasia skos:exactMatch NCIT:C84724 Gastric Antral Vascular Ectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006770 giant cell reparative granuloma skos:exactMatch NCIT:C121893 Giant Cell Lesion of Small Bones semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006777 hairy tongue skos:exactMatch NCIT:C35075 Hairy Tongue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006778 halo nevus skos:exactMatch NCIT:C7602 Halo Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006784 hemorrhagic disease of newborn skos:exactMatch NCIT:C111857 Hemorrhagic Disease of Newborn semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006787 hidrocystoma skos:exactMatch NCIT:C3760 Hidrocystoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006794 hypersensitivity vasculitis skos:exactMatch NCIT:C82863 Leukocytoclastic Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006795 hypersplenism skos:exactMatch NCIT:C34714 Hypersplenism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006796 hypertensive encephalopathy skos:exactMatch NCIT:C3503 Hypertensive Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006797 hypertensive retinopathy skos:exactMatch NCIT:C3514 Hypertensive Retinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006799 hypothalamic neoplasm skos:exactMatch NCIT:C3129 Hypothalamic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006801 ileal neoplasm skos:exactMatch NCIT:C3130 Ileal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006802 inappropriate ADH syndrome skos:exactMatch NCIT:C3988 Syndrome of Inappropriate Antidiuretic Hormone Secretion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006804 inflammatory breast carcinoma skos:exactMatch NCIT:C4001 Breast Inflammatory Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006806 intermediate uveitis skos:exactMatch NCIT:C35110 Intermediate Uveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006807 intestinal perforation skos:exactMatch NCIT:C39611 Intestinal Perforation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006813 intradermal nevus skos:exactMatch NCIT:C3804 Dermal Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006814 iritis skos:exactMatch NCIT:C50621 Iritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006816 arthropathy skos:exactMatch NCIT:C35760 Arthropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006817 juxtacortical osteosarcoma skos:exactMatch NCIT:C8969 Parosteal Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006823 Klinefelter syndrome skos:exactMatch NCIT:C34752 Klinefelter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006827 lateral medullary syndrome skos:exactMatch NCIT:C84807 Lateral Medullary Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006828 nasal cavity and paranasal sinus lethal midline granuloma skos:exactMatch NCIT:C8196 Nasal Cavity and Paranasal Sinus Lethal Midline Granuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006830 leukoplakia of penis skos:exactMatch NCIT:C3151 Penile Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006834 lip cancer skos:exactMatch NCIT:C7485 Malignant Lip Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006835 lipoid nephrosis skos:exactMatch NCIT:C34844 Minimal Change Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006840 lymphangiectasis skos:exactMatch NCIT:C97087 Lymphangiectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006841 lymphangioendothelioma skos:exactMatch NCIT:C3203 Acquired Progressive Lymphangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006842 lymphangiomyoma skos:exactMatch NCIT:C3204 Lymphangioleiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006843 macular holes skos:exactMatch NCIT:C34795 Macular Hole semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006849 mastitis skos:exactMatch NCIT:C53662 Mastitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006850 maxillary sinus neoplasm skos:exactMatch NCIT:C3219 Maxillary Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006851 meconium aspiration syndrome skos:exactMatch NCIT:C87093 Meconium Aspiration Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006853 mesenchymal chondrosarcoma skos:exactMatch NCIT:C3737 Mesenchymal Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006854 mesenchymoma skos:exactMatch NCIT:C3233 Mesenchymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006856 mesothelial neoplasm skos:exactMatch NCIT:C3786 Mesothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006858 mouth disorder skos:exactMatch NCIT:C3240 Oral Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006859 mucinous cystadenoma skos:exactMatch NCIT:C2973 Mucinous Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006861 myeloid sarcoma skos:exactMatch NCIT:C3520 Myeloid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006863 myxosarcoma skos:exactMatch NCIT:C3255 Myxosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006865 necrotizing ulcerative gingivitis skos:exactMatch NCIT:C34637 Necrotizing Ulcerative Gingivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006869 nodular goiter skos:exactMatch NCIT:C131437 Nodular Goiter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006873 nutritional deficiency disease skos:exactMatch NCIT:C3669 Malnutrition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006881 orbital cellulitis skos:exactMatch NCIT:C99000 Orbital Cellulitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006882 orchitis skos:exactMatch NCIT:C97145 Orchitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006883 malignant superior sulcus neoplasm skos:exactMatch NCIT:C7527 Malignant Superior Sulcus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006886 thyroid gland papillary and follicular carcinoma skos:exactMatch NCIT:C7380 Thyroid Gland Papillary and Follicular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006888 paraneoplastic polyneuropathy skos:exactMatch NCIT:C3981 Paraneoplastic Polyneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006889 paraphimosis skos:exactMatch NCIT:C34893 Paraphimosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006890 parathyroid gland adenoma skos:exactMatch NCIT:C156757 Parathyroid Gland Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006895 penile neoplasm skos:exactMatch NCIT:C3317 Penile Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006901 peritoneal neoplasm skos:exactMatch NCIT:C3322 Peritoneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006903 peroneal nerve paralysis skos:exactMatch NCIT:C27061 Peroneal Nerve Paralysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006904 phimosis skos:exactMatch NCIT:C26852 Phimosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006905 pigmented spindle cell nevus skos:exactMatch NCIT:C4751 Pigmented Spindle Cell Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006907 pilar sheath acanthoma skos:exactMatch NCIT:C4468 Pilar Sheath Acanthoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006908 pituitary apoplexy skos:exactMatch NCIT:C26853 Pituitary Gland Apoplexy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006913 pneumococcal meningitis skos:exactMatch NCIT:C157958 Pneumococcal Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006920 prediabetes syndrome skos:exactMatch NCIT:C122685 Prediabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006921 Actinomycetales infectious disease skos:exactMatch NCIT:C84534 Actinomycetales Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006926 haemophilus infectious disease skos:exactMatch NCIT:C34654 Hemophilus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006930 pseudobulbar palsy skos:exactMatch NCIT:C129934 Pseudobulbar Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006932 pulmonary edema skos:exactMatch NCIT:C26868 Pulmonary Edema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006935 pulmonary subvalvular stenosis skos:exactMatch NCIT:C34961 Congenital Infundibular Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006938 pyelitis skos:exactMatch NCIT:C34964 Pyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006939 pyelonephritis skos:exactMatch NCIT:C34965 Pyelonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006941 rat-bite fever skos:exactMatch NCIT:C34971 Rat-Bite Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006948 retinal artery occlusion skos:exactMatch NCIT:C34978 Retinal Artery Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006951 retinal vein occlusion skos:exactMatch NCIT:C34981 Retinal Vein Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006952 retinopathy of prematurity skos:exactMatch NCIT:C34982 Retinopathy of Prematurity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006955 rheumatic heart disease skos:exactMatch NCIT:C34882 Rheumatic Heart Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006956 Rickettsiosis skos:exactMatch NCIT:C34991 Rickettsiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006962 sebaceous adenocarcinoma skos:exactMatch NCIT:C40310 Sebaceous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006963 sebaceous gland neoplasm skos:exactMatch NCIT:C3363 Sebaceous Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006964 secondary hyperparathyroidism skos:exactMatch NCIT:C113335 Secondary Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006966 secondary Parkinson disease skos:exactMatch NCIT:C34899 Secondary Parkinsonism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006969 sialadenitis skos:exactMatch NCIT:C115165 Sialitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006969 sialadenitis skos:exactMatch NCIT:C26882 Sialadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006973 skin appendage carcinoma skos:exactMatch NCIT:C3775 Adnexal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006974 small cell sarcoma skos:exactMatch NCIT:C3746 Small Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006975 smooth muscle tumor skos:exactMatch NCIT:C3751 Smooth Muscle Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006976 somatostatinoma skos:exactMatch NCIT:C3379 Somatostatin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006980 struma ovarii skos:exactMatch NCIT:C7468 Struma Ovarii semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006981 subacute bacterial endocarditis skos:exactMatch NCIT:C34583 Subacute Bacterial Endocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006982 subacute thyroiditis skos:exactMatch NCIT:C35071 Subacute Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006982 subacute thyroiditis skos:exactMatch NCIT:C35828 Subacute Granulomatous Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006983 subclavian steal syndrome skos:exactMatch NCIT:C35044 Subclavian Steal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006987 subvalvular aortic stenosis skos:exactMatch NCIT:C85172 Subvalvular Aortic Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006989 suppurative periapical periodontitis skos:exactMatch NCIT:C34913 Periapical Dental Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006994 tarsal tunnel syndrome skos:exactMatch NCIT:C85183 Tarsal Tunnel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006995 tethered spinal cord syndrome skos:exactMatch NCIT:C99080 Tethered Spinal Cord Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006996 thyroid crisis skos:exactMatch NCIT:C112836 Thyroid Storm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006998 tonsil cancer skos:exactMatch NCIT:C7404 Malignant Tonsillar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0006999 tooth disorder skos:exactMatch NCIT:C35077 Dental Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007000 Treponema infectious disease skos:exactMatch NCIT:C85197 Treponemal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007002 trochlear nerve disorder skos:exactMatch NCIT:C78395 Trochlear Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007004 type III hypersensitivity disease skos:exactMatch NCIT:C114346 Type III Hypersensitivity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007009 ureterolithiasis skos:exactMatch NCIT:C114696 Ureterolithiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007012 variant Creutzfeldt-Jakob disease skos:exactMatch NCIT:C128438 Variant Creutzfeldt-Jakob Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007015 viral meningitis skos:exactMatch NCIT:C118298 Viral Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007016 vitamin A deficiency skos:exactMatch NCIT:C85220 Vitamin A Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007017 vitreous detachment skos:exactMatch NCIT:C50807 Vitreous Detachment semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007019 vulvovaginitis skos:exactMatch NCIT:C35131 Vulvovaginitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007022 xanthogranulomatous pyelonephritis skos:exactMatch NCIT:C123038 Xanthogranulomatous Pyelonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007023 Yersinia infectious disease skos:exactMatch NCIT:C128337 Yersiniosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007027 metabolic dysfunction-associated steatohepatitis skos:exactMatch NCIT:C84445 Nonalcoholic Steatohepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007029 branchio-oto-renal syndrome skos:exactMatch NCIT:C98983 Melnick-Fraser Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007032 prune belly syndrome skos:exactMatch NCIT:C85033 Prune Belly Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007033 abducens nerve palsy skos:exactMatch NCIT:C27592 Cranial Nerve VI Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007035 acanthosis nigricans skos:exactMatch NCIT:C26687 Acanthosis Nigricans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007036 Achard syndrome skos:exactMatch NCIT:C35809 Achard Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007037 Achondroplasia skos:exactMatch NCIT:C34345 Achondroplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007039 neurofibromatosis type 2 skos:exactMatch NCIT:C3274 Neurofibromatosis Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007041 Apert syndrome skos:exactMatch NCIT:C99099 Type I Acrocephalosyndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007042 Saethre-Chotzen syndrome skos:exactMatch NCIT:C75034 Type III Acrocephalosyndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007043 Pfeiffer syndrome skos:exactMatch NCIT:C99100 Type V Acrocephalosyndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007044 Acrodysostosis 1 with or without hormone resistance skos:exactMatch NCIT:C136464 Acrodysostosis 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007048 acrokeratosis verruciformis skos:exactMatch NCIT:C27519 Acrokeratosis Verruciformis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007056 acroosteolysis skos:exactMatch NCIT:C35545 Acroosteolysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007057 Acroosteolysis dominant type skos:exactMatch NCIT:C84745 Hajdu-Cheney Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007064 severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency skos:exactMatch NCIT:C3962 Adenosine Deaminase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007070 adiposis dolorosa skos:exactMatch NCIT:C84540 Adiposis Dolorosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007074 ainhum skos:exactMatch NCIT:C84544 Ainhum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007078 pseudohypoparathyroidism type 1A skos:exactMatch NCIT:C129721 Albright Hereditary Osteodystrophy with Multiple Hormone Resistance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007079 alcohol dependence skos:exactMatch NCIT:C93040 Alcohol Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007100 familial amyloid neuropathy skos:exactMatch NCIT:C84554 Familial Amyloid Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007105 frontotemporal dementia and/or amyotrophic lateral sclerosis 1 skos:exactMatch NCIT:C168756 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007108 anal canal carcinoma skos:exactMatch NCIT:C7489 Anal Canal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007110 Diamond-Blackfan anemia 1 skos:exactMatch NCIT:C176911 Diamond-Blackfan Anemia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007113 Angelman syndrome skos:exactMatch NCIT:C75462 Angelman Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007125 ankyloglossia skos:exactMatch NCIT:C124538 Ankyloglossia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007127 diffuse idiopathic skeletal hyperostosis skos:exactMatch NCIT:C84671 Diffuse Idiopathic Skeletal Hyperostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007130 congenital total pulmonary venous return anomaly skos:exactMatch NCIT:C98585 Total Anomalous Pulmonary Venous Return semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007142 Townes-Brocks syndrome skos:exactMatch NCIT:C99085 Townes-Brocks Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007145 aplasia cutis congenita skos:exactMatch NCIT:C98822 Aplasia Cutis Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007147 obstructive sleep apnea syndrome skos:exactMatch NCIT:C27168 Obstructive Sleep Apnea Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007154 arteriovenous malformations of the brain skos:exactMatch NCIT:C2936 Cerebral Arteriovenous Malformation/Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007160 Stickler syndrome type 1 skos:exactMatch NCIT:C168733 Stickler Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007179 autoimmune disease skos:exactMatch NCIT:C2889 Autoimmune Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007182 Machado-Joseph disease skos:exactMatch NCIT:C84830 Spinocerebellar Ataxia Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007186 gastroesophageal reflux disease skos:exactMatch NCIT:C26781 Gastroesophageal Reflux Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007187 nevoid basal cell carcinoma syndrome skos:exactMatch NCIT:C2892 Nevoid Basal Cell Carcinoma Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007191 Behcet disease skos:exactMatch NCIT:C34416 Behcet Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007197 bladder diverticulum skos:exactMatch NCIT:C160155 Bladder Diverticulum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007203 blue rubber bleb nevus skos:exactMatch NCIT:C4486 Blue Rubber Bleb Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007205 diaphyseal medullary stenosis-bone malignancy syndrome skos:exactMatch NCIT:C122660 Hardcastle's Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007233 second branchial cleft anomaly skos:exactMatch NCIT:C104813 Branchial Cleft Remnant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007238 amastia skos:exactMatch NCIT:C118459 Amastia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007240 progressive familial heart block, type 1A skos:exactMatch NCIT:C126651 Progressive Familial Heart Block, Type Ia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007243 Burkitt lymphoma skos:exactMatch NCIT:C2912 Burkitt Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007244 Caffey disease skos:exactMatch NCIT:C118423 Infantile Cortical Hyperostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007251 campomelic dysplasia skos:exactMatch NCIT:C84609 Campomelic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007254 breast cancer skos:exactMatch NCIT:C9335 Malignant Breast Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007256 hepatocellular carcinoma skos:exactMatch NCIT:C3099 Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007263 cardiac rhythm disease skos:exactMatch NCIT:C2881 Arrhythmia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007266 hypertrophic cardiomyopathy 2 skos:exactMatch NCIT:C142892 Familial Hypertrophic Cardiomyopathy Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007268 hypertrophic cardiomyopathy 4 skos:exactMatch NCIT:C133725 Familial Hypertrophic Cardiomyopathy Type 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007275 carpal tunnel syndrome skos:exactMatch NCIT:C34450 Carpal Tunnel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007276 cat-eye syndrome skos:exactMatch NCIT:C75477 Cat-Eye Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007293 leukocyte adhesion deficiency 1 skos:exactMatch NCIT:C4689 Leukocyte Adhesion Deficiency Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007294 central core myopathy skos:exactMatch NCIT:C83010 Central Core Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007295 childhood epilepsy with centrotemporal spikes skos:exactMatch NCIT:C116538 Benign Rolandic Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007296 spinocerebellar ataxia type 31 skos:exactMatch NCIT:C176901 Spinocerebellar Ataxia Type 31 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007303 cervical rib disease skos:exactMatch NCIT:C158329 Cervical Rib semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007307 Charcot-Marie-Tooth disease type 1B skos:exactMatch NCIT:C118782 Charcot-Marie-Tooth Disease Type 1B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007308 Charcot-Marie-Tooth disease type 2A1 skos:exactMatch NCIT:C134952 Charcot-Marie-Tooth Disease Type 2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007308 Charcot-Marie-Tooth disease type 2A1 skos:exactMatch NCIT:C150609 Charcot-Marie-Tooth Disease Type 2A1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007309 Charcot-Marie-Tooth disease type 1A skos:exactMatch NCIT:C75468 Charcot-Marie-Tooth Disease Type 1A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007315 cherubism skos:exactMatch NCIT:C84630 Cherubism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007318 Alagille syndrome skos:exactMatch NCIT:C35139 Alagille Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007329 cirrhosis, familial skos:exactMatch NCIT:C84411 Cryptogenic Cirrhosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007335 orofacial cleft 1 skos:exactMatch NCIT:C124838 Orofacial Cleft 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007340 cleidocranial dysplasia 1 skos:exactMatch NCIT:C75020 Cleidocranial Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007342 clubfoot skos:exactMatch NCIT:C84641 Clubfoot semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007345 aorta coarctation skos:exactMatch NCIT:C84567 Aortic Coarctation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007352 renal coloboma syndrome skos:exactMatch NCIT:C123230 Renal Coloboma Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007356 Lynch syndrome 1 skos:exactMatch NCIT:C6725 Lynch 1 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007362 cone-rod dystrophy 2 skos:exactMatch NCIT:C162399 Cone-Rod Dystrophy 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007363 congenital contractural arachnodactyly skos:exactMatch NCIT:C129865 Congenital Contractural Arachnodactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007369 hereditary coproporphyria skos:exactMatch NCIT:C84759 Hereditary Coproporphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007379 Meesmann corneal dystrophy skos:exactMatch NCIT:C84795 Meesmann Corneal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007400 Jackson-Weiss syndrome skos:exactMatch NCIT:C123814 Jackson-Weiss Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007404 Cri-du-chat syndrome skos:exactMatch NCIT:C34518 Cri du Chat Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007405 Crouzon syndrome skos:exactMatch NCIT:C84653 Craniofacial Dysostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007412 Beare-Stevenson cutis gyrata syndrome skos:exactMatch NCIT:C123813 Beare-Stevenson Cutis Gyrata Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007416 Balkan nephropathy skos:exactMatch NCIT:C123025 Aristolochic Acid Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007417 Darier disease skos:exactMatch NCIT:C84665 Darier Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007435 dentatorubral-pallidoluysian atrophy skos:exactMatch NCIT:C122653 Dentatorubral-Pallidoluysian Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007446 dermatosis papulosa nigra skos:exactMatch NCIT:C2984 Dermatosis Papulosa Nigra semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007450 neurohypophyseal diabetes insipidus skos:exactMatch NCIT:C84933 Neurogenic Diabetes Insipidus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007452 maturity-onset diabetes of the young type 1 skos:exactMatch NCIT:C129744 Hepatocyte Nuclear Factor 4-Alpha Associated Monogenic Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007453 maturity-onset diabetes of the young type 2 skos:exactMatch NCIT:C129741 Glucokinase-Associated Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007473 Duane retraction syndrome skos:exactMatch NCIT:C84678 Duane Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007478 autosomal dominant Kenny-Caffey syndrome skos:exactMatch NCIT:C130993 Kenny-Caffey Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007481 Leri-Weill dyschondrosteosis skos:exactMatch NCIT:C126560 Leri-Weill Dyschondrosteosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007483 dyschromatosis symmetrica hereditaria skos:exactMatch NCIT:C118435 Dyschromatosis Symmetrica Hereditaria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007485 dyskeratosis congenita, autosomal dominant 1 skos:exactMatch NCIT:C176921 Dyskeratosis Congenita, Autosomal Dominant 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007486 hereditary benign intraepithelial dyskeratosis skos:exactMatch NCIT:C3940 Hereditary Benign Intraepithelial Dyskeratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007488 Lewy body dementia skos:exactMatch NCIT:C84826 Lewy Body Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007492 early-onset generalized limb-onset dystonia skos:exactMatch NCIT:C116718 Early Onset Primary Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007496 dystonia 12 skos:exactMatch NCIT:C157577 Dystonia 12 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007523 Ehlers-Danlos syndrome, hypermobility type skos:exactMatch NCIT:C125698 Ehlers-Danlos Syndrome, Type III semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007525 Ehlers-Danlos syndrome, arthrochalasia type skos:exactMatch NCIT:C125701 Ehlers-Danlos Syndrome, Type VII semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007534 Beckwith-Wiedemann syndrome skos:exactMatch NCIT:C34415 Beckwith-Wiedemann Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007536 congenital lobar emphysema skos:exactMatch NCIT:C98895 Congenital Lobar Emphysema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007540 multiple endocrine neoplasia type 1 skos:exactMatch NCIT:C3225 Multiple Endocrine Neoplasia Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007542 Camurati-Engelmann disease skos:exactMatch NCIT:C84610 Camurati-Engelmann Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007547 epidermoid cysts skos:exactMatch NCIT:C3134 Epidermal Inclusion Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007564 pilomatrixoma skos:exactMatch NCIT:C7368 Pilomatricoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007565 familial cylindromatosis skos:exactMatch NCIT:C43352 Turban Tumor Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007566 multiple self-healing squamous epithelioma skos:exactMatch NCIT:C4461 Multiple Self Healing Epithelioma of Ferguson-Smith semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007571 primary erythermalgia skos:exactMatch NCIT:C125383 Primary Erythromelalgia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007576 esophageal cancer skos:exactMatch NCIT:C7478 Malignant Esophageal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007586 exostoses, multiple, type 2 skos:exactMatch NCIT:C18252 EXT2 Gene semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007589 exudative vitreoretinopathy 1 skos:exactMatch NCIT:C175048 Exudative Vitreoretinopathy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007600 primary Fanconi syndrome skos:exactMatch NCIT:C123229 Primary Fanconi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007603 Felty syndrome skos:exactMatch NCIT:C84712 Felty Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007606 fibrodysplasia ossificans progressiva skos:exactMatch NCIT:C3040 Fibrodysplasia Ossificans Progressiva semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007608 desmoid tumor skos:exactMatch NCIT:C9182 Desmoid Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007621 Floating-Harbor syndrome skos:exactMatch NCIT:C175241 Floating-Harbor Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007631 chromosome 16p12.1 deletion syndrome, 520kb skos:exactMatch NCIT:C129875 Chromosome 16p12.1 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007635 Frasier syndrome skos:exactMatch NCIT:C122805 Frasier Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007636 frontorhiny skos:exactMatch NCIT:C129028 Frontonasal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007644 IgAD1 skos:exactMatch NCIT:C123434 Immunoglobulin A Deficiency 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007648 hereditary diffuse gastric adenocarcinoma skos:exactMatch NCIT:C43295 Hereditary Gastric Diffuse Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007650 MALT lymphoma skos:exactMatch NCIT:C3898 Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007652 gastric mucosal hypertrophy skos:exactMatch NCIT:C67277 Giant Hypertrophic Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007656 Gerstmann-Straussler-Scheinker syndrome skos:exactMatch NCIT:C84727 Gerstmann-Straussler-Scheinker Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007661 Tourette syndrome skos:exactMatch NCIT:C35078 Tourette Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007665 obsolete glaucoma 1, open angle, E skos:exactMatch NCIT:C35394 Primary Open Angle Glaucoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007667 subependymoma skos:exactMatch NCIT:C3795 Subependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007669 renal cysts and diabetes syndrome skos:exactMatch NCIT:C123018 Renal Cysts and Diabetes Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007672 glomuvenous malformation skos:exactMatch NCIT:C5350 Hereditary Glomangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007686 gray platelet syndrome skos:exactMatch NCIT:C84741 Gray Platelet Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007688 Myhre syndrome skos:exactMatch NCIT:C123815 Myhre Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007699 Hashimoto thyroiditis skos:exactMatch NCIT:C27191 Hashimoto Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007708 Kasabach-Merritt syndrome skos:exactMatch NCIT:C3821 Hemangiomatosis with Thrombocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007710 facial hemiatrophy skos:exactMatch NCIT:C116916 Progressive Hemifacial Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007721 hiatus hernia skos:exactMatch NCIT:C98945 Hiatal Hernia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007727 autosomal dominant familial periodic fever skos:exactMatch NCIT:C119051 Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007732 Holt-Oram syndrome skos:exactMatch NCIT:C125592 Holt-Oram Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007734 holoprosencephaly 4 skos:exactMatch NCIT:C75475 Holoprosencephaly Type 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007739 Huntington disease skos:exactMatch NCIT:C82342 Huntington's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007741 congenital hydronephrosis skos:exactMatch NCIT:C102979 Congenital Hydronephrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007743 attention deficit-hyperactivity disorder skos:exactMatch NCIT:C97160 Attention Deficit Hyperactivity Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007745 Gilbert syndrome skos:exactMatch NCIT:C84729 Gilbert Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007758 epidermolytic palmoplantar keratoderma, 1 skos:exactMatch NCIT:C84693 Epidermolytic Palmoplantar Keratoderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007766 Morgagni-Stewart-Morel syndrome skos:exactMatch NCIT:C84772 Hyperostosis Frontalis Interna semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007768 hyperparathyroidism 2 with jaw tumors skos:exactMatch NCIT:C48287 Hyperparathyroidism-Jaw Tumor Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007778 obsolete hypertelorism skos:exactMatch NCIT:C34715 Hypertelorism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007790 Charcot-Marie-Tooth disease type 3 skos:exactMatch NCIT:C133087 Dejerine-Sottas Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007793 hypochondroplasia skos:exactMatch NCIT:C118697 Hypochondroplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007797 hypoparathyroidism-deafness-renal disease syndrome skos:exactMatch NCIT:C130983 Barakat Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007800 chromosome 18p deletion syndrome skos:exactMatch NCIT:C84521 Deletion 18p Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007803 multiple system atrophy skos:exactMatch NCIT:C84909 Multiple System Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007804 Pallister-Hall syndrome skos:exactMatch NCIT:C84987 Pallister-Hall Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007813 superficial epidermolytic ichthyosis skos:exactMatch NCIT:C84777 Ichthyosis Bullosa of Siemens semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007817 IgE responsiveness, atopic skos:exactMatch NCIT:C3116 Type I Hypersensitivity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007818 hyper-IgE recurrent infection syndrome 1, autosomal dominant skos:exactMatch NCIT:C126342 STAT3 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007827 inclusion body myositis skos:exactMatch NCIT:C84786 Inclusion Body Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007834 islet cell adenomatosis skos:exactMatch NCIT:C4375 Nesidioblastosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007838 Jacobsen syndrome skos:exactMatch NCIT:C75457 Jacobsen Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007863 Kleine-Levin syndrome skos:exactMatch NCIT:C84800 Kleine-Levin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007864 angioosteohypertrophic syndrome skos:exactMatch NCIT:C84801 Klippel-Trenaunay-Weber Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007874 trichorhinophalangeal syndrome type II skos:exactMatch NCIT:C75118 Trichorhinophalangeal Syndrome Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007878 congenital laryngomalacia skos:exactMatch NCIT:C98971 Laryngomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007879 larynx atresia skos:exactMatch NCIT:C98972 Laryngeal Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007880 congenital laryngeal web skos:exactMatch NCIT:C98970 Laryngeal Web semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007885 Legg-Calve-Perthes disease skos:exactMatch NCIT:C34766 Perthes Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007886 uterine corpus leiomyoma skos:exactMatch NCIT:C3434 Uterine Corpus Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007888 hereditary leiomyomatosis and renal cell cancer skos:exactMatch NCIT:C51302 Hereditary Leiomyomatosis and Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007893 Noonan syndrome with multiple lentigines skos:exactMatch NCIT:C84820 LEOPARD Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007896 acute monocytic leukemia skos:exactMatch NCIT:C4861 Acute Monocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007899 lichen sclerosus et atrophicus skos:exactMatch NCIT:C26817 Lichen Sclerosus et Atrophicus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007908 multiple symmetric lipomatosis skos:exactMatch NCIT:C4392 Cervical Symmetrical Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007915 systemic lupus erythematosus skos:exactMatch NCIT:C3201 Systemic Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007921 yellow nail syndrome skos:exactMatch NCIT:C85238 Yellow Nail Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007922 lymphedema-distichiasis syndrome skos:exactMatch NCIT:C128191 Lymphedema-Distichiasis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007924 Bannayan-Riley-Ruvalcaba syndrome skos:exactMatch NCIT:C3939 Bannayan-Riley-Ruvalcaba Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007925 myelodysplastic syndrome associated with isolated del(5q) skos:exactMatch NCIT:C6867 Myelodysplastic Syndrome with del(5q) semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007928 obsolete Fechtner syndrome skos:exactMatch NCIT:C131642 Fechtner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007929 obsolete Epstein syndrome skos:exactMatch NCIT:C131639 Epstein Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007935 cystoid macular edema skos:exactMatch NCIT:C34794 Cystoid Macular Edema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007938 46,XY sex reversal 4 skos:exactMatch NCIT:C132270 46,XY Sex Reversal 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007947 Marfan syndrome skos:exactMatch NCIT:C34807 Marfan Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007949 Marshall syndrome skos:exactMatch NCIT:C128115 Marshall Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007950 mastocytosis skos:exactMatch NCIT:C84269 Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007955 Meckel diverticulum skos:exactMatch NCIT:C12264 Meckel Diverticulum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007959 medulloblastoma skos:exactMatch NCIT:C3222 Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007962 megalodactyly skos:exactMatch NCIT:C48900 Macrodactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007964 melanoma, cutaneous malignant, susceptibility to, 2 skos:exactMatch NCIT:C7584 Dysplastic Nevus Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007969 Melkersson-Rosenthal syndrome skos:exactMatch NCIT:C84886 Melkersson-Rosenthal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007970 melorheostosis skos:exactMatch NCIT:C84887 Melorheostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007972 Meniere disease skos:exactMatch NCIT:C185243 Meniere Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007974 intellectual disability, autosomal dominant 1 skos:exactMatch NCIT:C141424 Mental Retardation, Autosomal Dominant 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007982 metaphyseal chondrodysplasia, Jansen type skos:exactMatch NCIT:C131868 Metaphyseal Chondrodysplasia, Jansen Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007986 metatropic dysplasia skos:exactMatch NCIT:C175209 Metatropic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007987 Kniest dysplasia skos:exactMatch NCIT:C125594 Kniest Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0007999 holoprosencephaly 2 skos:exactMatch NCIT:C74995 Holoprosencephaly Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008005 cardiospondylocarpofacial syndrome skos:exactMatch NCIT:C188216 Cardiospondylocarpofacial Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008006 Mobius syndrome skos:exactMatch NCIT:C84893 Mobius Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008009 monilethrix skos:exactMatch NCIT:C84894 Monilethrix semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008018 Muir-Torre syndrome skos:exactMatch NCIT:C84905 Muir-Torre Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008019 mullerian aplasia and hyperandrogenism skos:exactMatch NCIT:C120376 Mullerian Aplasia and Hyperandrogenism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008029 Bethlem myopathy skos:exactMatch NCIT:C126688 Bethlem Myopathy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008030 facioscapulohumeral muscular dystrophy 1 skos:exactMatch NCIT:C172704 Facioscapulohumeral Muscular Dystrophy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008031 facioscapulohumeral muscular dystrophy 2 skos:exactMatch NCIT:C172705 Facioscapulohumeral Muscular Dystrophy 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008038 ataxia-pancytopenia syndrome skos:exactMatch NCIT:C176909 Ataxia-Pancytopenia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008040 transient myeloproliferative syndrome skos:exactMatch NCIT:C82339 Transient Abnormal Myelopoiesis Associated with Down Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008048 autosomal dominant centronuclear myopathy skos:exactMatch NCIT:C126689 Centronuclear Myopathy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008054 juvenile dermatomyositis skos:exactMatch NCIT:C27576 Childhood Dermatomyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008056 myotonic dystrophy type 1 skos:exactMatch NCIT:C84679 Dystrophia Myotonica 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008061 nail-patella syndrome skos:exactMatch NCIT:C75120 Nail-Patella Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008062 narcolepsy 1 skos:exactMatch NCIT:C84618 Cataplexy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008070 nemaline myopathy 3 skos:exactMatch NCIT:C129870 Nemaline Myopathy 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008073 familial juvenile hyperuricemic nephropathy type 1 skos:exactMatch NCIT:C123172 Medullary Cystic Kidney Disease Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008075 schwannomatosis skos:exactMatch NCIT:C6557 Schwannomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008082 multiple endocrine neoplasia type 2B skos:exactMatch NCIT:C3227 Multiple Endocrine Neoplasia Type 2B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008083 ceroid lipofuscinosis, neuronal, 4 (Kufs type) skos:exactMatch NCIT:C128116 Neuronal Ceroid Lipofuscinosis Type 4B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008090 cyclic hematopoiesis skos:exactMatch NCIT:C3820 Cyclic Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008093 nevus, epidermal skos:exactMatch NCIT:C4088 Epidermal Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008094 familial multiple nevi flammei skos:exactMatch NCIT:C3840 Port Wine Stain semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008095 nevus anemicus skos:exactMatch NCIT:C3943 Nevus Anemicus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008097 linear nevus sebaceous syndrome skos:exactMatch NCIT:C4678 Organoid Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008104 Noonan syndrome 1 skos:exactMatch NCIT:C75459 Noonan Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008109 ocular cicatricial pemphigoid skos:exactMatch NCIT:C84939 Ocular Cicatricial Pemphigoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008114 obsessive-compulsive disorder skos:exactMatch NCIT:C88411 Obsessive Compulsive Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008119 spinocerebellar ataxia type 1 skos:exactMatch NCIT:C129982 Spinocerebellar Ataxia Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008145 Ollier disease skos:exactMatch NCIT:C3008 Enchondromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008146 osteogenesis imperfecta type 1 skos:exactMatch NCIT:C99003 Osteogenesis Imperfecta Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008147 osteogenesis imperfecta type 2 skos:exactMatch NCIT:C99001 Osteogenesis Imperfecta Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008148 osteogenesis imperfecta type 4 skos:exactMatch NCIT:C98576 Osteogenesis Imperfecta Type IV semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008167 dermoid cyst of ovary skos:exactMatch NCIT:C3856 Ovarian Dermoid Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008168 ovarian fibroma skos:exactMatch NCIT:C3498 Ovarian Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008170 ovarian cancer skos:exactMatch NCIT:C7431 Malignant Ovarian Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008171 nephrolithiasis skos:exactMatch NCIT:C114667 Nephrolithiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008177 extramammary Paget disease skos:exactMatch NCIT:C3302 Extramammary Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008178 inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 skos:exactMatch NCIT:C122663 Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008179 paroxysmal extreme pain disorder skos:exactMatch NCIT:C125385 Paroxysmal Extreme Pain Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008183 annular pancreas skos:exactMatch NCIT:C98813 Annular Pancreas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008185 hereditary chronic pancreatitis skos:exactMatch NCIT:C95436 Hereditary Pancreatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008195 paramyotonia congenita of Von Eulenburg skos:exactMatch NCIT:C122790 Paramyotonia Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008214 Pelger-Huet anomaly skos:exactMatch NCIT:C85002 Pelger-Huet Anomaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008218 Hailey-Hailey disease skos:exactMatch NCIT:C82865 Familial Benign Pemphigus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008219 pemphigus vulgaris skos:exactMatch NCIT:C34910 Pemphigus Vulgaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008221 prolidase deficiency skos:exactMatch NCIT:C85029 Prolidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008222 Andersen-Tawil syndrome skos:exactMatch NCIT:C84559 Long QT Syndrome 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008223 hypokalemic periodic paralysis skos:exactMatch NCIT:C84775 Hypokalemic Periodic Paralysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008224 hyperkalemic periodic paralysis skos:exactMatch NCIT:C123429 Hyperkalemic Periodic Paralysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008225 normokalemic periodic paralysis skos:exactMatch NCIT:C122791 Normokalemic Periodic Paralysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008228 pernicious anemia skos:exactMatch NCIT:C2871 Pernicious Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008231 Peyronie disease skos:exactMatch NCIT:C3316 Penile Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008234 multiple endocrine neoplasia type 2A skos:exactMatch NCIT:C3226 Multiple Endocrine Neoplasia Type 2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008243 Pick disease skos:exactMatch NCIT:C85008 Pick's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008244 piebaldism skos:exactMatch NCIT:C85009 Piebaldism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008262 Poland syndrome skos:exactMatch NCIT:C85017 Poland Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008274 polyostotic fibrous dysplasia skos:exactMatch NCIT:C34610 Polyostotic Fibrous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008277 stomach polyp skos:exactMatch NCIT:C3954 Gastric Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008280 Peutz-Jeghers syndrome skos:exactMatch NCIT:C3324 Peutz-Jeghers Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008283 Cronkhite-Canada syndrome skos:exactMatch NCIT:C7035 Gastric Cronkhite Canada Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008287 Greig cephalopolysyndactyly syndrome skos:exactMatch NCIT:C35255 Greig Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008294 acute intermittent porphyria skos:exactMatch NCIT:C84536 Acute Intermittent Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008297 variegate porphyria skos:exactMatch NCIT:C85219 Variegate Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008300 Prader-Willi syndrome skos:exactMatch NCIT:C75463 Prader-Willi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008310 Hutchinson-Gilford progeria syndrome skos:exactMatch NCIT:C34951 Progeria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008315 prostate cancer skos:exactMatch NCIT:C7378 Malignant Prostate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008318 Proteus syndrome skos:exactMatch NCIT:C85032 Proteus Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008319 protoporphyria, erythropoietic, 1 skos:exactMatch NCIT:C84698 Erythropoietic Protoporphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008322 pseudoachondroplasia skos:exactMatch NCIT:C118635 Pseudoachondroplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008323 Liddle syndrome skos:exactMatch NCIT:C84827 Liddle Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008327 exfoliation syndrome skos:exactMatch NCIT:C129025 Exfoliation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008329 autosomal dominant pseudohypoaldosteronism type 1 skos:exactMatch NCIT:C126810 Hyponatremic Mineralocorticoid Resistance due to Mineralocorticoid Receptor Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008332 platelet-type von Willebrand disease skos:exactMatch NCIT:C131681 Platelet-Type von Willebrand Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008340 ptosis, hereditary congenital, 1 skos:exactMatch NCIT:C27049 Congenital Eyelid Ptosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008343 pulmonary atresia with ventricular septal defect skos:exactMatch NCIT:C99033 Pulmonary Valve Atresia with Ventricular Septal Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008364 Raynaud disease skos:exactMatch NCIT:C116359 Secondary Raynaud Phenomenon semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008375 retinal detachment skos:exactMatch NCIT:C26874 Retinal Detachment semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008380 retinoblastoma skos:exactMatch NCIT:C7541 Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008383 rheumatoid arthritis skos:exactMatch NCIT:C2884 Rheumatoid Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008386 Axenfeld-Rieger syndrome type 1 skos:exactMatch NCIT:C75015 Rieger Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008393 Rubinstein-Taybi syndrome due to CREBBP mutations skos:exactMatch NCIT:C153290 Rubinstein-Taybi Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008394 Silver-Russell syndrome skos:exactMatch NCIT:C85068 Russell-Silver Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008401 pleomorphic adenoma skos:exactMatch NCIT:C8602 Pleomorphic Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008410 Scheuermann disease skos:exactMatch NCIT:C34999 Juvenile Osteochondrosis of Spine semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008420 seborrheic keratosis skos:exactMatch NCIT:C9006 Seborrheic Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008426 Shprintzen-Goldberg syndrome skos:exactMatch NCIT:C124840 Shprintzen-Goldberg Craniosynostosis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008428 septooptic dysplasia skos:exactMatch NCIT:C85063 Septo-Optic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008433 small cell lung carcinoma skos:exactMatch NCIT:C4917 Lung Small Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008434 Smith-Magenis syndrome skos:exactMatch NCIT:C75469 Smith-Magenis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008437 hereditary spastic paraplegia 3A skos:exactMatch NCIT:C142893 Spastic Paraplegia 3A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008438 hereditary spastic paraplegia 4 skos:exactMatch NCIT:C129981 Spastic Paraplegia 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008449 spina bifida skos:exactMatch NCIT:C101214 Spina Bifida semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008450 spinal arachnoiditis skos:exactMatch NCIT:C50749 Spinal Arachnoiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008451 neuronopathy, distal hereditary motor, autosomal dominant 1 skos:exactMatch NCIT:C132826 Distal Hereditary Motor Neuronopathy Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008457 spinocerebellar ataxia type 6 skos:exactMatch NCIT:C142838 Spinocerebellar Ataxia Type 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008458 spinocerebellar ataxia type 2 skos:exactMatch NCIT:C148315 Spinocerebellar Ataxia Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008464 split hand-foot malformation 1 skos:exactMatch NCIT:C75045 Split-Hand/Foot Malformation Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008475 spondylolisthesis skos:exactMatch NCIT:C35033 Spondylolisthesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008487 polycystic ovary syndrome skos:exactMatch NCIT:C26862 Polycystic Ovary Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008491 stiff-person syndrome skos:exactMatch NCIT:C85170 Stiff Person Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008492 stiff skin syndrome skos:exactMatch NCIT:C118636 Stiff Skin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008501 Sturge-Weber syndrome skos:exactMatch NCIT:C3391 Sturge-Weber Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008504 supravalvular aortic stenosis skos:exactMatch NCIT:C85176 Supravalvular Aortic Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008523 Blau syndrome skos:exactMatch NCIT:C116794 Blau Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008538 temporal arteritis skos:exactMatch NCIT:C35065 Temporal Arteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008541 spermatic cord torsion skos:exactMatch NCIT:C26885 Testicular Torsion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008542 tetralogy of fallot skos:exactMatch NCIT:C84505 Tetralogy of Fallot semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008546 thanatophoric dysplasia type 1 skos:exactMatch NCIT:C98583 Type 1 Thanatophoric Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008547 thanatophoric dysplasia type 2 skos:exactMatch NCIT:C98584 Type 2 Thanatophoric Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008553 platelet-type bleeding disorder 17 skos:exactMatch NCIT:C142084 Bleeding Disorder, Platelet-Type 17 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008555 thrombocytopenia 2 skos:exactMatch NCIT:C129035 Thrombocytopenia 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008558 autoimmune thrombocytopenic purpura skos:exactMatch NCIT:C3446 Primary Immune Thrombocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008564 DiGeorge syndrome skos:exactMatch NCIT:C2989 22q11.2 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008575 nicotine dependence skos:exactMatch NCIT:C54203 Nicotine Dependence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008582 tooth and nail syndrome skos:exactMatch NCIT:C40553 Tooth and Nail Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008583 inherited torticollis skos:exactMatch NCIT:C4811 Fibromatosis Colli semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008585 HELLP syndrome skos:exactMatch NCIT:C84750 HELLP Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008596 trichorhinophalangeal syndrome type I skos:exactMatch NCIT:C75109 Trichorhinophalangeal Syndrome Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008608 Down syndrome skos:exactMatch NCIT:C2993 Down Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008612 tuberous sclerosis 1 skos:exactMatch NCIT:C75122 Tuberous Sclerosis 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008627 ureter cancer skos:exactMatch NCIT:C7543 Malignant Ureter Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008628 ureterocele skos:exactMatch NCIT:C123159 Ureterocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008633 Muckle-Wells syndrome skos:exactMatch NCIT:C119054 Muckle-Wells Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008638 varicose disease skos:exactMatch NCIT:C35114 Varicose Vein semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008642 VACTERL/vater association skos:exactMatch NCIT:C99105 VACTERL Association semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008661 vitiligo skos:exactMatch NCIT:C26915 Vitiligo semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008666 volvulus of midgut skos:exactMatch NCIT:C98961 Intestinal Malrotation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008667 von Hippel-Lindau disease skos:exactMatch NCIT:C3105 Von Hippel Lindau Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008668 von Willebrand disease 1 skos:exactMatch NCIT:C131685 von Willebrand Disease, Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008670 Waardenburg syndrome type 1 skos:exactMatch NCIT:C75008 Waardenburg Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008671 Waardenburg syndrome type 2A skos:exactMatch NCIT:C75011 Waardenburg Syndrome Type 2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008675 Freeman-Sheldon syndrome skos:exactMatch NCIT:C98931 Freeman-Sheldon Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008678 Williams syndrome skos:exactMatch NCIT:C85232 Williams Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008681 WAGR syndrome skos:exactMatch NCIT:C3718 WAGR Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008682 Denys-Drash syndrome skos:exactMatch NCIT:C84668 Denys-Drash Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008684 Wolf-Hirschhorn syndrome skos:exactMatch NCIT:C35528 Wolf-Hirschhorn Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008685 Wolff-Parkinson-White syndrome skos:exactMatch NCIT:C35132 Wolff-Parkinson-White Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008692 abetalipoproteinemia skos:exactMatch NCIT:C84525 Abetalipoproteinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008703 acromesomelic dysplasia 2A skos:exactMatch NCIT:C3816 Type II Achondrogenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008708 acrocallosal syndrome skos:exactMatch NCIT:C84531 Acrocallosal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008713 acrodermatitis enteropathica skos:exactMatch NCIT:C128802 Acrodermatitis Enteropathica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008721 medium chain acyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C84538 Medium-Chain Acyl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008722 short chain acyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C84539 Acyl-CoA Dehydrogenase, Short-Chain Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008723 very long chain acyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C98647 Very Long-Chain Acyl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008726 Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis skos:exactMatch NCIT:C178415 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008727 congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency skos:exactMatch NCIT:C131088 3-Beta-Hydroxysteroid Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008728 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency skos:exactMatch NCIT:C131087 21-Hydroxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008729 congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency skos:exactMatch NCIT:C131085 11-Beta-Hydroxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008733 familial glucocorticoid deficiency skos:exactMatch NCIT:C120446 Isolated Glucocorticoid Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008736 peroxisome biogenesis disorder 2B skos:exactMatch NCIT:C155751 Peroxisome Biogenesis Disorder 2B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008737 congenital afibrinogenemia skos:exactMatch NCIT:C98130 Afibrinogenemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008738 aganglionosis, total intestinal skos:exactMatch NCIT:C101074 Total Intestinal Aganglionosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008740 agnathia-otocephaly complex skos:exactMatch NCIT:C124568 Otocephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008742 autosomal dominant severe congenital neutropenia skos:exactMatch NCIT:C166155 Autosomal Dominant Severe Congenital Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008745 oculocutaneous albinism type 1A skos:exactMatch NCIT:C168731 Oculocutaneous Albinism Type 1A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008748 Hermansky-Pudlak syndrome 1 skos:exactMatch NCIT:C150367 Hermansky-Pudlak Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008752 Alexander disease skos:exactMatch NCIT:C84545 Alexander Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008753 alkaptonuria skos:exactMatch NCIT:C84546 Alkaptonuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008758 mitochondrial DNA depletion syndrome 4a skos:exactMatch NCIT:C35257 Alper Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008760 beta-ketothiolase deficiency skos:exactMatch NCIT:C98841 Alpha-Methylacetoacetic Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008763 Alstrom syndrome skos:exactMatch NCIT:C84549 Alstrom Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008767 neuronal ceroid lipofuscinosis 3 skos:exactMatch NCIT:C61258 Neuronal Ceroid Lipofuscinosis Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008769 neuronal ceroid lipofuscinosis 2 skos:exactMatch NCIT:C85864 Neuronal Ceroid Lipofuscinosis Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008777 gelatinous drop-like corneal dystrophy skos:exactMatch NCIT:C142805 Gelatinous Drop-Like Corneal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008779 arthrogryposis skos:exactMatch NCIT:C84572 Arthrogryposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008783 Tangier disease skos:exactMatch NCIT:C85182 Tangier Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008813 arachnoid cyst skos:exactMatch NCIT:C3455 Arachnoid Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008814 hyperargininemia skos:exactMatch NCIT:C84568 Argininemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008815 argininosuccinic aciduria skos:exactMatch NCIT:C84569 Argininosuccinic Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008817 arterial calcification, generalized, of infancy, 1 skos:exactMatch NCIT:C128805 Generalized Arterial Calcification of Infancy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008824 fetal akinesia deformation sequence skos:exactMatch NCIT:C129071 Fetal Akinesia Deformation Sequence semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008829 chylous ascites skos:exactMatch NCIT:C34482 Chylous Peritoneal Effusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008830 aspartylglucosaminuria skos:exactMatch NCIT:C61273 Aspartylglycosaminuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008840 ataxia telangiectasia skos:exactMatch NCIT:C2887 Ataxia Telangiectasia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008846 atransferrinemia skos:exactMatch NCIT:C125693 Atransferrinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008855 MHC class II deficiency skos:exactMatch NCIT:C176823 MHC Class II Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008855 MHC class II deficiency skos:exactMatch NCIT:C3895 Bare Lymphocyte Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008856 immunodeficiency 27A skos:exactMatch NCIT:C176806 Immunodeficiency 27A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008858 Behr syndrome skos:exactMatch NCIT:C177251 Behr Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008863 sitosterolemia skos:exactMatch NCIT:C125694 Sitosterolemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008865 Bietti crystalline corneoretinal dystrophy skos:exactMatch NCIT:C179299 Bietti Crystalline Corneoretinal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008867 biliary atresia skos:exactMatch NCIT:C34421 Biliary Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008876 Bloom syndrome skos:exactMatch NCIT:C2903 Bloom Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008889 thromboangiitis obliterans skos:exactMatch NCIT:C35070 Buerger Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008890 progressive bulbar palsy skos:exactMatch NCIT:C85026 Progressive Bulbar Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008903 lung cancer skos:exactMatch NCIT:C7377 Malignant Lung Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008907 PMM2-congenital disorder of glycosylation skos:exactMatch NCIT:C126868 Congenital Disorder of Glycosylation Type Ia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008910 carboxypeptidase N deficiency skos:exactMatch NCIT:C132196 Carboxypeptidase N Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008915 dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome skos:exactMatch NCIT:C174217 Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008918 carnitine-acylcarnitine translocase deficiency skos:exactMatch NCIT:C133086 Carnitine-Acylcarnitine Translocase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008919 systemic primary carnitine deficiency disease skos:exactMatch NCIT:C98864 Primary Carnitine Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008921 carnosinemia skos:exactMatch NCIT:C125661 Carnosinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008926 COFS syndrome skos:exactMatch NCIT:C3817 Cerebrooculofacioskeletal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008939 isolated cerebellar hypoplasia/agenesis skos:exactMatch NCIT:C98890 Congenital Cerebellar Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008948 cerebrotendinous xanthomatosis skos:exactMatch NCIT:C84628 Cerebrotendinous Xanthomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008955 cerebrooculofacioskeletal syndrome 1 skos:exactMatch NCIT:C173085 Cerebrooculofacioskeletal Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008963 Chediak-Higashi syndrome skos:exactMatch NCIT:C2941 Chediak-Higashi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008965 CHARGE syndrome skos:exactMatch NCIT:C75100 CHARGE Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008966 Aagenaes syndrome skos:exactMatch NCIT:C35709 Aagenaes Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008970 chondrodysplasia Blomstrand type skos:exactMatch NCIT:C131420 Blomstrand Type Chondrodysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008977 chondrosarcoma skos:exactMatch NCIT:C2946 Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008978 chordoma skos:exactMatch NCIT:C2947 Chordoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0008988 citrullinemia type I skos:exactMatch NCIT:C150601 Citrullinemia Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009003 achromatopsia 2 skos:exactMatch NCIT:C168757 Achromatopsia 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009005 complement component C1r/C1s deficiency skos:exactMatch NCIT:C119991 C1r/C1s Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009006 complement component 2 deficiency skos:exactMatch NCIT:C119992 C2 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009016 band keratopathy skos:exactMatch NCIT:C118765 Band Keratopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009020 macular corneal dystrophy skos:exactMatch NCIT:C34793 Macular Corneal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009022 corpus callosum, agenesis of skos:exactMatch NCIT:C98905 Corpus Callosum Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009025 apparent mineralocorticoid excess skos:exactMatch NCIT:C123231 Syndrome of Apparent Mineralocorticoid Excess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009025 apparent mineralocorticoid excess skos:exactMatch NCIT:C131083 11 Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009026 Costello syndrome skos:exactMatch NCIT:C84652 Costello Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009031 craniodiaphyseal dysplasia skos:exactMatch NCIT:C131429 Craniodiaphyseal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009032 cranioectodermal dysplasia skos:exactMatch NCIT:C129305 Cranioectodermal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009033 temtamy syndrome skos:exactMatch NCIT:C148371 Temtamy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009044 Crigler-Najjar syndrome skos:exactMatch NCIT:C84656 Crigler-Najjar Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009046 Fraser syndrome skos:exactMatch NCIT:C118436 Fraser Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009047 cryptorchidism skos:exactMatch NCIT:C12326 Undescended Testes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009050 Cushing disease due to pituitary adenoma skos:exactMatch NCIT:C113210 Cushing Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009058 cystathioninuria skos:exactMatch NCIT:C129070 Cystathioninuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009061 cystic fibrosis skos:exactMatch NCIT:C2975 Cystic Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009067 cystinuria skos:exactMatch NCIT:C84664 Cystinuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009068 cytochrome-c oxidase deficiency disease skos:exactMatch NCIT:C98910 Cytochrome-C Oxidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009070 D-glyceric aciduria skos:exactMatch NCIT:C128804 D-Glyceric Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009072 Dandy-Walker syndrome skos:exactMatch NCIT:C75012 Dandy-Walker Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009076 autosomal recessive nonsyndromic hearing loss 1A skos:exactMatch NCIT:C129022 Deafness, Autosomal Recessive 1A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009106 diastematomyelia skos:exactMatch NCIT:C98913 Diastematomyelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009107 diastrophic dysplasia skos:exactMatch NCIT:C156311 Diastrophic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009109 lysinuric protein intolerance skos:exactMatch NCIT:C121563 Lysinuric Protein Intolerance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009113 hemolytic anemia due to diphosphoglycerate mutase deficiency skos:exactMatch NCIT:C131638 Bisphosphoglycerate Mutase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009114 congenital sucrase-isomaltase deficiency skos:exactMatch NCIT:C128190 Congenital Sucrase-Isomaltase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009124 Dubowitz syndrome skos:exactMatch NCIT:C125591 Dubowitz Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009126 duodenal atresia skos:exactMatch NCIT:C101025 Duodenal Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009130 Dyggve-Melchior-Clausen disease skos:exactMatch NCIT:C124844 Dyggve-Melchior-Clausen Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009131 Riley-Day syndrome skos:exactMatch NCIT:C84706 Familial Dysautonomia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009133 cerebellar ataxia, intellectual disability, and dysequilibrium skos:exactMatch NCIT:C114781 Dialysis Disequilibrium Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009136 dyskeratosis congenita, autosomal recessive 1 skos:exactMatch NCIT:C176925 Dyskeratosis Congenita, Autosomal Recessive 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009141 torsion dystonia 2 skos:exactMatch NCIT:C123415 Autosomal Recessive Torsion Dystonia 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009144 Ebstein anomaly skos:exactMatch NCIT:C84681 Ebstein Anomaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009151 cleft lip/palate-ectodermal dysplasia syndrome skos:exactMatch NCIT:C122656 Cleft Lip/Palate-Ectodermal Dysplasia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009162 Ellis-van Creveld syndrome skos:exactMatch NCIT:C84684 Ellis-Van Creveld Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009165 Aicardi-Goutieres syndrome 1 skos:exactMatch NCIT:C165501 Aicardi-Goutieres Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009169 endocardial fibroelastosis skos:exactMatch NCIT:C98922 Endocardial Fibroelastosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009172 enterocolitis skos:exactMatch NCIT:C79573 Enterocolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009175 eosinophilic fasciitis skos:exactMatch NCIT:C112116 Eosinophilic Fasciitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009176 epidermodysplasia verruciformis skos:exactMatch NCIT:C126877 Epidermodysplasia Verruciformis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009192 Wolcott-Rallison syndrome skos:exactMatch NCIT:C131007 Wolcott-Rallison Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009197 transient erythroblastopenia of childhood skos:exactMatch NCIT:C131683 Transient Erythroblastopenia of Childhood semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009210 congenital factor V deficiency skos:exactMatch NCIT:C98938 Hereditary Factor V Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009211 congenital factor VII deficiency skos:exactMatch NCIT:C131631 Factor VII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009212 congenital factor X deficiency skos:exactMatch NCIT:C98940 Hereditary Factor X Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009213 Fanconi anemia complementation group C skos:exactMatch NCIT:C125704 Fanconi Anemia, Complementation Group C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009214 Fanconi anemia complementation group D2 skos:exactMatch NCIT:C125706 Fanconi Anemia, Complementation Group D2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009215 Fanconi anemia complementation group A skos:exactMatch NCIT:C125702 Fanconi Anemia, Complementation Group A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009218 Farber lipogranulomatosis skos:exactMatch NCIT:C84710 Farber Lipogranulomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009234 congenital high-molecular-weight kininogen deficiency skos:exactMatch NCIT:C98946 High Molecular Weight Kininogen Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009237 focal epithelial hyperplasia skos:exactMatch NCIT:C97083 Focal Epithelial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009238 hereditary folate malabsorption skos:exactMatch NCIT:C156424 Hereditary Folate Malabsorption semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009249 hereditary fructose intolerance skos:exactMatch NCIT:C84720 Hereditary Fructose Intolerance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009251 fructose-1,6-bisphosphatase deficiency skos:exactMatch NCIT:C128119 Fructose-1,6-Bisphosphatase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009253 Fryns syndrome skos:exactMatch NCIT:C98932 Fryns Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009254 fucosidosis skos:exactMatch NCIT:C61274 Fucosidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009255 galactokinase deficiency skos:exactMatch NCIT:C114767 Galactokinase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009256 galactorrhea skos:exactMatch NCIT:C113343 Galactorrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009264 gastroschisis skos:exactMatch NCIT:C84725 Gastroschisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009275 neonatal hemochromatosis skos:exactMatch NCIT:C129980 Neonatal Hemochromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009276 Bernard-Soulier syndrome skos:exactMatch NCIT:C84595 Bernard-Soulier Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009277 glaucoma 3A skos:exactMatch NCIT:C148260 Primary Congenital Glaucoma 3A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009281 glutaryl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C99101 Glutaric Acidemia Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009282 multiple acyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C84907 Multiple Acyl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009288 glycogen storage disease Ib skos:exactMatch NCIT:C122661 Glycogen Storage Disease Type Ib semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009290 glycogen storage disease II skos:exactMatch NCIT:C84734 Glycogen Storage Disease Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009291 glycogen storage disease III skos:exactMatch NCIT:C84736 Glycogen Storage Disease Type III semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009292 glycogen storage disease due to glycogen branching enzyme deficiency skos:exactMatch NCIT:C84737 Glycogen Storage Disease Type IV semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009293 glycogen storage disease V skos:exactMatch NCIT:C84738 Glycogen Storage Disease Type V semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009294 glycogen storage disease VI skos:exactMatch NCIT:C126875 Glycogen Storage Disease Type VI semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009295 glycogen storage disease VII skos:exactMatch NCIT:C118437 Glycogen Storage Disease Type VII semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009299 46 XX gonadal dysgenesis skos:exactMatch NCIT:C120197 46,XX Gonadal Dysgenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009303 anti-glomerular basement membrane disease skos:exactMatch NCIT:C84566 Anti-Glomerular Basement Membrane Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009315 congenital factor XII deficiency skos:exactMatch NCIT:C131740 Factor XII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009318 Hallermann-Streiff syndrome skos:exactMatch NCIT:C84746 Hallermann Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009319 pantothenate kinase-associated neurodegeneration skos:exactMatch NCIT:C84988 Pantothenate Kinase-Associated Neurodegeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009324 Hartnup disease skos:exactMatch NCIT:C84748 Hartnup Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009330 hemangiopericytoma, malignant skos:exactMatch NCIT:C4301 Malignant Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009332 congenital hematological disorder skos:exactMatch NCIT:C104003 Congenital Hematological Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009341 Mowat-Wilson syndrome skos:exactMatch NCIT:C74999 Mowat-Wilson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009348 classic Hodgkin lymphoma skos:exactMatch NCIT:C7164 Classic Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009349 holoprosencephaly 1 skos:exactMatch NCIT:C75476 Holoprosencephaly Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009354 methylcobalamin deficiency type cblE skos:exactMatch NCIT:C142173 Homocystinuria-Megaloblastic Anemia, cblE Complementation Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009364 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 skos:exactMatch NCIT:C128118 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009369 non-immune hydrops fetalis skos:exactMatch NCIT:C111905 Non-Immune Hydrops Fetalis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009376 carbamoyl phosphate synthetase I deficiency disease skos:exactMatch NCIT:C84612 Carbamoyl-Phosphate Synthetase I Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009377 hyperammonemia due to N-acetylglutamate synthase deficiency skos:exactMatch NCIT:C129307 N-Acetylglutamate Synthase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009380 Dubin-Johnson syndrome skos:exactMatch NCIT:C34741 Dubin-Johnson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009387 familial lipoprotein lipase deficiency skos:exactMatch NCIT:C84771 Hyperlipoproteinemia, Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009388 hyperlysinemia skos:exactMatch NCIT:C123433 Hyperlysinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009393 ornithine translocase deficiency skos:exactMatch NCIT:C129029 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009394 juvenile Paget disease skos:exactMatch NCIT:C131861 Juvenile Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009395 hyperostosis corticalis generalisata skos:exactMatch NCIT:C131812 Endosteal Hyperostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009397 neonatal severe primary hyperparathyroidism skos:exactMatch NCIT:C131853 Neonatal Severe Primary Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009411 autoimmune polyendocrine syndrome type 1 skos:exactMatch NCIT:C129727 Autoimmune Polyglandular Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009412 scurvy skos:exactMatch NCIT:C35010 Vitamin C Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009426 hypoparathyroidism-retardation-dysmorphism syndrome skos:exactMatch NCIT:C133727 Hypoparathyroidism-Retardation-Dysmorphism Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009431 hereditary hypophosphatemic rickets with hypercalciuria skos:exactMatch NCIT:C131450 Hereditary Hypophosphatemic Rickets with Hypercalciuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009436 congenital hypothalamic hamartoma syndrome skos:exactMatch NCIT:C4385 Hypothalamic Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009439 autosomal recessive congenital ichthyosis 2 skos:exactMatch NCIT:C132827 Autosomal Recessive Congenital Ichthyosis 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009443 autosomal recessive congenital ichthyosis 4B skos:exactMatch NCIT:C98934 Harlequin Ichthyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009452 Vici syndrome skos:exactMatch NCIT:C138174 Vici Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009454 immunodeficiency-centromeric instability-facial anomalies syndrome 1 skos:exactMatch NCIT:C156430 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009458 Schimke immuno-osseous dysplasia skos:exactMatch NCIT:C135087 Schimke Immunoosseous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009468 pseudotumor cerebri skos:exactMatch NCIT:C85035 Pseudotumor Cerebri semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009475 isovaleric acidemia skos:exactMatch NCIT:C98964 Isovaleric Acidemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009476 atresia of small intestine skos:exactMatch NCIT:C98828 Small Intestine Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009478 combined immunodeficiency due to DOCK8 deficiency skos:exactMatch NCIT:C126343 DOCK8 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009484 primary ciliary dyskinesia 1 skos:exactMatch NCIT:C128117 Primary Ciliary Dyskinesia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009486 autosomal recessive Kenny-Caffey syndrome skos:exactMatch NCIT:C130992 Kenny-Caffey Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009490 Papillon-Lefevre disease skos:exactMatch NCIT:C84992 Papillon-Lefevre Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009499 Krabbe disease skos:exactMatch NCIT:C61254 Krabbe Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009509 Landau-Kleffner syndrome skos:exactMatch NCIT:C84806 Landau-Kleffner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009514 Laurence-Moon syndrome skos:exactMatch NCIT:C34760 Laurence-Moon Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009515 Norum disease skos:exactMatch NCIT:C84813 Lecithin Acyltransferase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009517 Donohue syndrome skos:exactMatch NCIT:C84676 Donohue Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009519 letterer-Siwe disease skos:exactMatch NCIT:C3160 Letterer-Siwe Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009520 3-hydroxy-3-methylglutaric aciduria skos:exactMatch NCIT:C84523 HMG-CoA Lyase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009525 split hand-foot malformation 3 skos:exactMatch NCIT:C75121 Split-Hand/Foot Malformation Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009527 lipase deficiency, combined skos:exactMatch NCIT:C126558 Combined Lipase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009530 lipoid proteinosis skos:exactMatch NCIT:C84829 Lipoid Proteinosis of Urbach and Wiethe semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009532 Miller-Dieker lissencephaly syndrome skos:exactMatch NCIT:C124852 Miller-Dieker Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009537 lymphoid interstitial pneumonia skos:exactMatch NCIT:C27558 Lymphocytic Interstitial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009557 mandibuloacral dysplasia with type A lipodystrophy skos:exactMatch NCIT:C123417 Mandibuloacral Dysplasia with Type A Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009561 alpha-mannosidosis skos:exactMatch NCIT:C84548 Alpha-Mannosidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009562 beta-mannosidosis skos:exactMatch NCIT:C84596 Beta-Mannosidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009563 maple syrup urine disease skos:exactMatch NCIT:C34806 Maple Syrup Urine Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009588 Langer mesomelic dysplasia skos:exactMatch NCIT:C126876 Langer Mesomelic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009595 cartilage-hair hypoplasia skos:exactMatch NCIT:C61245 Cartilage Hair Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009607 methionine adenosyltransferase deficiency skos:exactMatch NCIT:C123435 Methionine Adenosyltransferase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009610 3-methylglutaconic aciduria type 1 skos:exactMatch NCIT:C98683 3-Methylglutaconic Aciduria Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009612 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency skos:exactMatch NCIT:C148366 Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009613 methylmalonic aciduria, cblA type skos:exactMatch NCIT:C142171 Methylmalonic Aciduria, cblA Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009614 methylmalonic aciduria, cblB type skos:exactMatch NCIT:C142172 Methylmalonic Aciduria, cblB Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009623 Nijmegen breakage syndrome skos:exactMatch NCIT:C4692 Nijmegen Breakage Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009624 microcephaly and chorioretinopathy 1 skos:exactMatch NCIT:C129306 Microcephaly and Chorioretinopathy, Autosomal Recessive, Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009627 Galloway-Mowat syndrome skos:exactMatch NCIT:C132195 Galloway-Mowat Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009628 obsolete microcolon skos:exactMatch NCIT:C98987 Microcolon semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009637 inborn mitochondrial myopathy skos:exactMatch NCIT:C101328 Mitochondrial Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009646 monosomy 7 myelodysplasia and leukemia syndrome 1 skos:exactMatch NCIT:C176908 Monosomy 7 Myelodysplasia and Leukemia Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009650 mucolipidosis type II skos:exactMatch NCIT:C61270 I-Cell Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009652 GNPTG-mucolipidosis skos:exactMatch NCIT:C129978 Mucolipidosis Type III Gamma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009653 mucolipidosis type IV skos:exactMatch NCIT:C84896 Mucolipidosis Type IV semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009655 mucopolysaccharidosis type 3A skos:exactMatch NCIT:C84897 Mucopolysaccharidosis Type IIIA semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009656 mucopolysaccharidosis type 3B skos:exactMatch NCIT:C84898 Mucopolysaccharidosis Type IIIB semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009657 mucopolysaccharidosis type 3C skos:exactMatch NCIT:C84899 Mucopolysaccharidosis Type IIIC semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009658 mucopolysaccharidosis type 3D skos:exactMatch NCIT:C84900 Mucopolysaccharidosis Type IIID semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009659 mucopolysaccharidosis type 4A skos:exactMatch NCIT:C84901 Mucopolysaccharidosis Type IVA semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009660 mucopolysaccharidosis type 4B skos:exactMatch NCIT:C84902 Mucopolysaccharidosis Type IVB semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009661 mucopolysaccharidosis type 6 skos:exactMatch NCIT:C61264 Maroteaux-Lamy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009662 mucopolysaccharidosis type 7 skos:exactMatch NCIT:C84903 Sly Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009664 mulibrey nanism skos:exactMatch NCIT:C84906 Mulibrey Nanism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009665 biotinidase deficiency skos:exactMatch NCIT:C84598 Biotinidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009666 holocarboxylase synthetase deficiency skos:exactMatch NCIT:C98842 Holocarboxylase Synthetase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009667 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 skos:exactMatch NCIT:C126740 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009668 lethal multiple pterygium syndrome skos:exactMatch NCIT:C101038 Lethal Multiple Pterygium Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009669 spinal muscular atrophy, type 1 skos:exactMatch NCIT:C98670 Werdnig-Hoffmann Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009672 spinal muscular atrophy, type III skos:exactMatch NCIT:C118847 Spinal Muscular Atrophy Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009675 autosomal recessive limb-girdle muscular dystrophy type 2A skos:exactMatch NCIT:C142079 Limb-Girdle Muscular Dystrophy Type 2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009676 autosomal recessive limb-girdle muscular dystrophy type 2B skos:exactMatch NCIT:C142080 Limb-Girdle Muscular Dystrophy Type 2B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009678 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 skos:exactMatch NCIT:C126741 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009685 Miyoshi myopathy skos:exactMatch NCIT:C118846 Miyoshi Muscular Dystrophy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009688 myasthenia gravis skos:exactMatch NCIT:C60989 Myasthenia Gravis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009689 congenital myasthenic syndrome 6 skos:exactMatch NCIT:C132292 Presynaptic Congenital Myasthenic Syndrome 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009691 mycosis fungoides skos:exactMatch NCIT:C3246 Mycosis Fungoides semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009692 primary myelofibrosis skos:exactMatch NCIT:C2862 Primary Myelofibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009693 plasma cell myeloma skos:exactMatch NCIT:C3242 Multiple Myeloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009696 juvenile myoclonic epilepsy skos:exactMatch NCIT:C84796 Juvenile Myoclonic Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009697 Lafora disease skos:exactMatch NCIT:C84804 Lafora Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009705 carnitine palmitoyl transferase 1A deficiency skos:exactMatch NCIT:C98871 Carnitine Palmitoyltransferase I Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009710 Thomsen and Becker disease skos:exactMatch NCIT:C84912 Myotonia Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009711 congenital fiber-type disproportion myopathy skos:exactMatch NCIT:C120046 Congenital Fiber-Type Disproportion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009712 congenital multicore myopathy with external ophthalmoplegia skos:exactMatch NCIT:C150608 Minicore Myopathy with External Ophthalmoplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009717 Schwartz-Jampel syndrome skos:exactMatch NCIT:C35008 Schwartz-Jampel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009718 myxedema skos:exactMatch NCIT:C34834 Myxedema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009720 Keipert syndrome skos:exactMatch NCIT:C186306 Keipert Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009723 Leigh syndrome skos:exactMatch NCIT:C84814 Leigh Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009725 nemaline myopathy 2 skos:exactMatch NCIT:C118784 Nemaline Myopathy 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009728 nephronophthisis 1 skos:exactMatch NCIT:C74998 Nephronophthisis 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009732 congenital nephrotic syndrome, Finnish type skos:exactMatch NCIT:C122795 Nephrotic Syndrome - NPHS1 Associated semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009733 nephrotic syndrome, type 4 skos:exactMatch NCIT:C121198 Congenital Nephrotic Syndrome - Diffuse Mesangial Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009735 Netherton syndrome skos:exactMatch NCIT:C84922 Netherton Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009737 galactosialidosis skos:exactMatch NCIT:C129928 Galactosialidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009738 sialidosis type 2 skos:exactMatch NCIT:C125596 Neuraminidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009744 neuronal ceroid lipofuscinosis 1 skos:exactMatch NCIT:C85861 Neuronal Ceroid Lipofuscinosis Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009746 hereditary sensory and autonomic neuropathy type 4 skos:exactMatch NCIT:C118633 Neuropathy, Hereditary Sensory and Autonomic, Type IV semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009755 neutrophil actin dysfunction skos:exactMatch NCIT:C3694 Dysplastic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009756 Niemann-Pick disease type A skos:exactMatch NCIT:C126561 Niemann-Pick Disease, Type A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009757 Niemann-Pick disease, type C1 skos:exactMatch NCIT:C126864 Niemann-Pick Disease, Type C1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009761 cystic hygroma skos:exactMatch NCIT:C3724 Cystic Hygroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009796 ornithine aminotransferase deficiency skos:exactMatch NCIT:C84744 Gyrate Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009797 orotic aciduria skos:exactMatch NCIT:C98944 Hereditary Orotic Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009804 osteogenesis imperfecta type 3 skos:exactMatch NCIT:C99002 Osteogenesis Imperfecta Type III semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009807 osteosarcoma skos:exactMatch NCIT:C9145 Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009808 osteoid osteoma skos:exactMatch NCIT:C3297 Osteoid Osteoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009809 multicentric osteolysis, nodulosis, and arthropathy skos:exactMatch NCIT:C123437 Multicentric Osteolysis, Nodulosis, and Arthropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009813 chronic recurrent multifocal osteomyelitis skos:exactMatch NCIT:C119042 Chronic Recurrent Multifocal Osteomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009815 autosomal recessive osteopetrosis 1 skos:exactMatch NCIT:C167215 Autosomal Recessive Osteopetrosis 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009818 autosomal recessive osteopetrosis 3 skos:exactMatch NCIT:C118438 Osteopetrosis with Renal Tubular Acidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009820 osteoporosis-pseudoglioma syndrome skos:exactMatch NCIT:C130998 Osteoporosis Pseudoglioma Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009823 primary hyperoxaluria type 1 skos:exactMatch NCIT:C123212 Primary Hyperoxaluria Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009824 primary hyperoxaluria type 2 skos:exactMatch NCIT:C123213 Primary Hyperoxaluria Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009831 malignant pancreatic neoplasm skos:exactMatch NCIT:C9005 Malignant Pancreatic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009833 Shwachman-Diamond syndrome skos:exactMatch NCIT:C61235 Shwachman-Diamond Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009835 subacute sclerosing panencephalitis skos:exactMatch NCIT:C85171 Subacute Sclerosing Panencephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009837 choroid plexus papilloma skos:exactMatch NCIT:C3698 Choroid Plexus Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009838 Parana hard-skin syndrome skos:exactMatch NCIT:C126559 Hard Skin Syndrome Parana Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009855 d-bifunctional protein deficiency skos:exactMatch NCIT:C119676 D-Bifunctional Protein Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009856 Peters plus syndrome skos:exactMatch NCIT:C123436 Peters-Plus Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009857 persistent Mullerian duct syndrome skos:exactMatch NCIT:C120188 Persistent Mullerian Duct Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009861 phenylketonuria skos:exactMatch NCIT:C81315 Phenylketonuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009862 dihydropteridine reductase deficiency skos:exactMatch NCIT:C138173 Hyperphenylalaninemia, BH4-deficient C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009863 BH4-deficient hyperphenylalaninemia A skos:exactMatch NCIT:C138171 Hyperphenylalaninemia, BH4-deficient A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009865 glycogen storage disease due to phosphoglycerate mutase deficiency skos:exactMatch NCIT:C131647 Phosphoglycerate Mutase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009869 isolated Pierre-Robin syndrome skos:exactMatch NCIT:C85010 Pierre Robin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009874 Rabson-Mendenhall syndrome skos:exactMatch NCIT:C131000 Rabson-Mendenhall Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009877 Laron syndrome skos:exactMatch NCIT:C130994 Laron Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009887 desquamative interstitial pneumonia skos:exactMatch NCIT:C35288 Desquamative Interstitial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009889 autosomal recessive polycystic kidney disease skos:exactMatch NCIT:C84579 Autosomal Recessive Polycystic Kidney Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009891 acquired polycythemia vera skos:exactMatch NCIT:C3336 Polycythemia Vera semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009894 short-rib thoracic dysplasia 6 with or without polydactyly skos:exactMatch NCIT:C122654 Short-Rib Thoracic Dysplasia 6 with or without Polydactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009901 Bartsocas-Papas syndrome 1 skos:exactMatch NCIT:C168990 Bartsocas-Papas Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009902 cutaneous porphyria skos:exactMatch NCIT:C84697 Erythropoietic Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009904 Gitelman syndrome skos:exactMatch NCIT:C84730 Gitelman Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009910 Wiedemann-Rautenstrauch syndrome skos:exactMatch NCIT:C121565 Neonatal Progeroid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009916 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency skos:exactMatch NCIT:C120203 17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009919 peroxisomal acyl-CoA oxidase deficiency skos:exactMatch NCIT:C170437 Peroxisomal Acyl-CoA Oxidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009921 holoprosencephaly-postaxial polydactyly syndrome skos:exactMatch NCIT:C125418 Pseudotrisomy 13 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009923 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency skos:exactMatch NCIT:C98699 5 Alpha Steroid Reductase 2 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009924 vitamin D-dependent rickets, type 1 skos:exactMatch NCIT:C131073 Vitamin D 1 Alpha-Hydroxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009925 autosomal recessive inherited pseudoxanthoma elasticum skos:exactMatch NCIT:C85036 Pseudoxanthoma Elasticum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009926 autosomal recessive multiple pterygium syndrome skos:exactMatch NCIT:C101039 Escobar Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009930 obsolete pulmonary arteriovenous malformation skos:exactMatch NCIT:C99029 Pulmonary Arteriovenous Fistula semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009931 pulmonary atresia-intact ventricular septum syndrome skos:exactMatch NCIT:C99032 Pulmonary Valve Atresia with Intact Ventricular Septum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009933 congenital pulmonary lymphangiectasia skos:exactMatch NCIT:C99034 Congenital Pulmonary Lymphangiectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009934 alveolar capillary dysplasia with misalignment of pulmonary veins skos:exactMatch NCIT:C98809 Alveolar Capillary Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009937 pulmonary venoocclusive disease skos:exactMatch NCIT:C85039 Pulmonary Veno-Occlusive Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009940 pycnodysostosis skos:exactMatch NCIT:C131187 Pycnodysostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009948 pyropoikilocytosis, hereditary skos:exactMatch NCIT:C98943 Hereditary Pyropoikilocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009949 pyruvate carboxylase deficiency disease skos:exactMatch NCIT:C85040 Pyruvate Carboxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009950 pyruvate kinase deficiency of red cells skos:exactMatch NCIT:C99037 Pyruvate Kinase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009953 leukocyte adhesion deficiency type II skos:exactMatch NCIT:C4690 Leukocyte Adhesion Deficiency Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009965 Perlman syndrome skos:exactMatch NCIT:C103144 Perlman Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009973 reticular dysgenesis skos:exactMatch NCIT:C27070 Reticular Dysgenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009974 familial hemophagocytic lymphohistiocytosis type 1 skos:exactMatch NCIT:C61276 Familial Hemophagocytic Lymphohistiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009975 reticulum cell sarcoma skos:exactMatch NCIT:C27824 Reticulosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009990 Revesz syndrome skos:exactMatch NCIT:C152064 Revesz Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009993 embryonal rhabdomyosarcoma skos:exactMatch NCIT:C8971 Embryonal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0009994 alveolar rhabdomyosarcoma skos:exactMatch NCIT:C3749 Alveolar Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010002 Rothmund-Thomson syndrome skos:exactMatch NCIT:C3335 Rothmund-Thomson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010004 EEC syndrome skos:exactMatch NCIT:C148261 Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010006 Sandhoff disease skos:exactMatch NCIT:C85052 Sandhoff Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010010 Schinzel-Giedion syndrome skos:exactMatch NCIT:C129308 Schinzel-Giedion Midface-Retraction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010011 schizencephaly skos:exactMatch NCIT:C99056 Schizencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010012 autoimmune polyendocrinopathy type 2 skos:exactMatch NCIT:C129728 Autoimmune Polyglandular Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010017 sea-blue histiocyte syndrome skos:exactMatch NCIT:C85062 Sea-Blue Histiocyte Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010029 situs inversus skos:exactMatch NCIT:C87121 Situs Inversus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010030 Sjogren syndrome skos:exactMatch NCIT:C26883 Sjogren Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010031 Sjogren-Larsson syndrome skos:exactMatch NCIT:C85070 Sjogren-Larsson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010035 Smith-Lemli-Opitz syndrome skos:exactMatch NCIT:C85071 Smith-Lemli-Opitz Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010068 spondyloepimetaphyseal dysplasia, sponastrime type skos:exactMatch NCIT:C129031 Spondyloepimetaphyseal Dysplasia, Sponastrime Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010078 spondyloperipheral dysplasia skos:exactMatch NCIT:C135088 Spondyloperipheral Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010079 Canavan disease skos:exactMatch NCIT:C84611 Canavan Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010086 obsolete sudden infant death syndrome skos:exactMatch NCIT:C85173 Sudden Infant Death Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010088 mucosulfatidosis skos:exactMatch NCIT:C84908 Multiple Sulfatase Deficiency Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010099 Tay-Sachs disease AB variant skos:exactMatch NCIT:C133084 GM2-Gangliosidosis, AB Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010100 Tay-Sachs disease skos:exactMatch NCIT:C85184 Tay-Sachs Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010108 testicular germ cell tumor skos:exactMatch NCIT:C8591 Testicular Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010121 thrombocytopenia-absent radius syndrome skos:exactMatch NCIT:C99038 Radial Aplasia-Thrombocytopenia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010122 congenital thrombotic thrombocytopenic purpura skos:exactMatch NCIT:C131657 Congenital Thrombotic Thrombocytopenic Purpura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010130 dihydropyrimidine dehydrogenase deficiency skos:exactMatch NCIT:C84672 Dihydropyrimidine Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010131 thyroid hormone resistance, generalized, autosomal recessive skos:exactMatch NCIT:C85191 Thyroid Hormone Resistance Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010132 familial thyroid dyshormonogenesis skos:exactMatch NCIT:C121751 Thyroid Dyshormonogenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010133 thyroid dyshormonogenesis 2A skos:exactMatch NCIT:C121750 Thyroid Peroxidase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010134 Pendred syndrome skos:exactMatch NCIT:C121745 Pendred Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010138 thyrotoxicosis skos:exactMatch NCIT:C61469 Thyrotoxicosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010140 isolated thyrotropin-releasing hormone deficiency skos:exactMatch NCIT:C121741 Hypothalamic Hypothyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010148 Mounier-Kuhn syndrome skos:exactMatch NCIT:C85196 Tracheobronchomegaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010149 transcobalamin II deficiency skos:exactMatch NCIT:C142806 Transcobalamin II Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010150 head and neck squamous cell carcinoma skos:exactMatch NCIT:C34447 Head and Neck Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010159 mismatch repair cancer syndrome 1 skos:exactMatch NCIT:C130202 Constitutional Mismatch Repair Deficiency Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010160 tyrosinemia type II skos:exactMatch NCIT:C129032 Tyrosinemia Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010161 tyrosinemia type I skos:exactMatch NCIT:C98641 Tyrosinemia Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010168 Usher syndrome type 1 skos:exactMatch NCIT:C126327 Usher Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010176 orofaciodigital syndrome type 6 skos:exactMatch NCIT:C124841 Orofaciodigital Syndrome Type 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010178 congenital bilateral aplasia of vas deferens from CFTR mutation skos:exactMatch NCIT:C129303 Congenital Bilateral Aplasia of the Vas Deferens semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010184 methylmalonic aciduria and homocystinuria type cblC skos:exactMatch NCIT:C142174 Methylmalonic Aciduria and Homocystinuria, cblC Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010186 vitamin D-dependent rickets, type 2A skos:exactMatch NCIT:C131075 Vitamin D Dependent Rickets 2a semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010191 von Willebrand disease 3 skos:exactMatch NCIT:C85213 von Willebrand Disease, Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010193 Weaver syndrome skos:exactMatch NCIT:C125599 Weaver Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010196 Werner syndrome skos:exactMatch NCIT:C3447 Werner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010198 Wernicke-Korsakoff syndrome skos:exactMatch NCIT:C35764 Wernicke-Korsakoff Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010200 Wilson disease skos:exactMatch NCIT:C84756 Hepatolenticular Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010201 Winchester syndrome skos:exactMatch NCIT:C170731 Winchester Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010210 xeroderma pigmentosum group A skos:exactMatch NCIT:C3965 Xeroderma Pigmentosum, Complementation Group A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010211 xeroderma pigmentosum group C skos:exactMatch NCIT:C114770 Xeroderma Pigmentosum, Complementation Group C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010212 xeroderma pigmentosum group D skos:exactMatch NCIT:C3967 Xeroderma Pigmentosum, Complementation Group D semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010213 xeroderma pigmentosum group E skos:exactMatch NCIT:C114771 Xeroderma Pigmentosum, Complementation Group E semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010214 xeroderma pigmentosum variant type skos:exactMatch NCIT:C141367 Xeroderma Pigmentosum Variant Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010215 xeroderma pigmentosum group F skos:exactMatch NCIT:C3968 Xeroderma Pigmentosum, Complementation Group F semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010216 xeroderma pigmentosum group G skos:exactMatch NCIT:C3969 Xeroderma Pigmentosum, Complementation Group G semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010217 de Sanctis-Cacchione syndrome skos:exactMatch NCIT:C84666 De Sanctis-Cacchione Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010229 alopecia, congenital skos:exactMatch NCIT:C35790 Congenital Alopecia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010264 X-linked adrenal hypoplasia congenita skos:exactMatch NCIT:C123725 X-Linked Adrenal Hypoplasia Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010281 Danon disease skos:exactMatch NCIT:C84735 Glycogen Storage Disease Type IIb semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010283 syndromic X-linked intellectual disability Lubs type skos:exactMatch NCIT:C126747 Lubs X-Linked Mental Retardation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010293 ectodermal dysplasia and immune deficiency skos:exactMatch NCIT:C118844 Ectodermal Dysplasia and Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010298 Lesch-Nyhan syndrome skos:exactMatch NCIT:C61255 Lesch-Nyhan Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010305 creatine transporter deficiency skos:exactMatch NCIT:C125665 Cerebral Creatine Deficiency Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010308 thrombocytopenia, X-linked, with or without dyserythropoietic anemia skos:exactMatch NCIT:C136653 X-linked Thrombocytopenia, with or without Dyserythropoietic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010311 Becker muscular dystrophy skos:exactMatch NCIT:C84587 Becker's Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010315 T-B+ severe combined immunodeficiency due to gamma chain deficiency skos:exactMatch NCIT:C4682 X-Linked Severe Combined Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010351 Fanconi anemia complementation group B skos:exactMatch NCIT:C125703 Fanconi Anemia, Complementation Group B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010354 Allan-Herndon-Dudley syndrome skos:exactMatch NCIT:C118843 Allan-Herndon-Dudley Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010370 Cornelia de Lange syndrome 2 skos:exactMatch NCIT:C75485 X-Linked Cornelia De Lange Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010382 fragile X-associated tremor/ataxia syndrome skos:exactMatch NCIT:C126566 Fragile X Tremor/Ataxia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010383 fragile X syndrome skos:exactMatch NCIT:C84717 Fragile X Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010385 X-linked lymphoproliferative disease due to XIAP deficiency skos:exactMatch NCIT:C126295 X-linked Lymphoproliferative Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010392 glycogen storage disease due to phosphoglycerate kinase 1 deficiency skos:exactMatch NCIT:C126738 Phosphoglycerate Kinase 1 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010397 severe neonatal-onset encephalopathy with microcephaly skos:exactMatch NCIT:C132293 Severe Neonatal Encephalopathy Due to MECP2 Mutations semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010421 Bruton-type agammaglobulinemia skos:exactMatch NCIT:C3822 X-Linked Agammaglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010434 synovial sarcoma skos:exactMatch NCIT:C3400 Synovial Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010455 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia skos:exactMatch NCIT:C126336 X-Linked Immunodeficiency with Magnesium Defect, Epstein-Barr Virus Infection and Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010457 Ogden syndrome skos:exactMatch NCIT:C188215 Ogden Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010475 X-linked central congenital hypothyroidism with late-onset testicular enlargement skos:exactMatch NCIT:C130989 Immunoglobulin Superfamily Member 1 Deficiency Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010476 neurodegeneration with brain iron accumulation 5 skos:exactMatch NCIT:C175210 Neurodegeneration with Brain Iron Accumulation 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010497 intellectual disability, X-linked 102 skos:exactMatch NCIT:C129931 Mental Retardation, X-linked 102 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010507 Xq25 microduplication syndrome skos:exactMatch NCIT:C177544 Xq25 Microduplication Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010515 Meester-Loeys syndrome skos:exactMatch NCIT:C187989 Meester-Loeys Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010518 Wiskott-Aldrich syndrome skos:exactMatch NCIT:C3448 Wiskott-Aldrich Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010519 alpha thalassemia-X-linked intellectual disability syndrome skos:exactMatch NCIT:C118631 Alpha Thalassemia X-Linked Mental Retardation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010526 Fabry disease skos:exactMatch NCIT:C84701 Fabry Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010543 Barth syndrome skos:exactMatch NCIT:C84585 Barth Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010549 Charcot-Marie-Tooth disease X-linked dominant 1 skos:exactMatch NCIT:C129068 Charcot-Marie-Tooth Neuropathy X Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010557 choroideremia skos:exactMatch NCIT:C34469 Choroideremia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010559 MASA syndrome skos:exactMatch NCIT:C129930 MASA Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010561 Coffin-Lowry syndrome skos:exactMatch NCIT:C84643 Coffin-Lowry Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010562 colonic atresia skos:exactMatch NCIT:C101024 Colon Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010568 Aicardi syndrome skos:exactMatch NCIT:C35256 Aicardi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010574 syndromic X-linked intellectual disability 5 skos:exactMatch NCIT:C124839 Pettigrew Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010580 immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome skos:exactMatch NCIT:C131009 Immune Dysregulation, Polyendocrinopathy, and Enteropathy X-Linked Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010584 dyskeratosis congenita, X-linked skos:exactMatch NCIT:C126352 X-Linked Dyskeratosis Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010586 X-linked Ehlers-Danlos syndrome skos:exactMatch NCIT:C141423 Ehlers-Danlos Syndrome, Type V semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010589 Aarskog-Scott syndrome, X-linked skos:exactMatch NCIT:C129720 Aarskog Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010592 focal dermal hypoplasia skos:exactMatch NCIT:C84715 Focal Dermal Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010595 Sertoli cell-only syndrome skos:exactMatch NCIT:C168988 Sertoli Cell-Only Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010602 hemophilia A skos:exactMatch NCIT:C27146 Hemophilia A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010604 hemophilia B skos:exactMatch NCIT:C26721 Hemophilia B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010618 familial isolated hypoparathyroidism due to agenesis of parathyroid gland skos:exactMatch NCIT:C131079 X-Linked Hypoparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010619 X-linked dominant hypophosphatemic rickets skos:exactMatch NCIT:C85234 X-Linked Dominant Hypophosphatemic Rickets semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010622 recessive X-linked ichthyosis skos:exactMatch NCIT:C84779 X-Linked Ichthyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010626 hyper-IgM syndrome type 1 skos:exactMatch NCIT:C61244 CD40 Ligand Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010627 X-linked lymphoproliferative syndrome skos:exactMatch NCIT:C61246 X-Linked Lymphoproliferative Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010631 incontinentia pigmenti skos:exactMatch NCIT:C84787 Incontinentia Pigmenti semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010635 hypogonadotropic hypogonadism 1 with or without anosmia skos:exactMatch NCIT:C75480 Kallmann Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010643 acute leukemia skos:exactMatch NCIT:C9300 Acute Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010645 oculocerebrorenal syndrome skos:exactMatch NCIT:C84940 Oculocerebrorenal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010651 Menkes disease skos:exactMatch NCIT:C75486 Menkes Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010653 Renpenning syndrome skos:exactMatch NCIT:C165533 Renpenning Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010656 intellectual disability, X-linked 1 skos:exactMatch NCIT:C133729 Mental Retardation, X-linked 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010674 mucopolysaccharidosis type 2 skos:exactMatch NCIT:C61260 Hunter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010679 Duchenne muscular dystrophy skos:exactMatch NCIT:C75482 Duchenne Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010683 X-linked myotubular myopathy skos:exactMatch NCIT:C118781 X-Linked Centronuclear Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010691 Norrie disease skos:exactMatch NCIT:C118634 Norrie Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010702 orofaciodigital syndrome I skos:exactMatch NCIT:C75481 Orofaciodigital Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010703 ornithine carbamoyltransferase deficiency skos:exactMatch NCIT:C84957 Ornithine Carbamoyltransferase Deficiency Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010704 otopalatodigital syndrome type 1 skos:exactMatch NCIT:C118845 Otopalatodigital Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010714 Pelizeaus-Merzbacher spectrum disorder skos:exactMatch NCIT:C75487 Pelizaeus-Merzbacher Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010720 partial androgen insensitivity syndrome skos:exactMatch NCIT:C120192 Partial Androgen Insensitivity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010725 X-linked retinoschisis skos:exactMatch NCIT:C75483 Juvenile X-Linked Retinoschisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010726 Rett syndrome skos:exactMatch NCIT:C75488 Rett Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010731 Simpson-Golabi-Behmel syndrome skos:exactMatch NCIT:C131002 Simpson-Golabi-Behmel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010735 Kennedy disease skos:exactMatch NCIT:C85233 Spinal and Bulbar Muscular Atrophy, X-linked 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010742 pentalogy of Cantrell skos:exactMatch NCIT:C99011 Pentalogy of Cantrell semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010743 thrombocytopenia 1 skos:exactMatch NCIT:C176617 Thrombocytopenia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010745 beta-thalassemia-X-linked thrombocytopenia syndrome skos:exactMatch NCIT:C134941 X-Linked Thrombocytopenia with Beta-Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010747 X-linked dystonia-parkinsonism skos:exactMatch NCIT:C126330 X-Linked Dystonia Parkinsonism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010765 46,XY complete gonadal dysgenesis skos:exactMatch NCIT:C120198 46,XY Gonadal Dysgenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010768 gonadoblastoma skos:exactMatch NCIT:C3754 Gonadoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010771 histiocytoid cardiomyopathy skos:exactMatch NCIT:C45745 Conduction System Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010785 maternally-inherited diabetes and deafness skos:exactMatch NCIT:C131859 Mitochondrial Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010787 Kearns-Sayre syndrome skos:exactMatch NCIT:C84798 Kearns-Sayre Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010788 Leber hereditary optic neuropathy skos:exactMatch NCIT:C84808 Leber Hereditary Optic Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010789 MELAS syndrome skos:exactMatch NCIT:C84885 MELAS Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010790 MERRF syndrome skos:exactMatch NCIT:C84889 Myoclonic Epilepsy Associated with Ragged-Red Fibers semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010795 oncocytic neoplasm skos:exactMatch NCIT:C7072 Oncocytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010797 Pearson syndrome skos:exactMatch NCIT:C115326 Pearson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010805 bladder exstrophy skos:exactMatch NCIT:C123207 Bladder Exstrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010808 fatal familial insomnia skos:exactMatch NCIT:C84711 Fatal Familial Insomnia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010810 vitamin D hydroxylation-deficient rickets, type 1B skos:exactMatch NCIT:C131074 Vitamin D 25-Hydroxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010811 benign prostatic hyperplasia skos:exactMatch NCIT:C2897 Benign Prostatic Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010831 familial caudal dysgenesis skos:exactMatch NCIT:C99054 Sacral Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010837 primary hyperparathyroidism skos:exactMatch NCIT:C48280 Primary Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010838 gonadal agenesis skos:exactMatch NCIT:C27228 Gonadal Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010879 CODAS syndrome skos:exactMatch NCIT:C126744 Codas Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010886 2q37 microdeletion syndrome skos:exactMatch NCIT:C129021 Chromosome 2q37 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010888 adenomyosis skos:exactMatch NCIT:C6996 Uterine Corpus Adenomyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010894 maturity-onset diabetes of the young type 3 skos:exactMatch NCIT:C129742 Hepatocyte Nuclear Factor 1-Alpha-Associated Monogenic Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010896 pigment dispersion syndrome skos:exactMatch NCIT:C187288 Pigment Dispersion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010909 UV-sensitive syndrome 1 skos:exactMatch NCIT:C173106 UV-Sensitive Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010911 prolactin-producing pituitary gland adenoma skos:exactMatch NCIT:C3342 Lactotroph Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010913 Caroli disease skos:exactMatch NCIT:C84619 Caroli Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010931 vitamin D-dependent rickets, type 2B skos:exactMatch NCIT:C131076 Vitamin D Dependent Rickets 2b semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010953 Fanconi anemia complementation group E skos:exactMatch NCIT:C125709 Fanconi Anemia, Complementation Group E semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010979 Timothy syndrome skos:exactMatch NCIT:C142894 Long QT Syndrome 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0010998 ALG3-congenital disorder of glycosylation skos:exactMatch NCIT:C126870 Congenital Disorder of Glycosylation Type Id semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011014 pleuropulmonary blastoma skos:exactMatch NCIT:C5669 Pleuropulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011022 Potocki-Shaffer syndrome skos:exactMatch NCIT:C75456 Potocki-Shaffer Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011055 distal monosomy 10p skos:exactMatch NCIT:C130982 10p13-p14 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011057 cerebrovascular disorder skos:exactMatch NCIT:C2938 Cerebrovascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011091 Charcot-Marie-Tooth disease type 2D skos:exactMatch NCIT:C122659 Charcot-Marie-Tooth Disease Type 2D semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011093 mucopolysaccharidosis type 9 skos:exactMatch NCIT:C129073 Mucopolysaccharidosis Type IX semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011094 dilated cardiomyopathy 1C skos:exactMatch NCIT:C170436 Dilated Cardiomyopathy-1C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011101 peroxisome biogenesis disorder 1B skos:exactMatch NCIT:C155749 Peroxisome Biogenesis Disorder 1B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011113 Charcot-Marie-Tooth disease type 4C skos:exactMatch NCIT:C129864 Charcot-Marie-Tooth Disease Type 4C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011118 bilineal acute myeloid leukemia skos:exactMatch NCIT:C6923 Acute Bilineal Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011122 obesity disorder skos:exactMatch NCIT:C3283 Obesity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011125 trichothiodystrophy 1, photosensitive skos:exactMatch NCIT:C156433 Trichothiodystrophy 1, Photosensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011146 tetrasomy 12p skos:exactMatch NCIT:C75458 Pallister-Killian Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011147 chromosome 18q deletion syndrome skos:exactMatch NCIT:C84522 Deletion 18q Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011178 infantile convulsions and choreoathetosis skos:exactMatch NCIT:C126650 Infantile Convulsions and Paroxysmal Choreoathetosis, Familial semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011208 malignant atrophic papulosis skos:exactMatch NCIT:C84835 Malignant Atrophic Papulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011230 ossification of the posterior longitudinal ligament of the spine skos:exactMatch NCIT:C84975 Ossification of Posterior Longitudinal Ligament semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011264 torsion dystonia 6 skos:exactMatch NCIT:C156361 Torsion Dystonia 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011266 myotonic dystrophy type 2 skos:exactMatch NCIT:C84680 Dystrophia Myotonica 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011271 rigid spine muscular dystrophy 1 skos:exactMatch NCIT:C126691 Rigid Spine Muscular Dystrophy 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011274 Muenke syndrome skos:exactMatch NCIT:C84904 Muenke Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011281 congenital myasthenic syndrome 5 skos:exactMatch NCIT:C129304 Congenital Myasthenic Syndrome 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011291 ALG6-congenital disorder of glycosylation 1C skos:exactMatch NCIT:C126869 Congenital Disorder of Glycosylation Type Ic semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011325 Fanconi anemia complementation group F skos:exactMatch NCIT:C125707 Fanconi Anemia, Complementation Group F semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011327 neuronal intranuclear inclusion disease skos:exactMatch NCIT:C122655 Neuronal Intranuclear Inclusion Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011335 spondyloepimetaphyseal dysplasia with multiple dislocations skos:exactMatch NCIT:C125419 Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011338 Omenn syndrome skos:exactMatch NCIT:C61240 Omenn Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011366 ovarian germ cell tumor skos:exactMatch NCIT:C3873 Ovarian Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011368 papillary thyroid Microcarcinoma skos:exactMatch NCIT:C46004 Thyroid Gland Papillary Microcarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011374 hypercholesterolemia, familial, 4 skos:exactMatch NCIT:C128114 Hypercholesterolemia, Familial, 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011377 long QT syndrome 3 skos:exactMatch NCIT:C137959 Long QT Syndrome 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011382 sickle cell anemia skos:exactMatch NCIT:C34383 Sickle Cell Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011383 autoimmune lymphoproliferative syndrome type 2A skos:exactMatch NCIT:C39576 Autoimmune Lymphoproliferative Syndrome with Germline CASP10 Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011385 intervertebral disk degenerative disorder skos:exactMatch NCIT:C26983 Intervertebral Disc Degenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011399 alpha thalassemia spectrum skos:exactMatch NCIT:C34368 Alpha Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011405 poikiloderma with neutropenia skos:exactMatch NCIT:C177535 Poikiloderma with Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011424 Carney triad skos:exactMatch NCIT:C94833 Carney Triad semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011429 juvenile idiopathic arthritis skos:exactMatch NCIT:C114357 Juvenile Idiopathic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011438 acne skos:exactMatch NCIT:C27195 Acne semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011439 spinocerebellar ataxia type 12 skos:exactMatch NCIT:C154316 Spinocerebellar Ataxia Type 12 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011441 complex regional pain syndrome type 1 skos:exactMatch NCIT:C85042 Complex Regional Pain Syndrome I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011445 hereditary spastic paraplegia 11 skos:exactMatch NCIT:C148317 Spastic Paraplegia 11 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011449 Salla disease skos:exactMatch NCIT:C85067 Sialic Acid Storage Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011462 pyogenic arthritis-pyoderma gangrenosum-acne syndrome skos:exactMatch NCIT:C119055 Pyogenic Arthritis, Pyoderma Gangrenosum and Acne semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011465 infundibulocystic basal cell carcinoma skos:exactMatch NCIT:C27540 Skin Infundibulocystic Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011479 postural orthostatic tachycardia syndrome skos:exactMatch NCIT:C85020 Postural Orthostatic Tachycardia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011484 catecholaminergic polymorphic ventricular tachycardia 1 skos:exactMatch NCIT:C123414 Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011493 Stickler syndrome type 2 skos:exactMatch NCIT:C74985 Stickler Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011503 cortisone reductase deficiency 1 skos:exactMatch NCIT:C131849 Hexose-6-phosphate Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011510 Bohring-Opitz syndrome skos:exactMatch NCIT:C131533 Bohring-Opitz Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011514 tricuspid atresia skos:exactMatch NCIT:C85202 Tricuspid Valve Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011526 obsolete Sebastian syndrome skos:exactMatch NCIT:C131650 Sebastian Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011528 hyper-IgM syndrome type 2 skos:exactMatch NCIT:C129074 Immunodeficiency with Hyper-IgM Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011531 Noonan syndrome 2 skos:exactMatch NCIT:C176930 Noonan Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011558 Usher syndrome type 2C skos:exactMatch NCIT:C153174 Usher Syndrome Type 2C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011576 familial hyperaldosteronism type II skos:exactMatch NCIT:C127162 Familial Hyperaldosteronism Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011583 cerebral amyloid angiopathy, APP-related skos:exactMatch NCIT:C157147 Cerebral Amyloid Angiopathy, APP-Related semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011584 Fanconi anemia complementation group D1 skos:exactMatch NCIT:C125705 Fanconi Anemia, Complementation Group D1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011612 glycine encephalopathy skos:exactMatch NCIT:C84937 Glycine Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011628 propionic acidemia skos:exactMatch NCIT:C85030 Propionic Acidemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011632 amyotrophic lateral sclerosis type 21 skos:exactMatch NCIT:C168755 Amyotrophic Lateral Sclerosis 21 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011644 pars planitis skos:exactMatch NCIT:C34903 Pars Planitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011652 Phelan-McDermid syndrome skos:exactMatch NCIT:C157124 Phelan-McDermid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011655 alveolar soft part sarcoma skos:exactMatch NCIT:C3750 Alveolar Soft Part Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011655 alveolar soft part sarcoma skos:exactMatch NCIT:C7943 Adult Alveolar Soft Part Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011662 pathological gambling skos:exactMatch NCIT:C94335 Pathological Gambling semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011667 maturity-onset diabetes of the young type 4 skos:exactMatch NCIT:C129746 PDX1-Associated Monogenic Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011668 maturity-onset diabetes of the young type 6 skos:exactMatch NCIT:C129745 Neurogenic Differentiation Factor 1-Associated Monogenic Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011686 DNA ligase IV deficiency skos:exactMatch NCIT:C122657 LIG4 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011694 spinocerebellar ataxia type 15/16 skos:exactMatch NCIT:C150250 Spinocerebellar Ataxia Type 16 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011705 lymphangioleiomyomatosis skos:exactMatch NCIT:C3725 Lymphangioleiomyomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011709 split hand-foot malformation 5 skos:exactMatch NCIT:C75002 Split-Hand/Foot Malformation Type 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011713 melanoma-pancreatic cancer syndrome skos:exactMatch NCIT:C176904 Melanoma-Pancreatic Cancer Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011716 acute hemorrhagic leukoencephalitis skos:exactMatch NCIT:C84535 Acute Hemorrhagic Leukoencephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011717 hyperinsulinism-hyperammonemia syndrome skos:exactMatch NCIT:C131832 Glutamate Dehydrogenase 1 Hyperinsulinism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011719 gastrointestinal stromal tumor skos:exactMatch NCIT:C3868 Gastrointestinal Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011732 familial digital arthropathy-brachydactyly skos:exactMatch NCIT:C175208 Familial Digital Arthropathy-Brachydactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011738 bilateral frontoparietal polymicrogyria skos:exactMatch NCIT:C148367 Bilateral Frontoparietal Polymicrogyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011740 Carney-Stratakis syndrome skos:exactMatch NCIT:C94831 Carney-Stratakis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011743 Alzheimer disease 4 skos:exactMatch NCIT:C123413 Alzheimer's Disease 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011758 Hurler syndrome skos:exactMatch NCIT:C61261 Hurler Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011759 Hurler-Scheie syndrome skos:exactMatch NCIT:C122782 Hurler-Scheie Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011760 Scheie syndrome skos:exactMatch NCIT:C61265 Scheie Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011776 CINCA syndrome skos:exactMatch NCIT:C116380 Chronic Infantile Neurological Cutaneous and Articular Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011781 spinocerebellar ataxia type 17 skos:exactMatch NCIT:C179861 Spinocerebellar Ataxia Type 17 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011783 ALG12-congenital disorder of glycosylation skos:exactMatch NCIT:C126873 Congenital Disorder of Glycosylation Type Ig semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011784 Moyamoya disease 2 skos:exactMatch NCIT:C183312 Moyamoya Disease 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011786 allergic rhinitis skos:exactMatch NCIT:C79532 Allergic Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011787 autosomal recessive limb-girdle muscular dystrophy type 2I skos:exactMatch NCIT:C126739 Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C, 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011789 familial meningioma skos:exactMatch NCIT:C5301 Hereditary Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011806 osteofibrous dysplasia skos:exactMatch NCIT:C53970 Osteofibrous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011819 spinocerebellar ataxia type 19/22 skos:exactMatch NCIT:C163756 Spinocerebellar Ataxia Type 19/22 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011826 glucocorticoid deficiency 2 skos:exactMatch NCIT:C123728 Familial Glucocorticoid Deficiency Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011827 patent ductus arteriosus skos:exactMatch NCIT:C84492 Patent Ductus Arteriosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011849 psoriatic arthritis skos:exactMatch NCIT:C61277 Psoriatic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011871 Niemann-Pick disease type B skos:exactMatch NCIT:C126866 Niemann-Pick Disease, Type B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011872 Griscelli syndrome type 2 skos:exactMatch NCIT:C111814 Griscelli Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011873 Niemann-Pick disease, type C2 skos:exactMatch NCIT:C126865 Niemann-Pick Disease, Type C2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011885 tubulointerstitial nephritis and uveitis syndrome skos:exactMatch NCIT:C123021 Tubulointerstitial Nephritis and Uveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011894 Charcot-Marie-Tooth disease type 2E skos:exactMatch NCIT:C134953 Charcot-Marie-Tooth Disease Type 2E semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011899 Noonan syndrome-like disorder with loose anagen hair skos:exactMatch NCIT:C178129 Noonan Syndrome-Like Disorder with Loose Anagen Hair semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011908 juvenile myelomonocytic leukemia skos:exactMatch NCIT:C9233 Juvenile Myelomonocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011910 obsolete autosomal dominant limb-girdle muscular dystrophy type 1C skos:exactMatch NCIT:C148318 Limb-Girdle Muscular Dystrophy Type 1C semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011913 Alzheimer disease 3 skos:exactMatch NCIT:C123412 Alzheimer's Disease 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011925 congenital merosin-deficient muscular dystrophy 1A skos:exactMatch NCIT:C118783 Merosin-Deficient Congenital Muscular Dystrophy Type 1A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011927 tufted angioma skos:exactMatch NCIT:C4487 Tufted Angioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011929 chromosome 1p36 deletion syndrome skos:exactMatch NCIT:C74983 1p36 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011934 dermatofibrosarcoma protuberans skos:exactMatch NCIT:C4683 Dermatofibrosarcoma Protuberans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011959 sweet syndrome skos:exactMatch NCIT:C85177 Sweet Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011962 endometrial cancer skos:exactMatch NCIT:C27815 Malignant Endometrial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011964 DPAGT1-congenital disorder of glycosylation skos:exactMatch NCIT:C126874 Congenital Disorder of Glycosylation Type Ij semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011968 autosomal recessive limb-girdle muscular dystrophy type 2D skos:exactMatch NCIT:C142081 Limb-Girdle Muscular Dystrophy Type 2D semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011989 leishmaniasis skos:exactMatch NCIT:C34767 Leishmaniasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011996 chronic myelogenous leukemia, BCR-ABL1 positive skos:exactMatch NCIT:C3174 Chronic Myeloid Leukemia, BCR-ABL1 Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0011997 Hermansky-Pudlak syndrome 2 skos:exactMatch NCIT:C150368 Hermansky-Pudlak Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012000 specific phobia skos:exactMatch NCIT:C35284 Specific Phobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012003 autosomal recessive nonsyndromic hearing loss 39 skos:exactMatch NCIT:C129874 Deafness, Autosomal Recessive 39 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012004 parathyroid gland carcinoma skos:exactMatch NCIT:C4906 Parathyroid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012016 capillary malformation-arteriovenous malformation syndrome skos:exactMatch NCIT:C179668 Capillary Malformation-Arteriovenous Malformation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012041 familial adenomatous polyposis 2 skos:exactMatch NCIT:C96520 MUTYH-Associated Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012048 endogenous depression skos:exactMatch NCIT:C34532 Endogenous Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012078 Joubert syndrome 3 skos:exactMatch NCIT:C148259 Joubert Syndrome 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012081 15q11q13 microduplication syndrome skos:exactMatch NCIT:C126692 Chromosome 15q11-q13 Duplication Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012084 aromatic L-amino acid decarboxylase deficiency skos:exactMatch NCIT:C142085 Aromatic L-Amino-Acid Decarboxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012085 primary ciliary dyskinesia 3 skos:exactMatch NCIT:C172392 Primary Ciliary Dyskinesia 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012089 ichthyosis prematurity syndrome skos:exactMatch NCIT:C62590 Idiopathic Pneumonia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012104 acquired partial lipodystrophy skos:exactMatch NCIT:C129723 Acquired Partial Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012105 granulomatosis with polyangiitis skos:exactMatch NCIT:C123111 Pauci-Immune Glomerulonephritis associated with Granulomatosis with Polyangiitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012105 granulomatosis with polyangiitis skos:exactMatch NCIT:C3444 Granulomatosis with Polyangiitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012123 congenital disorder of glycosylation type 1E skos:exactMatch NCIT:C126871 Congenital Disorder of Glycosylation Type Ie semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012126 familial avascular necrosis of femoral head skos:exactMatch NCIT:C35480 Aseptic Necrosis of Femoral Head semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012172 mitochondrial trifunctional protein deficiency skos:exactMatch NCIT:C98991 Mitochondrial Trifunctional Protein Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012173 long chain 3-hydroxyacyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C129929 Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012184 Pierson syndrome skos:exactMatch NCIT:C128145 Pierson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012186 Fanconi anemia complementation group I skos:exactMatch NCIT:C129026 Fanconi Anemia, Complementation Group I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012187 Fanconi anemia complementation group J skos:exactMatch NCIT:C129027 Fanconi Anemia, Complementation Group J semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012191 hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 skos:exactMatch NCIT:C125663 Combined Oxidative Phosphorylation Deficiency 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012197 idiopathic aplastic anemia skos:exactMatch NCIT:C61230 Idiopathic Aplastic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012211 MPDU1-congenital disorder of glycosylation skos:exactMatch NCIT:C126872 Congenital Disorder of Glycosylation Type If semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012212 Loeys-Dietz syndrome 1 skos:exactMatch NCIT:C75119 Loeys-Dietz Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012231 Charcot-Marie-Tooth disease type 2A2 skos:exactMatch NCIT:C150646 Charcot-Marie-Tooth Disease Type 2A2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012240 congenital myopathy 23 skos:exactMatch NCIT:C164225 Nemaline Myopathy 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012248 autosomal recessive limb-girdle muscular dystrophy type 2K skos:exactMatch NCIT:C133730 Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C, 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012249 Lynch syndrome 2 skos:exactMatch NCIT:C6726 Lynch 2 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012252 rhabdoid tumor predisposition syndrome 1 skos:exactMatch NCIT:C178393 Rhabdoid Tumor Predisposition Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012268 AIDS skos:exactMatch NCIT:C2851 Acquired Immunodeficiency Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012275 fetal valproate syndrome skos:exactMatch NCIT:C98930 Fetal Valproate Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012295 complement component 5 deficiency skos:exactMatch NCIT:C9469 C5 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012308 Joubert syndrome with renal defect skos:exactMatch NCIT:C74997 Joubert Syndrome 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012316 Majeed syndrome skos:exactMatch NCIT:C119058 Majeed Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012322 holoprosencephaly 5 skos:exactMatch NCIT:C75460 Holoprosencephaly Type 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012355 autosomal recessive nonsyndromic hearing loss 28 skos:exactMatch NCIT:C129023 Deafness, Autosomal Recessive 28 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012371 Noonan syndrome 3 skos:exactMatch NCIT:C176931 Noonan Syndrome 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012383 primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency skos:exactMatch NCIT:C123729 Natural Killer Cell and Glucocorticoid Deficiency with DNA Repair Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012392 2-methylbutyryl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C98863 Butyryl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012396 exercise-induced hyperinsulinism skos:exactMatch NCIT:C131839 Monocarboxylate Transporter 1 Hyperinsulinism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012400 cortical dysplasia-focal epilepsy syndrome skos:exactMatch NCIT:C133743 Cortical Dysplasia-Focal Epilepsy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012420 autosomal recessive nonsyndromic hearing loss 49 skos:exactMatch NCIT:C129024 Deafness, Autosomal Recessive 49 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012427 Loeys-Dietz syndrome 2 skos:exactMatch NCIT:C114768 Loeys-Dietz Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012429 Aicardi-Goutieres syndrome 2 skos:exactMatch NCIT:C165673 Aicardi-Goutieres Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012435 3-methylglutaconic aciduria type 5 skos:exactMatch NCIT:C173146 3-Methylglutaconic Aciduria Type 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012456 congenital primary aphakia skos:exactMatch NCIT:C35172 Congenital Aphakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012481 mevalonic aciduria skos:exactMatch NCIT:C84890 Mevalonate Kinase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012503 thiopurine S-methyltransferase deficiency skos:exactMatch NCIT:C4389 Thiopurine Methyltransferase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012511 preterm premature rupture of the membranes skos:exactMatch NCIT:C92862 Preterm Premature Rupture of Membrane semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012518 congenital myasthenic syndrome 12 skos:exactMatch NCIT:C168997 Congenital Myasthenic Syndrome 12 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012520 insulin-resistance syndrome type A skos:exactMatch NCIT:C131836 Insulin Resistant Diabetes Mellitus with Acanthosis Nigricans and Hyperandrogenism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012521 herpes simplex encephalitis skos:exactMatch NCIT:C84762 Herpes Simplex Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012529 Diamond-Blackfan anemia 3 skos:exactMatch NCIT:C176912 Diamond-Blackfan Anemia 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012531 xeroderma pigmentosum group B skos:exactMatch NCIT:C3966 Xeroderma Pigmentosum, Complementation Group B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012547 Noonan syndrome 4 skos:exactMatch NCIT:C176932 Noonan Syndrome 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012552 multiple endocrine neoplasia type 4 skos:exactMatch NCIT:C157449 Multiple Endocrine Neoplasia Type 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012554 cerebrooculofacioskeletal syndrome 4 skos:exactMatch NCIT:C173104 Cerebrooculofacioskeletal Syndrome 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012574 Potocki-Lupski syndrome skos:exactMatch NCIT:C124846 Potocki-Lupski Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012589 Pitt-Hopkins syndrome skos:exactMatch NCIT:C129872 Pitt-Hopkins Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012590 XFE progeroid syndrome skos:exactMatch NCIT:C173111 XFE Progeroid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012640 Charcot-Marie-Tooth disease type 4J skos:exactMatch NCIT:C134954 Charcot-Marie-Tooth Disease Type 4J semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012648 isobutyryl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C129975 Isobutyryl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012669 Legius syndrome skos:exactMatch NCIT:C176941 Legius Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012672 cholelithiasis skos:exactMatch NCIT:C122822 Cholelithiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012690 Noonan syndrome 5 skos:exactMatch NCIT:C176933 Noonan Syndrome 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012694 Joubert syndrome 7 skos:exactMatch NCIT:C159653 Joubert Syndrome 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012703 lissencephaly due to TUBA1A mutation skos:exactMatch NCIT:C148461 Lissencephaly 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012724 familial cold autoinflammatory syndrome 2 skos:exactMatch NCIT:C119043 NALP12-Associated Hereditary Periodic Fever Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012727 mucocutaneous lymph node syndrome skos:exactMatch NCIT:C34825 Kawasaki Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012734 SERKAL syndrome skos:exactMatch NCIT:C123726 SERKAL Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012756 proximal 16p11.2 microdeletion syndrome skos:exactMatch NCIT:C120408 Chromosome 16p11.2 Deletion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012762 catecholaminergic polymorphic ventricular tachycardia 2 skos:exactMatch NCIT:C148368 Catecholaminergic Polymorphic Ventricular Tachycardia Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012789 dystonia 16 skos:exactMatch NCIT:C168729 Dystonia 16 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012806 ectodermal dysplasia and immunodeficiency 2 skos:exactMatch NCIT:C176826 Ectodermal Dysplasia and Immunodeficiency 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012809 histiocytoma, Angiomatoid fibrous skos:exactMatch NCIT:C6494 Angiomatoid Fibrous Histiocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012812 developmental and epileptic encephalopathy, 4 skos:exactMatch NCIT:C162472 Developmental and Epileptic Encephalopathy 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012817 Ewing sarcoma skos:exactMatch NCIT:C4817 Ewing Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012825 extraskeletal myxoid chondrosarcoma skos:exactMatch NCIT:C27502 Extraskeletal Myxoid Chondrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012833 Crouzon syndrome-acanthosis nigricans syndrome skos:exactMatch NCIT:C38145 Chronic Allograft Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012849 Joubert syndrome 9 skos:exactMatch NCIT:C181002 Joubert Syndrome 9 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012883 acute promyelocytic leukemia skos:exactMatch NCIT:C3182 Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012897 congenital factor XI deficiency skos:exactMatch NCIT:C84705 Hereditary Factor XI Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012912 pseudopseudohypoparathyroidism skos:exactMatch NCIT:C129722 Albright Hereditary Osteodystrophy without Multiple Hormone Resistance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012913 Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome skos:exactMatch NCIT:C122804 Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation-Obesity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012924 Diamond-Blackfan anemia 4 skos:exactMatch NCIT:C176913 Diamond-Blackfan Anemia 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012925 Diamond-Blackfan anemia 5 skos:exactMatch NCIT:C176914 Diamond-Blackfan Anemia 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012937 Diamond-Blackfan anemia 6 skos:exactMatch NCIT:C176915 Diamond-Blackfan Anemia 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012938 Diamond-Blackfan anemia 7 skos:exactMatch NCIT:C176916 Diamond-Blackfan Anemia 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0012939 Diamond-Blackfan anemia 8 skos:exactMatch NCIT:C176917 Diamond-Blackfan Anemia 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013000 porphyria due to ALA dehydratase deficiency skos:exactMatch NCIT:C133887 Acute Hepatic Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013021 sterile multifocal osteomyelitis with periostitis and pustulosis skos:exactMatch NCIT:C119056 Deficiency of the Interleukin-1 Receptor Antagonist semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013059 Aicardi-Goutieres syndrome 5 skos:exactMatch NCIT:C168564 Aicardi-Goutieres Syndrome 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013074 encephalocraniocutaneous lipomatosis skos:exactMatch NCIT:C4701 Encephalocraniocutaneous Lipomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013081 lymphoproliferative syndrome 1 skos:exactMatch NCIT:C126344 Lymphoproliferative Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013098 noise induced hearing loss skos:exactMatch NCIT:C34664 Noise Induced Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013118 Nijmegen breakage syndrome-like disorder skos:exactMatch NCIT:C153178 Nijmegen Breakage Syndrome-Like Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013127 asphyxiating thoracic dystrophy 3 skos:exactMatch NCIT:C163755 Short-Rib Thoracic Dysplasia 3 with or without Polydactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013129 cone dystrophy 4 skos:exactMatch NCIT:C164226 Achromatopsia 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013131 polycystic kidney disease 2 skos:exactMatch NCIT:C123166 Autosomal Dominant Polycystic Kidney Disease Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013153 inflammatory bowel disease 28 skos:exactMatch NCIT:C164676 Inflammatory Bowel Disease 28 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013154 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2 skos:exactMatch NCIT:C126742 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013158 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6 skos:exactMatch NCIT:C126743 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013160 muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2 skos:exactMatch NCIT:C126690 Congenital Muscular Dystrophy-Dystroglycanopathy with Mental Retardation Type B2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013171 purine nucleoside phosphorylase deficiency skos:exactMatch NCIT:C176817 Purine Nucleoside Phosphorylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013171 purine nucleoside phosphorylase deficiency skos:exactMatch NCIT:C3963 Purine-Nucleoside Phosphorylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013178 congenital muscular dystrophy due to LMNA mutation skos:exactMatch NCIT:C148369 Muscular Dystrophy Congenital, LMNA-Related semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013186 Noonan syndrome 6 skos:exactMatch NCIT:C176934 Noonan Syndrome 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013189 trichotillomania skos:exactMatch NCIT:C94336 Trichotillomania semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013199 tuberous sclerosis 2 skos:exactMatch NCIT:C75331 Tuberous Sclerosis 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013209 metabolic dysfunction-associated steatotic liver disease skos:exactMatch NCIT:C84444 Nonalcoholic Fatty Liver Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013216 Diamond-Blackfan anemia 9 skos:exactMatch NCIT:C176918 Diamond-Blackfan Anemia 9 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013217 Diamond-Blackfan anemia 10 skos:exactMatch NCIT:C176919 Diamond-Blackfan Anemia 10 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013224 rhabdoid tumor predisposition syndrome 2 skos:exactMatch NCIT:C178394 Rhabdoid Tumor Predisposition Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013227 congenital plasminogen activator inhibitor type 1 deficiency skos:exactMatch NCIT:C133884 Plasminogen Activator Inhibitor-1 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013252 Warsaw breakage syndrome skos:exactMatch NCIT:C164675 Warsaw Breakage Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013270 Rett syndrome, congenital variant skos:exactMatch NCIT:C176903 Rett Syndrome, Congenital Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013280 myxoid liposarcoma skos:exactMatch NCIT:C27781 Myxoid Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013282 alpha 1-antitrypsin deficiency skos:exactMatch NCIT:C84397 Alpha-1 Antitrypsin Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013296 myeloid neoplasm associated with FGFR1 rearrangement skos:exactMatch NCIT:C84277 Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013301 aromatase deficiency skos:exactMatch NCIT:C120144 P450-Aromatase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013310 congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency skos:exactMatch NCIT:C174439 Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013327 primary hyperoxaluria type 3 skos:exactMatch NCIT:C123214 Primary Hyperoxaluria Type III semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013333 odontoid hypoplasia skos:exactMatch NCIT:C86969 Odontoid Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013343 C1Q deficiency skos:exactMatch NCIT:C119990 C1q Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013361 congenital prothrombin deficiency skos:exactMatch NCIT:C131737 Factor II Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013364 Rubinstein-Taybi syndrome due to EP300 haploinsufficiency skos:exactMatch NCIT:C153291 Rubinstein-Taybi Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013367 long QT syndrome 2 skos:exactMatch NCIT:C137957 Long QT Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013372 long QT syndrome 5 skos:exactMatch NCIT:C172094 Long QT Syndrome 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013379 Noonan syndrome 7 skos:exactMatch NCIT:C176935 Noonan Syndrome 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013400 Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency skos:exactMatch NCIT:C131422 Cholesterol Side-Chain Cleavage Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013417 complement component 3 deficiency skos:exactMatch NCIT:C9468 C3 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013434 primary ciliary dyskinesia 14 skos:exactMatch NCIT:C148370 Primary Ciliary Dyskinesia 14 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013435 primary ciliary dyskinesia 15 skos:exactMatch NCIT:C155999 Primary Ciliary Dyskinesia 15 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013461 inosine triphosphatase deficiency skos:exactMatch NCIT:C129974 Inosine Triphosphatase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013481 chromosome 13q14 deletion syndrome skos:exactMatch NCIT:C36421 del(13q14) semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013512 hemoglobin H disease skos:exactMatch NCIT:C95504 Hemoglobin H Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013519 dyskeratosis congenita, autosomal recessive 2 skos:exactMatch NCIT:C176926 Dyskeratosis Congenita, Autosomal Recessive 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013520 dyskeratosis congenita, autosomal recessive 3 skos:exactMatch NCIT:C176927 Dyskeratosis Congenita, Autosomal Recessive 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013521 dyskeratosis congenita, autosomal dominant 2 skos:exactMatch NCIT:C176922 Dyskeratosis Congenita, Autosomal Dominant 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013522 dyskeratosis congenita, autosomal dominant 3 skos:exactMatch NCIT:C176923 Dyskeratosis Congenita, Autosomal Dominant 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013551 hereditary spastic paraplegia 47 skos:exactMatch NCIT:C164224 Spastic Paraplegia 47 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013558 Hermansky-Pudlak syndrome 6 skos:exactMatch NCIT:C150369 Hermansky-Pudlak Syndrome 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013563 multiple congenital anomalies-hypotonia-seizures syndrome 1 skos:exactMatch NCIT:C176896 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013565 Fanconi anemia complementation group G skos:exactMatch NCIT:C125708 Fanconi Anemia, Complementation Group G semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013571 acatalasia skos:exactMatch NCIT:C84526 Acatalasemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013582 mosaic variegated aneuploidy syndrome 2 skos:exactMatch NCIT:C168989 Mosaic Variegated Aneuploidy Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013594 spinocerebellar ataxia type 36 skos:exactMatch NCIT:C148316 Spinocerebellar Ataxia Type 36 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013600 insomnia skos:exactMatch NCIT:C28286 Insomnia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013626 psoriasis 14, pustular skos:exactMatch NCIT:C119057 Deficiency of the Interleukin-36 Receptor Antagonist semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013656 intellectual disability, autosomal dominant 9 skos:exactMatch NCIT:C133742 Mental Retardation, Autosomal Dominant 9 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013662 Barrett esophagus skos:exactMatch NCIT:C2891 Barrett Esophagus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013674 neurodegeneration with brain iron accumulation 4 skos:exactMatch NCIT:C175707 Neurodegeneration with Brain Iron Accumulation 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013681 alpha-methylacyl-CoA racemase deficiency skos:exactMatch NCIT:C119677 Alpha-Methylacyl-CoA Racemase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013688 linear and whorled nevoid hypermelanosis skos:exactMatch NCIT:C3924 Becker Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013700 pancreatic triacylglycerol lipase deficiency skos:exactMatch NCIT:C129030 Pancreatic Lipase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013730 graft versus host disease skos:exactMatch NCIT:C3063 Graft Versus Host Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013779 Wiskott-Aldrich syndrome 2 skos:exactMatch NCIT:C176820 Wiskott-Aldrich Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013785 intellectual disability, autosomal recessive 34 skos:exactMatch NCIT:C153179 Mental Retardation, Autosomal Recessive 34 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013808 Maffucci syndrome skos:exactMatch NCIT:C3213 Maffucci Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013824 Joubert syndrome 17 skos:exactMatch NCIT:C175702 Joubert Syndrome 17 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013829 UV-sensitive syndrome 2 skos:exactMatch NCIT:C173110 UV-Sensitive Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013834 UV-sensitive syndrome 3 skos:exactMatch NCIT:C173107 UV-Sensitive Syndrome 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013842 cortisone reductase deficiency 2 skos:exactMatch NCIT:C131084 11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013860 idiopathic membranous glomerulonephritis skos:exactMatch NCIT:C123060 Membranous Nephropathy - Idiopathic semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013867 Brown-Vialetto-van Laere syndrome 2 skos:exactMatch NCIT:C183529 Brown-Vialetto-Van Laere Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013869 adenine phosphoribosyltransferase deficiency skos:exactMatch NCIT:C121564 Adenine Phosphoribosyltransferase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013873 IMAGe syndrome skos:exactMatch NCIT:C130988 IMAGe Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013874 glucocorticoid deficiency 4 skos:exactMatch NCIT:C131452 Familial Glucocorticoid Deficiency Type 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013892 C3 glomerulonephritis skos:exactMatch NCIT:C123043 C3 Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013898 karyomegalic interstitial nephritis skos:exactMatch NCIT:C173626 Karyomegalic Interstitial Nephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013927 peroxisome biogenesis disorder 3A (Zellweger) skos:exactMatch NCIT:C155752 Peroxisome Biogenesis Disorder 3A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013930 peroxisome biogenesis disorder 4A (Zellweger) skos:exactMatch NCIT:C155754 Peroxisome Biogenesis Disorder 4A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013931 peroxisome biogenesis disorder 4B skos:exactMatch NCIT:C155755 Peroxisome Biogenesis Disorder 4B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013932 peroxisome biogenesis disorder 5A (Zellweger) skos:exactMatch NCIT:C155756 Peroxisome Biogenesis Disorder 5A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013933 peroxisome biogenesis disorder 5B skos:exactMatch NCIT:C155757 Peroxisome Biogenesis Disorder 5B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013936 peroxisome biogenesis disorder 6A (Zellweger) skos:exactMatch NCIT:C155758 Peroxisome Biogenesis Disorder 6A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013937 peroxisome biogenesis disorder 6B skos:exactMatch NCIT:C155759 Peroxisome Biogenesis Disorder 6B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013939 peroxisome biogenesis disorder 7B skos:exactMatch NCIT:C155761 Peroxisome Biogenesis Disorder 7B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013943 peroxisome biogenesis disorder 8B skos:exactMatch NCIT:C155763 Peroxisome Biogenesis Disorder 8B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013964 Diamond-Blackfan anemia 11 skos:exactMatch NCIT:C176920 Diamond-Blackfan Anemia 11 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0013992 obesity due to leptin receptor gene deficiency skos:exactMatch NCIT:C120386 Leptin Receptor Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014005 immunoglobulin-mediated membranoproliferative glomerulonephritis skos:exactMatch NCIT:C123055 Immune Complex Mediated Membranoproliferative Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014006 Schuurs-Hoeijmakers syndrome skos:exactMatch NCIT:C150555 Schuurs-Hoeijmakers Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014040 autosomal recessive osteopetrosis 8 skos:exactMatch NCIT:C150556 Autosomal Recessive Osteopetrosis 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014042 left ventricular noncompaction 7 skos:exactMatch NCIT:C157266 Left Ventricular Noncompaction 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014076 dyskeratosis congenita, autosomal recessive 5 skos:exactMatch NCIT:C176928 Dyskeratosis Congenita, Autosomal Recessive 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014138 nemaline myopathy 8 skos:exactMatch NCIT:C129871 Nemaline Myopathy 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014143 Noonan syndrome 8 skos:exactMatch NCIT:C176936 Noonan Syndrome 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014175 mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive skos:exactMatch NCIT:C129977 Mitochondrial DNA Depletion Syndrome 12 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014198 mitochondrial DNA depletion syndrome 13 skos:exactMatch NCIT:C172095 Mitochondrial DNA Depletion Syndrome 13 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014220 myopathy due to myoadenylate deaminase deficiency skos:exactMatch NCIT:C157504 Myopathy due to Myoadenylate Deaminase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014221 triosephosphate isomerase deficiency skos:exactMatch NCIT:C131652 Triosephosphate Isomerase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014244 hereditary sensory and autonomic neuropathy type 7 skos:exactMatch NCIT:C125388 Neuropathy, Hereditary Sensory and Autonomic, Type VII semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014247 familial episodic pain syndrome with predominantly lower limb involvement skos:exactMatch NCIT:C125390 Episodic Pain Syndrome, Familial, 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014292 leukoencephalopathy with mild cerebellar ataxia and white matter edema skos:exactMatch NCIT:C171603 Leukoencephalopathy with Ataxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014328 developmental and epileptic encephalopathy, 19 skos:exactMatch NCIT:C142802 Developmental and Epileptic Encephalopathy 19 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014367 Aicardi-Goutieres syndrome 7 skos:exactMatch NCIT:C168585 Aicardi-Goutieres Syndrome 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014378 primary ciliary dyskinesia 29 skos:exactMatch NCIT:C172393 Primary Ciliary Dyskinesia 29 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014448 hyperthyroxinemia, familial dysalbuminemic skos:exactMatch NCIT:C131813 Familial Dysalbuminemic Hyperthyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014449 congenital analbuminemia skos:exactMatch NCIT:C124851 Analbuminemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014452 familial dysfibrinogenemia skos:exactMatch NCIT:C131659 Dysfibrinogenemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014493 autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency skos:exactMatch NCIT:C126341 CTLA4 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014521 progressive myoclonic epilepsy type 7 skos:exactMatch NCIT:C142804 Epilepsy, Progressive Myoclonic 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014541 motor developmental delay due to 14q32.2 paternally expressed gene defect skos:exactMatch NCIT:C120409 Maternal Uniparental Disomy Chromosome 14 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014548 long QT syndrome 14 skos:exactMatch NCIT:C177534 Long QT Syndrome 14 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014600 dyskeratosis congenita, autosomal recessive 6 skos:exactMatch NCIT:C176929 Dyskeratosis Congenita, Autosomal Recessive 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014615 trichothiodystrophy 2, photosensitive skos:exactMatch NCIT:C173103 Trichothiodystrophy 2, Photosensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014619 trichothiodystrophy 3, photosensitive skos:exactMatch NCIT:C173099 Trichothiodystrophy 3, Photosensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014659 infantile liver failure syndrome 2 skos:exactMatch NCIT:C158135 Infantile Liver Failure Syndrome 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014690 dyskeratosis congenita, autosomal dominant 6 skos:exactMatch NCIT:C176924 Dyskeratosis Congenita, Autosomal Dominant 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014691 Noonan syndrome 9 skos:exactMatch NCIT:C176937 Noonan Syndrome 9 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014693 Noonan syndrome 10 skos:exactMatch NCIT:C176938 Noonan Syndrome 10 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014735 Charcot-Marie-Tooth disease type 2Y skos:exactMatch NCIT:C168974 Charcot-Marie-Tooth Disease Type 2Y semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014776 spinocerebellar ataxia type 42 skos:exactMatch NCIT:C171269 Spinocerebellar Ataxia Type 42 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014873 nevus comedonicus syndrome skos:exactMatch NCIT:C3946 Nevus Comedonicus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014888 MIRAGE syndrome skos:exactMatch NCIT:C147530 MIRAGE Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014900 autosomal recessive limb-girdle muscular dystrophy type 2Y skos:exactMatch NCIT:C181000 Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2Y semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014906 Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b; skos:exactMatch NCIT:C150647 Charcot-Marie-Tooth Disease Type 2A2B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0014977 autosomal recessive limb-girdle muscular dystrophy type 2R1 skos:exactMatch NCIT:C142082 Limb-Girdle Muscular Dystrophy Type 2Z semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015027 familial isolated hyperparathyroidism skos:exactMatch NCIT:C94830 Hereditary Isolated Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015028 48,XXYY syndrome skos:exactMatch NCIT:C89801 XXYY Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015031 extraneural perineurioma skos:exactMatch NCIT:C6912 Soft Tissue Perineurioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015032 intraneural perineurioma skos:exactMatch NCIT:C6911 Intraneural Perineurioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015040 myelodysplastic syndrome with excess blasts-1 skos:exactMatch NCIT:C7167 Myelodysplastic Syndrome with Excess Blasts-1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015041 myelodysplastic syndrome with excess blasts-2 skos:exactMatch NCIT:C7168 Myelodysplastic Syndrome/Acute Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015044 mu-heavy chain disease skos:exactMatch NCIT:C3892 Mu Heavy Chain Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015045 alpha-heavy chain disease skos:exactMatch NCIT:C3132 Alpha Heavy Chain Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015046 gamma-heavy chain disease skos:exactMatch NCIT:C3083 Gamma Heavy Chain Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015059 progressive non-fluent aphasia skos:exactMatch NCIT:C85025 Primary Progressive Nonfluent Aphasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015062 gastric neuroendocrine tumor, well differentiated, low or intermediate grade skos:exactMatch NCIT:C95871 Gastric Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015063 duodenal neuroendocrine tumor, well differentiated, low or intermediate grade skos:exactMatch NCIT:C135080 Duodenal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015064 jejunal neuroendocrine tumor, well differentiated, low or intermediate grade skos:exactMatch NCIT:C135090 Jejunal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015065 ileal neuroendocrine tumor, well differentiated, low or intermediate grade skos:exactMatch NCIT:C135092 Ileal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015066 neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade skos:exactMatch NCIT:C96422 Appendix Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015067 neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor skos:exactMatch NCIT:C135212 Colon Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015068 neuroendocrine tumor of rectum, well differentiated, low or intermediate grade skos:exactMatch NCIT:C135213 Rectal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015069 neuroendocrine tumor of the anal canal skos:exactMatch NCIT:C96540 Anal Canal Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015070 laryngeal neuroendocrine neoplasm skos:exactMatch NCIT:C6023 Laryngeal Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015072 liver neuroendocrine carcinoma skos:exactMatch NCIT:C96787 Liver Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015073 gallbladder neuroendocrine tumor, grade 1/2 skos:exactMatch NCIT:C96918 Gallbladder Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015074 thyroid tumor skos:exactMatch NCIT:C3414 Thyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015075 thyroid gland carcinoma skos:exactMatch NCIT:C4815 Thyroid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015104 porphyria cutanea tarda skos:exactMatch NCIT:C27725 Porphyria Cutanea Tarda semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015128 primary adrenal insufficiency skos:exactMatch NCIT:C113172 Primary Adrenal Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015129 chronic primary adrenal insufficiency skos:exactMatch NCIT:C26689 Addison's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015131 combined immunodeficiency skos:exactMatch NCIT:C27871 Congenital Combined Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015134 constitutional neutropenia skos:exactMatch NCIT:C61242 Congenital Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015137 periodic fever syndrome skos:exactMatch NCIT:C118240 Periodic Fever Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015167 amniotic band syndrome skos:exactMatch NCIT:C84552 Amniotic Band Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015183 short bowel syndrome skos:exactMatch NCIT:C99059 Short Bowel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015185 intestinal polyposis syndrome skos:exactMatch NCIT:C155954 Intestinal Polyposis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015193 hydrops fetalis skos:exactMatch NCIT:C84767 Hydrops Fetalis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015194 sideroblastic anemia skos:exactMatch NCIT:C36078 Sideroblastic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015200 anisakiasis skos:exactMatch NCIT:C128393 Anisakiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015228 pentasomy X skos:exactMatch NCIT:C89802 Penta X Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015229 Bardet-Biedl syndrome skos:exactMatch NCIT:C118632 Bardet-Biedl Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015231 Bartter syndrome skos:exactMatch NCIT:C34412 Bartter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015243 allergic bronchopulmonary aspergillosis skos:exactMatch NCIT:C84547 Allergic Bronchopulmonary Aspergillosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015247 opsoclonus-myoclonus syndrome skos:exactMatch NCIT:C4686 Opsoclonus Myoclonus Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015249 mitral atresia disorder skos:exactMatch NCIT:C98992 Mitral Valve Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015253 Diamond-Blackfan anemia skos:exactMatch NCIT:C61236 Congenital Pure Red Cell Aplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015254 schistosomiasis skos:exactMatch NCIT:C35000 Schistosomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015260 diphyllobothriasis skos:exactMatch NCIT:C128391 Diphyllobothriasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015263 Brugada syndrome skos:exactMatch NCIT:C142891 Brugada Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015264 cryptogenic organizing pneumonia skos:exactMatch NCIT:C62586 Cryptogenic Organizing Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015267 Feingold syndrome skos:exactMatch NCIT:C74987 Feingold Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015268 medullary sponge kidney skos:exactMatch NCIT:C34751 Medullary Sponge Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015277 medullary thyroid gland carcinoma skos:exactMatch NCIT:C3879 Thyroid Gland Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015278 familial pancreatic carcinoma skos:exactMatch NCIT:C43298 Hereditary Pancreatic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015279 chronic mucocutaneous candidiasis skos:exactMatch NCIT:C34444 Chronic Mucocutaneous Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015280 cardiofaciocutaneous syndrome skos:exactMatch NCIT:C84617 Cardiofaciocutaneous Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015285 Carney complex skos:exactMatch NCIT:C4705 Carney Complex semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015286 congenital disorder of glycosylation skos:exactMatch NCIT:C84615 Carbohydrate-Deficient Glycoprotein Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015288 herpes simplex virus keratitis skos:exactMatch NCIT:C34743 Dendritic Keratitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015294 nephrogenic systemic fibrosis skos:exactMatch NCIT:C84920 Nephrogenic Fibrosing Dermopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015304 arachnoiditis skos:exactMatch NCIT:C37913 Arachnoiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015328 obsolete rare bone development disorder skos:exactMatch NCIT:C34432 Bone Development Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015340 drug rash with eosinophilia and systemic symptoms skos:exactMatch NCIT:C112208 Drug Hypersensitivity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015342 acute transverse myelitis skos:exactMatch NCIT:C128378 Acute Transverse Myelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015347 multicentric reticulohistiocytosis skos:exactMatch NCIT:C27896 Multicentric Reticulohistiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015356 hereditary neoplastic syndrome skos:exactMatch NCIT:C3266 Hereditary Neoplastic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015364 hereditary sensory and autonomic neuropathy skos:exactMatch NCIT:C125386 Indifference to Pain, Congenital, Autosomal Recessive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015397 craniofacial microsomia skos:exactMatch NCIT:C84740 Goldenhar Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015403 non-involuting congenital hemangioma skos:exactMatch NCIT:C172208 Non-Involuting Congenital Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015404 rapidly involuting congenital hemangioma skos:exactMatch NCIT:C172207 Rapidly Involuting Congenital Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015411 facial cleft skos:exactMatch NCIT:C124510 Facial Cleft semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015426 Desbuquois dysplasia skos:exactMatch NCIT:C124056 Desbuquois Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015436 ring chromosome 20 skos:exactMatch NCIT:C169001 Ring Chromosome 20 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015439 ring chromosome 4 skos:exactMatch NCIT:C121983 ROSE Cluster 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015440 ring chromosome 6 skos:exactMatch NCIT:C121985 ROSE Cluster 6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015441 ring chromosome 7 skos:exactMatch NCIT:C121986 ROSE Cluster 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015443 chromosome 8-derived supernumerary ring/marker skos:exactMatch NCIT:C121988 ROSE Cluster 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015447 differentiated thyroid carcinoma skos:exactMatch NCIT:C7153 Differentiated Thyroid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015450 triatrial heart skos:exactMatch NCIT:C84651 Cor Triatriatum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015452 Coffin-Siris syndrome skos:exactMatch NCIT:C35321 Coffin-Siris Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015455 gonococcal conjunctivitis skos:exactMatch NCIT:C116816 Gonococcal Ophthalmia Neonatorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015459 nasopharyngeal carcinoma skos:exactMatch NCIT:C3871 Nasopharyngeal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015461 short rib-polydactyly syndrome skos:exactMatch NCIT:C85065 Short Rib-Polydactyly Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015469 craniosynostosis skos:exactMatch NCIT:C84655 Craniosynostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015474 cryptosporidiosis skos:exactMatch NCIT:C128408 Cryptosporidiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015484 cysticercosis skos:exactMatch NCIT:C34520 Cysticercosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015486 keratoconus skos:exactMatch NCIT:C26806 Keratoconus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015515 carnitine palmitoyltransferase II deficiency skos:exactMatch NCIT:C114766 Carnitine Palmitoyltransferase II Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015517 common variable immunodeficiency skos:exactMatch NCIT:C26725 Common Variable Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015523 epithelioid hemangioendothelioma skos:exactMatch NCIT:C3800 Epithelioid Hemangioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015524 hyperplastic polyposis syndrome skos:exactMatch NCIT:C165469 Colorectal Serrated Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015528 congenital epulis skos:exactMatch NCIT:C4675 Congenital Granular Cell Epulis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015530 trigeminal autonomic cephalalgia skos:exactMatch NCIT:C117074 Trigeminal Autonomic Cephalalgia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015534 juvenile xanthogranuloma skos:exactMatch NCIT:C3451 Juvenile Xanthogranuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015538 indeterminate dendritic cell tumor skos:exactMatch NCIT:C81767 Indeterminate Dendritic Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015540 hemophagocytic syndrome skos:exactMatch NCIT:C34792 Hemophagocytic Lymphohistiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015540 hemophagocytic syndrome skos:exactMatch NCIT:C35439 Hemophagocytic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015542 secondary hemophagocytic lymphohistiocytosis skos:exactMatch NCIT:C121184 Secondary Hemophagocytic Lymphohistiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015545 macrophage activation syndrome skos:exactMatch NCIT:C114471 Macrophage Activation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015564 Castleman disease skos:exactMatch NCIT:C3056 Castleman Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015573 subacute cutaneous lupus erythematosus skos:exactMatch NCIT:C117111 Subacute Cutaneous Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015589 paraneoplastic limbic encephalitis skos:exactMatch NCIT:C4350 Limbic Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015597 pustulosis palmaris et plantaris skos:exactMatch NCIT:C34888 Palmoplantar Pustulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015612 Dent disease skos:exactMatch NCIT:C123260 Dent Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015614 dermatitis herpetiformis skos:exactMatch NCIT:C26742 Dermatitis Herpetiformis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015626 Charcot-Marie-Tooth disease skos:exactMatch NCIT:C75467 Charcot-Marie-Tooth Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015628 von Willebrand disease type 2A skos:exactMatch NCIT:C131686 von Willebrand Disease, Type 2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015629 von Willebrand disease type 2B skos:exactMatch NCIT:C131687 von Willebrand Disease, Type 2B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015630 von Willebrand disease type 2M skos:exactMatch NCIT:C131688 von Willebrand Disease, Type 2M semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015631 von Willebrand disease type 2N skos:exactMatch NCIT:C131689 von Willebrand Disease, Type 2N semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015635 porokeratotic eccrine ostial and dermal duct nevus skos:exactMatch NCIT:C4740 Porokeratotic Eccrine Ostial and Dermal Duct Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015661 dextrocardia skos:exactMatch NCIT:C84669 Dextrocardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015663 diencephalic syndrome skos:exactMatch NCIT:C116955 Diencephalic Syndrome of Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015665 scleromyxedema skos:exactMatch NCIT:C85061 Scleromyxedema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015667 acute myeloid leukemia by FAB classification skos:exactMatch NCIT:C27753 Acute Myeloid Leukemia, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015681 childhood disintegrative disorder skos:exactMatch NCIT:C97164 Childhood Disintegrative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015686 primary peritoneal carcinoma skos:exactMatch NCIT:C40022 Primary Peritoneal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015687 chronic eosinophilic leukemia skos:exactMatch NCIT:C4563 Chronic Eosinophilic Leukemia, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015688 myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 skos:exactMatch NCIT:C84270 Myeloid/Lymphoid Neoplasms with Eosinophilia and Tyrosine Kinase Gene Fusions semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015689 myeloid neoplasm associated with PDGFRA rearrangement skos:exactMatch NCIT:C84275 Myeloid/Lymphoid Neoplasms with PDGFRA Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015690 myeloid neoplasm associated with PDGFRB rearrangement skos:exactMatch NCIT:C84276 Myeloid/Lymphoid Neoplasms with PDGFRB Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015691 hypereosinophilic syndrome skos:exactMatch NCIT:C27038 Idiopathic Hypereosinophilic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015692 refractory anemia with excess blasts in transformation skos:exactMatch NCIT:C27080 Refractory Anemia with Excess Blasts in Transformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015698 transient hypogammaglobulinemia of infancy skos:exactMatch NCIT:C27071 Transient Hypogammaglobulinemia of Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015713 idiopathic central precocious puberty skos:exactMatch NCIT:C120372 Idiopathic Central Precocious Puberty semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015725 mosaic trisomy 14 skos:exactMatch NCIT:C116319 Trisomy 14 Mosaicism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015733 low anorectal malformation skos:exactMatch NCIT:C98975 Low Anorectal Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015742 periventricular leukomalacia skos:exactMatch NCIT:C99013 Periventricular Leukomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015748 hereditary mucosal leukokeratosis skos:exactMatch NCIT:C84760 Hereditary Leukokeratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015759 B-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C3457 B-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015760 T-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C3466 T-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015762 progressive familial intrahepatic cholestasis skos:exactMatch NCIT:C84453 Progressive Familial Intrahepatic Cholestasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015766 cholera skos:exactMatch NCIT:C157812 Cholera semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015770 congenital hypogonadotropic hypogonadism skos:exactMatch NCIT:C120162 Congenital Hypogonadotropic Hypogonadism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015776 rhizomelic chondrodysplasia punctata skos:exactMatch NCIT:C85047 Rhizomelic Chondrodysplasia Punctata semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015779 45,X/46,XY mixed gonadal dysgenesis skos:exactMatch NCIT:C120199 45,X/46,XY Mixed Gonadal Dysgenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015780 dyskeratosis congenita skos:exactMatch NCIT:C111802 Dyskeratosis Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015792 transient congenital hypothyroidism skos:exactMatch NCIT:C113171 Transient Hypothyroxinemia of Prematurity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015796 acute lung injury skos:exactMatch NCIT:C155766 Acute Lung Injury semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015798 inflammatory myofibroblastic tumor skos:exactMatch NCIT:C6481 Inflammatory Myofibroblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015803 wound botulism skos:exactMatch NCIT:C128342 Wound Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015804 infant botulism skos:exactMatch NCIT:C128343 Infant Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015806 adult intestinal botulism skos:exactMatch NCIT:C128344 Adult Intestinal Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015808 folliculotropic mycosis fungoides skos:exactMatch NCIT:C35685 Folliculotropic Mycosis Fungoides semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015809 localized pagetoid reticulosis skos:exactMatch NCIT:C35794 Pagetoid Reticulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015813 primary cutaneous marginal zone B-cell lymphoma skos:exactMatch NCIT:C7230 Primary Cutaneous Marginal Zone Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015814 primary cutaneous follicle center lymphoma skos:exactMatch NCIT:C7217 Primary Cutaneous Follicle Center Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015863 polyembryoma skos:exactMatch NCIT:C66776 Gonadal Polyembryoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015864 mixed germ cell tumor skos:exactMatch NCIT:C4290 Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015867 vaginal carcinoma skos:exactMatch NCIT:C3917 Vaginal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015871 benign breast phyllodes tumor skos:exactMatch NCIT:C5196 Benign Breast Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015873 Paget disease of the nipple skos:exactMatch NCIT:C3301 Nipple Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015885 obsolete rare insulin-resistance syndrome skos:exactMatch NCIT:C113169 Insulin Resistance Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015892 growth hormone insensitivity syndrome skos:exactMatch NCIT:C129867 Growth Hormone Insensitivity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015903 hyperalphalipoproteinemia skos:exactMatch NCIT:C128806 Hyperalphalipoproteinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015909 aplastic anemia skos:exactMatch NCIT:C2870 Aplastic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015911 obsolete rare acquired hemolytic anemia skos:exactMatch NCIT:C34377 Acquired Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015912 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss skos:exactMatch NCIT:C131646 May-Hegglin Anomaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015912 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss skos:exactMatch NCIT:C158788 Macrothrombocytopenia and Granulocyte Inclusions with or without Nephritis or Sensorineural Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015925 interstitial lung disease skos:exactMatch NCIT:C164315 Interstitial Lung Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015926 pneumoconiosis skos:exactMatch NCIT:C26861 Pneumoconiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015943 eosinophilic granulomatosis with polyangiitis skos:exactMatch NCIT:C34481 Eosinophilic Granulomatosis with Polyangiitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015967 monogenic diabetes skos:exactMatch NCIT:C129739 Monogenic Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015974 severe combined immunodeficiency skos:exactMatch NCIT:C3472 Severe Combined Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015986 bilateral renal agenesis skos:exactMatch NCIT:C101219 Bilateral Renal Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015987 scimitar syndrome skos:exactMatch NCIT:C85056 Scimitar Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015988 multicystic dysplastic kidney skos:exactMatch NCIT:C123031 Multicystic Dysplastic Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015991 citrullinemia skos:exactMatch NCIT:C84639 Citrullinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015998 isolated ectopia lentis skos:exactMatch NCIT:C34566 Congenital Ectopic Lens semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0015999 primary pigmented nodular adrenocortical disease skos:exactMatch NCIT:C131196 Primary Pigmented Nodular Adrenal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016001 2-hydroxyglutaric aciduria skos:exactMatch NCIT:C128187 2-Hydroxyglutaric Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016002 Ehlers-Danlos syndrome, kyphoscoliotic type 1 skos:exactMatch NCIT:C125700 Ehlers-Danlos Syndrome, Type VI semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016004 aminopterin/methotrexate embryofetopathy skos:exactMatch NCIT:C98928 Fetal Methotrexate Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016006 Cockayne syndrome skos:exactMatch NCIT:C9460 Cockayne Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016008 fetal hydantoin syndrome skos:exactMatch NCIT:C98927 Fetal Hydantoin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016010 vitamin K-antagonist embryofetopathy skos:exactMatch NCIT:C98906 Fetal Warfarin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016011 fetal alcohol syndrome skos:exactMatch NCIT:C84713 Fetal Alcohol Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016012 diethylstilbestrol syndrome skos:exactMatch NCIT:C113422 Diethylstilbestrol Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016018 diabetic embryopathy skos:exactMatch NCIT:C113485 Diabetic Embryopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016019 Rasmussen subacute encephalitis skos:exactMatch NCIT:C125384 Rasmussen Subacute Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016022 early myoclonic encephalopathy skos:exactMatch NCIT:C116593 Early Myoclonic Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016027 benign neonatal seizures skos:exactMatch NCIT:C117307 Benign Familial Convulsion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016028 erythromelalgia skos:exactMatch NCIT:C34593 Erythromelalgia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016030 Evans syndrome skos:exactMatch NCIT:C61284 Evans Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016033 Cornelia de Lange syndrome skos:exactMatch NCIT:C75016 Cornelia De Lange Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016035 Nelson syndrome skos:exactMatch NCIT:C84917 Nelson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016037 superficial Fibromatosis skos:exactMatch NCIT:C6814 Superficial Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016038 calcified aponeurotic fibroma skos:exactMatch NCIT:C4818 Calcifying Aponeurotic Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016039 infantile digital fibromatosis skos:exactMatch NCIT:C3456 Inclusion Body Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016047 endophthalmitis skos:exactMatch NCIT:C34586 Endophthalmitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016060 laryngotracheoesophageal cleft skos:exactMatch NCIT:C98622 Larnygeotracheoesophageal Cleft semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016063 Cowden disease skos:exactMatch NCIT:C3076 Cowden Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016064 cleft palate skos:exactMatch NCIT:C87069 Cleft Palate semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016071 juvenile hyaline fibromatosis skos:exactMatch NCIT:C98297 Juvenile Hyaline Fibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016075 filariasis skos:exactMatch NCIT:C34611 Filariasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016085 Cole-Carpenter syndrome skos:exactMatch NCIT:C130985 Cole-Carpenter Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016093 borderline epithelial tumor of ovary skos:exactMatch NCIT:C4783 Borderline Ovarian Epithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016095 vaginal rhabdomyosarcoma skos:exactMatch NCIT:C128080 Vaginal Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016096 malignant non-dysgerminomatous germ cell tumor of ovary skos:exactMatch NCIT:C102870 Ovarian Non-Dysgerminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016103 isolated asymptomatic elevation of creatine phosphokinase skos:exactMatch NCIT:C148327 HyperCKmia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016104 obsolete infectious disease with peripheral neuropathy skos:exactMatch NCIT:C27589 Peripheral Nervous System Infectious Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016107 myotonic dystrophy skos:exactMatch NCIT:C84914 Myotonic Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016110 obsolete non-dystrophic myopathy skos:exactMatch NCIT:C122787 Non-Dystrophic Myotonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016129 eosinophilic gastroenteritis skos:exactMatch NCIT:C35330 Eosinophilic Gastroenteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016163 autosomal dominant cerebellar ataxia type II skos:exactMatch NCIT:C126562 Spinocerebellar Ataxia Type 7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016167 optic pathway glioma skos:exactMatch NCIT:C8567 Visual Pathway Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016168 cryopyrin-associated periodic syndrome skos:exactMatch NCIT:C84657 Cryopyrin-Associated Periodic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016175 cutis laxa skos:exactMatch NCIT:C84663 Cutis Laxa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016215 spastic quadriplegic cerebral palsy skos:exactMatch NCIT:C116904 Spastic Quadriplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016216 adult hepatocellular carcinoma skos:exactMatch NCIT:C7956 Adult Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016218 Guillain-Barre syndrome skos:exactMatch NCIT:C116345 Guillain-Barre Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016222 spindle cell hemangioma skos:exactMatch NCIT:C4754 Spindle Cell Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016236 kaposiform hemangioendothelioma skos:exactMatch NCIT:C27510 Kaposiform Hemangioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016238 solitary fibrous tumor skos:exactMatch NCIT:C7634 Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016239 cystinosis skos:exactMatch NCIT:C2976 Cystinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016240 hemimelia skos:exactMatch NCIT:C34674 Hemimelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016241 alternating hemiplegia of childhood skos:exactMatch NCIT:C35261 Congenital Adrenal Gland Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016242 hemoglobin C disease skos:exactMatch NCIT:C34675 Hemoglobin C Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016243 hemoglobin E disease skos:exactMatch NCIT:C35287 Hemoglobin E Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016244 atypical hemolytic-uremic syndrome skos:exactMatch NCIT:C123223 Atypical Hemolytic Uremic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016255 uterine corpus mixed epithelial and mesenchymal neoplasm skos:exactMatch NCIT:C40181 Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016258 uterine corpus carcinofibroma skos:exactMatch NCIT:C40182 Uterine Corpus Carcinofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016259 carcinosarcoma of the corpus uteri skos:exactMatch NCIT:C9180 Uterine Corpus Carcinosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016260 uterine corpus rhabdomyosarcoma skos:exactMatch NCIT:C127058 Uterine Corpus Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016262 leiomyosarcoma of the corpus uteri skos:exactMatch NCIT:C6340 Uterine Corpus Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016264 autoimmune hepatitis skos:exactMatch NCIT:C27029 Autoimmune Hepatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016281 46,XX ovotesticular disorder of sex development skos:exactMatch NCIT:C127167 Ovotesticular Differences of Sex Development semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016282 rhabdomyosarcoma of the cervix uteri skos:exactMatch NCIT:C128048 Cervical Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016283 leiomyosarcoma of the cervix uteri skos:exactMatch NCIT:C128047 Cervical Leiomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016295 neuronal ceroid lipofuscinosis skos:exactMatch NCIT:C61257 Neuronal Ceroid Lipofuscinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016296 holoprosencephaly skos:exactMatch NCIT:C74988 Holoprosencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016301 congenitally corrected transposition of the great arteries skos:exactMatch NCIT:C98902 Levo-Transposition of the Great Arteries semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016318 progressive multifocal leukoencephalopathy skos:exactMatch NCIT:C26815 Progressive Multifocal Leukoencephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016322 neuroendocrine cell hyperplasia of infancy skos:exactMatch NCIT:C120169 Neuroendocrine Cell Hyperplasia of Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016344 hydranencephaly skos:exactMatch NCIT:C98949 Hydranencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016349 congenital hydrocephalus skos:exactMatch NCIT:C98876 Congenital Hydrocephalus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016354 xeroderma pigmentosum-Cockayne syndrome complex skos:exactMatch NCIT:C156031 Xeroderma Pigmentosum-Cockayne Syndrome Complex semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016356 diffuse cutaneous systemic sclerosis skos:exactMatch NCIT:C116791 Diffuse Cutaneous Systemic Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016359 limited systemic sclerosis skos:exactMatch NCIT:C116789 Systemic Sclerosis without Skin Involvement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016362 attenuated familial adenomatous polyposis skos:exactMatch NCIT:C6729 Attenuated Familial Adenomatous Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016367 dermatomyositis skos:exactMatch NCIT:C26744 Dermatomyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016368 Rothmund-Thomson syndrome type 1 skos:exactMatch NCIT:C178826 Rothmund-Thomson Syndrome Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016369 Rothmund-Thomson syndrome type 2 skos:exactMatch NCIT:C178827 Rothmund-Thomson Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016383 nephrogenic diabetes insipidus skos:exactMatch NCIT:C84919 Nephrogenic Diabetes Insipidus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016391 neonatal diabetes mellitus skos:exactMatch NCIT:C99248 Neonatal Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016407 oligomeganephronia skos:exactMatch NCIT:C123202 Oligomeganephronia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016410 central congenital hypothyroidism skos:exactMatch NCIT:C113144 Central Hypothyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016419 hereditary breast carcinoma skos:exactMatch NCIT:C4503 Hereditary Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016440 elastofibroma dorsi skos:exactMatch NCIT:C4245 Elastofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016443 papular elastorrhexis skos:exactMatch NCIT:C4707 Eruptive Collagenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016453 foodborne botulism skos:exactMatch NCIT:C128341 Foodborne Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016463 syndromic agammaglobulinemia skos:exactMatch NCIT:C26931 Hypogammaglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016466 asbestosis skos:exactMatch NCIT:C84573 Asbestosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016467 isotretinoin syndrome skos:exactMatch NCIT:C98929 Fetal Retinoid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016471 pachyonychia congenita skos:exactMatch NCIT:C84986 Pachyonychia Congenita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016472 dracunculiasis skos:exactMatch NCIT:C84677 Dracunculiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016473 familial rhabdoid tumor skos:exactMatch NCIT:C93268 Rhabdoid Tumor Predisposition Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016474 drug-induced lupus erythematosus skos:exactMatch NCIT:C114354 Drug Induced Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016484 Usher syndrome type 2 skos:exactMatch NCIT:C126328 Usher Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016485 Usher syndrome type 3 skos:exactMatch NCIT:C126329 Usher Syndrome Type 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016486 beta-thalassemia major skos:exactMatch NCIT:C129699 Beta Thalassemia Major semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016489 delta-beta-thalassemia skos:exactMatch NCIT:C172823 Delta-Beta Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016505 aldosterone-producing adrenal cortex adenoma skos:exactMatch NCIT:C48451 Aldosterone-Producing Adrenal Cortical Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016512 Kabuki syndrome skos:exactMatch NCIT:C124837 Kabuki Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016516 Kenny-Caffey syndrome skos:exactMatch NCIT:C130991 Kenny-Caffey Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016525 familial hyperaldosteronism skos:exactMatch NCIT:C127160 Familial Hyperaldosteronism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016530 laryngocele skos:exactMatch NCIT:C97062 Laryngocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016532 Lennox-Gastaut syndrome skos:exactMatch NCIT:C84816 Lennox-Gastaut Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016535 hypohidrotic ectodermal dysplasia skos:exactMatch NCIT:C84562 Anhidrotic Ectodermal Dysplasia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016537 lymphoproliferative syndrome skos:exactMatch NCIT:C9308 Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016566 loiasis skos:exactMatch NCIT:C34784 Loiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016575 primary ciliary dyskinesia skos:exactMatch NCIT:C84797 Kartagener Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016576 split hand-foot malformation skos:exactMatch NCIT:C75000 Ectrodactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016580 congenital pulmonary airway malformation skos:exactMatch NCIT:C98892 Congenital Cystic Adenomatoid Malformation of the Lung semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016586 systemic mastocytosis skos:exactMatch NCIT:C9235 Systemic Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016587 arrhythmogenic right ventricular cardiomyopathy skos:exactMatch NCIT:C84571 Arrhythmogenic Right Ventricular Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016603 citrullinemia type II skos:exactMatch NCIT:C150603 Citrullinemia Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016607 odontohypophosphatasia skos:exactMatch NCIT:C131309 Odontohypophosphatasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016611 lipoblastoma skos:exactMatch NCIT:C27483 Lipoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016619 autosomal recessive hypohidrotic ectodermal dysplasia skos:exactMatch NCIT:C84580 Autosomal Recessive Hypohidrotic Ectodermal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016620 primary hypertrophic osteoarthropathy skos:exactMatch NCIT:C85023 Primary Hypertrophic Osteoarthropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016621 juvenile Huntington disease skos:exactMatch NCIT:C147072 Juvenile Huntington Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016642 meningioma skos:exactMatch NCIT:C3230 Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016654 ring chromosome 5 skos:exactMatch NCIT:C121984 ROSE Cluster 5 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016664 drug-induced vasculitis skos:exactMatch NCIT:C112204 Drug Induced Cutaneous Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016668 sickle cell-beta-thalassemia disease syndrome skos:exactMatch NCIT:C95539 Sickle Beta Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016680 high grade astrocytic tumor skos:exactMatch NCIT:C102897 High Grade Astrocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016681 gliosarcoma skos:exactMatch NCIT:C3796 Gliosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016682 giant cell glioblastoma skos:exactMatch NCIT:C4325 Giant Cell Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016683 gliomatosis cerebri skos:exactMatch NCIT:C4318 Gliomatosis Cerebri semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016684 anaplastic astrocytoma skos:exactMatch NCIT:C9477 Anaplastic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016686 diffuse astrocytoma skos:exactMatch NCIT:C7173 Diffuse Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016687 protoplasmic astrocytoma skos:exactMatch NCIT:C4320 Protoplasmic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016688 fibrillary astrocytoma skos:exactMatch NCIT:C4322 Fibrillary Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016689 gemistocytic astrocytoma skos:exactMatch NCIT:C4321 Gemistocytic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016690 pleomorphic xanthoastrocytoma skos:exactMatch NCIT:C4323 Pleomorphic Xanthoastrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016691 pilocytic astrocytoma skos:exactMatch NCIT:C4047 Pilocytic Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016692 pilomyxoid astrocytoma skos:exactMatch NCIT:C40315 Pilomyxoid Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016693 subependymal giant cell astrocytoma skos:exactMatch NCIT:C3696 Subependymal Giant Cell Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016695 oligodendroglioma skos:exactMatch NCIT:C3288 Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016696 anaplastic oligodendroglioma skos:exactMatch NCIT:C4326 Anaplastic Oligodendroglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016698 ependymoma skos:exactMatch NCIT:C3017 Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016699 myxopapillary ependymoma skos:exactMatch NCIT:C3697 Myxopapillary Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016700 anaplastic ependymoma skos:exactMatch NCIT:C4049 Anaplastic Ependymoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016702 oligoastrocytoma skos:exactMatch NCIT:C4050 Oligoastrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016703 anaplastic oligoastrocytoma skos:exactMatch NCIT:C6959 Anaplastic Oligoastrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016705 angiocentric glioma skos:exactMatch NCIT:C92552 Angiocentric Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016706 chordoid glioma of the third ventricle skos:exactMatch NCIT:C5592 Chordoid Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016707 astroblastoma skos:exactMatch NCIT:C4324 Astroblastoma, MN1-Altered semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016709 anaplastic/large cell medulloblastoma skos:exactMatch NCIT:C129436 Large Cell/Anaplastic Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016710 medulloblastoma with extensive nodularity skos:exactMatch NCIT:C5407 Medulloblastoma with Extensive Nodularity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016711 desmoplastic/nodular medulloblastoma skos:exactMatch NCIT:C4956 Desmoplastic/Nodular Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016712 classic medulloblastoma skos:exactMatch NCIT:C54039 Classic Medulloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016713 central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor skos:exactMatch NCIT:C129537 Central Nervous System Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016715 ependymoblastoma skos:exactMatch NCIT:C4915 Embryonal Tumor with Multilayered Rosettes, C19MC-Altered semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016717 choroid plexus neoplasm skos:exactMatch NCIT:C3473 Choroid Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016718 choroid plexus carcinoma skos:exactMatch NCIT:C4715 Choroid Plexus Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016722 pineoblastoma skos:exactMatch NCIT:C9344 Pineoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016723 pineocytoma skos:exactMatch NCIT:C6966 Pineocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016724 papillary tumor of the pineal region skos:exactMatch NCIT:C92624 Papillary Tumor of the Pineal Region semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016727 extraventricular neurocytoma skos:exactMatch NCIT:C92555 Extraventricular Neurocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016729 mixed neuronal-glial tumor skos:exactMatch NCIT:C4747 Glioneuronal and Neuronal Tumors semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016730 gangliocytoma skos:exactMatch NCIT:C6934 Gangliocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016733 ganglioglioma skos:exactMatch NCIT:C3788 Ganglioglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016734 anaplastic ganglioglioma skos:exactMatch NCIT:C4717 Anaplastic Ganglioglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016735 papillary glioneuronal tumor skos:exactMatch NCIT:C92554 Papillary Glioneuronal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016736 rosette-forming glioneuronal tumor of fourth ventricule skos:exactMatch NCIT:C129431 Rosette-Forming Glioneuronal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016739 yolk sac tumor of central nervous system skos:exactMatch NCIT:C7011 Central Nervous System Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016740 choriocarcinoma of the central nervous system skos:exactMatch NCIT:C7012 Central Nervous System Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016742 mixed germ cell tumor of central nervous system skos:exactMatch NCIT:C7016 Central Nervous System Mixed Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016743 tumor of meninges skos:exactMatch NCIT:C3229 Meningeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016746 meningeal melanocytoma skos:exactMatch NCIT:C4662 Meningeal Melanocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016747 primary melanoma of the central nervous system skos:exactMatch NCIT:C5505 Central Nervous System Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016748 hemangioblastoma skos:exactMatch NCIT:C3801 Hemangioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016751 malignant perineurioma skos:exactMatch NCIT:C66845 Malignant Peripheral Nerve Sheath Tumor with Perineurial Differentiation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016755 neurofibroma skos:exactMatch NCIT:C3272 Neurofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016757 malignant triton tumor skos:exactMatch NCIT:C4335 Malignant Triton Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016759 pontocerebellar hypoplasia type 2 skos:exactMatch NCIT:C124057 Pontocerebellar Hypoplasia Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016773 atrophic lichen planus skos:exactMatch NCIT:C34777 Atrophic Lichen Planus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016778 iatrogenic botulism skos:exactMatch NCIT:C128345 Iatrogenic Botulism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016785 complete hydatidiform mole skos:exactMatch NCIT:C4871 Complete Hydatidiform Mole semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016786 partial hydatidiform mole skos:exactMatch NCIT:C4293 Partial Hydatidiform Mole semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016787 epithelioid trophoblastic tumor skos:exactMatch NCIT:C6900 Epithelioid Trophoblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016812 dopa-responsive dystonia skos:exactMatch NCIT:C116719 Dopa-Responsive Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016820 Moyamoya disease skos:exactMatch NCIT:C84895 Moyamoya Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016823 mycetoma skos:exactMatch NCIT:C85505 Mycetoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016824 infantile myofibromatosis skos:exactMatch NCIT:C3742 Myofibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016830 Emery-Dreifuss muscular dystrophy skos:exactMatch NCIT:C84685 Emery-Dreifuss Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016971 limb-girdle muscular dystrophy skos:exactMatch NCIT:C84828 Limb-Girdle Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016974 thymoma type B skos:exactMatch NCIT:C7114 Thymoma Type B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016975 thymoma type AB skos:exactMatch NCIT:C6885 Thymoma Type AB semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016982 angiosarcoma skos:exactMatch NCIT:C3088 Angiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016984 nevus of Ota skos:exactMatch NCIT:C7583 Nevus of Ota semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016985 nevus of Ito skos:exactMatch NCIT:C7582 Nevus of Ito semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016987 neuroacanthocytosis skos:exactMatch NCIT:C84926 Neuroacanthocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016990 acquired prothrombin deficiency skos:exactMatch NCIT:C131622 Acquired Factor II Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017025 Langerhans cell histiocytosis specific to childhood skos:exactMatch NCIT:C114483 Childhood Langerhans Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017029 Langerhans cell histiocytosis specific to adulthood skos:exactMatch NCIT:C114929 Adult Langerhans Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017042 thanatophoric dysplasia skos:exactMatch NCIT:C85187 Thanatophoric Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017043 congenital mesoblastic nephroma skos:exactMatch NCIT:C6569 Congenital Mesoblastic Nephroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017048 pseudomyxoma peritonei skos:exactMatch NCIT:C3345 Pseudomyxoma Peritonei semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017050 intraocular medulloepithelioma skos:exactMatch NCIT:C66806 Ciliary Body Medulloepithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017069 spina bifida cystica skos:exactMatch NCIT:C101201 Myelomeningocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017078 cephalocele skos:exactMatch NCIT:C84687 Encephalocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017079 meningoencephalocele skos:exactMatch NCIT:C124517 Cranial Meningocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017094 cerebral cortical dysplasia skos:exactMatch NCIT:C42088 Cortical Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017124 noma skos:exactMatch NCIT:C34852 Gangrenous Stomatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017137 onchocerciasis skos:exactMatch NCIT:C34861 Onchocerciasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017138 Opitz G/BBB syndrome skos:exactMatch NCIT:C125487 Opitz G/BBB Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017148 heritable pulmonary arterial hypertension skos:exactMatch NCIT:C121945 Heritable Pulmonary Arterial Hypertension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017169 multiple endocrine neoplasia skos:exactMatch NCIT:C6432 Multiple Endocrine Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017178 osteochondritis dissecans skos:exactMatch NCIT:C34878 Osteochondritis Dissecans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017182 familial hyperinsulinism skos:exactMatch NCIT:C131425 Congenital Hyperinsulinism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017194 Blount disease skos:exactMatch NCIT:C118460 Blount's Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017198 osteopetrosis skos:exactMatch NCIT:C26840 Osteopetrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017207 primary organ-specific lymphoma skos:exactMatch NCIT:C7185 Lymphoma by Site semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017215 calciphylaxis skos:exactMatch NCIT:C84607 Calciphylaxis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017236 rapidly progressive glomerulonephritis skos:exactMatch NCIT:C35264 Rapidly Progressive Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017255 panuveitis skos:exactMatch NCIT:C84989 Panuveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017276 frontotemporal dementia skos:exactMatch NCIT:C84719 Frontotemporal Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017278 autoimmune polyendocrinopathy skos:exactMatch NCIT:C129726 Autoimmune Polyglandular Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017278 autoimmune polyendocrinopathy skos:exactMatch NCIT:C84576 Autoimmune Polyendocrinopathy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017285 penoscrotal transposition skos:exactMatch NCIT:C99010 Penoscrotal Transposition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017286 tempi syndrome skos:exactMatch NCIT:C121656 TEMPI Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017287 IgG4-related disease skos:exactMatch NCIT:C95992 IgG4-Related Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017292 well-differentiated fetal adenocarcinoma of the lung skos:exactMatch NCIT:C45509 Lung Fetal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017308 obsolete Marfan syndrome type 2 skos:exactMatch NCIT:C75007 Marfan Syndrome Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017314 Ehlers-Danlos syndrome, vascular type skos:exactMatch NCIT:C125699 Ehlers-Danlos Syndrome, Type IV semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017319 hereditary elliptocytosis skos:exactMatch NCIT:C35882 Hereditary Elliptocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017320 phosphoenolpyruvate carboxykinase deficiency skos:exactMatch NCIT:C99015 Phosphoenolpyruvate Carboxykinase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017323 hypocalcemic rickets skos:exactMatch NCIT:C131421 Calcium Deficiency Rickets semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017326 infective dermatitis associated with HTLV-1 skos:exactMatch NCIT:C129260 IDH Gene Family semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017340 juvenile nasopharyngeal angiofibroma skos:exactMatch NCIT:C27479 Sinonasal Tract Angiofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017346 Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly skos:exactMatch NCIT:C80281 EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017347 plasmablastic lymphoma skos:exactMatch NCIT:C7224 Plasmablastic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017349 myopericytoma skos:exactMatch NCIT:C50401 Myopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017359 3-methylglutaconic aciduria skos:exactMatch NCIT:C98678 3-Methylglutaconic Aciduria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017361 congenital rubella syndrome skos:exactMatch NCIT:C34992 Congenital Rubella semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017364 POEMS syndrome skos:exactMatch NCIT:C80303 POEMS Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017372 congenital varicella syndrome skos:exactMatch NCIT:C116800 Congenital Varicella Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017373 poliomyelitis skos:exactMatch NCIT:C35550 Acute Poliomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017376 reactive arthritis skos:exactMatch NCIT:C128332 Reactive Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017380 juvenile polyposis syndrome skos:exactMatch NCIT:C7754 Juvenile Polyposis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017384 acute generalized exanthematous pustulosis skos:exactMatch NCIT:C112122 Acute Generalized Exanthematous Pustulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017385 malignant migrating partial seizures of infancy skos:exactMatch NCIT:C125387 Migrating Partial Seizures in Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017386 pleomorphic rhabdomyosarcoma skos:exactMatch NCIT:C4258 Pleomorphic Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017387 epithelioid sarcoma skos:exactMatch NCIT:C3714 Epithelioid Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017408 rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome skos:exactMatch NCIT:C121944 Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017409 fetal cytomegalovirus syndrome skos:exactMatch NCIT:C122427 Congenital Cytomegaloviral Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017419 non-syndromic amelia skos:exactMatch NCIT:C34370 Amelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017435 popliteal pterygium syndrome skos:exactMatch NCIT:C118786 Autosomal Dominant Popliteal Pterygium Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017441 congenital absence of upper arm and forearm with hand present skos:exactMatch NCIT:C34928 Phocomelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017462 congenital pseudoarthrosis of the tibia skos:exactMatch NCIT:C132080 Congenital Pseudarthrosis of Tibia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017560 congenital genu recurvatum skos:exactMatch NCIT:C103184 Genu Recurvatum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017570 leukocyte adhesion deficiency skos:exactMatch NCIT:C27874 Leukocyte Adhesion Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017571 Proteus-like syndrome skos:exactMatch NCIT:C179930 Proteus-Like Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017572 tick-borne encephalitis skos:exactMatch NCIT:C34579 Tick-Borne Viral Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017575 mitochondrial neurogastrointestinal encephalomyopathy skos:exactMatch NCIT:C119678 Mitochondrial Neurogastrointestinal Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017576 46,XX disorder of sex development skos:exactMatch NCIT:C127169 46,XX Differences of Sex Development semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017582 pituitary adenocarcinoma skos:exactMatch NCIT:C4536 Metastatic Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017590 carcinoma of the ampulla of vater skos:exactMatch NCIT:C3908 Ampulla of Vater Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017594 indolent B-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C171299 Indolent B-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017595 aggressive B-cell non-Hodgkin lymphoma skos:exactMatch NCIT:C178541 Aggressive B-Cell Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017596 diffuse large B-cell lymphoma of the central nervous system skos:exactMatch NCIT:C71720 Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017597 T-cell/histiocyte rich large B cell lymphoma skos:exactMatch NCIT:C9496 T-Cell/Histiocyte-Rich Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017598 primary cutaneous anaplastic large cell lymphoma skos:exactMatch NCIT:C6860 Primary Cutaneous Anaplastic Large Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017599 splenic diffuse red pulp small B-cell lymphoma skos:exactMatch NCIT:C80309 Splenic Diffuse Red Pulp Small B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017600 hairy cell leukemia variant skos:exactMatch NCIT:C7401 Hairy Cell Leukemia Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017602 ALK-positive anaplastic large cell lymphoma skos:exactMatch NCIT:C37193 Anaplastic Large Cell Lymphoma, ALK-Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017603 ALK-negative anaplastic large cell lymphoma skos:exactMatch NCIT:C37194 Anaplastic Large Cell Lymphoma, ALK-Negative semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017604 marginal zone lymphoma skos:exactMatch NCIT:C4341 Marginal Zone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017607 caudal regression sequence skos:exactMatch NCIT:C124505 Caudal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017610 epidermolysis bullosa simplex skos:exactMatch NCIT:C84692 Epidermolysis Bullosa Simplex semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017611 pituitary tumor skos:exactMatch NCIT:C3330 Pituitary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017612 junctional epidermolysis bullosa skos:exactMatch NCIT:C90598 Junctional Epidermolysis Bullosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017623 PTEN hamartoma tumor syndrome skos:exactMatch NCIT:C179915 PTEN Hamartoma Tumor Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017648 Sydenham chorea skos:exactMatch NCIT:C168445 Sydenham Chorea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017767 rheumatic fever skos:exactMatch NCIT:C34984 Rheumatic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017768 reflex epilepsy skos:exactMatch NCIT:C85041 Reflex Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017771 Mayer-Rokitansky-Kuster-Hauser syndrome skos:exactMatch NCIT:C124853 Mayer-Rokitansky-Kuster-Hauser Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017773 hypoalphalipoproteinemia skos:exactMatch NCIT:C84774 Hypoalphalipoproteinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017775 melioidosis skos:exactMatch NCIT:C128336 Melioidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017776 nocardiosis skos:exactMatch NCIT:C171147 Nocardiosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017778 lamellar ichthyosis skos:exactMatch NCIT:C84805 Lamellar Ichthyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017790 gastric adenocarcinoma and proximal polyposis of the stomach skos:exactMatch NCIT:C172989 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017795 ameloblastoma skos:exactMatch NCIT:C4313 Ameloblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017799 Meigs syndrome skos:exactMatch NCIT:C3223 Meigs Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017807 growing teratoma syndrome skos:exactMatch NCIT:C118370 Growing Teratoma Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017814 primary bone lymphoma skos:exactMatch NCIT:C6620 Primary Bone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017816 primary systemic amyloidosis skos:exactMatch NCIT:C8299 Primary Systemic Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017827 malignant peripheral nerve sheath tumor skos:exactMatch NCIT:C3798 Malignant Peripheral Nerve Sheath Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017838 sclerosteosis skos:exactMatch NCIT:C131133 Sclerosteosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017842 Senior-Loken syndrome skos:exactMatch NCIT:C168588 Senior-Loken Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017843 congenital pulmonary sequestration skos:exactMatch NCIT:C97124 Bronchopulmonary Sequestration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017844 Sezary syndrome skos:exactMatch NCIT:C3366 Sezary Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017850 sirenomelia skos:exactMatch NCIT:C118455 Sirenomelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017851 erythrokeratodermia variabilis skos:exactMatch NCIT:C84696 Erythrokeratodermia Variabilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017853 hypersensitivity pneumonitis skos:exactMatch NCIT:C34369 Extrinsic Allergic Alveolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017858 acute erythroid leukemia skos:exactMatch NCIT:C8923 Acute Erythroid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017879 hantavirus pulmonary syndrome skos:exactMatch NCIT:C84747 Hantavirus Pulmonary Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017880 Rift valley fever skos:exactMatch NCIT:C128419 Rift Valley Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017884 papillary renal cell carcinoma skos:exactMatch NCIT:C6975 Papillary Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017885 chromophobe renal cell carcinoma skos:exactMatch NCIT:C4146 Chromophobe Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017887 renal cell carcinoma associated with neuroblastoma skos:exactMatch NCIT:C100051 Renal Cell Carcinoma Associated with Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017890 tubulocystic renal cell carcinoma skos:exactMatch NCIT:C126303 Tubulocystic Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017894 acute myeloid leukemia with CEBPA somatic mutations skos:exactMatch NCIT:C82433 Acute Myeloid Leukemia with CEBPA Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017895 familial papillary or follicular thyroid carcinoma skos:exactMatch NCIT:C118829 Hereditary Nonmedullary Thyroid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017909 inherited glutathione synthetase deficiency skos:exactMatch NCIT:C128193 Glutathione Synthetase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017919 exstrophy-epispadias complex skos:exactMatch NCIT:C99142 OEIS Complex semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017941 chikungunya skos:exactMatch NCIT:C128422 Chikungunya semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017979 autoimmune lymphoproliferative syndrome skos:exactMatch NCIT:C37864 Autoimmune Lymphoproliferative Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017987 syringomyelia skos:exactMatch NCIT:C85179 Syringomyelia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017989 His bundle tachycardia skos:exactMatch NCIT:C111646 Junctional Ectopic Tachycardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017991 Takayasu arteritis skos:exactMatch NCIT:C34391 Aortic Arch Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0017991 Takayasu arteritis skos:exactMatch NCIT:C35062 Takayasu Arteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018017 goblet cell carcinoma skos:exactMatch NCIT:C3689 Appendix Goblet Cell Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018024 hydroa vacciniforme skos:exactMatch NCIT:C84766 Hydroa Vacciniforme semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018029 congenital factor XIII deficiency skos:exactMatch NCIT:C131633 Factor XIII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018031 granulomatous slack skin disease skos:exactMatch NCIT:C35464 Granulomatous Slack Skin Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018034 thalidomide embryopathy skos:exactMatch NCIT:C99082 Thalidomide Embryopathy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018037 hyper-IgE syndrome skos:exactMatch NCIT:C3144 Hyperimmunoglobulin E Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018044 idiopathic hypersomnia skos:exactMatch NCIT:C116343 Idiopathic Hypersomnia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018053 trichothiodystrophy skos:exactMatch NCIT:C4924 Trichothiodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018055 pediatric hepatocellular carcinoma skos:exactMatch NCIT:C7955 Childhood Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018056 bullous lichen planus skos:exactMatch NCIT:C34778 Bullous Lichen Planus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018058 tracheal agenesis skos:exactMatch NCIT:C35376 Tracheal Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018066 trisomy X skos:exactMatch NCIT:C129718 47,XXX Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018067 triploidy skos:exactMatch NCIT:C85204 Triploidy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018068 trisomy 13 skos:exactMatch NCIT:C101223 Complete Trisomy 13 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018072 persistent truncus arteriosus skos:exactMatch NCIT:C98880 Persistent Truncus Arteriosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018075 neural tube defect skos:exactMatch NCIT:C84923 Neural Tube Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018076 tuberculosis skos:exactMatch NCIT:C3423 Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018077 tularemia skos:exactMatch NCIT:C85208 Tularemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018078 soft tissue sarcoma skos:exactMatch NCIT:C9306 Soft Tissue Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018079 thymic epithelial neoplasm skos:exactMatch NCIT:C6450 Thymic Epithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018087 viral hemorrhagic fever skos:exactMatch NCIT:C36170 Viral Hemorrhagic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018088 familial Mediterranean fever skos:exactMatch NCIT:C84707 Familial Mediterranean Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018089 double outlet right ventricle skos:exactMatch NCIT:C98916 Double Outlet Right Ventricle semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018092 Vogt-Koyanagi-Harada disease skos:exactMatch NCIT:C85218 Uveomeningoencephalitic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018094 Waardenburg syndrome skos:exactMatch NCIT:C85222 Waardenburg Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018096 Weill-Marchesani syndrome skos:exactMatch NCIT:C85226 Weill-Marchesani Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018097 West syndrome skos:exactMatch NCIT:C84788 West Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018100 familial primary hypomagnesemia skos:exactMatch NCIT:C123263 Familial Primary Hypomagnesemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018102 corneal dystrophy skos:exactMatch NCIT:C34513 Corneal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018105 Wolfram syndrome skos:exactMatch NCIT:C35133 Wolfram Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018116 galactosemia skos:exactMatch NCIT:C84723 Galactosemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018124 Oncogenic osteomalacia skos:exactMatch NCIT:C67235 Oncogenic Osteomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018149 GM1 gangliosidosis skos:exactMatch NCIT:C84739 GM1 Gangliosidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018150 Gaucher disease skos:exactMatch NCIT:C61268 Gaucher Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018151 coenzyme Q10 deficiency skos:exactMatch NCIT:C142083 Coenzyme Q10 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018153 Erdheim-Chester disease skos:exactMatch NCIT:C53972 Erdheim-Chester Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018155 lateral sclerosis skos:exactMatch NCIT:C129933 Primary Lateral Sclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018160 hereditary retinoblastoma skos:exactMatch NCIT:C8495 Hereditary Retinoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018166 oral submucous fibrosis skos:exactMatch NCIT:C34866 Oral Cavity Submucous Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018170 idiopathic nephrotic syndrome skos:exactMatch NCIT:C122796 Idiopathic Nephrotic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018171 malignant germ cell tumor of ovary skos:exactMatch NCIT:C4514 Malignant Ovarian Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018172 malignant sex cord stromal tumor of ovary skos:exactMatch NCIT:C8053 Malignant Ovarian Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018177 glioblastoma skos:exactMatch NCIT:C3058 Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018181 staphylococcal scalded skin syndrome skos:exactMatch NCIT:C85077 Staphylococcal Scalded Skin Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018184 gastric linitis plastica skos:exactMatch NCIT:C3190 Linitis Plastica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018193 testicular teratoma skos:exactMatch NCIT:C3877 Testicular Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018201 extragonadal germ cell tumor skos:exactMatch NCIT:C3918 Extragonadal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018214 generalized epilepsy with febrile seizures plus skos:exactMatch NCIT:C122811 Generalized Epilepsy with Febrile Seizures Plus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018221 immune hydrops fetalis skos:exactMatch NCIT:C111904 Immune Hydrops Fetalis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018223 systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood skos:exactMatch NCIT:C80374 Systemic EBV-Positive T-Cell Lymphoma of Childhood semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018224 hydroa vacciniforme-like lymphoma skos:exactMatch NCIT:C45327 Hydroa Vacciniforme Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018225 ALK-positive large B-cell lymphoma skos:exactMatch NCIT:C7225 ALK-Positive Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018229 Stevens-Johnson syndrome skos:exactMatch NCIT:C79484 Stevens-Johnson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018234 dysostosis skos:exactMatch NCIT:C34560 Dysostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018237 acrofacial dysostosis skos:exactMatch NCIT:C35795 Acrofacial Dysostosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018251 obsolete glycogen storage disease due to phosphorylase kinase deficiency skos:exactMatch NCIT:C122662 Glycogen Storage Disease Type IX semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018270 extraskeletal Ewing sarcoma skos:exactMatch NCIT:C7135 Extraskeletal Ewing Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018271 peripheral primitive neuroectodermal tumor skos:exactMatch NCIT:C9341 Peripheral Primitive Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018301 interstitial cystitis skos:exactMatch NCIT:C27189 Interstitial Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018305 chronic granulomatous disease skos:exactMatch NCIT:C26788 Chronic Granulomatous Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018308 liver mesenchymal hamartoma skos:exactMatch NCIT:C5751 Liver Mesenchymal Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018309 Hirschsprung disease skos:exactMatch NCIT:C34700 Hirschsprung Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018310 Langerhans cell histiocytosis skos:exactMatch NCIT:C3107 Langerhans Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018312 histoplasmosis skos:exactMatch NCIT:C77201 Histoplasmosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018326 transient neonatal myasthenia gravis skos:exactMatch NCIT:C117308 Transient Neonatal Myasthenia Gravis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018327 glomus tumor skos:exactMatch NCIT:C3060 Glomus Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018330 mucinous adenocarcinoma of the appendix skos:exactMatch NCIT:C43558 Appendix Mucinous Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018352 squamous cell carcinoma of penis skos:exactMatch NCIT:C7729 Penile Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018360 neonatal lupus erythematosus skos:exactMatch NCIT:C99236 Neonatal Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018364 malignant epithelial tumor of ovary skos:exactMatch NCIT:C40026 Malignant Ovarian Epithelial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018368 primary peritoneal serous/papillary carcinoma skos:exactMatch NCIT:C7695 Primary Peritoneal Serous Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018369 immature ovarian teratoma skos:exactMatch NCIT:C8111 Immature Ovarian Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018373 avascular necrosis skos:exactMatch NCIT:C34841 Avascular Necrosis of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018378 osteonecrosis of the jaw skos:exactMatch NCIT:C63924 Osteonecrosis of Jaw semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018381 osteochondrosis skos:exactMatch NCIT:C34879 Osteochondrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018439 eosinophilic colitis skos:exactMatch NCIT:C27053 Eosinophilic Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018447 chondromyxoid fibroma skos:exactMatch NCIT:C3830 Chondromyxoid Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018449 acquired cystic disease-associated renal cell carcinoma skos:exactMatch NCIT:C157718 Acquired Cystic Disease-Associated Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018453 familial atypical multiple mole melanoma syndrome skos:exactMatch NCIT:C27264 Hereditary Atypical Mole Melanoma Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018458 familial hypocalciuric hypercalcemia skos:exactMatch NCIT:C123262 Familial Hypocalciuric Hypercalcemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018470 renal agenesis skos:exactMatch NCIT:C99041 Renal Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018477 bilirubin encephalopathy skos:exactMatch NCIT:C84799 Kernicterus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018479 congenital adrenal hyperplasia skos:exactMatch NCIT:C34360 Congenital Adrenal Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018481 undifferentiated carcinoma of esophagus skos:exactMatch NCIT:C27422 Esophageal Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018492 hereditary clear cell renal cell carcinoma skos:exactMatch NCIT:C36260 Hereditary Clear Cell Renal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018493 malignant hyperthermia of anesthesia skos:exactMatch NCIT:C84869 Malignant Hyperthermia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018504 undifferentiated carcinoma of stomach skos:exactMatch NCIT:C5476 Gastric Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018509 squamous cell carcinoma of the small intestine skos:exactMatch NCIT:C43534 Small Intestinal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018510 small intestine neuroendocrine neoplasm skos:exactMatch NCIT:C5803 Small Intestinal Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018513 squamous cell carcinoma of colon skos:exactMatch NCIT:C5490 Colon Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018515 squamous cell carcinoma of rectum skos:exactMatch NCIT:C5554 Rectal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018521 squamous cell carcinoma of pancreas skos:exactMatch NCIT:C173813 Pancreatic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018523 pancreatic mucinous cystadenoma skos:exactMatch NCIT:C5718 Pancreatic Mucinous Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018525 solid pseudopapillary carcinoma of pancreas skos:exactMatch NCIT:C5728 Solid Pseudopapillary Carcinoma of the Pancreas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018531 carcinoma of liver and intrahepatic biliary tract skos:exactMatch NCIT:C7927 Liver Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018540 PFAPA syndrome skos:exactMatch NCIT:C116917 Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018542 severe congenital neutropenia skos:exactMatch NCIT:C166152 Severe Congenital Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018544 adrenoleukodystrophy skos:exactMatch NCIT:C61252 Adrenoleukodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018551 patent urachus skos:exactMatch NCIT:C99005 Patent Urachus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018553 urachal diverticulum skos:exactMatch NCIT:C123254 Urachal Diverticulum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018555 hypogonadotropic hypogonadism skos:exactMatch NCIT:C113347 Hypogonadotropic Hypogonadism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018556 Lambert-Eaton myasthenic syndrome skos:exactMatch NCIT:C3155 Lambert Eaton Myasthenic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018570 hypophosphatasia skos:exactMatch NCIT:C26798 Hypophosphatasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018592 cutaneous polyarteritis nodosa skos:exactMatch NCIT:C117295 Cutaneous Polyarteritis Nodosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018598 obsolete neonatal adrenoleukodystrophy skos:exactMatch NCIT:C99251 Neonatal Adrenoleukodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018604 familial colorectal cancer type X skos:exactMatch NCIT:C120084 Hereditary Colorectal Cancer Type X semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018607 combined hamartoma of the retina and retinal pigment epithelium skos:exactMatch NCIT:C174548 Combined Hamartoma of the Retina and Retinal Pigment Epithelium semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018612 congenital hypothyroidism skos:exactMatch NCIT:C26734 Congenital Hypothyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018613 AH amyloidosis skos:exactMatch NCIT:C158962 AH Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018616 central serous chorioretinopathy skos:exactMatch NCIT:C115124 Central Serous Chorioretinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018626 paratyphoid fever skos:exactMatch NCIT:C34897 Paratyphoid Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018630 hereditary nonpolyposis colon cancer skos:exactMatch NCIT:C120083 Hereditary Nonpolyposis Colorectal Cancer Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018634 hereditary amyloidosis skos:exactMatch NCIT:C84555 Familial Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018638 pseudohypoaldosteronism skos:exactMatch NCIT:C85034 Pseudohypoaldosteronism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018646 sclerosing cholangitis skos:exactMatch NCIT:C4828 Primary Sclerosing Cholangitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018648 Keratocystic odontogenic tumor skos:exactMatch NCIT:C54302 Odontogenic Keratocyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018649 obsolete cerebral visual impairment skos:exactMatch NCIT:C35275 Visual Cortex Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018653 Polymerase proofreading-related adenomatous polyposis skos:exactMatch NCIT:C162484 Polymerase Proofreading Associated Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018660 hemophilia skos:exactMatch NCIT:C3093 Hemophilia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018661 Zika virus infectious disease skos:exactMatch NCIT:C128423 Zika Virus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018664 ectopia cordis skos:exactMatch NCIT:C111643 Ectopia Cordis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018666 hepatoblastoma skos:exactMatch NCIT:C3728 Hepatoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018674 IgG4-related submandibular gland disease skos:exactMatch NCIT:C82887 Chronic Sclerosing Sialadenitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018677 visceral heterotaxy skos:exactMatch NCIT:C117273 Heterotaxy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018680 cutaneous pseudolymphoma skos:exactMatch NCIT:C62776 Cutaneous Pseudolymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018683 acquired ichthyosis skos:exactMatch NCIT:C112831 Ichthyosis Acquisita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018687 progressive muscular atrophy skos:exactMatch NCIT:C85027 Progressive Muscular Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018689 plasma cell leukemia skos:exactMatch NCIT:C3180 Plasma Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018690 Holmes-Adie syndrome skos:exactMatch NCIT:C34357 Holmes-Adie Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018694 isolated tracheo-esophageal fistula skos:exactMatch NCIT:C35080 Tracheoesophageal Fistula semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018712 composite hemangioendothelioma skos:exactMatch NCIT:C45475 Composite Hemangioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018713 retiform hemangioendothelioma skos:exactMatch NCIT:C27511 Retiform Hemangioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018714 primary intralymphatic angioendothelioma skos:exactMatch NCIT:C7526 Papillary Intralymphatic Angioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018715 congenital hemangioma skos:exactMatch NCIT:C3841 Congenital Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018716 partially involuting congenital hemangioma skos:exactMatch NCIT:C172209 Partially Involuting Congenital Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018734 verrucous hemangioma skos:exactMatch NCIT:C4299 Verrucous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018735 multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome skos:exactMatch NCIT:C60672 MALT1 wt Allele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018740 drug-induced methemoglobinemia skos:exactMatch NCIT:C101045 Drug Induced Methemoglobinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018744 oligodendroglial tumor skos:exactMatch NCIT:C6960 Oligodendroglial Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018746 mucous membrane pemphigoid skos:exactMatch NCIT:C34907 Benign Mucous Membrane Pemphigoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018747 acquired epidermolysis bullosa skos:exactMatch NCIT:C84690 Epidermolysis Bullosa Acquisita semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018768 familial cold autoinflammatory syndrome skos:exactMatch NCIT:C119053 Familial Cold Autoinflammatory Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018769 isosporiasis skos:exactMatch NCIT:C4076 Isosporiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018770 Jeune syndrome skos:exactMatch NCIT:C84794 Jeune Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018772 Joubert syndrome skos:exactMatch NCIT:C74996 Joubert Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018800 Kallmann syndrome skos:exactMatch NCIT:C75479 Hypogonadotropic Hypogonadism with Anosmia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018815 aneurysmal bone cyst skos:exactMatch NCIT:C3516 Aneurysmal Bone Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018830 Kimura disease skos:exactMatch NCIT:C26867 Kimura Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018838 lissencephaly spectrum disorders skos:exactMatch NCIT:C103921 Lissencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018840 isolated congenital hepatic fibrosis skos:exactMatch NCIT:C97071 Congenital Hepatic Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018842 primary effusion lymphoma skos:exactMatch NCIT:C6915 Primary Effusion Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018843 embryonal carcinoma of the central nervous system skos:exactMatch NCIT:C7010 Central Nervous System Embryonal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018844 urachal cyst skos:exactMatch NCIT:C85216 Urachal Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018846 penile agenesis skos:exactMatch NCIT:C99009 Penile Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018848 IgG4-related retroperitoneal fibrosis skos:exactMatch NCIT:C26876 Retroperitoneal Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018849 dentinogenesis imperfecta skos:exactMatch NCIT:C84667 Dentinogenesis Imperfecta semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018850 proliferating trichilemmal cyst skos:exactMatch NCIT:C27125 Proliferating Trichilemmal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018852 achromatopsia skos:exactMatch NCIT:C84528 Achromatopsia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018864 Kikuchi-Fujimoto disease skos:exactMatch NCIT:C71719 Kikuchi-Fujimoto Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018868 metachromatic leukodystrophy skos:exactMatch NCIT:C61251 Metachromatic Leukodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018871 acute myelomonocytic leukemia M4 skos:exactMatch NCIT:C7463 Acute Myelomonocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018872 acute megakaryoblastic leukemia skos:exactMatch NCIT:C3170 Acute Megakaryoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018874 acute myeloid leukemia skos:exactMatch NCIT:C3171 Acute Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018875 Li-Fraumeni syndrome skos:exactMatch NCIT:C3476 Li-Fraumeni Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018876 mantle cell lymphoma skos:exactMatch NCIT:C4337 Mantle Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018881 myelodysplastic syndrome skos:exactMatch NCIT:C3247 Myelodysplastic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018882 vasculitis skos:exactMatch NCIT:C26912 Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018883 Berardinelli-Seip congenital lipodystrophy skos:exactMatch NCIT:C84594 Berardinelli-Seip Congenital Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018893 Cobb syndrome skos:exactMatch NCIT:C4485 Cobb Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018895 Plummer-Vinson syndrome skos:exactMatch NCIT:C85016 Plummer-Vinson Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018896 thrombotic thrombocytopenic purpura skos:exactMatch NCIT:C78797 Thrombotic Thrombocytopenic Purpura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018898 primary cutaneous lymphoma skos:exactMatch NCIT:C7162 Primary Cutaneous Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018901 left ventricular noncompaction skos:exactMatch NCIT:C99544 Left Ventricular Non-Compaction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018902 hepatocellular adenoma skos:exactMatch NCIT:C3758 Hepatocellular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018905 diffuse large B-cell lymphoma skos:exactMatch NCIT:C8851 Diffuse Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018906 follicular lymphoma skos:exactMatch NCIT:C3209 Follicular Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018907 craniopharyngioma skos:exactMatch NCIT:C2964 Craniopharyngioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018908 non-Hodgkin lymphoma skos:exactMatch NCIT:C3211 Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018910 oculocutaneous albinism skos:exactMatch NCIT:C84941 Oculocutaneous Albinism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018911 maturity-onset diabetes of the young skos:exactMatch NCIT:C114769 Maturity-Onset Diabetes of the Young semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018912 Cushing syndrome skos:exactMatch NCIT:C2969 Cushing Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018913 malakoplakia skos:exactMatch NCIT:C84833 Malakoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018919 McCune-Albright syndrome skos:exactMatch NCIT:C48627 McCune-Albright Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018920 peripartum cardiomyopathy skos:exactMatch NCIT:C171602 Peripartum Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018921 Meckel syndrome skos:exactMatch NCIT:C98978 Meckel-Gruber Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018927 SUNCT syndrome skos:exactMatch NCIT:C85174 SUNCT Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018935 hairy cell leukemia skos:exactMatch NCIT:C7402 Hairy Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018936 osteoblastoma skos:exactMatch NCIT:C3294 Osteoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018937 mucopolysaccharidosis type 3 skos:exactMatch NCIT:C61262 Sanfilippo Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018938 mucopolysaccharidosis type 4 skos:exactMatch NCIT:C61263 Morquio Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018940 congenital myasthenic syndrome skos:exactMatch NCIT:C84647 Congenital Myasthenic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018943 myofibrillar myopathy skos:exactMatch NCIT:C83009 Myofibrillar Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018944 gestational trophoblastic neoplasm skos:exactMatch NCIT:C4699 Gestational Trophoblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018949 distal myopathy skos:exactMatch NCIT:C84675 Distal Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018950 3-methylcrotonyl-CoA carboxylase deficiency skos:exactMatch NCIT:C98674 Methylcrotonyl-CoA Carboxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018954 Loeys-Dietz syndrome skos:exactMatch NCIT:C75006 Loeys-Dietz Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018955 recurrent respiratory papillomatosis skos:exactMatch NCIT:C128637 Recurrent Respiratory Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018959 potassium-aggravated myotonia skos:exactMatch NCIT:C122788 Potassium Aggravated Myotonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018961 familial melanoma skos:exactMatch NCIT:C8498 Hereditary Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018963 hereditary methemoglobinemia skos:exactMatch NCIT:C98898 Congenital Methemoglobinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018965 Alport syndrome skos:exactMatch NCIT:C34842 Alport Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018968 iniencephaly skos:exactMatch NCIT:C124549 Iniencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018969 craniorachischisis skos:exactMatch NCIT:C98907 Craniorachischisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018975 neurofibromatosis type 1 skos:exactMatch NCIT:C3273 Neurofibromatosis Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018983 Tolosa-Hunt syndrome skos:exactMatch NCIT:C85193 Tolosa-Hunt Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018984 Oroya fever skos:exactMatch NCIT:C128441 Carrión Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018988 iridocorneal endothelial syndrome skos:exactMatch NCIT:C84792 Iridocorneal Endothelial Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018989 recurrent acute pancreatitis skos:exactMatch NCIT:C184324 Recurrent Acute Pancreatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018992 IgG4-related thyroid disease skos:exactMatch NCIT:C35827 Riedel Fibrosing Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018996 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 skos:exactMatch NCIT:C165500 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018997 Noonan syndrome skos:exactMatch NCIT:C34854 Noonan Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0018998 Leber congenital amaurosis skos:exactMatch NCIT:C129075 Leber Congenital Amaurosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019002 Lhermitte-Duclos disease skos:exactMatch NCIT:C8419 Dysplastic Cerebellar Gangliocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019003 multiple endocrine neoplasia type 2 skos:exactMatch NCIT:C123329 Multiple Endocrine Neoplasia Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019004 kidney Wilms tumor skos:exactMatch NCIT:C40407 Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019005 nephronophthisis skos:exactMatch NCIT:C123200 Nephronophthisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019010 congenital isolated hyperinsulinism skos:exactMatch NCIT:C122923 Persistent Hyperinsulinemic Hypoglycemia of Infancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019012 Carpenter syndrome skos:exactMatch NCIT:C98873 Type II Acrocephalopolysyndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019015 omphalocele skos:exactMatch NCIT:C98997 Omphalocele semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019018 Tako-tsubo cardiomyopathy skos:exactMatch NCIT:C85181 Takotsubo Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019019 osteogenesis imperfecta skos:exactMatch NCIT:C26837 Osteogenesis Imperfecta semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019023 cutaneous mastocytosis skos:exactMatch NCIT:C7137 Cutaneous Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019024 mast cell sarcoma skos:exactMatch NCIT:C9348 Mast Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019025 extracutaneous mastocytoma skos:exactMatch NCIT:C7136 Extracutaneous Mastocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019026 autosomal recessive osteopetrosis skos:exactMatch NCIT:C129733 Autosomal Recessive Osteopetrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019035 pancreatoblastoma skos:exactMatch NCIT:C4265 Pancreatoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019037 progressive supranuclear palsy skos:exactMatch NCIT:C85028 Progressive Supranuclear Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019040 chromosomal disorder skos:exactMatch NCIT:C34470 Chromosome Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019046 leukodystrophy skos:exactMatch NCIT:C61253 Leukodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019047 obsolete rare deafness skos:exactMatch NCIT:C36194 Complete Deafness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019050 inherited hemoglobinopathy skos:exactMatch NCIT:C3092 Hemoglobinopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019052 inborn errors of metabolism skos:exactMatch NCIT:C34816 Congenital Metabolic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019053 peroxisomal disease skos:exactMatch NCIT:C85005 Peroxisomal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019060 bone neoplasm skos:exactMatch NCIT:C9343 Bone Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019064 hereditary spastic paraplegia skos:exactMatch NCIT:C140267 Hereditary Spastic Paraplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019065 amyloidosis skos:exactMatch NCIT:C2868 Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019077 warty dyskeratoma skos:exactMatch NCIT:C4087 Warty Dyskeratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019082 bullous pemphigoid skos:exactMatch NCIT:C84389 Bullous Pemphigoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019086 carcinoma of esophagus skos:exactMatch NCIT:C3513 Esophageal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019087 cholangiocarcinoma skos:exactMatch NCIT:C4436 Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019088 post-transplant lymphoproliferative disease skos:exactMatch NCIT:C4727 Post-Transplant Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019091 bronchopulmonary dysplasia skos:exactMatch NCIT:C90599 Bronchopulmonary Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019095 plague skos:exactMatch NCIT:C85015 Plague semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019100 neuromyelitis optica skos:exactMatch NCIT:C84934 Neuromyelitis Optica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019104 Sandifer syndrome skos:exactMatch NCIT:C113397 Sandifer's Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019115 obesity due to melanocortin 4 receptor deficiency skos:exactMatch NCIT:C120394 Melanocortin 4 Receptor Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019118 inherited retinal dystrophy skos:exactMatch NCIT:C35194 Hereditary Retinal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019118 inherited retinal dystrophy skos:exactMatch NCIT:C35625 Retinal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019121 pneumocystosis skos:exactMatch NCIT:C3334 Pneumocystis Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019122 idiopathic acute eosinophilic pneumonia skos:exactMatch NCIT:C35301 Loffler Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019124 microscopic polyangiitis skos:exactMatch NCIT:C70549 Microscopic Polyarteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019125 relapsing polychondritis skos:exactMatch NCIT:C157268 Relapsing Polychondritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019127 polymyositis skos:exactMatch NCIT:C26925 Polymyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019134 central neurocytoma skos:exactMatch NCIT:C3791 Central Neurocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019136 Zygomycosis skos:exactMatch NCIT:C77212 Zygomycosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019142 inherited porphyria skos:exactMatch NCIT:C97096 Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019143 angiostrongyliasis skos:exactMatch NCIT:C128394 Angiostrongyliasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019145 hereditary thrombophilia due to congenital protein C deficiency skos:exactMatch NCIT:C99025 Protein C Deficiency Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019147 myiasis skos:exactMatch NCIT:C128400 Myiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019148 Wolman disease skos:exactMatch NCIT:C61271 Wolman Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019154 androgen insensitivity syndrome skos:exactMatch NCIT:C27226 Androgen Insensitivity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019157 myelodysplastic syndrome with ring sideroblasts skos:exactMatch NCIT:C4036 Myelodysplastic Syndrome with Ring Sideroblasts semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019159 Loeffler endocarditis skos:exactMatch NCIT:C27044 Eosinophilic Endomyocardial Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019161 pseudohypoaldosteronism type 1 skos:exactMatch NCIT:C123251 Pseudohypoaldosteronism Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019162 pseudohypoaldosteronism type 2 skos:exactMatch NCIT:C123252 Pseudohypoaldosteronism Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019167 immunoglobulin A vasculitis skos:exactMatch NCIT:C34963 Henoch-Schönlein Purpura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019168 pyomyositis skos:exactMatch NCIT:C128382 Pyomyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019169 pyruvate dehydrogenase deficiency skos:exactMatch NCIT:C103968 Pyruvate Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019170 polyarteritis nodosa skos:exactMatch NCIT:C26847 Polyarteritis Nodosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019172 aniridia skos:exactMatch NCIT:C84563 Aniridia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019173 rabies skos:exactMatch NCIT:C28182 Rabies semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019174 obsolete infantile Refsum disease skos:exactMatch NCIT:C84789 Infantile Refsum Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019175 primary lymphedema skos:exactMatch NCIT:C48829 Primary Lymphedema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019180 hereditary hemorrhagic telangiectasia skos:exactMatch NCIT:C35064 Hereditary Hemorrhagic Telangiectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019186 Q fever skos:exactMatch NCIT:C34970 Q Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019187 Axenfeld-Rieger syndrome skos:exactMatch NCIT:C131001 Rieger Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019188 Rubinstein-Taybi syndrome skos:exactMatch NCIT:C75466 Rubinstein-Taybi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019191 IgG4-related dacryoadenitis and sialadenitis skos:exactMatch NCIT:C34819 Mikulicz Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019193 acquired generalized lipodystrophy skos:exactMatch NCIT:C131089 Acquired Generalized Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019194 localized lipodystrophy skos:exactMatch NCIT:C131814 Focal Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019200 retinitis pigmentosa skos:exactMatch NCIT:C85045 Retinitis Pigmentosa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019202 myxofibrosarcoma skos:exactMatch NCIT:C6496 Myxofibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019203 acute interstitial pneumonia skos:exactMatch NCIT:C35806 Acute Interstitial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019207 DEND syndrome skos:exactMatch NCIT:C131845 K ATP Associated Developmental Delay, Epilepsy and Neonatal Diabetes semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019209 Japanese encephalitis skos:exactMatch NCIT:C34577 Japanese B Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019210 cutaneous neuroendocrine carcinoma skos:exactMatch NCIT:C9231 Merkel Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019214 inborn carbohydrate metabolic disorder skos:exactMatch NCIT:C97089 Carbohydrate Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019234 peroxisome biogenesis disorder skos:exactMatch NCIT:C146639 Peroxisome Biogenesis Disorders in the Zellweger Spectrum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019234 peroxisome biogenesis disorder skos:exactMatch NCIT:C155747 Peroxisome Biogenesis Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019248 mucolipidosis skos:exactMatch NCIT:C61267 Mucolipidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019249 mucopolysaccharidosis skos:exactMatch NCIT:C61259 Mucopolysaccharidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019255 sphingolipidosis skos:exactMatch NCIT:C117254 Sphingolipidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019266 SAPHO syndrome skos:exactMatch NCIT:C119049 Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019269 ichthyosis skos:exactMatch NCIT:C84776 Ichthyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019287 ectodermal dysplasia syndrome skos:exactMatch NCIT:C84683 Ectodermal Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019288 skin pigmentation disorder skos:exactMatch NCIT:C34557 Skin Pigmentation Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019293 skin vascular disease skos:exactMatch NCIT:C35254 Skin Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019297 lymphedema skos:exactMatch NCIT:C3207 Lymphedema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019312 Hermansky-Pudlak syndrome skos:exactMatch NCIT:C37261 Hermansky-Pudlak Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019315 diffuse cutaneous mastocytosis skos:exactMatch NCIT:C3218 Diffuse Cutaneous Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019316 maculopapular cutaneous mastocytosis skos:exactMatch NCIT:C3433 Urticaria Pigmentosa/Maculopapular Cutaneous Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019319 verrucous nevus skos:exactMatch NCIT:C4674 Verrucous Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019328 macrocystic lymphatic malformation skos:exactMatch NCIT:C53316 Cavernous Lymphangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019336 Gardner syndrome skos:exactMatch NCIT:C6728 Gardner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019338 sarcoidosis skos:exactMatch NCIT:C34995 Sarcoidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019339 47,XYY syndrome skos:exactMatch NCIT:C85237 47,XYY Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019340 scleroderma skos:exactMatch NCIT:C26746 Scleroderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019342 Seckel syndrome skos:exactMatch NCIT:C125488 Seckel Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019345 shigellosis skos:exactMatch NCIT:C157978 Shigellosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019349 Sotos syndrome skos:exactMatch NCIT:C75019 Sotos Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019350 hereditary spherocytosis skos:exactMatch NCIT:C97074 Hereditary Spherocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019353 Stargardt disease skos:exactMatch NCIT:C85078 Stargardt Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019354 Stickler syndrome skos:exactMatch NCIT:C74984 Stickler Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019359 Rocky mountain spotted fever skos:exactMatch NCIT:C128410 Rocky Mountain Spotted Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019362 epidemic louse-borne typhus skos:exactMatch NCIT:C84689 Epidemic Louse-Borne Typhus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019368 florid cemento-osseous dysplasia skos:exactMatch NCIT:C8381 Florid Cemento-Osseous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019372 solitary bone cyst skos:exactMatch NCIT:C2904 Simple Bone Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019373 desmoplastic small round cell tumor skos:exactMatch NCIT:C8300 Desmoplastic Small Round Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019380 western equine encephalitis skos:exactMatch NCIT:C85227 Western Equine Encephalomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019383 acute disseminated encephalomyelitis skos:exactMatch NCIT:C34578 Acute Disseminated Encephalomyelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019384 encephalitis lethargica skos:exactMatch NCIT:C26761 Encephalitis Lethargica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019384 encephalitis lethargica skos:exactMatch NCIT:C34576 Epidemic Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019390 Susac syndrome skos:exactMatch NCIT:C116363 Susac Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019391 Fanconi anemia skos:exactMatch NCIT:C62505 Fanconi Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019392 syringocystadenoma papilliferum skos:exactMatch NCIT:C4172 Syringocystadenoma Papilliferum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019402 beta thalassemia skos:exactMatch NCIT:C34375 Beta Thalassemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019403 congenital dyserythropoietic anemia skos:exactMatch NCIT:C84646 Congenital Dyserythropoietic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019404 perineurioma skos:exactMatch NCIT:C4973 Perineurioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019409 idiopathic juvenile osteoporosis skos:exactMatch NCIT:C119996 Pediatric Osteoporosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019433 oligoarticular juvenile idiopathic arthritis skos:exactMatch NCIT:C119032 Oligoarticular Juvenile Idiopathic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019434 systemic-onset juvenile idiopathic arthritis skos:exactMatch NCIT:C119031 Systemic Juvenile Idiopathic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019435 rheumatoid factor-positive polyarticular juvenile idiopathic arthritis skos:exactMatch NCIT:C119034 Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019436 psoriasis-related juvenile idiopathic arthritis skos:exactMatch NCIT:C114361 Juvenile Psoriatic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019437 enthesitis-related juvenile idiopathic arthritis skos:exactMatch NCIT:C119024 Enthesitis-Related Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019438 AL amyloidosis skos:exactMatch NCIT:C158963 AL Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019439 AA amyloidosis skos:exactMatch NCIT:C3818 Secondary Amyloidosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019444 trichinellosis skos:exactMatch NCIT:C85199 Trichinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019445 trichofolliculoma skos:exactMatch NCIT:C4112 Trichofolliculoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019451 chronic neutrophilic leukemia skos:exactMatch NCIT:C3179 Chronic Neutrophilic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019452 myeloproliferative neoplasm, unclassifiable skos:exactMatch NCIT:C27350 Myeloproliferative Neoplasm, Not Otherwise Specified semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019453 myelodysplastic syndrome with multilineage dysplasia skos:exactMatch NCIT:C8574 Myelodysplastic Syndrome, Not Otherwise Specified with Multilineage Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019454 myelodysplastic syndrome with excess blasts skos:exactMatch NCIT:C7506 Myelodysplastic Syndrome with Excess Blasts semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019455 acute panmyelosis with myelofibrosis skos:exactMatch NCIT:C4344 Acute Panmyelosis with Myelofibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019456 acute myeloid leukemia with multilineage dysplasia skos:exactMatch NCIT:C9289 Acute Myeloid Leukemia with Multilineage Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019457 therapy related acute myeloid leukemia and myelodysplastic syndrome skos:exactMatch NCIT:C25765 Secondary Acute Myeloid Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019458 acute basophilic leukemia skos:exactMatch NCIT:C3164 Acute Basophilic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019460 acute leukemia of ambiguous lineage skos:exactMatch NCIT:C7464 Acute Leukemia of Ambiguous Lineage semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019461 B-cell prolymphocytic leukemia skos:exactMatch NCIT:C4753 B-Cell Prolymphocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019462 splenic marginal zone lymphoma skos:exactMatch NCIT:C4663 Splenic Marginal Zone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019464 heavy chain disease skos:exactMatch NCIT:C3082 Heavy Chain Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019465 nodal marginal zone B-cell lymphoma skos:exactMatch NCIT:C8863 Nodal Marginal Zone Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019466 lymphomatoid granulomatosis skos:exactMatch NCIT:C7930 Lymphomatoid Granulomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019467 CD4+/CD56+ hematodermic neoplasm skos:exactMatch NCIT:C7203 Blastic Plasmacytoid Dendritic Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019468 T-cell prolymphocytic leukemia skos:exactMatch NCIT:C4752 T-Cell Prolymphocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019469 T-cell large granular lymphocyte leukemia skos:exactMatch NCIT:C4664 T-Cell Large Granular Lymphocyte Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019470 aggressive NK-cell leukemia skos:exactMatch NCIT:C8647 Aggressive NK-Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019471 adult T-cell leukemia/lymphoma skos:exactMatch NCIT:C3184 Adult T-Cell Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019472 extranodal nasal NK/T cell lymphoma skos:exactMatch NCIT:C4684 Nasal Type Extranodal NK/T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019473 enteropathy-associated T-cell lymphoma skos:exactMatch NCIT:C4737 Enteropathy-Associated T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019474 hepatosplenic T-cell lymphoma skos:exactMatch NCIT:C8459 Hepatosplenic T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019475 subcutaneous panniculitis-like T-cell lymphoma skos:exactMatch NCIT:C6918 Subcutaneous Panniculitis-Like T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019478 adult nodular lymphocyte predominant Hodgkin lymphoma skos:exactMatch NCIT:C7942 Adult Nodular Lymphocyte Predominant B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019479 histiocytic sarcoma skos:exactMatch NCIT:C27349 Histiocytic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019480 Langerhans cell sarcoma skos:exactMatch NCIT:C6921 Langerhans Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019483 methotrexate-associated lymphoproliferative disorders skos:exactMatch NCIT:C7184 Methotrexate-Associated Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019496 neuroendocrine neoplasm skos:exactMatch NCIT:C3809 Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019499 Turner syndrome skos:exactMatch NCIT:C26900 Turner Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019501 Usher syndrome skos:exactMatch NCIT:C85217 Usher Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019508 van der Woude syndrome skos:exactMatch NCIT:C74986 Van der Woude Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019509 cutaneous leukocytoclastic angiitis skos:exactMatch NCIT:C122919 Cutaneous Small Vessel Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019514 hepatic veno-occlusive disease skos:exactMatch NCIT:C26793 Sinusoidal Obstruction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019517 Waardenburg syndrome type 2 skos:exactMatch NCIT:C75009 Waardenburg Syndrome Type 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019518 Waardenburg-Shah syndrome skos:exactMatch NCIT:C124842 Waardenburg Syndrome Type 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019527 undifferentiated connective tissue syndrome skos:exactMatch NCIT:C116776 Undifferentiated Connective Tissue Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019530 non-syndromic syndactyly skos:exactMatch NCIT:C87125 Syndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019532 autoimmune hemolytic anemia, warm type skos:exactMatch NCIT:C162611 Warm Antibody Autoimmune Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019537 hemoglobin D disease skos:exactMatch NCIT:C35344 Hemoglobin D Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019538 Gaisbock syndrome skos:exactMatch NCIT:C27174 Stress Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019542 acute liver failure skos:exactMatch NCIT:C84396 Acute Liver Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019558 discoid lupus erythematosus skos:exactMatch NCIT:C26820 Discoid Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019560 lupus erythematosus tumidus skos:exactMatch NCIT:C117112 Lupus Erythematosus Tumidus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019561 lupus erythematosus panniculitis skos:exactMatch NCIT:C82884 Lupus Panniculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019562 localized scleroderma skos:exactMatch NCIT:C72069 Localized Scleroderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019563 CREST syndrome skos:exactMatch NCIT:C70646 CREST Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019567 Ehlers-Danlos syndrome, classic type, 1 skos:exactMatch NCIT:C125696 Ehlers-Danlos Syndrome, Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019568 Ehlers-Danlos syndrome, classic type, 2 skos:exactMatch NCIT:C125697 Ehlers-Danlos Syndrome, Type II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019569 Cockayne syndrome type 1 skos:exactMatch NCIT:C135725 Cockayne Syndrome Type A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019570 Cockayne syndrome type 2 skos:exactMatch NCIT:C135726 Cockayne Syndrome Type B semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019591 panhypopituitarism skos:exactMatch NCIT:C110940 Panhypopituitarism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019600 xeroderma pigmentosum skos:exactMatch NCIT:C3452 Xeroderma Pigmentosum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019609 Zellweger spectrum disorders skos:exactMatch NCIT:C85239 Zellweger Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019610 Zollinger-Ellison syndrome skos:exactMatch NCIT:C3453 Zollinger Ellison Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019613 non-functioning pituitary adenoma skos:exactMatch NCIT:C4348 Non-Functioning Pituitary Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019618 Sheehan syndrome skos:exactMatch NCIT:C35300 Sheehan Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019622 non-specific interstitial pneumonia skos:exactMatch NCIT:C35717 Nonspecific Interstitial Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019623 hereditary angioedema skos:exactMatch NCIT:C84758 Hereditary Angioedema semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019631 persistent hyperplastic primary vitreous skos:exactMatch NCIT:C161554 Persistent Hyperplastic Primary Vitreous semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019632 Lyme disease skos:exactMatch NCIT:C45161 Borrelia Burgdorferi Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019636 renal agenesis, unilateral skos:exactMatch NCIT:C101220 Unilateral Renal Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019640 posterior urethral valve skos:exactMatch NCIT:C99021 Posterior Urethral Valve semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019642 vitamin D-dependent rickets, type 2 skos:exactMatch NCIT:C131077 Vitamin D Dependent Rickets 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019648 achondrogenesis skos:exactMatch NCIT:C84527 Achondrogenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019665 monostotic fibrous dysplasia skos:exactMatch NCIT:C53971 Monostotic Fibrous Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019701 chondrodysplasia punctata skos:exactMatch NCIT:C84632 Chondrodysplasia Punctata semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019716 overgrowth syndrome skos:exactMatch NCIT:C94828 Overgrowth Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019722 glomerular disorder skos:exactMatch NCIT:C120887 Glomerulopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019728 heavy chain deposition disease skos:exactMatch NCIT:C7339 Heavy Chain Deposition Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019729 light and heavy chain deposition disease skos:exactMatch NCIT:C158965 Light and Heavy Chain Deposition Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019730 light chain deposition disease skos:exactMatch NCIT:C7727 Light Chain Deposition Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019734 juvenile polymyositis skos:exactMatch NCIT:C114358 Juvenile Polymyositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019735 polymyalgia rheumatica skos:exactMatch NCIT:C85018 Polymyalgia Rheumatica semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019736 dense deposit disease skos:exactMatch NCIT:C123039 Dense Deposit Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019737 thrombotic microangiopathy skos:exactMatch NCIT:C62605 Thrombotic Microangiopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019740 acquired thrombotic thrombocytopenic purpura skos:exactMatch NCIT:C131653 Acquired Thrombotic Thrombocytopenic Purpura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019751 autoinflammatory syndrome skos:exactMatch NCIT:C119050 Autoinflammatory Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019753 localized Castleman disease skos:exactMatch NCIT:C115200 Unicentric Castleman Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019754 multicentric Castleman disease skos:exactMatch NCIT:C27855 Multicentric Castleman Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019755 developmental defect during embryogenesis skos:exactMatch NCIT:C99267 Congenital Malformation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019759 epispadias skos:exactMatch NCIT:C98923 Epispadias semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019781 astrocytoma (excluding glioblastoma) skos:exactMatch NCIT:C60781 Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019787 autoimmune enteropathy skos:exactMatch NCIT:C94694 Autoimmune Enteropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019790 neuroleptic malignant syndrome skos:exactMatch NCIT:C94829 Neuroleptic Malignant Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019796 acrocephalosyndactyly skos:exactMatch NCIT:C34348 Acrocephalosyndactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019799 hepatoerythropoietic porphyria skos:exactMatch NCIT:C84754 Hepatoerythropoietic Porphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019801 acute adrenal insufficiency skos:exactMatch NCIT:C112840 Adrenal Crisis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019803 angioma serpiginosum skos:exactMatch NCIT:C3926 Angioma Serpiginosum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019804 tracheomalacia skos:exactMatch NCIT:C98634 Tracheomalacia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019805 twin to twin transfusion syndrome skos:exactMatch NCIT:C113824 Twin-Twin Transfusion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019806 primary progressive aphasia skos:exactMatch NCIT:C85024 Primary Progressive Aphasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019808 aortic valve atresia skos:exactMatch NCIT:C98818 Aortic Valve Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019809 congenital aortic valve insufficiency skos:exactMatch NCIT:C103936 Congenital Aortic Valve Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019810 toxic epidermal necrolysis skos:exactMatch NCIT:C79777 Toxic Epidermal Necrolysis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019828 pituitary stalk interruption syndrome skos:exactMatch NCIT:C121150 Pituitary Stalk Interruption Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019835 primary hypophysitis skos:exactMatch NCIT:C132055 Autoimmune Hypophysitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019862 levocardia skos:exactMatch NCIT:C111647 Levocardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019903 ring chromosome 2 skos:exactMatch NCIT:C121981 ROSE Cluster 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019904 ring chromosome 3 skos:exactMatch NCIT:C121982 ROSE Cluster 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019928 48,XXXY syndrome skos:exactMatch NCIT:C89799 XXXY Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019929 49,XXXXY syndrome skos:exactMatch NCIT:C185635 49,XXXXY Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019933 acromegaly skos:exactMatch NCIT:C84533 Acromegaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019944 Eisenmenger syndrome skos:exactMatch NCIT:C84390 Eisenmenger Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019947 rippling muscle disease 2 skos:exactMatch NCIT:C148325 Rippling Muscle Disease 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019954 pancreatic neuroendocrine tumor skos:exactMatch NCIT:C27720 Pancreatic Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019956 encephalitis skos:exactMatch NCIT:C26760 Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019957 PPoma skos:exactMatch NCIT:C67453 Pancreatic Polypeptide Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019959 glucagonoma skos:exactMatch NCIT:C95597 Pancreatic Glucagonoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019960 VIPoma skos:exactMatch NCIT:C26749 VIP-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019962 thyroid lymphoma skos:exactMatch NCIT:C5265 Thyroid Gland Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019978 Robinow syndrome skos:exactMatch NCIT:C85048 Robinow Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019991 immunotactoid glomerulopathy skos:exactMatch NCIT:C158968 Immunotactoid Glomerulopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019991 immunotactoid glomerulopathy skos:exactMatch NCIT:C96182 Fibrillary Glomerulonephritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0019992 pseudohypoparathyroidism skos:exactMatch NCIT:C99027 Pseudohypoparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020010 infectious disorder of the nervous system skos:exactMatch NCIT:C27590 Nervous System Infectious Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020040 46,XY disorder of sex development skos:exactMatch NCIT:C127171 46,XY Differences of Sex Development semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020066 Ehlers-Danlos syndrome skos:exactMatch NCIT:C34568 Ehlers-Danlos Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020067 infectious encephalitis skos:exactMatch NCIT:C79550 Infectious Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020074 progressive myoclonus epilepsy skos:exactMatch NCIT:C7636 Progressive Myoclonus Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020076 myeloproliferative neoplasm skos:exactMatch NCIT:C4345 Myeloproliferative Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020078 obsolete acute myeloid leukemia with recurrent genetic anomaly skos:exactMatch NCIT:C7175 Acute Myeloid Leukemia with Recurrent Genetic Abnormalities semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020088 familial partial lipodystrophy skos:exactMatch NCIT:C84708 Familial Partial Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020101 obsolete constitutional hemolytic anemia due to membrane defect skos:exactMatch NCIT:C101218 Hemolytic Anemia due to Membrane Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020108 autoimmune hemolytic anemia skos:exactMatch NCIT:C34378 Autoimmune Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020110 pulmonary agenesis skos:exactMatch NCIT:C99028 Pulmonary Agenesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020115 secondary polycythemia skos:exactMatch NCIT:C27178 Secondary Polycythemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020121 muscular dystrophy skos:exactMatch NCIT:C84910 Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020123 metabolic myopathy skos:exactMatch NCIT:C98985 Metabolic Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020153 cryptophthalmia skos:exactMatch NCIT:C124520 Cryptophthalmia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020179 palpebral nevus skos:exactMatch NCIT:C3880 Eyelid Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020204 conjunctival tumor skos:exactMatch NCIT:C2961 Conjunctival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020236 obsolete lens position anomaly skos:exactMatch NCIT:C125484 Ectopia Lentis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020242 hereditary macular dystrophy skos:exactMatch NCIT:C140264 Genetic Macular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020250 autosomal dominant optic atrophy skos:exactMatch NCIT:C84577 Autosomal Dominant Optic Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020283 uveitis skos:exactMatch NCIT:C26909 Uveitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020290 familial atrioventricular septal defect skos:exactMatch NCIT:C101029 Atrioventricular Septal Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020291 hypoplastic right heart syndrome skos:exactMatch NCIT:C99053 Hypoplastic Right Heart Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020295 congenital pulmonary veins anomaly skos:exactMatch NCIT:C110942 Congenital Anomaly of Pulmonary Veins semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020296 congenital arteriovenous fistula skos:exactMatch NCIT:C35377 Congenital Arteriovenous Fistula semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020311 chronic myelomonocytic leukemia skos:exactMatch NCIT:C3178 Chronic Myelomonocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020317 acute myeloid leukemia with 11q23 abnormalities skos:exactMatch NCIT:C82403 Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020320 acute myeloblastic leukemia with maturation skos:exactMatch NCIT:C3250 Acute Myeloid Leukemia with Maturation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020321 acute undifferentiated leukemia skos:exactMatch NCIT:C9298 Acute Undifferentiated Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020322 acute biphenotypic leukemia skos:exactMatch NCIT:C4673 Acute Biphenotypic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020323 primary mediastinal large B-cell lymphoma skos:exactMatch NCIT:C9280 Primary Mediastinal Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020324 intravascular large B-cell lymphoma skos:exactMatch NCIT:C4342 Intravascular Large B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020325 anaplastic large cell lymphoma skos:exactMatch NCIT:C3720 Anaplastic Large Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020326 lymphomatoid papulosis skos:exactMatch NCIT:C3721 Lymphomatoid Papulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020331 indolent systemic mastocytosis skos:exactMatch NCIT:C9286 Indolent Systemic Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020332 systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease skos:exactMatch NCIT:C9284 Systemic Mastocytosis with an Associated Myeloid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020333 aggressive systemic mastocytosis skos:exactMatch NCIT:C9285 Aggressive Systemic Mastocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020334 mast cell leukemia skos:exactMatch NCIT:C3169 Mast Cell Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020338 adult pure red cell aplasia skos:exactMatch NCIT:C70548 Acquired Pure Red Cell Aplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020347 acute inflammatory demyelinating polyradiculoneuropathy skos:exactMatch NCIT:C116926 Acute Inflammatory Demyelinating Polyradiculoneuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020348 acute motor and sensory axonal neuropathy skos:exactMatch NCIT:C116927 Acute Motor and Sensory Axonal Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020349 acute motor axonal neuropathy skos:exactMatch NCIT:C116929 Acute Motor Axonal Neuropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020356 coloboma of iris skos:exactMatch NCIT:C98879 Coloboma of the Iris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020357 coloboma of eyelid skos:exactMatch NCIT:C98878 Coloboma of the Eyelid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020366 congenital glaucoma skos:exactMatch NCIT:C50648 Congenital Glaucoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020370 Cogan-Reese syndrome skos:exactMatch NCIT:C84644 Cogan-Reese Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020404 shone complex skos:exactMatch NCIT:C99058 Shone Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020417 right aortic arch skos:exactMatch NCIT:C103917 Right Aortic Arch semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020420 pulmonary branch stenosis skos:exactMatch NCIT:C99144 Branch Pulmonary Artery Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020439 patent foramen ovale skos:exactMatch NCIT:C34619 Patent Foramen Ovale semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020453 congenital partial pulmonary venous return anomaly skos:exactMatch NCIT:C99004 Partial Anomalous Pulmonary Venous Return semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020479 pituitary gigantism skos:exactMatch NCIT:C93046 Gigantism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020481 myotonia fluctuans skos:exactMatch NCIT:C122789 Myotonia Fluctuans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020487 Pontiac fever skos:exactMatch NCIT:C128335 Pontiac Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020491 subcortical band heterotopia skos:exactMatch NCIT:C116933 Double Cortex Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020492 hemimegalencephaly skos:exactMatch NCIT:C177779 Hemimegalencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020500 Marburg hemorrhagic fever skos:exactMatch NCIT:C84883 Marburg Virus Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020501 Crimean-Congo hemorrhagic fever skos:exactMatch NCIT:C34682 Congo-Crimean Hemorrhagic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020502 yellow fever skos:exactMatch NCIT:C35547 Yellow Fever Virus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020511 precursor B-cell acute lymphoblastic leukemia skos:exactMatch NCIT:C8644 B Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020513 spermatocytic seminoma skos:exactMatch NCIT:C39921 Testicular Spermatocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020516 thymic neuroendocrine carcinoma skos:exactMatch NCIT:C171031 Thymic Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020517 eosinophilic granuloma skos:exactMatch NCIT:C3016 Eosinophilic Granuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020519 hand-Schuller-Christian disease skos:exactMatch NCIT:C6920 Hand-Schuller-Christian Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020520 adult pulmonary Langerhans cell histiocytosis skos:exactMatch NCIT:C142833 Pulmonary Langerhans Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020525 transient neonatal diabetes mellitus skos:exactMatch NCIT:C114899 Transient Neonatal Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020531 long chain acyl-CoA dehydrogenase deficiency skos:exactMatch NCIT:C84537 Long-Chain Acyl-CoA Dehydrogenase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020540 ovarian gynandroblastoma skos:exactMatch NCIT:C3072 Ovarian Gynandroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020541 maligant granulosa cell tumor of ovary skos:exactMatch NCIT:C8403 Malignant Ovarian Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020546 acute graft versus host disease skos:exactMatch NCIT:C4980 Acute Graft Versus Host Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020547 chronic graft versus host disease skos:exactMatch NCIT:C4981 Chronic Graft Versus Host Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020549 invasive hydatidiform mole skos:exactMatch NCIT:C6985 Invasive Hydatidiform Mole semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020550 gestational choriocarcinoma skos:exactMatch NCIT:C4646 Gestational Choriocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020552 placental site trophoblastic tumor skos:exactMatch NCIT:C3757 Placental Site Trophoblastic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020555 pleuropulmonary blastoma type 1 skos:exactMatch NCIT:C45626 Type I Pleuropulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020556 pleuropulmonary blastoma type 2 skos:exactMatch NCIT:C45627 Type II Pleuropulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020557 pleuropulmonary blastoma type 3 skos:exactMatch NCIT:C45628 Type III Pleuropulmonary Blastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020558 autosomal dominant Charcot-Marie-Tooth disease type 2K skos:exactMatch NCIT:C133886 Charcot-Marie-Tooth Disease Type 2K semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020560 atypical teratoid rhabdoid tumor skos:exactMatch NCIT:C6906 Atypical Teratoid/Rhabdoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020562 pleomorphic liposarcoma skos:exactMatch NCIT:C3705 Pleomorphic Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020563 dedifferentiated liposarcoma skos:exactMatch NCIT:C3704 Dedifferentiated Liposarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020567 apnea of prematurity skos:exactMatch NCIT:C98823 Apnea of Prematurity semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020572 complex regional pain syndrome type 2 skos:exactMatch NCIT:C121572 Complex Regional Pain Syndrome II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020574 central nervous system nongerminomatous germ cell tumor skos:exactMatch NCIT:C100093 Central Nervous System Nongerminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020575 polymorphic ventricular tachycardia skos:exactMatch NCIT:C111648 Polymorphic Ventricular Tachycardia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020576 cutaneous vasculitis skos:exactMatch NCIT:C112210 Cutaneous Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020577 childhood gonadal germ cell tumor skos:exactMatch NCIT:C114801 Childhood Gonadal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020579 mucositis skos:exactMatch NCIT:C115965 Mucositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020580 germinomatous germ cell tumor skos:exactMatch NCIT:C121618 Germinomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020581 benign PEComa skos:exactMatch NCIT:C121791 Benign PEComa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020582 benign uterine ligament neoplasm skos:exactMatch NCIT:C126493 Benign Uterine Ligament Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020584 anemia due to enzyme disorder skos:exactMatch NCIT:C35472 Anemia due to Enzyme Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020585 anemia due to erythrocyte enzyme disorder skos:exactMatch NCIT:C131630 Anemia due to Erythrocyte Enzyme Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020586 factor V deficiency skos:exactMatch NCIT:C131738 Factor V Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020587 factor XI deficiency skos:exactMatch NCIT:C131739 Factor XI Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020588 lung PEComa skos:exactMatch NCIT:C142783 Lung PEComa semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020589 cardiac germ cell tumor skos:exactMatch NCIT:C147005 Cardiac Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020590 mycobacterial infectious disease skos:exactMatch NCIT:C26831 Mycobacterial Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020591 obsolete disorder of peritoneum skos:exactMatch NCIT:C26848 Peritoneal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020592 disorder of pharynx skos:exactMatch NCIT:C26850 Pharyngeal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020593 trichoblastoma skos:exactMatch NCIT:C27132 Trichoblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020594 abducens nerve disorder skos:exactMatch NCIT:C27593 Abducens Nerve Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020595 obsolete disorder of retroperitoneum skos:exactMatch NCIT:C27667 Retroperitoneal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020596 mucin-producing carcinoma skos:exactMatch NCIT:C27825 Mucin-Producing Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020597 angiokeratoma of scrotum skos:exactMatch NCIT:C7752 Angiokeratoma of Fordyce semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020598 malabsorption syndrome skos:exactMatch NCIT:C3214 Malabsorption Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020599 acquired coagulation factor deficiency skos:exactMatch NCIT:C34347 Acquired Coagulation Factor Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020600 acute pharyngitis skos:exactMatch NCIT:C34355 Acute Pharyngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020601 mosquito-borne viral encephalitis skos:exactMatch NCIT:C34823 Mosquito-Borne Viral Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020633 anaplastic cancer skos:exactMatch NCIT:C36025 Anaplastic Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020634 grade III meningioma skos:exactMatch NCIT:C38938 Grade 3 Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020635 anaplastic meningioma skos:exactMatch NCIT:C4051 Anaplastic (Malignant) Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020638 superficial spreading melanoma skos:exactMatch NCIT:C9152 Low-CSD Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020640 autoimmune encephalitis skos:exactMatch NCIT:C122414 Autoimmune Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020641 respiratory tract neoplasm skos:exactMatch NCIT:C3355 Respiratory System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020642 polycystic kidney disease skos:exactMatch NCIT:C75464 Polycystic Kidney Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020644 lung non-Hodgkin lymphoma skos:exactMatch NCIT:C5684 Lung Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020645 autosomal dominant osteopetrosis skos:exactMatch NCIT:C129732 Autosomal Dominant Osteopetrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020646 ocular adnexal lymphoma skos:exactMatch NCIT:C88145 Ocular Adnexal Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020649 warty carcinoma of the penis skos:exactMatch NCIT:C6981 Penile Warty Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020653 vaginal adenocarcinoma skos:exactMatch NCIT:C7981 Vaginal Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020654 renal pelvis/ureter urothelial carcinoma skos:exactMatch NCIT:C7716 Renal Pelvis and Ureter Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020656 human papillomavirus-related penile squamous cell carcinoma skos:exactMatch NCIT:C27682 Penile Human Papillomavirus-Related Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020657 human papillomavirus-related squamous cell carcinoma skos:exactMatch NCIT:C27683 Human Papillomavirus-Related Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020660 osteoblastic osteosarcoma skos:exactMatch NCIT:C53953 Osteoblastic Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020661 undifferentiated round cell sarcoma skos:exactMatch NCIT:C121799 Undifferentiated Round Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020662 borderline ovarian serous tumor skos:exactMatch NCIT:C5226 Borderline Ovarian Serous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020663 malignant spindle cell neoplasm skos:exactMatch NCIT:C27091 Malignant Spindle Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020664 spindle cell neoplasm skos:exactMatch NCIT:C27263 Spindle Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020665 high grade malignant neoplasm skos:exactMatch NCIT:C36046 High Grade Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020669 paranasal sinus cancer skos:exactMatch NCIT:C7487 Malignant Paranasal Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020673 arterial occlusion skos:exactMatch NCIT:C35318 Arterial Occlusion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020675 ischemic bowel disorder skos:exactMatch NCIT:C35212 Ischemic Bowel Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020678 sensorineural hearing loss disorder skos:exactMatch NCIT:C26739 Sensorineural Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020679 conductive hearing loss disorder skos:exactMatch NCIT:C27645 Conductive Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020680 acute bronchiolitis skos:exactMatch NCIT:C39659 Acute Bronchiolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020681 Ehlers-Danlos syndrome, musculocontractural type 1 skos:exactMatch NCIT:C168975 Ehlers-Danlos Syndrome, Musculocontractural Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020685 infratentorial ependymal tumor skos:exactMatch NCIT:C131612 Infratentorial Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020686 acute tonsillitis skos:exactMatch NCIT:C97142 Acute Tonsillitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020687 supratentorial ependymal tumor skos:exactMatch NCIT:C131611 Supratentorial Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020689 AIDS dementia complex skos:exactMatch NCIT:C2864 AIDS Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020690 adult glioblastoma skos:exactMatch NCIT:C9094 Adult Glioblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020694 salivary gland epithelial myoepithelial carcinoma skos:exactMatch NCIT:C35701 Salivary Gland Epithelial-Myoepithelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020695 hypotonic cerebral palsy skos:exactMatch NCIT:C116906 Hypotonic Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020696 vitamin B12 deficiency skos:exactMatch NCIT:C131684 Vitamin B12 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020697 lung epithelial-myoepithelial carcinoma skos:exactMatch NCIT:C45545 Lung Epithelial-Myoepithelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020702 autosomal dominant epidermolytic ichthyosis skos:exactMatch NCIT:C62569 Epidermolytic Ichthyosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020703 erythroid neoplasm skos:exactMatch NCIT:C7064 Erythroid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020706 Heberden's node skos:exactMatch NCIT:C34671 Heberden's Node semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020707 central hearing loss skos:exactMatch NCIT:C34662 Central Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020708 brachial amyotrophic diplegia skos:exactMatch NCIT:C133085 Brachial Amyotrophic Diplegia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020710 amnionitis skos:exactMatch NCIT:C50459 Amnionitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020712 46,XY sex reversal 1 skos:exactMatch NCIT:C128188 46,XY Sex Reversal 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020725 anemia due to chronic disorder skos:exactMatch NCIT:C35659 Anemia due to Chronic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020726 tubulointerstitial kidney disease, autosomal dominant, 2 skos:exactMatch NCIT:C123171 Medullary Cystic Kidney Disease Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020731 arbovirus infection skos:exactMatch NCIT:C34396 Arthropod-Borne Viral Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020740 ectodermal dysplasia and immunodeficiency 1 skos:exactMatch NCIT:C176592 Ectodermal Dysplasia and Immunodeficiency 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020743 mixed phenotype acute leukemia skos:exactMatch NCIT:C82179 Mixed Phenotype Acute Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020744 Mobitz type I atrioventricular block skos:exactMatch NCIT:C62017 AV Block Second Degree Mobitz Type I semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020757 sporadic hemiplegic migraine skos:exactMatch NCIT:C117011 Sporadic Hemiplegic Migraine semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020760 skin squamous cell carcinoma in situ skos:exactMatch NCIT:C2906 Skin Squamous Cell Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020761 Bowen disease of the skin skos:exactMatch NCIT:C62571 Bowen Disease of the Skin semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020767 cauda equina syndrome with neurogenic bladder skos:exactMatch NCIT:C34453 Cauda Equina Syndrome with Neurogenic Bladder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020773 cerebrospinal fluid rhinorrhea skos:exactMatch NCIT:C84627 Cerebrospinal Fluid Rhinorrhea semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020779 cartilage development disorder skos:exactMatch NCIT:C34466 Cartilage Development Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020782 chronic gingivitis skos:exactMatch NCIT:C34474 Chronic Gingivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020794 colorectal medullary carcinoma skos:exactMatch NCIT:C43590 Colorectal Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020799 basal cell neoplasm skos:exactMatch NCIT:C3784 Basal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020800 demyelinating disease of central nervous system skos:exactMatch NCIT:C34526 Demyelinating Disorder of Central Nervous System semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020801 rectal medullary carcinoma skos:exactMatch NCIT:C60640 Rectal Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020804 basal cell carcinoma skos:exactMatch NCIT:C156767 Basal Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020804 basal cell carcinoma skos:exactMatch NCIT:C7586 Malignant Basal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020805 benign basal cell neoplasm skos:exactMatch NCIT:C4743 Benign Basal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020807 ovarian sertoli-stromal cell tumor skos:exactMatch NCIT:C39966 Ovarian Sertoli-Stromal Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020808 testicular sertoli cell tumor skos:exactMatch NCIT:C4672 Testicular Sertoli Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020809 benign sertoli cell tumor skos:exactMatch NCIT:C67012 Benign Sertoli Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020813 benign testicular sertoli cell tumor skos:exactMatch NCIT:C6522 Benign Testicular Sertoli Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020838 anterior nasal diphtheria skos:exactMatch NCIT:C34542 Anterior Nasal Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020842 obsolete medullary carcinoma skos:exactMatch NCIT:C8998 Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020843 pseudomembranous diphtheritic conjunctivitis skos:exactMatch NCIT:C34543 Pseudomembranous Diphtheritic Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020860 faucial diphtheria skos:exactMatch NCIT:C34545 Faucial Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020863 laryngeal diphtheria skos:exactMatch NCIT:C34546 Laryngeal Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020866 nasopharyngeal diphtheria skos:exactMatch NCIT:C34547 Nasopharyngeal Diphtheria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020920 escherichia coli infection skos:exactMatch NCIT:C34594 Escherichia coli Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020959 Mansonella ozzardi infection skos:exactMatch NCIT:C34612 Mansonella Ozzardi Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020971 gonococcal urethritis skos:exactMatch NCIT:C26787 Gonococcal Urethritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020977 granulomatous prostatitis skos:exactMatch NCIT:C26789 Granulomatous Prostatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020979 pilosebaceous hamartoma skos:exactMatch NCIT:C5565 Pilosebaceous Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020980 hair nevus skos:exactMatch NCIT:C3074 Hairy Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0020989 hereditary persistence of fetal hemoglobin skos:exactMatch NCIT:C129072 Hereditary Persistence of Fetal Hemoglobin semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021001 hemochromatosis type 1 skos:exactMatch NCIT:C84764 HFE-Associated Hereditary Hemochromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021003 polydactyly skos:exactMatch NCIT:C87110 Polydactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021009 salivary gland mucoepidermoid carcinoma skos:exactMatch NCIT:C5908 Salivary Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021010 skin lymphangiosarcoma skos:exactMatch NCIT:C4490 Skin Lymphangiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021013 trichothiodystrophy 4, nonphotosensitive skos:exactMatch NCIT:C146899 Trichothiodystrophy 4, Nonphotosensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021019 X-linked recessive ocular albinism skos:exactMatch NCIT:C118785 Ocular Albinism Type 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021023 complete androgen insensitivity syndrome skos:exactMatch NCIT:C120191 Complete Androgen Insensitivity Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021032 herpes zoster with dermatitis of eyelid skos:exactMatch NCIT:C34696 Herpes Zoster Dermatitis of Eyelid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021033 herpes zoster dermatitis skos:exactMatch NCIT:C35619 Herpes Zoster Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021036 keratosis pilaris skos:exactMatch NCIT:C124070 Keratosis Pilaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021038 Ewing sarcoma/peripheral primitive neuroectodermal tumor skos:exactMatch NCIT:C27291 Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021039 extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor skos:exactMatch NCIT:C27293 Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021040 pancreatic neoplasm skos:exactMatch NCIT:C3305 Pancreatic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021041 pleural solitary fibrous tumor skos:exactMatch NCIT:C4457 Pleural Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021042 glioma skos:exactMatch NCIT:C3059 Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021043 mixed neoplasm skos:exactMatch NCIT:C6930 Mixed Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021045 fibroepithelial neoplasm skos:exactMatch NCIT:C3743 Fibroepithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021046 breast fibroepithelial neoplasm skos:exactMatch NCIT:C40405 Breast Fibroepithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021047 breast phyllodes tumor skos:exactMatch NCIT:C7575 Breast Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021048 benign mastocytoma skos:exactMatch NCIT:C3217 Benign Mastocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021049 vulvar neoplasm skos:exactMatch NCIT:C3443 Vulvar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021050 vaginal neoplasm skos:exactMatch NCIT:C3437 Vaginal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021052 parasympathetic paraganglioma skos:exactMatch NCIT:C4217 Parasympathetic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021053 carotid body paraganglioma skos:exactMatch NCIT:C2932 Carotid Body Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021054 bone sarcoma skos:exactMatch NCIT:C9312 Bone Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021055 classic familial adenomatous polyposis skos:exactMatch NCIT:C3339 Familial Adenomatous Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021058 neoplastic syndrome skos:exactMatch NCIT:C54705 Neoplastic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021059 obsolete head or neck disorder/disorder skos:exactMatch NCIT:C27571 Head and Neck Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021060 RASopathy skos:exactMatch NCIT:C179667 RASopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021061 neurofibromatosis skos:exactMatch NCIT:C6727 Neurofibromatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021063 malignant colon neoplasm skos:exactMatch NCIT:C9242 Malignant Colon Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021064 jugulotympanic paraganglioma skos:exactMatch NCIT:C3061 Jugulotympanic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021065 pleural neoplasm skos:exactMatch NCIT:C3332 Pleural Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021066 urinary system neoplasm skos:exactMatch NCIT:C3431 Urinary System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021067 mediastinal germ cell tumor skos:exactMatch NCIT:C6437 Mediastinal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021068 ovarian neoplasm skos:exactMatch NCIT:C4984 Ovarian Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021069 malignant endocrine neoplasm skos:exactMatch NCIT:C3575 Malignant Endocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021070 sublingual gland carcinoma skos:exactMatch NCIT:C8397 Sublingual Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021071 laryngeal neoplasm skos:exactMatch NCIT:C3156 Laryngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021072 sympathetic paraganglioma skos:exactMatch NCIT:C4216 Sympathetic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021073 paraneoplastic syndrome skos:exactMatch NCIT:C3311 Paraneoplastic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021074 precancerous condition skos:exactMatch NCIT:C3341 Precancerous Condition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021075 neoplastic polyp skos:exactMatch NCIT:C7068 Neoplastic Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021076 pancreatic exocrine neoplasm skos:exactMatch NCIT:C4445 Pancreatic Exocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021077 cystic neoplasm skos:exactMatch NCIT:C6784 Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021078 glandular papilloma skos:exactMatch NCIT:C6880 Glandular Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021079 childhood neoplasm skos:exactMatch NCIT:C6283 Childhood Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021080 blood vessel neoplasm skos:exactMatch NCIT:C7387 Blood Vessel Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021081 anti-NMDA receptor encephalitis skos:exactMatch NCIT:C94853 Anti-NMDA Receptor Encephalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021084 vision disorder skos:exactMatch NCIT:C35126 Vision Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021085 gastric neoplasm skos:exactMatch NCIT:C3387 Gastric Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021086 gingival neoplasm skos:exactMatch NCIT:C3057 Gingival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021088 papillary meningioma skos:exactMatch NCIT:C3904 Papillary Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021089 peripheral nervous system cancer skos:exactMatch NCIT:C4961 Malignant Peripheral Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021090 lipid-rich breast carcinoma skos:exactMatch NCIT:C40365 Breast Lipid-Rich Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021091 papillary cystadenoma skos:exactMatch NCIT:C2974 Papillary Cystadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021092 fallopian tube neoplasm skos:exactMatch NCIT:C3032 Fallopian Tube Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021094 immunodeficiency disease skos:exactMatch NCIT:C3131 Immunodeficiency Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021096 papillary epithelial neoplasm skos:exactMatch NCIT:C8429 Papillary Epithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021097 intraductal breast papilloma skos:exactMatch NCIT:C3863 Breast Intraductal Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021098 papillomatosis skos:exactMatch NCIT:C3713 Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021099 intraductal papillomatosis skos:exactMatch NCIT:C7363 Intraductal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021100 breast neoplasm skos:exactMatch NCIT:C2910 Breast Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021101 appendix L-cell glucagon-like peptide-producing neuroendocrine tumor skos:exactMatch NCIT:C27445 Appendix L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021102 prostate phyllodes tumor skos:exactMatch NCIT:C7574 Prostate Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021107 narcolepsy skos:exactMatch NCIT:C84489 Narcolepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021108 meningitis skos:exactMatch NCIT:C26828 Meningitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021109 inverted urothelial papilloma skos:exactMatch NCIT:C6192 Inverted Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021110 sweat gland adenoma skos:exactMatch NCIT:C7560 Sweat Gland Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021111 ureter neoplasm skos:exactMatch NCIT:C3427 Ureter Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021112 scrotum cancer skos:exactMatch NCIT:C3560 Malignant Scrotal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021113 respiratory failure skos:exactMatch NCIT:C26872 Respiratory Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021114 Bartholin gland neoplasm skos:exactMatch NCIT:C6434 Bartholin Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021115 luminal B breast carcinoma skos:exactMatch NCIT:C53555 Luminal B Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021116 luminal A breast carcinoma skos:exactMatch NCIT:C53554 Luminal A Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021117 lung neoplasm skos:exactMatch NCIT:C3200 Lung Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021118 intestinal neoplasm skos:exactMatch NCIT:C3141 Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021119 non-functioning endocrine neoplasm skos:exactMatch NCIT:C94760 Non-Functioning Endocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021120 functioning endocrine neoplasm skos:exactMatch NCIT:C94759 Functioning Endocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021121 hemangioendothelioma skos:exactMatch NCIT:C3084 Hemangioendothelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021123 Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone skos:exactMatch NCIT:C35871 Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor of Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021125 disease characteristic skos:exactMatch NCIT:C41009 Qualifier semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021129 microphthalmia skos:exactMatch NCIT:C98989 Microphthalmos semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021131 frontal lobe ependymal tumor skos:exactMatch NCIT:C131573 Frontal Lobe Ependymal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021132 tertiary hyperparathyroidism skos:exactMatch NCIT:C114821 Tertiary Hyperparathyroidism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021133 acquired factor XIII deficiency skos:exactMatch NCIT:C131629 Acquired Factor XIII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021134 acquired factor X deficiency skos:exactMatch NCIT:C131626 Acquired Factor X Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021138 bone marrow cancer skos:exactMatch NCIT:C35501 Malignant Bone Marrow Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021143 melanocytic neoplasm skos:exactMatch NCIT:C7058 Melanocytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021144 ovarian clear cell tumor skos:exactMatch NCIT:C40076 Ovarian Clear Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021148 female reproductive system neoplasm skos:exactMatch NCIT:C3053 Female Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021156 hypophysitis skos:exactMatch NCIT:C12399 Pituitary Gland semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021163 kidney neoplasm skos:exactMatch NCIT:C3150 Kidney Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021165 Paget disease skos:exactMatch NCIT:C7073 Paget Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021166 inflammatory disease skos:exactMatch NCIT:C93210 Inflammatory Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021167 myositis disease skos:exactMatch NCIT:C27578 Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021168 hibernoma skos:exactMatch NCIT:C3702 Hibernoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021169 epithelioid hemangioma skos:exactMatch NCIT:C4298 Epithelioid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021175 herpetic vulvovaginitis skos:exactMatch NCIT:C34697 Herpetic Vulvovaginitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021178 injury skos:exactMatch NCIT:C3671 Injury semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021190 DNA repair disease skos:exactMatch NCIT:C7757 DNA Repair Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021192 odontogenic neoplasm skos:exactMatch NCIT:C3286 Odontogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021193 neuroepithelial neoplasm skos:exactMatch NCIT:C3787 Neuroepithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021200 obsolete rare disease skos:exactMatch NCIT:C4873 Rare Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021201 skin infection skos:exactMatch NCIT:C35025 Skin Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021205 disorder of ear skos:exactMatch NCIT:C26757 Ear Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021209 heart neoplasm skos:exactMatch NCIT:C3081 Heart Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021210 trachea neoplasm skos:exactMatch NCIT:C3419 Tracheal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021211 brain neoplasm skos:exactMatch NCIT:C2907 Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021218 placenta neoplasm skos:exactMatch NCIT:C4858 Placental Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021220 eye neoplasm skos:exactMatch NCIT:C3030 Eye Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021221 vestibulocochlear nerve neoplasm skos:exactMatch NCIT:C5120 Vestibulocochlear Nerve Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021222 lacrimal gland neoplasm skos:exactMatch NCIT:C4360 Lacrimal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021223 digestive system neoplasm skos:exactMatch NCIT:C3052 Digestive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021224 iris neoplasm skos:exactMatch NCIT:C3142 Iris Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021225 uvea neoplasm skos:exactMatch NCIT:C3436 Uveal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021227 adrenal gland neoplasm skos:exactMatch NCIT:C2859 Adrenal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021228 brainstem neoplasm skos:exactMatch NCIT:C4869 Brain Stem Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021229 ciliary body neoplasm skos:exactMatch NCIT:C4364 Ciliary Body Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021230 uterine cervix neoplasm skos:exactMatch NCIT:C2940 Cervical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021231 retina neoplasm skos:exactMatch NCIT:C4800 Retinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021232 pineal body neoplasm skos:exactMatch NCIT:C3328 Pineal Region Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021233 ear neoplasm skos:exactMatch NCIT:C3000 Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021234 spinal cord neoplasm skos:exactMatch NCIT:C3381 Spinal Cord Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021235 external ear neoplasm skos:exactMatch NCIT:C4652 External Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021237 adrenal medulla neoplasm skos:exactMatch NCIT:C4856 Adrenal Medulla Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021238 cornea neoplasm skos:exactMatch NCIT:C4361 Corneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021239 urethra neoplasm skos:exactMatch NCIT:C3428 Urethra Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021240 tongue neoplasm skos:exactMatch NCIT:C3416 Tongue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021241 buccal mucosa neoplasm skos:exactMatch NCIT:C4405 Buccal Mucosa Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021242 sublingual gland neoplasm skos:exactMatch NCIT:C3392 Sublingual Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021243 parotid gland neoplasm skos:exactMatch NCIT:C3314 Parotid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021244 submandibular gland neoplasm skos:exactMatch NCIT:C3393 Submandibular Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021245 oral cavity neoplasm skos:exactMatch NCIT:C7606 Oral Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021246 pharynx neoplasm skos:exactMatch NCIT:C3325 Pharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021248 nervous system neoplasm skos:exactMatch NCIT:C3268 Nervous System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021249 lip neoplasm skos:exactMatch NCIT:C3191 Lip Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021250 tonsil neoplasm skos:exactMatch NCIT:C3417 Tonsillar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021251 endometrium neoplasm skos:exactMatch NCIT:C3012 Endometrial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021253 gallbladder neoplasm skos:exactMatch NCIT:C3048 Gallbladder Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021254 corpus uteri neoplasm skos:exactMatch NCIT:C6300 Uterine Corpus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021258 choroid neoplasm skos:exactMatch NCIT:C2949 Choroid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021259 prostate neoplasm skos:exactMatch NCIT:C3343 Prostate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021271 villous adenoma of colon skos:exactMatch NCIT:C3495 Colon Villous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021273 leiomyoma of ciliary body skos:exactMatch NCIT:C4560 Ciliary Body Leiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021275 papilloma of eyelid skos:exactMatch NCIT:C4061 Eyelid Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021276 papilloma of buccal mucosa skos:exactMatch NCIT:C5819 Buccal Squamous Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021279 mucoepidermoid carcinoma of submandibular gland skos:exactMatch NCIT:C5939 Submandibular Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021280 mucoepidermoid carcinoma of parotid gland skos:exactMatch NCIT:C5938 Parotid Gland Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021281 cavernous hemangioma of retina skos:exactMatch NCIT:C4921 Retinal Cavernous Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021282 malignant teratoma of testis skos:exactMatch NCIT:C6353 Testicular Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021283 malignant teratoma of mediastinum skos:exactMatch NCIT:C4668 Mediastinal Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021284 carcinoma in situ of ureter skos:exactMatch NCIT:C4529 Stage 0is Ureter Cancer AJCC v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021285 carcinoma in situ of urethra skos:exactMatch NCIT:C4531 Stage 0is Urethral Cancer AJCC v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021287 carcinoma in situ of epiglottis skos:exactMatch NCIT:C4592 Stage 0 Epiglottic Carcinoma AJCC v6, v7, and v8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021288 carcinoma in situ of hypopharynx skos:exactMatch NCIT:C9101 Stage 0 Hypopharyngeal Carcinoma AJCC v6, v7, and v8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021289 carcinoma in situ of cecum skos:exactMatch NCIT:C4594 Cecum Carcinoma In Situ semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021290 carcinoma in situ of appendix skos:exactMatch NCIT:C4593 Stage 0 Appendix Carcinoma AJCC v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021291 carcinoma in situ of fundus of stomach skos:exactMatch NCIT:C4429 Gastric Fundus Carcinoma In Situ AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021292 carcinoma in situ of gastric body skos:exactMatch NCIT:C4430 Gastric Body Carcinoma In Situ AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021294 carcinoma in situ of gastric cardia skos:exactMatch NCIT:C4428 Gastric Cardia Carcinoma In Situ AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021296 carcinoma in situ of renal pelvis skos:exactMatch NCIT:C4597 Stage 0is Renal Pelvis Cancer AJCC v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021297 carcinoma in situ of nasopharynx skos:exactMatch NCIT:C9099 Stage 0 Nasopharyngeal Carcinoma AJCC v6, v7, and v8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021298 carcinoma in situ of oropharynx skos:exactMatch NCIT:C4590 Stage 0 Oropharyngeal Carcinoma AJCC v6 and v7 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021299 carcinoma in situ of extrahepatic bile duct skos:exactMatch NCIT:C4442 Stage 0 Extrahepatic Bile Duct Cancer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021300 adenoid cystic carcinoma of oropharynx skos:exactMatch NCIT:C6241 Oropharyngeal Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021301 adenoma of nipple skos:exactMatch NCIT:C4192 Nipple Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021303 adenoma of small intestine skos:exactMatch NCIT:C5340 Small Intestinal Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021309 malignant neoplasm of endocervix skos:exactMatch NCIT:C3553 Malignant Endocervical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021310 malignant tumor of neck skos:exactMatch NCIT:C4940 Malignant Neck Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021311 malignant tumor of parathyroid gland skos:exactMatch NCIT:C9322 Malignant Parathyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021312 malignant tumor of adrenal cortex skos:exactMatch NCIT:C9327 Malignant Adrenal Cortical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021313 eyelid cancer skos:exactMatch NCIT:C6786 Malignant Eyelid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021315 malignant tumor of nasopharynx skos:exactMatch NCIT:C9321 Malignant Nasopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021316 malignant tumor of minor salivary gland skos:exactMatch NCIT:C4410 Malignant Minor Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021317 cancer of cerebellum skos:exactMatch NCIT:C3569 Malignant Cerebellar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021320 malignant tumor of floor of mouth skos:exactMatch NCIT:C9318 Malignant Floor of the Mouth Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021321 malignant tumor of extrahepatic bile duct skos:exactMatch NCIT:C7483 Malignant Extrahepatic Bile Duct Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021322 malignant tumor of meninges skos:exactMatch NCIT:C4628 Malignant Meningeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021323 malignant neoplasm of chest wall skos:exactMatch NCIT:C4580 Malignant Chest Wall Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021324 malignant neoplasm of abdominal esophagus skos:exactMatch NCIT:C4764 Malignant Neoplasm of the Abdominal Esophagus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021325 malignant neoplasm of thoracic esophagus skos:exactMatch NCIT:C3532 Malignant Neoplasm of the Thoracic Esophagus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021326 malignant neoplasm of cervical esophagus skos:exactMatch NCIT:C4763 Malignant Neoplasm of the Cervical Esophagus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021327 carcinoma of urethra skos:exactMatch NCIT:C9106 Urethral Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021329 carcinoma of soft palate skos:exactMatch NCIT:C8395 Soft Palate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021331 carcinoma of parotid gland skos:exactMatch NCIT:C6791 Parotid Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021333 carcinoma of lip skos:exactMatch NCIT:C3490 Lip Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021335 carcinoma of duodenum skos:exactMatch NCIT:C4803 Duodenal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021337 tonsil carcinoma skos:exactMatch NCIT:C4825 Tonsillar Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021339 carcinoma of hard palate skos:exactMatch NCIT:C8394 Hard Palate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021343 carcinoma of floor of mouth skos:exactMatch NCIT:C9319 Floor of the Mouth Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021345 carcinoma of pharynx skos:exactMatch NCIT:C9466 Pharyngeal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021348 neoplasm of testis skos:exactMatch NCIT:C3404 Testicular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021350 neoplasm of thorax skos:exactMatch NCIT:C3406 Thoracic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021351 neoplasm of neck skos:exactMatch NCIT:C3260 Neck Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021353 tumor of uterus skos:exactMatch NCIT:C3435 Uterine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021354 tumor of adipose tissue skos:exactMatch NCIT:C4248 Lipomatous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021355 neoplasm of esophagus skos:exactMatch NCIT:C3028 Esophageal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021357 tumor of salivary gland skos:exactMatch NCIT:C3361 Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021358 neoplasm of hypopharynx skos:exactMatch NCIT:C3127 Hypopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021360 tumor of parathyroid gland skos:exactMatch NCIT:C3313 Parathyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021364 neoplasm of oropharynx skos:exactMatch NCIT:C3291 Oropharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021366 neoplasm of middle ear skos:exactMatch NCIT:C4412 Middle Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021368 neoplasm of major salivary gland skos:exactMatch NCIT:C4407 Major Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021370 neoplasm of minor salivary gland skos:exactMatch NCIT:C4409 Minor Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021372 neoplasm of temporal lobe skos:exactMatch NCIT:C5567 Temporal Lobe Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021373 neoplasm of parietal lobe skos:exactMatch NCIT:C5573 Parietal Lobe Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021374 neoplasm of cerebral hemisphere skos:exactMatch NCIT:C4874 Cerebral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021375 tumor of duodenum skos:exactMatch NCIT:C2995 Duodenal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021377 hypertrophic lichen planus skos:exactMatch NCIT:C34779 Hypertrophic Lichen Planus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021378 neoplasm of endocardium skos:exactMatch NCIT:C5346 Endocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021379 neoplasm of epicardium skos:exactMatch NCIT:C5347 Epicardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021380 neoplasm of myocardium skos:exactMatch NCIT:C5349 Myocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021381 neoplasm of pericardium skos:exactMatch NCIT:C4651 Pericardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021383 neoplasm of floor of mouth skos:exactMatch NCIT:C4401 Floor of the Mouth Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021385 extrahepatic bile duct neoplasm skos:exactMatch NCIT:C4441 Extrahepatic Bile Duct Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021386 neoplasm of mediastinum skos:exactMatch NCIT:C3221 Mediastinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021388 neoplasm of chest wall skos:exactMatch NCIT:C4929 Chest Wall Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021389 neoplasm of aortic body skos:exactMatch NCIT:C4218 Aorticopulmonary Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021390 polyp of ureter skos:exactMatch NCIT:C4530 Ureter Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021392 polyp of large intestine skos:exactMatch NCIT:C5679 Colorectal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021394 polyp of vagina skos:exactMatch NCIT:C3664 Vaginal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021396 polyp of vulva skos:exactMatch NCIT:C3978 Vulvar Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021398 polyp of rectum skos:exactMatch NCIT:C3351 Rectal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021400 polyp of colon skos:exactMatch NCIT:C2954 Colon Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021402 polyp of external auditory canal skos:exactMatch NCIT:C4366 External Ear Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021404 polyp of sphenoidal sinus skos:exactMatch NCIT:C3933 Sphenoid Sinus Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021408 polyp of frontal sinus skos:exactMatch NCIT:C4367 Frontal Sinus Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021412 polyp of maxillary sinus skos:exactMatch NCIT:C3931 Maxillary Sinus Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021416 polyp of gallbladder skos:exactMatch NCIT:C3909 Gallbladder Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021418 polyp of ethmoidal sinus skos:exactMatch NCIT:C3932 Ethmoid Sinus Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021420 polyp of vocal cord skos:exactMatch NCIT:C3440 Vocal Cord Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021424 hemangiopericytoma of skin skos:exactMatch NCIT:C4492 Skin Hemangiopericytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021427 squamous cell carcinoma of lip skos:exactMatch NCIT:C4042 Lip Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021429 squamous cell carcinoma of floor of mouth skos:exactMatch NCIT:C4041 Floor of Mouth Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021431 squamous cell carcinoma of buccal mucosa skos:exactMatch NCIT:C4040 Buccal Mucosa Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021437 lipoma of stomach skos:exactMatch NCIT:C5258 Gastric Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021439 benign neoplasm of pituitary gland skos:exactMatch NCIT:C4782 Benign Pituitary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021440 benign neoplasm of skin skos:exactMatch NCIT:C2896 Benign Skin Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021441 benign neoplasm of exocrine pancreas skos:exactMatch NCIT:C4613 Benign Exocrine Pancreas Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021443 benign neoplasm of lymph node skos:exactMatch NCIT:C3636 Benign Lymph Node Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021444 benign neoplasm of large intestine skos:exactMatch NCIT:C4610 Benign Colorectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021445 benign neoplasm of oral cavity skos:exactMatch NCIT:C7607 Benign Oral Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021446 benign neoplasm of epiglottis skos:exactMatch NCIT:C4606 Benign Epiglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021447 benign neoplasm of testis skos:exactMatch NCIT:C3612 Benign Testicular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021449 benign neoplasm of stomach skos:exactMatch NCIT:C3599 Benign Gastric Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021450 benign neoplasm of heart skos:exactMatch NCIT:C3605 Benign Cardiac Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021451 benign neoplasm of brain skos:exactMatch NCIT:C4781 Benign Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021452 benign neoplasm of cornea skos:exactMatch NCIT:C3623 Benign Corneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021453 benign neoplasm of retina skos:exactMatch NCIT:C3624 Benign Retinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021454 benign neoplasm of eye skos:exactMatch NCIT:C4780 Benign Eye Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021455 benign neoplasm of neck skos:exactMatch NCIT:C4884 Benign Neck Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021456 benign neoplasm of sternum skos:exactMatch NCIT:C8416 Benign Sternal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021457 benign neoplasm of pleura skos:exactMatch NCIT:C3603 Benign Pleural Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021458 benign neoplasm of penis skos:exactMatch NCIT:C3489 Benign Penile Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021459 benign neoplasm of esophagus skos:exactMatch NCIT:C3598 Benign Esophageal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021460 benign neoplasm of salivary gland skos:exactMatch NCIT:C4600 Benign Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021461 benign neoplasm of hypopharynx skos:exactMatch NCIT:C3596 Benign Hypopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021462 benign neoplasm of rectum skos:exactMatch NCIT:C4774 Benign Rectal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021463 benign neoplasm of parathyroid gland skos:exactMatch NCIT:C3630 Benign Parathyroid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021464 benign neoplasm of cecum skos:exactMatch NCIT:C4772 Benign Cecum Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021465 benign neoplasm of appendix skos:exactMatch NCIT:C4773 Benign Appendix Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021467 benign neoplasm of renal pelvis skos:exactMatch NCIT:C3616 Benign Renal Pelvis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021468 benign neoplasm of adrenal medulla skos:exactMatch NCIT:C4895 Benign Adrenal Medulla Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021469 benign neoplasm of anus skos:exactMatch NCIT:C4611 Benign Anal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021470 benign neoplasm of pancreas skos:exactMatch NCIT:C4612 Benign Pancreatic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021471 benign neoplasm of endometrium skos:exactMatch NCIT:C4894 Benign Endometrial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021472 benign neoplasm of scrotum skos:exactMatch NCIT:C3615 Benign Scrotal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021473 benign neoplasm of epididymis skos:exactMatch NCIT:C3614 Benign Epididymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021474 benign neoplasm of ear skos:exactMatch NCIT:C8417 Benign Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021475 benign neoplasm of nasal cavity skos:exactMatch NCIT:C4603 Benign Nasal Cavity Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021476 benign neoplasm of tongue skos:exactMatch NCIT:C3592 Benign Tongue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021477 benign neoplasm of sphenoidal sinus skos:exactMatch NCIT:C4422 Benign Sphenoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021478 benign neoplasm of nasopharynx skos:exactMatch NCIT:C3595 Benign Nasopharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021479 benign neoplasm of oropharynx skos:exactMatch NCIT:C4604 Benign Oropharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021480 benign neoplasm of soft palate skos:exactMatch NCIT:C4404 Benign Soft Palate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021481 benign neoplasm of submandibular gland skos:exactMatch NCIT:C4891 Benign Submandibular Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021482 benign neoplasm of middle ear skos:exactMatch NCIT:C4602 Benign Middle Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021483 benign neoplasm of frontal sinus skos:exactMatch NCIT:C4420 Benign Frontal Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021484 benign neoplasm of maxillary sinus skos:exactMatch NCIT:C4414 Benign Maxillary Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021485 benign neoplasm of iris skos:exactMatch NCIT:C4555 Benign Iris Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021486 benign neoplasm of ciliary body skos:exactMatch NCIT:C4779 Benign Ciliary Body Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021487 benign neoplasm of choroid skos:exactMatch NCIT:C3625 Benign Choroid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021488 benign neoplasm of lacrimal gland skos:exactMatch NCIT:C3621 Benign Lacrimal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021489 benign neoplasm of sweat gland skos:exactMatch NCIT:C4879 Benign Sweat Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021490 benign neoplasm of sebaceous gland skos:exactMatch NCIT:C8525 Benign Sebaceous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021491 benign neoplasm of gum skos:exactMatch NCIT:C4598 Benign Gingival Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021492 benign neoplasm of major salivary gland skos:exactMatch NCIT:C4771 Benign Major Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021493 benign neoplasm of minor salivary gland skos:exactMatch NCIT:C4411 Benign Minor Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021494 benign neoplasm of parotid gland skos:exactMatch NCIT:C4770 Benign Parotid Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021495 benign neoplasm of sublingual gland skos:exactMatch NCIT:C4601 Benign Sublingual Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021496 benign neoplasm of lip skos:exactMatch NCIT:C3591 Benign Lip Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021497 benign neoplasm of cerebrum skos:exactMatch NCIT:C8548 Benign Cerebral Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021498 benign neoplasm of placenta skos:exactMatch NCIT:C8545 Benign Placental Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021499 benign neoplasm of cerebellum skos:exactMatch NCIT:C4955 Benign Cerebellar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021500 benign neoplasm of spleen skos:exactMatch NCIT:C4902 Benign Splenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021501 benign neoplasm of small intestine skos:exactMatch NCIT:C3600 Benign Small Intestinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021503 benign neoplasm of gallbladder skos:exactMatch NCIT:C4440 Gallbladder Benign Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021505 benign neoplasm of endocardium skos:exactMatch NCIT:C4608 Benign Endocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021506 benign neoplasm of spinal cord skos:exactMatch NCIT:C3627 Benign Spinal Cord Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021507 benign neoplasm of brain stem skos:exactMatch NCIT:C8549 Benign Brain Stem Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021508 benign neoplasm of epicardium skos:exactMatch NCIT:C8535 Benign Epicardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021509 benign neoplasm of myocardium skos:exactMatch NCIT:C4607 Benign Myocardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021510 benign neoplasm of prostate skos:exactMatch NCIT:C3613 Benign Prostate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021511 benign neoplasm of adrenal gland skos:exactMatch NCIT:C3629 Benign Adrenal Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021512 benign neoplasm of thymus skos:exactMatch NCIT:C4458 Benign Thymus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021513 benign neoplasm of tonsil skos:exactMatch NCIT:C3594 Benign Tonsillar Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021514 benign neoplasm of pericardium skos:exactMatch NCIT:C8536 Benign Pericardial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021515 benign neoplasm of ethmoidal sinus skos:exactMatch NCIT:C4417 Benign Ethmoid Sinus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021516 benign neoplasm of glottis skos:exactMatch NCIT:C4605 Benign Glottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021517 benign neoplasm of trachea skos:exactMatch NCIT:C3602 Benign Tracheal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021518 benign neoplasm of hard palate skos:exactMatch NCIT:C4403 Benign Hard Palate Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021520 benign neoplasm of floor of mouth skos:exactMatch NCIT:C3593 Benign Floor of the Mouth Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021521 benign neoplasm of mediastinum skos:exactMatch NCIT:C3604 Benign Mediastinal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021522 benign neoplasm of lower jaw bone skos:exactMatch NCIT:C34417 Benign Neoplasm of Mandible semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021523 benign neoplasm of pharynx skos:exactMatch NCIT:C3597 Benign Pharyngeal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021524 benign neoplasm of buccal mucosa skos:exactMatch NCIT:C4406 Benign Buccal Mucosa Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021525 benign neoplasm of corpus uteri skos:exactMatch NCIT:C3608 Benign Uterine Corpus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021527 benign neoplasm of meninges skos:exactMatch NCIT:C4957 Benign Neoplasm of the Meninges semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021528 benign neoplasm of male breast skos:exactMatch NCIT:C4620 Benign Male Breast Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021529 benign neoplasm of chest wall skos:exactMatch NCIT:C8529 Benign Chest Wall Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021530 benign neoplasm of subglottis skos:exactMatch NCIT:C4427 Benign Subglottis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021531 fibroma of lung skos:exactMatch NCIT:C5658 Lung Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021532 fibroma of prostate skos:exactMatch NCIT:C3972 Prostate Fibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021533 intestinal neuroendocrine tumor G1 skos:exactMatch NCIT:C4637 Intestinal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021534 rectal neuroendocrine tumor G1 skos:exactMatch NCIT:C5547 Rectal Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021535 pancreatic neuroendocrine tumor G1 skos:exactMatch NCIT:C95584 Pancreatic Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021537 undifferentiated carcinoma of nasopharynx skos:exactMatch NCIT:C8023 Nasopharyngeal Undifferentiated Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021538 verrucous carcinoma of oral cavity skos:exactMatch NCIT:C8174 Oral Cavity Verrucous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021539 hamartoma of skin appendage skos:exactMatch NCIT:C5562 Skin Appendage Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021540 hamartoma of lung skos:exactMatch NCIT:C3497 Pulmonary Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021541 hemangioma of retina skos:exactMatch NCIT:C3634 Retinal Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021542 hemangioma of choroid skos:exactMatch NCIT:C4562 Choroid Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021543 hemangioma of gingiva skos:exactMatch NCIT:C4831 Gingival Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021545 myomatous neoplasm skos:exactMatch NCIT:C4063 Myomatous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021546 ependymal tumor of spinal cord skos:exactMatch NCIT:C131526 Ependymal Tumor of Spinal Cord semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021559 non-autoimmune hemolytic anemia skos:exactMatch NCIT:C34853 Non-Autoimmune Hemolytic Anemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021562 omphalitis skos:exactMatch NCIT:C116008 Omphalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021569 Emery-Dreifuss muscular dystrophy 2, autosomal dominant skos:exactMatch NCIT:C126745 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021576 fallopian tube endometrioid tumor skos:exactMatch NCIT:C40111 Fallopian Tube Endometrioid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021578 sternal neoplasm skos:exactMatch NCIT:C6730 Sternal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021582 lentigo skos:exactMatch NCIT:C3159 Lentigo semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021583 melanocytic skin neoplasm skos:exactMatch NCIT:C7161 Skin Melanocytic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021588 eyelid sebaceous gland carcinoma skos:exactMatch NCIT:C134831 Eyelid Sebaceous Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021605 benign eyelid neoplasm skos:exactMatch NCIT:C4354 Benign Eyelid Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021607 eyelid seborrheic keratosis skos:exactMatch NCIT:C4356 Eyelid Seborrheic Keratosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021627 eyelid capillary hemangioma skos:exactMatch NCIT:C4357 Eyelid Capillary Hemangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021629 uterine ligament neoplasm skos:exactMatch NCIT:C40133 Uterine Ligament Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021631 brain astrocytoma skos:exactMatch NCIT:C60780 Brain Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021632 primary brain neoplasm skos:exactMatch NCIT:C170814 Primary Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021632 primary brain neoplasm skos:exactMatch NCIT:C4952 Localized Brain Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021633 cerebral astrocytoma skos:exactMatch NCIT:C4951 Cerebral Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021634 epithelial skin neoplasm skos:exactMatch NCIT:C7342 Epithelial Skin Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021636 astrocytic tumor skos:exactMatch NCIT:C6958 Astrocytic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021637 low grade glioma skos:exactMatch NCIT:C132067 Low Grade Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021638 low grade astrocytic tumor skos:exactMatch NCIT:C116342 Low Grade Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021639 grade II glioma skos:exactMatch NCIT:C132505 WHO Grade 2 Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021640 grade III glioma skos:exactMatch NCIT:C127816 WHO Grade 3 Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021650 uterine corpus neuroendocrine neoplasm skos:exactMatch NCIT:C126771 Uterine Corpus Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021651 synpolydactyly skos:exactMatch NCIT:C75003 Synpolydactyly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021652 diffuse type adenocarcinoma skos:exactMatch NCIT:C4127 Diffuse Type Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021656 nongerminomatous germ cell tumor skos:exactMatch NCIT:C121619 Nongerminomatous Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021657 ovarian sex cord-stromal tumor skos:exactMatch NCIT:C4862 Ovarian Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021658 vascular ectasia skos:exactMatch NCIT:C45481 Vascular Ectasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021659 combined carcinoid and adenocarcinoma skos:exactMatch NCIT:C4139 Combined Carcinoid and Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021660 deep seated dermatophytosis skos:exactMatch NCIT:C35073 Deep Seated Dermatophytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021661 coronary atherosclerosis skos:exactMatch NCIT:C35505 Coronary Atherosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021662 bile duct neoplasm skos:exactMatch NCIT:C2898 Bile Duct Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021663 sarcomatoid squamous cell carcinoma skos:exactMatch NCIT:C27084 Spindle Cell Squamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021666 ear infection skos:exactMatch NCIT:C27193 Ear Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021680 streptococcal infection skos:exactMatch NCIT:C87062 Streptococcal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021681 sexually transmitted disease skos:exactMatch NCIT:C3365 Sexually Transmitted Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021718 polyneuritis skos:exactMatch NCIT:C26864 Polyneuritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021736 proctosigmoiditis skos:exactMatch NCIT:C34950 Proctosigmoiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021750 pyonephrosis skos:exactMatch NCIT:C123032 Pyonephrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021765 radiculitis skos:exactMatch NCIT:C78581 Radiculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021777 acute rheumatic heart disease skos:exactMatch NCIT:C34985 Acute Rheumatic Heart Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021783 streptococcal sore throat skos:exactMatch NCIT:C116003 Streptococcal Pharyngitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021812 adnexal spiradenoma/cylindroma of a sweat gland skos:exactMatch NCIT:C27094 Cylindroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021879 small cell variant anaplastic large cell lymphoma skos:exactMatch NCIT:C7208 Small Cell Variant Anaplastic Large Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021895 temporomandibular joint dysfunction syndrome skos:exactMatch NCIT:C35066 Temporomandibular Joint Dysfunction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021902 aortopulmonary window skos:exactMatch NCIT:C101050 Aortopulmonary Window semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021915 arakawa syndrome 2 skos:exactMatch NCIT:C99081 Arakawa Syndrome II semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021925 tracheobronchitis skos:exactMatch NCIT:C122784 Tracheobronchitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021929 traumatic myositis ossificans skos:exactMatch NCIT:C35081 Traumatic Myositis Ossificans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021932 infection by Trypanosoma gambiense skos:exactMatch NCIT:C35084 Gambian Trypanosomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021941 infection by Trypanosoma rhodesiense skos:exactMatch NCIT:C35085 Rhodesian Trypanosomiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021944 auditory neuropathy skos:exactMatch NCIT:C116364 Auditory Neuropathy Spectrum Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021945 hearing disorder skos:exactMatch NCIT:C3078 Hearing Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021953 tuberculous fibrosis of lung skos:exactMatch NCIT:C35088 Tuberculous Fibrosis of Lung semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021960 ureteritis skos:exactMatch NCIT:C78666 Ureteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0021977 basaloid follicular hamartoma skos:exactMatch NCIT:C4749 Basal Cell Nevus with Comedones semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022022 bowenoid papulosis skos:exactMatch NCIT:C8374 Bowenoid Papulosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022057 calcifying epithelial odontogenic tumor skos:exactMatch NCIT:C54301 Calcifying Epithelial Odontogenic Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022103 chronic prostatitis skos:exactMatch NCIT:C26930 Chronic Prostatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022220 Parinaud syndrome skos:exactMatch NCIT:C54102 Parinaud Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022293 vascular disorder of penis skos:exactMatch NCIT:C35218 Penile Vascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022308 corticobasal degeneration disorder skos:exactMatch NCIT:C129069 Corticobasal Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022394 cervical intraepithelial neoplasia skos:exactMatch NCIT:C3782 Cervical Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022430 persistent fetal circulation syndrome skos:exactMatch NCIT:C85006 Persistent Fetal Circulation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022435 Mauriac syndrome skos:exactMatch NCIT:C130997 Mauriac Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022538 leukoplakia of gingiva skos:exactMatch NCIT:C3881 Leukoplakia of Gingiva semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022578 childhood bladder carcinoma skos:exactMatch NCIT:C118816 Childhood Bladder Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022642 childhood carcinoid tumor skos:exactMatch NCIT:C118810 Childhood Neuroendocrine Tumor G1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022687 cerebellar degeneration skos:exactMatch NCIT:C84624 Cerebellar Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022697 athetoid cerebral palsy skos:exactMatch NCIT:C97169 Athetoid Cerebral Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022735 choroid plexus cyst skos:exactMatch NCIT:C4351 Choroid Plexus Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022749 non-neoplastic nevus skos:exactMatch NCIT:C3937 Non-Neoplastic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022772 classic Kaposi sarcoma skos:exactMatch NCIT:C9112 Classic Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022859 cor biloculare skos:exactMatch NCIT:C124591 Cor Biloculare semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022963 desmoplastic infantile astrocytoma skos:exactMatch NCIT:C9476 Desmoplastic Infantile Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022965 desmoplastic infantile ganglioglioma skos:exactMatch NCIT:C4738 Desmoplastic Infantile Ganglioglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022986 diffuse idiopathic pulmonary neuroendocrine cell hyperplasia skos:exactMatch NCIT:C7437 Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0022993 dipsogenic diabetes insipidus skos:exactMatch NCIT:C129735 Dipsogenic Diabetes Insipidus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023023 neonatal dacryocystitis skos:exactMatch NCIT:C116819 Neonatal Dacryocystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023054 klumpke's paralysis skos:exactMatch NCIT:C116724 Klumpke Palsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023089 erythroplakia skos:exactMatch NCIT:C3025 Erythroplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023122 familial prostate carcinoma skos:exactMatch NCIT:C103817 Hereditary Prostate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023153 tuberculous ascites skos:exactMatch NCIT:C27076 Tuberculous Ascites semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023161 viral myocarditis skos:exactMatch NCIT:C128381 Viral Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023164 viral pericarditis skos:exactMatch NCIT:C128405 Viral Pericarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023206 functional pancreatic neuroendocrine tumor skos:exactMatch NCIT:C45840 Functioning Pancreatic Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023232 giant cell myocarditis skos:exactMatch NCIT:C97055 Giant Cell Myocarditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023273 pigmented dermatofibrosarcoma protuberans skos:exactMatch NCIT:C9430 Pigmented Dermatofibrosarcoma Protuberans semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023283 ovarian granulosa cell tumor skos:exactMatch NCIT:C6261 Ovarian Granulosa Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023415 congenital candidiasis skos:exactMatch NCIT:C116811 Congenital Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023483 infectious myositis skos:exactMatch NCIT:C26984 Infectious Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023528 KSHV inflammatory cytokine syndrome skos:exactMatch NCIT:C125711 KSHV Inflammatory Cytokine Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023554 acquired testicular failure skos:exactMatch NCIT:C131091 Acquired Testicular Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023557 infective vaginitis skos:exactMatch NCIT:C84353 Vaginal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023595 congenital myotonic dystrophy skos:exactMatch NCIT:C123308 Congenital Myotonic Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023597 laryngeal papillomatosis skos:exactMatch NCIT:C157733 Laryngeal Papillomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023599 mesomelic dysplasia skos:exactMatch NCIT:C121156 Mesomelic Dysplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023601 non-classic congenital adrenal hyperplasia skos:exactMatch NCIT:C131442 Non-Classic Congenital Adrenal Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023603 hereditary disorder of connective tissue skos:exactMatch NCIT:C97075 Hereditary Connective Tissue Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023619 lentigo maligna melanoma skos:exactMatch NCIT:C9151 Lentigo Maligna Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023628 levator syndrome skos:exactMatch NCIT:C113615 Proctalgia Fugax semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023644 lip and oral cavity carcinoma skos:exactMatch NCIT:C9315 Lip and Oral Cavity Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023682 tympanic paraganglioma skos:exactMatch NCIT:C8428 Tympanic Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023726 mediastinal yolk sac tumor skos:exactMatch NCIT:C6443 Mediastinal Yolk Sac Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0023865 corneal infection skos:exactMatch NCIT:C83813 Corneal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024235 Brenner tumor skos:exactMatch NCIT:C39954 Brenner Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024237 inherited neurodegenerative disorder skos:exactMatch NCIT:C97073 Hereditary Neurodegenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024239 congenital anomaly of cardiovascular system skos:exactMatch NCIT:C35729 Congenital Cardiovascular Abnormality semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024240 eccrine carcinoma skos:exactMatch NCIT:C27255 Eccrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024245 ductal eccrine adenocarcinoma skos:exactMatch NCIT:C43345 Ductal Eccrine Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024246 syringofibroadenoma skos:exactMatch NCIT:C43356 Syringofibroadenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024247 benign eccrine neoplasm skos:exactMatch NCIT:C6797 Benign Eccrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024249 pityriasis lichenoides skos:exactMatch NCIT:C85013 Pityriasis Lichenoides semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024263 neonatal aspiration syndrome skos:exactMatch NCIT:C118312 Neonatal Aspiration Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024275 amebic dysentery skos:exactMatch NCIT:C34558 Amebic Colitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024276 glandular cell neoplasm skos:exactMatch NCIT:C7132 Glandular Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024278 proctocolitis skos:exactMatch NCIT:C77952 Proctocolitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024279 chronic endometritis skos:exactMatch NCIT:C102820 Chronic Endometritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024280 polyarticular arthritis skos:exactMatch NCIT:C26996 Polyarticular Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024281 juvenile chronic polyarthritis skos:exactMatch NCIT:C26979 Juvenile Chronic Polyarthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024282 mucinous ovarian cancer skos:exactMatch NCIT:C40033 Malignant Ovarian Mucinous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024286 benign blood vessel neoplasm skos:exactMatch NCIT:C8537 Benign Blood Vessel Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024287 congenital vascular malformation skos:exactMatch NCIT:C112117 Vascular Malformation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024290 enuresis skos:exactMatch NCIT:C34588 Enuresis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024292 gastrointestinal polyp skos:exactMatch NCIT:C35516 Gastrointestinal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024296 vascular neoplasm skos:exactMatch NCIT:C7388 Vascular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024298 vitamin deficiency disorder skos:exactMatch NCIT:C35772 Vitamin Deficiency Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024300 hypophosphatemic rickets skos:exactMatch NCIT:C131449 Hypophosphatemic Rickets semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024304 ichthyosis vulgaris skos:exactMatch NCIT:C84778 Ichthyosis Vulgaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024313 staphylococcal infection skos:exactMatch NCIT:C35038 Staphylococcal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024315 parasitic endophthalmitis skos:exactMatch NCIT:C34587 Parasitic Endophthalmitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024316 physiological malfunction arising from mental factor skos:exactMatch NCIT:C35186 Physiological Malfunction Arising from Mental Factor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024320 inner ear neoplasm skos:exactMatch NCIT:C39784 Inner Ear Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024323 glomangiomyoma skos:exactMatch NCIT:C4223 Glomangiomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024326 pleural adenomatoid tumor skos:exactMatch NCIT:C4499 Pleural Adenomatoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024327 chronic renal failure syndrome skos:exactMatch NCIT:C9438 Chronic Renal Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024330 infectious otitis media skos:exactMatch NCIT:C84354 Infectious Otitis Media semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024331 colorectal carcinoma skos:exactMatch NCIT:C2955 Colorectal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024332 perennial allergic rhinitis skos:exactMatch NCIT:C92189 Perennial Allergic Rhinitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024336 vulvar adenocarcinoma skos:exactMatch NCIT:C6380 Vulvar Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024337 urothelial neoplasm skos:exactMatch NCIT:C39852 Urothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024338 mucinous neoplasm skos:exactMatch NCIT:C7070 Mucinous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024339 lymph node neoplasm skos:exactMatch NCIT:C35497 Lymph Node Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024340 retinal neuroblastoma skos:exactMatch NCIT:C6956 Retinal Neuroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024341 retinal cell neoplasm skos:exactMatch NCIT:C7061 Retinal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024352 viral respiratory tract infection skos:exactMatch NCIT:C27219 Viral Respiratory Tract Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024354 cytomegalovirus pneumonia skos:exactMatch NCIT:C35360 Cytomegalovirus Pneumonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024361 circadian rhythm sleep disorder skos:exactMatch NCIT:C95071 Circadian Rhythm Sleep Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024386 large cell lung carcinoma, clear cell variant skos:exactMatch NCIT:C4451 Lung Large Cell Carcinoma, Clear Cell Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024387 benign ovarian sex cord-stromal tumor skos:exactMatch NCIT:C6803 Benign Ovarian Sex Cord-Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024419 enthesitis skos:exactMatch NCIT:C114470 Enthesitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024422 auditory perceptual disorders skos:exactMatch NCIT:C84575 Auditory Perceptual Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024429 Alice in Wonderland syndrome skos:exactMatch NCIT:C116362 Alice in Wonderland Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024432 nerve plexus disorder skos:exactMatch NCIT:C27744 Plexopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024457 neurodegeneration with brain iron accumulation 2A skos:exactMatch NCIT:C84927 Infantile Neuroaxonal Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024461 angiomatosis skos:exactMatch NCIT:C27503 Angiomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024469 chondrogenic neoplasm skos:exactMatch NCIT:C4755 Chondrogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024470 benign chondrogenic neoplasm skos:exactMatch NCIT:C8592 Benign Chondrogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024474 intraepithelial neoplasia skos:exactMatch NCIT:C8366 Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024475 squamous cell intraepithelial neoplasia skos:exactMatch NCIT:C8334 Squamous Cell Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024477 liver and intrahepatic bile duct neoplasm skos:exactMatch NCIT:C7103 Liver Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024477 liver and intrahepatic bile duct neoplasm skos:exactMatch NCIT:C7106 Liver Epithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024478 mesenchymal hamartoma skos:exactMatch NCIT:C40427 Mesenchymal Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024482 eccrine sweat gland hamartoma skos:exactMatch NCIT:C5564 Eccrine Sweat Gland Hamartoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024483 urothelial hyperplasia skos:exactMatch NCIT:C27877 Urothelial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024485 papillary urothelial hyperplasia skos:exactMatch NCIT:C27879 Papillary Urothelial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024487 nail infection skos:exactMatch NCIT:C78493 Nail Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024489 general tumor grading characteristic skos:exactMatch NCIT:C28076 Disease Grade Qualifier semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024491 tumor grade 1, general grading system skos:exactMatch NCIT:C28077 Grade 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024492 tumor grade 2, general grading system skos:exactMatch NCIT:C28078 Grade 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024493 tumor grade 3, general grading system skos:exactMatch NCIT:C28079 Grade 3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024494 tumor grade 4, general grading system skos:exactMatch NCIT:C28082 Grade 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024496 tumor grade 2 or 3, general grading system skos:exactMatch NCIT:C94678 Grade 2/3 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024497 tumor grade 3 or 4, general grading system skos:exactMatch NCIT:C14158 High Grade semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024499 vascular bone neoplasm skos:exactMatch NCIT:C6478 Vascular Bone Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024501 appendix neuroendocrine neoplasm skos:exactMatch NCIT:C60709 Appendix Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024502 gallbladder neuroendocrine neoplasm skos:exactMatch NCIT:C96917 Gallbladder Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024503 digestive system neuroendocrine neoplasm skos:exactMatch NCIT:C27721 Digestive System Neuroendocrine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024504 enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor skos:exactMatch NCIT:C4446 Pancreatic Serotonin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024537 Brown-Vialetto-van Laere syndrome 1 skos:exactMatch NCIT:C133724 Brown-Vialetto-Van Laere Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024538 basal ganglia calcification, idiopathic, 1 skos:exactMatch NCIT:C129973 Idiopathic Basal Ganglia Calcification 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024556 epilepsy, familial focal, with variable foci 1 skos:exactMatch NCIT:C161005 Familial Focal Epilepsy with Variable Foci 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024557 ataxia-telangiectasia-like disorder 1 skos:exactMatch NCIT:C132224 Ataxia-Telangiectasia-Like Disorder 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024571 AIDS-related disorder skos:exactMatch NCIT:C4991 AIDS-Related Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024572 immunodeficiency-related disorder skos:exactMatch NCIT:C35686 Immunodeficiency-Related Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024573 familial hypertrophic cardiomyopathy skos:exactMatch NCIT:C84773 Familial Hypertrophic Cardiomyopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024574 von Willebrand disease (hereditary or acquired) skos:exactMatch NCIT:C68677 von Willebrand Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024575 pregnancy disorder skos:exactMatch NCIT:C35169 Pregnancy Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024582 male reproductive system neoplasm skos:exactMatch NCIT:C3054 Male Reproductive System Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024583 obsolete hernia skos:exactMatch NCIT:C34685 Hernia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024609 vulvar squamous cell carcinoma skos:exactMatch NCIT:C4052 Vulvar Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024611 orbit neoplasm skos:exactMatch NCIT:C3290 Orbit Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024612 manic bipolar affective disorder skos:exactMatch NCIT:C34805 Manic Bipolar Affective Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024613 bipolar depression skos:exactMatch NCIT:C34424 Bipolar Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024614 neurotic depression skos:exactMatch NCIT:C35369 Neurotic Depression semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024615 T-cell and NK-cell neoplasm skos:exactMatch NCIT:C27908 T-Cell and NK-Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024617 xanthogranuloma skos:exactMatch NCIT:C27302 Reactive Xanthogranuloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024619 central nervous system infectious disorder skos:exactMatch NCIT:C27582 Central Nervous System Infectious Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024621 serous cystadenocarcinoma skos:exactMatch NCIT:C3778 Serous Cystadenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024622 thyroid gland adenocarcinoma skos:exactMatch NCIT:C27380 Thyroid Gland Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024623 otorhinolaryngologic disease skos:exactMatch NCIT:C118420 Otolaryngologic Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024633 hypertensive nephropathy skos:exactMatch NCIT:C4757 Hypertensive Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024637 malignant soft tissue neoplasm skos:exactMatch NCIT:C4867 Malignant Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024638 pancreatic gastrinoma skos:exactMatch NCIT:C95596 Pancreatic Gastrinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024639 gastric enterochromaffin cell serotonin-producing neuroendocrine tumor skos:exactMatch NCIT:C27443 Gastric Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024642 gastric neuroendocrine tumor G2 skos:exactMatch NCIT:C95880 Gastric Neuroendocrine Tumor G2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024643 myocardial disorder skos:exactMatch NCIT:C35544 Myocardial Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024644 myocardial ischemia skos:exactMatch NCIT:C50625 Ischemic Heart Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024645 retroperitoneal neoplasm skos:exactMatch NCIT:C3357 Retroperitoneal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024646 obsolete refractory skos:exactMatch NCIT:C39752 Refractory Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024647 urolithiasis skos:exactMatch NCIT:C114688 Urolithiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024648 optic tract meningioma skos:exactMatch NCIT:C5587 Visual Pathway Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024649 optic tract astrocytoma skos:exactMatch NCIT:C7533 Visual Pathway Astrocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024653 skull neoplasm skos:exactMatch NCIT:C3375 Skull Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024654 skull disorder skos:exactMatch NCIT:C27655 Skull Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024656 colorectal lymphoma skos:exactMatch NCIT:C96498 Colorectal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024658 extrahepatic bile duct sarcoma skos:exactMatch NCIT:C5029 Extrahepatic Bile Duct Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024659 colorectal Kaposi sarcoma skos:exactMatch NCIT:C96510 Colorectal Kaposi Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024660 tubular adenoma skos:exactMatch NCIT:C4133 Tubular Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024661 tubulovillous adenoma skos:exactMatch NCIT:C4143 Tubulovillous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024662 colorectal tubulovillous adenoma skos:exactMatch NCIT:C5675 Colorectal Tubulovillous Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024663 primary skin meningioma skos:exactMatch NCIT:C5277 Primary Cutaneous Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024664 hypertension, pregnancy-induced skos:exactMatch NCIT:C9243 Hypertension-Associated Pregnancy Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024666 benign epithelial skin neoplasm skos:exactMatch NCIT:C7341 Benign Epithelial Skin Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024673 skin lymphangioma skos:exactMatch NCIT:C27509 Skin Lymphangioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024674 Pancoast syndrome skos:exactMatch NCIT:C55815 Pancoast Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024675 adult kidney Wilms tumor skos:exactMatch NCIT:C6180 Adult Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024676 childhood kidney Wilms tumor skos:exactMatch NCIT:C27730 Childhood Kidney Wilms Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024677 pancreatic insulinoma skos:exactMatch NCIT:C95598 Pancreatic Insulinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024685 Philadelphia-positive myelogenous leukemia skos:exactMatch NCIT:C3177 Myeloid Leukemia, Philadelphia-Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024686 tenosynovial giant cell tumor, diffuse type skos:exactMatch NCIT:C3401 Tenosynovial Giant Cell Tumor, Diffuse Type semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024711 malignant mixed epithelial stromal tumor of the kidney skos:exactMatch NCIT:C37265 Malignant Mixed Epithelial and Stromal Tumor of the Kidney semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024715 benign synovial neoplasm skos:exactMatch NCIT:C3829 Benign Synovial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024744 childhood choroid plexus neoplasm skos:exactMatch NCIT:C42080 Childhood Choroid Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024746 immature teratoma skos:exactMatch NCIT:C4286 Immature Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024757 cardiovascular neoplasm skos:exactMatch NCIT:C4784 Cardiovascular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024797 adult brain stem neoplasm skos:exactMatch NCIT:C5967 Adult Brain Stem Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024813 pulmonary sulcus neoplasm skos:exactMatch NCIT:C27710 Pulmonary Sulcus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024857 immature extragonadal teratoma skos:exactMatch NCIT:C8884 Immature Extragonadal Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024861 mixed teratoma and seminoma skos:exactMatch NCIT:C9010 Mixed Teratoma and Seminoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024863 small size posterior uveal melanoma skos:exactMatch NCIT:C9089 Small Size Posterior Uveal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024864 medium/large size posterior uveal melanoma skos:exactMatch NCIT:C9090 Medium/Large Size Posterior Uveal Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024868 metastatic carcinoma in the adrenal medulla skos:exactMatch NCIT:C9276 Metastatic Carcinoma in the Adrenal Medulla semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024873 clitoral carcinoma skos:exactMatch NCIT:C9362 Clitoral Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024878 secondary carcinoma skos:exactMatch NCIT:C36310 Secondary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024879 metastatic carcinoma skos:exactMatch NCIT:C3482 Metastatic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024880 metastatic malignant neoplasm skos:exactMatch NCIT:C36263 Metastatic Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024881 secondary malignant neoplasm skos:exactMatch NCIT:C4968 Secondary Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024882 secondary neoplasm skos:exactMatch NCIT:C36255 Secondary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024883 metastatic neoplasm skos:exactMatch NCIT:C3261 Metastatic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024884 metastatic carcinoma in the bone skos:exactMatch NCIT:C36082 Metastatic Carcinoma in the Bone semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024885 malignant ovarian serous tumor skos:exactMatch NCIT:C40025 Malignant Ovarian Serous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024886 serous adenofibroma skos:exactMatch NCIT:C67090 Serous Adenofibroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024890 pineal parenchymal cell neoplasm skos:exactMatch NCIT:C6965 Pineal Parenchymal Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0024892 soft tissue amyloid neoplasm skos:exactMatch NCIT:C8323 Amyloid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0025303 anaplasmosis skos:exactMatch NCIT:C128425 Anaplasmosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0025419 furunculosis skos:exactMatch NCIT:C34629 Furunculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0025481 obsolete zoonosis skos:exactMatch NCIT:C35803 Zoonotic Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0026777 VEXAS syndrome skos:exactMatch NCIT:C181924 VEXAS Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0027026 Buschke Lowenstein tumor skos:exactMatch NCIT:C6371 Giant Condyloma Acuminatum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0027407 Kleefstra syndrome 1 skos:exactMatch NCIT:C129976 Kleefstra Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0027766 generalized lipodystrophy skos:exactMatch NCIT:C131815 Generalized Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0027767 partial lipodystrophy skos:exactMatch NCIT:C131296 Partial Lipodystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0027772 lung colloid adenocarcinoma skos:exactMatch NCIT:C45512 Lung Colloid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0028226 autosomal recessive severe congenital neutropenia skos:exactMatch NCIT:C176624 Autosomal Recessive Severe Congenital Neutropenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0030604 cystic partially differentiated nephroblastoma skos:exactMatch NCIT:C6897 Cystic Partially Differentiated Kidney Nephroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0030705 Trichomonas prostatitis skos:exactMatch NCIT:C35176 Trichomonas Prostatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0030706 Trichomonas cystitis skos:exactMatch NCIT:C35405 Trichomonas Cystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0030707 Trichomonas balanoposthitis skos:exactMatch NCIT:C35406 Trichomonas Balanoposthitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0030708 Trichomonas cervicitis skos:exactMatch NCIT:C35588 Trichomonas Cervicitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0031014 autoimmune gastritis skos:exactMatch NCIT:C95752 Autoimmune Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0031332 Glanzmann thrombasthenia 1 skos:exactMatch NCIT:C61249 Glanzmann Thrombasthenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0032572 cardiac, facial, and digital anomalies with developmental delay skos:exactMatch NCIT:C179868 Cardiac, Facial, and Digital Anomalies with Developmental Delay semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0032666 epidermodysplasia verruciformis, susceptibility to, 4 skos:exactMatch NCIT:C176608 Epidermodysplasia Verruciformis, Susceptibility to, 4 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0032786 Noonan syndrome 11 skos:exactMatch NCIT:C177119 Noonan Syndrome 11 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0032806 trichothiodystrophy 7, nonphotosensitive skos:exactMatch NCIT:C173102 Trichothiodystrophy 7, Nonphotosensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0032839 noonan syndrome 12 skos:exactMatch NCIT:C177120 Noonan Syndrome 12 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0033669 Noonan syndrome 13 skos:exactMatch NCIT:C177121 Noonan Syndrome 13 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0033821 fungal keratitis skos:exactMatch NCIT:C128370 Fungal Keratitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0033954 monoclonal mast cell activation syndrome skos:exactMatch NCIT:C181652 Monoclonal Mast Cell Activation Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035112 acute myeloid leukemia with BCR-ABL1 skos:exactMatch NCIT:C129785 Acute Myeloid Leukemia with BCR-ABL1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035121 myeloid/lymphoid neoplasm associated with JAK2 rearrangement skos:exactMatch NCIT:C129853 Myeloid/Lymphoid Neoplasms with JAK2 Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035450 aprosencephaly skos:exactMatch NCIT:C98824 Aprosencephaly semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035605 B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality skos:exactMatch NCIT:C80328 B Lymphoblastic Leukemia/Lymphoma with Recurrent Genetic Abnormalities semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035642 mixed phenotype acute leukemia with t(v;11q23.3) skos:exactMatch NCIT:C82203 Mixed Phenotype Acute Leukemia with KMT2A Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035735 acquired hemophilia A skos:exactMatch NCIT:C35345 Acquired Factor VIII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035737 acquired factor V deficiency skos:exactMatch NCIT:C131624 Acquired Factor V Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035738 acquired factor VII deficiency skos:exactMatch NCIT:C131625 Acquired Factor VII Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035740 acquired factor XI deficiency skos:exactMatch NCIT:C131627 Acquired Factor XI Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035940 B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2) skos:exactMatch NCIT:C80331 B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035941 B-lymphoblastic leukemia/lymphoma with t(v;11q23.3) skos:exactMatch NCIT:C80332 B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035942 B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1) skos:exactMatch NCIT:C80334 B Lymphoblastic Leukemia/Lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035943 B-lymphoblastic leukemia/lymphoma with hyperdiploidy skos:exactMatch NCIT:C80335 Hyperdiploid B Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035944 B-lymphoblastic leukemia/lymphoma with hypodiploidy skos:exactMatch NCIT:C80338 Hypodiploid B Lymphoblastic Leukemia/Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0035945 B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3) skos:exactMatch NCIT:C80340 B Lymphoblastic Leukemia/Lymphoma with t(5;14)(q31.1;q32.3); IL3-IGH semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036491 obsolete rare childhood malignant neoplasm skos:exactMatch NCIT:C114451 Rare Childhood Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036501 refractory malignant neoplasm skos:exactMatch NCIT:C120186 Refractory Malignant Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036511 childhood malignant kidney neoplasm skos:exactMatch NCIT:C123907 Childhood Malignant Kidney Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036591 adrenal cortex neoplasm skos:exactMatch NCIT:C2858 Adrenal Cortical Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036595 ovarian Sertoli-Leydig cell tumor skos:exactMatch NCIT:C2880 Ovarian Sertoli-Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036688 rhabdomyoma skos:exactMatch NCIT:C3358 Rhabdomyoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036696 spleen neoplasm skos:exactMatch NCIT:C3383 Splenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036779 axillary neoplasm skos:exactMatch NCIT:C35749 Axillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036781 benign axillary neoplasm skos:exactMatch NCIT:C35750 Benign Axillary Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036870 lymphatic vessel neoplasm skos:exactMatch NCIT:C3723 Lymphatic Vessel Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036915 benign ovarian mucinous tumor skos:exactMatch NCIT:C40039 Benign Ovarian Mucinous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036976 benign epithelial neoplasm skos:exactMatch NCIT:C4092 Benign Epithelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0036990 benign Leydig cell tumor skos:exactMatch NCIT:C4212 Benign Leydig Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037002 benign phyllodes tumor skos:exactMatch NCIT:C4274 Benign Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037003 malignant phyllodes tumor skos:exactMatch NCIT:C4275 Malignant Phyllodes Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037105 lung germ cell tumor skos:exactMatch NCIT:C45636 Lung Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037250 childhood testicular neoplasm skos:exactMatch NCIT:C5053 Childhood Testicular Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037252 thecoma skos:exactMatch NCIT:C3405 Thecoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037253 ovarian thecoma skos:exactMatch NCIT:C66989 Ovarian Thecoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037254 transitional cell neoplasm skos:exactMatch NCIT:C6783 Transitional Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037255 ovarian serous tumor skos:exactMatch NCIT:C8431 Ovarian Serous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037256 serous neoplasm skos:exactMatch NCIT:C7074 Serous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037735 sebaceous gland cancer skos:exactMatch NCIT:C8409 Malignant Sebaceous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037736 infratentorial neoplasm skos:exactMatch NCIT:C3139 Infratentorial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037737 peritoneal solitary fibrous tumor skos:exactMatch NCIT:C126357 Peritoneal Solitary Fibrous Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037740 malignant central nervous system mesenchymal, non-meningothelial neoplasm skos:exactMatch NCIT:C6758 Malignant Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037742 endometrioid stromal and related neoplasms skos:exactMatch NCIT:C8384 Endometrioid Stromal and Related Neoplasms semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037743 mediastinal soft tissue cancer skos:exactMatch NCIT:C6642 Malignant Mediastinal Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037745 fibromyxoid tumor skos:exactMatch NCIT:C66760 Fibromyxoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037746 malignant vaginal mixed epithelial and mesenchymal neoplasm skos:exactMatch NCIT:C40276 Malignant Vaginal Mixed Epithelial and Mesenchymal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037748 hyperlipoproteinemia skos:exactMatch NCIT:C34709 Hyperlipoproteinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0037858 inherited fatty acid metabolism disorder skos:exactMatch NCIT:C117115 Fatty Acid Metabolism Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040673 malignant peritoneal germ cell tumor skos:exactMatch NCIT:C136410 Malignant Peritoneal Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040675 myofibroblastoma skos:exactMatch NCIT:C49012 Myofibroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040676 great vessel cancer skos:exactMatch NCIT:C4575 Malignant Great Vessel Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040677 invasive carcinoma skos:exactMatch NCIT:C9480 Invasive Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040678 infiltrating urothelial carcinoma skos:exactMatch NCIT:C39853 Invasive Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040679 urothelial carcinoma skos:exactMatch NCIT:C4030 Urothelial Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040700 orbital dermoid cyst skos:exactMatch NCIT:C4548 Orbit Dermoid Cyst semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0040923 late latent syphilis skos:exactMatch NCIT:C128371 Late Latent Syphilis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0041161 obsolete endometrial hyperplasia skos:exactMatch NCIT:C3013 Endometrial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0041447 metastatic malignant neoplasm in the colon skos:exactMatch NCIT:C8411 Metastatic Malignant Neoplasm in the Colon semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042233 disseminated candidiasis skos:exactMatch NCIT:C116812 Disseminated Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042485 infective arthritis skos:exactMatch NCIT:C26700 Infective Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042487 uterine cervix carcinoma in situ skos:exactMatch NCIT:C4000 Stage 0 Cervical Cancer AJCC v6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042491 cervical squamous intraepithelial neoplasia skos:exactMatch NCIT:C7346 Cervical Squamous Intraepithelial Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042493 gastric non-hodgkin lymphoma skos:exactMatch NCIT:C27235 Gastric Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042494 childhood malignant melanoma skos:exactMatch NCIT:C131506 Childhood Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042727 sacrococcygeal teratoma skos:exactMatch NCIT:C99055 Sacrococcygeal Teratoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042963 wandering spleen skos:exactMatch NCIT:C85224 Wandering Spleen semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042976 vitamin B deficiency skos:exactMatch NCIT:C35129 Vitamin B Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042981 aortic valve stenosis skos:exactMatch NCIT:C50462 Aortic Valve Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042982 GATA2 deficiency with susceptibility to MDS/AML skos:exactMatch NCIT:C126349 GATA2 Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0042983 neurocutaneous syndrome skos:exactMatch NCIT:C84348 Phakomatosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043103 hypothyroidism due to iodide transport defect skos:exactMatch NCIT:C121747 Iodide Transport Defect semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043209 albinism skos:exactMatch NCIT:C84543 Albinism semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043218 neurovascular disorder skos:exactMatch NCIT:C117007 Neurovascular Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043219 migraine with brainstem aura skos:exactMatch NCIT:C117013 Basilar-Type Migraine semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043224 multi-infarct dementia skos:exactMatch NCIT:C34522 Multi-Infarct Dementia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043233 exfoliative dermatitis skos:exactMatch NCIT:C39646 Erythroderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043240 hemophilic arthropathy skos:exactMatch NCIT:C27039 Hemophilic Arthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043243 leukoplakia skos:exactMatch NCIT:C3186 Leukoplakia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043247 Mallory-Weiss syndrome skos:exactMatch NCIT:C84881 Mallory-Weiss Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043251 odontoma skos:exactMatch NCIT:C3287 Odontoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043275 TORCH syndrome skos:exactMatch NCIT:C98609 TORCH Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043280 Wallerian degeneration skos:exactMatch NCIT:C85223 Wallerian Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043287 superior vena cava syndrome skos:exactMatch NCIT:C3396 Superior Vena Cava Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043294 linear scleroderma skos:exactMatch NCIT:C116780 Linear Scleroderma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043300 actinic cheilitis skos:exactMatch NCIT:C183562 Actinic Cheilitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043303 hyperacusis skos:exactMatch NCIT:C116366 Hyperacusis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043310 amaurosis fugax skos:exactMatch NCIT:C84550 Amaurosis Fugax semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043320 piriformis syndrome skos:exactMatch NCIT:C85012 Piriformis Muscle Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043346 progressive transformation of germinal centers skos:exactMatch NCIT:C38408 Progressive Transformation of Germinal Centers semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043349 intravascular papillary endothelial hyperplasia skos:exactMatch NCIT:C4391 Intravascular Papillary Endothelial Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043355 collagenous gastritis skos:exactMatch NCIT:C122082 Collagenous Gastritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043358 engraftment syndrome skos:exactMatch NCIT:C63324 Engraftment Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043370 secondary adrenal insufficiency skos:exactMatch NCIT:C62602 Secondary Adrenal Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043377 juvenile spondyloarthropathy skos:exactMatch NCIT:C114347 Juvenile Spondyloarthritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043424 digestive system infectious disorder skos:exactMatch NCIT:C35503 Digestive System Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043455 humoral hypercalcemia of malignancy skos:exactMatch NCIT:C3496 Hypercalcemia of Malignancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043459 radiation-induced disorder skos:exactMatch NCIT:C26684 Radiation-Induced Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043465 achlorhydria skos:exactMatch NCIT:C2850 Achlorhydria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043468 acne keloid skos:exactMatch NCIT:C34346 Acne Keloid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043472 ectopic ACTH secretion syndrome skos:exactMatch NCIT:C4387 Ectopic ACTH Secretion Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043475 Adams-Stokes syndrome skos:exactMatch NCIT:C79765 Stokes-Adams Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043479 adenoviridae infectious disease skos:exactMatch NCIT:C115149 Adenovirus Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043494 arteritis skos:exactMatch NCIT:C34399 Arteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043512 traumatic encephalopathy skos:exactMatch NCIT:C35542 Traumatic Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043519 burn skos:exactMatch NCIT:C34441 Burn semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043537 cluster headache syndrome skos:exactMatch NCIT:C117077 Cluster Headache semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043541 viral conjunctivitis skos:exactMatch NCIT:C34509 Viral Conjunctivitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043544 nosocomial infection skos:exactMatch NCIT:C115164 Nosocomial Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043576 endarteritis skos:exactMatch NCIT:C34581 Endarteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043579 enteritis skos:exactMatch NCIT:C26765 Enteritis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043606 obsolete pathologic fracture skos:exactMatch NCIT:C3047 Pathologic Fracture semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043653 herpes labialis skos:exactMatch NCIT:C34695 Cold Sore semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043683 Leriche syndrome skos:exactMatch NCIT:C34773 Leriche Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043693 alcoholic liver diseases skos:exactMatch NCIT:C34783 Alcoholic Liver Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043707 obsolete mediastinal disorder skos:exactMatch NCIT:C26826 Mediastinal Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043726 multiple organ dysfunction syndrome skos:exactMatch NCIT:C179648 Multiple Organ Dysfunction Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043731 lytic metastatic bone lesion skos:exactMatch NCIT:C35371 Lytic Metastatic Bone Lesion semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043735 osteoradionecrosis skos:exactMatch NCIT:C63707 Osteoradionecrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043759 abdominal ectopic pregnancy skos:exactMatch NCIT:C92921 Abdominal Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043762 tubal pregnancy skos:exactMatch NCIT:C92946 Tubal Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043765 presbycusis skos:exactMatch NCIT:C116367 Presbycusis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043768 thrombocytopenic purpura skos:exactMatch NCIT:C26870 Thrombocytopenic Purpura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043771 radiodermatitis skos:exactMatch NCIT:C3349 Radiation-Induced Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043777 rhinophyma skos:exactMatch NCIT:C34989 Rhinophyma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043783 sclerema neonatorum skos:exactMatch NCIT:C35009 Sclerema Neonatorum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043786 serositis skos:exactMatch NCIT:C70428 Serositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043789 serum sickness skos:exactMatch NCIT:C79718 Serum Sickness semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043836 tuberculosis, spinal skos:exactMatch NCIT:C35087 Pott Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043839 ulcer disease skos:exactMatch NCIT:C3426 Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043862 voice disorders skos:exactMatch NCIT:C3441 Voice Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043875 tumor lysis syndrome skos:exactMatch NCIT:C3425 Tumor Lysis Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043878 hereditary optic atrophy skos:exactMatch NCIT:C34864 Hereditary Optic Atrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043881 obsolete acute eosinophilic leukemia skos:exactMatch NCIT:C26813 Acute Eosinophilic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043885 eye infectious disorder skos:exactMatch NCIT:C45372 Eye Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043892 prosthesis-related infectious disease skos:exactMatch NCIT:C79705 Prosthesis-Related Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043905 pneumonitis skos:exactMatch NCIT:C113159 Pneumonitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043923 lichen planus, oral skos:exactMatch NCIT:C7406 Oral Lichen Planus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043959 pseudolymphoma skos:exactMatch NCIT:C3825 Pseudolymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043985 central nervous system lupus skos:exactMatch NCIT:C116919 Central Nervous System Lupus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0043994 acute cholecystitis skos:exactMatch NCIT:C35152 Acute Cholecystitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044001 hearing loss, mixed conductive-sensorineural skos:exactMatch NCIT:C26974 Mixed Hearing Loss semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044014 postpartum thyroiditis skos:exactMatch NCIT:C114389 Postpartum Thyroiditis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044033 posterior leukoencephalopathy syndrome skos:exactMatch NCIT:C78598 Reversible Posterior Leukoencephalopathy Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044067 candidiasis, invasive skos:exactMatch NCIT:C116813 Invasive Candidiasis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044079 cardio-renal syndrome skos:exactMatch NCIT:C123225 Cardiorenal Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044092 collagenous sprue skos:exactMatch NCIT:C45426 Collagenous Sprue semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044098 ovarian ectopic pregnancy skos:exactMatch NCIT:C92945 Ovarian Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044101 pregnancy, cornual skos:exactMatch NCIT:C92761 Cornual Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044113 bullous systemic lupus erythematosus skos:exactMatch NCIT:C117104 Bullous Systemic Lupus Erythematosus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044137 vitreous body disorder skos:exactMatch NCIT:C45256 Vitreous Body Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044138 hyalitis skos:exactMatch NCIT:C50587 Hyalitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044141 panic disorder without agoraphobia skos:exactMatch NCIT:C97193 Panic Disorder without Agoraphobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044144 panic disorder with agoraphobia skos:exactMatch NCIT:C97194 Panic Disorder with Agoraphobia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044333 alcohol-induced Wernicke-Korsakoff's syndrome skos:exactMatch NCIT:C34366 Alcohol-Induced Wernicke-Korsakoff's Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044334 connective and soft tissue neoplasm skos:exactMatch NCIT:C3810 Connective and Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044335 benign soft tissue neoplasm skos:exactMatch NCIT:C4242 Benign Soft Tissue Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044336 colorectal signet ring cell carcinoma skos:exactMatch NCIT:C43586 Colorectal Signet Ring Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044337 stromal sarcoma skos:exactMatch NCIT:C6926 Stromal Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044339 lumbar disk degenerative disorder skos:exactMatch NCIT:C27154 Lumbar Disc Degenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044342 thoracic disk degenerative disorder skos:exactMatch NCIT:C27155 Thoracic Disc Degenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044343 cervical disk degenerative disorder skos:exactMatch NCIT:C27156 Cervical Disc Degenerative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044344 Schistosoma japonicum infectious disease skos:exactMatch NCIT:C35001 Schistosoma Japonicum Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044345 Schistosoma mansoni infectious disease skos:exactMatch NCIT:C35002 Schistosoma Mansoni Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044351 Schistosoma intercalatum infectious disease skos:exactMatch NCIT:C35364 Infection by Schistosoma Intercalatum semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044638 hypopharynx squamous cell carcinoma skos:exactMatch NCIT:C4043 Hypopharyngeal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044704 oropharynx squamous cell carcinoma skos:exactMatch NCIT:C8181 Oropharyngeal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044705 paranasal sinus squamous cell carcinoma skos:exactMatch NCIT:C8193 Paranasal Sinus Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044710 lip and oral cavity squamous cell carcinoma skos:exactMatch NCIT:C42690 Lip and Oral Cavity Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044719 erythema multiforme major skos:exactMatch NCIT:C3385 Erythema Multiforme Major semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044727 pancreatic carcinoma with mixed differentiation skos:exactMatch NCIT:C45843 Pancreatic Mixed Adenoneuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044740 salivary gland squamous cell carcinoma skos:exactMatch NCIT:C7991 Salivary Gland Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044743 major salivary gland cancer skos:exactMatch NCIT:C4762 Malignant Major Salivary Gland Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044744 prekallikrein deficiency skos:exactMatch NCIT:C99022 Prekallikrein Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044746 obsolete zoonotic bacterial infection skos:exactMatch NCIT:C35373 Zoonotic Bacterial Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044753 lumbar spinal stenosis skos:exactMatch NCIT:C177445 Lumbar Spinal Stenosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044764 benign choroid plexus neoplasm skos:exactMatch NCIT:C8405 Benign Choroid Plexus Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044765 steroid-resistant nephrotic syndrome skos:exactMatch NCIT:C122798 Nephrotic Syndrome of Childhood - Steroid Resistant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044767 childhood adrenal gland pheochromocytoma skos:exactMatch NCIT:C118822 Childhood Adrenal Gland Pheochromocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044768 vagus nerve paraganglioma skos:exactMatch NCIT:C8427 Vagal Paraganglioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044778 nodular lymphocyte predominant Hodgkin lymphoma skos:exactMatch NCIT:C7258 Nodular Lymphocyte Predominant B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044781 nephrotic syndrome of childhood - steroid sensitive skos:exactMatch NCIT:C122797 Nephrotic Syndrome of Childhood - Steroid Sensitive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044782 esophageal ulcer skos:exactMatch NCIT:C26950 Esophageal Ulcer semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044783 solid papillary breast carcinoma skos:exactMatch NCIT:C6870 Breast Solid Papillary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044784 myxoma skos:exactMatch NCIT:C6577 Myxoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044785 desmoplastic melanoma skos:exactMatch NCIT:C37257 Desmoplastic Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044786 solid pseudopapillary neoplasm of the pancreas skos:exactMatch NCIT:C37212 Solid Pseudopapillary Neoplasm of the Pancreas semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044787 nasal cavity and paranasal sinus squamous cell carcinoma skos:exactMatch NCIT:C68611 Sinonasal Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044788 perihilar intrahepatic cholangiocarcinoma skos:exactMatch NCIT:C96804 Large Duct Intrahepatic Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044789 digital papillary eccrine carcinoma skos:exactMatch NCIT:C27534 Digital Papillary Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044791 combined hepatocellular carcinoma and cholangiocarcinoma skos:exactMatch NCIT:C3828 Combined Hepatocellular Carcinoma and Cholangiocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044792 large congenital melanocytic nevus skos:exactMatch NCIT:C3944 Congenital Melanocytic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044792 large congenital melanocytic nevus skos:exactMatch NCIT:C4234 Giant Congenital Melanocytic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044793 spitz nevus skos:exactMatch NCIT:C27007 Spitz Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044794 benign melanocytic skin nevus skos:exactMatch NCIT:C7571 Benign Skin Melanocytic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044795 epithelioid cell nevus skos:exactMatch NCIT:C66757 Epithelioid Cell Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044796 spindle cell nevus skos:exactMatch NCIT:C66758 Spindle Cell Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044797 desmoplastic nevus skos:exactMatch NCIT:C4497 Desmoplastic Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044800 desmoplastic spitz nevus skos:exactMatch NCIT:C82864 Desmoplastic Spitz Nevus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044807 inherited dystonia skos:exactMatch NCIT:C35527 Familial Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044811 idiopathic torsion dystonia skos:exactMatch NCIT:C34564 Idiopathic Torsion Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044816 familial idiopathic torsion dystonia skos:exactMatch NCIT:C35437 Familial Idiopathic Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044817 acquired idiopathic torsion dystonia skos:exactMatch NCIT:C35438 Non-Familial Idiopathic Dystonia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044872 dysautonomia skos:exactMatch NCIT:C53439 Dysautonomia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044873 childhood myelodysplastic syndrome skos:exactMatch NCIT:C68744 Childhood Myelodysplastic Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044874 refractory cytopenia of childhood skos:exactMatch NCIT:C82596 Refractory Cytopenia of Childhood semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044875 coronary microvascular disorder skos:exactMatch NCIT:C84478 Coronary Microvascular Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044877 paraneoplastic cerebellar degeneration skos:exactMatch NCIT:C4685 Paraneoplastic Cerebellar Degeneration semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044878 adult germ cell tumor skos:exactMatch NCIT:C114777 Adult Germ Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044879 pancreatic mucinous-cystic neoplasm skos:exactMatch NCIT:C41247 Pancreatic Mucinous-Cystic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044881 hematopoietic and lymphoid cell neoplasm skos:exactMatch NCIT:C27134 Hematopoietic and Lymphoid Cell Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044884 tonsillar lymphoma skos:exactMatch NCIT:C5918 Tonsillar Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044885 tonsillar lipoma skos:exactMatch NCIT:C5989 Tonsillar Lipoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044887 central nervous system non-hodgkin lymphoma skos:exactMatch NCIT:C114779 Central Nervous System Non-Hodgkin Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044889 high grade B-cell lymphoma skos:exactMatch NCIT:C138211 High Grade B-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044903 myelofibrosis skos:exactMatch NCIT:C3248 Myelofibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044906 bladder urothelial papilloma skos:exactMatch NCIT:C39858 Bladder Urothelial Papilloma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044907 metastatic squamous cell carcinoma skos:exactMatch NCIT:C4104 Metastatic Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044912 metastatic malignant neoplasm in the spinal cord skos:exactMatch NCIT:C4585 Metastatic Malignant Neoplasm in the Spinal Cord semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044913 metastatic malignant neoplasm in the eye skos:exactMatch NCIT:C4586 Metastatic Malignant Neoplasm in the Eye semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044915 salivary duct carcinoma skos:exactMatch NCIT:C5904 Salivary Duct Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044916 extrarenal rhabdoid tumor skos:exactMatch NCIT:C6586 Extrarenal Rhabdoid Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044917 T-lymphoblastic lymphoma skos:exactMatch NCIT:C6919 T Lymphoblastic Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044919 malignant renal pelvis neoplasm skos:exactMatch NCIT:C7525 Malignant Renal Pelvis Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044921 atypical lymphoproliferative disorder skos:exactMatch NCIT:C7764 Atypical Lymphoproliferative Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044923 acute myeloid leukemia with mutated NPM1 skos:exactMatch NCIT:C82431 Acute Myeloid Leukemia with NPM1 Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044925 oral cavity carcinoma skos:exactMatch NCIT:C8990 Oral Cavity Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044926 oropharyngeal carcinoma skos:exactMatch NCIT:C9105 Oropharyngeal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044937 rectal carcinoma skos:exactMatch NCIT:C9382 Rectal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044956 paranasal sinus mucoepidermoid carcinoma skos:exactMatch NCIT:C6018 Paranasal Sinus Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044964 oral cavity mucoepidermoid carcinoma skos:exactMatch NCIT:C8177 Oral Cavity Mucoepidermoid Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0044983 benign lipomatous neoplasm skos:exactMatch NCIT:C4502 Benign Lipomatous Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045045 selective IgG immunodeficiency skos:exactMatch NCIT:C27142 Selective IgG Immunodeficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045048 toxemia of pregnancy skos:exactMatch NCIT:C34943 Toxemia of Pregnancy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045050 nuclear cataract skos:exactMatch NCIT:C135176 Nuclear Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045051 cortical cataract skos:exactMatch NCIT:C135177 Cortical Cataract semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045052 benign osteogenic neoplasm skos:exactMatch NCIT:C6602 Benign Osteogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045053 osteogenic neoplasm skos:exactMatch NCIT:C6603 Osteogenic Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045054 cancer-related condition skos:exactMatch NCIT:C8278 Cancer-Related Condition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045055 glycogen-rich carcinoma skos:exactMatch NCIT:C4153 Glycogen-Rich Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045056 grade II meningioma skos:exactMatch NCIT:C38937 Grade 2 Meningioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045057 delirium skos:exactMatch NCIT:C2981 Delirium semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045060 intraductal cribriform breast adenocarcinoma skos:exactMatch NCIT:C5138 Breast Ductal Carcinoma In Situ, Cribriform Pattern semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045063 major salivary gland adenoid cystic carcinoma skos:exactMatch NCIT:C5905 Major Salivary Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045068 minor salivary gland adenoid cystic carcinoma skos:exactMatch NCIT:C5936 Minor Salivary Gland Adenoid Cystic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045069 minor salivary gland carcinoma skos:exactMatch NCIT:C5957 Minor Salivary Gland Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045070 digestive system melanoma skos:exactMatch NCIT:C7091 Mucosal Melanoma of the Digestive System semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045071 mycosis fungoides variant skos:exactMatch NCIT:C39644 Mycosis Fungoides Variant semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0045072 ectopic hormone secretion syndrome associated with neoplasia skos:exactMatch NCIT:C4065 Ectopic Hormone Secretion Syndrome Associated with Neoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054588 Noonan syndrome-like disorder with loose anagen hair 2 skos:exactMatch NCIT:C176940 Noonan Syndrome-Like Disorder with Loose Anagen Hair 2 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054637 Noonan syndrome-like disorder with loose anagen hair 1 skos:exactMatch NCIT:C176939 Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054677 combined oxidative phosphorylation deficiency 33 skos:exactMatch NCIT:C174440 Combined Oxidative Phosphorylation Deficiency 33 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054697 immunodeficiency 11b with atopic dermatitis skos:exactMatch NCIT:C176630 Immunodeficiency 11B with Atopic Dermatitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054698 proteasome-associated autoinflammatory syndrome 1 skos:exactMatch NCIT:C176619 Proteasome-Associated Autoinflammatory Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054835 classic dopamine transporter deficiency syndrome skos:exactMatch NCIT:C129866 Dopamine Transporter Deficiency Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0054868 meconium ileus skos:exactMatch NCIT:C98979 Meconium Ileus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056796 obstructive nephropathy skos:exactMatch NCIT:C120902 Obstructive Nephropathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056805 benign peripheral nerve granular cell tumor skos:exactMatch NCIT:C5502 Benign Peripheral Nerve Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056806 non-small cell squamous lung carcinoma skos:exactMatch NCIT:C133254 Lung Non-Small Cell Squamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056813 hormone-resistant breast carcinoma skos:exactMatch NCIT:C114932 Hormone-Resistant Breast Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056814 hormone-resistant prostate carcinoma skos:exactMatch NCIT:C114933 Hormone-Resistant Prostate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056815 liver adenosquamous carcinoma skos:exactMatch NCIT:C118630 Liver Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056816 vulvar neuroendocrine carcinoma skos:exactMatch NCIT:C128243 Vulvar Neuroendocrine Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056817 rectal adenosquamous carcinoma skos:exactMatch NCIT:C43594 Rectal Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056818 skin adenosquamous carcinoma skos:exactMatch NCIT:C54250 Skin Adenosquamous Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056819 nasal cavity and paranasal sinus carcinoma skos:exactMatch NCIT:C54293 Sinonasal Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0056820 nasal cavity and paranasal sinus neoplasm skos:exactMatch NCIT:C7336 Sinonasal Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060765 fibroepithelial polyp skos:exactMatch NCIT:C3337 Fibroepithelial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060766 anal polyp skos:exactMatch NCIT:C3957 Anal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060768 gingival fibroepithelial polyp skos:exactMatch NCIT:C4693 Gingival Fibroepithelial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060774 vaginal fibroepithelial polyp skos:exactMatch NCIT:C4948 Vaginal Fibroepithelial Stromal Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060777 cervical fibroepithelial polyp skos:exactMatch NCIT:C40200 Cervical Fibroepithelial Polyp semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060778 adult Fanconi syndrome skos:exactMatch NCIT:C4377 Adult Fanconi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060779 acquired Fanconi syndrome skos:exactMatch NCIT:C78296 Acquired Fanconi Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060782 premalignant hematological system disease skos:exactMatch NCIT:C27274 Premalignant Hematologic Condition semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0060783 classic congenital adrenal hyperplasia skos:exactMatch NCIT:C131423 Classic Congenital Adrenal Hyperplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100017 pityriasis rubra pilaris skos:exactMatch NCIT:C85014 Pityriasis Rubra Pilaris semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100053 anaphylaxis skos:exactMatch NCIT:C107101 Anaphylaxis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100055 intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements skos:exactMatch NCIT:C178236 Intraosseous Spindle Cell Rhabdomyosarcoma with TFCP2/NCOA2 Rearrangements semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100060 congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements skos:exactMatch NCIT:C178232 Congenital/Infantile Spindle Cell Rhabdomyosarcoma with VGLL2/NCOA2/CITED2 Rearrangements semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100062 developmental and epileptic encephalopathy skos:exactMatch NCIT:C122814 Developmental and Epileptic Encephalopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100064 tyrosine hydroxylase deficiency skos:exactMatch NCIT:C157158 Tyrosine Hydroxylase Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100067 childhood spindle cell rhabdomyosarcoma skos:exactMatch NCIT:C123397 Childhood Spindle Cell Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100081 sleep disorder skos:exactMatch NCIT:C3376 Sleep Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100115 acute flaccid myelitis skos:exactMatch NCIT:C128379 Acute Flaccid Myelitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100116 Middle East respiratory syndrome skos:exactMatch NCIT:C128424 Middle East Respiratory Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100135 Dravet syndrome skos:exactMatch NCIT:C116573 Dravet Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100137 telomere syndrome skos:exactMatch NCIT:C152065 Telomere Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100151 nephropathic cystinosis skos:exactMatch NCIT:C129932 Nephropathic Cystinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100156 Imerslund-Grasbeck syndrome type 1 skos:exactMatch NCIT:C131677 Megaloblastic Anemia 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100159 pulmonary hypertension, neonatal skos:exactMatch NCIT:C4732 Neonatal Hypertension semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100163 COVID-19–associated multisystem inflammatory syndrome in children skos:exactMatch NCIT:C172127 Multisystem Inflammatory Syndrome in Children semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100164 permanent neonatal diabetes mellitus skos:exactMatch NCIT:C114902 Permanent Neonatal Diabetes Mellitus semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100186 GTP cyclohydrolase I deficiency with hyperphenylalaninemia skos:exactMatch NCIT:C141442 GTP Cyclohydrolase I Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100192 liver failure skos:exactMatch NCIT:C26922 Liver Failure semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100193 chronic liver failure skos:exactMatch NCIT:C84428 End Stage Liver Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100216 DICER1-related tumor predisposition skos:exactMatch NCIT:C123317 DICER1 Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100233 long COVID-19 skos:exactMatch NCIT:C179263 Post-Acute Sequelae of COVID-19 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100244 paroxysmal nocturnal hemoglobinuria skos:exactMatch NCIT:C61233 Paroxysmal Nocturnal Hemoglobinuria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100249 46,XX testicular disorder of sex development skos:exactMatch NCIT:C127170 46,XX Testicular Differences of Sex Development semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100250 46,XX sex reversal 1 skos:exactMatch NCIT:C179867 46,XX Sex Reversal 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100251 familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome skos:exactMatch NCIT:C131851 Hyperphosphatemic Familial Tumoral Calcinosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100253 Roberts-SC phocomelia syndrome skos:exactMatch NCIT:C4681 Roberts-SC Phocomelia Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100280 Waldenstrom macroglobulinemia skos:exactMatch NCIT:C80307 Waldenstrom Macroglobulinemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100285 extrahepatic biliary atresia skos:exactMatch NCIT:C97069 Extrahepatic Biliary Atresia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100290 colon serrated polyposis skos:exactMatch NCIT:C96470 Colon Serrated Polyposis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100291 early T cell progenitor acute lymphoblastic leukemia skos:exactMatch NCIT:C130043 Early T Precursor Acute Lymphoblastic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100310 hereditary cerebellar ataxia skos:exactMatch NCIT:C140268 Hereditary Cerebellar Ataxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100313 focal segmental glomerulosclerosis skos:exactMatch NCIT:C37308 Focal Segmental Glomerulosclerosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100316 long QT syndrome 1 skos:exactMatch NCIT:C85049 Long QT Syndrome 1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100339 Friedreich ataxia skos:exactMatch NCIT:C84718 Friedreich Ataxia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100342 malignant glioma skos:exactMatch NCIT:C4822 Malignant Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100345 lactose intolerance skos:exactMatch NCIT:C3154 Lactose Intolerance semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100347 carcinoid syndrome skos:exactMatch NCIT:C3215 Carcinoid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100354 megacystis-microcolon-intestinal hypoperistalsis syndrome 1 skos:exactMatch NCIT:C98982 MMIH Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100370 acute hepatitis B virus infection skos:exactMatch NCIT:C157781 Acute Hepatitis B Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100371 acute hepatitis C virus infection skos:exactMatch NCIT:C157782 Acute Hepatitis C Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100373 acute myeloid leukemia, inv(16)(p13.1;q22) skos:exactMatch NCIT:C9018 Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100374 acute myeloid leukemia, t(16;16)(p13.1;q22) skos:exactMatch NCIT:C9019 Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100375 acute myeloid leukemia, t(15;17)(q24;q21) skos:exactMatch NCIT:C36055 Acute Myeloid Leukemia with a Variant RARA Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100377 acute myeloid leukemia, t(10;11)(p12;q23) skos:exactMatch NCIT:C132101 Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100381 acute myeloid leukemia, t(6;11)(q27;q23) skos:exactMatch NCIT:C132105 Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100382 acute myeloid leukemia, t(6;9)(p23;q34.1) skos:exactMatch NCIT:C82423 Acute Myeloid Leukemia with t(6;9)(p22.3;q34.1); DEK-NUP214 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100389 acute myeloid leukemia, Trisomy 8 skos:exactMatch NCIT:C162775 Acute Myeloid Leukemia with Trisomy 8 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100395 acute myeloid leukemia, t(5;11)(q35;p15) skos:exactMatch NCIT:C131502 Childhood Acute Myeloid Leukemia with t(5;11)(q35;p15); NUP98-NSD1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100396 acute myeloid leukemia, t(7;12)(q36;p13) skos:exactMatch NCIT:C122690 Acute Myeloid Leukemia with t(7;12)(q36;p13); HLXB9-ETV6 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100398 acute myeloid leukemia, inv(3)(q21.3;q26.2) skos:exactMatch NCIT:C122716 Acute Myeloid Leukemia with inv(3) (q21.3;q26.2); GATA2, MECOM semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100399 acute myeloid leukemia, t(3;3)(q21.3;q26.2) skos:exactMatch NCIT:C122717 Acute Myeloid Leukemia with t(3;3) (q21.3;q26.2); GATA2, MECOM semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100404 acute myeloid leukemia, MLL gene rearrangement skos:exactMatch NCIT:C174129 Acute Myeloid Leukemia with KMT2A Rearrangement semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100407 acute myeloid leukemia, t(11;15)(p15;q35) skos:exactMatch NCIT:C131504 Childhood Acute Myeloid Leukemia with t(11;15)(p15;q35); NUP98-JARID1A semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100409 acute myeloid leukemia, t(3;5)(q25;q34) skos:exactMatch NCIT:C7600 Acute Myeloid Leukemia, Myelodysplasia-Related semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100414 acute myeloid leukemia, CEBPA gene mutation skos:exactMatch NCIT:C151898 Acute Myeloid Leukemia with Germline CEBPA Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100415 acute myeloid leukemia, FLT3 internal tandem duplication skos:exactMatch NCIT:C126748 Acute Myeloid Leukemia with FLT3/ITD Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100422 acute myeloid leukemia, RUNX1 gene mutation skos:exactMatch NCIT:C129786 Acute Myeloid Leukemia with RUNX1 Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100431 migraine without aura skos:exactMatch NCIT:C117004 Migraine Without Aura semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100470 reactive airway disease skos:exactMatch NCIT:C113673 Reactive Airway Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100471 vitamin D deficiency skos:exactMatch NCIT:C114830 Vitamin D Deficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100480 autoimmune primary adrenal insufficiency skos:exactMatch NCIT:C113814 Autoimmune Primary Adrenal Insufficiency semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100482 extensively drug-resistant tuberculosis skos:exactMatch NCIT:C128417 Extensively Drug-Resistant Tuberculosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100492 Bonnevie-Ullrich syndrome skos:exactMatch NCIT:C34434 Bonnevie-Ullrich Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100505 food dermatitis skos:exactMatch NCIT:C34534 Dermatitis due to Food taken Internally semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100514 familial ovarian carcinoma skos:exactMatch NCIT:C36102 Hereditary Ovarian Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100531 Emery-Dreifuss muscular dystrophy 1, X-linked skos:exactMatch NCIT:C168730 Emery-Dreifuss Muscular Dystrophy 1, X-Linked semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100534 SMARCB1-deficient kidney medullary carcinoma skos:exactMatch NCIT:C189247 SMARCB1-Deficient Kidney Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100542 clonal hematopoiesis skos:exactMatch NCIT:C162188 Clonal Hematopoiesis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0100550 orbital myositis skos:exactMatch NCIT:C117296 Orbital Myositis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0200000 uterine ligament adenosarcoma skos:exactMatch NCIT:C102570 Broad Ligament Adenosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600002 hemorrhagic fever skos:exactMatch NCIT:C36169 Hemorrhagic Fever semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600008 cytokine release syndrome skos:exactMatch NCIT:C78251 Cytokine Release Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600023 idiopathic inflammatory myopathy skos:exactMatch NCIT:C116796 Idiopathic Inflammatory Myopathy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600025 hydrosalpinx skos:exactMatch NCIT:C142886 Hydrosalpinx semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600029 restrictive pulmonary disease skos:exactMatch NCIT:C91762 Restrictive Lung Disease semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0600030 B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) skos:exactMatch NCIT:C80347 B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); TCF3-PBX1 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700048 hand-foot syndrome skos:exactMatch NCIT:C27177 Palmar-Plantar Erythrodysthesia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700051 liver abscess (disease) skos:exactMatch NCIT:C99089 Liver Abscess semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700058 Morton neuroma skos:exactMatch NCIT:C4075 Morton Neuroma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700064 aneuploidy skos:exactMatch NCIT:C2873 Aneuploidy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700078 triple-positive breast carcinoma skos:exactMatch NCIT:C118311 Hormone Receptor/HER2 Positive semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700081 newborn respiratory distress syndrome skos:exactMatch NCIT:C27560 Respiratory Distress Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700082 Robertsonian translocation Down syndrome skos:exactMatch NCIT:C188150 Robertsonian Translocation Down Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700086 uniparental disomy skos:exactMatch NCIT:C85215 Uniparental Disomy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700090 epilepsy, familial temporal lobe, 1 skos:exactMatch NCIT:C141441 Autosomal Dominant Lateral Temporal Lobe Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700091 ring chromosome disorder skos:exactMatch NCIT:C3360 Supernumerary Circular Chromosome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700092 neurodevelopmental disorder skos:exactMatch NCIT:C1535926 semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700092 neurodevelopmental disorder skos:exactMatch NCIT:C89338 Neurodevelopmental Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700134 bovine neoplasm skos:exactMatch NCIT:C134527 Bovine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700135 bovine leukemia skos:exactMatch NCIT:C131469 Bovine Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700136 bovine protoporphyria skos:exactMatch NCIT:C131472 Bovine Protoporphyria semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700137 bovine lymphosarcoma skos:exactMatch NCIT:C134767 Bovine Lymphosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700138 bovine rectal myxoma skos:exactMatch NCIT:C134768 Bovine Rectal Myxoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700139 canine neoplasm skos:exactMatch NCIT:C134526 Canine Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700140 canine osteosarcoma skos:exactMatch NCIT:C120045 Canine Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700141 canine melanoma skos:exactMatch NCIT:C120298 Canine Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700142 canine hemangiosarcoma skos:exactMatch NCIT:C122783 Canine Hemangiosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700143 canine mammary carcinoma skos:exactMatch NCIT:C124249 Canine Mammary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700144 canine leukemia skos:exactMatch NCIT:C128120 Canine Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700145 canine lymphoma skos:exactMatch NCIT:C128121 Canine Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700146 canine prostate carcinoma skos:exactMatch NCIT:C128122 Canine Prostate Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700147 canine histiocytic sarcoma skos:exactMatch NCIT:C128125 Canine Histiocytic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700148 canine transitional cell carcinoma skos:exactMatch NCIT:C128126 Canine Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700149 canine sarcoma skos:exactMatch NCIT:C128195 Canine Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700150 canine mastocytoma skos:exactMatch NCIT:C129077 Canine Mastocytoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700151 canine glioma skos:exactMatch NCIT:C129297 Canine Glioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700152 canine hepatocellular carcinoma skos:exactMatch NCIT:C129298 Canine Hepatocellular Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700153 canine lung adenocarcinoma skos:exactMatch NCIT:C129299 Canine Lung Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700154 canine rhabdomyosarcoma skos:exactMatch NCIT:C129300 Canine Rhabdomyosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700155 canine thyroid adenocarcinoma skos:exactMatch NCIT:C132275 Canine Thyroid Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700156 canine soft tissue sarcoma skos:exactMatch NCIT:C132276 Canine Soft Tissue Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700157 canine oral squamous cell carcinoma skos:exactMatch NCIT:C132823 Canine Oral Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700158 canine pancreatic carcinoma skos:exactMatch NCIT:C134944 Canine Pancreatic Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700159 canine acanthomatous epulis skos:exactMatch NCIT:C134956 Canine Acanthomatous Epulis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700160 canine mammary adenoma skos:exactMatch NCIT:C147073 Canine Mammary Adenoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700161 canine gastrointestinal stromal tumor skos:exactMatch NCIT:C158783 Canine Gastrointestinal Stromal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700162 canine granular cell tumor skos:exactMatch NCIT:C158784 Canine Granular Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700163 canine Langerhans cell histiocytosis skos:exactMatch NCIT:C158785 Canine Langerhans Cell Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700164 canine nephroblastoma skos:exactMatch NCIT:C158786 Canine Nephroblastoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700165 canine thyroid gland medullary carcinoma skos:exactMatch NCIT:C161006 Canine Thyroid Gland Medullary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700166 canine transmissible venereal tumor skos:exactMatch NCIT:C162473 Canine Transmissible Venereal Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700167 canine sebaceous gland epithelioma skos:exactMatch NCIT:C176701 Canine Sebaceous Gland Epithelioma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700168 canine oral melanoma skos:exactMatch NCIT:C185639 Canine Oral Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700169 canine cutaneous t-cell lymphoma skos:exactMatch NCIT:C186279 Canine Cutaneous T-Cell Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700171 horse melanoma skos:exactMatch NCIT:C134569 Horse Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700172 horse lymphoma skos:exactMatch NCIT:C134778 Horse Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700173 horse sarcoid skos:exactMatch NCIT:C134995 Horse Sarcoid semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700174 horse transitional cell carcinoma skos:exactMatch NCIT:C173624 Horse Transitional Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700176 feline lymphoma skos:exactMatch NCIT:C132193 Feline Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700177 feline mammary carcinoma skos:exactMatch NCIT:C132274 Feline Mammary Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700178 feline oral squamous cell carcinoma skos:exactMatch NCIT:C132824 Feline Oral Squamous Cell Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700179 feline osteosarcoma skos:exactMatch NCIT:C132825 Feline Osteosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700180 feline bronchioloalveolar lung carcinoma skos:exactMatch NCIT:C134559 Feline Bronchioloalveolar Lung Carcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700181 feline fibrosarcoma skos:exactMatch NCIT:C134560 Feline Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700182 feline erythroleukemia skos:exactMatch NCIT:C134770 Feline Erythroleukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700183 feline reticulum cell sarcoma skos:exactMatch NCIT:C135008 Feline Reticulum Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700184 feline large granular lymphocyte lymphoma skos:exactMatch NCIT:C135724 Feline Large Granular Lymphocyte Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700185 feline melanoma skos:exactMatch NCIT:C156362 Feline Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700186 feline histiocytic sarcoma skos:exactMatch NCIT:C157503 Feline Histiocytic Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700187 feline progressive histiocytosis skos:exactMatch NCIT:C176702 Feline Progressive Histiocytosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700188 feline synovial cell sarcoma skos:exactMatch NCIT:C181658 Feline Synovial Cell Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700189 chicken neoplasm skos:exactMatch NCIT:C135005 Chicken Neoplasm semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700190 chicken bursal lymphoma skos:exactMatch NCIT:C134556 Chicken Bursal Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700191 chicken fibrosarcoma skos:exactMatch NCIT:C134557 Chicken Fibrosarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700192 chicken hepatoma skos:exactMatch NCIT:C134558 Chicken Hepatoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700193 chicken monocytic leukemia skos:exactMatch NCIT:C134945 Chicken Monocytic Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700194 chicken lymphoma skos:exactMatch NCIT:C135004 Chicken Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700195 rous sarcoma skos:exactMatch NCIT:C17466 Rous Sarcoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700196 fish melanoma skos:exactMatch NCIT:C135006 Fish Melanoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700197 porcine leukemia skos:exactMatch NCIT:C141365 Porcine Leukemia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700198 porcine lymphoma skos:exactMatch NCIT:C134786 Porcine Lymphoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700199 sheep lung adenocarcinoma skos:exactMatch NCIT:C147532 Sheep Lung Adenocarcinoma semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700218 group B streptococcal infection skos:exactMatch NCIT:C87168 Group B Streptococcal Infection semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0700219 neoplastic meningitis skos:exactMatch NCIT:C3814 Metastatic Malignant Neoplasm in the Leptomeninges semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800026 central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease skos:exactMatch NCIT:C98889 Congenital Central Hypoventilation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800027 leukoencephalopathy, diffuse hereditary, with spheroids 1 skos:exactMatch NCIT:C153289 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800029 interstitial lung disease 2 skos:exactMatch NCIT:C35716 Idiopathic Pulmonary Fibrosis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800044 congenital disorder of deglycosylation 1 skos:exactMatch NCIT:C126746 Congenital Disorder of Deglycosylation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800106 disruptive behavior disorder skos:exactMatch NCIT:C99753 Disruptive Behavior Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800113 necrotizing vasculitis skos:exactMatch NCIT:C70635 Necrotizing Vasculitis semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800133 pulmonary hypoplasia skos:exactMatch NCIT:C99035 Pulmonary Hypoplasia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800177 frostbite skos:exactMatch NCIT:C34627 Frostbite semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800445 Birt-Hogg-Dube syndrome 1 skos:exactMatch NCIT:C28244 Birt-Hogg-Dube Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800448 leukoencephalopathy with vanishing white matter skos:exactMatch NCIT:C122664 Leukoencephalopathy with Vanishing White Matter semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800452 congenital amegakaryocytic thrombocytopenia 1 skos:exactMatch NCIT:C115207 Congenital Amegakaryocytic Thrombocytopenia semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800453 juvenile absence epilepsy skos:exactMatch NCIT:C129868 Juvenile Absence Epilepsy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0800486 metabolic bone disorder skos:exactMatch NCIT:C97045 Metabolic Bone Disorder semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0858921 EWSR1-negative small round cell tumor skos:exactMatch NCIT:C165671 EWSR1-Negative Small Round Cell Tumor semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0958176 oculopharyngeal muscular dystrophy 1 skos:exactMatch NCIT:C84942 Oculopharyngeal Muscular Dystrophy semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:8000010 antiphospholipid syndrome skos:exactMatch NCIT:C61283 Antiphospholipid Syndrome semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:8000023 type 3 autoimmune lymphoproliferative syndrome skos:exactMatch NCIT:C39577 Autoimmune Lymphoproliferative Syndrome-Unknown Underlying Mutation semapv:UnspecifiedMatching 0.95 MONDO:MONDO +MONDO:0016824 infantile myofibromatosis skos:exactMatch NCIT:C27498 Infantile Hemangiopericytoma semapv:LexicalMatching 0.8 oaklib ['oio:hasExactSynonym'] ['rdfs:label'] ['infantile hemangiopericytoma'] Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease. +MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch NCIT:C192096 Intratubular Embryonal Carcinoma semapv:LexicalMatching 0.8 oaklib ['oio:hasExactSynonym'] ['rdfs:label'] ['intratubular embryonal carcinoma'] +MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch NCIT:C192096 Intratubular Embryonal Carcinoma semapv:LexicalMatching 0.849779 oaklib ['rdfs:label'] ['rdfs:label'] ['intratubular embryonal carcinoma'] +MONDO:0850335 IDH-wildtype glioblastoma skos:exactMatch NCIT:C39750 Glioblastoma, IDH-Wildtype semapv:MappingChaining 0.475 This mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'. +MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch NCIT:C4182 Serous Surface Papillary Carcinoma semapv:MappingChaining 0.475 Generated by matching the object of a Mondo mapping to the object of a source mapping. +MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch NCIT:C39948 Malignant Testicular Sex Cord-Stromal Tumor semapv:MappingChaining 0.475 Generated by matching the object of a Mondo mapping to the object of a source mapping. +MONDO:0850303 supratentorial meningioma skos:exactMatch NCIT:C7048 Supratentorial Meningioma semapv:LexicalMatching 0.849779 oaklib rdfs:label rdfs:label supratentorial meningioma diff --git a/src/scripts/notebooks/mondo_paper_plots.ipynb b/src/scripts/notebooks/mondo_paper_plots.ipynb new file mode 100644 index 0000000000..2ff27739e8 --- /dev/null +++ b/src/scripts/notebooks/mondo_paper_plots.ipynb @@ -0,0 +1,745 @@ +{ + "cells": [ + { + "cell_type": "code", + "execution_count": 7, + "metadata": {}, + "outputs": [], + "source": [ + "import pandas as pd\n", + "\n", + "subsets_path = \"mondo_subsets.csv\"\n", + "synonyms_path = \"../../ontology/reports/all_synonym_data.tsv\"\n", + "mondo_mappings_path = \"../../ontology/mappings/mondo.sssom.tsv\"\n", + "\n", + "df_subsets = pd.read_csv(subsets_path, sep=\"\\t\")\n", + "df_synonyms = pd.read_csv(synonyms_path, sep=\"\\t\")\n", + "df_mappings = pd.read_csv(mondo_mappings_path, sep=\"\\t\", comment=\"#\")" + ] + }, + { + "cell_type": "code", + "execution_count": 8, + "metadata": {}, + "outputs": [ + { + "name": "stderr", + "output_type": "stream", + "text": [ + "/var/folders/vj/ks1_0k8x3t9ftrwcr0t9vjwr0000gn/T/ipykernel_37023/3810523524.py:11: FutureWarning: Downcasting behavior in `replace` is deprecated and will be removed in a future version. To retain the old behavior, explicitly call `result.infer_objects(copy=False)`. To opt-in to the future behavior, set `pd.set_option('future.no_silent_downcasting', True)`\n", + " df_gard_nr.replace({'yes': True, 'no': False}, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/data.py:303: FutureWarning: Downcasting object dtype arrays on .fillna, .ffill, .bfill is deprecated and will change in a future version. Call result.infer_objects(copy=False) instead. To opt-in to the future behavior, set `pd.set_option('future.no_silent_downcasting', True)`\n", + " df.fillna(False, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:795: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"linewidth\"].fillna(1, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:796: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"facecolor\"].fillna(self._facecolor, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:797: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"edgecolor\"].fillna(styles[\"facecolor\"], inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:798: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"linestyle\"].fillna(\"solid\", inplace=True)\n" + ] + }, + { + "data": { + "image/png": "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", + "text/plain": [ + "
" + ] + }, + "metadata": {}, + "output_type": "display_data" + } + ], + "source": [ + "# GARD analysis\n", + "from upsetplot import from_memberships\n", + "from matplotlib import pyplot\n", + "from upsetplot import plot\n", + "\n", + "#matplotlib.rcParams[\"font.size\"] = 6\n", + "\n", + "url_gard_not_rare = \"https://docs.google.com/spreadsheets/d/e/2PACX-1vTmFIVK1QUxd7NvOg1TjLMM8xGgNOWqCeLgZF6pFpIY79HU5FGNMxK7AZb5vjbxgA/pub?gid=900697982&single=true&output=tsv\"\n", + "\n", + "df_gard_nr = pd.read_csv(url_gard_not_rare, sep=\"\\t\")\n", + "df_gard_nr.replace({'yes': True, 'no': False}, inplace=True)\n", + "df_gard_nr.drop(columns=['?deprecated', '?label', '?gard', '?rare', '?general_grouping'], inplace=True)\n", + "\n", + "count_df = df_gard_nr.drop(columns='?mondo_id').groupby(list(df_gard_nr.columns[1:])).size().reset_index(name='count')\n", + "\n", + "memberships = []\n", + "counts = []\n", + "for _, row in count_df.iterrows():\n", + " record = []\n", + " for key in row.index:\n", + " if key == 'count':\n", + " counts.append(row[key])\n", + " else:\n", + " if row[key] == 1:\n", + " record.append(key)\n", + " memberships.append(record)\n", + "\n", + "subset_data = from_memberships(\n", + " data=counts,\n", + " memberships=memberships,\n", + ")\n", + "\n", + "subset_data.dropna(inplace=True)\n", + "\n", + "plot(subset_data, sort_by=\"cardinality\", show_percentages=\"{:.2%}\")\n", + "pyplot.show() " + ] + }, + { + "cell_type": "code", + "execution_count": 11, + "metadata": {}, + "outputs": [ + { + "data": { + "text/plain": [ + "array(['MONDO:0000005', 'MONDO:0000009', 'MONDO:0000014', ...,\n", + " 'MONDO:0020530', 'MONDO:0035547', 'MONDO:0035548'], dtype=object)" + ] + }, + "execution_count": 11, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "# Prepare subset data\n", + "\n", + "rare_subsets = [\n", + " #\"rare\",\n", + " \"nord_rare\",\n", + " \"gard_rare\",\n", + " \"mondo_rare\",\n", + " \"nando_rare\",\n", + " \"orphanet_rare\",\n", + " \"inferred_rare\"\n", + "]\n", + "\n", + "providers_compare = [\n", + " \"nord\",\n", + " \"gard\",\n", + " \"nando\",\n", + " \"orphanet\",\n", + " \"clingen\",\n", + " \"medgen\",\n", + " \"omim\",\n", + " \"doid\"\n", + "]\n", + "\n", + "df_rare = df_subsets[df_subsets[\"subset\"].isin([\"rare\"])]\n", + "\n", + "# Will be used throughout the notebook, dont change\n", + "rare = df_rare[\"id\"].unique()\n", + "rare" + ] + }, + { + "cell_type": "code", + "execution_count": 13, + "metadata": {}, + "outputs": [ + { + "name": "stderr", + "output_type": "stream", + "text": [ + "/var/folders/vj/ks1_0k8x3t9ftrwcr0t9vjwr0000gn/T/ipykernel_37023/3290211571.py:2: SettingWithCopyWarning: \n", + "A value is trying to be set on a copy of a slice from a DataFrame.\n", + "Try using .loc[row_indexer,col_indexer] = value instead\n", + "\n", + "See the caveats in the documentation: https://pandas.pydata.org/pandas-docs/stable/user_guide/indexing.html#returning-a-view-versus-a-copy\n", + " df_rare_subsets[\"subset\"] = df_rare_subsets[\"subset\"].apply(lambda x: x.replace(\"_rare\", \" \").title())\n" + ] + }, + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
idsubsetgroup
2MONDO:0000005Garddiseases
4MONDO:0000009Garddiseases
7MONDO:0000014Garddiseases
9MONDO:0000015Garddiseases
10MONDO:0000015Norddiseases
\n", + "
" + ], + "text/plain": [ + " id subset group\n", + "2 MONDO:0000005 Gard diseases\n", + "4 MONDO:0000009 Gard diseases\n", + "7 MONDO:0000014 Gard diseases\n", + "9 MONDO:0000015 Gard diseases\n", + "10 MONDO:0000015 Nord diseases" + ] + }, + "execution_count": 13, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "df_rare_subsets = df_subsets[df_subsets[\"subset\"].isin(rare_subsets)]\n", + "df_rare_subsets[\"subset\"] = df_rare_subsets[\"subset\"].apply(lambda x: x.replace(\"_rare\", \" \").title())\n", + "df_subset_upset = df_rare_subsets[[\"id\", \"subset\"]]\n", + "df_rare_subsets.head()" + ] + }, + { + "cell_type": "code", + "execution_count": 14, + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
?entity?synonym?synonym_property?xref?st1?st2idsynonym_type
0<http://purl.obolibrary.org/obo/MONDO_0042491>cervix squamous intraepithelial lesion<http://www.geneontology.org/formats/oboInOwl#...NCIT:C7346NaNNaNMONDO:0042491hasExactSynonym
1<http://purl.obolibrary.org/obo/MONDO_0003061>benign muscle tumour<http://www.geneontology.org/formats/oboInOwl#...NaNNaNNaNMONDO:0003061hasExactSynonym
2<http://purl.obolibrary.org/obo/MONDO_0013340>young-onset Parkinson disease caused by mutati...<http://www.geneontology.org/formats/oboInOwl#...MONDO:design_patternNaNNaNMONDO:0013340hasExactSynonym
3<http://purl.obolibrary.org/obo/MONDO_0007972>Mnire's vertigo<http://www.geneontology.org/formats/oboInOwl#...DOID:9849NaNNaNMONDO:0007972hasExactSynonym
4<http://purl.obolibrary.org/obo/MONDO_0012081>trisomy 15q11-q13<http://www.geneontology.org/formats/oboInOwl#...Orphanet:238446NaNNaNMONDO:0012081hasExactSynonym
...........................
169346<http://purl.obolibrary.org/obo/MONDO_0002243>hemorrhagic disease<http://www.w3.org/2000/01/rdf-schema#label>NaNNaNNaNMONDO:0002243label
169347<http://purl.obolibrary.org/obo/MONDO_1010172>alpha-mannosidosis, non-human animal<http://www.w3.org/2000/01/rdf-schema#label>NaNNaNNaNMONDO:1010172label
169348<http://purl.obolibrary.org/obo/MONDO_0100264>peroxisome biogenesis disorder due to PEX10 de...<http://www.w3.org/2000/01/rdf-schema#label>NaNNaNNaNMONDO:0100264label
169349<http://purl.obolibrary.org/obo/MONDO_0007118>isolated anhidrosis with normal sweat glands<http://www.w3.org/2000/01/rdf-schema#label>NaNNaNNaNMONDO:0007118label
169350<http://purl.obolibrary.org/obo/MONDO_0003770>thoracic spinal canal and spinal cord meningioma<http://www.w3.org/2000/01/rdf-schema#label>NaNNaNNaNMONDO:0003770label
\n", + "

169351 rows × 8 columns

\n", + "
" + ], + "text/plain": [ + " ?entity \\\n", + "0 \n", + "1 \n", + "2 \n", + "3 \n", + "4 \n", + "... ... \n", + "169346 \n", + "169347 \n", + "169348 \n", + "169349 \n", + "169350 \n", + "\n", + " ?synonym \\\n", + "0 cervix squamous intraepithelial lesion \n", + "1 benign muscle tumour \n", + "2 young-onset Parkinson disease caused by mutati... \n", + "3 Mnire's vertigo \n", + "4 trisomy 15q11-q13 \n", + "... ... \n", + "169346 hemorrhagic disease \n", + "169347 alpha-mannosidosis, non-human animal \n", + "169348 peroxisome biogenesis disorder due to PEX10 de... \n", + "169349 isolated anhidrosis with normal sweat glands \n", + "169350 thoracic spinal canal and spinal cord meningioma \n", + "\n", + " ?synonym_property \\\n", + "0 \n", + "169347 \n", + "169348 \n", + "169349 \n", + "169350 \n", + "\n", + " ?xref ?st1 ?st2 id synonym_type \n", + "0 NCIT:C7346 NaN NaN MONDO:0042491 hasExactSynonym \n", + "1 NaN NaN NaN MONDO:0003061 hasExactSynonym \n", + "2 MONDO:design_pattern NaN NaN MONDO:0013340 hasExactSynonym \n", + "3 DOID:9849 NaN NaN MONDO:0007972 hasExactSynonym \n", + "4 Orphanet:238446 NaN NaN MONDO:0012081 hasExactSynonym \n", + "... ... ... ... ... ... \n", + "169346 NaN NaN NaN MONDO:0002243 label \n", + "169347 NaN NaN NaN MONDO:1010172 label \n", + "169348 NaN NaN NaN MONDO:0100264 label \n", + "169349 NaN NaN NaN MONDO:0007118 label \n", + "169350 NaN NaN NaN MONDO:0003770 label \n", + "\n", + "[169351 rows x 8 columns]" + ] + }, + "execution_count": 14, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "df_synonyms[\"id\"] = df_synonyms[\"?entity\"].apply(lambda x: x.replace(\"\", \"\"))\n", + "df_synonyms[\"synonym_type\"] = df_synonyms[\"?synonym_property\"].apply(lambda x: x.replace(\"\", \"\"))\n", + "df_synonyms" + ] + }, + { + "cell_type": "code", + "execution_count": 16, + "metadata": {}, + "outputs": [ + { + "data": { + "image/png": "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", + "text/plain": [ + "
" + ] + }, + "metadata": {}, + "output_type": "display_data" + } + ], + "source": [ + "# Prepare synonyms data\n", + "\n", + "from matplotlib import pyplot as plt\n", + "\n", + "\n", + "df_synonyms_unique = df_synonyms[[\"id\", \"synonym_type\"]].drop_duplicates()\n", + "df_synonyms_unique['rare'] = df_synonyms_unique['id'].isin(rare)\n", + "df_synonyms_unique.head()\n", + "\n", + "# make bar plot of the synonym types\n", + "# Map rare values to specific colors\n", + "color_map = {True: 'red', False: 'blue'}\n", + "bar_colors = df_synonyms_unique['rare'].map(color_map)\n", + "\n", + "# Plot the bar plot with colored bars\n", + "ax = df_synonyms_unique['synonym_type'].value_counts().plot(kind='bar', color=bar_colors)\n", + "\n", + "# Optional: Add labels and title\n", + "ax.set_xlabel('Synonym Type')\n", + "ax.set_ylabel('Count')\n", + "ax.set_title('Value Counts of Synonym Type with Rare Highlighted')\n", + "\n", + "plt.show()\n" + ] + }, + { + "cell_type": "code", + "execution_count": 17, + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
idsynonym_typerare
0MONDO:0042491hasExactSynonymTrue
1MONDO:0003061hasExactSynonymFalse
2MONDO:0013340hasExactSynonymFalse
3MONDO:0007972hasExactSynonymTrue
4MONDO:0012081hasExactSynonymTrue
\n", + "
" + ], + "text/plain": [ + " id synonym_type rare\n", + "0 MONDO:0042491 hasExactSynonym True\n", + "1 MONDO:0003061 hasExactSynonym False\n", + "2 MONDO:0013340 hasExactSynonym False\n", + "3 MONDO:0007972 hasExactSynonym True\n", + "4 MONDO:0012081 hasExactSynonym True" + ] + }, + "execution_count": 17, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "df_synonyms_unique.head()" + ] + }, + { + "cell_type": "code", + "execution_count": 19, + "metadata": {}, + "outputs": [], + "source": [ + "def prepare_upset_membership_data(df_subset_upset):\n", + " from upsetplot import from_memberships\n", + " # Pivot the DataFrame to wide format\n", + " wide_df = df_subset_upset.pivot_table(index='id', columns='subset', aggfunc=lambda x: 1, fill_value=0)\n", + "\n", + " # Reset the index to move 'ID' from the index to a column\n", + " wide_df.reset_index(inplace=True)\n", + "\n", + " # Ensure that the column names are formatted correctly after pivoting\n", + " wide_df.columns.name = None\n", + "\n", + " # Drop the 'ID' column and count the unique combinations of subsets\n", + " count_df = wide_df.drop(columns='id').groupby(list(wide_df.columns[1:])).size().reset_index(name='count')\n", + "\n", + " memberships = []\n", + " counts = []\n", + " for _, row in count_df.iterrows():\n", + " record = []\n", + " for key in row.index:\n", + " if key == 'count':\n", + " counts.append(row[key])\n", + " else:\n", + " if row[key] == 1:\n", + " record.append(key)\n", + " memberships.append(record)\n", + " \n", + " data = from_memberships(\n", + " data=counts,\n", + " memberships=memberships,\n", + " )\n", + "\n", + " data.dropna(inplace=True)\n", + " return data" + ] + }, + { + "cell_type": "code", + "execution_count": 20, + "metadata": {}, + "outputs": [ + { + "name": "stderr", + "output_type": "stream", + "text": [ + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/data.py:303: FutureWarning: Downcasting object dtype arrays on .fillna, .ffill, .bfill is deprecated and will change in a future version. Call result.infer_objects(copy=False) instead. To opt-in to the future behavior, set `pd.set_option('future.no_silent_downcasting', True)`\n", + " df.fillna(False, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:795: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"linewidth\"].fillna(1, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:796: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"facecolor\"].fillna(self._facecolor, inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:797: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"edgecolor\"].fillna(styles[\"facecolor\"], inplace=True)\n", + "/Users/matentzn/.pyenv/versions/3.11.7/lib/python3.11/site-packages/upsetplot/plotting.py:798: FutureWarning: A value is trying to be set on a copy of a DataFrame or Series through chained assignment using an inplace method.\n", + "The behavior will change in pandas 3.0. This inplace method will never work because the intermediate object on which we are setting values always behaves as a copy.\n", + "\n", + "For example, when doing 'df[col].method(value, inplace=True)', try using 'df.method({col: value}, inplace=True)' or df[col] = df[col].method(value) instead, to perform the operation inplace on the original object.\n", + "\n", + "\n", + " styles[\"linestyle\"].fillna(\"solid\", inplace=True)\n" + ] + }, + { + "data": { + "image/png": "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", + "text/plain": [ + "
" + ] + }, + "metadata": {}, + "output_type": "display_data" + } + ], + "source": [ + "#!pip install upsetplot\n", + "\n", + "from matplotlib import pyplot\n", + "import matplotlib\n", + "from upsetplot import plot\n", + "\n", + "matplotlib.rcParams[\"font.size\"] = 6\n", + "\n", + "subset_data = prepare_upset_membership_data(df_subset_upset)\n", + "plot(subset_data, sort_by=\"cardinality\", show_percentages=\"{:.2%}\")\n", + "pyplot.show() " + ] + } + ], + "metadata": { + "kernelspec": { + "display_name": "Python 3", + "language": "python", + "name": "python3" + }, + "language_info": { + "codemirror_mode": { + "name": "ipython", + "version": 3 + }, + "file_extension": ".py", + "mimetype": "text/x-python", + "name": "python", + "nbconvert_exporter": "python", + "pygments_lexer": "ipython3", + "version": "3.11.7" + } + }, + "nbformat": 4, + "nbformat_minor": 2 +} diff --git a/src/scripts/notebooks/mondo_rd_paper.ipynb b/src/scripts/notebooks/mondo_rd_paper.ipynb new file mode 100644 index 0000000000..3268a130de --- /dev/null +++ b/src/scripts/notebooks/mondo_rd_paper.ipynb @@ -0,0 +1,554 @@ +{ + "cells": [ + { + "cell_type": "markdown", + "id": "ee7449b5-4256-456f-9d49-3672b9ccd298", + "metadata": {}, + "source": [ + "# Mondo RD subset analysis" + ] + }, + { + "cell_type": "code", + "execution_count": 1, + "id": "b6ca3bfd", + "metadata": {}, + "outputs": [], + "source": [ + "## Settings\n", + "\n", + "mondo_path = \"../../ontology/tmp/mondo_paper.db\"\n", + "mappings_path = \"../ontology/mappings/mondo.sssom.tsv\"\n", + "\n", + "oak_adapter = f\"sqlite:{mondo_path}\"\n" + ] + }, + { + "cell_type": "code", + "execution_count": 2, + "id": "5e2acff4", + "metadata": {}, + "outputs": [ + { + "name": "stdout", + "output_type": "stream", + "text": [ + "Requirement already satisfied: oaklib in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (0.6.6)\n", + "Requirement already satisfied: SPARQLWrapper in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (2.0.0)\n", + "Requirement already satisfied: SQLAlchemy>=1.4.32 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (2.0.30)\n", + "Requirement already satisfied: airium>=0.2.5 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.2.6)\n", + "Requirement already satisfied: appdirs>=1.4.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (1.4.4)\n", + "Requirement already satisfied: class-resolver>=0.4.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.4.3)\n", + "Requirement already satisfied: click in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (8.1.7)\n", + "Requirement already satisfied: curies>=0.6.6 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.7.9)\n", + "Requirement already satisfied: defusedxml<0.8.0,>=0.7.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.7.1)\n", + "Requirement already satisfied: eutils>=0.6.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.6.0)\n", + "Requirement already satisfied: funowl>=0.2.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.2.3)\n", + "Requirement already satisfied: jsonlines<5.0.0,>=4.0.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (4.0.0)\n", + "Requirement already satisfied: kgcl-rdflib==0.5.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.5.0)\n", + "Requirement already satisfied: kgcl-schema<0.7.0,>=0.6.8 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.6.8)\n", + "Requirement already satisfied: linkml-renderer>=0.3.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.3.0)\n", + "Requirement already satisfied: linkml-runtime>=1.5.3 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (1.7.5)\n", + "Requirement already satisfied: ndex2<4.0.0,>=3.5.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (3.8.0)\n", + "Requirement already satisfied: networkx>=2.7.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (3.3)\n", + "Requirement already satisfied: ols-client>=0.1.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.1.4)\n", + "Requirement already satisfied: ontoportal-client>=0.0.3 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.0.4)\n", + "Requirement already satisfied: prefixmaps>=0.1.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.2.4)\n", + "Requirement already satisfied: pronto>=2.5.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (2.5.7)\n", + "Requirement already satisfied: pydantic in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (2.7.1)\n", + "Requirement already satisfied: pysolr<4.0.0,>=3.9.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (3.9.0)\n", + "Requirement already satisfied: pystow>=0.5.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.5.4)\n", + "Requirement already satisfied: ratelimit>=2.2.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (2.2.1)\n", + "Requirement already satisfied: requests-cache<2.0.0,>=1.0.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (1.2.0)\n", + "Requirement already satisfied: semsql>=0.3.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.3.3)\n", + "Requirement already satisfied: sssom<0.5.0,>=0.4.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (0.4.9)\n", + "Requirement already satisfied: tenacity<9.0.0,>=8.2.3 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from oaklib) (8.3.0)\n", + "Requirement already satisfied: pytrie in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from curies>=0.6.6->oaklib) (0.4.0)\n", + "Requirement already satisfied: requests in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from curies>=0.6.6->oaklib) (2.31.0)\n", + "Requirement already satisfied: lxml in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from eutils>=0.6.0->oaklib) (5.2.2)\n", + "Requirement already satisfied: pytz in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from eutils>=0.6.0->oaklib) (2024.1)\n", + "Requirement already satisfied: bcp47 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (0.1.0)\n", + "Requirement already satisfied: jsonasobj in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (1.3.1)\n", + "Requirement already satisfied: pyjsg>=0.11.6 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (0.11.10)\n", + "Requirement already satisfied: rdflib-shim in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (1.0.3)\n", + "Requirement already satisfied: rdflib<8,>=6.2.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (7.0.0)\n", + "Requirement already satisfied: rfc3987 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from funowl>=0.2.0->oaklib) (1.3.8)\n", + "Requirement already satisfied: attrs>=19.2.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from jsonlines<5.0.0,>=4.0.0->oaklib) (23.2.0)\n", + "Requirement already satisfied: lark>=1.1.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from kgcl-schema<0.7.0,>=0.6.8->oaklib) (1.1.9)\n", + "Requirement already satisfied: deprecated in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (1.2.14)\n", + "Requirement already satisfied: hbreader in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (0.9.1)\n", + "Requirement already satisfied: json-flattener>=0.1.9 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (0.1.9)\n", + "Requirement already satisfied: jsonasobj2<2.dev0,>=1.0.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (1.0.4)\n", + "Requirement already satisfied: jsonschema>=3.2.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (4.22.0)\n", + "Requirement already satisfied: prefixcommons>=0.1.12 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (0.1.12)\n", + "Requirement already satisfied: pyyaml in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from linkml-runtime>=1.5.3->oaklib) (6.0.1)\n", + "Requirement already satisfied: six in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (1.16.0)\n", + "Requirement already satisfied: ijson in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (3.2.3)\n", + "Requirement already satisfied: requests-toolbelt in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (1.0.0)\n", + "Requirement already satisfied: urllib3>=1.16 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (2.2.1)\n", + "Requirement already satisfied: pandas in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (2.2.2)\n", + "Requirement already satisfied: numpy in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ndex2<4.0.0,>=3.5.0->oaklib) (1.26.4)\n", + "Requirement already satisfied: more-click in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ols-client>=0.1.1->oaklib) (0.1.2)\n", + "Requirement already satisfied: typing-extensions in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from ontoportal-client>=0.0.3->oaklib) (4.11.0)\n", + "Requirement already satisfied: chardet~=5.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pronto>=2.5.0->oaklib) (5.2.0)\n", + "Requirement already satisfied: fastobo~=0.12.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pronto>=2.5.0->oaklib) (0.12.3)\n", + "Requirement already satisfied: python-dateutil~=2.8 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pronto>=2.5.0->oaklib) (2.9.0.post0)\n", + "Requirement already satisfied: annotated-types>=0.4.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pydantic->oaklib) (0.6.0)\n", + "Requirement already satisfied: pydantic-core==2.18.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pydantic->oaklib) (2.18.2)\n", + "Requirement already satisfied: tqdm in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pystow>=0.5.0->oaklib) (4.66.4)\n", + "Requirement already satisfied: cattrs>=22.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests-cache<2.0.0,>=1.0.1->oaklib) (23.2.3)\n", + "Requirement already satisfied: platformdirs>=2.5 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests-cache<2.0.0,>=1.0.1->oaklib) (4.2.2)\n", + "Requirement already satisfied: url-normalize>=1.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests-cache<2.0.0,>=1.0.1->oaklib) (1.4.3)\n", + "Requirement already satisfied: SQLAlchemy-Utils<0.39.0,>=0.38.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from semsql>=0.3.1->oaklib) (0.38.3)\n", + "Requirement already satisfied: deprecation<3.0.0,>=2.1.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from sssom<0.5.0,>=0.4.4->oaklib) (2.1.0)\n", + "Requirement already satisfied: importlib-resources<7.0.0,>=6.1.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from sssom<0.5.0,>=0.4.4->oaklib) (6.4.0)\n", + "Requirement already satisfied: pansql>=0.0.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pansql[pansql]>=0.0.1->sssom<0.5.0,>=0.4.4->oaklib) (0.0.1)\n", + "Requirement already satisfied: scipy[scipy] in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from sssom<0.5.0,>=0.4.4->oaklib) (1.13.0)\n", + "Requirement already satisfied: sssom-schema<0.16.0,>=0.15.2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from sssom<0.5.0,>=0.4.4->oaklib) (0.15.2)\n", + "Requirement already satisfied: validators>=0.20.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from sssom<0.5.0,>=0.4.4->oaklib) (0.28.1)\n", + "Requirement already satisfied: packaging in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from deprecation<3.0.0,>=2.1.0->sssom<0.5.0,>=0.4.4->oaklib) (24.0)\n", + "Requirement already satisfied: jsonschema-specifications>=2023.03.6 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from jsonschema>=3.2.0->linkml-runtime>=1.5.3->oaklib) (2023.12.1)\n", + "Requirement already satisfied: referencing>=0.28.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from jsonschema>=3.2.0->linkml-runtime>=1.5.3->oaklib) (0.35.1)\n", + "Requirement already satisfied: rpds-py>=0.7.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from jsonschema>=3.2.0->linkml-runtime>=1.5.3->oaklib) (0.18.1)\n", + "\u001b[33mWARNING: networkx 3.3 does not provide the extra 'networkx'\u001b[0m\u001b[33m\n", + "\u001b[0mRequirement already satisfied: tzdata>=2022.7 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pandas->ndex2<4.0.0,>=3.5.0->oaklib) (2024.1)\n", + "\u001b[33mWARNING: pansql 0.0.1 does not provide the extra 'pansql'\u001b[0m\u001b[33m\n", + "\u001b[0mRequirement already satisfied: pytest-logging<2016.0.0,>=2015.11.4 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from prefixcommons>=0.1.12->linkml-runtime>=1.5.3->oaklib) (2015.11.4)\n", + "Requirement already satisfied: antlr4-python3-runtime~=4.9.3 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pyjsg>=0.11.6->funowl>=0.2.0->oaklib) (4.9.3)\n", + "Requirement already satisfied: isodate<0.7.0,>=0.6.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from rdflib<8,>=6.2.0->funowl>=0.2.0->oaklib) (0.6.1)\n", + "Requirement already satisfied: pyparsing<4,>=2.1.0 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from rdflib<8,>=6.2.0->funowl>=0.2.0->oaklib) (3.1.2)\n", + "Requirement already satisfied: charset-normalizer<4,>=2 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests->curies>=0.6.6->oaklib) (3.3.2)\n", + "Requirement already satisfied: idna<4,>=2.5 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests->curies>=0.6.6->oaklib) (3.7)\n", + "Requirement already satisfied: certifi>=2017.4.17 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from requests->curies>=0.6.6->oaklib) (2024.2.2)\n", + "Requirement already satisfied: wrapt<2,>=1.10 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from deprecated->linkml-runtime>=1.5.3->oaklib) (1.16.0)\n", + "Requirement already satisfied: sortedcontainers in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pytrie->curies>=0.6.6->oaklib) (2.4.0)\n", + "Requirement already satisfied: rdflib-jsonld==0.6.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from rdflib-shim->funowl>=0.2.0->oaklib) (0.6.1)\n", + "\u001b[33mWARNING: scipy 1.13.0 does not provide the extra 'scipy'\u001b[0m\u001b[33m\n", + "\u001b[0mRequirement already satisfied: pytest>=2.8.1 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pytest-logging<2016.0.0,>=2015.11.4->prefixcommons>=0.1.12->linkml-runtime>=1.5.3->oaklib) (8.2.0)\n", + "Requirement already satisfied: iniconfig in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pytest>=2.8.1->pytest-logging<2016.0.0,>=2015.11.4->prefixcommons>=0.1.12->linkml-runtime>=1.5.3->oaklib) (2.0.0)\n", + "Requirement already satisfied: pluggy<2.0,>=1.5 in /Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages (from pytest>=2.8.1->pytest-logging<2016.0.0,>=2015.11.4->prefixcommons>=0.1.12->linkml-runtime>=1.5.3->oaklib) (1.5.0)\n" + ] + } + ], + "source": [ + "# Install Python packages\n", + "#!pip install upsetplot\n", + "!pip install oaklib" + ] + }, + { + "cell_type": "code", + "execution_count": 3, + "id": "faddcbe6", + "metadata": {}, + "outputs": [ + { + "name": "stderr", + "output_type": "stream", + "text": [ + "/Users/matentzn/ws/mondo/.venv/lib/python3.11/site-packages/tqdm/auto.py:21: TqdmWarning: IProgress not found. Please update jupyter and ipywidgets. See https://ipywidgets.readthedocs.io/en/stable/user_install.html\n", + " from .autonotebook import tqdm as notebook_tqdm\n" + ] + } + ], + "source": [ + "# Load Imports\n", + "import pandas as pd\n", + "from pathlib import Path\n", + "from oaklib import get_adapter\n", + "from oaklib.mappers import OntologyMetadataMapper\n", + "from oaklib.datamodels.vocabulary import IS_A, PART_OF, SEMAPV, OWL_OBJECT_PROPERTY, OWL_ANNOTATION_PROPERTY\n", + "from typing import Tuple, List\n", + "\n", + "# Configure dataframe display\n", + "pd.set_option('display.max_columns', None)\n", + "# pd.set_option('display.max_rows', None)\n", + "pd.set_option('display.max_colwidth', None)\n", + "adapter = get_adapter(oak_adapter)\n" + ] + }, + { + "cell_type": "markdown", + "id": "808268d0", + "metadata": {}, + "source": [ + "[Back](#overview)\n", + "\n", + "---\n", + "\n", + "### Load Mondo using OAK pronto adapter\n" + ] + }, + { + "cell_type": "code", + "execution_count": 4, + "id": "05c0d034", + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
idsubsetgroup
0MONDO:0000001ordo_disorderdiseases
1MONDO:0000004otardiseases
2MONDO:0000005gard_rarediseases
3MONDO:0000005rarediseases
4MONDO:0000009gard_rarediseases
............
71403MONDO:0043797ordo_disorderinjuries
71404MONDO:0043797orphanet_rareinjuries
71405MONDO:0043797rareinjuries
71406MONDO:0044745otarinjuries
71407MONDO:0100075otarinjuries
\n", + "

71408 rows × 3 columns

\n", + "
" + ], + "text/plain": [ + " id subset group\n", + "0 MONDO:0000001 ordo_disorder diseases\n", + "1 MONDO:0000004 otar diseases\n", + "2 MONDO:0000005 gard_rare diseases\n", + "3 MONDO:0000005 rare diseases\n", + "4 MONDO:0000009 gard_rare diseases\n", + "... ... ... ...\n", + "71403 MONDO:0043797 ordo_disorder injuries\n", + "71404 MONDO:0043797 orphanet_rare injuries\n", + "71405 MONDO:0043797 rare injuries\n", + "71406 MONDO:0044745 otar injuries\n", + "71407 MONDO:0100075 otar injuries\n", + "\n", + "[71408 rows x 3 columns]" + ] + }, + "execution_count": 4, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "# Let's explore the ontology and get some initial data by getting all children of a class \n", + "\n", + "# Get all descendants for a CURIE\n", + "all_diseases = set(adapter.descendants([\"MONDO:0000001\"], predicates=[IS_A]))\n", + "all_characteristics = set(adapter.descendants([\"MONDO:0021125\"], predicates=[IS_A]))\n", + "all_susceptibilities = set(adapter.descendants([\"MONDO:0042489\"], predicates=[IS_A]))\n", + "all_injuries = set(adapter.descendants([\"MONDO:0021178\"], predicates=[IS_A]))\n", + "\n", + "all_mondo_terms = {\n", + " \"diseases\": all_diseases,\n", + " \"characteristics\": all_characteristics,\n", + " \"susceptibilities\": all_susceptibilities,\n", + " \"injuries\": all_injuries\n", + "}\n", + "\n", + "\n", + "\n", + "def get_subsets(adapter, mondo_terms_by_group: dict[str, List]) -> List[Tuple[str, List[str]]]:\n", + " \"\"\"Get subsets for a list of descendants.\"\"\" \n", + " data_subsets = []\n", + " for mondo_group, mondo_terms in mondo_terms_by_group.items(): \n", + " for e, subset in sorted(adapter.terms_subsets(mondo_terms)):\n", + " data_subsets.append({\n", + " \"id\": e,\n", + " \"subset\": subset,\n", + " \"group\": mondo_group\n", + " })\n", + " df = pd.DataFrame(data_subsets)\n", + " return df\n", + "\n", + "df_subsets = get_subsets(adapter, all_mondo_terms)\n", + "df_subsets.to_csv(\"mondo_subsets.csv\", sep=\"\\t\", index=False)\n", + "df_subsets\n" + ] + }, + { + "cell_type": "code", + "execution_count": 5, + "id": "09c110eb", + "metadata": {}, + "outputs": [ + { + "data": { + "text/html": [ + "
\n", + "\n", + "\n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + " \n", + "
idsynonymsynonym_typexrefspredicategroup
0MONDO:0000001conditionNoneNCIT:C2991hasExactSynonymdisease
1MONDO:0000001diseaseNoneNCIT:C2991hasExactSynonymdisease
2MONDO:0000001disease or disorderNoneNCIT:C2991hasExactSynonymdisease
3MONDO:0000001disease or disorder, non-neoplasticNoneNCIT:C2991hasExactSynonymdisease
4MONDO:0000001diseasesNoneNCIT:C2991hasExactSynonymdisease
5MONDO:0000001diseases and disordersNoneNCIT:C2991hasExactSynonymdisease
6MONDO:0000001disorderNoneNCIT:C2991hasExactSynonymdisease
7MONDO:0000001disordersNoneNCIT:C2991hasExactSynonymdisease
8MONDO:0000001medical conditionNonehasExactSynonymdisease
9MONDO:0000001other diseaseNoneNCIT:C2991hasExactSynonymdisease
\n", + "
" + ], + "text/plain": [ + " id synonym synonym_type \\\n", + "0 MONDO:0000001 condition None \n", + "1 MONDO:0000001 disease None \n", + "2 MONDO:0000001 disease or disorder None \n", + "3 MONDO:0000001 disease or disorder, non-neoplastic None \n", + "4 MONDO:0000001 diseases None \n", + "5 MONDO:0000001 diseases and disorders None \n", + "6 MONDO:0000001 disorder None \n", + "7 MONDO:0000001 disorders None \n", + "8 MONDO:0000001 medical condition None \n", + "9 MONDO:0000001 other disease None \n", + "\n", + " xrefs predicate group \n", + "0 NCIT:C2991 hasExactSynonym disease \n", + "1 NCIT:C2991 hasExactSynonym disease \n", + "2 NCIT:C2991 hasExactSynonym disease \n", + "3 NCIT:C2991 hasExactSynonym disease \n", + "4 NCIT:C2991 hasExactSynonym disease \n", + "5 NCIT:C2991 hasExactSynonym disease \n", + "6 NCIT:C2991 hasExactSynonym disease \n", + "7 NCIT:C2991 hasExactSynonym disease \n", + "8 hasExactSynonym disease \n", + "9 NCIT:C2991 hasExactSynonym disease " + ] + }, + "execution_count": 5, + "metadata": {}, + "output_type": "execute_result" + } + ], + "source": [ + "def get_synonyms(adapter, mondo_terms_by_group: dict[str, List]) -> List[Tuple[str, List[str]]]:\n", + " \"\"\"Get subsets for a list of descendants.\"\"\" \n", + " data_subsets = []\n", + " for mondo_group, mondo_terms in mondo_terms_by_group.items(): \n", + " for entity, spv in adapter.synonym_property_values(mondo_terms):\n", + " xrefs = \"|\".join(spv.xrefs)\n", + " synonym_type = spv.synonymType\n", + " synonym = spv.val\n", + " predicate = spv.pred\n", + " data_subsets.append({\n", + " \"id\": entity,\n", + " \"synonym\": synonym,\n", + " \"synonym_type\": synonym_type,\n", + " \"xrefs\": xrefs,\n", + " \"predicate\": predicate,\n", + " \"group\": mondo_group\n", + " })\n", + " df = pd.DataFrame(data_subsets)\n", + " return df\n", + "\n", + "#all_mondo_terms\n", + "df_synonyms = get_synonyms(adapter, {\"disease\":[\"MONDO:0000001\"]})\n", + "df_synonyms.to_csv(\"mondo_synonyms.csv\", sep=\"\\t\", index=False)\n", + "df_synonyms" + ] + } + ], + "metadata": { + "kernelspec": { + "display_name": "Python 3 (ipykernel)", + "language": "python", + "name": "python3" + }, + "language_info": { + "codemirror_mode": { + "name": "ipython", + "version": 3 + }, + "file_extension": ".py", + "mimetype": "text/x-python", + "name": "python", + "nbconvert_exporter": "python", + "pygments_lexer": "ipython3", + "version": "3.11.7" + } + }, + "nbformat": 4, + "nbformat_minor": 5 +} diff --git a/src/scripts/notebooks/mondo_subsets.csv b/src/scripts/notebooks/mondo_subsets.csv new file mode 100644 index 0000000000..1c92ca42a1 --- /dev/null +++ b/src/scripts/notebooks/mondo_subsets.csv @@ -0,0 +1,71409 @@ +id subset group +MONDO:0000001 ordo_disorder diseases +MONDO:0000004 otar diseases +MONDO:0000005 gard_rare diseases +MONDO:0000005 rare diseases +MONDO:0000009 gard_rare diseases +MONDO:0000009 otar diseases +MONDO:0000009 rare diseases +MONDO:0000014 gard_rare diseases +MONDO:0000014 rare diseases +MONDO:0000015 gard_rare diseases +MONDO:0000015 nord_rare diseases +MONDO:0000015 rare diseases +MONDO:0000023 gard_rare diseases +MONDO:0000023 nord_rare diseases +MONDO:0000023 ordo_disorder diseases +MONDO:0000023 orphanet_rare diseases +MONDO:0000023 otar diseases +MONDO:0000023 rare diseases +MONDO:0000030 clingen diseases +MONDO:0000030 gard_rare diseases +MONDO:0000030 otar diseases +MONDO:0000030 rare diseases +MONDO:0000032 otar diseases +MONDO:0000044 disease_grouping diseases +MONDO:0000044 gard_rare diseases +MONDO:0000044 nord_rare diseases +MONDO:0000044 ordo_group_of_disorders diseases +MONDO:0000044 otar diseases +MONDO:0000044 rare diseases +MONDO:0000045 gard_rare diseases +MONDO:0000045 nord_rare diseases +MONDO:0000045 otar diseases +MONDO:0000045 rare diseases +MONDO:0000050 gard_rare diseases +MONDO:0000050 nord_rare diseases +MONDO:0000050 ordo_disorder diseases +MONDO:0000050 orphanet_rare diseases +MONDO:0000050 otar diseases +MONDO:0000050 rare diseases +MONDO:0000060 gard_rare diseases +MONDO:0000060 otar diseases +MONDO:0000060 rare diseases +MONDO:0000062 otar diseases +MONDO:0000066 gard_rare diseases +MONDO:0000066 otar diseases +MONDO:0000066 rare diseases +MONDO:0000078 gard_rare diseases +MONDO:0000078 otar diseases +MONDO:0000078 rare diseases +MONDO:0000079 gard_rare diseases +MONDO:0000079 nord_rare diseases +MONDO:0000079 rare diseases +MONDO:0000082 otar diseases +MONDO:0000087 disease_grouping diseases +MONDO:0000087 gard_rare diseases +MONDO:0000087 nord_rare diseases +MONDO:0000087 ordo_group_of_disorders diseases +MONDO:0000087 otar diseases +MONDO:0000087 rare diseases +MONDO:0000088 disease_grouping diseases +MONDO:0000088 ordo_group_of_disorders diseases +MONDO:0000088 otar diseases +MONDO:0000090 gard_rare diseases +MONDO:0000090 otar diseases +MONDO:0000090 rare diseases +MONDO:0000104 gard_rare diseases +MONDO:0000104 nord_rare diseases +MONDO:0000104 rare diseases +MONDO:0000105 gard_rare diseases +MONDO:0000105 nord_rare diseases +MONDO:0000105 rare diseases +MONDO:0000107 gard_rare diseases +MONDO:0000107 nord_rare diseases +MONDO:0000107 ordo_disorder diseases +MONDO:0000107 ordo_malformation_syndrome diseases +MONDO:0000107 orphanet_rare diseases +MONDO:0000107 otar diseases +MONDO:0000107 rare diseases +MONDO:0000110 gard_rare diseases +MONDO:0000110 nord_rare diseases +MONDO:0000110 ordo_disorder diseases +MONDO:0000110 ordo_malformation_syndrome diseases +MONDO:0000110 orphanet_rare diseases +MONDO:0000110 otar diseases +MONDO:0000110 rare diseases +MONDO:0000115 otar diseases +MONDO:0000118 gard_rare diseases +MONDO:0000118 rare diseases +MONDO:0000119 otar diseases +MONDO:0000127 gard_rare diseases +MONDO:0000127 nord_rare diseases +MONDO:0000127 ordo_disorder diseases +MONDO:0000127 ordo_malformation_syndrome diseases +MONDO:0000127 orphanet_rare diseases +MONDO:0000127 otar diseases +MONDO:0000127 rare diseases +MONDO:0000128 gard_rare diseases +MONDO:0000128 nord_rare diseases +MONDO:0000128 otar diseases +MONDO:0000128 rare diseases +MONDO:0000129 otar diseases +MONDO:0000133 gard_rare diseases +MONDO:0000133 nord_rare diseases +MONDO:0000133 ordo_disorder diseases +MONDO:0000133 ordo_malformation_syndrome diseases +MONDO:0000133 orphanet_rare diseases +MONDO:0000133 otar diseases +MONDO:0000133 rare diseases +MONDO:0000136 gard_rare diseases +MONDO:0000136 nord_rare diseases +MONDO:0000136 ordo_disorder diseases +MONDO:0000136 orphanet_rare diseases +MONDO:0000136 otar diseases +MONDO:0000136 rare diseases +MONDO:0000137 otar diseases +MONDO:0000138 gard_rare diseases +MONDO:0000138 rare diseases +MONDO:0000141 gard_rare diseases +MONDO:0000141 nord_rare diseases +MONDO:0000141 ordo_disorder diseases +MONDO:0000141 ordo_malformation_syndrome diseases +MONDO:0000141 orphanet_rare diseases +MONDO:0000141 otar diseases +MONDO:0000141 rare diseases +MONDO:0000147 otar diseases +MONDO:0000148 gard_rare diseases +MONDO:0000148 otar diseases +MONDO:0000148 rare diseases +MONDO:0000151 otar diseases +MONDO:0000152 gard_rare diseases +MONDO:0000152 rare diseases +MONDO:0000153 disease_grouping diseases +MONDO:0000153 gard_rare diseases +MONDO:0000153 nord_rare diseases +MONDO:0000153 ordo_group_of_disorders diseases +MONDO:0000153 otar diseases +MONDO:0000153 rare diseases +MONDO:0000155 gard_rare diseases +MONDO:0000155 rare diseases +MONDO:0000156 gard_rare diseases +MONDO:0000156 nord_rare diseases +MONDO:0000156 otar diseases +MONDO:0000156 rare diseases +MONDO:0000158 otar diseases +MONDO:0000159 gard_rare diseases +MONDO:0000159 otar diseases +MONDO:0000159 rare diseases +MONDO:0000160 gard_rare diseases +MONDO:0000160 otar diseases +MONDO:0000160 rare diseases +MONDO:0000167 gard_rare diseases +MONDO:0000167 rare diseases +MONDO:0000169 obsoletion_candidate diseases +MONDO:0000170 gard_rare diseases +MONDO:0000170 nord_rare diseases +MONDO:0000170 ordo_disorder diseases +MONDO:0000170 ordo_malformation_syndrome diseases +MONDO:0000170 orphanet_rare diseases +MONDO:0000170 otar diseases +MONDO:0000170 rare diseases +MONDO:0000171 gard_rare diseases +MONDO:0000171 nord_rare diseases +MONDO:0000171 ordo_disorder diseases +MONDO:0000171 orphanet_rare diseases +MONDO:0000171 otar diseases +MONDO:0000171 rare diseases +MONDO:0000172 gard_rare diseases +MONDO:0000172 rare diseases +MONDO:0000173 gard_rare diseases +MONDO:0000173 otar diseases +MONDO:0000173 rare diseases +MONDO:0000179 gard_rare diseases +MONDO:0000179 nord_rare diseases +MONDO:0000179 ordo_disorder diseases +MONDO:0000179 ordo_malformation_syndrome diseases +MONDO:0000179 orphanet_rare diseases +MONDO:0000179 otar diseases +MONDO:0000179 rare diseases +MONDO:0000181 gard_rare diseases +MONDO:0000181 rare diseases +MONDO:0000182 gard_rare diseases +MONDO:0000182 nord_rare diseases +MONDO:0000182 rare diseases +MONDO:0000188 clingen diseases +MONDO:0000188 gard_rare diseases +MONDO:0000188 otar diseases +MONDO:0000188 rare diseases +MONDO:0000190 otar diseases +MONDO:0000192 gard_rare diseases +MONDO:0000192 otar diseases +MONDO:0000192 rare diseases +MONDO:0000193 gard_rare diseases +MONDO:0000193 nord_rare diseases +MONDO:0000193 ordo_disorder diseases +MONDO:0000193 ordo_malformation_syndrome diseases +MONDO:0000193 orphanet_rare diseases +MONDO:0000193 otar diseases +MONDO:0000193 rare diseases +MONDO:0000200 gard_rare diseases +MONDO:0000200 nord_rare diseases +MONDO:0000200 ordo_disorder diseases +MONDO:0000200 ordo_malformation_syndrome diseases +MONDO:0000200 orphanet_rare diseases +MONDO:0000200 otar diseases +MONDO:0000200 prototype_pattern diseases +MONDO:0000200 rare diseases +MONDO:0000208 gard_rare diseases +MONDO:0000208 nord_rare diseases +MONDO:0000208 rare diseases +MONDO:0000209 gard_rare diseases +MONDO:0000209 nord_rare diseases +MONDO:0000209 ordo_disorder diseases +MONDO:0000209 orphanet_rare diseases +MONDO:0000209 otar diseases +MONDO:0000209 rare diseases +MONDO:0000210 gard_rare diseases +MONDO:0000210 rare diseases +MONDO:0000211 gard_rare diseases +MONDO:0000211 nord_rare diseases +MONDO:0000211 ordo_disorder diseases +MONDO:0000211 orphanet_rare diseases +MONDO:0000211 otar diseases +MONDO:0000211 rare diseases +MONDO:0000212 gard_rare diseases +MONDO:0000212 nord_rare diseases +MONDO:0000212 ordo_disorder diseases +MONDO:0000212 orphanet_rare diseases +MONDO:0000212 otar diseases +MONDO:0000212 prototype_pattern diseases +MONDO:0000212 rare diseases +MONDO:0000214 gard_rare diseases +MONDO:0000214 rare diseases +MONDO:0000225 gard_rare diseases +MONDO:0000225 nord_rare diseases +MONDO:0000225 rare diseases +MONDO:0000226 otar diseases +MONDO:0000227 gard_rare diseases +MONDO:0000227 nord_rare diseases +MONDO:0000227 rare diseases +MONDO:0000229 gard_rare diseases +MONDO:0000229 rare diseases +MONDO:0000230 gard_rare diseases +MONDO:0000230 rare diseases +MONDO:0000231 gard_rare diseases +MONDO:0000231 rare diseases +MONDO:0000232 gard_rare diseases +MONDO:0000232 rare diseases +MONDO:0000233 gard_rare diseases +MONDO:0000233 rare diseases +MONDO:0000234 gard_rare diseases +MONDO:0000234 rare diseases +MONDO:0000240 gard_rare diseases +MONDO:0000240 rare diseases +MONDO:0000241 gard_rare diseases +MONDO:0000241 nord_rare diseases +MONDO:0000241 rare diseases +MONDO:0000248 gard_rare diseases +MONDO:0000248 rare diseases +MONDO:0000252 otar diseases +MONDO:0000256 otar diseases +MONDO:0000257 otar diseases +MONDO:0000259 inferred_rare diseases +MONDO:0000259 rare diseases +MONDO:0000263 otar diseases +MONDO:0000266 gard_rare diseases +MONDO:0000266 otar diseases +MONDO:0000266 rare diseases +MONDO:0000270 otar diseases +MONDO:0000271 gard_rare diseases +MONDO:0000271 rare diseases +MONDO:0000273 gard_rare diseases +MONDO:0000273 nord_rare diseases +MONDO:0000273 rare diseases +MONDO:0000276 gard_rare diseases +MONDO:0000276 nord_rare diseases +MONDO:0000276 rare diseases +MONDO:0000290 gard_rare diseases +MONDO:0000290 nord_rare diseases +MONDO:0000290 rare diseases +MONDO:0000291 gard_rare diseases +MONDO:0000291 nord_rare diseases +MONDO:0000291 rare diseases +MONDO:0000301 gard_rare diseases +MONDO:0000301 rare diseases +MONDO:0000302 gard_rare diseases +MONDO:0000302 nord_rare diseases +MONDO:0000302 rare diseases +MONDO:0000309 otar diseases +MONDO:0000310 gard_rare diseases +MONDO:0000310 nord_rare diseases +MONDO:0000310 rare diseases +MONDO:0000320 gard_rare diseases +MONDO:0000320 rare diseases +MONDO:0000321 gard_rare diseases +MONDO:0000321 rare diseases +MONDO:0000327 otar diseases +MONDO:0000330 gard_rare diseases +MONDO:0000330 nord_rare diseases +MONDO:0000330 ordo_disorder diseases +MONDO:0000330 orphanet_rare diseases +MONDO:0000330 rare diseases +MONDO:0000331 gard_rare diseases +MONDO:0000331 rare diseases +MONDO:0000332 gard_rare diseases +MONDO:0000332 nord_rare diseases +MONDO:0000332 rare diseases +MONDO:0000333 gard_rare diseases +MONDO:0000333 rare diseases +MONDO:0000334 otar diseases +MONDO:0000335 gard_rare diseases +MONDO:0000335 rare diseases +MONDO:0000336 gard_rare diseases +MONDO:0000336 rare diseases +MONDO:0000337 otar diseases +MONDO:0000339 gard_rare diseases +MONDO:0000339 rare diseases +MONDO:0000340 gard_rare diseases +MONDO:0000340 rare diseases +MONDO:0000341 gard_rare diseases +MONDO:0000341 otar diseases +MONDO:0000341 rare diseases +MONDO:0000351 gard_rare diseases +MONDO:0000351 otar diseases +MONDO:0000351 rare diseases +MONDO:0000355 gard_rare diseases +MONDO:0000355 nord_rare diseases +MONDO:0000355 ordo_disorder diseases +MONDO:0000355 orphanet_rare diseases +MONDO:0000355 otar diseases +MONDO:0000355 rare diseases +MONDO:0000358 otar diseases +MONDO:0000359 gard_rare diseases +MONDO:0000359 nord_rare diseases +MONDO:0000359 otar diseases +MONDO:0000359 rare diseases +MONDO:0000365 gard_rare diseases +MONDO:0000365 otar diseases +MONDO:0000365 rare diseases +MONDO:0000367 otar diseases +MONDO:0000368 gard_rare diseases +MONDO:0000368 otar diseases +MONDO:0000368 rare diseases +MONDO:0000369 gard_rare diseases +MONDO:0000369 otar diseases +MONDO:0000369 rare diseases +MONDO:0000373 gard_rare diseases +MONDO:0000373 rare diseases +MONDO:0000374 gard_rare diseases +MONDO:0000374 rare diseases +MONDO:0000376 otar diseases +MONDO:0000379 gard_rare diseases +MONDO:0000379 nord_rare diseases +MONDO:0000379 rare diseases +MONDO:0000380 gard_rare diseases +MONDO:0000380 nord_rare diseases +MONDO:0000380 otar diseases +MONDO:0000380 rare diseases +MONDO:0000381 gard_rare diseases +MONDO:0000381 rare diseases +MONDO:0000385 otar diseases +MONDO:0000386 gard_rare diseases +MONDO:0000386 otar diseases +MONDO:0000386 rare diseases +MONDO:0000387 otar diseases +MONDO:0000389 otar diseases +MONDO:0000390 gard_rare diseases +MONDO:0000390 otar diseases +MONDO:0000390 rare diseases +MONDO:0000393 gard_rare diseases +MONDO:0000393 rare diseases +MONDO:0000395 gard_rare diseases +MONDO:0000395 rare diseases +MONDO:0000396 otar diseases +MONDO:0000402 gard_rare diseases +MONDO:0000402 otar diseases +MONDO:0000402 rare diseases +MONDO:0000407 gard_rare diseases +MONDO:0000407 rare diseases +MONDO:0000408 gard_rare diseases +MONDO:0000408 nord_rare diseases +MONDO:0000408 rare diseases +MONDO:0000411 otar diseases +MONDO:0000421 gard_rare diseases +MONDO:0000421 rare diseases +MONDO:0000424 gard_rare diseases +MONDO:0000424 obsoletion_candidate diseases +MONDO:0000424 rare diseases +MONDO:0000425 otar diseases +MONDO:0000426 otar diseases +MONDO:0000429 otar diseases +MONDO:0000430 gard_rare diseases +MONDO:0000430 nord_rare diseases +MONDO:0000430 otar diseases +MONDO:0000430 rare diseases +MONDO:0000432 gard_rare diseases +MONDO:0000432 nord_rare diseases +MONDO:0000432 otar diseases +MONDO:0000432 rare diseases +MONDO:0000437 clingen diseases +MONDO:0000437 disease_grouping diseases +MONDO:0000437 gard_rare diseases +MONDO:0000437 mondo_rare diseases +MONDO:0000437 nord_rare diseases +MONDO:0000437 ordo_group_of_disorders diseases +MONDO:0000437 otar diseases +MONDO:0000437 rare diseases +MONDO:0000447 gard_rare diseases +MONDO:0000447 ordo_disorder diseases +MONDO:0000447 orphanet_rare diseases +MONDO:0000447 otar diseases +MONDO:0000447 rare diseases +MONDO:0000448 gard_rare diseases +MONDO:0000448 otar diseases +MONDO:0000448 rare diseases +MONDO:0000450 otar diseases +MONDO:0000451 otar diseases +MONDO:0000453 clingen diseases +MONDO:0000453 gard_rare diseases +MONDO:0000453 nord_rare diseases +MONDO:0000453 ordo_disorder diseases +MONDO:0000453 orphanet_rare diseases +MONDO:0000453 otar diseases +MONDO:0000453 prototype_pattern diseases +MONDO:0000453 rare diseases +MONDO:0000455 gard_rare diseases +MONDO:0000455 nord_rare diseases +MONDO:0000455 ordo_disorder diseases +MONDO:0000455 orphanet_rare diseases +MONDO:0000455 otar diseases +MONDO:0000455 rare diseases +MONDO:0000456 disease_grouping diseases +MONDO:0000456 gard_rare diseases +MONDO:0000456 ordo_group_of_disorders diseases +MONDO:0000456 otar diseases +MONDO:0000456 rare diseases +MONDO:0000457 gard_rare diseases +MONDO:0000457 rare diseases +MONDO:0000458 gard_rare diseases +MONDO:0000458 rare diseases +MONDO:0000459 gard_rare diseases +MONDO:0000459 rare diseases +MONDO:0000460 gard_rare diseases +MONDO:0000460 rare diseases +MONDO:0000461 otar diseases +MONDO:0000462 otar diseases +MONDO:0000463 gard_rare diseases +MONDO:0000463 nord_rare diseases +MONDO:0000463 ordo_disorder diseases +MONDO:0000463 ordo_malformation_syndrome diseases +MONDO:0000463 orphanet_rare diseases +MONDO:0000463 otar diseases +MONDO:0000463 rare diseases +MONDO:0000465 otar diseases +MONDO:0000468 otar diseases +MONDO:0000469 otar diseases +MONDO:0000470 otar diseases +MONDO:0000471 otar diseases +MONDO:0000473 otar diseases +MONDO:0000476 disease_grouping diseases +MONDO:0000476 gard_rare diseases +MONDO:0000476 ordo_group_of_disorders diseases +MONDO:0000476 otar diseases +MONDO:0000476 rare diseases +MONDO:0000477 otar diseases +MONDO:0000478 otar diseases +MONDO:0000480 gard_rare diseases +MONDO:0000480 rare diseases +MONDO:0000481 otar diseases +MONDO:0000485 otar diseases +MONDO:0000489 otar diseases +MONDO:0000490 gard_rare diseases +MONDO:0000490 otar diseases +MONDO:0000490 rare diseases +MONDO:0000494 gard_rare diseases +MONDO:0000494 otar diseases +MONDO:0000494 rare diseases +MONDO:0000498 gard_rare diseases +MONDO:0000498 nord_rare diseases +MONDO:0000498 rare diseases +MONDO:0000499 inferred_rare diseases +MONDO:0000499 rare diseases +MONDO:0000500 gard_rare diseases +MONDO:0000500 rare diseases +MONDO:0000502 otar diseases +MONDO:0000503 gard_rare diseases +MONDO:0000503 rare diseases +MONDO:0000507 clingen diseases +MONDO:0000507 gard_rare diseases +MONDO:0000507 nord_rare diseases +MONDO:0000507 ordo_disorder diseases +MONDO:0000507 orphanet_rare diseases +MONDO:0000507 otar diseases +MONDO:0000507 rare diseases +MONDO:0000508 clingen diseases +MONDO:0000508 otar diseases +MONDO:0000509 clingen diseases +MONDO:0000509 otar diseases +MONDO:0000510 gard_rare diseases +MONDO:0000510 rare diseases +MONDO:0000513 gard_rare diseases +MONDO:0000513 rare diseases +MONDO:0000514 gard_rare diseases +MONDO:0000514 otar diseases +MONDO:0000514 rare diseases +MONDO:0000515 gard_rare diseases +MONDO:0000515 otar diseases +MONDO:0000515 rare diseases +MONDO:0000516 gard_rare diseases +MONDO:0000516 rare diseases +MONDO:0000517 gard_rare diseases +MONDO:0000517 rare diseases +MONDO:0000518 gard_rare diseases +MONDO:0000518 nord_rare diseases +MONDO:0000518 rare diseases +MONDO:0000519 gard_rare diseases +MONDO:0000519 nord_rare diseases +MONDO:0000519 rare diseases +MONDO:0000520 gard_rare diseases +MONDO:0000520 rare diseases +MONDO:0000521 otar diseases +MONDO:0000524 gard_rare diseases +MONDO:0000524 nord_rare diseases +MONDO:0000524 rare diseases +MONDO:0000525 otar diseases +MONDO:0000527 otar diseases +MONDO:0000530 otar diseases +MONDO:0000531 gard_rare diseases +MONDO:0000531 rare diseases +MONDO:0000532 gard_rare diseases +MONDO:0000532 rare diseases +MONDO:0000534 gard_rare diseases +MONDO:0000534 rare diseases +MONDO:0000536 gard_rare diseases +MONDO:0000536 otar diseases +MONDO:0000536 rare diseases +MONDO:0000539 gard_rare diseases +MONDO:0000539 rare diseases +MONDO:0000540 gard_rare diseases +MONDO:0000540 otar diseases +MONDO:0000540 rare diseases +MONDO:0000541 gard_rare diseases +MONDO:0000541 rare diseases +MONDO:0000544 otar diseases +MONDO:0000545 gard_rare diseases +MONDO:0000545 rare diseases +MONDO:0000548 gard_rare diseases +MONDO:0000548 otar diseases +MONDO:0000548 rare diseases +MONDO:0000549 gard_rare diseases +MONDO:0000549 rare diseases +MONDO:0000550 gard_rare diseases +MONDO:0000550 otar diseases +MONDO:0000550 rare diseases +MONDO:0000551 gard_rare diseases +MONDO:0000551 otar diseases +MONDO:0000551 rare diseases +MONDO:0000552 otar diseases +MONDO:0000554 gard_rare diseases +MONDO:0000554 otar diseases +MONDO:0000554 rare diseases +MONDO:0000563 gard_rare diseases +MONDO:0000563 rare diseases +MONDO:0000565 gard_rare diseases +MONDO:0000565 nord_rare diseases +MONDO:0000565 ordo_disorder diseases +MONDO:0000565 orphanet_rare diseases +MONDO:0000565 otar diseases +MONDO:0000565 rare diseases +MONDO:0000568 otar diseases +MONDO:0000572 clingen diseases +MONDO:0000572 gard_rare diseases +MONDO:0000572 otar diseases +MONDO:0000572 rare diseases +MONDO:0000573 clingen diseases +MONDO:0000573 gard_rare diseases +MONDO:0000573 nord_rare diseases +MONDO:0000573 otar diseases +MONDO:0000573 rare diseases +MONDO:0000577 gard_rare diseases +MONDO:0000577 otar diseases +MONDO:0000577 rare diseases +MONDO:0000583 gard_rare diseases +MONDO:0000583 rare diseases +MONDO:0000584 gard_rare diseases +MONDO:0000584 obsoletion_candidate diseases +MONDO:0000584 rare diseases +MONDO:0000590 otar diseases +MONDO:0000591 clingen diseases +MONDO:0000591 gard_rare diseases +MONDO:0000591 otar diseases +MONDO:0000591 rare diseases +MONDO:0000592 otar diseases +MONDO:0000594 inferred_rare diseases +MONDO:0000594 otar diseases +MONDO:0000594 rare diseases +MONDO:0000595 otar diseases +MONDO:0000602 gard_rare diseases +MONDO:0000602 otar diseases +MONDO:0000602 rare diseases +MONDO:0000605 otar diseases +MONDO:0000607 gard_rare diseases +MONDO:0000607 otar diseases +MONDO:0000607 rare diseases +MONDO:0000608 otar diseases +MONDO:0000610 gard_rare diseases +MONDO:0000610 nord_rare diseases +MONDO:0000610 rare diseases +MONDO:0000612 otar diseases +MONDO:0000618 otar diseases +MONDO:0000620 otar diseases +MONDO:0000621 otar diseases +MONDO:0000624 otar diseases +MONDO:0000625 otar diseases +MONDO:0000628 otar diseases +MONDO:0000631 inferred_rare diseases +MONDO:0000631 otar diseases +MONDO:0000631 rare diseases +MONDO:0000632 otar diseases +MONDO:0000638 inferred_rare diseases +MONDO:0000638 otar diseases +MONDO:0000638 rare diseases +MONDO:0000639 gard_rare diseases +MONDO:0000639 rare diseases +MONDO:0000640 otar diseases +MONDO:0000645 nord_rare diseases +MONDO:0000645 ordo_disorder diseases +MONDO:0000645 orphanet_rare diseases +MONDO:0000645 rare diseases +MONDO:0000646 otar diseases +MONDO:0000647 otar diseases +MONDO:0000648 otar diseases +MONDO:0000650 otar diseases +MONDO:0000654 otar diseases +MONDO:0000659 gard_rare diseases +MONDO:0000659 nord_rare diseases +MONDO:0000659 rare diseases +MONDO:0000660 gard_rare diseases +MONDO:0000660 rare diseases +MONDO:0000661 otar diseases +MONDO:0000665 otar diseases +MONDO:0000675 otar diseases +MONDO:0000687 gard_rare diseases +MONDO:0000687 rare diseases +MONDO:0000688 disease_grouping diseases +MONDO:0000688 gard_rare diseases +MONDO:0000688 ordo_group_of_disorders diseases +MONDO:0000688 otar diseases +MONDO:0000688 rare diseases +MONDO:0000698 gard_rare diseases +MONDO:0000698 ordo_group_of_disorders diseases +MONDO:0000698 rare diseases +MONDO:0000700 clingen diseases +MONDO:0000700 gard_rare diseases +MONDO:0000700 nord_rare diseases +MONDO:0000700 otar diseases +MONDO:0000700 rare diseases +MONDO:0000701 otar diseases +MONDO:0000702 otar diseases +MONDO:0000703 otar diseases +MONDO:0000704 otar diseases +MONDO:0000709 otar diseases +MONDO:0000715 gard_rare diseases +MONDO:0000715 rare diseases +MONDO:0000721 otar diseases +MONDO:0000722 gard_rare diseases +MONDO:0000722 nord_rare diseases +MONDO:0000722 rare diseases +MONDO:0000724 otar diseases +MONDO:0000726 otar diseases +MONDO:0000727 gard_rare diseases +MONDO:0000727 otar diseases +MONDO:0000727 rare diseases +MONDO:0000728 otar diseases +MONDO:0000732 gard_rare diseases +MONDO:0000732 nord_rare diseases +MONDO:0000732 otar diseases +MONDO:0000732 rare diseases +MONDO:0000733 gard_rare diseases +MONDO:0000733 ordo_disorder diseases +MONDO:0000733 orphanet_rare diseases +MONDO:0000733 otar diseases +MONDO:0000733 rare diseases +MONDO:0000734 gard_rare diseases +MONDO:0000734 nord_rare diseases +MONDO:0000734 rare diseases +MONDO:0000736 gard_rare diseases +MONDO:0000736 nord_rare diseases +MONDO:0000736 ordo_disorder diseases +MONDO:0000736 orphanet_rare diseases +MONDO:0000736 otar diseases +MONDO:0000736 rare diseases +MONDO:0000744 otar diseases +MONDO:0000754 gard_rare diseases +MONDO:0000754 nord_rare diseases +MONDO:0000754 ordo_disorder diseases +MONDO:0000754 orphanet_rare diseases +MONDO:0000754 rare diseases +MONDO:0000756 gard_rare diseases +MONDO:0000756 rare diseases +MONDO:0000757 gard_rare diseases +MONDO:0000757 rare diseases +MONDO:0000761 gard_rare diseases +MONDO:0000761 otar diseases +MONDO:0000761 rare diseases +MONDO:0000762 gard_rare diseases +MONDO:0000762 rare diseases +MONDO:0000763 gard_rare diseases +MONDO:0000763 rare diseases +MONDO:0000764 gard_rare diseases +MONDO:0000764 nord_rare diseases +MONDO:0000764 otar diseases +MONDO:0000764 rare diseases +MONDO:0000766 gard_rare diseases +MONDO:0000766 otar diseases +MONDO:0000766 rare diseases +MONDO:0000771 otar diseases +MONDO:0000774 gard_rare diseases +MONDO:0000774 rare diseases +MONDO:0000775 otar diseases +MONDO:0000809 gard_rare diseases +MONDO:0000809 rare diseases +MONDO:0000812 otar diseases +MONDO:0000813 gard_rare diseases +MONDO:0000813 rare diseases +MONDO:0000814 gard_rare diseases +MONDO:0000814 otar diseases +MONDO:0000814 rare diseases +MONDO:0000816 inferred_rare diseases +MONDO:0000816 otar diseases +MONDO:0000816 rare diseases +MONDO:0000819 otar diseases +MONDO:0000820 otar diseases +MONDO:0000827 disease_grouping diseases +MONDO:0000827 ordo_group_of_disorders diseases +MONDO:0000827 otar diseases +MONDO:0000828 gard_rare diseases +MONDO:0000828 otar diseases +MONDO:0000828 rare diseases +MONDO:0000831 otar diseases +MONDO:0000833 otar diseases +MONDO:0000836 otar diseases +MONDO:0000837 otar diseases +MONDO:0000840 gard_rare diseases +MONDO:0000840 rare diseases +MONDO:0000845 gard_rare diseases +MONDO:0000845 nord_rare diseases +MONDO:0000845 ordo_disorder diseases +MONDO:0000845 ordo_malformation_syndrome diseases +MONDO:0000845 orphanet_rare diseases +MONDO:0000845 otar diseases +MONDO:0000845 rare diseases +MONDO:0000859 gard_rare diseases +MONDO:0000859 ordo_group_of_disorders diseases +MONDO:0000859 rare diseases +MONDO:0000863 gard_rare diseases +MONDO:0000863 nord_rare diseases +MONDO:0000863 ordo_disorder diseases +MONDO:0000863 orphanet_rare diseases +MONDO:0000863 otar diseases +MONDO:0000863 rare diseases +MONDO:0000866 gard_rare diseases +MONDO:0000866 obsoletion_candidate diseases +MONDO:0000866 otar diseases +MONDO:0000866 rare diseases +MONDO:0000870 gard_rare diseases +MONDO:0000870 nord_rare diseases +MONDO:0000870 otar diseases +MONDO:0000870 rare diseases +MONDO:0000871 gard_rare diseases +MONDO:0000871 otar diseases +MONDO:0000871 rare diseases +MONDO:0000872 gard_rare diseases +MONDO:0000872 otar diseases +MONDO:0000872 rare diseases +MONDO:0000873 gard_rare diseases +MONDO:0000873 otar diseases +MONDO:0000873 rare diseases +MONDO:0000874 gard_rare diseases +MONDO:0000874 rare diseases +MONDO:0000875 gard_rare diseases +MONDO:0000875 otar diseases +MONDO:0000875 rare diseases +MONDO:0000878 gard_rare diseases +MONDO:0000878 nord_rare diseases +MONDO:0000878 otar diseases +MONDO:0000878 rare diseases +MONDO:0000879 otar diseases +MONDO:0000884 gard_rare diseases +MONDO:0000884 obsoletion_candidate diseases +MONDO:0000884 rare diseases +MONDO:0000889 gard_rare diseases +MONDO:0000889 otar diseases +MONDO:0000889 rare diseases +MONDO:0000890 otar diseases +MONDO:0000891 gard_rare diseases +MONDO:0000891 rare diseases +MONDO:0000892 otar diseases +MONDO:0000893 gard_rare diseases +MONDO:0000893 rare diseases +MONDO:0000894 gard_rare diseases +MONDO:0000894 otar diseases +MONDO:0000894 rare diseases +MONDO:0000895 gard_rare diseases +MONDO:0000895 rare diseases +MONDO:0000901 gard_rare diseases +MONDO:0000901 rare diseases +MONDO:0000902 gard_rare diseases +MONDO:0000902 nord_rare diseases +MONDO:0000902 ordo_disorder diseases +MONDO:0000902 orphanet_rare diseases +MONDO:0000902 otar diseases +MONDO:0000902 rare diseases +MONDO:0000903 gard_rare diseases +MONDO:0000903 nord_rare diseases +MONDO:0000903 ordo_disorder diseases +MONDO:0000903 orphanet_rare diseases +MONDO:0000903 otar diseases +MONDO:0000903 rare diseases +MONDO:0000904 clingen diseases +MONDO:0000904 otar diseases +MONDO:0000908 gard_rare diseases +MONDO:0000908 nord_rare diseases +MONDO:0000908 rare diseases +MONDO:0000909 gard_rare diseases +MONDO:0000909 nord_rare diseases +MONDO:0000909 rare diseases +MONDO:0000910 gard_rare diseases +MONDO:0000910 nord_rare diseases +MONDO:0000910 rare diseases +MONDO:0000912 gard_rare diseases +MONDO:0000912 nord_rare diseases +MONDO:0000912 rare diseases +MONDO:0000913 gard_rare diseases +MONDO:0000913 nord_rare diseases +MONDO:0000913 rare diseases +MONDO:0000914 gard_rare diseases +MONDO:0000914 nord_rare diseases +MONDO:0000914 ordo_disorder diseases +MONDO:0000914 orphanet_rare diseases +MONDO:0000914 rare diseases +MONDO:0000916 otar diseases +MONDO:0000918 otar diseases +MONDO:0000919 gard_rare diseases +MONDO:0000919 otar diseases +MONDO:0000919 rare diseases +MONDO:0000920 gard_rare diseases +MONDO:0000920 otar diseases +MONDO:0000920 rare diseases +MONDO:0000921 otar diseases +MONDO:0000922 otar diseases +MONDO:0000923 otar diseases +MONDO:0000926 otar diseases +MONDO:0000927 inferred_rare diseases +MONDO:0000927 rare diseases +MONDO:0000928 gard_rare diseases +MONDO:0000928 nord_rare diseases +MONDO:0000928 rare diseases +MONDO:0000930 otar diseases +MONDO:0000931 otar diseases +MONDO:0000936 gard_rare diseases +MONDO:0000936 rare diseases +MONDO:0000937 gard_rare diseases +MONDO:0000937 rare diseases +MONDO:0000939 gard_rare diseases +MONDO:0000939 rare diseases +MONDO:0000942 otar diseases +MONDO:0000943 gard_rare diseases +MONDO:0000943 rare diseases +MONDO:0000944 otar diseases +MONDO:0000945 otar diseases +MONDO:0000951 gard_rare diseases +MONDO:0000951 otar diseases +MONDO:0000951 rare diseases +MONDO:0000952 gard_rare diseases +MONDO:0000952 rare diseases +MONDO:0000953 gard_rare diseases +MONDO:0000953 rare diseases +MONDO:0000954 gard_rare diseases +MONDO:0000954 rare diseases +MONDO:0000955 gard_rare diseases +MONDO:0000955 rare diseases +MONDO:0000956 gard_rare diseases +MONDO:0000956 nord_rare diseases +MONDO:0000956 otar diseases +MONDO:0000956 rare diseases +MONDO:0000958 gard_rare diseases +MONDO:0000958 rare diseases +MONDO:0000960 otar diseases +MONDO:0000962 otar diseases +MONDO:0000979 gard_rare diseases +MONDO:0000979 nord_rare diseases +MONDO:0000979 rare diseases +MONDO:0000981 gard_rare diseases +MONDO:0000981 rare diseases +MONDO:0000984 gard_rare diseases +MONDO:0000984 nord_rare diseases +MONDO:0000984 otar diseases +MONDO:0000984 rare diseases +MONDO:0000986 otar diseases +MONDO:0000989 otar diseases +MONDO:0000992 otar diseases +MONDO:0000994 gard_rare diseases +MONDO:0000994 rare diseases +MONDO:0000995 disease_grouping diseases +MONDO:0000995 gard_rare diseases +MONDO:0000995 ordo_group_of_disorders diseases +MONDO:0000995 otar diseases +MONDO:0000995 rare diseases +MONDO:0000996 gard_rare diseases +MONDO:0000996 rare diseases +MONDO:0001000 gard_rare diseases +MONDO:0001000 rare diseases +MONDO:0001001 gard_rare diseases +MONDO:0001001 rare diseases +MONDO:0001003 gard_rare diseases +MONDO:0001003 rare diseases +MONDO:0001004 gard_rare diseases +MONDO:0001004 rare diseases +MONDO:0001005 gard_rare diseases +MONDO:0001005 nord_rare diseases +MONDO:0001005 rare diseases +MONDO:0001014 gard_rare diseases +MONDO:0001014 otar diseases +MONDO:0001014 rare diseases +MONDO:0001020 otar diseases +MONDO:0001023 gard_rare diseases +MONDO:0001023 nord_rare diseases +MONDO:0001023 otar diseases +MONDO:0001023 rare diseases +MONDO:0001024 gard_rare diseases +MONDO:0001024 rare diseases +MONDO:0001029 gard_rare diseases +MONDO:0001029 nord_rare diseases +MONDO:0001029 ordo_disorder diseases +MONDO:0001029 orphanet_rare diseases +MONDO:0001029 otar diseases +MONDO:0001029 rare diseases +MONDO:0001030 gard_rare diseases +MONDO:0001030 rare diseases +MONDO:0001032 gard_rare diseases +MONDO:0001032 nord_rare diseases +MONDO:0001032 ordo_disorder diseases +MONDO:0001032 orphanet_rare diseases +MONDO:0001032 rare diseases +MONDO:0001035 gard_rare diseases +MONDO:0001035 rare diseases +MONDO:0001036 gard_rare diseases +MONDO:0001036 rare diseases +MONDO:0001040 otar diseases +MONDO:0001042 gard_rare diseases +MONDO:0001042 rare diseases +MONDO:0001045 otar diseases +MONDO:0001046 gard_rare diseases +MONDO:0001046 nord_rare diseases +MONDO:0001046 rare diseases +MONDO:0001056 otar diseases +MONDO:0001057 gard_rare diseases +MONDO:0001057 rare diseases +MONDO:0001059 gard_rare diseases +MONDO:0001059 otar diseases +MONDO:0001059 rare diseases +MONDO:0001063 otar diseases +MONDO:0001066 gard_rare diseases +MONDO:0001066 rare diseases +MONDO:0001067 gard_rare diseases +MONDO:0001067 rare diseases +MONDO:0001071 clingen diseases +MONDO:0001072 gard_rare diseases +MONDO:0001072 rare diseases +MONDO:0001073 gard_rare diseases +MONDO:0001073 rare diseases +MONDO:0001076 gard_rare diseases +MONDO:0001076 rare diseases +MONDO:0001078 otar diseases +MONDO:0001082 gard_rare diseases +MONDO:0001082 otar diseases +MONDO:0001082 rare diseases +MONDO:0001083 gard_rare diseases +MONDO:0001083 nord_rare diseases +MONDO:0001083 otar diseases +MONDO:0001083 rare diseases +MONDO:0001085 otar diseases +MONDO:0001087 otar diseases +MONDO:0001093 gard_rare diseases +MONDO:0001093 rare diseases +MONDO:0001095 gard_rare diseases +MONDO:0001095 otar diseases +MONDO:0001095 rare diseases +MONDO:0001096 gard_rare diseases +MONDO:0001096 rare diseases +MONDO:0001098 otar diseases +MONDO:0001104 otar diseases +MONDO:0001105 otar diseases +MONDO:0001106 otar diseases +MONDO:0001109 gard_rare diseases +MONDO:0001109 nord_rare diseases +MONDO:0001109 rare diseases +MONDO:0001110 otar diseases +MONDO:0001112 gard_rare diseases +MONDO:0001112 rare diseases +MONDO:0001113 gard_rare diseases +MONDO:0001113 nord_rare diseases +MONDO:0001113 rare diseases +MONDO:0001114 gard_rare diseases +MONDO:0001114 rare diseases +MONDO:0001115 gard_rare diseases +MONDO:0001115 otar diseases +MONDO:0001115 rare diseases +MONDO:0001117 gard_rare diseases +MONDO:0001117 otar diseases +MONDO:0001117 rare diseases +MONDO:0001118 gard_rare diseases +MONDO:0001118 rare diseases +MONDO:0001119 otar diseases +MONDO:0001126 otar diseases +MONDO:0001127 gard_rare diseases +MONDO:0001127 rare diseases +MONDO:0001128 otar diseases +MONDO:0001129 gard_rare diseases +MONDO:0001129 rare diseases +MONDO:0001130 gard_rare diseases +MONDO:0001130 rare diseases +MONDO:0001134 otar diseases +MONDO:0001142 otar diseases +MONDO:0001143 otar diseases +MONDO:0001144 gard_rare diseases +MONDO:0001144 rare diseases +MONDO:0001145 gard_rare diseases +MONDO:0001145 nord_rare diseases +MONDO:0001145 rare diseases +MONDO:0001146 otar diseases +MONDO:0001147 otar diseases +MONDO:0001148 gard_rare diseases +MONDO:0001148 nord_rare diseases +MONDO:0001148 rare diseases +MONDO:0001149 clingen diseases +MONDO:0001149 gard_rare diseases +MONDO:0001149 nord_rare diseases +MONDO:0001149 otar diseases +MONDO:0001149 rare diseases +MONDO:0001152 otar diseases +MONDO:0001154 gard_rare diseases +MONDO:0001154 nord_rare diseases +MONDO:0001154 rare diseases +MONDO:0001160 otar diseases +MONDO:0001161 otar diseases +MONDO:0001162 otar diseases +MONDO:0001163 otar diseases +MONDO:0001165 otar diseases +MONDO:0001166 otar diseases +MONDO:0001170 otar diseases +MONDO:0001176 otar diseases +MONDO:0001179 otar diseases +MONDO:0001184 gard_rare diseases +MONDO:0001184 nord_rare diseases +MONDO:0001184 rare diseases +MONDO:0001187 otar diseases +MONDO:0001188 gard_rare diseases +MONDO:0001188 nord_rare diseases +MONDO:0001188 rare diseases +MONDO:0001190 gard_rare diseases +MONDO:0001190 rare diseases +MONDO:0001195 disease_grouping diseases +MONDO:0001195 gard_rare diseases +MONDO:0001195 nord_rare diseases +MONDO:0001195 ordo_group_of_disorders diseases +MONDO:0001195 otar diseases +MONDO:0001195 rare diseases +MONDO:0001197 clingen diseases +MONDO:0001197 gard_rare diseases +MONDO:0001197 otar diseases +MONDO:0001197 rare diseases +MONDO:0001198 gard_rare diseases +MONDO:0001198 otar diseases +MONDO:0001198 rare diseases +MONDO:0001200 otar diseases +MONDO:0001204 gard_rare diseases +MONDO:0001204 rare diseases +MONDO:0001208 otar diseases +MONDO:0001209 otar diseases +MONDO:0001211 gard_rare diseases +MONDO:0001211 rare diseases +MONDO:0001212 otar diseases +MONDO:0001214 otar diseases +MONDO:0001220 gard_rare diseases +MONDO:0001220 nord_rare diseases +MONDO:0001220 otar diseases +MONDO:0001220 rare diseases +MONDO:0001221 otar diseases +MONDO:0001222 otar diseases +MONDO:0001223 otar diseases +MONDO:0001230 otar diseases +MONDO:0001235 otar diseases +MONDO:0001236 otar diseases +MONDO:0001237 gard_rare diseases +MONDO:0001237 rare diseases +MONDO:0001238 gard_rare diseases +MONDO:0001238 rare diseases +MONDO:0001239 gard_rare diseases +MONDO:0001239 nord_rare diseases +MONDO:0001239 rare diseases +MONDO:0001240 gard_rare diseases +MONDO:0001240 otar diseases +MONDO:0001240 rare diseases +MONDO:0001241 gard_rare diseases +MONDO:0001241 rare diseases +MONDO:0001242 gard_rare diseases +MONDO:0001242 rare diseases +MONDO:0001243 gard_rare diseases +MONDO:0001243 rare diseases +MONDO:0001245 otar diseases +MONDO:0001246 disease_grouping diseases +MONDO:0001246 gard_rare diseases +MONDO:0001246 nord_rare diseases +MONDO:0001246 ordo_group_of_disorders diseases +MONDO:0001246 otar diseases +MONDO:0001246 rare diseases +MONDO:0001247 otar diseases +MONDO:0001252 otar diseases +MONDO:0001255 gard_rare diseases +MONDO:0001255 rare diseases +MONDO:0001256 otar diseases +MONDO:0001259 otar diseases +MONDO:0001260 gard_rare diseases +MONDO:0001260 nord_rare diseases +MONDO:0001260 rare diseases +MONDO:0001261 gard_rare diseases +MONDO:0001261 nord_rare diseases +MONDO:0001261 rare diseases +MONDO:0001262 gard_rare diseases +MONDO:0001262 rare diseases +MONDO:0001263 gard_rare diseases +MONDO:0001263 rare diseases +MONDO:0001266 otar diseases +MONDO:0001269 otar diseases +MONDO:0001275 gard_rare diseases +MONDO:0001275 nord_rare diseases +MONDO:0001275 rare diseases +MONDO:0001277 gard_rare diseases +MONDO:0001277 rare diseases +MONDO:0001279 gard_rare diseases +MONDO:0001279 rare diseases +MONDO:0001280 disease_grouping diseases +MONDO:0001280 gard_rare diseases +MONDO:0001280 nord_rare diseases +MONDO:0001280 ordo_group_of_disorders diseases +MONDO:0001280 otar diseases +MONDO:0001280 rare diseases +MONDO:0001282 otar diseases +MONDO:0001285 otar diseases +MONDO:0001288 otar diseases +MONDO:0001290 gard_rare diseases +MONDO:0001290 rare diseases +MONDO:0001292 otar diseases +MONDO:0001294 gard_rare diseases +MONDO:0001294 otar diseases +MONDO:0001294 rare diseases +MONDO:0001297 otar diseases +MONDO:0001299 gard_rare diseases +MONDO:0001299 otar diseases +MONDO:0001299 rare diseases +MONDO:0001300 gard_rare diseases +MONDO:0001300 otar diseases +MONDO:0001300 rare diseases +MONDO:0001302 otar diseases +MONDO:0001307 gard_rare diseases +MONDO:0001307 rare diseases +MONDO:0001309 disease_grouping diseases +MONDO:0001309 gard_rare diseases +MONDO:0001309 ordo_group_of_disorders diseases +MONDO:0001309 rare diseases +MONDO:0001314 otar diseases +MONDO:0001316 gard_rare diseases +MONDO:0001316 otar diseases +MONDO:0001316 rare diseases +MONDO:0001318 otar diseases +MONDO:0001323 gard_rare diseases +MONDO:0001323 rare diseases +MONDO:0001325 disease_grouping diseases +MONDO:0001325 gard_rare diseases +MONDO:0001325 nord_rare diseases +MONDO:0001325 ordo_group_of_disorders diseases +MONDO:0001325 otar diseases +MONDO:0001325 rare diseases +MONDO:0001328 gard_rare diseases +MONDO:0001328 otar diseases +MONDO:0001328 rare diseases +MONDO:0001330 otar diseases +MONDO:0001332 otar diseases +MONDO:0001334 gard_rare diseases +MONDO:0001334 rare diseases +MONDO:0001336 gard_rare diseases +MONDO:0001336 otar diseases +MONDO:0001336 rare diseases +MONDO:0001340 otar diseases +MONDO:0001341 inferred_rare diseases +MONDO:0001341 otar diseases +MONDO:0001341 rare diseases +MONDO:0001342 gard_rare diseases +MONDO:0001342 otar diseases +MONDO:0001342 rare diseases +MONDO:0001343 otar diseases +MONDO:0001347 gard_rare diseases +MONDO:0001347 nord_rare diseases +MONDO:0001347 ordo_disorder diseases +MONDO:0001347 orphanet_rare diseases +MONDO:0001347 otar diseases +MONDO:0001347 rare diseases +MONDO:0001357 otar diseases +MONDO:0001358 otar diseases +MONDO:0001366 gard_rare diseases +MONDO:0001366 rare diseases +MONDO:0001367 gard_rare diseases +MONDO:0001367 rare diseases +MONDO:0001369 otar diseases +MONDO:0001370 otar diseases +MONDO:0001371 otar diseases +MONDO:0001374 gard_rare diseases +MONDO:0001374 otar diseases +MONDO:0001374 rare diseases +MONDO:0001377 otar diseases +MONDO:0001381 gard_rare diseases +MONDO:0001381 nord_rare diseases +MONDO:0001381 rare diseases +MONDO:0001382 otar diseases +MONDO:0001383 gard_rare diseases +MONDO:0001383 rare diseases +MONDO:0001384 otar diseases +MONDO:0001386 gard_rare diseases +MONDO:0001386 rare diseases +MONDO:0001387 gard_rare diseases +MONDO:0001387 nord_rare diseases +MONDO:0001387 rare diseases +MONDO:0001388 gard_rare diseases +MONDO:0001388 rare diseases +MONDO:0001391 gard_rare diseases +MONDO:0001391 rare diseases +MONDO:0001393 gard_rare diseases +MONDO:0001393 rare diseases +MONDO:0001394 gard_rare diseases +MONDO:0001394 rare diseases +MONDO:0001397 gard_rare diseases +MONDO:0001397 otar diseases +MONDO:0001397 rare diseases +MONDO:0001400 gard_rare diseases +MONDO:0001400 rare diseases +MONDO:0001402 otar diseases +MONDO:0001406 otar diseases +MONDO:0001407 otar diseases +MONDO:0001408 gard_rare diseases +MONDO:0001408 rare diseases +MONDO:0001409 otar diseases +MONDO:0001410 otar diseases +MONDO:0001411 gard_rare diseases +MONDO:0001411 rare diseases +MONDO:0001413 gard_rare diseases +MONDO:0001413 rare diseases +MONDO:0001414 otar diseases +MONDO:0001416 otar diseases +MONDO:0001417 gard_rare diseases +MONDO:0001417 nord_rare diseases +MONDO:0001417 rare diseases +MONDO:0001418 gard_rare diseases +MONDO:0001418 nord_rare diseases +MONDO:0001418 rare diseases +MONDO:0001419 otar diseases +MONDO:0001422 otar diseases +MONDO:0001423 otar diseases +MONDO:0001426 gard_rare diseases +MONDO:0001426 rare diseases +MONDO:0001433 otar diseases +MONDO:0001434 otar diseases +MONDO:0001436 otar diseases +MONDO:0001437 otar diseases +MONDO:0001438 gard_rare diseases +MONDO:0001438 otar diseases +MONDO:0001438 rare diseases +MONDO:0001442 otar diseases +MONDO:0001444 gard_rare diseases +MONDO:0001444 nord_rare diseases +MONDO:0001444 ordo_disorder diseases +MONDO:0001444 orphanet_rare diseases +MONDO:0001444 otar diseases +MONDO:0001444 rare diseases +MONDO:0001449 gard_rare diseases +MONDO:0001449 nord_rare diseases +MONDO:0001449 rare diseases +MONDO:0001458 gard_rare diseases +MONDO:0001458 rare diseases +MONDO:0001459 gard_rare diseases +MONDO:0001459 rare diseases +MONDO:0001470 gard_rare diseases +MONDO:0001470 rare diseases +MONDO:0001471 gard_rare diseases +MONDO:0001471 rare diseases +MONDO:0001472 gard_rare diseases +MONDO:0001472 rare diseases +MONDO:0001475 clingen diseases +MONDO:0001475 gard_rare diseases +MONDO:0001475 otar diseases +MONDO:0001475 rare diseases +MONDO:0001476 disease_grouping diseases +MONDO:0001476 otar diseases +MONDO:0001479 gard_rare diseases +MONDO:0001479 rare diseases +MONDO:0001481 gard_rare diseases +MONDO:0001481 rare diseases +MONDO:0001482 gard_rare diseases +MONDO:0001482 rare diseases +MONDO:0001487 gard_rare diseases +MONDO:0001487 otar diseases +MONDO:0001487 rare diseases +MONDO:0001490 gard_rare diseases +MONDO:0001490 nord_rare diseases +MONDO:0001490 rare diseases +MONDO:0001493 otar diseases +MONDO:0001498 otar diseases +MONDO:0001499 gard_rare diseases +MONDO:0001499 rare diseases +MONDO:0001501 gard_rare diseases +MONDO:0001501 rare diseases +MONDO:0001502 otar diseases +MONDO:0001505 otar diseases +MONDO:0001515 otar diseases +MONDO:0001516 gard_rare diseases +MONDO:0001516 nord_rare diseases +MONDO:0001516 otar diseases +MONDO:0001516 rare diseases +MONDO:0001517 otar diseases +MONDO:0001519 otar diseases +MONDO:0001528 otar diseases +MONDO:0001529 gard_rare diseases +MONDO:0001529 rare diseases +MONDO:0001531 gard_rare diseases +MONDO:0001531 otar diseases +MONDO:0001531 rare diseases +MONDO:0001537 gard_rare diseases +MONDO:0001537 rare diseases +MONDO:0001539 otar diseases +MONDO:0001540 gard_rare diseases +MONDO:0001540 nord_rare diseases +MONDO:0001540 rare diseases +MONDO:0001541 gard_rare diseases +MONDO:0001541 rare diseases +MONDO:0001542 gard_rare diseases +MONDO:0001542 rare diseases +MONDO:0001543 gard_rare diseases +MONDO:0001543 otar diseases +MONDO:0001543 rare diseases +MONDO:0001544 gard_rare diseases +MONDO:0001544 rare diseases +MONDO:0001549 disease_grouping diseases +MONDO:0001549 gard_rare diseases +MONDO:0001549 nord_rare diseases +MONDO:0001549 ordo_group_of_disorders diseases +MONDO:0001549 otar diseases +MONDO:0001549 rare diseases +MONDO:0001551 otar diseases +MONDO:0001557 otar diseases +MONDO:0001558 otar diseases +MONDO:0001560 otar diseases +MONDO:0001561 otar diseases +MONDO:0001563 otar diseases +MONDO:0001564 otar diseases +MONDO:0001566 otar diseases +MONDO:0001567 otar diseases +MONDO:0001569 gard_rare diseases +MONDO:0001569 nord_rare diseases +MONDO:0001569 ordo_subtype_of_a_disorder diseases +MONDO:0001569 rare diseases +MONDO:0001571 gard_rare diseases +MONDO:0001571 rare diseases +MONDO:0001572 otar diseases +MONDO:0001574 otar diseases +MONDO:0001576 otar diseases +MONDO:0001577 otar diseases +MONDO:0001580 otar diseases +MONDO:0001583 gard_rare diseases +MONDO:0001583 otar diseases +MONDO:0001583 rare diseases +MONDO:0001584 otar diseases +MONDO:0001586 clingen diseases +MONDO:0001586 gard_rare diseases +MONDO:0001586 nord_rare diseases +MONDO:0001586 ordo_disorder diseases +MONDO:0001586 orphanet_rare diseases +MONDO:0001586 otar diseases +MONDO:0001586 rare diseases +MONDO:0001590 otar diseases +MONDO:0001592 otar diseases +MONDO:0001593 otar diseases +MONDO:0001594 gard_rare diseases +MONDO:0001594 rare diseases +MONDO:0001595 gard_rare diseases +MONDO:0001595 ordo_disorder diseases +MONDO:0001595 orphanet_rare diseases +MONDO:0001595 otar diseases +MONDO:0001595 rare diseases +MONDO:0001597 otar diseases +MONDO:0001601 gard_rare diseases +MONDO:0001601 rare diseases +MONDO:0001602 gard_rare diseases +MONDO:0001602 rare diseases +MONDO:0001604 otar diseases +MONDO:0001606 gard_rare diseases +MONDO:0001606 rare diseases +MONDO:0001607 gard_rare diseases +MONDO:0001607 rare diseases +MONDO:0001609 gard_rare diseases +MONDO:0001609 nord_rare diseases +MONDO:0001609 rare diseases +MONDO:0001613 otar diseases +MONDO:0001614 gard_rare diseases +MONDO:0001614 rare diseases +MONDO:0001615 gard_rare diseases +MONDO:0001615 rare diseases +MONDO:0001616 otar diseases +MONDO:0001618 otar diseases +MONDO:0001620 gard_rare diseases +MONDO:0001620 nord_rare diseases +MONDO:0001620 rare diseases +MONDO:0001621 gard_rare diseases +MONDO:0001621 nord_rare diseases +MONDO:0001621 rare diseases +MONDO:0001627 otar diseases +MONDO:0001633 gard_rare diseases +MONDO:0001633 ordo_disorder diseases +MONDO:0001633 orphanet_rare diseases +MONDO:0001633 rare diseases +MONDO:0001638 gard_rare diseases +MONDO:0001638 rare diseases +MONDO:0001639 gard_rare diseases +MONDO:0001639 otar diseases +MONDO:0001639 rare diseases +MONDO:0001641 gard_rare diseases +MONDO:0001641 otar diseases +MONDO:0001641 rare diseases +MONDO:0001644 gard_rare diseases +MONDO:0001644 rare diseases +MONDO:0001645 gard_rare diseases +MONDO:0001645 rare diseases +MONDO:0001657 otar diseases +MONDO:0001658 otar diseases +MONDO:0001660 otar diseases +MONDO:0001664 gard_rare diseases +MONDO:0001664 rare diseases +MONDO:0001665 gard_rare diseases +MONDO:0001665 rare diseases +MONDO:0001666 gard_rare diseases +MONDO:0001666 rare diseases +MONDO:0001672 otar diseases +MONDO:0001673 otar diseases +MONDO:0001674 otar diseases +MONDO:0001676 gard_rare diseases +MONDO:0001676 otar diseases +MONDO:0001676 rare diseases +MONDO:0001678 gard_rare diseases +MONDO:0001678 rare diseases +MONDO:0001684 otar diseases +MONDO:0001691 gard_rare diseases +MONDO:0001691 rare diseases +MONDO:0001697 otar diseases +MONDO:0001700 gard_rare diseases +MONDO:0001700 otar diseases +MONDO:0001700 rare diseases +MONDO:0001702 gard_rare diseases +MONDO:0001702 rare diseases +MONDO:0001703 disease_grouping diseases +MONDO:0001703 ordo_group_of_disorders diseases +MONDO:0001703 otar diseases +MONDO:0001705 gard_rare diseases +MONDO:0001705 nord_rare diseases +MONDO:0001705 otar diseases +MONDO:0001705 rare diseases +MONDO:0001706 gard_rare diseases +MONDO:0001706 rare diseases +MONDO:0001707 gard_rare diseases +MONDO:0001707 rare diseases +MONDO:0001708 gard_rare diseases +MONDO:0001708 rare diseases +MONDO:0001709 gard_rare diseases +MONDO:0001709 rare diseases +MONDO:0001713 disease_grouping diseases +MONDO:0001713 gard_rare diseases +MONDO:0001713 nord_rare diseases +MONDO:0001713 ordo_group_of_disorders diseases +MONDO:0001713 otar diseases +MONDO:0001713 rare diseases +MONDO:0001714 gard_rare diseases +MONDO:0001714 nord_rare diseases +MONDO:0001714 rare diseases +MONDO:0001718 otar diseases +MONDO:0001724 otar diseases +MONDO:0001727 gard_rare diseases +MONDO:0001727 rare diseases +MONDO:0001728 gard_rare diseases +MONDO:0001728 rare diseases +MONDO:0001729 gard_rare diseases +MONDO:0001729 rare diseases +MONDO:0001730 otar diseases +MONDO:0001734 clingen diseases +MONDO:0001734 gard_rare diseases +MONDO:0001734 nord_rare diseases +MONDO:0001734 ordo_disorder diseases +MONDO:0001734 orphanet_rare diseases +MONDO:0001734 otar diseases +MONDO:0001734 rare diseases +MONDO:0001735 otar diseases +MONDO:0001737 gard_rare diseases +MONDO:0001737 rare diseases +MONDO:0001740 gard_rare diseases +MONDO:0001740 rare diseases +MONDO:0001741 otar diseases +MONDO:0001743 gard_rare diseases +MONDO:0001743 rare diseases +MONDO:0001744 otar diseases +MONDO:0001745 gard_rare diseases +MONDO:0001745 rare diseases +MONDO:0001748 gard_rare diseases +MONDO:0001748 otar diseases +MONDO:0001748 rare diseases +MONDO:0001751 otar diseases +MONDO:0001756 gard_rare diseases +MONDO:0001756 rare diseases +MONDO:0001757 gard_rare diseases +MONDO:0001757 rare diseases +MONDO:0001758 gard_rare diseases +MONDO:0001758 rare diseases +MONDO:0001760 gard_rare diseases +MONDO:0001760 rare diseases +MONDO:0001761 inferred_rare diseases +MONDO:0001761 rare diseases +MONDO:0001763 gard_rare diseases +MONDO:0001763 rare diseases +MONDO:0001764 gard_rare diseases +MONDO:0001764 rare diseases +MONDO:0001765 gard_rare diseases +MONDO:0001765 rare diseases +MONDO:0001773 gard_rare diseases +MONDO:0001773 rare diseases +MONDO:0001778 gard_rare diseases +MONDO:0001778 nord_rare diseases +MONDO:0001778 rare diseases +MONDO:0001780 otar diseases +MONDO:0001784 otar diseases +MONDO:0001785 otar diseases +MONDO:0001786 otar diseases +MONDO:0001789 gard_rare diseases +MONDO:0001789 rare diseases +MONDO:0001790 gard_rare diseases +MONDO:0001790 ordo_group_of_disorders diseases +MONDO:0001790 rare diseases +MONDO:0001795 otar diseases +MONDO:0001797 gard_rare diseases +MONDO:0001797 nord_rare diseases +MONDO:0001797 rare diseases +MONDO:0001798 otar diseases +MONDO:0001818 gard_rare diseases +MONDO:0001818 nord_rare diseases +MONDO:0001818 otar diseases +MONDO:0001818 rare diseases +MONDO:0001822 gard_rare diseases +MONDO:0001822 otar diseases +MONDO:0001822 rare diseases +MONDO:0001823 otar diseases +MONDO:0001824 gard_rare diseases +MONDO:0001824 otar diseases +MONDO:0001824 rare diseases +MONDO:0001825 otar diseases +MONDO:0001828 gard_rare diseases +MONDO:0001828 rare diseases +MONDO:0001829 gard_rare diseases +MONDO:0001829 rare diseases +MONDO:0001834 otar diseases +MONDO:0001835 otar diseases +MONDO:0001841 gard_rare diseases +MONDO:0001841 otar diseases +MONDO:0001841 rare diseases +MONDO:0001842 gard_rare diseases +MONDO:0001842 nord_rare diseases +MONDO:0001842 rare diseases +MONDO:0001843 gard_rare diseases +MONDO:0001843 rare diseases +MONDO:0001844 gard_rare diseases +MONDO:0001844 nord_rare diseases +MONDO:0001844 rare diseases +MONDO:0001845 gard_rare diseases +MONDO:0001845 nord_rare diseases +MONDO:0001845 rare diseases +MONDO:0001846 gard_rare diseases +MONDO:0001846 nord_rare diseases +MONDO:0001846 rare diseases +MONDO:0001847 otar diseases +MONDO:0001852 gard_rare diseases +MONDO:0001852 otar diseases +MONDO:0001852 rare diseases +MONDO:0001854 otar diseases +MONDO:0001857 gard_rare diseases +MONDO:0001857 rare diseases +MONDO:0001858 otar diseases +MONDO:0001859 gard_rare diseases +MONDO:0001859 otar diseases +MONDO:0001859 rare diseases +MONDO:0001868 clingen diseases +MONDO:0001868 otar diseases +MONDO:0001870 gard_rare diseases +MONDO:0001870 nord_rare diseases +MONDO:0001870 rare diseases +MONDO:0001871 gard_rare diseases +MONDO:0001871 nord_rare diseases +MONDO:0001871 rare diseases +MONDO:0001875 otar diseases +MONDO:0001879 otar diseases +MONDO:0001881 gard_rare diseases +MONDO:0001881 nord_rare diseases +MONDO:0001881 ordo_disorder diseases +MONDO:0001881 orphanet_rare diseases +MONDO:0001881 rare diseases +MONDO:0001888 gard_rare diseases +MONDO:0001888 rare diseases +MONDO:0001889 otar diseases +MONDO:0001892 gard_rare diseases +MONDO:0001892 nord_rare diseases +MONDO:0001892 rare diseases +MONDO:0001893 gard_rare diseases +MONDO:0001893 nord_rare diseases +MONDO:0001893 rare diseases +MONDO:0001894 gard_rare diseases +MONDO:0001894 nord_rare diseases +MONDO:0001894 rare diseases +MONDO:0001896 otar diseases +MONDO:0001898 otar diseases +MONDO:0001901 gard_rare diseases +MONDO:0001901 nord_rare diseases +MONDO:0001901 rare diseases +MONDO:0001902 gard_rare diseases +MONDO:0001902 otar diseases +MONDO:0001902 rare diseases +MONDO:0001903 gard_rare diseases +MONDO:0001903 otar diseases +MONDO:0001903 rare diseases +MONDO:0001904 gard_rare diseases +MONDO:0001904 rare diseases +MONDO:0001905 gard_rare diseases +MONDO:0001905 rare diseases +MONDO:0001907 gard_rare diseases +MONDO:0001907 rare diseases +MONDO:0001909 gard_rare diseases +MONDO:0001909 nord_rare diseases +MONDO:0001909 otar diseases +MONDO:0001909 rare diseases +MONDO:0001916 gard_rare diseases +MONDO:0001916 rare diseases +MONDO:0001923 gard_rare diseases +MONDO:0001923 rare diseases +MONDO:0001924 gard_rare diseases +MONDO:0001924 rare diseases +MONDO:0001925 gard_rare diseases +MONDO:0001925 rare diseases +MONDO:0001926 otar diseases +MONDO:0001933 otar diseases +MONDO:0001935 otar diseases +MONDO:0001938 otar diseases +MONDO:0001941 otar diseases +MONDO:0001942 otar diseases +MONDO:0001943 gard_rare diseases +MONDO:0001943 rare diseases +MONDO:0001944 gard_rare diseases +MONDO:0001944 rare diseases +MONDO:0001945 gard_rare diseases +MONDO:0001945 nord_rare diseases +MONDO:0001945 ordo_disorder diseases +MONDO:0001945 orphanet_rare diseases +MONDO:0001945 otar diseases +MONDO:0001945 rare diseases +MONDO:0001947 otar diseases +MONDO:0001949 otar diseases +MONDO:0001954 gard_rare diseases +MONDO:0001954 nord_rare diseases +MONDO:0001954 rare diseases +MONDO:0001956 gard_rare diseases +MONDO:0001956 ordo_disorder diseases +MONDO:0001956 orphanet_rare diseases +MONDO:0001956 otar diseases +MONDO:0001956 rare diseases +MONDO:0001957 gard_rare diseases +MONDO:0001957 rare diseases +MONDO:0001967 gard_rare diseases +MONDO:0001967 nord_rare diseases +MONDO:0001967 otar diseases +MONDO:0001967 rare diseases +MONDO:0001969 gard_rare diseases +MONDO:0001969 nord_rare diseases +MONDO:0001969 rare diseases +MONDO:0001971 gard_rare diseases +MONDO:0001971 nord_rare diseases +MONDO:0001971 ordo_disorder diseases +MONDO:0001971 orphanet_rare diseases +MONDO:0001971 rare diseases +MONDO:0001972 gard_rare diseases +MONDO:0001972 rare diseases +MONDO:0001973 gard_rare diseases +MONDO:0001973 rare diseases +MONDO:0001975 gard_rare diseases +MONDO:0001975 rare diseases +MONDO:0001976 gard_rare diseases +MONDO:0001976 nord_rare diseases +MONDO:0001976 rare diseases +MONDO:0001977 gard_rare diseases +MONDO:0001977 nord_rare diseases +MONDO:0001977 rare diseases +MONDO:0001979 otar diseases +MONDO:0001982 gard_rare diseases +MONDO:0001982 nord_rare diseases +MONDO:0001982 otar diseases +MONDO:0001982 rare diseases +MONDO:0001989 otar diseases +MONDO:0001990 gard_rare diseases +MONDO:0001990 rare diseases +MONDO:0001991 gard_rare diseases +MONDO:0001991 rare diseases +MONDO:0001994 gard_rare diseases +MONDO:0001994 nord_rare diseases +MONDO:0001994 rare diseases +MONDO:0001995 gard_rare diseases +MONDO:0001995 nord_rare diseases +MONDO:0001995 rare diseases +MONDO:0001998 otar diseases +MONDO:0001999 otar diseases +MONDO:0002000 gard_rare diseases +MONDO:0002000 rare diseases +MONDO:0002008 otar diseases +MONDO:0002009 otar diseases +MONDO:0002010 otar diseases +MONDO:0002012 gard_rare diseases +MONDO:0002012 otar diseases +MONDO:0002012 rare diseases +MONDO:0002013 disease_grouping diseases +MONDO:0002013 gard_rare diseases +MONDO:0002013 obsoletion_candidate diseases +MONDO:0002013 ordo_group_of_disorders diseases +MONDO:0002013 otar diseases +MONDO:0002013 rare diseases +MONDO:0002014 gard_rare diseases +MONDO:0002014 rare diseases +MONDO:0002021 otar diseases +MONDO:0002025 otar diseases +MONDO:0002025 rare_grouping diseases +MONDO:0002026 otar diseases +MONDO:0002028 otar diseases +MONDO:0002032 otar diseases +MONDO:0002033 otar diseases +MONDO:0002034 gard_rare diseases +MONDO:0002034 nord_rare diseases +MONDO:0002034 rare diseases +MONDO:0002035 gard_rare diseases +MONDO:0002035 rare diseases +MONDO:0002036 otar diseases +MONDO:0002037 otar diseases +MONDO:0002038 otar diseases +MONDO:0002039 otar diseases +MONDO:0002040 otar diseases +MONDO:0002041 otar diseases +MONDO:0002043 otar diseases +MONDO:0002045 otar diseases +MONDO:0002046 otar diseases +MONDO:0002047 gard_rare diseases +MONDO:0002047 rare diseases +MONDO:0002048 gard_rare diseases +MONDO:0002048 nord_rare diseases +MONDO:0002048 rare diseases +MONDO:0002049 gard_rare diseases +MONDO:0002049 rare diseases +MONDO:0002050 otar diseases +MONDO:0002051 otar diseases +MONDO:0002051 rare_grouping diseases +MONDO:0002052 otar diseases +MONDO:0002058 otar diseases +MONDO:0002060 otar diseases +MONDO:0002070 otar diseases +MONDO:0002073 gard_rare diseases +MONDO:0002073 nord_rare diseases +MONDO:0002073 rare diseases +MONDO:0002076 otar diseases +MONDO:0002078 otar diseases +MONDO:0002081 otar diseases +MONDO:0002081 rare_grouping diseases +MONDO:0002082 otar diseases +MONDO:0002083 gard_rare diseases +MONDO:0002083 nord_rare diseases +MONDO:0002083 otar diseases +MONDO:0002083 rare diseases +MONDO:0002087 otar diseases +MONDO:0002089 otar diseases +MONDO:0002090 otar diseases +MONDO:0002093 otar diseases +MONDO:0002095 otar diseases +MONDO:0002096 gard_rare diseases +MONDO:0002096 nord_rare diseases +MONDO:0002096 ordo_disorder diseases +MONDO:0002096 orphanet_rare diseases +MONDO:0002096 otar diseases +MONDO:0002096 rare diseases +MONDO:0002098 otar diseases +MONDO:0002099 gard_rare diseases +MONDO:0002099 rare diseases +MONDO:0002100 otar diseases +MONDO:0002102 otar diseases +MONDO:0002108 gard_rare diseases +MONDO:0002108 otar diseases +MONDO:0002108 rare diseases +MONDO:0002109 gard_rare diseases +MONDO:0002109 otar diseases +MONDO:0002109 rare diseases +MONDO:0002113 otar diseases +MONDO:0002114 gard_rare diseases +MONDO:0002114 nord_rare diseases +MONDO:0002114 rare diseases +MONDO:0002116 otar diseases +MONDO:0002117 gard_rare diseases +MONDO:0002117 rare diseases +MONDO:0002118 otar diseases +MONDO:0002118 rare_grouping diseases +MONDO:0002119 gard_rare diseases +MONDO:0002119 nord_rare diseases +MONDO:0002119 rare diseases +MONDO:0002120 gard_rare diseases +MONDO:0002120 otar diseases +MONDO:0002120 rare diseases +MONDO:0002121 gard_rare diseases +MONDO:0002121 rare diseases +MONDO:0002122 gard_rare diseases +MONDO:0002122 otar diseases +MONDO:0002122 rare diseases +MONDO:0002123 otar diseases +MONDO:0002125 otar diseases +MONDO:0002128 gard_rare diseases +MONDO:0002128 rare diseases +MONDO:0002129 gard_rare diseases +MONDO:0002129 otar diseases +MONDO:0002129 rare diseases +MONDO:0002130 gard_rare diseases +MONDO:0002130 rare diseases +MONDO:0002131 gard_rare diseases +MONDO:0002131 rare diseases +MONDO:0002132 gard_rare diseases +MONDO:0002132 rare diseases +MONDO:0002134 otar diseases +MONDO:0002135 otar diseases +MONDO:0002140 gard_rare diseases +MONDO:0002140 rare diseases +MONDO:0002141 gard_rare diseases +MONDO:0002141 rare diseases +MONDO:0002142 gard_rare diseases +MONDO:0002142 nord_rare diseases +MONDO:0002142 ordo_disorder diseases +MONDO:0002142 orphanet_rare diseases +MONDO:0002142 otar diseases +MONDO:0002142 rare diseases +MONDO:0002143 gard_rare diseases +MONDO:0002143 rare diseases +MONDO:0002145 disease_grouping diseases +MONDO:0002145 ordo_group_of_disorders diseases +MONDO:0002145 otar diseases +MONDO:0002146 otar diseases +MONDO:0002149 otar diseases +MONDO:0002150 otar diseases +MONDO:0002153 gard_rare diseases +MONDO:0002153 rare diseases +MONDO:0002156 otar diseases +MONDO:0002158 gard_rare diseases +MONDO:0002158 nord_rare diseases +MONDO:0002158 ordo_disorder diseases +MONDO:0002158 orphanet_rare diseases +MONDO:0002158 otar diseases +MONDO:0002158 rare diseases +MONDO:0002159 gard_rare diseases +MONDO:0002159 rare diseases +MONDO:0002162 gard_rare diseases +MONDO:0002162 rare diseases +MONDO:0002163 gard_rare diseases +MONDO:0002163 rare diseases +MONDO:0002164 gard_rare diseases +MONDO:0002164 rare diseases +MONDO:0002165 otar diseases +MONDO:0002166 gard_rare diseases +MONDO:0002166 rare diseases +MONDO:0002167 otar diseases +MONDO:0002169 otar diseases +MONDO:0002171 otar diseases +MONDO:0002173 otar diseases +MONDO:0002175 otar diseases +MONDO:0002177 otar diseases +MONDO:0002178 otar diseases +MONDO:0002181 otar diseases +MONDO:0002182 otar diseases +MONDO:0002183 otar diseases +MONDO:0002185 otar diseases +MONDO:0002187 otar diseases +MONDO:0002191 otar diseases +MONDO:0002195 otar diseases +MONDO:0002200 otar diseases +MONDO:0002203 otar diseases +MONDO:0002206 otar diseases +MONDO:0002207 gard_rare diseases +MONDO:0002207 rare diseases +MONDO:0002211 gard_rare diseases +MONDO:0002211 otar diseases +MONDO:0002211 rare diseases +MONDO:0002212 gard_rare diseases +MONDO:0002212 rare diseases +MONDO:0002214 gard_rare diseases +MONDO:0002214 rare diseases +MONDO:0002216 gard_rare diseases +MONDO:0002216 rare diseases +MONDO:0002217 gard_rare diseases +MONDO:0002217 otar diseases +MONDO:0002217 rare diseases +MONDO:0002220 otar diseases +MONDO:0002223 gard_rare diseases +MONDO:0002223 rare diseases +MONDO:0002224 gard_rare diseases +MONDO:0002224 rare diseases +MONDO:0002225 gard_rare diseases +MONDO:0002225 otar diseases +MONDO:0002225 rare diseases +MONDO:0002226 gard_rare diseases +MONDO:0002226 rare diseases +MONDO:0002227 gard_rare diseases +MONDO:0002227 rare diseases +MONDO:0002229 otar diseases +MONDO:0002230 gard_rare diseases +MONDO:0002230 rare diseases +MONDO:0002233 otar diseases +MONDO:0002234 otar diseases +MONDO:0002235 disease_grouping diseases +MONDO:0002235 otar diseases +MONDO:0002236 otar diseases +MONDO:0002241 gard_rare diseases +MONDO:0002241 otar diseases +MONDO:0002241 rare diseases +MONDO:0002242 gard_rare diseases +MONDO:0002242 otar diseases +MONDO:0002242 rare diseases +MONDO:0002243 gard_rare diseases +MONDO:0002243 otar diseases +MONDO:0002243 rare diseases +MONDO:0002244 clingen diseases +MONDO:0002244 gard_rare diseases +MONDO:0002244 otar diseases +MONDO:0002244 rare diseases +MONDO:0002245 gard_rare diseases +MONDO:0002245 otar diseases +MONDO:0002245 rare diseases +MONDO:0002247 gard_rare diseases +MONDO:0002247 otar diseases +MONDO:0002247 rare diseases +MONDO:0002249 gard_rare diseases +MONDO:0002249 otar diseases +MONDO:0002249 rare diseases +MONDO:0002253 otar diseases +MONDO:0002254 harrisons_view diseases +MONDO:0002254 rare_grouping diseases +MONDO:0002256 otar diseases +MONDO:0002257 otar diseases +MONDO:0002258 otar diseases +MONDO:0002259 otar diseases +MONDO:0002260 otar diseases +MONDO:0002262 gard_rare diseases +MONDO:0002262 rare diseases +MONDO:0002263 otar diseases +MONDO:0002266 gard_rare diseases +MONDO:0002266 nord_rare diseases +MONDO:0002266 rare diseases +MONDO:0002268 otar diseases +MONDO:0002269 otar diseases +MONDO:0002271 otar diseases +MONDO:0002272 gard_rare diseases +MONDO:0002272 rare diseases +MONDO:0002273 gard_rare diseases +MONDO:0002273 otar diseases +MONDO:0002273 rare diseases +MONDO:0002274 gard_rare diseases +MONDO:0002274 rare diseases +MONDO:0002277 otar diseases +MONDO:0002278 otar diseases +MONDO:0002279 otar diseases +MONDO:0002280 otar diseases +MONDO:0002281 otar diseases +MONDO:0002282 otar diseases +MONDO:0002283 otar diseases +MONDO:0002286 otar diseases +MONDO:0002289 otar diseases +MONDO:0002291 gard_rare diseases +MONDO:0002291 rare diseases +MONDO:0002293 gard_rare diseases +MONDO:0002293 rare diseases +MONDO:0002295 gard_rare diseases +MONDO:0002295 rare diseases +MONDO:0002297 otar diseases +MONDO:0002298 gard_rare diseases +MONDO:0002298 rare diseases +MONDO:0002299 gard_rare diseases +MONDO:0002299 rare diseases +MONDO:0002300 gard_rare diseases +MONDO:0002300 otar diseases +MONDO:0002300 rare diseases +MONDO:0002301 gard_rare diseases +MONDO:0002301 rare diseases +MONDO:0002303 gard_rare diseases +MONDO:0002303 nord_rare diseases +MONDO:0002303 ordo_disorder diseases +MONDO:0002303 orphanet_rare diseases +MONDO:0002303 rare diseases +MONDO:0002304 gard_rare diseases +MONDO:0002304 otar diseases +MONDO:0002304 rare diseases +MONDO:0002305 gard_rare diseases +MONDO:0002305 otar diseases +MONDO:0002305 rare diseases +MONDO:0002311 otar diseases +MONDO:0002312 otar diseases +MONDO:0002314 otar diseases +MONDO:0002316 gard_rare diseases +MONDO:0002316 otar diseases +MONDO:0002316 rare diseases +MONDO:0002319 otar diseases +MONDO:0002320 otar diseases +MONDO:0002321 gard_rare diseases +MONDO:0002321 otar diseases +MONDO:0002321 rare diseases +MONDO:0002326 otar diseases +MONDO:0002327 gard_rare diseases +MONDO:0002327 rare diseases +MONDO:0002328 otar diseases +MONDO:0002329 otar diseases +MONDO:0002330 otar diseases +MONDO:0002331 otar diseases +MONDO:0002332 gard_rare diseases +MONDO:0002332 otar diseases +MONDO:0002332 rare diseases +MONDO:0002333 gard_rare diseases +MONDO:0002333 rare diseases +MONDO:0002334 gard_rare diseases +MONDO:0002334 otar diseases +MONDO:0002334 rare diseases +MONDO:0002340 gard_rare diseases +MONDO:0002340 rare diseases +MONDO:0002341 gard_rare diseases +MONDO:0002341 otar diseases +MONDO:0002341 rare diseases +MONDO:0002342 otar diseases +MONDO:0002343 gard_rare diseases +MONDO:0002343 rare diseases +MONDO:0002345 otar diseases +MONDO:0002350 otar diseases +MONDO:0002351 otar diseases +MONDO:0002352 otar diseases +MONDO:0002353 otar diseases +MONDO:0002354 otar diseases +MONDO:0002355 otar diseases +MONDO:0002356 otar diseases +MONDO:0002356 rare_grouping diseases +MONDO:0002358 otar diseases +MONDO:0002359 gard_rare diseases +MONDO:0002359 otar diseases +MONDO:0002359 rare diseases +MONDO:0002360 otar diseases +MONDO:0002363 otar diseases +MONDO:0002367 otar diseases +MONDO:0002368 otar diseases +MONDO:0002369 otar diseases +MONDO:0002372 gard_rare diseases +MONDO:0002372 rare diseases +MONDO:0002375 otar diseases +MONDO:0002376 gard_rare diseases +MONDO:0002376 otar diseases +MONDO:0002376 rare diseases +MONDO:0002378 gard_rare diseases +MONDO:0002378 nord_rare diseases +MONDO:0002378 rare diseases +MONDO:0002379 gard_rare diseases +MONDO:0002379 rare diseases +MONDO:0002380 otar diseases +MONDO:0002381 otar diseases +MONDO:0002383 gard_rare diseases +MONDO:0002383 nord_rare diseases +MONDO:0002383 rare diseases +MONDO:0002387 gard_rare diseases +MONDO:0002387 nord_rare diseases +MONDO:0002387 rare diseases +MONDO:0002395 otar diseases +MONDO:0002397 gard_rare diseases +MONDO:0002397 otar diseases +MONDO:0002397 rare diseases +MONDO:0002400 otar diseases +MONDO:0002402 otar diseases +MONDO:0002404 otar diseases +MONDO:0002405 otar diseases +MONDO:0002406 otar diseases +MONDO:0002407 otar diseases +MONDO:0002408 gard_rare diseases +MONDO:0002408 otar diseases +MONDO:0002408 rare diseases +MONDO:0002409 otar diseases +MONDO:0002409 rare_grouping diseases +MONDO:0002412 disease_grouping diseases +MONDO:0002412 gard_rare diseases +MONDO:0002412 ordo_group_of_disorders diseases +MONDO:0002412 otar diseases +MONDO:0002412 rare diseases +MONDO:0002413 gard_rare diseases +MONDO:0002413 nord_rare diseases +MONDO:0002413 ordo_disorder diseases +MONDO:0002413 orphanet_rare diseases +MONDO:0002413 otar diseases +MONDO:0002413 rare diseases +MONDO:0002415 gard_rare diseases +MONDO:0002415 nord_rare diseases +MONDO:0002415 otar diseases +MONDO:0002415 rare diseases +MONDO:0002416 gard_rare diseases +MONDO:0002416 otar diseases +MONDO:0002416 rare diseases +MONDO:0002418 gard_rare diseases +MONDO:0002418 rare diseases +MONDO:0002420 otar diseases +MONDO:0002422 gard_rare diseases +MONDO:0002422 nord_rare diseases +MONDO:0002422 ordo_disorder diseases +MONDO:0002422 orphanet_rare diseases +MONDO:0002422 otar diseases +MONDO:0002422 rare diseases +MONDO:0002423 otar diseases +MONDO:0002426 gard_rare diseases +MONDO:0002426 nord_rare diseases +MONDO:0002426 otar diseases +MONDO:0002426 rare diseases +MONDO:0002427 otar diseases +MONDO:0002428 otar diseases +MONDO:0002429 disease_grouping diseases +MONDO:0002429 gard_rare diseases +MONDO:0002429 ordo_group_of_disorders diseases +MONDO:0002429 otar diseases +MONDO:0002429 rare diseases +MONDO:0002437 gard_rare diseases +MONDO:0002437 rare diseases +MONDO:0002438 gard_rare diseases +MONDO:0002438 nord_rare diseases +MONDO:0002438 rare diseases +MONDO:0002440 gard_rare diseases +MONDO:0002440 rare diseases +MONDO:0002441 clingen diseases +MONDO:0002441 gard_rare diseases +MONDO:0002441 nord_rare diseases +MONDO:0002441 ordo_disorder diseases +MONDO:0002441 orphanet_rare diseases +MONDO:0002441 otar diseases +MONDO:0002441 prototype_pattern diseases +MONDO:0002441 rare diseases +MONDO:0002442 clingen diseases +MONDO:0002444 otar diseases +MONDO:0002447 otar diseases +MONDO:0002448 gard_rare diseases +MONDO:0002448 rare diseases +MONDO:0002450 otar diseases +MONDO:0002451 inferred_rare diseases +MONDO:0002451 rare diseases +MONDO:0002457 clingen diseases +MONDO:0002457 gard_rare diseases +MONDO:0002457 nord_rare diseases +MONDO:0002457 ordo_disorder diseases +MONDO:0002457 ordo_malformation_syndrome diseases +MONDO:0002457 orphanet_rare diseases +MONDO:0002457 otar diseases +MONDO:0002457 prototype_pattern diseases +MONDO:0002457 rare diseases +MONDO:0002459 otar diseases +MONDO:0002461 gard_rare diseases +MONDO:0002461 rare diseases +MONDO:0002462 gard_rare diseases +MONDO:0002462 nord_rare diseases +MONDO:0002462 otar diseases +MONDO:0002462 rare diseases +MONDO:0002463 otar diseases +MONDO:0002464 otar diseases +MONDO:0002465 otar diseases +MONDO:0002466 otar diseases +MONDO:0002467 otar diseases +MONDO:0002468 gard_rare diseases +MONDO:0002468 otar diseases +MONDO:0002468 rare diseases +MONDO:0002470 gard_rare diseases +MONDO:0002470 nord_rare diseases +MONDO:0002470 otar diseases +MONDO:0002470 rare diseases +MONDO:0002471 otar diseases +MONDO:0002472 otar diseases +MONDO:0002473 otar diseases +MONDO:0002474 gard_rare diseases +MONDO:0002474 nord_rare diseases +MONDO:0002474 ordo_disorder diseases +MONDO:0002474 orphanet_rare diseases +MONDO:0002474 otar diseases +MONDO:0002474 rare diseases +MONDO:0002475 otar diseases +MONDO:0002476 otar diseases +MONDO:0002477 gard_rare diseases +MONDO:0002477 otar diseases +MONDO:0002477 rare diseases +MONDO:0002479 gard_rare diseases +MONDO:0002479 nord_rare diseases +MONDO:0002479 rare diseases +MONDO:0002480 otar diseases +MONDO:0002481 gard_rare diseases +MONDO:0002481 rare diseases +MONDO:0002485 gard_rare diseases +MONDO:0002485 rare diseases +MONDO:0002486 otar diseases +MONDO:0002487 gard_rare diseases +MONDO:0002487 rare diseases +MONDO:0002489 gard_rare diseases +MONDO:0002489 otar diseases +MONDO:0002489 rare diseases +MONDO:0002490 gard_rare diseases +MONDO:0002490 nord_rare diseases +MONDO:0002490 otar diseases +MONDO:0002490 rare diseases +MONDO:0002491 otar diseases +MONDO:0002492 otar diseases +MONDO:0002493 otar diseases +MONDO:0002494 otar diseases +MONDO:0002501 gard_rare diseases +MONDO:0002501 nord_rare diseases +MONDO:0002501 otar diseases +MONDO:0002501 rare diseases +MONDO:0002503 gard_rare diseases +MONDO:0002503 rare diseases +MONDO:0002505 gard_rare diseases +MONDO:0002505 rare diseases +MONDO:0002507 otar diseases +MONDO:0002508 otar diseases +MONDO:0002512 otar diseases +MONDO:0002513 otar diseases +MONDO:0002514 otar diseases +MONDO:0002515 otar diseases +MONDO:0002516 otar diseases +MONDO:0002517 gard_rare diseases +MONDO:0002517 rare diseases +MONDO:0002519 otar diseases +MONDO:0002520 disease_grouping diseases +MONDO:0002520 gard_rare diseases +MONDO:0002520 ordo_group_of_disorders diseases +MONDO:0002520 otar diseases +MONDO:0002520 rare diseases +MONDO:0002522 otar diseases +MONDO:0002523 otar diseases +MONDO:0002525 disease_grouping diseases +MONDO:0002525 gard_rare diseases +MONDO:0002525 ordo_group_of_disorders diseases +MONDO:0002525 otar diseases +MONDO:0002525 rare diseases +MONDO:0002526 gard_rare diseases +MONDO:0002526 rare diseases +MONDO:0002527 otar diseases +MONDO:0002528 otar diseases +MONDO:0002529 otar diseases +MONDO:0002531 otar diseases +MONDO:0002532 otar diseases +MONDO:0002533 otar diseases +MONDO:0002534 gard_rare diseases +MONDO:0002534 rare diseases +MONDO:0002537 otar diseases +MONDO:0002540 gard_rare diseases +MONDO:0002540 rare diseases +MONDO:0002541 gard_rare diseases +MONDO:0002541 rare diseases +MONDO:0002542 gard_rare diseases +MONDO:0002542 otar diseases +MONDO:0002542 rare diseases +MONDO:0002543 gard_rare diseases +MONDO:0002543 rare diseases +MONDO:0002544 gard_rare diseases +MONDO:0002544 nord_rare diseases +MONDO:0002544 rare diseases +MONDO:0002545 otar diseases +MONDO:0002546 gard_rare diseases +MONDO:0002546 nord_rare diseases +MONDO:0002546 ordo_disorder diseases +MONDO:0002546 orphanet_rare diseases +MONDO:0002546 otar diseases +MONDO:0002546 rare diseases +MONDO:0002547 gard_rare diseases +MONDO:0002547 otar diseases +MONDO:0002547 rare diseases +MONDO:0002548 gard_rare diseases +MONDO:0002548 otar diseases +MONDO:0002548 rare diseases +MONDO:0002549 gard_rare diseases +MONDO:0002549 rare diseases +MONDO:0002554 gard_rare diseases +MONDO:0002554 rare diseases +MONDO:0002555 gard_rare diseases +MONDO:0002555 rare diseases +MONDO:0002556 gard_rare diseases +MONDO:0002556 rare diseases +MONDO:0002558 gard_rare diseases +MONDO:0002558 otar diseases +MONDO:0002558 rare diseases +MONDO:0002559 gard_rare diseases +MONDO:0002559 rare diseases +MONDO:0002561 clingen diseases +MONDO:0002561 disease_grouping diseases +MONDO:0002561 gard_rare diseases +MONDO:0002561 ordo_group_of_disorders diseases +MONDO:0002561 otar diseases +MONDO:0002561 rare diseases +MONDO:0002562 otar diseases +MONDO:0002563 gard_rare diseases +MONDO:0002563 rare diseases +MONDO:0002564 otar diseases +MONDO:0002565 otar diseases +MONDO:0002571 gard_rare diseases +MONDO:0002571 nord_rare diseases +MONDO:0002571 ordo_disorder diseases +MONDO:0002571 orphanet_rare diseases +MONDO:0002571 otar diseases +MONDO:0002571 rare diseases +MONDO:0002572 otar diseases +MONDO:0002574 gard_rare diseases +MONDO:0002574 rare diseases +MONDO:0002576 gard_rare diseases +MONDO:0002576 rare diseases +MONDO:0002577 gard_rare diseases +MONDO:0002577 rare diseases +MONDO:0002578 gard_rare diseases +MONDO:0002578 nord_rare diseases +MONDO:0002578 rare diseases +MONDO:0002579 gard_rare diseases +MONDO:0002579 otar diseases +MONDO:0002579 rare diseases +MONDO:0002580 gard_rare diseases +MONDO:0002580 otar diseases +MONDO:0002580 rare diseases +MONDO:0002581 gard_rare diseases +MONDO:0002581 rare diseases +MONDO:0002582 gard_rare diseases +MONDO:0002582 rare diseases +MONDO:0002586 gard_rare diseases +MONDO:0002586 otar diseases +MONDO:0002586 rare diseases +MONDO:0002587 gard_rare diseases +MONDO:0002587 rare diseases +MONDO:0002588 gard_rare diseases +MONDO:0002588 nord_rare diseases +MONDO:0002588 ordo_histopathological_subtype diseases +MONDO:0002588 ordo_subtype_of_a_disorder diseases +MONDO:0002588 otar diseases +MONDO:0002588 rare diseases +MONDO:0002590 gard_rare diseases +MONDO:0002590 rare diseases +MONDO:0002592 gard_rare diseases +MONDO:0002592 rare diseases +MONDO:0002597 gard_rare diseases +MONDO:0002597 otar diseases +MONDO:0002597 rare diseases +MONDO:0002598 gard_rare diseases +MONDO:0002598 otar diseases +MONDO:0002598 rare diseases +MONDO:0002599 gard_rare diseases +MONDO:0002599 rare diseases +MONDO:0002601 gard_rare diseases +MONDO:0002601 otar diseases +MONDO:0002601 rare diseases +MONDO:0002602 otar diseases +MONDO:0002602 rare_grouping diseases +MONDO:0002603 gard_rare diseases +MONDO:0002603 otar diseases +MONDO:0002603 rare diseases +MONDO:0002604 otar diseases +MONDO:0002605 gard_rare diseases +MONDO:0002605 otar diseases +MONDO:0002605 rare diseases +MONDO:0002606 gard_rare diseases +MONDO:0002606 otar diseases +MONDO:0002606 rare diseases +MONDO:0002610 gard_rare diseases +MONDO:0002610 otar diseases +MONDO:0002610 rare diseases +MONDO:0002612 otar diseases +MONDO:0002614 otar diseases +MONDO:0002615 gard_rare diseases +MONDO:0002615 otar diseases +MONDO:0002615 rare diseases +MONDO:0002616 otar diseases +MONDO:0002617 gard_rare diseases +MONDO:0002617 rare diseases +MONDO:0002618 gard_rare diseases +MONDO:0002618 otar diseases +MONDO:0002618 rare diseases +MONDO:0002619 gard_rare diseases +MONDO:0002619 otar diseases +MONDO:0002619 rare diseases +MONDO:0002621 gard_rare diseases +MONDO:0002621 otar diseases +MONDO:0002621 rare diseases +MONDO:0002624 gard_rare diseases +MONDO:0002624 rare diseases +MONDO:0002625 gard_rare diseases +MONDO:0002625 nord_rare diseases +MONDO:0002625 rare diseases +MONDO:0002627 gard_rare diseases +MONDO:0002627 otar diseases +MONDO:0002627 rare diseases +MONDO:0002628 gard_rare diseases +MONDO:0002628 rare diseases +MONDO:0002629 gard_rare diseases +MONDO:0002629 nord_rare diseases +MONDO:0002629 ordo_disorder diseases +MONDO:0002629 orphanet_rare diseases +MONDO:0002629 otar diseases +MONDO:0002629 rare diseases +MONDO:0002630 gard_rare diseases +MONDO:0002630 otar diseases +MONDO:0002630 rare diseases +MONDO:0002631 gard_rare diseases +MONDO:0002631 rare diseases +MONDO:0002632 gard_rare diseases +MONDO:0002632 nord_rare diseases +MONDO:0002632 rare diseases +MONDO:0002633 otar diseases +MONDO:0002634 gard_rare diseases +MONDO:0002634 rare diseases +MONDO:0002635 otar diseases +MONDO:0002640 otar diseases +MONDO:0002643 gard_rare diseases +MONDO:0002643 otar diseases +MONDO:0002643 rare diseases +MONDO:0002644 gard_rare diseases +MONDO:0002644 rare diseases +MONDO:0002647 otar diseases +MONDO:0002651 gard_rare diseases +MONDO:0002651 rare diseases +MONDO:0002652 otar diseases +MONDO:0002653 gard_rare diseases +MONDO:0002653 ordo_disorder diseases +MONDO:0002653 orphanet_rare diseases +MONDO:0002653 rare diseases +MONDO:0002654 otar diseases +MONDO:0002656 otar diseases +MONDO:0002657 otar diseases +MONDO:0002659 otar diseases +MONDO:0002664 gard_rare diseases +MONDO:0002664 rare diseases +MONDO:0002665 gard_rare diseases +MONDO:0002665 otar diseases +MONDO:0002665 rare diseases +MONDO:0002667 gard_rare diseases +MONDO:0002667 rare diseases +MONDO:0002669 gard_rare diseases +MONDO:0002669 rare diseases +MONDO:0002670 gard_rare diseases +MONDO:0002670 otar diseases +MONDO:0002670 rare diseases +MONDO:0002675 gard_rare diseases +MONDO:0002675 rare diseases +MONDO:0002676 gard_rare diseases +MONDO:0002676 rare diseases +MONDO:0002677 gard_rare diseases +MONDO:0002677 nord_rare diseases +MONDO:0002677 rare diseases +MONDO:0002678 gard_rare diseases +MONDO:0002678 otar diseases +MONDO:0002678 rare diseases +MONDO:0002679 otar diseases +MONDO:0002681 gard_rare diseases +MONDO:0002681 otar diseases +MONDO:0002681 rare diseases +MONDO:0002683 gard_rare diseases +MONDO:0002683 rare diseases +MONDO:0002684 gard_rare diseases +MONDO:0002684 nord_rare diseases +MONDO:0002684 ordo_disorder diseases +MONDO:0002684 orphanet_rare diseases +MONDO:0002684 otar diseases +MONDO:0002684 rare diseases +MONDO:0002685 gard_rare diseases +MONDO:0002685 rare diseases +MONDO:0002687 gard_rare diseases +MONDO:0002687 nord_rare diseases +MONDO:0002687 ordo_disorder diseases +MONDO:0002687 orphanet_rare diseases +MONDO:0002687 rare diseases +MONDO:0002691 otar diseases +MONDO:0002697 gard_rare diseases +MONDO:0002697 nord_rare diseases +MONDO:0002697 ordo_disorder diseases +MONDO:0002697 orphanet_rare diseases +MONDO:0002697 rare diseases +MONDO:0002698 gard_rare diseases +MONDO:0002698 rare diseases +MONDO:0002701 gard_rare diseases +MONDO:0002701 otar diseases +MONDO:0002701 rare diseases +MONDO:0002702 gard_rare diseases +MONDO:0002702 otar diseases +MONDO:0002702 rare diseases +MONDO:0002703 gard_rare diseases +MONDO:0002703 rare diseases +MONDO:0002708 gard_rare diseases +MONDO:0002708 otar diseases +MONDO:0002708 rare diseases +MONDO:0002714 otar diseases +MONDO:0002715 otar diseases +MONDO:0002717 gard_rare diseases +MONDO:0002717 rare diseases +MONDO:0002718 gard_rare diseases +MONDO:0002718 nord_rare diseases +MONDO:0002718 ordo_subtype_of_a_disorder diseases +MONDO:0002718 otar diseases +MONDO:0002718 rare diseases +MONDO:0002720 gard_rare diseases +MONDO:0002720 otar diseases +MONDO:0002720 rare diseases +MONDO:0002721 otar diseases +MONDO:0002724 gard_rare diseases +MONDO:0002724 otar diseases +MONDO:0002724 rare diseases +MONDO:0002726 gard_rare diseases +MONDO:0002726 rare diseases +MONDO:0002728 gard_rare diseases +MONDO:0002728 nord_rare diseases +MONDO:0002728 ordo_disorder diseases +MONDO:0002728 orphanet_rare diseases +MONDO:0002728 otar diseases +MONDO:0002728 rare diseases +MONDO:0002729 gard_rare diseases +MONDO:0002729 otar diseases +MONDO:0002729 rare diseases +MONDO:0002730 otar diseases +MONDO:0002732 otar diseases +MONDO:0002735 gard_rare diseases +MONDO:0002735 nord_rare diseases +MONDO:0002735 ordo_disorder diseases +MONDO:0002735 orphanet_rare diseases +MONDO:0002735 rare diseases +MONDO:0002736 gard_rare diseases +MONDO:0002736 rare diseases +MONDO:0002739 gard_rare diseases +MONDO:0002739 rare diseases +MONDO:0002740 gard_rare diseases +MONDO:0002740 rare diseases +MONDO:0002741 gard_rare diseases +MONDO:0002741 rare diseases +MONDO:0002742 gard_rare diseases +MONDO:0002742 nord_rare diseases +MONDO:0002742 otar diseases +MONDO:0002742 rare diseases +MONDO:0002744 gard_rare diseases +MONDO:0002744 rare diseases +MONDO:0002746 gard_rare diseases +MONDO:0002746 otar diseases +MONDO:0002746 rare diseases +MONDO:0002747 otar diseases +MONDO:0002749 gard_rare diseases +MONDO:0002749 rare diseases +MONDO:0002751 otar diseases +MONDO:0002752 gard_rare diseases +MONDO:0002752 ordo_disorder diseases +MONDO:0002752 orphanet_rare diseases +MONDO:0002752 otar diseases +MONDO:0002752 rare diseases +MONDO:0002754 gard_rare diseases +MONDO:0002754 rare diseases +MONDO:0002755 gard_rare diseases +MONDO:0002755 rare diseases +MONDO:0002756 gard_rare diseases +MONDO:0002756 rare diseases +MONDO:0002758 gard_rare diseases +MONDO:0002758 rare diseases +MONDO:0002760 otar diseases +MONDO:0002761 gard_rare diseases +MONDO:0002761 rare diseases +MONDO:0002762 gard_rare diseases +MONDO:0002762 rare diseases +MONDO:0002764 otar diseases +MONDO:0002766 gard_rare diseases +MONDO:0002766 rare diseases +MONDO:0002768 gard_rare diseases +MONDO:0002768 rare diseases +MONDO:0002771 gard_rare diseases +MONDO:0002771 otar diseases +MONDO:0002771 rare diseases +MONDO:0002772 gard_rare diseases +MONDO:0002772 rare diseases +MONDO:0002775 otar diseases +MONDO:0002776 otar diseases +MONDO:0002778 gard_rare diseases +MONDO:0002778 rare diseases +MONDO:0002782 otar diseases +MONDO:0002783 gard_rare diseases +MONDO:0002783 nord_rare diseases +MONDO:0002783 rare diseases +MONDO:0002785 gard_rare diseases +MONDO:0002785 otar diseases +MONDO:0002785 rare diseases +MONDO:0002787 gard_rare diseases +MONDO:0002787 rare diseases +MONDO:0002788 gard_rare diseases +MONDO:0002788 rare diseases +MONDO:0002791 gard_rare diseases +MONDO:0002791 otar diseases +MONDO:0002791 rare diseases +MONDO:0002792 gard_rare diseases +MONDO:0002792 rare diseases +MONDO:0002794 gard_rare diseases +MONDO:0002794 rare diseases +MONDO:0002796 gard_rare diseases +MONDO:0002796 rare diseases +MONDO:0002797 gard_rare diseases +MONDO:0002797 rare diseases +MONDO:0002800 gard_rare diseases +MONDO:0002800 rare diseases +MONDO:0002801 gard_rare diseases +MONDO:0002801 rare diseases +MONDO:0002803 gard_rare diseases +MONDO:0002803 nord_rare diseases +MONDO:0002803 rare diseases +MONDO:0002805 otar diseases +MONDO:0002806 otar diseases +MONDO:0002807 otar diseases +MONDO:0002812 otar diseases +MONDO:0002813 otar diseases +MONDO:0002814 gard_rare diseases +MONDO:0002814 otar diseases +MONDO:0002814 rare diseases +MONDO:0002815 gard_rare diseases +MONDO:0002815 nord_rare diseases +MONDO:0002815 rare diseases +MONDO:0002816 otar diseases +MONDO:0002817 gard_rare diseases +MONDO:0002817 nord_rare diseases +MONDO:0002817 otar diseases +MONDO:0002817 rare diseases +MONDO:0002821 gard_rare diseases +MONDO:0002821 rare diseases +MONDO:0002824 gard_rare diseases +MONDO:0002824 nord_rare diseases +MONDO:0002824 rare diseases +MONDO:0002828 gard_rare diseases +MONDO:0002828 rare diseases +MONDO:0002829 gard_rare diseases +MONDO:0002829 otar diseases +MONDO:0002829 rare diseases +MONDO:0002831 gard_rare diseases +MONDO:0002831 rare diseases +MONDO:0002832 gard_rare diseases +MONDO:0002832 rare diseases +MONDO:0002833 gard_rare diseases +MONDO:0002833 rare diseases +MONDO:0002834 gard_rare diseases +MONDO:0002834 rare diseases +MONDO:0002836 gard_rare diseases +MONDO:0002836 otar diseases +MONDO:0002836 rare diseases +MONDO:0002837 gard_rare diseases +MONDO:0002837 rare diseases +MONDO:0002840 gard_rare diseases +MONDO:0002840 nord_rare diseases +MONDO:0002840 rare diseases +MONDO:0002847 gard_rare diseases +MONDO:0002847 rare diseases +MONDO:0002848 gard_rare diseases +MONDO:0002848 rare diseases +MONDO:0002849 gard_rare diseases +MONDO:0002849 rare diseases +MONDO:0002850 gard_rare diseases +MONDO:0002850 rare diseases +MONDO:0002851 gard_rare diseases +MONDO:0002851 rare diseases +MONDO:0002852 gard_rare diseases +MONDO:0002852 rare diseases +MONDO:0002853 gard_rare diseases +MONDO:0002853 nord_rare diseases +MONDO:0002853 rare diseases +MONDO:0002854 gard_rare diseases +MONDO:0002854 otar diseases +MONDO:0002854 rare diseases +MONDO:0002855 otar diseases +MONDO:0002856 gard_rare diseases +MONDO:0002856 nord_rare diseases +MONDO:0002856 rare diseases +MONDO:0002857 gard_rare diseases +MONDO:0002857 rare diseases +MONDO:0002858 gard_rare diseases +MONDO:0002858 nord_rare diseases +MONDO:0002858 rare diseases +MONDO:0002859 gard_rare diseases +MONDO:0002859 rare diseases +MONDO:0002860 gard_rare diseases +MONDO:0002860 nord_rare diseases +MONDO:0002860 rare diseases +MONDO:0002861 gard_rare diseases +MONDO:0002861 rare diseases +MONDO:0002862 gard_rare diseases +MONDO:0002862 rare diseases +MONDO:0002863 gard_rare diseases +MONDO:0002863 nord_rare diseases +MONDO:0002863 otar diseases +MONDO:0002863 rare diseases +MONDO:0002864 gard_rare diseases +MONDO:0002864 rare diseases +MONDO:0002865 gard_rare diseases +MONDO:0002865 rare diseases +MONDO:0002866 otar diseases +MONDO:0002869 otar diseases +MONDO:0002871 gard_rare diseases +MONDO:0002871 rare diseases +MONDO:0002872 otar diseases +MONDO:0002874 gard_rare diseases +MONDO:0002874 rare diseases +MONDO:0002876 gard_rare diseases +MONDO:0002876 nord_rare diseases +MONDO:0002876 ordo_disorder diseases +MONDO:0002876 orphanet_rare diseases +MONDO:0002876 otar diseases +MONDO:0002876 rare diseases +MONDO:0002877 gard_rare diseases +MONDO:0002877 nord_rare diseases +MONDO:0002877 ordo_disorder diseases +MONDO:0002877 orphanet_rare diseases +MONDO:0002877 otar diseases +MONDO:0002877 rare diseases +MONDO:0002878 gard_rare diseases +MONDO:0002878 nord_rare diseases +MONDO:0002878 ordo_disorder diseases +MONDO:0002878 orphanet_rare diseases +MONDO:0002878 otar diseases +MONDO:0002878 rare diseases +MONDO:0002879 gard_rare diseases +MONDO:0002879 otar diseases +MONDO:0002879 rare diseases +MONDO:0002880 gard_rare diseases +MONDO:0002880 rare diseases +MONDO:0002882 gard_rare diseases +MONDO:0002882 nord_rare diseases +MONDO:0002882 ordo_disorder diseases +MONDO:0002882 orphanet_rare diseases +MONDO:0002882 otar diseases +MONDO:0002882 rare diseases +MONDO:0002883 gard_rare diseases +MONDO:0002883 otar diseases +MONDO:0002883 rare diseases +MONDO:0002884 otar diseases +MONDO:0002887 otar diseases +MONDO:0002888 gard_rare diseases +MONDO:0002888 nord_rare diseases +MONDO:0002888 rare diseases +MONDO:0002889 gard_rare diseases +MONDO:0002889 otar diseases +MONDO:0002889 rare diseases +MONDO:0002892 gard_rare diseases +MONDO:0002892 nord_rare diseases +MONDO:0002892 rare diseases +MONDO:0002894 gard_rare diseases +MONDO:0002894 otar diseases +MONDO:0002894 rare diseases +MONDO:0002897 gard_rare diseases +MONDO:0002897 nord_rare diseases +MONDO:0002897 rare diseases +MONDO:0002898 otar diseases +MONDO:0002899 gard_rare diseases +MONDO:0002899 rare diseases +MONDO:0002900 gard_rare diseases +MONDO:0002900 rare diseases +MONDO:0002901 gard_rare diseases +MONDO:0002901 rare diseases +MONDO:0002907 otar diseases +MONDO:0002908 otar diseases +MONDO:0002910 gard_rare diseases +MONDO:0002910 rare diseases +MONDO:0002911 gard_rare diseases +MONDO:0002911 otar diseases +MONDO:0002911 rare diseases +MONDO:0002912 otar diseases +MONDO:0002913 otar diseases +MONDO:0002914 otar diseases +MONDO:0002916 gard_rare diseases +MONDO:0002916 rare diseases +MONDO:0002917 otar diseases +MONDO:0002918 gard_rare diseases +MONDO:0002918 nord_rare diseases +MONDO:0002918 rare diseases +MONDO:0002919 gard_rare diseases +MONDO:0002919 rare diseases +MONDO:0002920 gard_rare diseases +MONDO:0002920 rare diseases +MONDO:0002921 gard_rare diseases +MONDO:0002921 otar diseases +MONDO:0002921 rare diseases +MONDO:0002923 gard_rare diseases +MONDO:0002923 rare diseases +MONDO:0002924 otar diseases +MONDO:0002926 gard_rare diseases +MONDO:0002926 nord_rare diseases +MONDO:0002926 otar diseases +MONDO:0002926 rare diseases +MONDO:0002927 otar diseases +MONDO:0002928 otar diseases +MONDO:0002930 gard_rare diseases +MONDO:0002930 nord_rare diseases +MONDO:0002930 otar diseases +MONDO:0002930 rare diseases +MONDO:0002933 otar diseases +MONDO:0002935 gard_rare diseases +MONDO:0002935 rare diseases +MONDO:0002940 gard_rare diseases +MONDO:0002940 rare diseases +MONDO:0002943 gard_rare diseases +MONDO:0002943 rare diseases +MONDO:0002955 gard_rare diseases +MONDO:0002955 nord_rare diseases +MONDO:0002955 ordo_subtype_of_a_disorder diseases +MONDO:0002955 rare diseases +MONDO:0002959 otar diseases +MONDO:0002960 gard_rare diseases +MONDO:0002960 rare diseases +MONDO:0002966 gard_rare diseases +MONDO:0002966 rare diseases +MONDO:0002970 otar diseases +MONDO:0002971 otar diseases +MONDO:0002973 otar diseases +MONDO:0002974 otar diseases +MONDO:0002977 otar diseases +MONDO:0002978 gard_rare diseases +MONDO:0002978 rare diseases +MONDO:0002979 otar diseases +MONDO:0002981 gard_rare diseases +MONDO:0002981 nord_rare diseases +MONDO:0002981 rare diseases +MONDO:0002982 gard_rare diseases +MONDO:0002982 rare diseases +MONDO:0002989 otar diseases +MONDO:0002993 gard_rare diseases +MONDO:0002993 rare diseases +MONDO:0002994 gard_rare diseases +MONDO:0002994 rare diseases +MONDO:0002995 gard_rare diseases +MONDO:0002995 otar diseases +MONDO:0002995 rare diseases +MONDO:0002996 gard_rare diseases +MONDO:0002996 otar diseases +MONDO:0002996 rare diseases +MONDO:0002997 gard_rare diseases +MONDO:0002997 rare diseases +MONDO:0002998 gard_rare diseases +MONDO:0002998 otar diseases +MONDO:0002998 rare diseases +MONDO:0002999 gard_rare diseases +MONDO:0002999 nord_rare diseases +MONDO:0002999 rare diseases +MONDO:0003000 gard_rare diseases +MONDO:0003000 otar diseases +MONDO:0003000 rare diseases +MONDO:0003001 gard_rare diseases +MONDO:0003001 otar diseases +MONDO:0003001 rare diseases +MONDO:0003002 gard_rare diseases +MONDO:0003002 otar diseases +MONDO:0003002 rare diseases +MONDO:0003003 gard_rare diseases +MONDO:0003003 rare diseases +MONDO:0003004 otar diseases +MONDO:0003005 otar diseases +MONDO:0003007 gard_rare diseases +MONDO:0003007 rare diseases +MONDO:0003008 gard_rare diseases +MONDO:0003008 nord_rare diseases +MONDO:0003008 otar diseases +MONDO:0003008 rare diseases +MONDO:0003009 otar diseases +MONDO:0003010 gard_rare diseases +MONDO:0003010 nord_rare diseases +MONDO:0003010 ordo_histopathological_subtype diseases +MONDO:0003010 ordo_subtype_of_a_disorder diseases +MONDO:0003010 rare diseases +MONDO:0003011 gard_rare diseases +MONDO:0003011 nord_rare diseases +MONDO:0003011 ordo_disorder diseases +MONDO:0003011 orphanet_rare diseases +MONDO:0003011 rare diseases +MONDO:0003012 gard_rare diseases +MONDO:0003012 nord_rare diseases +MONDO:0003012 rare diseases +MONDO:0003014 otar diseases +MONDO:0003017 gard_rare diseases +MONDO:0003017 rare diseases +MONDO:0003019 otar diseases +MONDO:0003021 gard_rare diseases +MONDO:0003021 rare diseases +MONDO:0003022 gard_rare diseases +MONDO:0003022 rare diseases +MONDO:0003023 gard_rare diseases +MONDO:0003023 rare diseases +MONDO:0003024 gard_rare diseases +MONDO:0003024 nord_rare diseases +MONDO:0003024 rare diseases +MONDO:0003025 gard_rare diseases +MONDO:0003025 rare diseases +MONDO:0003026 gard_rare diseases +MONDO:0003026 rare diseases +MONDO:0003027 gard_rare diseases +MONDO:0003027 rare diseases +MONDO:0003028 gard_rare diseases +MONDO:0003028 rare diseases +MONDO:0003029 gard_rare diseases +MONDO:0003029 nord_rare diseases +MONDO:0003029 rare diseases +MONDO:0003030 gard_rare diseases +MONDO:0003030 rare diseases +MONDO:0003032 gard_rare diseases +MONDO:0003032 rare diseases +MONDO:0003033 gard_rare diseases +MONDO:0003033 nord_rare diseases +MONDO:0003033 rare diseases +MONDO:0003034 gard_rare diseases +MONDO:0003034 rare diseases +MONDO:0003035 gard_rare diseases +MONDO:0003035 otar diseases +MONDO:0003035 rare diseases +MONDO:0003036 gard_rare diseases +MONDO:0003036 nord_rare diseases +MONDO:0003036 otar diseases +MONDO:0003036 rare diseases +MONDO:0003037 otar diseases +MONDO:0003041 gard_rare diseases +MONDO:0003041 rare diseases +MONDO:0003042 gard_rare diseases +MONDO:0003042 rare diseases +MONDO:0003046 otar diseases +MONDO:0003047 gard_rare diseases +MONDO:0003047 rare diseases +MONDO:0003049 gard_rare diseases +MONDO:0003049 otar diseases +MONDO:0003049 rare diseases +MONDO:0003050 otar diseases +MONDO:0003053 gard_rare diseases +MONDO:0003053 rare diseases +MONDO:0003054 inferred_rare diseases +MONDO:0003054 rare diseases +MONDO:0003055 gard_rare diseases +MONDO:0003055 rare diseases +MONDO:0003056 gard_rare diseases +MONDO:0003056 rare diseases +MONDO:0003057 gard_rare diseases +MONDO:0003057 rare diseases +MONDO:0003058 gard_rare diseases +MONDO:0003058 rare diseases +MONDO:0003059 gard_rare diseases +MONDO:0003059 otar diseases +MONDO:0003059 rare diseases +MONDO:0003060 gard_rare diseases +MONDO:0003060 nord_rare diseases +MONDO:0003060 otar diseases +MONDO:0003060 rare diseases +MONDO:0003061 otar diseases +MONDO:0003062 otar diseases +MONDO:0003064 otar diseases +MONDO:0003072 otar diseases +MONDO:0003073 gard_rare diseases +MONDO:0003073 rare diseases +MONDO:0003075 gard_rare diseases +MONDO:0003075 rare diseases +MONDO:0003076 gard_rare diseases +MONDO:0003076 otar diseases +MONDO:0003076 rare diseases +MONDO:0003077 gard_rare diseases +MONDO:0003077 rare diseases +MONDO:0003078 gard_rare diseases +MONDO:0003078 rare diseases +MONDO:0003079 gard_rare diseases +MONDO:0003079 nord_rare diseases +MONDO:0003079 otar diseases +MONDO:0003079 rare diseases +MONDO:0003084 gard_rare diseases +MONDO:0003084 rare diseases +MONDO:0003085 otar diseases +MONDO:0003086 gard_rare diseases +MONDO:0003086 rare diseases +MONDO:0003087 gard_rare diseases +MONDO:0003087 rare diseases +MONDO:0003089 gard_rare diseases +MONDO:0003089 rare diseases +MONDO:0003090 gard_rare diseases +MONDO:0003090 otar diseases +MONDO:0003090 rare diseases +MONDO:0003091 gard_rare diseases +MONDO:0003091 rare diseases +MONDO:0003092 gard_rare diseases +MONDO:0003092 rare diseases +MONDO:0003093 gard_rare diseases +MONDO:0003093 rare diseases +MONDO:0003095 gard_rare diseases +MONDO:0003095 rare diseases +MONDO:0003100 gard_rare diseases +MONDO:0003100 rare diseases +MONDO:0003105 otar diseases +MONDO:0003109 gard_rare diseases +MONDO:0003109 rare diseases +MONDO:0003110 otar diseases +MONDO:0003111 gard_rare diseases +MONDO:0003111 nord_rare diseases +MONDO:0003111 ordo_disorder diseases +MONDO:0003111 orphanet_rare diseases +MONDO:0003111 otar diseases +MONDO:0003111 rare diseases +MONDO:0003112 gard_rare diseases +MONDO:0003112 rare diseases +MONDO:0003113 gard_rare diseases +MONDO:0003113 otar diseases +MONDO:0003113 rare diseases +MONDO:0003117 otar diseases +MONDO:0003120 gard_rare diseases +MONDO:0003120 rare diseases +MONDO:0003121 gard_rare diseases +MONDO:0003121 rare diseases +MONDO:0003122 gard_rare diseases +MONDO:0003122 nord_rare diseases +MONDO:0003122 otar diseases +MONDO:0003122 rare diseases +MONDO:0003124 gard_rare diseases +MONDO:0003124 nord_rare diseases +MONDO:0003124 rare diseases +MONDO:0003125 gard_rare diseases +MONDO:0003125 ordo_disorder diseases +MONDO:0003125 orphanet_rare diseases +MONDO:0003125 otar diseases +MONDO:0003125 rare diseases +MONDO:0003128 gard_rare diseases +MONDO:0003128 rare diseases +MONDO:0003129 gard_rare diseases +MONDO:0003129 rare diseases +MONDO:0003130 otar diseases +MONDO:0003133 gard_rare diseases +MONDO:0003133 rare diseases +MONDO:0003134 gard_rare diseases +MONDO:0003134 rare diseases +MONDO:0003135 gard_rare diseases +MONDO:0003135 rare diseases +MONDO:0003136 gard_rare diseases +MONDO:0003136 rare diseases +MONDO:0003137 gard_rare diseases +MONDO:0003137 rare diseases +MONDO:0003138 gard_rare diseases +MONDO:0003138 rare diseases +MONDO:0003139 gard_rare diseases +MONDO:0003139 rare diseases +MONDO:0003140 gard_rare diseases +MONDO:0003140 rare diseases +MONDO:0003142 otar diseases +MONDO:0003143 otar diseases +MONDO:0003144 gard_rare diseases +MONDO:0003144 nord_rare diseases +MONDO:0003144 rare diseases +MONDO:0003147 gard_rare diseases +MONDO:0003147 rare diseases +MONDO:0003150 otar diseases +MONDO:0003152 gard_rare diseases +MONDO:0003152 rare diseases +MONDO:0003153 gard_rare diseases +MONDO:0003153 rare diseases +MONDO:0003155 gard_rare diseases +MONDO:0003155 nord_rare diseases +MONDO:0003155 otar diseases +MONDO:0003155 rare diseases +MONDO:0003157 otar diseases +MONDO:0003158 otar diseases +MONDO:0003159 gard_rare diseases +MONDO:0003159 otar diseases +MONDO:0003159 rare diseases +MONDO:0003163 gard_rare diseases +MONDO:0003163 rare diseases +MONDO:0003165 gard_rare diseases +MONDO:0003165 otar diseases +MONDO:0003165 rare diseases +MONDO:0003168 gard_rare diseases +MONDO:0003168 otar diseases +MONDO:0003168 rare diseases +MONDO:0003169 gard_rare diseases +MONDO:0003169 otar diseases +MONDO:0003169 rare diseases +MONDO:0003170 gard_rare diseases +MONDO:0003170 rare diseases +MONDO:0003171 gard_rare diseases +MONDO:0003171 rare diseases +MONDO:0003173 gard_rare diseases +MONDO:0003173 otar diseases +MONDO:0003173 rare diseases +MONDO:0003174 gard_rare diseases +MONDO:0003174 otar diseases +MONDO:0003174 rare diseases +MONDO:0003175 gard_rare diseases +MONDO:0003175 otar diseases +MONDO:0003175 rare diseases +MONDO:0003177 gard_rare diseases +MONDO:0003177 rare diseases +MONDO:0003180 gard_rare diseases +MONDO:0003180 otar diseases +MONDO:0003180 rare diseases +MONDO:0003181 gard_rare diseases +MONDO:0003181 otar diseases +MONDO:0003181 rare diseases +MONDO:0003184 otar diseases +MONDO:0003185 gard_rare diseases +MONDO:0003185 otar diseases +MONDO:0003185 rare diseases +MONDO:0003186 gard_rare diseases +MONDO:0003186 rare diseases +MONDO:0003187 gard_rare diseases +MONDO:0003187 rare diseases +MONDO:0003190 otar diseases +MONDO:0003191 gard_rare diseases +MONDO:0003191 rare diseases +MONDO:0003193 gard_rare diseases +MONDO:0003193 otar diseases +MONDO:0003193 rare diseases +MONDO:0003194 otar diseases +MONDO:0003195 otar diseases +MONDO:0003196 gard_rare diseases +MONDO:0003196 nord_rare diseases +MONDO:0003196 otar diseases +MONDO:0003196 rare diseases +MONDO:0003197 gard_rare diseases +MONDO:0003197 otar diseases +MONDO:0003197 rare diseases +MONDO:0003198 gard_rare diseases +MONDO:0003198 nord_rare diseases +MONDO:0003198 ordo_disorder diseases +MONDO:0003198 orphanet_rare diseases +MONDO:0003198 otar diseases +MONDO:0003198 rare diseases +MONDO:0003199 otar diseases +MONDO:0003200 otar diseases +MONDO:0003202 gard_rare diseases +MONDO:0003202 rare diseases +MONDO:0003204 otar diseases +MONDO:0003205 gard_rare diseases +MONDO:0003205 nord_rare diseases +MONDO:0003205 rare diseases +MONDO:0003209 gard_rare diseases +MONDO:0003209 rare diseases +MONDO:0003210 gard_rare diseases +MONDO:0003210 nord_rare diseases +MONDO:0003210 otar diseases +MONDO:0003210 rare diseases +MONDO:0003212 otar diseases +MONDO:0003214 otar diseases +MONDO:0003215 otar diseases +MONDO:0003218 otar diseases +MONDO:0003219 otar diseases +MONDO:0003220 gard_rare diseases +MONDO:0003220 otar diseases +MONDO:0003220 rare diseases +MONDO:0003222 otar diseases +MONDO:0003223 gard_rare diseases +MONDO:0003223 otar diseases +MONDO:0003223 rare diseases +MONDO:0003225 gard_rare diseases +MONDO:0003225 otar diseases +MONDO:0003225 rare diseases +MONDO:0003231 gard_rare diseases +MONDO:0003231 rare diseases +MONDO:0003232 otar diseases +MONDO:0003233 otar diseases +MONDO:0003234 gard_rare diseases +MONDO:0003234 rare diseases +MONDO:0003235 gard_rare diseases +MONDO:0003235 otar diseases +MONDO:0003235 rare diseases +MONDO:0003236 otar diseases +MONDO:0003237 otar diseases +MONDO:0003240 otar diseases +MONDO:0003241 otar diseases +MONDO:0003243 gard_rare diseases +MONDO:0003243 otar diseases +MONDO:0003243 rare diseases +MONDO:0003245 gard_rare diseases +MONDO:0003245 rare diseases +MONDO:0003246 gard_rare diseases +MONDO:0003246 rare diseases +MONDO:0003250 inferred_rare diseases +MONDO:0003250 rare diseases +MONDO:0003251 gard_rare diseases +MONDO:0003251 rare diseases +MONDO:0003252 gard_rare diseases +MONDO:0003252 otar diseases +MONDO:0003252 rare diseases +MONDO:0003253 gard_rare diseases +MONDO:0003253 rare diseases +MONDO:0003254 gard_rare diseases +MONDO:0003254 rare diseases +MONDO:0003255 gard_rare diseases +MONDO:0003255 rare diseases +MONDO:0003256 gard_rare diseases +MONDO:0003256 otar diseases +MONDO:0003256 rare diseases +MONDO:0003257 gard_rare diseases +MONDO:0003257 otar diseases +MONDO:0003257 rare diseases +MONDO:0003261 gard_rare diseases +MONDO:0003261 rare diseases +MONDO:0003262 gard_rare diseases +MONDO:0003262 rare diseases +MONDO:0003264 otar diseases +MONDO:0003265 otar diseases +MONDO:0003266 disease_grouping diseases +MONDO:0003266 gard_rare diseases +MONDO:0003266 ordo_group_of_disorders diseases +MONDO:0003266 otar diseases +MONDO:0003266 rare diseases +MONDO:0003268 gard_rare diseases +MONDO:0003268 otar diseases +MONDO:0003268 rare diseases +MONDO:0003273 gard_rare diseases +MONDO:0003273 rare diseases +MONDO:0003274 otar diseases +MONDO:0003275 otar diseases +MONDO:0003276 otar diseases +MONDO:0003277 otar diseases +MONDO:0003281 gard_rare diseases +MONDO:0003281 nord_rare diseases +MONDO:0003281 rare diseases +MONDO:0003285 gard_rare diseases +MONDO:0003285 rare diseases +MONDO:0003291 gard_rare diseases +MONDO:0003291 otar diseases +MONDO:0003291 rare diseases +MONDO:0003295 otar diseases +MONDO:0003301 gard_rare diseases +MONDO:0003301 rare diseases +MONDO:0003302 gard_rare diseases +MONDO:0003302 rare diseases +MONDO:0003303 gard_rare diseases +MONDO:0003303 rare diseases +MONDO:0003304 gard_rare diseases +MONDO:0003304 rare diseases +MONDO:0003305 gard_rare diseases +MONDO:0003305 rare diseases +MONDO:0003306 gard_rare diseases +MONDO:0003306 rare diseases +MONDO:0003308 otar diseases +MONDO:0003311 otar diseases +MONDO:0003313 gard_rare diseases +MONDO:0003313 nord_rare diseases +MONDO:0003313 rare diseases +MONDO:0003316 gard_rare diseases +MONDO:0003316 rare diseases +MONDO:0003317 gard_rare diseases +MONDO:0003317 rare diseases +MONDO:0003318 gard_rare diseases +MONDO:0003318 rare diseases +MONDO:0003320 gard_rare diseases +MONDO:0003320 rare diseases +MONDO:0003321 gard_rare diseases +MONDO:0003321 otar diseases +MONDO:0003321 rare diseases +MONDO:0003322 gard_rare diseases +MONDO:0003322 rare diseases +MONDO:0003325 gard_rare diseases +MONDO:0003325 rare diseases +MONDO:0003326 gard_rare diseases +MONDO:0003326 nord_rare diseases +MONDO:0003326 rare diseases +MONDO:0003327 gard_rare diseases +MONDO:0003327 rare diseases +MONDO:0003328 gard_rare diseases +MONDO:0003328 rare diseases +MONDO:0003330 otar diseases +MONDO:0003331 gard_rare diseases +MONDO:0003331 rare diseases +MONDO:0003332 gard_rare diseases +MONDO:0003332 rare diseases +MONDO:0003333 nord_rare diseases +MONDO:0003333 rare diseases +MONDO:0003334 gard_rare diseases +MONDO:0003334 otar diseases +MONDO:0003334 rare diseases +MONDO:0003335 gard_rare diseases +MONDO:0003335 otar diseases +MONDO:0003335 rare diseases +MONDO:0003336 gard_rare diseases +MONDO:0003336 nord_rare diseases +MONDO:0003336 rare diseases +MONDO:0003337 gard_rare diseases +MONDO:0003337 rare diseases +MONDO:0003340 gard_rare diseases +MONDO:0003340 rare diseases +MONDO:0003341 gard_rare diseases +MONDO:0003341 rare diseases +MONDO:0003343 gard_rare diseases +MONDO:0003343 rare diseases +MONDO:0003345 gard_rare diseases +MONDO:0003345 nord_rare diseases +MONDO:0003345 ordo_disorder diseases +MONDO:0003345 orphanet_rare diseases +MONDO:0003345 otar diseases +MONDO:0003345 rare diseases +MONDO:0003346 gard_rare diseases +MONDO:0003346 otar diseases +MONDO:0003346 rare diseases +MONDO:0003347 gard_rare diseases +MONDO:0003347 rare diseases +MONDO:0003348 gard_rare diseases +MONDO:0003348 rare diseases +MONDO:0003349 gard_rare diseases +MONDO:0003349 rare diseases +MONDO:0003350 gard_rare diseases +MONDO:0003350 nord_rare diseases +MONDO:0003350 rare diseases +MONDO:0003351 gard_rare diseases +MONDO:0003351 rare diseases +MONDO:0003353 gard_rare diseases +MONDO:0003353 otar diseases +MONDO:0003353 rare diseases +MONDO:0003354 gard_rare diseases +MONDO:0003354 otar diseases +MONDO:0003354 rare diseases +MONDO:0003355 gard_rare diseases +MONDO:0003355 otar diseases +MONDO:0003355 rare diseases +MONDO:0003356 gard_rare diseases +MONDO:0003356 rare diseases +MONDO:0003357 gard_rare diseases +MONDO:0003357 rare diseases +MONDO:0003358 gard_rare diseases +MONDO:0003358 rare diseases +MONDO:0003359 gard_rare diseases +MONDO:0003359 rare diseases +MONDO:0003360 gard_rare diseases +MONDO:0003360 nord_rare diseases +MONDO:0003360 ordo_disorder diseases +MONDO:0003360 orphanet_rare diseases +MONDO:0003360 rare diseases +MONDO:0003361 gard_rare diseases +MONDO:0003361 rare diseases +MONDO:0003362 gard_rare diseases +MONDO:0003362 rare diseases +MONDO:0003363 gard_rare diseases +MONDO:0003363 rare diseases +MONDO:0003364 gard_rare diseases +MONDO:0003364 rare diseases +MONDO:0003365 gard_rare diseases +MONDO:0003365 rare diseases +MONDO:0003366 otar diseases +MONDO:0003367 gard_rare diseases +MONDO:0003367 rare diseases +MONDO:0003368 gard_rare diseases +MONDO:0003368 rare diseases +MONDO:0003369 gard_rare diseases +MONDO:0003369 rare diseases +MONDO:0003370 gard_rare diseases +MONDO:0003370 rare diseases +MONDO:0003371 gard_rare diseases +MONDO:0003371 rare diseases +MONDO:0003372 gard_rare diseases +MONDO:0003372 otar diseases +MONDO:0003372 rare diseases +MONDO:0003373 gard_rare diseases +MONDO:0003373 rare diseases +MONDO:0003374 gard_rare diseases +MONDO:0003374 rare diseases +MONDO:0003376 gard_rare diseases +MONDO:0003376 otar diseases +MONDO:0003376 rare diseases +MONDO:0003377 gard_rare diseases +MONDO:0003377 rare diseases +MONDO:0003378 gard_rare diseases +MONDO:0003378 rare diseases +MONDO:0003379 gard_rare diseases +MONDO:0003379 rare diseases +MONDO:0003381 otar diseases +MONDO:0003382 otar diseases +MONDO:0003383 gard_rare diseases +MONDO:0003383 rare diseases +MONDO:0003384 gard_rare diseases +MONDO:0003384 nord_rare diseases +MONDO:0003384 rare diseases +MONDO:0003388 gard_rare diseases +MONDO:0003388 rare diseases +MONDO:0003391 gard_rare diseases +MONDO:0003391 rare diseases +MONDO:0003392 gard_rare diseases +MONDO:0003392 rare diseases +MONDO:0003393 gard_rare diseases +MONDO:0003393 otar diseases +MONDO:0003393 rare diseases +MONDO:0003394 otar diseases +MONDO:0003395 gard_rare diseases +MONDO:0003395 rare diseases +MONDO:0003399 gard_rare diseases +MONDO:0003399 rare diseases +MONDO:0003400 gard_rare diseases +MONDO:0003400 nord_rare diseases +MONDO:0003400 rare diseases +MONDO:0003401 gard_rare diseases +MONDO:0003401 rare diseases +MONDO:0003402 gard_rare diseases +MONDO:0003402 otar diseases +MONDO:0003402 rare diseases +MONDO:0003403 gard_rare diseases +MONDO:0003403 otar diseases +MONDO:0003403 rare diseases +MONDO:0003404 gard_rare diseases +MONDO:0003404 rare diseases +MONDO:0003405 gard_rare diseases +MONDO:0003405 rare diseases +MONDO:0003406 otar diseases +MONDO:0003408 gard_rare diseases +MONDO:0003408 otar diseases +MONDO:0003408 rare diseases +MONDO:0003409 otar diseases +MONDO:0003410 gard_rare diseases +MONDO:0003410 rare diseases +MONDO:0003413 otar diseases +MONDO:0003414 gard_rare diseases +MONDO:0003414 mondo_rare diseases +MONDO:0003414 nord_rare diseases +MONDO:0003414 ordo_disorder diseases +MONDO:0003414 orphanet_rare diseases +MONDO:0003414 rare diseases +MONDO:0003424 otar diseases +MONDO:0003429 disease_grouping diseases +MONDO:0003429 gard_rare diseases +MONDO:0003429 ordo_group_of_disorders diseases +MONDO:0003429 otar diseases +MONDO:0003429 rare diseases +MONDO:0003430 gard_rare diseases +MONDO:0003430 nord_rare diseases +MONDO:0003430 rare diseases +MONDO:0003437 gard_rare diseases +MONDO:0003437 rare diseases +MONDO:0003438 gard_rare diseases +MONDO:0003438 otar diseases +MONDO:0003438 rare diseases +MONDO:0003441 otar diseases +MONDO:0003443 otar diseases +MONDO:0003446 otar diseases +MONDO:0003448 otar diseases +MONDO:0003453 otar diseases +MONDO:0003454 otar diseases +MONDO:0003455 otar diseases +MONDO:0003461 gard_rare diseases +MONDO:0003461 rare diseases +MONDO:0003465 gard_rare diseases +MONDO:0003465 nord_rare diseases +MONDO:0003465 rare diseases +MONDO:0003466 gard_rare diseases +MONDO:0003466 rare diseases +MONDO:0003467 gard_rare diseases +MONDO:0003467 rare diseases +MONDO:0003468 gard_rare diseases +MONDO:0003468 otar diseases +MONDO:0003468 rare diseases +MONDO:0003469 gard_rare diseases +MONDO:0003469 rare diseases +MONDO:0003470 gard_rare diseases +MONDO:0003470 rare diseases +MONDO:0003472 otar diseases +MONDO:0003473 gard_rare diseases +MONDO:0003473 otar diseases +MONDO:0003473 rare diseases +MONDO:0003474 gard_rare diseases +MONDO:0003474 rare diseases +MONDO:0003475 gard_rare diseases +MONDO:0003475 rare diseases +MONDO:0003476 gard_rare diseases +MONDO:0003476 rare diseases +MONDO:0003477 gard_rare diseases +MONDO:0003477 rare diseases +MONDO:0003478 gard_rare diseases +MONDO:0003478 otar diseases +MONDO:0003478 rare diseases +MONDO:0003480 gard_rare diseases +MONDO:0003480 rare diseases +MONDO:0003481 gard_rare diseases +MONDO:0003481 otar diseases +MONDO:0003481 rare diseases +MONDO:0003486 otar diseases +MONDO:0003490 gard_rare diseases +MONDO:0003490 rare diseases +MONDO:0003492 gard_rare diseases +MONDO:0003492 rare diseases +MONDO:0003493 gard_rare diseases +MONDO:0003493 otar diseases +MONDO:0003493 rare diseases +MONDO:0003494 gard_rare diseases +MONDO:0003494 otar diseases +MONDO:0003494 rare diseases +MONDO:0003500 gard_rare diseases +MONDO:0003500 rare diseases +MONDO:0003501 gard_rare diseases +MONDO:0003501 rare diseases +MONDO:0003503 gard_rare diseases +MONDO:0003503 rare diseases +MONDO:0003504 gard_rare diseases +MONDO:0003504 rare diseases +MONDO:0003505 gard_rare diseases +MONDO:0003505 nord_rare diseases +MONDO:0003505 rare diseases +MONDO:0003506 gard_rare diseases +MONDO:0003506 nord_rare diseases +MONDO:0003506 rare diseases +MONDO:0003507 gard_rare diseases +MONDO:0003507 nord_rare diseases +MONDO:0003507 otar diseases +MONDO:0003507 rare diseases +MONDO:0003508 gard_rare diseases +MONDO:0003508 nord_rare diseases +MONDO:0003508 otar diseases +MONDO:0003508 rare diseases +MONDO:0003509 gard_rare diseases +MONDO:0003509 rare diseases +MONDO:0003510 gard_rare diseases +MONDO:0003510 nord_rare diseases +MONDO:0003510 otar diseases +MONDO:0003510 rare diseases +MONDO:0003512 otar diseases +MONDO:0003513 gard_rare diseases +MONDO:0003513 rare diseases +MONDO:0003514 gard_rare diseases +MONDO:0003514 rare diseases +MONDO:0003515 gard_rare diseases +MONDO:0003515 rare diseases +MONDO:0003516 gard_rare diseases +MONDO:0003516 rare diseases +MONDO:0003517 gard_rare diseases +MONDO:0003517 rare diseases +MONDO:0003518 gard_rare diseases +MONDO:0003518 rare diseases +MONDO:0003519 otar diseases +MONDO:0003523 gard_rare diseases +MONDO:0003523 otar diseases +MONDO:0003523 rare diseases +MONDO:0003524 gard_rare diseases +MONDO:0003524 rare diseases +MONDO:0003525 gard_rare diseases +MONDO:0003525 rare diseases +MONDO:0003528 gard_rare diseases +MONDO:0003528 rare diseases +MONDO:0003531 otar diseases +MONDO:0003534 gard_rare diseases +MONDO:0003534 rare diseases +MONDO:0003535 gard_rare diseases +MONDO:0003535 rare diseases +MONDO:0003537 gard_rare diseases +MONDO:0003537 nord_rare diseases +MONDO:0003537 rare diseases +MONDO:0003538 gard_rare diseases +MONDO:0003538 rare diseases +MONDO:0003539 gard_rare diseases +MONDO:0003539 nord_rare diseases +MONDO:0003539 otar diseases +MONDO:0003539 rare diseases +MONDO:0003541 gard_rare diseases +MONDO:0003541 otar diseases +MONDO:0003541 rare diseases +MONDO:0003543 otar diseases +MONDO:0003544 otar diseases +MONDO:0003548 gard_rare diseases +MONDO:0003548 rare diseases +MONDO:0003549 gard_rare diseases +MONDO:0003549 rare diseases +MONDO:0003550 gard_rare diseases +MONDO:0003550 rare diseases +MONDO:0003551 gard_rare diseases +MONDO:0003551 rare diseases +MONDO:0003553 gard_rare diseases +MONDO:0003553 rare diseases +MONDO:0003554 gard_rare diseases +MONDO:0003554 rare diseases +MONDO:0003555 gard_rare diseases +MONDO:0003555 rare diseases +MONDO:0003556 otar diseases +MONDO:0003557 gard_rare diseases +MONDO:0003557 nord_rare diseases +MONDO:0003557 rare diseases +MONDO:0003561 gard_rare diseases +MONDO:0003561 otar diseases +MONDO:0003561 rare diseases +MONDO:0003563 gard_rare diseases +MONDO:0003563 rare diseases +MONDO:0003564 gard_rare diseases +MONDO:0003564 rare diseases +MONDO:0003569 otar diseases +MONDO:0003572 otar diseases +MONDO:0003578 gard_rare diseases +MONDO:0003578 otar diseases +MONDO:0003578 rare diseases +MONDO:0003581 gard_rare diseases +MONDO:0003581 otar diseases +MONDO:0003581 rare diseases +MONDO:0003582 gard_rare diseases +MONDO:0003582 nord_rare diseases +MONDO:0003582 ordo_disorder diseases +MONDO:0003582 orphanet_rare diseases +MONDO:0003582 otar diseases +MONDO:0003582 predisposition diseases +MONDO:0003582 rare diseases +MONDO:0003585 gard_rare diseases +MONDO:0003585 rare diseases +MONDO:0003586 gard_rare diseases +MONDO:0003586 rare diseases +MONDO:0003587 gard_rare diseases +MONDO:0003587 rare diseases +MONDO:0003588 gard_rare diseases +MONDO:0003588 rare diseases +MONDO:0003589 gard_rare diseases +MONDO:0003589 rare diseases +MONDO:0003590 gard_rare diseases +MONDO:0003590 rare diseases +MONDO:0003591 gard_rare diseases +MONDO:0003591 rare diseases +MONDO:0003592 gard_rare diseases +MONDO:0003592 rare diseases +MONDO:0003593 gard_rare diseases +MONDO:0003593 rare diseases +MONDO:0003594 gard_rare diseases +MONDO:0003594 nord_rare diseases +MONDO:0003594 otar diseases +MONDO:0003594 rare diseases +MONDO:0003595 gard_rare diseases +MONDO:0003595 rare diseases +MONDO:0003596 gard_rare diseases +MONDO:0003596 rare diseases +MONDO:0003598 gard_rare diseases +MONDO:0003598 rare diseases +MONDO:0003599 gard_rare diseases +MONDO:0003599 rare diseases +MONDO:0003600 gard_rare diseases +MONDO:0003600 rare diseases +MONDO:0003601 gard_rare diseases +MONDO:0003601 rare diseases +MONDO:0003602 gard_rare diseases +MONDO:0003602 rare diseases +MONDO:0003603 gard_rare diseases +MONDO:0003603 otar diseases +MONDO:0003603 rare diseases +MONDO:0003604 gard_rare diseases +MONDO:0003604 otar diseases +MONDO:0003604 rare diseases +MONDO:0003606 gard_rare diseases +MONDO:0003606 rare diseases +MONDO:0003607 gard_rare diseases +MONDO:0003607 rare diseases +MONDO:0003608 otar diseases +MONDO:0003615 gard_rare diseases +MONDO:0003615 otar diseases +MONDO:0003615 rare diseases +MONDO:0003619 otar diseases +MONDO:0003620 otar diseases +MONDO:0003620 rare_grouping diseases +MONDO:0003621 gard_rare diseases +MONDO:0003621 rare diseases +MONDO:0003622 gard_rare diseases +MONDO:0003622 rare diseases +MONDO:0003624 otar diseases +MONDO:0003626 gard_rare diseases +MONDO:0003626 rare diseases +MONDO:0003628 otar diseases +MONDO:0003630 gard_rare diseases +MONDO:0003630 nord_rare diseases +MONDO:0003630 ordo_disorder diseases +MONDO:0003630 orphanet_rare diseases +MONDO:0003630 rare diseases +MONDO:0003631 gard_rare diseases +MONDO:0003631 rare diseases +MONDO:0003632 otar diseases +MONDO:0003636 gard_rare diseases +MONDO:0003636 rare diseases +MONDO:0003637 gard_rare diseases +MONDO:0003637 rare diseases +MONDO:0003638 gard_rare diseases +MONDO:0003638 rare diseases +MONDO:0003641 gard_rare diseases +MONDO:0003641 rare diseases +MONDO:0003643 gard_rare diseases +MONDO:0003643 rare diseases +MONDO:0003644 gard_rare diseases +MONDO:0003644 rare diseases +MONDO:0003645 gard_rare diseases +MONDO:0003645 otar diseases +MONDO:0003645 rare diseases +MONDO:0003646 gard_rare diseases +MONDO:0003646 nord_rare diseases +MONDO:0003646 ordo_disorder diseases +MONDO:0003646 orphanet_rare diseases +MONDO:0003646 rare diseases +MONDO:0003648 otar diseases +MONDO:0003649 gard_rare diseases +MONDO:0003649 nord_rare diseases +MONDO:0003649 ordo_disorder diseases +MONDO:0003649 orphanet_rare diseases +MONDO:0003649 otar diseases +MONDO:0003649 rare diseases +MONDO:0003650 gard_rare diseases +MONDO:0003650 rare diseases +MONDO:0003651 gard_rare diseases +MONDO:0003651 rare diseases +MONDO:0003653 gard_rare diseases +MONDO:0003653 rare diseases +MONDO:0003654 gard_rare diseases +MONDO:0003654 rare diseases +MONDO:0003655 gard_rare diseases +MONDO:0003655 rare diseases +MONDO:0003656 otar diseases +MONDO:0003658 gard_rare diseases +MONDO:0003658 nord_rare diseases +MONDO:0003658 rare diseases +MONDO:0003659 gard_rare diseases +MONDO:0003659 otar diseases +MONDO:0003659 rare diseases +MONDO:0003660 gard_rare diseases +MONDO:0003660 otar diseases +MONDO:0003660 rare diseases +MONDO:0003661 gard_rare diseases +MONDO:0003661 otar diseases +MONDO:0003661 rare diseases +MONDO:0003663 gard_rare diseases +MONDO:0003663 rare diseases +MONDO:0003664 gard_rare diseases +MONDO:0003664 rare diseases +MONDO:0003665 gard_rare diseases +MONDO:0003665 otar diseases +MONDO:0003665 rare diseases +MONDO:0003666 gard_rare diseases +MONDO:0003666 rare diseases +MONDO:0003668 gard_rare diseases +MONDO:0003668 otar diseases +MONDO:0003668 rare diseases +MONDO:0003669 gard_rare diseases +MONDO:0003669 nord_rare diseases +MONDO:0003669 ordo_disorder diseases +MONDO:0003669 orphanet_rare diseases +MONDO:0003669 otar diseases +MONDO:0003669 rare diseases +MONDO:0003680 gard_rare diseases +MONDO:0003680 otar diseases +MONDO:0003680 rare diseases +MONDO:0003681 gard_rare diseases +MONDO:0003681 otar diseases +MONDO:0003681 rare diseases +MONDO:0003682 gard_rare diseases +MONDO:0003682 rare diseases +MONDO:0003684 gard_rare diseases +MONDO:0003684 nord_rare diseases +MONDO:0003684 otar diseases +MONDO:0003684 rare diseases +MONDO:0003685 gard_rare diseases +MONDO:0003685 rare diseases +MONDO:0003686 otar diseases +MONDO:0003688 otar diseases +MONDO:0003689 gard_rare diseases +MONDO:0003689 otar diseases +MONDO:0003689 rare diseases +MONDO:0003690 gard_rare diseases +MONDO:0003690 rare diseases +MONDO:0003697 gard_rare diseases +MONDO:0003697 rare diseases +MONDO:0003698 gard_rare diseases +MONDO:0003698 nord_rare diseases +MONDO:0003698 rare diseases +MONDO:0003699 otar diseases +MONDO:0003700 gard_rare diseases +MONDO:0003700 rare diseases +MONDO:0003701 gard_rare diseases +MONDO:0003701 rare diseases +MONDO:0003704 gard_rare diseases +MONDO:0003704 rare diseases +MONDO:0003705 gard_rare diseases +MONDO:0003705 rare diseases +MONDO:0003706 gard_rare diseases +MONDO:0003706 rare diseases +MONDO:0003707 gard_rare diseases +MONDO:0003707 rare diseases +MONDO:0003708 gard_rare diseases +MONDO:0003708 rare diseases +MONDO:0003709 otar diseases +MONDO:0003710 gard_rare diseases +MONDO:0003710 otar diseases +MONDO:0003710 rare diseases +MONDO:0003715 otar diseases +MONDO:0003716 gard_rare diseases +MONDO:0003716 rare diseases +MONDO:0003718 otar diseases +MONDO:0003719 otar diseases +MONDO:0003720 gard_rare diseases +MONDO:0003720 rare diseases +MONDO:0003721 gard_rare diseases +MONDO:0003721 rare diseases +MONDO:0003722 gard_rare diseases +MONDO:0003722 rare diseases +MONDO:0003725 otar diseases +MONDO:0003727 otar diseases +MONDO:0003728 gard_rare diseases +MONDO:0003728 rare diseases +MONDO:0003729 gard_rare diseases +MONDO:0003729 nord_rare diseases +MONDO:0003729 rare diseases +MONDO:0003730 gard_rare diseases +MONDO:0003730 rare diseases +MONDO:0003731 gard_rare diseases +MONDO:0003731 rare diseases +MONDO:0003732 gard_rare diseases +MONDO:0003732 rare diseases +MONDO:0003733 gard_rare diseases +MONDO:0003733 rare diseases +MONDO:0003734 gard_rare diseases +MONDO:0003734 rare diseases +MONDO:0003735 gard_rare diseases +MONDO:0003735 otar diseases +MONDO:0003735 rare diseases +MONDO:0003737 gard_rare diseases +MONDO:0003737 rare diseases +MONDO:0003738 gard_rare diseases +MONDO:0003738 rare diseases +MONDO:0003739 gard_rare diseases +MONDO:0003739 rare diseases +MONDO:0003741 gard_rare diseases +MONDO:0003741 nord_rare diseases +MONDO:0003741 rare diseases +MONDO:0003742 gard_rare diseases +MONDO:0003742 rare diseases +MONDO:0003744 gard_rare diseases +MONDO:0003744 otar diseases +MONDO:0003744 rare diseases +MONDO:0003745 gard_rare diseases +MONDO:0003745 rare diseases +MONDO:0003746 gard_rare diseases +MONDO:0003746 rare diseases +MONDO:0003747 gard_rare diseases +MONDO:0003747 rare diseases +MONDO:0003748 otar diseases +MONDO:0003749 otar diseases +MONDO:0003749 rare_grouping diseases +MONDO:0003750 gard_rare diseases +MONDO:0003750 rare diseases +MONDO:0003751 gard_rare diseases +MONDO:0003751 otar diseases +MONDO:0003751 rare diseases +MONDO:0003752 gard_rare diseases +MONDO:0003752 rare diseases +MONDO:0003754 otar diseases +MONDO:0003756 otar diseases +MONDO:0003757 otar diseases +MONDO:0003758 gard_rare diseases +MONDO:0003758 rare diseases +MONDO:0003759 gard_rare diseases +MONDO:0003759 rare diseases +MONDO:0003760 gard_rare diseases +MONDO:0003760 rare diseases +MONDO:0003761 gard_rare diseases +MONDO:0003761 otar diseases +MONDO:0003761 rare diseases +MONDO:0003762 gard_rare diseases +MONDO:0003762 nord_rare diseases +MONDO:0003762 rare diseases +MONDO:0003763 otar diseases +MONDO:0003764 gard_rare diseases +MONDO:0003764 nord_rare diseases +MONDO:0003764 rare diseases +MONDO:0003765 gard_rare diseases +MONDO:0003765 nord_rare diseases +MONDO:0003765 rare diseases +MONDO:0003767 otar diseases +MONDO:0003768 gard_rare diseases +MONDO:0003768 nord_rare diseases +MONDO:0003768 rare diseases +MONDO:0003770 gard_rare diseases +MONDO:0003770 rare diseases +MONDO:0003771 gard_rare diseases +MONDO:0003771 rare diseases +MONDO:0003772 gard_rare diseases +MONDO:0003772 rare diseases +MONDO:0003773 gard_rare diseases +MONDO:0003773 rare diseases +MONDO:0003774 gard_rare diseases +MONDO:0003774 rare diseases +MONDO:0003775 gard_rare diseases +MONDO:0003775 rare diseases +MONDO:0003778 disease_grouping diseases +MONDO:0003778 gard_rare diseases +MONDO:0003778 ordo_group_of_disorders diseases +MONDO:0003778 otar diseases +MONDO:0003778 rare diseases +MONDO:0003780 otar diseases +MONDO:0003781 otar diseases +MONDO:0003782 gard_rare diseases +MONDO:0003782 rare diseases +MONDO:0003783 gard_rare diseases +MONDO:0003783 otar diseases +MONDO:0003783 rare diseases +MONDO:0003785 gard_rare diseases +MONDO:0003785 rare diseases +MONDO:0003786 gard_rare diseases +MONDO:0003786 nord_rare diseases +MONDO:0003786 rare diseases +MONDO:0003787 gard_rare diseases +MONDO:0003787 rare diseases +MONDO:0003788 gard_rare diseases +MONDO:0003788 rare diseases +MONDO:0003789 gard_rare diseases +MONDO:0003789 nord_rare diseases +MONDO:0003789 ordo_disorder diseases +MONDO:0003789 orphanet_rare diseases +MONDO:0003789 otar diseases +MONDO:0003789 rare diseases +MONDO:0003790 gard_rare diseases +MONDO:0003790 rare diseases +MONDO:0003792 gard_rare diseases +MONDO:0003792 nord_rare diseases +MONDO:0003792 ordo_disorder diseases +MONDO:0003792 orphanet_rare diseases +MONDO:0003792 otar diseases +MONDO:0003792 rare diseases +MONDO:0003795 gard_rare diseases +MONDO:0003795 nord_rare diseases +MONDO:0003795 ordo_disorder diseases +MONDO:0003795 orphanet_rare diseases +MONDO:0003795 otar diseases +MONDO:0003795 rare diseases +MONDO:0003796 gard_rare diseases +MONDO:0003796 rare diseases +MONDO:0003799 otar diseases +MONDO:0003800 gard_rare diseases +MONDO:0003800 rare diseases +MONDO:0003803 otar diseases +MONDO:0003805 gard_rare diseases +MONDO:0003805 otar diseases +MONDO:0003805 rare diseases +MONDO:0003806 gard_rare diseases +MONDO:0003806 rare diseases +MONDO:0003808 gard_rare diseases +MONDO:0003808 rare diseases +MONDO:0003809 gard_rare diseases +MONDO:0003809 rare diseases +MONDO:0003812 gard_rare diseases +MONDO:0003812 otar diseases +MONDO:0003812 rare diseases +MONDO:0003818 gard_rare diseases +MONDO:0003818 rare diseases +MONDO:0003819 gard_rare diseases +MONDO:0003819 rare diseases +MONDO:0003820 gard_rare diseases +MONDO:0003820 rare diseases +MONDO:0003821 gard_rare diseases +MONDO:0003821 rare diseases +MONDO:0003826 gard_rare diseases +MONDO:0003826 rare diseases +MONDO:0003827 gard_rare diseases +MONDO:0003827 otar diseases +MONDO:0003827 rare diseases +MONDO:0003828 gard_rare diseases +MONDO:0003828 rare diseases +MONDO:0003832 disease_grouping diseases +MONDO:0003832 inferred_rare diseases +MONDO:0003832 ordo_group_of_disorders diseases +MONDO:0003832 otar diseases +MONDO:0003832 rare diseases +MONDO:0003834 otar diseases +MONDO:0003836 gard_rare diseases +MONDO:0003836 rare diseases +MONDO:0003837 gard_rare diseases +MONDO:0003837 rare diseases +MONDO:0003839 gard_rare diseases +MONDO:0003839 rare diseases +MONDO:0003842 gard_rare diseases +MONDO:0003842 rare diseases +MONDO:0003847 harrisons_view diseases +MONDO:0003847 otar diseases +MONDO:0003847 rare_grouping diseases +MONDO:0003848 gard_rare diseases +MONDO:0003848 rare diseases +MONDO:0003849 gard_rare diseases +MONDO:0003849 nord_rare diseases +MONDO:0003849 rare diseases +MONDO:0003850 gard_rare diseases +MONDO:0003850 rare diseases +MONDO:0003851 gard_rare diseases +MONDO:0003851 rare diseases +MONDO:0003852 gard_rare diseases +MONDO:0003852 rare diseases +MONDO:0003853 gard_rare diseases +MONDO:0003853 rare diseases +MONDO:0003856 gard_rare diseases +MONDO:0003856 rare diseases +MONDO:0003858 gard_rare diseases +MONDO:0003858 rare diseases +MONDO:0003859 gard_rare diseases +MONDO:0003859 rare diseases +MONDO:0003860 gard_rare diseases +MONDO:0003860 rare diseases +MONDO:0003861 gard_rare diseases +MONDO:0003861 rare diseases +MONDO:0003862 gard_rare diseases +MONDO:0003862 rare diseases +MONDO:0003863 gard_rare diseases +MONDO:0003863 rare diseases +MONDO:0003864 gard_rare diseases +MONDO:0003864 rare diseases +MONDO:0003865 otar diseases +MONDO:0003866 gard_rare diseases +MONDO:0003866 rare diseases +MONDO:0003868 gard_rare diseases +MONDO:0003868 rare diseases +MONDO:0003869 gard_rare diseases +MONDO:0003869 otar diseases +MONDO:0003869 rare diseases +MONDO:0003870 gard_rare diseases +MONDO:0003870 rare diseases +MONDO:0003874 gard_rare diseases +MONDO:0003874 rare diseases +MONDO:0003875 gard_rare diseases +MONDO:0003875 rare diseases +MONDO:0003878 gard_rare diseases +MONDO:0003878 rare diseases +MONDO:0003879 gard_rare diseases +MONDO:0003879 rare diseases +MONDO:0003881 gard_rare diseases +MONDO:0003881 rare diseases +MONDO:0003882 gard_rare diseases +MONDO:0003882 nord_rare diseases +MONDO:0003882 rare diseases +MONDO:0003888 gard_rare diseases +MONDO:0003888 rare diseases +MONDO:0003889 gard_rare diseases +MONDO:0003889 rare diseases +MONDO:0003890 gard_rare diseases +MONDO:0003890 otar diseases +MONDO:0003890 rare diseases +MONDO:0003892 gard_rare diseases +MONDO:0003892 otar diseases +MONDO:0003892 rare diseases +MONDO:0003894 gard_rare diseases +MONDO:0003894 rare diseases +MONDO:0003895 gard_rare diseases +MONDO:0003895 rare diseases +MONDO:0003898 gard_rare diseases +MONDO:0003898 rare diseases +MONDO:0003899 gard_rare diseases +MONDO:0003899 rare diseases +MONDO:0003900 otar diseases +MONDO:0003900 rare_grouping diseases +MONDO:0003901 gard_rare diseases +MONDO:0003901 otar diseases +MONDO:0003901 rare diseases +MONDO:0003902 gard_rare diseases +MONDO:0003902 rare diseases +MONDO:0003905 gard_rare diseases +MONDO:0003905 rare diseases +MONDO:0003906 gard_rare diseases +MONDO:0003906 rare diseases +MONDO:0003907 gard_rare diseases +MONDO:0003907 rare diseases +MONDO:0003908 gard_rare diseases +MONDO:0003908 rare diseases +MONDO:0003910 gard_rare diseases +MONDO:0003910 otar diseases +MONDO:0003910 rare diseases +MONDO:0003911 gard_rare diseases +MONDO:0003911 nord_rare diseases +MONDO:0003911 rare diseases +MONDO:0003912 gard_rare diseases +MONDO:0003912 nord_rare diseases +MONDO:0003912 rare diseases +MONDO:0003913 gard_rare diseases +MONDO:0003913 rare diseases +MONDO:0003915 gard_rare diseases +MONDO:0003915 otar diseases +MONDO:0003915 rare diseases +MONDO:0003916 otar diseases +MONDO:0003917 gard_rare diseases +MONDO:0003917 rare diseases +MONDO:0003918 gard_rare diseases +MONDO:0003918 rare diseases +MONDO:0003921 gard_rare diseases +MONDO:0003921 rare diseases +MONDO:0003922 gard_rare diseases +MONDO:0003922 otar diseases +MONDO:0003922 rare diseases +MONDO:0003923 gard_rare diseases +MONDO:0003923 rare diseases +MONDO:0003924 inferred_rare diseases +MONDO:0003924 otar diseases +MONDO:0003924 rare diseases +MONDO:0003925 gard_rare diseases +MONDO:0003925 rare diseases +MONDO:0003926 gard_rare diseases +MONDO:0003926 rare diseases +MONDO:0003927 gard_rare diseases +MONDO:0003927 rare diseases +MONDO:0003928 gard_rare diseases +MONDO:0003928 rare diseases +MONDO:0003930 gard_rare diseases +MONDO:0003930 rare diseases +MONDO:0003931 gard_rare diseases +MONDO:0003931 rare diseases +MONDO:0003932 gard_rare diseases +MONDO:0003932 rare diseases +MONDO:0003933 gard_rare diseases +MONDO:0003933 nord_rare diseases +MONDO:0003933 rare diseases +MONDO:0003937 otar diseases +MONDO:0003939 otar diseases +MONDO:0003939 rare_grouping diseases +MONDO:0003940 gard_rare diseases +MONDO:0003940 rare diseases +MONDO:0003941 gard_rare diseases +MONDO:0003941 rare diseases +MONDO:0003942 gard_rare diseases +MONDO:0003942 rare diseases +MONDO:0003947 gard_rare diseases +MONDO:0003947 otar diseases +MONDO:0003947 rare diseases +MONDO:0003952 gard_rare diseases +MONDO:0003952 nord_rare diseases +MONDO:0003952 rare diseases +MONDO:0003953 gard_rare diseases +MONDO:0003953 rare diseases +MONDO:0003957 gard_rare diseases +MONDO:0003957 nord_rare diseases +MONDO:0003957 rare diseases +MONDO:0003958 gard_rare diseases +MONDO:0003958 rare diseases +MONDO:0003959 gard_rare diseases +MONDO:0003959 rare diseases +MONDO:0003960 gard_rare diseases +MONDO:0003960 rare diseases +MONDO:0003964 gard_rare diseases +MONDO:0003964 rare diseases +MONDO:0003966 gard_rare diseases +MONDO:0003966 rare diseases +MONDO:0003973 gard_rare diseases +MONDO:0003973 rare diseases +MONDO:0003976 gard_rare diseases +MONDO:0003976 nord_rare diseases +MONDO:0003976 rare diseases +MONDO:0003978 gard_rare diseases +MONDO:0003978 otar diseases +MONDO:0003978 rare diseases +MONDO:0003980 gard_rare diseases +MONDO:0003980 rare diseases +MONDO:0003985 gard_rare diseases +MONDO:0003985 rare diseases +MONDO:0003987 gard_rare diseases +MONDO:0003987 otar diseases +MONDO:0003987 rare diseases +MONDO:0003988 gard_rare diseases +MONDO:0003988 rare diseases +MONDO:0003989 gard_rare diseases +MONDO:0003989 rare diseases +MONDO:0003992 gard_rare diseases +MONDO:0003992 rare diseases +MONDO:0003993 gard_rare diseases +MONDO:0003993 rare diseases +MONDO:0003994 gard_rare diseases +MONDO:0003994 rare diseases +MONDO:0003995 gard_rare diseases +MONDO:0003995 rare diseases +MONDO:0003996 otar diseases +MONDO:0003997 gard_rare diseases +MONDO:0003997 rare diseases +MONDO:0003999 gard_rare diseases +MONDO:0003999 rare diseases +MONDO:0004000 gard_rare diseases +MONDO:0004000 rare diseases +MONDO:0004001 gard_rare diseases +MONDO:0004001 nord_rare diseases +MONDO:0004001 otar diseases +MONDO:0004001 rare diseases +MONDO:0004004 gard_rare diseases +MONDO:0004004 rare diseases +MONDO:0004007 otar diseases +MONDO:0004009 gard_rare diseases +MONDO:0004009 rare diseases +MONDO:0004012 gard_rare diseases +MONDO:0004012 rare diseases +MONDO:0004013 gard_rare diseases +MONDO:0004013 rare diseases +MONDO:0004014 gard_rare diseases +MONDO:0004014 rare diseases +MONDO:0004015 gard_rare diseases +MONDO:0004015 rare diseases +MONDO:0004016 gard_rare diseases +MONDO:0004016 rare diseases +MONDO:0004017 gard_rare diseases +MONDO:0004017 rare diseases +MONDO:0004020 gard_rare diseases +MONDO:0004020 rare diseases +MONDO:0004021 gard_rare diseases +MONDO:0004021 otar diseases +MONDO:0004021 rare diseases +MONDO:0004022 gard_rare diseases +MONDO:0004022 rare diseases +MONDO:0004024 gard_rare diseases +MONDO:0004024 rare diseases +MONDO:0004028 gard_rare diseases +MONDO:0004028 rare diseases +MONDO:0004030 gard_rare diseases +MONDO:0004030 rare diseases +MONDO:0004031 gard_rare diseases +MONDO:0004031 obsoletion_candidate diseases +MONDO:0004031 rare diseases +MONDO:0004032 gard_rare diseases +MONDO:0004032 rare diseases +MONDO:0004034 gard_rare diseases +MONDO:0004034 nord_rare diseases +MONDO:0004034 rare diseases +MONDO:0004037 otar diseases +MONDO:0004038 otar diseases +MONDO:0004039 gard_rare diseases +MONDO:0004039 rare diseases +MONDO:0004041 otar diseases +MONDO:0004045 gard_rare diseases +MONDO:0004045 rare diseases +MONDO:0004046 gard_rare diseases +MONDO:0004046 rare diseases +MONDO:0004047 gard_rare diseases +MONDO:0004047 rare diseases +MONDO:0004048 gard_rare diseases +MONDO:0004048 rare diseases +MONDO:0004050 gard_rare diseases +MONDO:0004050 nord_rare diseases +MONDO:0004050 otar diseases +MONDO:0004050 rare diseases +MONDO:0004051 gard_rare diseases +MONDO:0004051 rare diseases +MONDO:0004052 gard_rare diseases +MONDO:0004052 rare diseases +MONDO:0004053 gard_rare diseases +MONDO:0004053 rare diseases +MONDO:0004056 gard_rare diseases +MONDO:0004056 rare diseases +MONDO:0004057 gard_rare diseases +MONDO:0004057 rare diseases +MONDO:0004060 gard_rare diseases +MONDO:0004060 rare diseases +MONDO:0004062 gard_rare diseases +MONDO:0004062 rare diseases +MONDO:0004063 gard_rare diseases +MONDO:0004063 nord_rare diseases +MONDO:0004063 rare diseases +MONDO:0004064 gard_rare diseases +MONDO:0004064 rare diseases +MONDO:0004065 gard_rare diseases +MONDO:0004065 rare diseases +MONDO:0004066 gard_rare diseases +MONDO:0004066 rare diseases +MONDO:0004067 gard_rare diseases +MONDO:0004067 rare diseases +MONDO:0004069 disease_grouping diseases +MONDO:0004069 gard_rare diseases +MONDO:0004069 ordo_group_of_disorders diseases +MONDO:0004069 otar diseases +MONDO:0004069 rare diseases +MONDO:0004071 gard_rare diseases +MONDO:0004071 nord_rare diseases +MONDO:0004071 rare diseases +MONDO:0004078 gard_rare diseases +MONDO:0004078 rare diseases +MONDO:0004080 gard_rare diseases +MONDO:0004080 rare diseases +MONDO:0004081 gard_rare diseases +MONDO:0004081 rare diseases +MONDO:0004082 gard_rare diseases +MONDO:0004082 rare diseases +MONDO:0004085 gard_rare diseases +MONDO:0004085 rare diseases +MONDO:0004086 gard_rare diseases +MONDO:0004086 nord_rare diseases +MONDO:0004086 rare diseases +MONDO:0004087 otar diseases +MONDO:0004088 gard_rare diseases +MONDO:0004088 rare diseases +MONDO:0004089 gard_rare diseases +MONDO:0004089 rare diseases +MONDO:0004090 gard_rare diseases +MONDO:0004090 rare diseases +MONDO:0004092 gard_rare diseases +MONDO:0004092 nord_rare diseases +MONDO:0004092 rare diseases +MONDO:0004093 gard_rare diseases +MONDO:0004093 otar diseases +MONDO:0004093 rare diseases +MONDO:0004094 gard_rare diseases +MONDO:0004094 rare diseases +MONDO:0004095 gard_rare diseases +MONDO:0004095 nord_rare diseases +MONDO:0004095 otar diseases +MONDO:0004095 rare diseases +MONDO:0004096 gard_rare diseases +MONDO:0004096 rare diseases +MONDO:0004098 gard_rare diseases +MONDO:0004098 rare diseases +MONDO:0004099 gard_rare diseases +MONDO:0004099 rare diseases +MONDO:0004100 gard_rare diseases +MONDO:0004100 rare diseases +MONDO:0004101 gard_rare diseases +MONDO:0004101 rare diseases +MONDO:0004102 gard_rare diseases +MONDO:0004102 rare diseases +MONDO:0004103 gard_rare diseases +MONDO:0004103 rare diseases +MONDO:0004104 gard_rare diseases +MONDO:0004104 rare diseases +MONDO:0004105 gard_rare diseases +MONDO:0004105 rare diseases +MONDO:0004106 gard_rare diseases +MONDO:0004106 rare diseases +MONDO:0004107 gard_rare diseases +MONDO:0004107 rare diseases +MONDO:0004108 gard_rare diseases +MONDO:0004108 rare diseases +MONDO:0004110 gard_rare diseases +MONDO:0004110 rare diseases +MONDO:0004111 gard_rare diseases +MONDO:0004111 otar diseases +MONDO:0004111 rare diseases +MONDO:0004114 gard_rare diseases +MONDO:0004114 nord_rare diseases +MONDO:0004114 ordo_disorder diseases +MONDO:0004114 orphanet_rare diseases +MONDO:0004114 otar diseases +MONDO:0004114 rare diseases +MONDO:0004116 gard_rare diseases +MONDO:0004116 otar diseases +MONDO:0004116 rare diseases +MONDO:0004117 gard_rare diseases +MONDO:0004117 rare diseases +MONDO:0004120 gard_rare diseases +MONDO:0004120 rare diseases +MONDO:0004122 gard_rare diseases +MONDO:0004122 otar diseases +MONDO:0004122 rare diseases +MONDO:0004124 gard_rare diseases +MONDO:0004124 rare diseases +MONDO:0004126 otar diseases +MONDO:0004127 gard_rare diseases +MONDO:0004127 rare diseases +MONDO:0004129 gard_rare diseases +MONDO:0004129 nord_rare diseases +MONDO:0004129 rare diseases +MONDO:0004130 gard_rare diseases +MONDO:0004130 rare diseases +MONDO:0004131 gard_rare diseases +MONDO:0004131 rare diseases +MONDO:0004132 gard_rare diseases +MONDO:0004132 nord_rare diseases +MONDO:0004132 ordo_disorder diseases +MONDO:0004132 orphanet_rare diseases +MONDO:0004132 rare diseases +MONDO:0004133 gard_rare diseases +MONDO:0004133 nord_rare diseases +MONDO:0004133 rare diseases +MONDO:0004139 otar diseases +MONDO:0004140 gard_rare diseases +MONDO:0004140 rare diseases +MONDO:0004142 gard_rare diseases +MONDO:0004142 rare diseases +MONDO:0004143 gard_rare diseases +MONDO:0004143 rare diseases +MONDO:0004144 gard_rare diseases +MONDO:0004144 rare diseases +MONDO:0004145 gard_rare diseases +MONDO:0004145 rare diseases +MONDO:0004146 gard_rare diseases +MONDO:0004146 nord_rare diseases +MONDO:0004146 rare diseases +MONDO:0004147 gard_rare diseases +MONDO:0004147 rare diseases +MONDO:0004148 gard_rare diseases +MONDO:0004148 rare diseases +MONDO:0004149 gard_rare diseases +MONDO:0004149 rare diseases +MONDO:0004150 gard_rare diseases +MONDO:0004150 ordo_disorder diseases +MONDO:0004150 orphanet_rare diseases +MONDO:0004150 rare diseases +MONDO:0004151 gard_rare diseases +MONDO:0004151 rare diseases +MONDO:0004152 gard_rare diseases +MONDO:0004152 rare diseases +MONDO:0004153 gard_rare diseases +MONDO:0004153 rare diseases +MONDO:0004155 gard_rare diseases +MONDO:0004155 rare diseases +MONDO:0004161 gard_rare diseases +MONDO:0004161 nord_rare diseases +MONDO:0004161 rare diseases +MONDO:0004162 gard_rare diseases +MONDO:0004162 rare diseases +MONDO:0004163 gard_rare diseases +MONDO:0004163 rare diseases +MONDO:0004165 gard_rare diseases +MONDO:0004165 rare diseases +MONDO:0004166 gard_rare diseases +MONDO:0004166 rare diseases +MONDO:0004168 gard_rare diseases +MONDO:0004168 nord_rare diseases +MONDO:0004168 rare diseases +MONDO:0004169 otar diseases +MONDO:0004172 gard_rare diseases +MONDO:0004172 rare diseases +MONDO:0004173 gard_rare diseases +MONDO:0004173 rare diseases +MONDO:0004176 gard_rare diseases +MONDO:0004176 rare diseases +MONDO:0004178 gard_rare diseases +MONDO:0004178 rare diseases +MONDO:0004183 gard_rare diseases +MONDO:0004183 otar diseases +MONDO:0004183 rare diseases +MONDO:0004184 otar diseases +MONDO:0004186 gard_rare diseases +MONDO:0004186 rare diseases +MONDO:0004187 gard_rare diseases +MONDO:0004187 nord_rare diseases +MONDO:0004187 ordo_disorder diseases +MONDO:0004187 orphanet_rare diseases +MONDO:0004187 otar diseases +MONDO:0004187 rare diseases +MONDO:0004188 gard_rare diseases +MONDO:0004188 rare diseases +MONDO:0004189 gard_rare diseases +MONDO:0004189 rare diseases +MONDO:0004192 otar diseases +MONDO:0004193 gard_rare diseases +MONDO:0004193 rare diseases +MONDO:0004195 gard_rare diseases +MONDO:0004195 rare diseases +MONDO:0004198 gard_rare diseases +MONDO:0004198 rare diseases +MONDO:0004199 gard_rare diseases +MONDO:0004199 rare diseases +MONDO:0004202 gard_rare diseases +MONDO:0004202 rare diseases +MONDO:0004205 gard_rare diseases +MONDO:0004205 rare diseases +MONDO:0004206 gard_rare diseases +MONDO:0004206 rare diseases +MONDO:0004207 gard_rare diseases +MONDO:0004207 rare diseases +MONDO:0004208 gard_rare diseases +MONDO:0004208 rare diseases +MONDO:0004210 gard_rare diseases +MONDO:0004210 rare diseases +MONDO:0004211 gard_rare diseases +MONDO:0004211 rare diseases +MONDO:0004212 gard_rare diseases +MONDO:0004212 rare diseases +MONDO:0004213 gard_rare diseases +MONDO:0004213 rare diseases +MONDO:0004216 gard_rare diseases +MONDO:0004216 nord_rare diseases +MONDO:0004216 ordo_subtype_of_a_disorder diseases +MONDO:0004216 rare diseases +MONDO:0004217 gard_rare diseases +MONDO:0004217 rare diseases +MONDO:0004218 gard_rare diseases +MONDO:0004218 nord_rare diseases +MONDO:0004218 rare diseases +MONDO:0004219 gard_rare diseases +MONDO:0004219 rare diseases +MONDO:0004221 gard_rare diseases +MONDO:0004221 rare diseases +MONDO:0004222 gard_rare diseases +MONDO:0004222 otar diseases +MONDO:0004222 rare diseases +MONDO:0004224 gard_rare diseases +MONDO:0004224 rare diseases +MONDO:0004225 gard_rare diseases +MONDO:0004225 rare diseases +MONDO:0004229 gard_rare diseases +MONDO:0004229 rare diseases +MONDO:0004231 gard_rare diseases +MONDO:0004231 rare diseases +MONDO:0004232 gard_rare diseases +MONDO:0004232 rare diseases +MONDO:0004233 gard_rare diseases +MONDO:0004233 rare diseases +MONDO:0004234 gard_rare diseases +MONDO:0004234 nord_rare diseases +MONDO:0004234 ordo_disorder diseases +MONDO:0004234 orphanet_rare diseases +MONDO:0004234 rare diseases +MONDO:0004235 otar diseases +MONDO:0004236 gard_rare diseases +MONDO:0004236 rare diseases +MONDO:0004238 gard_rare diseases +MONDO:0004238 nord_rare diseases +MONDO:0004238 rare diseases +MONDO:0004239 gard_rare diseases +MONDO:0004239 rare diseases +MONDO:0004241 gard_rare diseases +MONDO:0004241 nord_rare diseases +MONDO:0004241 ordo_disorder diseases +MONDO:0004241 orphanet_rare diseases +MONDO:0004241 rare diseases +MONDO:0004243 gard_rare diseases +MONDO:0004243 nord_rare diseases +MONDO:0004243 rare diseases +MONDO:0004244 gard_rare diseases +MONDO:0004244 rare diseases +MONDO:0004245 gard_rare diseases +MONDO:0004245 nord_rare diseases +MONDO:0004245 otar diseases +MONDO:0004245 rare diseases +MONDO:0004247 otar diseases +MONDO:0004248 gard_rare diseases +MONDO:0004248 rare diseases +MONDO:0004249 gard_rare diseases +MONDO:0004249 otar diseases +MONDO:0004249 rare diseases +MONDO:0004251 otar diseases +MONDO:0004252 gard_rare diseases +MONDO:0004252 rare diseases +MONDO:0004255 otar diseases +MONDO:0004256 gard_rare diseases +MONDO:0004256 rare diseases +MONDO:0004257 gard_rare diseases +MONDO:0004257 nord_rare diseases +MONDO:0004257 rare diseases +MONDO:0004259 otar diseases +MONDO:0004260 otar diseases +MONDO:0004263 gard_rare diseases +MONDO:0004263 nord_rare diseases +MONDO:0004263 rare diseases +MONDO:0004270 otar diseases +MONDO:0004272 gard_rare diseases +MONDO:0004272 rare diseases +MONDO:0004274 gard_rare diseases +MONDO:0004274 rare diseases +MONDO:0004275 gard_rare diseases +MONDO:0004275 rare diseases +MONDO:0004278 gard_rare diseases +MONDO:0004278 otar diseases +MONDO:0004278 rare diseases +MONDO:0004279 gard_rare diseases +MONDO:0004279 rare diseases +MONDO:0004280 gard_rare diseases +MONDO:0004280 rare diseases +MONDO:0004281 gard_rare diseases +MONDO:0004281 rare diseases +MONDO:0004283 gard_rare diseases +MONDO:0004283 rare diseases +MONDO:0004285 gard_rare diseases +MONDO:0004285 nord_rare diseases +MONDO:0004285 ordo_disorder diseases +MONDO:0004285 orphanet_rare diseases +MONDO:0004285 rare diseases +MONDO:0004289 gard_rare diseases +MONDO:0004289 nord_rare diseases +MONDO:0004289 rare diseases +MONDO:0004290 gard_rare diseases +MONDO:0004290 rare diseases +MONDO:0004291 gard_rare diseases +MONDO:0004291 nord_rare diseases +MONDO:0004291 rare diseases +MONDO:0004292 gard_rare diseases +MONDO:0004292 rare diseases +MONDO:0004293 gard_rare diseases +MONDO:0004293 nord_rare diseases +MONDO:0004293 rare diseases +MONDO:0004294 gard_rare diseases +MONDO:0004294 rare diseases +MONDO:0004296 gard_rare diseases +MONDO:0004296 rare diseases +MONDO:0004297 gard_rare diseases +MONDO:0004297 rare diseases +MONDO:0004298 otar diseases +MONDO:0004298 rare_grouping diseases +MONDO:0004299 gard_rare diseases +MONDO:0004299 rare diseases +MONDO:0004301 gard_rare diseases +MONDO:0004301 nord_rare diseases +MONDO:0004301 otar diseases +MONDO:0004301 rare diseases +MONDO:0004306 gard_rare diseases +MONDO:0004306 nord_rare diseases +MONDO:0004306 rare diseases +MONDO:0004307 gard_rare diseases +MONDO:0004307 rare diseases +MONDO:0004308 gard_rare diseases +MONDO:0004308 rare diseases +MONDO:0004310 gard_rare diseases +MONDO:0004310 rare diseases +MONDO:0004312 gard_rare diseases +MONDO:0004312 rare diseases +MONDO:0004313 gard_rare diseases +MONDO:0004313 rare diseases +MONDO:0004314 gard_rare diseases +MONDO:0004314 rare diseases +MONDO:0004315 gard_rare diseases +MONDO:0004315 rare diseases +MONDO:0004317 gard_rare diseases +MONDO:0004317 rare diseases +MONDO:0004318 gard_rare diseases +MONDO:0004318 rare diseases +MONDO:0004319 gard_rare diseases +MONDO:0004319 rare diseases +MONDO:0004320 gard_rare diseases +MONDO:0004320 rare diseases +MONDO:0004321 otar diseases +MONDO:0004322 gard_rare diseases +MONDO:0004322 rare diseases +MONDO:0004323 gard_rare diseases +MONDO:0004323 otar diseases +MONDO:0004323 rare diseases +MONDO:0004324 gard_rare diseases +MONDO:0004324 rare diseases +MONDO:0004325 gard_rare diseases +MONDO:0004325 rare diseases +MONDO:0004326 gard_rare diseases +MONDO:0004326 nord_rare diseases +MONDO:0004326 rare diseases +MONDO:0004327 gard_rare diseases +MONDO:0004327 rare diseases +MONDO:0004328 gard_rare diseases +MONDO:0004328 nord_rare diseases +MONDO:0004328 rare diseases +MONDO:0004329 gard_rare diseases +MONDO:0004329 nord_rare diseases +MONDO:0004329 rare diseases +MONDO:0004330 gard_rare diseases +MONDO:0004330 nord_rare diseases +MONDO:0004330 rare diseases +MONDO:0004331 otar diseases +MONDO:0004333 gard_rare diseases +MONDO:0004333 rare diseases +MONDO:0004334 gard_rare diseases +MONDO:0004334 nord_rare diseases +MONDO:0004334 ordo_disorder diseases +MONDO:0004334 orphanet_rare diseases +MONDO:0004334 rare diseases +MONDO:0004335 rare_grouping diseases +MONDO:0004337 gard_rare diseases +MONDO:0004337 rare diseases +MONDO:0004339 gard_rare diseases +MONDO:0004339 rare diseases +MONDO:0004343 gard_rare diseases +MONDO:0004343 rare diseases +MONDO:0004344 gard_rare diseases +MONDO:0004344 rare diseases +MONDO:0004345 gard_rare diseases +MONDO:0004345 nord_rare diseases +MONDO:0004345 rare diseases +MONDO:0004346 gard_rare diseases +MONDO:0004346 rare diseases +MONDO:0004348 otar diseases +MONDO:0004349 gard_rare diseases +MONDO:0004349 rare diseases +MONDO:0004350 gard_rare diseases +MONDO:0004350 rare diseases +MONDO:0004351 gard_rare diseases +MONDO:0004351 nord_rare diseases +MONDO:0004351 ordo_disorder diseases +MONDO:0004351 orphanet_rare diseases +MONDO:0004351 rare diseases +MONDO:0004352 gard_rare diseases +MONDO:0004352 rare diseases +MONDO:0004354 gard_rare diseases +MONDO:0004354 rare diseases +MONDO:0004355 gard_rare diseases +MONDO:0004355 otar diseases +MONDO:0004355 rare diseases +MONDO:0004357 otar diseases +MONDO:0004359 otar diseases +MONDO:0004360 gard_rare diseases +MONDO:0004360 rare diseases +MONDO:0004361 gard_rare diseases +MONDO:0004361 rare diseases +MONDO:0004363 gard_rare diseases +MONDO:0004363 rare diseases +MONDO:0004364 gard_rare diseases +MONDO:0004364 rare diseases +MONDO:0004365 gard_rare diseases +MONDO:0004365 rare diseases +MONDO:0004366 gard_rare diseases +MONDO:0004366 rare diseases +MONDO:0004367 gard_rare diseases +MONDO:0004367 rare diseases +MONDO:0004368 gard_rare diseases +MONDO:0004368 rare diseases +MONDO:0004370 gard_rare diseases +MONDO:0004370 rare diseases +MONDO:0004371 gard_rare diseases +MONDO:0004371 rare diseases +MONDO:0004372 gard_rare diseases +MONDO:0004372 rare diseases +MONDO:0004373 gard_rare diseases +MONDO:0004373 rare diseases +MONDO:0004374 gard_rare diseases +MONDO:0004374 rare diseases +MONDO:0004377 gard_rare diseases +MONDO:0004377 rare diseases +MONDO:0004378 gard_rare diseases +MONDO:0004378 rare diseases +MONDO:0004379 otar diseases +MONDO:0004380 gard_rare diseases +MONDO:0004380 ordo_disorder diseases +MONDO:0004380 orphanet_rare diseases +MONDO:0004380 otar diseases +MONDO:0004380 rare diseases +MONDO:0004382 otar diseases +MONDO:0004383 gard_rare diseases +MONDO:0004383 rare diseases +MONDO:0004384 gard_rare diseases +MONDO:0004384 rare diseases +MONDO:0004385 gard_rare diseases +MONDO:0004385 rare diseases +MONDO:0004386 otar diseases +MONDO:0004389 otar diseases +MONDO:0004392 gard_rare diseases +MONDO:0004392 nord_rare diseases +MONDO:0004392 otar diseases +MONDO:0004392 rare diseases +MONDO:0004393 gard_rare diseases +MONDO:0004393 rare diseases +MONDO:0004394 gard_rare diseases +MONDO:0004394 nord_rare diseases +MONDO:0004394 rare diseases +MONDO:0004396 gard_rare diseases +MONDO:0004396 rare diseases +MONDO:0004397 inferred_rare diseases +MONDO:0004397 rare diseases +MONDO:0004398 gard_rare diseases +MONDO:0004398 rare diseases +MONDO:0004400 gard_rare diseases +MONDO:0004400 rare diseases +MONDO:0004401 gard_rare diseases +MONDO:0004401 nord_rare diseases +MONDO:0004401 rare diseases +MONDO:0004402 gard_rare diseases +MONDO:0004402 rare diseases +MONDO:0004403 gard_rare diseases +MONDO:0004403 rare diseases +MONDO:0004404 gard_rare diseases +MONDO:0004404 rare diseases +MONDO:0004405 gard_rare diseases +MONDO:0004405 otar diseases +MONDO:0004405 rare diseases +MONDO:0004406 gard_rare diseases +MONDO:0004406 rare diseases +MONDO:0004407 gard_rare diseases +MONDO:0004407 rare diseases +MONDO:0004408 gard_rare diseases +MONDO:0004408 rare diseases +MONDO:0004410 gard_rare diseases +MONDO:0004410 nord_rare diseases +MONDO:0004410 rare diseases +MONDO:0004411 gard_rare diseases +MONDO:0004411 rare diseases +MONDO:0004413 gard_rare diseases +MONDO:0004413 rare diseases +MONDO:0004415 gard_rare diseases +MONDO:0004415 rare diseases +MONDO:0004416 gard_rare diseases +MONDO:0004416 rare diseases +MONDO:0004417 gard_rare diseases +MONDO:0004417 rare diseases +MONDO:0004418 gard_rare diseases +MONDO:0004418 rare diseases +MONDO:0004419 gard_rare diseases +MONDO:0004419 rare diseases +MONDO:0004422 gard_rare diseases +MONDO:0004422 rare diseases +MONDO:0004423 gard_rare diseases +MONDO:0004423 rare diseases +MONDO:0004425 otar diseases +MONDO:0004426 gard_rare diseases +MONDO:0004426 rare diseases +MONDO:0004427 otar diseases +MONDO:0004429 gard_rare diseases +MONDO:0004429 rare diseases +MONDO:0004430 gard_rare diseases +MONDO:0004430 rare diseases +MONDO:0004431 otar diseases +MONDO:0004432 gard_rare diseases +MONDO:0004432 rare diseases +MONDO:0004433 gard_rare diseases +MONDO:0004433 nord_rare diseases +MONDO:0004433 rare diseases +MONDO:0004435 gard_rare diseases +MONDO:0004435 otar diseases +MONDO:0004435 rare diseases +MONDO:0004436 gard_rare diseases +MONDO:0004436 rare diseases +MONDO:0004439 gard_rare diseases +MONDO:0004439 rare diseases +MONDO:0004440 gard_rare diseases +MONDO:0004440 rare diseases +MONDO:0004441 gard_rare diseases +MONDO:0004441 rare diseases +MONDO:0004442 gard_rare diseases +MONDO:0004442 rare diseases +MONDO:0004446 gard_rare diseases +MONDO:0004446 rare diseases +MONDO:0004447 gard_rare diseases +MONDO:0004447 rare diseases +MONDO:0004448 gard_rare diseases +MONDO:0004448 rare diseases +MONDO:0004451 gard_rare diseases +MONDO:0004451 rare diseases +MONDO:0004452 gard_rare diseases +MONDO:0004452 rare diseases +MONDO:0004453 gard_rare diseases +MONDO:0004453 rare diseases +MONDO:0004454 gard_rare diseases +MONDO:0004454 nord_rare diseases +MONDO:0004454 rare diseases +MONDO:0004455 gard_rare diseases +MONDO:0004455 rare diseases +MONDO:0004457 gard_rare diseases +MONDO:0004457 rare diseases +MONDO:0004458 otar diseases +MONDO:0004460 gard_rare diseases +MONDO:0004460 rare diseases +MONDO:0004463 gard_rare diseases +MONDO:0004463 rare diseases +MONDO:0004465 gard_rare diseases +MONDO:0004465 rare diseases +MONDO:0004467 gard_rare diseases +MONDO:0004467 rare diseases +MONDO:0004468 gard_rare diseases +MONDO:0004468 rare diseases +MONDO:0004471 otar diseases +MONDO:0004474 gard_rare diseases +MONDO:0004474 rare diseases +MONDO:0004475 gard_rare diseases +MONDO:0004475 rare diseases +MONDO:0004477 gard_rare diseases +MONDO:0004477 rare diseases +MONDO:0004478 gard_rare diseases +MONDO:0004478 rare diseases +MONDO:0004479 gard_rare diseases +MONDO:0004479 rare diseases +MONDO:0004481 gard_rare diseases +MONDO:0004481 rare diseases +MONDO:0004483 gard_rare diseases +MONDO:0004483 otar diseases +MONDO:0004483 rare diseases +MONDO:0004484 gard_rare diseases +MONDO:0004484 nord_rare diseases +MONDO:0004484 rare diseases +MONDO:0004485 gard_rare diseases +MONDO:0004485 rare diseases +MONDO:0004489 gard_rare diseases +MONDO:0004489 nord_rare diseases +MONDO:0004489 rare diseases +MONDO:0004491 gard_rare diseases +MONDO:0004491 rare diseases +MONDO:0004493 gard_rare diseases +MONDO:0004493 rare diseases +MONDO:0004494 gard_rare diseases +MONDO:0004494 rare diseases +MONDO:0004495 gard_rare diseases +MONDO:0004495 rare diseases +MONDO:0004496 gard_rare diseases +MONDO:0004496 nord_rare diseases +MONDO:0004496 otar diseases +MONDO:0004496 rare diseases +MONDO:0004498 gard_rare diseases +MONDO:0004498 rare diseases +MONDO:0004501 gard_rare diseases +MONDO:0004501 rare diseases +MONDO:0004502 gard_rare diseases +MONDO:0004502 rare diseases +MONDO:0004503 gard_rare diseases +MONDO:0004503 rare diseases +MONDO:0004504 gard_rare diseases +MONDO:0004504 rare diseases +MONDO:0004508 otar diseases +MONDO:0004510 gard_rare diseases +MONDO:0004510 rare diseases +MONDO:0004511 gard_rare diseases +MONDO:0004511 rare diseases +MONDO:0004512 gard_rare diseases +MONDO:0004512 rare diseases +MONDO:0004513 gard_rare diseases +MONDO:0004513 rare diseases +MONDO:0004514 otar diseases +MONDO:0004517 gard_rare diseases +MONDO:0004517 rare diseases +MONDO:0004520 gard_rare diseases +MONDO:0004520 rare diseases +MONDO:0004521 gard_rare diseases +MONDO:0004521 rare diseases +MONDO:0004522 otar diseases +MONDO:0004524 gard_rare diseases +MONDO:0004524 rare diseases +MONDO:0004528 gard_rare diseases +MONDO:0004528 otar diseases +MONDO:0004528 rare diseases +MONDO:0004530 gard_rare diseases +MONDO:0004530 rare diseases +MONDO:0004535 gard_rare diseases +MONDO:0004535 nord_rare diseases +MONDO:0004535 rare diseases +MONDO:0004537 gard_rare diseases +MONDO:0004537 rare diseases +MONDO:0004538 gard_rare diseases +MONDO:0004538 rare diseases +MONDO:0004540 gard_rare diseases +MONDO:0004540 rare diseases +MONDO:0004541 gard_rare diseases +MONDO:0004541 rare diseases +MONDO:0004542 gard_rare diseases +MONDO:0004542 nord_rare diseases +MONDO:0004542 ordo_disorder diseases +MONDO:0004542 orphanet_rare diseases +MONDO:0004542 rare diseases +MONDO:0004543 gard_rare diseases +MONDO:0004543 rare diseases +MONDO:0004544 gard_rare diseases +MONDO:0004544 rare diseases +MONDO:0004545 gard_rare diseases +MONDO:0004545 rare diseases +MONDO:0004546 gard_rare diseases +MONDO:0004546 rare diseases +MONDO:0004547 gard_rare diseases +MONDO:0004547 rare diseases +MONDO:0004548 gard_rare diseases +MONDO:0004548 nord_rare diseases +MONDO:0004548 rare diseases +MONDO:0004549 gard_rare diseases +MONDO:0004549 rare diseases +MONDO:0004552 gard_rare diseases +MONDO:0004552 rare diseases +MONDO:0004554 gard_rare diseases +MONDO:0004554 rare diseases +MONDO:0004555 gard_rare diseases +MONDO:0004555 rare diseases +MONDO:0004557 gard_rare diseases +MONDO:0004557 otar diseases +MONDO:0004557 rare diseases +MONDO:0004558 gard_rare diseases +MONDO:0004558 rare diseases +MONDO:0004559 gard_rare diseases +MONDO:0004559 rare diseases +MONDO:0004563 gard_rare diseases +MONDO:0004563 rare diseases +MONDO:0004565 otar diseases +MONDO:0004566 otar diseases +MONDO:0004567 otar diseases +MONDO:0004569 gard_rare diseases +MONDO:0004569 rare diseases +MONDO:0004571 otar diseases +MONDO:0004573 otar diseases +MONDO:0004579 otar diseases +MONDO:0004580 otar diseases +MONDO:0004582 gard_rare diseases +MONDO:0004582 nord_rare diseases +MONDO:0004582 otar diseases +MONDO:0004582 rare diseases +MONDO:0004584 gard_rare diseases +MONDO:0004584 nord_rare diseases +MONDO:0004584 rare diseases +MONDO:0004586 otar diseases +MONDO:0004587 obsoletion_candidate diseases +MONDO:0004587 otar diseases +MONDO:0004588 otar diseases +MONDO:0004593 otar diseases +MONDO:0004596 otar diseases +MONDO:0004600 gard_rare diseases +MONDO:0004600 otar diseases +MONDO:0004600 rare diseases +MONDO:0004603 otar diseases +MONDO:0004604 gard_rare diseases +MONDO:0004604 nord_rare diseases +MONDO:0004604 ordo_histopathological_subtype diseases +MONDO:0004604 ordo_subtype_of_a_disorder diseases +MONDO:0004604 rare diseases +MONDO:0004608 otar diseases +MONDO:0004609 otar diseases +MONDO:0004614 gard_rare diseases +MONDO:0004614 rare diseases +MONDO:0004615 gard_rare diseases +MONDO:0004615 rare diseases +MONDO:0004619 otar diseases +MONDO:0004620 gard_rare diseases +MONDO:0004620 nord_rare diseases +MONDO:0004620 ordo_histopathological_subtype diseases +MONDO:0004620 ordo_subtype_of_a_disorder diseases +MONDO:0004620 rare diseases +MONDO:0004625 gard_rare diseases +MONDO:0004625 otar diseases +MONDO:0004625 rare diseases +MONDO:0004627 otar diseases +MONDO:0004630 otar diseases +MONDO:0004633 gard_rare diseases +MONDO:0004633 nord_rare diseases +MONDO:0004633 ordo_histopathological_subtype diseases +MONDO:0004633 ordo_subtype_of_a_disorder diseases +MONDO:0004633 otar diseases +MONDO:0004633 rare diseases +MONDO:0004634 otar diseases +MONDO:0004638 gard_rare diseases +MONDO:0004638 nord_rare diseases +MONDO:0004638 rare diseases +MONDO:0004639 gard_rare diseases +MONDO:0004639 rare diseases +MONDO:0004640 otar diseases +MONDO:0004641 otar diseases +MONDO:0004643 gard_rare diseases +MONDO:0004643 nord_rare diseases +MONDO:0004643 otar diseases +MONDO:0004643 rare diseases +MONDO:0004644 gard_rare diseases +MONDO:0004644 rare diseases +MONDO:0004647 otar diseases +MONDO:0004648 otar diseases +MONDO:0004650 gard_rare diseases +MONDO:0004650 nord_rare diseases +MONDO:0004650 rare diseases +MONDO:0004651 otar diseases +MONDO:0004652 otar diseases +MONDO:0004653 gard_rare diseases +MONDO:0004653 nord_rare diseases +MONDO:0004653 ordo_disorder diseases +MONDO:0004653 orphanet_rare diseases +MONDO:0004653 rare diseases +MONDO:0004656 gard_rare diseases +MONDO:0004656 nord_rare diseases +MONDO:0004656 otar diseases +MONDO:0004656 rare diseases +MONDO:0004657 gard_rare diseases +MONDO:0004657 rare diseases +MONDO:0004658 otar diseases +MONDO:0004663 otar diseases +MONDO:0004664 otar diseases +MONDO:0004665 gard_rare diseases +MONDO:0004665 ordo_histopathological_subtype diseases +MONDO:0004665 ordo_subtype_of_a_disorder diseases +MONDO:0004665 otar diseases +MONDO:0004665 rare diseases +MONDO:0004668 otar diseases +MONDO:0004669 otar diseases +MONDO:0004670 otar diseases +MONDO:0004671 gard_rare diseases +MONDO:0004671 nord_rare diseases +MONDO:0004671 otar diseases +MONDO:0004671 rare diseases +MONDO:0004672 gard_rare diseases +MONDO:0004672 ordo_disorder diseases +MONDO:0004672 orphanet_rare diseases +MONDO:0004672 rare diseases +MONDO:0004674 gard_rare diseases +MONDO:0004674 otar diseases +MONDO:0004674 rare diseases +MONDO:0004675 gard_rare diseases +MONDO:0004675 otar diseases +MONDO:0004675 rare diseases +MONDO:0004678 otar diseases +MONDO:0004680 gard_rare diseases +MONDO:0004680 otar diseases +MONDO:0004680 rare diseases +MONDO:0004681 otar diseases +MONDO:0004682 gard_rare diseases +MONDO:0004682 rare diseases +MONDO:0004684 gard_rare diseases +MONDO:0004684 nord_rare diseases +MONDO:0004684 ordo_disorder diseases +MONDO:0004684 orphanet_rare diseases +MONDO:0004684 otar diseases +MONDO:0004684 rare diseases +MONDO:0004686 gard_rare diseases +MONDO:0004686 otar diseases +MONDO:0004686 rare diseases +MONDO:0004689 gard_rare diseases +MONDO:0004689 rare diseases +MONDO:0004691 clingen diseases +MONDO:0004691 gard_rare diseases +MONDO:0004691 nord_rare diseases +MONDO:0004691 ordo_disorder diseases +MONDO:0004691 orphanet_rare diseases +MONDO:0004691 otar diseases +MONDO:0004691 rare diseases +MONDO:0004693 otar diseases +MONDO:0004694 otar diseases +MONDO:0004695 gard_rare diseases +MONDO:0004695 otar diseases +MONDO:0004695 rare diseases +MONDO:0004697 otar diseases +MONDO:0004699 gard_rare diseases +MONDO:0004699 nord_rare diseases +MONDO:0004699 otar diseases +MONDO:0004699 rare diseases +MONDO:0004700 otar diseases +MONDO:0004701 otar diseases +MONDO:0004703 gard_rare diseases +MONDO:0004703 rare diseases +MONDO:0004705 gard_rare diseases +MONDO:0004705 otar diseases +MONDO:0004705 rare diseases +MONDO:0004707 gard_rare diseases +MONDO:0004707 rare diseases +MONDO:0004708 gard_rare diseases +MONDO:0004708 rare diseases +MONDO:0004710 otar diseases +MONDO:0004713 gard_rare diseases +MONDO:0004713 rare diseases +MONDO:0004714 gard_rare diseases +MONDO:0004714 rare diseases +MONDO:0004715 gard_rare diseases +MONDO:0004715 rare diseases +MONDO:0004717 otar diseases +MONDO:0004724 otar diseases +MONDO:0004725 otar diseases +MONDO:0004726 gard_rare diseases +MONDO:0004726 nord_rare diseases +MONDO:0004726 rare diseases +MONDO:0004728 otar diseases +MONDO:0004730 otar diseases +MONDO:0004731 otar diseases +MONDO:0004736 gard_rare diseases +MONDO:0004736 rare diseases +MONDO:0004737 gard_rare diseases +MONDO:0004737 otar diseases +MONDO:0004737 rare diseases +MONDO:0004739 disease_grouping diseases +MONDO:0004739 gard_rare diseases +MONDO:0004739 ordo_group_of_disorders diseases +MONDO:0004739 otar diseases +MONDO:0004739 rare diseases +MONDO:0004741 gard_rare diseases +MONDO:0004741 otar diseases +MONDO:0004741 rare diseases +MONDO:0004743 gard_rare diseases +MONDO:0004743 rare diseases +MONDO:0004745 gard_rare diseases +MONDO:0004745 nord_rare diseases +MONDO:0004745 ordo_disorder diseases +MONDO:0004745 orphanet_rare diseases +MONDO:0004745 rare diseases +MONDO:0004746 gard_rare diseases +MONDO:0004746 rare diseases +MONDO:0004748 otar diseases +MONDO:0004750 otar diseases +MONDO:0004751 otar diseases +MONDO:0004752 gard_rare diseases +MONDO:0004752 rare diseases +MONDO:0004756 otar diseases +MONDO:0004766 otar diseases +MONDO:0004768 otar diseases +MONDO:0004772 gard_rare diseases +MONDO:0004772 ordo_disorder diseases +MONDO:0004772 orphanet_rare diseases +MONDO:0004772 rare diseases +MONDO:0004773 gard_rare diseases +MONDO:0004773 rare diseases +MONDO:0004774 gard_rare diseases +MONDO:0004774 rare diseases +MONDO:0004775 gard_rare diseases +MONDO:0004775 rare diseases +MONDO:0004777 otar diseases +MONDO:0004781 otar diseases +MONDO:0004782 otar diseases +MONDO:0004784 otar diseases +MONDO:0004785 otar diseases +MONDO:0004789 otar diseases +MONDO:0004790 otar diseases +MONDO:0004792 gard_rare diseases +MONDO:0004792 rare diseases +MONDO:0004795 otar diseases +MONDO:0004796 gard_rare diseases +MONDO:0004796 otar diseases +MONDO:0004796 rare diseases +MONDO:0004797 gard_rare diseases +MONDO:0004797 rare diseases +MONDO:0004802 gard_rare diseases +MONDO:0004802 nord_rare diseases +MONDO:0004802 rare diseases +MONDO:0004803 gard_rare diseases +MONDO:0004803 rare diseases +MONDO:0004804 otar diseases +MONDO:0004805 gard_rare diseases +MONDO:0004805 otar diseases +MONDO:0004805 rare diseases +MONDO:0004815 gard_rare diseases +MONDO:0004815 rare diseases +MONDO:0004816 gard_rare diseases +MONDO:0004816 rare diseases +MONDO:0004817 gard_rare diseases +MONDO:0004817 rare diseases +MONDO:0004819 gard_rare diseases +MONDO:0004819 rare diseases +MONDO:0004820 gard_rare diseases +MONDO:0004820 otar diseases +MONDO:0004820 rare diseases +MONDO:0004822 otar diseases +MONDO:0004828 otar diseases +MONDO:0004829 gard_rare diseases +MONDO:0004829 otar diseases +MONDO:0004829 rare diseases +MONDO:0004830 otar diseases +MONDO:0004836 gard_rare diseases +MONDO:0004836 rare diseases +MONDO:0004837 gard_rare diseases +MONDO:0004837 rare diseases +MONDO:0004842 otar diseases +MONDO:0004846 otar diseases +MONDO:0004847 otar diseases +MONDO:0004848 otar diseases +MONDO:0004849 otar diseases +MONDO:0004851 gard_rare diseases +MONDO:0004851 nord_rare diseases +MONDO:0004851 rare diseases +MONDO:0004852 gard_rare diseases +MONDO:0004852 rare diseases +MONDO:0004853 gard_rare diseases +MONDO:0004853 rare diseases +MONDO:0004854 gard_rare diseases +MONDO:0004854 rare diseases +MONDO:0004855 gard_rare diseases +MONDO:0004855 otar diseases +MONDO:0004855 rare diseases +MONDO:0004857 gard_rare diseases +MONDO:0004857 otar diseases +MONDO:0004857 rare diseases +MONDO:0004862 gard_rare diseases +MONDO:0004862 rare diseases +MONDO:0004863 gard_rare diseases +MONDO:0004863 rare diseases +MONDO:0004866 otar diseases +MONDO:0004867 otar diseases +MONDO:0004868 otar diseases +MONDO:0004872 otar diseases +MONDO:0004877 gard_rare diseases +MONDO:0004877 nord_rare diseases +MONDO:0004877 rare diseases +MONDO:0004880 otar diseases +MONDO:0004881 gard_rare diseases +MONDO:0004881 rare diseases +MONDO:0004882 gard_rare diseases +MONDO:0004882 rare diseases +MONDO:0004884 otar diseases +MONDO:0004885 otar diseases +MONDO:0004889 gard_rare diseases +MONDO:0004889 rare diseases +MONDO:0004890 gard_rare diseases +MONDO:0004890 rare diseases +MONDO:0004891 otar diseases +MONDO:0004892 otar diseases +MONDO:0004900 gard_rare diseases +MONDO:0004900 otar diseases +MONDO:0004900 rare diseases +MONDO:0004905 otar diseases +MONDO:0004907 disease_grouping diseases +MONDO:0004907 ordo_group_of_disorders diseases +MONDO:0004907 otar diseases +MONDO:0004924 gard_rare diseases +MONDO:0004924 rare diseases +MONDO:0004928 otar diseases +MONDO:0004932 gard_rare diseases +MONDO:0004932 rare diseases +MONDO:0004933 gard_rare diseases +MONDO:0004933 nord_rare diseases +MONDO:0004933 ordo_disorder diseases +MONDO:0004933 ordo_morphological_anomaly diseases +MONDO:0004933 orphanet_rare diseases +MONDO:0004933 otar diseases +MONDO:0004933 rare diseases +MONDO:0004938 otar diseases +MONDO:0004941 gard_rare diseases +MONDO:0004941 nord_rare diseases +MONDO:0004941 otar diseases +MONDO:0004941 rare diseases +MONDO:0004942 gard_rare diseases +MONDO:0004942 nord_rare diseases +MONDO:0004942 rare diseases +MONDO:0004943 gard_rare diseases +MONDO:0004943 rare diseases +MONDO:0004944 gard_rare diseases +MONDO:0004944 nord_rare diseases +MONDO:0004944 otar diseases +MONDO:0004944 rare diseases +MONDO:0004947 gard_rare diseases +MONDO:0004947 otar diseases +MONDO:0004947 rare diseases +MONDO:0004948 gard_rare diseases +MONDO:0004948 nord_rare diseases +MONDO:0004948 ordo_disorder diseases +MONDO:0004948 orphanet_rare diseases +MONDO:0004948 otar diseases +MONDO:0004948 rare diseases +MONDO:0004949 gard_rare diseases +MONDO:0004949 otar diseases +MONDO:0004949 rare diseases +MONDO:0004950 otar diseases +MONDO:0004952 disease_grouping diseases +MONDO:0004952 gard_rare diseases +MONDO:0004952 nord_rare diseases +MONDO:0004952 ordo_group_of_disorders diseases +MONDO:0004952 otar diseases +MONDO:0004952 rare diseases +MONDO:0004953 otar diseases +MONDO:0004956 otar diseases +MONDO:0004957 otar diseases +MONDO:0004958 gard_rare diseases +MONDO:0004958 nord_rare diseases +MONDO:0004958 ordo_disorder diseases +MONDO:0004958 orphanet_rare diseases +MONDO:0004958 otar diseases +MONDO:0004958 rare diseases +MONDO:0004959 disease_grouping diseases +MONDO:0004959 gard_rare diseases +MONDO:0004959 ordo_group_of_disorders diseases +MONDO:0004959 otar diseases +MONDO:0004959 rare diseases +MONDO:0004960 gard_rare diseases +MONDO:0004960 otar diseases +MONDO:0004960 rare diseases +MONDO:0004963 gard_rare diseases +MONDO:0004963 otar diseases +MONDO:0004963 rare diseases +MONDO:0004964 gard_rare diseases +MONDO:0004964 obsoletion_candidate diseases +MONDO:0004964 otar diseases +MONDO:0004964 rare diseases +MONDO:0004965 otar diseases +MONDO:0004966 otar diseases +MONDO:0004967 disease_grouping diseases +MONDO:0004967 gard_rare diseases +MONDO:0004967 nord_rare diseases +MONDO:0004967 ordo_group_of_disorders diseases +MONDO:0004967 otar diseases +MONDO:0004967 rare diseases +MONDO:0004969 gard_rare diseases +MONDO:0004969 otar diseases +MONDO:0004969 rare diseases +MONDO:0004970 otar diseases +MONDO:0004971 gard_rare diseases +MONDO:0004971 nord_rare diseases +MONDO:0004971 otar diseases +MONDO:0004971 rare diseases +MONDO:0004972 otar diseases +MONDO:0004973 otar diseases +MONDO:0004974 gard_rare diseases +MONDO:0004974 nord_rare diseases +MONDO:0004974 otar diseases +MONDO:0004974 rare diseases +MONDO:0004975 otar diseases +MONDO:0004976 clingen diseases +MONDO:0004976 gard_rare diseases +MONDO:0004976 nord_rare diseases +MONDO:0004976 ordo_disorder diseases +MONDO:0004976 orphanet_rare diseases +MONDO:0004976 otar diseases +MONDO:0004976 rare diseases +MONDO:0004977 gard_rare diseases +MONDO:0004977 nord_rare diseases +MONDO:0004977 ordo_disorder diseases +MONDO:0004977 orphanet_rare diseases +MONDO:0004977 otar diseases +MONDO:0004977 rare diseases +MONDO:0004979 otar diseases +MONDO:0004980 otar diseases +MONDO:0004981 otar diseases +MONDO:0004982 otar diseases +MONDO:0004983 otar diseases +MONDO:0004984 otar diseases +MONDO:0004985 otar diseases +MONDO:0004986 otar diseases +MONDO:0004987 otar diseases +MONDO:0004988 otar diseases +MONDO:0004989 otar diseases +MONDO:0004990 otar diseases +MONDO:0004991 gard_rare diseases +MONDO:0004991 otar diseases +MONDO:0004991 rare diseases +MONDO:0004992 otar diseases +MONDO:0004993 otar diseases +MONDO:0004994 disease_grouping diseases +MONDO:0004994 ordo_group_of_disorders diseases +MONDO:0004994 otar diseases +MONDO:0004995 otar diseases +MONDO:0004995 rare_grouping diseases +MONDO:0004996 gard_rare diseases +MONDO:0004996 otar diseases +MONDO:0004996 rare diseases +MONDO:0004997 gard_rare diseases +MONDO:0004997 nord_rare diseases +MONDO:0004997 otar diseases +MONDO:0004997 rare diseases +MONDO:0005001 otar diseases +MONDO:0005002 otar diseases +MONDO:0005003 otar diseases +MONDO:0005004 otar diseases +MONDO:0005005 gard_rare diseases +MONDO:0005005 nord_rare diseases +MONDO:0005005 ordo_disorder diseases +MONDO:0005005 orphanet_rare diseases +MONDO:0005005 otar diseases +MONDO:0005005 rare diseases +MONDO:0005006 gard_rare diseases +MONDO:0005006 nord_rare diseases +MONDO:0005006 ordo_disorder diseases +MONDO:0005006 orphanet_rare diseases +MONDO:0005006 otar diseases +MONDO:0005006 rare diseases +MONDO:0005007 otar diseases +MONDO:0005008 otar diseases +MONDO:0005009 otar diseases +MONDO:0005010 otar diseases +MONDO:0005011 otar diseases +MONDO:0005012 otar diseases +MONDO:0005013 gard_rare diseases +MONDO:0005013 otar diseases +MONDO:0005013 rare diseases +MONDO:0005015 otar diseases +MONDO:0005016 otar diseases +MONDO:0005017 otar diseases +MONDO:0005019 gard_rare diseases +MONDO:0005019 otar diseases +MONDO:0005019 rare diseases +MONDO:0005020 otar diseases +MONDO:0005020 rare_grouping diseases +MONDO:0005021 clingen diseases +MONDO:0005021 disease_grouping diseases +MONDO:0005021 gard_rare diseases +MONDO:0005021 nord_rare diseases +MONDO:0005021 ordo_group_of_disorders diseases +MONDO:0005021 otar diseases +MONDO:0005021 rare diseases +MONDO:0005023 otar diseases +MONDO:0005025 otar diseases +MONDO:0005026 otar diseases +MONDO:0005027 clingen diseases +MONDO:0005027 otar diseases +MONDO:0005028 gard_rare diseases +MONDO:0005028 nord_rare diseases +MONDO:0005028 ordo_disorder diseases +MONDO:0005028 orphanet_rare diseases +MONDO:0005028 otar diseases +MONDO:0005028 rare diseases +MONDO:0005029 gard_rare diseases +MONDO:0005029 nord_rare diseases +MONDO:0005029 ordo_disorder diseases +MONDO:0005029 orphanet_rare diseases +MONDO:0005029 otar diseases +MONDO:0005029 rare diseases +MONDO:0005030 otar diseases +MONDO:0005031 otar diseases +MONDO:0005032 gard_rare diseases +MONDO:0005032 otar diseases +MONDO:0005032 rare diseases +MONDO:0005033 gard_rare diseases +MONDO:0005033 nord_rare diseases +MONDO:0005033 ordo_disorder diseases +MONDO:0005033 orphanet_rare diseases +MONDO:0005033 otar diseases +MONDO:0005033 rare diseases +MONDO:0005034 gard_rare diseases +MONDO:0005034 otar diseases +MONDO:0005034 rare diseases +MONDO:0005035 gard_rare diseases +MONDO:0005035 nord_rare diseases +MONDO:0005035 ordo_disorder diseases +MONDO:0005035 orphanet_rare diseases +MONDO:0005035 otar diseases +MONDO:0005035 rare diseases +MONDO:0005036 otar diseases +MONDO:0005037 otar diseases +MONDO:0005039 otar diseases +MONDO:0005039 rare_grouping diseases +MONDO:0005040 gard_rare diseases +MONDO:0005040 nord_rare diseases +MONDO:0005040 otar diseases +MONDO:0005040 rare diseases +MONDO:0005041 otar diseases +MONDO:0005043 otar diseases +MONDO:0005044 otar diseases +MONDO:0005045 clingen diseases +MONDO:0005045 disease_grouping diseases +MONDO:0005045 nord_rare diseases +MONDO:0005045 ordo_group_of_disorders diseases +MONDO:0005045 otar diseases +MONDO:0005045 rare diseases +MONDO:0005046 otar diseases +MONDO:0005046 rare_grouping diseases +MONDO:0005047 otar diseases +MONDO:0005048 gard_rare diseases +MONDO:0005048 ordo_disorder diseases +MONDO:0005048 orphanet_rare diseases +MONDO:0005048 otar diseases +MONDO:0005048 rare diseases +MONDO:0005050 otar diseases +MONDO:0005051 otar diseases +MONDO:0005052 otar diseases +MONDO:0005053 otar diseases +MONDO:0005055 gard_rare diseases +MONDO:0005055 nord_rare diseases +MONDO:0005055 ordo_disorder diseases +MONDO:0005055 orphanet_rare diseases +MONDO:0005055 otar diseases +MONDO:0005055 rare diseases +MONDO:0005056 otar diseases +MONDO:0005057 gard_rare diseases +MONDO:0005057 otar diseases +MONDO:0005057 rare diseases +MONDO:0005058 gard_rare diseases +MONDO:0005058 nord_rare diseases +MONDO:0005058 ordo_disorder diseases +MONDO:0005058 orphanet_rare diseases +MONDO:0005058 otar diseases +MONDO:0005058 rare diseases +MONDO:0005059 gard_rare diseases +MONDO:0005059 otar diseases +MONDO:0005059 rare diseases +MONDO:0005060 gard_rare diseases +MONDO:0005060 nord_rare diseases +MONDO:0005060 ordo_disorder diseases +MONDO:0005060 orphanet_rare diseases +MONDO:0005060 otar diseases +MONDO:0005060 rare diseases +MONDO:0005061 nord_rare diseases +MONDO:0005061 otar diseases +MONDO:0005061 rare diseases +MONDO:0005062 disease_grouping diseases +MONDO:0005062 inferred_rare diseases +MONDO:0005062 ordo_group_of_disorders diseases +MONDO:0005062 otar diseases +MONDO:0005062 rare diseases +MONDO:0005063 otar diseases +MONDO:0005065 otar diseases +MONDO:0005066 harrisons_view diseases +MONDO:0005066 otar diseases +MONDO:0005066 rare_grouping diseases +MONDO:0005067 gard_rare diseases +MONDO:0005067 otar diseases +MONDO:0005067 rare diseases +MONDO:0005068 otar diseases +MONDO:0005070 otar diseases +MONDO:0005071 otar diseases +MONDO:0005071 rare_grouping diseases +MONDO:0005072 gard_rare diseases +MONDO:0005072 nord_rare diseases +MONDO:0005072 ordo_disorder diseases +MONDO:0005072 orphanet_rare diseases +MONDO:0005072 otar diseases +MONDO:0005072 rare diseases +MONDO:0005073 otar diseases +MONDO:0005074 otar diseases +MONDO:0005075 gard_rare diseases +MONDO:0005075 otar diseases +MONDO:0005075 rare diseases +MONDO:0005076 otar diseases +MONDO:0005077 gard_rare diseases +MONDO:0005077 nord_rare diseases +MONDO:0005077 ordo_disorder diseases +MONDO:0005077 orphanet_rare diseases +MONDO:0005077 otar diseases +MONDO:0005077 rare diseases +MONDO:0005078 otar diseases +MONDO:0005079 otar diseases +MONDO:0005080 otar diseases +MONDO:0005081 gard_rare diseases +MONDO:0005081 ordo_disorder diseases +MONDO:0005081 orphanet_rare diseases +MONDO:0005081 otar diseases +MONDO:0005081 rare diseases +MONDO:0005082 otar diseases +MONDO:0005083 otar diseases +MONDO:0005084 otar diseases +MONDO:0005085 otar diseases +MONDO:0005086 disease_grouping diseases +MONDO:0005086 gard_rare diseases +MONDO:0005086 nord_rare diseases +MONDO:0005086 ordo_group_of_disorders diseases +MONDO:0005086 otar diseases +MONDO:0005086 rare diseases +MONDO:0005087 otar diseases +MONDO:0005087 rare_grouping diseases +MONDO:0005089 otar diseases +MONDO:0005090 otar diseases +MONDO:0005091 gard_rare diseases +MONDO:0005091 nord_rare diseases +MONDO:0005091 ordo_disorder diseases +MONDO:0005091 orphanet_rare diseases +MONDO:0005091 otar diseases +MONDO:0005091 rare diseases +MONDO:0005092 otar diseases +MONDO:0005093 otar diseases +MONDO:0005093 rare_grouping diseases +MONDO:0005094 otar diseases +MONDO:0005095 otar diseases +MONDO:0005096 otar diseases +MONDO:0005097 otar diseases +MONDO:0005098 otar diseases +MONDO:0005099 otar diseases +MONDO:0005100 gard_rare diseases +MONDO:0005100 nord_rare diseases +MONDO:0005100 ordo_disorder diseases +MONDO:0005100 orphanet_rare diseases +MONDO:0005100 otar diseases +MONDO:0005100 rare diseases +MONDO:0005101 otar diseases +MONDO:0005102 gard_rare diseases +MONDO:0005102 otar diseases +MONDO:0005102 rare diseases +MONDO:0005103 gard_rare diseases +MONDO:0005103 nord_rare diseases +MONDO:0005103 ordo_histopathological_subtype diseases +MONDO:0005103 ordo_subtype_of_a_disorder diseases +MONDO:0005103 otar diseases +MONDO:0005103 rare diseases +MONDO:0005105 otar diseases +MONDO:0005106 otar diseases +MONDO:0005108 otar diseases +MONDO:0005109 otar diseases +MONDO:0005110 gard_rare diseases +MONDO:0005110 otar diseases +MONDO:0005110 rare diseases +MONDO:0005111 otar diseases +MONDO:0005112 gard_rare diseases +MONDO:0005112 otar diseases +MONDO:0005112 rare diseases +MONDO:0005113 otar diseases +MONDO:0005114 otar diseases +MONDO:0005115 gard_rare diseases +MONDO:0005115 ordo_disorder diseases +MONDO:0005115 orphanet_rare diseases +MONDO:0005115 otar diseases +MONDO:0005115 rare diseases +MONDO:0005116 gard_rare diseases +MONDO:0005116 nord_rare diseases +MONDO:0005116 ordo_disorder diseases +MONDO:0005116 orphanet_rare diseases +MONDO:0005116 otar diseases +MONDO:0005116 rare diseases +MONDO:0005117 otar diseases +MONDO:0005118 gard_rare diseases +MONDO:0005118 otar diseases +MONDO:0005118 rare diseases +MONDO:0005119 otar diseases +MONDO:0005120 otar diseases +MONDO:0005121 otar diseases +MONDO:0005122 otar diseases +MONDO:0005124 gard_rare diseases +MONDO:0005124 nord_rare diseases +MONDO:0005124 ordo_disorder diseases +MONDO:0005124 orphanet_rare diseases +MONDO:0005124 otar diseases +MONDO:0005124 rare diseases +MONDO:0005125 gard_rare diseases +MONDO:0005125 otar diseases +MONDO:0005125 rare diseases +MONDO:0005126 gard_rare diseases +MONDO:0005126 otar diseases +MONDO:0005126 rare diseases +MONDO:0005127 gard_rare diseases +MONDO:0005127 otar diseases +MONDO:0005127 rare diseases +MONDO:0005129 otar diseases +MONDO:0005130 otar diseases +MONDO:0005131 otar diseases +MONDO:0005132 otar diseases +MONDO:0005133 otar diseases +MONDO:0005134 otar diseases +MONDO:0005135 otar diseases +MONDO:0005136 gard_rare diseases +MONDO:0005136 nord_rare diseases +MONDO:0005136 ordo_disorder diseases +MONDO:0005136 orphanet_rare diseases +MONDO:0005136 otar diseases +MONDO:0005136 rare diseases +MONDO:0005137 harrisons_view diseases +MONDO:0005137 otar diseases +MONDO:0005137 rare_grouping diseases +MONDO:0005138 otar diseases +MONDO:0005139 otar diseases +MONDO:0005140 gard_rare diseases +MONDO:0005140 otar diseases +MONDO:0005140 rare diseases +MONDO:0005141 otar diseases +MONDO:0005143 otar diseases +MONDO:0005144 clingen diseases +MONDO:0005144 gard_rare diseases +MONDO:0005144 nord_rare diseases +MONDO:0005144 otar diseases +MONDO:0005144 rare diseases +MONDO:0005145 gard_rare diseases +MONDO:0005145 nord_rare diseases +MONDO:0005145 otar diseases +MONDO:0005145 rare diseases +MONDO:0005146 otar diseases +MONDO:0005147 otar diseases +MONDO:0005148 otar diseases +MONDO:0005149 otar diseases +MONDO:0005150 inferred_rare diseases +MONDO:0005150 otar diseases +MONDO:0005150 rare diseases +MONDO:0005151 harrisons_view diseases +MONDO:0005151 otar diseases +MONDO:0005151 rare_grouping diseases +MONDO:0005152 otar diseases +MONDO:0005153 gard_rare diseases +MONDO:0005153 nord_rare diseases +MONDO:0005153 ordo_disorder diseases +MONDO:0005153 orphanet_rare diseases +MONDO:0005153 otar diseases +MONDO:0005153 rare diseases +MONDO:0005154 otar diseases +MONDO:0005155 otar diseases +MONDO:0005156 otar diseases +MONDO:0005157 gard_rare diseases +MONDO:0005157 otar diseases +MONDO:0005157 rare diseases +MONDO:0005159 otar diseases +MONDO:0005160 otar diseases +MONDO:0005161 otar diseases +MONDO:0005163 otar diseases +MONDO:0005164 gard_rare diseases +MONDO:0005164 nord_rare diseases +MONDO:0005164 ordo_disorder diseases +MONDO:0005164 orphanet_rare diseases +MONDO:0005164 otar diseases +MONDO:0005164 rare diseases +MONDO:0005165 otar diseases +MONDO:0005166 gard_rare diseases +MONDO:0005166 otar diseases +MONDO:0005166 rare diseases +MONDO:0005167 otar diseases +MONDO:0005168 gard_rare diseases +MONDO:0005168 rare diseases +MONDO:0005169 gard_rare diseases +MONDO:0005169 otar diseases +MONDO:0005169 rare diseases +MONDO:0005170 gard_rare diseases +MONDO:0005170 otar diseases +MONDO:0005170 rare diseases +MONDO:0005172 otar diseases +MONDO:0005172 rare_grouping diseases +MONDO:0005173 otar diseases +MONDO:0005174 otar diseases +MONDO:0005177 otar diseases +MONDO:0005178 otar diseases +MONDO:0005180 clingen diseases +MONDO:0005180 otar diseases +MONDO:0005181 disease_grouping diseases +MONDO:0005181 gard_rare diseases +MONDO:0005181 ordo_group_of_disorders diseases +MONDO:0005181 otar diseases +MONDO:0005181 rare diseases +MONDO:0005182 otar diseases +MONDO:0005183 otar diseases +MONDO:0005184 otar diseases +MONDO:0005186 otar diseases +MONDO:0005187 otar diseases +MONDO:0005188 gard_rare diseases +MONDO:0005188 rare diseases +MONDO:0005189 otar diseases +MONDO:0005191 otar diseases +MONDO:0005192 otar diseases +MONDO:0005193 otar diseases +MONDO:0005194 otar diseases +MONDO:0005195 otar diseases +MONDO:0005197 disease_grouping diseases +MONDO:0005197 gard_rare diseases +MONDO:0005197 nord_rare diseases +MONDO:0005197 ordo_group_of_disorders diseases +MONDO:0005197 otar diseases +MONDO:0005197 rare diseases +MONDO:0005198 gard_rare diseases +MONDO:0005198 nord_rare diseases +MONDO:0005198 ordo_disorder diseases +MONDO:0005198 orphanet_rare diseases +MONDO:0005198 otar diseases +MONDO:0005198 rare diseases +MONDO:0005200 gard_rare diseases +MONDO:0005200 otar diseases +MONDO:0005200 rare diseases +MONDO:0005201 disease_grouping diseases +MONDO:0005201 gard_rare diseases +MONDO:0005201 nord_rare diseases +MONDO:0005201 ordo_group_of_disorders diseases +MONDO:0005201 otar diseases +MONDO:0005201 rare diseases +MONDO:0005202 otar diseases +MONDO:0005204 gard_rare diseases +MONDO:0005204 rare diseases +MONDO:0005206 otar diseases +MONDO:0005207 gard_rare diseases +MONDO:0005207 nord_rare diseases +MONDO:0005207 otar diseases +MONDO:0005207 rare diseases +MONDO:0005208 otar diseases +MONDO:0005210 disease_grouping diseases +MONDO:0005210 gard_rare diseases +MONDO:0005210 nord_rare diseases +MONDO:0005210 ordo_group_of_disorders diseases +MONDO:0005210 otar diseases +MONDO:0005210 rare diseases +MONDO:0005211 gard_rare diseases +MONDO:0005211 otar diseases +MONDO:0005211 rare diseases +MONDO:0005212 gard_rare diseases +MONDO:0005212 nord_rare diseases +MONDO:0005212 ordo_disorder diseases +MONDO:0005212 orphanet_rare diseases +MONDO:0005212 otar diseases +MONDO:0005212 rare diseases +MONDO:0005213 otar diseases +MONDO:0005214 gard_rare diseases +MONDO:0005214 rare diseases +MONDO:0005215 gard_rare diseases +MONDO:0005215 nord_rare diseases +MONDO:0005215 ordo_disorder diseases +MONDO:0005215 orphanet_rare diseases +MONDO:0005215 otar diseases +MONDO:0005215 rare diseases +MONDO:0005216 otar diseases +MONDO:0005217 gard_rare diseases +MONDO:0005217 otar diseases +MONDO:0005217 rare diseases +MONDO:0005219 otar diseases +MONDO:0005220 gard_rare diseases +MONDO:0005220 nord_rare diseases +MONDO:0005220 ordo_disorder diseases +MONDO:0005220 orphanet_rare diseases +MONDO:0005220 otar diseases +MONDO:0005220 rare diseases +MONDO:0005221 gard_rare diseases +MONDO:0005221 otar diseases +MONDO:0005221 rare diseases +MONDO:0005223 gard_rare diseases +MONDO:0005223 nord_rare diseases +MONDO:0005223 ordo_disorder diseases +MONDO:0005223 orphanet_rare diseases +MONDO:0005223 otar diseases +MONDO:0005223 rare diseases +MONDO:0005224 gard_rare diseases +MONDO:0005224 nord_rare diseases +MONDO:0005224 ordo_disorder diseases +MONDO:0005224 orphanet_rare diseases +MONDO:0005224 otar diseases +MONDO:0005224 rare diseases +MONDO:0005227 otar diseases +MONDO:0005229 otar diseases +MONDO:0005230 otar diseases +MONDO:0005231 otar diseases +MONDO:0005232 otar diseases +MONDO:0005233 clingen diseases +MONDO:0005233 otar diseases +MONDO:0005235 gard_rare diseases +MONDO:0005235 otar diseases +MONDO:0005235 rare diseases +MONDO:0005236 otar diseases +MONDO:0005238 gard_rare diseases +MONDO:0005238 otar diseases +MONDO:0005238 rare diseases +MONDO:0005240 clingen diseases +MONDO:0005240 otar diseases +MONDO:0005242 otar diseases +MONDO:0005244 gard_rare diseases +MONDO:0005244 otar diseases +MONDO:0005244 rare diseases +MONDO:0005246 gard_rare diseases +MONDO:0005246 otar diseases +MONDO:0005246 rare diseases +MONDO:0005247 otar diseases +MONDO:0005249 otar diseases +MONDO:0005250 otar diseases +MONDO:0005252 otar diseases +MONDO:0005253 otar diseases +MONDO:0005254 otar diseases +MONDO:0005255 otar diseases +MONDO:0005256 otar diseases +MONDO:0005257 otar diseases +MONDO:0005258 clingen diseases +MONDO:0005258 inferred_rare diseases +MONDO:0005258 otar diseases +MONDO:0005258 rare diseases +MONDO:0005259 inferred_rare diseases +MONDO:0005259 otar diseases +MONDO:0005259 rare diseases +MONDO:0005260 inferred_rare diseases +MONDO:0005260 otar diseases +MONDO:0005260 rare diseases +MONDO:0005262 otar diseases +MONDO:0005264 otar diseases +MONDO:0005265 otar diseases +MONDO:0005266 otar diseases +MONDO:0005267 otar diseases +MONDO:0005267 rare_grouping diseases +MONDO:0005269 otar diseases +MONDO:0005271 otar diseases +MONDO:0005272 gard_rare diseases +MONDO:0005272 nord_rare diseases +MONDO:0005272 ordo_disorder diseases +MONDO:0005272 orphanet_rare diseases +MONDO:0005272 otar diseases +MONDO:0005272 rare diseases +MONDO:0005275 otar diseases +MONDO:0005276 otar diseases +MONDO:0005277 gard_rare diseases +MONDO:0005277 otar diseases +MONDO:0005277 rare diseases +MONDO:0005278 otar diseases +MONDO:0005279 otar diseases +MONDO:0005280 otar diseases +MONDO:0005281 otar diseases +MONDO:0005282 gard_rare diseases +MONDO:0005282 nord_rare diseases +MONDO:0005282 otar diseases +MONDO:0005282 rare diseases +MONDO:0005283 otar diseases +MONDO:0005284 otar diseases +MONDO:0005286 otar diseases +MONDO:0005287 otar diseases +MONDO:0005288 otar diseases +MONDO:0005289 gard_rare diseases +MONDO:0005289 otar diseases +MONDO:0005289 rare diseases +MONDO:0005291 otar diseases +MONDO:0005292 otar diseases +MONDO:0005293 otar diseases +MONDO:0005294 otar diseases +MONDO:0005295 otar diseases +MONDO:0005296 otar diseases +MONDO:0005297 otar diseases +MONDO:0005298 gard_rare diseases +MONDO:0005298 otar diseases +MONDO:0005298 rare diseases +MONDO:0005299 otar diseases +MONDO:0005300 otar diseases +MONDO:0005301 otar diseases +MONDO:0005303 otar diseases +MONDO:0005304 otar diseases +MONDO:0005306 otar diseases +MONDO:0005308 clingen diseases +MONDO:0005308 disease_grouping diseases +MONDO:0005308 gard_rare diseases +MONDO:0005308 ordo_group_of_disorders diseases +MONDO:0005308 otar diseases +MONDO:0005308 rare diseases +MONDO:0005310 otar diseases +MONDO:0005311 otar diseases +MONDO:0005312 gard_rare diseases +MONDO:0005312 nord_rare diseases +MONDO:0005312 ordo_disorder diseases +MONDO:0005312 orphanet_rare diseases +MONDO:0005312 otar diseases +MONDO:0005312 rare diseases +MONDO:0005313 gard_rare diseases +MONDO:0005313 nord_rare diseases +MONDO:0005313 ordo_disorder diseases +MONDO:0005313 orphanet_rare diseases +MONDO:0005313 otar diseases +MONDO:0005313 rare diseases +MONDO:0005314 otar diseases +MONDO:0005316 otar diseases +MONDO:0005318 otar diseases +MONDO:0005321 gard_rare diseases +MONDO:0005321 nord_rare diseases +MONDO:0005321 ordo_disorder diseases +MONDO:0005321 orphanet_rare diseases +MONDO:0005321 otar diseases +MONDO:0005321 rare diseases +MONDO:0005323 otar diseases +MONDO:0005324 otar diseases +MONDO:0005326 otar diseases +MONDO:0005328 otar diseases +MONDO:0005333 otar diseases +MONDO:0005335 otar diseases +MONDO:0005336 gard_rare diseases +MONDO:0005336 otar diseases +MONDO:0005336 rare diseases +MONDO:0005338 otar diseases +MONDO:0005339 gard_rare diseases +MONDO:0005339 otar diseases +MONDO:0005339 rare diseases +MONDO:0005340 gard_rare diseases +MONDO:0005340 nord_rare diseases +MONDO:0005340 otar diseases +MONDO:0005340 rare diseases +MONDO:0005341 otar diseases +MONDO:0005342 gard_rare diseases +MONDO:0005342 nord_rare diseases +MONDO:0005342 ordo_disorder diseases +MONDO:0005342 orphanet_rare diseases +MONDO:0005342 otar diseases +MONDO:0005342 rare diseases +MONDO:0005344 otar diseases +MONDO:0005345 ordo_morphological_anomaly diseases +MONDO:0005345 otar diseases +MONDO:0005346 otar diseases +MONDO:0005347 otar diseases +MONDO:0005348 otar diseases +MONDO:0005349 inferred_rare diseases +MONDO:0005349 otar diseases +MONDO:0005349 rare diseases +MONDO:0005350 otar diseases +MONDO:0005351 otar diseases +MONDO:0005352 otar diseases +MONDO:0005354 otar diseases +MONDO:0005355 otar diseases +MONDO:0005356 otar diseases +MONDO:0005357 gard_rare diseases +MONDO:0005357 nord_rare diseases +MONDO:0005357 otar diseases +MONDO:0005357 rare diseases +MONDO:0005358 gard_rare diseases +MONDO:0005358 otar diseases +MONDO:0005358 rare diseases +MONDO:0005359 otar diseases +MONDO:0005361 inferred_rare diseases +MONDO:0005361 otar diseases +MONDO:0005361 rare diseases +MONDO:0005362 otar diseases +MONDO:0005363 gard_rare diseases +MONDO:0005363 rare diseases +MONDO:0005364 otar diseases +MONDO:0005365 clingen diseases +MONDO:0005365 otar diseases +MONDO:0005366 otar diseases +MONDO:0005367 otar diseases +MONDO:0005369 gard_rare diseases +MONDO:0005369 otar diseases +MONDO:0005369 rare diseases +MONDO:0005371 otar diseases +MONDO:0005372 otar diseases +MONDO:0005373 otar diseases +MONDO:0005374 gard_rare diseases +MONDO:0005374 otar diseases +MONDO:0005374 rare diseases +MONDO:0005375 otar diseases +MONDO:0005376 gard_rare diseases +MONDO:0005376 otar diseases +MONDO:0005376 rare diseases +MONDO:0005377 otar diseases +MONDO:0005379 otar diseases +MONDO:0005380 disease_grouping diseases +MONDO:0005380 gard_rare diseases +MONDO:0005380 nord_rare diseases +MONDO:0005380 ordo_group_of_disorders diseases +MONDO:0005380 otar diseases +MONDO:0005380 rare diseases +MONDO:0005381 disease_grouping diseases +MONDO:0005381 otar diseases +MONDO:0005382 otar diseases +MONDO:0005383 otar diseases +MONDO:0005384 clingen diseases +MONDO:0005384 otar diseases +MONDO:0005385 otar diseases +MONDO:0005385 rare_grouping diseases +MONDO:0005386 otar diseases +MONDO:0005387 otar diseases +MONDO:0005388 gard_rare diseases +MONDO:0005388 nord_rare diseases +MONDO:0005388 ordo_disorder diseases +MONDO:0005388 orphanet_rare diseases +MONDO:0005388 otar diseases +MONDO:0005388 rare diseases +MONDO:0005391 otar diseases +MONDO:0005392 otar diseases +MONDO:0005393 otar diseases +MONDO:0005394 otar diseases +MONDO:0005395 clingen diseases +MONDO:0005395 otar diseases +MONDO:0005396 otar diseases +MONDO:0005397 otar diseases +MONDO:0005398 otar diseases +MONDO:0005399 otar diseases +MONDO:0005401 otar diseases +MONDO:0005402 gard_rare diseases +MONDO:0005402 otar diseases +MONDO:0005402 rare diseases +MONDO:0005404 otar diseases +MONDO:0005405 otar diseases +MONDO:0005406 otar diseases +MONDO:0005407 gard_rare diseases +MONDO:0005407 rare diseases +MONDO:0005408 otar diseases +MONDO:0005411 gard_rare diseases +MONDO:0005411 nord_rare diseases +MONDO:0005411 otar diseases +MONDO:0005411 rare diseases +MONDO:0005412 otar diseases +MONDO:0005413 otar diseases +MONDO:0005414 otar diseases +MONDO:0005416 otar diseases +MONDO:0005417 gard_rare diseases +MONDO:0005417 otar diseases +MONDO:0005417 rare diseases +MONDO:0005418 gard_rare diseases +MONDO:0005418 otar diseases +MONDO:0005418 rare diseases +MONDO:0005419 otar diseases +MONDO:0005420 otar diseases +MONDO:0005424 otar diseases +MONDO:0005425 otar diseases +MONDO:0005429 gard_rare diseases +MONDO:0005429 otar diseases +MONDO:0005429 rare diseases +MONDO:0005430 otar diseases +MONDO:0005433 otar diseases +MONDO:0005434 gard_rare diseases +MONDO:0005434 otar diseases +MONDO:0005434 rare diseases +MONDO:0005435 otar diseases +MONDO:0005437 gard_rare diseases +MONDO:0005437 otar diseases +MONDO:0005437 rare diseases +MONDO:0005438 gard_rare diseases +MONDO:0005438 otar diseases +MONDO:0005438 rare diseases +MONDO:0005439 gard_rare diseases +MONDO:0005439 otar diseases +MONDO:0005439 rare diseases +MONDO:0005440 gard_rare diseases +MONDO:0005440 nord_rare diseases +MONDO:0005440 ordo_disorder diseases +MONDO:0005440 orphanet_rare diseases +MONDO:0005440 otar diseases +MONDO:0005440 rare diseases +MONDO:0005441 otar diseases +MONDO:0005445 gard_rare diseases +MONDO:0005445 otar diseases +MONDO:0005445 rare diseases +MONDO:0005446 gard_rare diseases +MONDO:0005446 otar diseases +MONDO:0005446 rare diseases +MONDO:0005447 otar diseases +MONDO:0005448 otar diseases +MONDO:0005449 otar diseases +MONDO:0005451 otar diseases +MONDO:0005452 otar diseases +MONDO:0005453 clingen diseases +MONDO:0005453 otar diseases +MONDO:0005454 gard_rare diseases +MONDO:0005454 otar diseases +MONDO:0005454 rare diseases +MONDO:0005459 gard_rare diseases +MONDO:0005459 nord_rare diseases +MONDO:0005459 ordo_disorder diseases +MONDO:0005459 orphanet_rare diseases +MONDO:0005459 otar diseases +MONDO:0005459 rare diseases +MONDO:0005460 otar diseases +MONDO:0005461 otar diseases +MONDO:0005462 otar diseases +MONDO:0005463 otar diseases +MONDO:0005464 otar diseases +MONDO:0005465 otar diseases +MONDO:0005466 otar diseases +MONDO:0005468 otar diseases +MONDO:0005469 otar diseases +MONDO:0005473 otar diseases +MONDO:0005475 gard_rare diseases +MONDO:0005475 nord_rare diseases +MONDO:0005475 otar diseases +MONDO:0005475 rare diseases +MONDO:0005476 otar diseases +MONDO:0005477 otar diseases +MONDO:0005478 otar diseases +MONDO:0005479 otar diseases +MONDO:0005480 otar diseases +MONDO:0005483 gard_rare diseases +MONDO:0005483 otar diseases +MONDO:0005483 rare diseases +MONDO:0005484 otar diseases +MONDO:0005485 otar diseases +MONDO:0005486 gard_rare diseases +MONDO:0005486 ordo_disorder diseases +MONDO:0005486 ordo_morphological_anomaly diseases +MONDO:0005486 orphanet_rare diseases +MONDO:0005486 otar diseases +MONDO:0005486 rare diseases +MONDO:0005487 otar diseases +MONDO:0005488 otar diseases +MONDO:0005489 otar diseases +MONDO:0005490 otar diseases +MONDO:0005491 gard_rare diseases +MONDO:0005491 otar diseases +MONDO:0005491 rare diseases +MONDO:0005492 otar diseases +MONDO:0005494 otar diseases +MONDO:0005495 otar diseases +MONDO:0005496 gard_rare diseases +MONDO:0005496 otar diseases +MONDO:0005496 rare diseases +MONDO:0005497 otar diseases +MONDO:0005498 gard_rare diseases +MONDO:0005498 nord_rare diseases +MONDO:0005498 ordo_disorder diseases +MONDO:0005498 orphanet_rare diseases +MONDO:0005498 otar diseases +MONDO:0005498 rare diseases +MONDO:0005499 gard_rare diseases +MONDO:0005499 nord_rare diseases +MONDO:0005499 otar diseases +MONDO:0005499 rare diseases +MONDO:0005500 gard_rare diseases +MONDO:0005500 otar diseases +MONDO:0005500 rare diseases +MONDO:0005501 clingen diseases +MONDO:0005501 gard_rare diseases +MONDO:0005501 otar diseases +MONDO:0005501 rare diseases +MONDO:0005502 gard_rare diseases +MONDO:0005502 nord_rare diseases +MONDO:0005502 ordo_disorder diseases +MONDO:0005502 orphanet_rare diseases +MONDO:0005502 otar diseases +MONDO:0005502 rare diseases +MONDO:0005503 otar diseases +MONDO:0005504 gard_rare diseases +MONDO:0005504 nord_rare diseases +MONDO:0005504 ordo_disorder diseases +MONDO:0005504 orphanet_rare diseases +MONDO:0005504 otar diseases +MONDO:0005504 rare diseases +MONDO:0005505 gard_rare diseases +MONDO:0005505 nord_rare diseases +MONDO:0005505 ordo_disorder diseases +MONDO:0005505 orphanet_rare diseases +MONDO:0005505 otar diseases +MONDO:0005505 rare diseases +MONDO:0005507 gard_rare diseases +MONDO:0005507 otar diseases +MONDO:0005507 rare diseases +MONDO:0005508 gard_rare diseases +MONDO:0005508 nord_rare diseases +MONDO:0005508 ordo_disorder diseases +MONDO:0005508 orphanet_rare diseases +MONDO:0005508 otar diseases +MONDO:0005508 rare diseases +MONDO:0005509 otar diseases +MONDO:0005510 otar diseases +MONDO:0005511 gard_rare diseases +MONDO:0005511 nord_rare diseases +MONDO:0005511 otar diseases +MONDO:0005511 rare diseases +MONDO:0005512 gard_rare diseases +MONDO:0005512 nord_rare diseases +MONDO:0005512 ordo_disorder diseases +MONDO:0005512 orphanet_rare diseases +MONDO:0005512 otar diseases +MONDO:0005512 rare diseases +MONDO:0005514 gard_rare diseases +MONDO:0005514 nord_rare diseases +MONDO:0005514 ordo_disorder diseases +MONDO:0005514 ordo_malformation_syndrome diseases +MONDO:0005514 orphanet_rare diseases +MONDO:0005514 otar diseases +MONDO:0005514 rare diseases +MONDO:0005515 otar diseases +MONDO:0005516 otar diseases +MONDO:0005517 otar diseases +MONDO:0005518 gard_rare diseases +MONDO:0005518 otar diseases +MONDO:0005518 rare diseases +MONDO:0005519 otar diseases +MONDO:0005520 gard_rare diseases +MONDO:0005520 nord_rare diseases +MONDO:0005520 otar diseases +MONDO:0005520 rare diseases +MONDO:0005522 gard_rare diseases +MONDO:0005522 otar diseases +MONDO:0005522 rare diseases +MONDO:0005523 gard_rare diseases +MONDO:0005523 otar diseases +MONDO:0005523 rare diseases +MONDO:0005524 otar diseases +MONDO:0005525 gard_rare diseases +MONDO:0005525 otar diseases +MONDO:0005525 rare diseases +MONDO:0005526 gard_rare diseases +MONDO:0005526 nord_rare diseases +MONDO:0005526 ordo_disorder diseases +MONDO:0005526 orphanet_rare diseases +MONDO:0005526 otar diseases +MONDO:0005526 rare diseases +MONDO:0005527 otar diseases +MONDO:0005528 gard_rare diseases +MONDO:0005528 otar diseases +MONDO:0005528 rare diseases +MONDO:0005530 otar diseases +MONDO:0005531 otar diseases +MONDO:0005532 otar diseases +MONDO:0005533 otar diseases +MONDO:0005534 otar diseases +MONDO:0005536 otar diseases +MONDO:0005537 otar diseases +MONDO:0005538 otar diseases +MONDO:0005539 otar diseases +MONDO:0005541 otar diseases +MONDO:0005542 otar diseases +MONDO:0005543 gard_rare diseases +MONDO:0005543 nord_rare diseases +MONDO:0005543 ordo_subtype_of_a_disorder diseases +MONDO:0005543 rare diseases +MONDO:0005544 otar diseases +MONDO:0005545 otar diseases +MONDO:0005546 otar diseases +MONDO:0005549 gard_rare diseases +MONDO:0005549 otar diseases +MONDO:0005549 rare diseases +MONDO:0005550 otar diseases +MONDO:0005550 rare_grouping diseases +MONDO:0005551 otar diseases +MONDO:0005552 otar diseases +MONDO:0005554 otar diseases +MONDO:0005555 otar diseases +MONDO:0005556 gard_rare diseases +MONDO:0005556 nord_rare diseases +MONDO:0005556 otar diseases +MONDO:0005556 rare diseases +MONDO:0005557 otar diseases +MONDO:0005558 otar diseases +MONDO:0005559 merged_class diseases +MONDO:0005559 otar diseases +MONDO:0005560 otar diseases +MONDO:0005561 otar diseases +MONDO:0005563 gard_rare diseases +MONDO:0005563 nord_rare diseases +MONDO:0005563 ordo_disorder diseases +MONDO:0005563 orphanet_rare diseases +MONDO:0005563 otar diseases +MONDO:0005563 rare diseases +MONDO:0005564 otar diseases +MONDO:0005565 otar diseases +MONDO:0005566 otar diseases +MONDO:0005567 otar diseases +MONDO:0005568 otar diseases +MONDO:0005570 disease_grouping diseases +MONDO:0005570 ordo_group_of_disorders diseases +MONDO:0005570 otar diseases +MONDO:0005570 rare_grouping diseases +MONDO:0005571 disease_grouping diseases +MONDO:0005571 gard_rare diseases +MONDO:0005571 ordo_group_of_disorders diseases +MONDO:0005571 otar diseases +MONDO:0005571 rare diseases +MONDO:0005572 gard_rare diseases +MONDO:0005572 rare diseases +MONDO:0005574 otar diseases +MONDO:0005575 otar diseases +MONDO:0005576 otar diseases +MONDO:0005578 otar diseases +MONDO:0005579 otar diseases +MONDO:0005580 gard_rare diseases +MONDO:0005580 nord_rare diseases +MONDO:0005580 ordo_disorder diseases +MONDO:0005580 orphanet_rare diseases +MONDO:0005580 otar diseases +MONDO:0005580 rare diseases +MONDO:0005582 otar diseases +MONDO:0005583 otar diseases +MONDO:0005584 gard_rare diseases +MONDO:0005584 otar diseases +MONDO:0005584 rare diseases +MONDO:0005586 otar diseases +MONDO:0005589 otar diseases +MONDO:0005590 otar diseases +MONDO:0005593 otar diseases +MONDO:0005594 otar diseases +MONDO:0005595 gard_rare diseases +MONDO:0005595 nord_rare diseases +MONDO:0005595 ordo_disorder diseases +MONDO:0005595 orphanet_rare diseases +MONDO:0005595 otar diseases +MONDO:0005595 rare diseases +MONDO:0005596 otar diseases +MONDO:0005597 gard_rare diseases +MONDO:0005597 otar diseases +MONDO:0005597 rare diseases +MONDO:0005598 gard_rare diseases +MONDO:0005598 otar diseases +MONDO:0005598 rare diseases +MONDO:0005599 gard_rare diseases +MONDO:0005599 otar diseases +MONDO:0005599 rare diseases +MONDO:0005601 gard_rare diseases +MONDO:0005601 nord_rare diseases +MONDO:0005601 ordo_disorder diseases +MONDO:0005601 orphanet_rare diseases +MONDO:0005601 otar diseases +MONDO:0005601 rare diseases +MONDO:0005602 gard_rare diseases +MONDO:0005602 otar diseases +MONDO:0005602 rare diseases +MONDO:0005605 otar diseases +MONDO:0005606 otar diseases +MONDO:0005607 otar diseases +MONDO:0005608 otar diseases +MONDO:0005609 otar diseases +MONDO:0005610 otar diseases +MONDO:0005611 gard_rare diseases +MONDO:0005611 otar diseases +MONDO:0005611 rare diseases +MONDO:0005613 otar diseases +MONDO:0005614 gard_rare diseases +MONDO:0005614 otar diseases +MONDO:0005614 rare diseases +MONDO:0005615 gard_rare diseases +MONDO:0005615 nord_rare diseases +MONDO:0005615 ordo_disorder diseases +MONDO:0005615 orphanet_rare diseases +MONDO:0005615 otar diseases +MONDO:0005615 rare diseases +MONDO:0005616 gard_rare diseases +MONDO:0005616 otar diseases +MONDO:0005616 rare diseases +MONDO:0005617 otar diseases +MONDO:0005618 otar diseases +MONDO:0005619 gard_rare diseases +MONDO:0005619 nord_rare diseases +MONDO:0005619 ordo_disorder diseases +MONDO:0005619 orphanet_rare diseases +MONDO:0005619 otar diseases +MONDO:0005619 rare diseases +MONDO:0005620 gard_rare diseases +MONDO:0005620 nord_rare diseases +MONDO:0005620 ordo_disorder diseases +MONDO:0005620 orphanet_rare diseases +MONDO:0005620 otar diseases +MONDO:0005620 rare diseases +MONDO:0005621 otar diseases +MONDO:0005623 otar diseases +MONDO:0005624 otar diseases +MONDO:0005625 gard_rare diseases +MONDO:0005625 otar diseases +MONDO:0005625 rare diseases +MONDO:0005626 otar diseases +MONDO:0005627 otar diseases +MONDO:0005628 otar diseases +MONDO:0005629 gard_rare diseases +MONDO:0005629 nord_rare diseases +MONDO:0005629 ordo_disorder diseases +MONDO:0005629 orphanet_rare diseases +MONDO:0005629 otar diseases +MONDO:0005629 rare diseases +MONDO:0005631 gard_rare diseases +MONDO:0005631 nord_rare diseases +MONDO:0005631 ordo_disorder diseases +MONDO:0005631 orphanet_rare diseases +MONDO:0005631 otar diseases +MONDO:0005631 rare diseases +MONDO:0005632 otar diseases +MONDO:0005634 otar diseases +MONDO:0005635 otar diseases +MONDO:0005636 otar diseases +MONDO:0005638 otar diseases +MONDO:0005639 otar diseases +MONDO:0005640 otar diseases +MONDO:0005641 otar diseases +MONDO:0005642 otar diseases +MONDO:0005643 otar diseases +MONDO:0005644 otar diseases +MONDO:0005645 gard_rare diseases +MONDO:0005645 nord_rare diseases +MONDO:0005645 ordo_disorder diseases +MONDO:0005645 orphanet_rare diseases +MONDO:0005645 otar diseases +MONDO:0005645 rare diseases +MONDO:0005647 otar diseases +MONDO:0005648 otar diseases +MONDO:0005649 otar diseases +MONDO:0005650 otar diseases +MONDO:0005651 gard_rare diseases +MONDO:0005651 rare diseases +MONDO:0005652 otar diseases +MONDO:0005654 otar diseases +MONDO:0005655 otar diseases +MONDO:0005657 gard_rare diseases +MONDO:0005657 nord_rare diseases +MONDO:0005657 ordo_disorder diseases +MONDO:0005657 orphanet_rare diseases +MONDO:0005657 otar diseases +MONDO:0005657 rare diseases +MONDO:0005659 otar diseases +MONDO:0005661 gard_rare diseases +MONDO:0005661 nord_rare diseases +MONDO:0005661 ordo_disorder diseases +MONDO:0005661 orphanet_rare diseases +MONDO:0005661 otar diseases +MONDO:0005661 rare diseases +MONDO:0005662 gard_rare diseases +MONDO:0005662 nord_rare diseases +MONDO:0005662 ordo_disorder diseases +MONDO:0005662 orphanet_rare diseases +MONDO:0005662 otar diseases +MONDO:0005662 rare diseases +MONDO:0005664 otar diseases +MONDO:0005665 otar diseases +MONDO:0005667 otar diseases +MONDO:0005668 gard_rare diseases +MONDO:0005668 nord_rare diseases +MONDO:0005668 ordo_disorder diseases +MONDO:0005668 orphanet_rare diseases +MONDO:0005668 rare diseases +MONDO:0005670 gard_rare diseases +MONDO:0005670 nord_rare diseases +MONDO:0005670 otar diseases +MONDO:0005670 rare diseases +MONDO:0005671 otar diseases +MONDO:0005672 otar diseases +MONDO:0005673 otar diseases +MONDO:0005674 gard_rare diseases +MONDO:0005674 nord_rare diseases +MONDO:0005674 ordo_disorder diseases +MONDO:0005674 orphanet_rare diseases +MONDO:0005674 otar diseases +MONDO:0005674 rare diseases +MONDO:0005675 otar diseases +MONDO:0005676 otar diseases +MONDO:0005677 gard_rare diseases +MONDO:0005677 otar diseases +MONDO:0005677 rare diseases +MONDO:0005678 otar diseases +MONDO:0005680 gard_rare diseases +MONDO:0005680 nord_rare diseases +MONDO:0005680 ordo_subtype_of_a_disorder diseases +MONDO:0005680 otar diseases +MONDO:0005680 rare diseases +MONDO:0005682 otar diseases +MONDO:0005683 gard_rare diseases +MONDO:0005683 nord_rare diseases +MONDO:0005683 ordo_disorder diseases +MONDO:0005683 orphanet_rare diseases +MONDO:0005683 otar diseases +MONDO:0005683 rare diseases +MONDO:0005684 gard_rare diseases +MONDO:0005684 rare diseases +MONDO:0005687 otar diseases +MONDO:0005688 otar diseases +MONDO:0005689 otar diseases +MONDO:0005690 gard_rare diseases +MONDO:0005690 otar diseases +MONDO:0005690 rare diseases +MONDO:0005691 otar diseases +MONDO:0005692 gard_rare diseases +MONDO:0005692 nord_rare diseases +MONDO:0005692 ordo_disorder diseases +MONDO:0005692 orphanet_rare diseases +MONDO:0005692 otar diseases +MONDO:0005692 rare diseases +MONDO:0005693 otar diseases +MONDO:0005694 otar diseases +MONDO:0005695 gard_rare diseases +MONDO:0005695 rare diseases +MONDO:0005696 gard_rare diseases +MONDO:0005696 ordo_disorder diseases +MONDO:0005696 orphanet_rare diseases +MONDO:0005696 otar diseases +MONDO:0005696 rare diseases +MONDO:0005697 otar diseases +MONDO:0005698 otar diseases +MONDO:0005699 gard_rare diseases +MONDO:0005699 rare diseases +MONDO:0005700 otar diseases +MONDO:0005701 otar diseases +MONDO:0005705 gard_rare diseases +MONDO:0005705 ordo_disorder diseases +MONDO:0005705 orphanet_rare diseases +MONDO:0005705 otar diseases +MONDO:0005705 rare diseases +MONDO:0005706 gard_rare diseases +MONDO:0005706 nord_rare diseases +MONDO:0005706 ordo_disorder diseases +MONDO:0005706 orphanet_rare diseases +MONDO:0005706 otar diseases +MONDO:0005706 rare diseases +MONDO:0005707 otar diseases +MONDO:0005708 gard_rare diseases +MONDO:0005708 nord_rare diseases +MONDO:0005708 ordo_disorder diseases +MONDO:0005708 orphanet_rare diseases +MONDO:0005708 rare diseases +MONDO:0005709 otar diseases +MONDO:0005710 gard_rare diseases +MONDO:0005710 nord_rare diseases +MONDO:0005710 ordo_disorder diseases +MONDO:0005710 orphanet_rare diseases +MONDO:0005710 rare diseases +MONDO:0005711 gard_rare diseases +MONDO:0005711 nord_rare diseases +MONDO:0005711 ordo_disorder diseases +MONDO:0005711 ordo_morphological_anomaly diseases +MONDO:0005711 orphanet_rare diseases +MONDO:0005711 otar diseases +MONDO:0005711 rare diseases +MONDO:0005712 otar diseases +MONDO:0005714 gard_rare diseases +MONDO:0005714 nord_rare diseases +MONDO:0005714 ordo_disorder diseases +MONDO:0005714 orphanet_rare diseases +MONDO:0005714 otar diseases +MONDO:0005714 rare diseases +MONDO:0005715 gard_rare diseases +MONDO:0005715 nord_rare diseases +MONDO:0005715 ordo_disorder diseases +MONDO:0005715 orphanet_rare diseases +MONDO:0005715 otar diseases +MONDO:0005715 rare diseases +MONDO:0005716 otar diseases +MONDO:0005717 otar diseases +MONDO:0005718 otar diseases +MONDO:0005719 otar diseases +MONDO:0005720 otar diseases +MONDO:0005721 otar diseases +MONDO:0005722 otar diseases +MONDO:0005723 gard_rare diseases +MONDO:0005723 otar diseases +MONDO:0005723 rare diseases +MONDO:0005724 gard_rare diseases +MONDO:0005724 nord_rare diseases +MONDO:0005724 ordo_disorder diseases +MONDO:0005724 orphanet_rare diseases +MONDO:0005724 otar diseases +MONDO:0005724 rare diseases +MONDO:0005725 gard_rare diseases +MONDO:0005725 nord_rare diseases +MONDO:0005725 ordo_disorder diseases +MONDO:0005725 orphanet_rare diseases +MONDO:0005725 otar diseases +MONDO:0005725 rare diseases +MONDO:0005728 gard_rare diseases +MONDO:0005728 otar diseases +MONDO:0005728 rare diseases +MONDO:0005731 gard_rare diseases +MONDO:0005731 nord_rare diseases +MONDO:0005731 rare diseases +MONDO:0005736 gard_rare diseases +MONDO:0005736 nord_rare diseases +MONDO:0005736 ordo_disorder diseases +MONDO:0005736 orphanet_rare diseases +MONDO:0005736 otar diseases +MONDO:0005736 rare diseases +MONDO:0005737 gard_rare diseases +MONDO:0005737 nord_rare diseases +MONDO:0005737 ordo_disorder diseases +MONDO:0005737 orphanet_rare diseases +MONDO:0005737 otar diseases +MONDO:0005737 rare diseases +MONDO:0005738 otar diseases +MONDO:0005739 otar diseases +MONDO:0005740 otar diseases +MONDO:0005742 gard_rare diseases +MONDO:0005742 nord_rare diseases +MONDO:0005742 rare diseases +MONDO:0005743 gard_rare diseases +MONDO:0005743 nord_rare diseases +MONDO:0005743 otar diseases +MONDO:0005743 rare diseases +MONDO:0005744 gard_rare diseases +MONDO:0005744 nord_rare diseases +MONDO:0005744 ordo_disorder diseases +MONDO:0005744 orphanet_rare diseases +MONDO:0005744 otar diseases +MONDO:0005744 rare diseases +MONDO:0005746 otar diseases +MONDO:0005747 otar diseases +MONDO:0005749 otar diseases +MONDO:0005750 otar diseases +MONDO:0005752 gard_rare diseases +MONDO:0005752 otar diseases +MONDO:0005752 rare diseases +MONDO:0005753 otar diseases +MONDO:0005754 gard_rare diseases +MONDO:0005754 nord_rare diseases +MONDO:0005754 otar diseases +MONDO:0005754 rare diseases +MONDO:0005755 otar diseases +MONDO:0005756 otar diseases +MONDO:0005757 otar diseases +MONDO:0005758 otar diseases +MONDO:0005761 gard_rare diseases +MONDO:0005761 nord_rare diseases +MONDO:0005761 ordo_disorder diseases +MONDO:0005761 orphanet_rare diseases +MONDO:0005761 otar diseases +MONDO:0005761 rare diseases +MONDO:0005763 otar diseases +MONDO:0005764 gard_rare diseases +MONDO:0005764 nord_rare diseases +MONDO:0005764 ordo_disorder diseases +MONDO:0005764 orphanet_rare diseases +MONDO:0005764 otar diseases +MONDO:0005764 rare diseases +MONDO:0005765 otar diseases +MONDO:0005766 otar diseases +MONDO:0005767 gard_rare diseases +MONDO:0005767 nord_rare diseases +MONDO:0005767 otar diseases +MONDO:0005767 rare diseases +MONDO:0005768 gard_rare diseases +MONDO:0005768 otar diseases +MONDO:0005768 rare diseases +MONDO:0005769 gard_rare diseases +MONDO:0005769 nord_rare diseases +MONDO:0005769 ordo_disorder diseases +MONDO:0005769 orphanet_rare diseases +MONDO:0005769 otar diseases +MONDO:0005769 rare diseases +MONDO:0005770 otar diseases +MONDO:0005771 otar diseases +MONDO:0005773 gard_rare diseases +MONDO:0005773 nord_rare diseases +MONDO:0005773 ordo_disorder diseases +MONDO:0005773 orphanet_rare diseases +MONDO:0005773 otar diseases +MONDO:0005773 rare diseases +MONDO:0005774 otar diseases +MONDO:0005775 clingen diseases +MONDO:0005775 inferred_rare diseases +MONDO:0005775 otar diseases +MONDO:0005775 rare diseases +MONDO:0005776 otar diseases +MONDO:0005777 otar diseases +MONDO:0005779 otar diseases +MONDO:0005780 otar diseases +MONDO:0005783 otar diseases +MONDO:0005784 otar diseases +MONDO:0005785 otar diseases +MONDO:0005787 gard_rare diseases +MONDO:0005787 otar diseases +MONDO:0005787 rare diseases +MONDO:0005788 otar diseases +MONDO:0005789 gard_rare diseases +MONDO:0005789 nord_rare diseases +MONDO:0005789 ordo_disorder diseases +MONDO:0005789 orphanet_rare diseases +MONDO:0005789 otar diseases +MONDO:0005789 rare diseases +MONDO:0005790 otar diseases +MONDO:0005791 otar diseases +MONDO:0005792 otar diseases +MONDO:0005794 otar diseases +MONDO:0005796 otar diseases +MONDO:0005797 gard_rare diseases +MONDO:0005797 nord_rare diseases +MONDO:0005797 ordo_disorder diseases +MONDO:0005797 orphanet_rare diseases +MONDO:0005797 otar diseases +MONDO:0005797 rare diseases +MONDO:0005798 gard_rare diseases +MONDO:0005798 nord_rare diseases +MONDO:0005798 otar diseases +MONDO:0005798 rare diseases +MONDO:0005799 otar diseases +MONDO:0005801 gard_rare diseases +MONDO:0005801 nord_rare diseases +MONDO:0005801 otar diseases +MONDO:0005801 rare diseases +MONDO:0005802 gard_rare diseases +MONDO:0005802 nord_rare diseases +MONDO:0005802 ordo_disorder diseases +MONDO:0005802 orphanet_rare diseases +MONDO:0005802 otar diseases +MONDO:0005802 rare diseases +MONDO:0005803 disease_grouping diseases +MONDO:0005803 gard_rare diseases +MONDO:0005803 nord_rare diseases +MONDO:0005803 ordo_group_of_disorders diseases +MONDO:0005803 otar diseases +MONDO:0005803 rare diseases +MONDO:0005804 otar diseases +MONDO:0005805 gard_rare diseases +MONDO:0005805 rare diseases +MONDO:0005806 otar diseases +MONDO:0005807 gard_rare diseases +MONDO:0005807 rare diseases +MONDO:0005808 otar diseases +MONDO:0005810 otar diseases +MONDO:0005812 otar diseases +MONDO:0005813 gard_rare diseases +MONDO:0005813 otar diseases +MONDO:0005813 rare diseases +MONDO:0005814 otar diseases +MONDO:0005815 disease_grouping diseases +MONDO:0005815 gard_rare diseases +MONDO:0005815 ordo_group_of_disorders diseases +MONDO:0005815 otar diseases +MONDO:0005815 rare diseases +MONDO:0005817 gard_rare diseases +MONDO:0005817 nord_rare diseases +MONDO:0005817 ordo_clinical_syndrome diseases +MONDO:0005817 ordo_disorder diseases +MONDO:0005817 orphanet_rare diseases +MONDO:0005817 otar diseases +MONDO:0005817 rare diseases +MONDO:0005819 gard_rare diseases +MONDO:0005819 otar diseases +MONDO:0005819 rare diseases +MONDO:0005820 gard_rare diseases +MONDO:0005820 nord_rare diseases +MONDO:0005820 ordo_disorder diseases +MONDO:0005820 orphanet_rare diseases +MONDO:0005820 otar diseases +MONDO:0005820 rare diseases +MONDO:0005821 gard_rare diseases +MONDO:0005821 rare diseases +MONDO:0005822 otar diseases +MONDO:0005823 gard_rare diseases +MONDO:0005823 nord_rare diseases +MONDO:0005823 ordo_disorder diseases +MONDO:0005823 ordo_group_of_disorders diseases +MONDO:0005823 orphanet_rare diseases +MONDO:0005823 otar diseases +MONDO:0005823 rare diseases +MONDO:0005824 gard_rare diseases +MONDO:0005824 nord_rare diseases +MONDO:0005824 otar diseases +MONDO:0005824 rare diseases +MONDO:0005825 gard_rare diseases +MONDO:0005825 nord_rare diseases +MONDO:0005825 ordo_disorder diseases +MONDO:0005825 orphanet_rare diseases +MONDO:0005825 otar diseases +MONDO:0005825 rare diseases +MONDO:0005826 otar diseases +MONDO:0005827 otar diseases +MONDO:0005828 gard_rare diseases +MONDO:0005828 nord_rare diseases +MONDO:0005828 ordo_disorder diseases +MONDO:0005828 orphanet_rare diseases +MONDO:0005828 otar diseases +MONDO:0005828 rare diseases +MONDO:0005830 otar diseases +MONDO:0005831 gard_rare diseases +MONDO:0005831 otar diseases +MONDO:0005831 rare diseases +MONDO:0005832 gard_rare diseases +MONDO:0005832 otar diseases +MONDO:0005832 rare diseases +MONDO:0005833 otar diseases +MONDO:0005834 otar diseases +MONDO:0005835 clingen diseases +MONDO:0005835 gard_rare diseases +MONDO:0005835 nord_rare diseases +MONDO:0005835 ordo_disorder diseases +MONDO:0005835 orphanet_rare diseases +MONDO:0005835 otar diseases +MONDO:0005835 rare diseases +MONDO:0005836 otar diseases +MONDO:0005837 gard_rare diseases +MONDO:0005837 nord_rare diseases +MONDO:0005837 otar diseases +MONDO:0005837 rare diseases +MONDO:0005838 gard_rare diseases +MONDO:0005838 nord_rare diseases +MONDO:0005838 ordo_disorder diseases +MONDO:0005838 orphanet_rare diseases +MONDO:0005838 otar diseases +MONDO:0005838 rare diseases +MONDO:0005841 gard_rare diseases +MONDO:0005841 nord_rare diseases +MONDO:0005841 otar diseases +MONDO:0005841 rare diseases +MONDO:0005842 otar diseases +MONDO:0005843 otar diseases +MONDO:0005844 otar diseases +MONDO:0005845 gard_rare diseases +MONDO:0005845 otar diseases +MONDO:0005845 rare diseases +MONDO:0005846 gard_rare diseases +MONDO:0005846 nord_rare diseases +MONDO:0005846 ordo_disorder diseases +MONDO:0005846 orphanet_rare diseases +MONDO:0005846 otar diseases +MONDO:0005846 rare diseases +MONDO:0005847 otar diseases +MONDO:0005848 gard_rare diseases +MONDO:0005848 otar diseases +MONDO:0005848 rare diseases +MONDO:0005851 gard_rare diseases +MONDO:0005851 nord_rare diseases +MONDO:0005851 ordo_disorder diseases +MONDO:0005851 orphanet_rare diseases +MONDO:0005851 otar diseases +MONDO:0005851 rare diseases +MONDO:0005852 otar diseases +MONDO:0005853 otar diseases +MONDO:0005854 gard_rare diseases +MONDO:0005854 nord_rare diseases +MONDO:0005854 ordo_disorder diseases +MONDO:0005854 orphanet_rare diseases +MONDO:0005854 otar diseases +MONDO:0005854 rare diseases +MONDO:0005855 otar diseases +MONDO:0005857 otar diseases +MONDO:0005858 otar diseases +MONDO:0005859 gard_rare diseases +MONDO:0005859 otar diseases +MONDO:0005859 rare diseases +MONDO:0005861 gard_rare diseases +MONDO:0005861 otar diseases +MONDO:0005861 rare diseases +MONDO:0005864 otar diseases +MONDO:0005865 gard_rare diseases +MONDO:0005865 nord_rare diseases +MONDO:0005865 rare diseases +MONDO:0005866 otar diseases +MONDO:0005867 otar diseases +MONDO:0005868 gard_rare diseases +MONDO:0005868 otar diseases +MONDO:0005868 rare diseases +MONDO:0005870 otar diseases +MONDO:0005871 otar diseases +MONDO:0005872 otar diseases +MONDO:0005873 gard_rare diseases +MONDO:0005873 rare diseases +MONDO:0005874 gard_rare diseases +MONDO:0005874 otar diseases +MONDO:0005874 rare diseases +MONDO:0005875 otar diseases +MONDO:0005878 gard_rare diseases +MONDO:0005878 otar diseases +MONDO:0005878 rare diseases +MONDO:0005879 otar diseases +MONDO:0005881 otar diseases +MONDO:0005883 gard_rare diseases +MONDO:0005883 nord_rare diseases +MONDO:0005883 otar diseases +MONDO:0005883 rare diseases +MONDO:0005884 otar diseases +MONDO:0005885 otar diseases +MONDO:0005886 otar diseases +MONDO:0005887 gard_rare diseases +MONDO:0005887 rare diseases +MONDO:0005888 otar diseases +MONDO:0005890 otar diseases +MONDO:0005891 otar diseases +MONDO:0005892 otar diseases +MONDO:0005893 gard_rare diseases +MONDO:0005893 nord_rare diseases +MONDO:0005893 ordo_disorder diseases +MONDO:0005893 orphanet_rare diseases +MONDO:0005893 otar diseases +MONDO:0005893 rare diseases +MONDO:0005894 gard_rare diseases +MONDO:0005894 nord_rare diseases +MONDO:0005894 ordo_disorder diseases +MONDO:0005894 orphanet_rare diseases +MONDO:0005894 otar diseases +MONDO:0005894 rare diseases +MONDO:0005895 gard_rare diseases +MONDO:0005895 ordo_disorder diseases +MONDO:0005895 orphanet_rare diseases +MONDO:0005895 otar diseases +MONDO:0005895 rare diseases +MONDO:0005896 otar diseases +MONDO:0005898 otar diseases +MONDO:0005899 otar diseases +MONDO:0005900 otar diseases +MONDO:0005901 otar diseases +MONDO:0005903 gard_rare diseases +MONDO:0005903 otar diseases +MONDO:0005903 rare diseases +MONDO:0005904 otar diseases +MONDO:0005905 otar diseases +MONDO:0005906 otar diseases +MONDO:0005907 otar diseases +MONDO:0005909 otar diseases +MONDO:0005910 gard_rare diseases +MONDO:0005910 nord_rare diseases +MONDO:0005910 otar diseases +MONDO:0005910 rare diseases +MONDO:0005913 otar diseases +MONDO:0005914 otar diseases +MONDO:0005915 otar diseases +MONDO:0005916 otar diseases +MONDO:0005917 otar diseases +MONDO:0005918 otar diseases +MONDO:0005919 gard_rare diseases +MONDO:0005919 nord_rare diseases +MONDO:0005919 ordo_clinical_syndrome diseases +MONDO:0005919 ordo_disorder diseases +MONDO:0005919 orphanet_rare diseases +MONDO:0005919 otar diseases +MONDO:0005919 rare diseases +MONDO:0005920 gard_rare diseases +MONDO:0005920 otar diseases +MONDO:0005920 rare diseases +MONDO:0005921 gard_rare diseases +MONDO:0005921 otar diseases +MONDO:0005921 rare diseases +MONDO:0005922 gard_rare diseases +MONDO:0005922 otar diseases +MONDO:0005922 rare diseases +MONDO:0005923 otar diseases +MONDO:0005925 otar diseases +MONDO:0005927 otar diseases +MONDO:0005928 otar diseases +MONDO:0005929 otar diseases +MONDO:0005932 otar diseases +MONDO:0005933 gard_rare diseases +MONDO:0005933 nord_rare diseases +MONDO:0005933 ordo_disorder diseases +MONDO:0005933 orphanet_rare diseases +MONDO:0005933 otar diseases +MONDO:0005933 rare diseases +MONDO:0005936 otar diseases +MONDO:0005937 otar diseases +MONDO:0005938 gard_rare diseases +MONDO:0005938 otar diseases +MONDO:0005938 rare diseases +MONDO:0005939 otar diseases +MONDO:0005940 otar diseases +MONDO:0005941 otar diseases +MONDO:0005942 gard_rare diseases +MONDO:0005942 nord_rare diseases +MONDO:0005942 ordo_disorder diseases +MONDO:0005942 orphanet_rare diseases +MONDO:0005942 otar diseases +MONDO:0005942 rare diseases +MONDO:0005944 otar diseases +MONDO:0005945 otar diseases +MONDO:0005946 otar diseases +MONDO:0005947 gard_rare diseases +MONDO:0005947 rare diseases +MONDO:0005949 otar diseases +MONDO:0005950 gard_rare diseases +MONDO:0005950 otar diseases +MONDO:0005950 rare diseases +MONDO:0005952 otar diseases +MONDO:0005953 otar diseases +MONDO:0005954 gard_rare diseases +MONDO:0005954 rare diseases +MONDO:0005956 gard_rare diseases +MONDO:0005956 rare diseases +MONDO:0005957 gard_rare diseases +MONDO:0005957 rare diseases +MONDO:0005959 gard_rare diseases +MONDO:0005959 otar diseases +MONDO:0005959 rare diseases +MONDO:0005960 gard_rare diseases +MONDO:0005960 nord_rare diseases +MONDO:0005960 otar diseases +MONDO:0005960 rare diseases +MONDO:0005961 otar diseases +MONDO:0005962 gard_rare diseases +MONDO:0005962 otar diseases +MONDO:0005962 rare diseases +MONDO:0005963 otar diseases +MONDO:0005964 otar diseases +MONDO:0005965 otar diseases +MONDO:0005966 gard_rare diseases +MONDO:0005966 otar diseases +MONDO:0005966 rare diseases +MONDO:0005967 gard_rare diseases +MONDO:0005967 rare diseases +MONDO:0005968 gard_rare diseases +MONDO:0005968 nord_rare diseases +MONDO:0005968 ordo_disorder diseases +MONDO:0005968 orphanet_rare diseases +MONDO:0005968 otar diseases +MONDO:0005968 rare diseases +MONDO:0005969 gard_rare diseases +MONDO:0005969 nord_rare diseases +MONDO:0005969 ordo_disorder diseases +MONDO:0005969 orphanet_rare diseases +MONDO:0005969 otar diseases +MONDO:0005969 rare diseases +MONDO:0005970 otar diseases +MONDO:0005971 otar diseases +MONDO:0005972 otar diseases +MONDO:0005974 gard_rare diseases +MONDO:0005974 nord_rare diseases +MONDO:0005974 ordo_disorder diseases +MONDO:0005974 orphanet_rare diseases +MONDO:0005974 otar diseases +MONDO:0005974 rare diseases +MONDO:0005975 otar diseases +MONDO:0005976 otar diseases +MONDO:0005977 gard_rare diseases +MONDO:0005977 nord_rare diseases +MONDO:0005977 rare diseases +MONDO:0005978 otar diseases +MONDO:0005979 gard_rare diseases +MONDO:0005979 nord_rare diseases +MONDO:0005979 ordo_disorder diseases +MONDO:0005979 orphanet_rare diseases +MONDO:0005979 otar diseases +MONDO:0005979 rare diseases +MONDO:0005980 otar diseases +MONDO:0005981 gard_rare diseases +MONDO:0005981 nord_rare diseases +MONDO:0005981 otar diseases +MONDO:0005981 rare diseases +MONDO:0005982 otar diseases +MONDO:0005984 otar diseases +MONDO:0005988 gard_rare diseases +MONDO:0005988 nord_rare diseases +MONDO:0005988 ordo_disorder diseases +MONDO:0005988 orphanet_rare diseases +MONDO:0005988 otar diseases +MONDO:0005988 rare diseases +MONDO:0005989 otar diseases +MONDO:0005990 otar diseases +MONDO:0005991 gard_rare diseases +MONDO:0005991 nord_rare diseases +MONDO:0005991 ordo_disorder diseases +MONDO:0005991 orphanet_rare diseases +MONDO:0005991 otar diseases +MONDO:0005991 rare diseases +MONDO:0005995 otar diseases +MONDO:0005996 otar diseases +MONDO:0005997 otar diseases +MONDO:0005999 gard_rare diseases +MONDO:0005999 otar diseases +MONDO:0005999 rare diseases +MONDO:0006000 gard_rare diseases +MONDO:0006000 otar diseases +MONDO:0006000 rare diseases +MONDO:0006001 gard_rare diseases +MONDO:0006001 otar diseases +MONDO:0006001 rare diseases +MONDO:0006002 gard_rare diseases +MONDO:0006002 otar diseases +MONDO:0006002 rare diseases +MONDO:0006003 otar diseases +MONDO:0006004 otar diseases +MONDO:0006005 gard_rare diseases +MONDO:0006005 nord_rare diseases +MONDO:0006005 otar diseases +MONDO:0006005 rare diseases +MONDO:0006006 otar diseases +MONDO:0006007 otar diseases +MONDO:0006008 gard_rare diseases +MONDO:0006008 otar diseases +MONDO:0006008 rare diseases +MONDO:0006009 gard_rare diseases +MONDO:0006009 nord_rare diseases +MONDO:0006009 ordo_group_of_disorders diseases +MONDO:0006009 otar diseases +MONDO:0006009 rare diseases +MONDO:0006010 otar diseases +MONDO:0006011 otar diseases +MONDO:0006012 otar diseases +MONDO:0006014 otar diseases +MONDO:0006015 gard_rare diseases +MONDO:0006015 nord_rare diseases +MONDO:0006015 ordo_subtype_of_a_disorder diseases +MONDO:0006015 otar diseases +MONDO:0006015 rare diseases +MONDO:0006019 gard_rare diseases +MONDO:0006019 nord_rare diseases +MONDO:0006019 rare diseases +MONDO:0006021 otar diseases +MONDO:0006022 otar diseases +MONDO:0006025 otar diseases +MONDO:0006026 otar diseases +MONDO:0006027 gard_rare diseases +MONDO:0006027 nord_rare diseases +MONDO:0006027 rare diseases +MONDO:0006028 otar diseases +MONDO:0006029 otar diseases +MONDO:0006030 otar diseases +MONDO:0006031 otar diseases +MONDO:0006032 otar diseases +MONDO:0006033 gard_rare diseases +MONDO:0006033 nord_rare diseases +MONDO:0006033 ordo_disorder diseases +MONDO:0006033 orphanet_rare diseases +MONDO:0006033 otar diseases +MONDO:0006033 rare diseases +MONDO:0006034 gard_rare diseases +MONDO:0006034 otar diseases +MONDO:0006034 rare diseases +MONDO:0006035 otar diseases +MONDO:0006036 otar diseases +MONDO:0006037 gard_rare diseases +MONDO:0006037 nord_rare diseases +MONDO:0006037 ordo_disorder diseases +MONDO:0006037 ordo_malformation_syndrome diseases +MONDO:0006037 orphanet_rare diseases +MONDO:0006037 otar diseases +MONDO:0006037 rare diseases +MONDO:0006038 otar diseases +MONDO:0006039 otar diseases +MONDO:0006040 otar diseases +MONDO:0006041 gard_rare diseases +MONDO:0006041 otar diseases +MONDO:0006041 rare diseases +MONDO:0006042 gard_rare diseases +MONDO:0006042 nord_rare diseases +MONDO:0006042 otar diseases +MONDO:0006042 rare diseases +MONDO:0006043 gard_rare diseases +MONDO:0006043 nord_rare diseases +MONDO:0006043 ordo_disorder diseases +MONDO:0006043 orphanet_rare diseases +MONDO:0006043 otar diseases +MONDO:0006043 rare diseases +MONDO:0006044 otar diseases +MONDO:0006045 gard_rare diseases +MONDO:0006045 nord_rare diseases +MONDO:0006045 ordo_disorder diseases +MONDO:0006045 orphanet_rare diseases +MONDO:0006045 otar diseases +MONDO:0006045 rare diseases +MONDO:0006046 gard_rare diseases +MONDO:0006046 otar diseases +MONDO:0006046 rare diseases +MONDO:0006047 otar diseases +MONDO:0006049 gard_rare diseases +MONDO:0006049 otar diseases +MONDO:0006049 rare diseases +MONDO:0006050 otar diseases +MONDO:0006052 gard_rare diseases +MONDO:0006052 otar diseases +MONDO:0006052 rare diseases +MONDO:0006053 otar diseases +MONDO:0006054 otar diseases +MONDO:0006055 otar diseases +MONDO:0006056 gard_rare diseases +MONDO:0006056 otar diseases +MONDO:0006056 rare diseases +MONDO:0006058 otar diseases +MONDO:0006059 gard_rare diseases +MONDO:0006059 otar diseases +MONDO:0006059 rare diseases +MONDO:0006060 gard_rare diseases +MONDO:0006060 otar diseases +MONDO:0006060 rare diseases +MONDO:0006061 otar diseases +MONDO:0006065 inferred_rare diseases +MONDO:0006065 otar diseases +MONDO:0006065 rare diseases +MONDO:0006066 otar diseases +MONDO:0006067 otar diseases +MONDO:0006068 gard_rare diseases +MONDO:0006068 nord_rare diseases +MONDO:0006068 otar diseases +MONDO:0006068 rare diseases +MONDO:0006069 gard_rare diseases +MONDO:0006069 otar diseases +MONDO:0006069 rare diseases +MONDO:0006071 otar diseases +MONDO:0006073 otar diseases +MONDO:0006074 otar diseases +MONDO:0006075 gard_rare diseases +MONDO:0006075 otar diseases +MONDO:0006075 rare diseases +MONDO:0006076 gard_rare diseases +MONDO:0006076 otar diseases +MONDO:0006076 rare diseases +MONDO:0006077 otar diseases +MONDO:0006078 gard_rare diseases +MONDO:0006078 otar diseases +MONDO:0006078 rare diseases +MONDO:0006079 gard_rare diseases +MONDO:0006079 nord_rare diseases +MONDO:0006079 ordo_disorder diseases +MONDO:0006079 orphanet_rare diseases +MONDO:0006079 otar diseases +MONDO:0006079 rare diseases +MONDO:0006081 gard_rare diseases +MONDO:0006081 nord_rare diseases +MONDO:0006081 otar diseases +MONDO:0006081 rare diseases +MONDO:0006082 gard_rare diseases +MONDO:0006082 nord_rare diseases +MONDO:0006082 otar diseases +MONDO:0006082 rare diseases +MONDO:0006085 otar diseases +MONDO:0006086 otar diseases +MONDO:0006087 gard_rare diseases +MONDO:0006087 nord_rare diseases +MONDO:0006087 otar diseases +MONDO:0006087 rare diseases +MONDO:0006088 gard_rare diseases +MONDO:0006088 otar diseases +MONDO:0006088 rare diseases +MONDO:0006091 gard_rare diseases +MONDO:0006091 otar diseases +MONDO:0006091 rare diseases +MONDO:0006092 gard_rare diseases +MONDO:0006092 otar diseases +MONDO:0006092 rare diseases +MONDO:0006093 gard_rare diseases +MONDO:0006093 rare diseases +MONDO:0006094 gard_rare diseases +MONDO:0006094 nord_rare diseases +MONDO:0006094 otar diseases +MONDO:0006094 rare diseases +MONDO:0006095 gard_rare diseases +MONDO:0006095 otar diseases +MONDO:0006095 rare diseases +MONDO:0006096 otar diseases +MONDO:0006097 otar diseases +MONDO:0006098 otar diseases +MONDO:0006102 otar diseases +MONDO:0006103 nord_rare diseases +MONDO:0006103 otar diseases +MONDO:0006103 rare diseases +MONDO:0006104 inferred_rare diseases +MONDO:0006104 otar diseases +MONDO:0006104 rare diseases +MONDO:0006105 otar diseases +MONDO:0006106 otar diseases +MONDO:0006107 inferred_rare diseases +MONDO:0006107 otar diseases +MONDO:0006107 rare diseases +MONDO:0006108 otar diseases +MONDO:0006109 gard_rare diseases +MONDO:0006109 otar diseases +MONDO:0006109 rare diseases +MONDO:0006111 otar diseases +MONDO:0006112 gard_rare diseases +MONDO:0006112 otar diseases +MONDO:0006112 rare diseases +MONDO:0006115 gard_rare diseases +MONDO:0006115 nord_rare diseases +MONDO:0006115 otar diseases +MONDO:0006115 rare diseases +MONDO:0006116 otar diseases +MONDO:0006117 gard_rare diseases +MONDO:0006117 otar diseases +MONDO:0006117 rare diseases +MONDO:0006118 otar diseases +MONDO:0006119 gard_rare diseases +MONDO:0006119 rare diseases +MONDO:0006120 otar diseases +MONDO:0006121 otar diseases +MONDO:0006122 otar diseases +MONDO:0006123 otar diseases +MONDO:0006126 gard_rare diseases +MONDO:0006126 rare diseases +MONDO:0006128 gard_rare diseases +MONDO:0006128 otar diseases +MONDO:0006128 rare diseases +MONDO:0006130 otar diseases +MONDO:0006131 gard_rare diseases +MONDO:0006131 nord_rare diseases +MONDO:0006131 ordo_disorder diseases +MONDO:0006131 orphanet_rare diseases +MONDO:0006131 otar diseases +MONDO:0006131 rare diseases +MONDO:0006132 gard_rare diseases +MONDO:0006132 ordo_disorder diseases +MONDO:0006132 orphanet_rare diseases +MONDO:0006132 otar diseases +MONDO:0006132 rare diseases +MONDO:0006133 gard_rare diseases +MONDO:0006133 nord_rare diseases +MONDO:0006133 ordo_disorder diseases +MONDO:0006133 orphanet_rare diseases +MONDO:0006133 otar diseases +MONDO:0006133 rare diseases +MONDO:0006134 gard_rare diseases +MONDO:0006134 otar diseases +MONDO:0006134 rare diseases +MONDO:0006135 gard_rare diseases +MONDO:0006135 otar diseases +MONDO:0006135 rare diseases +MONDO:0006137 gard_rare diseases +MONDO:0006137 otar diseases +MONDO:0006137 rare diseases +MONDO:0006138 gard_rare diseases +MONDO:0006138 otar diseases +MONDO:0006138 rare diseases +MONDO:0006139 otar diseases +MONDO:0006140 gard_rare diseases +MONDO:0006140 otar diseases +MONDO:0006140 rare diseases +MONDO:0006141 gard_rare diseases +MONDO:0006141 rare diseases +MONDO:0006142 gard_rare diseases +MONDO:0006142 otar diseases +MONDO:0006142 rare diseases +MONDO:0006143 gard_rare diseases +MONDO:0006143 nord_rare diseases +MONDO:0006143 ordo_disorder diseases +MONDO:0006143 orphanet_rare diseases +MONDO:0006143 otar diseases +MONDO:0006143 rare diseases +MONDO:0006145 gard_rare diseases +MONDO:0006145 otar diseases +MONDO:0006145 rare diseases +MONDO:0006146 otar diseases +MONDO:0006149 otar diseases +MONDO:0006150 gard_rare diseases +MONDO:0006150 rare diseases +MONDO:0006151 otar diseases +MONDO:0006152 otar diseases +MONDO:0006153 otar diseases +MONDO:0006154 gard_rare diseases +MONDO:0006154 otar diseases +MONDO:0006154 rare diseases +MONDO:0006155 gard_rare diseases +MONDO:0006155 otar diseases +MONDO:0006155 rare diseases +MONDO:0006156 otar diseases +MONDO:0006157 otar diseases +MONDO:0006158 gard_rare diseases +MONDO:0006158 nord_rare diseases +MONDO:0006158 otar diseases +MONDO:0006158 rare diseases +MONDO:0006159 otar diseases +MONDO:0006160 otar diseases +MONDO:0006161 otar diseases +MONDO:0006162 gard_rare diseases +MONDO:0006162 otar diseases +MONDO:0006162 rare diseases +MONDO:0006163 otar diseases +MONDO:0006164 otar diseases +MONDO:0006165 otar diseases +MONDO:0006166 otar diseases +MONDO:0006167 gard_rare diseases +MONDO:0006167 otar diseases +MONDO:0006167 rare diseases +MONDO:0006169 otar diseases +MONDO:0006170 otar diseases +MONDO:0006172 gard_rare diseases +MONDO:0006172 nord_rare diseases +MONDO:0006172 otar diseases +MONDO:0006172 rare diseases +MONDO:0006173 gard_rare diseases +MONDO:0006173 otar diseases +MONDO:0006173 rare diseases +MONDO:0006174 gard_rare diseases +MONDO:0006174 otar diseases +MONDO:0006174 rare diseases +MONDO:0006176 otar diseases +MONDO:0006178 gard_rare diseases +MONDO:0006178 otar diseases +MONDO:0006178 rare diseases +MONDO:0006179 gard_rare diseases +MONDO:0006179 otar diseases +MONDO:0006179 rare diseases +MONDO:0006180 otar diseases +MONDO:0006181 otar diseases +MONDO:0006182 otar diseases +MONDO:0006183 gard_rare diseases +MONDO:0006183 nord_rare diseases +MONDO:0006183 ordo_disorder diseases +MONDO:0006183 orphanet_rare diseases +MONDO:0006183 otar diseases +MONDO:0006183 rare diseases +MONDO:0006184 otar diseases +MONDO:0006186 gard_rare diseases +MONDO:0006186 otar diseases +MONDO:0006186 rare diseases +MONDO:0006187 otar diseases +MONDO:0006188 gard_rare diseases +MONDO:0006188 nord_rare diseases +MONDO:0006188 rare diseases +MONDO:0006189 otar diseases +MONDO:0006190 otar diseases +MONDO:0006191 otar diseases +MONDO:0006192 otar diseases +MONDO:0006193 otar diseases +MONDO:0006195 otar diseases +MONDO:0006196 otar diseases +MONDO:0006197 gard_rare diseases +MONDO:0006197 otar diseases +MONDO:0006197 rare diseases +MONDO:0006198 otar diseases +MONDO:0006199 otar diseases +MONDO:0006200 gard_rare diseases +MONDO:0006200 otar diseases +MONDO:0006200 rare diseases +MONDO:0006201 gard_rare diseases +MONDO:0006201 otar diseases +MONDO:0006201 rare diseases +MONDO:0006202 gard_rare diseases +MONDO:0006202 otar diseases +MONDO:0006202 rare diseases +MONDO:0006203 gard_rare diseases +MONDO:0006203 otar diseases +MONDO:0006203 rare diseases +MONDO:0006206 gard_rare diseases +MONDO:0006206 otar diseases +MONDO:0006206 rare diseases +MONDO:0006207 gard_rare diseases +MONDO:0006207 otar diseases +MONDO:0006207 rare diseases +MONDO:0006208 gard_rare diseases +MONDO:0006208 otar diseases +MONDO:0006208 rare diseases +MONDO:0006209 otar diseases +MONDO:0006210 gard_rare diseases +MONDO:0006210 nord_rare diseases +MONDO:0006210 ordo_disorder diseases +MONDO:0006210 orphanet_rare diseases +MONDO:0006210 otar diseases +MONDO:0006210 rare diseases +MONDO:0006211 otar diseases +MONDO:0006212 otar diseases +MONDO:0006213 gard_rare diseases +MONDO:0006213 otar diseases +MONDO:0006213 rare diseases +MONDO:0006214 otar diseases +MONDO:0006215 gard_rare diseases +MONDO:0006215 otar diseases +MONDO:0006215 rare diseases +MONDO:0006216 otar diseases +MONDO:0006217 gard_rare diseases +MONDO:0006217 otar diseases +MONDO:0006217 rare diseases +MONDO:0006218 otar diseases +MONDO:0006219 gard_rare diseases +MONDO:0006219 otar diseases +MONDO:0006219 rare diseases +MONDO:0006220 gard_rare diseases +MONDO:0006220 otar diseases +MONDO:0006220 rare diseases +MONDO:0006221 otar diseases +MONDO:0006222 gard_rare diseases +MONDO:0006222 otar diseases +MONDO:0006222 rare diseases +MONDO:0006223 gard_rare diseases +MONDO:0006223 otar diseases +MONDO:0006223 rare diseases +MONDO:0006224 otar diseases +MONDO:0006225 gard_rare diseases +MONDO:0006225 otar diseases +MONDO:0006225 rare diseases +MONDO:0006226 gard_rare diseases +MONDO:0006226 otar diseases +MONDO:0006226 rare diseases +MONDO:0006227 gard_rare diseases +MONDO:0006227 otar diseases +MONDO:0006227 rare diseases +MONDO:0006228 otar diseases +MONDO:0006229 gard_rare diseases +MONDO:0006229 otar diseases +MONDO:0006229 rare diseases +MONDO:0006230 gard_rare diseases +MONDO:0006230 nord_rare diseases +MONDO:0006230 ordo_disorder diseases +MONDO:0006230 orphanet_rare diseases +MONDO:0006230 otar diseases +MONDO:0006230 rare diseases +MONDO:0006231 otar diseases +MONDO:0006232 otar diseases +MONDO:0006233 gard_rare diseases +MONDO:0006233 otar diseases +MONDO:0006233 rare diseases +MONDO:0006234 otar diseases +MONDO:0006235 gard_rare diseases +MONDO:0006235 nord_rare diseases +MONDO:0006235 otar diseases +MONDO:0006235 rare diseases +MONDO:0006237 gard_rare diseases +MONDO:0006237 nord_rare diseases +MONDO:0006237 otar diseases +MONDO:0006237 rare diseases +MONDO:0006238 disease_grouping diseases +MONDO:0006238 gard_rare diseases +MONDO:0006238 nord_rare diseases +MONDO:0006238 ordo_group_of_disorders diseases +MONDO:0006238 otar diseases +MONDO:0006238 rare diseases +MONDO:0006239 gard_rare diseases +MONDO:0006239 otar diseases +MONDO:0006239 rare diseases +MONDO:0006241 otar diseases +MONDO:0006243 otar diseases +MONDO:0006244 otar diseases +MONDO:0006245 otar diseases +MONDO:0006246 gard_rare diseases +MONDO:0006246 otar diseases +MONDO:0006246 rare diseases +MONDO:0006247 disease_grouping diseases +MONDO:0006247 gard_rare diseases +MONDO:0006247 nord_rare diseases +MONDO:0006247 ordo_group_of_disorders diseases +MONDO:0006247 otar diseases +MONDO:0006247 rare diseases +MONDO:0006248 gard_rare diseases +MONDO:0006248 ordo_disorder diseases +MONDO:0006248 orphanet_rare diseases +MONDO:0006248 otar diseases +MONDO:0006248 rare diseases +MONDO:0006249 otar diseases +MONDO:0006250 gard_rare diseases +MONDO:0006250 otar diseases +MONDO:0006250 rare diseases +MONDO:0006254 otar diseases +MONDO:0006255 gard_rare diseases +MONDO:0006255 otar diseases +MONDO:0006255 rare diseases +MONDO:0006256 otar diseases +MONDO:0006257 gard_rare diseases +MONDO:0006257 nord_rare diseases +MONDO:0006257 otar diseases +MONDO:0006257 rare diseases +MONDO:0006258 otar diseases +MONDO:0006260 gard_rare diseases +MONDO:0006260 nord_rare diseases +MONDO:0006260 ordo_disorder diseases +MONDO:0006260 orphanet_rare diseases +MONDO:0006260 otar diseases +MONDO:0006260 rare diseases +MONDO:0006262 gard_rare diseases +MONDO:0006262 otar diseases +MONDO:0006262 rare diseases +MONDO:0006264 gard_rare diseases +MONDO:0006264 otar diseases +MONDO:0006264 rare diseases +MONDO:0006265 gard_rare diseases +MONDO:0006265 otar diseases +MONDO:0006265 rare diseases +MONDO:0006266 otar diseases +MONDO:0006267 gard_rare diseases +MONDO:0006267 rare diseases +MONDO:0006268 gard_rare diseases +MONDO:0006268 otar diseases +MONDO:0006268 rare diseases +MONDO:0006270 otar diseases +MONDO:0006272 gard_rare diseases +MONDO:0006272 rare diseases +MONDO:0006273 gard_rare diseases +MONDO:0006273 otar diseases +MONDO:0006273 rare diseases +MONDO:0006274 gard_rare diseases +MONDO:0006274 otar diseases +MONDO:0006274 rare diseases +MONDO:0006275 otar diseases +MONDO:0006276 gard_rare diseases +MONDO:0006276 nord_rare diseases +MONDO:0006276 otar diseases +MONDO:0006276 rare diseases +MONDO:0006277 gard_rare diseases +MONDO:0006277 ordo_disorder diseases +MONDO:0006277 orphanet_rare diseases +MONDO:0006277 otar diseases +MONDO:0006277 rare diseases +MONDO:0006278 otar diseases +MONDO:0006279 otar diseases +MONDO:0006280 otar diseases +MONDO:0006281 gard_rare diseases +MONDO:0006281 otar diseases +MONDO:0006281 rare diseases +MONDO:0006282 otar diseases +MONDO:0006283 otar diseases +MONDO:0006284 otar diseases +MONDO:0006285 otar diseases +MONDO:0006286 gard_rare diseases +MONDO:0006286 otar diseases +MONDO:0006286 rare diseases +MONDO:0006287 gard_rare diseases +MONDO:0006287 otar diseases +MONDO:0006287 rare diseases +MONDO:0006288 gard_rare diseases +MONDO:0006288 nord_rare diseases +MONDO:0006288 otar diseases +MONDO:0006288 rare diseases +MONDO:0006290 gard_rare diseases +MONDO:0006290 nord_rare diseases +MONDO:0006290 otar diseases +MONDO:0006290 rare diseases +MONDO:0006291 gard_rare diseases +MONDO:0006291 rare diseases +MONDO:0006292 gard_rare diseases +MONDO:0006292 nord_rare diseases +MONDO:0006292 ordo_disorder diseases +MONDO:0006292 orphanet_rare diseases +MONDO:0006292 otar diseases +MONDO:0006292 rare diseases +MONDO:0006294 otar diseases +MONDO:0006295 otar diseases +MONDO:0006297 gard_rare diseases +MONDO:0006297 otar diseases +MONDO:0006297 rare diseases +MONDO:0006298 gard_rare diseases +MONDO:0006298 otar diseases +MONDO:0006298 rare diseases +MONDO:0006300 gard_rare diseases +MONDO:0006300 otar diseases +MONDO:0006300 rare diseases +MONDO:0006301 otar diseases +MONDO:0006302 otar diseases +MONDO:0006303 gard_rare diseases +MONDO:0006303 otar diseases +MONDO:0006303 rare diseases +MONDO:0006304 otar diseases +MONDO:0006306 otar diseases +MONDO:0006307 otar diseases +MONDO:0006309 otar diseases +MONDO:0006311 gard_rare diseases +MONDO:0006311 otar diseases +MONDO:0006311 rare diseases +MONDO:0006312 otar diseases +MONDO:0006313 otar diseases +MONDO:0006314 otar diseases +MONDO:0006316 otar diseases +MONDO:0006317 gard_rare diseases +MONDO:0006317 otar diseases +MONDO:0006317 rare diseases +MONDO:0006320 otar diseases +MONDO:0006321 gard_rare diseases +MONDO:0006321 otar diseases +MONDO:0006321 rare diseases +MONDO:0006322 otar diseases +MONDO:0006324 otar diseases +MONDO:0006325 otar diseases +MONDO:0006327 otar diseases +MONDO:0006328 otar diseases +MONDO:0006329 gard_rare diseases +MONDO:0006329 otar diseases +MONDO:0006329 rare diseases +MONDO:0006330 otar diseases +MONDO:0006335 gard_rare diseases +MONDO:0006335 nord_rare diseases +MONDO:0006335 ordo_disorder diseases +MONDO:0006335 orphanet_rare diseases +MONDO:0006335 otar diseases +MONDO:0006335 rare diseases +MONDO:0006336 gard_rare diseases +MONDO:0006336 otar diseases +MONDO:0006336 rare diseases +MONDO:0006337 otar diseases +MONDO:0006339 gard_rare diseases +MONDO:0006339 nord_rare diseases +MONDO:0006339 ordo_disorder diseases +MONDO:0006339 orphanet_rare diseases +MONDO:0006339 otar diseases +MONDO:0006339 rare diseases +MONDO:0006340 otar diseases +MONDO:0006343 gard_rare diseases +MONDO:0006343 otar diseases +MONDO:0006343 rare diseases +MONDO:0006344 gard_rare diseases +MONDO:0006344 otar diseases +MONDO:0006344 rare diseases +MONDO:0006345 gard_rare diseases +MONDO:0006345 otar diseases +MONDO:0006345 rare diseases +MONDO:0006346 gard_rare diseases +MONDO:0006346 nord_rare diseases +MONDO:0006346 ordo_disorder diseases +MONDO:0006346 orphanet_rare diseases +MONDO:0006346 otar diseases +MONDO:0006346 rare diseases +MONDO:0006347 gard_rare diseases +MONDO:0006347 otar diseases +MONDO:0006347 rare diseases +MONDO:0006348 gard_rare diseases +MONDO:0006348 otar diseases +MONDO:0006348 rare diseases +MONDO:0006349 otar diseases +MONDO:0006350 gard_rare diseases +MONDO:0006350 otar diseases +MONDO:0006350 rare diseases +MONDO:0006351 otar diseases +MONDO:0006352 gard_rare diseases +MONDO:0006352 rare diseases +MONDO:0006353 gard_rare diseases +MONDO:0006353 rare diseases +MONDO:0006354 otar diseases +MONDO:0006355 otar diseases +MONDO:0006356 gard_rare diseases +MONDO:0006356 otar diseases +MONDO:0006356 rare diseases +MONDO:0006357 otar diseases +MONDO:0006358 gard_rare diseases +MONDO:0006358 otar diseases +MONDO:0006358 rare diseases +MONDO:0006359 gard_rare diseases +MONDO:0006359 nord_rare diseases +MONDO:0006359 ordo_disorder diseases +MONDO:0006359 orphanet_rare diseases +MONDO:0006359 otar diseases +MONDO:0006359 rare diseases +MONDO:0006360 gard_rare diseases +MONDO:0006360 nord_rare diseases +MONDO:0006360 otar diseases +MONDO:0006360 rare diseases +MONDO:0006362 otar diseases +MONDO:0006363 gard_rare diseases +MONDO:0006363 nord_rare diseases +MONDO:0006363 ordo_disorder diseases +MONDO:0006363 orphanet_rare diseases +MONDO:0006363 otar diseases +MONDO:0006363 rare diseases +MONDO:0006364 otar diseases +MONDO:0006365 otar diseases +MONDO:0006367 gard_rare diseases +MONDO:0006367 rare diseases +MONDO:0006368 otar diseases +MONDO:0006369 gard_rare diseases +MONDO:0006369 ordo_disorder diseases +MONDO:0006369 orphanet_rare diseases +MONDO:0006369 otar diseases +MONDO:0006369 rare diseases +MONDO:0006372 gard_rare diseases +MONDO:0006372 nord_rare diseases +MONDO:0006372 ordo_disorder diseases +MONDO:0006372 orphanet_rare diseases +MONDO:0006372 otar diseases +MONDO:0006372 rare diseases +MONDO:0006373 disease_grouping diseases +MONDO:0006373 gard_rare diseases +MONDO:0006373 ordo_group_of_disorders diseases +MONDO:0006373 otar diseases +MONDO:0006373 rare diseases +MONDO:0006374 gard_rare diseases +MONDO:0006374 nord_rare diseases +MONDO:0006374 otar diseases +MONDO:0006374 rare diseases +MONDO:0006375 otar diseases +MONDO:0006377 gard_rare diseases +MONDO:0006377 otar diseases +MONDO:0006377 rare diseases +MONDO:0006378 gard_rare diseases +MONDO:0006378 otar diseases +MONDO:0006378 rare diseases +MONDO:0006380 gard_rare diseases +MONDO:0006380 otar diseases +MONDO:0006380 rare diseases +MONDO:0006381 gard_rare diseases +MONDO:0006381 otar diseases +MONDO:0006381 rare diseases +MONDO:0006382 otar diseases +MONDO:0006383 gard_rare diseases +MONDO:0006383 nord_rare diseases +MONDO:0006383 ordo_disorder diseases +MONDO:0006383 orphanet_rare diseases +MONDO:0006383 otar diseases +MONDO:0006383 rare diseases +MONDO:0006385 gard_rare diseases +MONDO:0006385 otar diseases +MONDO:0006385 rare diseases +MONDO:0006386 gard_rare diseases +MONDO:0006386 otar diseases +MONDO:0006386 rare diseases +MONDO:0006387 gard_rare diseases +MONDO:0006387 otar diseases +MONDO:0006387 rare diseases +MONDO:0006388 gard_rare diseases +MONDO:0006388 otar diseases +MONDO:0006388 rare diseases +MONDO:0006389 gard_rare diseases +MONDO:0006389 otar diseases +MONDO:0006389 rare diseases +MONDO:0006390 gard_rare diseases +MONDO:0006390 otar diseases +MONDO:0006390 rare diseases +MONDO:0006391 otar diseases +MONDO:0006392 otar diseases +MONDO:0006393 otar diseases +MONDO:0006394 otar diseases +MONDO:0006395 otar diseases +MONDO:0006396 otar diseases +MONDO:0006397 gard_rare diseases +MONDO:0006397 nord_rare diseases +MONDO:0006397 otar diseases +MONDO:0006397 rare diseases +MONDO:0006398 gard_rare diseases +MONDO:0006398 otar diseases +MONDO:0006398 rare diseases +MONDO:0006400 otar diseases +MONDO:0006401 gard_rare diseases +MONDO:0006401 rare diseases +MONDO:0006402 gard_rare diseases +MONDO:0006402 otar diseases +MONDO:0006402 rare diseases +MONDO:0006403 otar diseases +MONDO:0006404 otar diseases +MONDO:0006405 gard_rare diseases +MONDO:0006405 otar diseases +MONDO:0006405 rare diseases +MONDO:0006406 otar diseases +MONDO:0006407 gard_rare diseases +MONDO:0006407 otar diseases +MONDO:0006407 rare diseases +MONDO:0006408 gard_rare diseases +MONDO:0006408 otar diseases +MONDO:0006408 rare diseases +MONDO:0006409 otar diseases +MONDO:0006410 otar diseases +MONDO:0006411 otar diseases +MONDO:0006412 gard_rare diseases +MONDO:0006412 nord_rare diseases +MONDO:0006412 ordo_disorder diseases +MONDO:0006412 orphanet_rare diseases +MONDO:0006412 otar diseases +MONDO:0006412 rare diseases +MONDO:0006414 gard_rare diseases +MONDO:0006414 otar diseases +MONDO:0006414 rare diseases +MONDO:0006416 gard_rare diseases +MONDO:0006416 rare diseases +MONDO:0006417 gard_rare diseases +MONDO:0006417 otar diseases +MONDO:0006417 rare diseases +MONDO:0006418 gard_rare diseases +MONDO:0006418 otar diseases +MONDO:0006418 rare diseases +MONDO:0006420 gard_rare diseases +MONDO:0006420 nord_rare diseases +MONDO:0006420 rare diseases +MONDO:0006421 otar diseases +MONDO:0006422 otar diseases +MONDO:0006423 otar diseases +MONDO:0006424 otar diseases +MONDO:0006426 otar diseases +MONDO:0006427 otar diseases +MONDO:0006428 gard_rare diseases +MONDO:0006428 otar diseases +MONDO:0006428 rare diseases +MONDO:0006429 gard_rare diseases +MONDO:0006429 rare diseases +MONDO:0006430 gard_rare diseases +MONDO:0006430 otar diseases +MONDO:0006430 rare diseases +MONDO:0006432 gard_rare diseases +MONDO:0006432 rare diseases +MONDO:0006435 otar diseases +MONDO:0006436 gard_rare diseases +MONDO:0006436 otar diseases +MONDO:0006436 rare diseases +MONDO:0006438 otar diseases +MONDO:0006442 otar diseases +MONDO:0006444 gard_rare diseases +MONDO:0006444 nord_rare diseases +MONDO:0006444 otar diseases +MONDO:0006444 rare diseases +MONDO:0006446 gard_rare diseases +MONDO:0006446 nord_rare diseases +MONDO:0006446 otar diseases +MONDO:0006446 rare diseases +MONDO:0006447 gard_rare diseases +MONDO:0006447 nord_rare diseases +MONDO:0006447 ordo_disorder diseases +MONDO:0006447 orphanet_rare diseases +MONDO:0006447 otar diseases +MONDO:0006447 rare diseases +MONDO:0006450 gard_rare diseases +MONDO:0006450 otar diseases +MONDO:0006450 rare diseases +MONDO:0006451 gard_rare diseases +MONDO:0006451 nord_rare diseases +MONDO:0006451 ordo_disorder diseases +MONDO:0006451 orphanet_rare diseases +MONDO:0006451 otar diseases +MONDO:0006451 rare diseases +MONDO:0006452 gard_rare diseases +MONDO:0006452 otar diseases +MONDO:0006452 rare diseases +MONDO:0006455 gard_rare diseases +MONDO:0006455 otar diseases +MONDO:0006455 rare diseases +MONDO:0006456 gard_rare diseases +MONDO:0006456 nord_rare diseases +MONDO:0006456 ordo_disorder diseases +MONDO:0006456 orphanet_rare diseases +MONDO:0006456 otar diseases +MONDO:0006456 rare diseases +MONDO:0006458 gard_rare diseases +MONDO:0006458 otar diseases +MONDO:0006458 rare diseases +MONDO:0006459 gard_rare diseases +MONDO:0006459 otar diseases +MONDO:0006459 rare diseases +MONDO:0006460 otar diseases +MONDO:0006462 gard_rare diseases +MONDO:0006462 otar diseases +MONDO:0006462 rare diseases +MONDO:0006463 gard_rare diseases +MONDO:0006463 otar diseases +MONDO:0006463 rare diseases +MONDO:0006464 gard_rare diseases +MONDO:0006464 otar diseases +MONDO:0006464 rare diseases +MONDO:0006465 obsoletion_candidate diseases +MONDO:0006465 otar diseases +MONDO:0006466 gard_rare diseases +MONDO:0006466 otar diseases +MONDO:0006466 rare diseases +MONDO:0006467 gard_rare diseases +MONDO:0006467 otar diseases +MONDO:0006467 rare diseases +MONDO:0006468 gard_rare diseases +MONDO:0006468 nord_rare diseases +MONDO:0006468 ordo_disorder diseases +MONDO:0006468 orphanet_rare diseases +MONDO:0006468 otar diseases +MONDO:0006468 rare diseases +MONDO:0006469 gard_rare diseases +MONDO:0006469 rare diseases +MONDO:0006470 gard_rare diseases +MONDO:0006470 otar diseases +MONDO:0006470 rare diseases +MONDO:0006471 gard_rare diseases +MONDO:0006471 otar diseases +MONDO:0006471 rare diseases +MONDO:0006474 gard_rare diseases +MONDO:0006474 nord_rare diseases +MONDO:0006474 otar diseases +MONDO:0006474 rare diseases +MONDO:0006476 gard_rare diseases +MONDO:0006476 otar diseases +MONDO:0006476 rare diseases +MONDO:0006477 gard_rare diseases +MONDO:0006477 otar diseases +MONDO:0006477 rare diseases +MONDO:0006478 otar diseases +MONDO:0006479 gard_rare diseases +MONDO:0006479 ordo_disorder diseases +MONDO:0006479 orphanet_rare diseases +MONDO:0006479 otar diseases +MONDO:0006479 rare diseases +MONDO:0006480 gard_rare diseases +MONDO:0006480 otar diseases +MONDO:0006480 rare diseases +MONDO:0006481 otar diseases +MONDO:0006482 gard_rare diseases +MONDO:0006482 rare diseases +MONDO:0006483 otar diseases +MONDO:0006484 otar diseases +MONDO:0006485 otar diseases +MONDO:0006486 gard_rare diseases +MONDO:0006486 nord_rare diseases +MONDO:0006486 ordo_disorder diseases +MONDO:0006486 orphanet_rare diseases +MONDO:0006486 otar diseases +MONDO:0006486 rare diseases +MONDO:0006487 gard_rare diseases +MONDO:0006487 rare diseases +MONDO:0006489 otar diseases +MONDO:0006490 gard_rare diseases +MONDO:0006490 otar diseases +MONDO:0006490 rare diseases +MONDO:0006491 otar diseases +MONDO:0006493 otar diseases +MONDO:0006496 otar diseases +MONDO:0006497 otar diseases +MONDO:0006498 otar diseases +MONDO:0006499 otar diseases +MONDO:0006500 otar diseases +MONDO:0006502 otar diseases +MONDO:0006504 otar diseases +MONDO:0006505 otar diseases +MONDO:0006506 gard_rare diseases +MONDO:0006506 otar diseases +MONDO:0006506 rare diseases +MONDO:0006507 gard_rare diseases +MONDO:0006507 otar diseases +MONDO:0006507 rare diseases +MONDO:0006509 otar diseases +MONDO:0006510 otar diseases +MONDO:0006512 otar diseases +MONDO:0006513 otar diseases +MONDO:0006515 otar diseases +MONDO:0006517 otar diseases +MONDO:0006518 gard_rare diseases +MONDO:0006518 nord_rare diseases +MONDO:0006518 otar diseases +MONDO:0006518 rare diseases +MONDO:0006519 otar diseases +MONDO:0006520 otar diseases +MONDO:0006521 otar diseases +MONDO:0006523 otar diseases +MONDO:0006524 otar diseases +MONDO:0006525 otar diseases +MONDO:0006526 otar diseases +MONDO:0006527 otar diseases +MONDO:0006530 otar diseases +MONDO:0006531 otar diseases +MONDO:0006532 otar diseases +MONDO:0006533 otar diseases +MONDO:0006534 otar diseases +MONDO:0006536 gard_rare diseases +MONDO:0006536 nord_rare diseases +MONDO:0006536 otar diseases +MONDO:0006536 rare diseases +MONDO:0006540 otar diseases +MONDO:0006541 gard_rare diseases +MONDO:0006541 nord_rare diseases +MONDO:0006541 otar diseases +MONDO:0006541 rare diseases +MONDO:0006543 disease_grouping diseases +MONDO:0006543 gard_rare diseases +MONDO:0006543 nord_rare diseases +MONDO:0006543 ordo_group_of_disorders diseases +MONDO:0006543 otar diseases +MONDO:0006543 rare diseases +MONDO:0006544 otar diseases +MONDO:0006545 otar diseases +MONDO:0006546 otar diseases +MONDO:0006547 otar diseases +MONDO:0006549 otar diseases +MONDO:0006551 gard_rare diseases +MONDO:0006551 otar diseases +MONDO:0006551 rare diseases +MONDO:0006552 otar diseases +MONDO:0006554 otar diseases +MONDO:0006555 otar diseases +MONDO:0006556 otar diseases +MONDO:0006557 gard_rare diseases +MONDO:0006557 rare diseases +MONDO:0006558 gard_rare diseases +MONDO:0006558 nord_rare diseases +MONDO:0006558 ordo_disorder diseases +MONDO:0006558 orphanet_rare diseases +MONDO:0006558 otar diseases +MONDO:0006558 rare diseases +MONDO:0006559 otar diseases +MONDO:0006563 otar diseases +MONDO:0006564 otar diseases +MONDO:0006565 gard_rare diseases +MONDO:0006565 rare diseases +MONDO:0006566 otar diseases +MONDO:0006567 gard_rare diseases +MONDO:0006567 rare diseases +MONDO:0006570 otar diseases +MONDO:0006572 otar diseases +MONDO:0006573 otar diseases +MONDO:0006574 otar diseases +MONDO:0006578 otar diseases +MONDO:0006579 otar diseases +MONDO:0006581 otar diseases +MONDO:0006583 gard_rare diseases +MONDO:0006583 nord_rare diseases +MONDO:0006583 ordo_disorder diseases +MONDO:0006583 orphanet_rare diseases +MONDO:0006583 otar diseases +MONDO:0006583 rare diseases +MONDO:0006585 otar diseases +MONDO:0006589 otar diseases +MONDO:0006590 otar diseases +MONDO:0006591 otar diseases +MONDO:0006592 otar diseases +MONDO:0006593 otar diseases +MONDO:0006594 gard_rare diseases +MONDO:0006594 nord_rare diseases +MONDO:0006594 otar diseases +MONDO:0006594 rare diseases +MONDO:0006596 gard_rare diseases +MONDO:0006596 rare diseases +MONDO:0006597 gard_rare diseases +MONDO:0006597 otar diseases +MONDO:0006597 rare diseases +MONDO:0006598 gard_rare diseases +MONDO:0006598 otar diseases +MONDO:0006598 rare diseases +MONDO:0006599 otar diseases +MONDO:0006601 otar diseases +MONDO:0006602 disease_grouping diseases +MONDO:0006602 gard_rare diseases +MONDO:0006602 nord_rare diseases +MONDO:0006602 ordo_group_of_disorders diseases +MONDO:0006602 otar diseases +MONDO:0006602 rare diseases +MONDO:0006603 otar diseases +MONDO:0006604 otar diseases +MONDO:0006606 gard_rare diseases +MONDO:0006606 nord_rare diseases +MONDO:0006606 ordo_disorder diseases +MONDO:0006606 orphanet_rare diseases +MONDO:0006606 otar diseases +MONDO:0006606 rare diseases +MONDO:0006607 otar diseases +MONDO:0006608 otar diseases +MONDO:0006610 otar diseases +MONDO:0006611 gard_rare diseases +MONDO:0006611 otar diseases +MONDO:0006611 rare diseases +MONDO:0006614 gard_rare diseases +MONDO:0006614 nord_rare diseases +MONDO:0006614 ordo_disorder diseases +MONDO:0006614 orphanet_rare diseases +MONDO:0006614 otar diseases +MONDO:0006614 rare diseases +MONDO:0006616 otar diseases +MONDO:0006617 otar diseases +MONDO:0006618 otar diseases +MONDO:0006619 otar diseases +MONDO:0006621 gard_rare diseases +MONDO:0006621 rare diseases +MONDO:0006622 gard_rare diseases +MONDO:0006622 nord_rare diseases +MONDO:0006622 rare diseases +MONDO:0006624 otar diseases +MONDO:0006625 otar diseases +MONDO:0006626 gard_rare diseases +MONDO:0006626 otar diseases +MONDO:0006626 rare diseases +MONDO:0006629 otar diseases +MONDO:0006630 otar diseases +MONDO:0006632 otar diseases +MONDO:0006633 otar diseases +MONDO:0006634 gard_rare diseases +MONDO:0006634 otar diseases +MONDO:0006634 rare diseases +MONDO:0006635 otar diseases +MONDO:0006637 otar diseases +MONDO:0006638 gard_rare diseases +MONDO:0006638 otar diseases +MONDO:0006638 rare diseases +MONDO:0006639 gard_rare diseases +MONDO:0006639 nord_rare diseases +MONDO:0006639 ordo_disorder diseases +MONDO:0006639 orphanet_rare diseases +MONDO:0006639 otar diseases +MONDO:0006639 rare diseases +MONDO:0006640 otar diseases +MONDO:0006641 otar diseases +MONDO:0006642 otar diseases +MONDO:0006643 gard_rare diseases +MONDO:0006643 nord_rare diseases +MONDO:0006643 otar diseases +MONDO:0006643 rare diseases +MONDO:0006644 otar diseases +MONDO:0006645 gard_rare diseases +MONDO:0006645 otar diseases +MONDO:0006645 rare diseases +MONDO:0006646 otar diseases +MONDO:0006647 otar diseases +MONDO:0006648 gard_rare diseases +MONDO:0006648 rare diseases +MONDO:0006649 gard_rare diseases +MONDO:0006649 nord_rare diseases +MONDO:0006649 otar diseases +MONDO:0006649 rare diseases +MONDO:0006650 otar diseases +MONDO:0006651 disease_grouping diseases +MONDO:0006651 gard_rare diseases +MONDO:0006651 ordo_group_of_disorders diseases +MONDO:0006651 otar diseases +MONDO:0006651 rare diseases +MONDO:0006652 otar diseases +MONDO:0006653 gard_rare diseases +MONDO:0006653 otar diseases +MONDO:0006653 rare diseases +MONDO:0006654 gard_rare diseases +MONDO:0006654 otar diseases +MONDO:0006654 rare diseases +MONDO:0006656 gard_rare diseases +MONDO:0006656 otar diseases +MONDO:0006656 rare diseases +MONDO:0006658 otar diseases +MONDO:0006659 otar diseases +MONDO:0006660 otar diseases +MONDO:0006662 otar diseases +MONDO:0006663 gard_rare diseases +MONDO:0006663 ordo_disorder diseases +MONDO:0006663 orphanet_rare diseases +MONDO:0006663 otar diseases +MONDO:0006663 rare diseases +MONDO:0006664 gard_rare diseases +MONDO:0006664 nord_rare diseases +MONDO:0006664 ordo_disorder diseases +MONDO:0006664 ordo_morphological_anomaly diseases +MONDO:0006664 orphanet_rare diseases +MONDO:0006664 otar diseases +MONDO:0006664 rare diseases +MONDO:0006665 otar diseases +MONDO:0006666 otar diseases +MONDO:0006668 otar diseases +MONDO:0006669 gard_rare diseases +MONDO:0006669 otar diseases +MONDO:0006669 rare diseases +MONDO:0006670 gard_rare diseases +MONDO:0006670 otar diseases +MONDO:0006670 rare diseases +MONDO:0006671 otar diseases +MONDO:0006672 otar diseases +MONDO:0006673 gard_rare diseases +MONDO:0006673 otar diseases +MONDO:0006673 rare diseases +MONDO:0006676 otar diseases +MONDO:0006677 otar diseases +MONDO:0006678 otar diseases +MONDO:0006679 otar diseases +MONDO:0006680 otar diseases +MONDO:0006681 otar diseases +MONDO:0006682 gard_rare diseases +MONDO:0006682 otar diseases +MONDO:0006682 rare diseases +MONDO:0006683 gard_rare diseases +MONDO:0006683 otar diseases +MONDO:0006683 rare diseases +MONDO:0006684 otar diseases +MONDO:0006686 otar diseases +MONDO:0006687 gard_rare diseases +MONDO:0006687 ordo_disorder diseases +MONDO:0006687 orphanet_rare diseases +MONDO:0006687 otar diseases +MONDO:0006687 rare diseases +MONDO:0006688 gard_rare diseases +MONDO:0006688 otar diseases +MONDO:0006688 rare diseases +MONDO:0006690 otar diseases +MONDO:0006692 otar diseases +MONDO:0006693 otar diseases +MONDO:0006694 otar diseases +MONDO:0006698 otar diseases +MONDO:0006699 otar diseases +MONDO:0006701 gard_rare diseases +MONDO:0006701 otar diseases +MONDO:0006701 rare diseases +MONDO:0006702 gard_rare diseases +MONDO:0006702 ordo_disorder diseases +MONDO:0006702 orphanet_rare diseases +MONDO:0006702 otar diseases +MONDO:0006702 rare diseases +MONDO:0006704 otar diseases +MONDO:0006710 otar diseases +MONDO:0006711 otar diseases +MONDO:0006712 otar diseases +MONDO:0006713 otar diseases +MONDO:0006714 otar diseases +MONDO:0006715 otar diseases +MONDO:0006716 otar diseases +MONDO:0006717 gard_rare diseases +MONDO:0006717 otar diseases +MONDO:0006717 rare diseases +MONDO:0006718 otar diseases +MONDO:0006720 otar diseases +MONDO:0006721 otar diseases +MONDO:0006722 otar diseases +MONDO:0006723 otar diseases +MONDO:0006726 gard_rare diseases +MONDO:0006726 otar diseases +MONDO:0006726 rare diseases +MONDO:0006727 otar diseases +MONDO:0006729 gard_rare diseases +MONDO:0006729 rare diseases +MONDO:0006732 otar diseases +MONDO:0006733 otar diseases +MONDO:0006734 otar diseases +MONDO:0006735 otar diseases +MONDO:0006736 otar diseases +MONDO:0006737 otar diseases +MONDO:0006738 otar diseases +MONDO:0006739 otar diseases +MONDO:0006740 otar diseases +MONDO:0006741 otar diseases +MONDO:0006742 otar diseases +MONDO:0006743 gard_rare diseases +MONDO:0006743 rare diseases +MONDO:0006744 gard_rare diseases +MONDO:0006744 otar diseases +MONDO:0006744 rare diseases +MONDO:0006745 gard_rare diseases +MONDO:0006745 nord_rare diseases +MONDO:0006745 ordo_disorder diseases +MONDO:0006745 orphanet_rare diseases +MONDO:0006745 otar diseases +MONDO:0006745 rare diseases +MONDO:0006746 gard_rare diseases +MONDO:0006746 nord_rare diseases +MONDO:0006746 otar diseases +MONDO:0006746 rare diseases +MONDO:0006747 otar diseases +MONDO:0006748 otar diseases +MONDO:0006752 otar diseases +MONDO:0006753 gard_rare diseases +MONDO:0006753 otar diseases +MONDO:0006753 rare diseases +MONDO:0006755 otar diseases +MONDO:0006757 otar diseases +MONDO:0006758 otar diseases +MONDO:0006759 gard_rare diseases +MONDO:0006759 rare diseases +MONDO:0006760 gard_rare diseases +MONDO:0006760 otar diseases +MONDO:0006760 rare diseases +MONDO:0006761 otar diseases +MONDO:0006762 otar diseases +MONDO:0006763 otar diseases +MONDO:0006764 gard_rare diseases +MONDO:0006764 otar diseases +MONDO:0006764 rare diseases +MONDO:0006765 otar diseases +MONDO:0006767 otar diseases +MONDO:0006769 otar diseases +MONDO:0006770 gard_rare diseases +MONDO:0006770 otar diseases +MONDO:0006770 rare diseases +MONDO:0006771 otar diseases +MONDO:0006774 otar diseases +MONDO:0006778 otar diseases +MONDO:0006779 otar diseases +MONDO:0006781 otar diseases +MONDO:0006783 otar diseases +MONDO:0006784 gard_rare diseases +MONDO:0006784 otar diseases +MONDO:0006784 rare diseases +MONDO:0006786 otar diseases +MONDO:0006787 otar diseases +MONDO:0006788 gard_rare diseases +MONDO:0006788 obsoletion_candidate diseases +MONDO:0006788 rare diseases +MONDO:0006789 gard_rare diseases +MONDO:0006789 nord_rare diseases +MONDO:0006789 otar diseases +MONDO:0006789 rare diseases +MONDO:0006790 otar diseases +MONDO:0006791 otar diseases +MONDO:0006792 gard_rare diseases +MONDO:0006792 nord_rare diseases +MONDO:0006792 rare diseases +MONDO:0006793 otar diseases +MONDO:0006794 gard_rare diseases +MONDO:0006794 nord_rare diseases +MONDO:0006794 otar diseases +MONDO:0006794 rare diseases +MONDO:0006795 gard_rare diseases +MONDO:0006795 otar diseases +MONDO:0006795 rare diseases +MONDO:0006796 otar diseases +MONDO:0006797 otar diseases +MONDO:0006798 otar diseases +MONDO:0006799 otar diseases +MONDO:0006800 otar diseases +MONDO:0006801 otar diseases +MONDO:0006802 otar diseases +MONDO:0006803 otar diseases +MONDO:0006804 otar diseases +MONDO:0006805 otar diseases +MONDO:0006806 gard_rare diseases +MONDO:0006806 nord_rare diseases +MONDO:0006806 ordo_disorder diseases +MONDO:0006806 orphanet_rare diseases +MONDO:0006806 otar diseases +MONDO:0006806 rare diseases +MONDO:0006807 otar diseases +MONDO:0006808 otar diseases +MONDO:0006809 otar diseases +MONDO:0006810 otar diseases +MONDO:0006811 otar diseases +MONDO:0006812 otar diseases +MONDO:0006813 otar diseases +MONDO:0006814 gard_rare diseases +MONDO:0006814 otar diseases +MONDO:0006814 rare diseases +MONDO:0006815 gard_rare diseases +MONDO:0006815 otar diseases +MONDO:0006815 rare diseases +MONDO:0006816 otar diseases +MONDO:0006817 gard_rare diseases +MONDO:0006817 otar diseases +MONDO:0006817 rare diseases +MONDO:0006823 inferred_rare diseases +MONDO:0006823 otar diseases +MONDO:0006823 rare diseases +MONDO:0006824 otar diseases +MONDO:0006825 gard_rare diseases +MONDO:0006825 nord_rare diseases +MONDO:0006825 ordo_disorder diseases +MONDO:0006825 orphanet_rare diseases +MONDO:0006825 otar diseases +MONDO:0006825 rare diseases +MONDO:0006826 otar diseases +MONDO:0006827 otar diseases +MONDO:0006828 otar diseases +MONDO:0006829 gard_rare diseases +MONDO:0006829 otar diseases +MONDO:0006829 rare diseases +MONDO:0006831 gard_rare diseases +MONDO:0006831 otar diseases +MONDO:0006831 rare diseases +MONDO:0006834 otar diseases +MONDO:0006835 gard_rare diseases +MONDO:0006835 nord_rare diseases +MONDO:0006835 otar diseases +MONDO:0006835 rare diseases +MONDO:0006836 gard_rare diseases +MONDO:0006836 otar diseases +MONDO:0006836 rare diseases +MONDO:0006837 otar diseases +MONDO:0006838 gard_rare diseases +MONDO:0006838 otar diseases +MONDO:0006838 rare diseases +MONDO:0006839 gard_rare diseases +MONDO:0006839 nord_rare diseases +MONDO:0006839 rare diseases +MONDO:0006840 otar diseases +MONDO:0006841 gard_rare diseases +MONDO:0006841 otar diseases +MONDO:0006841 rare diseases +MONDO:0006842 gard_rare diseases +MONDO:0006842 otar diseases +MONDO:0006842 rare diseases +MONDO:0006843 otar diseases +MONDO:0006844 otar diseases +MONDO:0006845 gard_rare diseases +MONDO:0006845 rare diseases +MONDO:0006846 otar diseases +MONDO:0006847 gard_rare diseases +MONDO:0006847 rare diseases +MONDO:0006848 otar diseases +MONDO:0006849 otar diseases +MONDO:0006850 gard_rare diseases +MONDO:0006850 nord_rare diseases +MONDO:0006850 otar diseases +MONDO:0006850 rare diseases +MONDO:0006851 gard_rare diseases +MONDO:0006851 ordo_disorder diseases +MONDO:0006851 orphanet_rare diseases +MONDO:0006851 otar diseases +MONDO:0006851 rare diseases +MONDO:0006853 gard_rare diseases +MONDO:0006853 otar diseases +MONDO:0006853 rare diseases +MONDO:0006854 otar diseases +MONDO:0006855 otar diseases +MONDO:0006856 otar diseases +MONDO:0006857 otar diseases +MONDO:0006858 otar diseases +MONDO:0006858 rare_grouping diseases +MONDO:0006859 otar diseases +MONDO:0006861 gard_rare diseases +MONDO:0006861 nord_rare diseases +MONDO:0006861 ordo_disorder diseases +MONDO:0006861 orphanet_rare diseases +MONDO:0006861 otar diseases +MONDO:0006861 rare diseases +MONDO:0006862 gard_rare diseases +MONDO:0006862 otar diseases +MONDO:0006862 rare diseases +MONDO:0006863 gard_rare diseases +MONDO:0006863 otar diseases +MONDO:0006863 rare diseases +MONDO:0006865 otar diseases +MONDO:0006866 gard_rare diseases +MONDO:0006866 rare diseases +MONDO:0006869 otar diseases +MONDO:0006871 gard_rare diseases +MONDO:0006871 otar diseases +MONDO:0006871 rare diseases +MONDO:0006873 otar diseases +MONDO:0006874 otar diseases +MONDO:0006875 otar diseases +MONDO:0006876 gard_rare diseases +MONDO:0006876 otar diseases +MONDO:0006876 rare diseases +MONDO:0006877 otar diseases +MONDO:0006878 otar diseases +MONDO:0006879 gard_rare diseases +MONDO:0006879 otar diseases +MONDO:0006879 rare diseases +MONDO:0006881 otar diseases +MONDO:0006882 otar diseases +MONDO:0006883 otar diseases +MONDO:0006884 gard_rare diseases +MONDO:0006884 rare diseases +MONDO:0006886 gard_rare diseases +MONDO:0006886 otar diseases +MONDO:0006886 rare diseases +MONDO:0006887 otar diseases +MONDO:0006888 gard_rare diseases +MONDO:0006888 rare diseases +MONDO:0006889 otar diseases +MONDO:0006890 otar diseases +MONDO:0006891 otar diseases +MONDO:0006893 otar diseases +MONDO:0006894 otar diseases +MONDO:0006895 otar diseases +MONDO:0006896 otar diseases +MONDO:0006897 otar diseases +MONDO:0006898 otar diseases +MONDO:0006899 otar diseases +MONDO:0006900 otar diseases +MONDO:0006901 otar diseases +MONDO:0006903 otar diseases +MONDO:0006904 otar diseases +MONDO:0006908 gard_rare diseases +MONDO:0006908 nord_rare diseases +MONDO:0006908 ordo_disorder diseases +MONDO:0006908 orphanet_rare diseases +MONDO:0006908 otar diseases +MONDO:0006908 rare diseases +MONDO:0006909 otar diseases +MONDO:0006912 otar diseases +MONDO:0006913 gard_rare diseases +MONDO:0006913 nord_rare diseases +MONDO:0006913 ordo_disorder diseases +MONDO:0006913 orphanet_rare diseases +MONDO:0006913 otar diseases +MONDO:0006913 rare diseases +MONDO:0006915 gard_rare diseases +MONDO:0006915 otar diseases +MONDO:0006915 rare diseases +MONDO:0006916 otar diseases +MONDO:0006917 otar diseases +MONDO:0006918 gard_rare diseases +MONDO:0006918 otar diseases +MONDO:0006918 rare diseases +MONDO:0006919 otar diseases +MONDO:0006920 otar diseases +MONDO:0006921 otar diseases +MONDO:0006922 gard_rare diseases +MONDO:0006922 nord_rare diseases +MONDO:0006922 rare diseases +MONDO:0006926 otar diseases +MONDO:0006927 gard_rare diseases +MONDO:0006927 otar diseases +MONDO:0006927 rare diseases +MONDO:0006930 otar diseases +MONDO:0006932 otar diseases +MONDO:0006935 otar diseases +MONDO:0006936 otar diseases +MONDO:0006937 otar diseases +MONDO:0006939 otar diseases +MONDO:0006940 gard_rare diseases +MONDO:0006940 otar diseases +MONDO:0006940 rare diseases +MONDO:0006941 gard_rare diseases +MONDO:0006941 nord_rare diseases +MONDO:0006941 ordo_disorder diseases +MONDO:0006941 orphanet_rare diseases +MONDO:0006941 otar diseases +MONDO:0006941 rare diseases +MONDO:0006945 otar diseases +MONDO:0006946 gard_rare diseases +MONDO:0006946 otar diseases +MONDO:0006946 rare diseases +MONDO:0006947 otar diseases +MONDO:0006948 otar diseases +MONDO:0006949 otar diseases +MONDO:0006950 gard_rare diseases +MONDO:0006950 otar diseases +MONDO:0006950 rare diseases +MONDO:0006951 otar diseases +MONDO:0006952 gard_rare diseases +MONDO:0006952 nord_rare diseases +MONDO:0006952 ordo_disorder diseases +MONDO:0006952 orphanet_rare diseases +MONDO:0006952 otar diseases +MONDO:0006952 rare diseases +MONDO:0006953 gard_rare diseases +MONDO:0006953 otar diseases +MONDO:0006953 rare diseases +MONDO:0006955 otar diseases +MONDO:0006956 disease_grouping diseases +MONDO:0006956 gard_rare diseases +MONDO:0006956 ordo_group_of_disorders diseases +MONDO:0006956 otar diseases +MONDO:0006956 rare diseases +MONDO:0006957 otar diseases +MONDO:0006960 gard_rare diseases +MONDO:0006960 otar diseases +MONDO:0006960 rare diseases +MONDO:0006961 gard_rare diseases +MONDO:0006961 otar diseases +MONDO:0006961 rare diseases +MONDO:0006962 otar diseases +MONDO:0006963 otar diseases +MONDO:0006964 otar diseases +MONDO:0006965 otar diseases +MONDO:0006966 otar diseases +MONDO:0006968 otar diseases +MONDO:0006969 otar diseases +MONDO:0006970 otar diseases +MONDO:0006971 otar diseases +MONDO:0006973 otar diseases +MONDO:0006974 otar diseases +MONDO:0006975 otar diseases +MONDO:0006976 gard_rare diseases +MONDO:0006976 nord_rare diseases +MONDO:0006976 ordo_disorder diseases +MONDO:0006976 orphanet_rare diseases +MONDO:0006976 otar diseases +MONDO:0006976 rare diseases +MONDO:0006977 otar diseases +MONDO:0006978 gard_rare diseases +MONDO:0006978 nord_rare diseases +MONDO:0006978 otar diseases +MONDO:0006978 rare diseases +MONDO:0006980 gard_rare diseases +MONDO:0006980 nord_rare diseases +MONDO:0006980 otar diseases +MONDO:0006980 rare diseases +MONDO:0006981 gard_rare diseases +MONDO:0006981 otar diseases +MONDO:0006981 rare diseases +MONDO:0006982 otar diseases +MONDO:0006984 gard_rare diseases +MONDO:0006984 nord_rare diseases +MONDO:0006984 otar diseases +MONDO:0006984 rare diseases +MONDO:0006987 gard_rare diseases +MONDO:0006987 nord_rare diseases +MONDO:0006987 otar diseases +MONDO:0006987 rare diseases +MONDO:0006988 gard_rare diseases +MONDO:0006988 nord_rare diseases +MONDO:0006988 otar diseases +MONDO:0006988 rare diseases +MONDO:0006989 otar diseases +MONDO:0006990 gard_rare diseases +MONDO:0006990 rare diseases +MONDO:0006992 otar diseases +MONDO:0006993 otar diseases +MONDO:0006994 gard_rare diseases +MONDO:0006994 otar diseases +MONDO:0006994 rare diseases +MONDO:0006995 otar diseases +MONDO:0006996 otar diseases +MONDO:0006997 gard_rare diseases +MONDO:0006997 rare diseases +MONDO:0006998 otar diseases +MONDO:0006999 otar diseases +MONDO:0007000 otar diseases +MONDO:0007001 gard_rare diseases +MONDO:0007001 ordo_morphological_anomaly diseases +MONDO:0007001 otar diseases +MONDO:0007001 rare diseases +MONDO:0007004 otar diseases +MONDO:0007005 otar diseases +MONDO:0007006 gard_rare diseases +MONDO:0007006 otar diseases +MONDO:0007006 rare diseases +MONDO:0007007 otar diseases +MONDO:0007008 otar diseases +MONDO:0007009 otar diseases +MONDO:0007011 gard_rare diseases +MONDO:0007011 otar diseases +MONDO:0007011 rare diseases +MONDO:0007012 gard_rare diseases +MONDO:0007012 nord_rare diseases +MONDO:0007012 ordo_disorder diseases +MONDO:0007012 orphanet_rare diseases +MONDO:0007012 otar diseases +MONDO:0007012 rare diseases +MONDO:0007014 otar diseases +MONDO:0007015 gard_rare diseases +MONDO:0007015 otar diseases +MONDO:0007015 rare diseases +MONDO:0007016 otar diseases +MONDO:0007017 gard_rare diseases +MONDO:0007017 otar diseases +MONDO:0007017 rare diseases +MONDO:0007018 otar diseases +MONDO:0007019 otar diseases +MONDO:0007022 otar diseases +MONDO:0007023 otar diseases +MONDO:0007024 otar diseases +MONDO:0007025 otar diseases +MONDO:0007027 otar diseases +MONDO:0007028 otar diseases +MONDO:0007029 clingen diseases +MONDO:0007029 gard_rare diseases +MONDO:0007029 nord_rare diseases +MONDO:0007029 ordo_disorder diseases +MONDO:0007029 ordo_malformation_syndrome diseases +MONDO:0007029 orphanet_rare diseases +MONDO:0007029 otar diseases +MONDO:0007029 rare diseases +MONDO:0007030 gard_rare diseases +MONDO:0007030 nord_rare diseases +MONDO:0007030 rare diseases +MONDO:0007031 gard_rare diseases +MONDO:0007031 nord_rare diseases +MONDO:0007031 ordo_disorder diseases +MONDO:0007031 orphanet_rare diseases +MONDO:0007031 prototype_pattern diseases +MONDO:0007031 rare diseases +MONDO:0007032 gard_rare diseases +MONDO:0007032 nord_rare diseases +MONDO:0007032 ordo_disorder diseases +MONDO:0007032 ordo_malformation_syndrome diseases +MONDO:0007032 orphanet_rare diseases +MONDO:0007032 otar diseases +MONDO:0007032 rare diseases +MONDO:0007034 clingen diseases +MONDO:0007034 gard_rare diseases +MONDO:0007034 nord_rare diseases +MONDO:0007034 ordo_disorder diseases +MONDO:0007034 ordo_malformation_syndrome diseases +MONDO:0007034 orphanet_rare diseases +MONDO:0007034 otar diseases +MONDO:0007034 rare diseases +MONDO:0007035 otar diseases +MONDO:0007037 clingen diseases +MONDO:0007037 gard_rare diseases +MONDO:0007037 nord_rare diseases +MONDO:0007037 ordo_disorder diseases +MONDO:0007037 orphanet_rare diseases +MONDO:0007037 otar diseases +MONDO:0007037 rare diseases +MONDO:0007039 clingen diseases +MONDO:0007039 gard_rare diseases +MONDO:0007039 nord_rare diseases +MONDO:0007039 ordo_disorder diseases +MONDO:0007039 orphanet_rare diseases +MONDO:0007039 otar diseases +MONDO:0007039 rare diseases +MONDO:0007040 gard_rare diseases +MONDO:0007040 rare diseases +MONDO:0007041 clingen diseases +MONDO:0007041 gard_rare diseases +MONDO:0007041 nord_rare diseases +MONDO:0007041 ordo_disorder diseases +MONDO:0007041 ordo_malformation_syndrome diseases +MONDO:0007041 orphanet_rare diseases +MONDO:0007041 otar diseases +MONDO:0007041 rare diseases +MONDO:0007042 clingen diseases +MONDO:0007042 gard_rare diseases +MONDO:0007042 nord_rare diseases +MONDO:0007042 ordo_disorder diseases +MONDO:0007042 ordo_malformation_syndrome diseases +MONDO:0007042 orphanet_rare diseases +MONDO:0007042 otar diseases +MONDO:0007042 rare diseases +MONDO:0007043 clingen diseases +MONDO:0007043 gard_rare diseases +MONDO:0007043 nord_rare diseases +MONDO:0007043 ordo_disorder diseases +MONDO:0007043 ordo_malformation_syndrome diseases +MONDO:0007043 orphanet_rare diseases +MONDO:0007043 otar diseases +MONDO:0007043 rare diseases +MONDO:0007044 gard_rare diseases +MONDO:0007044 nord_rare diseases +MONDO:0007044 rare diseases +MONDO:0007045 gard_rare diseases +MONDO:0007045 nord_rare diseases +MONDO:0007045 ordo_disorder diseases +MONDO:0007045 ordo_malformation_syndrome diseases +MONDO:0007045 orphanet_rare diseases +MONDO:0007045 otar diseases +MONDO:0007045 rare diseases +MONDO:0007046 otar diseases +MONDO:0007047 gard_rare diseases +MONDO:0007047 nord_rare diseases +MONDO:0007047 ordo_disorder diseases +MONDO:0007047 orphanet_rare diseases +MONDO:0007047 otar diseases +MONDO:0007047 rare diseases +MONDO:0007048 gard_rare diseases +MONDO:0007048 nord_rare diseases +MONDO:0007048 ordo_disorder diseases +MONDO:0007048 orphanet_rare diseases +MONDO:0007048 otar diseases +MONDO:0007048 rare diseases +MONDO:0007051 gard_rare diseases +MONDO:0007051 ordo_malformation_syndrome diseases +MONDO:0007051 otar diseases +MONDO:0007051 rare diseases +MONDO:0007052 gard_rare diseases +MONDO:0007052 rare diseases +MONDO:0007055 gard_rare diseases +MONDO:0007055 nord_rare diseases +MONDO:0007055 ordo_disorder diseases +MONDO:0007055 ordo_malformation_syndrome diseases +MONDO:0007055 orphanet_rare diseases +MONDO:0007055 otar diseases +MONDO:0007055 rare diseases +MONDO:0007056 gard_rare diseases +MONDO:0007056 nord_rare diseases +MONDO:0007056 otar diseases +MONDO:0007056 rare diseases +MONDO:0007057 gard_rare diseases +MONDO:0007057 nord_rare diseases +MONDO:0007057 ordo_disorder diseases +MONDO:0007057 ordo_malformation_syndrome diseases +MONDO:0007057 orphanet_rare diseases +MONDO:0007057 otar diseases +MONDO:0007057 rare diseases +MONDO:0007058 gard_rare diseases +MONDO:0007058 nord_rare diseases +MONDO:0007058 ordo_disorder diseases +MONDO:0007058 ordo_malformation_syndrome diseases +MONDO:0007058 orphanet_rare diseases +MONDO:0007058 otar diseases +MONDO:0007058 rare diseases +MONDO:0007059 gard_rare diseases +MONDO:0007059 ordo_disorder diseases +MONDO:0007059 ordo_malformation_syndrome diseases +MONDO:0007059 orphanet_rare diseases +MONDO:0007059 otar diseases +MONDO:0007059 rare diseases +MONDO:0007060 gard_rare diseases +MONDO:0007060 rare diseases +MONDO:0007062 gard_rare diseases +MONDO:0007062 nord_rare diseases +MONDO:0007062 ordo_disorder diseases +MONDO:0007062 orphanet_rare diseases +MONDO:0007062 otar diseases +MONDO:0007062 rare diseases +MONDO:0007064 clingen diseases +MONDO:0007064 gard_rare diseases +MONDO:0007064 nord_rare diseases +MONDO:0007064 ordo_disorder diseases +MONDO:0007064 orphanet_rare diseases +MONDO:0007064 otar diseases +MONDO:0007064 rare diseases +MONDO:0007066 gard_rare diseases +MONDO:0007066 nord_rare diseases +MONDO:0007066 otar diseases +MONDO:0007066 rare diseases +MONDO:0007067 gard_rare diseases +MONDO:0007067 otar diseases +MONDO:0007067 rare diseases +MONDO:0007068 clingen diseases +MONDO:0007068 gard_rare diseases +MONDO:0007068 nord_rare diseases +MONDO:0007068 ordo_disorder diseases +MONDO:0007068 orphanet_rare diseases +MONDO:0007068 otar diseases +MONDO:0007068 rare diseases +MONDO:0007070 gard_rare diseases +MONDO:0007070 nord_rare diseases +MONDO:0007070 ordo_disorder diseases +MONDO:0007070 orphanet_rare diseases +MONDO:0007070 otar diseases +MONDO:0007070 rare diseases +MONDO:0007071 gard_rare diseases +MONDO:0007071 rare diseases +MONDO:0007072 gard_rare diseases +MONDO:0007072 nord_rare diseases +MONDO:0007072 ordo_disorder diseases +MONDO:0007072 ordo_malformation_syndrome diseases +MONDO:0007072 orphanet_rare diseases +MONDO:0007072 otar diseases +MONDO:0007072 rare diseases +MONDO:0007073 gard_rare diseases +MONDO:0007073 nord_rare diseases +MONDO:0007073 ordo_disorder diseases +MONDO:0007073 ordo_malformation_syndrome diseases +MONDO:0007073 orphanet_rare diseases +MONDO:0007073 otar diseases +MONDO:0007073 rare diseases +MONDO:0007075 gard_rare diseases +MONDO:0007075 nord_rare diseases +MONDO:0007075 rare diseases +MONDO:0007077 gard_rare diseases +MONDO:0007077 nord_rare diseases +MONDO:0007077 ordo_disorder diseases +MONDO:0007077 ordo_malformation_syndrome diseases +MONDO:0007077 orphanet_rare diseases +MONDO:0007077 otar diseases +MONDO:0007077 rare diseases +MONDO:0007078 gard_rare diseases +MONDO:0007078 nord_rare diseases +MONDO:0007078 ordo_disorder diseases +MONDO:0007078 orphanet_rare diseases +MONDO:0007078 otar diseases +MONDO:0007078 rare diseases +MONDO:0007079 otar diseases +MONDO:0007080 gard_rare diseases +MONDO:0007080 nord_rare diseases +MONDO:0007080 ordo_disorder diseases +MONDO:0007080 orphanet_rare diseases +MONDO:0007080 otar diseases +MONDO:0007080 rare diseases +MONDO:0007082 gard_rare diseases +MONDO:0007082 nord_rare diseases +MONDO:0007082 rare diseases +MONDO:0007083 gard_rare diseases +MONDO:0007083 nord_rare diseases +MONDO:0007083 ordo_disorder diseases +MONDO:0007083 orphanet_rare diseases +MONDO:0007083 otar diseases +MONDO:0007083 rare diseases +MONDO:0007084 gard_rare diseases +MONDO:0007084 rare diseases +MONDO:0007085 gard_rare diseases +MONDO:0007085 nord_rare diseases +MONDO:0007085 ordo_disorder diseases +MONDO:0007085 orphanet_rare diseases +MONDO:0007085 otar diseases +MONDO:0007085 rare diseases +MONDO:0007086 gard_rare diseases +MONDO:0007086 nord_rare diseases +MONDO:0007086 ordo_etiological_subtype diseases +MONDO:0007086 ordo_subtype_of_a_disorder diseases +MONDO:0007086 otar diseases +MONDO:0007086 rare diseases +MONDO:0007087 gard_rare diseases +MONDO:0007087 rare diseases +MONDO:0007088 gard_rare diseases +MONDO:0007088 rare diseases +MONDO:0007089 gard_rare diseases +MONDO:0007089 rare diseases +MONDO:0007092 gard_rare diseases +MONDO:0007092 rare diseases +MONDO:0007093 gard_rare diseases +MONDO:0007093 nord_rare diseases +MONDO:0007093 ordo_subtype_of_a_disorder diseases +MONDO:0007093 otar diseases +MONDO:0007093 rare diseases +MONDO:0007094 gard_rare diseases +MONDO:0007094 rare diseases +MONDO:0007095 gard_rare diseases +MONDO:0007095 nord_rare diseases +MONDO:0007095 ordo_disorder diseases +MONDO:0007095 ordo_malformation_syndrome diseases +MONDO:0007095 orphanet_rare diseases +MONDO:0007095 otar diseases +MONDO:0007095 rare diseases +MONDO:0007097 gard_rare diseases +MONDO:0007097 nord_rare diseases +MONDO:0007097 ordo_disorder diseases +MONDO:0007097 orphanet_rare diseases +MONDO:0007097 otar diseases +MONDO:0007097 rare diseases +MONDO:0007098 gard_rare diseases +MONDO:0007098 nord_rare diseases +MONDO:0007098 ordo_subtype_of_a_disorder diseases +MONDO:0007098 otar diseases +MONDO:0007098 rare diseases +MONDO:0007099 gard_rare diseases +MONDO:0007099 nord_rare diseases +MONDO:0007099 ordo_disorder diseases +MONDO:0007099 orphanet_rare diseases +MONDO:0007099 otar diseases +MONDO:0007099 rare diseases +MONDO:0007100 gard_rare diseases +MONDO:0007100 nord_rare diseases +MONDO:0007100 ordo_group_of_disorders diseases +MONDO:0007100 otar diseases +MONDO:0007100 rare diseases +MONDO:0007101 gard_rare diseases +MONDO:0007101 ordo_disorder diseases +MONDO:0007101 orphanet_rare diseases +MONDO:0007101 otar diseases +MONDO:0007101 rare diseases +MONDO:0007103 clingen diseases +MONDO:0007103 gard_rare diseases +MONDO:0007103 nord_rare diseases +MONDO:0007103 rare diseases +MONDO:0007104 gard_rare diseases +MONDO:0007104 nord_rare diseases +MONDO:0007104 ordo_disorder diseases +MONDO:0007104 orphanet_rare diseases +MONDO:0007104 rare diseases +MONDO:0007105 clingen diseases +MONDO:0007105 gard_rare diseases +MONDO:0007105 nord_rare diseases +MONDO:0007105 otar diseases +MONDO:0007105 rare diseases +MONDO:0007108 disease_grouping diseases +MONDO:0007108 gard_rare diseases +MONDO:0007108 nord_rare diseases +MONDO:0007108 ordo_group_of_disorders diseases +MONDO:0007108 rare diseases +MONDO:0007109 gard_rare diseases +MONDO:0007109 nord_rare diseases +MONDO:0007109 ordo_disorder diseases +MONDO:0007109 orphanet_rare diseases +MONDO:0007109 otar diseases +MONDO:0007109 rare diseases +MONDO:0007110 gard_rare diseases +MONDO:0007110 nord_rare diseases +MONDO:0007110 rare diseases +MONDO:0007111 gard_rare diseases +MONDO:0007111 nord_rare diseases +MONDO:0007111 rare diseases +MONDO:0007112 gard_rare diseases +MONDO:0007112 nord_rare diseases +MONDO:0007112 ordo_disorder diseases +MONDO:0007112 ordo_morphological_anomaly diseases +MONDO:0007112 orphanet_rare diseases +MONDO:0007112 otar diseases +MONDO:0007112 rare diseases +MONDO:0007113 clingen diseases +MONDO:0007113 gard_rare diseases +MONDO:0007113 nord_rare diseases +MONDO:0007113 ordo_disorder diseases +MONDO:0007113 ordo_malformation_syndrome diseases +MONDO:0007113 orphanet_rare diseases +MONDO:0007113 otar diseases +MONDO:0007113 rare diseases +MONDO:0007114 gard_rare diseases +MONDO:0007114 nord_rare diseases +MONDO:0007114 ordo_disorder diseases +MONDO:0007114 ordo_malformation_syndrome diseases +MONDO:0007114 orphanet_rare diseases +MONDO:0007114 otar diseases +MONDO:0007114 rare diseases +MONDO:0007115 gard_rare diseases +MONDO:0007115 nord_rare diseases +MONDO:0007115 rare diseases +MONDO:0007116 gard_rare diseases +MONDO:0007116 ordo_disorder diseases +MONDO:0007116 orphanet_rare diseases +MONDO:0007116 otar diseases +MONDO:0007116 rare diseases +MONDO:0007118 gard_rare diseases +MONDO:0007118 nord_rare diseases +MONDO:0007118 ordo_disorder diseases +MONDO:0007118 orphanet_rare diseases +MONDO:0007118 rare diseases +MONDO:0007119 gard_rare diseases +MONDO:0007119 nord_rare diseases +MONDO:0007119 ordo_disorder diseases +MONDO:0007119 ordo_morphological_anomaly diseases +MONDO:0007119 orphanet_rare diseases +MONDO:0007119 otar diseases +MONDO:0007119 prototype_pattern diseases +MONDO:0007119 rare diseases +MONDO:0007120 gard_rare diseases +MONDO:0007120 ordo_disorder diseases +MONDO:0007120 ordo_malformation_syndrome diseases +MONDO:0007120 orphanet_rare diseases +MONDO:0007120 otar diseases +MONDO:0007120 rare diseases +MONDO:0007123 gard_rare diseases +MONDO:0007123 ordo_malformation_syndrome diseases +MONDO:0007123 ordo_subtype_of_a_disorder diseases +MONDO:0007123 otar diseases +MONDO:0007123 rare diseases +MONDO:0007124 gard_rare diseases +MONDO:0007124 nord_rare diseases +MONDO:0007124 ordo_disorder diseases +MONDO:0007124 ordo_malformation_syndrome diseases +MONDO:0007124 orphanet_rare diseases +MONDO:0007124 otar diseases +MONDO:0007124 rare diseases +MONDO:0007127 gard_rare diseases +MONDO:0007127 nord_rare diseases +MONDO:0007127 ordo_disorder diseases +MONDO:0007127 ordo_malformation_syndrome diseases +MONDO:0007127 orphanet_rare diseases +MONDO:0007127 otar diseases +MONDO:0007127 rare diseases +MONDO:0007129 gard_rare diseases +MONDO:0007129 rare diseases +MONDO:0007130 gard_rare diseases +MONDO:0007130 nord_rare diseases +MONDO:0007130 ordo_disorder diseases +MONDO:0007130 ordo_morphological_anomaly diseases +MONDO:0007130 orphanet_rare diseases +MONDO:0007130 rare diseases +MONDO:0007131 gard_rare diseases +MONDO:0007131 ordo_disorder diseases +MONDO:0007131 ordo_malformation_syndrome diseases +MONDO:0007131 orphanet_rare diseases +MONDO:0007131 otar diseases +MONDO:0007131 rare diseases +MONDO:0007133 gard_rare diseases +MONDO:0007133 nord_rare diseases +MONDO:0007133 rare diseases +MONDO:0007134 clingen diseases +MONDO:0007134 gard_rare diseases +MONDO:0007134 nord_rare diseases +MONDO:0007134 ordo_disorder diseases +MONDO:0007134 ordo_malformation_syndrome diseases +MONDO:0007134 orphanet_rare diseases +MONDO:0007134 otar diseases +MONDO:0007134 rare diseases +MONDO:0007135 gard_rare diseases +MONDO:0007135 rare diseases +MONDO:0007136 gard_rare diseases +MONDO:0007136 prototype_pattern diseases +MONDO:0007136 rare diseases +MONDO:0007137 gard_rare diseases +MONDO:0007137 nord_rare diseases +MONDO:0007137 ordo_disorder diseases +MONDO:0007137 orphanet_rare diseases +MONDO:0007137 rare diseases +MONDO:0007138 gard_rare diseases +MONDO:0007138 nord_rare diseases +MONDO:0007138 rare diseases +MONDO:0007142 gard_rare diseases +MONDO:0007142 nord_rare diseases +MONDO:0007142 ordo_disorder diseases +MONDO:0007142 ordo_malformation_syndrome diseases +MONDO:0007142 orphanet_rare diseases +MONDO:0007142 otar diseases +MONDO:0007142 prototype_pattern diseases +MONDO:0007142 rare diseases +MONDO:0007143 gard_rare diseases +MONDO:0007143 ordo_disorder diseases +MONDO:0007143 ordo_malformation_syndrome diseases +MONDO:0007143 orphanet_rare diseases +MONDO:0007143 otar diseases +MONDO:0007143 rare diseases +MONDO:0007145 gard_rare diseases +MONDO:0007145 nord_rare diseases +MONDO:0007145 ordo_disorder diseases +MONDO:0007145 ordo_malformation_syndrome diseases +MONDO:0007145 orphanet_rare diseases +MONDO:0007145 otar diseases +MONDO:0007145 rare diseases +MONDO:0007147 otar diseases +MONDO:0007150 otar diseases +MONDO:0007152 gard_rare diseases +MONDO:0007152 nord_rare diseases +MONDO:0007152 otar diseases +MONDO:0007152 rare diseases +MONDO:0007154 gard_rare diseases +MONDO:0007154 nord_rare diseases +MONDO:0007154 ordo_disorder diseases +MONDO:0007154 ordo_morphological_anomaly diseases +MONDO:0007154 orphanet_rare diseases +MONDO:0007154 otar diseases +MONDO:0007154 rare diseases +MONDO:0007157 gard_rare diseases +MONDO:0007157 nord_rare diseases +MONDO:0007157 rare diseases +MONDO:0007158 gard_rare diseases +MONDO:0007158 nord_rare diseases +MONDO:0007158 ordo_disorder diseases +MONDO:0007158 ordo_malformation_syndrome diseases +MONDO:0007158 orphanet_rare diseases +MONDO:0007158 otar diseases +MONDO:0007158 rare diseases +MONDO:0007159 gard_rare diseases +MONDO:0007159 nord_rare diseases +MONDO:0007159 ordo_disorder diseases +MONDO:0007159 ordo_malformation_syndrome diseases +MONDO:0007159 orphanet_rare diseases +MONDO:0007159 otar diseases +MONDO:0007159 rare diseases +MONDO:0007160 clingen diseases +MONDO:0007160 gard_rare diseases +MONDO:0007160 nord_rare diseases +MONDO:0007160 ordo_subtype_of_a_disorder diseases +MONDO:0007160 otar diseases +MONDO:0007160 rare diseases +MONDO:0007161 gard_rare diseases +MONDO:0007161 rare diseases +MONDO:0007163 gard_rare diseases +MONDO:0007163 nord_rare diseases +MONDO:0007163 ordo_disorder diseases +MONDO:0007163 orphanet_rare diseases +MONDO:0007163 otar diseases +MONDO:0007163 rare diseases +MONDO:0007164 gard_rare diseases +MONDO:0007164 nord_rare diseases +MONDO:0007164 ordo_disorder diseases +MONDO:0007164 orphanet_rare diseases +MONDO:0007164 otar diseases +MONDO:0007164 rare diseases +MONDO:0007165 gard_rare diseases +MONDO:0007165 nord_rare diseases +MONDO:0007165 ordo_disorder diseases +MONDO:0007165 orphanet_rare diseases +MONDO:0007165 otar diseases +MONDO:0007165 rare diseases +MONDO:0007166 gard_rare diseases +MONDO:0007166 rare diseases +MONDO:0007167 gard_rare diseases +MONDO:0007167 nord_rare diseases +MONDO:0007167 ordo_disorder diseases +MONDO:0007167 ordo_malformation_syndrome diseases +MONDO:0007167 orphanet_rare diseases +MONDO:0007167 otar diseases +MONDO:0007167 rare diseases +MONDO:0007168 gard_rare diseases +MONDO:0007168 nord_rare diseases +MONDO:0007168 ordo_disorder diseases +MONDO:0007168 ordo_malformation_syndrome diseases +MONDO:0007168 orphanet_rare diseases +MONDO:0007168 otar diseases +MONDO:0007168 rare diseases +MONDO:0007170 gard_rare diseases +MONDO:0007170 nord_rare diseases +MONDO:0007170 rare diseases +MONDO:0007171 gard_rare diseases +MONDO:0007171 nord_rare diseases +MONDO:0007171 rare diseases +MONDO:0007172 gard_rare diseases +MONDO:0007172 nord_rare diseases +MONDO:0007172 otar diseases +MONDO:0007172 rare diseases +MONDO:0007173 gard_rare diseases +MONDO:0007173 nord_rare diseases +MONDO:0007173 ordo_disorder diseases +MONDO:0007173 ordo_malformation_syndrome diseases +MONDO:0007173 orphanet_rare diseases +MONDO:0007173 otar diseases +MONDO:0007173 rare diseases +MONDO:0007174 gard_rare diseases +MONDO:0007174 nord_rare diseases +MONDO:0007174 ordo_disorder diseases +MONDO:0007174 orphanet_rare diseases +MONDO:0007174 otar diseases +MONDO:0007174 rare diseases +MONDO:0007176 gard_rare diseases +MONDO:0007176 nord_rare diseases +MONDO:0007176 ordo_disorder diseases +MONDO:0007176 orphanet_rare diseases +MONDO:0007176 otar diseases +MONDO:0007176 rare diseases +MONDO:0007177 gard_rare diseases +MONDO:0007177 nord_rare diseases +MONDO:0007177 ordo_disorder diseases +MONDO:0007177 ordo_malformation_syndrome diseases +MONDO:0007177 orphanet_rare diseases +MONDO:0007177 otar diseases +MONDO:0007177 rare diseases +MONDO:0007179 clingen diseases +MONDO:0007179 otar diseases +MONDO:0007182 gard_rare diseases +MONDO:0007182 nord_rare diseases +MONDO:0007182 ordo_disorder diseases +MONDO:0007182 orphanet_rare diseases +MONDO:0007182 otar diseases +MONDO:0007182 rare diseases +MONDO:0007184 gard_rare diseases +MONDO:0007184 nord_rare diseases +MONDO:0007184 rare diseases +MONDO:0007185 gard_rare diseases +MONDO:0007185 ordo_disorder diseases +MONDO:0007185 ordo_malformation_syndrome diseases +MONDO:0007185 orphanet_rare diseases +MONDO:0007185 otar diseases +MONDO:0007185 rare diseases +MONDO:0007186 otar diseases +MONDO:0007187 clingen diseases +MONDO:0007187 gard_rare diseases +MONDO:0007187 nord_rare diseases +MONDO:0007187 ordo_disorder diseases +MONDO:0007187 ordo_malformation_syndrome diseases +MONDO:0007187 orphanet_rare diseases +MONDO:0007187 otar diseases +MONDO:0007187 rare diseases +MONDO:0007188 gard_rare diseases +MONDO:0007188 nord_rare diseases +MONDO:0007188 ordo_disorder diseases +MONDO:0007188 ordo_morphological_anomaly diseases +MONDO:0007188 orphanet_rare diseases +MONDO:0007188 otar diseases +MONDO:0007188 rare diseases +MONDO:0007190 inferred_rare diseases +MONDO:0007190 predisposition diseases +MONDO:0007190 rare diseases +MONDO:0007191 gard_rare diseases +MONDO:0007191 ordo_disorder diseases +MONDO:0007191 orphanet_rare diseases +MONDO:0007191 otar diseases +MONDO:0007191 rare diseases +MONDO:0007193 gard_rare diseases +MONDO:0007193 nord_rare diseases +MONDO:0007193 rare diseases +MONDO:0007194 gard_rare diseases +MONDO:0007194 nord_rare diseases +MONDO:0007194 ordo_disorder diseases +MONDO:0007194 ordo_morphological_anomaly diseases +MONDO:0007194 orphanet_rare diseases +MONDO:0007194 otar diseases +MONDO:0007194 rare diseases +MONDO:0007195 gard_rare diseases +MONDO:0007195 nord_rare diseases +MONDO:0007195 rare diseases +MONDO:0007197 otar diseases +MONDO:0007198 gard_rare diseases +MONDO:0007198 nord_rare diseases +MONDO:0007198 ordo_disorder diseases +MONDO:0007198 ordo_malformation_syndrome diseases +MONDO:0007198 orphanet_rare diseases +MONDO:0007198 otar diseases +MONDO:0007198 rare diseases +MONDO:0007200 gard_rare diseases +MONDO:0007200 nord_rare diseases +MONDO:0007200 ordo_disorder diseases +MONDO:0007200 ordo_malformation_syndrome diseases +MONDO:0007200 orphanet_rare diseases +MONDO:0007200 otar diseases +MONDO:0007200 rare diseases +MONDO:0007201 gard_rare diseases +MONDO:0007201 nord_rare diseases +MONDO:0007201 ordo_disorder diseases +MONDO:0007201 ordo_malformation_syndrome diseases +MONDO:0007201 orphanet_rare diseases +MONDO:0007201 otar diseases +MONDO:0007201 rare diseases +MONDO:0007202 gard_rare diseases +MONDO:0007202 ordo_disorder diseases +MONDO:0007202 orphanet_rare diseases +MONDO:0007202 otar diseases +MONDO:0007202 rare diseases +MONDO:0007203 gard_rare diseases +MONDO:0007203 nord_rare diseases +MONDO:0007203 ordo_disorder diseases +MONDO:0007203 ordo_malformation_syndrome diseases +MONDO:0007203 orphanet_rare diseases +MONDO:0007203 otar diseases +MONDO:0007203 rare diseases +MONDO:0007204 gard_rare diseases +MONDO:0007204 nord_rare diseases +MONDO:0007204 rare diseases +MONDO:0007205 clingen diseases +MONDO:0007205 gard_rare diseases +MONDO:0007205 nord_rare diseases +MONDO:0007205 ordo_disorder diseases +MONDO:0007205 orphanet_rare diseases +MONDO:0007205 otar diseases +MONDO:0007205 rare diseases +MONDO:0007207 gard_rare diseases +MONDO:0007207 nord_rare diseases +MONDO:0007207 ordo_disorder diseases +MONDO:0007207 ordo_malformation_syndrome diseases +MONDO:0007207 orphanet_rare diseases +MONDO:0007207 otar diseases +MONDO:0007207 rare diseases +MONDO:0007208 gard_rare diseases +MONDO:0007208 nord_rare diseases +MONDO:0007208 ordo_disorder diseases +MONDO:0007208 orphanet_rare diseases +MONDO:0007208 otar diseases +MONDO:0007208 rare diseases +MONDO:0007209 gard_rare diseases +MONDO:0007209 nord_rare diseases +MONDO:0007209 ordo_disorder diseases +MONDO:0007209 ordo_malformation_syndrome diseases +MONDO:0007209 orphanet_rare diseases +MONDO:0007209 otar diseases +MONDO:0007209 rare diseases +MONDO:0007211 gard_rare diseases +MONDO:0007211 nord_rare diseases +MONDO:0007211 ordo_disorder diseases +MONDO:0007211 ordo_malformation_syndrome diseases +MONDO:0007211 orphanet_rare diseases +MONDO:0007211 otar diseases +MONDO:0007211 rare diseases +MONDO:0007212 gard_rare diseases +MONDO:0007212 ordo_disorder diseases +MONDO:0007212 ordo_malformation_syndrome diseases +MONDO:0007212 orphanet_rare diseases +MONDO:0007212 rare diseases +MONDO:0007213 ordo_malformation_syndrome diseases +MONDO:0007214 gard_rare diseases +MONDO:0007214 ordo_disorder diseases +MONDO:0007214 ordo_malformation_syndrome diseases +MONDO:0007214 orphanet_rare diseases +MONDO:0007214 otar diseases +MONDO:0007214 rare diseases +MONDO:0007215 gard_rare diseases +MONDO:0007215 nord_rare diseases +MONDO:0007215 ordo_disorder diseases +MONDO:0007215 ordo_malformation_syndrome diseases +MONDO:0007215 orphanet_rare diseases +MONDO:0007215 otar diseases +MONDO:0007215 rare diseases +MONDO:0007216 gard_rare diseases +MONDO:0007216 nord_rare diseases +MONDO:0007216 ordo_disorder diseases +MONDO:0007216 ordo_malformation_syndrome diseases +MONDO:0007216 orphanet_rare diseases +MONDO:0007216 otar diseases +MONDO:0007216 rare diseases +MONDO:0007217 gard_rare diseases +MONDO:0007217 nord_rare diseases +MONDO:0007217 rare diseases +MONDO:0007218 gard_rare diseases +MONDO:0007218 nord_rare diseases +MONDO:0007218 ordo_disorder diseases +MONDO:0007218 ordo_malformation_syndrome diseases +MONDO:0007218 orphanet_rare diseases +MONDO:0007218 otar diseases +MONDO:0007218 rare diseases +MONDO:0007219 gard_rare diseases +MONDO:0007219 nord_rare diseases +MONDO:0007219 ordo_disorder diseases +MONDO:0007219 ordo_malformation_syndrome diseases +MONDO:0007219 orphanet_rare diseases +MONDO:0007219 otar diseases +MONDO:0007219 rare diseases +MONDO:0007220 gard_rare diseases +MONDO:0007220 nord_rare diseases +MONDO:0007220 ordo_subtype_of_a_disorder diseases +MONDO:0007220 otar diseases +MONDO:0007220 rare diseases +MONDO:0007221 gard_rare diseases +MONDO:0007221 nord_rare diseases +MONDO:0007221 ordo_disorder diseases +MONDO:0007221 ordo_malformation_syndrome diseases +MONDO:0007221 orphanet_rare diseases +MONDO:0007221 otar diseases +MONDO:0007221 rare diseases +MONDO:0007222 gard_rare diseases +MONDO:0007222 nord_rare diseases +MONDO:0007222 rare diseases +MONDO:0007223 gard_rare diseases +MONDO:0007223 nord_rare diseases +MONDO:0007223 rare diseases +MONDO:0007224 gard_rare diseases +MONDO:0007224 rare diseases +MONDO:0007225 gard_rare diseases +MONDO:0007225 nord_rare diseases +MONDO:0007225 ordo_disorder diseases +MONDO:0007225 ordo_malformation_syndrome diseases +MONDO:0007225 orphanet_rare diseases +MONDO:0007225 otar diseases +MONDO:0007225 rare diseases +MONDO:0007226 gard_rare diseases +MONDO:0007226 ordo_disorder diseases +MONDO:0007226 ordo_malformation_syndrome diseases +MONDO:0007226 orphanet_rare diseases +MONDO:0007226 otar diseases +MONDO:0007226 rare diseases +MONDO:0007227 gard_rare diseases +MONDO:0007227 nord_rare diseases +MONDO:0007227 ordo_disorder diseases +MONDO:0007227 ordo_malformation_syndrome diseases +MONDO:0007227 orphanet_rare diseases +MONDO:0007227 otar diseases +MONDO:0007227 rare diseases +MONDO:0007230 gard_rare diseases +MONDO:0007230 nord_rare diseases +MONDO:0007230 ordo_disorder diseases +MONDO:0007230 ordo_malformation_syndrome diseases +MONDO:0007230 orphanet_rare diseases +MONDO:0007230 rare diseases +MONDO:0007231 gard_rare diseases +MONDO:0007231 ordo_disorder diseases +MONDO:0007231 ordo_malformation_syndrome diseases +MONDO:0007231 orphanet_rare diseases +MONDO:0007231 otar diseases +MONDO:0007231 rare diseases +MONDO:0007232 gard_rare diseases +MONDO:0007232 nord_rare diseases +MONDO:0007232 ordo_disorder diseases +MONDO:0007232 ordo_malformation_syndrome diseases +MONDO:0007232 orphanet_rare diseases +MONDO:0007232 otar diseases +MONDO:0007232 rare diseases +MONDO:0007233 gard_rare diseases +MONDO:0007233 nord_rare diseases +MONDO:0007233 ordo_disorder diseases +MONDO:0007233 ordo_morphological_anomaly diseases +MONDO:0007233 orphanet_rare diseases +MONDO:0007233 rare diseases +MONDO:0007235 gard_rare diseases +MONDO:0007235 nord_rare diseases +MONDO:0007235 ordo_disorder diseases +MONDO:0007235 ordo_malformation_syndrome diseases +MONDO:0007235 orphanet_rare diseases +MONDO:0007235 otar diseases +MONDO:0007235 rare diseases +MONDO:0007236 gard_rare diseases +MONDO:0007236 rare diseases +MONDO:0007237 gard_rare diseases +MONDO:0007237 nord_rare diseases +MONDO:0007237 ordo_disorder diseases +MONDO:0007237 ordo_morphological_anomaly diseases +MONDO:0007237 orphanet_rare diseases +MONDO:0007237 rare diseases +MONDO:0007238 gard_rare diseases +MONDO:0007238 nord_rare diseases +MONDO:0007238 rare diseases +MONDO:0007239 gard_rare diseases +MONDO:0007239 nord_rare diseases +MONDO:0007239 otar diseases +MONDO:0007239 rare diseases +MONDO:0007240 gard_rare diseases +MONDO:0007240 rare diseases +MONDO:0007243 gard_rare diseases +MONDO:0007243 nord_rare diseases +MONDO:0007243 ordo_disorder diseases +MONDO:0007243 orphanet_rare diseases +MONDO:0007243 otar diseases +MONDO:0007243 rare diseases +MONDO:0007244 clingen diseases +MONDO:0007244 gard_rare diseases +MONDO:0007244 nord_rare diseases +MONDO:0007244 ordo_disorder diseases +MONDO:0007244 ordo_malformation_syndrome diseases +MONDO:0007244 orphanet_rare diseases +MONDO:0007244 otar diseases +MONDO:0007244 rare diseases +MONDO:0007245 gard_rare diseases +MONDO:0007245 nord_rare diseases +MONDO:0007245 ordo_disorder diseases +MONDO:0007245 ordo_malformation_syndrome diseases +MONDO:0007245 orphanet_rare diseases +MONDO:0007245 otar diseases +MONDO:0007245 rare diseases +MONDO:0007247 gard_rare diseases +MONDO:0007247 nord_rare diseases +MONDO:0007247 rare diseases +MONDO:0007248 gard_rare diseases +MONDO:0007248 nord_rare diseases +MONDO:0007248 ordo_disorder diseases +MONDO:0007248 orphanet_rare diseases +MONDO:0007248 rare diseases +MONDO:0007249 gard_rare diseases +MONDO:0007249 nord_rare diseases +MONDO:0007249 ordo_disorder diseases +MONDO:0007249 ordo_malformation_syndrome diseases +MONDO:0007249 orphanet_rare diseases +MONDO:0007249 otar diseases +MONDO:0007249 rare diseases +MONDO:0007250 gard_rare diseases +MONDO:0007250 nord_rare diseases +MONDO:0007250 ordo_disorder diseases +MONDO:0007250 ordo_morphological_anomaly diseases +MONDO:0007250 orphanet_rare diseases +MONDO:0007250 otar diseases +MONDO:0007250 rare diseases +MONDO:0007251 clingen diseases +MONDO:0007251 gard_rare diseases +MONDO:0007251 nord_rare diseases +MONDO:0007251 ordo_disorder diseases +MONDO:0007251 ordo_malformation_syndrome diseases +MONDO:0007251 orphanet_rare diseases +MONDO:0007251 otar diseases +MONDO:0007251 rare diseases +MONDO:0007252 gard_rare diseases +MONDO:0007252 nord_rare diseases +MONDO:0007252 ordo_disorder diseases +MONDO:0007252 ordo_malformation_syndrome diseases +MONDO:0007252 orphanet_rare diseases +MONDO:0007252 otar diseases +MONDO:0007252 rare diseases +MONDO:0007254 otar diseases +MONDO:0007256 gard_rare diseases +MONDO:0007256 nord_rare diseases +MONDO:0007256 ordo_group_of_disorders diseases +MONDO:0007256 otar diseases +MONDO:0007256 rare diseases +MONDO:0007257 gard_rare diseases +MONDO:0007257 nord_rare diseases +MONDO:0007257 rare diseases +MONDO:0007259 gard_rare diseases +MONDO:0007259 nord_rare diseases +MONDO:0007259 ordo_disorder diseases +MONDO:0007259 orphanet_rare diseases +MONDO:0007259 otar diseases +MONDO:0007259 rare diseases +MONDO:0007260 n_of_one diseases +MONDO:0007263 otar diseases +MONDO:0007265 gard_rare diseases +MONDO:0007265 nord_rare diseases +MONDO:0007265 rare diseases +MONDO:0007266 gard_rare diseases +MONDO:0007266 nord_rare diseases +MONDO:0007266 otar diseases +MONDO:0007266 rare diseases +MONDO:0007267 gard_rare diseases +MONDO:0007267 nord_rare diseases +MONDO:0007267 rare diseases +MONDO:0007268 gard_rare diseases +MONDO:0007268 nord_rare diseases +MONDO:0007268 otar diseases +MONDO:0007268 rare diseases +MONDO:0007269 gard_rare diseases +MONDO:0007269 nord_rare diseases +MONDO:0007269 ordo_disorder diseases +MONDO:0007269 orphanet_rare diseases +MONDO:0007269 otar diseases +MONDO:0007269 rare diseases +MONDO:0007270 gard_rare diseases +MONDO:0007270 nord_rare diseases +MONDO:0007270 rare diseases +MONDO:0007271 gard_rare diseases +MONDO:0007271 nord_rare diseases +MONDO:0007271 ordo_disorder diseases +MONDO:0007271 orphanet_rare diseases +MONDO:0007271 otar diseases +MONDO:0007271 rare diseases +MONDO:0007272 gard_rare diseases +MONDO:0007272 nord_rare diseases +MONDO:0007272 ordo_disorder diseases +MONDO:0007272 orphanet_rare diseases +MONDO:0007272 otar diseases +MONDO:0007272 rare diseases +MONDO:0007273 gard_rare diseases +MONDO:0007273 nord_rare diseases +MONDO:0007273 rare diseases +MONDO:0007275 inferred_rare diseases +MONDO:0007275 otar diseases +MONDO:0007275 rare diseases +MONDO:0007276 gard_rare diseases +MONDO:0007276 nord_rare diseases +MONDO:0007276 ordo_disorder diseases +MONDO:0007276 ordo_malformation_syndrome diseases +MONDO:0007276 orphanet_rare diseases +MONDO:0007276 otar diseases +MONDO:0007276 rare diseases +MONDO:0007277 gard_rare diseases +MONDO:0007277 ordo_disorder diseases +MONDO:0007277 ordo_malformation_syndrome diseases +MONDO:0007277 orphanet_rare diseases +MONDO:0007277 otar diseases +MONDO:0007277 rare diseases +MONDO:0007278 gard_rare diseases +MONDO:0007278 nord_rare diseases +MONDO:0007278 rare diseases +MONDO:0007279 gard_rare diseases +MONDO:0007279 nord_rare diseases +MONDO:0007279 rare diseases +MONDO:0007280 gard_rare diseases +MONDO:0007280 nord_rare diseases +MONDO:0007280 otar diseases +MONDO:0007280 rare diseases +MONDO:0007281 gard_rare diseases +MONDO:0007281 rare diseases +MONDO:0007282 gard_rare diseases +MONDO:0007282 nord_rare diseases +MONDO:0007282 rare diseases +MONDO:0007283 gard_rare diseases +MONDO:0007283 nord_rare diseases +MONDO:0007283 rare diseases +MONDO:0007284 gard_rare diseases +MONDO:0007284 nord_rare diseases +MONDO:0007284 rare diseases +MONDO:0007285 gard_rare diseases +MONDO:0007285 rare diseases +MONDO:0007286 gard_rare diseases +MONDO:0007286 nord_rare diseases +MONDO:0007286 rare diseases +MONDO:0007287 gard_rare diseases +MONDO:0007287 nord_rare diseases +MONDO:0007287 rare diseases +MONDO:0007288 gard_rare diseases +MONDO:0007288 nord_rare diseases +MONDO:0007288 rare diseases +MONDO:0007289 gard_rare diseases +MONDO:0007289 nord_rare diseases +MONDO:0007289 otar diseases +MONDO:0007289 rare diseases +MONDO:0007290 gard_rare diseases +MONDO:0007290 nord_rare diseases +MONDO:0007290 otar diseases +MONDO:0007290 rare diseases +MONDO:0007293 gard_rare diseases +MONDO:0007293 nord_rare diseases +MONDO:0007293 ordo_subtype_of_a_disorder diseases +MONDO:0007293 otar diseases +MONDO:0007293 rare diseases +MONDO:0007294 gard_rare diseases +MONDO:0007294 nord_rare diseases +MONDO:0007294 ordo_disorder diseases +MONDO:0007294 orphanet_rare diseases +MONDO:0007294 otar diseases +MONDO:0007294 rare diseases +MONDO:0007295 gard_rare diseases +MONDO:0007295 nord_rare diseases +MONDO:0007295 ordo_disorder diseases +MONDO:0007295 orphanet_rare diseases +MONDO:0007295 otar diseases +MONDO:0007295 rare diseases +MONDO:0007296 gard_rare diseases +MONDO:0007296 nord_rare diseases +MONDO:0007296 ordo_disorder diseases +MONDO:0007296 orphanet_rare diseases +MONDO:0007296 otar diseases +MONDO:0007296 rare diseases +MONDO:0007297 gard_rare diseases +MONDO:0007297 nord_rare diseases +MONDO:0007297 ordo_subtype_of_a_disorder diseases +MONDO:0007297 otar diseases +MONDO:0007297 rare diseases +MONDO:0007298 clingen diseases +MONDO:0007298 gard_rare diseases +MONDO:0007298 nord_rare diseases +MONDO:0007298 ordo_disorder diseases +MONDO:0007298 orphanet_rare diseases +MONDO:0007298 otar diseases +MONDO:0007298 rare diseases +MONDO:0007300 gard_rare diseases +MONDO:0007300 nord_rare diseases +MONDO:0007300 rare diseases +MONDO:0007301 gard_rare diseases +MONDO:0007301 nord_rare diseases +MONDO:0007301 ordo_disorder diseases +MONDO:0007301 ordo_malformation_syndrome diseases +MONDO:0007301 orphanet_rare diseases +MONDO:0007301 otar diseases +MONDO:0007301 rare diseases +MONDO:0007306 gard_rare diseases +MONDO:0007306 nord_rare diseases +MONDO:0007306 rare diseases +MONDO:0007307 gard_rare diseases +MONDO:0007307 nord_rare diseases +MONDO:0007307 ordo_disorder diseases +MONDO:0007307 orphanet_rare diseases +MONDO:0007307 otar diseases +MONDO:0007307 rare diseases +MONDO:0007308 clingen diseases +MONDO:0007308 gard_rare diseases +MONDO:0007308 nord_rare diseases +MONDO:0007308 ordo_disorder diseases +MONDO:0007308 orphanet_rare diseases +MONDO:0007308 otar diseases +MONDO:0007308 prototype_pattern diseases +MONDO:0007308 rare diseases +MONDO:0007309 clingen diseases +MONDO:0007309 gard_rare diseases +MONDO:0007309 nord_rare diseases +MONDO:0007309 ordo_disorder diseases +MONDO:0007309 orphanet_rare diseases +MONDO:0007309 otar diseases +MONDO:0007309 rare diseases +MONDO:0007310 gard_rare diseases +MONDO:0007310 rare diseases +MONDO:0007311 gard_rare diseases +MONDO:0007311 nord_rare diseases +MONDO:0007311 ordo_disorder diseases +MONDO:0007311 orphanet_rare diseases +MONDO:0007311 otar diseases +MONDO:0007311 rare diseases +MONDO:0007312 gard_rare diseases +MONDO:0007312 rare diseases +MONDO:0007313 gard_rare diseases +MONDO:0007313 nord_rare diseases +MONDO:0007313 ordo_disorder diseases +MONDO:0007313 orphanet_rare diseases +MONDO:0007313 rare diseases +MONDO:0007315 gard_rare diseases +MONDO:0007315 nord_rare diseases +MONDO:0007315 ordo_disorder diseases +MONDO:0007315 ordo_malformation_syndrome diseases +MONDO:0007315 orphanet_rare diseases +MONDO:0007315 otar diseases +MONDO:0007315 rare diseases +MONDO:0007316 gard_rare diseases +MONDO:0007316 nord_rare diseases +MONDO:0007316 ordo_disorder diseases +MONDO:0007316 ordo_morphological_anomaly diseases +MONDO:0007316 orphanet_rare diseases +MONDO:0007316 otar diseases +MONDO:0007316 rare diseases +MONDO:0007318 gard_rare diseases +MONDO:0007318 nord_rare diseases +MONDO:0007318 ordo_disorder diseases +MONDO:0007318 ordo_malformation_syndrome diseases +MONDO:0007318 orphanet_rare diseases +MONDO:0007318 otar diseases +MONDO:0007318 rare diseases +MONDO:0007319 gard_rare diseases +MONDO:0007319 nord_rare diseases +MONDO:0007319 ordo_disorder diseases +MONDO:0007319 orphanet_rare diseases +MONDO:0007319 otar diseases +MONDO:0007319 rare diseases +MONDO:0007321 gard_rare diseases +MONDO:0007321 nord_rare diseases +MONDO:0007321 ordo_malformation_syndrome diseases +MONDO:0007321 otar diseases +MONDO:0007321 rare diseases +MONDO:0007322 gard_rare diseases +MONDO:0007322 nord_rare diseases +MONDO:0007322 ordo_disorder diseases +MONDO:0007322 ordo_malformation_syndrome diseases +MONDO:0007322 orphanet_rare diseases +MONDO:0007322 otar diseases +MONDO:0007322 rare diseases +MONDO:0007325 gard_rare diseases +MONDO:0007325 nord_rare diseases +MONDO:0007325 rare diseases +MONDO:0007327 gard_rare diseases +MONDO:0007327 rare diseases +MONDO:0007329 gard_rare diseases +MONDO:0007329 nord_rare diseases +MONDO:0007329 otar diseases +MONDO:0007329 rare diseases +MONDO:0007330 gard_rare diseases +MONDO:0007330 nord_rare diseases +MONDO:0007330 ordo_disorder diseases +MONDO:0007330 orphanet_rare diseases +MONDO:0007330 otar diseases +MONDO:0007330 rare diseases +MONDO:0007332 gard_rare diseases +MONDO:0007332 nord_rare diseases +MONDO:0007332 rare diseases +MONDO:0007333 gard_rare diseases +MONDO:0007333 rare diseases +MONDO:0007334 gard_rare diseases +MONDO:0007334 nord_rare diseases +MONDO:0007334 ordo_disorder diseases +MONDO:0007334 ordo_malformation_syndrome diseases +MONDO:0007334 orphanet_rare diseases +MONDO:0007334 otar diseases +MONDO:0007334 rare diseases +MONDO:0007336 gard_rare diseases +MONDO:0007336 otar diseases +MONDO:0007336 rare diseases +MONDO:0007337 gard_rare diseases +MONDO:0007337 nord_rare diseases +MONDO:0007337 ordo_disorder diseases +MONDO:0007337 ordo_malformation_syndrome diseases +MONDO:0007337 orphanet_rare diseases +MONDO:0007337 otar diseases +MONDO:0007337 rare diseases +MONDO:0007338 gard_rare diseases +MONDO:0007338 nord_rare diseases +MONDO:0007338 ordo_disorder diseases +MONDO:0007338 ordo_morphological_anomaly diseases +MONDO:0007338 orphanet_rare diseases +MONDO:0007338 rare diseases +MONDO:0007339 gard_rare diseases +MONDO:0007339 nord_rare diseases +MONDO:0007339 ordo_disorder diseases +MONDO:0007339 ordo_malformation_syndrome diseases +MONDO:0007339 orphanet_rare diseases +MONDO:0007339 prototype_pattern diseases +MONDO:0007339 rare diseases +MONDO:0007340 gard_rare diseases +MONDO:0007340 nord_rare diseases +MONDO:0007340 ordo_disorder diseases +MONDO:0007340 ordo_malformation_syndrome diseases +MONDO:0007340 orphanet_rare diseases +MONDO:0007340 otar diseases +MONDO:0007340 rare diseases +MONDO:0007341 gard_rare diseases +MONDO:0007341 ordo_disorder diseases +MONDO:0007341 ordo_malformation_syndrome diseases +MONDO:0007341 orphanet_rare diseases +MONDO:0007341 otar diseases +MONDO:0007341 rare diseases +MONDO:0007342 gard_rare diseases +MONDO:0007342 otar diseases +MONDO:0007342 rare diseases +MONDO:0007343 gard_rare diseases +MONDO:0007343 nord_rare diseases +MONDO:0007343 ordo_disorder diseases +MONDO:0007343 ordo_morphological_anomaly diseases +MONDO:0007343 orphanet_rare diseases +MONDO:0007343 otar diseases +MONDO:0007343 rare diseases +MONDO:0007344 gard_rare diseases +MONDO:0007344 nord_rare diseases +MONDO:0007344 rare diseases +MONDO:0007345 gard_rare diseases +MONDO:0007345 nord_rare diseases +MONDO:0007345 ordo_disorder diseases +MONDO:0007345 ordo_morphological_anomaly diseases +MONDO:0007345 orphanet_rare diseases +MONDO:0007345 otar diseases +MONDO:0007345 rare diseases +MONDO:0007346 gard_rare diseases +MONDO:0007346 nord_rare diseases +MONDO:0007346 ordo_disorder diseases +MONDO:0007346 ordo_malformation_syndrome diseases +MONDO:0007346 orphanet_rare diseases +MONDO:0007346 otar diseases +MONDO:0007346 rare diseases +MONDO:0007349 gard_rare diseases +MONDO:0007349 nord_rare diseases +MONDO:0007349 otar diseases +MONDO:0007349 rare diseases +MONDO:0007350 otar diseases +MONDO:0007351 gard_rare diseases +MONDO:0007351 nord_rare diseases +MONDO:0007351 ordo_disorder diseases +MONDO:0007351 ordo_morphological_anomaly diseases +MONDO:0007351 orphanet_rare diseases +MONDO:0007351 otar diseases +MONDO:0007351 rare diseases +MONDO:0007352 gard_rare diseases +MONDO:0007352 nord_rare diseases +MONDO:0007352 ordo_disorder diseases +MONDO:0007352 ordo_malformation_syndrome diseases +MONDO:0007352 orphanet_rare diseases +MONDO:0007352 otar diseases +MONDO:0007352 rare diseases +MONDO:0007353 gard_rare diseases +MONDO:0007353 nord_rare diseases +MONDO:0007353 ordo_disorder diseases +MONDO:0007353 ordo_malformation_syndrome diseases +MONDO:0007353 orphanet_rare diseases +MONDO:0007353 otar diseases +MONDO:0007353 rare diseases +MONDO:0007354 gard_rare diseases +MONDO:0007354 ordo_disorder diseases +MONDO:0007354 ordo_morphological_anomaly diseases +MONDO:0007354 orphanet_rare diseases +MONDO:0007354 otar diseases +MONDO:0007354 rare diseases +MONDO:0007355 gard_rare diseases +MONDO:0007355 nord_rare diseases +MONDO:0007355 ordo_disorder diseases +MONDO:0007355 ordo_malformation_syndrome diseases +MONDO:0007355 orphanet_rare diseases +MONDO:0007355 otar diseases +MONDO:0007355 rare diseases +MONDO:0007356 gard_rare diseases +MONDO:0007356 nord_rare diseases +MONDO:0007356 rare diseases +MONDO:0007360 gard_rare diseases +MONDO:0007360 nord_rare diseases +MONDO:0007360 rare diseases +MONDO:0007361 gard_rare diseases +MONDO:0007361 rare diseases +MONDO:0007362 gard_rare diseases +MONDO:0007362 nord_rare diseases +MONDO:0007362 rare diseases +MONDO:0007363 gard_rare diseases +MONDO:0007363 nord_rare diseases +MONDO:0007363 ordo_disorder diseases +MONDO:0007363 ordo_malformation_syndrome diseases +MONDO:0007363 orphanet_rare diseases +MONDO:0007363 otar diseases +MONDO:0007363 rare diseases +MONDO:0007364 gard_rare diseases +MONDO:0007364 nord_rare diseases +MONDO:0007364 rare diseases +MONDO:0007365 gard_rare diseases +MONDO:0007365 rare diseases +MONDO:0007366 gard_rare diseases +MONDO:0007366 nord_rare diseases +MONDO:0007366 rare diseases +MONDO:0007368 gard_rare diseases +MONDO:0007368 nord_rare diseases +MONDO:0007368 ordo_disorder diseases +MONDO:0007368 orphanet_rare diseases +MONDO:0007368 otar diseases +MONDO:0007368 rare diseases +MONDO:0007369 gard_rare diseases +MONDO:0007369 nord_rare diseases +MONDO:0007369 ordo_disorder diseases +MONDO:0007369 orphanet_rare diseases +MONDO:0007369 otar diseases +MONDO:0007369 rare diseases +MONDO:0007372 gard_rare diseases +MONDO:0007372 rare diseases +MONDO:0007374 gard_rare diseases +MONDO:0007374 nord_rare diseases +MONDO:0007374 ordo_disorder diseases +MONDO:0007374 orphanet_rare diseases +MONDO:0007374 otar diseases +MONDO:0007374 rare diseases +MONDO:0007375 gard_rare diseases +MONDO:0007375 nord_rare diseases +MONDO:0007375 ordo_disorder diseases +MONDO:0007375 orphanet_rare diseases +MONDO:0007375 otar diseases +MONDO:0007375 rare diseases +MONDO:0007376 gard_rare diseases +MONDO:0007376 nord_rare diseases +MONDO:0007376 ordo_disorder diseases +MONDO:0007376 orphanet_rare diseases +MONDO:0007376 otar diseases +MONDO:0007376 rare diseases +MONDO:0007377 gard_rare diseases +MONDO:0007377 nord_rare diseases +MONDO:0007377 ordo_disorder diseases +MONDO:0007377 orphanet_rare diseases +MONDO:0007377 otar diseases +MONDO:0007377 rare diseases +MONDO:0007378 gard_rare diseases +MONDO:0007378 nord_rare diseases +MONDO:0007378 rare diseases +MONDO:0007379 gard_rare diseases +MONDO:0007379 nord_rare diseases +MONDO:0007379 ordo_disorder diseases +MONDO:0007379 orphanet_rare diseases +MONDO:0007379 otar diseases +MONDO:0007379 rare diseases +MONDO:0007380 gard_rare diseases +MONDO:0007380 nord_rare diseases +MONDO:0007380 ordo_disorder diseases +MONDO:0007380 orphanet_rare diseases +MONDO:0007380 otar diseases +MONDO:0007380 rare diseases +MONDO:0007381 gard_rare diseases +MONDO:0007381 nord_rare diseases +MONDO:0007381 ordo_disorder diseases +MONDO:0007381 orphanet_rare diseases +MONDO:0007381 otar diseases +MONDO:0007381 rare diseases +MONDO:0007382 gard_rare diseases +MONDO:0007382 nord_rare diseases +MONDO:0007382 ordo_disorder diseases +MONDO:0007382 ordo_malformation_syndrome diseases +MONDO:0007382 orphanet_rare diseases +MONDO:0007382 otar diseases +MONDO:0007382 rare diseases +MONDO:0007383 gard_rare diseases +MONDO:0007383 ordo_disorder diseases +MONDO:0007383 ordo_malformation_syndrome diseases +MONDO:0007383 orphanet_rare diseases +MONDO:0007383 otar diseases +MONDO:0007383 rare diseases +MONDO:0007384 gard_rare diseases +MONDO:0007384 nord_rare diseases +MONDO:0007384 ordo_disorder diseases +MONDO:0007384 orphanet_rare diseases +MONDO:0007384 rare diseases +MONDO:0007385 gard_rare diseases +MONDO:0007385 nord_rare diseases +MONDO:0007385 ordo_disorder diseases +MONDO:0007385 orphanet_rare diseases +MONDO:0007385 rare diseases +MONDO:0007387 gard_rare diseases +MONDO:0007387 nord_rare diseases +MONDO:0007387 rare diseases +MONDO:0007388 gard_rare diseases +MONDO:0007388 nord_rare diseases +MONDO:0007388 ordo_disorder diseases +MONDO:0007388 ordo_malformation_syndrome diseases +MONDO:0007388 orphanet_rare diseases +MONDO:0007388 rare diseases +MONDO:0007389 gard_rare diseases +MONDO:0007389 nord_rare diseases +MONDO:0007389 rare diseases +MONDO:0007391 otar diseases +MONDO:0007392 gard_rare diseases +MONDO:0007392 ordo_disorder diseases +MONDO:0007392 ordo_malformation_syndrome diseases +MONDO:0007392 orphanet_rare diseases +MONDO:0007392 otar diseases +MONDO:0007392 rare diseases +MONDO:0007395 gard_rare diseases +MONDO:0007395 nord_rare diseases +MONDO:0007395 ordo_disorder diseases +MONDO:0007395 ordo_malformation_syndrome diseases +MONDO:0007395 orphanet_rare diseases +MONDO:0007395 otar diseases +MONDO:0007395 rare diseases +MONDO:0007396 gard_rare diseases +MONDO:0007396 ordo_disorder diseases +MONDO:0007396 ordo_malformation_syndrome diseases +MONDO:0007396 orphanet_rare diseases +MONDO:0007396 otar diseases +MONDO:0007396 rare diseases +MONDO:0007397 gard_rare diseases +MONDO:0007397 nord_rare diseases +MONDO:0007397 rare diseases +MONDO:0007398 gard_rare diseases +MONDO:0007398 ordo_disorder diseases +MONDO:0007398 ordo_malformation_syndrome diseases +MONDO:0007398 orphanet_rare diseases +MONDO:0007398 rare diseases +MONDO:0007399 clingen diseases +MONDO:0007399 gard_rare diseases +MONDO:0007399 nord_rare diseases +MONDO:0007399 otar diseases +MONDO:0007399 rare diseases +MONDO:0007400 gard_rare diseases +MONDO:0007400 nord_rare diseases +MONDO:0007400 ordo_disorder diseases +MONDO:0007400 ordo_malformation_syndrome diseases +MONDO:0007400 orphanet_rare diseases +MONDO:0007400 otar diseases +MONDO:0007400 rare diseases +MONDO:0007401 gard_rare diseases +MONDO:0007401 nord_rare diseases +MONDO:0007401 ordo_disorder diseases +MONDO:0007401 ordo_malformation_syndrome diseases +MONDO:0007401 orphanet_rare diseases +MONDO:0007401 otar diseases +MONDO:0007401 rare diseases +MONDO:0007403 gard_rare diseases +MONDO:0007403 nord_rare diseases +MONDO:0007403 ordo_disorder diseases +MONDO:0007403 orphanet_rare diseases +MONDO:0007403 otar diseases +MONDO:0007403 rare diseases +MONDO:0007404 gard_rare diseases +MONDO:0007404 nord_rare diseases +MONDO:0007404 ordo_disorder diseases +MONDO:0007404 ordo_malformation_syndrome diseases +MONDO:0007404 orphanet_rare diseases +MONDO:0007404 otar diseases +MONDO:0007404 rare diseases +MONDO:0007405 clingen diseases +MONDO:0007405 gard_rare diseases +MONDO:0007405 nord_rare diseases +MONDO:0007405 ordo_disorder diseases +MONDO:0007405 ordo_malformation_syndrome diseases +MONDO:0007405 orphanet_rare diseases +MONDO:0007405 otar diseases +MONDO:0007405 rare diseases +MONDO:0007407 gard_rare diseases +MONDO:0007407 nord_rare diseases +MONDO:0007407 ordo_disorder diseases +MONDO:0007407 orphanet_rare diseases +MONDO:0007407 rare diseases +MONDO:0007409 gard_rare diseases +MONDO:0007409 ordo_disorder diseases +MONDO:0007409 ordo_malformation_syndrome diseases +MONDO:0007409 orphanet_rare diseases +MONDO:0007409 otar diseases +MONDO:0007409 rare diseases +MONDO:0007410 gard_rare diseases +MONDO:0007410 nord_rare diseases +MONDO:0007410 ordo_disorder diseases +MONDO:0007410 ordo_morphological_anomaly diseases +MONDO:0007410 orphanet_rare diseases +MONDO:0007410 otar diseases +MONDO:0007410 rare diseases +MONDO:0007411 gard_rare diseases +MONDO:0007411 nord_rare diseases +MONDO:0007411 rare diseases +MONDO:0007412 clingen diseases +MONDO:0007412 gard_rare diseases +MONDO:0007412 nord_rare diseases +MONDO:0007412 ordo_disorder diseases +MONDO:0007412 ordo_malformation_syndrome diseases +MONDO:0007412 orphanet_rare diseases +MONDO:0007412 otar diseases +MONDO:0007412 rare diseases +MONDO:0007413 gard_rare diseases +MONDO:0007413 ordo_disorder diseases +MONDO:0007413 ordo_malformation_syndrome diseases +MONDO:0007413 orphanet_rare diseases +MONDO:0007413 rare diseases +MONDO:0007414 gard_rare diseases +MONDO:0007414 nord_rare diseases +MONDO:0007414 ordo_disorder diseases +MONDO:0007414 ordo_malformation_syndrome diseases +MONDO:0007414 orphanet_rare diseases +MONDO:0007414 otar diseases +MONDO:0007414 rare diseases +MONDO:0007415 gard_rare diseases +MONDO:0007415 nord_rare diseases +MONDO:0007415 otar diseases +MONDO:0007415 rare diseases +MONDO:0007416 otar diseases +MONDO:0007417 gard_rare diseases +MONDO:0007417 nord_rare diseases +MONDO:0007417 ordo_disorder diseases +MONDO:0007417 orphanet_rare diseases +MONDO:0007417 otar diseases +MONDO:0007417 rare diseases +MONDO:0007418 merged_class diseases +MONDO:0007420 gard_rare diseases +MONDO:0007420 nord_rare diseases +MONDO:0007420 ordo_disorder diseases +MONDO:0007420 ordo_malformation_syndrome diseases +MONDO:0007420 orphanet_rare diseases +MONDO:0007420 otar diseases +MONDO:0007420 rare diseases +MONDO:0007421 gard_rare diseases +MONDO:0007421 ordo_disorder diseases +MONDO:0007421 ordo_malformation_syndrome diseases +MONDO:0007421 orphanet_rare diseases +MONDO:0007421 otar diseases +MONDO:0007421 rare diseases +MONDO:0007422 gard_rare diseases +MONDO:0007422 nord_rare diseases +MONDO:0007422 ordo_disorder diseases +MONDO:0007422 orphanet_rare diseases +MONDO:0007422 otar diseases +MONDO:0007422 rare diseases +MONDO:0007424 gard_rare diseases +MONDO:0007424 nord_rare diseases +MONDO:0007424 otar diseases +MONDO:0007424 rare diseases +MONDO:0007428 gard_rare diseases +MONDO:0007428 ordo_disorder diseases +MONDO:0007428 ordo_malformation_syndrome diseases +MONDO:0007428 orphanet_rare diseases +MONDO:0007428 otar diseases +MONDO:0007428 rare diseases +MONDO:0007429 gard_rare diseases +MONDO:0007429 nord_rare diseases +MONDO:0007429 rare diseases +MONDO:0007432 gard_rare diseases +MONDO:0007432 nord_rare diseases +MONDO:0007432 otar diseases +MONDO:0007432 prototype_pattern diseases +MONDO:0007432 rare diseases +MONDO:0007434 gard_rare diseases +MONDO:0007434 nord_rare diseases +MONDO:0007434 ordo_disorder diseases +MONDO:0007434 orphanet_rare diseases +MONDO:0007434 otar diseases +MONDO:0007434 rare diseases +MONDO:0007435 gard_rare diseases +MONDO:0007435 nord_rare diseases +MONDO:0007435 ordo_disorder diseases +MONDO:0007435 orphanet_rare diseases +MONDO:0007435 otar diseases +MONDO:0007435 rare diseases +MONDO:0007436 gard_rare diseases +MONDO:0007436 nord_rare diseases +MONDO:0007436 ordo_subtype_of_a_disorder diseases +MONDO:0007436 otar diseases +MONDO:0007436 rare diseases +MONDO:0007437 gard_rare diseases +MONDO:0007437 ordo_subtype_of_a_disorder diseases +MONDO:0007437 otar diseases +MONDO:0007437 rare diseases +MONDO:0007438 gard_rare diseases +MONDO:0007438 ordo_disorder diseases +MONDO:0007438 orphanet_rare diseases +MONDO:0007438 otar diseases +MONDO:0007438 rare diseases +MONDO:0007441 gard_rare diseases +MONDO:0007441 nord_rare diseases +MONDO:0007441 ordo_subtype_of_a_disorder diseases +MONDO:0007441 otar diseases +MONDO:0007441 rare diseases +MONDO:0007442 gard_rare diseases +MONDO:0007442 nord_rare diseases +MONDO:0007442 ordo_subtype_of_a_disorder diseases +MONDO:0007442 otar diseases +MONDO:0007442 rare diseases +MONDO:0007443 gard_rare diseases +MONDO:0007443 nord_rare diseases +MONDO:0007443 ordo_disorder diseases +MONDO:0007443 ordo_morphological_anomaly diseases +MONDO:0007443 orphanet_rare diseases +MONDO:0007443 otar diseases +MONDO:0007443 rare diseases +MONDO:0007445 gard_rare diseases +MONDO:0007445 nord_rare diseases +MONDO:0007445 ordo_disorder diseases +MONDO:0007445 orphanet_rare diseases +MONDO:0007445 otar diseases +MONDO:0007445 rare diseases +MONDO:0007446 otar diseases +MONDO:0007447 gard_rare diseases +MONDO:0007447 nord_rare diseases +MONDO:0007447 ordo_disorder diseases +MONDO:0007447 orphanet_rare diseases +MONDO:0007447 rare diseases +MONDO:0007448 otar diseases +MONDO:0007449 gard_rare diseases +MONDO:0007449 nord_rare diseases +MONDO:0007449 ordo_disorder diseases +MONDO:0007449 ordo_malformation_syndrome diseases +MONDO:0007449 orphanet_rare diseases +MONDO:0007449 otar diseases +MONDO:0007449 rare diseases +MONDO:0007450 gard_rare diseases +MONDO:0007450 nord_rare diseases +MONDO:0007450 ordo_subtype_of_a_disorder diseases +MONDO:0007450 otar diseases +MONDO:0007450 rare diseases +MONDO:0007451 gard_rare diseases +MONDO:0007451 nord_rare diseases +MONDO:0007451 otar diseases +MONDO:0007451 rare diseases +MONDO:0007452 gard_rare diseases +MONDO:0007452 nord_rare diseases +MONDO:0007452 rare diseases +MONDO:0007453 gard_rare diseases +MONDO:0007453 nord_rare diseases +MONDO:0007453 rare diseases +MONDO:0007458 gard_rare diseases +MONDO:0007458 nord_rare diseases +MONDO:0007458 rare diseases +MONDO:0007461 gard_rare diseases +MONDO:0007461 ordo_disorder diseases +MONDO:0007461 ordo_malformation_syndrome diseases +MONDO:0007461 orphanet_rare diseases +MONDO:0007461 otar diseases +MONDO:0007461 rare diseases +MONDO:0007470 gard_rare diseases +MONDO:0007470 nord_rare diseases +MONDO:0007470 ordo_disorder diseases +MONDO:0007470 ordo_malformation_syndrome diseases +MONDO:0007470 orphanet_rare diseases +MONDO:0007470 otar diseases +MONDO:0007470 rare diseases +MONDO:0007471 clingen diseases +MONDO:0007471 gard_rare diseases +MONDO:0007471 nord_rare diseases +MONDO:0007471 ordo_disorder diseases +MONDO:0007471 orphanet_rare diseases +MONDO:0007471 otar diseases +MONDO:0007471 rare diseases +MONDO:0007472 gard_rare diseases +MONDO:0007472 rare diseases +MONDO:0007473 gard_rare diseases +MONDO:0007473 nord_rare diseases +MONDO:0007473 ordo_disorder diseases +MONDO:0007473 ordo_malformation_syndrome diseases +MONDO:0007473 orphanet_rare diseases +MONDO:0007473 otar diseases +MONDO:0007473 prototype_pattern diseases +MONDO:0007473 rare diseases +MONDO:0007477 gard_rare diseases +MONDO:0007477 nord_rare diseases +MONDO:0007477 ordo_disorder diseases +MONDO:0007477 ordo_malformation_syndrome diseases +MONDO:0007477 orphanet_rare diseases +MONDO:0007477 otar diseases +MONDO:0007477 prototype_pattern diseases +MONDO:0007477 rare diseases +MONDO:0007478 gard_rare diseases +MONDO:0007478 nord_rare diseases +MONDO:0007478 ordo_etiological_subtype diseases +MONDO:0007478 ordo_subtype_of_a_disorder diseases +MONDO:0007478 otar diseases +MONDO:0007478 rare diseases +MONDO:0007481 gard_rare diseases +MONDO:0007481 nord_rare diseases +MONDO:0007481 ordo_disorder diseases +MONDO:0007481 ordo_malformation_syndrome diseases +MONDO:0007481 orphanet_rare diseases +MONDO:0007481 otar diseases +MONDO:0007481 rare diseases +MONDO:0007482 gard_rare diseases +MONDO:0007482 ordo_disorder diseases +MONDO:0007482 ordo_malformation_syndrome diseases +MONDO:0007482 orphanet_rare diseases +MONDO:0007482 otar diseases +MONDO:0007482 rare diseases +MONDO:0007483 gard_rare diseases +MONDO:0007483 ordo_disorder diseases +MONDO:0007483 orphanet_rare diseases +MONDO:0007483 otar diseases +MONDO:0007483 rare diseases +MONDO:0007485 gard_rare diseases +MONDO:0007485 nord_rare diseases +MONDO:0007485 prototype_pattern diseases +MONDO:0007485 rare diseases +MONDO:0007486 gard_rare diseases +MONDO:0007486 nord_rare diseases +MONDO:0007486 ordo_disorder diseases +MONDO:0007486 orphanet_rare diseases +MONDO:0007486 otar diseases +MONDO:0007486 rare diseases +MONDO:0007488 inferred_rare diseases +MONDO:0007488 otar diseases +MONDO:0007488 rare diseases +MONDO:0007489 gard_rare diseases +MONDO:0007489 nord_rare diseases +MONDO:0007489 ordo_disorder diseases +MONDO:0007489 ordo_malformation_syndrome diseases +MONDO:0007489 orphanet_rare diseases +MONDO:0007489 otar diseases +MONDO:0007489 rare diseases +MONDO:0007490 gard_rare diseases +MONDO:0007490 nord_rare diseases +MONDO:0007490 ordo_disorder diseases +MONDO:0007490 ordo_malformation_syndrome diseases +MONDO:0007490 orphanet_rare diseases +MONDO:0007490 rare diseases +MONDO:0007492 gard_rare diseases +MONDO:0007492 nord_rare diseases +MONDO:0007492 ordo_disorder diseases +MONDO:0007492 orphanet_rare diseases +MONDO:0007492 otar diseases +MONDO:0007492 rare diseases +MONDO:0007493 gard_rare diseases +MONDO:0007493 nord_rare diseases +MONDO:0007493 ordo_disorder diseases +MONDO:0007493 orphanet_rare diseases +MONDO:0007493 otar diseases +MONDO:0007493 rare diseases +MONDO:0007495 gard_rare diseases +MONDO:0007495 nord_rare diseases +MONDO:0007495 ordo_disorder diseases +MONDO:0007495 orphanet_rare diseases +MONDO:0007495 otar diseases +MONDO:0007495 rare diseases +MONDO:0007496 gard_rare diseases +MONDO:0007496 nord_rare diseases +MONDO:0007496 ordo_disorder diseases +MONDO:0007496 orphanet_rare diseases +MONDO:0007496 otar diseases +MONDO:0007496 rare diseases +MONDO:0007500 otar diseases +MONDO:0007503 gard_rare diseases +MONDO:0007503 nord_rare diseases +MONDO:0007503 rare diseases +MONDO:0007504 gard_rare diseases +MONDO:0007504 ordo_disorder diseases +MONDO:0007504 ordo_malformation_syndrome diseases +MONDO:0007504 orphanet_rare diseases +MONDO:0007504 otar diseases +MONDO:0007504 rare diseases +MONDO:0007507 gard_rare diseases +MONDO:0007507 nord_rare diseases +MONDO:0007507 ordo_disorder diseases +MONDO:0007507 orphanet_rare diseases +MONDO:0007507 otar diseases +MONDO:0007507 rare diseases +MONDO:0007508 gard_rare diseases +MONDO:0007508 nord_rare diseases +MONDO:0007508 rare diseases +MONDO:0007508 speculative diseases +MONDO:0007509 gard_rare diseases +MONDO:0007509 nord_rare diseases +MONDO:0007509 otar diseases +MONDO:0007509 rare diseases +MONDO:0007510 clingen diseases +MONDO:0007510 do_inheritance_inconsistent diseases +MONDO:0007510 gard_rare diseases +MONDO:0007510 nord_rare diseases +MONDO:0007510 ordo_disorder diseases +MONDO:0007510 orphanet_rare diseases +MONDO:0007510 otar diseases +MONDO:0007510 rare diseases +MONDO:0007511 gard_rare diseases +MONDO:0007511 nord_rare diseases +MONDO:0007511 ordo_disorder diseases +MONDO:0007511 ordo_malformation_syndrome diseases +MONDO:0007511 orphanet_rare diseases +MONDO:0007511 otar diseases +MONDO:0007511 rare diseases +MONDO:0007514 gard_rare diseases +MONDO:0007514 rare diseases +MONDO:0007519 gard_rare diseases +MONDO:0007519 nord_rare diseases +MONDO:0007519 ordo_disorder diseases +MONDO:0007519 ordo_malformation_syndrome diseases +MONDO:0007519 orphanet_rare diseases +MONDO:0007519 rare diseases +MONDO:0007520 gard_rare diseases +MONDO:0007520 nord_rare diseases +MONDO:0007520 rare diseases +MONDO:0007522 clingen diseases +MONDO:0007522 gard_rare diseases +MONDO:0007522 nord_rare diseases +MONDO:0007522 ordo_disorder diseases +MONDO:0007522 orphanet_rare diseases +MONDO:0007522 otar diseases +MONDO:0007522 rare diseases +MONDO:0007523 gard_rare diseases +MONDO:0007523 ordo_disorder diseases +MONDO:0007523 orphanet_rare diseases +MONDO:0007523 otar diseases +MONDO:0007523 rare diseases +MONDO:0007524 gard_rare diseases +MONDO:0007524 rare diseases +MONDO:0007525 clingen diseases +MONDO:0007525 gard_rare diseases +MONDO:0007525 nord_rare diseases +MONDO:0007525 ordo_disorder diseases +MONDO:0007525 orphanet_rare diseases +MONDO:0007525 otar diseases +MONDO:0007525 rare diseases +MONDO:0007526 gard_rare diseases +MONDO:0007526 nord_rare diseases +MONDO:0007526 ordo_subtype_of_a_disorder diseases +MONDO:0007526 otar diseases +MONDO:0007526 rare diseases +MONDO:0007527 gard_rare diseases +MONDO:0007527 nord_rare diseases +MONDO:0007527 ordo_disorder diseases +MONDO:0007527 orphanet_rare diseases +MONDO:0007527 otar diseases +MONDO:0007527 rare diseases +MONDO:0007528 gard_rare diseases +MONDO:0007528 rare diseases +MONDO:0007529 gard_rare diseases +MONDO:0007529 nord_rare diseases +MONDO:0007529 ordo_disorder diseases +MONDO:0007529 orphanet_rare diseases +MONDO:0007529 rare diseases +MONDO:0007533 gard_rare diseases +MONDO:0007533 nord_rare diseases +MONDO:0007533 otar diseases +MONDO:0007533 rare diseases +MONDO:0007534 gard_rare diseases +MONDO:0007534 nord_rare diseases +MONDO:0007534 ordo_disorder diseases +MONDO:0007534 ordo_malformation_syndrome diseases +MONDO:0007534 orphanet_rare diseases +MONDO:0007534 otar diseases +MONDO:0007534 rare diseases +MONDO:0007536 gard_rare diseases +MONDO:0007536 nord_rare diseases +MONDO:0007536 ordo_disorder diseases +MONDO:0007536 ordo_morphological_anomaly diseases +MONDO:0007536 orphanet_rare diseases +MONDO:0007536 otar diseases +MONDO:0007536 rare diseases +MONDO:0007537 gard_rare diseases +MONDO:0007537 nord_rare diseases +MONDO:0007537 ordo_disorder diseases +MONDO:0007537 ordo_malformation_syndrome diseases +MONDO:0007537 orphanet_rare diseases +MONDO:0007537 otar diseases +MONDO:0007537 rare diseases +MONDO:0007538 gard_rare diseases +MONDO:0007538 otar diseases +MONDO:0007538 rare diseases +MONDO:0007539 gard_rare diseases +MONDO:0007539 nord_rare diseases +MONDO:0007539 ordo_disorder diseases +MONDO:0007539 orphanet_rare diseases +MONDO:0007539 rare diseases +MONDO:0007540 clingen diseases +MONDO:0007540 gard_rare diseases +MONDO:0007540 nord_rare diseases +MONDO:0007540 ordo_disorder diseases +MONDO:0007540 orphanet_rare diseases +MONDO:0007540 otar diseases +MONDO:0007540 rare diseases +MONDO:0007542 gard_rare diseases +MONDO:0007542 nord_rare diseases +MONDO:0007542 ordo_disorder diseases +MONDO:0007542 ordo_malformation_syndrome diseases +MONDO:0007542 orphanet_rare diseases +MONDO:0007542 otar diseases +MONDO:0007542 rare diseases +MONDO:0007546 gard_rare diseases +MONDO:0007546 nord_rare diseases +MONDO:0007546 rare diseases +MONDO:0007548 gard_rare diseases +MONDO:0007548 nord_rare diseases +MONDO:0007548 ordo_disorder diseases +MONDO:0007548 orphanet_rare diseases +MONDO:0007548 otar diseases +MONDO:0007548 rare diseases +MONDO:0007549 gard_rare diseases +MONDO:0007549 nord_rare diseases +MONDO:0007549 ordo_disorder diseases +MONDO:0007549 orphanet_rare diseases +MONDO:0007549 otar diseases +MONDO:0007549 rare diseases +MONDO:0007550 gard_rare diseases +MONDO:0007550 nord_rare diseases +MONDO:0007550 ordo_disorder diseases +MONDO:0007550 orphanet_rare diseases +MONDO:0007550 otar diseases +MONDO:0007550 rare diseases +MONDO:0007551 gard_rare diseases +MONDO:0007551 nord_rare diseases +MONDO:0007551 ordo_disorder diseases +MONDO:0007551 orphanet_rare diseases +MONDO:0007551 otar diseases +MONDO:0007551 rare diseases +MONDO:0007552 gard_rare diseases +MONDO:0007552 nord_rare diseases +MONDO:0007552 ordo_subtype_of_a_disorder diseases +MONDO:0007552 otar diseases +MONDO:0007552 rare diseases +MONDO:0007554 gard_rare diseases +MONDO:0007554 nord_rare diseases +MONDO:0007554 ordo_disorder diseases +MONDO:0007554 orphanet_rare diseases +MONDO:0007554 otar diseases +MONDO:0007554 rare diseases +MONDO:0007555 gard_rare diseases +MONDO:0007555 nord_rare diseases +MONDO:0007555 ordo_disorder diseases +MONDO:0007555 orphanet_rare diseases +MONDO:0007555 otar diseases +MONDO:0007555 rare diseases +MONDO:0007556 gard_rare diseases +MONDO:0007556 nord_rare diseases +MONDO:0007556 ordo_disorder diseases +MONDO:0007556 orphanet_rare diseases +MONDO:0007556 otar diseases +MONDO:0007556 rare diseases +MONDO:0007558 gard_rare diseases +MONDO:0007558 nord_rare diseases +MONDO:0007558 ordo_disorder diseases +MONDO:0007558 orphanet_rare diseases +MONDO:0007558 otar diseases +MONDO:0007558 rare diseases +MONDO:0007559 gard_rare diseases +MONDO:0007559 rare diseases +MONDO:0007560 gard_rare diseases +MONDO:0007560 nord_rare diseases +MONDO:0007560 ordo_disorder diseases +MONDO:0007560 orphanet_rare diseases +MONDO:0007560 rare diseases +MONDO:0007561 gard_rare diseases +MONDO:0007561 nord_rare diseases +MONDO:0007561 ordo_disorder diseases +MONDO:0007561 orphanet_rare diseases +MONDO:0007561 otar diseases +MONDO:0007561 rare diseases +MONDO:0007562 gard_rare diseases +MONDO:0007562 nord_rare diseases +MONDO:0007562 ordo_disorder diseases +MONDO:0007562 orphanet_rare diseases +MONDO:0007562 otar diseases +MONDO:0007562 rare diseases +MONDO:0007564 gard_rare diseases +MONDO:0007564 nord_rare diseases +MONDO:0007564 ordo_disorder diseases +MONDO:0007564 ordo_malformation_syndrome diseases +MONDO:0007564 orphanet_rare diseases +MONDO:0007564 otar diseases +MONDO:0007564 rare diseases +MONDO:0007565 gard_rare diseases +MONDO:0007565 nord_rare diseases +MONDO:0007565 ordo_subtype_of_a_disorder diseases +MONDO:0007565 otar diseases +MONDO:0007565 rare diseases +MONDO:0007566 clingen diseases +MONDO:0007566 gard_rare diseases +MONDO:0007566 nord_rare diseases +MONDO:0007566 ordo_disorder diseases +MONDO:0007566 orphanet_rare diseases +MONDO:0007566 otar diseases +MONDO:0007566 rare diseases +MONDO:0007568 gard_rare diseases +MONDO:0007568 nord_rare diseases +MONDO:0007568 rare diseases +MONDO:0007570 gard_rare diseases +MONDO:0007570 nord_rare diseases +MONDO:0007570 ordo_disorder diseases +MONDO:0007570 orphanet_rare diseases +MONDO:0007570 otar diseases +MONDO:0007570 rare diseases +MONDO:0007571 gard_rare diseases +MONDO:0007571 nord_rare diseases +MONDO:0007571 ordo_disorder diseases +MONDO:0007571 orphanet_rare diseases +MONDO:0007571 otar diseases +MONDO:0007571 rare diseases +MONDO:0007572 gard_rare diseases +MONDO:0007572 nord_rare diseases +MONDO:0007572 ordo_disorder diseases +MONDO:0007572 orphanet_rare diseases +MONDO:0007572 otar diseases +MONDO:0007572 rare diseases +MONDO:0007573 inferred_rare diseases +MONDO:0007573 rare diseases +MONDO:0007574 gard_rare diseases +MONDO:0007574 nord_rare diseases +MONDO:0007574 ordo_disorder diseases +MONDO:0007574 orphanet_rare diseases +MONDO:0007574 otar diseases +MONDO:0007574 rare diseases +MONDO:0007576 otar diseases +MONDO:0007584 gard_rare diseases +MONDO:0007584 ordo_disorder diseases +MONDO:0007584 ordo_malformation_syndrome diseases +MONDO:0007584 orphanet_rare diseases +MONDO:0007584 otar diseases +MONDO:0007584 rare diseases +MONDO:0007585 clingen diseases +MONDO:0007585 gard_rare diseases +MONDO:0007585 nord_rare diseases +MONDO:0007585 otar diseases +MONDO:0007585 rare diseases +MONDO:0007586 clingen diseases +MONDO:0007586 gard_rare diseases +MONDO:0007586 nord_rare diseases +MONDO:0007586 otar diseases +MONDO:0007586 rare diseases +MONDO:0007587 gard_rare diseases +MONDO:0007587 nord_rare diseases +MONDO:0007587 ordo_disorder diseases +MONDO:0007587 ordo_malformation_syndrome diseases +MONDO:0007587 orphanet_rare diseases +MONDO:0007587 rare diseases +MONDO:0007588 gard_rare diseases +MONDO:0007588 ordo_disorder diseases +MONDO:0007588 ordo_malformation_syndrome diseases +MONDO:0007588 orphanet_rare diseases +MONDO:0007588 rare diseases +MONDO:0007589 gard_rare diseases +MONDO:0007589 nord_rare diseases +MONDO:0007589 rare diseases +MONDO:0007590 gard_rare diseases +MONDO:0007590 nord_rare diseases +MONDO:0007590 ordo_disorder diseases +MONDO:0007590 ordo_malformation_syndrome diseases +MONDO:0007590 orphanet_rare diseases +MONDO:0007590 otar diseases +MONDO:0007590 rare diseases +MONDO:0007592 gard_rare diseases +MONDO:0007592 nord_rare diseases +MONDO:0007592 ordo_disorder diseases +MONDO:0007592 orphanet_rare diseases +MONDO:0007592 rare diseases +MONDO:0007594 gard_rare diseases +MONDO:0007594 rare diseases +MONDO:0007595 gard_rare diseases +MONDO:0007595 nord_rare diseases +MONDO:0007595 rare diseases +MONDO:0007600 gard_rare diseases +MONDO:0007600 ordo_disorder diseases +MONDO:0007600 orphanet_rare diseases +MONDO:0007600 otar diseases +MONDO:0007600 rare diseases +MONDO:0007601 gard_rare diseases +MONDO:0007601 nord_rare diseases +MONDO:0007601 rare diseases +MONDO:0007603 gard_rare diseases +MONDO:0007603 nord_rare diseases +MONDO:0007603 ordo_disorder diseases +MONDO:0007603 orphanet_rare diseases +MONDO:0007603 otar diseases +MONDO:0007603 rare diseases +MONDO:0007604 gard_rare diseases +MONDO:0007604 nord_rare diseases +MONDO:0007604 ordo_disorder diseases +MONDO:0007604 ordo_malformation_syndrome diseases +MONDO:0007604 orphanet_rare diseases +MONDO:0007604 otar diseases +MONDO:0007604 rare diseases +MONDO:0007606 gard_rare diseases +MONDO:0007606 nord_rare diseases +MONDO:0007606 ordo_disorder diseases +MONDO:0007606 orphanet_rare diseases +MONDO:0007606 otar diseases +MONDO:0007606 rare diseases +MONDO:0007608 gard_rare diseases +MONDO:0007608 nord_rare diseases +MONDO:0007608 ordo_disorder diseases +MONDO:0007608 orphanet_rare diseases +MONDO:0007608 otar diseases +MONDO:0007608 rare diseases +MONDO:0007609 gard_rare diseases +MONDO:0007609 nord_rare diseases +MONDO:0007609 rare diseases +MONDO:0007610 gard_rare diseases +MONDO:0007610 nord_rare diseases +MONDO:0007610 ordo_disorder diseases +MONDO:0007610 ordo_malformation_syndrome diseases +MONDO:0007610 orphanet_rare diseases +MONDO:0007610 otar diseases +MONDO:0007610 rare diseases +MONDO:0007612 gard_rare diseases +MONDO:0007612 nord_rare diseases +MONDO:0007612 ordo_disorder diseases +MONDO:0007612 ordo_malformation_syndrome diseases +MONDO:0007612 orphanet_rare diseases +MONDO:0007612 otar diseases +MONDO:0007612 rare diseases +MONDO:0007614 clingen diseases +MONDO:0007614 gard_rare diseases +MONDO:0007614 nord_rare diseases +MONDO:0007614 ordo_disorder diseases +MONDO:0007614 orphanet_rare diseases +MONDO:0007614 otar diseases +MONDO:0007614 prototype_pattern diseases +MONDO:0007614 rare diseases +MONDO:0007615 gard_rare diseases +MONDO:0007615 nord_rare diseases +MONDO:0007615 ordo_disorder diseases +MONDO:0007615 ordo_malformation_syndrome diseases +MONDO:0007615 orphanet_rare diseases +MONDO:0007615 otar diseases +MONDO:0007615 rare diseases +MONDO:0007617 gard_rare diseases +MONDO:0007617 nord_rare diseases +MONDO:0007617 rare diseases +MONDO:0007618 gard_rare diseases +MONDO:0007618 nord_rare diseases +MONDO:0007618 ordo_disorder diseases +MONDO:0007618 ordo_malformation_syndrome diseases +MONDO:0007618 orphanet_rare diseases +MONDO:0007618 rare diseases +MONDO:0007619 gard_rare diseases +MONDO:0007619 nord_rare diseases +MONDO:0007619 ordo_disorder diseases +MONDO:0007619 orphanet_rare diseases +MONDO:0007619 otar diseases +MONDO:0007619 rare diseases +MONDO:0007620 gard_rare diseases +MONDO:0007620 nord_rare diseases +MONDO:0007620 ordo_subtype_of_a_disorder diseases +MONDO:0007620 otar diseases +MONDO:0007620 rare diseases +MONDO:0007621 clingen diseases +MONDO:0007621 gard_rare diseases +MONDO:0007621 nord_rare diseases +MONDO:0007621 ordo_disorder diseases +MONDO:0007621 ordo_malformation_syndrome diseases +MONDO:0007621 orphanet_rare diseases +MONDO:0007621 otar diseases +MONDO:0007621 rare diseases +MONDO:0007624 gard_rare diseases +MONDO:0007624 ordo_disorder diseases +MONDO:0007624 orphanet_rare diseases +MONDO:0007624 otar diseases +MONDO:0007624 rare diseases +MONDO:0007626 gard_rare diseases +MONDO:0007626 nord_rare diseases +MONDO:0007626 ordo_disorder diseases +MONDO:0007626 orphanet_rare diseases +MONDO:0007626 otar diseases +MONDO:0007626 rare diseases +MONDO:0007627 gard_rare diseases +MONDO:0007627 nord_rare diseases +MONDO:0007627 ordo_subtype_of_a_disorder diseases +MONDO:0007627 otar diseases +MONDO:0007627 rare diseases +MONDO:0007628 gard_rare diseases +MONDO:0007628 rare diseases +MONDO:0007630 gard_rare diseases +MONDO:0007630 nord_rare diseases +MONDO:0007630 ordo_disorder diseases +MONDO:0007630 orphanet_rare diseases +MONDO:0007630 otar diseases +MONDO:0007630 rare diseases +MONDO:0007631 gard_rare diseases +MONDO:0007631 nord_rare diseases +MONDO:0007631 otar diseases +MONDO:0007631 rare diseases +MONDO:0007634 otar diseases +MONDO:0007635 gard_rare diseases +MONDO:0007635 nord_rare diseases +MONDO:0007635 ordo_disorder diseases +MONDO:0007635 orphanet_rare diseases +MONDO:0007635 otar diseases +MONDO:0007635 rare diseases +MONDO:0007636 clingen diseases +MONDO:0007636 gard_rare diseases +MONDO:0007636 nord_rare diseases +MONDO:0007636 ordo_disorder diseases +MONDO:0007636 ordo_malformation_syndrome diseases +MONDO:0007636 orphanet_rare diseases +MONDO:0007636 otar diseases +MONDO:0007636 rare diseases +MONDO:0007637 gard_rare diseases +MONDO:0007637 nord_rare diseases +MONDO:0007637 rare diseases +MONDO:0007639 gard_rare diseases +MONDO:0007639 nord_rare diseases +MONDO:0007639 ordo_disorder diseases +MONDO:0007639 orphanet_rare diseases +MONDO:0007639 otar diseases +MONDO:0007639 rare diseases +MONDO:0007640 clingen diseases +MONDO:0007640 gard_rare diseases +MONDO:0007640 nord_rare diseases +MONDO:0007640 ordo_disorder diseases +MONDO:0007640 orphanet_rare diseases +MONDO:0007640 otar diseases +MONDO:0007640 rare diseases +MONDO:0007642 gard_rare diseases +MONDO:0007642 nord_rare diseases +MONDO:0007642 ordo_disorder diseases +MONDO:0007642 ordo_morphological_anomaly diseases +MONDO:0007642 orphanet_rare diseases +MONDO:0007642 rare diseases +MONDO:0007644 gard_rare diseases +MONDO:0007644 nord_rare diseases +MONDO:0007644 rare diseases +MONDO:0007646 gard_rare diseases +MONDO:0007646 nord_rare diseases +MONDO:0007646 ordo_disorder diseases +MONDO:0007646 orphanet_rare diseases +MONDO:0007646 otar diseases +MONDO:0007646 rare diseases +MONDO:0007648 clingen diseases +MONDO:0007648 gard_rare diseases +MONDO:0007648 nord_rare diseases +MONDO:0007648 ordo_disorder diseases +MONDO:0007648 orphanet_rare diseases +MONDO:0007648 otar diseases +MONDO:0007648 rare diseases +MONDO:0007650 gard_rare diseases +MONDO:0007650 nord_rare diseases +MONDO:0007650 ordo_disorder diseases +MONDO:0007650 orphanet_rare diseases +MONDO:0007650 otar diseases +MONDO:0007650 rare diseases +MONDO:0007651 gard_rare diseases +MONDO:0007651 nord_rare diseases +MONDO:0007651 ordo_disorder diseases +MONDO:0007651 orphanet_rare diseases +MONDO:0007651 rare diseases +MONDO:0007652 gard_rare diseases +MONDO:0007652 nord_rare diseases +MONDO:0007652 ordo_disorder diseases +MONDO:0007652 orphanet_rare diseases +MONDO:0007652 otar diseases +MONDO:0007652 rare diseases +MONDO:0007653 gard_rare diseases +MONDO:0007653 nord_rare diseases +MONDO:0007653 otar diseases +MONDO:0007653 prototype_pattern diseases +MONDO:0007653 rare diseases +MONDO:0007656 gard_rare diseases +MONDO:0007656 nord_rare diseases +MONDO:0007656 ordo_disorder diseases +MONDO:0007656 orphanet_rare diseases +MONDO:0007656 otar diseases +MONDO:0007656 rare diseases +MONDO:0007660 gard_rare diseases +MONDO:0007660 nord_rare diseases +MONDO:0007660 ordo_disorder diseases +MONDO:0007660 orphanet_rare diseases +MONDO:0007660 rare diseases +MONDO:0007661 otar diseases +MONDO:0007662 gard_rare diseases +MONDO:0007662 nord_rare diseases +MONDO:0007662 rare diseases +MONDO:0007663 gard_rare diseases +MONDO:0007663 rare diseases +MONDO:0007664 gard_rare diseases +MONDO:0007664 otar diseases +MONDO:0007664 rare diseases +MONDO:0007666 gard_rare diseases +MONDO:0007666 ordo_disorder diseases +MONDO:0007666 orphanet_rare diseases +MONDO:0007666 otar diseases +MONDO:0007666 rare diseases +MONDO:0007667 gard_rare diseases +MONDO:0007667 nord_rare diseases +MONDO:0007667 ordo_disorder diseases +MONDO:0007667 ordo_histopathological_subtype diseases +MONDO:0007667 orphanet_rare diseases +MONDO:0007667 otar diseases +MONDO:0007667 prototype_pattern diseases +MONDO:0007667 rare diseases +MONDO:0007669 clingen diseases +MONDO:0007669 gard_rare diseases +MONDO:0007669 nord_rare diseases +MONDO:0007669 ordo_subtype_of_a_disorder diseases +MONDO:0007669 otar diseases +MONDO:0007669 rare diseases +MONDO:0007670 gard_rare diseases +MONDO:0007670 nord_rare diseases +MONDO:0007670 ordo_disorder diseases +MONDO:0007670 orphanet_rare diseases +MONDO:0007670 rare diseases +MONDO:0007671 gard_rare diseases +MONDO:0007671 nord_rare diseases +MONDO:0007671 ordo_disorder diseases +MONDO:0007671 orphanet_rare diseases +MONDO:0007671 otar diseases +MONDO:0007671 prototype_pattern diseases +MONDO:0007671 rare diseases +MONDO:0007672 gard_rare diseases +MONDO:0007672 nord_rare diseases +MONDO:0007672 ordo_disorder diseases +MONDO:0007672 ordo_malformation_syndrome diseases +MONDO:0007672 orphanet_rare diseases +MONDO:0007672 otar diseases +MONDO:0007672 rare diseases +MONDO:0007679 gard_rare diseases +MONDO:0007679 nord_rare diseases +MONDO:0007679 ordo_disorder diseases +MONDO:0007679 ordo_malformation_syndrome diseases +MONDO:0007679 orphanet_rare diseases +MONDO:0007679 otar diseases +MONDO:0007679 rare diseases +MONDO:0007680 gard_rare diseases +MONDO:0007680 nord_rare diseases +MONDO:0007680 ordo_disorder diseases +MONDO:0007680 ordo_malformation_syndrome diseases +MONDO:0007680 orphanet_rare diseases +MONDO:0007680 otar diseases +MONDO:0007680 rare diseases +MONDO:0007681 gard_rare diseases +MONDO:0007681 nord_rare diseases +MONDO:0007681 ordo_disorder diseases +MONDO:0007681 orphanet_rare diseases +MONDO:0007681 otar diseases +MONDO:0007681 rare diseases +MONDO:0007683 gard_rare diseases +MONDO:0007683 ordo_disorder diseases +MONDO:0007683 ordo_malformation_syndrome diseases +MONDO:0007683 orphanet_rare diseases +MONDO:0007683 otar diseases +MONDO:0007683 rare diseases +MONDO:0007686 clingen diseases +MONDO:0007686 gard_rare diseases +MONDO:0007686 nord_rare diseases +MONDO:0007686 ordo_disorder diseases +MONDO:0007686 orphanet_rare diseases +MONDO:0007686 otar diseases +MONDO:0007686 rare diseases +MONDO:0007688 clingen diseases +MONDO:0007688 gard_rare diseases +MONDO:0007688 nord_rare diseases +MONDO:0007688 ordo_disorder diseases +MONDO:0007688 ordo_malformation_syndrome diseases +MONDO:0007688 orphanet_rare diseases +MONDO:0007688 otar diseases +MONDO:0007688 rare diseases +MONDO:0007690 gard_rare diseases +MONDO:0007690 nord_rare diseases +MONDO:0007690 ordo_disorder diseases +MONDO:0007690 orphanet_rare diseases +MONDO:0007690 otar diseases +MONDO:0007690 rare diseases +MONDO:0007691 gard_rare diseases +MONDO:0007691 nord_rare diseases +MONDO:0007691 otar diseases +MONDO:0007691 rare diseases +MONDO:0007693 gard_rare diseases +MONDO:0007693 nord_rare diseases +MONDO:0007693 ordo_disorder diseases +MONDO:0007693 ordo_malformation_syndrome diseases +MONDO:0007693 orphanet_rare diseases +MONDO:0007693 otar diseases +MONDO:0007693 rare diseases +MONDO:0007696 gard_rare diseases +MONDO:0007696 ordo_disorder diseases +MONDO:0007696 ordo_malformation_syndrome diseases +MONDO:0007696 orphanet_rare diseases +MONDO:0007696 otar diseases +MONDO:0007696 rare diseases +MONDO:0007698 gard_rare diseases +MONDO:0007698 nord_rare diseases +MONDO:0007698 ordo_disorder diseases +MONDO:0007698 ordo_malformation_syndrome diseases +MONDO:0007698 orphanet_rare diseases +MONDO:0007698 otar diseases +MONDO:0007698 rare diseases +MONDO:0007699 otar diseases +MONDO:0007700 clingen diseases +MONDO:0007700 gard_rare diseases +MONDO:0007700 nord_rare diseases +MONDO:0007700 ordo_disorder diseases +MONDO:0007700 orphanet_rare diseases +MONDO:0007700 otar diseases +MONDO:0007700 rare diseases +MONDO:0007701 gard_rare diseases +MONDO:0007701 nord_rare diseases +MONDO:0007701 rare diseases +MONDO:0007702 gard_rare diseases +MONDO:0007702 nord_rare diseases +MONDO:0007702 ordo_disorder diseases +MONDO:0007702 ordo_malformation_syndrome diseases +MONDO:0007702 orphanet_rare diseases +MONDO:0007702 otar diseases +MONDO:0007702 rare diseases +MONDO:0007705 gard_rare diseases +MONDO:0007705 nord_rare diseases +MONDO:0007705 otar diseases +MONDO:0007705 rare diseases +MONDO:0007706 ordo_malformation_syndrome diseases +MONDO:0007706 otar diseases +MONDO:0007708 gard_rare diseases +MONDO:0007708 nord_rare diseases +MONDO:0007708 ordo_clinical_situation diseases +MONDO:0007708 ordo_disorder diseases +MONDO:0007708 orphanet_rare diseases +MONDO:0007708 rare diseases +MONDO:0007710 gard_rare diseases +MONDO:0007710 nord_rare diseases +MONDO:0007710 ordo_disorder diseases +MONDO:0007710 orphanet_rare diseases +MONDO:0007710 rare diseases +MONDO:0007711 gard_rare diseases +MONDO:0007711 nord_rare diseases +MONDO:0007711 ordo_disorder diseases +MONDO:0007711 ordo_malformation_syndrome diseases +MONDO:0007711 orphanet_rare diseases +MONDO:0007711 otar diseases +MONDO:0007711 rare diseases +MONDO:0007712 gard_rare diseases +MONDO:0007712 nord_rare diseases +MONDO:0007712 ordo_disorder diseases +MONDO:0007712 ordo_malformation_syndrome diseases +MONDO:0007712 orphanet_rare diseases +MONDO:0007712 otar diseases +MONDO:0007712 rare diseases +MONDO:0007713 gard_rare diseases +MONDO:0007713 nord_rare diseases +MONDO:0007713 ordo_disorder diseases +MONDO:0007713 orphanet_rare diseases +MONDO:0007713 rare diseases +MONDO:0007716 gard_rare diseases +MONDO:0007716 nord_rare diseases +MONDO:0007716 ordo_disorder diseases +MONDO:0007716 orphanet_rare diseases +MONDO:0007716 otar diseases +MONDO:0007716 rare diseases +MONDO:0007718 gard_rare diseases +MONDO:0007718 nord_rare diseases +MONDO:0007718 rare diseases +MONDO:0007719 gard_rare diseases +MONDO:0007719 prototype_pattern diseases +MONDO:0007719 rare diseases +MONDO:0007724 gard_rare diseases +MONDO:0007724 ordo_malformation_syndrome diseases +MONDO:0007724 rare diseases +MONDO:0007725 gard_rare diseases +MONDO:0007725 nord_rare diseases +MONDO:0007725 ordo_disorder diseases +MONDO:0007725 orphanet_rare diseases +MONDO:0007725 rare diseases +MONDO:0007726 gard_rare diseases +MONDO:0007726 nord_rare diseases +MONDO:0007726 ordo_disorder diseases +MONDO:0007726 orphanet_rare diseases +MONDO:0007726 otar diseases +MONDO:0007726 rare diseases +MONDO:0007727 gard_rare diseases +MONDO:0007727 nord_rare diseases +MONDO:0007727 ordo_disorder diseases +MONDO:0007727 orphanet_rare diseases +MONDO:0007727 otar diseases +MONDO:0007727 rare diseases +MONDO:0007728 otar diseases +MONDO:0007729 prototype_pattern diseases +MONDO:0007732 clingen diseases +MONDO:0007732 gard_rare diseases +MONDO:0007732 nord_rare diseases +MONDO:0007732 ordo_disorder diseases +MONDO:0007732 ordo_malformation_syndrome diseases +MONDO:0007732 orphanet_rare diseases +MONDO:0007732 otar diseases +MONDO:0007732 rare diseases +MONDO:0007733 gard_rare diseases +MONDO:0007733 nord_rare diseases +MONDO:0007733 otar diseases +MONDO:0007733 rare diseases +MONDO:0007734 gard_rare diseases +MONDO:0007734 nord_rare diseases +MONDO:0007734 rare diseases +MONDO:0007735 gard_rare diseases +MONDO:0007735 nord_rare diseases +MONDO:0007735 ordo_disorder diseases +MONDO:0007735 orphanet_rare diseases +MONDO:0007735 otar diseases +MONDO:0007735 rare diseases +MONDO:0007737 gard_rare diseases +MONDO:0007737 nord_rare diseases +MONDO:0007737 ordo_disorder diseases +MONDO:0007737 ordo_morphological_anomaly diseases +MONDO:0007737 orphanet_rare diseases +MONDO:0007737 otar diseases +MONDO:0007737 rare diseases +MONDO:0007738 gard_rare diseases +MONDO:0007738 nord_rare diseases +MONDO:0007738 ordo_disorder diseases +MONDO:0007738 orphanet_rare diseases +MONDO:0007738 otar diseases +MONDO:0007738 rare diseases +MONDO:0007739 clingen diseases +MONDO:0007739 gard_rare diseases +MONDO:0007739 nord_rare diseases +MONDO:0007739 ordo_disorder diseases +MONDO:0007739 orphanet_rare diseases +MONDO:0007739 otar diseases +MONDO:0007739 rare diseases +MONDO:0007740 clingen diseases +MONDO:0007740 gard_rare diseases +MONDO:0007740 nord_rare diseases +MONDO:0007740 ordo_disorder diseases +MONDO:0007740 orphanet_rare diseases +MONDO:0007740 otar diseases +MONDO:0007740 rare diseases +MONDO:0007741 ordo_morphological_anomaly diseases +MONDO:0007741 otar diseases +MONDO:0007743 otar diseases +MONDO:0007744 gard_rare diseases +MONDO:0007744 nord_rare diseases +MONDO:0007744 ordo_disorder diseases +MONDO:0007744 orphanet_rare diseases +MONDO:0007744 otar diseases +MONDO:0007744 rare diseases +MONDO:0007745 inferred_rare diseases +MONDO:0007745 otar diseases +MONDO:0007745 rare diseases +MONDO:0007747 gard_rare diseases +MONDO:0007747 nord_rare diseases +MONDO:0007747 ordo_disorder diseases +MONDO:0007747 orphanet_rare diseases +MONDO:0007747 otar diseases +MONDO:0007747 rare diseases +MONDO:0007748 gard_rare diseases +MONDO:0007748 nord_rare diseases +MONDO:0007748 rare diseases +MONDO:0007750 clingen diseases +MONDO:0007750 gard_rare diseases +MONDO:0007750 otar diseases +MONDO:0007750 rare diseases +MONDO:0007751 clingen diseases +MONDO:0007751 gard_rare diseases +MONDO:0007751 otar diseases +MONDO:0007751 rare diseases +MONDO:0007753 otar diseases +MONDO:0007756 gard_rare diseases +MONDO:0007756 nord_rare diseases +MONDO:0007756 ordo_disorder diseases +MONDO:0007756 orphanet_rare diseases +MONDO:0007756 otar diseases +MONDO:0007756 rare diseases +MONDO:0007757 gard_rare diseases +MONDO:0007757 nord_rare diseases +MONDO:0007757 ordo_disorder diseases +MONDO:0007757 orphanet_rare diseases +MONDO:0007757 otar diseases +MONDO:0007757 rare diseases +MONDO:0007758 gard_rare diseases +MONDO:0007758 nord_rare diseases +MONDO:0007758 ordo_disorder diseases +MONDO:0007758 orphanet_rare diseases +MONDO:0007758 otar diseases +MONDO:0007758 rare diseases +MONDO:0007759 gard_rare diseases +MONDO:0007759 rare diseases +MONDO:0007762 gard_rare diseases +MONDO:0007762 nord_rare diseases +MONDO:0007762 ordo_subtype_of_a_disorder diseases +MONDO:0007762 otar diseases +MONDO:0007762 rare diseases +MONDO:0007763 gard_rare diseases +MONDO:0007763 nord_rare diseases +MONDO:0007763 otar diseases +MONDO:0007763 rare diseases +MONDO:0007764 gard_rare diseases +MONDO:0007764 nord_rare diseases +MONDO:0007764 ordo_disorder diseases +MONDO:0007764 ordo_malformation_syndrome diseases +MONDO:0007764 orphanet_rare diseases +MONDO:0007764 otar diseases +MONDO:0007764 rare diseases +MONDO:0007765 gard_rare diseases +MONDO:0007765 nord_rare diseases +MONDO:0007765 ordo_disorder diseases +MONDO:0007765 orphanet_rare diseases +MONDO:0007765 otar diseases +MONDO:0007765 rare diseases +MONDO:0007766 gard_rare diseases +MONDO:0007766 nord_rare diseases +MONDO:0007766 ordo_disorder diseases +MONDO:0007766 ordo_malformation_syndrome diseases +MONDO:0007766 orphanet_rare diseases +MONDO:0007766 otar diseases +MONDO:0007766 rare diseases +MONDO:0007767 gard_rare diseases +MONDO:0007767 nord_rare diseases +MONDO:0007767 rare diseases +MONDO:0007768 clingen diseases +MONDO:0007768 gard_rare diseases +MONDO:0007768 nord_rare diseases +MONDO:0007768 ordo_disorder diseases +MONDO:0007768 orphanet_rare diseases +MONDO:0007768 otar diseases +MONDO:0007768 rare diseases +MONDO:0007771 gard_rare diseases +MONDO:0007771 nord_rare diseases +MONDO:0007771 otar diseases +MONDO:0007771 rare diseases +MONDO:0007772 gard_rare diseases +MONDO:0007772 nord_rare diseases +MONDO:0007772 ordo_etiological_subtype diseases +MONDO:0007772 ordo_subtype_of_a_disorder diseases +MONDO:0007772 otar diseases +MONDO:0007772 rare diseases +MONDO:0007776 gard_rare diseases +MONDO:0007776 nord_rare diseases +MONDO:0007776 otar diseases +MONDO:0007776 rare diseases +MONDO:0007777 clingen diseases +MONDO:0007781 otar diseases +MONDO:0007784 gard_rare diseases +MONDO:0007784 nord_rare diseases +MONDO:0007784 otar diseases +MONDO:0007784 rare diseases +MONDO:0007787 gard_rare diseases +MONDO:0007787 nord_rare diseases +MONDO:0007787 ordo_subtype_of_a_disorder diseases +MONDO:0007787 otar diseases +MONDO:0007787 rare diseases +MONDO:0007788 gard_rare diseases +MONDO:0007788 nord_rare diseases +MONDO:0007788 rare diseases +MONDO:0007790 gard_rare diseases +MONDO:0007790 nord_rare diseases +MONDO:0007790 ordo_disorder diseases +MONDO:0007790 orphanet_rare diseases +MONDO:0007790 otar diseases +MONDO:0007790 rare diseases +MONDO:0007791 clingen diseases +MONDO:0007791 gard_rare diseases +MONDO:0007791 nord_rare diseases +MONDO:0007791 ordo_etiological_subtype diseases +MONDO:0007791 ordo_subtype_of_a_disorder diseases +MONDO:0007791 otar diseases +MONDO:0007791 rare diseases +MONDO:0007792 gard_rare diseases +MONDO:0007792 nord_rare diseases +MONDO:0007792 ordo_etiological_subtype diseases +MONDO:0007792 ordo_subtype_of_a_disorder diseases +MONDO:0007792 otar diseases +MONDO:0007792 rare diseases +MONDO:0007793 clingen diseases +MONDO:0007793 gard_rare diseases +MONDO:0007793 nord_rare diseases +MONDO:0007793 ordo_disorder diseases +MONDO:0007793 orphanet_rare diseases +MONDO:0007793 otar diseases +MONDO:0007793 rare diseases +MONDO:0007794 gard_rare diseases +MONDO:0007794 nord_rare diseases +MONDO:0007794 rare diseases +MONDO:0007795 gard_rare diseases +MONDO:0007795 nord_rare diseases +MONDO:0007795 ordo_disorder diseases +MONDO:0007795 ordo_malformation_syndrome diseases +MONDO:0007795 orphanet_rare diseases +MONDO:0007795 otar diseases +MONDO:0007795 rare diseases +MONDO:0007796 gard_rare diseases +MONDO:0007796 nord_rare diseases +MONDO:0007796 otar diseases +MONDO:0007796 rare diseases +MONDO:0007797 clingen diseases +MONDO:0007797 gard_rare diseases +MONDO:0007797 nord_rare diseases +MONDO:0007797 ordo_disorder diseases +MONDO:0007797 ordo_malformation_syndrome diseases +MONDO:0007797 orphanet_rare diseases +MONDO:0007797 otar diseases +MONDO:0007797 rare diseases +MONDO:0007800 disease_grouping diseases +MONDO:0007800 gard_rare diseases +MONDO:0007800 nord_rare diseases +MONDO:0007800 ordo_disorder diseases +MONDO:0007800 ordo_group_of_disorders diseases +MONDO:0007800 orphanet_rare diseases +MONDO:0007800 otar diseases +MONDO:0007800 rare diseases +MONDO:0007802 gard_rare diseases +MONDO:0007802 nord_rare diseases +MONDO:0007802 rare diseases +MONDO:0007803 gard_rare diseases +MONDO:0007803 nord_rare diseases +MONDO:0007803 ordo_disorder diseases +MONDO:0007803 orphanet_rare diseases +MONDO:0007803 otar diseases +MONDO:0007803 rare diseases +MONDO:0007804 gard_rare diseases +MONDO:0007804 nord_rare diseases +MONDO:0007804 ordo_disorder diseases +MONDO:0007804 ordo_malformation_syndrome diseases +MONDO:0007804 orphanet_rare diseases +MONDO:0007804 otar diseases +MONDO:0007804 rare diseases +MONDO:0007805 gard_rare diseases +MONDO:0007805 nord_rare diseases +MONDO:0007805 rare diseases +MONDO:0007808 gard_rare diseases +MONDO:0007808 nord_rare diseases +MONDO:0007808 ordo_disorder diseases +MONDO:0007808 orphanet_rare diseases +MONDO:0007808 otar diseases +MONDO:0007808 rare diseases +MONDO:0007809 gard_rare diseases +MONDO:0007809 otar diseases +MONDO:0007809 rare diseases +MONDO:0007810 inferred_rare diseases +MONDO:0007810 rare diseases +MONDO:0007811 otar diseases +MONDO:0007812 gard_rare diseases +MONDO:0007812 nord_rare diseases +MONDO:0007812 otar diseases +MONDO:0007812 rare diseases +MONDO:0007813 gard_rare diseases +MONDO:0007813 nord_rare diseases +MONDO:0007813 ordo_disorder diseases +MONDO:0007813 orphanet_rare diseases +MONDO:0007813 otar diseases +MONDO:0007813 rare diseases +MONDO:0007814 gard_rare diseases +MONDO:0007814 nord_rare diseases +MONDO:0007814 rare diseases +MONDO:0007817 otar diseases +MONDO:0007818 clingen diseases +MONDO:0007818 gard_rare diseases +MONDO:0007818 ordo_disorder diseases +MONDO:0007818 orphanet_rare diseases +MONDO:0007818 otar diseases +MONDO:0007818 rare diseases +MONDO:0007819 gard_rare diseases +MONDO:0007819 nord_rare diseases +MONDO:0007819 otar diseases +MONDO:0007819 rare diseases +MONDO:0007820 gard_rare diseases +MONDO:0007820 nord_rare diseases +MONDO:0007820 ordo_disorder diseases +MONDO:0007820 ordo_morphological_anomaly diseases +MONDO:0007820 orphanet_rare diseases +MONDO:0007820 otar diseases +MONDO:0007820 rare diseases +MONDO:0007827 gard_rare diseases +MONDO:0007827 nord_rare diseases +MONDO:0007827 ordo_disorder diseases +MONDO:0007827 orphanet_rare diseases +MONDO:0007827 otar diseases +MONDO:0007827 rare diseases +MONDO:0007829 gard_rare diseases +MONDO:0007829 nord_rare diseases +MONDO:0007829 rare diseases +MONDO:0007834 otar diseases +MONDO:0007836 gard_rare diseases +MONDO:0007836 nord_rare diseases +MONDO:0007836 ordo_disorder diseases +MONDO:0007836 ordo_malformation_syndrome diseases +MONDO:0007836 orphanet_rare diseases +MONDO:0007836 otar diseases +MONDO:0007836 rare diseases +MONDO:0007837 gard_rare diseases +MONDO:0007837 nord_rare diseases +MONDO:0007837 ordo_disorder diseases +MONDO:0007837 ordo_malformation_syndrome diseases +MONDO:0007837 orphanet_rare diseases +MONDO:0007837 otar diseases +MONDO:0007837 rare diseases +MONDO:0007838 gard_rare diseases +MONDO:0007838 nord_rare diseases +MONDO:0007838 ordo_disorder diseases +MONDO:0007838 ordo_malformation_syndrome diseases +MONDO:0007838 orphanet_rare diseases +MONDO:0007838 otar diseases +MONDO:0007838 rare diseases +MONDO:0007839 gard_rare diseases +MONDO:0007839 nord_rare diseases +MONDO:0007839 ordo_disorder diseases +MONDO:0007839 ordo_malformation_syndrome diseases +MONDO:0007839 orphanet_rare diseases +MONDO:0007839 otar diseases +MONDO:0007839 rare diseases +MONDO:0007841 gard_rare diseases +MONDO:0007841 nord_rare diseases +MONDO:0007841 ordo_disorder diseases +MONDO:0007841 orphanet_rare diseases +MONDO:0007841 otar diseases +MONDO:0007841 rare diseases +MONDO:0007842 gard_rare diseases +MONDO:0007842 ordo_disorder diseases +MONDO:0007842 orphanet_rare diseases +MONDO:0007842 otar diseases +MONDO:0007842 rare diseases +MONDO:0007843 clingen diseases +MONDO:0007843 gard_rare diseases +MONDO:0007843 nord_rare diseases +MONDO:0007843 rare diseases +MONDO:0007844 gard_rare diseases +MONDO:0007844 otar diseases +MONDO:0007844 rare diseases +MONDO:0007845 inferred_rare diseases +MONDO:0007845 predisposition diseases +MONDO:0007845 rare diseases +MONDO:0007846 clingen diseases +MONDO:0007846 gard_rare diseases +MONDO:0007846 nord_rare diseases +MONDO:0007846 ordo_disorder diseases +MONDO:0007846 ordo_malformation_syndrome diseases +MONDO:0007846 orphanet_rare diseases +MONDO:0007846 otar diseases +MONDO:0007846 rare diseases +MONDO:0007848 gard_rare diseases +MONDO:0007848 nord_rare diseases +MONDO:0007848 ordo_disorder diseases +MONDO:0007848 orphanet_rare diseases +MONDO:0007848 otar diseases +MONDO:0007848 rare diseases +MONDO:0007849 gard_rare diseases +MONDO:0007849 ordo_disorder diseases +MONDO:0007849 orphanet_rare diseases +MONDO:0007849 otar diseases +MONDO:0007849 rare diseases +MONDO:0007850 gard_rare diseases +MONDO:0007850 nord_rare diseases +MONDO:0007850 rare diseases +MONDO:0007851 gard_rare diseases +MONDO:0007851 nord_rare diseases +MONDO:0007851 rare diseases +MONDO:0007852 gard_rare diseases +MONDO:0007852 nord_rare diseases +MONDO:0007852 ordo_disorder diseases +MONDO:0007852 orphanet_rare diseases +MONDO:0007852 otar diseases +MONDO:0007852 rare diseases +MONDO:0007853 gard_rare diseases +MONDO:0007853 nord_rare diseases +MONDO:0007853 ordo_disorder diseases +MONDO:0007853 orphanet_rare diseases +MONDO:0007853 otar diseases +MONDO:0007853 rare diseases +MONDO:0007854 gard_rare diseases +MONDO:0007854 nord_rare diseases +MONDO:0007854 ordo_disorder diseases +MONDO:0007854 orphanet_rare diseases +MONDO:0007854 otar diseases +MONDO:0007854 rare diseases +MONDO:0007856 clingen diseases +MONDO:0007856 gard_rare diseases +MONDO:0007856 nord_rare diseases +MONDO:0007856 ordo_disorder diseases +MONDO:0007856 orphanet_rare diseases +MONDO:0007856 otar diseases +MONDO:0007856 rare diseases +MONDO:0007857 gard_rare diseases +MONDO:0007857 nord_rare diseases +MONDO:0007857 ordo_disorder diseases +MONDO:0007857 orphanet_rare diseases +MONDO:0007857 otar diseases +MONDO:0007857 rare diseases +MONDO:0007858 gard_rare diseases +MONDO:0007858 nord_rare diseases +MONDO:0007858 rare diseases +MONDO:0007859 gard_rare diseases +MONDO:0007859 nord_rare diseases +MONDO:0007859 otar diseases +MONDO:0007859 rare diseases +MONDO:0007860 gard_rare diseases +MONDO:0007860 nord_rare diseases +MONDO:0007860 ordo_disorder diseases +MONDO:0007860 orphanet_rare diseases +MONDO:0007860 otar diseases +MONDO:0007860 rare diseases +MONDO:0007861 gard_rare diseases +MONDO:0007861 nord_rare diseases +MONDO:0007861 ordo_morphological_anomaly diseases +MONDO:0007861 otar diseases +MONDO:0007861 rare diseases +MONDO:0007862 gard_rare diseases +MONDO:0007862 nord_rare diseases +MONDO:0007862 ordo_subtype_of_a_disorder diseases +MONDO:0007862 otar diseases +MONDO:0007862 rare diseases +MONDO:0007863 gard_rare diseases +MONDO:0007863 nord_rare diseases +MONDO:0007863 ordo_disorder diseases +MONDO:0007863 orphanet_rare diseases +MONDO:0007863 otar diseases +MONDO:0007863 rare diseases +MONDO:0007864 gard_rare diseases +MONDO:0007864 nord_rare diseases +MONDO:0007864 ordo_disorder diseases +MONDO:0007864 ordo_group_of_disorders diseases +MONDO:0007864 orphanet_rare diseases +MONDO:0007864 otar diseases +MONDO:0007864 rare diseases +MONDO:0007866 gard_rare diseases +MONDO:0007866 nord_rare diseases +MONDO:0007866 ordo_disorder diseases +MONDO:0007866 orphanet_rare diseases +MONDO:0007866 otar diseases +MONDO:0007866 rare diseases +MONDO:0007867 gard_rare diseases +MONDO:0007867 rare diseases +MONDO:0007868 gard_rare diseases +MONDO:0007868 nord_rare diseases +MONDO:0007868 rare diseases +MONDO:0007871 gard_rare diseases +MONDO:0007871 nord_rare diseases +MONDO:0007871 ordo_disorder diseases +MONDO:0007871 ordo_morphological_anomaly diseases +MONDO:0007871 orphanet_rare diseases +MONDO:0007871 rare diseases +MONDO:0007872 gard_rare diseases +MONDO:0007872 nord_rare diseases +MONDO:0007872 ordo_disorder diseases +MONDO:0007872 ordo_malformation_syndrome diseases +MONDO:0007872 orphanet_rare diseases +MONDO:0007872 otar diseases +MONDO:0007872 rare diseases +MONDO:0007874 gard_rare diseases +MONDO:0007874 nord_rare diseases +MONDO:0007874 ordo_disorder diseases +MONDO:0007874 ordo_malformation_syndrome diseases +MONDO:0007874 orphanet_rare diseases +MONDO:0007874 otar diseases +MONDO:0007874 rare diseases +MONDO:0007875 gard_rare diseases +MONDO:0007875 nord_rare diseases +MONDO:0007875 ordo_disorder diseases +MONDO:0007875 ordo_malformation_syndrome diseases +MONDO:0007875 orphanet_rare diseases +MONDO:0007875 otar diseases +MONDO:0007875 rare diseases +MONDO:0007876 gard_rare diseases +MONDO:0007876 nord_rare diseases +MONDO:0007876 ordo_disorder diseases +MONDO:0007876 ordo_malformation_syndrome diseases +MONDO:0007876 orphanet_rare diseases +MONDO:0007876 rare diseases +MONDO:0007878 gard_rare diseases +MONDO:0007878 nord_rare diseases +MONDO:0007878 ordo_disorder diseases +MONDO:0007878 ordo_malformation_syndrome diseases +MONDO:0007878 orphanet_rare diseases +MONDO:0007878 otar diseases +MONDO:0007878 rare diseases +MONDO:0007879 gard_rare diseases +MONDO:0007879 nord_rare diseases +MONDO:0007879 ordo_disorder diseases +MONDO:0007879 ordo_malformation_syndrome diseases +MONDO:0007879 orphanet_rare diseases +MONDO:0007879 otar diseases +MONDO:0007879 rare diseases +MONDO:0007880 gard_rare diseases +MONDO:0007880 nord_rare diseases +MONDO:0007880 ordo_disorder diseases +MONDO:0007880 ordo_malformation_syndrome diseases +MONDO:0007880 orphanet_rare diseases +MONDO:0007880 otar diseases +MONDO:0007880 rare diseases +MONDO:0007881 gard_rare diseases +MONDO:0007881 nord_rare diseases +MONDO:0007881 rare diseases +MONDO:0007883 gard_rare diseases +MONDO:0007883 ordo_disorder diseases +MONDO:0007883 orphanet_rare diseases +MONDO:0007883 otar diseases +MONDO:0007883 rare diseases +MONDO:0007885 gard_rare diseases +MONDO:0007885 nord_rare diseases +MONDO:0007885 ordo_disorder diseases +MONDO:0007885 orphanet_rare diseases +MONDO:0007885 otar diseases +MONDO:0007885 rare diseases +MONDO:0007886 gard_rare diseases +MONDO:0007886 nord_rare diseases +MONDO:0007886 otar diseases +MONDO:0007886 rare diseases +MONDO:0007887 gard_rare diseases +MONDO:0007887 nord_rare diseases +MONDO:0007887 rare diseases +MONDO:0007888 clingen diseases +MONDO:0007888 gard_rare diseases +MONDO:0007888 nord_rare diseases +MONDO:0007888 ordo_disorder diseases +MONDO:0007888 orphanet_rare diseases +MONDO:0007888 otar diseases +MONDO:0007888 rare diseases +MONDO:0007891 gard_rare diseases +MONDO:0007891 nord_rare diseases +MONDO:0007891 ordo_disorder diseases +MONDO:0007891 orphanet_rare diseases +MONDO:0007891 otar diseases +MONDO:0007891 rare diseases +MONDO:0007892 gard_rare diseases +MONDO:0007892 nord_rare diseases +MONDO:0007892 ordo_disorder diseases +MONDO:0007892 ordo_malformation_syndrome diseases +MONDO:0007892 orphanet_rare diseases +MONDO:0007892 otar diseases +MONDO:0007892 rare diseases +MONDO:0007893 clingen diseases +MONDO:0007893 gard_rare diseases +MONDO:0007893 nord_rare diseases +MONDO:0007893 ordo_disorder diseases +MONDO:0007893 ordo_malformation_syndrome diseases +MONDO:0007893 orphanet_rare diseases +MONDO:0007893 otar diseases +MONDO:0007893 rare diseases +MONDO:0007894 gard_rare diseases +MONDO:0007894 nord_rare diseases +MONDO:0007894 ordo_disorder diseases +MONDO:0007894 ordo_malformation_syndrome diseases +MONDO:0007894 orphanet_rare diseases +MONDO:0007894 otar diseases +MONDO:0007894 rare diseases +MONDO:0007895 clingen diseases +MONDO:0007895 gard_rare diseases +MONDO:0007895 nord_rare diseases +MONDO:0007895 ordo_disorder diseases +MONDO:0007895 ordo_malformation_syndrome diseases +MONDO:0007895 orphanet_rare diseases +MONDO:0007895 otar diseases +MONDO:0007895 rare diseases +MONDO:0007896 gard_rare diseases +MONDO:0007896 nord_rare diseases +MONDO:0007896 ordo_disorder diseases +MONDO:0007896 orphanet_rare diseases +MONDO:0007896 otar diseases +MONDO:0007896 rare diseases +MONDO:0007899 otar diseases +MONDO:0007900 gard_rare diseases +MONDO:0007900 rare diseases +MONDO:0007904 gard_rare diseases +MONDO:0007904 nord_rare diseases +MONDO:0007904 ordo_disorder diseases +MONDO:0007904 ordo_malformation_syndrome diseases +MONDO:0007904 orphanet_rare diseases +MONDO:0007904 rare diseases +MONDO:0007906 gard_rare diseases +MONDO:0007906 nord_rare diseases +MONDO:0007906 ordo_disorder diseases +MONDO:0007906 orphanet_rare diseases +MONDO:0007906 otar diseases +MONDO:0007906 rare diseases +MONDO:0007907 gard_rare diseases +MONDO:0007907 nord_rare diseases +MONDO:0007907 rare diseases +MONDO:0007908 gard_rare diseases +MONDO:0007908 nord_rare diseases +MONDO:0007908 ordo_disorder diseases +MONDO:0007908 orphanet_rare diseases +MONDO:0007908 otar diseases +MONDO:0007908 rare diseases +MONDO:0007909 gard_rare diseases +MONDO:0007909 nord_rare diseases +MONDO:0007909 ordo_disorder diseases +MONDO:0007909 orphanet_rare diseases +MONDO:0007909 otar diseases +MONDO:0007909 rare diseases +MONDO:0007915 gard_rare diseases +MONDO:0007915 nord_rare diseases +MONDO:0007915 ordo_disorder diseases +MONDO:0007915 orphanet_rare diseases +MONDO:0007915 otar diseases +MONDO:0007915 rare diseases +MONDO:0007916 gard_rare diseases +MONDO:0007916 nord_rare diseases +MONDO:0007916 ordo_disorder diseases +MONDO:0007916 orphanet_rare diseases +MONDO:0007916 otar diseases +MONDO:0007916 rare diseases +MONDO:0007917 gard_rare diseases +MONDO:0007917 ordo_disorder diseases +MONDO:0007917 ordo_malformation_syndrome diseases +MONDO:0007917 orphanet_rare diseases +MONDO:0007917 otar diseases +MONDO:0007917 rare diseases +MONDO:0007918 clingen diseases +MONDO:0007918 gard_rare diseases +MONDO:0007918 nord_rare diseases +MONDO:0007918 ordo_disorder diseases +MONDO:0007918 ordo_malformation_syndrome diseases +MONDO:0007918 orphanet_rare diseases +MONDO:0007918 otar diseases +MONDO:0007918 rare diseases +MONDO:0007919 clingen diseases +MONDO:0007919 gard_rare diseases +MONDO:0007919 nord_rare diseases +MONDO:0007919 ordo_disorder diseases +MONDO:0007919 orphanet_rare diseases +MONDO:0007919 rare diseases +MONDO:0007920 gard_rare diseases +MONDO:0007920 nord_rare diseases +MONDO:0007920 ordo_disorder diseases +MONDO:0007920 orphanet_rare diseases +MONDO:0007920 otar diseases +MONDO:0007920 rare diseases +MONDO:0007921 gard_rare diseases +MONDO:0007921 nord_rare diseases +MONDO:0007921 ordo_disorder diseases +MONDO:0007921 orphanet_rare diseases +MONDO:0007921 otar diseases +MONDO:0007921 rare diseases +MONDO:0007922 gard_rare diseases +MONDO:0007922 nord_rare diseases +MONDO:0007922 ordo_disorder diseases +MONDO:0007922 ordo_malformation_syndrome diseases +MONDO:0007922 orphanet_rare diseases +MONDO:0007922 otar diseases +MONDO:0007922 rare diseases +MONDO:0007924 gard_rare diseases +MONDO:0007924 nord_rare diseases +MONDO:0007924 ordo_disorder diseases +MONDO:0007924 ordo_malformation_syndrome diseases +MONDO:0007924 orphanet_rare diseases +MONDO:0007924 otar diseases +MONDO:0007924 rare diseases +MONDO:0007925 gard_rare diseases +MONDO:0007925 nord_rare diseases +MONDO:0007925 ordo_disorder diseases +MONDO:0007925 orphanet_rare diseases +MONDO:0007925 rare diseases +MONDO:0007927 gard_rare diseases +MONDO:0007927 nord_rare diseases +MONDO:0007927 ordo_disorder diseases +MONDO:0007927 ordo_malformation_syndrome diseases +MONDO:0007927 orphanet_rare diseases +MONDO:0007927 otar diseases +MONDO:0007927 rare diseases +MONDO:0007930 gard_rare diseases +MONDO:0007930 nord_rare diseases +MONDO:0007930 rare diseases +MONDO:0007931 gard_rare diseases +MONDO:0007931 nord_rare diseases +MONDO:0007931 ordo_disorder diseases +MONDO:0007931 orphanet_rare diseases +MONDO:0007931 otar diseases +MONDO:0007931 rare diseases +MONDO:0007932 gard_rare diseases +MONDO:0007932 nord_rare diseases +MONDO:0007932 rare diseases +MONDO:0007933 gard_rare diseases +MONDO:0007933 nord_rare diseases +MONDO:0007933 rare diseases +MONDO:0007934 gard_rare diseases +MONDO:0007934 nord_rare diseases +MONDO:0007934 ordo_disorder diseases +MONDO:0007934 orphanet_rare diseases +MONDO:0007934 otar diseases +MONDO:0007934 rare diseases +MONDO:0007935 gard_rare diseases +MONDO:0007935 nord_rare diseases +MONDO:0007935 ordo_disorder diseases +MONDO:0007935 orphanet_rare diseases +MONDO:0007935 otar diseases +MONDO:0007935 rare diseases +MONDO:0007936 gard_rare diseases +MONDO:0007936 rare diseases +MONDO:0007937 clingen diseases +MONDO:0007937 gard_rare diseases +MONDO:0007937 nord_rare diseases +MONDO:0007937 ordo_disorder diseases +MONDO:0007937 orphanet_rare diseases +MONDO:0007937 otar diseases +MONDO:0007937 rare diseases +MONDO:0007938 gard_rare diseases +MONDO:0007938 nord_rare diseases +MONDO:0007938 rare diseases +MONDO:0007943 gard_rare diseases +MONDO:0007943 nord_rare diseases +MONDO:0007943 ordo_disorder diseases +MONDO:0007943 ordo_malformation_syndrome diseases +MONDO:0007943 orphanet_rare diseases +MONDO:0007943 otar diseases +MONDO:0007943 rare diseases +MONDO:0007944 gard_rare diseases +MONDO:0007944 nord_rare diseases +MONDO:0007944 rare diseases +MONDO:0007946 gard_rare diseases +MONDO:0007946 nord_rare diseases +MONDO:0007946 ordo_disorder diseases +MONDO:0007946 orphanet_rare diseases +MONDO:0007946 otar diseases +MONDO:0007946 rare diseases +MONDO:0007947 clingen diseases +MONDO:0007947 gard_rare diseases +MONDO:0007947 nord_rare diseases +MONDO:0007947 ordo_disorder diseases +MONDO:0007947 ordo_subtype_of_a_disorder diseases +MONDO:0007947 orphanet_rare diseases +MONDO:0007947 otar diseases +MONDO:0007947 prototype_pattern diseases +MONDO:0007947 rare diseases +MONDO:0007949 gard_rare diseases +MONDO:0007949 nord_rare diseases +MONDO:0007949 ordo_disorder diseases +MONDO:0007949 ordo_malformation_syndrome diseases +MONDO:0007949 orphanet_rare diseases +MONDO:0007949 otar diseases +MONDO:0007949 rare diseases +MONDO:0007950 disease_grouping diseases +MONDO:0007950 gard_rare diseases +MONDO:0007950 nord_rare diseases +MONDO:0007950 ordo_group_of_disorders diseases +MONDO:0007950 otar diseases +MONDO:0007950 rare diseases +MONDO:0007953 gard_rare diseases +MONDO:0007953 nord_rare diseases +MONDO:0007953 ordo_disorder diseases +MONDO:0007953 ordo_malformation_syndrome diseases +MONDO:0007953 orphanet_rare diseases +MONDO:0007953 otar diseases +MONDO:0007953 rare diseases +MONDO:0007955 otar diseases +MONDO:0007956 gard_rare diseases +MONDO:0007956 nord_rare diseases +MONDO:0007956 ordo_disorder diseases +MONDO:0007956 ordo_malformation_syndrome diseases +MONDO:0007956 orphanet_rare diseases +MONDO:0007956 otar diseases +MONDO:0007956 rare diseases +MONDO:0007958 gard_rare diseases +MONDO:0007958 nord_rare diseases +MONDO:0007958 ordo_disorder diseases +MONDO:0007958 orphanet_rare diseases +MONDO:0007958 otar diseases +MONDO:0007958 rare diseases +MONDO:0007959 clingen diseases +MONDO:0007959 gard_rare diseases +MONDO:0007959 nord_rare diseases +MONDO:0007959 ordo_disorder diseases +MONDO:0007959 orphanet_rare diseases +MONDO:0007959 otar diseases +MONDO:0007959 rare diseases +MONDO:0007961 gard_rare diseases +MONDO:0007961 nord_rare diseases +MONDO:0007961 rare diseases +MONDO:0007962 gard_rare diseases +MONDO:0007962 nord_rare diseases +MONDO:0007962 otar diseases +MONDO:0007962 rare diseases +MONDO:0007963 inferred_rare diseases +MONDO:0007963 predisposition diseases +MONDO:0007963 rare diseases +MONDO:0007964 nord_rare diseases +MONDO:0007964 predisposition diseases +MONDO:0007964 rare diseases +MONDO:0007965 gard_rare diseases +MONDO:0007965 nord_rare diseases +MONDO:0007965 rare diseases +MONDO:0007966 gard_rare diseases +MONDO:0007966 predisposition diseases +MONDO:0007966 rare diseases +MONDO:0007967 gard_rare diseases +MONDO:0007967 nord_rare diseases +MONDO:0007967 ordo_disorder diseases +MONDO:0007967 orphanet_rare diseases +MONDO:0007967 rare diseases +MONDO:0007969 gard_rare diseases +MONDO:0007969 nord_rare diseases +MONDO:0007969 ordo_disorder diseases +MONDO:0007969 ordo_malformation_syndrome diseases +MONDO:0007969 orphanet_rare diseases +MONDO:0007969 otar diseases +MONDO:0007969 rare diseases +MONDO:0007970 gard_rare diseases +MONDO:0007970 nord_rare diseases +MONDO:0007970 ordo_disorder diseases +MONDO:0007970 ordo_malformation_syndrome diseases +MONDO:0007970 orphanet_rare diseases +MONDO:0007970 otar diseases +MONDO:0007970 rare diseases +MONDO:0007971 gard_rare diseases +MONDO:0007971 nord_rare diseases +MONDO:0007971 ordo_disorder diseases +MONDO:0007971 ordo_malformation_syndrome diseases +MONDO:0007971 orphanet_rare diseases +MONDO:0007971 otar diseases +MONDO:0007971 rare diseases +MONDO:0007972 nord_rare diseases +MONDO:0007972 otar diseases +MONDO:0007972 rare diseases +MONDO:0007974 gard_rare diseases +MONDO:0007974 rare diseases +MONDO:0007975 gard_rare diseases +MONDO:0007975 nord_rare diseases +MONDO:0007975 rare diseases +MONDO:0007977 gard_rare diseases +MONDO:0007977 nord_rare diseases +MONDO:0007977 ordo_disorder diseases +MONDO:0007977 ordo_malformation_syndrome diseases +MONDO:0007977 orphanet_rare diseases +MONDO:0007977 otar diseases +MONDO:0007977 rare diseases +MONDO:0007979 gard_rare diseases +MONDO:0007979 nord_rare diseases +MONDO:0007979 ordo_disorder diseases +MONDO:0007979 ordo_malformation_syndrome diseases +MONDO:0007979 orphanet_rare diseases +MONDO:0007979 otar diseases +MONDO:0007979 rare diseases +MONDO:0007982 gard_rare diseases +MONDO:0007982 nord_rare diseases +MONDO:0007982 ordo_disorder diseases +MONDO:0007982 orphanet_rare diseases +MONDO:0007982 otar diseases +MONDO:0007982 rare diseases +MONDO:0007983 gard_rare diseases +MONDO:0007983 nord_rare diseases +MONDO:0007983 ordo_disorder diseases +MONDO:0007983 orphanet_rare diseases +MONDO:0007983 otar diseases +MONDO:0007983 rare diseases +MONDO:0007984 gard_rare diseases +MONDO:0007984 nord_rare diseases +MONDO:0007984 ordo_disorder diseases +MONDO:0007984 ordo_malformation_syndrome diseases +MONDO:0007984 orphanet_rare diseases +MONDO:0007984 otar diseases +MONDO:0007984 rare diseases +MONDO:0007986 gard_rare diseases +MONDO:0007986 nord_rare diseases +MONDO:0007986 ordo_disorder diseases +MONDO:0007986 orphanet_rare diseases +MONDO:0007986 otar diseases +MONDO:0007986 rare diseases +MONDO:0007987 clingen diseases +MONDO:0007987 gard_rare diseases +MONDO:0007987 nord_rare diseases +MONDO:0007987 ordo_disorder diseases +MONDO:0007987 orphanet_rare diseases +MONDO:0007987 otar diseases +MONDO:0007987 rare diseases +MONDO:0007988 gard_rare diseases +MONDO:0007988 nord_rare diseases +MONDO:0007988 ordo_etiological_subtype diseases +MONDO:0007988 ordo_subtype_of_a_disorder diseases +MONDO:0007988 otar diseases +MONDO:0007988 rare diseases +MONDO:0007989 gard_rare diseases +MONDO:0007989 nord_rare diseases +MONDO:0007989 ordo_disorder diseases +MONDO:0007989 ordo_malformation_syndrome diseases +MONDO:0007989 orphanet_rare diseases +MONDO:0007989 otar diseases +MONDO:0007989 rare diseases +MONDO:0007990 gard_rare diseases +MONDO:0007990 nord_rare diseases +MONDO:0007990 ordo_disorder diseases +MONDO:0007990 orphanet_rare diseases +MONDO:0007990 otar diseases +MONDO:0007990 rare diseases +MONDO:0007991 gard_rare diseases +MONDO:0007991 ordo_disorder diseases +MONDO:0007991 ordo_malformation_syndrome diseases +MONDO:0007991 orphanet_rare diseases +MONDO:0007991 otar diseases +MONDO:0007991 rare diseases +MONDO:0007992 gard_rare diseases +MONDO:0007992 ordo_disorder diseases +MONDO:0007992 ordo_malformation_syndrome diseases +MONDO:0007992 orphanet_rare diseases +MONDO:0007992 otar diseases +MONDO:0007992 rare diseases +MONDO:0007993 gard_rare diseases +MONDO:0007993 nord_rare diseases +MONDO:0007993 ordo_disorder diseases +MONDO:0007993 ordo_malformation_syndrome diseases +MONDO:0007993 orphanet_rare diseases +MONDO:0007993 rare diseases +MONDO:0007994 gard_rare diseases +MONDO:0007994 nord_rare diseases +MONDO:0007994 rare diseases +MONDO:0007995 gard_rare diseases +MONDO:0007995 nord_rare diseases +MONDO:0007995 rare diseases +MONDO:0007998 gard_rare diseases +MONDO:0007998 ordo_disorder diseases +MONDO:0007998 ordo_malformation_syndrome diseases +MONDO:0007998 orphanet_rare diseases +MONDO:0007998 rare diseases +MONDO:0007999 gard_rare diseases +MONDO:0007999 nord_rare diseases +MONDO:0007999 rare diseases +MONDO:0008002 gard_rare diseases +MONDO:0008002 nord_rare diseases +MONDO:0008002 otar diseases +MONDO:0008002 rare diseases +MONDO:0008003 gard_rare diseases +MONDO:0008003 nord_rare diseases +MONDO:0008003 ordo_disorder diseases +MONDO:0008003 orphanet_rare diseases +MONDO:0008003 otar diseases +MONDO:0008003 rare diseases +MONDO:0008004 gard_rare diseases +MONDO:0008004 nord_rare diseases +MONDO:0008004 ordo_disorder diseases +MONDO:0008004 ordo_morphological_anomaly diseases +MONDO:0008004 orphanet_rare diseases +MONDO:0008004 rare diseases +MONDO:0008005 gard_rare diseases +MONDO:0008005 nord_rare diseases +MONDO:0008005 ordo_disorder diseases +MONDO:0008005 ordo_malformation_syndrome diseases +MONDO:0008005 orphanet_rare diseases +MONDO:0008005 otar diseases +MONDO:0008005 rare diseases +MONDO:0008006 gard_rare diseases +MONDO:0008006 nord_rare diseases +MONDO:0008006 ordo_disorder diseases +MONDO:0008006 orphanet_rare diseases +MONDO:0008006 otar diseases +MONDO:0008006 rare diseases +MONDO:0008007 gard_rare diseases +MONDO:0008007 ordo_disorder diseases +MONDO:0008007 ordo_malformation_syndrome diseases +MONDO:0008007 orphanet_rare diseases +MONDO:0008007 otar diseases +MONDO:0008007 rare diseases +MONDO:0008008 gard_rare diseases +MONDO:0008008 nord_rare diseases +MONDO:0008008 ordo_disorder diseases +MONDO:0008008 ordo_malformation_syndrome diseases +MONDO:0008008 orphanet_rare diseases +MONDO:0008008 otar diseases +MONDO:0008008 rare diseases +MONDO:0008009 gard_rare diseases +MONDO:0008009 nord_rare diseases +MONDO:0008009 ordo_disorder diseases +MONDO:0008009 orphanet_rare diseases +MONDO:0008009 otar diseases +MONDO:0008009 rare diseases +MONDO:0008013 disease_grouping diseases +MONDO:0008013 gard_rare diseases +MONDO:0008013 nord_rare diseases +MONDO:0008013 ordo_disorder diseases +MONDO:0008013 ordo_malformation_syndrome diseases +MONDO:0008013 orphanet_rare diseases +MONDO:0008013 otar diseases +MONDO:0008013 rare diseases +MONDO:0008015 gard_rare diseases +MONDO:0008015 rare diseases +MONDO:0008016 gard_rare diseases +MONDO:0008016 nord_rare diseases +MONDO:0008016 ordo_disorder diseases +MONDO:0008016 ordo_malformation_syndrome diseases +MONDO:0008016 orphanet_rare diseases +MONDO:0008016 otar diseases +MONDO:0008016 rare diseases +MONDO:0008017 gard_rare diseases +MONDO:0008017 nord_rare diseases +MONDO:0008017 ordo_disorder diseases +MONDO:0008017 ordo_malformation_syndrome diseases +MONDO:0008017 orphanet_rare diseases +MONDO:0008017 otar diseases +MONDO:0008017 rare diseases +MONDO:0008018 gard_rare diseases +MONDO:0008018 nord_rare diseases +MONDO:0008018 otar diseases +MONDO:0008018 rare diseases +MONDO:0008019 gard_rare diseases +MONDO:0008019 nord_rare diseases +MONDO:0008019 ordo_disorder diseases +MONDO:0008019 ordo_malformation_syndrome diseases +MONDO:0008019 orphanet_rare diseases +MONDO:0008019 otar diseases +MONDO:0008019 rare diseases +MONDO:0008021 gard_rare diseases +MONDO:0008021 rare diseases +MONDO:0008023 gard_rare diseases +MONDO:0008023 nord_rare diseases +MONDO:0008023 ordo_disorder diseases +MONDO:0008023 orphanet_rare diseases +MONDO:0008023 otar diseases +MONDO:0008023 rare diseases +MONDO:0008024 clingen diseases +MONDO:0008024 gard_rare diseases +MONDO:0008024 nord_rare diseases +MONDO:0008024 rare diseases +MONDO:0008025 gard_rare diseases +MONDO:0008025 nord_rare diseases +MONDO:0008025 rare diseases +MONDO:0008026 gard_rare diseases +MONDO:0008026 nord_rare diseases +MONDO:0008026 ordo_subtype_of_a_disorder diseases +MONDO:0008026 otar diseases +MONDO:0008026 rare diseases +MONDO:0008028 gard_rare diseases +MONDO:0008028 rare diseases +MONDO:0008029 gard_rare diseases +MONDO:0008029 ordo_disorder diseases +MONDO:0008029 orphanet_rare diseases +MONDO:0008029 otar diseases +MONDO:0008029 prototype_pattern diseases +MONDO:0008029 rare diseases +MONDO:0008030 gard_rare diseases +MONDO:0008030 nord_rare diseases +MONDO:0008030 rare diseases +MONDO:0008031 gard_rare diseases +MONDO:0008031 nord_rare diseases +MONDO:0008031 rare diseases +MONDO:0008034 gard_rare diseases +MONDO:0008034 rare diseases +MONDO:0008036 gard_rare diseases +MONDO:0008036 rare diseases +MONDO:0008038 gard_rare diseases +MONDO:0008038 nord_rare diseases +MONDO:0008038 ordo_disorder diseases +MONDO:0008038 ordo_malformation_syndrome diseases +MONDO:0008038 orphanet_rare diseases +MONDO:0008038 otar diseases +MONDO:0008038 rare diseases +MONDO:0008039 gard_rare diseases +MONDO:0008039 nord_rare diseases +MONDO:0008039 ordo_disorder diseases +MONDO:0008039 orphanet_rare diseases +MONDO:0008039 otar diseases +MONDO:0008039 rare diseases +MONDO:0008040 gard_rare diseases +MONDO:0008040 nord_rare diseases +MONDO:0008040 ordo_disorder diseases +MONDO:0008040 orphanet_rare diseases +MONDO:0008040 rare diseases +MONDO:0008041 gard_rare diseases +MONDO:0008041 nord_rare diseases +MONDO:0008041 rare diseases +MONDO:0008043 gard_rare diseases +MONDO:0008043 nord_rare diseases +MONDO:0008043 ordo_disorder diseases +MONDO:0008043 ordo_malformation_syndrome diseases +MONDO:0008043 orphanet_rare diseases +MONDO:0008043 otar diseases +MONDO:0008043 rare diseases +MONDO:0008044 gard_rare diseases +MONDO:0008044 nord_rare diseases +MONDO:0008044 rare diseases +MONDO:0008045 gard_rare diseases +MONDO:0008045 nord_rare diseases +MONDO:0008045 ordo_disorder diseases +MONDO:0008045 orphanet_rare diseases +MONDO:0008045 otar diseases +MONDO:0008045 rare diseases +MONDO:0008046 gard_rare diseases +MONDO:0008046 ordo_disorder diseases +MONDO:0008046 orphanet_rare diseases +MONDO:0008046 otar diseases +MONDO:0008046 rare diseases +MONDO:0008047 clingen diseases +MONDO:0008047 gard_rare diseases +MONDO:0008047 nord_rare diseases +MONDO:0008047 ordo_disorder diseases +MONDO:0008047 orphanet_rare diseases +MONDO:0008047 otar diseases +MONDO:0008047 rare diseases +MONDO:0008048 clingen diseases +MONDO:0008048 gard_rare diseases +MONDO:0008048 nord_rare diseases +MONDO:0008048 ordo_disorder diseases +MONDO:0008048 orphanet_rare diseases +MONDO:0008048 otar diseases +MONDO:0008048 prototype_pattern diseases +MONDO:0008048 rare diseases +MONDO:0008049 gard_rare diseases +MONDO:0008049 rare diseases +MONDO:0008050 clingen diseases +MONDO:0008050 gard_rare diseases +MONDO:0008050 nord_rare diseases +MONDO:0008050 ordo_disorder diseases +MONDO:0008050 orphanet_rare diseases +MONDO:0008050 otar diseases +MONDO:0008050 rare diseases +MONDO:0008051 clingen diseases +MONDO:0008051 gard_rare diseases +MONDO:0008051 nord_rare diseases +MONDO:0008051 ordo_disorder diseases +MONDO:0008051 orphanet_rare diseases +MONDO:0008051 otar diseases +MONDO:0008051 prototype_pattern diseases +MONDO:0008051 rare diseases +MONDO:0008054 gard_rare diseases +MONDO:0008054 nord_rare diseases +MONDO:0008054 ordo_disorder diseases +MONDO:0008054 orphanet_rare diseases +MONDO:0008054 otar diseases +MONDO:0008054 rare diseases +MONDO:0008055 gard_rare diseases +MONDO:0008055 rare diseases +MONDO:0008056 gard_rare diseases +MONDO:0008056 nord_rare diseases +MONDO:0008056 ordo_disorder diseases +MONDO:0008056 orphanet_rare diseases +MONDO:0008056 otar diseases +MONDO:0008056 rare diseases +MONDO:0008057 clingen diseases +MONDO:0008057 gard_rare diseases +MONDO:0008057 otar diseases +MONDO:0008057 rare diseases +MONDO:0008058 gard_rare diseases +MONDO:0008058 ordo_disorder diseases +MONDO:0008058 orphanet_rare diseases +MONDO:0008058 rare diseases +MONDO:0008059 gard_rare diseases +MONDO:0008059 nord_rare diseases +MONDO:0008059 ordo_disorder diseases +MONDO:0008059 orphanet_rare diseases +MONDO:0008059 otar diseases +MONDO:0008059 rare diseases +MONDO:0008060 gard_rare diseases +MONDO:0008060 nord_rare diseases +MONDO:0008060 ordo_disorder diseases +MONDO:0008060 orphanet_rare diseases +MONDO:0008060 otar diseases +MONDO:0008060 rare diseases +MONDO:0008061 clingen diseases +MONDO:0008061 gard_rare diseases +MONDO:0008061 nord_rare diseases +MONDO:0008061 ordo_disorder diseases +MONDO:0008061 ordo_malformation_syndrome diseases +MONDO:0008061 orphanet_rare diseases +MONDO:0008061 otar diseases +MONDO:0008061 rare diseases +MONDO:0008062 gard_rare diseases +MONDO:0008062 nord_rare diseases +MONDO:0008062 rare diseases +MONDO:0008067 inferred_rare diseases +MONDO:0008067 predisposition diseases +MONDO:0008067 rare diseases +MONDO:0008069 gard_rare diseases +MONDO:0008069 nord_rare diseases +MONDO:0008069 rare diseases +MONDO:0008070 gard_rare diseases +MONDO:0008070 ordo_disorder diseases +MONDO:0008070 orphanet_rare diseases +MONDO:0008070 rare diseases +MONDO:0008071 gard_rare diseases +MONDO:0008071 nord_rare diseases +MONDO:0008071 ordo_disorder diseases +MONDO:0008071 orphanet_rare diseases +MONDO:0008071 otar diseases +MONDO:0008071 rare diseases +MONDO:0008073 gard_rare diseases +MONDO:0008073 nord_rare diseases +MONDO:0008073 ordo_subtype_of_a_disorder diseases +MONDO:0008073 otar diseases +MONDO:0008073 prototype_pattern diseases +MONDO:0008073 rare diseases +MONDO:0008075 gard_rare diseases +MONDO:0008075 nord_rare diseases +MONDO:0008075 ordo_disorder diseases +MONDO:0008075 orphanet_rare diseases +MONDO:0008075 otar diseases +MONDO:0008075 rare diseases +MONDO:0008076 gard_rare diseases +MONDO:0008076 rare diseases +MONDO:0008078 gard_rare diseases +MONDO:0008078 nord_rare diseases +MONDO:0008078 rare diseases +MONDO:0008080 gard_rare diseases +MONDO:0008080 nord_rare diseases +MONDO:0008080 rare diseases +MONDO:0008081 gard_rare diseases +MONDO:0008081 nord_rare diseases +MONDO:0008081 rare diseases +MONDO:0008082 clingen diseases +MONDO:0008082 gard_rare diseases +MONDO:0008082 nord_rare diseases +MONDO:0008082 ordo_subtype_of_a_disorder diseases +MONDO:0008082 otar diseases +MONDO:0008082 rare diseases +MONDO:0008083 gard_rare diseases +MONDO:0008083 nord_rare diseases +MONDO:0008083 ordo_etiological_subtype diseases +MONDO:0008083 otar diseases +MONDO:0008083 rare diseases +MONDO:0008086 gard_rare diseases +MONDO:0008086 nord_rare diseases +MONDO:0008086 rare diseases +MONDO:0008087 gard_rare diseases +MONDO:0008087 nord_rare diseases +MONDO:0008087 ordo_disorder diseases +MONDO:0008087 ordo_malformation_syndrome diseases +MONDO:0008087 orphanet_rare diseases +MONDO:0008087 otar diseases +MONDO:0008087 rare diseases +MONDO:0008090 gard_rare diseases +MONDO:0008090 nord_rare diseases +MONDO:0008090 ordo_disorder diseases +MONDO:0008090 orphanet_rare diseases +MONDO:0008090 otar diseases +MONDO:0008090 rare diseases +MONDO:0008092 gard_rare diseases +MONDO:0008092 nord_rare diseases +MONDO:0008092 ordo_disorder diseases +MONDO:0008092 orphanet_rare diseases +MONDO:0008092 otar diseases +MONDO:0008092 rare diseases +MONDO:0008093 gard_rare diseases +MONDO:0008093 nord_rare diseases +MONDO:0008093 otar diseases +MONDO:0008093 rare diseases +MONDO:0008094 gard_rare diseases +MONDO:0008094 nord_rare diseases +MONDO:0008094 ordo_disorder diseases +MONDO:0008094 ordo_morphological_anomaly diseases +MONDO:0008094 orphanet_rare diseases +MONDO:0008094 otar diseases +MONDO:0008094 rare diseases +MONDO:0008097 gard_rare diseases +MONDO:0008097 nord_rare diseases +MONDO:0008097 ordo_disorder diseases +MONDO:0008097 orphanet_rare diseases +MONDO:0008097 otar diseases +MONDO:0008097 rare diseases +MONDO:0008098 gard_rare diseases +MONDO:0008098 nord_rare diseases +MONDO:0008098 ordo_disorder diseases +MONDO:0008098 ordo_malformation_syndrome diseases +MONDO:0008098 orphanet_rare diseases +MONDO:0008098 otar diseases +MONDO:0008098 rare diseases +MONDO:0008099 gard_rare diseases +MONDO:0008099 rare diseases +MONDO:0008101 gard_rare diseases +MONDO:0008101 nord_rare diseases +MONDO:0008101 ordo_disorder diseases +MONDO:0008101 ordo_morphological_anomaly diseases +MONDO:0008101 orphanet_rare diseases +MONDO:0008101 rare diseases +MONDO:0008102 gard_rare diseases +MONDO:0008102 rare diseases +MONDO:0008104 gard_rare diseases +MONDO:0008104 nord_rare diseases +MONDO:0008104 rare diseases +MONDO:0008108 gard_rare diseases +MONDO:0008108 nord_rare diseases +MONDO:0008108 ordo_disorder diseases +MONDO:0008108 ordo_malformation_syndrome diseases +MONDO:0008108 orphanet_rare diseases +MONDO:0008108 otar diseases +MONDO:0008108 rare diseases +MONDO:0008109 gard_rare diseases +MONDO:0008109 ordo_disorder diseases +MONDO:0008109 orphanet_rare diseases +MONDO:0008109 otar diseases +MONDO:0008109 rare diseases +MONDO:0008111 gard_rare diseases +MONDO:0008111 nord_rare diseases +MONDO:0008111 ordo_disorder diseases +MONDO:0008111 ordo_malformation_syndrome diseases +MONDO:0008111 orphanet_rare diseases +MONDO:0008111 otar diseases +MONDO:0008111 rare diseases +MONDO:0008113 gard_rare diseases +MONDO:0008113 nord_rare diseases +MONDO:0008113 ordo_disorder diseases +MONDO:0008113 ordo_malformation_syndrome diseases +MONDO:0008113 orphanet_rare diseases +MONDO:0008113 otar diseases +MONDO:0008113 rare diseases +MONDO:0008114 otar diseases +MONDO:0008115 gard_rare diseases +MONDO:0008115 nord_rare diseases +MONDO:0008115 ordo_subtype_of_a_disorder diseases +MONDO:0008115 otar diseases +MONDO:0008115 rare diseases +MONDO:0008116 gard_rare diseases +MONDO:0008116 nord_rare diseases +MONDO:0008116 ordo_disorder diseases +MONDO:0008116 orphanet_rare diseases +MONDO:0008116 otar diseases +MONDO:0008116 rare diseases +MONDO:0008118 gard_rare diseases +MONDO:0008118 nord_rare diseases +MONDO:0008118 ordo_disorder diseases +MONDO:0008118 ordo_malformation_syndrome diseases +MONDO:0008118 orphanet_rare diseases +MONDO:0008118 otar diseases +MONDO:0008118 rare diseases +MONDO:0008119 gard_rare diseases +MONDO:0008119 nord_rare diseases +MONDO:0008119 ordo_disorder diseases +MONDO:0008119 orphanet_rare diseases +MONDO:0008119 otar diseases +MONDO:0008119 rare diseases +MONDO:0008123 gard_rare diseases +MONDO:0008123 nord_rare diseases +MONDO:0008123 ordo_subtype_of_a_disorder diseases +MONDO:0008123 otar diseases +MONDO:0008123 rare diseases +MONDO:0008124 gard_rare diseases +MONDO:0008124 nord_rare diseases +MONDO:0008124 rare diseases +MONDO:0008125 gard_rare diseases +MONDO:0008125 rare diseases +MONDO:0008127 gard_rare diseases +MONDO:0008127 ordo_disorder diseases +MONDO:0008127 ordo_malformation_syndrome diseases +MONDO:0008127 orphanet_rare diseases +MONDO:0008127 otar diseases +MONDO:0008127 rare diseases +MONDO:0008130 gard_rare diseases +MONDO:0008130 ordo_disorder diseases +MONDO:0008130 ordo_malformation_syndrome diseases +MONDO:0008130 orphanet_rare diseases +MONDO:0008130 otar diseases +MONDO:0008130 rare diseases +MONDO:0008131 gard_rare diseases +MONDO:0008131 nord_rare diseases +MONDO:0008131 rare diseases +MONDO:0008132 gard_rare diseases +MONDO:0008132 rare diseases +MONDO:0008133 gard_rare diseases +MONDO:0008133 nord_rare diseases +MONDO:0008133 ordo_disorder diseases +MONDO:0008133 orphanet_rare diseases +MONDO:0008133 otar diseases +MONDO:0008133 rare diseases +MONDO:0008134 gard_rare diseases +MONDO:0008134 nord_rare diseases +MONDO:0008134 ordo_disorder diseases +MONDO:0008134 orphanet_rare diseases +MONDO:0008134 otar diseases +MONDO:0008134 rare diseases +MONDO:0008135 clingen diseases +MONDO:0008135 gard_rare diseases +MONDO:0008135 otar diseases +MONDO:0008135 rare diseases +MONDO:0008136 gard_rare diseases +MONDO:0008136 nord_rare diseases +MONDO:0008136 ordo_disorder diseases +MONDO:0008136 orphanet_rare diseases +MONDO:0008136 otar diseases +MONDO:0008136 rare diseases +MONDO:0008137 gard_rare diseases +MONDO:0008137 nord_rare diseases +MONDO:0008137 ordo_disorder diseases +MONDO:0008137 ordo_malformation_syndrome diseases +MONDO:0008137 orphanet_rare diseases +MONDO:0008137 otar diseases +MONDO:0008137 rare diseases +MONDO:0008138 gard_rare diseases +MONDO:0008138 nord_rare diseases +MONDO:0008138 ordo_disorder diseases +MONDO:0008138 ordo_malformation_syndrome diseases +MONDO:0008138 orphanet_rare diseases +MONDO:0008138 otar diseases +MONDO:0008138 rare diseases +MONDO:0008139 gard_rare diseases +MONDO:0008139 ordo_disorder diseases +MONDO:0008139 ordo_malformation_syndrome diseases +MONDO:0008139 orphanet_rare diseases +MONDO:0008139 otar diseases +MONDO:0008139 rare diseases +MONDO:0008142 gard_rare diseases +MONDO:0008142 nord_rare diseases +MONDO:0008142 ordo_disorder diseases +MONDO:0008142 orphanet_rare diseases +MONDO:0008142 otar diseases +MONDO:0008142 rare diseases +MONDO:0008145 gard_rare diseases +MONDO:0008145 nord_rare diseases +MONDO:0008145 ordo_disorder diseases +MONDO:0008145 orphanet_rare diseases +MONDO:0008145 otar diseases +MONDO:0008145 rare diseases +MONDO:0008146 clingen diseases +MONDO:0008146 gard_rare diseases +MONDO:0008146 nord_rare diseases +MONDO:0008146 ordo_subtype_of_a_disorder diseases +MONDO:0008146 otar diseases +MONDO:0008146 rare diseases +MONDO:0008147 clingen diseases +MONDO:0008147 gard_rare diseases +MONDO:0008147 nord_rare diseases +MONDO:0008147 ordo_subtype_of_a_disorder diseases +MONDO:0008147 otar diseases +MONDO:0008147 rare diseases +MONDO:0008148 clingen diseases +MONDO:0008148 gard_rare diseases +MONDO:0008148 nord_rare diseases +MONDO:0008148 ordo_subtype_of_a_disorder diseases +MONDO:0008148 otar diseases +MONDO:0008148 rare diseases +MONDO:0008149 gard_rare diseases +MONDO:0008149 rare diseases +MONDO:0008150 clingen diseases +MONDO:0008150 gard_rare diseases +MONDO:0008150 nord_rare diseases +MONDO:0008150 ordo_disorder diseases +MONDO:0008150 ordo_malformation_syndrome diseases +MONDO:0008150 orphanet_rare diseases +MONDO:0008150 otar diseases +MONDO:0008150 rare diseases +MONDO:0008151 gard_rare diseases +MONDO:0008151 nord_rare diseases +MONDO:0008151 ordo_disorder diseases +MONDO:0008151 ordo_malformation_syndrome diseases +MONDO:0008151 orphanet_rare diseases +MONDO:0008151 otar diseases +MONDO:0008151 rare diseases +MONDO:0008152 gard_rare diseases +MONDO:0008152 nord_rare diseases +MONDO:0008152 ordo_disorder diseases +MONDO:0008152 ordo_malformation_syndrome diseases +MONDO:0008152 orphanet_rare diseases +MONDO:0008152 otar diseases +MONDO:0008152 rare diseases +MONDO:0008153 gard_rare diseases +MONDO:0008153 nord_rare diseases +MONDO:0008153 ordo_disorder diseases +MONDO:0008153 ordo_malformation_syndrome diseases +MONDO:0008153 orphanet_rare diseases +MONDO:0008153 otar diseases +MONDO:0008153 rare diseases +MONDO:0008154 gard_rare diseases +MONDO:0008154 rare diseases +MONDO:0008155 gard_rare diseases +MONDO:0008155 nord_rare diseases +MONDO:0008155 ordo_disorder diseases +MONDO:0008155 ordo_malformation_syndrome diseases +MONDO:0008155 orphanet_rare diseases +MONDO:0008155 otar diseases +MONDO:0008155 rare diseases +MONDO:0008156 gard_rare diseases +MONDO:0008156 nord_rare diseases +MONDO:0008156 ordo_disorder diseases +MONDO:0008156 ordo_malformation_syndrome diseases +MONDO:0008156 orphanet_rare diseases +MONDO:0008156 otar diseases +MONDO:0008156 rare diseases +MONDO:0008157 gard_rare diseases +MONDO:0008157 nord_rare diseases +MONDO:0008157 ordo_malformation_syndrome diseases +MONDO:0008157 otar diseases +MONDO:0008157 rare diseases +MONDO:0008158 gard_rare diseases +MONDO:0008158 ordo_disorder diseases +MONDO:0008158 ordo_malformation_syndrome diseases +MONDO:0008158 orphanet_rare diseases +MONDO:0008158 otar diseases +MONDO:0008158 rare diseases +MONDO:0008159 gard_rare diseases +MONDO:0008159 otar diseases +MONDO:0008159 rare diseases +MONDO:0008161 gard_rare diseases +MONDO:0008161 nord_rare diseases +MONDO:0008161 ordo_disorder diseases +MONDO:0008161 ordo_malformation_syndrome diseases +MONDO:0008161 orphanet_rare diseases +MONDO:0008161 otar diseases +MONDO:0008161 rare diseases +MONDO:0008163 gard_rare diseases +MONDO:0008163 nord_rare diseases +MONDO:0008163 ordo_disorder diseases +MONDO:0008163 ordo_malformation_syndrome diseases +MONDO:0008163 orphanet_rare diseases +MONDO:0008163 otar diseases +MONDO:0008163 prototype_pattern diseases +MONDO:0008163 rare diseases +MONDO:0008164 gard_rare diseases +MONDO:0008164 rare diseases +MONDO:0008165 gard_rare diseases +MONDO:0008165 nord_rare diseases +MONDO:0008165 ordo_disorder diseases +MONDO:0008165 orphanet_rare diseases +MONDO:0008165 otar diseases +MONDO:0008165 rare diseases +MONDO:0008167 gard_rare diseases +MONDO:0008167 nord_rare diseases +MONDO:0008167 rare diseases +MONDO:0008168 gard_rare diseases +MONDO:0008168 nord_rare diseases +MONDO:0008168 ordo_disorder diseases +MONDO:0008168 orphanet_rare diseases +MONDO:0008168 rare diseases +MONDO:0008170 gard_rare diseases +MONDO:0008170 ordo_group_of_disorders diseases +MONDO:0008170 otar diseases +MONDO:0008170 rare diseases +MONDO:0008171 otar diseases +MONDO:0008172 gard_rare diseases +MONDO:0008172 nord_rare diseases +MONDO:0008172 rare diseases +MONDO:0008173 gard_rare diseases +MONDO:0008173 nord_rare diseases +MONDO:0008173 rare diseases +MONDO:0008174 gard_rare diseases +MONDO:0008174 nord_rare diseases +MONDO:0008174 rare diseases +MONDO:0008175 gard_rare diseases +MONDO:0008175 nord_rare diseases +MONDO:0008175 ordo_disorder diseases +MONDO:0008175 ordo_malformation_syndrome diseases +MONDO:0008175 orphanet_rare diseases +MONDO:0008175 otar diseases +MONDO:0008175 rare diseases +MONDO:0008176 gard_rare diseases +MONDO:0008176 rare diseases +MONDO:0008177 gard_rare diseases +MONDO:0008177 nord_rare diseases +MONDO:0008177 ordo_disorder diseases +MONDO:0008177 orphanet_rare diseases +MONDO:0008177 otar diseases +MONDO:0008177 rare diseases +MONDO:0008178 gard_rare diseases +MONDO:0008178 otar diseases +MONDO:0008178 rare diseases +MONDO:0008179 gard_rare diseases +MONDO:0008179 nord_rare diseases +MONDO:0008179 ordo_disorder diseases +MONDO:0008179 orphanet_rare diseases +MONDO:0008179 otar diseases +MONDO:0008179 rare diseases +MONDO:0008180 gard_rare diseases +MONDO:0008180 nord_rare diseases +MONDO:0008180 ordo_disorder diseases +MONDO:0008180 ordo_malformation_syndrome diseases +MONDO:0008180 orphanet_rare diseases +MONDO:0008180 rare diseases +MONDO:0008182 gard_rare diseases +MONDO:0008182 nord_rare diseases +MONDO:0008182 ordo_disorder diseases +MONDO:0008182 ordo_malformation_syndrome diseases +MONDO:0008182 orphanet_rare diseases +MONDO:0008182 otar diseases +MONDO:0008182 rare diseases +MONDO:0008183 gard_rare diseases +MONDO:0008183 nord_rare diseases +MONDO:0008183 ordo_disorder diseases +MONDO:0008183 ordo_morphological_anomaly diseases +MONDO:0008183 orphanet_rare diseases +MONDO:0008183 otar diseases +MONDO:0008183 rare diseases +MONDO:0008184 gard_rare diseases +MONDO:0008184 nord_rare diseases +MONDO:0008184 rare diseases +MONDO:0008185 clingen diseases +MONDO:0008185 gard_rare diseases +MONDO:0008185 nord_rare diseases +MONDO:0008185 ordo_disorder diseases +MONDO:0008185 orphanet_rare diseases +MONDO:0008185 otar diseases +MONDO:0008185 predisposition diseases +MONDO:0008185 rare diseases +MONDO:0008192 gard_rare diseases +MONDO:0008192 nord_rare diseases +MONDO:0008192 otar diseases +MONDO:0008192 rare diseases +MONDO:0008193 gard_rare diseases +MONDO:0008193 rare diseases +MONDO:0008195 gard_rare diseases +MONDO:0008195 nord_rare diseases +MONDO:0008195 ordo_disorder diseases +MONDO:0008195 orphanet_rare diseases +MONDO:0008195 otar diseases +MONDO:0008195 rare diseases +MONDO:0008196 gard_rare diseases +MONDO:0008196 nord_rare diseases +MONDO:0008196 ordo_disorder diseases +MONDO:0008196 ordo_malformation_syndrome diseases +MONDO:0008196 orphanet_rare diseases +MONDO:0008196 otar diseases +MONDO:0008196 rare diseases +MONDO:0008197 gard_rare diseases +MONDO:0008197 nord_rare diseases +MONDO:0008197 rare diseases +MONDO:0008198 gard_rare diseases +MONDO:0008198 nord_rare diseases +MONDO:0008198 ordo_disorder diseases +MONDO:0008198 ordo_malformation_syndrome diseases +MONDO:0008198 orphanet_rare diseases +MONDO:0008198 otar diseases +MONDO:0008198 rare diseases +MONDO:0008199 gard_rare diseases +MONDO:0008199 nord_rare diseases +MONDO:0008199 ordo_disorder diseases +MONDO:0008199 orphanet_rare diseases +MONDO:0008199 otar diseases +MONDO:0008199 rare diseases +MONDO:0008200 gard_rare diseases +MONDO:0008200 nord_rare diseases +MONDO:0008200 rare diseases +MONDO:0008201 gard_rare diseases +MONDO:0008201 nord_rare diseases +MONDO:0008201 ordo_disorder diseases +MONDO:0008201 orphanet_rare diseases +MONDO:0008201 otar diseases +MONDO:0008201 rare diseases +MONDO:0008205 gard_rare diseases +MONDO:0008205 nord_rare diseases +MONDO:0008205 ordo_disorder diseases +MONDO:0008205 ordo_morphological_anomaly diseases +MONDO:0008205 orphanet_rare diseases +MONDO:0008205 otar diseases +MONDO:0008205 rare diseases +MONDO:0008206 gard_rare diseases +MONDO:0008206 nord_rare diseases +MONDO:0008206 ordo_disorder diseases +MONDO:0008206 orphanet_rare diseases +MONDO:0008206 otar diseases +MONDO:0008206 rare diseases +MONDO:0008207 gard_rare diseases +MONDO:0008207 nord_rare diseases +MONDO:0008207 otar diseases +MONDO:0008207 rare diseases +MONDO:0008209 gard_rare diseases +MONDO:0008209 nord_rare diseases +MONDO:0008209 ordo_disorder diseases +MONDO:0008209 ordo_malformation_syndrome diseases +MONDO:0008209 orphanet_rare diseases +MONDO:0008209 otar diseases +MONDO:0008209 rare diseases +MONDO:0008210 gard_rare diseases +MONDO:0008210 nord_rare diseases +MONDO:0008210 otar diseases +MONDO:0008210 rare diseases +MONDO:0008211 gard_rare diseases +MONDO:0008211 nord_rare diseases +MONDO:0008211 ordo_disorder diseases +MONDO:0008211 ordo_malformation_syndrome diseases +MONDO:0008211 orphanet_rare diseases +MONDO:0008211 otar diseases +MONDO:0008211 rare diseases +MONDO:0008214 gard_rare diseases +MONDO:0008214 otar diseases +MONDO:0008214 rare diseases +MONDO:0008215 gard_rare diseases +MONDO:0008215 nord_rare diseases +MONDO:0008215 ordo_disorder diseases +MONDO:0008215 orphanet_rare diseases +MONDO:0008215 otar diseases +MONDO:0008215 rare diseases +MONDO:0008217 gard_rare diseases +MONDO:0008217 nord_rare diseases +MONDO:0008217 ordo_disorder diseases +MONDO:0008217 ordo_malformation_syndrome diseases +MONDO:0008217 orphanet_rare diseases +MONDO:0008217 otar diseases +MONDO:0008217 rare diseases +MONDO:0008218 gard_rare diseases +MONDO:0008218 nord_rare diseases +MONDO:0008218 ordo_disorder diseases +MONDO:0008218 orphanet_rare diseases +MONDO:0008218 otar diseases +MONDO:0008218 rare diseases +MONDO:0008219 gard_rare diseases +MONDO:0008219 nord_rare diseases +MONDO:0008219 ordo_disorder diseases +MONDO:0008219 orphanet_rare diseases +MONDO:0008219 otar diseases +MONDO:0008219 rare diseases +MONDO:0008221 gard_rare diseases +MONDO:0008221 nord_rare diseases +MONDO:0008221 ordo_disorder diseases +MONDO:0008221 orphanet_rare diseases +MONDO:0008221 otar diseases +MONDO:0008221 rare diseases +MONDO:0008222 gard_rare diseases +MONDO:0008222 nord_rare diseases +MONDO:0008222 ordo_disorder diseases +MONDO:0008222 orphanet_rare diseases +MONDO:0008222 otar diseases +MONDO:0008222 rare diseases +MONDO:0008223 gard_rare diseases +MONDO:0008223 nord_rare diseases +MONDO:0008223 ordo_disorder diseases +MONDO:0008223 orphanet_rare diseases +MONDO:0008223 otar diseases +MONDO:0008223 rare diseases +MONDO:0008224 gard_rare diseases +MONDO:0008224 nord_rare diseases +MONDO:0008224 ordo_disorder diseases +MONDO:0008224 orphanet_rare diseases +MONDO:0008224 otar diseases +MONDO:0008224 rare diseases +MONDO:0008225 gard_rare diseases +MONDO:0008225 rare diseases +MONDO:0008226 gard_rare diseases +MONDO:0008226 otar diseases +MONDO:0008226 rare diseases +MONDO:0008227 gard_rare diseases +MONDO:0008227 nord_rare diseases +MONDO:0008227 ordo_malformation_syndrome diseases +MONDO:0008227 otar diseases +MONDO:0008227 rare diseases +MONDO:0008228 gard_rare diseases +MONDO:0008228 nord_rare diseases +MONDO:0008228 otar diseases +MONDO:0008228 rare diseases +MONDO:0008233 gard_rare diseases +MONDO:0008233 nord_rare diseases +MONDO:0008233 rare diseases +MONDO:0008234 clingen diseases +MONDO:0008234 gard_rare diseases +MONDO:0008234 nord_rare diseases +MONDO:0008234 ordo_subtype_of_a_disorder diseases +MONDO:0008234 otar diseases +MONDO:0008234 rare diseases +MONDO:0008237 gard_rare diseases +MONDO:0008237 nord_rare diseases +MONDO:0008237 ordo_disorder diseases +MONDO:0008237 ordo_malformation_syndrome diseases +MONDO:0008237 orphanet_rare diseases +MONDO:0008237 otar diseases +MONDO:0008237 rare diseases +MONDO:0008243 gard_rare diseases +MONDO:0008243 otar diseases +MONDO:0008243 rare diseases +MONDO:0008244 gard_rare diseases +MONDO:0008244 nord_rare diseases +MONDO:0008244 ordo_disorder diseases +MONDO:0008244 orphanet_rare diseases +MONDO:0008244 otar diseases +MONDO:0008244 rare diseases +MONDO:0008245 gard_rare diseases +MONDO:0008245 nord_rare diseases +MONDO:0008245 ordo_disorder diseases +MONDO:0008245 ordo_malformation_syndrome diseases +MONDO:0008245 orphanet_rare diseases +MONDO:0008245 otar diseases +MONDO:0008245 rare diseases +MONDO:0008246 gard_rare diseases +MONDO:0008246 nord_rare diseases +MONDO:0008246 ordo_disorder diseases +MONDO:0008246 orphanet_rare diseases +MONDO:0008246 otar diseases +MONDO:0008246 rare diseases +MONDO:0008247 gard_rare diseases +MONDO:0008247 ordo_disorder diseases +MONDO:0008247 ordo_malformation_syndrome diseases +MONDO:0008247 orphanet_rare diseases +MONDO:0008247 otar diseases +MONDO:0008247 rare diseases +MONDO:0008248 otar diseases +MONDO:0008250 gard_rare diseases +MONDO:0008250 nord_rare diseases +MONDO:0008250 ordo_subtype_of_a_disorder diseases +MONDO:0008250 otar diseases +MONDO:0008250 rare diseases +MONDO:0008251 gard_rare diseases +MONDO:0008251 ordo_disorder diseases +MONDO:0008251 orphanet_rare diseases +MONDO:0008251 otar diseases +MONDO:0008251 rare diseases +MONDO:0008259 gard_rare diseases +MONDO:0008259 nord_rare diseases +MONDO:0008259 ordo_disorder diseases +MONDO:0008259 orphanet_rare diseases +MONDO:0008259 otar diseases +MONDO:0008259 rare diseases +MONDO:0008260 gard_rare diseases +MONDO:0008260 nord_rare diseases +MONDO:0008260 ordo_disorder diseases +MONDO:0008260 orphanet_rare diseases +MONDO:0008260 otar diseases +MONDO:0008260 rare diseases +MONDO:0008261 gard_rare diseases +MONDO:0008261 nord_rare diseases +MONDO:0008261 ordo_disorder diseases +MONDO:0008261 orphanet_rare diseases +MONDO:0008261 rare diseases +MONDO:0008262 gard_rare diseases +MONDO:0008262 nord_rare diseases +MONDO:0008262 ordo_disorder diseases +MONDO:0008262 ordo_malformation_syndrome diseases +MONDO:0008262 orphanet_rare diseases +MONDO:0008262 otar diseases +MONDO:0008262 rare diseases +MONDO:0008263 gard_rare diseases +MONDO:0008263 nord_rare diseases +MONDO:0008263 rare diseases +MONDO:0008264 clingen diseases +MONDO:0008264 gard_rare diseases +MONDO:0008264 nord_rare diseases +MONDO:0008264 ordo_disorder diseases +MONDO:0008264 orphanet_rare diseases +MONDO:0008264 otar diseases +MONDO:0008264 rare diseases +MONDO:0008265 clingen diseases +MONDO:0008265 gard_rare diseases +MONDO:0008265 nord_rare diseases +MONDO:0008265 ordo_malformation_syndrome diseases +MONDO:0008265 otar diseases +MONDO:0008265 rare diseases +MONDO:0008266 gard_rare diseases +MONDO:0008266 nord_rare diseases +MONDO:0008266 otar diseases +MONDO:0008266 rare diseases +MONDO:0008267 gard_rare diseases +MONDO:0008267 nord_rare diseases +MONDO:0008267 ordo_disorder diseases +MONDO:0008267 ordo_malformation_syndrome diseases +MONDO:0008267 orphanet_rare diseases +MONDO:0008267 otar diseases +MONDO:0008267 rare diseases +MONDO:0008268 gard_rare diseases +MONDO:0008268 ordo_disorder diseases +MONDO:0008268 ordo_malformation_syndrome diseases +MONDO:0008268 orphanet_rare diseases +MONDO:0008268 otar diseases +MONDO:0008268 rare diseases +MONDO:0008269 gard_rare diseases +MONDO:0008269 nord_rare diseases +MONDO:0008269 ordo_disorder diseases +MONDO:0008269 ordo_morphological_anomaly diseases +MONDO:0008269 orphanet_rare diseases +MONDO:0008269 otar diseases +MONDO:0008269 rare diseases +MONDO:0008270 gard_rare diseases +MONDO:0008270 nord_rare diseases +MONDO:0008270 ordo_disorder diseases +MONDO:0008270 ordo_morphological_anomaly diseases +MONDO:0008270 orphanet_rare diseases +MONDO:0008270 otar diseases +MONDO:0008270 rare diseases +MONDO:0008271 gard_rare diseases +MONDO:0008271 nord_rare diseases +MONDO:0008271 ordo_disorder diseases +MONDO:0008271 ordo_morphological_anomaly diseases +MONDO:0008271 orphanet_rare diseases +MONDO:0008271 otar diseases +MONDO:0008271 rare diseases +MONDO:0008272 gard_rare diseases +MONDO:0008272 nord_rare diseases +MONDO:0008272 ordo_disorder diseases +MONDO:0008272 ordo_morphological_anomaly diseases +MONDO:0008272 orphanet_rare diseases +MONDO:0008272 otar diseases +MONDO:0008272 rare diseases +MONDO:0008273 gard_rare diseases +MONDO:0008273 nord_rare diseases +MONDO:0008273 ordo_disorder diseases +MONDO:0008273 orphanet_rare diseases +MONDO:0008273 rare diseases +MONDO:0008274 gard_rare diseases +MONDO:0008274 ordo_subtype_of_a_disorder diseases +MONDO:0008274 otar diseases +MONDO:0008274 rare diseases +MONDO:0008275 gard_rare diseases +MONDO:0008275 nord_rare diseases +MONDO:0008275 ordo_disorder diseases +MONDO:0008275 orphanet_rare diseases +MONDO:0008275 otar diseases +MONDO:0008275 rare diseases +MONDO:0008276 gard_rare diseases +MONDO:0008276 nord_rare diseases +MONDO:0008276 ordo_subtype_of_a_disorder diseases +MONDO:0008276 otar diseases +MONDO:0008276 rare diseases +MONDO:0008277 otar diseases +MONDO:0008278 clingen diseases +MONDO:0008278 gard_rare diseases +MONDO:0008278 nord_rare diseases +MONDO:0008278 otar diseases +MONDO:0008278 rare diseases +MONDO:0008280 clingen diseases +MONDO:0008280 gard_rare diseases +MONDO:0008280 nord_rare diseases +MONDO:0008280 ordo_disorder diseases +MONDO:0008280 orphanet_rare diseases +MONDO:0008280 otar diseases +MONDO:0008280 rare diseases +MONDO:0008283 gard_rare diseases +MONDO:0008283 nord_rare diseases +MONDO:0008283 ordo_disorder diseases +MONDO:0008283 orphanet_rare diseases +MONDO:0008283 otar diseases +MONDO:0008283 rare diseases +MONDO:0008285 gard_rare diseases +MONDO:0008285 rare diseases +MONDO:0008286 gard_rare diseases +MONDO:0008286 nord_rare diseases +MONDO:0008286 ordo_disorder diseases +MONDO:0008286 ordo_malformation_syndrome diseases +MONDO:0008286 orphanet_rare diseases +MONDO:0008286 otar diseases +MONDO:0008286 rare diseases +MONDO:0008287 gard_rare diseases +MONDO:0008287 nord_rare diseases +MONDO:0008287 ordo_disorder diseases +MONDO:0008287 ordo_malformation_syndrome diseases +MONDO:0008287 orphanet_rare diseases +MONDO:0008287 otar diseases +MONDO:0008287 rare diseases +MONDO:0008289 gard_rare diseases +MONDO:0008289 nord_rare diseases +MONDO:0008289 ordo_disorder diseases +MONDO:0008289 orphanet_rare diseases +MONDO:0008289 otar diseases +MONDO:0008289 rare diseases +MONDO:0008290 gard_rare diseases +MONDO:0008290 nord_rare diseases +MONDO:0008290 rare diseases +MONDO:0008291 gard_rare diseases +MONDO:0008291 nord_rare diseases +MONDO:0008291 ordo_disorder diseases +MONDO:0008291 orphanet_rare diseases +MONDO:0008291 otar diseases +MONDO:0008291 rare diseases +MONDO:0008292 gard_rare diseases +MONDO:0008292 nord_rare diseases +MONDO:0008292 ordo_disorder diseases +MONDO:0008292 orphanet_rare diseases +MONDO:0008292 otar diseases +MONDO:0008292 rare diseases +MONDO:0008293 gard_rare diseases +MONDO:0008293 nord_rare diseases +MONDO:0008293 rare diseases +MONDO:0008294 clingen diseases +MONDO:0008294 gard_rare diseases +MONDO:0008294 nord_rare diseases +MONDO:0008294 ordo_disorder diseases +MONDO:0008294 orphanet_rare diseases +MONDO:0008294 otar diseases +MONDO:0008294 rare diseases +MONDO:0008295 gard_rare diseases +MONDO:0008295 nord_rare diseases +MONDO:0008295 ordo_subtype_of_a_disorder diseases +MONDO:0008295 otar diseases +MONDO:0008295 rare diseases +MONDO:0008296 gard_rare diseases +MONDO:0008296 nord_rare diseases +MONDO:0008296 ordo_subtype_of_a_disorder diseases +MONDO:0008296 otar diseases +MONDO:0008296 rare diseases +MONDO:0008297 gard_rare diseases +MONDO:0008297 nord_rare diseases +MONDO:0008297 ordo_disorder diseases +MONDO:0008297 orphanet_rare diseases +MONDO:0008297 otar diseases +MONDO:0008297 rare diseases +MONDO:0008298 gard_rare diseases +MONDO:0008298 ordo_disorder diseases +MONDO:0008298 ordo_malformation_syndrome diseases +MONDO:0008298 orphanet_rare diseases +MONDO:0008298 otar diseases +MONDO:0008298 rare diseases +MONDO:0008300 gard_rare diseases +MONDO:0008300 nord_rare diseases +MONDO:0008300 ordo_disorder diseases +MONDO:0008300 orphanet_rare diseases +MONDO:0008300 otar diseases +MONDO:0008300 rare diseases +MONDO:0008301 gard_rare diseases +MONDO:0008301 nord_rare diseases +MONDO:0008301 ordo_disorder diseases +MONDO:0008301 ordo_malformation_syndrome diseases +MONDO:0008301 orphanet_rare diseases +MONDO:0008301 otar diseases +MONDO:0008301 rare diseases +MONDO:0008302 gard_rare diseases +MONDO:0008302 rare diseases +MONDO:0008303 gard_rare diseases +MONDO:0008303 nord_rare diseases +MONDO:0008303 ordo_disorder diseases +MONDO:0008303 orphanet_rare diseases +MONDO:0008303 rare diseases +MONDO:0008305 gard_rare diseases +MONDO:0008305 nord_rare diseases +MONDO:0008305 ordo_disorder diseases +MONDO:0008305 ordo_malformation_syndrome diseases +MONDO:0008305 orphanet_rare diseases +MONDO:0008305 otar diseases +MONDO:0008305 rare diseases +MONDO:0008306 gard_rare diseases +MONDO:0008306 nord_rare diseases +MONDO:0008306 ordo_subtype_of_a_disorder diseases +MONDO:0008306 otar diseases +MONDO:0008306 rare diseases +MONDO:0008309 gard_rare diseases +MONDO:0008309 rare diseases +MONDO:0008310 gard_rare diseases +MONDO:0008310 nord_rare diseases +MONDO:0008310 ordo_disorder diseases +MONDO:0008310 orphanet_rare diseases +MONDO:0008310 otar diseases +MONDO:0008310 prototype_pattern diseases +MONDO:0008310 rare diseases +MONDO:0008311 gard_rare diseases +MONDO:0008311 nord_rare diseases +MONDO:0008311 ordo_disorder diseases +MONDO:0008311 ordo_malformation_syndrome diseases +MONDO:0008311 orphanet_rare diseases +MONDO:0008311 otar diseases +MONDO:0008311 rare diseases +MONDO:0008312 gard_rare diseases +MONDO:0008312 nord_rare diseases +MONDO:0008312 ordo_disorder diseases +MONDO:0008312 ordo_malformation_syndrome diseases +MONDO:0008312 orphanet_rare diseases +MONDO:0008312 otar diseases +MONDO:0008312 rare diseases +MONDO:0008315 otar diseases +MONDO:0008316 gard_rare diseases +MONDO:0008316 nord_rare diseases +MONDO:0008316 rare diseases +MONDO:0008318 gard_rare diseases +MONDO:0008318 nord_rare diseases +MONDO:0008318 ordo_disorder diseases +MONDO:0008318 ordo_malformation_syndrome diseases +MONDO:0008318 orphanet_rare diseases +MONDO:0008318 otar diseases +MONDO:0008318 rare diseases +MONDO:0008319 clingen diseases +MONDO:0008319 gard_rare diseases +MONDO:0008319 nord_rare diseases +MONDO:0008319 rare diseases +MONDO:0008322 clingen diseases +MONDO:0008322 gard_rare diseases +MONDO:0008322 nord_rare diseases +MONDO:0008322 ordo_disorder diseases +MONDO:0008322 orphanet_rare diseases +MONDO:0008322 otar diseases +MONDO:0008322 rare diseases +MONDO:0008323 clingen diseases +MONDO:0008323 gard_rare diseases +MONDO:0008323 nord_rare diseases +MONDO:0008323 ordo_disorder diseases +MONDO:0008323 orphanet_rare diseases +MONDO:0008323 otar diseases +MONDO:0008323 rare diseases +MONDO:0008327 inferred_rare diseases +MONDO:0008327 otar diseases +MONDO:0008327 rare diseases +MONDO:0008328 gard_rare diseases +MONDO:0008328 rare diseases +MONDO:0008329 clingen diseases +MONDO:0008329 gard_rare diseases +MONDO:0008329 nord_rare diseases +MONDO:0008329 ordo_subtype_of_a_disorder diseases +MONDO:0008329 otar diseases +MONDO:0008329 rare diseases +MONDO:0008332 clingen diseases +MONDO:0008332 gard_rare diseases +MONDO:0008332 nord_rare diseases +MONDO:0008332 ordo_disorder diseases +MONDO:0008332 orphanet_rare diseases +MONDO:0008332 otar diseases +MONDO:0008332 rare diseases +MONDO:0008333 gard_rare diseases +MONDO:0008333 rare diseases +MONDO:0008335 gard_rare diseases +MONDO:0008335 nord_rare diseases +MONDO:0008335 ordo_disorder diseases +MONDO:0008335 ordo_malformation_syndrome diseases +MONDO:0008335 orphanet_rare diseases +MONDO:0008335 otar diseases +MONDO:0008335 rare diseases +MONDO:0008337 gard_rare diseases +MONDO:0008337 nord_rare diseases +MONDO:0008337 ordo_disorder diseases +MONDO:0008337 ordo_morphological_anomaly diseases +MONDO:0008337 orphanet_rare diseases +MONDO:0008337 otar diseases +MONDO:0008337 rare diseases +MONDO:0008338 gard_rare diseases +MONDO:0008338 nord_rare diseases +MONDO:0008338 ordo_disorder diseases +MONDO:0008338 ordo_malformation_syndrome diseases +MONDO:0008338 orphanet_rare diseases +MONDO:0008338 otar diseases +MONDO:0008338 rare diseases +MONDO:0008339 clingen diseases +MONDO:0008339 gard_rare diseases +MONDO:0008339 nord_rare diseases +MONDO:0008339 ordo_disorder diseases +MONDO:0008339 ordo_malformation_syndrome diseases +MONDO:0008339 orphanet_rare diseases +MONDO:0008339 otar diseases +MONDO:0008339 rare diseases +MONDO:0008340 gard_rare diseases +MONDO:0008340 nord_rare diseases +MONDO:0008340 ordo_disorder diseases +MONDO:0008340 orphanet_rare diseases +MONDO:0008340 otar diseases +MONDO:0008340 rare diseases +MONDO:0008341 gard_rare diseases +MONDO:0008341 ordo_disorder diseases +MONDO:0008341 ordo_malformation_syndrome diseases +MONDO:0008341 orphanet_rare diseases +MONDO:0008341 otar diseases +MONDO:0008341 rare diseases +MONDO:0008343 gard_rare diseases +MONDO:0008343 nord_rare diseases +MONDO:0008343 ordo_disorder diseases +MONDO:0008343 ordo_morphological_anomaly diseases +MONDO:0008343 orphanet_rare diseases +MONDO:0008343 otar diseases +MONDO:0008343 rare diseases +MONDO:0008346 gard_rare diseases +MONDO:0008346 nord_rare diseases +MONDO:0008346 ordo_disorder diseases +MONDO:0008346 orphanet_rare diseases +MONDO:0008346 rare diseases +MONDO:0008348 gard_rare diseases +MONDO:0008348 nord_rare diseases +MONDO:0008348 ordo_disorder diseases +MONDO:0008348 orphanet_rare diseases +MONDO:0008348 rare diseases +MONDO:0008353 gard_rare diseases +MONDO:0008353 nord_rare diseases +MONDO:0008353 ordo_disorder diseases +MONDO:0008353 orphanet_rare diseases +MONDO:0008353 rare diseases +MONDO:0008357 gard_rare diseases +MONDO:0008357 nord_rare diseases +MONDO:0008357 ordo_disorder diseases +MONDO:0008357 ordo_malformation_syndrome diseases +MONDO:0008357 orphanet_rare diseases +MONDO:0008357 otar diseases +MONDO:0008357 rare diseases +MONDO:0008358 gard_rare diseases +MONDO:0008358 nord_rare diseases +MONDO:0008358 ordo_disorder diseases +MONDO:0008358 ordo_malformation_syndrome diseases +MONDO:0008358 orphanet_rare diseases +MONDO:0008358 rare diseases +MONDO:0008359 gard_rare diseases +MONDO:0008359 nord_rare diseases +MONDO:0008359 ordo_disorder diseases +MONDO:0008359 ordo_malformation_syndrome diseases +MONDO:0008359 orphanet_rare diseases +MONDO:0008359 otar diseases +MONDO:0008359 rare diseases +MONDO:0008364 otar diseases +MONDO:0008365 gard_rare diseases +MONDO:0008365 nord_rare diseases +MONDO:0008365 ordo_disorder diseases +MONDO:0008365 ordo_malformation_syndrome diseases +MONDO:0008365 orphanet_rare diseases +MONDO:0008365 otar diseases +MONDO:0008365 rare diseases +MONDO:0008368 gard_rare diseases +MONDO:0008368 nord_rare diseases +MONDO:0008368 ordo_subtype_of_a_disorder diseases +MONDO:0008368 otar diseases +MONDO:0008368 rare diseases +MONDO:0008369 gard_rare diseases +MONDO:0008369 nord_rare diseases +MONDO:0008369 ordo_disorder diseases +MONDO:0008369 orphanet_rare diseases +MONDO:0008369 otar diseases +MONDO:0008369 rare diseases +MONDO:0008371 gard_rare diseases +MONDO:0008371 nord_rare diseases +MONDO:0008371 ordo_disorder diseases +MONDO:0008371 orphanet_rare diseases +MONDO:0008371 otar diseases +MONDO:0008371 rare diseases +MONDO:0008372 gard_rare diseases +MONDO:0008372 nord_rare diseases +MONDO:0008372 rare diseases +MONDO:0008373 gard_rare diseases +MONDO:0008373 nord_rare diseases +MONDO:0008373 ordo_disorder diseases +MONDO:0008373 orphanet_rare diseases +MONDO:0008373 otar diseases +MONDO:0008373 rare diseases +MONDO:0008374 gard_rare diseases +MONDO:0008374 nord_rare diseases +MONDO:0008374 rare diseases +MONDO:0008375 otar diseases +MONDO:0008377 gard_rare diseases +MONDO:0008377 nord_rare diseases +MONDO:0008377 rare diseases +MONDO:0008378 gard_rare diseases +MONDO:0008378 nord_rare diseases +MONDO:0008378 rare diseases +MONDO:0008379 gard_rare diseases +MONDO:0008379 nord_rare diseases +MONDO:0008379 rare diseases +MONDO:0008380 clingen diseases +MONDO:0008380 gard_rare diseases +MONDO:0008380 ordo_disorder diseases +MONDO:0008380 orphanet_rare diseases +MONDO:0008380 otar diseases +MONDO:0008380 rare diseases +MONDO:0008381 gard_rare diseases +MONDO:0008381 nord_rare diseases +MONDO:0008381 rare diseases +MONDO:0008382 gard_rare diseases +MONDO:0008382 rare diseases +MONDO:0008383 otar diseases +MONDO:0008385 n_of_one diseases +MONDO:0008386 gard_rare diseases +MONDO:0008386 nord_rare diseases +MONDO:0008386 rare diseases +MONDO:0008387 gard_rare diseases +MONDO:0008387 nord_rare diseases +MONDO:0008387 ordo_disorder diseases +MONDO:0008387 orphanet_rare diseases +MONDO:0008387 otar diseases +MONDO:0008387 rare diseases +MONDO:0008388 gard_rare diseases +MONDO:0008388 nord_rare diseases +MONDO:0008388 ordo_disorder diseases +MONDO:0008388 orphanet_rare diseases +MONDO:0008388 otar diseases +MONDO:0008388 rare diseases +MONDO:0008389 clingen diseases +MONDO:0008389 gard_rare diseases +MONDO:0008389 nord_rare diseases +MONDO:0008389 ordo_subtype_of_a_disorder diseases +MONDO:0008389 otar diseases +MONDO:0008389 rare diseases +MONDO:0008390 gard_rare diseases +MONDO:0008390 nord_rare diseases +MONDO:0008390 ordo_disorder diseases +MONDO:0008390 orphanet_rare diseases +MONDO:0008390 otar diseases +MONDO:0008390 rare diseases +MONDO:0008391 gard_rare diseases +MONDO:0008391 rare diseases +MONDO:0008392 gard_rare diseases +MONDO:0008392 nord_rare diseases +MONDO:0008392 ordo_disorder diseases +MONDO:0008392 orphanet_rare diseases +MONDO:0008392 otar diseases +MONDO:0008392 rare diseases +MONDO:0008393 gard_rare diseases +MONDO:0008393 nord_rare diseases +MONDO:0008393 ordo_subtype_of_a_disorder diseases +MONDO:0008393 otar diseases +MONDO:0008393 rare diseases +MONDO:0008394 gard_rare diseases +MONDO:0008394 nord_rare diseases +MONDO:0008394 ordo_disorder diseases +MONDO:0008394 orphanet_rare diseases +MONDO:0008394 otar diseases +MONDO:0008394 rare diseases +MONDO:0008395 gard_rare diseases +MONDO:0008395 nord_rare diseases +MONDO:0008395 ordo_disorder diseases +MONDO:0008395 ordo_malformation_syndrome diseases +MONDO:0008395 orphanet_rare diseases +MONDO:0008395 otar diseases +MONDO:0008395 rare diseases +MONDO:0008396 gard_rare diseases +MONDO:0008396 nord_rare diseases +MONDO:0008396 ordo_disorder diseases +MONDO:0008396 ordo_malformation_syndrome diseases +MONDO:0008396 orphanet_rare diseases +MONDO:0008396 otar diseases +MONDO:0008396 rare diseases +MONDO:0008397 gard_rare diseases +MONDO:0008397 nord_rare diseases +MONDO:0008397 ordo_disorder diseases +MONDO:0008397 orphanet_rare diseases +MONDO:0008397 otar diseases +MONDO:0008397 rare diseases +MONDO:0008401 gard_rare diseases +MONDO:0008401 nord_rare diseases +MONDO:0008401 ordo_histopathological_subtype diseases +MONDO:0008401 ordo_subtype_of_a_disorder diseases +MONDO:0008401 rare diseases +MONDO:0008402 gard_rare diseases +MONDO:0008402 nord_rare diseases +MONDO:0008402 ordo_disorder diseases +MONDO:0008402 ordo_malformation_syndrome diseases +MONDO:0008402 orphanet_rare diseases +MONDO:0008402 otar diseases +MONDO:0008402 rare diseases +MONDO:0008403 gard_rare diseases +MONDO:0008403 nord_rare diseases +MONDO:0008403 ordo_disorder diseases +MONDO:0008403 ordo_malformation_syndrome diseases +MONDO:0008403 orphanet_rare diseases +MONDO:0008403 otar diseases +MONDO:0008403 rare diseases +MONDO:0008404 gard_rare diseases +MONDO:0008404 nord_rare diseases +MONDO:0008404 ordo_disorder diseases +MONDO:0008404 ordo_malformation_syndrome diseases +MONDO:0008404 orphanet_rare diseases +MONDO:0008404 otar diseases +MONDO:0008404 rare diseases +MONDO:0008407 gard_rare diseases +MONDO:0008407 nord_rare diseases +MONDO:0008407 ordo_disorder diseases +MONDO:0008407 orphanet_rare diseases +MONDO:0008407 otar diseases +MONDO:0008407 rare diseases +MONDO:0008408 gard_rare diseases +MONDO:0008408 nord_rare diseases +MONDO:0008408 ordo_disorder diseases +MONDO:0008408 orphanet_rare diseases +MONDO:0008408 otar diseases +MONDO:0008408 rare diseases +MONDO:0008409 gard_rare diseases +MONDO:0008409 nord_rare diseases +MONDO:0008409 ordo_subtype_of_a_disorder diseases +MONDO:0008409 otar diseases +MONDO:0008409 rare diseases +MONDO:0008410 nord_rare diseases +MONDO:0008410 ordo_malformation_syndrome diseases +MONDO:0008410 otar diseases +MONDO:0008410 rare diseases +MONDO:0008411 gard_rare diseases +MONDO:0008411 nord_rare diseases +MONDO:0008411 ordo_disorder diseases +MONDO:0008411 ordo_malformation_syndrome diseases +MONDO:0008411 orphanet_rare diseases +MONDO:0008411 otar diseases +MONDO:0008411 rare diseases +MONDO:0008412 gard_rare diseases +MONDO:0008412 rare diseases +MONDO:0008416 gard_rare diseases +MONDO:0008416 nord_rare diseases +MONDO:0008416 ordo_disorder diseases +MONDO:0008416 orphanet_rare diseases +MONDO:0008416 otar diseases +MONDO:0008416 rare diseases +MONDO:0008417 gard_rare diseases +MONDO:0008417 rare diseases +MONDO:0008418 gard_rare diseases +MONDO:0008418 rare diseases +MONDO:0008420 otar diseases +MONDO:0008421 gard_rare diseases +MONDO:0008421 ordo_disorder diseases +MONDO:0008421 ordo_malformation_syndrome diseases +MONDO:0008421 orphanet_rare diseases +MONDO:0008421 rare diseases +MONDO:0008422 gard_rare diseases +MONDO:0008422 nord_rare diseases +MONDO:0008422 rare diseases +MONDO:0008423 gard_rare diseases +MONDO:0008423 rare diseases +MONDO:0008425 gard_rare diseases +MONDO:0008425 nord_rare diseases +MONDO:0008425 ordo_disorder diseases +MONDO:0008425 ordo_malformation_syndrome diseases +MONDO:0008425 orphanet_rare diseases +MONDO:0008425 otar diseases +MONDO:0008425 rare diseases +MONDO:0008426 clingen diseases +MONDO:0008426 gard_rare diseases +MONDO:0008426 nord_rare diseases +MONDO:0008426 ordo_disorder diseases +MONDO:0008426 ordo_malformation_syndrome diseases +MONDO:0008426 orphanet_rare diseases +MONDO:0008426 otar diseases +MONDO:0008426 rare diseases +MONDO:0008428 gard_rare diseases +MONDO:0008428 nord_rare diseases +MONDO:0008428 ordo_disorder diseases +MONDO:0008428 ordo_malformation_syndrome diseases +MONDO:0008428 orphanet_rare diseases +MONDO:0008428 otar diseases +MONDO:0008428 rare diseases +MONDO:0008429 gard_rare diseases +MONDO:0008429 nord_rare diseases +MONDO:0008429 ordo_disorder diseases +MONDO:0008429 ordo_malformation_syndrome diseases +MONDO:0008429 orphanet_rare diseases +MONDO:0008429 otar diseases +MONDO:0008429 rare diseases +MONDO:0008433 gard_rare diseases +MONDO:0008433 ordo_disorder diseases +MONDO:0008433 orphanet_rare diseases +MONDO:0008433 otar diseases +MONDO:0008433 rare diseases +MONDO:0008434 clingen diseases +MONDO:0008434 gard_rare diseases +MONDO:0008434 nord_rare diseases +MONDO:0008434 ordo_disorder diseases +MONDO:0008434 ordo_malformation_syndrome diseases +MONDO:0008434 orphanet_rare diseases +MONDO:0008434 otar diseases +MONDO:0008434 rare diseases +MONDO:0008436 gard_rare diseases +MONDO:0008436 nord_rare diseases +MONDO:0008436 ordo_disorder diseases +MONDO:0008436 orphanet_rare diseases +MONDO:0008436 otar diseases +MONDO:0008436 rare diseases +MONDO:0008437 gard_rare diseases +MONDO:0008437 nord_rare diseases +MONDO:0008437 ordo_disorder diseases +MONDO:0008437 orphanet_rare diseases +MONDO:0008437 otar diseases +MONDO:0008437 rare diseases +MONDO:0008438 gard_rare diseases +MONDO:0008438 nord_rare diseases +MONDO:0008438 ordo_disorder diseases +MONDO:0008438 orphanet_rare diseases +MONDO:0008438 otar diseases +MONDO:0008438 rare diseases +MONDO:0008439 gard_rare diseases +MONDO:0008439 rare diseases +MONDO:0008440 gard_rare diseases +MONDO:0008440 ordo_clinical_syndrome diseases +MONDO:0008440 ordo_disorder diseases +MONDO:0008440 orphanet_rare diseases +MONDO:0008440 otar diseases +MONDO:0008440 rare diseases +MONDO:0008442 gard_rare diseases +MONDO:0008442 ordo_disorder diseases +MONDO:0008442 orphanet_rare diseases +MONDO:0008442 otar diseases +MONDO:0008442 rare diseases +MONDO:0008443 gard_rare diseases +MONDO:0008443 ordo_disorder diseases +MONDO:0008443 orphanet_rare diseases +MONDO:0008443 otar diseases +MONDO:0008443 rare diseases +MONDO:0008445 gard_rare diseases +MONDO:0008445 nord_rare diseases +MONDO:0008445 ordo_disorder diseases +MONDO:0008445 ordo_malformation_syndrome diseases +MONDO:0008445 orphanet_rare diseases +MONDO:0008445 rare diseases +MONDO:0008447 gard_rare diseases +MONDO:0008447 nord_rare diseases +MONDO:0008447 rare diseases +MONDO:0008449 otar diseases +MONDO:0008450 gard_rare diseases +MONDO:0008450 rare diseases +MONDO:0008451 gard_rare diseases +MONDO:0008451 nord_rare diseases +MONDO:0008451 ordo_disorder diseases +MONDO:0008451 orphanet_rare diseases +MONDO:0008451 otar diseases +MONDO:0008451 rare diseases +MONDO:0008452 gard_rare diseases +MONDO:0008452 otar diseases +MONDO:0008452 rare diseases +MONDO:0008453 gard_rare diseases +MONDO:0008453 nord_rare diseases +MONDO:0008453 ordo_disorder diseases +MONDO:0008453 orphanet_rare diseases +MONDO:0008453 otar diseases +MONDO:0008453 rare diseases +MONDO:0008454 gard_rare diseases +MONDO:0008454 rare diseases +MONDO:0008455 gard_rare diseases +MONDO:0008455 rare diseases +MONDO:0008457 gard_rare diseases +MONDO:0008457 nord_rare diseases +MONDO:0008457 ordo_disorder diseases +MONDO:0008457 orphanet_rare diseases +MONDO:0008457 otar diseases +MONDO:0008457 rare diseases +MONDO:0008458 gard_rare diseases +MONDO:0008458 nord_rare diseases +MONDO:0008458 ordo_disorder diseases +MONDO:0008458 orphanet_rare diseases +MONDO:0008458 otar diseases +MONDO:0008458 predisposition diseases +MONDO:0008458 rare diseases +MONDO:0008460 gard_rare diseases +MONDO:0008460 nord_rare diseases +MONDO:0008460 ordo_disorder diseases +MONDO:0008460 ordo_malformation_syndrome diseases +MONDO:0008460 orphanet_rare diseases +MONDO:0008460 otar diseases +MONDO:0008460 rare diseases +MONDO:0008464 gard_rare diseases +MONDO:0008464 nord_rare diseases +MONDO:0008464 rare diseases +MONDO:0008465 gard_rare diseases +MONDO:0008465 nord_rare diseases +MONDO:0008465 ordo_disorder diseases +MONDO:0008465 ordo_malformation_syndrome diseases +MONDO:0008465 orphanet_rare diseases +MONDO:0008465 otar diseases +MONDO:0008465 rare diseases +MONDO:0008466 gard_rare diseases +MONDO:0008466 nord_rare diseases +MONDO:0008466 ordo_disorder diseases +MONDO:0008466 ordo_malformation_syndrome diseases +MONDO:0008466 orphanet_rare diseases +MONDO:0008466 otar diseases +MONDO:0008466 rare diseases +MONDO:0008467 gard_rare diseases +MONDO:0008467 nord_rare diseases +MONDO:0008467 ordo_disorder diseases +MONDO:0008467 ordo_malformation_syndrome diseases +MONDO:0008467 orphanet_rare diseases +MONDO:0008467 otar diseases +MONDO:0008467 rare diseases +MONDO:0008469 gard_rare diseases +MONDO:0008469 nord_rare diseases +MONDO:0008469 ordo_disorder diseases +MONDO:0008469 orphanet_rare diseases +MONDO:0008469 rare diseases +MONDO:0008470 gard_rare diseases +MONDO:0008470 rare diseases +MONDO:0008471 clingen diseases +MONDO:0008471 gard_rare diseases +MONDO:0008471 nord_rare diseases +MONDO:0008471 ordo_disorder diseases +MONDO:0008471 orphanet_rare diseases +MONDO:0008471 otar diseases +MONDO:0008471 rare diseases +MONDO:0008472 gard_rare diseases +MONDO:0008472 ordo_disorder diseases +MONDO:0008472 ordo_malformation_syndrome diseases +MONDO:0008472 orphanet_rare diseases +MONDO:0008472 rare diseases +MONDO:0008473 gard_rare diseases +MONDO:0008473 nord_rare diseases +MONDO:0008473 ordo_disorder diseases +MONDO:0008473 orphanet_rare diseases +MONDO:0008473 otar diseases +MONDO:0008473 rare diseases +MONDO:0008474 gard_rare diseases +MONDO:0008474 nord_rare diseases +MONDO:0008474 rare diseases +MONDO:0008475 otar diseases +MONDO:0008476 gard_rare diseases +MONDO:0008476 nord_rare diseases +MONDO:0008476 ordo_disorder diseases +MONDO:0008476 orphanet_rare diseases +MONDO:0008476 otar diseases +MONDO:0008476 rare diseases +MONDO:0008477 gard_rare diseases +MONDO:0008477 nord_rare diseases +MONDO:0008477 ordo_disorder diseases +MONDO:0008477 orphanet_rare diseases +MONDO:0008477 otar diseases +MONDO:0008477 rare diseases +MONDO:0008478 gard_rare diseases +MONDO:0008478 nord_rare diseases +MONDO:0008478 ordo_disorder diseases +MONDO:0008478 orphanet_rare diseases +MONDO:0008478 otar diseases +MONDO:0008478 rare diseases +MONDO:0008479 gard_rare diseases +MONDO:0008479 nord_rare diseases +MONDO:0008479 ordo_disorder diseases +MONDO:0008479 orphanet_rare diseases +MONDO:0008479 otar diseases +MONDO:0008479 rare diseases +MONDO:0008481 otar diseases +MONDO:0008482 gard_rare diseases +MONDO:0008482 nord_rare diseases +MONDO:0008482 ordo_disorder diseases +MONDO:0008482 ordo_morphological_anomaly diseases +MONDO:0008482 orphanet_rare diseases +MONDO:0008482 rare diseases +MONDO:0008484 gard_rare diseases +MONDO:0008484 nord_rare diseases +MONDO:0008484 ordo_disorder diseases +MONDO:0008484 ordo_malformation_syndrome diseases +MONDO:0008484 orphanet_rare diseases +MONDO:0008484 otar diseases +MONDO:0008484 rare diseases +MONDO:0008485 gard_rare diseases +MONDO:0008485 nord_rare diseases +MONDO:0008485 ordo_disorder diseases +MONDO:0008485 orphanet_rare diseases +MONDO:0008485 otar diseases +MONDO:0008485 rare diseases +MONDO:0008486 gard_rare diseases +MONDO:0008486 nord_rare diseases +MONDO:0008486 ordo_disorder diseases +MONDO:0008486 ordo_malformation_syndrome diseases +MONDO:0008486 orphanet_rare diseases +MONDO:0008486 otar diseases +MONDO:0008486 rare diseases +MONDO:0008487 otar diseases +MONDO:0008488 gard_rare diseases +MONDO:0008488 nord_rare diseases +MONDO:0008488 ordo_disorder diseases +MONDO:0008488 ordo_malformation_syndrome diseases +MONDO:0008488 orphanet_rare diseases +MONDO:0008488 otar diseases +MONDO:0008488 rare diseases +MONDO:0008490 gard_rare diseases +MONDO:0008490 nord_rare diseases +MONDO:0008490 ordo_disorder diseases +MONDO:0008490 ordo_malformation_syndrome diseases +MONDO:0008490 orphanet_rare diseases +MONDO:0008490 otar diseases +MONDO:0008490 rare diseases +MONDO:0008491 gard_rare diseases +MONDO:0008491 nord_rare diseases +MONDO:0008491 ordo_disorder diseases +MONDO:0008491 orphanet_rare diseases +MONDO:0008491 otar diseases +MONDO:0008491 rare diseases +MONDO:0008492 gard_rare diseases +MONDO:0008492 nord_rare diseases +MONDO:0008492 ordo_disorder diseases +MONDO:0008492 orphanet_rare diseases +MONDO:0008492 otar diseases +MONDO:0008492 rare diseases +MONDO:0008493 gard_rare diseases +MONDO:0008493 nord_rare diseases +MONDO:0008493 ordo_disorder diseases +MONDO:0008493 orphanet_rare diseases +MONDO:0008493 otar diseases +MONDO:0008493 rare diseases +MONDO:0008494 gard_rare diseases +MONDO:0008494 nord_rare diseases +MONDO:0008494 ordo_disorder diseases +MONDO:0008494 orphanet_rare diseases +MONDO:0008494 otar diseases +MONDO:0008494 rare diseases +MONDO:0008495 gard_rare diseases +MONDO:0008495 nord_rare diseases +MONDO:0008495 ordo_disorder diseases +MONDO:0008495 orphanet_rare diseases +MONDO:0008495 otar diseases +MONDO:0008495 rare diseases +MONDO:0008497 gard_rare diseases +MONDO:0008497 nord_rare diseases +MONDO:0008497 ordo_disorder diseases +MONDO:0008497 orphanet_rare diseases +MONDO:0008497 otar diseases +MONDO:0008497 rare diseases +MONDO:0008499 gard_rare diseases +MONDO:0008499 nord_rare diseases +MONDO:0008499 ordo_disorder diseases +MONDO:0008499 ordo_malformation_syndrome diseases +MONDO:0008499 orphanet_rare diseases +MONDO:0008499 otar diseases +MONDO:0008499 rare diseases +MONDO:0008501 gard_rare diseases +MONDO:0008501 nord_rare diseases +MONDO:0008501 ordo_disorder diseases +MONDO:0008501 ordo_malformation_syndrome diseases +MONDO:0008501 orphanet_rare diseases +MONDO:0008501 otar diseases +MONDO:0008501 rare diseases +MONDO:0008502 gard_rare diseases +MONDO:0008502 nord_rare diseases +MONDO:0008502 rare diseases +MONDO:0008503 gard_rare diseases +MONDO:0008503 nord_rare diseases +MONDO:0008503 ordo_disorder diseases +MONDO:0008503 ordo_malformation_syndrome diseases +MONDO:0008503 orphanet_rare diseases +MONDO:0008503 rare diseases +MONDO:0008504 gard_rare diseases +MONDO:0008504 nord_rare diseases +MONDO:0008504 ordo_disorder diseases +MONDO:0008504 ordo_morphological_anomaly diseases +MONDO:0008504 orphanet_rare diseases +MONDO:0008504 otar diseases +MONDO:0008504 rare diseases +MONDO:0008508 n_of_one diseases +MONDO:0008509 gard_rare diseases +MONDO:0008509 nord_rare diseases +MONDO:0008509 ordo_disorder diseases +MONDO:0008509 ordo_morphological_anomaly diseases +MONDO:0008509 orphanet_rare diseases +MONDO:0008509 otar diseases +MONDO:0008509 rare diseases +MONDO:0008510 gard_rare diseases +MONDO:0008510 ordo_disorder diseases +MONDO:0008510 ordo_malformation_syndrome diseases +MONDO:0008510 orphanet_rare diseases +MONDO:0008510 otar diseases +MONDO:0008510 rare diseases +MONDO:0008511 gard_rare diseases +MONDO:0008511 nord_rare diseases +MONDO:0008511 ordo_disorder diseases +MONDO:0008511 ordo_malformation_syndrome diseases +MONDO:0008511 orphanet_rare diseases +MONDO:0008511 otar diseases +MONDO:0008511 prototype_pattern diseases +MONDO:0008511 rare diseases +MONDO:0008512 gard_rare diseases +MONDO:0008512 nord_rare diseases +MONDO:0008512 ordo_disorder diseases +MONDO:0008512 ordo_morphological_anomaly diseases +MONDO:0008512 orphanet_rare diseases +MONDO:0008512 otar diseases +MONDO:0008512 rare diseases +MONDO:0008513 gard_rare diseases +MONDO:0008513 nord_rare diseases +MONDO:0008513 ordo_subtype_of_a_disorder diseases +MONDO:0008513 otar diseases +MONDO:0008513 rare diseases +MONDO:0008514 gard_rare diseases +MONDO:0008514 nord_rare diseases +MONDO:0008514 ordo_disorder diseases +MONDO:0008514 ordo_morphological_anomaly diseases +MONDO:0008514 orphanet_rare diseases +MONDO:0008514 otar diseases +MONDO:0008514 rare diseases +MONDO:0008515 gard_rare diseases +MONDO:0008515 nord_rare diseases +MONDO:0008515 ordo_disorder diseases +MONDO:0008515 ordo_morphological_anomaly diseases +MONDO:0008515 orphanet_rare diseases +MONDO:0008515 otar diseases +MONDO:0008515 rare diseases +MONDO:0008516 gard_rare diseases +MONDO:0008516 nord_rare diseases +MONDO:0008516 ordo_disorder diseases +MONDO:0008516 ordo_morphological_anomaly diseases +MONDO:0008516 orphanet_rare diseases +MONDO:0008516 otar diseases +MONDO:0008516 rare diseases +MONDO:0008517 gard_rare diseases +MONDO:0008517 ordo_disorder diseases +MONDO:0008517 ordo_malformation_syndrome diseases +MONDO:0008517 orphanet_rare diseases +MONDO:0008517 otar diseases +MONDO:0008517 rare diseases +MONDO:0008518 gard_rare diseases +MONDO:0008518 nord_rare diseases +MONDO:0008518 rare diseases +MONDO:0008519 gard_rare diseases +MONDO:0008519 nord_rare diseases +MONDO:0008519 rare diseases +MONDO:0008520 gard_rare diseases +MONDO:0008520 nord_rare diseases +MONDO:0008520 ordo_disorder diseases +MONDO:0008520 ordo_malformation_syndrome diseases +MONDO:0008520 orphanet_rare diseases +MONDO:0008520 otar diseases +MONDO:0008520 rare diseases +MONDO:0008521 gard_rare diseases +MONDO:0008521 nord_rare diseases +MONDO:0008521 ordo_disorder diseases +MONDO:0008521 ordo_malformation_syndrome diseases +MONDO:0008521 orphanet_rare diseases +MONDO:0008521 otar diseases +MONDO:0008521 rare diseases +MONDO:0008523 clingen diseases +MONDO:0008523 gard_rare diseases +MONDO:0008523 nord_rare diseases +MONDO:0008523 ordo_disorder diseases +MONDO:0008523 orphanet_rare diseases +MONDO:0008523 otar diseases +MONDO:0008523 rare diseases +MONDO:0008525 gard_rare diseases +MONDO:0008525 rare diseases +MONDO:0008534 gard_rare diseases +MONDO:0008534 nord_rare diseases +MONDO:0008534 ordo_disorder diseases +MONDO:0008534 orphanet_rare diseases +MONDO:0008534 rare diseases +MONDO:0008535 clingen diseases +MONDO:0008535 gard_rare diseases +MONDO:0008535 nord_rare diseases +MONDO:0008535 otar diseases +MONDO:0008535 rare diseases +MONDO:0008537 disease_grouping diseases +MONDO:0008537 gard_rare diseases +MONDO:0008537 ordo_group_of_disorders diseases +MONDO:0008537 otar diseases +MONDO:0008537 rare diseases +MONDO:0008538 gard_rare diseases +MONDO:0008538 nord_rare diseases +MONDO:0008538 ordo_disorder diseases +MONDO:0008538 orphanet_rare diseases +MONDO:0008538 otar diseases +MONDO:0008538 rare diseases +MONDO:0008540 gard_rare diseases +MONDO:0008540 ordo_disorder diseases +MONDO:0008540 ordo_malformation_syndrome diseases +MONDO:0008540 orphanet_rare diseases +MONDO:0008540 otar diseases +MONDO:0008540 rare diseases +MONDO:0008542 gard_rare diseases +MONDO:0008542 nord_rare diseases +MONDO:0008542 ordo_disorder diseases +MONDO:0008542 ordo_malformation_syndrome diseases +MONDO:0008542 orphanet_rare diseases +MONDO:0008542 rare diseases +MONDO:0008544 gard_rare diseases +MONDO:0008544 nord_rare diseases +MONDO:0008544 ordo_disorder diseases +MONDO:0008544 ordo_malformation_syndrome diseases +MONDO:0008544 orphanet_rare diseases +MONDO:0008544 otar diseases +MONDO:0008544 rare diseases +MONDO:0008545 gard_rare diseases +MONDO:0008545 nord_rare diseases +MONDO:0008545 rare diseases +MONDO:0008546 clingen diseases +MONDO:0008546 gard_rare diseases +MONDO:0008546 nord_rare diseases +MONDO:0008546 ordo_subtype_of_a_disorder diseases +MONDO:0008546 otar diseases +MONDO:0008546 rare diseases +MONDO:0008547 clingen diseases +MONDO:0008547 gard_rare diseases +MONDO:0008547 nord_rare diseases +MONDO:0008547 ordo_subtype_of_a_disorder diseases +MONDO:0008547 otar diseases +MONDO:0008547 rare diseases +MONDO:0008551 gard_rare diseases +MONDO:0008551 nord_rare diseases +MONDO:0008551 ordo_disorder diseases +MONDO:0008551 ordo_malformation_syndrome diseases +MONDO:0008551 orphanet_rare diseases +MONDO:0008551 otar diseases +MONDO:0008551 rare diseases +MONDO:0008552 clingen diseases +MONDO:0008552 gard_rare diseases +MONDO:0008552 nord_rare diseases +MONDO:0008552 rare diseases +MONDO:0008553 clingen diseases +MONDO:0008553 gard_rare diseases +MONDO:0008553 nord_rare diseases +MONDO:0008553 otar diseases +MONDO:0008553 rare diseases +MONDO:0008554 clingen diseases +MONDO:0008554 gard_rare diseases +MONDO:0008554 nord_rare diseases +MONDO:0008554 rare diseases +MONDO:0008555 clingen diseases +MONDO:0008555 gard_rare diseases +MONDO:0008555 nord_rare diseases +MONDO:0008555 rare diseases +MONDO:0008556 gard_rare diseases +MONDO:0008556 nord_rare diseases +MONDO:0008556 rare diseases +MONDO:0008557 gard_rare diseases +MONDO:0008557 nord_rare diseases +MONDO:0008557 ordo_disorder diseases +MONDO:0008557 orphanet_rare diseases +MONDO:0008557 otar diseases +MONDO:0008557 rare diseases +MONDO:0008558 gard_rare diseases +MONDO:0008558 nord_rare diseases +MONDO:0008558 ordo_disorder diseases +MONDO:0008558 orphanet_rare diseases +MONDO:0008558 otar diseases +MONDO:0008558 rare diseases +MONDO:0008559 clingen diseases +MONDO:0008559 gard_rare diseases +MONDO:0008559 nord_rare diseases +MONDO:0008559 otar diseases +MONDO:0008559 rare diseases +MONDO:0008560 clingen diseases +MONDO:0008560 gard_rare diseases +MONDO:0008560 nord_rare diseases +MONDO:0008560 otar diseases +MONDO:0008560 rare diseases +MONDO:0008562 gard_rare diseases +MONDO:0008562 nord_rare diseases +MONDO:0008562 ordo_disorder diseases +MONDO:0008562 ordo_malformation_syndrome diseases +MONDO:0008562 orphanet_rare diseases +MONDO:0008562 otar diseases +MONDO:0008562 rare diseases +MONDO:0008563 gard_rare diseases +MONDO:0008563 nord_rare diseases +MONDO:0008563 ordo_disorder diseases +MONDO:0008563 ordo_malformation_syndrome diseases +MONDO:0008563 orphanet_rare diseases +MONDO:0008563 otar diseases +MONDO:0008563 rare diseases +MONDO:0008564 gard_rare diseases +MONDO:0008564 nord_rare diseases +MONDO:0008564 rare diseases +MONDO:0008565 gard_rare diseases +MONDO:0008565 nord_rare diseases +MONDO:0008565 ordo_disorder diseases +MONDO:0008565 ordo_morphological_anomaly diseases +MONDO:0008565 orphanet_rare diseases +MONDO:0008565 rare diseases +MONDO:0008566 gard_rare diseases +MONDO:0008566 nord_rare diseases +MONDO:0008566 rare diseases +MONDO:0008567 gard_rare diseases +MONDO:0008567 nord_rare diseases +MONDO:0008567 rare diseases +MONDO:0008569 gard_rare diseases +MONDO:0008569 rare diseases +MONDO:0008571 gard_rare diseases +MONDO:0008571 nord_rare diseases +MONDO:0008571 rare diseases +MONDO:0008572 gard_rare diseases +MONDO:0008572 nord_rare diseases +MONDO:0008572 ordo_disorder diseases +MONDO:0008572 ordo_malformation_syndrome diseases +MONDO:0008572 orphanet_rare diseases +MONDO:0008572 rare diseases +MONDO:0008575 otar diseases +MONDO:0008582 gard_rare diseases +MONDO:0008582 nord_rare diseases +MONDO:0008582 ordo_disorder diseases +MONDO:0008582 ordo_malformation_syndrome diseases +MONDO:0008582 orphanet_rare diseases +MONDO:0008582 otar diseases +MONDO:0008582 rare diseases +MONDO:0008583 gard_rare diseases +MONDO:0008583 nord_rare diseases +MONDO:0008583 rare diseases +MONDO:0008585 gard_rare diseases +MONDO:0008585 nord_rare diseases +MONDO:0008585 ordo_disorder diseases +MONDO:0008585 orphanet_rare diseases +MONDO:0008585 otar diseases +MONDO:0008585 rare diseases +MONDO:0008586 gard_rare diseases +MONDO:0008586 nord_rare diseases +MONDO:0008586 ordo_disorder diseases +MONDO:0008586 ordo_morphological_anomaly diseases +MONDO:0008586 orphanet_rare diseases +MONDO:0008586 rare diseases +MONDO:0008587 gard_rare diseases +MONDO:0008587 ordo_disorder diseases +MONDO:0008587 orphanet_rare diseases +MONDO:0008587 rare diseases +MONDO:0008588 gard_rare diseases +MONDO:0008588 nord_rare diseases +MONDO:0008588 ordo_disorder diseases +MONDO:0008588 orphanet_rare diseases +MONDO:0008588 otar diseases +MONDO:0008588 rare diseases +MONDO:0008591 gard_rare diseases +MONDO:0008591 ordo_disorder diseases +MONDO:0008591 orphanet_rare diseases +MONDO:0008591 rare diseases +MONDO:0008592 gard_rare diseases +MONDO:0008592 nord_rare diseases +MONDO:0008592 ordo_disorder diseases +MONDO:0008592 ordo_malformation_syndrome diseases +MONDO:0008592 orphanet_rare diseases +MONDO:0008592 otar diseases +MONDO:0008592 rare diseases +MONDO:0008593 otar diseases +MONDO:0008594 gard_rare diseases +MONDO:0008594 nord_rare diseases +MONDO:0008594 ordo_disorder diseases +MONDO:0008594 orphanet_rare diseases +MONDO:0008594 rare diseases +MONDO:0008596 gard_rare diseases +MONDO:0008596 nord_rare diseases +MONDO:0008596 otar diseases +MONDO:0008596 rare diseases +MONDO:0008597 gard_rare diseases +MONDO:0008597 nord_rare diseases +MONDO:0008597 otar diseases +MONDO:0008597 rare diseases +MONDO:0008598 gard_rare diseases +MONDO:0008598 ordo_disorder diseases +MONDO:0008598 ordo_malformation_syndrome diseases +MONDO:0008598 orphanet_rare diseases +MONDO:0008598 otar diseases +MONDO:0008598 rare diseases +MONDO:0008599 gard_rare diseases +MONDO:0008599 nord_rare diseases +MONDO:0008599 ordo_disorder diseases +MONDO:0008599 orphanet_rare diseases +MONDO:0008599 otar diseases +MONDO:0008599 rare diseases +MONDO:0008601 gard_rare diseases +MONDO:0008601 rare diseases +MONDO:0008602 gard_rare diseases +MONDO:0008602 rare diseases +MONDO:0008603 gard_rare diseases +MONDO:0008603 nord_rare diseases +MONDO:0008603 rare diseases +MONDO:0008606 gard_rare diseases +MONDO:0008606 ordo_malformation_syndrome diseases +MONDO:0008606 rare diseases +MONDO:0008607 gard_rare diseases +MONDO:0008607 nord_rare diseases +MONDO:0008607 ordo_disorder diseases +MONDO:0008607 ordo_malformation_syndrome diseases +MONDO:0008607 orphanet_rare diseases +MONDO:0008607 otar diseases +MONDO:0008607 rare diseases +MONDO:0008608 ordo_disorder diseases +MONDO:0008608 ordo_malformation_syndrome diseases +MONDO:0008608 orphanet_rare diseases +MONDO:0008608 otar diseases +MONDO:0008608 rare diseases +MONDO:0008610 gard_rare diseases +MONDO:0008610 nord_rare diseases +MONDO:0008610 ordo_disorder diseases +MONDO:0008610 orphanet_rare diseases +MONDO:0008610 otar diseases +MONDO:0008610 rare diseases +MONDO:0008611 gard_rare diseases +MONDO:0008611 ordo_disorder diseases +MONDO:0008611 ordo_malformation_syndrome diseases +MONDO:0008611 orphanet_rare diseases +MONDO:0008611 otar diseases +MONDO:0008611 rare diseases +MONDO:0008612 gard_rare diseases +MONDO:0008612 nord_rare diseases +MONDO:0008612 rare diseases +MONDO:0008618 gard_rare diseases +MONDO:0008618 nord_rare diseases +MONDO:0008618 ordo_disorder diseases +MONDO:0008618 ordo_malformation_syndrome diseases +MONDO:0008618 orphanet_rare diseases +MONDO:0008618 otar diseases +MONDO:0008618 rare diseases +MONDO:0008619 gard_rare diseases +MONDO:0008619 nord_rare diseases +MONDO:0008619 ordo_disorder diseases +MONDO:0008619 orphanet_rare diseases +MONDO:0008619 otar diseases +MONDO:0008619 rare diseases +MONDO:0008620 gard_rare diseases +MONDO:0008620 nord_rare diseases +MONDO:0008620 ordo_disorder diseases +MONDO:0008620 ordo_malformation_syndrome diseases +MONDO:0008620 orphanet_rare diseases +MONDO:0008620 otar diseases +MONDO:0008620 rare diseases +MONDO:0008621 gard_rare diseases +MONDO:0008621 nord_rare diseases +MONDO:0008621 ordo_disorder diseases +MONDO:0008621 orphanet_rare diseases +MONDO:0008621 otar diseases +MONDO:0008621 rare diseases +MONDO:0008622 gard_rare diseases +MONDO:0008622 nord_rare diseases +MONDO:0008622 ordo_disorder diseases +MONDO:0008622 ordo_malformation_syndrome diseases +MONDO:0008622 orphanet_rare diseases +MONDO:0008622 otar diseases +MONDO:0008622 rare diseases +MONDO:0008624 gard_rare diseases +MONDO:0008624 ordo_disorder diseases +MONDO:0008624 ordo_malformation_syndrome diseases +MONDO:0008624 orphanet_rare diseases +MONDO:0008624 otar diseases +MONDO:0008624 rare diseases +MONDO:0008627 otar diseases +MONDO:0008628 otar diseases +MONDO:0008630 otar diseases +MONDO:0008633 gard_rare diseases +MONDO:0008633 nord_rare diseases +MONDO:0008633 ordo_disorder diseases +MONDO:0008633 orphanet_rare diseases +MONDO:0008633 otar diseases +MONDO:0008633 rare diseases +MONDO:0008636 gard_rare diseases +MONDO:0008636 ordo_disorder diseases +MONDO:0008636 ordo_malformation_syndrome diseases +MONDO:0008636 orphanet_rare diseases +MONDO:0008636 otar diseases +MONDO:0008636 rare diseases +MONDO:0008637 gard_rare diseases +MONDO:0008637 ordo_disorder diseases +MONDO:0008637 ordo_morphological_anomaly diseases +MONDO:0008637 orphanet_rare diseases +MONDO:0008637 rare diseases +MONDO:0008638 otar diseases +MONDO:0008640 gard_rare diseases +MONDO:0008640 rare diseases +MONDO:0008641 gard_rare diseases +MONDO:0008641 nord_rare diseases +MONDO:0008641 ordo_disorder diseases +MONDO:0008641 orphanet_rare diseases +MONDO:0008641 otar diseases +MONDO:0008641 rare diseases +MONDO:0008642 gard_rare diseases +MONDO:0008642 nord_rare diseases +MONDO:0008642 ordo_disorder diseases +MONDO:0008642 ordo_malformation_syndrome diseases +MONDO:0008642 orphanet_rare diseases +MONDO:0008642 otar diseases +MONDO:0008642 rare diseases +MONDO:0008644 gard_rare diseases +MONDO:0008644 nord_rare diseases +MONDO:0008644 rare diseases +MONDO:0008645 gard_rare diseases +MONDO:0008645 ordo_disorder diseases +MONDO:0008645 ordo_malformation_syndrome diseases +MONDO:0008645 orphanet_rare diseases +MONDO:0008645 otar diseases +MONDO:0008645 rare diseases +MONDO:0008647 gard_rare diseases +MONDO:0008647 nord_rare diseases +MONDO:0008647 rare diseases +MONDO:0008648 gard_rare diseases +MONDO:0008648 nord_rare diseases +MONDO:0008648 otar diseases +MONDO:0008648 rare diseases +MONDO:0008650 gard_rare diseases +MONDO:0008650 ordo_disorder diseases +MONDO:0008650 ordo_malformation_syndrome diseases +MONDO:0008650 orphanet_rare diseases +MONDO:0008650 otar diseases +MONDO:0008650 rare diseases +MONDO:0008652 gard_rare diseases +MONDO:0008652 nord_rare diseases +MONDO:0008652 ordo_disorder diseases +MONDO:0008652 ordo_morphological_anomaly diseases +MONDO:0008652 orphanet_rare diseases +MONDO:0008652 otar diseases +MONDO:0008652 rare diseases +MONDO:0008653 gard_rare diseases +MONDO:0008653 nord_rare diseases +MONDO:0008653 rare diseases +MONDO:0008654 gard_rare diseases +MONDO:0008654 rare diseases +MONDO:0008659 gard_rare diseases +MONDO:0008659 nord_rare diseases +MONDO:0008659 ordo_disorder diseases +MONDO:0008659 orphanet_rare diseases +MONDO:0008659 otar diseases +MONDO:0008659 rare diseases +MONDO:0008660 gard_rare diseases +MONDO:0008660 nord_rare diseases +MONDO:0008660 ordo_disorder diseases +MONDO:0008660 orphanet_rare diseases +MONDO:0008660 otar diseases +MONDO:0008660 rare diseases +MONDO:0008661 otar diseases +MONDO:0008662 gard_rare diseases +MONDO:0008662 nord_rare diseases +MONDO:0008662 ordo_disorder diseases +MONDO:0008662 orphanet_rare diseases +MONDO:0008662 otar diseases +MONDO:0008662 rare diseases +MONDO:0008663 gard_rare diseases +MONDO:0008663 nord_rare diseases +MONDO:0008663 ordo_disorder diseases +MONDO:0008663 orphanet_rare diseases +MONDO:0008663 otar diseases +MONDO:0008663 rare diseases +MONDO:0008665 gard_rare diseases +MONDO:0008665 ordo_disorder diseases +MONDO:0008665 ordo_malformation_syndrome diseases +MONDO:0008665 orphanet_rare diseases +MONDO:0008665 otar diseases +MONDO:0008665 rare diseases +MONDO:0008666 otar diseases +MONDO:0008667 clingen diseases +MONDO:0008667 gard_rare diseases +MONDO:0008667 nord_rare diseases +MONDO:0008667 ordo_disorder diseases +MONDO:0008667 orphanet_rare diseases +MONDO:0008667 otar diseases +MONDO:0008667 rare diseases +MONDO:0008668 gard_rare diseases +MONDO:0008668 nord_rare diseases +MONDO:0008668 ordo_subtype_of_a_disorder diseases +MONDO:0008668 otar diseases +MONDO:0008668 rare diseases +MONDO:0008670 gard_rare diseases +MONDO:0008670 nord_rare diseases +MONDO:0008670 ordo_subtype_of_a_disorder diseases +MONDO:0008670 otar diseases +MONDO:0008670 rare diseases +MONDO:0008671 gard_rare diseases +MONDO:0008671 rare diseases +MONDO:0008672 gard_rare diseases +MONDO:0008672 otar diseases +MONDO:0008672 rare diseases +MONDO:0008673 gard_rare diseases +MONDO:0008673 nord_rare diseases +MONDO:0008673 ordo_disorder diseases +MONDO:0008673 ordo_malformation_syndrome diseases +MONDO:0008673 orphanet_rare diseases +MONDO:0008673 otar diseases +MONDO:0008673 rare diseases +MONDO:0008675 gard_rare diseases +MONDO:0008675 nord_rare diseases +MONDO:0008675 ordo_disorder diseases +MONDO:0008675 ordo_malformation_syndrome diseases +MONDO:0008675 orphanet_rare diseases +MONDO:0008675 rare diseases +MONDO:0008676 gard_rare diseases +MONDO:0008676 nord_rare diseases +MONDO:0008676 otar diseases +MONDO:0008676 rare diseases +MONDO:0008678 gard_rare diseases +MONDO:0008678 nord_rare diseases +MONDO:0008678 ordo_disorder diseases +MONDO:0008678 ordo_malformation_syndrome diseases +MONDO:0008678 orphanet_rare diseases +MONDO:0008678 otar diseases +MONDO:0008678 rare diseases +MONDO:0008679 clingen diseases +MONDO:0008679 gard_rare diseases +MONDO:0008679 nord_rare diseases +MONDO:0008679 otar diseases +MONDO:0008679 rare diseases +MONDO:0008680 gard_rare diseases +MONDO:0008680 nord_rare diseases +MONDO:0008680 rare diseases +MONDO:0008681 gard_rare diseases +MONDO:0008681 nord_rare diseases +MONDO:0008681 ordo_disorder diseases +MONDO:0008681 ordo_malformation_syndrome diseases +MONDO:0008681 orphanet_rare diseases +MONDO:0008681 otar diseases +MONDO:0008681 rare diseases +MONDO:0008682 clingen diseases +MONDO:0008682 gard_rare diseases +MONDO:0008682 nord_rare diseases +MONDO:0008682 ordo_disorder diseases +MONDO:0008682 orphanet_rare diseases +MONDO:0008682 otar diseases +MONDO:0008682 rare diseases +MONDO:0008683 gard_rare diseases +MONDO:0008683 nord_rare diseases +MONDO:0008683 rare diseases +MONDO:0008684 gard_rare diseases +MONDO:0008684 nord_rare diseases +MONDO:0008684 ordo_disorder diseases +MONDO:0008684 ordo_malformation_syndrome diseases +MONDO:0008684 orphanet_rare diseases +MONDO:0008684 otar diseases +MONDO:0008684 rare diseases +MONDO:0008685 inferred_rare diseases +MONDO:0008685 otar diseases +MONDO:0008685 rare diseases +MONDO:0008686 gard_rare diseases +MONDO:0008686 nord_rare diseases +MONDO:0008686 ordo_disorder diseases +MONDO:0008686 orphanet_rare diseases +MONDO:0008686 otar diseases +MONDO:0008686 rare diseases +MONDO:0008688 gard_rare diseases +MONDO:0008688 nord_rare diseases +MONDO:0008688 ordo_disorder diseases +MONDO:0008688 orphanet_rare diseases +MONDO:0008688 otar diseases +MONDO:0008688 rare diseases +MONDO:0008689 clingen diseases +MONDO:0008689 gard_rare diseases +MONDO:0008689 nord_rare diseases +MONDO:0008689 otar diseases +MONDO:0008689 rare diseases +MONDO:0008690 gard_rare diseases +MONDO:0008690 nord_rare diseases +MONDO:0008690 rare diseases +MONDO:0008692 gard_rare diseases +MONDO:0008692 nord_rare diseases +MONDO:0008692 ordo_disorder diseases +MONDO:0008692 orphanet_rare diseases +MONDO:0008692 otar diseases +MONDO:0008692 rare diseases +MONDO:0008693 gard_rare diseases +MONDO:0008693 nord_rare diseases +MONDO:0008693 ordo_disorder diseases +MONDO:0008693 ordo_malformation_syndrome diseases +MONDO:0008693 orphanet_rare diseases +MONDO:0008693 otar diseases +MONDO:0008693 rare diseases +MONDO:0008694 gard_rare diseases +MONDO:0008694 ordo_disorder diseases +MONDO:0008694 ordo_malformation_syndrome diseases +MONDO:0008694 orphanet_rare diseases +MONDO:0008694 otar diseases +MONDO:0008694 rare diseases +MONDO:0008695 gard_rare diseases +MONDO:0008695 nord_rare diseases +MONDO:0008695 ordo_disorder diseases +MONDO:0008695 orphanet_rare diseases +MONDO:0008695 otar diseases +MONDO:0008695 rare diseases +MONDO:0008696 gard_rare diseases +MONDO:0008696 nord_rare diseases +MONDO:0008696 ordo_disorder diseases +MONDO:0008696 orphanet_rare diseases +MONDO:0008696 otar diseases +MONDO:0008696 rare diseases +MONDO:0008699 gard_rare diseases +MONDO:0008699 nord_rare diseases +MONDO:0008699 ordo_disorder diseases +MONDO:0008699 ordo_malformation_syndrome diseases +MONDO:0008699 orphanet_rare diseases +MONDO:0008699 otar diseases +MONDO:0008699 rare diseases +MONDO:0008700 gard_rare diseases +MONDO:0008700 nord_rare diseases +MONDO:0008700 ordo_disorder diseases +MONDO:0008700 ordo_morphological_anomaly diseases +MONDO:0008700 orphanet_rare diseases +MONDO:0008700 otar diseases +MONDO:0008700 rare diseases +MONDO:0008701 gard_rare diseases +MONDO:0008701 nord_rare diseases +MONDO:0008701 ordo_subtype_of_a_disorder diseases +MONDO:0008701 otar diseases +MONDO:0008701 rare diseases +MONDO:0008702 clingen diseases +MONDO:0008702 gard_rare diseases +MONDO:0008702 nord_rare diseases +MONDO:0008702 ordo_subtype_of_a_disorder diseases +MONDO:0008702 otar diseases +MONDO:0008702 rare diseases +MONDO:0008703 gard_rare diseases +MONDO:0008703 nord_rare diseases +MONDO:0008703 ordo_disorder diseases +MONDO:0008703 ordo_malformation_syndrome diseases +MONDO:0008703 orphanet_rare diseases +MONDO:0008703 otar diseases +MONDO:0008703 rare diseases +MONDO:0008704 gard_rare diseases +MONDO:0008704 nord_rare diseases +MONDO:0008704 ordo_disorder diseases +MONDO:0008704 orphanet_rare diseases +MONDO:0008704 otar diseases +MONDO:0008704 rare diseases +MONDO:0008705 gard_rare diseases +MONDO:0008705 ordo_disorder diseases +MONDO:0008705 orphanet_rare diseases +MONDO:0008705 rare diseases +MONDO:0008706 gard_rare diseases +MONDO:0008706 nord_rare diseases +MONDO:0008706 ordo_disorder diseases +MONDO:0008706 ordo_malformation_syndrome diseases +MONDO:0008706 orphanet_rare diseases +MONDO:0008706 otar diseases +MONDO:0008706 rare diseases +MONDO:0008707 gard_rare diseases +MONDO:0008707 nord_rare diseases +MONDO:0008707 ordo_disorder diseases +MONDO:0008707 ordo_malformation_syndrome diseases +MONDO:0008707 orphanet_rare diseases +MONDO:0008707 otar diseases +MONDO:0008707 rare diseases +MONDO:0008708 gard_rare diseases +MONDO:0008708 nord_rare diseases +MONDO:0008708 ordo_disorder diseases +MONDO:0008708 ordo_malformation_syndrome diseases +MONDO:0008708 orphanet_rare diseases +MONDO:0008708 otar diseases +MONDO:0008708 rare diseases +MONDO:0008709 gard_rare diseases +MONDO:0008709 nord_rare diseases +MONDO:0008709 ordo_disorder diseases +MONDO:0008709 ordo_malformation_syndrome diseases +MONDO:0008709 orphanet_rare diseases +MONDO:0008709 otar diseases +MONDO:0008709 rare diseases +MONDO:0008710 clingen diseases +MONDO:0008710 gard_rare diseases +MONDO:0008710 nord_rare diseases +MONDO:0008710 otar diseases +MONDO:0008710 rare diseases +MONDO:0008711 gard_rare diseases +MONDO:0008711 ordo_disorder diseases +MONDO:0008711 ordo_malformation_syndrome diseases +MONDO:0008711 orphanet_rare diseases +MONDO:0008711 rare diseases +MONDO:0008712 gard_rare diseases +MONDO:0008712 ordo_disorder diseases +MONDO:0008712 ordo_malformation_syndrome diseases +MONDO:0008712 orphanet_rare diseases +MONDO:0008712 otar diseases +MONDO:0008712 rare diseases +MONDO:0008713 gard_rare diseases +MONDO:0008713 nord_rare diseases +MONDO:0008713 ordo_disorder diseases +MONDO:0008713 orphanet_rare diseases +MONDO:0008713 otar diseases +MONDO:0008713 rare diseases +MONDO:0008714 gard_rare diseases +MONDO:0008714 nord_rare diseases +MONDO:0008714 ordo_disorder diseases +MONDO:0008714 ordo_malformation_syndrome diseases +MONDO:0008714 orphanet_rare diseases +MONDO:0008714 otar diseases +MONDO:0008714 rare diseases +MONDO:0008715 gard_rare diseases +MONDO:0008715 nord_rare diseases +MONDO:0008715 ordo_disorder diseases +MONDO:0008715 ordo_malformation_syndrome diseases +MONDO:0008715 orphanet_rare diseases +MONDO:0008715 otar diseases +MONDO:0008715 rare diseases +MONDO:0008716 gard_rare diseases +MONDO:0008716 nord_rare diseases +MONDO:0008716 ordo_disorder diseases +MONDO:0008716 ordo_malformation_syndrome diseases +MONDO:0008716 orphanet_rare diseases +MONDO:0008716 otar diseases +MONDO:0008716 rare diseases +MONDO:0008717 gard_rare diseases +MONDO:0008717 nord_rare diseases +MONDO:0008717 ordo_disorder diseases +MONDO:0008717 ordo_malformation_syndrome diseases +MONDO:0008717 orphanet_rare diseases +MONDO:0008717 otar diseases +MONDO:0008717 rare diseases +MONDO:0008718 gard_rare diseases +MONDO:0008718 nord_rare diseases +MONDO:0008718 ordo_disorder diseases +MONDO:0008718 orphanet_rare diseases +MONDO:0008718 otar diseases +MONDO:0008718 rare diseases +MONDO:0008719 gard_rare diseases +MONDO:0008719 rare diseases +MONDO:0008720 gard_rare diseases +MONDO:0008720 nord_rare diseases +MONDO:0008720 ordo_disorder diseases +MONDO:0008720 orphanet_rare diseases +MONDO:0008720 otar diseases +MONDO:0008720 rare diseases +MONDO:0008721 clingen diseases +MONDO:0008721 gard_rare diseases +MONDO:0008721 ordo_disorder diseases +MONDO:0008721 orphanet_rare diseases +MONDO:0008721 otar diseases +MONDO:0008721 rare diseases +MONDO:0008722 clingen diseases +MONDO:0008722 gard_rare diseases +MONDO:0008722 nord_rare diseases +MONDO:0008722 ordo_disorder diseases +MONDO:0008722 orphanet_rare diseases +MONDO:0008722 otar diseases +MONDO:0008722 rare diseases +MONDO:0008723 clingen diseases +MONDO:0008723 gard_rare diseases +MONDO:0008723 nord_rare diseases +MONDO:0008723 ordo_disorder diseases +MONDO:0008723 orphanet_rare diseases +MONDO:0008723 otar diseases +MONDO:0008723 rare diseases +MONDO:0008724 gard_rare diseases +MONDO:0008724 nord_rare diseases +MONDO:0008724 ordo_disorder diseases +MONDO:0008724 ordo_malformation_syndrome diseases +MONDO:0008724 orphanet_rare diseases +MONDO:0008724 otar diseases +MONDO:0008724 rare diseases +MONDO:0008725 gard_rare diseases +MONDO:0008725 nord_rare diseases +MONDO:0008725 ordo_disorder diseases +MONDO:0008725 orphanet_rare diseases +MONDO:0008725 otar diseases +MONDO:0008725 rare diseases +MONDO:0008726 clingen diseases +MONDO:0008726 gard_rare diseases +MONDO:0008726 nord_rare diseases +MONDO:0008726 ordo_subtype_of_a_disorder diseases +MONDO:0008726 rare diseases +MONDO:0008727 gard_rare diseases +MONDO:0008727 nord_rare diseases +MONDO:0008727 ordo_disorder diseases +MONDO:0008727 orphanet_rare diseases +MONDO:0008727 otar diseases +MONDO:0008727 rare diseases +MONDO:0008728 gard_rare diseases +MONDO:0008728 nord_rare diseases +MONDO:0008728 ordo_disorder diseases +MONDO:0008728 orphanet_rare diseases +MONDO:0008728 otar diseases +MONDO:0008728 rare diseases +MONDO:0008729 gard_rare diseases +MONDO:0008729 nord_rare diseases +MONDO:0008729 ordo_disorder diseases +MONDO:0008729 orphanet_rare diseases +MONDO:0008729 otar diseases +MONDO:0008729 rare diseases +MONDO:0008730 gard_rare diseases +MONDO:0008730 nord_rare diseases +MONDO:0008730 ordo_disorder diseases +MONDO:0008730 orphanet_rare diseases +MONDO:0008730 otar diseases +MONDO:0008730 rare diseases +MONDO:0008731 gard_rare diseases +MONDO:0008731 ordo_disorder diseases +MONDO:0008731 orphanet_rare diseases +MONDO:0008731 otar diseases +MONDO:0008731 rare diseases +MONDO:0008732 gard_rare diseases +MONDO:0008732 nord_rare diseases +MONDO:0008732 rare diseases +MONDO:0008733 gard_rare diseases +MONDO:0008733 nord_rare diseases +MONDO:0008733 ordo_disorder diseases +MONDO:0008733 orphanet_rare diseases +MONDO:0008733 otar diseases +MONDO:0008733 rare diseases +MONDO:0008734 gard_rare diseases +MONDO:0008734 nord_rare diseases +MONDO:0008734 otar diseases +MONDO:0008734 rare diseases +MONDO:0008735 gard_rare diseases +MONDO:0008735 nord_rare diseases +MONDO:0008735 rare diseases +MONDO:0008736 gard_rare diseases +MONDO:0008736 nord_rare diseases +MONDO:0008736 rare diseases +MONDO:0008737 gard_rare diseases +MONDO:0008737 nord_rare diseases +MONDO:0008737 ordo_subtype_of_a_disorder diseases +MONDO:0008737 otar diseases +MONDO:0008737 rare diseases +MONDO:0008738 n_of_one diseases +MONDO:0008740 gard_rare diseases +MONDO:0008740 nord_rare diseases +MONDO:0008740 ordo_disorder diseases +MONDO:0008740 ordo_malformation_syndrome diseases +MONDO:0008740 orphanet_rare diseases +MONDO:0008740 otar diseases +MONDO:0008740 rare diseases +MONDO:0008741 gard_rare diseases +MONDO:0008741 nord_rare diseases +MONDO:0008741 ordo_disorder diseases +MONDO:0008741 ordo_malformation_syndrome diseases +MONDO:0008741 orphanet_rare diseases +MONDO:0008741 otar diseases +MONDO:0008741 rare diseases +MONDO:0008742 gard_rare diseases +MONDO:0008742 nord_rare diseases +MONDO:0008742 ordo_disorder diseases +MONDO:0008742 orphanet_rare diseases +MONDO:0008742 otar diseases +MONDO:0008742 rare diseases +MONDO:0008743 gard_rare diseases +MONDO:0008743 ordo_disorder diseases +MONDO:0008743 ordo_malformation_syndrome diseases +MONDO:0008743 orphanet_rare diseases +MONDO:0008743 otar diseases +MONDO:0008743 rare diseases +MONDO:0008744 gard_rare diseases +MONDO:0008744 nord_rare diseases +MONDO:0008744 ordo_disorder diseases +MONDO:0008744 ordo_malformation_syndrome diseases +MONDO:0008744 orphanet_rare diseases +MONDO:0008744 otar diseases +MONDO:0008744 rare diseases +MONDO:0008745 gard_rare diseases +MONDO:0008745 nord_rare diseases +MONDO:0008745 ordo_subtype_of_a_disorder diseases +MONDO:0008745 otar diseases +MONDO:0008745 rare diseases +MONDO:0008746 clingen diseases +MONDO:0008746 gard_rare diseases +MONDO:0008746 nord_rare diseases +MONDO:0008746 ordo_disorder diseases +MONDO:0008746 orphanet_rare diseases +MONDO:0008746 otar diseases +MONDO:0008746 rare diseases +MONDO:0008747 gard_rare diseases +MONDO:0008747 nord_rare diseases +MONDO:0008747 ordo_disorder diseases +MONDO:0008747 orphanet_rare diseases +MONDO:0008747 otar diseases +MONDO:0008747 rare diseases +MONDO:0008748 clingen diseases +MONDO:0008748 gard_rare diseases +MONDO:0008748 nord_rare diseases +MONDO:0008748 rare diseases +MONDO:0008749 gard_rare diseases +MONDO:0008749 nord_rare diseases +MONDO:0008749 ordo_disorder diseases +MONDO:0008749 orphanet_rare diseases +MONDO:0008749 otar diseases +MONDO:0008749 rare diseases +MONDO:0008750 gard_rare diseases +MONDO:0008750 ordo_disorder diseases +MONDO:0008750 ordo_malformation_syndrome diseases +MONDO:0008750 orphanet_rare diseases +MONDO:0008750 otar diseases +MONDO:0008750 rare diseases +MONDO:0008751 gard_rare diseases +MONDO:0008751 nord_rare diseases +MONDO:0008751 rare diseases +MONDO:0008752 gard_rare diseases +MONDO:0008752 nord_rare diseases +MONDO:0008752 ordo_disorder diseases +MONDO:0008752 orphanet_rare diseases +MONDO:0008752 otar diseases +MONDO:0008752 rare diseases +MONDO:0008753 clingen diseases +MONDO:0008753 gard_rare diseases +MONDO:0008753 nord_rare diseases +MONDO:0008753 ordo_disorder diseases +MONDO:0008753 orphanet_rare diseases +MONDO:0008753 otar diseases +MONDO:0008753 rare diseases +MONDO:0008754 gard_rare diseases +MONDO:0008754 nord_rare diseases +MONDO:0008754 ordo_disorder diseases +MONDO:0008754 ordo_malformation_syndrome diseases +MONDO:0008754 orphanet_rare diseases +MONDO:0008754 otar diseases +MONDO:0008754 rare diseases +MONDO:0008755 gard_rare diseases +MONDO:0008755 nord_rare diseases +MONDO:0008755 ordo_disorder diseases +MONDO:0008755 ordo_malformation_syndrome diseases +MONDO:0008755 orphanet_rare diseases +MONDO:0008755 otar diseases +MONDO:0008755 rare diseases +MONDO:0008756 gard_rare diseases +MONDO:0008756 nord_rare diseases +MONDO:0008756 ordo_disorder diseases +MONDO:0008756 orphanet_rare diseases +MONDO:0008756 otar diseases +MONDO:0008756 rare diseases +MONDO:0008757 gard_rare diseases +MONDO:0008757 nord_rare diseases +MONDO:0008757 ordo_disorder diseases +MONDO:0008757 orphanet_rare diseases +MONDO:0008757 otar diseases +MONDO:0008757 rare diseases +MONDO:0008758 gard_rare diseases +MONDO:0008758 nord_rare diseases +MONDO:0008758 ordo_disorder diseases +MONDO:0008758 orphanet_rare diseases +MONDO:0008758 otar diseases +MONDO:0008758 rare diseases +MONDO:0008759 gard_rare diseases +MONDO:0008759 nord_rare diseases +MONDO:0008759 ordo_disorder diseases +MONDO:0008759 orphanet_rare diseases +MONDO:0008759 otar diseases +MONDO:0008759 rare diseases +MONDO:0008760 clingen diseases +MONDO:0008760 gard_rare diseases +MONDO:0008760 nord_rare diseases +MONDO:0008760 ordo_disorder diseases +MONDO:0008760 orphanet_rare diseases +MONDO:0008760 otar diseases +MONDO:0008760 rare diseases +MONDO:0008762 gard_rare diseases +MONDO:0008762 nord_rare diseases +MONDO:0008762 ordo_etiological_subtype diseases +MONDO:0008762 ordo_subtype_of_a_disorder diseases +MONDO:0008762 otar diseases +MONDO:0008762 rare diseases +MONDO:0008763 clingen diseases +MONDO:0008763 gard_rare diseases +MONDO:0008763 nord_rare diseases +MONDO:0008763 ordo_disorder diseases +MONDO:0008763 orphanet_rare diseases +MONDO:0008763 otar diseases +MONDO:0008763 rare diseases +MONDO:0008764 gard_rare diseases +MONDO:0008764 nord_rare diseases +MONDO:0008764 rare diseases +MONDO:0008765 gard_rare diseases +MONDO:0008765 nord_rare diseases +MONDO:0008765 rare diseases +MONDO:0008766 gard_rare diseases +MONDO:0008766 ordo_disorder diseases +MONDO:0008766 orphanet_rare diseases +MONDO:0008766 otar diseases +MONDO:0008766 rare diseases +MONDO:0008767 gard_rare diseases +MONDO:0008767 nord_rare diseases +MONDO:0008767 ordo_etiological_subtype diseases +MONDO:0008767 otar diseases +MONDO:0008767 rare diseases +MONDO:0008768 gard_rare diseases +MONDO:0008768 nord_rare diseases +MONDO:0008768 ordo_etiological_subtype diseases +MONDO:0008768 otar diseases +MONDO:0008768 rare diseases +MONDO:0008769 gard_rare diseases +MONDO:0008769 nord_rare diseases +MONDO:0008769 ordo_etiological_subtype diseases +MONDO:0008769 otar diseases +MONDO:0008769 rare diseases +MONDO:0008770 gard_rare diseases +MONDO:0008770 rare diseases +MONDO:0008771 gard_rare diseases +MONDO:0008771 nord_rare diseases +MONDO:0008771 ordo_disorder diseases +MONDO:0008771 ordo_malformation_syndrome diseases +MONDO:0008771 orphanet_rare diseases +MONDO:0008771 otar diseases +MONDO:0008771 rare diseases +MONDO:0008772 gard_rare diseases +MONDO:0008772 rare diseases +MONDO:0008774 clingen diseases +MONDO:0008774 gard_rare diseases +MONDO:0008774 nord_rare diseases +MONDO:0008774 ordo_disorder diseases +MONDO:0008774 orphanet_rare diseases +MONDO:0008774 otar diseases +MONDO:0008774 rare diseases +MONDO:0008777 gard_rare diseases +MONDO:0008777 nord_rare diseases +MONDO:0008777 ordo_disorder diseases +MONDO:0008777 orphanet_rare diseases +MONDO:0008777 otar diseases +MONDO:0008777 rare diseases +MONDO:0008779 otar diseases +MONDO:0008780 gard_rare diseases +MONDO:0008780 nord_rare diseases +MONDO:0008780 otar diseases +MONDO:0008780 rare diseases +MONDO:0008781 gard_rare diseases +MONDO:0008781 nord_rare diseases +MONDO:0008781 rare diseases +MONDO:0008782 gard_rare diseases +MONDO:0008782 nord_rare diseases +MONDO:0008782 rare diseases +MONDO:0008783 gard_rare diseases +MONDO:0008783 nord_rare diseases +MONDO:0008783 ordo_disorder diseases +MONDO:0008783 orphanet_rare diseases +MONDO:0008783 otar diseases +MONDO:0008783 rare diseases +MONDO:0008785 gard_rare diseases +MONDO:0008785 nord_rare diseases +MONDO:0008785 rare diseases +MONDO:0008786 gard_rare diseases +MONDO:0008786 nord_rare diseases +MONDO:0008786 rare diseases +MONDO:0008787 gard_rare diseases +MONDO:0008787 nord_rare diseases +MONDO:0008787 ordo_disorder diseases +MONDO:0008787 orphanet_rare diseases +MONDO:0008787 otar diseases +MONDO:0008787 rare diseases +MONDO:0008788 gard_rare diseases +MONDO:0008788 nord_rare diseases +MONDO:0008788 ordo_disorder diseases +MONDO:0008788 orphanet_rare diseases +MONDO:0008788 otar diseases +MONDO:0008788 rare diseases +MONDO:0008789 gard_rare diseases +MONDO:0008789 rare diseases +MONDO:0008790 gard_rare diseases +MONDO:0008790 rare diseases +MONDO:0008791 gard_rare diseases +MONDO:0008791 nord_rare diseases +MONDO:0008791 ordo_disorder diseases +MONDO:0008791 ordo_morphological_anomaly diseases +MONDO:0008791 orphanet_rare diseases +MONDO:0008791 otar diseases +MONDO:0008791 rare diseases +MONDO:0008792 gard_rare diseases +MONDO:0008792 nord_rare diseases +MONDO:0008792 ordo_disorder diseases +MONDO:0008792 orphanet_rare diseases +MONDO:0008792 otar diseases +MONDO:0008792 rare diseases +MONDO:0008795 clingen diseases +MONDO:0008795 gard_rare diseases +MONDO:0008795 nord_rare diseases +MONDO:0008795 ordo_disorder diseases +MONDO:0008795 ordo_malformation_syndrome diseases +MONDO:0008795 orphanet_rare diseases +MONDO:0008795 otar diseases +MONDO:0008795 rare diseases +MONDO:0008796 gard_rare diseases +MONDO:0008796 ordo_disorder diseases +MONDO:0008796 ordo_malformation_syndrome diseases +MONDO:0008796 orphanet_rare diseases +MONDO:0008796 otar diseases +MONDO:0008796 rare diseases +MONDO:0008797 gard_rare diseases +MONDO:0008797 nord_rare diseases +MONDO:0008797 ordo_disorder diseases +MONDO:0008797 ordo_morphological_anomaly diseases +MONDO:0008797 orphanet_rare diseases +MONDO:0008797 otar diseases +MONDO:0008797 rare diseases +MONDO:0008798 gard_rare diseases +MONDO:0008798 nord_rare diseases +MONDO:0008798 ordo_subtype_of_a_disorder diseases +MONDO:0008798 otar diseases +MONDO:0008798 rare diseases +MONDO:0008799 gard_rare diseases +MONDO:0008799 nord_rare diseases +MONDO:0008799 ordo_disorder diseases +MONDO:0008799 ordo_malformation_syndrome diseases +MONDO:0008799 orphanet_rare diseases +MONDO:0008799 otar diseases +MONDO:0008799 rare diseases +MONDO:0008800 gard_rare diseases +MONDO:0008800 nord_rare diseases +MONDO:0008800 ordo_disorder diseases +MONDO:0008800 ordo_malformation_syndrome diseases +MONDO:0008800 orphanet_rare diseases +MONDO:0008800 otar diseases +MONDO:0008800 rare diseases +MONDO:0008803 gard_rare diseases +MONDO:0008803 nord_rare diseases +MONDO:0008803 ordo_disorder diseases +MONDO:0008803 ordo_malformation_syndrome diseases +MONDO:0008803 orphanet_rare diseases +MONDO:0008803 otar diseases +MONDO:0008803 rare diseases +MONDO:0008806 gard_rare diseases +MONDO:0008806 ordo_disorder diseases +MONDO:0008806 ordo_malformation_syndrome diseases +MONDO:0008806 orphanet_rare diseases +MONDO:0008806 otar diseases +MONDO:0008806 rare diseases +MONDO:0008808 gard_rare diseases +MONDO:0008808 ordo_disorder diseases +MONDO:0008808 orphanet_rare diseases +MONDO:0008808 otar diseases +MONDO:0008808 rare diseases +MONDO:0008809 gard_rare diseases +MONDO:0008809 ordo_disorder diseases +MONDO:0008809 ordo_malformation_syndrome diseases +MONDO:0008809 orphanet_rare diseases +MONDO:0008809 otar diseases +MONDO:0008809 rare diseases +MONDO:0008810 gard_rare diseases +MONDO:0008810 nord_rare diseases +MONDO:0008810 ordo_subtype_of_a_disorder diseases +MONDO:0008810 otar diseases +MONDO:0008810 rare diseases +MONDO:0008811 gard_rare diseases +MONDO:0008811 nord_rare diseases +MONDO:0008811 ordo_disorder diseases +MONDO:0008811 ordo_malformation_syndrome diseases +MONDO:0008811 orphanet_rare diseases +MONDO:0008811 rare diseases +MONDO:0008812 gard_rare diseases +MONDO:0008812 nord_rare diseases +MONDO:0008812 ordo_disorder diseases +MONDO:0008812 ordo_malformation_syndrome diseases +MONDO:0008812 orphanet_rare diseases +MONDO:0008812 otar diseases +MONDO:0008812 rare diseases +MONDO:0008813 gard_rare diseases +MONDO:0008813 ordo_disorder diseases +MONDO:0008813 ordo_morphological_anomaly diseases +MONDO:0008813 orphanet_rare diseases +MONDO:0008813 otar diseases +MONDO:0008813 rare diseases +MONDO:0008814 clingen diseases +MONDO:0008814 gard_rare diseases +MONDO:0008814 nord_rare diseases +MONDO:0008814 ordo_disorder diseases +MONDO:0008814 orphanet_rare diseases +MONDO:0008814 otar diseases +MONDO:0008814 rare diseases +MONDO:0008815 clingen diseases +MONDO:0008815 gard_rare diseases +MONDO:0008815 nord_rare diseases +MONDO:0008815 ordo_disorder diseases +MONDO:0008815 orphanet_rare diseases +MONDO:0008815 otar diseases +MONDO:0008815 rare diseases +MONDO:0008816 gard_rare diseases +MONDO:0008816 nord_rare diseases +MONDO:0008816 ordo_morphological_anomaly diseases +MONDO:0008816 otar diseases +MONDO:0008816 rare diseases +MONDO:0008817 gard_rare diseases +MONDO:0008817 nord_rare diseases +MONDO:0008817 rare diseases +MONDO:0008818 gard_rare diseases +MONDO:0008818 nord_rare diseases +MONDO:0008818 ordo_disorder diseases +MONDO:0008818 ordo_malformation_syndrome diseases +MONDO:0008818 orphanet_rare diseases +MONDO:0008818 otar diseases +MONDO:0008818 rare diseases +MONDO:0008822 clingen diseases +MONDO:0008822 gard_rare diseases +MONDO:0008822 nord_rare diseases +MONDO:0008822 rare diseases +MONDO:0008823 gard_rare diseases +MONDO:0008823 nord_rare diseases +MONDO:0008823 ordo_disorder diseases +MONDO:0008823 orphanet_rare diseases +MONDO:0008823 otar diseases +MONDO:0008823 rare diseases +MONDO:0008824 gard_rare diseases +MONDO:0008824 nord_rare diseases +MONDO:0008824 ordo_malformation_syndrome diseases +MONDO:0008824 otar diseases +MONDO:0008824 rare diseases +MONDO:0008825 gard_rare diseases +MONDO:0008825 nord_rare diseases +MONDO:0008825 ordo_disorder diseases +MONDO:0008825 ordo_malformation_syndrome diseases +MONDO:0008825 orphanet_rare diseases +MONDO:0008825 otar diseases +MONDO:0008825 rare diseases +MONDO:0008826 gard_rare diseases +MONDO:0008826 ordo_disorder diseases +MONDO:0008826 ordo_malformation_syndrome diseases +MONDO:0008826 orphanet_rare diseases +MONDO:0008826 otar diseases +MONDO:0008826 rare diseases +MONDO:0008827 gard_rare diseases +MONDO:0008827 nord_rare diseases +MONDO:0008827 ordo_disorder diseases +MONDO:0008827 orphanet_rare diseases +MONDO:0008827 otar diseases +MONDO:0008827 rare diseases +MONDO:0008828 clingen diseases +MONDO:0008828 gard_rare diseases +MONDO:0008828 nord_rare diseases +MONDO:0008828 ordo_disorder diseases +MONDO:0008828 orphanet_rare diseases +MONDO:0008828 otar diseases +MONDO:0008828 rare diseases +MONDO:0008829 gard_rare diseases +MONDO:0008829 nord_rare diseases +MONDO:0008829 ordo_disorder diseases +MONDO:0008829 orphanet_rare diseases +MONDO:0008829 rare diseases +MONDO:0008830 clingen diseases +MONDO:0008830 gard_rare diseases +MONDO:0008830 nord_rare diseases +MONDO:0008830 ordo_disorder diseases +MONDO:0008830 orphanet_rare diseases +MONDO:0008830 otar diseases +MONDO:0008830 rare diseases +MONDO:0008831 gard_rare diseases +MONDO:0008831 nord_rare diseases +MONDO:0008831 rare diseases +MONDO:0008832 gard_rare diseases +MONDO:0008832 nord_rare diseases +MONDO:0008832 ordo_disorder diseases +MONDO:0008832 ordo_malformation_syndrome diseases +MONDO:0008832 orphanet_rare diseases +MONDO:0008832 otar diseases +MONDO:0008832 rare diseases +MONDO:0008833 gard_rare diseases +MONDO:0008833 rare diseases +MONDO:0008838 gard_rare diseases +MONDO:0008838 nord_rare diseases +MONDO:0008838 ordo_disorder diseases +MONDO:0008838 ordo_malformation_syndrome diseases +MONDO:0008838 orphanet_rare diseases +MONDO:0008838 otar diseases +MONDO:0008838 rare diseases +MONDO:0008840 clingen diseases +MONDO:0008840 gard_rare diseases +MONDO:0008840 nord_rare diseases +MONDO:0008840 ordo_disorder diseases +MONDO:0008840 orphanet_rare diseases +MONDO:0008840 otar diseases +MONDO:0008840 rare diseases +MONDO:0008841 gard_rare diseases +MONDO:0008841 rare diseases +MONDO:0008842 gard_rare diseases +MONDO:0008842 nord_rare diseases +MONDO:0008842 ordo_disorder diseases +MONDO:0008842 orphanet_rare diseases +MONDO:0008842 otar diseases +MONDO:0008842 rare diseases +MONDO:0008843 gard_rare diseases +MONDO:0008843 ordo_disorder diseases +MONDO:0008843 ordo_malformation_syndrome diseases +MONDO:0008843 orphanet_rare diseases +MONDO:0008843 otar diseases +MONDO:0008843 rare diseases +MONDO:0008846 gard_rare diseases +MONDO:0008846 nord_rare diseases +MONDO:0008846 ordo_disorder diseases +MONDO:0008846 orphanet_rare diseases +MONDO:0008846 otar diseases +MONDO:0008846 rare diseases +MONDO:0008847 gard_rare diseases +MONDO:0008847 nord_rare diseases +MONDO:0008847 ordo_disorder diseases +MONDO:0008847 orphanet_rare diseases +MONDO:0008847 otar diseases +MONDO:0008847 rare diseases +MONDO:0008848 otar diseases +MONDO:0008849 gard_rare diseases +MONDO:0008849 nord_rare diseases +MONDO:0008849 ordo_disorder diseases +MONDO:0008849 orphanet_rare diseases +MONDO:0008849 otar diseases +MONDO:0008849 rare diseases +MONDO:0008850 gard_rare diseases +MONDO:0008850 ordo_disorder diseases +MONDO:0008850 ordo_malformation_syndrome diseases +MONDO:0008850 orphanet_rare diseases +MONDO:0008850 otar diseases +MONDO:0008850 rare diseases +MONDO:0008853 gard_rare diseases +MONDO:0008853 nord_rare diseases +MONDO:0008853 ordo_disorder diseases +MONDO:0008853 ordo_malformation_syndrome diseases +MONDO:0008853 orphanet_rare diseases +MONDO:0008853 otar diseases +MONDO:0008853 rare diseases +MONDO:0008854 gard_rare diseases +MONDO:0008854 nord_rare diseases +MONDO:0008854 rare diseases +MONDO:0008855 clingen diseases +MONDO:0008855 gard_rare diseases +MONDO:0008855 nord_rare diseases +MONDO:0008855 ordo_disorder diseases +MONDO:0008855 orphanet_rare diseases +MONDO:0008855 otar diseases +MONDO:0008855 rare diseases +MONDO:0008857 gard_rare diseases +MONDO:0008857 ordo_disorder diseases +MONDO:0008857 ordo_malformation_syndrome diseases +MONDO:0008857 orphanet_rare diseases +MONDO:0008857 otar diseases +MONDO:0008857 rare diseases +MONDO:0008858 gard_rare diseases +MONDO:0008858 nord_rare diseases +MONDO:0008858 ordo_malformation_syndrome diseases +MONDO:0008858 otar diseases +MONDO:0008858 rare diseases +MONDO:0008861 gard_rare diseases +MONDO:0008861 rare diseases +MONDO:0008862 gard_rare diseases +MONDO:0008862 otar diseases +MONDO:0008862 rare diseases +MONDO:0008863 clingen diseases +MONDO:0008863 gard_rare diseases +MONDO:0008863 nord_rare diseases +MONDO:0008863 ordo_disorder diseases +MONDO:0008863 orphanet_rare diseases +MONDO:0008863 otar diseases +MONDO:0008863 rare diseases +MONDO:0008864 gard_rare diseases +MONDO:0008864 nord_rare diseases +MONDO:0008864 ordo_disorder diseases +MONDO:0008864 orphanet_rare diseases +MONDO:0008864 otar diseases +MONDO:0008864 rare diseases +MONDO:0008865 clingen diseases +MONDO:0008865 gard_rare diseases +MONDO:0008865 nord_rare diseases +MONDO:0008865 ordo_disorder diseases +MONDO:0008865 orphanet_rare diseases +MONDO:0008865 otar diseases +MONDO:0008865 rare diseases +MONDO:0008866 gard_rare diseases +MONDO:0008866 nord_rare diseases +MONDO:0008866 rare diseases +MONDO:0008867 gard_rare diseases +MONDO:0008867 nord_rare diseases +MONDO:0008867 ordo_disorder diseases +MONDO:0008867 ordo_morphological_anomaly diseases +MONDO:0008867 orphanet_rare diseases +MONDO:0008867 otar diseases +MONDO:0008867 rare diseases +MONDO:0008869 gard_rare diseases +MONDO:0008869 nord_rare diseases +MONDO:0008869 otar diseases +MONDO:0008869 rare diseases +MONDO:0008870 gard_rare diseases +MONDO:0008870 ordo_disorder diseases +MONDO:0008870 ordo_malformation_syndrome diseases +MONDO:0008870 orphanet_rare diseases +MONDO:0008870 otar diseases +MONDO:0008870 rare diseases +MONDO:0008871 gard_rare diseases +MONDO:0008871 nord_rare diseases +MONDO:0008871 rare diseases +MONDO:0008872 gard_rare diseases +MONDO:0008872 nord_rare diseases +MONDO:0008872 ordo_disorder diseases +MONDO:0008872 ordo_malformation_syndrome diseases +MONDO:0008872 orphanet_rare diseases +MONDO:0008872 otar diseases +MONDO:0008872 rare diseases +MONDO:0008873 gard_rare diseases +MONDO:0008873 nord_rare diseases +MONDO:0008873 rare diseases +MONDO:0008874 gard_rare diseases +MONDO:0008874 ordo_disorder diseases +MONDO:0008874 ordo_malformation_syndrome diseases +MONDO:0008874 orphanet_rare diseases +MONDO:0008874 otar diseases +MONDO:0008874 rare diseases +MONDO:0008875 gard_rare diseases +MONDO:0008875 nord_rare diseases +MONDO:0008875 ordo_disorder diseases +MONDO:0008875 ordo_malformation_syndrome diseases +MONDO:0008875 orphanet_rare diseases +MONDO:0008875 otar diseases +MONDO:0008875 rare diseases +MONDO:0008876 clingen diseases +MONDO:0008876 gard_rare diseases +MONDO:0008876 nord_rare diseases +MONDO:0008876 ordo_disorder diseases +MONDO:0008876 orphanet_rare diseases +MONDO:0008876 otar diseases +MONDO:0008876 rare diseases +MONDO:0008877 gard_rare diseases +MONDO:0008877 nord_rare diseases +MONDO:0008877 ordo_disorder diseases +MONDO:0008877 orphanet_rare diseases +MONDO:0008877 otar diseases +MONDO:0008877 rare diseases +MONDO:0008878 gard_rare diseases +MONDO:0008878 nord_rare diseases +MONDO:0008878 ordo_disorder diseases +MONDO:0008878 ordo_malformation_syndrome diseases +MONDO:0008878 orphanet_rare diseases +MONDO:0008878 otar diseases +MONDO:0008878 rare diseases +MONDO:0008879 gard_rare diseases +MONDO:0008879 nord_rare diseases +MONDO:0008879 ordo_disorder diseases +MONDO:0008879 ordo_malformation_syndrome diseases +MONDO:0008879 orphanet_rare diseases +MONDO:0008879 otar diseases +MONDO:0008879 rare diseases +MONDO:0008881 gard_rare diseases +MONDO:0008881 nord_rare diseases +MONDO:0008881 ordo_disorder diseases +MONDO:0008881 ordo_malformation_syndrome diseases +MONDO:0008881 orphanet_rare diseases +MONDO:0008881 otar diseases +MONDO:0008881 rare diseases +MONDO:0008882 gard_rare diseases +MONDO:0008882 ordo_morphological_anomaly diseases +MONDO:0008882 otar diseases +MONDO:0008882 rare diseases +MONDO:0008884 gard_rare diseases +MONDO:0008884 ordo_disorder diseases +MONDO:0008884 ordo_malformation_syndrome diseases +MONDO:0008884 orphanet_rare diseases +MONDO:0008884 rare diseases +MONDO:0008885 gard_rare diseases +MONDO:0008885 nord_rare diseases +MONDO:0008885 ordo_disorder diseases +MONDO:0008885 ordo_malformation_syndrome diseases +MONDO:0008885 orphanet_rare diseases +MONDO:0008885 otar diseases +MONDO:0008885 rare diseases +MONDO:0008887 gard_rare diseases +MONDO:0008887 nord_rare diseases +MONDO:0008887 otar diseases +MONDO:0008887 rare diseases +MONDO:0008888 gard_rare diseases +MONDO:0008888 nord_rare diseases +MONDO:0008888 ordo_disorder diseases +MONDO:0008888 ordo_morphological_anomaly diseases +MONDO:0008888 orphanet_rare diseases +MONDO:0008888 rare diseases +MONDO:0008889 gard_rare diseases +MONDO:0008889 nord_rare diseases +MONDO:0008889 ordo_disorder diseases +MONDO:0008889 orphanet_rare diseases +MONDO:0008889 otar diseases +MONDO:0008889 rare diseases +MONDO:0008890 gard_rare diseases +MONDO:0008890 nord_rare diseases +MONDO:0008890 otar diseases +MONDO:0008890 rare diseases +MONDO:0008891 gard_rare diseases +MONDO:0008891 nord_rare diseases +MONDO:0008891 ordo_disorder diseases +MONDO:0008891 ordo_malformation_syndrome diseases +MONDO:0008891 orphanet_rare diseases +MONDO:0008891 otar diseases +MONDO:0008891 rare diseases +MONDO:0008892 gard_rare diseases +MONDO:0008892 nord_rare diseases +MONDO:0008892 ordo_subtype_of_a_disorder diseases +MONDO:0008892 otar diseases +MONDO:0008892 rare diseases +MONDO:0008893 gard_rare diseases +MONDO:0008893 nord_rare diseases +MONDO:0008893 ordo_disorder diseases +MONDO:0008893 ordo_malformation_syndrome diseases +MONDO:0008893 orphanet_rare diseases +MONDO:0008893 otar diseases +MONDO:0008893 rare diseases +MONDO:0008894 gard_rare diseases +MONDO:0008894 nord_rare diseases +MONDO:0008894 ordo_disorder diseases +MONDO:0008894 ordo_malformation_syndrome diseases +MONDO:0008894 orphanet_rare diseases +MONDO:0008894 otar diseases +MONDO:0008894 rare diseases +MONDO:0008895 gard_rare diseases +MONDO:0008895 nord_rare diseases +MONDO:0008895 ordo_disorder diseases +MONDO:0008895 orphanet_rare diseases +MONDO:0008895 otar diseases +MONDO:0008895 rare diseases +MONDO:0008896 gard_rare diseases +MONDO:0008896 nord_rare diseases +MONDO:0008896 ordo_disorder diseases +MONDO:0008896 ordo_malformation_syndrome diseases +MONDO:0008896 orphanet_rare diseases +MONDO:0008896 otar diseases +MONDO:0008896 rare diseases +MONDO:0008898 gard_rare diseases +MONDO:0008898 nord_rare diseases +MONDO:0008898 ordo_disorder diseases +MONDO:0008898 ordo_malformation_syndrome diseases +MONDO:0008898 orphanet_rare diseases +MONDO:0008898 otar diseases +MONDO:0008898 rare diseases +MONDO:0008899 gard_rare diseases +MONDO:0008899 nord_rare diseases +MONDO:0008899 ordo_disorder diseases +MONDO:0008899 ordo_malformation_syndrome diseases +MONDO:0008899 orphanet_rare diseases +MONDO:0008899 otar diseases +MONDO:0008899 rare diseases +MONDO:0008900 gard_rare diseases +MONDO:0008900 nord_rare diseases +MONDO:0008900 ordo_disorder diseases +MONDO:0008900 ordo_malformation_syndrome diseases +MONDO:0008900 orphanet_rare diseases +MONDO:0008900 rare diseases +MONDO:0008901 gard_rare diseases +MONDO:0008901 nord_rare diseases +MONDO:0008901 ordo_disorder diseases +MONDO:0008901 ordo_malformation_syndrome diseases +MONDO:0008901 orphanet_rare diseases +MONDO:0008901 otar diseases +MONDO:0008901 rare diseases +MONDO:0008903 otar diseases +MONDO:0008904 gard_rare diseases +MONDO:0008904 rare diseases +MONDO:0008907 gard_rare diseases +MONDO:0008907 nord_rare diseases +MONDO:0008907 ordo_disorder diseases +MONDO:0008907 orphanet_rare diseases +MONDO:0008907 otar diseases +MONDO:0008907 rare diseases +MONDO:0008908 gard_rare diseases +MONDO:0008908 nord_rare diseases +MONDO:0008908 ordo_disorder diseases +MONDO:0008908 orphanet_rare diseases +MONDO:0008908 otar diseases +MONDO:0008908 rare diseases +MONDO:0008911 gard_rare diseases +MONDO:0008911 nord_rare diseases +MONDO:0008911 rare diseases +MONDO:0008913 otar diseases +MONDO:0008915 gard_rare diseases +MONDO:0008915 nord_rare diseases +MONDO:0008915 ordo_disorder diseases +MONDO:0008915 ordo_malformation_syndrome diseases +MONDO:0008915 orphanet_rare diseases +MONDO:0008915 otar diseases +MONDO:0008915 rare diseases +MONDO:0008917 gard_rare diseases +MONDO:0008917 ordo_disorder diseases +MONDO:0008917 ordo_malformation_syndrome diseases +MONDO:0008917 orphanet_rare diseases +MONDO:0008917 otar diseases +MONDO:0008917 rare diseases +MONDO:0008918 clingen diseases +MONDO:0008918 gard_rare diseases +MONDO:0008918 nord_rare diseases +MONDO:0008918 ordo_disorder diseases +MONDO:0008918 orphanet_rare diseases +MONDO:0008918 otar diseases +MONDO:0008918 rare diseases +MONDO:0008919 clingen diseases +MONDO:0008919 gard_rare diseases +MONDO:0008919 nord_rare diseases +MONDO:0008919 ordo_disorder diseases +MONDO:0008919 orphanet_rare diseases +MONDO:0008919 otar diseases +MONDO:0008919 rare diseases +MONDO:0008921 gard_rare diseases +MONDO:0008921 nord_rare diseases +MONDO:0008921 ordo_disorder diseases +MONDO:0008921 orphanet_rare diseases +MONDO:0008921 otar diseases +MONDO:0008921 rare diseases +MONDO:0008922 gard_rare diseases +MONDO:0008922 nord_rare diseases +MONDO:0008922 ordo_disorder diseases +MONDO:0008922 orphanet_rare diseases +MONDO:0008922 otar diseases +MONDO:0008922 rare diseases +MONDO:0008923 gard_rare diseases +MONDO:0008923 nord_rare diseases +MONDO:0008923 ordo_disorder diseases +MONDO:0008923 orphanet_rare diseases +MONDO:0008923 otar diseases +MONDO:0008923 rare diseases +MONDO:0008924 gard_rare diseases +MONDO:0008924 otar diseases +MONDO:0008924 rare diseases +MONDO:0008925 gard_rare diseases +MONDO:0008925 nord_rare diseases +MONDO:0008925 otar diseases +MONDO:0008925 rare diseases +MONDO:0008926 gard_rare diseases +MONDO:0008926 nord_rare diseases +MONDO:0008926 ordo_subtype_of_a_disorder diseases +MONDO:0008926 otar diseases +MONDO:0008926 prototype_pattern diseases +MONDO:0008926 rare diseases +MONDO:0008927 gard_rare diseases +MONDO:0008927 nord_rare diseases +MONDO:0008927 ordo_disorder diseases +MONDO:0008927 orphanet_rare diseases +MONDO:0008927 rare diseases +MONDO:0008928 gard_rare diseases +MONDO:0008928 ordo_disorder diseases +MONDO:0008928 orphanet_rare diseases +MONDO:0008928 otar diseases +MONDO:0008928 rare diseases +MONDO:0008931 gard_rare diseases +MONDO:0008931 nord_rare diseases +MONDO:0008931 ordo_disorder diseases +MONDO:0008931 ordo_malformation_syndrome diseases +MONDO:0008931 orphanet_rare diseases +MONDO:0008931 otar diseases +MONDO:0008931 rare diseases +MONDO:0008934 gard_rare diseases +MONDO:0008934 nord_rare diseases +MONDO:0008934 ordo_disorder diseases +MONDO:0008934 ordo_malformation_syndrome diseases +MONDO:0008934 orphanet_rare diseases +MONDO:0008934 otar diseases +MONDO:0008934 rare diseases +MONDO:0008935 gard_rare diseases +MONDO:0008935 nord_rare diseases +MONDO:0008935 ordo_disorder diseases +MONDO:0008935 orphanet_rare diseases +MONDO:0008935 otar diseases +MONDO:0008935 rare diseases +MONDO:0008938 gard_rare diseases +MONDO:0008938 nord_rare diseases +MONDO:0008938 ordo_disorder diseases +MONDO:0008938 orphanet_rare diseases +MONDO:0008938 otar diseases +MONDO:0008938 rare diseases +MONDO:0008939 gard_rare diseases +MONDO:0008939 nord_rare diseases +MONDO:0008939 ordo_disorder diseases +MONDO:0008939 ordo_morphological_anomaly diseases +MONDO:0008939 orphanet_rare diseases +MONDO:0008939 otar diseases +MONDO:0008939 rare diseases +MONDO:0008941 gard_rare diseases +MONDO:0008941 ordo_disorder diseases +MONDO:0008941 ordo_malformation_syndrome diseases +MONDO:0008941 orphanet_rare diseases +MONDO:0008941 otar diseases +MONDO:0008941 rare diseases +MONDO:0008943 gard_rare diseases +MONDO:0008943 nord_rare diseases +MONDO:0008943 ordo_disorder diseases +MONDO:0008943 orphanet_rare diseases +MONDO:0008943 otar diseases +MONDO:0008943 rare diseases +MONDO:0008944 clingen diseases +MONDO:0008944 gard_rare diseases +MONDO:0008944 nord_rare diseases +MONDO:0008944 rare diseases +MONDO:0008945 gard_rare diseases +MONDO:0008945 otar diseases +MONDO:0008945 rare diseases +MONDO:0008945 speculative diseases +MONDO:0008947 gard_rare diseases +MONDO:0008947 nord_rare diseases +MONDO:0008947 ordo_disorder diseases +MONDO:0008947 orphanet_rare diseases +MONDO:0008947 otar diseases +MONDO:0008947 rare diseases +MONDO:0008948 gard_rare diseases +MONDO:0008948 nord_rare diseases +MONDO:0008948 ordo_disorder diseases +MONDO:0008948 orphanet_rare diseases +MONDO:0008948 otar diseases +MONDO:0008948 rare diseases +MONDO:0008950 gard_rare diseases +MONDO:0008950 rare diseases +MONDO:0008953 gard_rare diseases +MONDO:0008953 nord_rare diseases +MONDO:0008953 otar diseases +MONDO:0008953 rare diseases +MONDO:0008954 gard_rare diseases +MONDO:0008954 nord_rare diseases +MONDO:0008954 otar diseases +MONDO:0008954 rare diseases +MONDO:0008955 gard_rare diseases +MONDO:0008955 nord_rare diseases +MONDO:0008955 rare diseases +MONDO:0008958 gard_rare diseases +MONDO:0008958 nord_rare diseases +MONDO:0008958 rare diseases +MONDO:0008959 gard_rare diseases +MONDO:0008959 ordo_disorder diseases +MONDO:0008959 orphanet_rare diseases +MONDO:0008959 otar diseases +MONDO:0008959 rare diseases +MONDO:0008960 gard_rare diseases +MONDO:0008960 nord_rare diseases +MONDO:0008960 ordo_disorder diseases +MONDO:0008960 ordo_malformation_syndrome diseases +MONDO:0008960 orphanet_rare diseases +MONDO:0008960 otar diseases +MONDO:0008960 rare diseases +MONDO:0008961 gard_rare diseases +MONDO:0008961 nord_rare diseases +MONDO:0008961 ordo_disorder diseases +MONDO:0008961 orphanet_rare diseases +MONDO:0008961 otar diseases +MONDO:0008961 rare diseases +MONDO:0008962 clingen diseases +MONDO:0008962 gard_rare diseases +MONDO:0008962 nord_rare diseases +MONDO:0008962 ordo_subtype_of_a_disorder diseases +MONDO:0008962 otar diseases +MONDO:0008962 rare diseases +MONDO:0008963 clingen diseases +MONDO:0008963 gard_rare diseases +MONDO:0008963 nord_rare diseases +MONDO:0008963 ordo_disorder diseases +MONDO:0008963 orphanet_rare diseases +MONDO:0008963 otar diseases +MONDO:0008963 rare diseases +MONDO:0008964 gard_rare diseases +MONDO:0008964 nord_rare diseases +MONDO:0008964 ordo_disorder diseases +MONDO:0008964 orphanet_rare diseases +MONDO:0008964 otar diseases +MONDO:0008964 rare diseases +MONDO:0008965 clingen diseases +MONDO:0008965 gard_rare diseases +MONDO:0008965 nord_rare diseases +MONDO:0008965 ordo_disorder diseases +MONDO:0008965 ordo_malformation_syndrome diseases +MONDO:0008965 orphanet_rare diseases +MONDO:0008965 otar diseases +MONDO:0008965 rare diseases +MONDO:0008966 gard_rare diseases +MONDO:0008966 nord_rare diseases +MONDO:0008966 ordo_disorder diseases +MONDO:0008966 orphanet_rare diseases +MONDO:0008966 otar diseases +MONDO:0008966 rare diseases +MONDO:0008967 gard_rare diseases +MONDO:0008967 nord_rare diseases +MONDO:0008967 ordo_disorder diseases +MONDO:0008967 orphanet_rare diseases +MONDO:0008967 otar diseases +MONDO:0008967 rare diseases +MONDO:0008970 gard_rare diseases +MONDO:0008970 nord_rare diseases +MONDO:0008970 ordo_disorder diseases +MONDO:0008970 ordo_malformation_syndrome diseases +MONDO:0008970 orphanet_rare diseases +MONDO:0008970 otar diseases +MONDO:0008970 rare diseases +MONDO:0008971 gard_rare diseases +MONDO:0008971 nord_rare diseases +MONDO:0008971 rare diseases +MONDO:0008972 gard_rare diseases +MONDO:0008972 nord_rare diseases +MONDO:0008972 ordo_etiological_subtype diseases +MONDO:0008972 ordo_subtype_of_a_disorder diseases +MONDO:0008972 otar diseases +MONDO:0008972 rare diseases +MONDO:0008973 gard_rare diseases +MONDO:0008973 nord_rare diseases +MONDO:0008973 ordo_disorder diseases +MONDO:0008973 ordo_malformation_syndrome diseases +MONDO:0008973 orphanet_rare diseases +MONDO:0008973 rare diseases +MONDO:0008974 gard_rare diseases +MONDO:0008974 nord_rare diseases +MONDO:0008974 ordo_disorder diseases +MONDO:0008974 orphanet_rare diseases +MONDO:0008974 otar diseases +MONDO:0008974 rare diseases +MONDO:0008975 clingen diseases +MONDO:0008975 gard_rare diseases +MONDO:0008975 nord_rare diseases +MONDO:0008975 ordo_disorder diseases +MONDO:0008975 orphanet_rare diseases +MONDO:0008975 otar diseases +MONDO:0008975 rare diseases +MONDO:0008977 gard_rare diseases +MONDO:0008977 nord_rare diseases +MONDO:0008977 ordo_disorder diseases +MONDO:0008977 orphanet_rare diseases +MONDO:0008977 otar diseases +MONDO:0008977 rare diseases +MONDO:0008978 gard_rare diseases +MONDO:0008978 nord_rare diseases +MONDO:0008978 ordo_disorder diseases +MONDO:0008978 orphanet_rare diseases +MONDO:0008978 otar diseases +MONDO:0008978 rare diseases +MONDO:0008979 gard_rare diseases +MONDO:0008979 nord_rare diseases +MONDO:0008979 otar diseases +MONDO:0008979 rare diseases +MONDO:0008980 gard_rare diseases +MONDO:0008980 nord_rare diseases +MONDO:0008980 ordo_disorder diseases +MONDO:0008980 orphanet_rare diseases +MONDO:0008980 otar diseases +MONDO:0008980 rare diseases +MONDO:0008981 gard_rare diseases +MONDO:0008981 nord_rare diseases +MONDO:0008981 ordo_disorder diseases +MONDO:0008981 orphanet_rare diseases +MONDO:0008981 rare diseases +MONDO:0008982 gard_rare diseases +MONDO:0008982 nord_rare diseases +MONDO:0008982 ordo_disorder diseases +MONDO:0008982 orphanet_rare diseases +MONDO:0008982 otar diseases +MONDO:0008982 rare diseases +MONDO:0008984 gard_rare diseases +MONDO:0008984 rare diseases +MONDO:0008985 gard_rare diseases +MONDO:0008985 rare diseases +MONDO:0008988 clingen diseases +MONDO:0008988 gard_rare diseases +MONDO:0008988 nord_rare diseases +MONDO:0008988 ordo_disorder diseases +MONDO:0008988 orphanet_rare diseases +MONDO:0008988 otar diseases +MONDO:0008988 rare diseases +MONDO:0008990 gard_rare diseases +MONDO:0008990 nord_rare diseases +MONDO:0008990 otar diseases +MONDO:0008990 rare diseases +MONDO:0008991 gard_rare diseases +MONDO:0008991 ordo_disorder diseases +MONDO:0008991 ordo_malformation_syndrome diseases +MONDO:0008991 orphanet_rare diseases +MONDO:0008991 otar diseases +MONDO:0008991 rare diseases +MONDO:0008992 gard_rare diseases +MONDO:0008992 nord_rare diseases +MONDO:0008992 ordo_disorder diseases +MONDO:0008992 ordo_malformation_syndrome diseases +MONDO:0008992 orphanet_rare diseases +MONDO:0008992 otar diseases +MONDO:0008992 rare diseases +MONDO:0008993 gard_rare diseases +MONDO:0008993 ordo_disorder diseases +MONDO:0008993 ordo_malformation_syndrome diseases +MONDO:0008993 orphanet_rare diseases +MONDO:0008993 otar diseases +MONDO:0008993 rare diseases +MONDO:0008994 gard_rare diseases +MONDO:0008994 rare diseases +MONDO:0008995 gard_rare diseases +MONDO:0008995 nord_rare diseases +MONDO:0008995 ordo_disorder diseases +MONDO:0008995 ordo_malformation_syndrome diseases +MONDO:0008995 orphanet_rare diseases +MONDO:0008995 otar diseases +MONDO:0008995 rare diseases +MONDO:0008998 gard_rare diseases +MONDO:0008998 nord_rare diseases +MONDO:0008998 ordo_subtype_of_a_disorder diseases +MONDO:0008998 otar diseases +MONDO:0008998 rare diseases +MONDO:0008999 clingen diseases +MONDO:0008999 gard_rare diseases +MONDO:0008999 nord_rare diseases +MONDO:0008999 ordo_disorder diseases +MONDO:0008999 ordo_malformation_syndrome diseases +MONDO:0008999 orphanet_rare diseases +MONDO:0008999 otar diseases +MONDO:0008999 rare diseases +MONDO:0009000 gard_rare diseases +MONDO:0009000 nord_rare diseases +MONDO:0009000 ordo_disorder diseases +MONDO:0009000 orphanet_rare diseases +MONDO:0009000 otar diseases +MONDO:0009000 rare diseases +MONDO:0009001 gard_rare diseases +MONDO:0009001 ordo_disorder diseases +MONDO:0009001 ordo_malformation_syndrome diseases +MONDO:0009001 orphanet_rare diseases +MONDO:0009001 otar diseases +MONDO:0009001 rare diseases +MONDO:0009003 gard_rare diseases +MONDO:0009003 nord_rare diseases +MONDO:0009003 rare diseases +MONDO:0009005 gard_rare diseases +MONDO:0009005 rare diseases +MONDO:0009006 gard_rare diseases +MONDO:0009006 rare diseases +MONDO:0009007 clingen diseases +MONDO:0009007 gard_rare diseases +MONDO:0009007 nord_rare diseases +MONDO:0009007 ordo_disorder diseases +MONDO:0009007 ordo_malformation_syndrome diseases +MONDO:0009007 orphanet_rare diseases +MONDO:0009007 otar diseases +MONDO:0009007 rare diseases +MONDO:0009008 gard_rare diseases +MONDO:0009008 nord_rare diseases +MONDO:0009008 ordo_disorder diseases +MONDO:0009008 ordo_malformation_syndrome diseases +MONDO:0009008 orphanet_rare diseases +MONDO:0009008 otar diseases +MONDO:0009008 rare diseases +MONDO:0009009 clingen diseases +MONDO:0009009 gard_rare diseases +MONDO:0009009 nord_rare diseases +MONDO:0009009 ordo_disorder diseases +MONDO:0009009 orphanet_rare diseases +MONDO:0009009 otar diseases +MONDO:0009009 rare diseases +MONDO:0009010 gard_rare diseases +MONDO:0009010 nord_rare diseases +MONDO:0009010 ordo_disorder diseases +MONDO:0009010 ordo_morphological_anomaly diseases +MONDO:0009010 orphanet_rare diseases +MONDO:0009010 rare diseases +MONDO:0009012 gard_rare diseases +MONDO:0009012 nord_rare diseases +MONDO:0009012 ordo_disorder diseases +MONDO:0009012 ordo_malformation_syndrome diseases +MONDO:0009012 orphanet_rare diseases +MONDO:0009012 otar diseases +MONDO:0009012 rare diseases +MONDO:0009014 gard_rare diseases +MONDO:0009014 rare diseases +MONDO:0009015 gard_rare diseases +MONDO:0009015 nord_rare diseases +MONDO:0009015 ordo_disorder diseases +MONDO:0009015 ordo_malformation_syndrome diseases +MONDO:0009015 orphanet_rare diseases +MONDO:0009015 otar diseases +MONDO:0009015 rare diseases +MONDO:0009016 gard_rare diseases +MONDO:0009016 nord_rare diseases +MONDO:0009016 rare diseases +MONDO:0009018 gard_rare diseases +MONDO:0009018 ordo_disorder diseases +MONDO:0009018 orphanet_rare diseases +MONDO:0009018 rare diseases +MONDO:0009019 gard_rare diseases +MONDO:0009019 nord_rare diseases +MONDO:0009019 ordo_disorder diseases +MONDO:0009019 orphanet_rare diseases +MONDO:0009019 otar diseases +MONDO:0009019 rare diseases +MONDO:0009020 gard_rare diseases +MONDO:0009020 nord_rare diseases +MONDO:0009020 ordo_disorder diseases +MONDO:0009020 orphanet_rare diseases +MONDO:0009020 otar diseases +MONDO:0009020 rare diseases +MONDO:0009021 gard_rare diseases +MONDO:0009021 nord_rare diseases +MONDO:0009021 ordo_disorder diseases +MONDO:0009021 ordo_malformation_syndrome diseases +MONDO:0009021 orphanet_rare diseases +MONDO:0009021 otar diseases +MONDO:0009021 rare diseases +MONDO:0009024 gard_rare diseases +MONDO:0009024 ordo_disorder diseases +MONDO:0009024 ordo_malformation_syndrome diseases +MONDO:0009024 orphanet_rare diseases +MONDO:0009024 otar diseases +MONDO:0009024 rare diseases +MONDO:0009025 gard_rare diseases +MONDO:0009025 nord_rare diseases +MONDO:0009025 ordo_disorder diseases +MONDO:0009025 orphanet_rare diseases +MONDO:0009025 otar diseases +MONDO:0009025 rare diseases +MONDO:0009026 clingen diseases +MONDO:0009026 gard_rare diseases +MONDO:0009026 nord_rare diseases +MONDO:0009026 ordo_disorder diseases +MONDO:0009026 ordo_malformation_syndrome diseases +MONDO:0009026 orphanet_rare diseases +MONDO:0009026 otar diseases +MONDO:0009026 rare diseases +MONDO:0009028 gard_rare diseases +MONDO:0009028 nord_rare diseases +MONDO:0009028 ordo_disorder diseases +MONDO:0009028 ordo_malformation_syndrome diseases +MONDO:0009028 orphanet_rare diseases +MONDO:0009028 otar diseases +MONDO:0009028 rare diseases +MONDO:0009031 gard_rare diseases +MONDO:0009031 nord_rare diseases +MONDO:0009031 ordo_disorder diseases +MONDO:0009031 ordo_malformation_syndrome diseases +MONDO:0009031 orphanet_rare diseases +MONDO:0009031 otar diseases +MONDO:0009031 rare diseases +MONDO:0009032 gard_rare diseases +MONDO:0009032 nord_rare diseases +MONDO:0009032 ordo_disorder diseases +MONDO:0009032 ordo_malformation_syndrome diseases +MONDO:0009032 orphanet_rare diseases +MONDO:0009032 otar diseases +MONDO:0009032 rare diseases +MONDO:0009033 gard_rare diseases +MONDO:0009033 nord_rare diseases +MONDO:0009033 ordo_disorder diseases +MONDO:0009033 ordo_malformation_syndrome diseases +MONDO:0009033 orphanet_rare diseases +MONDO:0009033 otar diseases +MONDO:0009033 rare diseases +MONDO:0009034 gard_rare diseases +MONDO:0009034 nord_rare diseases +MONDO:0009034 ordo_disorder diseases +MONDO:0009034 ordo_malformation_syndrome diseases +MONDO:0009034 orphanet_rare diseases +MONDO:0009034 otar diseases +MONDO:0009034 rare diseases +MONDO:0009035 gard_rare diseases +MONDO:0009035 nord_rare diseases +MONDO:0009035 rare diseases +MONDO:0009036 gard_rare diseases +MONDO:0009036 nord_rare diseases +MONDO:0009036 ordo_disorder diseases +MONDO:0009036 ordo_malformation_syndrome diseases +MONDO:0009036 orphanet_rare diseases +MONDO:0009036 otar diseases +MONDO:0009036 rare diseases +MONDO:0009038 gard_rare diseases +MONDO:0009038 ordo_malformation_syndrome diseases +MONDO:0009038 otar diseases +MONDO:0009038 rare diseases +MONDO:0009039 gard_rare diseases +MONDO:0009039 nord_rare diseases +MONDO:0009039 ordo_disorder diseases +MONDO:0009039 ordo_malformation_syndrome diseases +MONDO:0009039 orphanet_rare diseases +MONDO:0009039 otar diseases +MONDO:0009039 rare diseases +MONDO:0009042 gard_rare diseases +MONDO:0009042 nord_rare diseases +MONDO:0009042 ordo_disorder diseases +MONDO:0009042 ordo_malformation_syndrome diseases +MONDO:0009042 orphanet_rare diseases +MONDO:0009042 otar diseases +MONDO:0009042 rare diseases +MONDO:0009043 gard_rare diseases +MONDO:0009043 nord_rare diseases +MONDO:0009043 otar diseases +MONDO:0009043 rare diseases +MONDO:0009044 gard_rare diseases +MONDO:0009044 nord_rare diseases +MONDO:0009044 ordo_disorder diseases +MONDO:0009044 orphanet_rare diseases +MONDO:0009044 otar diseases +MONDO:0009044 rare diseases +MONDO:0009045 gard_rare diseases +MONDO:0009045 ordo_disorder diseases +MONDO:0009045 ordo_malformation_syndrome diseases +MONDO:0009045 orphanet_rare diseases +MONDO:0009045 otar diseases +MONDO:0009045 rare diseases +MONDO:0009046 clingen diseases +MONDO:0009046 gard_rare diseases +MONDO:0009046 nord_rare diseases +MONDO:0009046 ordo_disorder diseases +MONDO:0009046 ordo_malformation_syndrome diseases +MONDO:0009046 orphanet_rare diseases +MONDO:0009046 otar diseases +MONDO:0009046 prototype_pattern diseases +MONDO:0009046 rare diseases +MONDO:0009047 otar diseases +MONDO:0009049 gard_rare diseases +MONDO:0009049 nord_rare diseases +MONDO:0009049 ordo_disorder diseases +MONDO:0009049 orphanet_rare diseases +MONDO:0009049 otar diseases +MONDO:0009049 prototype_pattern diseases +MONDO:0009049 rare diseases +MONDO:0009050 gard_rare diseases +MONDO:0009050 nord_rare diseases +MONDO:0009050 ordo_disorder diseases +MONDO:0009050 orphanet_rare diseases +MONDO:0009050 rare diseases +MONDO:0009051 gard_rare diseases +MONDO:0009051 ordo_disorder diseases +MONDO:0009051 orphanet_rare diseases +MONDO:0009051 rare diseases +MONDO:0009052 gard_rare diseases +MONDO:0009052 nord_rare diseases +MONDO:0009052 rare diseases +MONDO:0009053 gard_rare diseases +MONDO:0009053 nord_rare diseases +MONDO:0009053 ordo_etiological_subtype diseases +MONDO:0009053 ordo_subtype_of_a_disorder diseases +MONDO:0009053 otar diseases +MONDO:0009053 rare diseases +MONDO:0009054 gard_rare diseases +MONDO:0009054 nord_rare diseases +MONDO:0009054 ordo_subtype_of_a_disorder diseases +MONDO:0009054 otar diseases +MONDO:0009054 rare diseases +MONDO:0009055 gard_rare diseases +MONDO:0009055 nord_rare diseases +MONDO:0009055 ordo_disorder diseases +MONDO:0009055 ordo_malformation_syndrome diseases +MONDO:0009055 orphanet_rare diseases +MONDO:0009055 rare diseases +MONDO:0009058 clingen diseases +MONDO:0009058 gard_rare diseases +MONDO:0009058 mostly_harmless diseases +MONDO:0009058 ordo_disorder diseases +MONDO:0009058 orphanet_rare diseases +MONDO:0009058 otar diseases +MONDO:0009058 rare diseases +MONDO:0009061 gard_rare diseases +MONDO:0009061 nord_rare diseases +MONDO:0009061 ordo_disorder diseases +MONDO:0009061 orphanet_rare diseases +MONDO:0009061 otar diseases +MONDO:0009061 rare diseases +MONDO:0009062 gard_rare diseases +MONDO:0009062 ordo_disorder diseases +MONDO:0009062 orphanet_rare diseases +MONDO:0009062 otar diseases +MONDO:0009062 rare diseases +MONDO:0009063 gard_rare diseases +MONDO:0009063 nord_rare diseases +MONDO:0009063 ordo_disorder diseases +MONDO:0009063 orphanet_rare diseases +MONDO:0009063 otar diseases +MONDO:0009063 rare diseases +MONDO:0009064 gard_rare diseases +MONDO:0009064 nord_rare diseases +MONDO:0009064 ordo_subtype_of_a_disorder diseases +MONDO:0009064 otar diseases +MONDO:0009064 rare diseases +MONDO:0009066 gard_rare diseases +MONDO:0009066 nord_rare diseases +MONDO:0009066 ordo_subtype_of_a_disorder diseases +MONDO:0009066 rare diseases +MONDO:0009067 clingen diseases +MONDO:0009067 gard_rare diseases +MONDO:0009067 nord_rare diseases +MONDO:0009067 ordo_disorder diseases +MONDO:0009067 orphanet_rare diseases +MONDO:0009067 otar diseases +MONDO:0009067 rare diseases +MONDO:0009068 gard_rare diseases +MONDO:0009068 nord_rare diseases +MONDO:0009068 obsoletion_candidate diseases +MONDO:0009068 ordo_disorder diseases +MONDO:0009068 orphanet_rare diseases +MONDO:0009068 otar diseases +MONDO:0009068 rare diseases +MONDO:0009069 gard_rare diseases +MONDO:0009069 nord_rare diseases +MONDO:0009069 ordo_disorder diseases +MONDO:0009069 orphanet_rare diseases +MONDO:0009069 otar diseases +MONDO:0009069 rare diseases +MONDO:0009070 gard_rare diseases +MONDO:0009070 ordo_disorder diseases +MONDO:0009070 orphanet_rare diseases +MONDO:0009070 otar diseases +MONDO:0009070 rare diseases +MONDO:0009071 gard_rare diseases +MONDO:0009071 nord_rare diseases +MONDO:0009071 ordo_disorder diseases +MONDO:0009071 ordo_malformation_syndrome diseases +MONDO:0009071 orphanet_rare diseases +MONDO:0009071 otar diseases +MONDO:0009071 rare diseases +MONDO:0009072 gard_rare diseases +MONDO:0009072 nord_rare diseases +MONDO:0009072 ordo_disorder diseases +MONDO:0009072 ordo_morphological_anomaly diseases +MONDO:0009072 orphanet_rare diseases +MONDO:0009072 otar diseases +MONDO:0009072 rare diseases +MONDO:0009073 clingen diseases +MONDO:0009073 gard_rare diseases +MONDO:0009073 nord_rare diseases +MONDO:0009073 rare diseases +MONDO:0009074 gard_rare diseases +MONDO:0009074 ordo_disorder diseases +MONDO:0009074 ordo_malformation_syndrome diseases +MONDO:0009074 orphanet_rare diseases +MONDO:0009074 rare diseases +MONDO:0009075 gard_rare diseases +MONDO:0009075 nord_rare diseases +MONDO:0009075 ordo_disorder diseases +MONDO:0009075 ordo_malformation_syndrome diseases +MONDO:0009075 orphanet_rare diseases +MONDO:0009075 otar diseases +MONDO:0009075 rare diseases +MONDO:0009076 gard_rare diseases +MONDO:0009076 nord_rare diseases +MONDO:0009076 rare diseases +MONDO:0009079 clingen diseases +MONDO:0009079 gard_rare diseases +MONDO:0009079 nord_rare diseases +MONDO:0009079 ordo_disorder diseases +MONDO:0009079 ordo_malformation_syndrome diseases +MONDO:0009079 orphanet_rare diseases +MONDO:0009079 otar diseases +MONDO:0009079 rare diseases +MONDO:0009080 gard_rare diseases +MONDO:0009080 nord_rare diseases +MONDO:0009080 ordo_disorder diseases +MONDO:0009080 ordo_malformation_syndrome diseases +MONDO:0009080 orphanet_rare diseases +MONDO:0009080 otar diseases +MONDO:0009080 rare diseases +MONDO:0009081 gard_rare diseases +MONDO:0009081 rare diseases +MONDO:0009082 clingen diseases +MONDO:0009082 gard_rare diseases +MONDO:0009082 nord_rare diseases +MONDO:0009082 ordo_disorder diseases +MONDO:0009082 orphanet_rare diseases +MONDO:0009082 otar diseases +MONDO:0009082 rare diseases +MONDO:0009083 gard_rare diseases +MONDO:0009083 nord_rare diseases +MONDO:0009083 ordo_disorder diseases +MONDO:0009083 ordo_malformation_syndrome diseases +MONDO:0009083 orphanet_rare diseases +MONDO:0009083 rare diseases +MONDO:0009084 gard_rare diseases +MONDO:0009084 ordo_disorder diseases +MONDO:0009084 ordo_malformation_syndrome diseases +MONDO:0009084 orphanet_rare diseases +MONDO:0009084 otar diseases +MONDO:0009084 rare diseases +MONDO:0009085 gard_rare diseases +MONDO:0009085 ordo_disorder diseases +MONDO:0009085 ordo_malformation_syndrome diseases +MONDO:0009085 orphanet_rare diseases +MONDO:0009085 otar diseases +MONDO:0009085 rare diseases +MONDO:0009086 gard_rare diseases +MONDO:0009086 nord_rare diseases +MONDO:0009086 ordo_disorder diseases +MONDO:0009086 orphanet_rare diseases +MONDO:0009086 otar diseases +MONDO:0009086 rare diseases +MONDO:0009089 gard_rare diseases +MONDO:0009089 ordo_disorder diseases +MONDO:0009089 ordo_malformation_syndrome diseases +MONDO:0009089 orphanet_rare diseases +MONDO:0009089 otar diseases +MONDO:0009089 rare diseases +MONDO:0009090 gard_rare diseases +MONDO:0009090 nord_rare diseases +MONDO:0009090 rare diseases +MONDO:0009091 gard_rare diseases +MONDO:0009091 nord_rare diseases +MONDO:0009091 ordo_disorder diseases +MONDO:0009091 ordo_malformation_syndrome diseases +MONDO:0009091 orphanet_rare diseases +MONDO:0009091 otar diseases +MONDO:0009091 rare diseases +MONDO:0009092 gard_rare diseases +MONDO:0009092 nord_rare diseases +MONDO:0009092 ordo_disorder diseases +MONDO:0009092 ordo_malformation_syndrome diseases +MONDO:0009092 orphanet_rare diseases +MONDO:0009092 otar diseases +MONDO:0009092 rare diseases +MONDO:0009093 gard_rare diseases +MONDO:0009093 nord_rare diseases +MONDO:0009093 ordo_disorder diseases +MONDO:0009093 orphanet_rare diseases +MONDO:0009093 rare diseases +MONDO:0009094 gard_rare diseases +MONDO:0009094 nord_rare diseases +MONDO:0009094 ordo_disorder diseases +MONDO:0009094 orphanet_rare diseases +MONDO:0009094 otar diseases +MONDO:0009094 rare diseases +MONDO:0009095 gard_rare diseases +MONDO:0009095 ordo_disorder diseases +MONDO:0009095 ordo_malformation_syndrome diseases +MONDO:0009095 orphanet_rare diseases +MONDO:0009095 otar diseases +MONDO:0009095 rare diseases +MONDO:0009097 gard_rare diseases +MONDO:0009097 nord_rare diseases +MONDO:0009097 otar diseases +MONDO:0009097 rare diseases +MONDO:0009099 gard_rare diseases +MONDO:0009099 nord_rare diseases +MONDO:0009099 ordo_disorder diseases +MONDO:0009099 orphanet_rare diseases +MONDO:0009099 rare diseases +MONDO:0009101 gard_rare diseases +MONDO:0009101 rare diseases +MONDO:0009103 gard_rare diseases +MONDO:0009103 rare diseases +MONDO:0009104 gard_rare diseases +MONDO:0009104 nord_rare diseases +MONDO:0009104 ordo_disorder diseases +MONDO:0009104 ordo_malformation_syndrome diseases +MONDO:0009104 orphanet_rare diseases +MONDO:0009104 otar diseases +MONDO:0009104 rare diseases +MONDO:0009105 gard_rare diseases +MONDO:0009105 nord_rare diseases +MONDO:0009105 ordo_disorder diseases +MONDO:0009105 orphanet_rare diseases +MONDO:0009105 otar diseases +MONDO:0009105 rare diseases +MONDO:0009106 gard_rare diseases +MONDO:0009106 nord_rare diseases +MONDO:0009106 ordo_disorder diseases +MONDO:0009106 ordo_morphological_anomaly diseases +MONDO:0009106 orphanet_rare diseases +MONDO:0009106 otar diseases +MONDO:0009106 rare diseases +MONDO:0009107 clingen diseases +MONDO:0009107 gard_rare diseases +MONDO:0009107 nord_rare diseases +MONDO:0009107 ordo_disorder diseases +MONDO:0009107 orphanet_rare diseases +MONDO:0009107 otar diseases +MONDO:0009107 rare diseases +MONDO:0009108 gard_rare diseases +MONDO:0009108 nord_rare diseases +MONDO:0009108 otar diseases +MONDO:0009108 rare diseases +MONDO:0009109 clingen diseases +MONDO:0009109 gard_rare diseases +MONDO:0009109 nord_rare diseases +MONDO:0009109 ordo_disorder diseases +MONDO:0009109 orphanet_rare diseases +MONDO:0009109 otar diseases +MONDO:0009109 rare diseases +MONDO:0009110 clingen diseases +MONDO:0009110 gard_rare diseases +MONDO:0009110 nord_rare diseases +MONDO:0009110 ordo_disorder diseases +MONDO:0009110 orphanet_rare diseases +MONDO:0009110 otar diseases +MONDO:0009110 rare diseases +MONDO:0009111 gard_rare diseases +MONDO:0009111 nord_rare diseases +MONDO:0009111 ordo_disorder diseases +MONDO:0009111 orphanet_rare diseases +MONDO:0009111 otar diseases +MONDO:0009111 rare diseases +MONDO:0009112 gard_rare diseases +MONDO:0009112 nord_rare diseases +MONDO:0009112 ordo_etiological_subtype diseases +MONDO:0009112 ordo_subtype_of_a_disorder diseases +MONDO:0009112 otar diseases +MONDO:0009112 rare diseases +MONDO:0009113 gard_rare diseases +MONDO:0009113 nord_rare diseases +MONDO:0009113 ordo_disorder diseases +MONDO:0009113 orphanet_rare diseases +MONDO:0009113 otar diseases +MONDO:0009113 rare diseases +MONDO:0009114 gard_rare diseases +MONDO:0009114 nord_rare diseases +MONDO:0009114 ordo_disorder diseases +MONDO:0009114 orphanet_rare diseases +MONDO:0009114 otar diseases +MONDO:0009114 rare diseases +MONDO:0009115 gard_rare diseases +MONDO:0009115 nord_rare diseases +MONDO:0009115 ordo_disorder diseases +MONDO:0009115 orphanet_rare diseases +MONDO:0009115 otar diseases +MONDO:0009115 rare diseases +MONDO:0009120 gard_rare diseases +MONDO:0009120 nord_rare diseases +MONDO:0009120 ordo_disorder diseases +MONDO:0009120 ordo_malformation_syndrome diseases +MONDO:0009120 orphanet_rare diseases +MONDO:0009120 rare diseases +MONDO:0009121 gard_rare diseases +MONDO:0009121 nord_rare diseases +MONDO:0009121 ordo_disorder diseases +MONDO:0009121 ordo_malformation_syndrome diseases +MONDO:0009121 orphanet_rare diseases +MONDO:0009121 otar diseases +MONDO:0009121 rare diseases +MONDO:0009123 gard_rare diseases +MONDO:0009123 nord_rare diseases +MONDO:0009123 ordo_disorder diseases +MONDO:0009123 orphanet_rare diseases +MONDO:0009123 otar diseases +MONDO:0009123 rare diseases +MONDO:0009124 gard_rare diseases +MONDO:0009124 nord_rare diseases +MONDO:0009124 ordo_disorder diseases +MONDO:0009124 ordo_malformation_syndrome diseases +MONDO:0009124 orphanet_rare diseases +MONDO:0009124 otar diseases +MONDO:0009124 rare diseases +MONDO:0009126 gard_rare diseases +MONDO:0009126 nord_rare diseases +MONDO:0009126 ordo_disorder diseases +MONDO:0009126 ordo_morphological_anomaly diseases +MONDO:0009126 orphanet_rare diseases +MONDO:0009126 otar diseases +MONDO:0009126 rare diseases +MONDO:0009130 gard_rare diseases +MONDO:0009130 nord_rare diseases +MONDO:0009130 ordo_disorder diseases +MONDO:0009130 orphanet_rare diseases +MONDO:0009130 otar diseases +MONDO:0009130 rare diseases +MONDO:0009131 gard_rare diseases +MONDO:0009131 nord_rare diseases +MONDO:0009131 ordo_disorder diseases +MONDO:0009131 orphanet_rare diseases +MONDO:0009131 otar diseases +MONDO:0009131 rare diseases +MONDO:0009133 gard_rare diseases +MONDO:0009133 nord_rare diseases +MONDO:0009133 ordo_disorder diseases +MONDO:0009133 orphanet_rare diseases +MONDO:0009133 otar diseases +MONDO:0009133 prototype_pattern diseases +MONDO:0009133 rare diseases +MONDO:0009134 gard_rare diseases +MONDO:0009134 nord_rare diseases +MONDO:0009134 ordo_disorder diseases +MONDO:0009134 orphanet_rare diseases +MONDO:0009134 otar diseases +MONDO:0009134 rare diseases +MONDO:0009135 gard_rare diseases +MONDO:0009135 nord_rare diseases +MONDO:0009135 rare diseases +MONDO:0009136 gard_rare diseases +MONDO:0009136 nord_rare diseases +MONDO:0009136 prototype_pattern diseases +MONDO:0009136 rare diseases +MONDO:0009138 gard_rare diseases +MONDO:0009138 nord_rare diseases +MONDO:0009138 ordo_disorder diseases +MONDO:0009138 ordo_malformation_syndrome diseases +MONDO:0009138 orphanet_rare diseases +MONDO:0009138 otar diseases +MONDO:0009138 rare diseases +MONDO:0009139 gard_rare diseases +MONDO:0009139 nord_rare diseases +MONDO:0009139 ordo_disorder diseases +MONDO:0009139 orphanet_rare diseases +MONDO:0009139 otar diseases +MONDO:0009139 rare diseases +MONDO:0009140 clingen diseases +MONDO:0009140 gard_rare diseases +MONDO:0009140 nord_rare diseases +MONDO:0009140 ordo_disorder diseases +MONDO:0009140 orphanet_rare diseases +MONDO:0009140 otar diseases +MONDO:0009140 rare diseases +MONDO:0009141 gard_rare diseases +MONDO:0009141 nord_rare diseases +MONDO:0009141 ordo_disorder diseases +MONDO:0009141 orphanet_rare diseases +MONDO:0009141 otar diseases +MONDO:0009141 rare diseases +MONDO:0009143 gard_rare diseases +MONDO:0009143 nord_rare diseases +MONDO:0009143 rare diseases +MONDO:0009144 gard_rare diseases +MONDO:0009144 nord_rare diseases +MONDO:0009144 ordo_disorder diseases +MONDO:0009144 ordo_morphological_anomaly diseases +MONDO:0009144 orphanet_rare diseases +MONDO:0009144 otar diseases +MONDO:0009144 rare diseases +MONDO:0009145 gard_rare diseases +MONDO:0009145 nord_rare diseases +MONDO:0009145 ordo_disorder diseases +MONDO:0009145 orphanet_rare diseases +MONDO:0009145 otar diseases +MONDO:0009145 rare diseases +MONDO:0009146 gard_rare diseases +MONDO:0009146 ordo_disorder diseases +MONDO:0009146 ordo_malformation_syndrome diseases +MONDO:0009146 orphanet_rare diseases +MONDO:0009146 otar diseases +MONDO:0009146 rare diseases +MONDO:0009147 gard_rare diseases +MONDO:0009147 nord_rare diseases +MONDO:0009147 rare diseases +MONDO:0009148 gard_rare diseases +MONDO:0009148 nord_rare diseases +MONDO:0009148 rare diseases +MONDO:0009148 speculative diseases +MONDO:0009149 gard_rare diseases +MONDO:0009149 nord_rare diseases +MONDO:0009149 ordo_disorder diseases +MONDO:0009149 ordo_malformation_syndrome diseases +MONDO:0009149 orphanet_rare diseases +MONDO:0009149 otar diseases +MONDO:0009149 rare diseases +MONDO:0009150 gard_rare diseases +MONDO:0009150 nord_rare diseases +MONDO:0009150 ordo_disorder diseases +MONDO:0009150 ordo_malformation_syndrome diseases +MONDO:0009150 orphanet_rare diseases +MONDO:0009150 otar diseases +MONDO:0009150 rare diseases +MONDO:0009151 disease_grouping diseases +MONDO:0009151 gard_rare diseases +MONDO:0009151 nord_rare diseases +MONDO:0009151 ordo_disorder diseases +MONDO:0009151 ordo_malformation_syndrome diseases +MONDO:0009151 orphanet_rare diseases +MONDO:0009151 otar diseases +MONDO:0009151 rare diseases +MONDO:0009152 gard_rare diseases +MONDO:0009152 rare diseases +MONDO:0009153 gard_rare diseases +MONDO:0009153 rare diseases +MONDO:0009154 gard_rare diseases +MONDO:0009154 nord_rare diseases +MONDO:0009154 rare diseases +MONDO:0009155 clingen diseases +MONDO:0009155 gard_rare diseases +MONDO:0009155 nord_rare diseases +MONDO:0009155 ordo_disorder diseases +MONDO:0009155 ordo_malformation_syndrome diseases +MONDO:0009155 orphanet_rare diseases +MONDO:0009155 otar diseases +MONDO:0009155 rare diseases +MONDO:0009156 gard_rare diseases +MONDO:0009156 ordo_disorder diseases +MONDO:0009156 ordo_malformation_syndrome diseases +MONDO:0009156 orphanet_rare diseases +MONDO:0009156 otar diseases +MONDO:0009156 rare diseases +MONDO:0009157 gard_rare diseases +MONDO:0009157 nord_rare diseases +MONDO:0009157 rare diseases +MONDO:0009158 gard_rare diseases +MONDO:0009158 otar diseases +MONDO:0009158 rare diseases +MONDO:0009159 clingen diseases +MONDO:0009159 gard_rare diseases +MONDO:0009159 nord_rare diseases +MONDO:0009159 ordo_disorder diseases +MONDO:0009159 orphanet_rare diseases +MONDO:0009159 otar diseases +MONDO:0009159 rare diseases +MONDO:0009161 gard_rare diseases +MONDO:0009161 nord_rare diseases +MONDO:0009161 ordo_disorder diseases +MONDO:0009161 orphanet_rare diseases +MONDO:0009161 otar diseases +MONDO:0009161 rare diseases +MONDO:0009162 gard_rare diseases +MONDO:0009162 nord_rare diseases +MONDO:0009162 ordo_disorder diseases +MONDO:0009162 ordo_malformation_syndrome diseases +MONDO:0009162 orphanet_rare diseases +MONDO:0009162 otar diseases +MONDO:0009162 rare diseases +MONDO:0009165 gard_rare diseases +MONDO:0009165 nord_rare diseases +MONDO:0009165 rare diseases +MONDO:0009166 gard_rare diseases +MONDO:0009166 nord_rare diseases +MONDO:0009166 ordo_disorder diseases +MONDO:0009166 ordo_malformation_syndrome diseases +MONDO:0009166 orphanet_rare diseases +MONDO:0009166 otar diseases +MONDO:0009166 rare diseases +MONDO:0009167 gard_rare diseases +MONDO:0009167 nord_rare diseases +MONDO:0009167 ordo_disorder diseases +MONDO:0009167 ordo_malformation_syndrome diseases +MONDO:0009167 orphanet_rare diseases +MONDO:0009167 otar diseases +MONDO:0009167 rare diseases +MONDO:0009168 gard_rare diseases +MONDO:0009168 nord_rare diseases +MONDO:0009168 ordo_disorder diseases +MONDO:0009168 ordo_malformation_syndrome diseases +MONDO:0009168 orphanet_rare diseases +MONDO:0009168 otar diseases +MONDO:0009168 rare diseases +MONDO:0009169 gard_rare diseases +MONDO:0009169 nord_rare diseases +MONDO:0009169 ordo_disorder diseases +MONDO:0009169 orphanet_rare diseases +MONDO:0009169 otar diseases +MONDO:0009169 rare diseases +MONDO:0009172 otar diseases +MONDO:0009173 gard_rare diseases +MONDO:0009173 nord_rare diseases +MONDO:0009173 ordo_disorder diseases +MONDO:0009173 orphanet_rare diseases +MONDO:0009173 otar diseases +MONDO:0009173 rare diseases +MONDO:0009174 gard_rare diseases +MONDO:0009174 nord_rare diseases +MONDO:0009174 ordo_disorder diseases +MONDO:0009174 orphanet_rare diseases +MONDO:0009174 rare diseases +MONDO:0009175 gard_rare diseases +MONDO:0009175 nord_rare diseases +MONDO:0009175 ordo_disorder diseases +MONDO:0009175 orphanet_rare diseases +MONDO:0009175 rare diseases +MONDO:0009176 gard_rare diseases +MONDO:0009176 nord_rare diseases +MONDO:0009176 ordo_disorder diseases +MONDO:0009176 orphanet_rare diseases +MONDO:0009176 otar diseases +MONDO:0009176 rare diseases +MONDO:0009177 gard_rare diseases +MONDO:0009177 nord_rare diseases +MONDO:0009177 ordo_disorder diseases +MONDO:0009177 orphanet_rare diseases +MONDO:0009177 rare diseases +MONDO:0009178 gard_rare diseases +MONDO:0009178 nord_rare diseases +MONDO:0009178 rare diseases +MONDO:0009179 clingen diseases +MONDO:0009179 gard_rare diseases +MONDO:0009179 nord_rare diseases +MONDO:0009179 ordo_disorder diseases +MONDO:0009179 orphanet_rare diseases +MONDO:0009179 otar diseases +MONDO:0009179 rare diseases +MONDO:0009180 gard_rare diseases +MONDO:0009180 nord_rare diseases +MONDO:0009180 otar diseases +MONDO:0009180 rare diseases +MONDO:0009181 gard_rare diseases +MONDO:0009181 nord_rare diseases +MONDO:0009181 ordo_disorder diseases +MONDO:0009181 orphanet_rare diseases +MONDO:0009181 otar diseases +MONDO:0009181 rare diseases +MONDO:0009182 gard_rare diseases +MONDO:0009182 nord_rare diseases +MONDO:0009182 ordo_disorder diseases +MONDO:0009182 orphanet_rare diseases +MONDO:0009182 otar diseases +MONDO:0009182 rare diseases +MONDO:0009183 gard_rare diseases +MONDO:0009183 nord_rare diseases +MONDO:0009183 ordo_disorder diseases +MONDO:0009183 orphanet_rare diseases +MONDO:0009183 otar diseases +MONDO:0009183 rare diseases +MONDO:0009185 clingen diseases +MONDO:0009185 gard_rare diseases +MONDO:0009185 nord_rare diseases +MONDO:0009185 ordo_disorder diseases +MONDO:0009185 ordo_malformation_syndrome diseases +MONDO:0009185 orphanet_rare diseases +MONDO:0009185 otar diseases +MONDO:0009185 rare diseases +MONDO:0009187 gard_rare diseases +MONDO:0009187 ordo_disorder diseases +MONDO:0009187 orphanet_rare diseases +MONDO:0009187 rare diseases +MONDO:0009188 gard_rare diseases +MONDO:0009188 ordo_disorder diseases +MONDO:0009188 orphanet_rare diseases +MONDO:0009188 otar diseases +MONDO:0009188 rare diseases +MONDO:0009189 gard_rare diseases +MONDO:0009189 nord_rare diseases +MONDO:0009189 ordo_disorder diseases +MONDO:0009189 orphanet_rare diseases +MONDO:0009189 otar diseases +MONDO:0009189 rare diseases +MONDO:0009191 gard_rare diseases +MONDO:0009191 nord_rare diseases +MONDO:0009191 ordo_disorder diseases +MONDO:0009191 orphanet_rare diseases +MONDO:0009191 otar diseases +MONDO:0009191 rare diseases +MONDO:0009192 gard_rare diseases +MONDO:0009192 nord_rare diseases +MONDO:0009192 ordo_disorder diseases +MONDO:0009192 orphanet_rare diseases +MONDO:0009192 otar diseases +MONDO:0009192 rare diseases +MONDO:0009194 gard_rare diseases +MONDO:0009194 nord_rare diseases +MONDO:0009194 ordo_disorder diseases +MONDO:0009194 orphanet_rare diseases +MONDO:0009194 rare diseases +MONDO:0009196 gard_rare diseases +MONDO:0009196 nord_rare diseases +MONDO:0009196 ordo_disorder diseases +MONDO:0009196 ordo_malformation_syndrome diseases +MONDO:0009196 orphanet_rare diseases +MONDO:0009196 otar diseases +MONDO:0009196 rare diseases +MONDO:0009197 gard_rare diseases +MONDO:0009197 nord_rare diseases +MONDO:0009197 ordo_disorder diseases +MONDO:0009197 orphanet_rare diseases +MONDO:0009197 rare diseases +MONDO:0009198 gard_rare diseases +MONDO:0009198 nord_rare diseases +MONDO:0009198 ordo_disorder diseases +MONDO:0009198 orphanet_rare diseases +MONDO:0009198 otar diseases +MONDO:0009198 rare diseases +MONDO:0009200 gard_rare diseases +MONDO:0009200 ordo_disorder diseases +MONDO:0009200 ordo_malformation_syndrome diseases +MONDO:0009200 orphanet_rare diseases +MONDO:0009200 rare diseases +MONDO:0009202 gard_rare diseases +MONDO:0009202 ordo_disorder diseases +MONDO:0009202 ordo_malformation_syndrome diseases +MONDO:0009202 orphanet_rare diseases +MONDO:0009202 rare diseases +MONDO:0009203 gard_rare diseases +MONDO:0009203 nord_rare diseases +MONDO:0009203 ordo_subtype_of_a_disorder diseases +MONDO:0009203 otar diseases +MONDO:0009203 rare diseases +MONDO:0009204 gard_rare diseases +MONDO:0009204 nord_rare diseases +MONDO:0009204 ordo_disorder diseases +MONDO:0009204 ordo_malformation_syndrome diseases +MONDO:0009204 orphanet_rare diseases +MONDO:0009204 otar diseases +MONDO:0009204 rare diseases +MONDO:0009205 gard_rare diseases +MONDO:0009205 nord_rare diseases +MONDO:0009205 ordo_disorder diseases +MONDO:0009205 ordo_malformation_syndrome diseases +MONDO:0009205 orphanet_rare diseases +MONDO:0009205 otar diseases +MONDO:0009205 rare diseases +MONDO:0009206 clingen diseases +MONDO:0009206 gard_rare diseases +MONDO:0009206 nord_rare diseases +MONDO:0009206 otar diseases +MONDO:0009206 rare diseases +MONDO:0009207 gard_rare diseases +MONDO:0009207 rare diseases +MONDO:0009209 gard_rare diseases +MONDO:0009209 nord_rare diseases +MONDO:0009209 ordo_disorder diseases +MONDO:0009209 ordo_malformation_syndrome diseases +MONDO:0009209 orphanet_rare diseases +MONDO:0009209 otar diseases +MONDO:0009209 rare diseases +MONDO:0009210 clingen diseases +MONDO:0009210 gard_rare diseases +MONDO:0009210 nord_rare diseases +MONDO:0009210 ordo_disorder diseases +MONDO:0009210 orphanet_rare diseases +MONDO:0009210 otar diseases +MONDO:0009210 rare diseases +MONDO:0009211 gard_rare diseases +MONDO:0009211 nord_rare diseases +MONDO:0009211 ordo_disorder diseases +MONDO:0009211 orphanet_rare diseases +MONDO:0009211 otar diseases +MONDO:0009211 rare diseases +MONDO:0009212 clingen diseases +MONDO:0009212 gard_rare diseases +MONDO:0009212 nord_rare diseases +MONDO:0009212 ordo_disorder diseases +MONDO:0009212 orphanet_rare diseases +MONDO:0009212 otar diseases +MONDO:0009212 rare diseases +MONDO:0009213 clingen diseases +MONDO:0009213 gard_rare diseases +MONDO:0009213 nord_rare diseases +MONDO:0009213 otar diseases +MONDO:0009213 rare diseases +MONDO:0009214 clingen diseases +MONDO:0009214 gard_rare diseases +MONDO:0009214 nord_rare diseases +MONDO:0009214 otar diseases +MONDO:0009214 rare diseases +MONDO:0009215 clingen diseases +MONDO:0009215 gard_rare diseases +MONDO:0009215 nord_rare diseases +MONDO:0009215 rare diseases +MONDO:0009216 gard_rare diseases +MONDO:0009216 nord_rare diseases +MONDO:0009216 ordo_disorder diseases +MONDO:0009216 orphanet_rare diseases +MONDO:0009216 otar diseases +MONDO:0009216 rare diseases +MONDO:0009218 gard_rare diseases +MONDO:0009218 nord_rare diseases +MONDO:0009218 ordo_disorder diseases +MONDO:0009218 orphanet_rare diseases +MONDO:0009218 otar diseases +MONDO:0009218 rare diseases +MONDO:0009219 gard_rare diseases +MONDO:0009219 rare diseases +MONDO:0009221 gard_rare diseases +MONDO:0009221 nord_rare diseases +MONDO:0009221 ordo_disorder diseases +MONDO:0009221 ordo_malformation_syndrome diseases +MONDO:0009221 orphanet_rare diseases +MONDO:0009221 otar diseases +MONDO:0009221 rare diseases +MONDO:0009222 gard_rare diseases +MONDO:0009222 nord_rare diseases +MONDO:0009222 ordo_disorder diseases +MONDO:0009222 ordo_malformation_syndrome diseases +MONDO:0009222 orphanet_rare diseases +MONDO:0009222 otar diseases +MONDO:0009222 rare diseases +MONDO:0009223 gard_rare diseases +MONDO:0009223 nord_rare diseases +MONDO:0009223 ordo_subtype_of_a_disorder diseases +MONDO:0009223 otar diseases +MONDO:0009223 rare diseases +MONDO:0009224 gard_rare diseases +MONDO:0009224 nord_rare diseases +MONDO:0009224 ordo_disorder diseases +MONDO:0009224 ordo_malformation_syndrome diseases +MONDO:0009224 orphanet_rare diseases +MONDO:0009224 rare diseases +MONDO:0009226 gard_rare diseases +MONDO:0009226 nord_rare diseases +MONDO:0009226 rare diseases +MONDO:0009227 gard_rare diseases +MONDO:0009227 nord_rare diseases +MONDO:0009227 rare diseases +MONDO:0009228 gard_rare diseases +MONDO:0009228 ordo_disorder diseases +MONDO:0009228 ordo_malformation_syndrome diseases +MONDO:0009228 orphanet_rare diseases +MONDO:0009228 otar diseases +MONDO:0009228 rare diseases +MONDO:0009229 gard_rare diseases +MONDO:0009229 nord_rare diseases +MONDO:0009229 ordo_disorder diseases +MONDO:0009229 orphanet_rare diseases +MONDO:0009229 otar diseases +MONDO:0009229 rare diseases +MONDO:0009230 gard_rare diseases +MONDO:0009230 nord_rare diseases +MONDO:0009230 rare diseases +MONDO:0009231 gard_rare diseases +MONDO:0009231 nord_rare diseases +MONDO:0009231 ordo_disorder diseases +MONDO:0009231 ordo_malformation_syndrome diseases +MONDO:0009231 orphanet_rare diseases +MONDO:0009231 otar diseases +MONDO:0009231 rare diseases +MONDO:0009232 gard_rare diseases +MONDO:0009232 nord_rare diseases +MONDO:0009232 ordo_disorder diseases +MONDO:0009232 ordo_malformation_syndrome diseases +MONDO:0009232 orphanet_rare diseases +MONDO:0009232 otar diseases +MONDO:0009232 rare diseases +MONDO:0009233 gard_rare diseases +MONDO:0009233 ordo_disorder diseases +MONDO:0009233 ordo_malformation_syndrome diseases +MONDO:0009233 orphanet_rare diseases +MONDO:0009233 otar diseases +MONDO:0009233 rare diseases +MONDO:0009234 clingen diseases +MONDO:0009234 gard_rare diseases +MONDO:0009234 nord_rare diseases +MONDO:0009234 ordo_disorder diseases +MONDO:0009234 orphanet_rare diseases +MONDO:0009234 otar diseases +MONDO:0009234 rare diseases +MONDO:0009235 gard_rare diseases +MONDO:0009235 nord_rare diseases +MONDO:0009235 ordo_disorder diseases +MONDO:0009235 orphanet_rare diseases +MONDO:0009235 otar diseases +MONDO:0009235 rare diseases +MONDO:0009236 gard_rare diseases +MONDO:0009236 nord_rare diseases +MONDO:0009236 ordo_disorder diseases +MONDO:0009236 ordo_malformation_syndrome diseases +MONDO:0009236 orphanet_rare diseases +MONDO:0009236 rare diseases +MONDO:0009237 otar diseases +MONDO:0009238 gard_rare diseases +MONDO:0009238 nord_rare diseases +MONDO:0009238 ordo_disorder diseases +MONDO:0009238 orphanet_rare diseases +MONDO:0009238 otar diseases +MONDO:0009238 rare diseases +MONDO:0009239 gard_rare diseases +MONDO:0009239 nord_rare diseases +MONDO:0009239 ordo_disorder diseases +MONDO:0009239 orphanet_rare diseases +MONDO:0009239 otar diseases +MONDO:0009239 rare diseases +MONDO:0009240 gard_rare diseases +MONDO:0009240 nord_rare diseases +MONDO:0009240 ordo_disorder diseases +MONDO:0009240 orphanet_rare diseases +MONDO:0009240 otar diseases +MONDO:0009240 rare diseases +MONDO:0009241 gard_rare diseases +MONDO:0009241 nord_rare diseases +MONDO:0009241 ordo_disorder diseases +MONDO:0009241 ordo_malformation_syndrome diseases +MONDO:0009241 orphanet_rare diseases +MONDO:0009241 otar diseases +MONDO:0009241 rare diseases +MONDO:0009242 gard_rare diseases +MONDO:0009242 nord_rare diseases +MONDO:0009242 ordo_disorder diseases +MONDO:0009242 orphanet_rare diseases +MONDO:0009242 otar diseases +MONDO:0009242 prototype_pattern diseases +MONDO:0009242 rare diseases +MONDO:0009247 gard_rare diseases +MONDO:0009247 nord_rare diseases +MONDO:0009247 ordo_disorder diseases +MONDO:0009247 ordo_malformation_syndrome diseases +MONDO:0009247 orphanet_rare diseases +MONDO:0009247 otar diseases +MONDO:0009247 rare diseases +MONDO:0009249 gard_rare diseases +MONDO:0009249 nord_rare diseases +MONDO:0009249 ordo_disorder diseases +MONDO:0009249 orphanet_rare diseases +MONDO:0009249 otar diseases +MONDO:0009249 rare diseases +MONDO:0009251 gard_rare diseases +MONDO:0009251 ordo_disorder diseases +MONDO:0009251 orphanet_rare diseases +MONDO:0009251 otar diseases +MONDO:0009251 rare diseases +MONDO:0009252 gard_rare diseases +MONDO:0009252 nord_rare diseases +MONDO:0009252 ordo_disorder diseases +MONDO:0009252 orphanet_rare diseases +MONDO:0009252 otar diseases +MONDO:0009252 rare diseases +MONDO:0009253 gard_rare diseases +MONDO:0009253 nord_rare diseases +MONDO:0009253 ordo_disorder diseases +MONDO:0009253 ordo_malformation_syndrome diseases +MONDO:0009253 orphanet_rare diseases +MONDO:0009253 otar diseases +MONDO:0009253 rare diseases +MONDO:0009254 clingen diseases +MONDO:0009254 gard_rare diseases +MONDO:0009254 nord_rare diseases +MONDO:0009254 ordo_disorder diseases +MONDO:0009254 orphanet_rare diseases +MONDO:0009254 otar diseases +MONDO:0009254 rare diseases +MONDO:0009255 clingen diseases +MONDO:0009255 gard_rare diseases +MONDO:0009255 nord_rare diseases +MONDO:0009255 ordo_disorder diseases +MONDO:0009255 orphanet_rare diseases +MONDO:0009255 otar diseases +MONDO:0009255 rare diseases +MONDO:0009257 clingen diseases +MONDO:0009257 gard_rare diseases +MONDO:0009257 nord_rare diseases +MONDO:0009257 ordo_disorder diseases +MONDO:0009257 orphanet_rare diseases +MONDO:0009257 otar diseases +MONDO:0009257 rare diseases +MONDO:0009258 gard_rare diseases +MONDO:0009258 nord_rare diseases +MONDO:0009258 ordo_disorder diseases +MONDO:0009258 orphanet_rare diseases +MONDO:0009258 otar diseases +MONDO:0009258 rare diseases +MONDO:0009259 gard_rare diseases +MONDO:0009259 nord_rare diseases +MONDO:0009259 ordo_disorder diseases +MONDO:0009259 orphanet_rare diseases +MONDO:0009259 otar diseases +MONDO:0009259 rare diseases +MONDO:0009260 gard_rare diseases +MONDO:0009260 nord_rare diseases +MONDO:0009260 ordo_subtype_of_a_disorder diseases +MONDO:0009260 otar diseases +MONDO:0009260 rare diseases +MONDO:0009261 gard_rare diseases +MONDO:0009261 nord_rare diseases +MONDO:0009261 ordo_subtype_of_a_disorder diseases +MONDO:0009261 otar diseases +MONDO:0009261 rare diseases +MONDO:0009262 gard_rare diseases +MONDO:0009262 nord_rare diseases +MONDO:0009262 ordo_subtype_of_a_disorder diseases +MONDO:0009262 otar diseases +MONDO:0009262 rare diseases +MONDO:0009263 gard_rare diseases +MONDO:0009263 nord_rare diseases +MONDO:0009263 ordo_disorder diseases +MONDO:0009263 ordo_malformation_syndrome diseases +MONDO:0009263 orphanet_rare diseases +MONDO:0009263 otar diseases +MONDO:0009263 rare diseases +MONDO:0009264 gard_rare diseases +MONDO:0009264 nord_rare diseases +MONDO:0009264 ordo_disorder diseases +MONDO:0009264 ordo_morphological_anomaly diseases +MONDO:0009264 orphanet_rare diseases +MONDO:0009264 otar diseases +MONDO:0009264 rare diseases +MONDO:0009265 gard_rare diseases +MONDO:0009265 nord_rare diseases +MONDO:0009265 ordo_subtype_of_a_disorder diseases +MONDO:0009265 otar diseases +MONDO:0009265 rare diseases +MONDO:0009266 gard_rare diseases +MONDO:0009266 nord_rare diseases +MONDO:0009266 ordo_subtype_of_a_disorder diseases +MONDO:0009266 otar diseases +MONDO:0009266 rare diseases +MONDO:0009267 gard_rare diseases +MONDO:0009267 nord_rare diseases +MONDO:0009267 ordo_subtype_of_a_disorder diseases +MONDO:0009267 otar diseases +MONDO:0009267 rare diseases +MONDO:0009268 gard_rare diseases +MONDO:0009268 nord_rare diseases +MONDO:0009268 ordo_subtype_of_a_disorder diseases +MONDO:0009268 otar diseases +MONDO:0009268 rare diseases +MONDO:0009269 gard_rare diseases +MONDO:0009269 nord_rare diseases +MONDO:0009269 rare diseases +MONDO:0009270 gard_rare diseases +MONDO:0009270 nord_rare diseases +MONDO:0009270 ordo_disorder diseases +MONDO:0009270 ordo_malformation_syndrome diseases +MONDO:0009270 orphanet_rare diseases +MONDO:0009270 otar diseases +MONDO:0009270 rare diseases +MONDO:0009271 gard_rare diseases +MONDO:0009271 nord_rare diseases +MONDO:0009271 ordo_disorder diseases +MONDO:0009271 ordo_malformation_syndrome diseases +MONDO:0009271 orphanet_rare diseases +MONDO:0009271 otar diseases +MONDO:0009271 rare diseases +MONDO:0009272 gard_rare diseases +MONDO:0009272 ordo_disorder diseases +MONDO:0009272 ordo_malformation_syndrome diseases +MONDO:0009272 orphanet_rare diseases +MONDO:0009272 otar diseases +MONDO:0009272 rare diseases +MONDO:0009273 gard_rare diseases +MONDO:0009273 otar diseases +MONDO:0009273 rare diseases +MONDO:0009274 clingen diseases +MONDO:0009274 gard_rare diseases +MONDO:0009274 nord_rare diseases +MONDO:0009274 ordo_disorder diseases +MONDO:0009274 ordo_malformation_syndrome diseases +MONDO:0009274 orphanet_rare diseases +MONDO:0009274 otar diseases +MONDO:0009274 rare diseases +MONDO:0009275 gard_rare diseases +MONDO:0009275 nord_rare diseases +MONDO:0009275 ordo_disorder diseases +MONDO:0009275 orphanet_rare diseases +MONDO:0009275 otar diseases +MONDO:0009275 rare diseases +MONDO:0009276 clingen diseases +MONDO:0009276 gard_rare diseases +MONDO:0009276 nord_rare diseases +MONDO:0009276 ordo_disorder diseases +MONDO:0009276 orphanet_rare diseases +MONDO:0009276 otar diseases +MONDO:0009276 rare diseases +MONDO:0009277 gard_rare diseases +MONDO:0009277 ordo_disorder diseases +MONDO:0009277 orphanet_rare diseases +MONDO:0009277 rare diseases +MONDO:0009279 gard_rare diseases +MONDO:0009279 nord_rare diseases +MONDO:0009279 ordo_disorder diseases +MONDO:0009279 orphanet_rare diseases +MONDO:0009279 otar diseases +MONDO:0009279 rare diseases +MONDO:0009281 clingen diseases +MONDO:0009281 gard_rare diseases +MONDO:0009281 nord_rare diseases +MONDO:0009281 ordo_disorder diseases +MONDO:0009281 orphanet_rare diseases +MONDO:0009281 otar diseases +MONDO:0009281 rare diseases +MONDO:0009282 clingen diseases +MONDO:0009282 gard_rare diseases +MONDO:0009282 nord_rare diseases +MONDO:0009282 ordo_disorder diseases +MONDO:0009282 orphanet_rare diseases +MONDO:0009282 otar diseases +MONDO:0009282 rare diseases +MONDO:0009283 clingen diseases +MONDO:0009283 gard_rare diseases +MONDO:0009283 nord_rare diseases +MONDO:0009283 ordo_disorder diseases +MONDO:0009283 orphanet_rare diseases +MONDO:0009283 otar diseases +MONDO:0009283 rare diseases +MONDO:0009284 gard_rare diseases +MONDO:0009284 nord_rare diseases +MONDO:0009284 ordo_subtype_of_a_disorder diseases +MONDO:0009284 otar diseases +MONDO:0009284 rare diseases +MONDO:0009285 gard_rare diseases +MONDO:0009285 nord_rare diseases +MONDO:0009285 ordo_disorder diseases +MONDO:0009285 orphanet_rare diseases +MONDO:0009285 otar diseases +MONDO:0009285 rare diseases +MONDO:0009287 gard_rare diseases +MONDO:0009287 nord_rare diseases +MONDO:0009287 ordo_subtype_of_a_disorder diseases +MONDO:0009287 otar diseases +MONDO:0009287 rare diseases +MONDO:0009288 gard_rare diseases +MONDO:0009288 nord_rare diseases +MONDO:0009288 ordo_subtype_of_a_disorder diseases +MONDO:0009288 otar diseases +MONDO:0009288 rare diseases +MONDO:0009290 clingen diseases +MONDO:0009290 gard_rare diseases +MONDO:0009290 nord_rare diseases +MONDO:0009290 ordo_disorder diseases +MONDO:0009290 orphanet_rare diseases +MONDO:0009290 otar diseases +MONDO:0009290 rare diseases +MONDO:0009291 clingen diseases +MONDO:0009291 gard_rare diseases +MONDO:0009291 ordo_disorder diseases +MONDO:0009291 orphanet_rare diseases +MONDO:0009291 otar diseases +MONDO:0009291 rare diseases +MONDO:0009292 clingen diseases +MONDO:0009292 gard_rare diseases +MONDO:0009292 nord_rare diseases +MONDO:0009292 ordo_disorder diseases +MONDO:0009292 orphanet_rare diseases +MONDO:0009292 otar diseases +MONDO:0009292 rare diseases +MONDO:0009293 gard_rare diseases +MONDO:0009293 nord_rare diseases +MONDO:0009293 ordo_disorder diseases +MONDO:0009293 orphanet_rare diseases +MONDO:0009293 otar diseases +MONDO:0009293 rare diseases +MONDO:0009294 gard_rare diseases +MONDO:0009294 nord_rare diseases +MONDO:0009294 ordo_disorder diseases +MONDO:0009294 orphanet_rare diseases +MONDO:0009294 otar diseases +MONDO:0009294 rare diseases +MONDO:0009295 gard_rare diseases +MONDO:0009295 nord_rare diseases +MONDO:0009295 ordo_disorder diseases +MONDO:0009295 orphanet_rare diseases +MONDO:0009295 otar diseases +MONDO:0009295 rare diseases +MONDO:0009296 gard_rare diseases +MONDO:0009296 rare diseases +MONDO:0009297 gard_rare diseases +MONDO:0009297 nord_rare diseases +MONDO:0009297 ordo_disorder diseases +MONDO:0009297 orphanet_rare diseases +MONDO:0009297 otar diseases +MONDO:0009297 rare diseases +MONDO:0009299 gard_rare diseases +MONDO:0009299 nord_rare diseases +MONDO:0009299 ordo_disorder diseases +MONDO:0009299 ordo_malformation_syndrome diseases +MONDO:0009299 orphanet_rare diseases +MONDO:0009299 otar diseases +MONDO:0009299 rare diseases +MONDO:0009300 gard_rare diseases +MONDO:0009300 nord_rare diseases +MONDO:0009300 ordo_subtype_of_a_disorder diseases +MONDO:0009300 rare diseases +MONDO:0009301 gard_rare diseases +MONDO:0009301 nord_rare diseases +MONDO:0009301 rare diseases +MONDO:0009302 gard_rare diseases +MONDO:0009302 nord_rare diseases +MONDO:0009302 ordo_disorder diseases +MONDO:0009302 ordo_malformation_syndrome diseases +MONDO:0009302 orphanet_rare diseases +MONDO:0009302 otar diseases +MONDO:0009302 rare diseases +MONDO:0009303 gard_rare diseases +MONDO:0009303 nord_rare diseases +MONDO:0009303 ordo_disorder diseases +MONDO:0009303 orphanet_rare diseases +MONDO:0009303 otar diseases +MONDO:0009303 rare diseases +MONDO:0009305 otar diseases +MONDO:0009306 gard_rare diseases +MONDO:0009306 nord_rare diseases +MONDO:0009306 ordo_disorder diseases +MONDO:0009306 orphanet_rare diseases +MONDO:0009306 otar diseases +MONDO:0009306 rare diseases +MONDO:0009307 gard_rare diseases +MONDO:0009307 rare diseases +MONDO:0009308 gard_rare diseases +MONDO:0009308 nord_rare diseases +MONDO:0009308 rare diseases +MONDO:0009309 gard_rare diseases +MONDO:0009309 nord_rare diseases +MONDO:0009309 rare diseases +MONDO:0009310 gard_rare diseases +MONDO:0009310 nord_rare diseases +MONDO:0009310 rare diseases +MONDO:0009312 gard_rare diseases +MONDO:0009312 nord_rare diseases +MONDO:0009312 ordo_disorder diseases +MONDO:0009312 orphanet_rare diseases +MONDO:0009312 otar diseases +MONDO:0009312 rare diseases +MONDO:0009313 gard_rare diseases +MONDO:0009313 nord_rare diseases +MONDO:0009313 ordo_disorder diseases +MONDO:0009313 ordo_malformation_syndrome diseases +MONDO:0009313 orphanet_rare diseases +MONDO:0009313 rare diseases +MONDO:0009315 clingen diseases +MONDO:0009315 gard_rare diseases +MONDO:0009315 nord_rare diseases +MONDO:0009315 ordo_disorder diseases +MONDO:0009315 orphanet_rare diseases +MONDO:0009315 otar diseases +MONDO:0009315 rare diseases +MONDO:0009318 gard_rare diseases +MONDO:0009318 nord_rare diseases +MONDO:0009318 ordo_disorder diseases +MONDO:0009318 ordo_malformation_syndrome diseases +MONDO:0009318 orphanet_rare diseases +MONDO:0009318 otar diseases +MONDO:0009318 rare diseases +MONDO:0009319 gard_rare diseases +MONDO:0009319 nord_rare diseases +MONDO:0009319 ordo_disorder diseases +MONDO:0009319 orphanet_rare diseases +MONDO:0009319 otar diseases +MONDO:0009319 rare diseases +MONDO:0009320 gard_rare diseases +MONDO:0009320 nord_rare diseases +MONDO:0009320 ordo_disorder diseases +MONDO:0009320 ordo_malformation_syndrome diseases +MONDO:0009320 orphanet_rare diseases +MONDO:0009320 otar diseases +MONDO:0009320 rare diseases +MONDO:0009321 gard_rare diseases +MONDO:0009321 ordo_disorder diseases +MONDO:0009321 ordo_malformation_syndrome diseases +MONDO:0009321 orphanet_rare diseases +MONDO:0009321 otar diseases +MONDO:0009321 rare diseases +MONDO:0009324 clingen diseases +MONDO:0009324 gard_rare diseases +MONDO:0009324 nord_rare diseases +MONDO:0009324 ordo_disorder diseases +MONDO:0009324 orphanet_rare diseases +MONDO:0009324 otar diseases +MONDO:0009324 rare diseases +MONDO:0009326 gard_rare diseases +MONDO:0009326 mondo_rare diseases +MONDO:0009326 nord_rare diseases +MONDO:0009326 ordo_disorder diseases +MONDO:0009326 orphanet_rare diseases +MONDO:0009326 otar diseases +MONDO:0009326 rare diseases +MONDO:0009327 gard_rare diseases +MONDO:0009327 nord_rare diseases +MONDO:0009327 rare diseases +MONDO:0009329 gard_rare diseases +MONDO:0009329 nord_rare diseases +MONDO:0009329 ordo_disorder diseases +MONDO:0009329 orphanet_rare diseases +MONDO:0009329 otar diseases +MONDO:0009329 rare diseases +MONDO:0009330 gard_rare diseases +MONDO:0009330 rare diseases +MONDO:0009331 gard_rare diseases +MONDO:0009331 nord_rare diseases +MONDO:0009331 ordo_disorder diseases +MONDO:0009331 ordo_morphological_anomaly diseases +MONDO:0009331 orphanet_rare diseases +MONDO:0009331 otar diseases +MONDO:0009331 rare diseases +MONDO:0009332 gard_rare diseases +MONDO:0009332 rare diseases +MONDO:0009333 gard_rare diseases +MONDO:0009333 nord_rare diseases +MONDO:0009333 ordo_disorder diseases +MONDO:0009333 ordo_malformation_syndrome diseases +MONDO:0009333 orphanet_rare diseases +MONDO:0009333 otar diseases +MONDO:0009333 rare diseases +MONDO:0009334 gard_rare diseases +MONDO:0009334 rare diseases +MONDO:0009336 gard_rare diseases +MONDO:0009336 rare diseases +MONDO:0009337 gard_rare diseases +MONDO:0009337 nord_rare diseases +MONDO:0009337 rare diseases +MONDO:0009338 gard_rare diseases +MONDO:0009338 nord_rare diseases +MONDO:0009338 ordo_disorder diseases +MONDO:0009338 orphanet_rare diseases +MONDO:0009338 otar diseases +MONDO:0009338 rare diseases +MONDO:0009339 gard_rare diseases +MONDO:0009339 nord_rare diseases +MONDO:0009339 ordo_disorder diseases +MONDO:0009339 orphanet_rare diseases +MONDO:0009339 otar diseases +MONDO:0009339 rare diseases +MONDO:0009340 gard_rare diseases +MONDO:0009340 nord_rare diseases +MONDO:0009340 ordo_disorder diseases +MONDO:0009340 orphanet_rare diseases +MONDO:0009340 otar diseases +MONDO:0009340 rare diseases +MONDO:0009341 clingen diseases +MONDO:0009341 gard_rare diseases +MONDO:0009341 nord_rare diseases +MONDO:0009341 ordo_disorder diseases +MONDO:0009341 ordo_malformation_syndrome diseases +MONDO:0009341 orphanet_rare diseases +MONDO:0009341 otar diseases +MONDO:0009341 rare diseases +MONDO:0009342 gard_rare diseases +MONDO:0009342 ordo_disorder diseases +MONDO:0009342 ordo_malformation_syndrome diseases +MONDO:0009342 orphanet_rare diseases +MONDO:0009342 otar diseases +MONDO:0009342 rare diseases +MONDO:0009344 gard_rare diseases +MONDO:0009344 ordo_disorder diseases +MONDO:0009344 ordo_malformation_syndrome diseases +MONDO:0009344 orphanet_rare diseases +MONDO:0009344 otar diseases +MONDO:0009344 rare diseases +MONDO:0009345 clingen diseases +MONDO:0009345 gard_rare diseases +MONDO:0009345 mostly_harmless diseases +MONDO:0009345 nord_rare diseases +MONDO:0009345 ordo_disorder diseases +MONDO:0009345 orphanet_rare diseases +MONDO:0009345 otar diseases +MONDO:0009345 rare diseases +MONDO:0009346 gard_rare diseases +MONDO:0009346 nord_rare diseases +MONDO:0009346 ordo_disorder diseases +MONDO:0009346 orphanet_rare diseases +MONDO:0009346 otar diseases +MONDO:0009346 rare diseases +MONDO:0009348 gard_rare diseases +MONDO:0009348 nord_rare diseases +MONDO:0009348 ordo_disorder diseases +MONDO:0009348 orphanet_rare diseases +MONDO:0009348 otar diseases +MONDO:0009348 rare diseases +MONDO:0009349 gard_rare diseases +MONDO:0009349 nord_rare diseases +MONDO:0009349 ordo_morphological_anomaly diseases +MONDO:0009349 rare diseases +MONDO:0009350 gard_rare diseases +MONDO:0009350 ordo_disorder diseases +MONDO:0009350 ordo_malformation_syndrome diseases +MONDO:0009350 orphanet_rare diseases +MONDO:0009350 otar diseases +MONDO:0009350 rare diseases +MONDO:0009351 gard_rare diseases +MONDO:0009351 otar diseases +MONDO:0009351 rare diseases +MONDO:0009352 clingen diseases +MONDO:0009352 gard_rare diseases +MONDO:0009352 nord_rare diseases +MONDO:0009352 ordo_disorder diseases +MONDO:0009352 orphanet_rare diseases +MONDO:0009352 otar diseases +MONDO:0009352 rare diseases +MONDO:0009353 clingen diseases +MONDO:0009353 gard_rare diseases +MONDO:0009353 nord_rare diseases +MONDO:0009353 ordo_disorder diseases +MONDO:0009353 orphanet_rare diseases +MONDO:0009353 otar diseases +MONDO:0009353 rare diseases +MONDO:0009354 clingen diseases +MONDO:0009354 gard_rare diseases +MONDO:0009354 nord_rare diseases +MONDO:0009354 ordo_subtype_of_a_disorder diseases +MONDO:0009354 otar diseases +MONDO:0009354 rare diseases +MONDO:0009356 gard_rare diseases +MONDO:0009356 nord_rare diseases +MONDO:0009356 rare diseases +MONDO:0009357 gard_rare diseases +MONDO:0009357 rare diseases +MONDO:0009359 gard_rare diseases +MONDO:0009359 nord_rare diseases +MONDO:0009359 ordo_disorder diseases +MONDO:0009359 ordo_malformation_syndrome diseases +MONDO:0009359 orphanet_rare diseases +MONDO:0009359 otar diseases +MONDO:0009359 rare diseases +MONDO:0009360 gard_rare diseases +MONDO:0009360 nord_rare diseases +MONDO:0009360 rare diseases +MONDO:0009361 gard_rare diseases +MONDO:0009361 nord_rare diseases +MONDO:0009361 rare diseases +MONDO:0009362 gard_rare diseases +MONDO:0009362 ordo_disorder diseases +MONDO:0009362 ordo_malformation_syndrome diseases +MONDO:0009362 orphanet_rare diseases +MONDO:0009362 otar diseases +MONDO:0009362 rare diseases +MONDO:0009363 gard_rare diseases +MONDO:0009363 ordo_disorder diseases +MONDO:0009363 ordo_malformation_syndrome diseases +MONDO:0009363 orphanet_rare diseases +MONDO:0009363 otar diseases +MONDO:0009363 rare diseases +MONDO:0009364 gard_rare diseases +MONDO:0009364 nord_rare diseases +MONDO:0009364 otar diseases +MONDO:0009364 rare diseases +MONDO:0009365 gard_rare diseases +MONDO:0009365 nord_rare diseases +MONDO:0009365 rare diseases +MONDO:0009366 clingen diseases +MONDO:0009366 otar diseases +MONDO:0009367 gard_rare diseases +MONDO:0009367 nord_rare diseases +MONDO:0009367 ordo_disorder diseases +MONDO:0009367 ordo_malformation_syndrome diseases +MONDO:0009367 orphanet_rare diseases +MONDO:0009367 otar diseases +MONDO:0009367 rare diseases +MONDO:0009368 gard_rare diseases +MONDO:0009368 rare diseases +MONDO:0009369 gard_rare diseases +MONDO:0009369 nord_rare diseases +MONDO:0009369 ordo_subtype_of_a_disorder diseases +MONDO:0009369 rare diseases +MONDO:0009370 gard_rare diseases +MONDO:0009370 nord_rare diseases +MONDO:0009370 ordo_disorder diseases +MONDO:0009370 orphanet_rare diseases +MONDO:0009370 otar diseases +MONDO:0009370 rare diseases +MONDO:0009371 clingen diseases +MONDO:0009371 gard_rare diseases +MONDO:0009371 nord_rare diseases +MONDO:0009371 ordo_disorder diseases +MONDO:0009371 orphanet_rare diseases +MONDO:0009371 otar diseases +MONDO:0009371 rare diseases +MONDO:0009372 gard_rare diseases +MONDO:0009372 nord_rare diseases +MONDO:0009372 ordo_disorder diseases +MONDO:0009372 orphanet_rare diseases +MONDO:0009372 otar diseases +MONDO:0009372 rare diseases +MONDO:0009373 gard_rare diseases +MONDO:0009373 nord_rare diseases +MONDO:0009373 ordo_disorder diseases +MONDO:0009373 orphanet_rare diseases +MONDO:0009373 otar diseases +MONDO:0009373 rare diseases +MONDO:0009374 clingen diseases +MONDO:0009374 mostly_harmless diseases +MONDO:0009374 otar diseases +MONDO:0009376 clingen diseases +MONDO:0009376 gard_rare diseases +MONDO:0009376 nord_rare diseases +MONDO:0009376 ordo_disorder diseases +MONDO:0009376 orphanet_rare diseases +MONDO:0009376 otar diseases +MONDO:0009376 rare diseases +MONDO:0009377 clingen diseases +MONDO:0009377 gard_rare diseases +MONDO:0009377 nord_rare diseases +MONDO:0009377 ordo_disorder diseases +MONDO:0009377 orphanet_rare diseases +MONDO:0009377 otar diseases +MONDO:0009377 rare diseases +MONDO:0009378 gard_rare diseases +MONDO:0009378 nord_rare diseases +MONDO:0009378 ordo_disorder diseases +MONDO:0009378 orphanet_rare diseases +MONDO:0009378 otar diseases +MONDO:0009378 rare diseases +MONDO:0009379 gard_rare diseases +MONDO:0009379 nord_rare diseases +MONDO:0009379 ordo_disorder diseases +MONDO:0009379 orphanet_rare diseases +MONDO:0009379 otar diseases +MONDO:0009379 rare diseases +MONDO:0009380 gard_rare diseases +MONDO:0009380 nord_rare diseases +MONDO:0009380 ordo_disorder diseases +MONDO:0009380 orphanet_rare diseases +MONDO:0009380 otar diseases +MONDO:0009380 rare diseases +MONDO:0009381 gard_rare diseases +MONDO:0009381 rare diseases +MONDO:0009382 gard_rare diseases +MONDO:0009382 rare diseases +MONDO:0009383 gard_rare diseases +MONDO:0009383 nord_rare diseases +MONDO:0009383 ordo_disorder diseases +MONDO:0009383 orphanet_rare diseases +MONDO:0009383 otar diseases +MONDO:0009383 rare diseases +MONDO:0009384 gard_rare diseases +MONDO:0009384 otar diseases +MONDO:0009384 rare diseases +MONDO:0009387 gard_rare diseases +MONDO:0009387 nord_rare diseases +MONDO:0009387 ordo_subtype_of_a_disorder diseases +MONDO:0009387 otar diseases +MONDO:0009387 rare diseases +MONDO:0009388 clingen diseases +MONDO:0009388 gard_rare diseases +MONDO:0009388 nord_rare diseases +MONDO:0009388 ordo_disorder diseases +MONDO:0009388 orphanet_rare diseases +MONDO:0009388 otar diseases +MONDO:0009388 rare diseases +MONDO:0009389 gard_rare diseases +MONDO:0009389 rare diseases +MONDO:0009393 clingen diseases +MONDO:0009393 gard_rare diseases +MONDO:0009393 nord_rare diseases +MONDO:0009393 ordo_disorder diseases +MONDO:0009393 orphanet_rare diseases +MONDO:0009393 otar diseases +MONDO:0009393 rare diseases +MONDO:0009394 gard_rare diseases +MONDO:0009394 nord_rare diseases +MONDO:0009394 ordo_disorder diseases +MONDO:0009394 ordo_malformation_syndrome diseases +MONDO:0009394 orphanet_rare diseases +MONDO:0009394 otar diseases +MONDO:0009394 rare diseases +MONDO:0009395 gard_rare diseases +MONDO:0009395 nord_rare diseases +MONDO:0009395 ordo_disorder diseases +MONDO:0009395 ordo_malformation_syndrome diseases +MONDO:0009395 orphanet_rare diseases +MONDO:0009395 otar diseases +MONDO:0009395 rare diseases +MONDO:0009397 clingen diseases +MONDO:0009397 gard_rare diseases +MONDO:0009397 nord_rare diseases +MONDO:0009397 ordo_disorder diseases +MONDO:0009397 orphanet_rare diseases +MONDO:0009397 otar diseases +MONDO:0009397 rare diseases +MONDO:0009398 gard_rare diseases +MONDO:0009398 nord_rare diseases +MONDO:0009398 rare diseases +MONDO:0009400 clingen diseases +MONDO:0009400 gard_rare diseases +MONDO:0009400 ordo_disorder diseases +MONDO:0009400 orphanet_rare diseases +MONDO:0009400 otar diseases +MONDO:0009400 rare diseases +MONDO:0009401 clingen diseases +MONDO:0009401 gard_rare diseases +MONDO:0009401 nord_rare diseases +MONDO:0009401 ordo_disorder diseases +MONDO:0009401 orphanet_rare diseases +MONDO:0009401 otar diseases +MONDO:0009401 rare diseases +MONDO:0009402 gard_rare diseases +MONDO:0009402 nord_rare diseases +MONDO:0009402 ordo_disorder diseases +MONDO:0009402 ordo_malformation_syndrome diseases +MONDO:0009402 orphanet_rare diseases +MONDO:0009402 otar diseases +MONDO:0009402 rare diseases +MONDO:0009404 gard_rare diseases +MONDO:0009404 nord_rare diseases +MONDO:0009404 ordo_disorder diseases +MONDO:0009404 ordo_malformation_syndrome diseases +MONDO:0009404 orphanet_rare diseases +MONDO:0009404 otar diseases +MONDO:0009404 rare diseases +MONDO:0009405 gard_rare diseases +MONDO:0009405 nord_rare diseases +MONDO:0009405 ordo_disorder diseases +MONDO:0009405 orphanet_rare diseases +MONDO:0009405 otar diseases +MONDO:0009405 rare diseases +MONDO:0009406 gard_rare diseases +MONDO:0009406 nord_rare diseases +MONDO:0009406 ordo_disorder diseases +MONDO:0009406 ordo_malformation_syndrome diseases +MONDO:0009406 orphanet_rare diseases +MONDO:0009406 otar diseases +MONDO:0009406 rare diseases +MONDO:0009411 gard_rare diseases +MONDO:0009411 nord_rare diseases +MONDO:0009411 ordo_disorder diseases +MONDO:0009411 orphanet_rare diseases +MONDO:0009411 otar diseases +MONDO:0009411 rare diseases +MONDO:0009412 otar diseases +MONDO:0009413 clingen diseases +MONDO:0009413 gard_rare diseases +MONDO:0009413 nord_rare diseases +MONDO:0009413 otar diseases +MONDO:0009413 rare diseases +MONDO:0009414 gard_rare diseases +MONDO:0009414 ordo_disorder diseases +MONDO:0009414 orphanet_rare diseases +MONDO:0009414 otar diseases +MONDO:0009414 rare diseases +MONDO:0009416 gard_rare diseases +MONDO:0009416 nord_rare diseases +MONDO:0009416 ordo_disorder diseases +MONDO:0009416 orphanet_rare diseases +MONDO:0009416 otar diseases +MONDO:0009416 rare diseases +MONDO:0009417 gard_rare diseases +MONDO:0009417 ordo_disorder diseases +MONDO:0009417 ordo_malformation_syndrome diseases +MONDO:0009417 orphanet_rare diseases +MONDO:0009417 otar diseases +MONDO:0009417 rare diseases +MONDO:0009419 clingen diseases +MONDO:0009419 gard_rare diseases +MONDO:0009419 nord_rare diseases +MONDO:0009419 ordo_disorder diseases +MONDO:0009419 orphanet_rare diseases +MONDO:0009419 otar diseases +MONDO:0009419 rare diseases +MONDO:0009420 gard_rare diseases +MONDO:0009420 nord_rare diseases +MONDO:0009420 ordo_disorder diseases +MONDO:0009420 orphanet_rare diseases +MONDO:0009420 otar diseases +MONDO:0009420 rare diseases +MONDO:0009423 clingen diseases +MONDO:0009424 gard_rare diseases +MONDO:0009424 nord_rare diseases +MONDO:0009424 ordo_subtype_of_a_disorder diseases +MONDO:0009424 rare diseases +MONDO:0009425 gard_rare diseases +MONDO:0009425 nord_rare diseases +MONDO:0009425 ordo_disorder diseases +MONDO:0009425 ordo_malformation_syndrome diseases +MONDO:0009425 orphanet_rare diseases +MONDO:0009425 otar diseases +MONDO:0009425 rare diseases +MONDO:0009426 gard_rare diseases +MONDO:0009426 nord_rare diseases +MONDO:0009426 ordo_disorder diseases +MONDO:0009426 ordo_malformation_syndrome diseases +MONDO:0009426 orphanet_rare diseases +MONDO:0009426 otar diseases +MONDO:0009426 rare diseases +MONDO:0009430 gard_rare diseases +MONDO:0009430 nord_rare diseases +MONDO:0009430 rare diseases +MONDO:0009431 gard_rare diseases +MONDO:0009431 nord_rare diseases +MONDO:0009431 ordo_disorder diseases +MONDO:0009431 orphanet_rare diseases +MONDO:0009431 otar diseases +MONDO:0009431 rare diseases +MONDO:0009433 gard_rare diseases +MONDO:0009433 nord_rare diseases +MONDO:0009433 rare diseases +MONDO:0009434 gard_rare diseases +MONDO:0009434 rare diseases +MONDO:0009435 gard_rare diseases +MONDO:0009435 ordo_disorder diseases +MONDO:0009435 ordo_malformation_syndrome diseases +MONDO:0009435 orphanet_rare diseases +MONDO:0009435 rare diseases +MONDO:0009436 gard_rare diseases +MONDO:0009436 otar diseases +MONDO:0009436 rare diseases +MONDO:0009437 gard_rare diseases +MONDO:0009437 nord_rare diseases +MONDO:0009437 ordo_disorder diseases +MONDO:0009437 ordo_malformation_syndrome diseases +MONDO:0009437 orphanet_rare diseases +MONDO:0009437 otar diseases +MONDO:0009437 rare diseases +MONDO:0009438 gard_rare diseases +MONDO:0009438 rare diseases +MONDO:0009439 gard_rare diseases +MONDO:0009439 nord_rare diseases +MONDO:0009439 rare diseases +MONDO:0009440 gard_rare diseases +MONDO:0009440 nord_rare diseases +MONDO:0009440 otar diseases +MONDO:0009440 rare diseases +MONDO:0009441 gard_rare diseases +MONDO:0009441 nord_rare diseases +MONDO:0009441 rare diseases +MONDO:0009443 gard_rare diseases +MONDO:0009443 nord_rare diseases +MONDO:0009443 ordo_disorder diseases +MONDO:0009443 orphanet_rare diseases +MONDO:0009443 otar diseases +MONDO:0009443 rare diseases +MONDO:0009444 gard_rare diseases +MONDO:0009444 ordo_disorder diseases +MONDO:0009444 orphanet_rare diseases +MONDO:0009444 otar diseases +MONDO:0009444 rare diseases +MONDO:0009445 gard_rare diseases +MONDO:0009445 ordo_disorder diseases +MONDO:0009445 orphanet_rare diseases +MONDO:0009445 otar diseases +MONDO:0009445 rare diseases +MONDO:0009446 gard_rare diseases +MONDO:0009446 ordo_disorder diseases +MONDO:0009446 ordo_malformation_syndrome diseases +MONDO:0009446 orphanet_rare diseases +MONDO:0009446 otar diseases +MONDO:0009446 rare diseases +MONDO:0009448 clingen diseases +MONDO:0009448 gard_rare diseases +MONDO:0009448 nord_rare diseases +MONDO:0009448 ordo_disorder diseases +MONDO:0009448 orphanet_rare diseases +MONDO:0009448 otar diseases +MONDO:0009448 rare diseases +MONDO:0009449 gard_rare diseases +MONDO:0009449 rare diseases +MONDO:0009450 gard_rare diseases +MONDO:0009450 rare diseases +MONDO:0009451 gard_rare diseases +MONDO:0009451 nord_rare diseases +MONDO:0009451 ordo_disorder diseases +MONDO:0009451 orphanet_rare diseases +MONDO:0009451 otar diseases +MONDO:0009451 rare diseases +MONDO:0009452 gard_rare diseases +MONDO:0009452 nord_rare diseases +MONDO:0009452 ordo_disorder diseases +MONDO:0009452 ordo_malformation_syndrome diseases +MONDO:0009452 orphanet_rare diseases +MONDO:0009452 otar diseases +MONDO:0009452 rare diseases +MONDO:0009453 obsoletion_candidate diseases +MONDO:0009453 otar diseases +MONDO:0009454 clingen diseases +MONDO:0009454 gard_rare diseases +MONDO:0009454 nord_rare diseases +MONDO:0009454 rare diseases +MONDO:0009456 gard_rare diseases +MONDO:0009456 rare diseases +MONDO:0009458 clingen diseases +MONDO:0009458 gard_rare diseases +MONDO:0009458 nord_rare diseases +MONDO:0009458 ordo_disorder diseases +MONDO:0009458 orphanet_rare diseases +MONDO:0009458 otar diseases +MONDO:0009458 rare diseases +MONDO:0009459 gard_rare diseases +MONDO:0009459 nord_rare diseases +MONDO:0009459 ordo_disorder diseases +MONDO:0009459 orphanet_rare diseases +MONDO:0009459 otar diseases +MONDO:0009459 rare diseases +MONDO:0009461 gard_rare diseases +MONDO:0009461 nord_rare diseases +MONDO:0009461 ordo_subtype_of_a_disorder diseases +MONDO:0009461 otar diseases +MONDO:0009461 rare diseases +MONDO:0009464 gard_rare diseases +MONDO:0009464 rare diseases +MONDO:0009465 clingen diseases +MONDO:0009465 gard_rare diseases +MONDO:0009465 nord_rare diseases +MONDO:0009465 ordo_disorder diseases +MONDO:0009465 ordo_morphological_anomaly diseases +MONDO:0009465 orphanet_rare diseases +MONDO:0009465 otar diseases +MONDO:0009465 rare diseases +MONDO:0009467 ordo_malformation_syndrome diseases +MONDO:0009467 otar diseases +MONDO:0009468 gard_rare diseases +MONDO:0009468 nord_rare diseases +MONDO:0009468 ordo_disorder diseases +MONDO:0009468 orphanet_rare diseases +MONDO:0009468 otar diseases +MONDO:0009468 rare diseases +MONDO:0009469 gard_rare diseases +MONDO:0009469 nord_rare diseases +MONDO:0009469 ordo_subtype_of_a_disorder diseases +MONDO:0009469 otar diseases +MONDO:0009469 rare diseases +MONDO:0009470 gard_rare diseases +MONDO:0009470 nord_rare diseases +MONDO:0009470 rare diseases +MONDO:0009471 gard_rare diseases +MONDO:0009471 nord_rare diseases +MONDO:0009471 rare diseases +MONDO:0009473 gard_rare diseases +MONDO:0009473 nord_rare diseases +MONDO:0009473 ordo_disorder diseases +MONDO:0009473 ordo_malformation_syndrome diseases +MONDO:0009473 orphanet_rare diseases +MONDO:0009473 otar diseases +MONDO:0009473 rare diseases +MONDO:0009475 clingen diseases +MONDO:0009475 gard_rare diseases +MONDO:0009475 nord_rare diseases +MONDO:0009475 ordo_disorder diseases +MONDO:0009475 orphanet_rare diseases +MONDO:0009475 otar diseases +MONDO:0009475 rare diseases +MONDO:0009476 gard_rare diseases +MONDO:0009476 nord_rare diseases +MONDO:0009476 ordo_disorder diseases +MONDO:0009476 ordo_morphological_anomaly diseases +MONDO:0009476 orphanet_rare diseases +MONDO:0009476 otar diseases +MONDO:0009476 rare diseases +MONDO:0009477 gard_rare diseases +MONDO:0009477 nord_rare diseases +MONDO:0009477 ordo_disorder diseases +MONDO:0009477 ordo_malformation_syndrome diseases +MONDO:0009477 orphanet_rare diseases +MONDO:0009477 otar diseases +MONDO:0009477 rare diseases +MONDO:0009478 clingen diseases +MONDO:0009478 gard_rare diseases +MONDO:0009478 nord_rare diseases +MONDO:0009478 ordo_disorder diseases +MONDO:0009478 orphanet_rare diseases +MONDO:0009478 otar diseases +MONDO:0009478 rare diseases +MONDO:0009479 gard_rare diseases +MONDO:0009479 nord_rare diseases +MONDO:0009479 ordo_disorder diseases +MONDO:0009479 ordo_malformation_syndrome diseases +MONDO:0009479 orphanet_rare diseases +MONDO:0009479 otar diseases +MONDO:0009479 rare diseases +MONDO:0009480 gard_rare diseases +MONDO:0009480 nord_rare diseases +MONDO:0009480 ordo_disorder diseases +MONDO:0009480 orphanet_rare diseases +MONDO:0009480 otar diseases +MONDO:0009480 rare diseases +MONDO:0009482 clingen diseases +MONDO:0009482 gard_rare diseases +MONDO:0009482 rare diseases +MONDO:0009483 gard_rare diseases +MONDO:0009483 nord_rare diseases +MONDO:0009483 ordo_disorder diseases +MONDO:0009483 ordo_malformation_syndrome diseases +MONDO:0009483 orphanet_rare diseases +MONDO:0009483 otar diseases +MONDO:0009483 rare diseases +MONDO:0009484 clingen diseases +MONDO:0009484 gard_rare diseases +MONDO:0009484 nord_rare diseases +MONDO:0009484 rare diseases +MONDO:0009485 clingen diseases +MONDO:0009485 gard_rare diseases +MONDO:0009485 nord_rare diseases +MONDO:0009485 ordo_disorder diseases +MONDO:0009485 ordo_malformation_syndrome diseases +MONDO:0009485 orphanet_rare diseases +MONDO:0009485 otar diseases +MONDO:0009485 rare diseases +MONDO:0009486 gard_rare diseases +MONDO:0009486 nord_rare diseases +MONDO:0009486 ordo_etiological_subtype diseases +MONDO:0009486 ordo_subtype_of_a_disorder diseases +MONDO:0009486 otar diseases +MONDO:0009486 rare diseases +MONDO:0009489 gard_rare diseases +MONDO:0009489 nord_rare diseases +MONDO:0009489 ordo_disorder diseases +MONDO:0009489 orphanet_rare diseases +MONDO:0009489 otar diseases +MONDO:0009489 rare diseases +MONDO:0009490 gard_rare diseases +MONDO:0009490 nord_rare diseases +MONDO:0009490 ordo_disorder diseases +MONDO:0009490 orphanet_rare diseases +MONDO:0009490 otar diseases +MONDO:0009490 rare diseases +MONDO:0009491 gard_rare diseases +MONDO:0009491 nord_rare diseases +MONDO:0009491 ordo_disorder diseases +MONDO:0009491 orphanet_rare diseases +MONDO:0009491 otar diseases +MONDO:0009491 rare diseases +MONDO:0009492 gard_rare diseases +MONDO:0009492 nord_rare diseases +MONDO:0009492 ordo_disorder diseases +MONDO:0009492 orphanet_rare diseases +MONDO:0009492 otar diseases +MONDO:0009492 rare diseases +MONDO:0009493 gard_rare diseases +MONDO:0009493 nord_rare diseases +MONDO:0009493 ordo_disorder diseases +MONDO:0009493 ordo_malformation_syndrome diseases +MONDO:0009493 orphanet_rare diseases +MONDO:0009493 otar diseases +MONDO:0009493 rare diseases +MONDO:0009495 gard_rare diseases +MONDO:0009495 nord_rare diseases +MONDO:0009495 ordo_disorder diseases +MONDO:0009495 ordo_malformation_syndrome diseases +MONDO:0009495 orphanet_rare diseases +MONDO:0009495 otar diseases +MONDO:0009495 rare diseases +MONDO:0009498 gard_rare diseases +MONDO:0009498 ordo_disorder diseases +MONDO:0009498 ordo_malformation_syndrome diseases +MONDO:0009498 orphanet_rare diseases +MONDO:0009498 otar diseases +MONDO:0009498 rare diseases +MONDO:0009499 clingen diseases +MONDO:0009499 gard_rare diseases +MONDO:0009499 nord_rare diseases +MONDO:0009499 ordo_disorder diseases +MONDO:0009499 orphanet_rare diseases +MONDO:0009499 otar diseases +MONDO:0009499 rare diseases +MONDO:0009501 gard_rare diseases +MONDO:0009501 nord_rare diseases +MONDO:0009501 ordo_disorder diseases +MONDO:0009501 orphanet_rare diseases +MONDO:0009501 otar diseases +MONDO:0009501 rare diseases +MONDO:0009502 gard_rare diseases +MONDO:0009502 nord_rare diseases +MONDO:0009502 ordo_subtype_of_a_disorder diseases +MONDO:0009502 otar diseases +MONDO:0009502 rare diseases +MONDO:0009503 gard_rare diseases +MONDO:0009503 nord_rare diseases +MONDO:0009503 ordo_subtype_of_a_disorder diseases +MONDO:0009503 otar diseases +MONDO:0009503 rare diseases +MONDO:0009504 gard_rare diseases +MONDO:0009504 nord_rare diseases +MONDO:0009504 ordo_disorder diseases +MONDO:0009504 orphanet_rare diseases +MONDO:0009504 otar diseases +MONDO:0009504 rare diseases +MONDO:0009505 gard_rare diseases +MONDO:0009505 otar diseases +MONDO:0009505 rare diseases +MONDO:0009506 gard_rare diseases +MONDO:0009506 nord_rare diseases +MONDO:0009506 ordo_disorder diseases +MONDO:0009506 orphanet_rare diseases +MONDO:0009506 otar diseases +MONDO:0009506 rare diseases +MONDO:0009507 gard_rare diseases +MONDO:0009507 ordo_disorder diseases +MONDO:0009507 ordo_malformation_syndrome diseases +MONDO:0009507 orphanet_rare diseases +MONDO:0009507 otar diseases +MONDO:0009507 rare diseases +MONDO:0009509 gard_rare diseases +MONDO:0009509 nord_rare diseases +MONDO:0009509 ordo_disorder diseases +MONDO:0009509 orphanet_rare diseases +MONDO:0009509 otar diseases +MONDO:0009509 rare diseases +MONDO:0009511 gard_rare diseases +MONDO:0009511 nord_rare diseases +MONDO:0009511 ordo_disorder diseases +MONDO:0009511 ordo_malformation_syndrome diseases +MONDO:0009511 orphanet_rare diseases +MONDO:0009511 otar diseases +MONDO:0009511 rare diseases +MONDO:0009512 gard_rare diseases +MONDO:0009512 ordo_disorder diseases +MONDO:0009512 ordo_malformation_syndrome diseases +MONDO:0009512 orphanet_rare diseases +MONDO:0009512 otar diseases +MONDO:0009512 rare diseases +MONDO:0009513 gard_rare diseases +MONDO:0009513 nord_rare diseases +MONDO:0009513 ordo_disorder diseases +MONDO:0009513 orphanet_rare diseases +MONDO:0009513 otar diseases +MONDO:0009513 rare diseases +MONDO:0009514 gard_rare diseases +MONDO:0009514 nord_rare diseases +MONDO:0009514 ordo_disorder diseases +MONDO:0009514 ordo_malformation_syndrome diseases +MONDO:0009514 orphanet_rare diseases +MONDO:0009514 otar diseases +MONDO:0009514 rare diseases +MONDO:0009515 gard_rare diseases +MONDO:0009515 nord_rare diseases +MONDO:0009515 ordo_subtype_of_a_disorder diseases +MONDO:0009515 otar diseases +MONDO:0009515 rare diseases +MONDO:0009516 gard_rare diseases +MONDO:0009516 ordo_disorder diseases +MONDO:0009516 ordo_malformation_syndrome diseases +MONDO:0009516 orphanet_rare diseases +MONDO:0009516 otar diseases +MONDO:0009516 rare diseases +MONDO:0009517 gard_rare diseases +MONDO:0009517 nord_rare diseases +MONDO:0009517 ordo_disorder diseases +MONDO:0009517 ordo_malformation_syndrome diseases +MONDO:0009517 orphanet_rare diseases +MONDO:0009517 otar diseases +MONDO:0009517 rare diseases +MONDO:0009519 gard_rare diseases +MONDO:0009519 rare diseases +MONDO:0009520 clingen diseases +MONDO:0009520 gard_rare diseases +MONDO:0009520 nord_rare diseases +MONDO:0009520 ordo_disorder diseases +MONDO:0009520 orphanet_rare diseases +MONDO:0009520 otar diseases +MONDO:0009520 rare diseases +MONDO:0009522 gard_rare diseases +MONDO:0009522 nord_rare diseases +MONDO:0009522 ordo_disorder diseases +MONDO:0009522 ordo_malformation_syndrome diseases +MONDO:0009522 orphanet_rare diseases +MONDO:0009522 otar diseases +MONDO:0009522 rare diseases +MONDO:0009523 gard_rare diseases +MONDO:0009523 ordo_disorder diseases +MONDO:0009523 orphanet_rare diseases +MONDO:0009523 rare diseases +MONDO:0009524 gard_rare diseases +MONDO:0009524 nord_rare diseases +MONDO:0009524 ordo_disorder diseases +MONDO:0009524 ordo_malformation_syndrome diseases +MONDO:0009524 orphanet_rare diseases +MONDO:0009524 otar diseases +MONDO:0009524 rare diseases +MONDO:0009525 gard_rare diseases +MONDO:0009525 nord_rare diseases +MONDO:0009525 ordo_disorder diseases +MONDO:0009525 ordo_malformation_syndrome diseases +MONDO:0009525 orphanet_rare diseases +MONDO:0009525 otar diseases +MONDO:0009525 rare diseases +MONDO:0009526 gard_rare diseases +MONDO:0009526 nord_rare diseases +MONDO:0009526 ordo_malformation_syndrome diseases +MONDO:0009526 rare diseases +MONDO:0009527 gard_rare diseases +MONDO:0009527 nord_rare diseases +MONDO:0009527 ordo_etiological_subtype diseases +MONDO:0009527 ordo_subtype_of_a_disorder diseases +MONDO:0009527 rare diseases +MONDO:0009528 gard_rare diseases +MONDO:0009528 nord_rare diseases +MONDO:0009528 ordo_disorder diseases +MONDO:0009528 orphanet_rare diseases +MONDO:0009528 otar diseases +MONDO:0009528 rare diseases +MONDO:0009529 clingen diseases +MONDO:0009529 gard_rare diseases +MONDO:0009529 nord_rare diseases +MONDO:0009529 ordo_subtype_of_a_disorder diseases +MONDO:0009529 otar diseases +MONDO:0009529 rare diseases +MONDO:0009530 gard_rare diseases +MONDO:0009530 nord_rare diseases +MONDO:0009530 ordo_disorder diseases +MONDO:0009530 ordo_malformation_syndrome diseases +MONDO:0009530 orphanet_rare diseases +MONDO:0009530 otar diseases +MONDO:0009530 rare diseases +MONDO:0009532 gard_rare diseases +MONDO:0009532 nord_rare diseases +MONDO:0009532 ordo_disorder diseases +MONDO:0009532 ordo_malformation_syndrome diseases +MONDO:0009532 orphanet_rare diseases +MONDO:0009532 otar diseases +MONDO:0009532 rare diseases +MONDO:0009533 gard_rare diseases +MONDO:0009533 nord_rare diseases +MONDO:0009533 ordo_disorder diseases +MONDO:0009533 ordo_malformation_syndrome diseases +MONDO:0009533 orphanet_rare diseases +MONDO:0009533 otar diseases +MONDO:0009533 rare diseases +MONDO:0009534 gard_rare diseases +MONDO:0009534 rare diseases +MONDO:0009536 gard_rare diseases +MONDO:0009536 rare diseases +MONDO:0009537 gard_rare diseases +MONDO:0009537 nord_rare diseases +MONDO:0009537 ordo_disorder diseases +MONDO:0009537 orphanet_rare diseases +MONDO:0009537 rare diseases +MONDO:0009539 gard_rare diseases +MONDO:0009539 nord_rare diseases +MONDO:0009539 rare diseases +MONDO:0009540 gard_rare diseases +MONDO:0009540 nord_rare diseases +MONDO:0009540 rare diseases +MONDO:0009543 gard_rare diseases +MONDO:0009543 ordo_disorder diseases +MONDO:0009543 ordo_malformation_syndrome diseases +MONDO:0009543 orphanet_rare diseases +MONDO:0009543 otar diseases +MONDO:0009543 rare diseases +MONDO:0009544 gard_rare diseases +MONDO:0009544 nord_rare diseases +MONDO:0009544 otar diseases +MONDO:0009544 rare diseases +MONDO:0009547 gard_rare diseases +MONDO:0009547 ordo_disorder diseases +MONDO:0009547 ordo_malformation_syndrome diseases +MONDO:0009547 orphanet_rare diseases +MONDO:0009547 otar diseases +MONDO:0009547 rare diseases +MONDO:0009548 gard_rare diseases +MONDO:0009548 nord_rare diseases +MONDO:0009548 ordo_subtype_of_a_disorder diseases +MONDO:0009548 otar diseases +MONDO:0009548 rare diseases +MONDO:0009549 gard_rare diseases +MONDO:0009549 nord_rare diseases +MONDO:0009549 ordo_disorder diseases +MONDO:0009549 orphanet_rare diseases +MONDO:0009549 otar diseases +MONDO:0009549 rare diseases +MONDO:0009550 gard_rare diseases +MONDO:0009550 nord_rare diseases +MONDO:0009550 ordo_subtype_of_a_disorder diseases +MONDO:0009550 otar diseases +MONDO:0009550 rare diseases +MONDO:0009552 gard_rare diseases +MONDO:0009552 nord_rare diseases +MONDO:0009552 ordo_disorder diseases +MONDO:0009552 orphanet_rare diseases +MONDO:0009552 otar diseases +MONDO:0009552 rare diseases +MONDO:0009554 gard_rare diseases +MONDO:0009554 nord_rare diseases +MONDO:0009554 rare diseases +MONDO:0009556 clingen diseases +MONDO:0009556 gard_rare diseases +MONDO:0009556 nord_rare diseases +MONDO:0009556 ordo_disorder diseases +MONDO:0009556 orphanet_rare diseases +MONDO:0009556 otar diseases +MONDO:0009556 rare diseases +MONDO:0009557 gard_rare diseases +MONDO:0009557 nord_rare diseases +MONDO:0009557 ordo_subtype_of_a_disorder diseases +MONDO:0009557 otar diseases +MONDO:0009557 rare diseases +MONDO:0009558 gard_rare diseases +MONDO:0009558 nord_rare diseases +MONDO:0009558 rare diseases +MONDO:0009559 otar diseases +MONDO:0009560 gard_rare diseases +MONDO:0009560 nord_rare diseases +MONDO:0009560 ordo_disorder diseases +MONDO:0009560 ordo_malformation_syndrome diseases +MONDO:0009560 orphanet_rare diseases +MONDO:0009560 otar diseases +MONDO:0009560 rare diseases +MONDO:0009561 clingen diseases +MONDO:0009561 gard_rare diseases +MONDO:0009561 nord_rare diseases +MONDO:0009561 ordo_disorder diseases +MONDO:0009561 orphanet_rare diseases +MONDO:0009561 otar diseases +MONDO:0009561 rare diseases +MONDO:0009562 clingen diseases +MONDO:0009562 gard_rare diseases +MONDO:0009562 nord_rare diseases +MONDO:0009562 ordo_disorder diseases +MONDO:0009562 orphanet_rare diseases +MONDO:0009562 otar diseases +MONDO:0009562 rare diseases +MONDO:0009563 clingen diseases +MONDO:0009563 gard_rare diseases +MONDO:0009563 nord_rare diseases +MONDO:0009563 ordo_disorder diseases +MONDO:0009563 orphanet_rare diseases +MONDO:0009563 otar diseases +MONDO:0009563 prototype_pattern diseases +MONDO:0009563 rare diseases +MONDO:0009564 gard_rare diseases +MONDO:0009564 nord_rare diseases +MONDO:0009564 ordo_disorder diseases +MONDO:0009564 ordo_malformation_syndrome diseases +MONDO:0009564 orphanet_rare diseases +MONDO:0009564 otar diseases +MONDO:0009564 rare diseases +MONDO:0009565 gard_rare diseases +MONDO:0009565 ordo_disorder diseases +MONDO:0009565 ordo_malformation_syndrome diseases +MONDO:0009565 orphanet_rare diseases +MONDO:0009565 otar diseases +MONDO:0009565 rare diseases +MONDO:0009566 gard_rare diseases +MONDO:0009566 ordo_disorder diseases +MONDO:0009566 ordo_malformation_syndrome diseases +MONDO:0009566 orphanet_rare diseases +MONDO:0009566 otar diseases +MONDO:0009566 rare diseases +MONDO:0009567 clingen diseases +MONDO:0009567 gard_rare diseases +MONDO:0009567 nord_rare diseases +MONDO:0009567 ordo_disorder diseases +MONDO:0009567 orphanet_rare diseases +MONDO:0009567 otar diseases +MONDO:0009567 rare diseases +MONDO:0009568 gard_rare diseases +MONDO:0009568 nord_rare diseases +MONDO:0009568 ordo_disorder diseases +MONDO:0009568 orphanet_rare diseases +MONDO:0009568 otar diseases +MONDO:0009568 rare diseases +MONDO:0009569 gard_rare diseases +MONDO:0009569 nord_rare diseases +MONDO:0009569 ordo_disorder diseases +MONDO:0009569 ordo_malformation_syndrome diseases +MONDO:0009569 orphanet_rare diseases +MONDO:0009569 otar diseases +MONDO:0009569 rare diseases +MONDO:0009570 gard_rare diseases +MONDO:0009570 nord_rare diseases +MONDO:0009570 ordo_disorder diseases +MONDO:0009570 ordo_malformation_syndrome diseases +MONDO:0009570 orphanet_rare diseases +MONDO:0009570 otar diseases +MONDO:0009570 rare diseases +MONDO:0009571 gard_rare diseases +MONDO:0009571 nord_rare diseases +MONDO:0009571 rare diseases +MONDO:0009572 gard_rare diseases +MONDO:0009572 nord_rare diseases +MONDO:0009572 rare diseases +MONDO:0009575 gard_rare diseases +MONDO:0009575 nord_rare diseases +MONDO:0009575 ordo_disorder diseases +MONDO:0009575 orphanet_rare diseases +MONDO:0009575 otar diseases +MONDO:0009575 rare diseases +MONDO:0009576 otar diseases +MONDO:0009577 gard_rare diseases +MONDO:0009577 nord_rare diseases +MONDO:0009577 ordo_disorder diseases +MONDO:0009577 ordo_malformation_syndrome diseases +MONDO:0009577 orphanet_rare diseases +MONDO:0009577 otar diseases +MONDO:0009577 rare diseases +MONDO:0009578 gard_rare diseases +MONDO:0009578 nord_rare diseases +MONDO:0009578 ordo_disorder diseases +MONDO:0009578 orphanet_rare diseases +MONDO:0009578 otar diseases +MONDO:0009578 rare diseases +MONDO:0009579 clingen diseases +MONDO:0009579 gard_rare diseases +MONDO:0009579 nord_rare diseases +MONDO:0009579 ordo_disorder diseases +MONDO:0009579 orphanet_rare diseases +MONDO:0009579 otar diseases +MONDO:0009579 rare diseases +MONDO:0009580 gard_rare diseases +MONDO:0009580 nord_rare diseases +MONDO:0009580 otar diseases +MONDO:0009580 rare diseases +MONDO:0009581 gard_rare diseases +MONDO:0009581 ordo_disorder diseases +MONDO:0009581 ordo_malformation_syndrome diseases +MONDO:0009581 orphanet_rare diseases +MONDO:0009581 otar diseases +MONDO:0009581 rare diseases +MONDO:0009582 gard_rare diseases +MONDO:0009582 nord_rare diseases +MONDO:0009582 ordo_disorder diseases +MONDO:0009582 ordo_malformation_syndrome diseases +MONDO:0009582 orphanet_rare diseases +MONDO:0009582 otar diseases +MONDO:0009582 rare diseases +MONDO:0009583 gard_rare diseases +MONDO:0009583 nord_rare diseases +MONDO:0009583 ordo_disorder diseases +MONDO:0009583 ordo_malformation_syndrome diseases +MONDO:0009583 orphanet_rare diseases +MONDO:0009583 otar diseases +MONDO:0009583 rare diseases +MONDO:0009584 gard_rare diseases +MONDO:0009584 nord_rare diseases +MONDO:0009584 ordo_disorder diseases +MONDO:0009584 ordo_malformation_syndrome diseases +MONDO:0009584 orphanet_rare diseases +MONDO:0009584 otar diseases +MONDO:0009584 rare diseases +MONDO:0009585 clingen diseases +MONDO:0009585 gard_rare diseases +MONDO:0009585 nord_rare diseases +MONDO:0009585 ordo_disorder diseases +MONDO:0009585 orphanet_rare diseases +MONDO:0009585 otar diseases +MONDO:0009585 rare diseases +MONDO:0009588 gard_rare diseases +MONDO:0009588 nord_rare diseases +MONDO:0009588 ordo_disorder diseases +MONDO:0009588 ordo_malformation_syndrome diseases +MONDO:0009588 orphanet_rare diseases +MONDO:0009588 otar diseases +MONDO:0009588 rare diseases +MONDO:0009589 gard_rare diseases +MONDO:0009589 ordo_disorder diseases +MONDO:0009589 ordo_malformation_syndrome diseases +MONDO:0009589 orphanet_rare diseases +MONDO:0009589 otar diseases +MONDO:0009589 rare diseases +MONDO:0009590 clingen diseases +MONDO:0009590 gard_rare diseases +MONDO:0009590 nord_rare diseases +MONDO:0009590 rare diseases +MONDO:0009591 gard_rare diseases +MONDO:0009591 nord_rare diseases +MONDO:0009591 ordo_subtype_of_a_disorder diseases +MONDO:0009591 otar diseases +MONDO:0009591 rare diseases +MONDO:0009592 gard_rare diseases +MONDO:0009592 nord_rare diseases +MONDO:0009592 ordo_disorder diseases +MONDO:0009592 orphanet_rare diseases +MONDO:0009592 otar diseases +MONDO:0009592 rare diseases +MONDO:0009593 gard_rare diseases +MONDO:0009593 nord_rare diseases +MONDO:0009593 ordo_disorder diseases +MONDO:0009593 ordo_malformation_syndrome diseases +MONDO:0009593 orphanet_rare diseases +MONDO:0009593 otar diseases +MONDO:0009593 rare diseases +MONDO:0009594 gard_rare diseases +MONDO:0009594 nord_rare diseases +MONDO:0009594 ordo_disorder diseases +MONDO:0009594 orphanet_rare diseases +MONDO:0009594 rare diseases +MONDO:0009595 clingen diseases +MONDO:0009595 gard_rare diseases +MONDO:0009595 nord_rare diseases +MONDO:0009595 ordo_disorder diseases +MONDO:0009595 orphanet_rare diseases +MONDO:0009595 otar diseases +MONDO:0009595 rare diseases +MONDO:0009597 gard_rare diseases +MONDO:0009597 nord_rare diseases +MONDO:0009597 ordo_disorder diseases +MONDO:0009597 orphanet_rare diseases +MONDO:0009597 otar diseases +MONDO:0009597 rare diseases +MONDO:0009598 gard_rare diseases +MONDO:0009598 nord_rare diseases +MONDO:0009598 ordo_disorder diseases +MONDO:0009598 orphanet_rare diseases +MONDO:0009598 otar diseases +MONDO:0009598 rare diseases +MONDO:0009599 gard_rare diseases +MONDO:0009599 nord_rare diseases +MONDO:0009599 ordo_disorder diseases +MONDO:0009599 ordo_malformation_syndrome diseases +MONDO:0009599 orphanet_rare diseases +MONDO:0009599 otar diseases +MONDO:0009599 rare diseases +MONDO:0009601 gard_rare diseases +MONDO:0009601 nord_rare diseases +MONDO:0009601 otar diseases +MONDO:0009601 rare diseases +MONDO:0009603 clingen diseases +MONDO:0009603 gard_rare diseases +MONDO:0009603 nord_rare diseases +MONDO:0009603 ordo_disorder diseases +MONDO:0009603 orphanet_rare diseases +MONDO:0009603 otar diseases +MONDO:0009603 rare diseases +MONDO:0009604 gard_rare diseases +MONDO:0009604 nord_rare diseases +MONDO:0009604 rare diseases +MONDO:0009605 gard_rare diseases +MONDO:0009605 nord_rare diseases +MONDO:0009605 rare diseases +MONDO:0009606 gard_rare diseases +MONDO:0009606 nord_rare diseases +MONDO:0009606 rare diseases +MONDO:0009607 clingen diseases +MONDO:0009607 gard_rare diseases +MONDO:0009607 nord_rare diseases +MONDO:0009607 ordo_disorder diseases +MONDO:0009607 orphanet_rare diseases +MONDO:0009607 otar diseases +MONDO:0009607 rare diseases +MONDO:0009609 clingen diseases +MONDO:0009609 gard_rare diseases +MONDO:0009609 nord_rare diseases +MONDO:0009609 ordo_subtype_of_a_disorder diseases +MONDO:0009609 otar diseases +MONDO:0009609 rare diseases +MONDO:0009610 clingen diseases +MONDO:0009610 gard_rare diseases +MONDO:0009610 nord_rare diseases +MONDO:0009610 ordo_disorder diseases +MONDO:0009610 orphanet_rare diseases +MONDO:0009610 otar diseases +MONDO:0009610 rare diseases +MONDO:0009611 gard_rare diseases +MONDO:0009611 nord_rare diseases +MONDO:0009611 ordo_disorder diseases +MONDO:0009611 orphanet_rare diseases +MONDO:0009611 otar diseases +MONDO:0009611 rare diseases +MONDO:0009612 clingen diseases +MONDO:0009612 gard_rare diseases +MONDO:0009612 ordo_disorder diseases +MONDO:0009612 orphanet_rare diseases +MONDO:0009612 otar diseases +MONDO:0009612 rare diseases +MONDO:0009613 clingen diseases +MONDO:0009613 gard_rare diseases +MONDO:0009613 nord_rare diseases +MONDO:0009613 ordo_subtype_of_a_disorder diseases +MONDO:0009613 otar diseases +MONDO:0009613 rare diseases +MONDO:0009614 clingen diseases +MONDO:0009614 gard_rare diseases +MONDO:0009614 nord_rare diseases +MONDO:0009614 ordo_subtype_of_a_disorder diseases +MONDO:0009614 otar diseases +MONDO:0009614 rare diseases +MONDO:0009615 clingen diseases +MONDO:0009615 gard_rare diseases +MONDO:0009615 nord_rare diseases +MONDO:0009615 ordo_disorder diseases +MONDO:0009615 orphanet_rare diseases +MONDO:0009615 otar diseases +MONDO:0009615 rare diseases +MONDO:0009616 gard_rare diseases +MONDO:0009616 ordo_disorder diseases +MONDO:0009616 ordo_malformation_syndrome diseases +MONDO:0009616 orphanet_rare diseases +MONDO:0009616 otar diseases +MONDO:0009616 rare diseases +MONDO:0009617 gard_rare diseases +MONDO:0009617 nord_rare diseases +MONDO:0009617 otar diseases +MONDO:0009617 rare diseases +MONDO:0009618 gard_rare diseases +MONDO:0009618 nord_rare diseases +MONDO:0009618 ordo_disorder diseases +MONDO:0009618 ordo_malformation_syndrome diseases +MONDO:0009618 orphanet_rare diseases +MONDO:0009618 otar diseases +MONDO:0009618 rare diseases +MONDO:0009619 gard_rare diseases +MONDO:0009619 nord_rare diseases +MONDO:0009619 ordo_subtype_of_a_disorder diseases +MONDO:0009619 otar diseases +MONDO:0009619 rare diseases +MONDO:0009620 gard_rare diseases +MONDO:0009620 nord_rare diseases +MONDO:0009620 ordo_disorder diseases +MONDO:0009620 ordo_malformation_syndrome diseases +MONDO:0009620 orphanet_rare diseases +MONDO:0009620 otar diseases +MONDO:0009620 rare diseases +MONDO:0009621 gard_rare diseases +MONDO:0009621 ordo_disorder diseases +MONDO:0009621 ordo_malformation_syndrome diseases +MONDO:0009621 orphanet_rare diseases +MONDO:0009621 otar diseases +MONDO:0009621 rare diseases +MONDO:0009622 gard_rare diseases +MONDO:0009622 nord_rare diseases +MONDO:0009622 ordo_disorder diseases +MONDO:0009622 ordo_malformation_syndrome diseases +MONDO:0009622 orphanet_rare diseases +MONDO:0009622 otar diseases +MONDO:0009622 rare diseases +MONDO:0009623 clingen diseases +MONDO:0009623 gard_rare diseases +MONDO:0009623 nord_rare diseases +MONDO:0009623 ordo_disorder diseases +MONDO:0009623 ordo_malformation_syndrome diseases +MONDO:0009623 orphanet_rare diseases +MONDO:0009623 otar diseases +MONDO:0009623 rare diseases +MONDO:0009624 clingen diseases +MONDO:0009624 gard_rare diseases +MONDO:0009624 nord_rare diseases +MONDO:0009624 ordo_disorder diseases +MONDO:0009624 ordo_malformation_syndrome diseases +MONDO:0009624 orphanet_rare diseases +MONDO:0009624 otar diseases +MONDO:0009624 rare diseases +MONDO:0009625 gard_rare diseases +MONDO:0009625 rare diseases +MONDO:0009626 gard_rare diseases +MONDO:0009626 nord_rare diseases +MONDO:0009626 ordo_disorder diseases +MONDO:0009626 ordo_malformation_syndrome diseases +MONDO:0009626 orphanet_rare diseases +MONDO:0009626 otar diseases +MONDO:0009626 prototype_pattern diseases +MONDO:0009626 rare diseases +MONDO:0009627 gard_rare diseases +MONDO:0009627 nord_rare diseases +MONDO:0009627 ordo_disorder diseases +MONDO:0009627 ordo_malformation_syndrome diseases +MONDO:0009627 orphanet_rare diseases +MONDO:0009627 otar diseases +MONDO:0009627 prototype_pattern diseases +MONDO:0009627 rare diseases +MONDO:0009629 gard_rare diseases +MONDO:0009629 nord_rare diseases +MONDO:0009629 rare diseases +MONDO:0009630 gard_rare diseases +MONDO:0009630 nord_rare diseases +MONDO:0009630 rare diseases +MONDO:0009633 otar diseases +MONDO:0009635 gard_rare diseases +MONDO:0009635 nord_rare diseases +MONDO:0009635 ordo_disorder diseases +MONDO:0009635 orphanet_rare diseases +MONDO:0009635 otar diseases +MONDO:0009635 rare diseases +MONDO:0009636 gard_rare diseases +MONDO:0009636 nord_rare diseases +MONDO:0009636 ordo_disorder diseases +MONDO:0009636 orphanet_rare diseases +MONDO:0009636 otar diseases +MONDO:0009636 rare diseases +MONDO:0009637 disease_grouping diseases +MONDO:0009637 gard_rare diseases +MONDO:0009637 ordo_group_of_disorders diseases +MONDO:0009637 otar diseases +MONDO:0009637 rare diseases +MONDO:0009638 gard_rare diseases +MONDO:0009638 rare diseases +MONDO:0009642 gard_rare diseases +MONDO:0009642 nord_rare diseases +MONDO:0009642 ordo_disorder diseases +MONDO:0009642 ordo_malformation_syndrome diseases +MONDO:0009642 orphanet_rare diseases +MONDO:0009642 otar diseases +MONDO:0009642 rare diseases +MONDO:0009643 clingen diseases +MONDO:0009643 gard_rare diseases +MONDO:0009643 nord_rare diseases +MONDO:0009643 ordo_etiological_subtype diseases +MONDO:0009643 ordo_subtype_of_a_disorder diseases +MONDO:0009643 otar diseases +MONDO:0009643 rare diseases +MONDO:0009644 clingen diseases +MONDO:0009644 gard_rare diseases +MONDO:0009644 nord_rare diseases +MONDO:0009644 ordo_etiological_subtype diseases +MONDO:0009644 ordo_subtype_of_a_disorder diseases +MONDO:0009644 otar diseases +MONDO:0009644 rare diseases +MONDO:0009645 gard_rare diseases +MONDO:0009645 rare diseases +MONDO:0009646 gard_rare diseases +MONDO:0009646 nord_rare diseases +MONDO:0009646 rare diseases +MONDO:0009647 gard_rare diseases +MONDO:0009647 nord_rare diseases +MONDO:0009647 rare diseases +MONDO:0009648 gard_rare diseases +MONDO:0009648 nord_rare diseases +MONDO:0009648 ordo_disorder diseases +MONDO:0009648 orphanet_rare diseases +MONDO:0009648 rare diseases +MONDO:0009649 gard_rare diseases +MONDO:0009649 nord_rare diseases +MONDO:0009649 rare diseases +MONDO:0009650 gard_rare diseases +MONDO:0009650 nord_rare diseases +MONDO:0009650 ordo_disorder diseases +MONDO:0009650 orphanet_rare diseases +MONDO:0009650 otar diseases +MONDO:0009650 rare diseases +MONDO:0009652 clingen diseases +MONDO:0009652 gard_rare diseases +MONDO:0009652 nord_rare diseases +MONDO:0009652 ordo_subtype_of_a_disorder diseases +MONDO:0009652 otar diseases +MONDO:0009652 rare diseases +MONDO:0009653 clingen diseases +MONDO:0009653 gard_rare diseases +MONDO:0009653 nord_rare diseases +MONDO:0009653 ordo_disorder diseases +MONDO:0009653 orphanet_rare diseases +MONDO:0009653 otar diseases +MONDO:0009653 rare diseases +MONDO:0009655 clingen diseases +MONDO:0009655 gard_rare diseases +MONDO:0009655 nord_rare diseases +MONDO:0009655 ordo_etiological_subtype diseases +MONDO:0009655 ordo_subtype_of_a_disorder diseases +MONDO:0009655 otar diseases +MONDO:0009655 rare diseases +MONDO:0009656 gard_rare diseases +MONDO:0009656 nord_rare diseases +MONDO:0009656 ordo_etiological_subtype diseases +MONDO:0009656 ordo_subtype_of_a_disorder diseases +MONDO:0009656 otar diseases +MONDO:0009656 rare diseases +MONDO:0009657 gard_rare diseases +MONDO:0009657 nord_rare diseases +MONDO:0009657 ordo_etiological_subtype diseases +MONDO:0009657 ordo_subtype_of_a_disorder diseases +MONDO:0009657 otar diseases +MONDO:0009657 rare diseases +MONDO:0009658 clingen diseases +MONDO:0009658 gard_rare diseases +MONDO:0009658 nord_rare diseases +MONDO:0009658 ordo_etiological_subtype diseases +MONDO:0009658 ordo_subtype_of_a_disorder diseases +MONDO:0009658 otar diseases +MONDO:0009658 rare diseases +MONDO:0009659 clingen diseases +MONDO:0009659 gard_rare diseases +MONDO:0009659 nord_rare diseases +MONDO:0009659 ordo_subtype_of_a_disorder diseases +MONDO:0009659 otar diseases +MONDO:0009659 rare diseases +MONDO:0009660 gard_rare diseases +MONDO:0009660 nord_rare diseases +MONDO:0009660 ordo_subtype_of_a_disorder diseases +MONDO:0009660 otar diseases +MONDO:0009660 rare diseases +MONDO:0009661 clingen diseases +MONDO:0009661 gard_rare diseases +MONDO:0009661 nord_rare diseases +MONDO:0009661 ordo_disorder diseases +MONDO:0009661 orphanet_rare diseases +MONDO:0009661 otar diseases +MONDO:0009661 rare diseases +MONDO:0009662 clingen diseases +MONDO:0009662 gard_rare diseases +MONDO:0009662 nord_rare diseases +MONDO:0009662 ordo_disorder diseases +MONDO:0009662 orphanet_rare diseases +MONDO:0009662 otar diseases +MONDO:0009662 rare diseases +MONDO:0009664 clingen diseases +MONDO:0009664 gard_rare diseases +MONDO:0009664 nord_rare diseases +MONDO:0009664 ordo_disorder diseases +MONDO:0009664 ordo_malformation_syndrome diseases +MONDO:0009664 orphanet_rare diseases +MONDO:0009664 otar diseases +MONDO:0009664 rare diseases +MONDO:0009665 clingen diseases +MONDO:0009665 gard_rare diseases +MONDO:0009665 nord_rare diseases +MONDO:0009665 ordo_disorder diseases +MONDO:0009665 orphanet_rare diseases +MONDO:0009665 otar diseases +MONDO:0009665 rare diseases +MONDO:0009666 clingen diseases +MONDO:0009666 gard_rare diseases +MONDO:0009666 nord_rare diseases +MONDO:0009666 ordo_disorder diseases +MONDO:0009666 orphanet_rare diseases +MONDO:0009666 otar diseases +MONDO:0009666 rare diseases +MONDO:0009667 gard_rare diseases +MONDO:0009667 nord_rare diseases +MONDO:0009667 otar diseases +MONDO:0009667 rare diseases +MONDO:0009668 gard_rare diseases +MONDO:0009668 nord_rare diseases +MONDO:0009668 ordo_disorder diseases +MONDO:0009668 ordo_malformation_syndrome diseases +MONDO:0009668 orphanet_rare diseases +MONDO:0009668 otar diseases +MONDO:0009668 rare diseases +MONDO:0009669 gard_rare diseases +MONDO:0009669 nord_rare diseases +MONDO:0009669 ordo_subtype_of_a_disorder diseases +MONDO:0009669 otar diseases +MONDO:0009669 rare diseases +MONDO:0009670 gard_rare diseases +MONDO:0009670 nord_rare diseases +MONDO:0009670 ordo_disorder diseases +MONDO:0009670 ordo_malformation_syndrome diseases +MONDO:0009670 orphanet_rare diseases +MONDO:0009670 otar diseases +MONDO:0009670 rare diseases +MONDO:0009671 gard_rare diseases +MONDO:0009671 ordo_disorder diseases +MONDO:0009671 orphanet_rare diseases +MONDO:0009671 otar diseases +MONDO:0009671 rare diseases +MONDO:0009672 gard_rare diseases +MONDO:0009672 nord_rare diseases +MONDO:0009672 ordo_subtype_of_a_disorder diseases +MONDO:0009672 otar diseases +MONDO:0009672 rare diseases +MONDO:0009673 gard_rare diseases +MONDO:0009673 nord_rare diseases +MONDO:0009673 ordo_subtype_of_a_disorder diseases +MONDO:0009673 otar diseases +MONDO:0009673 rare diseases +MONDO:0009675 gard_rare diseases +MONDO:0009675 nord_rare diseases +MONDO:0009675 ordo_disorder diseases +MONDO:0009675 orphanet_rare diseases +MONDO:0009675 otar diseases +MONDO:0009675 rare diseases +MONDO:0009676 gard_rare diseases +MONDO:0009676 nord_rare diseases +MONDO:0009676 ordo_disorder diseases +MONDO:0009676 orphanet_rare diseases +MONDO:0009676 otar diseases +MONDO:0009676 rare diseases +MONDO:0009677 gard_rare diseases +MONDO:0009677 nord_rare diseases +MONDO:0009677 ordo_disorder diseases +MONDO:0009677 orphanet_rare diseases +MONDO:0009677 otar diseases +MONDO:0009677 rare diseases +MONDO:0009678 gard_rare diseases +MONDO:0009678 nord_rare diseases +MONDO:0009678 ordo_disorder diseases +MONDO:0009678 orphanet_rare diseases +MONDO:0009678 otar diseases +MONDO:0009678 rare diseases +MONDO:0009679 gard_rare diseases +MONDO:0009679 rare diseases +MONDO:0009680 gard_rare diseases +MONDO:0009680 nord_rare diseases +MONDO:0009680 ordo_disorder diseases +MONDO:0009680 orphanet_rare diseases +MONDO:0009680 otar diseases +MONDO:0009680 rare diseases +MONDO:0009681 gard_rare diseases +MONDO:0009681 rare diseases +MONDO:0009682 gard_rare diseases +MONDO:0009682 rare diseases +MONDO:0009683 gard_rare diseases +MONDO:0009683 nord_rare diseases +MONDO:0009683 ordo_disorder diseases +MONDO:0009683 orphanet_rare diseases +MONDO:0009683 otar diseases +MONDO:0009683 rare diseases +MONDO:0009685 gard_rare diseases +MONDO:0009685 nord_rare diseases +MONDO:0009685 ordo_disorder diseases +MONDO:0009685 orphanet_rare diseases +MONDO:0009685 otar diseases +MONDO:0009685 prototype_pattern diseases +MONDO:0009685 rare diseases +MONDO:0009687 gard_rare diseases +MONDO:0009687 rare diseases +MONDO:0009688 gard_rare diseases +MONDO:0009688 nord_rare diseases +MONDO:0009688 ordo_disorder diseases +MONDO:0009688 orphanet_rare diseases +MONDO:0009688 otar diseases +MONDO:0009688 rare diseases +MONDO:0009689 gard_rare diseases +MONDO:0009689 nord_rare diseases +MONDO:0009689 rare diseases +MONDO:0009690 gard_rare diseases +MONDO:0009690 nord_rare diseases +MONDO:0009690 rare diseases +MONDO:0009691 gard_rare diseases +MONDO:0009691 nord_rare diseases +MONDO:0009691 ordo_disorder diseases +MONDO:0009691 orphanet_rare diseases +MONDO:0009691 otar diseases +MONDO:0009691 rare diseases +MONDO:0009692 gard_rare diseases +MONDO:0009692 nord_rare diseases +MONDO:0009692 ordo_disorder diseases +MONDO:0009692 orphanet_rare diseases +MONDO:0009692 otar diseases +MONDO:0009692 rare diseases +MONDO:0009693 gard_rare diseases +MONDO:0009693 nord_rare diseases +MONDO:0009693 ordo_disorder diseases +MONDO:0009693 orphanet_rare diseases +MONDO:0009693 otar diseases +MONDO:0009693 rare diseases +MONDO:0009694 gard_rare diseases +MONDO:0009694 nord_rare diseases +MONDO:0009694 ordo_disorder diseases +MONDO:0009694 orphanet_rare diseases +MONDO:0009694 otar diseases +MONDO:0009694 rare diseases +MONDO:0009695 gard_rare diseases +MONDO:0009695 rare diseases +MONDO:0009696 gard_rare diseases +MONDO:0009696 nord_rare diseases +MONDO:0009696 ordo_disorder diseases +MONDO:0009696 orphanet_rare diseases +MONDO:0009696 otar diseases +MONDO:0009696 predisposition diseases +MONDO:0009696 rare diseases +MONDO:0009697 clingen diseases +MONDO:0009697 gard_rare diseases +MONDO:0009697 nord_rare diseases +MONDO:0009697 ordo_disorder diseases +MONDO:0009697 orphanet_rare diseases +MONDO:0009697 otar diseases +MONDO:0009697 rare diseases +MONDO:0009698 clingen diseases +MONDO:0009698 gard_rare diseases +MONDO:0009698 nord_rare diseases +MONDO:0009698 ordo_disorder diseases +MONDO:0009698 ordo_malformation_syndrome diseases +MONDO:0009698 orphanet_rare diseases +MONDO:0009698 otar diseases +MONDO:0009698 rare diseases +MONDO:0009699 gard_rare diseases +MONDO:0009699 nord_rare diseases +MONDO:0009699 ordo_disorder diseases +MONDO:0009699 orphanet_rare diseases +MONDO:0009699 otar diseases +MONDO:0009699 rare diseases +MONDO:0009703 clingen diseases +MONDO:0009703 gard_rare diseases +MONDO:0009703 otar diseases +MONDO:0009703 rare diseases +MONDO:0009704 gard_rare diseases +MONDO:0009704 nord_rare diseases +MONDO:0009704 ordo_subtype_of_a_disorder diseases +MONDO:0009704 otar diseases +MONDO:0009704 rare diseases +MONDO:0009705 clingen diseases +MONDO:0009705 gard_rare diseases +MONDO:0009705 nord_rare diseases +MONDO:0009705 ordo_disorder diseases +MONDO:0009705 orphanet_rare diseases +MONDO:0009705 otar diseases +MONDO:0009705 rare diseases +MONDO:0009706 gard_rare diseases +MONDO:0009706 nord_rare diseases +MONDO:0009706 ordo_disorder diseases +MONDO:0009706 orphanet_rare diseases +MONDO:0009706 otar diseases +MONDO:0009706 rare diseases +MONDO:0009708 gard_rare diseases +MONDO:0009708 ordo_subtype_of_a_disorder diseases +MONDO:0009708 rare diseases +MONDO:0009709 gard_rare diseases +MONDO:0009709 otar diseases +MONDO:0009709 rare diseases +MONDO:0009710 gard_rare diseases +MONDO:0009710 nord_rare diseases +MONDO:0009710 ordo_disorder diseases +MONDO:0009710 orphanet_rare diseases +MONDO:0009710 otar diseases +MONDO:0009710 rare diseases +MONDO:0009711 gard_rare diseases +MONDO:0009711 nord_rare diseases +MONDO:0009711 ordo_disorder diseases +MONDO:0009711 orphanet_rare diseases +MONDO:0009711 otar diseases +MONDO:0009711 rare diseases +MONDO:0009712 gard_rare diseases +MONDO:0009712 nord_rare diseases +MONDO:0009712 ordo_subtype_of_a_disorder diseases +MONDO:0009712 otar diseases +MONDO:0009712 rare diseases +MONDO:0009714 gard_rare diseases +MONDO:0009714 nord_rare diseases +MONDO:0009714 obsoletion_candidate diseases +MONDO:0009714 ordo_disorder diseases +MONDO:0009714 orphanet_rare diseases +MONDO:0009714 otar diseases +MONDO:0009714 rare diseases +MONDO:0009715 gard_rare diseases +MONDO:0009715 rare diseases +MONDO:0009716 gard_rare diseases +MONDO:0009716 ordo_disorder diseases +MONDO:0009716 ordo_malformation_syndrome diseases +MONDO:0009716 orphanet_rare diseases +MONDO:0009716 otar diseases +MONDO:0009716 rare diseases +MONDO:0009717 gard_rare diseases +MONDO:0009717 nord_rare diseases +MONDO:0009717 ordo_disorder diseases +MONDO:0009717 orphanet_rare diseases +MONDO:0009717 otar diseases +MONDO:0009717 prototype_pattern diseases +MONDO:0009717 rare diseases +MONDO:0009718 otar diseases +MONDO:0009719 gard_rare diseases +MONDO:0009719 nord_rare diseases +MONDO:0009719 ordo_disorder diseases +MONDO:0009719 orphanet_rare diseases +MONDO:0009719 otar diseases +MONDO:0009719 rare diseases +MONDO:0009720 gard_rare diseases +MONDO:0009720 nord_rare diseases +MONDO:0009720 ordo_disorder diseases +MONDO:0009720 ordo_malformation_syndrome diseases +MONDO:0009720 orphanet_rare diseases +MONDO:0009720 otar diseases +MONDO:0009720 rare diseases +MONDO:0009721 gard_rare diseases +MONDO:0009721 ordo_disorder diseases +MONDO:0009721 ordo_malformation_syndrome diseases +MONDO:0009721 orphanet_rare diseases +MONDO:0009721 otar diseases +MONDO:0009721 rare diseases +MONDO:0009722 clingen diseases +MONDO:0009722 gard_rare diseases +MONDO:0009722 ordo_disorder diseases +MONDO:0009722 ordo_malformation_syndrome diseases +MONDO:0009722 orphanet_rare diseases +MONDO:0009722 otar diseases +MONDO:0009722 rare diseases +MONDO:0009723 clingen diseases +MONDO:0009723 disease_grouping diseases +MONDO:0009723 gard_rare diseases +MONDO:0009723 nord_rare diseases +MONDO:0009723 ordo_disorder diseases +MONDO:0009723 orphanet_rare diseases +MONDO:0009723 otar diseases +MONDO:0009723 rare diseases +MONDO:0009724 gard_rare diseases +MONDO:0009724 ordo_disorder diseases +MONDO:0009724 orphanet_rare diseases +MONDO:0009724 otar diseases +MONDO:0009724 rare diseases +MONDO:0009725 clingen diseases +MONDO:0009725 gard_rare diseases +MONDO:0009725 rare diseases +MONDO:0009726 gard_rare diseases +MONDO:0009726 nord_rare diseases +MONDO:0009726 ordo_disorder diseases +MONDO:0009726 orphanet_rare diseases +MONDO:0009726 otar diseases +MONDO:0009726 rare diseases +MONDO:0009727 clingen diseases +MONDO:0009727 gard_rare diseases +MONDO:0009727 nord_rare diseases +MONDO:0009727 ordo_disorder diseases +MONDO:0009727 ordo_malformation_syndrome diseases +MONDO:0009727 orphanet_rare diseases +MONDO:0009727 otar diseases +MONDO:0009727 rare diseases +MONDO:0009728 clingen diseases +MONDO:0009728 gard_rare diseases +MONDO:0009728 nord_rare diseases +MONDO:0009728 ordo_subtype_of_a_disorder diseases +MONDO:0009728 otar diseases +MONDO:0009728 rare diseases +MONDO:0009729 gard_rare diseases +MONDO:0009729 nord_rare diseases +MONDO:0009729 ordo_disorder diseases +MONDO:0009729 ordo_malformation_syndrome diseases +MONDO:0009729 orphanet_rare diseases +MONDO:0009729 rare diseases +MONDO:0009731 gard_rare diseases +MONDO:0009731 ordo_disorder diseases +MONDO:0009731 ordo_malformation_syndrome diseases +MONDO:0009731 orphanet_rare diseases +MONDO:0009731 otar diseases +MONDO:0009731 rare diseases +MONDO:0009732 gard_rare diseases +MONDO:0009732 nord_rare diseases +MONDO:0009732 ordo_disorder diseases +MONDO:0009732 orphanet_rare diseases +MONDO:0009732 otar diseases +MONDO:0009732 rare diseases +MONDO:0009733 gard_rare diseases +MONDO:0009733 rare diseases +MONDO:0009734 gard_rare diseases +MONDO:0009734 nord_rare diseases +MONDO:0009734 otar diseases +MONDO:0009734 rare diseases +MONDO:0009735 gard_rare diseases +MONDO:0009735 nord_rare diseases +MONDO:0009735 ordo_disorder diseases +MONDO:0009735 orphanet_rare diseases +MONDO:0009735 otar diseases +MONDO:0009735 rare diseases +MONDO:0009736 gard_rare diseases +MONDO:0009736 nord_rare diseases +MONDO:0009736 ordo_subtype_of_a_disorder diseases +MONDO:0009736 rare diseases +MONDO:0009737 clingen diseases +MONDO:0009737 gard_rare diseases +MONDO:0009737 nord_rare diseases +MONDO:0009737 ordo_disorder diseases +MONDO:0009737 orphanet_rare diseases +MONDO:0009737 otar diseases +MONDO:0009737 rare diseases +MONDO:0009738 gard_rare diseases +MONDO:0009738 nord_rare diseases +MONDO:0009738 ordo_disorder diseases +MONDO:0009738 orphanet_rare diseases +MONDO:0009738 otar diseases +MONDO:0009738 rare diseases +MONDO:0009740 gard_rare diseases +MONDO:0009740 nord_rare diseases +MONDO:0009740 ordo_disorder diseases +MONDO:0009740 ordo_malformation_syndrome diseases +MONDO:0009740 orphanet_rare diseases +MONDO:0009740 otar diseases +MONDO:0009740 rare diseases +MONDO:0009741 inferred_rare diseases +MONDO:0009741 predisposition diseases +MONDO:0009741 rare diseases +MONDO:0009742 gard_rare diseases +MONDO:0009742 nord_rare diseases +MONDO:0009742 ordo_disorder diseases +MONDO:0009742 ordo_malformation_syndrome diseases +MONDO:0009742 orphanet_rare diseases +MONDO:0009742 otar diseases +MONDO:0009742 rare diseases +MONDO:0009744 clingen diseases +MONDO:0009744 gard_rare diseases +MONDO:0009744 nord_rare diseases +MONDO:0009744 ordo_etiological_subtype diseases +MONDO:0009744 otar diseases +MONDO:0009744 rare diseases +MONDO:0009745 gard_rare diseases +MONDO:0009745 nord_rare diseases +MONDO:0009745 ordo_etiological_subtype diseases +MONDO:0009745 otar diseases +MONDO:0009745 rare diseases +MONDO:0009746 clingen diseases +MONDO:0009746 gard_rare diseases +MONDO:0009746 nord_rare diseases +MONDO:0009746 ordo_disorder diseases +MONDO:0009746 orphanet_rare diseases +MONDO:0009746 otar diseases +MONDO:0009746 rare diseases +MONDO:0009747 gard_rare diseases +MONDO:0009747 nord_rare diseases +MONDO:0009747 ordo_disorder diseases +MONDO:0009747 orphanet_rare diseases +MONDO:0009747 otar diseases +MONDO:0009747 rare diseases +MONDO:0009748 gard_rare diseases +MONDO:0009748 nord_rare diseases +MONDO:0009748 ordo_disorder diseases +MONDO:0009748 orphanet_rare diseases +MONDO:0009748 otar diseases +MONDO:0009748 rare diseases +MONDO:0009749 clingen diseases +MONDO:0009749 gard_rare diseases +MONDO:0009749 nord_rare diseases +MONDO:0009749 ordo_disorder diseases +MONDO:0009749 orphanet_rare diseases +MONDO:0009749 rare diseases +MONDO:0009751 gard_rare diseases +MONDO:0009751 nord_rare diseases +MONDO:0009751 rare diseases +MONDO:0009754 gard_rare diseases +MONDO:0009754 rare diseases +MONDO:0009755 gard_rare diseases +MONDO:0009755 nord_rare diseases +MONDO:0009755 rare diseases +MONDO:0009756 gard_rare diseases +MONDO:0009756 nord_rare diseases +MONDO:0009756 ordo_disorder diseases +MONDO:0009756 orphanet_rare diseases +MONDO:0009756 otar diseases +MONDO:0009756 rare diseases +MONDO:0009757 clingen diseases +MONDO:0009757 gard_rare diseases +MONDO:0009757 rare diseases +MONDO:0009758 gard_rare diseases +MONDO:0009758 rare diseases +MONDO:0009759 clingen diseases +MONDO:0009759 gard_rare diseases +MONDO:0009759 nord_rare diseases +MONDO:0009759 rare diseases +MONDO:0009760 gard_rare diseases +MONDO:0009760 nord_rare diseases +MONDO:0009760 ordo_subtype_of_a_disorder diseases +MONDO:0009760 otar diseases +MONDO:0009760 rare diseases +MONDO:0009761 gard_rare diseases +MONDO:0009761 otar diseases +MONDO:0009761 rare diseases +MONDO:0009763 otar diseases +MONDO:0009764 gard_rare diseases +MONDO:0009764 nord_rare diseases +MONDO:0009764 ordo_disorder diseases +MONDO:0009764 orphanet_rare diseases +MONDO:0009764 otar diseases +MONDO:0009764 rare diseases +MONDO:0009766 gard_rare diseases +MONDO:0009766 ordo_disorder diseases +MONDO:0009766 orphanet_rare diseases +MONDO:0009766 rare diseases +MONDO:0009767 gard_rare diseases +MONDO:0009767 nord_rare diseases +MONDO:0009767 ordo_disorder diseases +MONDO:0009767 ordo_malformation_syndrome diseases +MONDO:0009767 orphanet_rare diseases +MONDO:0009767 otar diseases +MONDO:0009767 rare diseases +MONDO:0009768 gard_rare diseases +MONDO:0009768 nord_rare diseases +MONDO:0009768 rare diseases +MONDO:0009769 gard_rare diseases +MONDO:0009769 nord_rare diseases +MONDO:0009769 ordo_disorder diseases +MONDO:0009769 ordo_malformation_syndrome diseases +MONDO:0009769 orphanet_rare diseases +MONDO:0009769 otar diseases +MONDO:0009769 rare diseases +MONDO:0009770 gard_rare diseases +MONDO:0009770 nord_rare diseases +MONDO:0009770 otar diseases +MONDO:0009770 rare diseases +MONDO:0009771 gard_rare diseases +MONDO:0009771 ordo_disorder diseases +MONDO:0009771 ordo_malformation_syndrome diseases +MONDO:0009771 orphanet_rare diseases +MONDO:0009771 otar diseases +MONDO:0009771 rare diseases +MONDO:0009772 gard_rare diseases +MONDO:0009772 nord_rare diseases +MONDO:0009772 ordo_disorder diseases +MONDO:0009772 ordo_malformation_syndrome diseases +MONDO:0009772 orphanet_rare diseases +MONDO:0009772 rare diseases +MONDO:0009773 gard_rare diseases +MONDO:0009773 nord_rare diseases +MONDO:0009773 ordo_disorder diseases +MONDO:0009773 orphanet_rare diseases +MONDO:0009773 otar diseases +MONDO:0009773 rare diseases +MONDO:0009774 gard_rare diseases +MONDO:0009774 nord_rare diseases +MONDO:0009774 ordo_subtype_of_a_disorder diseases +MONDO:0009774 otar diseases +MONDO:0009774 rare diseases +MONDO:0009775 gard_rare diseases +MONDO:0009775 nord_rare diseases +MONDO:0009775 rare diseases +MONDO:0009776 gard_rare diseases +MONDO:0009776 otar diseases +MONDO:0009776 rare diseases +MONDO:0009777 gard_rare diseases +MONDO:0009777 nord_rare diseases +MONDO:0009777 ordo_disorder diseases +MONDO:0009777 ordo_malformation_syndrome diseases +MONDO:0009777 orphanet_rare diseases +MONDO:0009777 otar diseases +MONDO:0009777 rare diseases +MONDO:0009779 gard_rare diseases +MONDO:0009779 nord_rare diseases +MONDO:0009779 ordo_subtype_of_a_disorder diseases +MONDO:0009779 otar diseases +MONDO:0009779 rare diseases +MONDO:0009780 gard_rare diseases +MONDO:0009780 ordo_disorder diseases +MONDO:0009780 ordo_malformation_syndrome diseases +MONDO:0009780 orphanet_rare diseases +MONDO:0009780 otar diseases +MONDO:0009780 rare diseases +MONDO:0009781 gard_rare diseases +MONDO:0009781 nord_rare diseases +MONDO:0009781 rare diseases +MONDO:0009783 gard_rare diseases +MONDO:0009783 rare diseases +MONDO:0009785 gard_rare diseases +MONDO:0009785 nord_rare diseases +MONDO:0009785 ordo_disorder diseases +MONDO:0009785 orphanet_rare diseases +MONDO:0009785 otar diseases +MONDO:0009785 rare diseases +MONDO:0009786 gard_rare diseases +MONDO:0009786 nord_rare diseases +MONDO:0009786 otar diseases +MONDO:0009786 rare diseases +MONDO:0009787 gard_rare diseases +MONDO:0009787 nord_rare diseases +MONDO:0009787 ordo_disorder diseases +MONDO:0009787 orphanet_rare diseases +MONDO:0009787 otar diseases +MONDO:0009787 rare diseases +MONDO:0009791 other_hierarchy diseases +MONDO:0009792 gard_rare diseases +MONDO:0009792 ordo_disorder diseases +MONDO:0009792 ordo_malformation_syndrome diseases +MONDO:0009792 orphanet_rare diseases +MONDO:0009792 rare diseases +MONDO:0009793 gard_rare diseases +MONDO:0009793 nord_rare diseases +MONDO:0009793 ordo_disorder diseases +MONDO:0009793 ordo_malformation_syndrome diseases +MONDO:0009793 orphanet_rare diseases +MONDO:0009793 otar diseases +MONDO:0009793 rare diseases +MONDO:0009794 gard_rare diseases +MONDO:0009794 nord_rare diseases +MONDO:0009794 ordo_disorder diseases +MONDO:0009794 ordo_malformation_syndrome diseases +MONDO:0009794 orphanet_rare diseases +MONDO:0009794 otar diseases +MONDO:0009794 rare diseases +MONDO:0009795 gard_rare diseases +MONDO:0009795 nord_rare diseases +MONDO:0009795 ordo_disorder diseases +MONDO:0009795 ordo_malformation_syndrome diseases +MONDO:0009795 orphanet_rare diseases +MONDO:0009795 otar diseases +MONDO:0009795 rare diseases +MONDO:0009796 clingen diseases +MONDO:0009796 gard_rare diseases +MONDO:0009796 nord_rare diseases +MONDO:0009796 ordo_disorder diseases +MONDO:0009796 orphanet_rare diseases +MONDO:0009796 otar diseases +MONDO:0009796 rare diseases +MONDO:0009797 gard_rare diseases +MONDO:0009797 nord_rare diseases +MONDO:0009797 ordo_disorder diseases +MONDO:0009797 orphanet_rare diseases +MONDO:0009797 otar diseases +MONDO:0009797 rare diseases +MONDO:0009798 gard_rare diseases +MONDO:0009798 nord_rare diseases +MONDO:0009798 ordo_disorder diseases +MONDO:0009798 ordo_malformation_syndrome diseases +MONDO:0009798 orphanet_rare diseases +MONDO:0009798 otar diseases +MONDO:0009798 rare diseases +MONDO:0009800 gard_rare diseases +MONDO:0009800 nord_rare diseases +MONDO:0009800 rare diseases +MONDO:0009801 gard_rare diseases +MONDO:0009801 nord_rare diseases +MONDO:0009801 ordo_disorder diseases +MONDO:0009801 ordo_malformation_syndrome diseases +MONDO:0009801 orphanet_rare diseases +MONDO:0009801 otar diseases +MONDO:0009801 rare diseases +MONDO:0009803 gard_rare diseases +MONDO:0009803 ordo_disorder diseases +MONDO:0009803 ordo_malformation_syndrome diseases +MONDO:0009803 orphanet_rare diseases +MONDO:0009803 otar diseases +MONDO:0009803 rare diseases +MONDO:0009804 clingen diseases +MONDO:0009804 gard_rare diseases +MONDO:0009804 nord_rare diseases +MONDO:0009804 ordo_subtype_of_a_disorder diseases +MONDO:0009804 otar diseases +MONDO:0009804 rare diseases +MONDO:0009805 gard_rare diseases +MONDO:0009805 nord_rare diseases +MONDO:0009805 rare diseases +MONDO:0009806 gard_rare diseases +MONDO:0009806 nord_rare diseases +MONDO:0009806 rare diseases +MONDO:0009807 otar diseases +MONDO:0009808 gard_rare diseases +MONDO:0009808 rare diseases +MONDO:0009809 gard_rare diseases +MONDO:0009809 nord_rare diseases +MONDO:0009809 rare diseases +MONDO:0009810 gard_rare diseases +MONDO:0009810 ordo_disorder diseases +MONDO:0009810 ordo_malformation_syndrome diseases +MONDO:0009810 orphanet_rare diseases +MONDO:0009810 otar diseases +MONDO:0009810 rare diseases +MONDO:0009813 gard_rare diseases +MONDO:0009813 nord_rare diseases +MONDO:0009813 ordo_disorder diseases +MONDO:0009813 orphanet_rare diseases +MONDO:0009813 rare diseases +MONDO:0009814 gard_rare diseases +MONDO:0009814 ordo_disorder diseases +MONDO:0009814 ordo_malformation_syndrome diseases +MONDO:0009814 orphanet_rare diseases +MONDO:0009814 otar diseases +MONDO:0009814 rare diseases +MONDO:0009815 clingen diseases +MONDO:0009815 gard_rare diseases +MONDO:0009815 nord_rare diseases +MONDO:0009815 otar diseases +MONDO:0009815 rare diseases +MONDO:0009816 gard_rare diseases +MONDO:0009816 nord_rare diseases +MONDO:0009816 otar diseases +MONDO:0009816 rare diseases +MONDO:0009817 gard_rare diseases +MONDO:0009817 nord_rare diseases +MONDO:0009817 rare diseases +MONDO:0009818 gard_rare diseases +MONDO:0009818 nord_rare diseases +MONDO:0009818 ordo_disorder diseases +MONDO:0009818 orphanet_rare diseases +MONDO:0009818 otar diseases +MONDO:0009818 rare diseases +MONDO:0009820 gard_rare diseases +MONDO:0009820 nord_rare diseases +MONDO:0009820 ordo_disorder diseases +MONDO:0009820 orphanet_rare diseases +MONDO:0009820 otar diseases +MONDO:0009820 rare diseases +MONDO:0009821 gard_rare diseases +MONDO:0009821 nord_rare diseases +MONDO:0009821 ordo_disorder diseases +MONDO:0009821 ordo_malformation_syndrome diseases +MONDO:0009821 orphanet_rare diseases +MONDO:0009821 otar diseases +MONDO:0009821 rare diseases +MONDO:0009822 gard_rare diseases +MONDO:0009822 nord_rare diseases +MONDO:0009822 ordo_disorder diseases +MONDO:0009822 ordo_malformation_syndrome diseases +MONDO:0009822 orphanet_rare diseases +MONDO:0009822 rare diseases +MONDO:0009823 gard_rare diseases +MONDO:0009823 nord_rare diseases +MONDO:0009823 ordo_subtype_of_a_disorder diseases +MONDO:0009823 otar diseases +MONDO:0009823 rare diseases +MONDO:0009824 gard_rare diseases +MONDO:0009824 nord_rare diseases +MONDO:0009824 ordo_subtype_of_a_disorder diseases +MONDO:0009824 otar diseases +MONDO:0009824 rare diseases +MONDO:0009825 gard_rare diseases +MONDO:0009825 nord_rare diseases +MONDO:0009825 ordo_disorder diseases +MONDO:0009825 orphanet_rare diseases +MONDO:0009825 otar diseases +MONDO:0009825 rare diseases +MONDO:0009830 gard_rare diseases +MONDO:0009830 ordo_disorder diseases +MONDO:0009830 orphanet_rare diseases +MONDO:0009830 otar diseases +MONDO:0009830 rare diseases +MONDO:0009831 otar diseases +MONDO:0009832 gard_rare diseases +MONDO:0009832 nord_rare diseases +MONDO:0009832 ordo_disorder diseases +MONDO:0009832 ordo_morphological_anomaly diseases +MONDO:0009832 orphanet_rare diseases +MONDO:0009832 otar diseases +MONDO:0009832 prototype_pattern diseases +MONDO:0009832 rare diseases +MONDO:0009833 clingen diseases +MONDO:0009833 gard_rare diseases +MONDO:0009833 nord_rare diseases +MONDO:0009833 ordo_disorder diseases +MONDO:0009833 orphanet_rare diseases +MONDO:0009833 otar diseases +MONDO:0009833 rare diseases +MONDO:0009835 gard_rare diseases +MONDO:0009835 nord_rare diseases +MONDO:0009835 ordo_disorder diseases +MONDO:0009835 orphanet_rare diseases +MONDO:0009835 otar diseases +MONDO:0009835 rare diseases +MONDO:0009837 gard_rare diseases +MONDO:0009837 nord_rare diseases +MONDO:0009837 ordo_disorder diseases +MONDO:0009837 orphanet_rare diseases +MONDO:0009837 rare diseases +MONDO:0009838 gard_rare diseases +MONDO:0009838 ordo_disorder diseases +MONDO:0009838 orphanet_rare diseases +MONDO:0009838 otar diseases +MONDO:0009838 rare diseases +MONDO:0009839 gard_rare diseases +MONDO:0009839 nord_rare diseases +MONDO:0009839 ordo_subtype_of_a_disorder diseases +MONDO:0009839 otar diseases +MONDO:0009839 rare diseases +MONDO:0009841 gard_rare diseases +MONDO:0009841 nord_rare diseases +MONDO:0009841 ordo_disorder diseases +MONDO:0009841 orphanet_rare diseases +MONDO:0009841 otar diseases +MONDO:0009841 rare diseases +MONDO:0009842 gard_rare diseases +MONDO:0009842 nord_rare diseases +MONDO:0009842 rare diseases +MONDO:0009843 gard_rare diseases +MONDO:0009843 nord_rare diseases +MONDO:0009843 ordo_subtype_of_a_disorder diseases +MONDO:0009843 otar diseases +MONDO:0009843 rare diseases +MONDO:0009844 gard_rare diseases +MONDO:0009844 nord_rare diseases +MONDO:0009844 otar diseases +MONDO:0009844 rare diseases +MONDO:0009845 gard_rare diseases +MONDO:0009845 nord_rare diseases +MONDO:0009845 ordo_disorder diseases +MONDO:0009845 ordo_malformation_syndrome diseases +MONDO:0009845 orphanet_rare diseases +MONDO:0009845 otar diseases +MONDO:0009845 rare diseases +MONDO:0009846 gard_rare diseases +MONDO:0009846 mostly_harmless diseases +MONDO:0009846 nord_rare diseases +MONDO:0009846 ordo_disorder diseases +MONDO:0009846 orphanet_rare diseases +MONDO:0009846 otar diseases +MONDO:0009846 rare diseases +MONDO:0009848 gard_rare diseases +MONDO:0009848 nord_rare diseases +MONDO:0009848 ordo_disorder diseases +MONDO:0009848 orphanet_rare diseases +MONDO:0009848 rare diseases +MONDO:0009849 gard_rare diseases +MONDO:0009849 nord_rare diseases +MONDO:0009849 ordo_subtype_of_a_disorder diseases +MONDO:0009849 otar diseases +MONDO:0009849 rare diseases +MONDO:0009852 gard_rare diseases +MONDO:0009852 nord_rare diseases +MONDO:0009852 ordo_disorder diseases +MONDO:0009852 orphanet_rare diseases +MONDO:0009852 otar diseases +MONDO:0009852 rare diseases +MONDO:0009853 gard_rare diseases +MONDO:0009853 nord_rare diseases +MONDO:0009853 ordo_disorder diseases +MONDO:0009853 orphanet_rare diseases +MONDO:0009853 otar diseases +MONDO:0009853 rare diseases +MONDO:0009855 clingen diseases +MONDO:0009855 gard_rare diseases +MONDO:0009855 nord_rare diseases +MONDO:0009855 ordo_disorder diseases +MONDO:0009855 orphanet_rare diseases +MONDO:0009855 otar diseases +MONDO:0009855 rare diseases +MONDO:0009856 gard_rare diseases +MONDO:0009856 nord_rare diseases +MONDO:0009856 ordo_disorder diseases +MONDO:0009856 ordo_malformation_syndrome diseases +MONDO:0009856 orphanet_rare diseases +MONDO:0009856 otar diseases +MONDO:0009856 rare diseases +MONDO:0009857 gard_rare diseases +MONDO:0009857 nord_rare diseases +MONDO:0009857 ordo_disorder diseases +MONDO:0009857 ordo_malformation_syndrome diseases +MONDO:0009857 orphanet_rare diseases +MONDO:0009857 otar diseases +MONDO:0009857 rare diseases +MONDO:0009858 gard_rare diseases +MONDO:0009858 ordo_disorder diseases +MONDO:0009858 ordo_malformation_syndrome diseases +MONDO:0009858 orphanet_rare diseases +MONDO:0009858 otar diseases +MONDO:0009858 rare diseases +MONDO:0009859 gard_rare diseases +MONDO:0009859 ordo_disorder diseases +MONDO:0009859 ordo_malformation_syndrome diseases +MONDO:0009859 orphanet_rare diseases +MONDO:0009859 otar diseases +MONDO:0009859 rare diseases +MONDO:0009861 clingen diseases +MONDO:0009861 gard_rare diseases +MONDO:0009861 nord_rare diseases +MONDO:0009861 ordo_disorder diseases +MONDO:0009861 orphanet_rare diseases +MONDO:0009861 otar diseases +MONDO:0009861 rare diseases +MONDO:0009862 clingen diseases +MONDO:0009862 gard_rare diseases +MONDO:0009862 nord_rare diseases +MONDO:0009862 ordo_subtype_of_a_disorder diseases +MONDO:0009862 otar diseases +MONDO:0009862 rare diseases +MONDO:0009863 clingen diseases +MONDO:0009863 gard_rare diseases +MONDO:0009863 nord_rare diseases +MONDO:0009863 ordo_subtype_of_a_disorder diseases +MONDO:0009863 otar diseases +MONDO:0009863 rare diseases +MONDO:0009864 gard_rare diseases +MONDO:0009864 otar diseases +MONDO:0009864 rare diseases +MONDO:0009865 gard_rare diseases +MONDO:0009865 nord_rare diseases +MONDO:0009865 ordo_disorder diseases +MONDO:0009865 orphanet_rare diseases +MONDO:0009865 otar diseases +MONDO:0009865 rare diseases +MONDO:0009866 gard_rare diseases +MONDO:0009866 nord_rare diseases +MONDO:0009866 otar diseases +MONDO:0009866 rare diseases +MONDO:0009867 gard_rare diseases +MONDO:0009867 nord_rare diseases +MONDO:0009867 ordo_disorder diseases +MONDO:0009867 orphanet_rare diseases +MONDO:0009867 otar diseases +MONDO:0009867 rare diseases +MONDO:0009868 gard_rare diseases +MONDO:0009868 nord_rare diseases +MONDO:0009868 ordo_disorder diseases +MONDO:0009868 orphanet_rare diseases +MONDO:0009868 otar diseases +MONDO:0009868 rare diseases +MONDO:0009869 clingen diseases +MONDO:0009869 gard_rare diseases +MONDO:0009869 nord_rare diseases +MONDO:0009869 ordo_disorder diseases +MONDO:0009869 ordo_malformation_syndrome diseases +MONDO:0009869 orphanet_rare diseases +MONDO:0009869 otar diseases +MONDO:0009869 rare diseases +MONDO:0009870 gard_rare diseases +MONDO:0009870 nord_rare diseases +MONDO:0009870 ordo_disorder diseases +MONDO:0009870 orphanet_rare diseases +MONDO:0009870 otar diseases +MONDO:0009870 rare diseases +MONDO:0009871 gard_rare diseases +MONDO:0009871 nord_rare diseases +MONDO:0009871 ordo_disorder diseases +MONDO:0009871 ordo_malformation_syndrome diseases +MONDO:0009871 orphanet_rare diseases +MONDO:0009871 otar diseases +MONDO:0009871 rare diseases +MONDO:0009872 clingen diseases +MONDO:0009872 gard_rare diseases +MONDO:0009872 nord_rare diseases +MONDO:0009872 ordo_disorder diseases +MONDO:0009872 orphanet_rare diseases +MONDO:0009872 otar diseases +MONDO:0009872 rare diseases +MONDO:0009873 gard_rare diseases +MONDO:0009873 ordo_disorder diseases +MONDO:0009873 ordo_malformation_syndrome diseases +MONDO:0009873 orphanet_rare diseases +MONDO:0009873 rare diseases +MONDO:0009874 gard_rare diseases +MONDO:0009874 nord_rare diseases +MONDO:0009874 ordo_disorder diseases +MONDO:0009874 ordo_malformation_syndrome diseases +MONDO:0009874 orphanet_rare diseases +MONDO:0009874 otar diseases +MONDO:0009874 rare diseases +MONDO:0009875 gard_rare diseases +MONDO:0009875 rare diseases +MONDO:0009876 gard_rare diseases +MONDO:0009876 nord_rare diseases +MONDO:0009876 ordo_subtype_of_a_disorder diseases +MONDO:0009876 otar diseases +MONDO:0009876 rare diseases +MONDO:0009877 gard_rare diseases +MONDO:0009877 nord_rare diseases +MONDO:0009877 ordo_disorder diseases +MONDO:0009877 orphanet_rare diseases +MONDO:0009877 otar diseases +MONDO:0009877 rare diseases +MONDO:0009878 gard_rare diseases +MONDO:0009878 nord_rare diseases +MONDO:0009878 rare diseases +MONDO:0009879 gard_rare diseases +MONDO:0009879 nord_rare diseases +MONDO:0009879 ordo_subtype_of_a_disorder diseases +MONDO:0009879 otar diseases +MONDO:0009879 rare diseases +MONDO:0009880 gard_rare diseases +MONDO:0009880 nord_rare diseases +MONDO:0009880 ordo_disorder diseases +MONDO:0009880 orphanet_rare diseases +MONDO:0009880 otar diseases +MONDO:0009880 rare diseases +MONDO:0009883 clingen diseases +MONDO:0009883 gard_rare diseases +MONDO:0009883 nord_rare diseases +MONDO:0009883 ordo_disorder diseases +MONDO:0009883 orphanet_rare diseases +MONDO:0009883 otar diseases +MONDO:0009883 rare diseases +MONDO:0009885 clingen diseases +MONDO:0009885 gard_rare diseases +MONDO:0009885 nord_rare diseases +MONDO:0009885 ordo_disorder diseases +MONDO:0009885 orphanet_rare diseases +MONDO:0009885 otar diseases +MONDO:0009885 rare diseases +MONDO:0009887 gard_rare diseases +MONDO:0009887 nord_rare diseases +MONDO:0009887 ordo_disorder diseases +MONDO:0009887 orphanet_rare diseases +MONDO:0009887 rare diseases +MONDO:0009889 clingen diseases +MONDO:0009889 gard_rare diseases +MONDO:0009889 nord_rare diseases +MONDO:0009889 ordo_disorder diseases +MONDO:0009889 orphanet_rare diseases +MONDO:0009889 otar diseases +MONDO:0009889 rare diseases +MONDO:0009890 gard_rare diseases +MONDO:0009890 nord_rare diseases +MONDO:0009890 rare diseases +MONDO:0009891 gard_rare diseases +MONDO:0009891 nord_rare diseases +MONDO:0009891 ordo_disorder diseases +MONDO:0009891 orphanet_rare diseases +MONDO:0009891 otar diseases +MONDO:0009891 rare diseases +MONDO:0009892 gard_rare diseases +MONDO:0009892 nord_rare diseases +MONDO:0009892 ordo_disorder diseases +MONDO:0009892 orphanet_rare diseases +MONDO:0009892 otar diseases +MONDO:0009892 rare diseases +MONDO:0009893 gard_rare diseases +MONDO:0009893 nord_rare diseases +MONDO:0009893 rare diseases +MONDO:0009894 gard_rare diseases +MONDO:0009894 nord_rare diseases +MONDO:0009894 otar diseases +MONDO:0009894 rare diseases +MONDO:0009895 gard_rare diseases +MONDO:0009895 nord_rare diseases +MONDO:0009895 ordo_disorder diseases +MONDO:0009895 ordo_malformation_syndrome diseases +MONDO:0009895 orphanet_rare diseases +MONDO:0009895 otar diseases +MONDO:0009895 rare diseases +MONDO:0009897 gard_rare diseases +MONDO:0009897 nord_rare diseases +MONDO:0009897 ordo_subtype_of_a_disorder diseases +MONDO:0009897 otar diseases +MONDO:0009897 rare diseases +MONDO:0009900 gard_rare diseases +MONDO:0009900 nord_rare diseases +MONDO:0009900 ordo_disorder diseases +MONDO:0009900 ordo_malformation_syndrome diseases +MONDO:0009900 orphanet_rare diseases +MONDO:0009900 otar diseases +MONDO:0009900 rare diseases +MONDO:0009901 gard_rare diseases +MONDO:0009901 nord_rare diseases +MONDO:0009901 ordo_disorder diseases +MONDO:0009901 ordo_malformation_syndrome diseases +MONDO:0009901 orphanet_rare diseases +MONDO:0009901 otar diseases +MONDO:0009901 rare diseases +MONDO:0009902 gard_rare diseases +MONDO:0009902 nord_rare diseases +MONDO:0009902 ordo_disorder diseases +MONDO:0009902 orphanet_rare diseases +MONDO:0009902 otar diseases +MONDO:0009902 rare diseases +MONDO:0009903 gard_rare diseases +MONDO:0009903 nord_rare diseases +MONDO:0009903 ordo_disorder diseases +MONDO:0009903 ordo_malformation_syndrome diseases +MONDO:0009903 orphanet_rare diseases +MONDO:0009903 otar diseases +MONDO:0009903 rare diseases +MONDO:0009904 gard_rare diseases +MONDO:0009904 nord_rare diseases +MONDO:0009904 ordo_disorder diseases +MONDO:0009904 orphanet_rare diseases +MONDO:0009904 otar diseases +MONDO:0009904 rare diseases +MONDO:0009905 gard_rare diseases +MONDO:0009905 nord_rare diseases +MONDO:0009905 ordo_disorder diseases +MONDO:0009905 ordo_malformation_syndrome diseases +MONDO:0009905 orphanet_rare diseases +MONDO:0009905 otar diseases +MONDO:0009905 rare diseases +MONDO:0009906 gard_rare diseases +MONDO:0009906 nord_rare diseases +MONDO:0009906 rare diseases +MONDO:0009908 clingen diseases +MONDO:0009908 gard_rare diseases +MONDO:0009908 ordo_subtype_of_a_disorder diseases +MONDO:0009908 otar diseases +MONDO:0009908 rare diseases +MONDO:0009910 gard_rare diseases +MONDO:0009910 nord_rare diseases +MONDO:0009910 ordo_disorder diseases +MONDO:0009910 ordo_malformation_syndrome diseases +MONDO:0009910 orphanet_rare diseases +MONDO:0009910 otar diseases +MONDO:0009910 rare diseases +MONDO:0009914 gard_rare diseases +MONDO:0009914 nord_rare diseases +MONDO:0009914 ordo_disorder diseases +MONDO:0009914 ordo_malformation_syndrome diseases +MONDO:0009914 orphanet_rare diseases +MONDO:0009914 otar diseases +MONDO:0009914 rare diseases +MONDO:0009915 gard_rare diseases +MONDO:0009915 ordo_disorder diseases +MONDO:0009915 ordo_malformation_syndrome diseases +MONDO:0009915 orphanet_rare diseases +MONDO:0009915 otar diseases +MONDO:0009915 rare diseases +MONDO:0009916 gard_rare diseases +MONDO:0009916 nord_rare diseases +MONDO:0009916 ordo_disorder diseases +MONDO:0009916 orphanet_rare diseases +MONDO:0009916 otar diseases +MONDO:0009916 rare diseases +MONDO:0009917 clingen diseases +MONDO:0009917 gard_rare diseases +MONDO:0009917 nord_rare diseases +MONDO:0009917 ordo_subtype_of_a_disorder diseases +MONDO:0009917 otar diseases +MONDO:0009917 rare diseases +MONDO:0009918 gard_rare diseases +MONDO:0009918 nord_rare diseases +MONDO:0009918 rare diseases +MONDO:0009919 clingen diseases +MONDO:0009919 gard_rare diseases +MONDO:0009919 ordo_disorder diseases +MONDO:0009919 orphanet_rare diseases +MONDO:0009919 otar diseases +MONDO:0009919 rare diseases +MONDO:0009920 gard_rare diseases +MONDO:0009920 nord_rare diseases +MONDO:0009920 ordo_disorder diseases +MONDO:0009920 ordo_malformation_syndrome diseases +MONDO:0009920 orphanet_rare diseases +MONDO:0009920 otar diseases +MONDO:0009920 rare diseases +MONDO:0009921 gard_rare diseases +MONDO:0009921 nord_rare diseases +MONDO:0009921 ordo_disorder diseases +MONDO:0009921 ordo_malformation_syndrome diseases +MONDO:0009921 orphanet_rare diseases +MONDO:0009921 otar diseases +MONDO:0009921 rare diseases +MONDO:0009923 gard_rare diseases +MONDO:0009923 nord_rare diseases +MONDO:0009923 ordo_disorder diseases +MONDO:0009923 orphanet_rare diseases +MONDO:0009923 otar diseases +MONDO:0009923 rare diseases +MONDO:0009924 gard_rare diseases +MONDO:0009924 nord_rare diseases +MONDO:0009924 ordo_disorder diseases +MONDO:0009924 orphanet_rare diseases +MONDO:0009924 otar diseases +MONDO:0009924 rare diseases +MONDO:0009925 gard_rare diseases +MONDO:0009925 nord_rare diseases +MONDO:0009925 ordo_disorder diseases +MONDO:0009925 orphanet_rare diseases +MONDO:0009925 otar diseases +MONDO:0009925 rare diseases +MONDO:0009926 gard_rare diseases +MONDO:0009926 nord_rare diseases +MONDO:0009926 ordo_disorder diseases +MONDO:0009926 ordo_malformation_syndrome diseases +MONDO:0009926 orphanet_rare diseases +MONDO:0009926 otar diseases +MONDO:0009926 rare diseases +MONDO:0009927 gard_rare diseases +MONDO:0009927 nord_rare diseases +MONDO:0009927 otar diseases +MONDO:0009927 rare diseases +MONDO:0009928 gard_rare diseases +MONDO:0009928 nord_rare diseases +MONDO:0009928 ordo_disorder diseases +MONDO:0009928 orphanet_rare diseases +MONDO:0009928 otar diseases +MONDO:0009928 rare diseases +MONDO:0009929 gard_rare diseases +MONDO:0009929 nord_rare diseases +MONDO:0009929 ordo_disorder diseases +MONDO:0009929 orphanet_rare diseases +MONDO:0009929 otar diseases +MONDO:0009929 rare diseases +MONDO:0009931 gard_rare diseases +MONDO:0009931 nord_rare diseases +MONDO:0009931 ordo_disorder diseases +MONDO:0009931 ordo_morphological_anomaly diseases +MONDO:0009931 orphanet_rare diseases +MONDO:0009931 rare diseases +MONDO:0009933 gard_rare diseases +MONDO:0009933 nord_rare diseases +MONDO:0009933 ordo_disorder diseases +MONDO:0009933 orphanet_rare diseases +MONDO:0009933 otar diseases +MONDO:0009933 rare diseases +MONDO:0009934 gard_rare diseases +MONDO:0009934 nord_rare diseases +MONDO:0009934 ordo_disorder diseases +MONDO:0009934 orphanet_rare diseases +MONDO:0009934 otar diseases +MONDO:0009934 rare diseases +MONDO:0009935 gard_rare diseases +MONDO:0009935 nord_rare diseases +MONDO:0009935 rare diseases +MONDO:0009936 gard_rare diseases +MONDO:0009936 nord_rare diseases +MONDO:0009936 ordo_disorder diseases +MONDO:0009936 ordo_malformation_syndrome diseases +MONDO:0009936 orphanet_rare diseases +MONDO:0009936 otar diseases +MONDO:0009936 rare diseases +MONDO:0009937 gard_rare diseases +MONDO:0009937 nord_rare diseases +MONDO:0009937 ordo_disorder diseases +MONDO:0009937 orphanet_rare diseases +MONDO:0009937 otar diseases +MONDO:0009937 prototype_pattern diseases +MONDO:0009937 rare diseases +MONDO:0009938 gard_rare diseases +MONDO:0009938 nord_rare diseases +MONDO:0009938 rare diseases +MONDO:0009940 clingen diseases +MONDO:0009940 gard_rare diseases +MONDO:0009940 nord_rare diseases +MONDO:0009940 ordo_disorder diseases +MONDO:0009940 orphanet_rare diseases +MONDO:0009940 otar diseases +MONDO:0009940 rare diseases +MONDO:0009942 gard_rare diseases +MONDO:0009942 nord_rare diseases +MONDO:0009942 ordo_disorder diseases +MONDO:0009942 ordo_malformation_syndrome diseases +MONDO:0009942 orphanet_rare diseases +MONDO:0009942 otar diseases +MONDO:0009942 rare diseases +MONDO:0009943 gard_rare diseases +MONDO:0009943 nord_rare diseases +MONDO:0009943 ordo_disorder diseases +MONDO:0009943 orphanet_rare diseases +MONDO:0009943 otar diseases +MONDO:0009943 rare diseases +MONDO:0009945 clingen diseases +MONDO:0009945 gard_rare diseases +MONDO:0009945 nord_rare diseases +MONDO:0009945 ordo_disorder diseases +MONDO:0009945 orphanet_rare diseases +MONDO:0009945 otar diseases +MONDO:0009945 rare diseases +MONDO:0009946 gard_rare diseases +MONDO:0009946 nord_rare diseases +MONDO:0009946 ordo_disorder diseases +MONDO:0009946 orphanet_rare diseases +MONDO:0009946 otar diseases +MONDO:0009946 rare diseases +MONDO:0009947 gard_rare diseases +MONDO:0009947 nord_rare diseases +MONDO:0009947 ordo_subtype_of_a_disorder diseases +MONDO:0009947 otar diseases +MONDO:0009947 rare diseases +MONDO:0009948 gard_rare diseases +MONDO:0009948 nord_rare diseases +MONDO:0009948 otar diseases +MONDO:0009948 rare diseases +MONDO:0009949 gard_rare diseases +MONDO:0009949 nord_rare diseases +MONDO:0009949 ordo_disorder diseases +MONDO:0009949 orphanet_rare diseases +MONDO:0009949 otar diseases +MONDO:0009949 rare diseases +MONDO:0009950 gard_rare diseases +MONDO:0009950 nord_rare diseases +MONDO:0009950 ordo_disorder diseases +MONDO:0009950 orphanet_rare diseases +MONDO:0009950 otar diseases +MONDO:0009950 rare diseases +MONDO:0009952 gard_rare diseases +MONDO:0009952 nord_rare diseases +MONDO:0009952 ordo_disorder diseases +MONDO:0009952 ordo_malformation_syndrome diseases +MONDO:0009952 orphanet_rare diseases +MONDO:0009952 otar diseases +MONDO:0009952 rare diseases +MONDO:0009953 gard_rare diseases +MONDO:0009953 nord_rare diseases +MONDO:0009953 ordo_subtype_of_a_disorder diseases +MONDO:0009953 otar diseases +MONDO:0009953 rare diseases +MONDO:0009954 gard_rare diseases +MONDO:0009954 nord_rare diseases +MONDO:0009954 ordo_disorder diseases +MONDO:0009954 ordo_malformation_syndrome diseases +MONDO:0009954 orphanet_rare diseases +MONDO:0009954 otar diseases +MONDO:0009954 rare diseases +MONDO:0009955 gard_rare diseases +MONDO:0009955 nord_rare diseases +MONDO:0009955 ordo_disorder diseases +MONDO:0009955 ordo_malformation_syndrome diseases +MONDO:0009955 orphanet_rare diseases +MONDO:0009955 otar diseases +MONDO:0009955 rare diseases +MONDO:0009958 gard_rare diseases +MONDO:0009958 nord_rare diseases +MONDO:0009958 ordo_disorder diseases +MONDO:0009958 orphanet_rare diseases +MONDO:0009958 otar diseases +MONDO:0009958 rare diseases +MONDO:0009959 gard_rare diseases +MONDO:0009959 nord_rare diseases +MONDO:0009959 otar diseases +MONDO:0009959 rare diseases +MONDO:0009962 gard_rare diseases +MONDO:0009962 nord_rare diseases +MONDO:0009962 rare diseases +MONDO:0009963 gard_rare diseases +MONDO:0009963 nord_rare diseases +MONDO:0009963 ordo_disorder diseases +MONDO:0009963 ordo_malformation_syndrome diseases +MONDO:0009963 orphanet_rare diseases +MONDO:0009963 otar diseases +MONDO:0009963 rare diseases +MONDO:0009964 gard_rare diseases +MONDO:0009964 nord_rare diseases +MONDO:0009964 ordo_disorder diseases +MONDO:0009964 orphanet_rare diseases +MONDO:0009964 otar diseases +MONDO:0009964 rare diseases +MONDO:0009965 clingen diseases +MONDO:0009965 gard_rare diseases +MONDO:0009965 nord_rare diseases +MONDO:0009965 ordo_disorder diseases +MONDO:0009965 ordo_malformation_syndrome diseases +MONDO:0009965 orphanet_rare diseases +MONDO:0009965 otar diseases +MONDO:0009965 rare diseases +MONDO:0009966 gard_rare diseases +MONDO:0009966 nord_rare diseases +MONDO:0009966 ordo_disorder diseases +MONDO:0009966 ordo_malformation_syndrome diseases +MONDO:0009966 orphanet_rare diseases +MONDO:0009966 otar diseases +MONDO:0009966 rare diseases +MONDO:0009967 gard_rare diseases +MONDO:0009967 rare diseases +MONDO:0009968 clingen diseases +MONDO:0009968 gard_rare diseases +MONDO:0009968 nord_rare diseases +MONDO:0009968 otar diseases +MONDO:0009968 rare diseases +MONDO:0009969 gard_rare diseases +MONDO:0009969 ordo_malformation_syndrome diseases +MONDO:0009969 otar diseases +MONDO:0009969 rare diseases +MONDO:0009970 clingen diseases +MONDO:0009970 gard_rare diseases +MONDO:0009970 ordo_etiological_subtype diseases +MONDO:0009970 ordo_subtype_of_a_disorder diseases +MONDO:0009970 otar diseases +MONDO:0009970 rare diseases +MONDO:0009971 gard_rare diseases +MONDO:0009971 nord_rare diseases +MONDO:0009971 ordo_disorder diseases +MONDO:0009971 orphanet_rare diseases +MONDO:0009971 otar diseases +MONDO:0009971 rare diseases +MONDO:0009973 clingen diseases +MONDO:0009973 gard_rare diseases +MONDO:0009973 nord_rare diseases +MONDO:0009973 ordo_disorder diseases +MONDO:0009973 orphanet_rare diseases +MONDO:0009973 otar diseases +MONDO:0009973 rare diseases +MONDO:0009974 gard_rare diseases +MONDO:0009974 nord_rare diseases +MONDO:0009974 otar diseases +MONDO:0009974 prototype_pattern diseases +MONDO:0009974 rare diseases +MONDO:0009975 gard_rare diseases +MONDO:0009975 nord_rare diseases +MONDO:0009975 ordo_disorder diseases +MONDO:0009975 orphanet_rare diseases +MONDO:0009975 otar diseases +MONDO:0009975 rare diseases +MONDO:0009978 gard_rare diseases +MONDO:0009978 nord_rare diseases +MONDO:0009978 ordo_disorder diseases +MONDO:0009978 ordo_malformation_syndrome diseases +MONDO:0009978 orphanet_rare diseases +MONDO:0009978 otar diseases +MONDO:0009978 rare diseases +MONDO:0009979 gard_rare diseases +MONDO:0009979 nord_rare diseases +MONDO:0009979 ordo_disorder diseases +MONDO:0009979 orphanet_rare diseases +MONDO:0009979 otar diseases +MONDO:0009979 rare diseases +MONDO:0009983 gard_rare diseases +MONDO:0009983 nord_rare diseases +MONDO:0009983 ordo_disorder diseases +MONDO:0009983 ordo_malformation_syndrome diseases +MONDO:0009983 orphanet_rare diseases +MONDO:0009983 otar diseases +MONDO:0009983 rare diseases +MONDO:0009984 gard_rare diseases +MONDO:0009984 nord_rare diseases +MONDO:0009984 rare diseases +MONDO:0009985 gard_rare diseases +MONDO:0009985 nord_rare diseases +MONDO:0009985 ordo_malformation_syndrome diseases +MONDO:0009985 rare diseases +MONDO:0009987 gard_rare diseases +MONDO:0009987 nord_rare diseases +MONDO:0009987 rare diseases +MONDO:0009988 gard_rare diseases +MONDO:0009988 nord_rare diseases +MONDO:0009988 rare diseases +MONDO:0009990 gard_rare diseases +MONDO:0009990 nord_rare diseases +MONDO:0009990 ordo_disorder diseases +MONDO:0009990 ordo_malformation_syndrome diseases +MONDO:0009990 orphanet_rare diseases +MONDO:0009990 otar diseases +MONDO:0009990 rare diseases +MONDO:0009992 clingen diseases +MONDO:0009992 gard_rare diseases +MONDO:0009992 rare diseases +MONDO:0009993 gard_rare diseases +MONDO:0009993 nord_rare diseases +MONDO:0009993 ordo_subtype_of_a_disorder diseases +MONDO:0009993 otar diseases +MONDO:0009993 rare diseases +MONDO:0009994 gard_rare diseases +MONDO:0009994 nord_rare diseases +MONDO:0009994 ordo_subtype_of_a_disorder diseases +MONDO:0009994 otar diseases +MONDO:0009994 rare diseases +MONDO:0009996 gard_rare diseases +MONDO:0009996 nord_rare diseases +MONDO:0009996 ordo_disorder diseases +MONDO:0009996 ordo_malformation_syndrome diseases +MONDO:0009996 orphanet_rare diseases +MONDO:0009996 otar diseases +MONDO:0009996 rare diseases +MONDO:0009998 gard_rare diseases +MONDO:0009998 nord_rare diseases +MONDO:0009998 ordo_disorder diseases +MONDO:0009998 ordo_malformation_syndrome diseases +MONDO:0009998 orphanet_rare diseases +MONDO:0009998 otar diseases +MONDO:0009998 rare diseases +MONDO:0009999 gard_rare diseases +MONDO:0009999 nord_rare diseases +MONDO:0009999 ordo_subtype_of_a_disorder diseases +MONDO:0009999 otar diseases +MONDO:0009999 rare diseases +MONDO:0010000 otar diseases +MONDO:0010001 gard_rare diseases +MONDO:0010001 ordo_disorder diseases +MONDO:0010001 ordo_malformation_syndrome diseases +MONDO:0010001 orphanet_rare diseases +MONDO:0010001 otar diseases +MONDO:0010001 rare diseases +MONDO:0010002 clingen diseases +MONDO:0010002 gard_rare diseases +MONDO:0010002 nord_rare diseases +MONDO:0010002 ordo_disorder diseases +MONDO:0010002 orphanet_rare diseases +MONDO:0010002 otar diseases +MONDO:0010002 rare diseases +MONDO:0010004 gard_rare diseases +MONDO:0010004 nord_rare diseases +MONDO:0010004 ordo_disorder diseases +MONDO:0010004 ordo_malformation_syndrome diseases +MONDO:0010004 orphanet_rare diseases +MONDO:0010004 otar diseases +MONDO:0010004 rare diseases +MONDO:0010005 gard_rare diseases +MONDO:0010005 ordo_disorder diseases +MONDO:0010005 orphanet_rare diseases +MONDO:0010005 otar diseases +MONDO:0010005 rare diseases +MONDO:0010006 clingen diseases +MONDO:0010006 gard_rare diseases +MONDO:0010006 nord_rare diseases +MONDO:0010006 ordo_disorder diseases +MONDO:0010006 orphanet_rare diseases +MONDO:0010006 otar diseases +MONDO:0010006 rare diseases +MONDO:0010007 gard_rare diseases +MONDO:0010007 nord_rare diseases +MONDO:0010007 ordo_disorder diseases +MONDO:0010007 ordo_malformation_syndrome diseases +MONDO:0010007 orphanet_rare diseases +MONDO:0010007 otar diseases +MONDO:0010007 rare diseases +MONDO:0010008 clingen diseases +MONDO:0010008 gard_rare diseases +MONDO:0010008 nord_rare diseases +MONDO:0010008 ordo_disorder diseases +MONDO:0010008 orphanet_rare diseases +MONDO:0010008 otar diseases +MONDO:0010008 rare diseases +MONDO:0010010 clingen diseases +MONDO:0010010 gard_rare diseases +MONDO:0010010 nord_rare diseases +MONDO:0010010 ordo_disorder diseases +MONDO:0010010 ordo_malformation_syndrome diseases +MONDO:0010010 orphanet_rare diseases +MONDO:0010010 otar diseases +MONDO:0010010 rare diseases +MONDO:0010011 gard_rare diseases +MONDO:0010011 nord_rare diseases +MONDO:0010011 ordo_disorder diseases +MONDO:0010011 orphanet_rare diseases +MONDO:0010011 otar diseases +MONDO:0010011 rare diseases +MONDO:0010012 gard_rare diseases +MONDO:0010012 nord_rare diseases +MONDO:0010012 ordo_disorder diseases +MONDO:0010012 orphanet_rare diseases +MONDO:0010012 rare diseases +MONDO:0010013 gard_rare diseases +MONDO:0010013 nord_rare diseases +MONDO:0010013 ordo_disorder diseases +MONDO:0010013 ordo_malformation_syndrome diseases +MONDO:0010013 orphanet_rare diseases +MONDO:0010013 otar diseases +MONDO:0010013 rare diseases +MONDO:0010014 gard_rare diseases +MONDO:0010014 nord_rare diseases +MONDO:0010014 ordo_disorder diseases +MONDO:0010014 ordo_malformation_syndrome diseases +MONDO:0010014 orphanet_rare diseases +MONDO:0010014 otar diseases +MONDO:0010014 rare diseases +MONDO:0010015 clingen diseases +MONDO:0010015 gard_rare diseases +MONDO:0010015 nord_rare diseases +MONDO:0010015 ordo_disorder diseases +MONDO:0010015 ordo_malformation_syndrome diseases +MONDO:0010015 orphanet_rare diseases +MONDO:0010015 otar diseases +MONDO:0010015 rare diseases +MONDO:0010016 gard_rare diseases +MONDO:0010016 nord_rare diseases +MONDO:0010016 rare diseases +MONDO:0010017 gard_rare diseases +MONDO:0010017 nord_rare diseases +MONDO:0010017 ordo_disorder diseases +MONDO:0010017 orphanet_rare diseases +MONDO:0010017 otar diseases +MONDO:0010017 rare diseases +MONDO:0010019 gard_rare diseases +MONDO:0010019 nord_rare diseases +MONDO:0010019 rare diseases +MONDO:0010020 gard_rare diseases +MONDO:0010020 nord_rare diseases +MONDO:0010020 rare diseases +MONDO:0010021 gard_rare diseases +MONDO:0010021 nord_rare diseases +MONDO:0010021 rare diseases +MONDO:0010023 clingen diseases +MONDO:0010023 gard_rare diseases +MONDO:0010023 nord_rare diseases +MONDO:0010023 ordo_disorder diseases +MONDO:0010023 orphanet_rare diseases +MONDO:0010023 otar diseases +MONDO:0010023 rare diseases +MONDO:0010024 gard_rare diseases +MONDO:0010024 nord_rare diseases +MONDO:0010024 ordo_disorder diseases +MONDO:0010024 ordo_malformation_syndrome diseases +MONDO:0010024 orphanet_rare diseases +MONDO:0010024 otar diseases +MONDO:0010024 rare diseases +MONDO:0010026 clingen diseases +MONDO:0010026 gard_rare diseases +MONDO:0010026 nord_rare diseases +MONDO:0010026 ordo_disorder diseases +MONDO:0010026 ordo_malformation_syndrome diseases +MONDO:0010026 orphanet_rare diseases +MONDO:0010026 otar diseases +MONDO:0010026 rare diseases +MONDO:0010027 gard_rare diseases +MONDO:0010027 nord_rare diseases +MONDO:0010027 ordo_subtype_of_a_disorder diseases +MONDO:0010027 otar diseases +MONDO:0010027 rare diseases +MONDO:0010028 gard_rare diseases +MONDO:0010028 nord_rare diseases +MONDO:0010028 ordo_disorder diseases +MONDO:0010028 orphanet_rare diseases +MONDO:0010028 otar diseases +MONDO:0010028 rare diseases +MONDO:0010029 gard_rare diseases +MONDO:0010029 nord_rare diseases +MONDO:0010029 ordo_disorder diseases +MONDO:0010029 ordo_morphological_anomaly diseases +MONDO:0010029 orphanet_rare diseases +MONDO:0010029 otar diseases +MONDO:0010029 rare diseases +MONDO:0010030 gard_rare diseases +MONDO:0010030 ordo_disorder diseases +MONDO:0010030 orphanet_rare diseases +MONDO:0010030 otar diseases +MONDO:0010030 rare diseases +MONDO:0010031 gard_rare diseases +MONDO:0010031 nord_rare diseases +MONDO:0010031 ordo_disorder diseases +MONDO:0010031 orphanet_rare diseases +MONDO:0010031 otar diseases +MONDO:0010031 rare diseases +MONDO:0010033 gard_rare diseases +MONDO:0010033 nord_rare diseases +MONDO:0010033 ordo_disorder diseases +MONDO:0010033 orphanet_rare diseases +MONDO:0010033 otar diseases +MONDO:0010033 rare diseases +MONDO:0010035 clingen diseases +MONDO:0010035 gard_rare diseases +MONDO:0010035 nord_rare diseases +MONDO:0010035 ordo_disorder diseases +MONDO:0010035 ordo_malformation_syndrome diseases +MONDO:0010035 orphanet_rare diseases +MONDO:0010035 otar diseases +MONDO:0010035 rare diseases +MONDO:0010036 gard_rare diseases +MONDO:0010036 nord_rare diseases +MONDO:0010036 rare diseases +MONDO:0010038 gard_rare diseases +MONDO:0010038 nord_rare diseases +MONDO:0010038 ordo_disorder diseases +MONDO:0010038 orphanet_rare diseases +MONDO:0010038 otar diseases +MONDO:0010038 rare diseases +MONDO:0010039 gard_rare diseases +MONDO:0010039 nord_rare diseases +MONDO:0010039 ordo_disorder diseases +MONDO:0010039 ordo_malformation_syndrome diseases +MONDO:0010039 orphanet_rare diseases +MONDO:0010039 otar diseases +MONDO:0010039 rare diseases +MONDO:0010041 gard_rare diseases +MONDO:0010041 nord_rare diseases +MONDO:0010041 ordo_disorder diseases +MONDO:0010041 orphanet_rare diseases +MONDO:0010041 otar diseases +MONDO:0010041 rare diseases +MONDO:0010043 gard_rare diseases +MONDO:0010043 nord_rare diseases +MONDO:0010043 ordo_disorder diseases +MONDO:0010043 orphanet_rare diseases +MONDO:0010043 otar diseases +MONDO:0010043 rare diseases +MONDO:0010044 gard_rare diseases +MONDO:0010044 nord_rare diseases +MONDO:0010044 ordo_disorder diseases +MONDO:0010044 orphanet_rare diseases +MONDO:0010044 otar diseases +MONDO:0010044 rare diseases +MONDO:0010046 gard_rare diseases +MONDO:0010046 nord_rare diseases +MONDO:0010046 ordo_disorder diseases +MONDO:0010046 orphanet_rare diseases +MONDO:0010046 otar diseases +MONDO:0010046 rare diseases +MONDO:0010047 gard_rare diseases +MONDO:0010047 nord_rare diseases +MONDO:0010047 ordo_disorder diseases +MONDO:0010047 orphanet_rare diseases +MONDO:0010047 otar diseases +MONDO:0010047 rare diseases +MONDO:0010049 gard_rare diseases +MONDO:0010049 nord_rare diseases +MONDO:0010049 ordo_disorder diseases +MONDO:0010049 orphanet_rare diseases +MONDO:0010049 otar diseases +MONDO:0010049 rare diseases +MONDO:0010051 gard_rare diseases +MONDO:0010051 ordo_disorder diseases +MONDO:0010051 orphanet_rare diseases +MONDO:0010051 otar diseases +MONDO:0010051 rare diseases +MONDO:0010052 gard_rare diseases +MONDO:0010052 predisposition diseases +MONDO:0010052 rare diseases +MONDO:0010053 gard_rare diseases +MONDO:0010053 nord_rare diseases +MONDO:0010053 rare diseases +MONDO:0010056 gard_rare diseases +MONDO:0010056 nord_rare diseases +MONDO:0010056 ordo_subtype_of_a_disorder diseases +MONDO:0010056 otar diseases +MONDO:0010056 rare diseases +MONDO:0010057 gard_rare diseases +MONDO:0010057 rare diseases +MONDO:0010058 gard_rare diseases +MONDO:0010058 rare diseases +MONDO:0010060 gard_rare diseases +MONDO:0010060 nord_rare diseases +MONDO:0010060 ordo_disorder diseases +MONDO:0010060 orphanet_rare diseases +MONDO:0010060 otar diseases +MONDO:0010060 rare diseases +MONDO:0010061 gard_rare diseases +MONDO:0010061 nord_rare diseases +MONDO:0010061 ordo_disorder diseases +MONDO:0010061 orphanet_rare diseases +MONDO:0010061 otar diseases +MONDO:0010061 rare diseases +MONDO:0010062 gard_rare diseases +MONDO:0010062 ordo_disorder diseases +MONDO:0010062 orphanet_rare diseases +MONDO:0010062 otar diseases +MONDO:0010062 rare diseases +MONDO:0010063 gard_rare diseases +MONDO:0010063 ordo_disorder diseases +MONDO:0010063 ordo_malformation_syndrome diseases +MONDO:0010063 orphanet_rare diseases +MONDO:0010063 otar diseases +MONDO:0010063 rare diseases +MONDO:0010064 gard_rare diseases +MONDO:0010064 ordo_disorder diseases +MONDO:0010064 orphanet_rare diseases +MONDO:0010064 otar diseases +MONDO:0010064 rare diseases +MONDO:0010065 gard_rare diseases +MONDO:0010065 rare diseases +MONDO:0010066 gard_rare diseases +MONDO:0010066 nord_rare diseases +MONDO:0010066 ordo_disorder diseases +MONDO:0010066 ordo_morphological_anomaly diseases +MONDO:0010066 orphanet_rare diseases +MONDO:0010066 otar diseases +MONDO:0010066 rare diseases +MONDO:0010068 gard_rare diseases +MONDO:0010068 nord_rare diseases +MONDO:0010068 ordo_disorder diseases +MONDO:0010068 orphanet_rare diseases +MONDO:0010068 otar diseases +MONDO:0010068 rare diseases +MONDO:0010069 gard_rare diseases +MONDO:0010069 nord_rare diseases +MONDO:0010069 ordo_malformation_syndrome diseases +MONDO:0010069 otar diseases +MONDO:0010069 rare diseases +MONDO:0010070 gard_rare diseases +MONDO:0010070 nord_rare diseases +MONDO:0010070 otar diseases +MONDO:0010070 rare diseases +MONDO:0010072 gard_rare diseases +MONDO:0010072 nord_rare diseases +MONDO:0010072 rare diseases +MONDO:0010073 gard_rare diseases +MONDO:0010073 nord_rare diseases +MONDO:0010073 ordo_disorder diseases +MONDO:0010073 orphanet_rare diseases +MONDO:0010073 otar diseases +MONDO:0010073 rare diseases +MONDO:0010074 gard_rare diseases +MONDO:0010074 nord_rare diseases +MONDO:0010074 otar diseases +MONDO:0010074 rare diseases +MONDO:0010075 gard_rare diseases +MONDO:0010075 nord_rare diseases +MONDO:0010075 ordo_disorder diseases +MONDO:0010075 orphanet_rare diseases +MONDO:0010075 otar diseases +MONDO:0010075 rare diseases +MONDO:0010076 gard_rare diseases +MONDO:0010076 nord_rare diseases +MONDO:0010076 ordo_disorder diseases +MONDO:0010076 orphanet_rare diseases +MONDO:0010076 otar diseases +MONDO:0010076 rare diseases +MONDO:0010077 clingen diseases +MONDO:0010077 gard_rare diseases +MONDO:0010077 nord_rare diseases +MONDO:0010077 ordo_disorder diseases +MONDO:0010077 orphanet_rare diseases +MONDO:0010077 otar diseases +MONDO:0010077 rare diseases +MONDO:0010078 clingen diseases +MONDO:0010078 gard_rare diseases +MONDO:0010078 nord_rare diseases +MONDO:0010078 ordo_disorder diseases +MONDO:0010078 orphanet_rare diseases +MONDO:0010078 otar diseases +MONDO:0010078 rare diseases +MONDO:0010079 clingen diseases +MONDO:0010079 gard_rare diseases +MONDO:0010079 nord_rare diseases +MONDO:0010079 ordo_disorder diseases +MONDO:0010079 orphanet_rare diseases +MONDO:0010079 otar diseases +MONDO:0010079 rare diseases +MONDO:0010080 gard_rare diseases +MONDO:0010080 nord_rare diseases +MONDO:0010080 ordo_disorder diseases +MONDO:0010080 orphanet_rare diseases +MONDO:0010080 otar diseases +MONDO:0010080 rare diseases +MONDO:0010081 gard_rare diseases +MONDO:0010081 nord_rare diseases +MONDO:0010081 rare diseases +MONDO:0010082 gard_rare diseases +MONDO:0010082 nord_rare diseases +MONDO:0010082 ordo_disorder diseases +MONDO:0010082 ordo_malformation_syndrome diseases +MONDO:0010082 orphanet_rare diseases +MONDO:0010082 rare diseases +MONDO:0010083 clingen diseases +MONDO:0010083 gard_rare diseases +MONDO:0010083 nord_rare diseases +MONDO:0010083 ordo_disorder diseases +MONDO:0010083 orphanet_rare diseases +MONDO:0010083 otar diseases +MONDO:0010083 rare diseases +MONDO:0010085 gard_rare diseases +MONDO:0010085 ordo_disorder diseases +MONDO:0010085 orphanet_rare diseases +MONDO:0010085 rare diseases +MONDO:0010087 gard_rare diseases +MONDO:0010087 ordo_disorder diseases +MONDO:0010087 ordo_morphological_anomaly diseases +MONDO:0010087 orphanet_rare diseases +MONDO:0010087 rare diseases +MONDO:0010088 clingen diseases +MONDO:0010088 gard_rare diseases +MONDO:0010088 nord_rare diseases +MONDO:0010088 ordo_disorder diseases +MONDO:0010088 orphanet_rare diseases +MONDO:0010088 otar diseases +MONDO:0010088 rare diseases +MONDO:0010089 clingen diseases +MONDO:0010089 gard_rare diseases +MONDO:0010089 nord_rare diseases +MONDO:0010089 ordo_subtype_of_a_disorder diseases +MONDO:0010089 otar diseases +MONDO:0010089 rare diseases +MONDO:0010090 gard_rare diseases +MONDO:0010090 nord_rare diseases +MONDO:0010090 ordo_disorder diseases +MONDO:0010090 ordo_malformation_syndrome diseases +MONDO:0010090 orphanet_rare diseases +MONDO:0010090 otar diseases +MONDO:0010090 rare diseases +MONDO:0010091 gard_rare diseases +MONDO:0010091 nord_rare diseases +MONDO:0010091 ordo_disorder diseases +MONDO:0010091 ordo_malformation_syndrome diseases +MONDO:0010091 orphanet_rare diseases +MONDO:0010091 otar diseases +MONDO:0010091 rare diseases +MONDO:0010092 gard_rare diseases +MONDO:0010092 nord_rare diseases +MONDO:0010092 ordo_disorder diseases +MONDO:0010092 ordo_malformation_syndrome diseases +MONDO:0010092 orphanet_rare diseases +MONDO:0010092 otar diseases +MONDO:0010092 rare diseases +MONDO:0010094 gard_rare diseases +MONDO:0010094 nord_rare diseases +MONDO:0010094 ordo_disorder diseases +MONDO:0010094 ordo_malformation_syndrome diseases +MONDO:0010094 orphanet_rare diseases +MONDO:0010094 otar diseases +MONDO:0010094 rare diseases +MONDO:0010095 gard_rare diseases +MONDO:0010095 ordo_disorder diseases +MONDO:0010095 orphanet_rare diseases +MONDO:0010095 otar diseases +MONDO:0010095 rare diseases +MONDO:0010097 gard_rare diseases +MONDO:0010097 nord_rare diseases +MONDO:0010097 rare diseases +MONDO:0010098 ordo_morphological_anomaly diseases +MONDO:0010098 otar diseases +MONDO:0010099 clingen diseases +MONDO:0010099 gard_rare diseases +MONDO:0010099 nord_rare diseases +MONDO:0010099 ordo_disorder diseases +MONDO:0010099 orphanet_rare diseases +MONDO:0010099 otar diseases +MONDO:0010099 rare diseases +MONDO:0010100 clingen diseases +MONDO:0010100 gard_rare diseases +MONDO:0010100 nord_rare diseases +MONDO:0010100 ordo_disorder diseases +MONDO:0010100 orphanet_rare diseases +MONDO:0010100 otar diseases +MONDO:0010100 rare diseases +MONDO:0010101 gard_rare diseases +MONDO:0010101 nord_rare diseases +MONDO:0010101 ordo_disorder diseases +MONDO:0010101 ordo_malformation_syndrome diseases +MONDO:0010101 orphanet_rare diseases +MONDO:0010101 otar diseases +MONDO:0010101 rare diseases +MONDO:0010102 gard_rare diseases +MONDO:0010102 nord_rare diseases +MONDO:0010102 ordo_malformation_syndrome diseases +MONDO:0010102 rare diseases +MONDO:0010104 gard_rare diseases +MONDO:0010104 ordo_disorder diseases +MONDO:0010104 ordo_malformation_syndrome diseases +MONDO:0010104 orphanet_rare diseases +MONDO:0010104 otar diseases +MONDO:0010104 rare diseases +MONDO:0010105 gard_rare diseases +MONDO:0010105 nord_rare diseases +MONDO:0010105 rare diseases +MONDO:0010108 disease_grouping diseases +MONDO:0010108 gard_rare diseases +MONDO:0010108 nord_rare diseases +MONDO:0010108 ordo_group_of_disorders diseases +MONDO:0010108 otar diseases +MONDO:0010108 rare diseases +MONDO:0010110 gard_rare diseases +MONDO:0010110 nord_rare diseases +MONDO:0010110 ordo_disorder diseases +MONDO:0010110 ordo_malformation_syndrome diseases +MONDO:0010110 orphanet_rare diseases +MONDO:0010110 otar diseases +MONDO:0010110 rare diseases +MONDO:0010111 gard_rare diseases +MONDO:0010111 nord_rare diseases +MONDO:0010111 ordo_disorder diseases +MONDO:0010111 ordo_malformation_syndrome diseases +MONDO:0010111 orphanet_rare diseases +MONDO:0010111 otar diseases +MONDO:0010111 rare diseases +MONDO:0010112 gard_rare diseases +MONDO:0010112 nord_rare diseases +MONDO:0010112 rare diseases +MONDO:0010114 gard_rare diseases +MONDO:0010114 nord_rare diseases +MONDO:0010114 rare diseases +MONDO:0010115 gard_rare diseases +MONDO:0010115 ordo_disorder diseases +MONDO:0010115 ordo_malformation_syndrome diseases +MONDO:0010115 orphanet_rare diseases +MONDO:0010115 rare diseases +MONDO:0010116 gard_rare diseases +MONDO:0010116 ordo_disorder diseases +MONDO:0010116 orphanet_rare diseases +MONDO:0010116 otar diseases +MONDO:0010116 rare diseases +MONDO:0010117 gard_rare diseases +MONDO:0010117 nord_rare diseases +MONDO:0010117 rare diseases +MONDO:0010118 gard_rare diseases +MONDO:0010118 n_of_one diseases +MONDO:0010118 rare diseases +MONDO:0010120 clingen diseases +MONDO:0010120 gard_rare diseases +MONDO:0010120 nord_rare diseases +MONDO:0010120 otar diseases +MONDO:0010120 rare diseases +MONDO:0010121 clingen diseases +MONDO:0010121 gard_rare diseases +MONDO:0010121 nord_rare diseases +MONDO:0010121 ordo_disorder diseases +MONDO:0010121 ordo_malformation_syndrome diseases +MONDO:0010121 orphanet_rare diseases +MONDO:0010121 otar diseases +MONDO:0010121 rare diseases +MONDO:0010122 clingen diseases +MONDO:0010122 gard_rare diseases +MONDO:0010122 nord_rare diseases +MONDO:0010122 ordo_subtype_of_a_disorder diseases +MONDO:0010122 otar diseases +MONDO:0010122 rare diseases +MONDO:0010125 gard_rare diseases +MONDO:0010125 ordo_disorder diseases +MONDO:0010125 ordo_malformation_syndrome diseases +MONDO:0010125 orphanet_rare diseases +MONDO:0010125 otar diseases +MONDO:0010125 rare diseases +MONDO:0010127 gard_rare diseases +MONDO:0010127 nord_rare diseases +MONDO:0010127 otar diseases +MONDO:0010127 rare diseases +MONDO:0010128 gard_rare diseases +MONDO:0010128 ordo_disorder diseases +MONDO:0010128 ordo_malformation_syndrome diseases +MONDO:0010128 orphanet_rare diseases +MONDO:0010128 otar diseases +MONDO:0010128 rare diseases +MONDO:0010129 gard_rare diseases +MONDO:0010129 ordo_disorder diseases +MONDO:0010129 ordo_malformation_syndrome diseases +MONDO:0010129 orphanet_rare diseases +MONDO:0010129 otar diseases +MONDO:0010129 rare diseases +MONDO:0010130 gard_rare diseases +MONDO:0010130 nord_rare diseases +MONDO:0010130 ordo_disorder diseases +MONDO:0010130 orphanet_rare diseases +MONDO:0010130 otar diseases +MONDO:0010130 rare diseases +MONDO:0010131 gard_rare diseases +MONDO:0010131 nord_rare diseases +MONDO:0010131 rare diseases +MONDO:0010132 gard_rare diseases +MONDO:0010132 nord_rare diseases +MONDO:0010132 ordo_disorder diseases +MONDO:0010132 orphanet_rare diseases +MONDO:0010132 otar diseases +MONDO:0010132 rare diseases +MONDO:0010133 gard_rare diseases +MONDO:0010133 nord_rare diseases +MONDO:0010133 rare diseases +MONDO:0010134 clingen diseases +MONDO:0010134 gard_rare diseases +MONDO:0010134 nord_rare diseases +MONDO:0010134 ordo_disorder diseases +MONDO:0010134 ordo_malformation_syndrome diseases +MONDO:0010134 orphanet_rare diseases +MONDO:0010134 otar diseases +MONDO:0010134 rare diseases +MONDO:0010135 gard_rare diseases +MONDO:0010135 nord_rare diseases +MONDO:0010135 rare diseases +MONDO:0010136 gard_rare diseases +MONDO:0010136 nord_rare diseases +MONDO:0010136 rare diseases +MONDO:0010137 gard_rare diseases +MONDO:0010137 nord_rare diseases +MONDO:0010137 rare diseases +MONDO:0010138 otar diseases +MONDO:0010138 predisposition diseases +MONDO:0010139 gard_rare diseases +MONDO:0010139 nord_rare diseases +MONDO:0010139 ordo_disorder diseases +MONDO:0010139 orphanet_rare diseases +MONDO:0010139 otar diseases +MONDO:0010139 rare diseases +MONDO:0010140 gard_rare diseases +MONDO:0010140 nord_rare diseases +MONDO:0010140 ordo_disorder diseases +MONDO:0010140 orphanet_rare diseases +MONDO:0010140 otar diseases +MONDO:0010140 rare diseases +MONDO:0010142 gard_rare diseases +MONDO:0010142 nord_rare diseases +MONDO:0010142 ordo_disorder diseases +MONDO:0010142 orphanet_rare diseases +MONDO:0010142 otar diseases +MONDO:0010142 rare diseases +MONDO:0010144 gard_rare diseases +MONDO:0010144 nord_rare diseases +MONDO:0010144 ordo_disorder diseases +MONDO:0010144 ordo_morphological_anomaly diseases +MONDO:0010144 orphanet_rare diseases +MONDO:0010144 otar diseases +MONDO:0010144 rare diseases +MONDO:0010146 gard_rare diseases +MONDO:0010146 nord_rare diseases +MONDO:0010146 ordo_disorder diseases +MONDO:0010146 orphanet_rare diseases +MONDO:0010146 rare diseases +MONDO:0010148 gard_rare diseases +MONDO:0010148 nord_rare diseases +MONDO:0010148 ordo_clinical_syndrome diseases +MONDO:0010148 ordo_disorder diseases +MONDO:0010148 orphanet_rare diseases +MONDO:0010148 rare diseases +MONDO:0010149 gard_rare diseases +MONDO:0010149 nord_rare diseases +MONDO:0010149 ordo_disorder diseases +MONDO:0010149 orphanet_rare diseases +MONDO:0010149 otar diseases +MONDO:0010149 rare diseases +MONDO:0010150 gard_rare diseases +MONDO:0010150 nord_rare diseases +MONDO:0010150 otar diseases +MONDO:0010150 rare diseases +MONDO:0010151 gard_rare diseases +MONDO:0010151 rare diseases +MONDO:0010152 gard_rare diseases +MONDO:0010152 nord_rare diseases +MONDO:0010152 ordo_disorder diseases +MONDO:0010152 ordo_malformation_syndrome diseases +MONDO:0010152 orphanet_rare diseases +MONDO:0010152 otar diseases +MONDO:0010152 rare diseases +MONDO:0010153 gard_rare diseases +MONDO:0010153 ordo_disorder diseases +MONDO:0010153 ordo_malformation_syndrome diseases +MONDO:0010153 orphanet_rare diseases +MONDO:0010153 rare diseases +MONDO:0010154 gard_rare diseases +MONDO:0010154 ordo_disorder diseases +MONDO:0010154 ordo_malformation_syndrome diseases +MONDO:0010154 orphanet_rare diseases +MONDO:0010154 rare diseases +MONDO:0010155 clingen diseases +MONDO:0010155 gard_rare diseases +MONDO:0010155 nord_rare diseases +MONDO:0010155 ordo_disorder diseases +MONDO:0010155 orphanet_rare diseases +MONDO:0010155 otar diseases +MONDO:0010155 rare diseases +MONDO:0010156 clingen diseases +MONDO:0010156 gard_rare diseases +MONDO:0010156 nord_rare diseases +MONDO:0010156 ordo_disorder diseases +MONDO:0010156 orphanet_rare diseases +MONDO:0010156 otar diseases +MONDO:0010156 rare diseases +MONDO:0010159 clingen diseases +MONDO:0010159 gard_rare diseases +MONDO:0010159 nord_rare diseases +MONDO:0010159 otar diseases +MONDO:0010159 rare diseases +MONDO:0010160 clingen diseases +MONDO:0010160 gard_rare diseases +MONDO:0010160 nord_rare diseases +MONDO:0010160 ordo_disorder diseases +MONDO:0010160 orphanet_rare diseases +MONDO:0010160 otar diseases +MONDO:0010160 rare diseases +MONDO:0010161 clingen diseases +MONDO:0010161 gard_rare diseases +MONDO:0010161 nord_rare diseases +MONDO:0010161 ordo_disorder diseases +MONDO:0010161 orphanet_rare diseases +MONDO:0010161 otar diseases +MONDO:0010161 rare diseases +MONDO:0010162 clingen diseases +MONDO:0010162 gard_rare diseases +MONDO:0010162 nord_rare diseases +MONDO:0010162 ordo_disorder diseases +MONDO:0010162 orphanet_rare diseases +MONDO:0010162 otar diseases +MONDO:0010162 rare diseases +MONDO:0010164 gard_rare diseases +MONDO:0010164 nord_rare diseases +MONDO:0010164 ordo_disorder diseases +MONDO:0010164 ordo_malformation_syndrome diseases +MONDO:0010164 orphanet_rare diseases +MONDO:0010164 otar diseases +MONDO:0010164 rare diseases +MONDO:0010165 gard_rare diseases +MONDO:0010165 ordo_disorder diseases +MONDO:0010165 ordo_malformation_syndrome diseases +MONDO:0010165 orphanet_rare diseases +MONDO:0010165 otar diseases +MONDO:0010165 rare diseases +MONDO:0010167 clingen diseases +MONDO:0010167 gard_rare diseases +MONDO:0010167 nord_rare diseases +MONDO:0010167 ordo_disorder diseases +MONDO:0010167 orphanet_rare diseases +MONDO:0010167 otar diseases +MONDO:0010167 rare diseases +MONDO:0010168 clingen diseases +MONDO:0010168 gard_rare diseases +MONDO:0010168 nord_rare diseases +MONDO:0010168 ordo_subtype_of_a_disorder diseases +MONDO:0010168 otar diseases +MONDO:0010168 rare diseases +MONDO:0010169 gard_rare diseases +MONDO:0010169 nord_rare diseases +MONDO:0010169 otar diseases +MONDO:0010169 rare diseases +MONDO:0010170 gard_rare diseases +MONDO:0010170 nord_rare diseases +MONDO:0010170 rare diseases +MONDO:0010171 gard_rare diseases +MONDO:0010171 nord_rare diseases +MONDO:0010171 otar diseases +MONDO:0010171 rare diseases +MONDO:0010172 gard_rare diseases +MONDO:0010172 ordo_disorder diseases +MONDO:0010172 ordo_malformation_syndrome diseases +MONDO:0010172 orphanet_rare diseases +MONDO:0010172 otar diseases +MONDO:0010172 rare diseases +MONDO:0010173 gard_rare diseases +MONDO:0010173 nord_rare diseases +MONDO:0010173 ordo_subtype_of_a_disorder diseases +MONDO:0010173 otar diseases +MONDO:0010173 rare diseases +MONDO:0010176 gard_rare diseases +MONDO:0010176 nord_rare diseases +MONDO:0010176 ordo_disorder diseases +MONDO:0010176 orphanet_rare diseases +MONDO:0010176 otar diseases +MONDO:0010176 rare diseases +MONDO:0010177 gard_rare diseases +MONDO:0010177 ordo_disorder diseases +MONDO:0010177 ordo_malformation_syndrome diseases +MONDO:0010177 orphanet_rare diseases +MONDO:0010177 rare diseases +MONDO:0010178 gard_rare diseases +MONDO:0010178 nord_rare diseases +MONDO:0010178 otar diseases +MONDO:0010178 rare diseases +MONDO:0010179 gard_rare diseases +MONDO:0010179 nord_rare diseases +MONDO:0010179 ordo_disorder diseases +MONDO:0010179 ordo_morphological_anomaly diseases +MONDO:0010179 orphanet_rare diseases +MONDO:0010179 rare diseases +MONDO:0010180 gard_rare diseases +MONDO:0010180 nord_rare diseases +MONDO:0010180 ordo_disorder diseases +MONDO:0010180 ordo_malformation_syndrome diseases +MONDO:0010180 orphanet_rare diseases +MONDO:0010180 otar diseases +MONDO:0010180 rare diseases +MONDO:0010181 gard_rare diseases +MONDO:0010181 nord_rare diseases +MONDO:0010181 ordo_disorder diseases +MONDO:0010181 orphanet_rare diseases +MONDO:0010181 otar diseases +MONDO:0010181 rare diseases +MONDO:0010182 gard_rare diseases +MONDO:0010182 rare diseases +MONDO:0010183 clingen diseases +MONDO:0010183 gard_rare diseases +MONDO:0010183 nord_rare diseases +MONDO:0010183 ordo_subtype_of_a_disorder diseases +MONDO:0010183 otar diseases +MONDO:0010183 rare diseases +MONDO:0010184 clingen diseases +MONDO:0010184 gard_rare diseases +MONDO:0010184 nord_rare diseases +MONDO:0010184 ordo_subtype_of_a_disorder diseases +MONDO:0010184 otar diseases +MONDO:0010184 rare diseases +MONDO:0010185 gard_rare diseases +MONDO:0010185 nord_rare diseases +MONDO:0010185 ordo_subtype_of_a_disorder diseases +MONDO:0010185 otar diseases +MONDO:0010185 rare diseases +MONDO:0010186 gard_rare diseases +MONDO:0010186 nord_rare diseases +MONDO:0010186 rare diseases +MONDO:0010187 clingen diseases +MONDO:0010187 gard_rare diseases +MONDO:0010187 nord_rare diseases +MONDO:0010187 otar diseases +MONDO:0010187 prototype_pattern diseases +MONDO:0010187 rare diseases +MONDO:0010188 gard_rare diseases +MONDO:0010188 nord_rare diseases +MONDO:0010188 ordo_disorder diseases +MONDO:0010188 orphanet_rare diseases +MONDO:0010188 otar diseases +MONDO:0010188 rare diseases +MONDO:0010190 gard_rare diseases +MONDO:0010190 nord_rare diseases +MONDO:0010190 rare diseases +MONDO:0010191 gard_rare diseases +MONDO:0010191 nord_rare diseases +MONDO:0010191 ordo_subtype_of_a_disorder diseases +MONDO:0010191 otar diseases +MONDO:0010191 rare diseases +MONDO:0010192 clingen diseases +MONDO:0010192 gard_rare diseases +MONDO:0010192 nord_rare diseases +MONDO:0010192 rare diseases +MONDO:0010193 clingen diseases +MONDO:0010193 gard_rare diseases +MONDO:0010193 nord_rare diseases +MONDO:0010193 ordo_disorder diseases +MONDO:0010193 ordo_malformation_syndrome diseases +MONDO:0010193 orphanet_rare diseases +MONDO:0010193 otar diseases +MONDO:0010193 rare diseases +MONDO:0010194 gard_rare diseases +MONDO:0010194 nord_rare diseases +MONDO:0010194 rare diseases +MONDO:0010196 clingen diseases +MONDO:0010196 gard_rare diseases +MONDO:0010196 nord_rare diseases +MONDO:0010196 ordo_disorder diseases +MONDO:0010196 orphanet_rare diseases +MONDO:0010196 otar diseases +MONDO:0010196 rare diseases +MONDO:0010197 gard_rare diseases +MONDO:0010197 nord_rare diseases +MONDO:0010197 rare diseases +MONDO:0010198 otar diseases +MONDO:0010199 gard_rare diseases +MONDO:0010199 ordo_disorder diseases +MONDO:0010199 ordo_malformation_syndrome diseases +MONDO:0010199 orphanet_rare diseases +MONDO:0010199 otar diseases +MONDO:0010199 rare diseases +MONDO:0010200 clingen diseases +MONDO:0010200 gard_rare diseases +MONDO:0010200 nord_rare diseases +MONDO:0010200 ordo_disorder diseases +MONDO:0010200 orphanet_rare diseases +MONDO:0010200 otar diseases +MONDO:0010200 rare diseases +MONDO:0010201 gard_rare diseases +MONDO:0010201 nord_rare diseases +MONDO:0010201 rare diseases +MONDO:0010203 gard_rare diseases +MONDO:0010203 ordo_disorder diseases +MONDO:0010203 ordo_malformation_syndrome diseases +MONDO:0010203 orphanet_rare diseases +MONDO:0010203 otar diseases +MONDO:0010203 rare diseases +MONDO:0010206 gard_rare diseases +MONDO:0010206 nord_rare diseases +MONDO:0010206 rare diseases +MONDO:0010207 ordo_malformation_syndrome diseases +MONDO:0010207 otar diseases +MONDO:0010208 gard_rare diseases +MONDO:0010208 nord_rare diseases +MONDO:0010208 ordo_subtype_of_a_disorder diseases +MONDO:0010208 otar diseases +MONDO:0010208 rare diseases +MONDO:0010209 gard_rare diseases +MONDO:0010209 nord_rare diseases +MONDO:0010209 ordo_etiological_subtype diseases +MONDO:0010209 ordo_subtype_of_a_disorder diseases +MONDO:0010209 otar diseases +MONDO:0010209 rare diseases +MONDO:0010210 clingen diseases +MONDO:0010210 gard_rare diseases +MONDO:0010210 nord_rare diseases +MONDO:0010210 otar diseases +MONDO:0010210 rare diseases +MONDO:0010211 clingen diseases +MONDO:0010211 gard_rare diseases +MONDO:0010211 nord_rare diseases +MONDO:0010211 otar diseases +MONDO:0010211 rare diseases +MONDO:0010212 clingen diseases +MONDO:0010212 gard_rare diseases +MONDO:0010212 nord_rare diseases +MONDO:0010212 otar diseases +MONDO:0010212 rare diseases +MONDO:0010213 clingen diseases +MONDO:0010213 gard_rare diseases +MONDO:0010213 nord_rare diseases +MONDO:0010213 otar diseases +MONDO:0010213 rare diseases +MONDO:0010214 clingen diseases +MONDO:0010214 gard_rare diseases +MONDO:0010214 nord_rare diseases +MONDO:0010214 ordo_disorder diseases +MONDO:0010214 orphanet_rare diseases +MONDO:0010214 otar diseases +MONDO:0010214 rare diseases +MONDO:0010215 clingen diseases +MONDO:0010215 gard_rare diseases +MONDO:0010215 nord_rare diseases +MONDO:0010215 otar diseases +MONDO:0010215 rare diseases +MONDO:0010216 clingen diseases +MONDO:0010216 gard_rare diseases +MONDO:0010216 nord_rare diseases +MONDO:0010216 otar diseases +MONDO:0010216 rare diseases +MONDO:0010217 gard_rare diseases +MONDO:0010217 nord_rare diseases +MONDO:0010217 otar diseases +MONDO:0010217 rare diseases +MONDO:0010218 gard_rare diseases +MONDO:0010218 nord_rare diseases +MONDO:0010218 rare diseases +MONDO:0010220 gard_rare diseases +MONDO:0010220 nord_rare diseases +MONDO:0010220 ordo_disorder diseases +MONDO:0010220 orphanet_rare diseases +MONDO:0010220 otar diseases +MONDO:0010220 rare diseases +MONDO:0010221 gard_rare diseases +MONDO:0010221 nord_rare diseases +MONDO:0010221 ordo_disorder diseases +MONDO:0010221 ordo_malformation_syndrome diseases +MONDO:0010221 orphanet_rare diseases +MONDO:0010221 otar diseases +MONDO:0010221 rare diseases +MONDO:0010222 clingen diseases +MONDO:0010222 gard_rare diseases +MONDO:0010222 nord_rare diseases +MONDO:0010222 ordo_etiological_subtype diseases +MONDO:0010222 otar diseases +MONDO:0010222 rare diseases +MONDO:0010223 gard_rare diseases +MONDO:0010223 nord_rare diseases +MONDO:0010223 rare diseases +MONDO:0010224 gard_rare diseases +MONDO:0010224 nord_rare diseases +MONDO:0010224 ordo_disorder diseases +MONDO:0010224 ordo_malformation_syndrome diseases +MONDO:0010224 orphanet_rare diseases +MONDO:0010224 otar diseases +MONDO:0010224 rare diseases +MONDO:0010225 gard_rare diseases +MONDO:0010225 nord_rare diseases +MONDO:0010225 ordo_subtype_of_a_disorder diseases +MONDO:0010225 otar diseases +MONDO:0010225 rare diseases +MONDO:0010226 gard_rare diseases +MONDO:0010226 nord_rare diseases +MONDO:0010226 rare diseases +MONDO:0010227 gard_rare diseases +MONDO:0010227 nord_rare diseases +MONDO:0010227 rare diseases +MONDO:0010228 gard_rare diseases +MONDO:0010228 nord_rare diseases +MONDO:0010228 rare diseases +MONDO:0010229 gard_rare diseases +MONDO:0010229 rare diseases +MONDO:0010230 gard_rare diseases +MONDO:0010230 nord_rare diseases +MONDO:0010230 rare diseases +MONDO:0010231 gard_rare diseases +MONDO:0010231 nord_rare diseases +MONDO:0010231 rare diseases +MONDO:0010232 gard_rare diseases +MONDO:0010232 nord_rare diseases +MONDO:0010232 rare diseases +MONDO:0010233 gard_rare diseases +MONDO:0010233 nord_rare diseases +MONDO:0010233 otar diseases +MONDO:0010233 rare diseases +MONDO:0010235 gard_rare diseases +MONDO:0010235 nord_rare diseases +MONDO:0010235 ordo_disorder diseases +MONDO:0010235 ordo_malformation_syndrome diseases +MONDO:0010235 orphanet_rare diseases +MONDO:0010235 otar diseases +MONDO:0010235 rare diseases +MONDO:0010236 gard_rare diseases +MONDO:0010236 nord_rare diseases +MONDO:0010236 rare diseases +MONDO:0010237 gard_rare diseases +MONDO:0010237 ordo_disorder diseases +MONDO:0010237 ordo_malformation_syndrome diseases +MONDO:0010237 orphanet_rare diseases +MONDO:0010237 otar diseases +MONDO:0010237 rare diseases +MONDO:0010238 gard_rare diseases +MONDO:0010238 nord_rare diseases +MONDO:0010238 rare diseases +MONDO:0010239 gard_rare diseases +MONDO:0010239 nord_rare diseases +MONDO:0010239 ordo_disorder diseases +MONDO:0010239 orphanet_rare diseases +MONDO:0010239 otar diseases +MONDO:0010239 rare diseases +MONDO:0010241 gard_rare diseases +MONDO:0010241 rare diseases +MONDO:0010242 gard_rare diseases +MONDO:0010242 nord_rare diseases +MONDO:0010242 rare diseases +MONDO:0010243 gard_rare diseases +MONDO:0010243 nord_rare diseases +MONDO:0010243 ordo_disorder diseases +MONDO:0010243 orphanet_rare diseases +MONDO:0010243 otar diseases +MONDO:0010243 rare diseases +MONDO:0010245 gard_rare diseases +MONDO:0010245 nord_rare diseases +MONDO:0010245 rare diseases +MONDO:0010246 gard_rare diseases +MONDO:0010246 nord_rare diseases +MONDO:0010246 ordo_disorder diseases +MONDO:0010246 orphanet_rare diseases +MONDO:0010246 otar diseases +MONDO:0010246 rare diseases +MONDO:0010247 gard_rare diseases +MONDO:0010247 nord_rare diseases +MONDO:0010247 ordo_subtype_of_a_disorder diseases +MONDO:0010247 otar diseases +MONDO:0010247 rare diseases +MONDO:0010248 gard_rare diseases +MONDO:0010248 nord_rare diseases +MONDO:0010248 ordo_disorder diseases +MONDO:0010248 orphanet_rare diseases +MONDO:0010248 otar diseases +MONDO:0010248 rare diseases +MONDO:0010250 gard_rare diseases +MONDO:0010250 nord_rare diseases +MONDO:0010250 ordo_disorder diseases +MONDO:0010250 ordo_malformation_syndrome diseases +MONDO:0010250 orphanet_rare diseases +MONDO:0010250 rare diseases +MONDO:0010251 gard_rare diseases +MONDO:0010251 nord_rare diseases +MONDO:0010251 rare diseases +MONDO:0010252 gard_rare diseases +MONDO:0010252 nord_rare diseases +MONDO:0010252 rare diseases +MONDO:0010256 gard_rare diseases +MONDO:0010256 nord_rare diseases +MONDO:0010256 otar diseases +MONDO:0010256 rare diseases +MONDO:0010257 gard_rare diseases +MONDO:0010257 rare diseases +MONDO:0010258 clingen diseases +MONDO:0010258 gard_rare diseases +MONDO:0010258 nord_rare diseases +MONDO:0010258 ordo_disorder diseases +MONDO:0010258 ordo_malformation_syndrome diseases +MONDO:0010258 orphanet_rare diseases +MONDO:0010258 otar diseases +MONDO:0010258 rare diseases +MONDO:0010259 gard_rare diseases +MONDO:0010259 nord_rare diseases +MONDO:0010259 rare diseases +MONDO:0010261 clingen diseases +MONDO:0010261 gard_rare diseases +MONDO:0010261 nord_rare diseases +MONDO:0010261 ordo_disorder diseases +MONDO:0010261 ordo_malformation_syndrome diseases +MONDO:0010261 orphanet_rare diseases +MONDO:0010261 otar diseases +MONDO:0010261 rare diseases +MONDO:0010263 gard_rare diseases +MONDO:0010263 nord_rare diseases +MONDO:0010263 ordo_disorder diseases +MONDO:0010263 orphanet_rare diseases +MONDO:0010263 otar diseases +MONDO:0010263 rare diseases +MONDO:0010264 gard_rare diseases +MONDO:0010264 nord_rare diseases +MONDO:0010264 ordo_disorder diseases +MONDO:0010264 orphanet_rare diseases +MONDO:0010264 otar diseases +MONDO:0010264 rare diseases +MONDO:0010265 gard_rare diseases +MONDO:0010265 nord_rare diseases +MONDO:0010265 ordo_malformation_syndrome diseases +MONDO:0010265 otar diseases +MONDO:0010265 rare diseases +MONDO:0010266 gard_rare diseases +MONDO:0010266 nord_rare diseases +MONDO:0010266 otar diseases +MONDO:0010266 rare diseases +MONDO:0010268 gard_rare diseases +MONDO:0010268 nord_rare diseases +MONDO:0010268 ordo_disorder diseases +MONDO:0010268 ordo_malformation_syndrome diseases +MONDO:0010268 orphanet_rare diseases +MONDO:0010268 otar diseases +MONDO:0010268 rare diseases +MONDO:0010269 gard_rare diseases +MONDO:0010269 nord_rare diseases +MONDO:0010269 ordo_disorder diseases +MONDO:0010269 orphanet_rare diseases +MONDO:0010269 otar diseases +MONDO:0010269 rare diseases +MONDO:0010270 gard_rare diseases +MONDO:0010270 nord_rare diseases +MONDO:0010270 ordo_disorder diseases +MONDO:0010270 ordo_malformation_syndrome diseases +MONDO:0010270 orphanet_rare diseases +MONDO:0010270 otar diseases +MONDO:0010270 rare diseases +MONDO:0010271 gard_rare diseases +MONDO:0010271 nord_rare diseases +MONDO:0010271 ordo_disorder diseases +MONDO:0010271 orphanet_rare diseases +MONDO:0010271 rare diseases +MONDO:0010273 gard_rare diseases +MONDO:0010273 rare diseases +MONDO:0010274 gard_rare diseases +MONDO:0010274 nord_rare diseases +MONDO:0010274 rare diseases +MONDO:0010275 gard_rare diseases +MONDO:0010275 nord_rare diseases +MONDO:0010275 ordo_disorder diseases +MONDO:0010275 orphanet_rare diseases +MONDO:0010275 otar diseases +MONDO:0010275 rare diseases +MONDO:0010277 gard_rare diseases +MONDO:0010277 nord_rare diseases +MONDO:0010277 ordo_disorder diseases +MONDO:0010277 ordo_malformation_syndrome diseases +MONDO:0010277 orphanet_rare diseases +MONDO:0010277 otar diseases +MONDO:0010277 rare diseases +MONDO:0010278 clingen diseases +MONDO:0010278 gard_rare diseases +MONDO:0010278 nord_rare diseases +MONDO:0010278 ordo_disorder diseases +MONDO:0010278 ordo_malformation_syndrome diseases +MONDO:0010278 orphanet_rare diseases +MONDO:0010278 otar diseases +MONDO:0010278 rare diseases +MONDO:0010279 gard_rare diseases +MONDO:0010279 nord_rare diseases +MONDO:0010279 ordo_disorder diseases +MONDO:0010279 ordo_malformation_syndrome diseases +MONDO:0010279 orphanet_rare diseases +MONDO:0010279 otar diseases +MONDO:0010279 rare diseases +MONDO:0010280 gard_rare diseases +MONDO:0010280 rare diseases +MONDO:0010281 clingen diseases +MONDO:0010281 gard_rare diseases +MONDO:0010281 nord_rare diseases +MONDO:0010281 ordo_disorder diseases +MONDO:0010281 orphanet_rare diseases +MONDO:0010281 otar diseases +MONDO:0010281 rare diseases +MONDO:0010283 gard_rare diseases +MONDO:0010283 nord_rare diseases +MONDO:0010283 ordo_disorder diseases +MONDO:0010283 ordo_malformation_syndrome diseases +MONDO:0010283 orphanet_rare diseases +MONDO:0010283 otar diseases +MONDO:0010283 rare diseases +MONDO:0010284 gard_rare diseases +MONDO:0010284 nord_rare diseases +MONDO:0010284 ordo_disorder diseases +MONDO:0010284 ordo_malformation_syndrome diseases +MONDO:0010284 orphanet_rare diseases +MONDO:0010284 otar diseases +MONDO:0010284 rare diseases +MONDO:0010285 gard_rare diseases +MONDO:0010285 nord_rare diseases +MONDO:0010285 ordo_disorder diseases +MONDO:0010285 ordo_malformation_syndrome diseases +MONDO:0010285 orphanet_rare diseases +MONDO:0010285 rare diseases +MONDO:0010286 clingen diseases +MONDO:0010286 gard_rare diseases +MONDO:0010286 nord_rare diseases +MONDO:0010286 ordo_disorder diseases +MONDO:0010286 ordo_malformation_syndrome diseases +MONDO:0010286 orphanet_rare diseases +MONDO:0010286 otar diseases +MONDO:0010286 rare diseases +MONDO:0010287 gard_rare diseases +MONDO:0010287 ordo_disorder diseases +MONDO:0010287 orphanet_rare diseases +MONDO:0010287 otar diseases +MONDO:0010287 rare diseases +MONDO:0010288 gard_rare diseases +MONDO:0010288 ordo_disorder diseases +MONDO:0010288 orphanet_rare diseases +MONDO:0010288 otar diseases +MONDO:0010288 rare diseases +MONDO:0010289 gard_rare diseases +MONDO:0010289 nord_rare diseases +MONDO:0010289 rare diseases +MONDO:0010292 gard_rare diseases +MONDO:0010292 otar diseases +MONDO:0010292 rare diseases +MONDO:0010293 gard_rare diseases +MONDO:0010293 nord_rare diseases +MONDO:0010293 ordo_disorder diseases +MONDO:0010293 orphanet_rare diseases +MONDO:0010293 otar diseases +MONDO:0010293 rare diseases +MONDO:0010294 clingen diseases +MONDO:0010294 gard_rare diseases +MONDO:0010294 nord_rare diseases +MONDO:0010294 ordo_disorder diseases +MONDO:0010294 orphanet_rare diseases +MONDO:0010294 otar diseases +MONDO:0010294 rare diseases +MONDO:0010295 gard_rare diseases +MONDO:0010295 nord_rare diseases +MONDO:0010295 ordo_disorder diseases +MONDO:0010295 orphanet_rare diseases +MONDO:0010295 otar diseases +MONDO:0010295 rare diseases +MONDO:0010296 clingen diseases +MONDO:0010296 gard_rare diseases +MONDO:0010296 nord_rare diseases +MONDO:0010296 rare diseases +MONDO:0010298 clingen diseases +MONDO:0010298 gard_rare diseases +MONDO:0010298 nord_rare diseases +MONDO:0010298 ordo_disorder diseases +MONDO:0010298 orphanet_rare diseases +MONDO:0010298 otar diseases +MONDO:0010298 rare diseases +MONDO:0010299 gard_rare diseases +MONDO:0010299 nord_rare diseases +MONDO:0010299 ordo_disorder diseases +MONDO:0010299 orphanet_rare diseases +MONDO:0010299 otar diseases +MONDO:0010299 rare diseases +MONDO:0010300 gard_rare diseases +MONDO:0010300 nord_rare diseases +MONDO:0010300 rare diseases +MONDO:0010302 gard_rare diseases +MONDO:0010302 nord_rare diseases +MONDO:0010302 otar diseases +MONDO:0010302 rare diseases +MONDO:0010305 clingen diseases +MONDO:0010305 gard_rare diseases +MONDO:0010305 nord_rare diseases +MONDO:0010305 ordo_disorder diseases +MONDO:0010305 orphanet_rare diseases +MONDO:0010305 otar diseases +MONDO:0010305 rare diseases +MONDO:0010306 clingen diseases +MONDO:0010306 gard_rare diseases +MONDO:0010306 nord_rare diseases +MONDO:0010306 ordo_disorder diseases +MONDO:0010306 ordo_malformation_syndrome diseases +MONDO:0010306 orphanet_rare diseases +MONDO:0010306 otar diseases +MONDO:0010306 rare diseases +MONDO:0010307 gard_rare diseases +MONDO:0010307 nord_rare diseases +MONDO:0010307 rare diseases +MONDO:0010308 gard_rare diseases +MONDO:0010308 nord_rare diseases +MONDO:0010308 otar diseases +MONDO:0010308 rare diseases +MONDO:0010309 gard_rare diseases +MONDO:0010309 nord_rare diseases +MONDO:0010309 rare diseases +MONDO:0010310 gard_rare diseases +MONDO:0010310 nord_rare diseases +MONDO:0010310 ordo_disorder diseases +MONDO:0010310 ordo_malformation_syndrome diseases +MONDO:0010310 orphanet_rare diseases +MONDO:0010310 otar diseases +MONDO:0010310 rare diseases +MONDO:0010311 gard_rare diseases +MONDO:0010311 nord_rare diseases +MONDO:0010311 ordo_disorder diseases +MONDO:0010311 orphanet_rare diseases +MONDO:0010311 otar diseases +MONDO:0010311 rare diseases +MONDO:0010313 gard_rare diseases +MONDO:0010313 nord_rare diseases +MONDO:0010313 rare diseases +MONDO:0010314 gard_rare diseases +MONDO:0010314 nord_rare diseases +MONDO:0010314 rare diseases +MONDO:0010315 clingen diseases +MONDO:0010315 gard_rare diseases +MONDO:0010315 nord_rare diseases +MONDO:0010315 ordo_disorder diseases +MONDO:0010315 orphanet_rare diseases +MONDO:0010315 otar diseases +MONDO:0010315 rare diseases +MONDO:0010317 gard_rare diseases +MONDO:0010317 nord_rare diseases +MONDO:0010317 otar diseases +MONDO:0010317 rare diseases +MONDO:0010318 otar diseases +MONDO:0010319 gard_rare diseases +MONDO:0010319 nord_rare diseases +MONDO:0010319 ordo_disorder diseases +MONDO:0010319 orphanet_rare diseases +MONDO:0010319 otar diseases +MONDO:0010319 rare diseases +MONDO:0010320 gard_rare diseases +MONDO:0010320 nord_rare diseases +MONDO:0010320 rare diseases +MONDO:0010322 gard_rare diseases +MONDO:0010322 nord_rare diseases +MONDO:0010322 rare diseases +MONDO:0010323 gard_rare diseases +MONDO:0010323 ordo_disorder diseases +MONDO:0010323 ordo_malformation_syndrome diseases +MONDO:0010323 orphanet_rare diseases +MONDO:0010323 otar diseases +MONDO:0010323 rare diseases +MONDO:0010324 gard_rare diseases +MONDO:0010324 nord_rare diseases +MONDO:0010324 rare diseases +MONDO:0010325 gard_rare diseases +MONDO:0010325 nord_rare diseases +MONDO:0010325 ordo_disorder diseases +MONDO:0010325 ordo_malformation_syndrome diseases +MONDO:0010325 orphanet_rare diseases +MONDO:0010325 otar diseases +MONDO:0010325 rare diseases +MONDO:0010326 gard_rare diseases +MONDO:0010326 nord_rare diseases +MONDO:0010326 rare diseases +MONDO:0010327 clingen diseases +MONDO:0010327 gard_rare diseases +MONDO:0010327 nord_rare diseases +MONDO:0010327 ordo_disorder diseases +MONDO:0010327 orphanet_rare diseases +MONDO:0010327 otar diseases +MONDO:0010327 rare diseases +MONDO:0010328 gard_rare diseases +MONDO:0010328 nord_rare diseases +MONDO:0010328 ordo_disorder diseases +MONDO:0010328 orphanet_rare diseases +MONDO:0010328 otar diseases +MONDO:0010328 rare diseases +MONDO:0010329 gard_rare diseases +MONDO:0010329 nord_rare diseases +MONDO:0010329 rare diseases +MONDO:0010332 gard_rare diseases +MONDO:0010332 nord_rare diseases +MONDO:0010332 ordo_disorder diseases +MONDO:0010332 ordo_malformation_syndrome diseases +MONDO:0010332 orphanet_rare diseases +MONDO:0010332 otar diseases +MONDO:0010332 rare diseases +MONDO:0010333 clingen diseases +MONDO:0010333 gard_rare diseases +MONDO:0010333 ordo_disorder diseases +MONDO:0010333 ordo_malformation_syndrome diseases +MONDO:0010333 orphanet_rare diseases +MONDO:0010333 otar diseases +MONDO:0010333 rare diseases +MONDO:0010334 clingen diseases +MONDO:0010334 gard_rare diseases +MONDO:0010334 ordo_disorder diseases +MONDO:0010334 ordo_malformation_syndrome diseases +MONDO:0010334 orphanet_rare diseases +MONDO:0010334 otar diseases +MONDO:0010334 rare diseases +MONDO:0010335 gard_rare diseases +MONDO:0010335 nord_rare diseases +MONDO:0010335 rare diseases +MONDO:0010336 gard_rare diseases +MONDO:0010336 nord_rare diseases +MONDO:0010336 ordo_disorder diseases +MONDO:0010336 ordo_malformation_syndrome diseases +MONDO:0010336 orphanet_rare diseases +MONDO:0010336 otar diseases +MONDO:0010336 rare diseases +MONDO:0010337 clingen diseases +MONDO:0010337 gard_rare diseases +MONDO:0010337 nord_rare diseases +MONDO:0010337 ordo_disorder diseases +MONDO:0010337 orphanet_rare diseases +MONDO:0010337 otar diseases +MONDO:0010337 rare diseases +MONDO:0010338 clingen diseases +MONDO:0010338 gard_rare diseases +MONDO:0010338 nord_rare diseases +MONDO:0010338 ordo_disorder diseases +MONDO:0010338 orphanet_rare diseases +MONDO:0010338 otar diseases +MONDO:0010338 rare diseases +MONDO:0010339 gard_rare diseases +MONDO:0010339 ordo_disorder diseases +MONDO:0010339 orphanet_rare diseases +MONDO:0010339 otar diseases +MONDO:0010339 rare diseases +MONDO:0010344 gard_rare diseases +MONDO:0010344 nord_rare diseases +MONDO:0010344 rare diseases +MONDO:0010347 gard_rare diseases +MONDO:0010347 nord_rare diseases +MONDO:0010347 rare diseases +MONDO:0010349 gard_rare diseases +MONDO:0010349 nord_rare diseases +MONDO:0010349 rare diseases +MONDO:0010350 gard_rare diseases +MONDO:0010350 nord_rare diseases +MONDO:0010350 rare diseases +MONDO:0010351 clingen diseases +MONDO:0010351 gard_rare diseases +MONDO:0010351 nord_rare diseases +MONDO:0010351 rare diseases +MONDO:0010352 gard_rare diseases +MONDO:0010352 nord_rare diseases +MONDO:0010352 rare diseases +MONDO:0010353 gard_rare diseases +MONDO:0010353 nord_rare diseases +MONDO:0010353 ordo_disorder diseases +MONDO:0010353 ordo_malformation_syndrome diseases +MONDO:0010353 orphanet_rare diseases +MONDO:0010353 otar diseases +MONDO:0010353 rare diseases +MONDO:0010354 clingen diseases +MONDO:0010354 gard_rare diseases +MONDO:0010354 nord_rare diseases +MONDO:0010354 ordo_disorder diseases +MONDO:0010354 orphanet_rare diseases +MONDO:0010354 otar diseases +MONDO:0010354 rare diseases +MONDO:0010355 gard_rare diseases +MONDO:0010355 nord_rare diseases +MONDO:0010355 ordo_disorder diseases +MONDO:0010355 ordo_malformation_syndrome diseases +MONDO:0010355 orphanet_rare diseases +MONDO:0010355 otar diseases +MONDO:0010355 rare diseases +MONDO:0010356 gard_rare diseases +MONDO:0010356 nord_rare diseases +MONDO:0010356 ordo_disorder diseases +MONDO:0010356 orphanet_rare diseases +MONDO:0010356 otar diseases +MONDO:0010356 rare diseases +MONDO:0010358 gard_rare diseases +MONDO:0010358 nord_rare diseases +MONDO:0010358 rare diseases +MONDO:0010359 gard_rare diseases +MONDO:0010359 nord_rare diseases +MONDO:0010359 ordo_subtype_of_a_disorder diseases +MONDO:0010359 otar diseases +MONDO:0010359 rare diseases +MONDO:0010360 gard_rare diseases +MONDO:0010360 rare diseases +MONDO:0010361 gard_rare diseases +MONDO:0010361 nord_rare diseases +MONDO:0010361 rare diseases +MONDO:0010362 gard_rare diseases +MONDO:0010362 nord_rare diseases +MONDO:0010362 ordo_disorder diseases +MONDO:0010362 orphanet_rare diseases +MONDO:0010362 otar diseases +MONDO:0010362 rare diseases +MONDO:0010363 gard_rare diseases +MONDO:0010363 nord_rare diseases +MONDO:0010363 rare diseases +MONDO:0010364 gard_rare diseases +MONDO:0010364 nord_rare diseases +MONDO:0010364 ordo_disorder diseases +MONDO:0010364 orphanet_rare diseases +MONDO:0010364 otar diseases +MONDO:0010364 rare diseases +MONDO:0010365 gard_rare diseases +MONDO:0010365 rare diseases +MONDO:0010367 gard_rare diseases +MONDO:0010367 nord_rare diseases +MONDO:0010367 ordo_disorder diseases +MONDO:0010367 orphanet_rare diseases +MONDO:0010367 otar diseases +MONDO:0010367 rare diseases +MONDO:0010370 gard_rare diseases +MONDO:0010370 nord_rare diseases +MONDO:0010370 rare diseases +MONDO:0010371 gard_rare diseases +MONDO:0010371 nord_rare diseases +MONDO:0010371 ordo_disorder diseases +MONDO:0010371 orphanet_rare diseases +MONDO:0010371 otar diseases +MONDO:0010371 rare diseases +MONDO:0010373 gard_rare diseases +MONDO:0010373 nord_rare diseases +MONDO:0010373 rare diseases +MONDO:0010374 gard_rare diseases +MONDO:0010374 nord_rare diseases +MONDO:0010374 rare diseases +MONDO:0010375 gard_rare diseases +MONDO:0010375 nord_rare diseases +MONDO:0010375 ordo_disorder diseases +MONDO:0010375 orphanet_rare diseases +MONDO:0010375 otar diseases +MONDO:0010375 rare diseases +MONDO:0010378 clingen diseases +MONDO:0010378 gard_rare diseases +MONDO:0010378 nord_rare diseases +MONDO:0010378 ordo_disorder diseases +MONDO:0010378 orphanet_rare diseases +MONDO:0010378 otar diseases +MONDO:0010378 rare diseases +MONDO:0010379 clingen diseases +MONDO:0010379 gard_rare diseases +MONDO:0010379 nord_rare diseases +MONDO:0010379 ordo_disorder diseases +MONDO:0010379 orphanet_rare diseases +MONDO:0010379 otar diseases +MONDO:0010379 rare diseases +MONDO:0010382 gard_rare diseases +MONDO:0010382 nord_rare diseases +MONDO:0010382 ordo_disorder diseases +MONDO:0010382 ordo_malformation_syndrome diseases +MONDO:0010382 orphanet_rare diseases +MONDO:0010382 otar diseases +MONDO:0010382 rare diseases +MONDO:0010383 clingen diseases +MONDO:0010383 gard_rare diseases +MONDO:0010383 nord_rare diseases +MONDO:0010383 ordo_disorder diseases +MONDO:0010383 ordo_malformation_syndrome diseases +MONDO:0010383 orphanet_rare diseases +MONDO:0010383 otar diseases +MONDO:0010383 rare diseases +MONDO:0010384 gard_rare diseases +MONDO:0010384 nord_rare diseases +MONDO:0010384 rare diseases +MONDO:0010385 gard_rare diseases +MONDO:0010385 nord_rare diseases +MONDO:0010385 ordo_disorder diseases +MONDO:0010385 orphanet_rare diseases +MONDO:0010385 rare diseases +MONDO:0010386 gard_rare diseases +MONDO:0010386 ordo_etiological_subtype diseases +MONDO:0010386 ordo_subtype_of_a_disorder diseases +MONDO:0010386 otar diseases +MONDO:0010386 predisposition diseases +MONDO:0010386 rare diseases +MONDO:0010388 gard_rare diseases +MONDO:0010388 nord_rare diseases +MONDO:0010388 rare diseases +MONDO:0010390 gard_rare diseases +MONDO:0010390 nord_rare diseases +MONDO:0010390 ordo_disorder diseases +MONDO:0010390 orphanet_rare diseases +MONDO:0010390 otar diseases +MONDO:0010390 rare diseases +MONDO:0010391 gard_rare diseases +MONDO:0010391 nord_rare diseases +MONDO:0010391 rare diseases +MONDO:0010392 gard_rare diseases +MONDO:0010392 nord_rare diseases +MONDO:0010392 ordo_disorder diseases +MONDO:0010392 orphanet_rare diseases +MONDO:0010392 otar diseases +MONDO:0010392 rare diseases +MONDO:0010393 gard_rare diseases +MONDO:0010393 nord_rare diseases +MONDO:0010393 otar diseases +MONDO:0010393 rare diseases +MONDO:0010395 clingen diseases +MONDO:0010395 gard_rare diseases +MONDO:0010395 nord_rare diseases +MONDO:0010395 ordo_disorder diseases +MONDO:0010395 orphanet_rare diseases +MONDO:0010395 otar diseases +MONDO:0010395 rare diseases +MONDO:0010396 gard_rare diseases +MONDO:0010396 nord_rare diseases +MONDO:0010396 ordo_disorder diseases +MONDO:0010396 orphanet_rare diseases +MONDO:0010396 rare diseases +MONDO:0010397 gard_rare diseases +MONDO:0010397 nord_rare diseases +MONDO:0010397 ordo_disorder diseases +MONDO:0010397 orphanet_rare diseases +MONDO:0010397 otar diseases +MONDO:0010397 rare diseases +MONDO:0010398 gard_rare diseases +MONDO:0010398 nord_rare diseases +MONDO:0010398 rare diseases +MONDO:0010399 gard_rare diseases +MONDO:0010399 nord_rare diseases +MONDO:0010399 ordo_disorder diseases +MONDO:0010399 orphanet_rare diseases +MONDO:0010399 otar diseases +MONDO:0010399 rare diseases +MONDO:0010400 gard_rare diseases +MONDO:0010400 nord_rare diseases +MONDO:0010400 ordo_disorder diseases +MONDO:0010400 orphanet_rare diseases +MONDO:0010400 rare diseases +MONDO:0010401 gard_rare diseases +MONDO:0010401 nord_rare diseases +MONDO:0010401 ordo_disorder diseases +MONDO:0010401 orphanet_rare diseases +MONDO:0010401 otar diseases +MONDO:0010401 rare diseases +MONDO:0010403 gard_rare diseases +MONDO:0010403 nord_rare diseases +MONDO:0010403 ordo_disorder diseases +MONDO:0010403 ordo_malformation_syndrome diseases +MONDO:0010403 orphanet_rare diseases +MONDO:0010403 rare diseases +MONDO:0010404 gard_rare diseases +MONDO:0010404 nord_rare diseases +MONDO:0010404 ordo_disorder diseases +MONDO:0010404 orphanet_rare diseases +MONDO:0010404 otar diseases +MONDO:0010404 rare diseases +MONDO:0010405 gard_rare diseases +MONDO:0010405 rare diseases +MONDO:0010406 gard_rare diseases +MONDO:0010406 nord_rare diseases +MONDO:0010406 rare diseases +MONDO:0010407 gard_rare diseases +MONDO:0010407 nord_rare diseases +MONDO:0010407 ordo_malformation_syndrome diseases +MONDO:0010407 otar diseases +MONDO:0010407 rare diseases +MONDO:0010408 gard_rare diseases +MONDO:0010408 nord_rare diseases +MONDO:0010408 ordo_disorder diseases +MONDO:0010408 ordo_malformation_syndrome diseases +MONDO:0010408 orphanet_rare diseases +MONDO:0010408 otar diseases +MONDO:0010408 rare diseases +MONDO:0010409 gard_rare diseases +MONDO:0010409 nord_rare diseases +MONDO:0010409 ordo_disorder diseases +MONDO:0010409 ordo_malformation_syndrome diseases +MONDO:0010409 orphanet_rare diseases +MONDO:0010409 rare diseases +MONDO:0010410 gard_rare diseases +MONDO:0010410 rare diseases +MONDO:0010412 gard_rare diseases +MONDO:0010412 nord_rare diseases +MONDO:0010412 ordo_disorder diseases +MONDO:0010412 orphanet_rare diseases +MONDO:0010412 otar diseases +MONDO:0010412 rare diseases +MONDO:0010413 gard_rare diseases +MONDO:0010413 nord_rare diseases +MONDO:0010413 rare diseases +MONDO:0010414 gard_rare diseases +MONDO:0010414 rare diseases +MONDO:0010415 gard_rare diseases +MONDO:0010415 rare diseases +MONDO:0010417 gard_rare diseases +MONDO:0010417 nord_rare diseases +MONDO:0010417 ordo_disorder diseases +MONDO:0010417 orphanet_rare diseases +MONDO:0010417 otar diseases +MONDO:0010417 rare diseases +MONDO:0010418 gard_rare diseases +MONDO:0010418 nord_rare diseases +MONDO:0010418 ordo_disorder diseases +MONDO:0010418 orphanet_rare diseases +MONDO:0010418 otar diseases +MONDO:0010418 rare diseases +MONDO:0010420 clingen diseases +MONDO:0010420 gard_rare diseases +MONDO:0010420 nord_rare diseases +MONDO:0010420 ordo_disorder diseases +MONDO:0010420 orphanet_rare diseases +MONDO:0010420 rare diseases +MONDO:0010421 clingen diseases +MONDO:0010421 gard_rare diseases +MONDO:0010421 nord_rare diseases +MONDO:0010421 ordo_subtype_of_a_disorder diseases +MONDO:0010421 otar diseases +MONDO:0010421 rare diseases +MONDO:0010423 gard_rare diseases +MONDO:0010423 nord_rare diseases +MONDO:0010423 rare diseases +MONDO:0010424 gard_rare diseases +MONDO:0010424 nord_rare diseases +MONDO:0010424 rare diseases +MONDO:0010425 gard_rare diseases +MONDO:0010425 nord_rare diseases +MONDO:0010425 ordo_disorder diseases +MONDO:0010425 orphanet_rare diseases +MONDO:0010425 otar diseases +MONDO:0010425 rare diseases +MONDO:0010426 gard_rare diseases +MONDO:0010426 nord_rare diseases +MONDO:0010426 ordo_disorder diseases +MONDO:0010426 orphanet_rare diseases +MONDO:0010426 otar diseases +MONDO:0010426 rare diseases +MONDO:0010427 clingen diseases +MONDO:0010427 gard_rare diseases +MONDO:0010427 nord_rare diseases +MONDO:0010427 otar diseases +MONDO:0010427 rare diseases +MONDO:0010428 gard_rare diseases +MONDO:0010428 nord_rare diseases +MONDO:0010428 ordo_disorder diseases +MONDO:0010428 ordo_malformation_syndrome diseases +MONDO:0010428 orphanet_rare diseases +MONDO:0010428 rare diseases +MONDO:0010429 gard_rare diseases +MONDO:0010429 nord_rare diseases +MONDO:0010429 rare diseases +MONDO:0010430 gard_rare diseases +MONDO:0010430 nord_rare diseases +MONDO:0010430 rare diseases +MONDO:0010431 gard_rare diseases +MONDO:0010431 nord_rare diseases +MONDO:0010431 rare diseases +MONDO:0010432 clingen diseases +MONDO:0010432 gard_rare diseases +MONDO:0010432 nord_rare diseases +MONDO:0010432 otar diseases +MONDO:0010432 rare diseases +MONDO:0010434 gard_rare diseases +MONDO:0010434 nord_rare diseases +MONDO:0010434 ordo_disorder diseases +MONDO:0010434 orphanet_rare diseases +MONDO:0010434 otar diseases +MONDO:0010434 rare diseases +MONDO:0010435 otar diseases +MONDO:0010436 gard_rare diseases +MONDO:0010436 nord_rare diseases +MONDO:0010436 otar diseases +MONDO:0010436 rare diseases +MONDO:0010437 gard_rare diseases +MONDO:0010437 nord_rare diseases +MONDO:0010437 ordo_disorder diseases +MONDO:0010437 orphanet_rare diseases +MONDO:0010437 otar diseases +MONDO:0010437 rare diseases +MONDO:0010438 gard_rare diseases +MONDO:0010438 nord_rare diseases +MONDO:0010438 otar diseases +MONDO:0010438 rare diseases +MONDO:0010441 clingen diseases +MONDO:0010441 gard_rare diseases +MONDO:0010441 nord_rare diseases +MONDO:0010441 ordo_disorder diseases +MONDO:0010441 ordo_malformation_syndrome diseases +MONDO:0010441 orphanet_rare diseases +MONDO:0010441 otar diseases +MONDO:0010441 rare diseases +MONDO:0010442 gard_rare diseases +MONDO:0010442 nord_rare diseases +MONDO:0010442 rare diseases +MONDO:0010443 gard_rare diseases +MONDO:0010443 nord_rare diseases +MONDO:0010443 rare diseases +MONDO:0010444 gard_rare diseases +MONDO:0010444 nord_rare diseases +MONDO:0010444 ordo_disorder diseases +MONDO:0010444 orphanet_rare diseases +MONDO:0010444 otar diseases +MONDO:0010444 rare diseases +MONDO:0010446 gard_rare diseases +MONDO:0010446 nord_rare diseases +MONDO:0010446 ordo_disorder diseases +MONDO:0010446 orphanet_rare diseases +MONDO:0010446 otar diseases +MONDO:0010446 rare diseases +MONDO:0010447 gard_rare diseases +MONDO:0010447 nord_rare diseases +MONDO:0010447 rare diseases +MONDO:0010448 gard_rare diseases +MONDO:0010448 nord_rare diseases +MONDO:0010448 ordo_disorder diseases +MONDO:0010448 orphanet_rare diseases +MONDO:0010448 otar diseases +MONDO:0010448 rare diseases +MONDO:0010450 gard_rare diseases +MONDO:0010450 nord_rare diseases +MONDO:0010450 rare diseases +MONDO:0010451 gard_rare diseases +MONDO:0010451 nord_rare diseases +MONDO:0010451 rare diseases +MONDO:0010452 gard_rare diseases +MONDO:0010452 nord_rare diseases +MONDO:0010452 rare diseases +MONDO:0010453 gard_rare diseases +MONDO:0010453 nord_rare diseases +MONDO:0010453 rare diseases +MONDO:0010454 gard_rare diseases +MONDO:0010454 nord_rare diseases +MONDO:0010454 rare diseases +MONDO:0010455 gard_rare diseases +MONDO:0010455 nord_rare diseases +MONDO:0010455 ordo_disorder diseases +MONDO:0010455 orphanet_rare diseases +MONDO:0010455 otar diseases +MONDO:0010455 rare diseases +MONDO:0010456 gard_rare diseases +MONDO:0010456 nord_rare diseases +MONDO:0010456 rare diseases +MONDO:0010457 gard_rare diseases +MONDO:0010457 nord_rare diseases +MONDO:0010457 ordo_disorder diseases +MONDO:0010457 ordo_malformation_syndrome diseases +MONDO:0010457 orphanet_rare diseases +MONDO:0010457 otar diseases +MONDO:0010457 rare diseases +MONDO:0010458 gard_rare diseases +MONDO:0010458 nord_rare diseases +MONDO:0010458 rare diseases +MONDO:0010459 clingen diseases +MONDO:0010459 gard_rare diseases +MONDO:0010459 nord_rare diseases +MONDO:0010459 otar diseases +MONDO:0010459 rare diseases +MONDO:0010460 gard_rare diseases +MONDO:0010460 nord_rare diseases +MONDO:0010460 ordo_disorder diseases +MONDO:0010460 orphanet_rare diseases +MONDO:0010460 otar diseases +MONDO:0010460 rare diseases +MONDO:0010461 clingen diseases +MONDO:0010461 gard_rare diseases +MONDO:0010461 nord_rare diseases +MONDO:0010461 ordo_disorder diseases +MONDO:0010461 orphanet_rare diseases +MONDO:0010461 otar diseases +MONDO:0010461 rare diseases +MONDO:0010462 gard_rare diseases +MONDO:0010462 nord_rare diseases +MONDO:0010462 rare diseases +MONDO:0010463 gard_rare diseases +MONDO:0010463 nord_rare diseases +MONDO:0010463 ordo_disorder diseases +MONDO:0010463 orphanet_rare diseases +MONDO:0010463 otar diseases +MONDO:0010463 rare diseases +MONDO:0010464 gard_rare diseases +MONDO:0010464 nord_rare diseases +MONDO:0010464 ordo_disorder diseases +MONDO:0010464 orphanet_rare diseases +MONDO:0010464 otar diseases +MONDO:0010464 rare diseases +MONDO:0010465 clingen diseases +MONDO:0010465 gard_rare diseases +MONDO:0010465 nord_rare diseases +MONDO:0010465 rare diseases +MONDO:0010466 gard_rare diseases +MONDO:0010466 nord_rare diseases +MONDO:0010466 ordo_disorder diseases +MONDO:0010466 ordo_malformation_syndrome diseases +MONDO:0010466 orphanet_rare diseases +MONDO:0010466 otar diseases +MONDO:0010466 rare diseases +MONDO:0010467 gard_rare diseases +MONDO:0010467 nord_rare diseases +MONDO:0010467 ordo_disorder diseases +MONDO:0010467 ordo_malformation_syndrome diseases +MONDO:0010467 orphanet_rare diseases +MONDO:0010467 otar diseases +MONDO:0010467 rare diseases +MONDO:0010468 gard_rare diseases +MONDO:0010468 nord_rare diseases +MONDO:0010468 rare diseases +MONDO:0010471 gard_rare diseases +MONDO:0010471 nord_rare diseases +MONDO:0010471 rare diseases +MONDO:0010472 gard_rare diseases +MONDO:0010472 nord_rare diseases +MONDO:0010472 ordo_disorder diseases +MONDO:0010472 orphanet_rare diseases +MONDO:0010472 otar diseases +MONDO:0010472 rare diseases +MONDO:0010473 gard_rare diseases +MONDO:0010473 nord_rare diseases +MONDO:0010473 ordo_disorder diseases +MONDO:0010473 orphanet_rare diseases +MONDO:0010473 otar diseases +MONDO:0010473 rare diseases +MONDO:0010474 gard_rare diseases +MONDO:0010474 nord_rare diseases +MONDO:0010474 rare diseases +MONDO:0010475 gard_rare diseases +MONDO:0010475 nord_rare diseases +MONDO:0010475 ordo_disorder diseases +MONDO:0010475 orphanet_rare diseases +MONDO:0010475 otar diseases +MONDO:0010475 rare diseases +MONDO:0010476 gard_rare diseases +MONDO:0010476 nord_rare diseases +MONDO:0010476 ordo_disorder diseases +MONDO:0010476 orphanet_rare diseases +MONDO:0010476 otar diseases +MONDO:0010476 rare diseases +MONDO:0010477 gard_rare diseases +MONDO:0010477 nord_rare diseases +MONDO:0010477 ordo_disorder diseases +MONDO:0010477 ordo_malformation_syndrome diseases +MONDO:0010477 orphanet_rare diseases +MONDO:0010477 otar diseases +MONDO:0010477 rare diseases +MONDO:0010478 gard_rare diseases +MONDO:0010478 nord_rare diseases +MONDO:0010478 ordo_disorder diseases +MONDO:0010478 ordo_inheritance_inconsistent diseases +MONDO:0010478 orphanet_rare diseases +MONDO:0010478 otar diseases +MONDO:0010478 rare diseases +MONDO:0010479 gard_rare diseases +MONDO:0010479 nord_rare diseases +MONDO:0010479 ordo_disorder diseases +MONDO:0010479 orphanet_rare diseases +MONDO:0010479 otar diseases +MONDO:0010479 rare diseases +MONDO:0010480 clingen diseases +MONDO:0010480 gard_rare diseases +MONDO:0010480 nord_rare diseases +MONDO:0010480 ordo_disorder diseases +MONDO:0010480 orphanet_rare diseases +MONDO:0010480 rare diseases +MONDO:0010481 gard_rare diseases +MONDO:0010481 otar diseases +MONDO:0010481 rare diseases +MONDO:0010482 gard_rare diseases +MONDO:0010482 nord_rare diseases +MONDO:0010482 ordo_disorder diseases +MONDO:0010482 orphanet_rare diseases +MONDO:0010482 otar diseases +MONDO:0010482 rare diseases +MONDO:0010483 gard_rare diseases +MONDO:0010483 nord_rare diseases +MONDO:0010483 ordo_disorder diseases +MONDO:0010483 ordo_malformation_syndrome diseases +MONDO:0010483 orphanet_rare diseases +MONDO:0010483 otar diseases +MONDO:0010483 rare diseases +MONDO:0010484 clingen diseases +MONDO:0010484 gard_rare diseases +MONDO:0010484 nord_rare diseases +MONDO:0010484 rare diseases +MONDO:0010485 gard_rare diseases +MONDO:0010485 nord_rare diseases +MONDO:0010485 ordo_disorder diseases +MONDO:0010485 ordo_malformation_syndrome diseases +MONDO:0010485 orphanet_rare diseases +MONDO:0010485 rare diseases +MONDO:0010486 gard_rare diseases +MONDO:0010486 nord_rare diseases +MONDO:0010486 rare diseases +MONDO:0010487 gard_rare diseases +MONDO:0010487 nord_rare diseases +MONDO:0010487 rare diseases +MONDO:0010488 gard_rare diseases +MONDO:0010488 nord_rare diseases +MONDO:0010488 rare diseases +MONDO:0010489 gard_rare diseases +MONDO:0010489 nord_rare diseases +MONDO:0010489 rare diseases +MONDO:0010490 gard_rare diseases +MONDO:0010490 nord_rare diseases +MONDO:0010490 ordo_disorder diseases +MONDO:0010490 orphanet_rare diseases +MONDO:0010490 otar diseases +MONDO:0010490 rare diseases +MONDO:0010491 gard_rare diseases +MONDO:0010491 nord_rare diseases +MONDO:0010491 ordo_etiological_subtype diseases +MONDO:0010491 rare diseases +MONDO:0010492 gard_rare diseases +MONDO:0010492 nord_rare diseases +MONDO:0010492 rare diseases +MONDO:0010493 gard_rare diseases +MONDO:0010493 nord_rare diseases +MONDO:0010493 rare diseases +MONDO:0010494 gard_rare diseases +MONDO:0010494 nord_rare diseases +MONDO:0010494 rare diseases +MONDO:0010495 gard_rare diseases +MONDO:0010495 nord_rare diseases +MONDO:0010495 rare diseases +MONDO:0010496 gard_rare diseases +MONDO:0010496 nord_rare diseases +MONDO:0010496 ordo_disorder diseases +MONDO:0010496 ordo_malformation_syndrome diseases +MONDO:0010496 orphanet_rare diseases +MONDO:0010496 rare diseases +MONDO:0010497 gard_rare diseases +MONDO:0010497 nord_rare diseases +MONDO:0010497 rare diseases +MONDO:0010498 clingen diseases +MONDO:0010498 gard_rare diseases +MONDO:0010498 nord_rare diseases +MONDO:0010498 ordo_disorder diseases +MONDO:0010498 ordo_malformation_syndrome diseases +MONDO:0010498 orphanet_rare diseases +MONDO:0010498 otar diseases +MONDO:0010498 rare diseases +MONDO:0010499 clingen diseases +MONDO:0010499 gard_rare diseases +MONDO:0010499 nord_rare diseases +MONDO:0010499 rare diseases +MONDO:0010500 gard_rare diseases +MONDO:0010500 nord_rare diseases +MONDO:0010500 rare diseases +MONDO:0010501 gard_rare diseases +MONDO:0010501 nord_rare diseases +MONDO:0010501 ordo_disorder diseases +MONDO:0010501 ordo_malformation_syndrome diseases +MONDO:0010501 orphanet_rare diseases +MONDO:0010501 rare diseases +MONDO:0010502 gard_rare diseases +MONDO:0010502 nord_rare diseases +MONDO:0010502 rare diseases +MONDO:0010503 gard_rare diseases +MONDO:0010503 nord_rare diseases +MONDO:0010503 ordo_subtype_of_a_disorder diseases +MONDO:0010503 rare diseases +MONDO:0010504 gard_rare diseases +MONDO:0010504 otar diseases +MONDO:0010504 rare diseases +MONDO:0010505 gard_rare diseases +MONDO:0010505 nord_rare diseases +MONDO:0010505 ordo_disorder diseases +MONDO:0010505 ordo_malformation_syndrome diseases +MONDO:0010505 orphanet_rare diseases +MONDO:0010505 otar diseases +MONDO:0010505 rare diseases +MONDO:0010506 gard_rare diseases +MONDO:0010506 nord_rare diseases +MONDO:0010506 rare diseases +MONDO:0010507 gard_rare diseases +MONDO:0010507 nord_rare diseases +MONDO:0010507 ordo_disorder diseases +MONDO:0010507 ordo_malformation_syndrome diseases +MONDO:0010507 orphanet_rare diseases +MONDO:0010507 rare diseases +MONDO:0010508 gard_rare diseases +MONDO:0010508 nord_rare diseases +MONDO:0010508 rare diseases +MONDO:0010509 gard_rare diseases +MONDO:0010509 nord_rare diseases +MONDO:0010509 rare diseases +MONDO:0010510 gard_rare diseases +MONDO:0010510 nord_rare diseases +MONDO:0010510 rare diseases +MONDO:0010511 gard_rare diseases +MONDO:0010511 nord_rare diseases +MONDO:0010511 rare diseases +MONDO:0010512 gard_rare diseases +MONDO:0010512 nord_rare diseases +MONDO:0010512 otar diseases +MONDO:0010512 rare diseases +MONDO:0010514 clingen diseases +MONDO:0010514 gard_rare diseases +MONDO:0010514 nord_rare diseases +MONDO:0010514 ordo_disorder diseases +MONDO:0010514 orphanet_rare diseases +MONDO:0010514 rare diseases +MONDO:0010515 gard_rare diseases +MONDO:0010515 nord_rare diseases +MONDO:0010515 rare diseases +MONDO:0010516 gard_rare diseases +MONDO:0010516 nord_rare diseases +MONDO:0010516 rare diseases +MONDO:0010517 gard_rare diseases +MONDO:0010517 nord_rare diseases +MONDO:0010517 rare diseases +MONDO:0010518 clingen diseases +MONDO:0010518 gard_rare diseases +MONDO:0010518 nord_rare diseases +MONDO:0010518 ordo_disorder diseases +MONDO:0010518 orphanet_rare diseases +MONDO:0010518 otar diseases +MONDO:0010518 rare diseases +MONDO:0010519 do_inheritance_inconsistent diseases +MONDO:0010519 gard_rare diseases +MONDO:0010519 nord_rare diseases +MONDO:0010519 ordo_disorder diseases +MONDO:0010519 orphanet_rare diseases +MONDO:0010519 otar diseases +MONDO:0010519 rare diseases +MONDO:0010520 gard_rare diseases +MONDO:0010520 nord_rare diseases +MONDO:0010520 ordo_etiological_subtype diseases +MONDO:0010520 ordo_subtype_of_a_disorder diseases +MONDO:0010520 otar diseases +MONDO:0010520 rare diseases +MONDO:0010521 gard_rare diseases +MONDO:0010521 rare diseases +MONDO:0010522 gard_rare diseases +MONDO:0010522 rare diseases +MONDO:0010523 gard_rare diseases +MONDO:0010523 nord_rare diseases +MONDO:0010523 ordo_disorder diseases +MONDO:0010523 orphanet_rare diseases +MONDO:0010523 otar diseases +MONDO:0010523 rare diseases +MONDO:0010524 gard_rare diseases +MONDO:0010524 nord_rare diseases +MONDO:0010524 ordo_disorder diseases +MONDO:0010524 orphanet_rare diseases +MONDO:0010524 otar diseases +MONDO:0010524 rare diseases +MONDO:0010525 gard_rare diseases +MONDO:0010525 rare diseases +MONDO:0010526 clingen diseases +MONDO:0010526 gard_rare diseases +MONDO:0010526 nord_rare diseases +MONDO:0010526 ordo_disorder diseases +MONDO:0010526 orphanet_rare diseases +MONDO:0010526 otar diseases +MONDO:0010526 rare diseases +MONDO:0010529 gard_rare diseases +MONDO:0010529 nord_rare diseases +MONDO:0010529 ordo_disorder diseases +MONDO:0010529 ordo_malformation_syndrome diseases +MONDO:0010529 orphanet_rare diseases +MONDO:0010529 otar diseases +MONDO:0010529 rare diseases +MONDO:0010531 gard_rare diseases +MONDO:0010531 ordo_disorder diseases +MONDO:0010531 ordo_malformation_syndrome diseases +MONDO:0010531 orphanet_rare diseases +MONDO:0010531 otar diseases +MONDO:0010531 rare diseases +MONDO:0010532 gard_rare diseases +MONDO:0010532 nord_rare diseases +MONDO:0010532 ordo_disorder diseases +MONDO:0010532 orphanet_rare diseases +MONDO:0010532 otar diseases +MONDO:0010532 rare diseases +MONDO:0010533 gard_rare diseases +MONDO:0010533 nord_rare diseases +MONDO:0010533 ordo_disorder diseases +MONDO:0010533 orphanet_rare diseases +MONDO:0010533 otar diseases +MONDO:0010533 rare diseases +MONDO:0010534 gard_rare diseases +MONDO:0010534 nord_rare diseases +MONDO:0010534 ordo_disorder diseases +MONDO:0010534 orphanet_rare diseases +MONDO:0010534 otar diseases +MONDO:0010534 rare diseases +MONDO:0010535 gard_rare diseases +MONDO:0010535 nord_rare diseases +MONDO:0010535 ordo_disorder diseases +MONDO:0010535 orphanet_rare diseases +MONDO:0010535 otar diseases +MONDO:0010535 rare diseases +MONDO:0010537 clingen diseases +MONDO:0010537 gard_rare diseases +MONDO:0010537 nord_rare diseases +MONDO:0010537 ordo_disorder diseases +MONDO:0010537 ordo_malformation_syndrome diseases +MONDO:0010537 orphanet_rare diseases +MONDO:0010537 otar diseases +MONDO:0010537 rare diseases +MONDO:0010538 gard_rare diseases +MONDO:0010538 nord_rare diseases +MONDO:0010538 ordo_disorder diseases +MONDO:0010538 ordo_malformation_syndrome diseases +MONDO:0010538 orphanet_rare diseases +MONDO:0010538 rare diseases +MONDO:0010539 gard_rare diseases +MONDO:0010539 nord_rare diseases +MONDO:0010539 ordo_disorder diseases +MONDO:0010539 ordo_malformation_syndrome diseases +MONDO:0010539 orphanet_rare diseases +MONDO:0010539 otar diseases +MONDO:0010539 rare diseases +MONDO:0010540 gard_rare diseases +MONDO:0010540 nord_rare diseases +MONDO:0010540 ordo_disorder diseases +MONDO:0010540 orphanet_rare diseases +MONDO:0010540 otar diseases +MONDO:0010540 rare diseases +MONDO:0010541 gard_rare diseases +MONDO:0010541 nord_rare diseases +MONDO:0010541 ordo_disorder diseases +MONDO:0010541 orphanet_rare diseases +MONDO:0010541 otar diseases +MONDO:0010541 rare diseases +MONDO:0010542 gard_rare diseases +MONDO:0010542 nord_rare diseases +MONDO:0010542 otar diseases +MONDO:0010542 rare diseases +MONDO:0010543 clingen diseases +MONDO:0010543 gard_rare diseases +MONDO:0010543 nord_rare diseases +MONDO:0010543 ordo_disorder diseases +MONDO:0010543 orphanet_rare diseases +MONDO:0010543 otar diseases +MONDO:0010543 rare diseases +MONDO:0010544 gard_rare diseases +MONDO:0010544 nord_rare diseases +MONDO:0010544 rare diseases +MONDO:0010545 clingen diseases +MONDO:0010545 gard_rare diseases +MONDO:0010545 nord_rare diseases +MONDO:0010545 ordo_disorder diseases +MONDO:0010545 ordo_malformation_syndrome diseases +MONDO:0010545 orphanet_rare diseases +MONDO:0010545 otar diseases +MONDO:0010545 rare diseases +MONDO:0010547 gard_rare diseases +MONDO:0010547 nord_rare diseases +MONDO:0010547 ordo_disorder diseases +MONDO:0010547 orphanet_rare diseases +MONDO:0010547 otar diseases +MONDO:0010547 rare diseases +MONDO:0010548 gard_rare diseases +MONDO:0010548 nord_rare diseases +MONDO:0010548 rare diseases +MONDO:0010549 clingen diseases +MONDO:0010549 gard_rare diseases +MONDO:0010549 nord_rare diseases +MONDO:0010549 ordo_disorder diseases +MONDO:0010549 orphanet_rare diseases +MONDO:0010549 otar diseases +MONDO:0010549 rare diseases +MONDO:0010550 gard_rare diseases +MONDO:0010550 nord_rare diseases +MONDO:0010550 ordo_disorder diseases +MONDO:0010550 orphanet_rare diseases +MONDO:0010550 otar diseases +MONDO:0010550 rare diseases +MONDO:0010551 gard_rare diseases +MONDO:0010551 nord_rare diseases +MONDO:0010551 ordo_disorder diseases +MONDO:0010551 orphanet_rare diseases +MONDO:0010551 otar diseases +MONDO:0010551 rare diseases +MONDO:0010554 gard_rare diseases +MONDO:0010554 nord_rare diseases +MONDO:0010554 ordo_disorder diseases +MONDO:0010554 ordo_malformation_syndrome diseases +MONDO:0010554 orphanet_rare diseases +MONDO:0010554 otar diseases +MONDO:0010554 rare diseases +MONDO:0010555 clingen diseases +MONDO:0010555 gard_rare diseases +MONDO:0010555 nord_rare diseases +MONDO:0010555 ordo_disorder diseases +MONDO:0010555 ordo_malformation_syndrome diseases +MONDO:0010555 orphanet_rare diseases +MONDO:0010555 otar diseases +MONDO:0010555 prototype_pattern diseases +MONDO:0010555 rare diseases +MONDO:0010556 gard_rare diseases +MONDO:0010556 nord_rare diseases +MONDO:0010556 otar diseases +MONDO:0010556 prototype_pattern diseases +MONDO:0010556 rare diseases +MONDO:0010557 clingen diseases +MONDO:0010557 gard_rare diseases +MONDO:0010557 nord_rare diseases +MONDO:0010557 ordo_disorder diseases +MONDO:0010557 orphanet_rare diseases +MONDO:0010557 otar diseases +MONDO:0010557 rare diseases +MONDO:0010558 gard_rare diseases +MONDO:0010558 nord_rare diseases +MONDO:0010558 ordo_disorder diseases +MONDO:0010558 ordo_malformation_syndrome diseases +MONDO:0010558 orphanet_rare diseases +MONDO:0010558 otar diseases +MONDO:0010558 rare diseases +MONDO:0010559 gard_rare diseases +MONDO:0010559 nord_rare diseases +MONDO:0010559 ordo_subtype_of_a_disorder diseases +MONDO:0010559 otar diseases +MONDO:0010559 rare diseases +MONDO:0010560 gard_rare diseases +MONDO:0010560 nord_rare diseases +MONDO:0010560 ordo_disorder diseases +MONDO:0010560 ordo_malformation_syndrome diseases +MONDO:0010560 orphanet_rare diseases +MONDO:0010560 otar diseases +MONDO:0010560 rare diseases +MONDO:0010561 clingen diseases +MONDO:0010561 gard_rare diseases +MONDO:0010561 nord_rare diseases +MONDO:0010561 ordo_disorder diseases +MONDO:0010561 ordo_malformation_syndrome diseases +MONDO:0010561 orphanet_rare diseases +MONDO:0010561 otar diseases +MONDO:0010561 rare diseases +MONDO:0010562 gard_rare diseases +MONDO:0010562 nord_rare diseases +MONDO:0010562 ordo_disorder diseases +MONDO:0010562 ordo_morphological_anomaly diseases +MONDO:0010562 orphanet_rare diseases +MONDO:0010562 otar diseases +MONDO:0010562 rare diseases +MONDO:0010563 gard_rare diseases +MONDO:0010563 nord_rare diseases +MONDO:0010563 ordo_disorder diseases +MONDO:0010563 orphanet_rare diseases +MONDO:0010563 otar diseases +MONDO:0010563 rare diseases +MONDO:0010564 inferred_rare diseases +MONDO:0010564 otar diseases +MONDO:0010564 rare diseases +MONDO:0010565 otar diseases +MONDO:0010566 gard_rare diseases +MONDO:0010566 nord_rare diseases +MONDO:0010566 rare diseases +MONDO:0010567 gard_rare diseases +MONDO:0010567 nord_rare diseases +MONDO:0010567 rare diseases +MONDO:0010568 gard_rare diseases +MONDO:0010568 nord_rare diseases +MONDO:0010568 ordo_disorder diseases +MONDO:0010568 orphanet_rare diseases +MONDO:0010568 otar diseases +MONDO:0010568 rare diseases +MONDO:0010569 gard_rare diseases +MONDO:0010569 nord_rare diseases +MONDO:0010569 ordo_subtype_of_a_disorder diseases +MONDO:0010569 otar diseases +MONDO:0010569 rare diseases +MONDO:0010570 clingen diseases +MONDO:0010570 gard_rare diseases +MONDO:0010570 nord_rare diseases +MONDO:0010570 ordo_disorder diseases +MONDO:0010570 ordo_malformation_syndrome diseases +MONDO:0010570 orphanet_rare diseases +MONDO:0010570 otar diseases +MONDO:0010570 rare diseases +MONDO:0010571 gard_rare diseases +MONDO:0010571 nord_rare diseases +MONDO:0010571 ordo_disorder diseases +MONDO:0010571 orphanet_rare diseases +MONDO:0010571 otar diseases +MONDO:0010571 rare diseases +MONDO:0010572 gard_rare diseases +MONDO:0010572 nord_rare diseases +MONDO:0010572 ordo_disorder diseases +MONDO:0010572 orphanet_rare diseases +MONDO:0010572 otar diseases +MONDO:0010572 rare diseases +MONDO:0010574 gard_rare diseases +MONDO:0010574 nord_rare diseases +MONDO:0010574 ordo_disorder diseases +MONDO:0010574 ordo_malformation_syndrome diseases +MONDO:0010574 orphanet_rare diseases +MONDO:0010574 otar diseases +MONDO:0010574 rare diseases +MONDO:0010575 gard_rare diseases +MONDO:0010575 nord_rare diseases +MONDO:0010575 ordo_disorder diseases +MONDO:0010575 ordo_malformation_syndrome diseases +MONDO:0010575 orphanet_rare diseases +MONDO:0010575 otar diseases +MONDO:0010575 rare diseases +MONDO:0010576 gard_rare diseases +MONDO:0010576 nord_rare diseases +MONDO:0010576 otar diseases +MONDO:0010576 rare diseases +MONDO:0010577 gard_rare diseases +MONDO:0010577 nord_rare diseases +MONDO:0010577 rare diseases +MONDO:0010578 clingen diseases +MONDO:0010578 gard_rare diseases +MONDO:0010578 nord_rare diseases +MONDO:0010578 ordo_disorder diseases +MONDO:0010578 orphanet_rare diseases +MONDO:0010578 otar diseases +MONDO:0010578 rare diseases +MONDO:0010579 gard_rare diseases +MONDO:0010579 nord_rare diseases +MONDO:0010579 ordo_disorder diseases +MONDO:0010579 orphanet_rare diseases +MONDO:0010579 otar diseases +MONDO:0010579 rare diseases +MONDO:0010580 gard_rare diseases +MONDO:0010580 nord_rare diseases +MONDO:0010580 ordo_disorder diseases +MONDO:0010580 orphanet_rare diseases +MONDO:0010580 otar diseases +MONDO:0010580 rare diseases +MONDO:0010581 gard_rare diseases +MONDO:0010581 nord_rare diseases +MONDO:0010581 rare diseases +MONDO:0010583 gard_rare diseases +MONDO:0010583 rare diseases +MONDO:0010584 clingen diseases +MONDO:0010584 gard_rare diseases +MONDO:0010584 nord_rare diseases +MONDO:0010584 otar diseases +MONDO:0010584 rare diseases +MONDO:0010585 gard_rare diseases +MONDO:0010585 nord_rare diseases +MONDO:0010585 ordo_etiological_subtype diseases +MONDO:0010585 ordo_subtype_of_a_disorder diseases +MONDO:0010585 otar diseases +MONDO:0010585 rare diseases +MONDO:0010586 gard_rare diseases +MONDO:0010586 ordo_disorder diseases +MONDO:0010586 orphanet_rare diseases +MONDO:0010586 otar diseases +MONDO:0010586 rare diseases +MONDO:0010587 gard_rare diseases +MONDO:0010587 rare diseases +MONDO:0010588 gard_rare diseases +MONDO:0010588 nord_rare diseases +MONDO:0010588 rare diseases +MONDO:0010589 clingen diseases +MONDO:0010589 gard_rare diseases +MONDO:0010589 nord_rare diseases +MONDO:0010589 otar diseases +MONDO:0010589 rare diseases +MONDO:0010590 gard_rare diseases +MONDO:0010590 nord_rare diseases +MONDO:0010590 ordo_disorder diseases +MONDO:0010590 orphanet_rare diseases +MONDO:0010590 rare diseases +MONDO:0010591 gard_rare diseases +MONDO:0010591 nord_rare diseases +MONDO:0010591 ordo_disorder diseases +MONDO:0010591 orphanet_rare diseases +MONDO:0010591 otar diseases +MONDO:0010591 rare diseases +MONDO:0010592 clingen diseases +MONDO:0010592 gard_rare diseases +MONDO:0010592 nord_rare diseases +MONDO:0010592 ordo_disorder diseases +MONDO:0010592 ordo_malformation_syndrome diseases +MONDO:0010592 orphanet_rare diseases +MONDO:0010592 otar diseases +MONDO:0010592 rare diseases +MONDO:0010595 gard_rare diseases +MONDO:0010595 nord_rare diseases +MONDO:0010595 obsoletion_candidate diseases +MONDO:0010595 otar diseases +MONDO:0010595 rare diseases +MONDO:0010596 gard_rare diseases +MONDO:0010596 nord_rare diseases +MONDO:0010596 rare diseases +MONDO:0010598 gard_rare diseases +MONDO:0010598 nord_rare diseases +MONDO:0010598 rare diseases +MONDO:0010600 gard_rare diseases +MONDO:0010600 nord_rare diseases +MONDO:0010600 rare diseases +MONDO:0010602 clingen diseases +MONDO:0010602 gard_rare diseases +MONDO:0010602 nord_rare diseases +MONDO:0010602 ordo_disorder diseases +MONDO:0010602 orphanet_rare diseases +MONDO:0010602 otar diseases +MONDO:0010602 rare diseases +MONDO:0010603 gard_rare diseases +MONDO:0010603 nord_rare diseases +MONDO:0010603 rare diseases +MONDO:0010604 clingen diseases +MONDO:0010604 gard_rare diseases +MONDO:0010604 nord_rare diseases +MONDO:0010604 ordo_disorder diseases +MONDO:0010604 orphanet_rare diseases +MONDO:0010604 otar diseases +MONDO:0010604 rare diseases +MONDO:0010606 gard_rare diseases +MONDO:0010606 rare diseases +MONDO:0010607 gard_rare diseases +MONDO:0010607 nord_rare diseases +MONDO:0010607 rare diseases +MONDO:0010610 gard_rare diseases +MONDO:0010610 nord_rare diseases +MONDO:0010610 ordo_disorder diseases +MONDO:0010610 ordo_malformation_syndrome diseases +MONDO:0010610 orphanet_rare diseases +MONDO:0010610 rare diseases +MONDO:0010611 gard_rare diseases +MONDO:0010611 nord_rare diseases +MONDO:0010611 ordo_subtype_of_a_disorder diseases +MONDO:0010611 otar diseases +MONDO:0010611 rare diseases +MONDO:0010612 gard_rare diseases +MONDO:0010612 nord_rare diseases +MONDO:0010612 ordo_disorder diseases +MONDO:0010612 ordo_malformation_syndrome diseases +MONDO:0010612 orphanet_rare diseases +MONDO:0010612 otar diseases +MONDO:0010612 rare diseases +MONDO:0010613 clingen diseases +MONDO:0010613 disease_grouping diseases +MONDO:0010613 gard_rare diseases +MONDO:0010613 ordo_group_of_disorders diseases +MONDO:0010613 otar diseases +MONDO:0010613 rare diseases +MONDO:0010614 gard_rare diseases +MONDO:0010614 nord_rare diseases +MONDO:0010614 ordo_subtype_of_a_disorder diseases +MONDO:0010614 otar diseases +MONDO:0010614 rare diseases +MONDO:0010615 clingen diseases +MONDO:0010615 gard_rare diseases +MONDO:0010615 nord_rare diseases +MONDO:0010615 ordo_subtype_of_a_disorder diseases +MONDO:0010615 otar diseases +MONDO:0010615 rare diseases +MONDO:0010617 gard_rare diseases +MONDO:0010617 ordo_disorder diseases +MONDO:0010617 ordo_malformation_syndrome diseases +MONDO:0010617 orphanet_rare diseases +MONDO:0010617 otar diseases +MONDO:0010617 rare diseases +MONDO:0010618 gard_rare diseases +MONDO:0010618 nord_rare diseases +MONDO:0010618 ordo_subtype_of_a_disorder diseases +MONDO:0010618 otar diseases +MONDO:0010618 rare diseases +MONDO:0010619 gard_rare diseases +MONDO:0010619 nord_rare diseases +MONDO:0010619 ordo_disorder diseases +MONDO:0010619 orphanet_rare diseases +MONDO:0010619 otar diseases +MONDO:0010619 rare diseases +MONDO:0010620 gard_rare diseases +MONDO:0010620 nord_rare diseases +MONDO:0010620 rare diseases +MONDO:0010621 gard_rare diseases +MONDO:0010621 nord_rare diseases +MONDO:0010621 ordo_disorder diseases +MONDO:0010621 orphanet_rare diseases +MONDO:0010621 otar diseases +MONDO:0010621 rare diseases +MONDO:0010622 gard_rare diseases +MONDO:0010622 nord_rare diseases +MONDO:0010622 ordo_disorder diseases +MONDO:0010622 orphanet_rare diseases +MONDO:0010622 otar diseases +MONDO:0010622 rare diseases +MONDO:0010625 gard_rare diseases +MONDO:0010625 rare diseases +MONDO:0010626 clingen diseases +MONDO:0010626 gard_rare diseases +MONDO:0010626 nord_rare diseases +MONDO:0010626 ordo_subtype_of_a_disorder diseases +MONDO:0010626 otar diseases +MONDO:0010626 rare diseases +MONDO:0010627 gard_rare diseases +MONDO:0010627 nord_rare diseases +MONDO:0010627 ordo_group_of_disorders diseases +MONDO:0010627 otar diseases +MONDO:0010627 prototype_pattern diseases +MONDO:0010627 rare diseases +MONDO:0010631 clingen diseases +MONDO:0010631 gard_rare diseases +MONDO:0010631 nord_rare diseases +MONDO:0010631 ordo_disorder diseases +MONDO:0010631 ordo_malformation_syndrome diseases +MONDO:0010631 orphanet_rare diseases +MONDO:0010631 otar diseases +MONDO:0010631 rare diseases +MONDO:0010632 gard_rare diseases +MONDO:0010632 nord_rare diseases +MONDO:0010632 otar diseases +MONDO:0010632 rare diseases +MONDO:0010633 gard_rare diseases +MONDO:0010633 rare diseases +MONDO:0010635 clingen diseases +MONDO:0010635 gard_rare diseases +MONDO:0010635 otar diseases +MONDO:0010635 rare diseases +MONDO:0010637 gard_rare diseases +MONDO:0010637 nord_rare diseases +MONDO:0010637 rare diseases +MONDO:0010638 gard_rare diseases +MONDO:0010638 ordo_disorder diseases +MONDO:0010638 ordo_malformation_syndrome diseases +MONDO:0010638 orphanet_rare diseases +MONDO:0010638 otar diseases +MONDO:0010638 rare diseases +MONDO:0010639 gard_rare diseases +MONDO:0010639 nord_rare diseases +MONDO:0010639 ordo_disorder diseases +MONDO:0010639 ordo_malformation_syndrome diseases +MONDO:0010639 orphanet_rare diseases +MONDO:0010639 otar diseases +MONDO:0010639 rare diseases +MONDO:0010641 gard_rare diseases +MONDO:0010641 nord_rare diseases +MONDO:0010641 ordo_subtype_of_a_disorder diseases +MONDO:0010641 otar diseases +MONDO:0010641 rare diseases +MONDO:0010642 gard_rare diseases +MONDO:0010642 rare diseases +MONDO:0010643 gard_rare diseases +MONDO:0010643 nord_rare diseases +MONDO:0010643 otar diseases +MONDO:0010643 rare diseases +MONDO:0010644 gard_rare diseases +MONDO:0010644 rare diseases +MONDO:0010645 clingen diseases +MONDO:0010645 gard_rare diseases +MONDO:0010645 nord_rare diseases +MONDO:0010645 ordo_disorder diseases +MONDO:0010645 ordo_malformation_syndrome diseases +MONDO:0010645 orphanet_rare diseases +MONDO:0010645 otar diseases +MONDO:0010645 rare diseases +MONDO:0010646 gard_rare diseases +MONDO:0010646 nord_rare diseases +MONDO:0010646 rare diseases +MONDO:0010647 gard_rare diseases +MONDO:0010647 rare diseases +MONDO:0010649 gard_rare diseases +MONDO:0010649 nord_rare diseases +MONDO:0010649 ordo_disorder diseases +MONDO:0010649 ordo_morphological_anomaly diseases +MONDO:0010649 orphanet_rare diseases +MONDO:0010649 otar diseases +MONDO:0010649 rare diseases +MONDO:0010650 gard_rare diseases +MONDO:0010650 nord_rare diseases +MONDO:0010650 ordo_disorder diseases +MONDO:0010650 ordo_malformation_syndrome diseases +MONDO:0010650 orphanet_rare diseases +MONDO:0010650 otar diseases +MONDO:0010650 rare diseases +MONDO:0010651 clingen diseases +MONDO:0010651 gard_rare diseases +MONDO:0010651 nord_rare diseases +MONDO:0010651 ordo_disorder diseases +MONDO:0010651 orphanet_rare diseases +MONDO:0010651 otar diseases +MONDO:0010651 rare diseases +MONDO:0010652 gard_rare diseases +MONDO:0010652 nord_rare diseases +MONDO:0010652 ordo_disorder diseases +MONDO:0010652 orphanet_rare diseases +MONDO:0010652 otar diseases +MONDO:0010652 rare diseases +MONDO:0010653 clingen diseases +MONDO:0010653 gard_rare diseases +MONDO:0010653 ordo_disorder diseases +MONDO:0010653 ordo_malformation_syndrome diseases +MONDO:0010653 orphanet_rare diseases +MONDO:0010653 otar diseases +MONDO:0010653 rare diseases +MONDO:0010654 gard_rare diseases +MONDO:0010654 ordo_disorder diseases +MONDO:0010654 ordo_malformation_syndrome diseases +MONDO:0010654 orphanet_rare diseases +MONDO:0010654 otar diseases +MONDO:0010654 rare diseases +MONDO:0010655 gard_rare diseases +MONDO:0010655 nord_rare diseases +MONDO:0010655 ordo_disorder diseases +MONDO:0010655 ordo_malformation_syndrome diseases +MONDO:0010655 orphanet_rare diseases +MONDO:0010655 otar diseases +MONDO:0010655 rare diseases +MONDO:0010656 gard_rare diseases +MONDO:0010656 nord_rare diseases +MONDO:0010656 ordo_disorder diseases +MONDO:0010656 orphanet_rare diseases +MONDO:0010656 rare diseases +MONDO:0010657 gard_rare diseases +MONDO:0010657 nord_rare diseases +MONDO:0010657 ordo_subtype_of_a_disorder diseases +MONDO:0010657 otar diseases +MONDO:0010657 rare diseases +MONDO:0010658 gard_rare diseases +MONDO:0010658 nord_rare diseases +MONDO:0010658 ordo_disorder diseases +MONDO:0010658 ordo_malformation_syndrome diseases +MONDO:0010658 orphanet_rare diseases +MONDO:0010658 otar diseases +MONDO:0010658 rare diseases +MONDO:0010659 gard_rare diseases +MONDO:0010659 nord_rare diseases +MONDO:0010659 ordo_disorder diseases +MONDO:0010659 orphanet_rare diseases +MONDO:0010659 otar diseases +MONDO:0010659 rare diseases +MONDO:0010660 gard_rare diseases +MONDO:0010660 nord_rare diseases +MONDO:0010660 rare diseases +MONDO:0010661 gard_rare diseases +MONDO:0010661 ordo_disorder diseases +MONDO:0010661 ordo_malformation_syndrome diseases +MONDO:0010661 orphanet_rare diseases +MONDO:0010661 otar diseases +MONDO:0010661 rare diseases +MONDO:0010662 gard_rare diseases +MONDO:0010662 nord_rare diseases +MONDO:0010662 ordo_disorder diseases +MONDO:0010662 ordo_malformation_syndrome diseases +MONDO:0010662 orphanet_rare diseases +MONDO:0010662 otar diseases +MONDO:0010662 rare diseases +MONDO:0010663 disease_grouping diseases +MONDO:0010663 gard_rare diseases +MONDO:0010663 ordo_malformation_syndrome diseases +MONDO:0010663 otar diseases +MONDO:0010663 rare diseases +MONDO:0010664 clingen diseases +MONDO:0010664 gard_rare diseases +MONDO:0010664 nord_rare diseases +MONDO:0010664 ordo_disorder diseases +MONDO:0010664 orphanet_rare diseases +MONDO:0010664 otar diseases +MONDO:0010664 rare diseases +MONDO:0010665 gard_rare diseases +MONDO:0010665 nord_rare diseases +MONDO:0010665 ordo_disorder diseases +MONDO:0010665 ordo_malformation_syndrome diseases +MONDO:0010665 orphanet_rare diseases +MONDO:0010665 otar diseases +MONDO:0010665 rare diseases +MONDO:0010667 gard_rare diseases +MONDO:0010667 ordo_disorder diseases +MONDO:0010667 ordo_malformation_syndrome diseases +MONDO:0010667 orphanet_rare diseases +MONDO:0010667 otar diseases +MONDO:0010667 rare diseases +MONDO:0010668 gard_rare diseases +MONDO:0010668 nord_rare diseases +MONDO:0010668 ordo_disorder diseases +MONDO:0010668 ordo_malformation_syndrome diseases +MONDO:0010668 orphanet_rare diseases +MONDO:0010668 otar diseases +MONDO:0010668 rare diseases +MONDO:0010669 gard_rare diseases +MONDO:0010669 nord_rare diseases +MONDO:0010669 ordo_disorder diseases +MONDO:0010669 ordo_morphological_anomaly diseases +MONDO:0010669 orphanet_rare diseases +MONDO:0010669 otar diseases +MONDO:0010669 rare diseases +MONDO:0010671 gard_rare diseases +MONDO:0010671 nord_rare diseases +MONDO:0010671 ordo_disorder diseases +MONDO:0010671 ordo_malformation_syndrome diseases +MONDO:0010671 orphanet_rare diseases +MONDO:0010671 rare diseases +MONDO:0010672 gard_rare diseases +MONDO:0010672 nord_rare diseases +MONDO:0010672 ordo_disorder diseases +MONDO:0010672 ordo_malformation_syndrome diseases +MONDO:0010672 orphanet_rare diseases +MONDO:0010672 otar diseases +MONDO:0010672 rare diseases +MONDO:0010674 clingen diseases +MONDO:0010674 gard_rare diseases +MONDO:0010674 nord_rare diseases +MONDO:0010674 ordo_disorder diseases +MONDO:0010674 ordo_group_of_disorders diseases +MONDO:0010674 orphanet_rare diseases +MONDO:0010674 otar diseases +MONDO:0010674 rare diseases +MONDO:0010675 gard_rare diseases +MONDO:0010675 rare diseases +MONDO:0010676 gard_rare diseases +MONDO:0010676 rare diseases +MONDO:0010677 gard_rare diseases +MONDO:0010677 rare diseases +MONDO:0010678 gard_rare diseases +MONDO:0010678 rare diseases +MONDO:0010679 gard_rare diseases +MONDO:0010679 nord_rare diseases +MONDO:0010679 ordo_disorder diseases +MONDO:0010679 orphanet_rare diseases +MONDO:0010679 otar diseases +MONDO:0010679 rare diseases +MONDO:0010680 gard_rare diseases +MONDO:0010680 nord_rare diseases +MONDO:0010680 ordo_etiological_subtype diseases +MONDO:0010680 ordo_subtype_of_a_disorder diseases +MONDO:0010680 otar diseases +MONDO:0010680 rare diseases +MONDO:0010683 clingen diseases +MONDO:0010683 gard_rare diseases +MONDO:0010683 nord_rare diseases +MONDO:0010683 ordo_disorder diseases +MONDO:0010683 orphanet_rare diseases +MONDO:0010683 otar diseases +MONDO:0010683 rare diseases +MONDO:0010684 gard_rare diseases +MONDO:0010684 nord_rare diseases +MONDO:0010684 ordo_disorder diseases +MONDO:0010684 orphanet_rare diseases +MONDO:0010684 otar diseases +MONDO:0010684 rare diseases +MONDO:0010686 gard_rare diseases +MONDO:0010686 nord_rare diseases +MONDO:0010686 ordo_disorder diseases +MONDO:0010686 ordo_malformation_syndrome diseases +MONDO:0010686 orphanet_rare diseases +MONDO:0010686 otar diseases +MONDO:0010686 rare diseases +MONDO:0010687 gard_rare diseases +MONDO:0010687 rare diseases +MONDO:0010688 gard_rare diseases +MONDO:0010688 rare diseases +MONDO:0010689 gard_rare diseases +MONDO:0010689 nord_rare diseases +MONDO:0010689 ordo_disorder diseases +MONDO:0010689 orphanet_rare diseases +MONDO:0010689 otar diseases +MONDO:0010689 rare diseases +MONDO:0010690 gard_rare diseases +MONDO:0010690 nord_rare diseases +MONDO:0010690 rare diseases +MONDO:0010691 clingen diseases +MONDO:0010691 gard_rare diseases +MONDO:0010691 nord_rare diseases +MONDO:0010691 ordo_disorder diseases +MONDO:0010691 ordo_malformation_syndrome diseases +MONDO:0010691 orphanet_rare diseases +MONDO:0010691 otar diseases +MONDO:0010691 rare diseases +MONDO:0010696 gard_rare diseases +MONDO:0010696 rare diseases +MONDO:0010698 gard_rare diseases +MONDO:0010698 nord_rare diseases +MONDO:0010698 ordo_disorder diseases +MONDO:0010698 orphanet_rare diseases +MONDO:0010698 otar diseases +MONDO:0010698 rare diseases +MONDO:0010699 gard_rare diseases +MONDO:0010699 nord_rare diseases +MONDO:0010699 ordo_disorder diseases +MONDO:0010699 orphanet_rare diseases +MONDO:0010699 otar diseases +MONDO:0010699 rare diseases +MONDO:0010702 gard_rare diseases +MONDO:0010702 nord_rare diseases +MONDO:0010702 ordo_disorder diseases +MONDO:0010702 ordo_malformation_syndrome diseases +MONDO:0010702 orphanet_rare diseases +MONDO:0010702 otar diseases +MONDO:0010702 rare diseases +MONDO:0010703 clingen diseases +MONDO:0010703 gard_rare diseases +MONDO:0010703 nord_rare diseases +MONDO:0010703 ordo_disorder diseases +MONDO:0010703 orphanet_rare diseases +MONDO:0010703 otar diseases +MONDO:0010703 rare diseases +MONDO:0010704 gard_rare diseases +MONDO:0010704 nord_rare diseases +MONDO:0010704 ordo_disorder diseases +MONDO:0010704 orphanet_rare diseases +MONDO:0010704 otar diseases +MONDO:0010704 rare diseases +MONDO:0010706 gard_rare diseases +MONDO:0010706 nord_rare diseases +MONDO:0010706 ordo_disorder diseases +MONDO:0010706 orphanet_rare diseases +MONDO:0010706 rare diseases +MONDO:0010708 gard_rare diseases +MONDO:0010708 ordo_disorder diseases +MONDO:0010708 ordo_malformation_syndrome diseases +MONDO:0010708 orphanet_rare diseases +MONDO:0010708 rare diseases +MONDO:0010709 clingen diseases +MONDO:0010709 gard_rare diseases +MONDO:0010709 ordo_disorder diseases +MONDO:0010709 orphanet_rare diseases +MONDO:0010709 otar diseases +MONDO:0010709 rare diseases +MONDO:0010710 gard_rare diseases +MONDO:0010710 nord_rare diseases +MONDO:0010710 ordo_disorder diseases +MONDO:0010710 ordo_malformation_syndrome diseases +MONDO:0010710 orphanet_rare diseases +MONDO:0010710 otar diseases +MONDO:0010710 rare diseases +MONDO:0010711 gard_rare diseases +MONDO:0010711 nord_rare diseases +MONDO:0010711 ordo_disorder diseases +MONDO:0010711 ordo_malformation_syndrome diseases +MONDO:0010711 orphanet_rare diseases +MONDO:0010711 otar diseases +MONDO:0010711 rare diseases +MONDO:0010712 gard_rare diseases +MONDO:0010712 nord_rare diseases +MONDO:0010712 rare diseases +MONDO:0010713 gard_rare diseases +MONDO:0010713 nord_rare diseases +MONDO:0010713 ordo_disorder diseases +MONDO:0010713 orphanet_rare diseases +MONDO:0010713 otar diseases +MONDO:0010713 rare diseases +MONDO:0010714 clingen diseases +MONDO:0010714 gard_rare diseases +MONDO:0010714 nord_rare diseases +MONDO:0010714 ordo_disorder diseases +MONDO:0010714 orphanet_rare diseases +MONDO:0010714 otar diseases +MONDO:0010714 rare diseases +MONDO:0010716 gard_rare diseases +MONDO:0010716 nord_rare diseases +MONDO:0010716 ordo_disorder diseases +MONDO:0010716 ordo_malformation_syndrome diseases +MONDO:0010716 orphanet_rare diseases +MONDO:0010716 otar diseases +MONDO:0010716 rare diseases +MONDO:0010717 gard_rare diseases +MONDO:0010717 nord_rare diseases +MONDO:0010717 ordo_subtype_of_a_disorder diseases +MONDO:0010717 otar diseases +MONDO:0010717 rare diseases +MONDO:0010718 gard_rare diseases +MONDO:0010718 ordo_disorder diseases +MONDO:0010718 ordo_malformation_syndrome diseases +MONDO:0010718 orphanet_rare diseases +MONDO:0010718 otar diseases +MONDO:0010718 rare diseases +MONDO:0010720 gard_rare diseases +MONDO:0010720 nord_rare diseases +MONDO:0010720 ordo_disorder diseases +MONDO:0010720 orphanet_rare diseases +MONDO:0010720 otar diseases +MONDO:0010720 rare diseases +MONDO:0010722 gard_rare diseases +MONDO:0010722 nord_rare diseases +MONDO:0010722 ordo_disorder diseases +MONDO:0010722 orphanet_rare diseases +MONDO:0010722 otar diseases +MONDO:0010722 rare diseases +MONDO:0010723 gard_rare diseases +MONDO:0010723 nord_rare diseases +MONDO:0010723 rare diseases +MONDO:0010725 clingen diseases +MONDO:0010725 gard_rare diseases +MONDO:0010725 nord_rare diseases +MONDO:0010725 ordo_disorder diseases +MONDO:0010725 ordo_malformation_syndrome diseases +MONDO:0010725 orphanet_rare diseases +MONDO:0010725 otar diseases +MONDO:0010725 rare diseases +MONDO:0010726 clingen diseases +MONDO:0010726 gard_rare diseases +MONDO:0010726 nord_rare diseases +MONDO:0010726 ordo_disorder diseases +MONDO:0010726 orphanet_rare diseases +MONDO:0010726 otar diseases +MONDO:0010726 rare diseases +MONDO:0010727 gard_rare diseases +MONDO:0010727 rare diseases +MONDO:0010728 gard_rare diseases +MONDO:0010728 ordo_disorder diseases +MONDO:0010728 ordo_malformation_syndrome diseases +MONDO:0010728 orphanet_rare diseases +MONDO:0010728 otar diseases +MONDO:0010728 rare diseases +MONDO:0010729 gard_rare diseases +MONDO:0010729 nord_rare diseases +MONDO:0010729 ordo_disorder diseases +MONDO:0010729 ordo_malformation_syndrome diseases +MONDO:0010729 orphanet_rare diseases +MONDO:0010729 otar diseases +MONDO:0010729 rare diseases +MONDO:0010730 clingen diseases +MONDO:0010730 gard_rare diseases +MONDO:0010730 nord_rare diseases +MONDO:0010730 otar diseases +MONDO:0010730 rare diseases +MONDO:0010731 clingen diseases +MONDO:0010731 gard_rare diseases +MONDO:0010731 nord_rare diseases +MONDO:0010731 ordo_disorder diseases +MONDO:0010731 ordo_malformation_syndrome diseases +MONDO:0010731 orphanet_rare diseases +MONDO:0010731 otar diseases +MONDO:0010731 rare diseases +MONDO:0010732 gard_rare diseases +MONDO:0010732 ordo_disorder diseases +MONDO:0010732 ordo_malformation_syndrome diseases +MONDO:0010732 orphanet_rare diseases +MONDO:0010732 otar diseases +MONDO:0010732 rare diseases +MONDO:0010733 gard_rare diseases +MONDO:0010733 nord_rare diseases +MONDO:0010733 ordo_disorder diseases +MONDO:0010733 orphanet_rare diseases +MONDO:0010733 otar diseases +MONDO:0010733 rare diseases +MONDO:0010735 gard_rare diseases +MONDO:0010735 nord_rare diseases +MONDO:0010735 ordo_disorder diseases +MONDO:0010735 orphanet_rare diseases +MONDO:0010735 otar diseases +MONDO:0010735 rare diseases +MONDO:0010736 gard_rare diseases +MONDO:0010736 nord_rare diseases +MONDO:0010736 rare diseases +MONDO:0010737 gard_rare diseases +MONDO:0010737 nord_rare diseases +MONDO:0010737 rare diseases +MONDO:0010738 gard_rare diseases +MONDO:0010738 nord_rare diseases +MONDO:0010738 ordo_disorder diseases +MONDO:0010738 orphanet_rare diseases +MONDO:0010738 otar diseases +MONDO:0010738 rare diseases +MONDO:0010741 gard_rare diseases +MONDO:0010741 rare diseases +MONDO:0010742 gard_rare diseases +MONDO:0010742 nord_rare diseases +MONDO:0010742 ordo_disorder diseases +MONDO:0010742 ordo_malformation_syndrome diseases +MONDO:0010742 orphanet_rare diseases +MONDO:0010742 otar diseases +MONDO:0010742 rare diseases +MONDO:0010743 gard_rare diseases +MONDO:0010743 nord_rare diseases +MONDO:0010743 ordo_etiological_subtype diseases +MONDO:0010743 ordo_subtype_of_a_disorder diseases +MONDO:0010743 otar diseases +MONDO:0010743 rare diseases +MONDO:0010745 gard_rare diseases +MONDO:0010745 nord_rare diseases +MONDO:0010745 ordo_disorder diseases +MONDO:0010745 orphanet_rare diseases +MONDO:0010745 otar diseases +MONDO:0010745 rare diseases +MONDO:0010747 gard_rare diseases +MONDO:0010747 nord_rare diseases +MONDO:0010747 ordo_disorder diseases +MONDO:0010747 orphanet_rare diseases +MONDO:0010747 otar diseases +MONDO:0010747 rare diseases +MONDO:0010748 gard_rare diseases +MONDO:0010748 nord_rare diseases +MONDO:0010748 ordo_disorder diseases +MONDO:0010748 ordo_malformation_syndrome diseases +MONDO:0010748 orphanet_rare diseases +MONDO:0010748 otar diseases +MONDO:0010748 rare diseases +MONDO:0010749 gard_rare diseases +MONDO:0010749 ordo_disorder diseases +MONDO:0010749 ordo_malformation_syndrome diseases +MONDO:0010749 orphanet_rare diseases +MONDO:0010749 otar diseases +MONDO:0010749 rare diseases +MONDO:0010750 gard_rare diseases +MONDO:0010750 ordo_disorder diseases +MONDO:0010750 ordo_malformation_syndrome diseases +MONDO:0010750 orphanet_rare diseases +MONDO:0010750 otar diseases +MONDO:0010750 rare diseases +MONDO:0010752 gard_rare diseases +MONDO:0010752 nord_rare diseases +MONDO:0010752 otar diseases +MONDO:0010752 rare diseases +MONDO:0010753 gard_rare diseases +MONDO:0010753 nord_rare diseases +MONDO:0010753 ordo_disorder diseases +MONDO:0010753 ordo_morphological_anomaly diseases +MONDO:0010753 orphanet_rare diseases +MONDO:0010753 otar diseases +MONDO:0010753 rare diseases +MONDO:0010754 gard_rare diseases +MONDO:0010754 ordo_disorder diseases +MONDO:0010754 ordo_malformation_syndrome diseases +MONDO:0010754 orphanet_rare diseases +MONDO:0010754 otar diseases +MONDO:0010754 rare diseases +MONDO:0010755 gard_rare diseases +MONDO:0010755 rare diseases +MONDO:0010756 gard_rare diseases +MONDO:0010756 nord_rare diseases +MONDO:0010756 rare diseases +MONDO:0010758 gard_rare diseases +MONDO:0010758 nord_rare diseases +MONDO:0010758 ordo_disorder diseases +MONDO:0010758 ordo_malformation_syndrome diseases +MONDO:0010758 orphanet_rare diseases +MONDO:0010758 otar diseases +MONDO:0010758 rare diseases +MONDO:0010759 gard_rare diseases +MONDO:0010759 nord_rare diseases +MONDO:0010759 ordo_disorder diseases +MONDO:0010759 ordo_malformation_syndrome diseases +MONDO:0010759 orphanet_rare diseases +MONDO:0010759 otar diseases +MONDO:0010759 rare diseases +MONDO:0010761 gard_rare diseases +MONDO:0010761 nord_rare diseases +MONDO:0010761 rare diseases +MONDO:0010762 gard_rare diseases +MONDO:0010762 rare diseases +MONDO:0010763 gard_rare diseases +MONDO:0010763 nord_rare diseases +MONDO:0010763 rare diseases +MONDO:0010764 gard_rare diseases +MONDO:0010764 nord_rare diseases +MONDO:0010764 rare diseases +MONDO:0010765 gard_rare diseases +MONDO:0010765 nord_rare diseases +MONDO:0010765 ordo_disorder diseases +MONDO:0010765 ordo_malformation_syndrome diseases +MONDO:0010765 orphanet_rare diseases +MONDO:0010765 otar diseases +MONDO:0010765 prototype_pattern diseases +MONDO:0010765 rare diseases +MONDO:0010767 gard_rare diseases +MONDO:0010767 nord_rare diseases +MONDO:0010767 rare diseases +MONDO:0010771 gard_rare diseases +MONDO:0010771 nord_rare diseases +MONDO:0010771 ordo_disorder diseases +MONDO:0010771 orphanet_rare diseases +MONDO:0010771 otar diseases +MONDO:0010771 rare diseases +MONDO:0010772 gard_rare diseases +MONDO:0010772 nord_rare diseases +MONDO:0010772 rare diseases +MONDO:0010773 gard_rare diseases +MONDO:0010773 nord_rare diseases +MONDO:0010773 ordo_disorder diseases +MONDO:0010773 orphanet_rare diseases +MONDO:0010773 otar diseases +MONDO:0010773 rare diseases +MONDO:0010774 gard_rare diseases +MONDO:0010774 nord_rare diseases +MONDO:0010774 rare diseases +MONDO:0010775 gard_rare diseases +MONDO:0010775 nord_rare diseases +MONDO:0010775 rare diseases +MONDO:0010779 gard_rare diseases +MONDO:0010779 nord_rare diseases +MONDO:0010779 ordo_etiological_subtype diseases +MONDO:0010779 ordo_subtype_of_a_disorder diseases +MONDO:0010779 otar diseases +MONDO:0010779 rare diseases +MONDO:0010780 gard_rare diseases +MONDO:0010780 nord_rare diseases +MONDO:0010780 ordo_disorder diseases +MONDO:0010780 orphanet_rare diseases +MONDO:0010780 otar diseases +MONDO:0010780 rare diseases +MONDO:0010781 gard_rare diseases +MONDO:0010781 rare diseases +MONDO:0010782 gard_rare diseases +MONDO:0010782 nord_rare diseases +MONDO:0010782 rare diseases +MONDO:0010785 gard_rare diseases +MONDO:0010785 nord_rare diseases +MONDO:0010785 ordo_disorder diseases +MONDO:0010785 orphanet_rare diseases +MONDO:0010785 otar diseases +MONDO:0010785 rare diseases +MONDO:0010786 gard_rare diseases +MONDO:0010786 nord_rare diseases +MONDO:0010786 ordo_disorder diseases +MONDO:0010786 orphanet_rare diseases +MONDO:0010786 rare diseases +MONDO:0010787 gard_rare diseases +MONDO:0010787 nord_rare diseases +MONDO:0010787 ordo_disorder diseases +MONDO:0010787 orphanet_rare diseases +MONDO:0010787 otar diseases +MONDO:0010787 rare diseases +MONDO:0010788 gard_rare diseases +MONDO:0010788 nord_rare diseases +MONDO:0010788 ordo_disorder diseases +MONDO:0010788 orphanet_rare diseases +MONDO:0010788 otar diseases +MONDO:0010788 rare diseases +MONDO:0010789 gard_rare diseases +MONDO:0010789 ordo_disorder diseases +MONDO:0010789 orphanet_rare diseases +MONDO:0010789 otar diseases +MONDO:0010789 rare diseases +MONDO:0010790 gard_rare diseases +MONDO:0010790 nord_rare diseases +MONDO:0010790 ordo_disorder diseases +MONDO:0010790 orphanet_rare diseases +MONDO:0010790 otar diseases +MONDO:0010790 rare diseases +MONDO:0010791 gard_rare diseases +MONDO:0010791 rare diseases +MONDO:0010792 gard_rare diseases +MONDO:0010792 nord_rare diseases +MONDO:0010792 ordo_disorder diseases +MONDO:0010792 orphanet_rare diseases +MONDO:0010792 otar diseases +MONDO:0010792 rare diseases +MONDO:0010794 gard_rare diseases +MONDO:0010794 nord_rare diseases +MONDO:0010794 ordo_disorder diseases +MONDO:0010794 orphanet_rare diseases +MONDO:0010794 otar diseases +MONDO:0010794 rare diseases +MONDO:0010795 otar diseases +MONDO:0010796 otar diseases +MONDO:0010797 gard_rare diseases +MONDO:0010797 nord_rare diseases +MONDO:0010797 ordo_disorder diseases +MONDO:0010797 orphanet_rare diseases +MONDO:0010797 otar diseases +MONDO:0010797 rare diseases +MONDO:0010799 gard_rare diseases +MONDO:0010799 nord_rare diseases +MONDO:0010799 ordo_etiological_subtype diseases +MONDO:0010799 otar diseases +MONDO:0010799 predisposition diseases +MONDO:0010799 rare diseases +MONDO:0010800 gard_rare diseases +MONDO:0010800 rare diseases +MONDO:0010801 gard_rare diseases +MONDO:0010801 nord_rare diseases +MONDO:0010801 ordo_disorder diseases +MONDO:0010801 ordo_malformation_syndrome diseases +MONDO:0010801 orphanet_rare diseases +MONDO:0010801 otar diseases +MONDO:0010801 rare diseases +MONDO:0010802 gard_rare diseases +MONDO:0010802 nord_rare diseases +MONDO:0010802 ordo_disorder diseases +MONDO:0010802 orphanet_rare diseases +MONDO:0010802 otar diseases +MONDO:0010802 rare diseases +MONDO:0010803 gard_rare diseases +MONDO:0010803 nord_rare diseases +MONDO:0010803 ordo_disorder diseases +MONDO:0010803 ordo_malformation_syndrome diseases +MONDO:0010803 orphanet_rare diseases +MONDO:0010803 otar diseases +MONDO:0010803 rare diseases +MONDO:0010805 gard_rare diseases +MONDO:0010805 nord_rare diseases +MONDO:0010805 ordo_subtype_of_a_disorder diseases +MONDO:0010805 otar diseases +MONDO:0010805 rare diseases +MONDO:0010806 gard_rare diseases +MONDO:0010806 nord_rare diseases +MONDO:0010806 rare diseases +MONDO:0010807 gard_rare diseases +MONDO:0010807 nord_rare diseases +MONDO:0010807 rare diseases +MONDO:0010808 gard_rare diseases +MONDO:0010808 nord_rare diseases +MONDO:0010808 ordo_disorder diseases +MONDO:0010808 orphanet_rare diseases +MONDO:0010808 otar diseases +MONDO:0010808 rare diseases +MONDO:0010809 gard_rare diseases +MONDO:0010809 nord_rare diseases +MONDO:0010809 rare diseases +MONDO:0010810 gard_rare diseases +MONDO:0010810 nord_rare diseases +MONDO:0010810 rare diseases +MONDO:0010811 otar diseases +MONDO:0010813 otar diseases +MONDO:0010814 gard_rare diseases +MONDO:0010814 nord_rare diseases +MONDO:0010814 ordo_disorder diseases +MONDO:0010814 ordo_malformation_syndrome diseases +MONDO:0010814 orphanet_rare diseases +MONDO:0010814 otar diseases +MONDO:0010814 rare diseases +MONDO:0010815 gard_rare diseases +MONDO:0010815 rare diseases +MONDO:0010816 gard_rare diseases +MONDO:0010816 nord_rare diseases +MONDO:0010816 ordo_disorder diseases +MONDO:0010816 orphanet_rare diseases +MONDO:0010816 rare diseases +MONDO:0010817 gard_rare diseases +MONDO:0010817 nord_rare diseases +MONDO:0010817 otar diseases +MONDO:0010817 rare diseases +MONDO:0010818 gard_rare diseases +MONDO:0010818 nord_rare diseases +MONDO:0010818 rare diseases +MONDO:0010819 clingen diseases +MONDO:0010819 gard_rare diseases +MONDO:0010819 nord_rare diseases +MONDO:0010819 rare diseases +MONDO:0010820 gard_rare diseases +MONDO:0010820 rare diseases +MONDO:0010821 gard_rare diseases +MONDO:0010821 nord_rare diseases +MONDO:0010821 ordo_clinical_syndrome diseases +MONDO:0010821 ordo_disorder diseases +MONDO:0010821 orphanet_rare diseases +MONDO:0010821 rare diseases +MONDO:0010822 gard_rare diseases +MONDO:0010822 nord_rare diseases +MONDO:0010822 rare diseases +MONDO:0010823 gard_rare diseases +MONDO:0010823 nord_rare diseases +MONDO:0010823 ordo_etiological_subtype diseases +MONDO:0010823 ordo_subtype_of_a_disorder diseases +MONDO:0010823 otar diseases +MONDO:0010823 rare diseases +MONDO:0010824 gard_rare diseases +MONDO:0010824 nord_rare diseases +MONDO:0010824 ordo_disorder diseases +MONDO:0010824 orphanet_rare diseases +MONDO:0010824 rare diseases +MONDO:0010825 gard_rare diseases +MONDO:0010825 ordo_disorder diseases +MONDO:0010825 ordo_malformation_syndrome diseases +MONDO:0010825 orphanet_rare diseases +MONDO:0010825 otar diseases +MONDO:0010825 rare diseases +MONDO:0010826 gard_rare diseases +MONDO:0010826 nord_rare diseases +MONDO:0010826 ordo_disorder diseases +MONDO:0010826 orphanet_rare diseases +MONDO:0010826 otar diseases +MONDO:0010826 predisposition diseases +MONDO:0010826 rare diseases +MONDO:0010827 gard_rare diseases +MONDO:0010827 nord_rare diseases +MONDO:0010827 rare diseases +MONDO:0010828 gard_rare diseases +MONDO:0010828 nord_rare diseases +MONDO:0010828 rare diseases +MONDO:0010829 gard_rare diseases +MONDO:0010829 nord_rare diseases +MONDO:0010829 ordo_disorder diseases +MONDO:0010829 orphanet_rare diseases +MONDO:0010829 otar diseases +MONDO:0010829 rare diseases +MONDO:0010830 gard_rare diseases +MONDO:0010830 nord_rare diseases +MONDO:0010830 ordo_etiological_subtype diseases +MONDO:0010830 otar diseases +MONDO:0010830 rare diseases +MONDO:0010831 gard_rare diseases +MONDO:0010831 nord_rare diseases +MONDO:0010831 ordo_disorder diseases +MONDO:0010831 ordo_malformation_syndrome diseases +MONDO:0010831 orphanet_rare diseases +MONDO:0010831 otar diseases +MONDO:0010831 rare diseases +MONDO:0010832 gard_rare diseases +MONDO:0010832 nord_rare diseases +MONDO:0010832 rare diseases +MONDO:0010835 gard_rare diseases +MONDO:0010835 ordo_disorder diseases +MONDO:0010835 ordo_malformation_syndrome diseases +MONDO:0010835 orphanet_rare diseases +MONDO:0010835 otar diseases +MONDO:0010835 rare diseases +MONDO:0010836 gard_rare diseases +MONDO:0010836 nord_rare diseases +MONDO:0010836 rare diseases +MONDO:0010837 otar diseases +MONDO:0010839 gard_rare diseases +MONDO:0010839 nord_rare diseases +MONDO:0010839 ordo_disorder diseases +MONDO:0010839 orphanet_rare diseases +MONDO:0010839 otar diseases +MONDO:0010839 rare diseases +MONDO:0010840 gard_rare diseases +MONDO:0010840 nord_rare diseases +MONDO:0010840 ordo_disorder diseases +MONDO:0010840 ordo_malformation_syndrome diseases +MONDO:0010840 orphanet_rare diseases +MONDO:0010840 otar diseases +MONDO:0010840 rare diseases +MONDO:0010841 gard_rare diseases +MONDO:0010841 rare diseases +MONDO:0010842 gard_rare diseases +MONDO:0010842 nord_rare diseases +MONDO:0010842 ordo_disorder diseases +MONDO:0010842 ordo_malformation_syndrome diseases +MONDO:0010842 orphanet_rare diseases +MONDO:0010842 otar diseases +MONDO:0010842 rare diseases +MONDO:0010844 gard_rare diseases +MONDO:0010844 nord_rare diseases +MONDO:0010844 rare diseases +MONDO:0010846 gard_rare diseases +MONDO:0010846 nord_rare diseases +MONDO:0010846 rare diseases +MONDO:0010847 gard_rare diseases +MONDO:0010847 nord_rare diseases +MONDO:0010847 ordo_disorder diseases +MONDO:0010847 orphanet_rare diseases +MONDO:0010847 otar diseases +MONDO:0010847 rare diseases +MONDO:0010848 gard_rare diseases +MONDO:0010848 nord_rare diseases +MONDO:0010848 ordo_disorder diseases +MONDO:0010848 orphanet_rare diseases +MONDO:0010848 otar diseases +MONDO:0010848 rare diseases +MONDO:0010849 clingen diseases +MONDO:0010849 gard_rare diseases +MONDO:0010849 nord_rare diseases +MONDO:0010849 ordo_disorder diseases +MONDO:0010849 orphanet_rare diseases +MONDO:0010849 rare diseases +MONDO:0010850 gard_rare diseases +MONDO:0010850 nord_rare diseases +MONDO:0010850 ordo_disorder diseases +MONDO:0010850 ordo_morphological_anomaly diseases +MONDO:0010850 orphanet_rare diseases +MONDO:0010850 otar diseases +MONDO:0010850 rare diseases +MONDO:0010851 gard_rare diseases +MONDO:0010851 nord_rare diseases +MONDO:0010851 ordo_disorder diseases +MONDO:0010851 ordo_malformation_syndrome diseases +MONDO:0010851 orphanet_rare diseases +MONDO:0010851 otar diseases +MONDO:0010851 rare diseases +MONDO:0010852 gard_rare diseases +MONDO:0010852 nord_rare diseases +MONDO:0010852 rare diseases +MONDO:0010854 gard_rare diseases +MONDO:0010854 nord_rare diseases +MONDO:0010854 ordo_disorder diseases +MONDO:0010854 ordo_malformation_syndrome diseases +MONDO:0010854 orphanet_rare diseases +MONDO:0010854 otar diseases +MONDO:0010854 rare diseases +MONDO:0010855 gard_rare diseases +MONDO:0010855 nord_rare diseases +MONDO:0010855 ordo_disorder diseases +MONDO:0010855 ordo_malformation_syndrome diseases +MONDO:0010855 orphanet_rare diseases +MONDO:0010855 otar diseases +MONDO:0010855 rare diseases +MONDO:0010856 gard_rare diseases +MONDO:0010856 nord_rare diseases +MONDO:0010856 ordo_disorder diseases +MONDO:0010856 orphanet_rare diseases +MONDO:0010856 otar diseases +MONDO:0010856 rare diseases +MONDO:0010857 gard_rare diseases +MONDO:0010857 nord_rare diseases +MONDO:0010857 ordo_disorder diseases +MONDO:0010857 orphanet_rare diseases +MONDO:0010857 otar diseases +MONDO:0010857 rare diseases +MONDO:0010858 gard_rare diseases +MONDO:0010858 nord_rare diseases +MONDO:0010858 ordo_disorder diseases +MONDO:0010858 ordo_malformation_syndrome diseases +MONDO:0010858 orphanet_rare diseases +MONDO:0010858 otar diseases +MONDO:0010858 rare diseases +MONDO:0010860 gard_rare diseases +MONDO:0010860 nord_rare diseases +MONDO:0010860 rare diseases +MONDO:0010865 gard_rare diseases +MONDO:0010865 nord_rare diseases +MONDO:0010865 ordo_disorder diseases +MONDO:0010865 ordo_malformation_syndrome diseases +MONDO:0010865 orphanet_rare diseases +MONDO:0010865 otar diseases +MONDO:0010865 rare diseases +MONDO:0010866 gard_rare diseases +MONDO:0010866 nord_rare diseases +MONDO:0010866 ordo_disorder diseases +MONDO:0010866 ordo_malformation_syndrome diseases +MONDO:0010866 orphanet_rare diseases +MONDO:0010866 otar diseases +MONDO:0010866 rare diseases +MONDO:0010867 gard_rare diseases +MONDO:0010867 ordo_disorder diseases +MONDO:0010867 ordo_malformation_syndrome diseases +MONDO:0010867 orphanet_rare diseases +MONDO:0010867 otar diseases +MONDO:0010867 rare diseases +MONDO:0010868 gard_rare diseases +MONDO:0010868 rare diseases +MONDO:0010869 gard_rare diseases +MONDO:0010869 rare diseases +MONDO:0010870 clingen diseases +MONDO:0010870 gard_rare diseases +MONDO:0010870 nord_rare diseases +MONDO:0010870 ordo_disorder diseases +MONDO:0010870 orphanet_rare diseases +MONDO:0010870 otar diseases +MONDO:0010870 rare diseases +MONDO:0010873 gard_rare diseases +MONDO:0010873 rare diseases +MONDO:0010876 gard_rare diseases +MONDO:0010876 nord_rare diseases +MONDO:0010876 otar diseases +MONDO:0010876 rare diseases +MONDO:0010877 gard_rare diseases +MONDO:0010877 nord_rare diseases +MONDO:0010877 ordo_disorder diseases +MONDO:0010877 orphanet_rare diseases +MONDO:0010877 otar diseases +MONDO:0010877 rare diseases +MONDO:0010878 gard_rare diseases +MONDO:0010878 nord_rare diseases +MONDO:0010878 ordo_disorder diseases +MONDO:0010878 orphanet_rare diseases +MONDO:0010878 otar diseases +MONDO:0010878 rare diseases +MONDO:0010879 gard_rare diseases +MONDO:0010879 nord_rare diseases +MONDO:0010879 ordo_disorder diseases +MONDO:0010879 ordo_malformation_syndrome diseases +MONDO:0010879 orphanet_rare diseases +MONDO:0010879 otar diseases +MONDO:0010879 rare diseases +MONDO:0010880 clingen diseases +MONDO:0010880 gard_rare diseases +MONDO:0010880 nord_rare diseases +MONDO:0010880 rare diseases +MONDO:0010881 gard_rare diseases +MONDO:0010881 nord_rare diseases +MONDO:0010881 ordo_disorder diseases +MONDO:0010881 ordo_malformation_syndrome diseases +MONDO:0010881 orphanet_rare diseases +MONDO:0010881 otar diseases +MONDO:0010881 rare diseases +MONDO:0010882 gard_rare diseases +MONDO:0010882 nord_rare diseases +MONDO:0010882 ordo_disorder diseases +MONDO:0010882 ordo_malformation_syndrome diseases +MONDO:0010882 orphanet_rare diseases +MONDO:0010882 otar diseases +MONDO:0010882 rare diseases +MONDO:0010883 gard_rare diseases +MONDO:0010883 ordo_disorder diseases +MONDO:0010883 ordo_malformation_syndrome diseases +MONDO:0010883 orphanet_rare diseases +MONDO:0010883 rare diseases +MONDO:0010884 gard_rare diseases +MONDO:0010884 nord_rare diseases +MONDO:0010884 rare diseases +MONDO:0010885 otar diseases +MONDO:0010886 gard_rare diseases +MONDO:0010886 nord_rare diseases +MONDO:0010886 ordo_disorder diseases +MONDO:0010886 ordo_malformation_syndrome diseases +MONDO:0010886 orphanet_rare diseases +MONDO:0010886 otar diseases +MONDO:0010886 rare diseases +MONDO:0010887 gard_rare diseases +MONDO:0010887 nord_rare diseases +MONDO:0010887 ordo_disorder diseases +MONDO:0010887 orphanet_rare diseases +MONDO:0010887 otar diseases +MONDO:0010887 rare diseases +MONDO:0010888 otar diseases +MONDO:0010889 gard_rare diseases +MONDO:0010889 nord_rare diseases +MONDO:0010889 ordo_disorder diseases +MONDO:0010889 ordo_malformation_syndrome diseases +MONDO:0010889 orphanet_rare diseases +MONDO:0010889 rare diseases +MONDO:0010890 gard_rare diseases +MONDO:0010890 nord_rare diseases +MONDO:0010890 ordo_disorder diseases +MONDO:0010890 ordo_malformation_syndrome diseases +MONDO:0010890 orphanet_rare diseases +MONDO:0010890 otar diseases +MONDO:0010890 rare diseases +MONDO:0010891 gard_rare diseases +MONDO:0010891 ordo_disorder diseases +MONDO:0010891 ordo_malformation_syndrome diseases +MONDO:0010891 orphanet_rare diseases +MONDO:0010891 otar diseases +MONDO:0010891 rare diseases +MONDO:0010894 gard_rare diseases +MONDO:0010894 nord_rare diseases +MONDO:0010894 rare diseases +MONDO:0010895 otar diseases +MONDO:0010896 gard_rare diseases +MONDO:0010896 nord_rare diseases +MONDO:0010896 otar diseases +MONDO:0010896 rare diseases +MONDO:0010898 clingen diseases +MONDO:0010898 gard_rare diseases +MONDO:0010898 nord_rare diseases +MONDO:0010898 ordo_disorder diseases +MONDO:0010898 orphanet_rare diseases +MONDO:0010898 otar diseases +MONDO:0010898 rare diseases +MONDO:0010899 gard_rare diseases +MONDO:0010899 nord_rare diseases +MONDO:0010899 rare diseases +MONDO:0010900 gard_rare diseases +MONDO:0010900 nord_rare diseases +MONDO:0010900 rare diseases +MONDO:0010901 gard_rare diseases +MONDO:0010901 nord_rare diseases +MONDO:0010901 ordo_disorder diseases +MONDO:0010901 ordo_malformation_syndrome diseases +MONDO:0010901 orphanet_rare diseases +MONDO:0010901 rare diseases +MONDO:0010902 gard_rare diseases +MONDO:0010902 ordo_disorder diseases +MONDO:0010902 orphanet_rare diseases +MONDO:0010902 otar diseases +MONDO:0010902 rare diseases +MONDO:0010903 gard_rare diseases +MONDO:0010903 nord_rare diseases +MONDO:0010903 rare diseases +MONDO:0010905 gard_rare diseases +MONDO:0010905 nord_rare diseases +MONDO:0010905 rare diseases +MONDO:0010906 gard_rare diseases +MONDO:0010906 rare diseases +MONDO:0010907 clingen diseases +MONDO:0010907 gard_rare diseases +MONDO:0010907 nord_rare diseases +MONDO:0010907 ordo_disorder diseases +MONDO:0010907 orphanet_rare diseases +MONDO:0010907 otar diseases +MONDO:0010907 rare diseases +MONDO:0010908 gard_rare diseases +MONDO:0010908 nord_rare diseases +MONDO:0010908 ordo_disorder diseases +MONDO:0010908 orphanet_rare diseases +MONDO:0010908 otar diseases +MONDO:0010908 rare diseases +MONDO:0010909 gard_rare diseases +MONDO:0010909 nord_rare diseases +MONDO:0010909 rare diseases +MONDO:0010911 gard_rare diseases +MONDO:0010911 ordo_disorder diseases +MONDO:0010911 orphanet_rare diseases +MONDO:0010911 otar diseases +MONDO:0010911 rare diseases +MONDO:0010912 gard_rare diseases +MONDO:0010912 nord_rare diseases +MONDO:0010912 rare diseases +MONDO:0010913 gard_rare diseases +MONDO:0010913 nord_rare diseases +MONDO:0010913 ordo_disorder diseases +MONDO:0010913 ordo_malformation_syndrome diseases +MONDO:0010913 orphanet_rare diseases +MONDO:0010913 otar diseases +MONDO:0010913 rare diseases +MONDO:0010914 gard_rare diseases +MONDO:0010914 nord_rare diseases +MONDO:0010914 ordo_subtype_of_a_disorder diseases +MONDO:0010914 otar diseases +MONDO:0010914 rare diseases +MONDO:0010915 gard_rare diseases +MONDO:0010915 nord_rare diseases +MONDO:0010915 rare diseases +MONDO:0010916 clingen diseases +MONDO:0010916 gard_rare diseases +MONDO:0010916 nord_rare diseases +MONDO:0010916 otar diseases +MONDO:0010916 rare diseases +MONDO:0010917 gard_rare diseases +MONDO:0010917 rare diseases +MONDO:0010920 gard_rare diseases +MONDO:0010920 nord_rare diseases +MONDO:0010920 ordo_disorder diseases +MONDO:0010920 ordo_morphological_anomaly diseases +MONDO:0010920 orphanet_rare diseases +MONDO:0010920 otar diseases +MONDO:0010920 rare diseases +MONDO:0010921 gard_rare diseases +MONDO:0010921 nord_rare diseases +MONDO:0010921 ordo_disorder diseases +MONDO:0010921 ordo_morphological_anomaly diseases +MONDO:0010921 orphanet_rare diseases +MONDO:0010921 rare diseases +MONDO:0010922 gard_rare diseases +MONDO:0010922 nord_rare diseases +MONDO:0010922 ordo_disorder diseases +MONDO:0010922 orphanet_rare diseases +MONDO:0010922 rare diseases +MONDO:0010923 gard_rare diseases +MONDO:0010923 nord_rare diseases +MONDO:0010923 ordo_disorder diseases +MONDO:0010923 orphanet_rare diseases +MONDO:0010923 rare diseases +MONDO:0010924 gard_rare diseases +MONDO:0010924 nord_rare diseases +MONDO:0010924 ordo_disorder diseases +MONDO:0010924 orphanet_rare diseases +MONDO:0010924 otar diseases +MONDO:0010924 prototype_pattern diseases +MONDO:0010924 rare diseases +MONDO:0010925 gard_rare diseases +MONDO:0010925 ordo_disorder diseases +MONDO:0010925 ordo_malformation_syndrome diseases +MONDO:0010925 orphanet_rare diseases +MONDO:0010925 otar diseases +MONDO:0010925 rare diseases +MONDO:0010926 gard_rare diseases +MONDO:0010926 ordo_etiological_subtype diseases +MONDO:0010926 ordo_subtype_of_a_disorder diseases +MONDO:0010926 otar diseases +MONDO:0010926 rare diseases +MONDO:0010927 gard_rare diseases +MONDO:0010927 rare diseases +MONDO:0010929 clingen diseases +MONDO:0010929 gard_rare diseases +MONDO:0010929 nord_rare diseases +MONDO:0010929 rare diseases +MONDO:0010930 gard_rare diseases +MONDO:0010930 nord_rare diseases +MONDO:0010930 ordo_disorder diseases +MONDO:0010930 ordo_malformation_syndrome diseases +MONDO:0010930 orphanet_rare diseases +MONDO:0010930 otar diseases +MONDO:0010930 rare diseases +MONDO:0010931 gard_rare diseases +MONDO:0010931 nord_rare diseases +MONDO:0010931 rare diseases +MONDO:0010932 gard_rare diseases +MONDO:0010932 nord_rare diseases +MONDO:0010932 ordo_disorder diseases +MONDO:0010932 orphanet_rare diseases +MONDO:0010932 otar diseases +MONDO:0010932 rare diseases +MONDO:0010933 gard_rare diseases +MONDO:0010933 nord_rare diseases +MONDO:0010933 otar diseases +MONDO:0010933 rare diseases +MONDO:0010936 clingen diseases +MONDO:0010936 gard_rare diseases +MONDO:0010936 nord_rare diseases +MONDO:0010936 rare diseases +MONDO:0010938 clingen diseases +MONDO:0010938 gard_rare diseases +MONDO:0010938 nord_rare diseases +MONDO:0010938 ordo_disorder diseases +MONDO:0010938 orphanet_rare diseases +MONDO:0010938 otar diseases +MONDO:0010938 rare diseases +MONDO:0010939 gard_rare diseases +MONDO:0010939 nord_rare diseases +MONDO:0010939 ordo_disorder diseases +MONDO:0010939 orphanet_rare diseases +MONDO:0010939 otar diseases +MONDO:0010939 rare diseases +MONDO:0010945 gard_rare diseases +MONDO:0010945 nord_rare diseases +MONDO:0010945 rare diseases +MONDO:0010946 gard_rare diseases +MONDO:0010946 nord_rare diseases +MONDO:0010946 rare diseases +MONDO:0010947 gard_rare diseases +MONDO:0010947 nord_rare diseases +MONDO:0010947 ordo_disorder diseases +MONDO:0010947 orphanet_rare diseases +MONDO:0010947 rare diseases +MONDO:0010948 gard_rare diseases +MONDO:0010948 nord_rare diseases +MONDO:0010948 rare diseases +MONDO:0010949 gard_rare diseases +MONDO:0010949 nord_rare diseases +MONDO:0010949 ordo_disorder diseases +MONDO:0010949 orphanet_rare diseases +MONDO:0010949 otar diseases +MONDO:0010949 rare diseases +MONDO:0010951 gard_rare diseases +MONDO:0010951 nord_rare diseases +MONDO:0010951 rare diseases +MONDO:0010952 gard_rare diseases +MONDO:0010952 nord_rare diseases +MONDO:0010952 ordo_disorder diseases +MONDO:0010952 orphanet_rare diseases +MONDO:0010952 otar diseases +MONDO:0010952 rare diseases +MONDO:0010953 clingen diseases +MONDO:0010953 gard_rare diseases +MONDO:0010953 nord_rare diseases +MONDO:0010953 otar diseases +MONDO:0010953 rare diseases +MONDO:0010954 gard_rare diseases +MONDO:0010954 rare diseases +MONDO:0010958 gard_rare diseases +MONDO:0010958 rare diseases +MONDO:0010959 gard_rare diseases +MONDO:0010959 nord_rare diseases +MONDO:0010959 ordo_disorder diseases +MONDO:0010959 ordo_malformation_syndrome diseases +MONDO:0010959 orphanet_rare diseases +MONDO:0010959 otar diseases +MONDO:0010959 rare diseases +MONDO:0010961 gard_rare diseases +MONDO:0010961 nord_rare diseases +MONDO:0010961 ordo_subtype_of_a_disorder diseases +MONDO:0010961 otar diseases +MONDO:0010961 rare diseases +MONDO:0010962 gard_rare diseases +MONDO:0010962 nord_rare diseases +MONDO:0010962 ordo_disorder diseases +MONDO:0010962 ordo_inheritance_inconsistent diseases +MONDO:0010962 orphanet_rare diseases +MONDO:0010962 rare diseases +MONDO:0010963 gard_rare diseases +MONDO:0010963 nord_rare diseases +MONDO:0010963 rare diseases +MONDO:0010964 gard_rare diseases +MONDO:0010964 nord_rare diseases +MONDO:0010964 rare diseases +MONDO:0010965 gard_rare diseases +MONDO:0010965 nord_rare diseases +MONDO:0010965 rare diseases +MONDO:0010966 clingen diseases +MONDO:0010966 gard_rare diseases +MONDO:0010966 nord_rare diseases +MONDO:0010966 ordo_subtype_of_a_disorder diseases +MONDO:0010966 otar diseases +MONDO:0010966 rare diseases +MONDO:0010967 clingen diseases +MONDO:0010967 gard_rare diseases +MONDO:0010967 nord_rare diseases +MONDO:0010967 otar diseases +MONDO:0010967 rare diseases +MONDO:0010968 gard_rare diseases +MONDO:0010968 rare diseases +MONDO:0010969 gard_rare diseases +MONDO:0010969 nord_rare diseases +MONDO:0010969 rare diseases +MONDO:0010971 ordo_malformation_syndrome diseases +MONDO:0010971 otar diseases +MONDO:0010972 gard_rare diseases +MONDO:0010972 nord_rare diseases +MONDO:0010972 ordo_disorder diseases +MONDO:0010972 ordo_malformation_syndrome diseases +MONDO:0010972 orphanet_rare diseases +MONDO:0010972 otar diseases +MONDO:0010972 rare diseases +MONDO:0010973 gard_rare diseases +MONDO:0010973 nord_rare diseases +MONDO:0010973 rare diseases +MONDO:0010974 gard_rare diseases +MONDO:0010974 rare diseases +MONDO:0010976 gard_rare diseases +MONDO:0010976 nord_rare diseases +MONDO:0010976 ordo_disorder diseases +MONDO:0010976 orphanet_rare diseases +MONDO:0010976 otar diseases +MONDO:0010976 rare diseases +MONDO:0010977 gard_rare diseases +MONDO:0010977 nord_rare diseases +MONDO:0010977 ordo_disorder diseases +MONDO:0010977 orphanet_rare diseases +MONDO:0010977 otar diseases +MONDO:0010977 rare diseases +MONDO:0010979 gard_rare diseases +MONDO:0010979 nord_rare diseases +MONDO:0010979 ordo_disorder diseases +MONDO:0010979 orphanet_rare diseases +MONDO:0010979 otar diseases +MONDO:0010979 rare diseases +MONDO:0010981 gard_rare diseases +MONDO:0010981 ordo_disorder diseases +MONDO:0010981 ordo_malformation_syndrome diseases +MONDO:0010981 orphanet_rare diseases +MONDO:0010981 rare diseases +MONDO:0010983 gard_rare diseases +MONDO:0010983 nord_rare diseases +MONDO:0010983 ordo_disorder diseases +MONDO:0010983 orphanet_rare diseases +MONDO:0010983 otar diseases +MONDO:0010983 rare diseases +MONDO:0010984 gard_rare diseases +MONDO:0010984 nord_rare diseases +MONDO:0010984 rare diseases +MONDO:0010985 gard_rare diseases +MONDO:0010985 nord_rare diseases +MONDO:0010985 rare diseases +MONDO:0010986 clingen diseases +MONDO:0010986 gard_rare diseases +MONDO:0010986 nord_rare diseases +MONDO:0010986 otar diseases +MONDO:0010986 rare diseases +MONDO:0010987 gard_rare diseases +MONDO:0010987 nord_rare diseases +MONDO:0010987 rare diseases +MONDO:0010988 gard_rare diseases +MONDO:0010988 nord_rare diseases +MONDO:0010988 ordo_disorder diseases +MONDO:0010988 orphanet_rare diseases +MONDO:0010988 otar diseases +MONDO:0010988 rare diseases +MONDO:0010989 gard_rare diseases +MONDO:0010989 ordo_subtype_of_a_disorder diseases +MONDO:0010989 otar diseases +MONDO:0010989 rare diseases +MONDO:0010991 gard_rare diseases +MONDO:0010991 nord_rare diseases +MONDO:0010991 rare diseases +MONDO:0010992 gard_rare diseases +MONDO:0010992 nord_rare diseases +MONDO:0010992 ordo_malformation_syndrome diseases +MONDO:0010992 rare diseases +MONDO:0010993 gard_rare diseases +MONDO:0010993 nord_rare diseases +MONDO:0010993 ordo_disorder diseases +MONDO:0010993 ordo_malformation_syndrome diseases +MONDO:0010993 orphanet_rare diseases +MONDO:0010993 otar diseases +MONDO:0010993 rare diseases +MONDO:0010995 gard_rare diseases +MONDO:0010995 nord_rare diseases +MONDO:0010995 ordo_disorder diseases +MONDO:0010995 orphanet_rare diseases +MONDO:0010995 otar diseases +MONDO:0010995 rare diseases +MONDO:0010996 gard_rare diseases +MONDO:0010996 nord_rare diseases +MONDO:0010996 rare diseases +MONDO:0010997 gard_rare diseases +MONDO:0010997 nord_rare diseases +MONDO:0010997 ordo_subtype_of_a_disorder diseases +MONDO:0010997 otar diseases +MONDO:0010997 rare diseases +MONDO:0010998 clingen diseases +MONDO:0010998 gard_rare diseases +MONDO:0010998 nord_rare diseases +MONDO:0010998 ordo_disorder diseases +MONDO:0010998 orphanet_rare diseases +MONDO:0010998 otar diseases +MONDO:0010998 rare diseases +MONDO:0010999 gard_rare diseases +MONDO:0010999 nord_rare diseases +MONDO:0010999 ordo_disorder diseases +MONDO:0010999 ordo_malformation_syndrome diseases +MONDO:0010999 orphanet_rare diseases +MONDO:0010999 otar diseases +MONDO:0010999 rare diseases +MONDO:0011001 clingen diseases +MONDO:0011001 gard_rare diseases +MONDO:0011001 rare diseases +MONDO:0011002 gard_rare diseases +MONDO:0011002 nord_rare diseases +MONDO:0011002 rare diseases +MONDO:0011003 gard_rare diseases +MONDO:0011003 nord_rare diseases +MONDO:0011003 rare diseases +MONDO:0011004 gard_rare diseases +MONDO:0011004 nord_rare diseases +MONDO:0011004 ordo_disorder diseases +MONDO:0011004 ordo_malformation_syndrome diseases +MONDO:0011004 orphanet_rare diseases +MONDO:0011004 otar diseases +MONDO:0011004 rare diseases +MONDO:0011006 gard_rare diseases +MONDO:0011006 nord_rare diseases +MONDO:0011006 ordo_disorder diseases +MONDO:0011006 orphanet_rare diseases +MONDO:0011006 rare diseases +MONDO:0011007 gard_rare diseases +MONDO:0011007 nord_rare diseases +MONDO:0011007 ordo_disorder diseases +MONDO:0011007 ordo_malformation_syndrome diseases +MONDO:0011007 orphanet_rare diseases +MONDO:0011007 otar diseases +MONDO:0011007 rare diseases +MONDO:0011008 gard_rare diseases +MONDO:0011008 ordo_disorder diseases +MONDO:0011008 ordo_malformation_syndrome diseases +MONDO:0011008 orphanet_rare diseases +MONDO:0011008 otar diseases +MONDO:0011008 rare diseases +MONDO:0011010 gard_rare diseases +MONDO:0011010 nord_rare diseases +MONDO:0011010 ordo_disorder diseases +MONDO:0011010 ordo_malformation_syndrome diseases +MONDO:0011010 orphanet_rare diseases +MONDO:0011010 otar diseases +MONDO:0011010 rare diseases +MONDO:0011011 gard_rare diseases +MONDO:0011011 nord_rare diseases +MONDO:0011011 ordo_disorder diseases +MONDO:0011011 ordo_malformation_syndrome diseases +MONDO:0011011 orphanet_rare diseases +MONDO:0011011 otar diseases +MONDO:0011011 rare diseases +MONDO:0011012 gard_rare diseases +MONDO:0011012 nord_rare diseases +MONDO:0011012 ordo_disorder diseases +MONDO:0011012 orphanet_rare diseases +MONDO:0011012 otar diseases +MONDO:0011012 rare diseases +MONDO:0011013 clingen diseases +MONDO:0011013 gard_rare diseases +MONDO:0011013 otar diseases +MONDO:0011013 rare diseases +MONDO:0011014 gard_rare diseases +MONDO:0011014 nord_rare diseases +MONDO:0011014 ordo_disorder diseases +MONDO:0011014 orphanet_rare diseases +MONDO:0011014 otar diseases +MONDO:0011014 rare diseases +MONDO:0011015 gard_rare diseases +MONDO:0011015 nord_rare diseases +MONDO:0011015 rare diseases +MONDO:0011017 gard_rare diseases +MONDO:0011017 nord_rare diseases +MONDO:0011017 ordo_disorder diseases +MONDO:0011017 orphanet_rare diseases +MONDO:0011017 otar diseases +MONDO:0011017 rare diseases +MONDO:0011018 gard_rare diseases +MONDO:0011018 nord_rare diseases +MONDO:0011018 ordo_disorder diseases +MONDO:0011018 ordo_malformation_syndrome diseases +MONDO:0011018 orphanet_rare diseases +MONDO:0011018 otar diseases +MONDO:0011018 rare diseases +MONDO:0011019 gard_rare diseases +MONDO:0011019 nord_rare diseases +MONDO:0011019 ordo_disorder diseases +MONDO:0011019 orphanet_rare diseases +MONDO:0011019 otar diseases +MONDO:0011019 rare diseases +MONDO:0011020 gard_rare diseases +MONDO:0011020 ordo_disorder diseases +MONDO:0011020 ordo_malformation_syndrome diseases +MONDO:0011020 orphanet_rare diseases +MONDO:0011020 otar diseases +MONDO:0011020 rare diseases +MONDO:0011021 gard_rare diseases +MONDO:0011021 nord_rare diseases +MONDO:0011021 rare diseases +MONDO:0011022 gard_rare diseases +MONDO:0011022 nord_rare diseases +MONDO:0011022 ordo_disorder diseases +MONDO:0011022 ordo_malformation_syndrome diseases +MONDO:0011022 orphanet_rare diseases +MONDO:0011022 otar diseases +MONDO:0011022 rare diseases +MONDO:0011023 clingen diseases +MONDO:0011023 gard_rare diseases +MONDO:0011023 nord_rare diseases +MONDO:0011023 ordo_disorder diseases +MONDO:0011023 orphanet_rare diseases +MONDO:0011023 otar diseases +MONDO:0011023 rare diseases +MONDO:0011024 gard_rare diseases +MONDO:0011024 otar diseases +MONDO:0011024 rare diseases +MONDO:0011025 gard_rare diseases +MONDO:0011025 nord_rare diseases +MONDO:0011025 ordo_disorder diseases +MONDO:0011025 orphanet_rare diseases +MONDO:0011025 otar diseases +MONDO:0011025 rare diseases +MONDO:0011026 gard_rare diseases +MONDO:0011026 nord_rare diseases +MONDO:0011026 otar diseases +MONDO:0011026 rare diseases +MONDO:0011027 gard_rare diseases +MONDO:0011027 rare diseases +MONDO:0011028 gard_rare diseases +MONDO:0011028 nord_rare diseases +MONDO:0011028 ordo_disorder diseases +MONDO:0011028 orphanet_rare diseases +MONDO:0011028 otar diseases +MONDO:0011028 rare diseases +MONDO:0011031 gard_rare diseases +MONDO:0011031 nord_rare diseases +MONDO:0011031 rare diseases +MONDO:0011032 gard_rare diseases +MONDO:0011032 nord_rare diseases +MONDO:0011032 rare diseases +MONDO:0011034 gard_rare diseases +MONDO:0011034 ordo_disorder diseases +MONDO:0011034 ordo_malformation_syndrome diseases +MONDO:0011034 orphanet_rare diseases +MONDO:0011034 otar diseases +MONDO:0011034 rare diseases +MONDO:0011035 gard_rare diseases +MONDO:0011035 nord_rare diseases +MONDO:0011035 ordo_disorder diseases +MONDO:0011035 ordo_malformation_syndrome diseases +MONDO:0011035 orphanet_rare diseases +MONDO:0011035 otar diseases +MONDO:0011035 rare diseases +MONDO:0011036 gard_rare diseases +MONDO:0011036 ordo_disorder diseases +MONDO:0011036 ordo_malformation_syndrome diseases +MONDO:0011036 orphanet_rare diseases +MONDO:0011036 rare diseases +MONDO:0011038 gard_rare diseases +MONDO:0011038 nord_rare diseases +MONDO:0011038 ordo_disorder diseases +MONDO:0011038 orphanet_rare diseases +MONDO:0011038 otar diseases +MONDO:0011038 rare diseases +MONDO:0011041 gard_rare diseases +MONDO:0011041 nord_rare diseases +MONDO:0011041 ordo_disorder diseases +MONDO:0011041 ordo_malformation_syndrome diseases +MONDO:0011041 orphanet_rare diseases +MONDO:0011041 otar diseases +MONDO:0011041 rare diseases +MONDO:0011045 gard_rare diseases +MONDO:0011045 nord_rare diseases +MONDO:0011045 ordo_disorder diseases +MONDO:0011045 ordo_malformation_syndrome diseases +MONDO:0011045 orphanet_rare diseases +MONDO:0011045 otar diseases +MONDO:0011045 rare diseases +MONDO:0011046 gard_rare diseases +MONDO:0011046 ordo_disorder diseases +MONDO:0011046 ordo_malformation_syndrome diseases +MONDO:0011046 orphanet_rare diseases +MONDO:0011046 otar diseases +MONDO:0011046 rare diseases +MONDO:0011047 gard_rare diseases +MONDO:0011047 ordo_disorder diseases +MONDO:0011047 ordo_malformation_syndrome diseases +MONDO:0011047 orphanet_rare diseases +MONDO:0011047 otar diseases +MONDO:0011047 rare diseases +MONDO:0011048 gard_rare diseases +MONDO:0011048 ordo_disorder diseases +MONDO:0011048 ordo_malformation_syndrome diseases +MONDO:0011048 orphanet_rare diseases +MONDO:0011048 otar diseases +MONDO:0011048 rare diseases +MONDO:0011049 gard_rare diseases +MONDO:0011049 nord_rare diseases +MONDO:0011049 ordo_disorder diseases +MONDO:0011049 ordo_malformation_syndrome diseases +MONDO:0011049 orphanet_rare diseases +MONDO:0011049 otar diseases +MONDO:0011049 rare diseases +MONDO:0011050 gard_rare diseases +MONDO:0011050 ordo_disorder diseases +MONDO:0011050 ordo_malformation_syndrome diseases +MONDO:0011050 orphanet_rare diseases +MONDO:0011050 otar diseases +MONDO:0011050 rare diseases +MONDO:0011051 gard_rare diseases +MONDO:0011051 nord_rare diseases +MONDO:0011051 ordo_subtype_of_a_disorder diseases +MONDO:0011051 rare diseases +MONDO:0011053 clingen diseases +MONDO:0011053 gard_rare diseases +MONDO:0011053 nord_rare diseases +MONDO:0011053 ordo_disorder diseases +MONDO:0011053 ordo_malformation_syndrome diseases +MONDO:0011053 orphanet_rare diseases +MONDO:0011053 otar diseases +MONDO:0011053 rare diseases +MONDO:0011054 gard_rare diseases +MONDO:0011054 nord_rare diseases +MONDO:0011054 ordo_disorder diseases +MONDO:0011054 ordo_malformation_syndrome diseases +MONDO:0011054 orphanet_rare diseases +MONDO:0011054 otar diseases +MONDO:0011054 rare diseases +MONDO:0011055 gard_rare diseases +MONDO:0011055 nord_rare diseases +MONDO:0011055 ordo_disorder diseases +MONDO:0011055 ordo_malformation_syndrome diseases +MONDO:0011055 orphanet_rare diseases +MONDO:0011055 otar diseases +MONDO:0011055 rare diseases +MONDO:0011056 gard_rare diseases +MONDO:0011056 nord_rare diseases +MONDO:0011056 rare diseases +MONDO:0011057 otar diseases +MONDO:0011058 gard_rare diseases +MONDO:0011058 nord_rare diseases +MONDO:0011058 rare diseases +MONDO:0011059 gard_rare diseases +MONDO:0011059 ordo_disorder diseases +MONDO:0011059 ordo_malformation_syndrome diseases +MONDO:0011059 orphanet_rare diseases +MONDO:0011059 otar diseases +MONDO:0011059 rare diseases +MONDO:0011060 gard_rare diseases +MONDO:0011060 nord_rare diseases +MONDO:0011060 ordo_disorder diseases +MONDO:0011060 orphanet_rare diseases +MONDO:0011060 otar diseases +MONDO:0011060 rare diseases +MONDO:0011061 gard_rare diseases +MONDO:0011061 rare diseases +MONDO:0011062 gard_rare diseases +MONDO:0011062 nord_rare diseases +MONDO:0011062 ordo_disorder diseases +MONDO:0011062 ordo_malformation_syndrome diseases +MONDO:0011062 orphanet_rare diseases +MONDO:0011062 otar diseases +MONDO:0011062 rare diseases +MONDO:0011063 gard_rare diseases +MONDO:0011063 ordo_disorder diseases +MONDO:0011063 ordo_malformation_syndrome diseases +MONDO:0011063 orphanet_rare diseases +MONDO:0011063 otar diseases +MONDO:0011063 rare diseases +MONDO:0011064 gard_rare diseases +MONDO:0011064 nord_rare diseases +MONDO:0011064 ordo_malformation_syndrome diseases +MONDO:0011064 rare diseases +MONDO:0011065 gard_rare diseases +MONDO:0011065 nord_rare diseases +MONDO:0011065 ordo_disorder diseases +MONDO:0011065 ordo_malformation_syndrome diseases +MONDO:0011065 orphanet_rare diseases +MONDO:0011065 otar diseases +MONDO:0011065 rare diseases +MONDO:0011066 gard_rare diseases +MONDO:0011066 nord_rare diseases +MONDO:0011066 ordo_disorder diseases +MONDO:0011066 orphanet_rare diseases +MONDO:0011066 otar diseases +MONDO:0011066 rare diseases +MONDO:0011067 gard_rare diseases +MONDO:0011067 nord_rare diseases +MONDO:0011067 rare diseases +MONDO:0011070 gard_rare diseases +MONDO:0011070 nord_rare diseases +MONDO:0011070 rare diseases +MONDO:0011071 clingen diseases +MONDO:0011071 gard_rare diseases +MONDO:0011071 nord_rare diseases +MONDO:0011071 ordo_disorder diseases +MONDO:0011071 orphanet_rare diseases +MONDO:0011071 otar diseases +MONDO:0011071 rare diseases +MONDO:0011072 gard_rare diseases +MONDO:0011072 rare diseases +MONDO:0011073 gard_rare diseases +MONDO:0011073 nord_rare diseases +MONDO:0011073 ordo_disorder diseases +MONDO:0011073 orphanet_rare diseases +MONDO:0011073 rare diseases +MONDO:0011074 gard_rare diseases +MONDO:0011074 nord_rare diseases +MONDO:0011074 otar diseases +MONDO:0011074 rare diseases +MONDO:0011075 gard_rare diseases +MONDO:0011075 nord_rare diseases +MONDO:0011075 rare diseases +MONDO:0011076 gard_rare diseases +MONDO:0011076 ordo_disorder diseases +MONDO:0011076 orphanet_rare diseases +MONDO:0011076 otar diseases +MONDO:0011076 rare diseases +MONDO:0011078 gard_rare diseases +MONDO:0011078 ordo_disorder diseases +MONDO:0011078 orphanet_rare diseases +MONDO:0011078 rare diseases +MONDO:0011079 gard_rare diseases +MONDO:0011079 nord_rare diseases +MONDO:0011079 ordo_disorder diseases +MONDO:0011079 ordo_malformation_syndrome diseases +MONDO:0011079 orphanet_rare diseases +MONDO:0011079 otar diseases +MONDO:0011079 rare diseases +MONDO:0011080 gard_rare diseases +MONDO:0011080 nord_rare diseases +MONDO:0011080 ordo_disorder diseases +MONDO:0011080 ordo_malformation_syndrome diseases +MONDO:0011080 orphanet_rare diseases +MONDO:0011080 otar diseases +MONDO:0011080 rare diseases +MONDO:0011081 gard_rare diseases +MONDO:0011081 ordo_disorder diseases +MONDO:0011081 ordo_malformation_syndrome diseases +MONDO:0011081 orphanet_rare diseases +MONDO:0011081 otar diseases +MONDO:0011081 rare diseases +MONDO:0011082 gard_rare diseases +MONDO:0011082 nord_rare diseases +MONDO:0011082 ordo_disorder diseases +MONDO:0011082 ordo_malformation_syndrome diseases +MONDO:0011082 orphanet_rare diseases +MONDO:0011082 otar diseases +MONDO:0011082 rare diseases +MONDO:0011083 gard_rare diseases +MONDO:0011083 nord_rare diseases +MONDO:0011083 ordo_disorder diseases +MONDO:0011083 ordo_malformation_syndrome diseases +MONDO:0011083 orphanet_rare diseases +MONDO:0011083 otar diseases +MONDO:0011083 rare diseases +MONDO:0011085 gard_rare diseases +MONDO:0011085 nord_rare diseases +MONDO:0011085 ordo_disorder diseases +MONDO:0011085 orphanet_rare diseases +MONDO:0011085 otar diseases +MONDO:0011085 rare diseases +MONDO:0011086 gard_rare diseases +MONDO:0011086 nord_rare diseases +MONDO:0011086 ordo_disorder diseases +MONDO:0011086 orphanet_rare diseases +MONDO:0011086 otar diseases +MONDO:0011086 rare diseases +MONDO:0011088 gard_rare diseases +MONDO:0011088 nord_rare diseases +MONDO:0011088 rare diseases +MONDO:0011090 gard_rare diseases +MONDO:0011090 nord_rare diseases +MONDO:0011090 ordo_disorder diseases +MONDO:0011090 ordo_morphological_anomaly diseases +MONDO:0011090 orphanet_rare diseases +MONDO:0011090 otar diseases +MONDO:0011090 rare diseases +MONDO:0011091 clingen diseases +MONDO:0011091 gard_rare diseases +MONDO:0011091 nord_rare diseases +MONDO:0011091 ordo_disorder diseases +MONDO:0011091 orphanet_rare diseases +MONDO:0011091 otar diseases +MONDO:0011091 rare diseases +MONDO:0011093 clingen diseases +MONDO:0011093 gard_rare diseases +MONDO:0011093 nord_rare diseases +MONDO:0011093 ordo_disorder diseases +MONDO:0011093 orphanet_rare diseases +MONDO:0011093 otar diseases +MONDO:0011093 rare diseases +MONDO:0011094 gard_rare diseases +MONDO:0011094 nord_rare diseases +MONDO:0011094 rare diseases +MONDO:0011095 gard_rare diseases +MONDO:0011095 nord_rare diseases +MONDO:0011095 rare diseases +MONDO:0011096 clingen diseases +MONDO:0011096 gard_rare diseases +MONDO:0011096 nord_rare diseases +MONDO:0011096 ordo_subtype_of_a_disorder diseases +MONDO:0011096 otar diseases +MONDO:0011096 rare diseases +MONDO:0011097 gard_rare diseases +MONDO:0011097 nord_rare diseases +MONDO:0011097 rare diseases +MONDO:0011098 gard_rare diseases +MONDO:0011098 rare diseases +MONDO:0011099 gard_rare diseases +MONDO:0011099 nord_rare diseases +MONDO:0011099 ordo_disorder diseases +MONDO:0011099 orphanet_rare diseases +MONDO:0011099 otar diseases +MONDO:0011099 rare diseases +MONDO:0011101 gard_rare diseases +MONDO:0011101 nord_rare diseases +MONDO:0011101 otar diseases +MONDO:0011101 rare diseases +MONDO:0011102 gard_rare diseases +MONDO:0011102 nord_rare diseases +MONDO:0011102 rare diseases +MONDO:0011103 gard_rare diseases +MONDO:0011103 nord_rare diseases +MONDO:0011103 rare diseases +MONDO:0011104 gard_rare diseases +MONDO:0011104 rare diseases +MONDO:0011105 gard_rare diseases +MONDO:0011105 nord_rare diseases +MONDO:0011105 rare diseases +MONDO:0011106 gard_rare diseases +MONDO:0011106 nord_rare diseases +MONDO:0011106 ordo_disorder diseases +MONDO:0011106 ordo_malformation_syndrome diseases +MONDO:0011106 orphanet_rare diseases +MONDO:0011106 otar diseases +MONDO:0011106 rare diseases +MONDO:0011107 gard_rare diseases +MONDO:0011107 nord_rare diseases +MONDO:0011107 ordo_disorder diseases +MONDO:0011107 ordo_malformation_syndrome diseases +MONDO:0011107 orphanet_rare diseases +MONDO:0011107 otar diseases +MONDO:0011107 rare diseases +MONDO:0011109 gard_rare diseases +MONDO:0011109 nord_rare diseases +MONDO:0011109 ordo_disorder diseases +MONDO:0011109 orphanet_rare diseases +MONDO:0011109 otar diseases +MONDO:0011109 rare diseases +MONDO:0011110 ordo_malformation_syndrome diseases +MONDO:0011112 gard_rare diseases +MONDO:0011112 nord_rare diseases +MONDO:0011112 rare diseases +MONDO:0011113 gard_rare diseases +MONDO:0011113 nord_rare diseases +MONDO:0011113 ordo_disorder diseases +MONDO:0011113 orphanet_rare diseases +MONDO:0011113 otar diseases +MONDO:0011113 rare diseases +MONDO:0011114 gard_rare diseases +MONDO:0011114 nord_rare diseases +MONDO:0011114 ordo_subtype_of_a_disorder diseases +MONDO:0011114 otar diseases +MONDO:0011114 rare diseases +MONDO:0011116 gard_rare diseases +MONDO:0011116 nord_rare diseases +MONDO:0011116 ordo_disorder diseases +MONDO:0011116 ordo_malformation_syndrome diseases +MONDO:0011116 orphanet_rare diseases +MONDO:0011116 otar diseases +MONDO:0011116 rare diseases +MONDO:0011118 gard_rare diseases +MONDO:0011118 rare diseases +MONDO:0011119 disease_grouping diseases +MONDO:0011119 gard_rare diseases +MONDO:0011119 ordo_group_of_disorders diseases +MONDO:0011119 otar diseases +MONDO:0011119 rare diseases +MONDO:0011120 gard_rare diseases +MONDO:0011120 nord_rare diseases +MONDO:0011120 rare diseases +MONDO:0011121 gard_rare diseases +MONDO:0011121 nord_rare diseases +MONDO:0011121 rare diseases +MONDO:0011122 otar diseases +MONDO:0011124 gard_rare diseases +MONDO:0011124 ordo_disorder diseases +MONDO:0011124 orphanet_rare diseases +MONDO:0011124 otar diseases +MONDO:0011124 rare diseases +MONDO:0011125 gard_rare diseases +MONDO:0011125 nord_rare diseases +MONDO:0011125 rare diseases +MONDO:0011128 gard_rare diseases +MONDO:0011128 nord_rare diseases +MONDO:0011128 ordo_disorder diseases +MONDO:0011128 ordo_malformation_syndrome diseases +MONDO:0011128 orphanet_rare diseases +MONDO:0011128 otar diseases +MONDO:0011128 rare diseases +MONDO:0011129 gard_rare diseases +MONDO:0011129 rare diseases +MONDO:0011131 gard_rare diseases +MONDO:0011131 nord_rare diseases +MONDO:0011131 ordo_malformation_syndrome diseases +MONDO:0011131 otar diseases +MONDO:0011131 rare diseases +MONDO:0011132 clingen diseases +MONDO:0011132 gard_rare diseases +MONDO:0011132 ordo_disorder diseases +MONDO:0011132 orphanet_rare diseases +MONDO:0011132 otar diseases +MONDO:0011132 rare diseases +MONDO:0011133 gard_rare diseases +MONDO:0011133 ordo_disorder diseases +MONDO:0011133 ordo_malformation_syndrome diseases +MONDO:0011133 orphanet_rare diseases +MONDO:0011133 otar diseases +MONDO:0011133 rare diseases +MONDO:0011134 gard_rare diseases +MONDO:0011134 nord_rare diseases +MONDO:0011134 ordo_disorder diseases +MONDO:0011134 ordo_malformation_syndrome diseases +MONDO:0011134 orphanet_rare diseases +MONDO:0011134 otar diseases +MONDO:0011134 rare diseases +MONDO:0011136 clingen diseases +MONDO:0011136 gard_rare diseases +MONDO:0011136 nord_rare diseases +MONDO:0011136 ordo_disorder diseases +MONDO:0011136 orphanet_rare diseases +MONDO:0011136 otar diseases +MONDO:0011136 rare diseases +MONDO:0011137 gard_rare diseases +MONDO:0011137 nord_rare diseases +MONDO:0011137 rare diseases +MONDO:0011139 gard_rare diseases +MONDO:0011139 rare diseases +MONDO:0011142 gard_rare diseases +MONDO:0011142 nord_rare diseases +MONDO:0011142 ordo_disorder diseases +MONDO:0011142 orphanet_rare diseases +MONDO:0011142 otar diseases +MONDO:0011142 rare diseases +MONDO:0011143 gard_rare diseases +MONDO:0011143 nord_rare diseases +MONDO:0011143 rare diseases +MONDO:0011144 gard_rare diseases +MONDO:0011144 nord_rare diseases +MONDO:0011144 ordo_etiological_subtype diseases +MONDO:0011144 otar diseases +MONDO:0011144 rare diseases +MONDO:0011145 gard_rare diseases +MONDO:0011145 nord_rare diseases +MONDO:0011145 ordo_disorder diseases +MONDO:0011145 orphanet_rare diseases +MONDO:0011145 otar diseases +MONDO:0011145 rare diseases +MONDO:0011146 gard_rare diseases +MONDO:0011146 nord_rare diseases +MONDO:0011146 ordo_disorder diseases +MONDO:0011146 ordo_malformation_syndrome diseases +MONDO:0011146 orphanet_rare diseases +MONDO:0011146 otar diseases +MONDO:0011146 rare diseases +MONDO:0011147 disease_grouping diseases +MONDO:0011147 gard_rare diseases +MONDO:0011147 nord_rare diseases +MONDO:0011147 ordo_disorder diseases +MONDO:0011147 ordo_group_of_disorders diseases +MONDO:0011147 ordo_malformation_syndrome diseases +MONDO:0011147 orphanet_rare diseases +MONDO:0011147 otar diseases +MONDO:0011147 rare diseases +MONDO:0011149 gard_rare diseases +MONDO:0011149 rare diseases +MONDO:0011150 gard_rare diseases +MONDO:0011150 nord_rare diseases +MONDO:0011150 ordo_disorder diseases +MONDO:0011150 orphanet_rare diseases +MONDO:0011150 otar diseases +MONDO:0011150 rare diseases +MONDO:0011151 gard_rare diseases +MONDO:0011151 nord_rare diseases +MONDO:0011151 rare diseases +MONDO:0011152 gard_rare diseases +MONDO:0011152 nord_rare diseases +MONDO:0011152 ordo_subtype_of_a_disorder diseases +MONDO:0011152 otar diseases +MONDO:0011152 rare diseases +MONDO:0011153 gard_rare diseases +MONDO:0011153 nord_rare diseases +MONDO:0011153 otar diseases +MONDO:0011153 rare diseases +MONDO:0011154 gard_rare diseases +MONDO:0011154 ordo_disorder diseases +MONDO:0011154 ordo_malformation_syndrome diseases +MONDO:0011154 orphanet_rare diseases +MONDO:0011154 otar diseases +MONDO:0011154 rare diseases +MONDO:0011156 gard_rare diseases +MONDO:0011156 nord_rare diseases +MONDO:0011156 ordo_subtype_of_a_disorder diseases +MONDO:0011156 otar diseases +MONDO:0011156 rare diseases +MONDO:0011157 gard_rare diseases +MONDO:0011157 nord_rare diseases +MONDO:0011157 ordo_disorder diseases +MONDO:0011157 ordo_malformation_syndrome diseases +MONDO:0011157 orphanet_rare diseases +MONDO:0011157 otar diseases +MONDO:0011157 rare diseases +MONDO:0011158 gard_rare diseases +MONDO:0011158 nord_rare diseases +MONDO:0011158 rare diseases +MONDO:0011159 gard_rare diseases +MONDO:0011159 nord_rare diseases +MONDO:0011159 rare diseases +MONDO:0011160 gard_rare diseases +MONDO:0011160 nord_rare diseases +MONDO:0011160 rare diseases +MONDO:0011162 gard_rare diseases +MONDO:0011162 nord_rare diseases +MONDO:0011162 rare diseases +MONDO:0011165 clingen diseases +MONDO:0011165 gard_rare diseases +MONDO:0011165 nord_rare diseases +MONDO:0011165 rare diseases +MONDO:0011166 gard_rare diseases +MONDO:0011166 nord_rare diseases +MONDO:0011166 ordo_disorder diseases +MONDO:0011166 ordo_malformation_syndrome diseases +MONDO:0011166 orphanet_rare diseases +MONDO:0011166 otar diseases +MONDO:0011166 rare diseases +MONDO:0011169 gard_rare diseases +MONDO:0011169 nord_rare diseases +MONDO:0011169 ordo_disorder diseases +MONDO:0011169 orphanet_rare diseases +MONDO:0011169 otar diseases +MONDO:0011169 rare diseases +MONDO:0011170 gard_rare diseases +MONDO:0011170 nord_rare diseases +MONDO:0011170 ordo_disorder diseases +MONDO:0011170 orphanet_rare diseases +MONDO:0011170 otar diseases +MONDO:0011170 rare diseases +MONDO:0011171 gard_rare diseases +MONDO:0011171 ordo_disorder diseases +MONDO:0011171 ordo_malformation_syndrome diseases +MONDO:0011171 orphanet_rare diseases +MONDO:0011171 otar diseases +MONDO:0011171 rare diseases +MONDO:0011173 clingen diseases +MONDO:0011173 gard_rare diseases +MONDO:0011173 nord_rare diseases +MONDO:0011173 otar diseases +MONDO:0011173 rare diseases +MONDO:0011175 gard_rare diseases +MONDO:0011175 nord_rare diseases +MONDO:0011175 rare diseases +MONDO:0011176 gard_rare diseases +MONDO:0011176 nord_rare diseases +MONDO:0011176 ordo_disorder diseases +MONDO:0011176 orphanet_rare diseases +MONDO:0011176 otar diseases +MONDO:0011176 rare diseases +MONDO:0011177 gard_rare diseases +MONDO:0011177 nord_rare diseases +MONDO:0011177 rare diseases +MONDO:0011178 clingen diseases +MONDO:0011178 gard_rare diseases +MONDO:0011178 nord_rare diseases +MONDO:0011178 ordo_disorder diseases +MONDO:0011178 orphanet_rare diseases +MONDO:0011178 otar diseases +MONDO:0011178 rare diseases +MONDO:0011181 gard_rare diseases +MONDO:0011181 nord_rare diseases +MONDO:0011181 rare diseases +MONDO:0011182 clingen diseases +MONDO:0011182 inferred_rare diseases +MONDO:0011182 otar diseases +MONDO:0011182 rare diseases +MONDO:0011183 gard_rare diseases +MONDO:0011183 nord_rare diseases +MONDO:0011183 rare diseases +MONDO:0011184 gard_rare diseases +MONDO:0011184 nord_rare diseases +MONDO:0011184 ordo_disorder diseases +MONDO:0011184 orphanet_rare diseases +MONDO:0011184 otar diseases +MONDO:0011184 rare diseases +MONDO:0011185 gard_rare diseases +MONDO:0011185 nord_rare diseases +MONDO:0011185 ordo_disorder diseases +MONDO:0011185 orphanet_rare diseases +MONDO:0011185 otar diseases +MONDO:0011185 rare diseases +MONDO:0011186 gard_rare diseases +MONDO:0011186 nord_rare diseases +MONDO:0011186 rare diseases +MONDO:0011187 gard_rare diseases +MONDO:0011187 nord_rare diseases +MONDO:0011187 rare diseases +MONDO:0011188 gard_rare diseases +MONDO:0011188 nord_rare diseases +MONDO:0011188 rare diseases +MONDO:0011189 gard_rare diseases +MONDO:0011189 nord_rare diseases +MONDO:0011189 rare diseases +MONDO:0011190 clingen diseases +MONDO:0011190 gard_rare diseases +MONDO:0011190 nord_rare diseases +MONDO:0011190 ordo_subtype_of_a_disorder diseases +MONDO:0011190 otar diseases +MONDO:0011190 rare diseases +MONDO:0011191 otar diseases +MONDO:0011192 gard_rare diseases +MONDO:0011192 nord_rare diseases +MONDO:0011192 rare diseases +MONDO:0011193 gard_rare diseases +MONDO:0011193 nord_rare diseases +MONDO:0011193 otar diseases +MONDO:0011193 rare diseases +MONDO:0011194 gard_rare diseases +MONDO:0011194 rare diseases +MONDO:0011195 gard_rare diseases +MONDO:0011195 nord_rare diseases +MONDO:0011195 rare diseases +MONDO:0011196 gard_rare diseases +MONDO:0011196 nord_rare diseases +MONDO:0011196 rare diseases +MONDO:0011197 gard_rare diseases +MONDO:0011197 nord_rare diseases +MONDO:0011197 ordo_disorder diseases +MONDO:0011197 orphanet_rare diseases +MONDO:0011197 rare diseases +MONDO:0011198 gard_rare diseases +MONDO:0011198 nord_rare diseases +MONDO:0011198 ordo_disorder diseases +MONDO:0011198 orphanet_rare diseases +MONDO:0011198 otar diseases +MONDO:0011198 rare diseases +MONDO:0011199 gard_rare diseases +MONDO:0011199 rare diseases +MONDO:0011200 gard_rare diseases +MONDO:0011200 nord_rare diseases +MONDO:0011200 otar diseases +MONDO:0011200 rare diseases +MONDO:0011202 gard_rare diseases +MONDO:0011202 nord_rare diseases +MONDO:0011202 ordo_disorder diseases +MONDO:0011202 orphanet_rare diseases +MONDO:0011202 otar diseases +MONDO:0011202 rare diseases +MONDO:0011203 gard_rare diseases +MONDO:0011203 rare diseases +MONDO:0011208 gard_rare diseases +MONDO:0011208 nord_rare diseases +MONDO:0011208 ordo_subtype_of_a_disorder diseases +MONDO:0011208 otar diseases +MONDO:0011208 rare diseases +MONDO:0011211 gard_rare diseases +MONDO:0011211 nord_rare diseases +MONDO:0011211 ordo_disorder diseases +MONDO:0011211 orphanet_rare diseases +MONDO:0011211 otar diseases +MONDO:0011211 rare diseases +MONDO:0011213 gard_rare diseases +MONDO:0011213 nord_rare diseases +MONDO:0011213 ordo_disorder diseases +MONDO:0011213 ordo_malformation_syndrome diseases +MONDO:0011213 orphanet_rare diseases +MONDO:0011213 otar diseases +MONDO:0011213 rare diseases +MONDO:0011214 clingen diseases +MONDO:0011214 gard_rare diseases +MONDO:0011214 nord_rare diseases +MONDO:0011214 ordo_subtype_of_a_disorder diseases +MONDO:0011214 otar diseases +MONDO:0011214 rare diseases +MONDO:0011215 gard_rare diseases +MONDO:0011215 nord_rare diseases +MONDO:0011215 ordo_disorder diseases +MONDO:0011215 ordo_malformation_syndrome diseases +MONDO:0011215 orphanet_rare diseases +MONDO:0011215 otar diseases +MONDO:0011215 rare diseases +MONDO:0011216 gard_rare diseases +MONDO:0011216 nord_rare diseases +MONDO:0011216 otar diseases +MONDO:0011216 rare diseases +MONDO:0011217 gard_rare diseases +MONDO:0011217 nord_rare diseases +MONDO:0011217 ordo_disorder diseases +MONDO:0011217 orphanet_rare diseases +MONDO:0011217 otar diseases +MONDO:0011217 rare diseases +MONDO:0011218 gard_rare diseases +MONDO:0011218 nord_rare diseases +MONDO:0011218 ordo_disorder diseases +MONDO:0011218 orphanet_rare diseases +MONDO:0011218 otar diseases +MONDO:0011218 rare diseases +MONDO:0011219 gard_rare diseases +MONDO:0011219 nord_rare diseases +MONDO:0011219 ordo_disorder diseases +MONDO:0011219 ordo_malformation_syndrome diseases +MONDO:0011219 orphanet_rare diseases +MONDO:0011219 otar diseases +MONDO:0011219 rare diseases +MONDO:0011220 gard_rare diseases +MONDO:0011220 rare diseases +MONDO:0011223 gard_rare diseases +MONDO:0011223 nord_rare diseases +MONDO:0011223 ordo_disorder diseases +MONDO:0011223 orphanet_rare diseases +MONDO:0011223 otar diseases +MONDO:0011223 rare diseases +MONDO:0011224 gard_rare diseases +MONDO:0011224 nord_rare diseases +MONDO:0011224 ordo_disorder diseases +MONDO:0011224 orphanet_rare diseases +MONDO:0011224 otar diseases +MONDO:0011224 rare diseases +MONDO:0011225 clingen diseases +MONDO:0011225 gard_rare diseases +MONDO:0011225 nord_rare diseases +MONDO:0011225 ordo_disorder diseases +MONDO:0011225 orphanet_rare diseases +MONDO:0011225 otar diseases +MONDO:0011225 rare diseases +MONDO:0011226 gard_rare diseases +MONDO:0011226 nord_rare diseases +MONDO:0011226 rare diseases +MONDO:0011227 gard_rare diseases +MONDO:0011227 nord_rare diseases +MONDO:0011227 ordo_disorder diseases +MONDO:0011227 ordo_malformation_syndrome diseases +MONDO:0011227 orphanet_rare diseases +MONDO:0011227 otar diseases +MONDO:0011227 rare diseases +MONDO:0011229 gard_rare diseases +MONDO:0011229 nord_rare diseases +MONDO:0011229 ordo_disorder diseases +MONDO:0011229 orphanet_rare diseases +MONDO:0011229 otar diseases +MONDO:0011229 rare diseases +MONDO:0011230 otar diseases +MONDO:0011231 otar diseases +MONDO:0011232 gard_rare diseases +MONDO:0011232 nord_rare diseases +MONDO:0011232 rare diseases +MONDO:0011233 gard_rare diseases +MONDO:0011233 nord_rare diseases +MONDO:0011233 rare diseases +MONDO:0011234 gard_rare diseases +MONDO:0011234 nord_rare diseases +MONDO:0011234 rare diseases +MONDO:0011235 gard_rare diseases +MONDO:0011235 nord_rare diseases +MONDO:0011235 ordo_disorder diseases +MONDO:0011235 ordo_malformation_syndrome diseases +MONDO:0011235 orphanet_rare diseases +MONDO:0011235 otar diseases +MONDO:0011235 rare diseases +MONDO:0011236 gard_rare diseases +MONDO:0011236 nord_rare diseases +MONDO:0011236 ordo_disorder diseases +MONDO:0011236 orphanet_rare diseases +MONDO:0011236 otar diseases +MONDO:0011236 rare diseases +MONDO:0011238 gard_rare diseases +MONDO:0011238 nord_rare diseases +MONDO:0011238 otar diseases +MONDO:0011238 rare diseases +MONDO:0011239 gard_rare diseases +MONDO:0011239 nord_rare diseases +MONDO:0011239 ordo_disorder diseases +MONDO:0011239 orphanet_rare diseases +MONDO:0011239 rare diseases +MONDO:0011240 gard_rare diseases +MONDO:0011240 nord_rare diseases +MONDO:0011240 ordo_disorder diseases +MONDO:0011240 ordo_malformation_syndrome diseases +MONDO:0011240 orphanet_rare diseases +MONDO:0011240 otar diseases +MONDO:0011240 rare diseases +MONDO:0011242 clingen diseases +MONDO:0011242 gard_rare diseases +MONDO:0011242 nord_rare diseases +MONDO:0011242 otar diseases +MONDO:0011242 rare diseases +MONDO:0011243 gard_rare diseases +MONDO:0011243 nord_rare diseases +MONDO:0011243 ordo_disorder diseases +MONDO:0011243 ordo_malformation_syndrome diseases +MONDO:0011243 orphanet_rare diseases +MONDO:0011243 otar diseases +MONDO:0011243 rare diseases +MONDO:0011244 clingen diseases +MONDO:0011244 gard_rare diseases +MONDO:0011244 nord_rare diseases +MONDO:0011244 ordo_disorder diseases +MONDO:0011244 ordo_malformation_syndrome diseases +MONDO:0011244 orphanet_rare diseases +MONDO:0011244 otar diseases +MONDO:0011244 rare diseases +MONDO:0011245 gard_rare diseases +MONDO:0011245 nord_rare diseases +MONDO:0011245 rare diseases +MONDO:0011246 gard_rare diseases +MONDO:0011246 nord_rare diseases +MONDO:0011246 ordo_disorder diseases +MONDO:0011246 orphanet_rare diseases +MONDO:0011246 otar diseases +MONDO:0011246 rare diseases +MONDO:0011248 gard_rare diseases +MONDO:0011248 nord_rare diseases +MONDO:0011248 ordo_disorder diseases +MONDO:0011248 ordo_malformation_syndrome diseases +MONDO:0011248 orphanet_rare diseases +MONDO:0011248 otar diseases +MONDO:0011248 rare diseases +MONDO:0011249 gard_rare diseases +MONDO:0011249 nord_rare diseases +MONDO:0011249 rare diseases +MONDO:0011252 gard_rare diseases +MONDO:0011252 nord_rare diseases +MONDO:0011252 ordo_disorder diseases +MONDO:0011252 orphanet_rare diseases +MONDO:0011252 otar diseases +MONDO:0011252 rare diseases +MONDO:0011253 gard_rare diseases +MONDO:0011253 nord_rare diseases +MONDO:0011253 ordo_disorder diseases +MONDO:0011253 ordo_malformation_syndrome diseases +MONDO:0011253 orphanet_rare diseases +MONDO:0011253 rare diseases +MONDO:0011255 gard_rare diseases +MONDO:0011255 nord_rare diseases +MONDO:0011255 ordo_disorder diseases +MONDO:0011255 orphanet_rare diseases +MONDO:0011255 otar diseases +MONDO:0011255 rare diseases +MONDO:0011257 gard_rare diseases +MONDO:0011257 nord_rare diseases +MONDO:0011257 ordo_disorder diseases +MONDO:0011257 orphanet_rare diseases +MONDO:0011257 otar diseases +MONDO:0011257 rare diseases +MONDO:0011258 gard_rare diseases +MONDO:0011258 nord_rare diseases +MONDO:0011258 rare diseases +MONDO:0011259 gard_rare diseases +MONDO:0011259 nord_rare diseases +MONDO:0011259 rare diseases +MONDO:0011260 gard_rare diseases +MONDO:0011260 nord_rare diseases +MONDO:0011260 predisposition diseases +MONDO:0011260 rare diseases +MONDO:0011261 gard_rare diseases +MONDO:0011261 n_of_one diseases +MONDO:0011261 ordo_disorder diseases +MONDO:0011261 orphanet_rare diseases +MONDO:0011261 rare diseases +MONDO:0011262 gard_rare diseases +MONDO:0011262 nord_rare diseases +MONDO:0011262 ordo_disorder diseases +MONDO:0011262 ordo_malformation_syndrome diseases +MONDO:0011262 orphanet_rare diseases +MONDO:0011262 rare diseases +MONDO:0011264 gard_rare diseases +MONDO:0011264 nord_rare diseases +MONDO:0011264 ordo_disorder diseases +MONDO:0011264 orphanet_rare diseases +MONDO:0011264 otar diseases +MONDO:0011264 rare diseases +MONDO:0011265 gard_rare diseases +MONDO:0011265 rare diseases +MONDO:0011266 gard_rare diseases +MONDO:0011266 nord_rare diseases +MONDO:0011266 ordo_disorder diseases +MONDO:0011266 orphanet_rare diseases +MONDO:0011266 otar diseases +MONDO:0011266 rare diseases +MONDO:0011268 gard_rare diseases +MONDO:0011268 nord_rare diseases +MONDO:0011268 rare diseases +MONDO:0011270 gard_rare diseases +MONDO:0011270 rare diseases +MONDO:0011271 gard_rare diseases +MONDO:0011271 otar diseases +MONDO:0011271 rare diseases +MONDO:0011272 gard_rare diseases +MONDO:0011272 nord_rare diseases +MONDO:0011272 rare diseases +MONDO:0011273 gard_rare diseases +MONDO:0011273 nord_rare diseases +MONDO:0011273 ordo_disorder diseases +MONDO:0011273 ordo_malformation_syndrome diseases +MONDO:0011273 orphanet_rare diseases +MONDO:0011273 otar diseases +MONDO:0011273 rare diseases +MONDO:0011274 clingen diseases +MONDO:0011274 gard_rare diseases +MONDO:0011274 nord_rare diseases +MONDO:0011274 ordo_disorder diseases +MONDO:0011274 ordo_malformation_syndrome diseases +MONDO:0011274 orphanet_rare diseases +MONDO:0011274 otar diseases +MONDO:0011274 rare diseases +MONDO:0011275 gard_rare diseases +MONDO:0011275 nord_rare diseases +MONDO:0011275 ordo_disorder diseases +MONDO:0011275 ordo_malformation_syndrome diseases +MONDO:0011275 orphanet_rare diseases +MONDO:0011275 otar diseases +MONDO:0011275 rare diseases +MONDO:0011279 gard_rare diseases +MONDO:0011279 nord_rare diseases +MONDO:0011279 rare diseases +MONDO:0011281 gard_rare diseases +MONDO:0011281 nord_rare diseases +MONDO:0011281 rare diseases +MONDO:0011283 gard_rare diseases +MONDO:0011283 otar diseases +MONDO:0011283 rare diseases +MONDO:0011285 gard_rare diseases +MONDO:0011285 nord_rare diseases +MONDO:0011285 rare diseases +MONDO:0011286 gard_rare diseases +MONDO:0011286 nord_rare diseases +MONDO:0011286 rare diseases +MONDO:0011287 gard_rare diseases +MONDO:0011287 nord_rare diseases +MONDO:0011287 ordo_disorder diseases +MONDO:0011287 ordo_malformation_syndrome diseases +MONDO:0011287 orphanet_rare diseases +MONDO:0011287 otar diseases +MONDO:0011287 rare diseases +MONDO:0011291 clingen diseases +MONDO:0011291 gard_rare diseases +MONDO:0011291 nord_rare diseases +MONDO:0011291 ordo_disorder diseases +MONDO:0011291 orphanet_rare diseases +MONDO:0011291 otar diseases +MONDO:0011291 rare diseases +MONDO:0011296 gard_rare diseases +MONDO:0011296 nord_rare diseases +MONDO:0011296 rare diseases +MONDO:0011297 gard_rare diseases +MONDO:0011297 nord_rare diseases +MONDO:0011297 rare diseases +MONDO:0011299 gard_rare diseases +MONDO:0011299 nord_rare diseases +MONDO:0011299 ordo_disorder diseases +MONDO:0011299 orphanet_rare diseases +MONDO:0011299 otar diseases +MONDO:0011299 rare diseases +MONDO:0011301 gard_rare diseases +MONDO:0011301 nord_rare diseases +MONDO:0011301 ordo_disorder diseases +MONDO:0011301 orphanet_rare diseases +MONDO:0011301 otar diseases +MONDO:0011301 rare diseases +MONDO:0011303 gard_rare diseases +MONDO:0011303 nord_rare diseases +MONDO:0011303 ordo_histopathological_subtype diseases +MONDO:0011303 otar diseases +MONDO:0011303 rare diseases +MONDO:0011304 gard_rare diseases +MONDO:0011304 nord_rare diseases +MONDO:0011304 rare diseases +MONDO:0011305 gard_rare diseases +MONDO:0011305 nord_rare diseases +MONDO:0011305 rare diseases +MONDO:0011308 gard_rare diseases +MONDO:0011308 nord_rare diseases +MONDO:0011308 ordo_disorder diseases +MONDO:0011308 orphanet_rare diseases +MONDO:0011308 otar diseases +MONDO:0011308 rare diseases +MONDO:0011309 gard_rare diseases +MONDO:0011309 nord_rare diseases +MONDO:0011309 ordo_disorder diseases +MONDO:0011309 orphanet_rare diseases +MONDO:0011309 otar diseases +MONDO:0011309 rare diseases +MONDO:0011312 gard_rare diseases +MONDO:0011312 nord_rare diseases +MONDO:0011312 rare diseases +MONDO:0011313 gard_rare diseases +MONDO:0011313 nord_rare diseases +MONDO:0011313 rare diseases +MONDO:0011320 gard_rare diseases +MONDO:0011320 ordo_disorder diseases +MONDO:0011320 ordo_malformation_syndrome diseases +MONDO:0011320 orphanet_rare diseases +MONDO:0011320 otar diseases +MONDO:0011320 rare diseases +MONDO:0011323 clingen diseases +MONDO:0011323 otar diseases +MONDO:0011325 clingen diseases +MONDO:0011325 gard_rare diseases +MONDO:0011325 nord_rare diseases +MONDO:0011325 rare diseases +MONDO:0011326 gard_rare diseases +MONDO:0011326 rare diseases +MONDO:0011327 gard_rare diseases +MONDO:0011327 nord_rare diseases +MONDO:0011327 ordo_disorder diseases +MONDO:0011327 orphanet_rare diseases +MONDO:0011327 otar diseases +MONDO:0011327 rare diseases +MONDO:0011330 gard_rare diseases +MONDO:0011330 nord_rare diseases +MONDO:0011330 ordo_disorder diseases +MONDO:0011330 orphanet_rare diseases +MONDO:0011330 otar diseases +MONDO:0011330 rare diseases +MONDO:0011331 gard_rare diseases +MONDO:0011331 nord_rare diseases +MONDO:0011331 ordo_disorder diseases +MONDO:0011331 orphanet_rare diseases +MONDO:0011331 rare diseases +MONDO:0011334 gard_rare diseases +MONDO:0011334 nord_rare diseases +MONDO:0011334 ordo_disorder diseases +MONDO:0011334 ordo_malformation_syndrome diseases +MONDO:0011334 orphanet_rare diseases +MONDO:0011334 otar diseases +MONDO:0011334 rare diseases +MONDO:0011335 gard_rare diseases +MONDO:0011335 nord_rare diseases +MONDO:0011335 ordo_disorder diseases +MONDO:0011335 orphanet_rare diseases +MONDO:0011335 otar diseases +MONDO:0011335 rare diseases +MONDO:0011336 clingen diseases +MONDO:0011336 gard_rare diseases +MONDO:0011336 nord_rare diseases +MONDO:0011336 rare diseases +MONDO:0011337 clingen diseases +MONDO:0011337 gard_rare diseases +MONDO:0011337 nord_rare diseases +MONDO:0011337 rare diseases +MONDO:0011338 gard_rare diseases +MONDO:0011338 nord_rare diseases +MONDO:0011338 ordo_disorder diseases +MONDO:0011338 orphanet_rare diseases +MONDO:0011338 otar diseases +MONDO:0011338 rare diseases +MONDO:0011339 clingen diseases +MONDO:0011339 gard_rare diseases +MONDO:0011339 nord_rare diseases +MONDO:0011339 ordo_disorder diseases +MONDO:0011339 orphanet_rare diseases +MONDO:0011339 otar diseases +MONDO:0011339 rare diseases +MONDO:0011340 gard_rare diseases +MONDO:0011340 nord_rare diseases +MONDO:0011340 ordo_disorder diseases +MONDO:0011340 ordo_morphological_anomaly diseases +MONDO:0011340 orphanet_rare diseases +MONDO:0011340 otar diseases +MONDO:0011340 rare diseases +MONDO:0011342 gard_rare diseases +MONDO:0011342 nord_rare diseases +MONDO:0011342 ordo_disorder diseases +MONDO:0011342 orphanet_rare diseases +MONDO:0011342 otar diseases +MONDO:0011342 rare diseases +MONDO:0011346 clingen diseases +MONDO:0011346 gard_rare diseases +MONDO:0011346 nord_rare diseases +MONDO:0011346 ordo_etiological_subtype diseases +MONDO:0011346 ordo_subtype_of_a_disorder diseases +MONDO:0011346 otar diseases +MONDO:0011346 rare diseases +MONDO:0011347 gard_rare diseases +MONDO:0011347 nord_rare diseases +MONDO:0011347 rare diseases +MONDO:0011348 disease_grouping diseases +MONDO:0011348 ordo_group_of_disorders diseases +MONDO:0011350 gard_rare diseases +MONDO:0011350 nord_rare diseases +MONDO:0011350 rare diseases +MONDO:0011351 gard_rare diseases +MONDO:0011351 nord_rare diseases +MONDO:0011351 rare diseases +MONDO:0011354 gard_rare diseases +MONDO:0011354 nord_rare diseases +MONDO:0011354 rare diseases +MONDO:0011355 gard_rare diseases +MONDO:0011355 nord_rare diseases +MONDO:0011355 rare diseases +MONDO:0011359 gard_rare diseases +MONDO:0011359 nord_rare diseases +MONDO:0011359 ordo_disorder diseases +MONDO:0011359 ordo_malformation_syndrome diseases +MONDO:0011359 orphanet_rare diseases +MONDO:0011359 otar diseases +MONDO:0011359 rare diseases +MONDO:0011360 gard_rare diseases +MONDO:0011360 nord_rare diseases +MONDO:0011360 rare diseases +MONDO:0011361 inferred_rare diseases +MONDO:0011361 predisposition diseases +MONDO:0011361 rare diseases +MONDO:0011362 clingen diseases +MONDO:0011362 gard_rare diseases +MONDO:0011362 nord_rare diseases +MONDO:0011362 ordo_disorder diseases +MONDO:0011362 orphanet_rare diseases +MONDO:0011362 otar diseases +MONDO:0011362 rare diseases +MONDO:0011363 gard_rare diseases +MONDO:0011363 rare diseases +MONDO:0011364 gard_rare diseases +MONDO:0011364 nord_rare diseases +MONDO:0011364 rare diseases +MONDO:0011365 gard_rare diseases +MONDO:0011365 nord_rare diseases +MONDO:0011365 ordo_disorder diseases +MONDO:0011365 ordo_malformation_syndrome diseases +MONDO:0011365 orphanet_rare diseases +MONDO:0011365 otar diseases +MONDO:0011365 rare diseases +MONDO:0011366 gard_rare diseases +MONDO:0011366 otar diseases +MONDO:0011366 rare diseases +MONDO:0011368 gard_rare diseases +MONDO:0011368 nord_rare diseases +MONDO:0011368 rare diseases +MONDO:0011369 clingen diseases +MONDO:0011369 gard_rare diseases +MONDO:0011369 otar diseases +MONDO:0011369 rare diseases +MONDO:0011370 gard_rare diseases +MONDO:0011370 nord_rare diseases +MONDO:0011370 rare diseases +MONDO:0011371 gard_rare diseases +MONDO:0011371 rare diseases +MONDO:0011372 gard_rare diseases +MONDO:0011372 nord_rare diseases +MONDO:0011372 rare diseases +MONDO:0011374 clingen diseases +MONDO:0011374 gard_rare diseases +MONDO:0011374 rare diseases +MONDO:0011375 gard_rare diseases +MONDO:0011375 rare diseases +MONDO:0011376 gard_rare diseases +MONDO:0011376 otar diseases +MONDO:0011376 rare diseases +MONDO:0011377 gard_rare diseases +MONDO:0011377 otar diseases +MONDO:0011377 rare diseases +MONDO:0011381 clingen diseases +MONDO:0011381 gard_rare diseases +MONDO:0011381 nord_rare diseases +MONDO:0011381 ordo_subtype_of_a_disorder diseases +MONDO:0011381 otar diseases +MONDO:0011381 rare diseases +MONDO:0011382 gard_rare diseases +MONDO:0011382 nord_rare diseases +MONDO:0011382 ordo_disorder diseases +MONDO:0011382 orphanet_rare diseases +MONDO:0011382 otar diseases +MONDO:0011382 rare diseases +MONDO:0011383 gard_rare diseases +MONDO:0011383 nord_rare diseases +MONDO:0011383 otar diseases +MONDO:0011383 rare diseases +MONDO:0011385 otar diseases +MONDO:0011389 gard_rare diseases +MONDO:0011389 nord_rare diseases +MONDO:0011389 rare diseases +MONDO:0011390 gard_rare diseases +MONDO:0011390 nord_rare diseases +MONDO:0011390 rare diseases +MONDO:0011391 gard_rare diseases +MONDO:0011391 nord_rare diseases +MONDO:0011391 ordo_disorder diseases +MONDO:0011391 orphanet_rare diseases +MONDO:0011391 otar diseases +MONDO:0011391 rare diseases +MONDO:0011392 gard_rare diseases +MONDO:0011392 nord_rare diseases +MONDO:0011392 rare diseases +MONDO:0011393 gard_rare diseases +MONDO:0011393 nord_rare diseases +MONDO:0011393 otar diseases +MONDO:0011393 rare diseases +MONDO:0011395 gard_rare diseases +MONDO:0011395 nord_rare diseases +MONDO:0011395 rare diseases +MONDO:0011396 gard_rare diseases +MONDO:0011396 nord_rare diseases +MONDO:0011396 ordo_disorder diseases +MONDO:0011396 orphanet_rare diseases +MONDO:0011396 otar diseases +MONDO:0011396 rare diseases +MONDO:0011397 clingen diseases +MONDO:0011397 gard_rare diseases +MONDO:0011397 nord_rare diseases +MONDO:0011397 ordo_disorder diseases +MONDO:0011397 orphanet_rare diseases +MONDO:0011397 otar diseases +MONDO:0011397 rare diseases +MONDO:0011398 gard_rare diseases +MONDO:0011398 nord_rare diseases +MONDO:0011398 ordo_disorder diseases +MONDO:0011398 orphanet_rare diseases +MONDO:0011398 otar diseases +MONDO:0011398 rare diseases +MONDO:0011399 clingen diseases +MONDO:0011399 gard_rare diseases +MONDO:0011399 nord_rare diseases +MONDO:0011399 ordo_disorder diseases +MONDO:0011399 orphanet_rare diseases +MONDO:0011399 otar diseases +MONDO:0011399 rare diseases +MONDO:0011400 gard_rare diseases +MONDO:0011400 nord_rare diseases +MONDO:0011400 rare diseases +MONDO:0011401 gard_rare diseases +MONDO:0011401 rare diseases +MONDO:0011402 gard_rare diseases +MONDO:0011402 nord_rare diseases +MONDO:0011402 ordo_disorder diseases +MONDO:0011402 ordo_malformation_syndrome diseases +MONDO:0011402 orphanet_rare diseases +MONDO:0011402 otar diseases +MONDO:0011402 rare diseases +MONDO:0011403 gard_rare diseases +MONDO:0011403 nord_rare diseases +MONDO:0011403 rare diseases +MONDO:0011405 gard_rare diseases +MONDO:0011405 nord_rare diseases +MONDO:0011405 ordo_disorder diseases +MONDO:0011405 orphanet_rare diseases +MONDO:0011405 otar diseases +MONDO:0011405 rare diseases +MONDO:0011407 gard_rare diseases +MONDO:0011407 nord_rare diseases +MONDO:0011407 rare diseases +MONDO:0011408 gard_rare diseases +MONDO:0011408 nord_rare diseases +MONDO:0011408 ordo_disorder diseases +MONDO:0011408 orphanet_rare diseases +MONDO:0011408 otar diseases +MONDO:0011408 rare diseases +MONDO:0011411 clingen diseases +MONDO:0011411 gard_rare diseases +MONDO:0011411 nord_rare diseases +MONDO:0011411 ordo_disorder diseases +MONDO:0011411 ordo_malformation_syndrome diseases +MONDO:0011411 orphanet_rare diseases +MONDO:0011411 otar diseases +MONDO:0011411 rare diseases +MONDO:0011412 gard_rare diseases +MONDO:0011412 nord_rare diseases +MONDO:0011412 ordo_disorder diseases +MONDO:0011412 orphanet_rare diseases +MONDO:0011412 otar diseases +MONDO:0011412 rare diseases +MONDO:0011413 gard_rare diseases +MONDO:0011413 rare diseases +MONDO:0011414 gard_rare diseases +MONDO:0011414 nord_rare diseases +MONDO:0011414 ordo_disorder diseases +MONDO:0011414 ordo_morphological_anomaly diseases +MONDO:0011414 orphanet_rare diseases +MONDO:0011414 otar diseases +MONDO:0011414 rare diseases +MONDO:0011415 gard_rare diseases +MONDO:0011415 nord_rare diseases +MONDO:0011415 rare diseases +MONDO:0011416 gard_rare diseases +MONDO:0011416 rare diseases +MONDO:0011417 gard_rare diseases +MONDO:0011417 nord_rare diseases +MONDO:0011417 ordo_disorder diseases +MONDO:0011417 orphanet_rare diseases +MONDO:0011417 otar diseases +MONDO:0011417 rare diseases +MONDO:0011420 gard_rare diseases +MONDO:0011420 nord_rare diseases +MONDO:0011420 ordo_disorder diseases +MONDO:0011420 orphanet_rare diseases +MONDO:0011420 otar diseases +MONDO:0011420 rare diseases +MONDO:0011421 gard_rare diseases +MONDO:0011421 prototype_pattern diseases +MONDO:0011421 rare diseases +MONDO:0011422 gard_rare diseases +MONDO:0011422 nord_rare diseases +MONDO:0011422 ordo_subtype_of_a_disorder diseases +MONDO:0011422 otar diseases +MONDO:0011422 rare diseases +MONDO:0011423 gard_rare diseases +MONDO:0011423 nord_rare diseases +MONDO:0011423 ordo_disorder diseases +MONDO:0011423 orphanet_rare diseases +MONDO:0011423 otar diseases +MONDO:0011423 rare diseases +MONDO:0011424 gard_rare diseases +MONDO:0011424 nord_rare diseases +MONDO:0011424 ordo_disorder diseases +MONDO:0011424 orphanet_rare diseases +MONDO:0011424 otar diseases +MONDO:0011424 rare diseases +MONDO:0011425 gard_rare diseases +MONDO:0011425 nord_rare diseases +MONDO:0011425 rare diseases +MONDO:0011426 gard_rare diseases +MONDO:0011426 nord_rare diseases +MONDO:0011426 ordo_disorder diseases +MONDO:0011426 orphanet_rare diseases +MONDO:0011426 otar diseases +MONDO:0011426 rare diseases +MONDO:0011428 gard_rare diseases +MONDO:0011428 nord_rare diseases +MONDO:0011428 otar diseases +MONDO:0011428 rare diseases +MONDO:0011429 disease_grouping diseases +MONDO:0011429 gard_rare diseases +MONDO:0011429 nord_rare diseases +MONDO:0011429 ordo_group_of_disorders diseases +MONDO:0011429 otar diseases +MONDO:0011429 rare diseases +MONDO:0011430 gard_rare diseases +MONDO:0011430 nord_rare diseases +MONDO:0011430 ordo_subtype_of_a_disorder diseases +MONDO:0011430 otar diseases +MONDO:0011430 rare diseases +MONDO:0011431 gard_rare diseases +MONDO:0011431 nord_rare diseases +MONDO:0011431 otar diseases +MONDO:0011431 rare diseases +MONDO:0011432 gard_rare diseases +MONDO:0011432 nord_rare diseases +MONDO:0011432 ordo_disorder diseases +MONDO:0011432 ordo_malformation_syndrome diseases +MONDO:0011432 orphanet_rare diseases +MONDO:0011432 otar diseases +MONDO:0011432 rare diseases +MONDO:0011435 clingen diseases +MONDO:0011435 gard_rare diseases +MONDO:0011435 nord_rare diseases +MONDO:0011435 rare diseases +MONDO:0011436 gard_rare diseases +MONDO:0011436 nord_rare diseases +MONDO:0011436 ordo_disorder diseases +MONDO:0011436 orphanet_rare diseases +MONDO:0011436 otar diseases +MONDO:0011436 rare diseases +MONDO:0011437 gard_rare diseases +MONDO:0011437 nord_rare diseases +MONDO:0011437 rare diseases +MONDO:0011438 otar diseases +MONDO:0011439 gard_rare diseases +MONDO:0011439 nord_rare diseases +MONDO:0011439 ordo_disorder diseases +MONDO:0011439 orphanet_rare diseases +MONDO:0011439 otar diseases +MONDO:0011439 rare diseases +MONDO:0011441 gard_rare diseases +MONDO:0011441 nord_rare diseases +MONDO:0011441 ordo_subtype_of_a_disorder diseases +MONDO:0011441 otar diseases +MONDO:0011441 rare diseases +MONDO:0011442 gard_rare diseases +MONDO:0011442 nord_rare diseases +MONDO:0011442 rare diseases +MONDO:0011444 gard_rare diseases +MONDO:0011444 nord_rare diseases +MONDO:0011444 rare diseases +MONDO:0011445 clingen diseases +MONDO:0011445 gard_rare diseases +MONDO:0011445 nord_rare diseases +MONDO:0011445 ordo_disorder diseases +MONDO:0011445 orphanet_rare diseases +MONDO:0011445 otar diseases +MONDO:0011445 rare diseases +MONDO:0011448 gard_rare diseases +MONDO:0011448 nord_rare diseases +MONDO:0011448 ordo_disorder diseases +MONDO:0011448 orphanet_rare diseases +MONDO:0011448 otar diseases +MONDO:0011448 rare diseases +MONDO:0011449 gard_rare diseases +MONDO:0011449 nord_rare diseases +MONDO:0011449 ordo_subtype_of_a_disorder diseases +MONDO:0011449 otar diseases +MONDO:0011449 rare diseases +MONDO:0011450 clingen diseases +MONDO:0011450 gard_rare diseases +MONDO:0011450 nord_rare diseases +MONDO:0011450 predisposition diseases +MONDO:0011450 rare diseases +MONDO:0011451 gard_rare diseases +MONDO:0011451 nord_rare diseases +MONDO:0011451 rare diseases +MONDO:0011452 gard_rare diseases +MONDO:0011452 nord_rare diseases +MONDO:0011452 rare diseases +MONDO:0011454 gard_rare diseases +MONDO:0011454 ordo_disorder diseases +MONDO:0011454 ordo_malformation_syndrome diseases +MONDO:0011454 orphanet_rare diseases +MONDO:0011454 otar diseases +MONDO:0011454 rare diseases +MONDO:0011456 gard_rare diseases +MONDO:0011456 nord_rare diseases +MONDO:0011456 rare diseases +MONDO:0011457 gard_rare diseases +MONDO:0011457 nord_rare diseases +MONDO:0011457 otar diseases +MONDO:0011457 prototype_pattern diseases +MONDO:0011457 rare diseases +MONDO:0011458 gard_rare diseases +MONDO:0011458 nord_rare diseases +MONDO:0011458 rare diseases +MONDO:0011459 clingen diseases +MONDO:0011459 gard_rare diseases +MONDO:0011459 nord_rare diseases +MONDO:0011459 otar diseases +MONDO:0011459 rare diseases +MONDO:0011460 gard_rare diseases +MONDO:0011460 nord_rare diseases +MONDO:0011460 rare diseases +MONDO:0011461 gard_rare diseases +MONDO:0011461 rare diseases +MONDO:0011462 gard_rare diseases +MONDO:0011462 nord_rare diseases +MONDO:0011462 ordo_disorder diseases +MONDO:0011462 orphanet_rare diseases +MONDO:0011462 otar diseases +MONDO:0011462 rare diseases +MONDO:0011463 gard_rare diseases +MONDO:0011463 ordo_disorder diseases +MONDO:0011463 orphanet_rare diseases +MONDO:0011463 rare diseases +MONDO:0011464 gard_rare diseases +MONDO:0011464 nord_rare diseases +MONDO:0011464 ordo_disorder diseases +MONDO:0011464 orphanet_rare diseases +MONDO:0011464 otar diseases +MONDO:0011464 rare diseases +MONDO:0011465 gard_rare diseases +MONDO:0011465 nord_rare diseases +MONDO:0011465 rare diseases +MONDO:0011466 gard_rare diseases +MONDO:0011466 nord_rare diseases +MONDO:0011466 ordo_disorder diseases +MONDO:0011466 orphanet_rare diseases +MONDO:0011466 otar diseases +MONDO:0011466 rare diseases +MONDO:0011468 gard_rare diseases +MONDO:0011468 nord_rare diseases +MONDO:0011468 ordo_disorder diseases +MONDO:0011468 orphanet_rare diseases +MONDO:0011468 otar diseases +MONDO:0011468 rare diseases +MONDO:0011470 gard_rare diseases +MONDO:0011470 rare diseases +MONDO:0011472 gard_rare diseases +MONDO:0011472 nord_rare diseases +MONDO:0011472 ordo_disorder diseases +MONDO:0011472 orphanet_rare diseases +MONDO:0011472 otar diseases +MONDO:0011472 rare diseases +MONDO:0011473 gard_rare diseases +MONDO:0011473 nord_rare diseases +MONDO:0011473 rare diseases +MONDO:0011474 gard_rare diseases +MONDO:0011474 rare diseases +MONDO:0011475 clingen diseases +MONDO:0011475 gard_rare diseases +MONDO:0011475 nord_rare diseases +MONDO:0011475 ordo_disorder diseases +MONDO:0011475 orphanet_rare diseases +MONDO:0011475 otar diseases +MONDO:0011475 rare diseases +MONDO:0011476 clingen diseases +MONDO:0011476 gard_rare diseases +MONDO:0011476 nord_rare diseases +MONDO:0011476 ordo_disorder diseases +MONDO:0011476 orphanet_rare diseases +MONDO:0011476 otar diseases +MONDO:0011476 rare diseases +MONDO:0011477 gard_rare diseases +MONDO:0011477 rare diseases +MONDO:0011479 gard_rare diseases +MONDO:0011479 nord_rare diseases +MONDO:0011479 ordo_disorder diseases +MONDO:0011479 orphanet_rare diseases +MONDO:0011479 otar diseases +MONDO:0011479 rare diseases +MONDO:0011480 gard_rare diseases +MONDO:0011480 nord_rare diseases +MONDO:0011480 rare diseases +MONDO:0011481 clingen diseases +MONDO:0011481 gard_rare diseases +MONDO:0011481 nord_rare diseases +MONDO:0011481 ordo_disorder diseases +MONDO:0011481 ordo_malformation_syndrome diseases +MONDO:0011481 orphanet_rare diseases +MONDO:0011481 otar diseases +MONDO:0011481 rare diseases +MONDO:0011482 gard_rare diseases +MONDO:0011482 nord_rare diseases +MONDO:0011482 rare diseases +MONDO:0011484 gard_rare diseases +MONDO:0011484 nord_rare diseases +MONDO:0011484 otar diseases +MONDO:0011484 rare diseases +MONDO:0011485 gard_rare diseases +MONDO:0011485 nord_rare diseases +MONDO:0011485 rare diseases +MONDO:0011486 gard_rare diseases +MONDO:0011486 nord_rare diseases +MONDO:0011486 ordo_disorder diseases +MONDO:0011486 orphanet_rare diseases +MONDO:0011486 otar diseases +MONDO:0011486 rare diseases +MONDO:0011487 gard_rare diseases +MONDO:0011487 nord_rare diseases +MONDO:0011487 ordo_disorder diseases +MONDO:0011487 orphanet_rare diseases +MONDO:0011487 otar diseases +MONDO:0011487 rare diseases +MONDO:0011488 gard_rare diseases +MONDO:0011488 nord_rare diseases +MONDO:0011488 rare diseases +MONDO:0011489 gard_rare diseases +MONDO:0011489 nord_rare diseases +MONDO:0011489 ordo_disorder diseases +MONDO:0011489 orphanet_rare diseases +MONDO:0011489 otar diseases +MONDO:0011489 rare diseases +MONDO:0011490 gard_rare diseases +MONDO:0011490 nord_rare diseases +MONDO:0011490 ordo_disorder diseases +MONDO:0011490 orphanet_rare diseases +MONDO:0011490 rare diseases +MONDO:0011493 gard_rare diseases +MONDO:0011493 nord_rare diseases +MONDO:0011493 ordo_subtype_of_a_disorder diseases +MONDO:0011493 otar diseases +MONDO:0011493 rare diseases +MONDO:0011496 gard_rare diseases +MONDO:0011496 nord_rare diseases +MONDO:0011496 ordo_disorder diseases +MONDO:0011496 orphanet_rare diseases +MONDO:0011496 otar diseases +MONDO:0011496 rare diseases +MONDO:0011497 gard_rare diseases +MONDO:0011497 nord_rare diseases +MONDO:0011497 ordo_subtype_of_a_disorder diseases +MONDO:0011497 otar diseases +MONDO:0011497 rare diseases +MONDO:0011500 gard_rare diseases +MONDO:0011500 nord_rare diseases +MONDO:0011500 ordo_disorder diseases +MONDO:0011500 orphanet_rare diseases +MONDO:0011500 otar diseases +MONDO:0011500 rare diseases +MONDO:0011501 gard_rare diseases +MONDO:0011501 nord_rare diseases +MONDO:0011501 ordo_disorder diseases +MONDO:0011501 ordo_malformation_syndrome diseases +MONDO:0011501 orphanet_rare diseases +MONDO:0011501 otar diseases +MONDO:0011501 rare diseases +MONDO:0011502 gard_rare diseases +MONDO:0011502 rare diseases +MONDO:0011503 gard_rare diseases +MONDO:0011503 nord_rare diseases +MONDO:0011503 rare diseases +MONDO:0011504 gard_rare diseases +MONDO:0011504 nord_rare diseases +MONDO:0011504 ordo_disorder diseases +MONDO:0011504 ordo_malformation_syndrome diseases +MONDO:0011504 orphanet_rare diseases +MONDO:0011504 otar diseases +MONDO:0011504 rare diseases +MONDO:0011505 clingen diseases +MONDO:0011505 gard_rare diseases +MONDO:0011505 nord_rare diseases +MONDO:0011505 rare diseases +MONDO:0011506 gard_rare diseases +MONDO:0011506 nord_rare diseases +MONDO:0011506 ordo_disorder diseases +MONDO:0011506 orphanet_rare diseases +MONDO:0011506 otar diseases +MONDO:0011506 rare diseases +MONDO:0011508 gard_rare diseases +MONDO:0011508 nord_rare diseases +MONDO:0011508 rare diseases +MONDO:0011510 clingen diseases +MONDO:0011510 gard_rare diseases +MONDO:0011510 nord_rare diseases +MONDO:0011510 ordo_disorder diseases +MONDO:0011510 ordo_malformation_syndrome diseases +MONDO:0011510 orphanet_rare diseases +MONDO:0011510 otar diseases +MONDO:0011510 rare diseases +MONDO:0011512 clingen diseases +MONDO:0011512 gard_rare diseases +MONDO:0011512 nord_rare diseases +MONDO:0011512 ordo_disorder diseases +MONDO:0011512 orphanet_rare diseases +MONDO:0011512 otar diseases +MONDO:0011512 rare diseases +MONDO:0011513 gard_rare diseases +MONDO:0011513 rare diseases +MONDO:0011514 gard_rare diseases +MONDO:0011514 nord_rare diseases +MONDO:0011514 ordo_disorder diseases +MONDO:0011514 ordo_morphological_anomaly diseases +MONDO:0011514 orphanet_rare diseases +MONDO:0011514 rare diseases +MONDO:0011517 clingen diseases +MONDO:0011517 gard_rare diseases +MONDO:0011517 nord_rare diseases +MONDO:0011517 ordo_disorder diseases +MONDO:0011517 orphanet_rare diseases +MONDO:0011517 otar diseases +MONDO:0011517 rare diseases +MONDO:0011518 clingen diseases +MONDO:0011518 gard_rare diseases +MONDO:0011518 nord_rare diseases +MONDO:0011518 ordo_disorder diseases +MONDO:0011518 ordo_malformation_syndrome diseases +MONDO:0011518 orphanet_rare diseases +MONDO:0011518 otar diseases +MONDO:0011518 rare diseases +MONDO:0011519 gard_rare diseases +MONDO:0011519 nord_rare diseases +MONDO:0011519 rare diseases +MONDO:0011522 gard_rare diseases +MONDO:0011522 ordo_disorder diseases +MONDO:0011522 orphanet_rare diseases +MONDO:0011522 rare diseases +MONDO:0011523 gard_rare diseases +MONDO:0011523 nord_rare diseases +MONDO:0011523 rare diseases +MONDO:0011524 gard_rare diseases +MONDO:0011524 nord_rare diseases +MONDO:0011524 ordo_disorder diseases +MONDO:0011524 orphanet_rare diseases +MONDO:0011524 otar diseases +MONDO:0011524 rare diseases +MONDO:0011525 gard_rare diseases +MONDO:0011525 rare diseases +MONDO:0011527 gard_rare diseases +MONDO:0011527 nord_rare diseases +MONDO:0011527 ordo_disorder diseases +MONDO:0011527 orphanet_rare diseases +MONDO:0011527 otar diseases +MONDO:0011527 rare diseases +MONDO:0011528 clingen diseases +MONDO:0011528 gard_rare diseases +MONDO:0011528 nord_rare diseases +MONDO:0011528 ordo_subtype_of_a_disorder diseases +MONDO:0011528 otar diseases +MONDO:0011528 rare diseases +MONDO:0011529 gard_rare diseases +MONDO:0011529 nord_rare diseases +MONDO:0011529 ordo_disorder diseases +MONDO:0011529 orphanet_rare diseases +MONDO:0011529 otar diseases +MONDO:0011529 rare diseases +MONDO:0011530 gard_rare diseases +MONDO:0011530 nord_rare diseases +MONDO:0011530 ordo_disorder diseases +MONDO:0011530 ordo_malformation_syndrome diseases +MONDO:0011530 orphanet_rare diseases +MONDO:0011530 otar diseases +MONDO:0011530 rare diseases +MONDO:0011531 gard_rare diseases +MONDO:0011531 nord_rare diseases +MONDO:0011531 rare diseases +MONDO:0011532 gard_rare diseases +MONDO:0011532 nord_rare diseases +MONDO:0011532 ordo_disorder diseases +MONDO:0011532 orphanet_rare diseases +MONDO:0011532 otar diseases +MONDO:0011532 rare diseases +MONDO:0011533 gard_rare diseases +MONDO:0011533 nord_rare diseases +MONDO:0011533 ordo_disorder diseases +MONDO:0011533 ordo_malformation_syndrome diseases +MONDO:0011533 orphanet_rare diseases +MONDO:0011533 otar diseases +MONDO:0011533 rare diseases +MONDO:0011534 gard_rare diseases +MONDO:0011534 nord_rare diseases +MONDO:0011534 ordo_disorder diseases +MONDO:0011534 orphanet_rare diseases +MONDO:0011534 otar diseases +MONDO:0011534 rare diseases +MONDO:0011535 gard_rare diseases +MONDO:0011535 nord_rare diseases +MONDO:0011535 rare diseases +MONDO:0011536 gard_rare diseases +MONDO:0011536 rare diseases +MONDO:0011537 gard_rare diseases +MONDO:0011537 nord_rare diseases +MONDO:0011537 ordo_disorder diseases +MONDO:0011537 orphanet_rare diseases +MONDO:0011537 otar diseases +MONDO:0011537 rare diseases +MONDO:0011539 clingen diseases +MONDO:0011539 gard_rare diseases +MONDO:0011539 nord_rare diseases +MONDO:0011539 ordo_disorder diseases +MONDO:0011539 orphanet_rare diseases +MONDO:0011539 otar diseases +MONDO:0011539 rare diseases +MONDO:0011540 gard_rare diseases +MONDO:0011540 nord_rare diseases +MONDO:0011540 ordo_disorder diseases +MONDO:0011540 orphanet_rare diseases +MONDO:0011540 otar diseases +MONDO:0011540 rare diseases +MONDO:0011541 clingen diseases +MONDO:0011541 gard_rare diseases +MONDO:0011541 nord_rare diseases +MONDO:0011541 ordo_disorder diseases +MONDO:0011541 orphanet_rare diseases +MONDO:0011541 otar diseases +MONDO:0011541 rare diseases +MONDO:0011544 gard_rare diseases +MONDO:0011544 nord_rare diseases +MONDO:0011544 rare diseases +MONDO:0011545 gard_rare diseases +MONDO:0011545 nord_rare diseases +MONDO:0011545 rare diseases +MONDO:0011546 gard_rare diseases +MONDO:0011546 nord_rare diseases +MONDO:0011546 rare diseases +MONDO:0011547 gard_rare diseases +MONDO:0011547 nord_rare diseases +MONDO:0011547 rare diseases +MONDO:0011549 gard_rare diseases +MONDO:0011549 nord_rare diseases +MONDO:0011549 rare diseases +MONDO:0011551 gard_rare diseases +MONDO:0011551 nord_rare diseases +MONDO:0011551 ordo_disorder diseases +MONDO:0011551 orphanet_rare diseases +MONDO:0011551 otar diseases +MONDO:0011551 rare diseases +MONDO:0011553 gard_rare diseases +MONDO:0011553 nord_rare diseases +MONDO:0011553 rare diseases +MONDO:0011555 gard_rare diseases +MONDO:0011555 nord_rare diseases +MONDO:0011555 ordo_disorder diseases +MONDO:0011555 ordo_malformation_syndrome diseases +MONDO:0011555 orphanet_rare diseases +MONDO:0011555 otar diseases +MONDO:0011555 rare diseases +MONDO:0011557 gard_rare diseases +MONDO:0011557 n_of_one diseases +MONDO:0011557 rare diseases +MONDO:0011558 gard_rare diseases +MONDO:0011558 nord_rare diseases +MONDO:0011558 rare diseases +MONDO:0011559 gard_rare diseases +MONDO:0011559 nord_rare diseases +MONDO:0011559 ordo_subtype_of_a_disorder diseases +MONDO:0011559 otar diseases +MONDO:0011559 rare diseases +MONDO:0011561 gard_rare diseases +MONDO:0011561 rare diseases +MONDO:0011562 gard_rare diseases +MONDO:0011562 nord_rare diseases +MONDO:0011562 rare diseases +MONDO:0011563 gard_rare diseases +MONDO:0011563 nord_rare diseases +MONDO:0011563 rare diseases +MONDO:0011564 gard_rare diseases +MONDO:0011564 nord_rare diseases +MONDO:0011564 rare diseases +MONDO:0011565 gard_rare diseases +MONDO:0011565 otar diseases +MONDO:0011565 rare diseases +MONDO:0011566 gard_rare diseases +MONDO:0011566 rare diseases +MONDO:0011567 gard_rare diseases +MONDO:0011567 nord_rare diseases +MONDO:0011567 rare diseases +MONDO:0011568 gard_rare diseases +MONDO:0011568 nord_rare diseases +MONDO:0011568 rare diseases +MONDO:0011569 gard_rare diseases +MONDO:0011569 nord_rare diseases +MONDO:0011569 ordo_disorder diseases +MONDO:0011569 orphanet_rare diseases +MONDO:0011569 otar diseases +MONDO:0011569 rare diseases +MONDO:0011570 clingen diseases +MONDO:0011570 gard_rare diseases +MONDO:0011570 nord_rare diseases +MONDO:0011570 ordo_disorder diseases +MONDO:0011570 orphanet_rare diseases +MONDO:0011570 otar diseases +MONDO:0011570 rare diseases +MONDO:0011571 gard_rare diseases +MONDO:0011571 otar diseases +MONDO:0011571 rare diseases +MONDO:0011575 gard_rare diseases +MONDO:0011575 nord_rare diseases +MONDO:0011575 ordo_disorder diseases +MONDO:0011575 ordo_malformation_syndrome diseases +MONDO:0011575 orphanet_rare diseases +MONDO:0011575 otar diseases +MONDO:0011575 rare diseases +MONDO:0011576 gard_rare diseases +MONDO:0011576 nord_rare diseases +MONDO:0011576 ordo_disorder diseases +MONDO:0011576 orphanet_rare diseases +MONDO:0011576 otar diseases +MONDO:0011576 rare diseases +MONDO:0011577 clingen diseases +MONDO:0011577 gard_rare diseases +MONDO:0011577 otar diseases +MONDO:0011577 rare diseases +MONDO:0011578 gard_rare diseases +MONDO:0011578 nord_rare diseases +MONDO:0011578 ordo_disorder diseases +MONDO:0011578 orphanet_rare diseases +MONDO:0011578 otar diseases +MONDO:0011578 rare diseases +MONDO:0011579 gard_rare diseases +MONDO:0011579 nord_rare diseases +MONDO:0011579 ordo_disorder diseases +MONDO:0011579 orphanet_rare diseases +MONDO:0011579 otar diseases +MONDO:0011579 rare diseases +MONDO:0011580 gard_rare diseases +MONDO:0011580 nord_rare diseases +MONDO:0011580 rare diseases +MONDO:0011581 clingen diseases +MONDO:0011581 gard_rare diseases +MONDO:0011581 nord_rare diseases +MONDO:0011581 ordo_disorder diseases +MONDO:0011581 orphanet_rare diseases +MONDO:0011581 otar diseases +MONDO:0011581 rare diseases +MONDO:0011582 gard_rare diseases +MONDO:0011582 nord_rare diseases +MONDO:0011582 ordo_disorder diseases +MONDO:0011582 orphanet_rare diseases +MONDO:0011582 otar diseases +MONDO:0011582 rare diseases +MONDO:0011583 gard_rare diseases +MONDO:0011583 nord_rare diseases +MONDO:0011583 otar diseases +MONDO:0011583 rare diseases +MONDO:0011584 clingen diseases +MONDO:0011584 gard_rare diseases +MONDO:0011584 nord_rare diseases +MONDO:0011584 ordo_disorder diseases +MONDO:0011584 orphanet_rare diseases +MONDO:0011584 otar diseases +MONDO:0011584 rare diseases +MONDO:0011585 gard_rare diseases +MONDO:0011585 nord_rare diseases +MONDO:0011585 ordo_disorder diseases +MONDO:0011585 orphanet_rare diseases +MONDO:0011585 otar diseases +MONDO:0011585 rare diseases +MONDO:0011586 gard_rare diseases +MONDO:0011586 rare diseases +MONDO:0011587 gard_rare diseases +MONDO:0011587 nord_rare diseases +MONDO:0011587 rare diseases +MONDO:0011588 clingen diseases +MONDO:0011588 gard_rare diseases +MONDO:0011588 nord_rare diseases +MONDO:0011588 rare diseases +MONDO:0011589 gard_rare diseases +MONDO:0011589 nord_rare diseases +MONDO:0011589 rare diseases +MONDO:0011591 gard_rare diseases +MONDO:0011591 nord_rare diseases +MONDO:0011591 rare diseases +MONDO:0011592 gard_rare diseases +MONDO:0011592 nord_rare diseases +MONDO:0011592 rare diseases +MONDO:0011593 gard_rare diseases +MONDO:0011593 nord_rare diseases +MONDO:0011593 rare diseases +MONDO:0011595 gard_rare diseases +MONDO:0011595 nord_rare diseases +MONDO:0011595 ordo_disorder diseases +MONDO:0011595 orphanet_rare diseases +MONDO:0011595 rare diseases +MONDO:0011599 gard_rare diseases +MONDO:0011599 nord_rare diseases +MONDO:0011599 ordo_disorder diseases +MONDO:0011599 orphanet_rare diseases +MONDO:0011599 otar diseases +MONDO:0011599 rare diseases +MONDO:0011600 gard_rare diseases +MONDO:0011600 nord_rare diseases +MONDO:0011600 rare diseases +MONDO:0011601 gard_rare diseases +MONDO:0011601 nord_rare diseases +MONDO:0011601 ordo_disorder diseases +MONDO:0011601 orphanet_rare diseases +MONDO:0011601 otar diseases +MONDO:0011601 rare diseases +MONDO:0011602 gard_rare diseases +MONDO:0011602 nord_rare diseases +MONDO:0011602 rare diseases +MONDO:0011603 gard_rare diseases +MONDO:0011603 nord_rare diseases +MONDO:0011603 ordo_disorder diseases +MONDO:0011603 orphanet_rare diseases +MONDO:0011603 otar diseases +MONDO:0011603 rare diseases +MONDO:0011604 gard_rare diseases +MONDO:0011604 nord_rare diseases +MONDO:0011604 ordo_disorder diseases +MONDO:0011604 ordo_malformation_syndrome diseases +MONDO:0011604 orphanet_rare diseases +MONDO:0011604 otar diseases +MONDO:0011604 rare diseases +MONDO:0011605 gard_rare diseases +MONDO:0011605 nord_rare diseases +MONDO:0011605 ordo_disorder diseases +MONDO:0011605 orphanet_rare diseases +MONDO:0011605 otar diseases +MONDO:0011605 rare diseases +MONDO:0011606 gard_rare diseases +MONDO:0011606 rare diseases +MONDO:0011610 clingen diseases +MONDO:0011610 gard_rare diseases +MONDO:0011610 n_of_one diseases +MONDO:0011610 nord_rare diseases +MONDO:0011610 ordo_disorder diseases +MONDO:0011610 orphanet_rare diseases +MONDO:0011610 otar diseases +MONDO:0011610 rare diseases +MONDO:0011612 clingen diseases +MONDO:0011612 gard_rare diseases +MONDO:0011612 nord_rare diseases +MONDO:0011612 ordo_disorder diseases +MONDO:0011612 orphanet_rare diseases +MONDO:0011612 otar diseases +MONDO:0011612 rare diseases +MONDO:0011613 gard_rare diseases +MONDO:0011613 rare diseases +MONDO:0011614 clingen diseases +MONDO:0011614 gard_rare diseases +MONDO:0011614 nord_rare diseases +MONDO:0011614 ordo_disorder diseases +MONDO:0011614 orphanet_rare diseases +MONDO:0011614 otar diseases +MONDO:0011614 rare diseases +MONDO:0011615 gard_rare diseases +MONDO:0011615 nord_rare diseases +MONDO:0011615 ordo_subtype_of_a_disorder diseases +MONDO:0011615 otar diseases +MONDO:0011615 rare diseases +MONDO:0011616 gard_rare diseases +MONDO:0011616 nord_rare diseases +MONDO:0011616 rare diseases +MONDO:0011620 gard_rare diseases +MONDO:0011620 nord_rare diseases +MONDO:0011620 ordo_disorder diseases +MONDO:0011620 ordo_malformation_syndrome diseases +MONDO:0011620 orphanet_rare diseases +MONDO:0011620 otar diseases +MONDO:0011620 rare diseases +MONDO:0011621 gard_rare diseases +MONDO:0011621 nord_rare diseases +MONDO:0011621 ordo_disorder diseases +MONDO:0011621 ordo_malformation_syndrome diseases +MONDO:0011621 orphanet_rare diseases +MONDO:0011621 otar diseases +MONDO:0011621 rare diseases +MONDO:0011624 gard_rare diseases +MONDO:0011624 nord_rare diseases +MONDO:0011624 ordo_disorder diseases +MONDO:0011624 orphanet_rare diseases +MONDO:0011624 otar diseases +MONDO:0011624 rare diseases +MONDO:0011625 gard_rare diseases +MONDO:0011625 nord_rare diseases +MONDO:0011625 rare diseases +MONDO:0011628 clingen diseases +MONDO:0011628 gard_rare diseases +MONDO:0011628 nord_rare diseases +MONDO:0011628 ordo_disorder diseases +MONDO:0011628 orphanet_rare diseases +MONDO:0011628 otar diseases +MONDO:0011628 rare diseases +MONDO:0011629 clingen diseases +MONDO:0011629 gard_rare diseases +MONDO:0011629 nord_rare diseases +MONDO:0011629 ordo_disorder diseases +MONDO:0011629 orphanet_rare diseases +MONDO:0011629 otar diseases +MONDO:0011629 rare diseases +MONDO:0011630 gard_rare diseases +MONDO:0011630 nord_rare diseases +MONDO:0011630 rare diseases +MONDO:0011631 gard_rare diseases +MONDO:0011631 nord_rare diseases +MONDO:0011631 ordo_disorder diseases +MONDO:0011631 orphanet_rare diseases +MONDO:0011631 otar diseases +MONDO:0011631 rare diseases +MONDO:0011632 clingen diseases +MONDO:0011632 gard_rare diseases +MONDO:0011632 nord_rare diseases +MONDO:0011632 rare diseases +MONDO:0011633 gard_rare diseases +MONDO:0011633 nord_rare diseases +MONDO:0011633 ordo_disorder diseases +MONDO:0011633 orphanet_rare diseases +MONDO:0011633 otar diseases +MONDO:0011633 rare diseases +MONDO:0011634 gard_rare diseases +MONDO:0011634 otar diseases +MONDO:0011634 rare diseases +MONDO:0011636 gard_rare diseases +MONDO:0011636 nord_rare diseases +MONDO:0011636 rare diseases +MONDO:0011638 gard_rare diseases +MONDO:0011638 nord_rare diseases +MONDO:0011638 ordo_disorder diseases +MONDO:0011638 orphanet_rare diseases +MONDO:0011638 otar diseases +MONDO:0011638 rare diseases +MONDO:0011639 gard_rare diseases +MONDO:0011639 nord_rare diseases +MONDO:0011639 rare diseases +MONDO:0011640 gard_rare diseases +MONDO:0011640 nord_rare diseases +MONDO:0011640 ordo_disorder diseases +MONDO:0011640 ordo_malformation_syndrome diseases +MONDO:0011640 orphanet_rare diseases +MONDO:0011640 otar diseases +MONDO:0011640 rare diseases +MONDO:0011644 gard_rare diseases +MONDO:0011644 otar diseases +MONDO:0011644 rare diseases +MONDO:0011647 gard_rare diseases +MONDO:0011647 rare diseases +MONDO:0011648 gard_rare diseases +MONDO:0011648 nord_rare diseases +MONDO:0011648 rare diseases +MONDO:0011652 clingen diseases +MONDO:0011652 gard_rare diseases +MONDO:0011652 nord_rare diseases +MONDO:0011652 ordo_disorder diseases +MONDO:0011652 ordo_malformation_syndrome diseases +MONDO:0011652 orphanet_rare diseases +MONDO:0011652 otar diseases +MONDO:0011652 rare diseases +MONDO:0011653 gard_rare diseases +MONDO:0011653 nord_rare diseases +MONDO:0011653 rare diseases +MONDO:0011655 gard_rare diseases +MONDO:0011655 nord_rare diseases +MONDO:0011655 ordo_disorder diseases +MONDO:0011655 orphanet_rare diseases +MONDO:0011655 otar diseases +MONDO:0011655 rare diseases +MONDO:0011657 gard_rare diseases +MONDO:0011657 nord_rare diseases +MONDO:0011657 rare diseases +MONDO:0011658 gard_rare diseases +MONDO:0011658 rare diseases +MONDO:0011659 gard_rare diseases +MONDO:0011659 nord_rare diseases +MONDO:0011659 rare diseases +MONDO:0011660 gard_rare diseases +MONDO:0011660 nord_rare diseases +MONDO:0011660 rare diseases +MONDO:0011661 otar diseases +MONDO:0011662 otar diseases +MONDO:0011663 gard_rare diseases +MONDO:0011663 nord_rare diseases +MONDO:0011663 ordo_disorder diseases +MONDO:0011663 orphanet_rare diseases +MONDO:0011663 otar diseases +MONDO:0011663 rare diseases +MONDO:0011664 gard_rare diseases +MONDO:0011664 nord_rare diseases +MONDO:0011664 ordo_disorder diseases +MONDO:0011664 orphanet_rare diseases +MONDO:0011664 otar diseases +MONDO:0011664 rare diseases +MONDO:0011667 gard_rare diseases +MONDO:0011667 nord_rare diseases +MONDO:0011667 otar diseases +MONDO:0011667 rare diseases +MONDO:0011668 gard_rare diseases +MONDO:0011668 nord_rare diseases +MONDO:0011668 otar diseases +MONDO:0011668 rare diseases +MONDO:0011669 disease_grouping diseases +MONDO:0011669 gard_rare diseases +MONDO:0011669 nord_rare diseases +MONDO:0011669 ordo_disorder diseases +MONDO:0011669 ordo_group_of_disorders diseases +MONDO:0011669 orphanet_rare diseases +MONDO:0011669 otar diseases +MONDO:0011669 rare diseases +MONDO:0011670 gard_rare diseases +MONDO:0011670 nord_rare diseases +MONDO:0011670 ordo_disorder diseases +MONDO:0011670 orphanet_rare diseases +MONDO:0011670 otar diseases +MONDO:0011670 rare diseases +MONDO:0011671 gard_rare diseases +MONDO:0011671 nord_rare diseases +MONDO:0011671 ordo_disorder diseases +MONDO:0011671 orphanet_rare diseases +MONDO:0011671 otar diseases +MONDO:0011671 rare diseases +MONDO:0011672 gard_rare diseases +MONDO:0011672 nord_rare diseases +MONDO:0011672 ordo_disorder diseases +MONDO:0011672 orphanet_rare diseases +MONDO:0011672 rare diseases +MONDO:0011673 gard_rare diseases +MONDO:0011673 nord_rare diseases +MONDO:0011673 rare diseases +MONDO:0011674 gard_rare diseases +MONDO:0011674 nord_rare diseases +MONDO:0011674 ordo_disorder diseases +MONDO:0011674 orphanet_rare diseases +MONDO:0011674 otar diseases +MONDO:0011674 rare diseases +MONDO:0011675 gard_rare diseases +MONDO:0011675 nord_rare diseases +MONDO:0011675 ordo_disorder diseases +MONDO:0011675 orphanet_rare diseases +MONDO:0011675 otar diseases +MONDO:0011675 rare diseases +MONDO:0011676 gard_rare diseases +MONDO:0011676 nord_rare diseases +MONDO:0011676 ordo_disorder diseases +MONDO:0011676 ordo_malformation_syndrome diseases +MONDO:0011676 orphanet_rare diseases +MONDO:0011676 otar diseases +MONDO:0011676 rare diseases +MONDO:0011678 gard_rare diseases +MONDO:0011678 nord_rare diseases +MONDO:0011678 rare diseases +MONDO:0011679 gard_rare diseases +MONDO:0011679 otar diseases +MONDO:0011679 rare diseases +MONDO:0011680 gard_rare diseases +MONDO:0011680 nord_rare diseases +MONDO:0011680 rare diseases +MONDO:0011681 gard_rare diseases +MONDO:0011681 nord_rare diseases +MONDO:0011681 ordo_disorder diseases +MONDO:0011681 orphanet_rare diseases +MONDO:0011681 otar diseases +MONDO:0011681 rare diseases +MONDO:0011682 gard_rare diseases +MONDO:0011682 nord_rare diseases +MONDO:0011682 ordo_disorder diseases +MONDO:0011682 orphanet_rare diseases +MONDO:0011682 otar diseases +MONDO:0011682 rare diseases +MONDO:0011683 gard_rare diseases +MONDO:0011683 nord_rare diseases +MONDO:0011683 ordo_disorder diseases +MONDO:0011683 orphanet_rare diseases +MONDO:0011683 otar diseases +MONDO:0011683 rare diseases +MONDO:0011686 clingen diseases +MONDO:0011686 gard_rare diseases +MONDO:0011686 nord_rare diseases +MONDO:0011686 ordo_disorder diseases +MONDO:0011686 orphanet_rare diseases +MONDO:0011686 otar diseases +MONDO:0011686 rare diseases +MONDO:0011687 clingen diseases +MONDO:0011687 gard_rare diseases +MONDO:0011687 nord_rare diseases +MONDO:0011687 ordo_disorder diseases +MONDO:0011687 orphanet_rare diseases +MONDO:0011687 otar diseases +MONDO:0011687 rare diseases +MONDO:0011688 gard_rare diseases +MONDO:0011688 otar diseases +MONDO:0011688 rare diseases +MONDO:0011690 n_of_one diseases +MONDO:0011690 speculative diseases +MONDO:0011691 gard_rare diseases +MONDO:0011691 nord_rare diseases +MONDO:0011691 rare diseases +MONDO:0011694 gard_rare diseases +MONDO:0011694 nord_rare diseases +MONDO:0011694 ordo_disorder diseases +MONDO:0011694 orphanet_rare diseases +MONDO:0011694 otar diseases +MONDO:0011694 rare diseases +MONDO:0011695 inferred_rare diseases +MONDO:0011695 predisposition diseases +MONDO:0011695 rare diseases +MONDO:0011696 inferred_rare diseases +MONDO:0011696 predisposition diseases +MONDO:0011696 rare diseases +MONDO:0011697 gard_rare diseases +MONDO:0011697 rare diseases +MONDO:0011698 clingen diseases +MONDO:0011698 gard_rare diseases +MONDO:0011698 nord_rare diseases +MONDO:0011698 ordo_disorder diseases +MONDO:0011698 orphanet_rare diseases +MONDO:0011698 otar diseases +MONDO:0011698 rare diseases +MONDO:0011702 gard_rare diseases +MONDO:0011702 nord_rare diseases +MONDO:0011702 rare diseases +MONDO:0011703 gard_rare diseases +MONDO:0011703 nord_rare diseases +MONDO:0011703 rare diseases +MONDO:0011705 gard_rare diseases +MONDO:0011705 nord_rare diseases +MONDO:0011705 otar diseases +MONDO:0011705 rare diseases +MONDO:0011706 clingen diseases +MONDO:0011706 gard_rare diseases +MONDO:0011706 nord_rare diseases +MONDO:0011706 ordo_disorder diseases +MONDO:0011706 orphanet_rare diseases +MONDO:0011706 otar diseases +MONDO:0011706 rare diseases +MONDO:0011708 gard_rare diseases +MONDO:0011708 nord_rare diseases +MONDO:0011708 rare diseases +MONDO:0011709 gard_rare diseases +MONDO:0011709 nord_rare diseases +MONDO:0011709 rare diseases +MONDO:0011712 gard_rare diseases +MONDO:0011712 rare diseases +MONDO:0011713 clingen diseases +MONDO:0011713 gard_rare diseases +MONDO:0011713 nord_rare diseases +MONDO:0011713 rare diseases +MONDO:0011714 gard_rare diseases +MONDO:0011714 rare diseases +MONDO:0011715 gard_rare diseases +MONDO:0011715 nord_rare diseases +MONDO:0011715 rare diseases +MONDO:0011716 gard_rare diseases +MONDO:0011716 nord_rare diseases +MONDO:0011716 otar diseases +MONDO:0011716 rare diseases +MONDO:0011717 clingen diseases +MONDO:0011717 gard_rare diseases +MONDO:0011717 nord_rare diseases +MONDO:0011717 ordo_disorder diseases +MONDO:0011717 orphanet_rare diseases +MONDO:0011717 otar diseases +MONDO:0011717 rare diseases +MONDO:0011718 clingen diseases +MONDO:0011718 gard_rare diseases +MONDO:0011718 nord_rare diseases +MONDO:0011718 rare diseases +MONDO:0011719 clingen diseases +MONDO:0011719 gard_rare diseases +MONDO:0011719 nord_rare diseases +MONDO:0011719 ordo_disorder diseases +MONDO:0011719 orphanet_rare diseases +MONDO:0011719 otar diseases +MONDO:0011719 rare diseases +MONDO:0011720 gard_rare diseases +MONDO:0011720 rare diseases +MONDO:0011721 gard_rare diseases +MONDO:0011721 nord_rare diseases +MONDO:0011721 ordo_disorder diseases +MONDO:0011721 orphanet_rare diseases +MONDO:0011721 otar diseases +MONDO:0011721 rare diseases +MONDO:0011722 gard_rare diseases +MONDO:0011722 nord_rare diseases +MONDO:0011722 ordo_disorder diseases +MONDO:0011722 orphanet_rare diseases +MONDO:0011722 otar diseases +MONDO:0011722 rare diseases +MONDO:0011723 gard_rare diseases +MONDO:0011723 nord_rare diseases +MONDO:0011723 ordo_disorder diseases +MONDO:0011723 ordo_malformation_syndrome diseases +MONDO:0011723 orphanet_rare diseases +MONDO:0011723 rare diseases +MONDO:0011724 gard_rare diseases +MONDO:0011724 nord_rare diseases +MONDO:0011724 ordo_disorder diseases +MONDO:0011724 orphanet_rare diseases +MONDO:0011724 otar diseases +MONDO:0011724 rare diseases +MONDO:0011725 gard_rare diseases +MONDO:0011725 nord_rare diseases +MONDO:0011725 ordo_subtype_of_a_disorder diseases +MONDO:0011725 otar diseases +MONDO:0011725 rare diseases +MONDO:0011728 otar diseases +MONDO:0011730 gard_rare diseases +MONDO:0011730 nord_rare diseases +MONDO:0011730 ordo_disorder diseases +MONDO:0011730 orphanet_rare diseases +MONDO:0011730 otar diseases +MONDO:0011730 rare diseases +MONDO:0011731 gard_rare diseases +MONDO:0011731 nord_rare diseases +MONDO:0011731 ordo_disorder diseases +MONDO:0011731 orphanet_rare diseases +MONDO:0011731 otar diseases +MONDO:0011731 rare diseases +MONDO:0011732 gard_rare diseases +MONDO:0011732 nord_rare diseases +MONDO:0011732 ordo_disorder diseases +MONDO:0011732 ordo_malformation_syndrome diseases +MONDO:0011732 orphanet_rare diseases +MONDO:0011732 otar diseases +MONDO:0011732 rare diseases +MONDO:0011735 clingen diseases +MONDO:0011735 gard_rare diseases +MONDO:0011735 nord_rare diseases +MONDO:0011735 ordo_subtype_of_a_disorder diseases +MONDO:0011735 otar diseases +MONDO:0011735 rare diseases +MONDO:0011737 gard_rare diseases +MONDO:0011737 rare diseases +MONDO:0011738 clingen diseases +MONDO:0011738 gard_rare diseases +MONDO:0011738 nord_rare diseases +MONDO:0011738 ordo_subtype_of_a_disorder diseases +MONDO:0011738 otar diseases +MONDO:0011738 rare diseases +MONDO:0011739 inferred_rare diseases +MONDO:0011739 predisposition diseases +MONDO:0011739 rare diseases +MONDO:0011740 gard_rare diseases +MONDO:0011740 nord_rare diseases +MONDO:0011740 ordo_disorder diseases +MONDO:0011740 orphanet_rare diseases +MONDO:0011740 otar diseases +MONDO:0011740 rare diseases +MONDO:0011743 gard_rare diseases +MONDO:0011743 rare diseases +MONDO:0011744 gard_rare diseases +MONDO:0011744 nord_rare diseases +MONDO:0011744 ordo_disorder diseases +MONDO:0011744 orphanet_rare diseases +MONDO:0011744 otar diseases +MONDO:0011744 rare diseases +MONDO:0011748 gard_rare diseases +MONDO:0011748 nord_rare diseases +MONDO:0011748 rare diseases +MONDO:0011749 gard_rare diseases +MONDO:0011749 nord_rare diseases +MONDO:0011749 ordo_subtype_of_a_disorder diseases +MONDO:0011749 otar diseases +MONDO:0011749 rare diseases +MONDO:0011752 clingen diseases +MONDO:0011752 gard_rare diseases +MONDO:0011752 nord_rare diseases +MONDO:0011752 rare diseases +MONDO:0011754 gard_rare diseases +MONDO:0011754 nord_rare diseases +MONDO:0011754 ordo_etiological_subtype diseases +MONDO:0011754 rare diseases +MONDO:0011755 gard_rare diseases +MONDO:0011755 nord_rare diseases +MONDO:0011755 rare diseases +MONDO:0011756 gard_rare diseases +MONDO:0011756 nord_rare diseases +MONDO:0011756 rare diseases +MONDO:0011757 gard_rare diseases +MONDO:0011757 nord_rare diseases +MONDO:0011757 rare diseases +MONDO:0011758 gard_rare diseases +MONDO:0011758 nord_rare diseases +MONDO:0011758 ordo_subtype_of_a_disorder diseases +MONDO:0011758 otar diseases +MONDO:0011758 rare diseases +MONDO:0011759 gard_rare diseases +MONDO:0011759 nord_rare diseases +MONDO:0011759 ordo_subtype_of_a_disorder diseases +MONDO:0011759 otar diseases +MONDO:0011759 rare diseases +MONDO:0011760 gard_rare diseases +MONDO:0011760 nord_rare diseases +MONDO:0011760 ordo_subtype_of_a_disorder diseases +MONDO:0011760 otar diseases +MONDO:0011760 rare diseases +MONDO:0011761 gard_rare diseases +MONDO:0011761 nord_rare diseases +MONDO:0011761 rare diseases +MONDO:0011762 gard_rare diseases +MONDO:0011762 nord_rare diseases +MONDO:0011762 rare diseases +MONDO:0011764 gard_rare diseases +MONDO:0011764 nord_rare diseases +MONDO:0011764 rare diseases +MONDO:0011765 gard_rare diseases +MONDO:0011765 nord_rare diseases +MONDO:0011765 ordo_disorder diseases +MONDO:0011765 orphanet_rare diseases +MONDO:0011765 otar diseases +MONDO:0011765 rare diseases +MONDO:0011766 gard_rare diseases +MONDO:0011766 nord_rare diseases +MONDO:0011766 ordo_disorder diseases +MONDO:0011766 ordo_malformation_syndrome diseases +MONDO:0011766 orphanet_rare diseases +MONDO:0011766 otar diseases +MONDO:0011766 rare diseases +MONDO:0011767 gard_rare diseases +MONDO:0011767 nord_rare diseases +MONDO:0011767 rare diseases +MONDO:0011768 gard_rare diseases +MONDO:0011768 rare diseases +MONDO:0011770 gard_rare diseases +MONDO:0011770 nord_rare diseases +MONDO:0011770 rare diseases +MONDO:0011771 gard_rare diseases +MONDO:0011771 nord_rare diseases +MONDO:0011771 ordo_disorder diseases +MONDO:0011771 orphanet_rare diseases +MONDO:0011771 otar diseases +MONDO:0011771 rare diseases +MONDO:0011772 gard_rare diseases +MONDO:0011772 nord_rare diseases +MONDO:0011772 ordo_disorder diseases +MONDO:0011772 orphanet_rare diseases +MONDO:0011772 otar diseases +MONDO:0011772 rare diseases +MONDO:0011773 gard_rare diseases +MONDO:0011773 nord_rare diseases +MONDO:0011773 ordo_disorder diseases +MONDO:0011773 orphanet_rare diseases +MONDO:0011773 otar diseases +MONDO:0011773 prototype_pattern diseases +MONDO:0011773 rare diseases +MONDO:0011774 gard_rare diseases +MONDO:0011774 nord_rare diseases +MONDO:0011774 rare diseases +MONDO:0011775 gard_rare diseases +MONDO:0011775 predisposition diseases +MONDO:0011775 rare diseases +MONDO:0011776 gard_rare diseases +MONDO:0011776 nord_rare diseases +MONDO:0011776 ordo_disorder diseases +MONDO:0011776 orphanet_rare diseases +MONDO:0011776 otar diseases +MONDO:0011776 rare diseases +MONDO:0011777 gard_rare diseases +MONDO:0011777 rare diseases +MONDO:0011778 gard_rare diseases +MONDO:0011778 nord_rare diseases +MONDO:0011778 ordo_disorder diseases +MONDO:0011778 orphanet_rare diseases +MONDO:0011778 otar diseases +MONDO:0011778 rare diseases +MONDO:0011781 gard_rare diseases +MONDO:0011781 nord_rare diseases +MONDO:0011781 ordo_disorder diseases +MONDO:0011781 orphanet_rare diseases +MONDO:0011781 otar diseases +MONDO:0011781 rare diseases +MONDO:0011782 otar diseases +MONDO:0011783 clingen diseases +MONDO:0011783 gard_rare diseases +MONDO:0011783 nord_rare diseases +MONDO:0011783 ordo_disorder diseases +MONDO:0011783 orphanet_rare diseases +MONDO:0011783 otar diseases +MONDO:0011783 rare diseases +MONDO:0011784 gard_rare diseases +MONDO:0011784 nord_rare diseases +MONDO:0011784 rare diseases +MONDO:0011785 gard_rare diseases +MONDO:0011785 ordo_disorder diseases +MONDO:0011785 orphanet_rare diseases +MONDO:0011785 otar diseases +MONDO:0011785 rare diseases +MONDO:0011786 otar diseases +MONDO:0011787 gard_rare diseases +MONDO:0011787 nord_rare diseases +MONDO:0011787 ordo_disorder diseases +MONDO:0011787 orphanet_rare diseases +MONDO:0011787 otar diseases +MONDO:0011787 rare diseases +MONDO:0011788 gard_rare diseases +MONDO:0011788 ordo_disorder diseases +MONDO:0011788 ordo_malformation_syndrome diseases +MONDO:0011788 orphanet_rare diseases +MONDO:0011788 otar diseases +MONDO:0011788 rare diseases +MONDO:0011789 clingen diseases +MONDO:0011789 gard_rare diseases +MONDO:0011789 nord_rare diseases +MONDO:0011789 otar diseases +MONDO:0011789 rare diseases +MONDO:0011790 gard_rare diseases +MONDO:0011790 nord_rare diseases +MONDO:0011790 ordo_disorder diseases +MONDO:0011790 ordo_malformation_syndrome diseases +MONDO:0011790 orphanet_rare diseases +MONDO:0011790 otar diseases +MONDO:0011790 rare diseases +MONDO:0011792 gard_rare diseases +MONDO:0011792 nord_rare diseases +MONDO:0011792 rare diseases +MONDO:0011795 gard_rare diseases +MONDO:0011795 ordo_disorder diseases +MONDO:0011795 ordo_malformation_syndrome diseases +MONDO:0011795 orphanet_rare diseases +MONDO:0011795 otar diseases +MONDO:0011795 rare diseases +MONDO:0011797 gard_rare diseases +MONDO:0011797 nord_rare diseases +MONDO:0011797 ordo_disorder diseases +MONDO:0011797 orphanet_rare diseases +MONDO:0011797 otar diseases +MONDO:0011797 rare diseases +MONDO:0011799 gard_rare diseases +MONDO:0011799 nord_rare diseases +MONDO:0011799 rare diseases +MONDO:0011800 gard_rare diseases +MONDO:0011800 rare diseases +MONDO:0011801 gard_rare diseases +MONDO:0011801 nord_rare diseases +MONDO:0011801 ordo_disorder diseases +MONDO:0011801 orphanet_rare diseases +MONDO:0011801 otar diseases +MONDO:0011801 rare diseases +MONDO:0011802 gard_rare diseases +MONDO:0011802 nord_rare diseases +MONDO:0011802 rare diseases +MONDO:0011803 gard_rare diseases +MONDO:0011803 nord_rare diseases +MONDO:0011803 ordo_disorder diseases +MONDO:0011803 orphanet_rare diseases +MONDO:0011803 otar diseases +MONDO:0011803 rare diseases +MONDO:0011804 gard_rare diseases +MONDO:0011804 nord_rare diseases +MONDO:0011804 ordo_disorder diseases +MONDO:0011804 orphanet_rare diseases +MONDO:0011804 otar diseases +MONDO:0011804 rare diseases +MONDO:0011806 gard_rare diseases +MONDO:0011806 nord_rare diseases +MONDO:0011806 ordo_disorder diseases +MONDO:0011806 orphanet_rare diseases +MONDO:0011806 rare diseases +MONDO:0011808 gard_rare diseases +MONDO:0011808 nord_rare diseases +MONDO:0011808 rare diseases +MONDO:0011810 gard_rare diseases +MONDO:0011810 nord_rare diseases +MONDO:0011810 ordo_disorder diseases +MONDO:0011810 orphanet_rare diseases +MONDO:0011810 otar diseases +MONDO:0011810 prototype_pattern diseases +MONDO:0011810 rare diseases +MONDO:0011811 gard_rare diseases +MONDO:0011811 nord_rare diseases +MONDO:0011811 ordo_disorder diseases +MONDO:0011811 orphanet_rare diseases +MONDO:0011811 otar diseases +MONDO:0011811 rare diseases +MONDO:0011812 gard_rare diseases +MONDO:0011812 nord_rare diseases +MONDO:0011812 ordo_disorder diseases +MONDO:0011812 ordo_malformation_syndrome diseases +MONDO:0011812 orphanet_rare diseases +MONDO:0011812 otar diseases +MONDO:0011812 rare diseases +MONDO:0011813 gard_rare diseases +MONDO:0011813 nord_rare diseases +MONDO:0011813 rare diseases +MONDO:0011814 gard_rare diseases +MONDO:0011814 nord_rare diseases +MONDO:0011814 rare diseases +MONDO:0011816 gard_rare diseases +MONDO:0011816 nord_rare diseases +MONDO:0011816 ordo_disorder diseases +MONDO:0011816 orphanet_rare diseases +MONDO:0011816 otar diseases +MONDO:0011816 rare diseases +MONDO:0011818 gard_rare diseases +MONDO:0011818 nord_rare diseases +MONDO:0011818 ordo_subtype_of_a_disorder diseases +MONDO:0011818 otar diseases +MONDO:0011818 rare diseases +MONDO:0011819 gard_rare diseases +MONDO:0011819 nord_rare diseases +MONDO:0011819 ordo_disorder diseases +MONDO:0011819 orphanet_rare diseases +MONDO:0011819 otar diseases +MONDO:0011819 rare diseases +MONDO:0011821 gard_rare diseases +MONDO:0011821 nord_rare diseases +MONDO:0011821 rare diseases +MONDO:0011822 gard_rare diseases +MONDO:0011822 nord_rare diseases +MONDO:0011822 ordo_subtype_of_a_disorder diseases +MONDO:0011822 otar diseases +MONDO:0011822 rare diseases +MONDO:0011823 gard_rare diseases +MONDO:0011823 nord_rare diseases +MONDO:0011823 ordo_disorder diseases +MONDO:0011823 ordo_malformation_syndrome diseases +MONDO:0011823 orphanet_rare diseases +MONDO:0011823 otar diseases +MONDO:0011823 rare diseases +MONDO:0011826 gard_rare diseases +MONDO:0011826 nord_rare diseases +MONDO:0011826 rare diseases +MONDO:0011827 gard_rare diseases +MONDO:0011827 nord_rare diseases +MONDO:0011827 prototype_pattern diseases +MONDO:0011827 rare diseases +MONDO:0011828 gard_rare diseases +MONDO:0011828 nord_rare diseases +MONDO:0011828 rare diseases +MONDO:0011829 gard_rare diseases +MONDO:0011829 nord_rare diseases +MONDO:0011829 rare diseases +MONDO:0011830 gard_rare diseases +MONDO:0011830 nord_rare diseases +MONDO:0011830 ordo_disorder diseases +MONDO:0011830 orphanet_rare diseases +MONDO:0011830 otar diseases +MONDO:0011830 rare diseases +MONDO:0011831 gard_rare diseases +MONDO:0011831 nord_rare diseases +MONDO:0011831 otar diseases +MONDO:0011831 rare diseases +MONDO:0011832 gard_rare diseases +MONDO:0011832 nord_rare diseases +MONDO:0011832 rare diseases +MONDO:0011833 gard_rare diseases +MONDO:0011833 nord_rare diseases +MONDO:0011833 ordo_disorder diseases +MONDO:0011833 orphanet_rare diseases +MONDO:0011833 otar diseases +MONDO:0011833 rare diseases +MONDO:0011834 gard_rare diseases +MONDO:0011834 nord_rare diseases +MONDO:0011834 ordo_disorder diseases +MONDO:0011834 orphanet_rare diseases +MONDO:0011834 otar diseases +MONDO:0011834 rare diseases +MONDO:0011835 gard_rare diseases +MONDO:0011835 nord_rare diseases +MONDO:0011835 ordo_disorder diseases +MONDO:0011835 orphanet_rare diseases +MONDO:0011835 otar diseases +MONDO:0011835 rare diseases +MONDO:0011836 gard_rare diseases +MONDO:0011836 rare diseases +MONDO:0011837 clingen diseases +MONDO:0011837 gard_rare diseases +MONDO:0011837 nord_rare diseases +MONDO:0011837 otar diseases +MONDO:0011837 rare diseases +MONDO:0011838 gard_rare diseases +MONDO:0011838 nord_rare diseases +MONDO:0011838 ordo_disorder diseases +MONDO:0011838 orphanet_rare diseases +MONDO:0011838 otar diseases +MONDO:0011838 rare diseases +MONDO:0011839 gard_rare diseases +MONDO:0011839 nord_rare diseases +MONDO:0011839 rare diseases +MONDO:0011840 gard_rare diseases +MONDO:0011840 nord_rare diseases +MONDO:0011840 rare diseases +MONDO:0011841 gard_rare diseases +MONDO:0011841 nord_rare diseases +MONDO:0011841 ordo_disorder diseases +MONDO:0011841 orphanet_rare diseases +MONDO:0011841 otar diseases +MONDO:0011841 rare diseases +MONDO:0011842 gard_rare diseases +MONDO:0011842 otar diseases +MONDO:0011842 rare diseases +MONDO:0011843 gard_rare diseases +MONDO:0011843 nord_rare diseases +MONDO:0011843 rare diseases +MONDO:0011844 gard_rare diseases +MONDO:0011844 nord_rare diseases +MONDO:0011844 rare diseases +MONDO:0011849 otar diseases +MONDO:0011849 predisposition diseases +MONDO:0011852 gard_rare diseases +MONDO:0011852 rare diseases +MONDO:0011853 otar diseases +MONDO:0011855 gard_rare diseases +MONDO:0011855 nord_rare diseases +MONDO:0011855 ordo_disorder diseases +MONDO:0011855 orphanet_rare diseases +MONDO:0011855 otar diseases +MONDO:0011855 rare diseases +MONDO:0011856 gard_rare diseases +MONDO:0011856 ordo_disorder diseases +MONDO:0011856 orphanet_rare diseases +MONDO:0011856 rare diseases +MONDO:0011857 gard_rare diseases +MONDO:0011857 nord_rare diseases +MONDO:0011857 rare diseases +MONDO:0011862 gard_rare diseases +MONDO:0011862 ordo_disorder diseases +MONDO:0011862 orphanet_rare diseases +MONDO:0011862 otar diseases +MONDO:0011862 rare diseases +MONDO:0011864 clingen diseases +MONDO:0011864 gard_rare diseases +MONDO:0011864 nord_rare diseases +MONDO:0011864 rare diseases +MONDO:0011866 gard_rare diseases +MONDO:0011866 nord_rare diseases +MONDO:0011866 rare diseases +MONDO:0011868 gard_rare diseases +MONDO:0011868 nord_rare diseases +MONDO:0011868 ordo_disorder diseases +MONDO:0011868 ordo_malformation_syndrome diseases +MONDO:0011868 orphanet_rare diseases +MONDO:0011868 otar diseases +MONDO:0011868 rare diseases +MONDO:0011869 gard_rare diseases +MONDO:0011869 nord_rare diseases +MONDO:0011869 otar diseases +MONDO:0011869 rare diseases +MONDO:0011870 gard_rare diseases +MONDO:0011870 nord_rare diseases +MONDO:0011870 ordo_disorder diseases +MONDO:0011870 orphanet_rare diseases +MONDO:0011870 otar diseases +MONDO:0011870 rare diseases +MONDO:0011871 gard_rare diseases +MONDO:0011871 nord_rare diseases +MONDO:0011871 ordo_disorder diseases +MONDO:0011871 orphanet_rare diseases +MONDO:0011871 otar diseases +MONDO:0011871 rare diseases +MONDO:0011872 clingen diseases +MONDO:0011872 gard_rare diseases +MONDO:0011872 nord_rare diseases +MONDO:0011872 ordo_subtype_of_a_disorder diseases +MONDO:0011872 otar diseases +MONDO:0011872 rare diseases +MONDO:0011873 clingen diseases +MONDO:0011873 gard_rare diseases +MONDO:0011873 rare diseases +MONDO:0011874 gard_rare diseases +MONDO:0011874 nord_rare diseases +MONDO:0011874 ordo_disorder diseases +MONDO:0011874 orphanet_rare diseases +MONDO:0011874 otar diseases +MONDO:0011874 rare diseases +MONDO:0011877 gard_rare diseases +MONDO:0011877 nord_rare diseases +MONDO:0011877 ordo_disorder diseases +MONDO:0011877 ordo_malformation_syndrome diseases +MONDO:0011877 orphanet_rare diseases +MONDO:0011877 otar diseases +MONDO:0011877 rare diseases +MONDO:0011879 gard_rare diseases +MONDO:0011879 nord_rare diseases +MONDO:0011879 rare diseases +MONDO:0011880 gard_rare diseases +MONDO:0011880 nord_rare diseases +MONDO:0011880 rare diseases +MONDO:0011881 gard_rare diseases +MONDO:0011881 nord_rare diseases +MONDO:0011881 rare diseases +MONDO:0011882 gard_rare diseases +MONDO:0011882 nord_rare diseases +MONDO:0011882 ordo_disorder diseases +MONDO:0011882 orphanet_rare diseases +MONDO:0011882 otar diseases +MONDO:0011882 rare diseases +MONDO:0011883 gard_rare diseases +MONDO:0011883 nord_rare diseases +MONDO:0011883 ordo_disorder diseases +MONDO:0011883 orphanet_rare diseases +MONDO:0011883 otar diseases +MONDO:0011883 rare diseases +MONDO:0011884 gard_rare diseases +MONDO:0011884 nord_rare diseases +MONDO:0011884 ordo_disorder diseases +MONDO:0011884 orphanet_rare diseases +MONDO:0011884 rare diseases +MONDO:0011885 gard_rare diseases +MONDO:0011885 nord_rare diseases +MONDO:0011885 ordo_disorder diseases +MONDO:0011885 orphanet_rare diseases +MONDO:0011885 rare diseases +MONDO:0011886 gard_rare diseases +MONDO:0011886 nord_rare diseases +MONDO:0011886 ordo_disorder diseases +MONDO:0011886 orphanet_rare diseases +MONDO:0011886 rare diseases +MONDO:0011888 gard_rare diseases +MONDO:0011888 nord_rare diseases +MONDO:0011888 ordo_disorder diseases +MONDO:0011888 orphanet_rare diseases +MONDO:0011888 otar diseases +MONDO:0011888 rare diseases +MONDO:0011889 gard_rare diseases +MONDO:0011889 nord_rare diseases +MONDO:0011889 ordo_disorder diseases +MONDO:0011889 orphanet_rare diseases +MONDO:0011889 otar diseases +MONDO:0011889 rare diseases +MONDO:0011890 gard_rare diseases +MONDO:0011890 nord_rare diseases +MONDO:0011890 ordo_disorder diseases +MONDO:0011890 orphanet_rare diseases +MONDO:0011890 otar diseases +MONDO:0011890 rare diseases +MONDO:0011891 gard_rare diseases +MONDO:0011891 nord_rare diseases +MONDO:0011891 predisposition diseases +MONDO:0011891 rare diseases +MONDO:0011893 gard_rare diseases +MONDO:0011893 nord_rare diseases +MONDO:0011893 rare diseases +MONDO:0011894 gard_rare diseases +MONDO:0011894 nord_rare diseases +MONDO:0011894 ordo_disorder diseases +MONDO:0011894 orphanet_rare diseases +MONDO:0011894 otar diseases +MONDO:0011894 rare diseases +MONDO:0011895 gard_rare diseases +MONDO:0011895 nord_rare diseases +MONDO:0011895 ordo_disorder diseases +MONDO:0011895 orphanet_rare diseases +MONDO:0011895 otar diseases +MONDO:0011895 rare diseases +MONDO:0011897 gard_rare diseases +MONDO:0011897 nord_rare diseases +MONDO:0011897 ordo_subtype_of_a_disorder diseases +MONDO:0011897 otar diseases +MONDO:0011897 rare diseases +MONDO:0011898 gard_rare diseases +MONDO:0011898 nord_rare diseases +MONDO:0011898 rare diseases +MONDO:0011899 clingen diseases +MONDO:0011899 gard_rare diseases +MONDO:0011899 nord_rare diseases +MONDO:0011899 ordo_disorder diseases +MONDO:0011899 ordo_malformation_syndrome diseases +MONDO:0011899 orphanet_rare diseases +MONDO:0011899 otar diseases +MONDO:0011899 prototype_pattern diseases +MONDO:0011899 rare diseases +MONDO:0011900 gard_rare diseases +MONDO:0011900 nord_rare diseases +MONDO:0011900 rare diseases +MONDO:0011901 gard_rare diseases +MONDO:0011901 nord_rare diseases +MONDO:0011901 ordo_disorder diseases +MONDO:0011901 orphanet_rare diseases +MONDO:0011901 otar diseases +MONDO:0011901 rare diseases +MONDO:0011902 gard_rare diseases +MONDO:0011902 nord_rare diseases +MONDO:0011902 ordo_disorder diseases +MONDO:0011902 orphanet_rare diseases +MONDO:0011902 otar diseases +MONDO:0011902 rare diseases +MONDO:0011903 gard_rare diseases +MONDO:0011903 nord_rare diseases +MONDO:0011903 ordo_disorder diseases +MONDO:0011903 orphanet_rare diseases +MONDO:0011903 otar diseases +MONDO:0011903 rare diseases +MONDO:0011904 gard_rare diseases +MONDO:0011904 nord_rare diseases +MONDO:0011904 ordo_disorder diseases +MONDO:0011904 orphanet_rare diseases +MONDO:0011904 rare diseases +MONDO:0011906 clingen diseases +MONDO:0011906 gard_rare diseases +MONDO:0011906 nord_rare diseases +MONDO:0011906 ordo_disorder diseases +MONDO:0011906 orphanet_rare diseases +MONDO:0011906 otar diseases +MONDO:0011906 rare diseases +MONDO:0011907 gard_rare diseases +MONDO:0011907 nord_rare diseases +MONDO:0011907 ordo_disorder diseases +MONDO:0011907 ordo_malformation_syndrome diseases +MONDO:0011907 orphanet_rare diseases +MONDO:0011907 otar diseases +MONDO:0011907 rare diseases +MONDO:0011908 gard_rare diseases +MONDO:0011908 nord_rare diseases +MONDO:0011908 ordo_disorder diseases +MONDO:0011908 orphanet_rare diseases +MONDO:0011908 otar diseases +MONDO:0011908 rare diseases +MONDO:0011909 gard_rare diseases +MONDO:0011909 nord_rare diseases +MONDO:0011909 ordo_disorder diseases +MONDO:0011909 orphanet_rare diseases +MONDO:0011909 otar diseases +MONDO:0011909 rare diseases +MONDO:0011911 gard_rare diseases +MONDO:0011911 nord_rare diseases +MONDO:0011911 ordo_disorder diseases +MONDO:0011911 ordo_malformation_syndrome diseases +MONDO:0011911 orphanet_rare diseases +MONDO:0011911 otar diseases +MONDO:0011911 rare diseases +MONDO:0011912 gard_rare diseases +MONDO:0011912 nord_rare diseases +MONDO:0011912 rare diseases +MONDO:0011913 gard_rare diseases +MONDO:0011913 rare diseases +MONDO:0011914 gard_rare diseases +MONDO:0011914 nord_rare diseases +MONDO:0011914 rare diseases +MONDO:0011915 gard_rare diseases +MONDO:0011915 nord_rare diseases +MONDO:0011915 rare diseases +MONDO:0011916 gard_rare diseases +MONDO:0011916 nord_rare diseases +MONDO:0011916 ordo_disorder diseases +MONDO:0011916 orphanet_rare diseases +MONDO:0011916 otar diseases +MONDO:0011916 rare diseases +MONDO:0011920 gard_rare diseases +MONDO:0011920 nord_rare diseases +MONDO:0011920 rare diseases +MONDO:0011921 clingen diseases +MONDO:0011921 gard_rare diseases +MONDO:0011921 nord_rare diseases +MONDO:0011921 rare diseases +MONDO:0011922 gard_rare diseases +MONDO:0011922 nord_rare diseases +MONDO:0011922 ordo_disorder diseases +MONDO:0011922 orphanet_rare diseases +MONDO:0011922 rare diseases +MONDO:0011925 gard_rare diseases +MONDO:0011925 nord_rare diseases +MONDO:0011925 ordo_disorder diseases +MONDO:0011925 ordo_malformation_syndrome diseases +MONDO:0011925 orphanet_rare diseases +MONDO:0011925 otar diseases +MONDO:0011925 rare diseases +MONDO:0011927 gard_rare diseases +MONDO:0011927 nord_rare diseases +MONDO:0011927 ordo_disorder diseases +MONDO:0011927 orphanet_rare diseases +MONDO:0011927 otar diseases +MONDO:0011927 rare diseases +MONDO:0011928 gard_rare diseases +MONDO:0011928 nord_rare diseases +MONDO:0011928 ordo_disorder diseases +MONDO:0011928 ordo_malformation_syndrome diseases +MONDO:0011928 orphanet_rare diseases +MONDO:0011928 otar diseases +MONDO:0011928 rare diseases +MONDO:0011929 gard_rare diseases +MONDO:0011929 nord_rare diseases +MONDO:0011929 ordo_disorder diseases +MONDO:0011929 ordo_malformation_syndrome diseases +MONDO:0011929 orphanet_rare diseases +MONDO:0011929 otar diseases +MONDO:0011929 rare diseases +MONDO:0011930 gard_rare diseases +MONDO:0011930 nord_rare diseases +MONDO:0011930 rare diseases +MONDO:0011931 gard_rare diseases +MONDO:0011931 predisposition diseases +MONDO:0011931 rare diseases +MONDO:0011932 gard_rare diseases +MONDO:0011932 nord_rare diseases +MONDO:0011932 rare diseases +MONDO:0011933 gard_rare diseases +MONDO:0011933 nord_rare diseases +MONDO:0011933 ordo_disorder diseases +MONDO:0011933 orphanet_rare diseases +MONDO:0011933 otar diseases +MONDO:0011933 rare diseases +MONDO:0011934 gard_rare diseases +MONDO:0011934 nord_rare diseases +MONDO:0011934 ordo_disorder diseases +MONDO:0011934 orphanet_rare diseases +MONDO:0011934 otar diseases +MONDO:0011934 rare diseases +MONDO:0011935 gard_rare diseases +MONDO:0011935 nord_rare diseases +MONDO:0011935 rare diseases +MONDO:0011936 gard_rare diseases +MONDO:0011936 nord_rare diseases +MONDO:0011936 ordo_disorder diseases +MONDO:0011936 ordo_malformation_syndrome diseases +MONDO:0011936 orphanet_rare diseases +MONDO:0011936 otar diseases +MONDO:0011936 rare diseases +MONDO:0011937 gard_rare diseases +MONDO:0011937 nord_rare diseases +MONDO:0011937 rare diseases +MONDO:0011938 gard_rare diseases +MONDO:0011938 nord_rare diseases +MONDO:0011938 rare diseases +MONDO:0011939 gard_rare diseases +MONDO:0011939 nord_rare diseases +MONDO:0011939 ordo_disorder diseases +MONDO:0011939 ordo_malformation_syndrome diseases +MONDO:0011939 orphanet_rare diseases +MONDO:0011939 otar diseases +MONDO:0011939 rare diseases +MONDO:0011945 gard_rare diseases +MONDO:0011945 nord_rare diseases +MONDO:0011945 ordo_subtype_of_a_disorder diseases +MONDO:0011945 otar diseases +MONDO:0011945 rare diseases +MONDO:0011946 gard_rare diseases +MONDO:0011946 nord_rare diseases +MONDO:0011946 ordo_disorder diseases +MONDO:0011946 ordo_malformation_syndrome diseases +MONDO:0011946 orphanet_rare diseases +MONDO:0011946 otar diseases +MONDO:0011946 rare diseases +MONDO:0011948 gard_rare diseases +MONDO:0011948 nord_rare diseases +MONDO:0011948 ordo_disorder diseases +MONDO:0011948 ordo_malformation_syndrome diseases +MONDO:0011948 orphanet_rare diseases +MONDO:0011948 otar diseases +MONDO:0011948 rare diseases +MONDO:0011950 gard_rare diseases +MONDO:0011950 nord_rare diseases +MONDO:0011950 ordo_disorder diseases +MONDO:0011950 orphanet_rare diseases +MONDO:0011950 otar diseases +MONDO:0011950 rare diseases +MONDO:0011951 clingen diseases +MONDO:0011951 gard_rare diseases +MONDO:0011951 nord_rare diseases +MONDO:0011951 rare diseases +MONDO:0011952 gard_rare diseases +MONDO:0011952 nord_rare diseases +MONDO:0011952 rare diseases +MONDO:0011953 gard_rare diseases +MONDO:0011953 nord_rare diseases +MONDO:0011953 ordo_disorder diseases +MONDO:0011953 orphanet_rare diseases +MONDO:0011953 otar diseases +MONDO:0011953 predisposition diseases +MONDO:0011953 rare diseases +MONDO:0011954 inferred_rare diseases +MONDO:0011954 predisposition diseases +MONDO:0011954 rare diseases +MONDO:0011955 gard_rare diseases +MONDO:0011955 rare diseases +MONDO:0011957 gard_rare diseases +MONDO:0011957 nord_rare diseases +MONDO:0011957 ordo_disorder diseases +MONDO:0011957 orphanet_rare diseases +MONDO:0011957 otar diseases +MONDO:0011957 rare diseases +MONDO:0011959 gard_rare diseases +MONDO:0011959 nord_rare diseases +MONDO:0011959 ordo_disorder diseases +MONDO:0011959 orphanet_rare diseases +MONDO:0011959 otar diseases +MONDO:0011959 rare diseases +MONDO:0011961 gard_rare diseases +MONDO:0011961 nord_rare diseases +MONDO:0011961 ordo_disorder diseases +MONDO:0011961 orphanet_rare diseases +MONDO:0011961 otar diseases +MONDO:0011961 rare diseases +MONDO:0011962 otar diseases +MONDO:0011963 gard_rare diseases +MONDO:0011963 nord_rare diseases +MONDO:0011963 rare diseases +MONDO:0011964 gard_rare diseases +MONDO:0011964 nord_rare diseases +MONDO:0011964 ordo_disorder diseases +MONDO:0011964 orphanet_rare diseases +MONDO:0011964 otar diseases +MONDO:0011964 rare diseases +MONDO:0011965 gard_rare diseases +MONDO:0011965 nord_rare diseases +MONDO:0011965 otar diseases +MONDO:0011965 rare diseases +MONDO:0011966 gard_rare diseases +MONDO:0011966 nord_rare diseases +MONDO:0011966 rare diseases +MONDO:0011967 gard_rare diseases +MONDO:0011967 nord_rare diseases +MONDO:0011967 rare diseases +MONDO:0011968 gard_rare diseases +MONDO:0011968 nord_rare diseases +MONDO:0011968 ordo_disorder diseases +MONDO:0011968 orphanet_rare diseases +MONDO:0011968 otar diseases +MONDO:0011968 rare diseases +MONDO:0011969 gard_rare diseases +MONDO:0011969 nord_rare diseases +MONDO:0011969 ordo_disorder diseases +MONDO:0011969 orphanet_rare diseases +MONDO:0011969 otar diseases +MONDO:0011969 rare diseases +MONDO:0011970 gard_rare diseases +MONDO:0011970 nord_rare diseases +MONDO:0011970 ordo_disorder diseases +MONDO:0011970 orphanet_rare diseases +MONDO:0011970 otar diseases +MONDO:0011970 rare diseases +MONDO:0011971 clingen diseases +MONDO:0011971 gard_rare diseases +MONDO:0011971 nord_rare diseases +MONDO:0011971 ordo_subtype_of_a_disorder diseases +MONDO:0011971 otar diseases +MONDO:0011971 rare diseases +MONDO:0011972 gard_rare diseases +MONDO:0011972 nord_rare diseases +MONDO:0011972 ordo_disorder diseases +MONDO:0011972 orphanet_rare diseases +MONDO:0011972 otar diseases +MONDO:0011972 rare diseases +MONDO:0011973 otar diseases +MONDO:0011974 gard_rare diseases +MONDO:0011974 nord_rare diseases +MONDO:0011974 rare diseases +MONDO:0011975 gard_rare diseases +MONDO:0011975 nord_rare diseases +MONDO:0011975 ordo_etiological_subtype diseases +MONDO:0011975 ordo_subtype_of_a_disorder diseases +MONDO:0011975 otar diseases +MONDO:0011975 rare diseases +MONDO:0011976 gard_rare diseases +MONDO:0011976 ordo_disorder diseases +MONDO:0011976 orphanet_rare diseases +MONDO:0011976 otar diseases +MONDO:0011976 rare diseases +MONDO:0011977 gard_rare diseases +MONDO:0011977 nord_rare diseases +MONDO:0011977 ordo_disorder diseases +MONDO:0011977 ordo_malformation_syndrome diseases +MONDO:0011977 orphanet_rare diseases +MONDO:0011977 otar diseases +MONDO:0011977 rare diseases +MONDO:0011978 n_of_one diseases +MONDO:0011979 gard_rare diseases +MONDO:0011979 nord_rare diseases +MONDO:0011979 ordo_disorder diseases +MONDO:0011979 orphanet_rare diseases +MONDO:0011979 otar diseases +MONDO:0011979 rare diseases +MONDO:0011984 gard_rare diseases +MONDO:0011984 nord_rare diseases +MONDO:0011984 ordo_subtype_of_a_disorder diseases +MONDO:0011984 otar diseases +MONDO:0011984 rare diseases +MONDO:0011985 gard_rare diseases +MONDO:0011985 nord_rare diseases +MONDO:0011985 ordo_subtype_of_a_disorder diseases +MONDO:0011985 otar diseases +MONDO:0011985 rare diseases +MONDO:0011986 gard_rare diseases +MONDO:0011986 nord_rare diseases +MONDO:0011986 ordo_disorder diseases +MONDO:0011986 orphanet_rare diseases +MONDO:0011986 rare diseases +MONDO:0011987 gard_rare diseases +MONDO:0011987 nord_rare diseases +MONDO:0011987 rare diseases +MONDO:0011988 clingen diseases +MONDO:0011988 gard_rare diseases +MONDO:0011988 nord_rare diseases +MONDO:0011988 ordo_disorder diseases +MONDO:0011988 orphanet_rare diseases +MONDO:0011988 otar diseases +MONDO:0011988 rare diseases +MONDO:0011989 gard_rare diseases +MONDO:0011989 nord_rare diseases +MONDO:0011989 ordo_disorder diseases +MONDO:0011989 orphanet_rare diseases +MONDO:0011989 otar diseases +MONDO:0011989 rare diseases +MONDO:0011990 gard_rare diseases +MONDO:0011990 nord_rare diseases +MONDO:0011990 rare diseases +MONDO:0011991 gard_rare diseases +MONDO:0011991 nord_rare diseases +MONDO:0011991 rare diseases +MONDO:0011992 gard_rare diseases +MONDO:0011992 ordo_disorder diseases +MONDO:0011992 orphanet_rare diseases +MONDO:0011992 otar diseases +MONDO:0011992 rare diseases +MONDO:0011994 gard_rare diseases +MONDO:0011994 nord_rare diseases +MONDO:0011994 rare diseases +MONDO:0011995 gard_rare diseases +MONDO:0011995 ordo_disorder diseases +MONDO:0011995 ordo_malformation_syndrome diseases +MONDO:0011995 orphanet_rare diseases +MONDO:0011995 otar diseases +MONDO:0011995 rare diseases +MONDO:0011996 gard_rare diseases +MONDO:0011996 nord_rare diseases +MONDO:0011996 ordo_disorder diseases +MONDO:0011996 orphanet_rare diseases +MONDO:0011996 otar diseases +MONDO:0011996 rare diseases +MONDO:0011997 clingen diseases +MONDO:0011997 gard_rare diseases +MONDO:0011997 nord_rare diseases +MONDO:0011997 ordo_subtype_of_a_disorder diseases +MONDO:0011997 otar diseases +MONDO:0011997 rare diseases +MONDO:0011998 clingen diseases +MONDO:0011998 gard_rare diseases +MONDO:0011998 nord_rare diseases +MONDO:0011998 ordo_disorder diseases +MONDO:0011998 orphanet_rare diseases +MONDO:0011998 otar diseases +MONDO:0011998 rare diseases +MONDO:0011999 gard_rare diseases +MONDO:0011999 rare diseases +MONDO:0012000 otar diseases +MONDO:0012002 gard_rare diseases +MONDO:0012002 nord_rare diseases +MONDO:0012002 rare diseases +MONDO:0012003 gard_rare diseases +MONDO:0012003 nord_rare diseases +MONDO:0012003 rare diseases +MONDO:0012004 gard_rare diseases +MONDO:0012004 ordo_disorder diseases +MONDO:0012004 orphanet_rare diseases +MONDO:0012004 otar diseases +MONDO:0012004 rare diseases +MONDO:0012006 gard_rare diseases +MONDO:0012006 rare diseases +MONDO:0012008 gard_rare diseases +MONDO:0012008 nord_rare diseases +MONDO:0012008 ordo_disorder diseases +MONDO:0012008 ordo_malformation_syndrome diseases +MONDO:0012008 orphanet_rare diseases +MONDO:0012008 otar diseases +MONDO:0012008 rare diseases +MONDO:0012012 gard_rare diseases +MONDO:0012012 nord_rare diseases +MONDO:0012012 ordo_disorder diseases +MONDO:0012012 orphanet_rare diseases +MONDO:0012012 otar diseases +MONDO:0012012 rare diseases +MONDO:0012013 gard_rare diseases +MONDO:0012013 nord_rare diseases +MONDO:0012013 ordo_disorder diseases +MONDO:0012013 ordo_malformation_syndrome diseases +MONDO:0012013 orphanet_rare diseases +MONDO:0012013 otar diseases +MONDO:0012013 rare diseases +MONDO:0012014 gard_rare diseases +MONDO:0012014 nord_rare diseases +MONDO:0012014 ordo_disorder diseases +MONDO:0012014 orphanet_rare diseases +MONDO:0012014 otar diseases +MONDO:0012014 rare diseases +MONDO:0012016 gard_rare diseases +MONDO:0012016 nord_rare diseases +MONDO:0012016 ordo_disorder diseases +MONDO:0012016 ordo_malformation_syndrome diseases +MONDO:0012016 orphanet_rare diseases +MONDO:0012016 otar diseases +MONDO:0012016 rare diseases +MONDO:0012019 gard_rare diseases +MONDO:0012019 nord_rare diseases +MONDO:0012019 ordo_disorder diseases +MONDO:0012019 orphanet_rare diseases +MONDO:0012019 otar diseases +MONDO:0012019 rare diseases +MONDO:0012020 gard_rare diseases +MONDO:0012020 nord_rare diseases +MONDO:0012020 ordo_disorder diseases +MONDO:0012020 ordo_malformation_syndrome diseases +MONDO:0012020 orphanet_rare diseases +MONDO:0012020 otar diseases +MONDO:0012020 rare diseases +MONDO:0012023 gard_rare diseases +MONDO:0012023 nord_rare diseases +MONDO:0012023 rare diseases +MONDO:0012024 gard_rare diseases +MONDO:0012024 nord_rare diseases +MONDO:0012024 rare diseases +MONDO:0012025 gard_rare diseases +MONDO:0012025 nord_rare diseases +MONDO:0012025 rare diseases +MONDO:0012029 gard_rare diseases +MONDO:0012029 nord_rare diseases +MONDO:0012029 rare diseases +MONDO:0012030 gard_rare diseases +MONDO:0012030 nord_rare diseases +MONDO:0012030 rare diseases +MONDO:0012031 gard_rare diseases +MONDO:0012031 nord_rare diseases +MONDO:0012031 otar diseases +MONDO:0012031 rare diseases +MONDO:0012032 gard_rare diseases +MONDO:0012032 ordo_disorder diseases +MONDO:0012032 ordo_malformation_syndrome diseases +MONDO:0012032 orphanet_rare diseases +MONDO:0012032 otar diseases +MONDO:0012032 rare diseases +MONDO:0012033 clingen diseases +MONDO:0012033 gard_rare diseases +MONDO:0012033 nord_rare diseases +MONDO:0012033 ordo_disorder diseases +MONDO:0012033 orphanet_rare diseases +MONDO:0012033 otar diseases +MONDO:0012033 rare diseases +MONDO:0012034 gard_rare diseases +MONDO:0012034 nord_rare diseases +MONDO:0012034 ordo_disorder diseases +MONDO:0012034 orphanet_rare diseases +MONDO:0012034 otar diseases +MONDO:0012034 rare diseases +MONDO:0012035 gard_rare diseases +MONDO:0012035 ordo_disorder diseases +MONDO:0012035 ordo_malformation_syndrome diseases +MONDO:0012035 orphanet_rare diseases +MONDO:0012035 rare diseases +MONDO:0012037 gard_rare diseases +MONDO:0012037 nord_rare diseases +MONDO:0012037 rare diseases +MONDO:0012041 clingen diseases +MONDO:0012041 gard_rare diseases +MONDO:0012041 nord_rare diseases +MONDO:0012041 ordo_subtype_of_a_disorder diseases +MONDO:0012041 otar diseases +MONDO:0012041 rare diseases +MONDO:0012043 gard_rare diseases +MONDO:0012043 nord_rare diseases +MONDO:0012043 ordo_disorder diseases +MONDO:0012043 orphanet_rare diseases +MONDO:0012043 otar diseases +MONDO:0012043 rare diseases +MONDO:0012044 gard_rare diseases +MONDO:0012044 nord_rare diseases +MONDO:0012044 rare diseases +MONDO:0012046 gard_rare diseases +MONDO:0012046 rare diseases +MONDO:0012049 gard_rare diseases +MONDO:0012049 nord_rare diseases +MONDO:0012049 rare diseases +MONDO:0012052 gard_rare diseases +MONDO:0012052 nord_rare diseases +MONDO:0012052 ordo_disorder diseases +MONDO:0012052 orphanet_rare diseases +MONDO:0012052 otar diseases +MONDO:0012052 rare diseases +MONDO:0012053 gard_rare diseases +MONDO:0012053 nord_rare diseases +MONDO:0012053 rare diseases +MONDO:0012055 gard_rare diseases +MONDO:0012055 nord_rare diseases +MONDO:0012055 ordo_disorder diseases +MONDO:0012055 ordo_malformation_syndrome diseases +MONDO:0012055 orphanet_rare diseases +MONDO:0012055 otar diseases +MONDO:0012055 rare diseases +MONDO:0012056 gard_rare diseases +MONDO:0012056 nord_rare diseases +MONDO:0012056 rare diseases +MONDO:0012059 gard_rare diseases +MONDO:0012059 nord_rare diseases +MONDO:0012059 rare diseases +MONDO:0012060 gard_rare diseases +MONDO:0012060 nord_rare diseases +MONDO:0012060 rare diseases +MONDO:0012061 gard_rare diseases +MONDO:0012061 nord_rare diseases +MONDO:0012061 ordo_disorder diseases +MONDO:0012061 orphanet_rare diseases +MONDO:0012061 otar diseases +MONDO:0012061 rare diseases +MONDO:0012062 gard_rare diseases +MONDO:0012062 nord_rare diseases +MONDO:0012062 rare diseases +MONDO:0012063 gard_rare diseases +MONDO:0012063 ordo_disorder diseases +MONDO:0012063 ordo_malformation_syndrome diseases +MONDO:0012063 orphanet_rare diseases +MONDO:0012063 otar diseases +MONDO:0012063 rare diseases +MONDO:0012064 gard_rare diseases +MONDO:0012064 ordo_disorder diseases +MONDO:0012064 ordo_malformation_syndrome diseases +MONDO:0012064 orphanet_rare diseases +MONDO:0012064 otar diseases +MONDO:0012064 rare diseases +MONDO:0012066 gard_rare diseases +MONDO:0012066 rare diseases +MONDO:0012069 gard_rare diseases +MONDO:0012069 nord_rare diseases +MONDO:0012069 rare diseases +MONDO:0012071 gard_rare diseases +MONDO:0012071 nord_rare diseases +MONDO:0012071 rare diseases +MONDO:0012072 gard_rare diseases +MONDO:0012072 nord_rare diseases +MONDO:0012072 ordo_disorder diseases +MONDO:0012072 orphanet_rare diseases +MONDO:0012072 otar diseases +MONDO:0012072 rare diseases +MONDO:0012073 gard_rare diseases +MONDO:0012073 nord_rare diseases +MONDO:0012073 ordo_disorder diseases +MONDO:0012073 orphanet_rare diseases +MONDO:0012073 otar diseases +MONDO:0012073 rare diseases +MONDO:0012074 clingen diseases +MONDO:0012074 gard_rare diseases +MONDO:0012074 nord_rare diseases +MONDO:0012074 ordo_subtype_of_a_disorder diseases +MONDO:0012074 otar diseases +MONDO:0012074 rare diseases +MONDO:0012075 clingen diseases +MONDO:0012075 gard_rare diseases +MONDO:0012075 nord_rare diseases +MONDO:0012075 ordo_disorder diseases +MONDO:0012075 orphanet_rare diseases +MONDO:0012075 otar diseases +MONDO:0012075 rare diseases +MONDO:0012077 clingen diseases +MONDO:0012077 gard_rare diseases +MONDO:0012077 nord_rare diseases +MONDO:0012077 rare diseases +MONDO:0012078 clingen diseases +MONDO:0012078 gard_rare diseases +MONDO:0012078 nord_rare diseases +MONDO:0012078 rare diseases +MONDO:0012080 gard_rare diseases +MONDO:0012080 nord_rare diseases +MONDO:0012080 rare diseases +MONDO:0012081 gard_rare diseases +MONDO:0012081 nord_rare diseases +MONDO:0012081 ordo_disorder diseases +MONDO:0012081 ordo_malformation_syndrome diseases +MONDO:0012081 orphanet_rare diseases +MONDO:0012081 otar diseases +MONDO:0012081 predisposition diseases +MONDO:0012081 rare diseases +MONDO:0012083 gard_rare diseases +MONDO:0012083 nord_rare diseases +MONDO:0012083 rare diseases +MONDO:0012084 clingen diseases +MONDO:0012084 gard_rare diseases +MONDO:0012084 nord_rare diseases +MONDO:0012084 ordo_disorder diseases +MONDO:0012084 orphanet_rare diseases +MONDO:0012084 otar diseases +MONDO:0012084 rare diseases +MONDO:0012085 clingen diseases +MONDO:0012085 gard_rare diseases +MONDO:0012085 nord_rare diseases +MONDO:0012085 rare diseases +MONDO:0012086 gard_rare diseases +MONDO:0012086 nord_rare diseases +MONDO:0012086 rare diseases +MONDO:0012087 gard_rare diseases +MONDO:0012087 nord_rare diseases +MONDO:0012087 rare diseases +MONDO:0012088 clingen diseases +MONDO:0012088 gard_rare diseases +MONDO:0012088 nord_rare diseases +MONDO:0012088 otar diseases +MONDO:0012088 rare diseases +MONDO:0012089 gard_rare diseases +MONDO:0012089 nord_rare diseases +MONDO:0012089 ordo_disorder diseases +MONDO:0012089 orphanet_rare diseases +MONDO:0012089 otar diseases +MONDO:0012089 rare diseases +MONDO:0012090 gard_rare diseases +MONDO:0012090 nord_rare diseases +MONDO:0012090 rare diseases +MONDO:0012091 gard_rare diseases +MONDO:0012091 nord_rare diseases +MONDO:0012091 rare diseases +MONDO:0012092 gard_rare diseases +MONDO:0012092 nord_rare diseases +MONDO:0012092 ordo_disorder diseases +MONDO:0012092 orphanet_rare diseases +MONDO:0012092 otar diseases +MONDO:0012092 rare diseases +MONDO:0012093 gard_rare diseases +MONDO:0012093 rare diseases +MONDO:0012094 gard_rare diseases +MONDO:0012094 rare diseases +MONDO:0012095 gard_rare diseases +MONDO:0012095 nord_rare diseases +MONDO:0012095 ordo_disorder diseases +MONDO:0012095 ordo_malformation_syndrome diseases +MONDO:0012095 orphanet_rare diseases +MONDO:0012095 otar diseases +MONDO:0012095 rare diseases +MONDO:0012096 gard_rare diseases +MONDO:0012096 nord_rare diseases +MONDO:0012096 ordo_disorder diseases +MONDO:0012096 orphanet_rare diseases +MONDO:0012096 otar diseases +MONDO:0012096 rare diseases +MONDO:0012097 gard_rare diseases +MONDO:0012097 nord_rare diseases +MONDO:0012097 rare diseases +MONDO:0012098 gard_rare diseases +MONDO:0012098 nord_rare diseases +MONDO:0012098 ordo_disorder diseases +MONDO:0012098 orphanet_rare diseases +MONDO:0012098 otar diseases +MONDO:0012098 rare diseases +MONDO:0012099 gard_rare diseases +MONDO:0012099 nord_rare diseases +MONDO:0012099 ordo_disorder diseases +MONDO:0012099 orphanet_rare diseases +MONDO:0012099 otar diseases +MONDO:0012099 rare diseases +MONDO:0012101 gard_rare diseases +MONDO:0012101 rare diseases +MONDO:0012102 gard_rare diseases +MONDO:0012102 rare diseases +MONDO:0012103 gard_rare diseases +MONDO:0012103 nord_rare diseases +MONDO:0012103 ordo_disorder diseases +MONDO:0012103 orphanet_rare diseases +MONDO:0012103 otar diseases +MONDO:0012103 rare diseases +MONDO:0012104 gard_rare diseases +MONDO:0012104 nord_rare diseases +MONDO:0012104 ordo_disorder diseases +MONDO:0012104 orphanet_rare diseases +MONDO:0012104 otar diseases +MONDO:0012104 rare diseases +MONDO:0012105 gard_rare diseases +MONDO:0012105 nord_rare diseases +MONDO:0012105 ordo_disorder diseases +MONDO:0012105 orphanet_rare diseases +MONDO:0012105 otar diseases +MONDO:0012105 rare diseases +MONDO:0012106 gard_rare diseases +MONDO:0012106 nord_rare diseases +MONDO:0012106 rare diseases +MONDO:0012108 gard_rare diseases +MONDO:0012108 nord_rare diseases +MONDO:0012108 ordo_disorder diseases +MONDO:0012108 orphanet_rare diseases +MONDO:0012108 otar diseases +MONDO:0012108 rare diseases +MONDO:0012110 gard_rare diseases +MONDO:0012110 nord_rare diseases +MONDO:0012110 ordo_disorder diseases +MONDO:0012110 orphanet_rare diseases +MONDO:0012110 otar diseases +MONDO:0012110 rare diseases +MONDO:0012111 gard_rare diseases +MONDO:0012111 nord_rare diseases +MONDO:0012111 rare diseases +MONDO:0012112 clingen diseases +MONDO:0012112 gard_rare diseases +MONDO:0012112 nord_rare diseases +MONDO:0012112 otar diseases +MONDO:0012112 rare diseases +MONDO:0012114 gard_rare diseases +MONDO:0012114 n_of_one diseases +MONDO:0012114 rare diseases +MONDO:0012116 gard_rare diseases +MONDO:0012116 nord_rare diseases +MONDO:0012116 ordo_disorder diseases +MONDO:0012116 orphanet_rare diseases +MONDO:0012116 otar diseases +MONDO:0012116 rare diseases +MONDO:0012117 gard_rare diseases +MONDO:0012117 nord_rare diseases +MONDO:0012117 ordo_disorder diseases +MONDO:0012117 orphanet_rare diseases +MONDO:0012117 otar diseases +MONDO:0012117 rare diseases +MONDO:0012118 gard_rare diseases +MONDO:0012118 nord_rare diseases +MONDO:0012118 ordo_disorder diseases +MONDO:0012118 orphanet_rare diseases +MONDO:0012118 otar diseases +MONDO:0012118 rare diseases +MONDO:0012120 gard_rare diseases +MONDO:0012120 nord_rare diseases +MONDO:0012120 ordo_subtype_of_a_disorder diseases +MONDO:0012120 otar diseases +MONDO:0012120 rare diseases +MONDO:0012121 gard_rare diseases +MONDO:0012121 rare diseases +MONDO:0012122 gard_rare diseases +MONDO:0012122 nord_rare diseases +MONDO:0012122 rare diseases +MONDO:0012123 clingen diseases +MONDO:0012123 gard_rare diseases +MONDO:0012123 nord_rare diseases +MONDO:0012123 ordo_disorder diseases +MONDO:0012123 orphanet_rare diseases +MONDO:0012123 otar diseases +MONDO:0012123 rare diseases +MONDO:0012124 gard_rare diseases +MONDO:0012124 nord_rare diseases +MONDO:0012124 ordo_disorder diseases +MONDO:0012124 ordo_malformation_syndrome diseases +MONDO:0012124 orphanet_rare diseases +MONDO:0012124 otar diseases +MONDO:0012124 rare diseases +MONDO:0012125 gard_rare diseases +MONDO:0012125 nord_rare diseases +MONDO:0012125 ordo_subtype_of_a_disorder diseases +MONDO:0012125 otar diseases +MONDO:0012125 rare diseases +MONDO:0012126 gard_rare diseases +MONDO:0012126 nord_rare diseases +MONDO:0012126 ordo_disorder diseases +MONDO:0012126 orphanet_rare diseases +MONDO:0012126 otar diseases +MONDO:0012126 prototype_pattern diseases +MONDO:0012126 rare diseases +MONDO:0012127 gard_rare diseases +MONDO:0012127 nord_rare diseases +MONDO:0012127 ordo_disorder diseases +MONDO:0012127 orphanet_rare diseases +MONDO:0012127 otar diseases +MONDO:0012127 rare diseases +MONDO:0012128 gard_rare diseases +MONDO:0012128 nord_rare diseases +MONDO:0012128 rare diseases +MONDO:0012130 gard_rare diseases +MONDO:0012130 nord_rare diseases +MONDO:0012130 ordo_disorder diseases +MONDO:0012130 orphanet_rare diseases +MONDO:0012130 otar diseases +MONDO:0012130 rare diseases +MONDO:0012131 gard_rare diseases +MONDO:0012131 nord_rare diseases +MONDO:0012131 ordo_disorder diseases +MONDO:0012131 orphanet_rare diseases +MONDO:0012131 rare diseases +MONDO:0012132 clingen diseases +MONDO:0012132 gard_rare diseases +MONDO:0012132 predisposition diseases +MONDO:0012132 rare diseases +MONDO:0012136 gard_rare diseases +MONDO:0012136 nord_rare diseases +MONDO:0012136 ordo_subtype_of_a_disorder diseases +MONDO:0012136 otar diseases +MONDO:0012136 rare diseases +MONDO:0012137 gard_rare diseases +MONDO:0012137 nord_rare diseases +MONDO:0012137 ordo_disorder diseases +MONDO:0012137 orphanet_rare diseases +MONDO:0012137 otar diseases +MONDO:0012137 rare diseases +MONDO:0012138 gard_rare diseases +MONDO:0012138 otar diseases +MONDO:0012138 rare diseases +MONDO:0012139 gard_rare diseases +MONDO:0012139 nord_rare diseases +MONDO:0012139 rare diseases +MONDO:0012142 gard_rare diseases +MONDO:0012142 rare diseases +MONDO:0012143 gard_rare diseases +MONDO:0012143 nord_rare diseases +MONDO:0012143 ordo_disorder diseases +MONDO:0012143 orphanet_rare diseases +MONDO:0012143 otar diseases +MONDO:0012143 rare diseases +MONDO:0012144 inferred_rare diseases +MONDO:0012144 rare diseases +MONDO:0012145 gard_rare diseases +MONDO:0012145 nord_rare diseases +MONDO:0012145 rare diseases +MONDO:0012146 gard_rare diseases +MONDO:0012146 nord_rare diseases +MONDO:0012146 rare diseases +MONDO:0012154 gard_rare diseases +MONDO:0012154 nord_rare diseases +MONDO:0012154 rare diseases +MONDO:0012155 gard_rare diseases +MONDO:0012155 nord_rare diseases +MONDO:0012155 ordo_disorder diseases +MONDO:0012155 ordo_morphological_anomaly diseases +MONDO:0012155 orphanet_rare diseases +MONDO:0012155 otar diseases +MONDO:0012155 rare diseases +MONDO:0012156 gard_rare diseases +MONDO:0012156 nord_rare diseases +MONDO:0012156 rare diseases +MONDO:0012157 gard_rare diseases +MONDO:0012157 nord_rare diseases +MONDO:0012157 rare diseases +MONDO:0012158 gard_rare diseases +MONDO:0012158 nord_rare diseases +MONDO:0012158 rare diseases +MONDO:0012159 gard_rare diseases +MONDO:0012159 rare diseases +MONDO:0012160 clingen diseases +MONDO:0012160 gard_rare diseases +MONDO:0012160 nord_rare diseases +MONDO:0012160 ordo_disorder diseases +MONDO:0012160 orphanet_rare diseases +MONDO:0012160 otar diseases +MONDO:0012160 rare diseases +MONDO:0012162 gard_rare diseases +MONDO:0012162 nord_rare diseases +MONDO:0012162 rare diseases +MONDO:0012163 clingen diseases +MONDO:0012163 gard_rare diseases +MONDO:0012163 nord_rare diseases +MONDO:0012163 otar diseases +MONDO:0012163 rare diseases +MONDO:0012164 gard_rare diseases +MONDO:0012164 nord_rare diseases +MONDO:0012164 ordo_disorder diseases +MONDO:0012164 ordo_malformation_syndrome diseases +MONDO:0012164 orphanet_rare diseases +MONDO:0012164 otar diseases +MONDO:0012164 rare diseases +MONDO:0012165 gard_rare diseases +MONDO:0012165 nord_rare diseases +MONDO:0012165 ordo_disorder diseases +MONDO:0012165 ordo_malformation_syndrome diseases +MONDO:0012165 orphanet_rare diseases +MONDO:0012165 otar diseases +MONDO:0012165 rare diseases +MONDO:0012166 gard_rare diseases +MONDO:0012166 nord_rare diseases +MONDO:0012166 rare diseases +MONDO:0012167 gard_rare diseases +MONDO:0012167 nord_rare diseases +MONDO:0012167 rare diseases +MONDO:0012169 gard_rare diseases +MONDO:0012169 nord_rare diseases +MONDO:0012169 rare diseases +MONDO:0012170 gard_rare diseases +MONDO:0012170 nord_rare diseases +MONDO:0012170 rare diseases +MONDO:0012172 clingen diseases +MONDO:0012172 gard_rare diseases +MONDO:0012172 nord_rare diseases +MONDO:0012172 ordo_disorder diseases +MONDO:0012172 orphanet_rare diseases +MONDO:0012172 otar diseases +MONDO:0012172 rare diseases +MONDO:0012173 clingen diseases +MONDO:0012173 gard_rare diseases +MONDO:0012173 nord_rare diseases +MONDO:0012173 ordo_disorder diseases +MONDO:0012173 orphanet_rare diseases +MONDO:0012173 otar diseases +MONDO:0012173 rare diseases +MONDO:0012176 gard_rare diseases +MONDO:0012176 nord_rare diseases +MONDO:0012176 ordo_disorder diseases +MONDO:0012176 ordo_malformation_syndrome diseases +MONDO:0012176 orphanet_rare diseases +MONDO:0012176 otar diseases +MONDO:0012176 rare diseases +MONDO:0012177 gard_rare diseases +MONDO:0012177 nord_rare diseases +MONDO:0012177 ordo_disorder diseases +MONDO:0012177 orphanet_rare diseases +MONDO:0012177 otar diseases +MONDO:0012177 rare diseases +MONDO:0012179 gard_rare diseases +MONDO:0012179 nord_rare diseases +MONDO:0012179 rare diseases +MONDO:0012180 gard_rare diseases +MONDO:0012180 nord_rare diseases +MONDO:0012180 rare diseases +MONDO:0012181 gard_rare diseases +MONDO:0012181 nord_rare diseases +MONDO:0012181 ordo_disorder diseases +MONDO:0012181 orphanet_rare diseases +MONDO:0012181 otar diseases +MONDO:0012181 rare diseases +MONDO:0012183 clingen diseases +MONDO:0012183 inferred_rare diseases +MONDO:0012183 predisposition diseases +MONDO:0012183 rare diseases +MONDO:0012184 gard_rare diseases +MONDO:0012184 nord_rare diseases +MONDO:0012184 ordo_disorder diseases +MONDO:0012184 ordo_malformation_syndrome diseases +MONDO:0012184 orphanet_rare diseases +MONDO:0012184 otar diseases +MONDO:0012184 rare diseases +MONDO:0012185 gard_rare diseases +MONDO:0012185 nord_rare diseases +MONDO:0012185 ordo_disorder diseases +MONDO:0012185 orphanet_rare diseases +MONDO:0012185 otar diseases +MONDO:0012185 rare diseases +MONDO:0012186 clingen diseases +MONDO:0012186 gard_rare diseases +MONDO:0012186 nord_rare diseases +MONDO:0012186 otar diseases +MONDO:0012186 rare diseases +MONDO:0012187 clingen diseases +MONDO:0012187 gard_rare diseases +MONDO:0012187 nord_rare diseases +MONDO:0012187 otar diseases +MONDO:0012187 rare diseases +MONDO:0012188 gard_rare diseases +MONDO:0012188 nord_rare diseases +MONDO:0012188 ordo_etiological_subtype diseases +MONDO:0012188 otar diseases +MONDO:0012188 rare diseases +MONDO:0012190 gard_rare diseases +MONDO:0012190 nord_rare diseases +MONDO:0012190 ordo_disorder diseases +MONDO:0012190 orphanet_rare diseases +MONDO:0012190 otar diseases +MONDO:0012190 rare diseases +MONDO:0012191 gard_rare diseases +MONDO:0012191 nord_rare diseases +MONDO:0012191 ordo_disorder diseases +MONDO:0012191 orphanet_rare diseases +MONDO:0012191 otar diseases +MONDO:0012191 rare diseases +MONDO:0012192 gard_rare diseases +MONDO:0012192 nord_rare diseases +MONDO:0012192 ordo_disorder diseases +MONDO:0012192 ordo_malformation_syndrome diseases +MONDO:0012192 orphanet_rare diseases +MONDO:0012192 otar diseases +MONDO:0012192 rare diseases +MONDO:0012193 gard_rare diseases +MONDO:0012193 nord_rare diseases +MONDO:0012193 ordo_disorder diseases +MONDO:0012193 orphanet_rare diseases +MONDO:0012193 otar diseases +MONDO:0012193 rare diseases +MONDO:0012194 gard_rare diseases +MONDO:0012194 nord_rare diseases +MONDO:0012194 rare diseases +MONDO:0012195 gard_rare diseases +MONDO:0012195 nord_rare diseases +MONDO:0012195 ordo_disorder diseases +MONDO:0012195 ordo_malformation_syndrome diseases +MONDO:0012195 orphanet_rare diseases +MONDO:0012195 otar diseases +MONDO:0012195 rare diseases +MONDO:0012196 gard_rare diseases +MONDO:0012196 nord_rare diseases +MONDO:0012196 rare diseases +MONDO:0012197 gard_rare diseases +MONDO:0012197 nord_rare diseases +MONDO:0012197 ordo_disorder diseases +MONDO:0012197 orphanet_rare diseases +MONDO:0012197 otar diseases +MONDO:0012197 rare diseases +MONDO:0012198 gard_rare diseases +MONDO:0012198 nord_rare diseases +MONDO:0012198 ordo_disorder diseases +MONDO:0012198 orphanet_rare diseases +MONDO:0012198 otar diseases +MONDO:0012198 rare diseases +MONDO:0012199 gard_rare diseases +MONDO:0012199 nord_rare diseases +MONDO:0012199 rare diseases +MONDO:0012200 gard_rare diseases +MONDO:0012200 nord_rare diseases +MONDO:0012200 rare diseases +MONDO:0012203 gard_rare diseases +MONDO:0012203 nord_rare diseases +MONDO:0012203 ordo_disorder diseases +MONDO:0012203 orphanet_rare diseases +MONDO:0012203 otar diseases +MONDO:0012203 rare diseases +MONDO:0012204 gard_rare diseases +MONDO:0012204 nord_rare diseases +MONDO:0012204 ordo_disorder diseases +MONDO:0012204 orphanet_rare diseases +MONDO:0012204 otar diseases +MONDO:0012204 rare diseases +MONDO:0012205 gard_rare diseases +MONDO:0012205 nord_rare diseases +MONDO:0012205 otar diseases +MONDO:0012205 rare diseases +MONDO:0012206 clingen diseases +MONDO:0012206 gard_rare diseases +MONDO:0012206 nord_rare diseases +MONDO:0012206 ordo_disorder diseases +MONDO:0012206 orphanet_rare diseases +MONDO:0012206 otar diseases +MONDO:0012206 rare diseases +MONDO:0012208 gard_rare diseases +MONDO:0012208 nord_rare diseases +MONDO:0012208 ordo_disorder diseases +MONDO:0012208 orphanet_rare diseases +MONDO:0012208 otar diseases +MONDO:0012208 rare diseases +MONDO:0012209 gard_rare diseases +MONDO:0012209 nord_rare diseases +MONDO:0012209 ordo_disorder diseases +MONDO:0012209 ordo_malformation_syndrome diseases +MONDO:0012209 orphanet_rare diseases +MONDO:0012209 otar diseases +MONDO:0012209 rare diseases +MONDO:0012211 gard_rare diseases +MONDO:0012211 nord_rare diseases +MONDO:0012211 ordo_disorder diseases +MONDO:0012211 orphanet_rare diseases +MONDO:0012211 otar diseases +MONDO:0012211 rare diseases +MONDO:0012212 gard_rare diseases +MONDO:0012212 nord_rare diseases +MONDO:0012212 rare diseases +MONDO:0012213 gard_rare diseases +MONDO:0012213 nord_rare diseases +MONDO:0012213 ordo_disorder diseases +MONDO:0012213 orphanet_rare diseases +MONDO:0012213 otar diseases +MONDO:0012213 rare diseases +MONDO:0012214 gard_rare diseases +MONDO:0012214 nord_rare diseases +MONDO:0012214 rare diseases +MONDO:0012215 gard_rare diseases +MONDO:0012215 nord_rare diseases +MONDO:0012215 ordo_disorder diseases +MONDO:0012215 orphanet_rare diseases +MONDO:0012215 otar diseases +MONDO:0012215 rare diseases +MONDO:0012216 clingen diseases +MONDO:0012216 gard_rare diseases +MONDO:0012216 nord_rare diseases +MONDO:0012216 ordo_disorder diseases +MONDO:0012216 orphanet_rare diseases +MONDO:0012216 otar diseases +MONDO:0012216 rare diseases +MONDO:0012217 gard_rare diseases +MONDO:0012217 nord_rare diseases +MONDO:0012217 rare diseases +MONDO:0012219 gard_rare diseases +MONDO:0012219 nord_rare diseases +MONDO:0012219 rare diseases +MONDO:0012220 gard_rare diseases +MONDO:0012220 nord_rare diseases +MONDO:0012220 ordo_subtype_of_a_disorder diseases +MONDO:0012220 otar diseases +MONDO:0012220 rare diseases +MONDO:0012221 gard_rare diseases +MONDO:0012221 nord_rare diseases +MONDO:0012221 ordo_subtype_of_a_disorder diseases +MONDO:0012221 otar diseases +MONDO:0012221 rare diseases +MONDO:0012222 gard_rare diseases +MONDO:0012222 nord_rare diseases +MONDO:0012222 ordo_subtype_of_a_disorder diseases +MONDO:0012222 otar diseases +MONDO:0012222 rare diseases +MONDO:0012225 gard_rare diseases +MONDO:0012225 nord_rare diseases +MONDO:0012225 rare diseases +MONDO:0012231 gard_rare diseases +MONDO:0012231 nord_rare diseases +MONDO:0012231 ordo_disorder diseases +MONDO:0012231 orphanet_rare diseases +MONDO:0012231 otar diseases +MONDO:0012231 rare diseases +MONDO:0012235 gard_rare diseases +MONDO:0012235 nord_rare diseases +MONDO:0012235 ordo_disorder diseases +MONDO:0012235 orphanet_rare diseases +MONDO:0012235 otar diseases +MONDO:0012235 rare diseases +MONDO:0012236 gard_rare diseases +MONDO:0012236 nord_rare diseases +MONDO:0012236 rare diseases +MONDO:0012237 clingen diseases +MONDO:0012237 gard_rare diseases +MONDO:0012237 otar diseases +MONDO:0012237 rare diseases +MONDO:0012238 gard_rare diseases +MONDO:0012238 otar diseases +MONDO:0012238 rare diseases +MONDO:0012239 gard_rare diseases +MONDO:0012239 otar diseases +MONDO:0012239 rare diseases +MONDO:0012240 gard_rare diseases +MONDO:0012240 rare diseases +MONDO:0012241 gard_rare diseases +MONDO:0012241 otar diseases +MONDO:0012241 rare diseases +MONDO:0012243 clingen diseases +MONDO:0012244 gard_rare diseases +MONDO:0012244 rare diseases +MONDO:0012245 gard_rare diseases +MONDO:0012245 nord_rare diseases +MONDO:0012245 rare diseases +MONDO:0012246 gard_rare diseases +MONDO:0012246 nord_rare diseases +MONDO:0012246 ordo_disorder diseases +MONDO:0012246 orphanet_rare diseases +MONDO:0012246 otar diseases +MONDO:0012246 rare diseases +MONDO:0012247 gard_rare diseases +MONDO:0012247 nord_rare diseases +MONDO:0012247 ordo_disorder diseases +MONDO:0012247 orphanet_rare diseases +MONDO:0012247 otar diseases +MONDO:0012247 rare diseases +MONDO:0012248 gard_rare diseases +MONDO:0012248 nord_rare diseases +MONDO:0012248 ordo_disorder diseases +MONDO:0012248 orphanet_rare diseases +MONDO:0012248 otar diseases +MONDO:0012248 rare diseases +MONDO:0012249 gard_rare diseases +MONDO:0012249 nord_rare diseases +MONDO:0012249 rare diseases +MONDO:0012250 gard_rare diseases +MONDO:0012250 nord_rare diseases +MONDO:0012250 ordo_disorder diseases +MONDO:0012250 orphanet_rare diseases +MONDO:0012250 otar diseases +MONDO:0012250 rare diseases +MONDO:0012251 clingen diseases +MONDO:0012251 gard_rare diseases +MONDO:0012251 nord_rare diseases +MONDO:0012251 ordo_disorder diseases +MONDO:0012251 orphanet_rare diseases +MONDO:0012251 otar diseases +MONDO:0012251 rare diseases +MONDO:0012252 clingen diseases +MONDO:0012252 gard_rare diseases +MONDO:0012252 nord_rare diseases +MONDO:0012252 rare diseases +MONDO:0012253 gard_rare diseases +MONDO:0012253 nord_rare diseases +MONDO:0012253 ordo_disorder diseases +MONDO:0012253 orphanet_rare diseases +MONDO:0012253 otar diseases +MONDO:0012253 rare diseases +MONDO:0012254 gard_rare diseases +MONDO:0012254 nord_rare diseases +MONDO:0012254 ordo_disorder diseases +MONDO:0012254 orphanet_rare diseases +MONDO:0012254 otar diseases +MONDO:0012254 rare diseases +MONDO:0012255 gard_rare diseases +MONDO:0012255 nord_rare diseases +MONDO:0012255 rare diseases +MONDO:0012256 gard_rare diseases +MONDO:0012256 nord_rare diseases +MONDO:0012256 ordo_disorder diseases +MONDO:0012256 orphanet_rare diseases +MONDO:0012256 otar diseases +MONDO:0012256 rare diseases +MONDO:0012257 gard_rare diseases +MONDO:0012257 ordo_malformation_syndrome diseases +MONDO:0012257 rare diseases +MONDO:0012258 gard_rare diseases +MONDO:0012258 nord_rare diseases +MONDO:0012258 ordo_disorder diseases +MONDO:0012258 orphanet_rare diseases +MONDO:0012258 otar diseases +MONDO:0012258 rare diseases +MONDO:0012260 gard_rare diseases +MONDO:0012260 nord_rare diseases +MONDO:0012260 rare diseases +MONDO:0012262 gard_rare diseases +MONDO:0012262 nord_rare diseases +MONDO:0012262 rare diseases +MONDO:0012264 gard_rare diseases +MONDO:0012264 nord_rare diseases +MONDO:0012264 rare diseases +MONDO:0012265 gard_rare diseases +MONDO:0012265 nord_rare diseases +MONDO:0012265 rare diseases +MONDO:0012266 gard_rare diseases +MONDO:0012266 nord_rare diseases +MONDO:0012266 rare diseases +MONDO:0012267 gard_rare diseases +MONDO:0012267 nord_rare diseases +MONDO:0012267 rare diseases +MONDO:0012268 otar diseases +MONDO:0012269 gard_rare diseases +MONDO:0012269 nord_rare diseases +MONDO:0012269 ordo_disorder diseases +MONDO:0012269 ordo_malformation_syndrome diseases +MONDO:0012269 orphanet_rare diseases +MONDO:0012269 otar diseases +MONDO:0012269 rare diseases +MONDO:0012270 gard_rare diseases +MONDO:0012270 nord_rare diseases +MONDO:0012270 rare diseases +MONDO:0012271 gard_rare diseases +MONDO:0012271 nord_rare diseases +MONDO:0012271 ordo_disorder diseases +MONDO:0012271 ordo_morphological_anomaly diseases +MONDO:0012271 orphanet_rare diseases +MONDO:0012271 otar diseases +MONDO:0012271 rare diseases +MONDO:0012273 gard_rare diseases +MONDO:0012273 nord_rare diseases +MONDO:0012273 rare diseases +MONDO:0012274 gard_rare diseases +MONDO:0012274 nord_rare diseases +MONDO:0012274 otar diseases +MONDO:0012274 rare diseases +MONDO:0012275 gard_rare diseases +MONDO:0012275 nord_rare diseases +MONDO:0012275 ordo_disorder diseases +MONDO:0012275 ordo_malformation_syndrome diseases +MONDO:0012275 orphanet_rare diseases +MONDO:0012275 rare diseases +MONDO:0012276 clingen diseases +MONDO:0012276 gard_rare diseases +MONDO:0012276 nord_rare diseases +MONDO:0012276 ordo_disorder diseases +MONDO:0012276 orphanet_rare diseases +MONDO:0012276 otar diseases +MONDO:0012276 rare diseases +MONDO:0012277 gard_rare diseases +MONDO:0012277 nord_rare diseases +MONDO:0012277 ordo_disorder diseases +MONDO:0012277 orphanet_rare diseases +MONDO:0012277 otar diseases +MONDO:0012277 rare diseases +MONDO:0012278 gard_rare diseases +MONDO:0012278 nord_rare diseases +MONDO:0012278 rare diseases +MONDO:0012280 gard_rare diseases +MONDO:0012280 nord_rare diseases +MONDO:0012280 ordo_disorder diseases +MONDO:0012280 ordo_malformation_syndrome diseases +MONDO:0012280 orphanet_rare diseases +MONDO:0012280 otar diseases +MONDO:0012280 rare diseases +MONDO:0012282 gard_rare diseases +MONDO:0012282 nord_rare diseases +MONDO:0012282 ordo_malformation_syndrome diseases +MONDO:0012282 otar diseases +MONDO:0012282 rare diseases +MONDO:0012285 gard_rare diseases +MONDO:0012285 nord_rare diseases +MONDO:0012285 rare diseases +MONDO:0012286 gard_rare diseases +MONDO:0012286 rare diseases +MONDO:0012287 gard_rare diseases +MONDO:0012287 nord_rare diseases +MONDO:0012287 rare diseases +MONDO:0012289 clingen diseases +MONDO:0012289 gard_rare diseases +MONDO:0012289 ordo_disorder diseases +MONDO:0012289 orphanet_rare diseases +MONDO:0012289 otar diseases +MONDO:0012289 rare diseases +MONDO:0012290 gard_rare diseases +MONDO:0012290 nord_rare diseases +MONDO:0012290 ordo_disorder diseases +MONDO:0012290 orphanet_rare diseases +MONDO:0012290 otar diseases +MONDO:0012290 rare diseases +MONDO:0012291 gard_rare diseases +MONDO:0012291 nord_rare diseases +MONDO:0012291 rare diseases +MONDO:0012293 gard_rare diseases +MONDO:0012293 nord_rare diseases +MONDO:0012293 rare diseases +MONDO:0012295 gard_rare diseases +MONDO:0012295 rare diseases +MONDO:0012296 gard_rare diseases +MONDO:0012296 nord_rare diseases +MONDO:0012296 ordo_morphological_anomaly diseases +MONDO:0012296 otar diseases +MONDO:0012296 rare diseases +MONDO:0012297 gard_rare diseases +MONDO:0012297 nord_rare diseases +MONDO:0012297 ordo_disorder diseases +MONDO:0012297 orphanet_rare diseases +MONDO:0012297 otar diseases +MONDO:0012297 rare diseases +MONDO:0012299 gard_rare diseases +MONDO:0012299 nord_rare diseases +MONDO:0012299 rare diseases +MONDO:0012300 gard_rare diseases +MONDO:0012300 rare diseases +MONDO:0012301 gard_rare diseases +MONDO:0012301 nord_rare diseases +MONDO:0012301 ordo_disorder diseases +MONDO:0012301 orphanet_rare diseases +MONDO:0012301 otar diseases +MONDO:0012301 rare diseases +MONDO:0012302 gard_rare diseases +MONDO:0012302 nord_rare diseases +MONDO:0012302 rare diseases +MONDO:0012304 gard_rare diseases +MONDO:0012304 rare diseases +MONDO:0012305 gard_rare diseases +MONDO:0012305 rare diseases +MONDO:0012306 gard_rare diseases +MONDO:0012306 nord_rare diseases +MONDO:0012306 rare diseases +MONDO:0012307 gard_rare diseases +MONDO:0012307 nord_rare diseases +MONDO:0012307 ordo_disorder diseases +MONDO:0012307 ordo_malformation_syndrome diseases +MONDO:0012307 orphanet_rare diseases +MONDO:0012307 otar diseases +MONDO:0012307 rare diseases +MONDO:0012308 gard_rare diseases +MONDO:0012308 nord_rare diseases +MONDO:0012308 ordo_disorder diseases +MONDO:0012308 orphanet_rare diseases +MONDO:0012308 otar diseases +MONDO:0012308 rare diseases +MONDO:0012309 gard_rare diseases +MONDO:0012309 nord_rare diseases +MONDO:0012309 rare diseases +MONDO:0012310 gard_rare diseases +MONDO:0012310 nord_rare diseases +MONDO:0012310 rare diseases +MONDO:0012312 gard_rare diseases +MONDO:0012312 rare diseases +MONDO:0012313 gard_rare diseases +MONDO:0012313 rare diseases +MONDO:0012314 gard_rare diseases +MONDO:0012314 rare diseases +MONDO:0012315 gard_rare diseases +MONDO:0012315 nord_rare diseases +MONDO:0012315 ordo_disorder diseases +MONDO:0012315 ordo_malformation_syndrome diseases +MONDO:0012315 orphanet_rare diseases +MONDO:0012315 otar diseases +MONDO:0012315 rare diseases +MONDO:0012316 gard_rare diseases +MONDO:0012316 nord_rare diseases +MONDO:0012316 ordo_disorder diseases +MONDO:0012316 orphanet_rare diseases +MONDO:0012316 otar diseases +MONDO:0012316 rare diseases +MONDO:0012317 gard_rare diseases +MONDO:0012317 nord_rare diseases +MONDO:0012317 rare diseases +MONDO:0012318 inferred_rare diseases +MONDO:0012318 predisposition diseases +MONDO:0012318 rare diseases +MONDO:0012320 gard_rare diseases +MONDO:0012320 nord_rare diseases +MONDO:0012320 otar diseases +MONDO:0012320 rare diseases +MONDO:0012321 gard_rare diseases +MONDO:0012321 rare diseases +MONDO:0012322 gard_rare diseases +MONDO:0012322 nord_rare diseases +MONDO:0012322 otar diseases +MONDO:0012322 rare diseases +MONDO:0012323 gard_rare diseases +MONDO:0012323 nord_rare diseases +MONDO:0012323 ordo_disorder diseases +MONDO:0012323 orphanet_rare diseases +MONDO:0012323 otar diseases +MONDO:0012323 rare diseases +MONDO:0012324 gard_rare diseases +MONDO:0012324 nord_rare diseases +MONDO:0012324 ordo_disorder diseases +MONDO:0012324 ordo_malformation_syndrome diseases +MONDO:0012324 orphanet_rare diseases +MONDO:0012324 otar diseases +MONDO:0012324 rare diseases +MONDO:0012326 gard_rare diseases +MONDO:0012326 nord_rare diseases +MONDO:0012326 rare diseases +MONDO:0012327 gard_rare diseases +MONDO:0012327 nord_rare diseases +MONDO:0012327 rare diseases +MONDO:0012328 otar diseases +MONDO:0012330 gard_rare diseases +MONDO:0012330 ordo_disorder diseases +MONDO:0012330 ordo_malformation_syndrome diseases +MONDO:0012330 orphanet_rare diseases +MONDO:0012330 otar diseases +MONDO:0012330 rare diseases +MONDO:0012333 gard_rare diseases +MONDO:0012333 nord_rare diseases +MONDO:0012333 rare diseases +MONDO:0012334 gard_rare diseases +MONDO:0012334 ordo_disorder diseases +MONDO:0012334 orphanet_rare diseases +MONDO:0012334 otar diseases +MONDO:0012334 rare diseases +MONDO:0012335 gard_rare diseases +MONDO:0012335 nord_rare diseases +MONDO:0012335 ordo_malformation_syndrome diseases +MONDO:0012335 ordo_subtype_of_a_disorder diseases +MONDO:0012335 otar diseases +MONDO:0012335 rare diseases +MONDO:0012336 gard_rare diseases +MONDO:0012336 nord_rare diseases +MONDO:0012336 rare diseases +MONDO:0012342 gard_rare diseases +MONDO:0012342 nord_rare diseases +MONDO:0012342 ordo_disorder diseases +MONDO:0012342 ordo_malformation_syndrome diseases +MONDO:0012342 orphanet_rare diseases +MONDO:0012342 otar diseases +MONDO:0012342 rare diseases +MONDO:0012343 gard_rare diseases +MONDO:0012343 nord_rare diseases +MONDO:0012343 rare diseases +MONDO:0012344 gard_rare diseases +MONDO:0012344 rare diseases +MONDO:0012345 gard_rare diseases +MONDO:0012345 nord_rare diseases +MONDO:0012345 ordo_disorder diseases +MONDO:0012345 orphanet_rare diseases +MONDO:0012345 otar diseases +MONDO:0012345 rare diseases +MONDO:0012346 gard_rare diseases +MONDO:0012346 rare diseases +MONDO:0012348 clingen diseases +MONDO:0012348 gard_rare diseases +MONDO:0012348 nord_rare diseases +MONDO:0012348 rare diseases +MONDO:0012349 gard_rare diseases +MONDO:0012349 nord_rare diseases +MONDO:0012349 rare diseases +MONDO:0012350 gard_rare diseases +MONDO:0012350 nord_rare diseases +MONDO:0012350 otar diseases +MONDO:0012350 rare diseases +MONDO:0012351 gard_rare diseases +MONDO:0012351 nord_rare diseases +MONDO:0012351 ordo_subtype_of_a_disorder diseases +MONDO:0012351 rare diseases +MONDO:0012353 gard_rare diseases +MONDO:0012353 nord_rare diseases +MONDO:0012353 rare diseases +MONDO:0012354 clingen diseases +MONDO:0012354 gard_rare diseases +MONDO:0012354 nord_rare diseases +MONDO:0012354 ordo_disorder diseases +MONDO:0012354 orphanet_rare diseases +MONDO:0012354 otar diseases +MONDO:0012354 rare diseases +MONDO:0012355 gard_rare diseases +MONDO:0012355 nord_rare diseases +MONDO:0012355 rare diseases +MONDO:0012359 gard_rare diseases +MONDO:0012359 nord_rare diseases +MONDO:0012359 ordo_disorder diseases +MONDO:0012359 orphanet_rare diseases +MONDO:0012359 otar diseases +MONDO:0012359 rare diseases +MONDO:0012360 gard_rare diseases +MONDO:0012360 nord_rare diseases +MONDO:0012360 rare diseases +MONDO:0012362 gard_rare diseases +MONDO:0012362 nord_rare diseases +MONDO:0012362 rare diseases +MONDO:0012363 gard_rare diseases +MONDO:0012363 nord_rare diseases +MONDO:0012363 otar diseases +MONDO:0012363 rare diseases +MONDO:0012364 gard_rare diseases +MONDO:0012364 nord_rare diseases +MONDO:0012364 rare diseases +MONDO:0012367 gard_rare diseases +MONDO:0012367 nord_rare diseases +MONDO:0012367 rare diseases +MONDO:0012368 clingen diseases +MONDO:0012368 gard_rare diseases +MONDO:0012368 nord_rare diseases +MONDO:0012368 ordo_disorder diseases +MONDO:0012368 orphanet_rare diseases +MONDO:0012368 otar diseases +MONDO:0012368 rare diseases +MONDO:0012370 gard_rare diseases +MONDO:0012370 nord_rare diseases +MONDO:0012370 rare diseases +MONDO:0012371 gard_rare diseases +MONDO:0012371 nord_rare diseases +MONDO:0012371 rare diseases +MONDO:0012375 gard_rare diseases +MONDO:0012375 nord_rare diseases +MONDO:0012375 rare diseases +MONDO:0012376 gard_rare diseases +MONDO:0012376 nord_rare diseases +MONDO:0012376 rare diseases +MONDO:0012378 gard_rare diseases +MONDO:0012378 nord_rare diseases +MONDO:0012378 rare diseases +MONDO:0012380 gard_rare diseases +MONDO:0012380 nord_rare diseases +MONDO:0012380 rare diseases +MONDO:0012381 gard_rare diseases +MONDO:0012381 nord_rare diseases +MONDO:0012381 ordo_disorder diseases +MONDO:0012381 orphanet_rare diseases +MONDO:0012381 otar diseases +MONDO:0012381 rare diseases +MONDO:0012382 gard_rare diseases +MONDO:0012382 nord_rare diseases +MONDO:0012382 ordo_disorder diseases +MONDO:0012382 orphanet_rare diseases +MONDO:0012382 otar diseases +MONDO:0012382 rare diseases +MONDO:0012383 clingen diseases +MONDO:0012383 gard_rare diseases +MONDO:0012383 nord_rare diseases +MONDO:0012383 ordo_disorder diseases +MONDO:0012383 orphanet_rare diseases +MONDO:0012383 otar diseases +MONDO:0012383 rare diseases +MONDO:0012387 gard_rare diseases +MONDO:0012387 ordo_disorder diseases +MONDO:0012387 orphanet_rare diseases +MONDO:0012387 otar diseases +MONDO:0012387 rare diseases +MONDO:0012391 gard_rare diseases +MONDO:0012391 nord_rare diseases +MONDO:0012391 ordo_disorder diseases +MONDO:0012391 ordo_subtype_of_a_disorder diseases +MONDO:0012391 orphanet_rare diseases +MONDO:0012391 otar diseases +MONDO:0012391 rare diseases +MONDO:0012392 clingen diseases +MONDO:0012392 gard_rare diseases +MONDO:0012392 nord_rare diseases +MONDO:0012392 ordo_disorder diseases +MONDO:0012392 orphanet_rare diseases +MONDO:0012392 otar diseases +MONDO:0012392 rare diseases +MONDO:0012393 clingen diseases +MONDO:0012393 gard_rare diseases +MONDO:0012393 nord_rare diseases +MONDO:0012393 ordo_disorder diseases +MONDO:0012393 orphanet_rare diseases +MONDO:0012393 otar diseases +MONDO:0012393 rare diseases +MONDO:0012394 gard_rare diseases +MONDO:0012394 nord_rare diseases +MONDO:0012394 rare diseases +MONDO:0012395 gard_rare diseases +MONDO:0012395 rare diseases +MONDO:0012396 gard_rare diseases +MONDO:0012396 nord_rare diseases +MONDO:0012396 ordo_disorder diseases +MONDO:0012396 orphanet_rare diseases +MONDO:0012396 otar diseases +MONDO:0012396 rare diseases +MONDO:0012398 gard_rare diseases +MONDO:0012398 rare diseases +MONDO:0012399 gard_rare diseases +MONDO:0012399 nord_rare diseases +MONDO:0012399 ordo_disorder diseases +MONDO:0012399 ordo_malformation_syndrome diseases +MONDO:0012399 orphanet_rare diseases +MONDO:0012399 otar diseases +MONDO:0012399 rare diseases +MONDO:0012400 gard_rare diseases +MONDO:0012400 nord_rare diseases +MONDO:0012400 ordo_disorder diseases +MONDO:0012400 orphanet_rare diseases +MONDO:0012400 otar diseases +MONDO:0012400 rare diseases +MONDO:0012401 gard_rare diseases +MONDO:0012401 nord_rare diseases +MONDO:0012401 ordo_disorder diseases +MONDO:0012401 orphanet_rare diseases +MONDO:0012401 otar diseases +MONDO:0012401 rare diseases +MONDO:0012405 gard_rare diseases +MONDO:0012405 nord_rare diseases +MONDO:0012405 rare diseases +MONDO:0012406 gard_rare diseases +MONDO:0012406 nord_rare diseases +MONDO:0012406 rare diseases +MONDO:0012407 clingen diseases +MONDO:0012407 gard_rare diseases +MONDO:0012407 ordo_disorder diseases +MONDO:0012407 orphanet_rare diseases +MONDO:0012407 otar diseases +MONDO:0012407 rare diseases +MONDO:0012408 gard_rare diseases +MONDO:0012408 nord_rare diseases +MONDO:0012408 rare diseases +MONDO:0012409 gard_rare diseases +MONDO:0012409 nord_rare diseases +MONDO:0012409 rare diseases +MONDO:0012410 gard_rare diseases +MONDO:0012410 ordo_disorder diseases +MONDO:0012410 orphanet_rare diseases +MONDO:0012410 otar diseases +MONDO:0012410 rare diseases +MONDO:0012411 gard_rare diseases +MONDO:0012411 nord_rare diseases +MONDO:0012411 ordo_disorder diseases +MONDO:0012411 orphanet_rare diseases +MONDO:0012411 otar diseases +MONDO:0012411 rare diseases +MONDO:0012412 gard_rare diseases +MONDO:0012412 rare diseases +MONDO:0012413 gard_rare diseases +MONDO:0012413 nord_rare diseases +MONDO:0012413 ordo_disorder diseases +MONDO:0012413 ordo_malformation_syndrome diseases +MONDO:0012413 orphanet_rare diseases +MONDO:0012413 otar diseases +MONDO:0012413 rare diseases +MONDO:0012414 gard_rare diseases +MONDO:0012414 nord_rare diseases +MONDO:0012414 ordo_etiological_subtype diseases +MONDO:0012414 otar diseases +MONDO:0012414 rare diseases +MONDO:0012415 gard_rare diseases +MONDO:0012415 rare diseases +MONDO:0012417 gard_rare diseases +MONDO:0012417 nord_rare diseases +MONDO:0012417 ordo_disorder diseases +MONDO:0012417 ordo_malformation_syndrome diseases +MONDO:0012417 orphanet_rare diseases +MONDO:0012417 otar diseases +MONDO:0012417 rare diseases +MONDO:0012418 gard_rare diseases +MONDO:0012418 nord_rare diseases +MONDO:0012418 rare diseases +MONDO:0012419 gard_rare diseases +MONDO:0012419 nord_rare diseases +MONDO:0012419 rare diseases +MONDO:0012420 gard_rare diseases +MONDO:0012420 nord_rare diseases +MONDO:0012420 rare diseases +MONDO:0012421 gard_rare diseases +MONDO:0012421 nord_rare diseases +MONDO:0012421 rare diseases +MONDO:0012423 clingen diseases +MONDO:0012423 gard_rare diseases +MONDO:0012423 nord_rare diseases +MONDO:0012423 ordo_disorder diseases +MONDO:0012423 orphanet_rare diseases +MONDO:0012423 otar diseases +MONDO:0012423 rare diseases +MONDO:0012425 gard_rare diseases +MONDO:0012425 nord_rare diseases +MONDO:0012425 rare diseases +MONDO:0012426 clingen diseases +MONDO:0012426 gard_rare diseases +MONDO:0012426 nord_rare diseases +MONDO:0012426 otar diseases +MONDO:0012426 rare diseases +MONDO:0012427 clingen diseases +MONDO:0012427 gard_rare diseases +MONDO:0012427 nord_rare diseases +MONDO:0012427 rare diseases +MONDO:0012429 gard_rare diseases +MONDO:0012429 nord_rare diseases +MONDO:0012429 rare diseases +MONDO:0012430 gard_rare diseases +MONDO:0012430 nord_rare diseases +MONDO:0012430 rare diseases +MONDO:0012431 gard_rare diseases +MONDO:0012431 otar diseases +MONDO:0012431 rare diseases +MONDO:0012432 gard_rare diseases +MONDO:0012432 nord_rare diseases +MONDO:0012432 rare diseases +MONDO:0012433 gard_rare diseases +MONDO:0012433 nord_rare diseases +MONDO:0012433 rare diseases +MONDO:0012434 gard_rare diseases +MONDO:0012434 nord_rare diseases +MONDO:0012434 rare diseases +MONDO:0012435 clingen diseases +MONDO:0012435 gard_rare diseases +MONDO:0012435 nord_rare diseases +MONDO:0012435 ordo_disorder diseases +MONDO:0012435 orphanet_rare diseases +MONDO:0012435 otar diseases +MONDO:0012435 rare diseases +MONDO:0012436 gard_rare diseases +MONDO:0012436 nord_rare diseases +MONDO:0012436 ordo_disorder diseases +MONDO:0012436 orphanet_rare diseases +MONDO:0012436 otar diseases +MONDO:0012436 rare diseases +MONDO:0012437 gard_rare diseases +MONDO:0012437 nord_rare diseases +MONDO:0012437 rare diseases +MONDO:0012438 gard_rare diseases +MONDO:0012438 nord_rare diseases +MONDO:0012438 ordo_malformation_syndrome diseases +MONDO:0012438 otar diseases +MONDO:0012438 rare diseases +MONDO:0012439 gard_rare diseases +MONDO:0012439 nord_rare diseases +MONDO:0012439 ordo_etiological_subtype diseases +MONDO:0012439 ordo_subtype_of_a_disorder diseases +MONDO:0012439 otar diseases +MONDO:0012439 rare diseases +MONDO:0012442 gard_rare diseases +MONDO:0012442 nord_rare diseases +MONDO:0012442 rare diseases +MONDO:0012443 gard_rare diseases +MONDO:0012443 nord_rare diseases +MONDO:0012443 rare diseases +MONDO:0012444 gard_rare diseases +MONDO:0012444 nord_rare diseases +MONDO:0012444 rare diseases +MONDO:0012445 gard_rare diseases +MONDO:0012445 nord_rare diseases +MONDO:0012445 rare diseases +MONDO:0012446 gard_rare diseases +MONDO:0012446 nord_rare diseases +MONDO:0012446 ordo_disorder diseases +MONDO:0012446 orphanet_rare diseases +MONDO:0012446 otar diseases +MONDO:0012446 rare diseases +MONDO:0012447 gard_rare diseases +MONDO:0012447 nord_rare diseases +MONDO:0012447 ordo_subtype_of_a_disorder diseases +MONDO:0012447 rare diseases +MONDO:0012448 clingen diseases +MONDO:0012448 gard_rare diseases +MONDO:0012448 otar diseases +MONDO:0012448 rare diseases +MONDO:0012449 gard_rare diseases +MONDO:0012449 nord_rare diseases +MONDO:0012449 ordo_disorder diseases +MONDO:0012449 orphanet_rare diseases +MONDO:0012449 otar diseases +MONDO:0012449 rare diseases +MONDO:0012450 gard_rare diseases +MONDO:0012450 nord_rare diseases +MONDO:0012450 ordo_disorder diseases +MONDO:0012450 orphanet_rare diseases +MONDO:0012450 otar diseases +MONDO:0012450 rare diseases +MONDO:0012451 gard_rare diseases +MONDO:0012451 nord_rare diseases +MONDO:0012451 rare diseases +MONDO:0012452 gard_rare diseases +MONDO:0012452 nord_rare diseases +MONDO:0012452 rare diseases +MONDO:0012453 gard_rare diseases +MONDO:0012453 nord_rare diseases +MONDO:0012453 ordo_disorder diseases +MONDO:0012453 orphanet_rare diseases +MONDO:0012453 otar diseases +MONDO:0012453 rare diseases +MONDO:0012455 clingen diseases +MONDO:0012455 gard_rare diseases +MONDO:0012455 nord_rare diseases +MONDO:0012455 ordo_disorder diseases +MONDO:0012455 ordo_malformation_syndrome diseases +MONDO:0012455 orphanet_rare diseases +MONDO:0012455 otar diseases +MONDO:0012455 prototype_pattern diseases +MONDO:0012455 rare diseases +MONDO:0012456 gard_rare diseases +MONDO:0012456 nord_rare diseases +MONDO:0012456 ordo_disorder diseases +MONDO:0012456 ordo_malformation_syndrome diseases +MONDO:0012456 orphanet_rare diseases +MONDO:0012456 otar diseases +MONDO:0012456 rare diseases +MONDO:0012460 gard_rare diseases +MONDO:0012460 nord_rare diseases +MONDO:0012460 rare diseases +MONDO:0012462 gard_rare diseases +MONDO:0012462 ordo_disorder diseases +MONDO:0012462 ordo_malformation_syndrome diseases +MONDO:0012462 orphanet_rare diseases +MONDO:0012462 otar diseases +MONDO:0012462 rare diseases +MONDO:0012463 gard_rare diseases +MONDO:0012463 nord_rare diseases +MONDO:0012463 rare diseases +MONDO:0012464 gard_rare diseases +MONDO:0012464 nord_rare diseases +MONDO:0012464 rare diseases +MONDO:0012465 gard_rare diseases +MONDO:0012465 nord_rare diseases +MONDO:0012465 ordo_disorder diseases +MONDO:0012465 orphanet_rare diseases +MONDO:0012465 otar diseases +MONDO:0012465 rare diseases +MONDO:0012467 gard_rare diseases +MONDO:0012467 nord_rare diseases +MONDO:0012467 rare diseases +MONDO:0012470 gard_rare diseases +MONDO:0012470 rare diseases +MONDO:0012471 gard_rare diseases +MONDO:0012471 nord_rare diseases +MONDO:0012471 rare diseases +MONDO:0012472 gard_rare diseases +MONDO:0012472 nord_rare diseases +MONDO:0012472 rare diseases +MONDO:0012474 gard_rare diseases +MONDO:0012474 nord_rare diseases +MONDO:0012474 rare diseases +MONDO:0012475 gard_rare diseases +MONDO:0012475 nord_rare diseases +MONDO:0012475 ordo_disorder diseases +MONDO:0012475 orphanet_rare diseases +MONDO:0012475 otar diseases +MONDO:0012475 rare diseases +MONDO:0012476 gard_rare diseases +MONDO:0012476 nord_rare diseases +MONDO:0012476 ordo_disorder diseases +MONDO:0012476 orphanet_rare diseases +MONDO:0012476 otar diseases +MONDO:0012476 rare diseases +MONDO:0012477 gard_rare diseases +MONDO:0012477 nord_rare diseases +MONDO:0012477 rare diseases +MONDO:0012479 gard_rare diseases +MONDO:0012479 nord_rare diseases +MONDO:0012479 ordo_disorder diseases +MONDO:0012479 orphanet_rare diseases +MONDO:0012479 otar diseases +MONDO:0012479 rare diseases +MONDO:0012480 gard_rare diseases +MONDO:0012480 nord_rare diseases +MONDO:0012480 rare diseases +MONDO:0012481 gard_rare diseases +MONDO:0012481 nord_rare diseases +MONDO:0012481 ordo_subtype_of_a_disorder diseases +MONDO:0012481 otar diseases +MONDO:0012481 rare diseases +MONDO:0012483 gard_rare diseases +MONDO:0012483 nord_rare diseases +MONDO:0012483 rare diseases +MONDO:0012485 gard_rare diseases +MONDO:0012485 nord_rare diseases +MONDO:0012485 rare diseases +MONDO:0012487 gard_rare diseases +MONDO:0012487 nord_rare diseases +MONDO:0012487 rare diseases +MONDO:0012489 gard_rare diseases +MONDO:0012489 nord_rare diseases +MONDO:0012489 rare diseases +MONDO:0012490 gard_rare diseases +MONDO:0012490 rare diseases +MONDO:0012491 gard_rare diseases +MONDO:0012491 predisposition diseases +MONDO:0012491 rare diseases +MONDO:0012495 gard_rare diseases +MONDO:0012495 nord_rare diseases +MONDO:0012495 ordo_disorder diseases +MONDO:0012495 orphanet_rare diseases +MONDO:0012495 otar diseases +MONDO:0012495 rare diseases +MONDO:0012496 clingen diseases +MONDO:0012496 gard_rare diseases +MONDO:0012496 nord_rare diseases +MONDO:0012496 ordo_disorder diseases +MONDO:0012496 ordo_malformation_syndrome diseases +MONDO:0012496 orphanet_rare diseases +MONDO:0012496 otar diseases +MONDO:0012496 rare diseases +MONDO:0012497 gard_rare diseases +MONDO:0012497 rare diseases +MONDO:0012498 gard_rare diseases +MONDO:0012498 rare diseases +MONDO:0012500 gard_rare diseases +MONDO:0012500 nord_rare diseases +MONDO:0012500 rare diseases +MONDO:0012502 gard_rare diseases +MONDO:0012502 nord_rare diseases +MONDO:0012502 ordo_subtype_of_a_disorder diseases +MONDO:0012502 otar diseases +MONDO:0012502 rare diseases +MONDO:0012503 gard_rare diseases +MONDO:0012503 otar diseases +MONDO:0012503 rare diseases +MONDO:0012504 clingen diseases +MONDO:0012504 gard_rare diseases +MONDO:0012504 nord_rare diseases +MONDO:0012504 ordo_disorder diseases +MONDO:0012504 orphanet_rare diseases +MONDO:0012504 otar diseases +MONDO:0012504 rare diseases +MONDO:0012505 gard_rare diseases +MONDO:0012505 nord_rare diseases +MONDO:0012505 rare diseases +MONDO:0012506 gard_rare diseases +MONDO:0012506 nord_rare diseases +MONDO:0012506 rare diseases +MONDO:0012507 gard_rare diseases +MONDO:0012507 nord_rare diseases +MONDO:0012507 rare diseases +MONDO:0012508 gard_rare diseases +MONDO:0012508 ordo_disorder diseases +MONDO:0012508 ordo_malformation_syndrome diseases +MONDO:0012508 orphanet_rare diseases +MONDO:0012508 otar diseases +MONDO:0012508 rare diseases +MONDO:0012509 gard_rare diseases +MONDO:0012509 nord_rare diseases +MONDO:0012509 rare diseases +MONDO:0012510 gard_rare diseases +MONDO:0012510 nord_rare diseases +MONDO:0012510 ordo_disorder diseases +MONDO:0012510 orphanet_rare diseases +MONDO:0012510 otar diseases +MONDO:0012510 rare diseases +MONDO:0012511 otar diseases +MONDO:0012512 gard_rare diseases +MONDO:0012512 nord_rare diseases +MONDO:0012512 ordo_disorder diseases +MONDO:0012512 orphanet_rare diseases +MONDO:0012512 otar diseases +MONDO:0012512 rare diseases +MONDO:0012513 gard_rare diseases +MONDO:0012513 nord_rare diseases +MONDO:0012513 rare diseases +MONDO:0012514 gard_rare diseases +MONDO:0012514 nord_rare diseases +MONDO:0012514 ordo_disorder diseases +MONDO:0012514 ordo_malformation_syndrome diseases +MONDO:0012514 orphanet_rare diseases +MONDO:0012514 otar diseases +MONDO:0012514 rare diseases +MONDO:0012515 gard_rare diseases +MONDO:0012515 rare diseases +MONDO:0012516 clingen diseases +MONDO:0012516 gard_rare diseases +MONDO:0012516 nord_rare diseases +MONDO:0012516 ordo_disorder diseases +MONDO:0012516 ordo_malformation_syndrome diseases +MONDO:0012516 orphanet_rare diseases +MONDO:0012516 otar diseases +MONDO:0012516 rare diseases +MONDO:0012517 clingen diseases +MONDO:0012517 gard_rare diseases +MONDO:0012517 nord_rare diseases +MONDO:0012517 ordo_subtype_of_a_disorder diseases +MONDO:0012517 otar diseases +MONDO:0012517 rare diseases +MONDO:0012518 gard_rare diseases +MONDO:0012518 nord_rare diseases +MONDO:0012518 rare diseases +MONDO:0012519 gard_rare diseases +MONDO:0012519 nord_rare diseases +MONDO:0012519 ordo_subtype_of_a_disorder diseases +MONDO:0012519 otar diseases +MONDO:0012519 rare diseases +MONDO:0012520 gard_rare diseases +MONDO:0012520 nord_rare diseases +MONDO:0012520 ordo_disorder diseases +MONDO:0012520 orphanet_rare diseases +MONDO:0012520 otar diseases +MONDO:0012520 rare diseases +MONDO:0012521 gard_rare diseases +MONDO:0012521 nord_rare diseases +MONDO:0012521 ordo_disorder diseases +MONDO:0012521 orphanet_rare diseases +MONDO:0012521 otar diseases +MONDO:0012521 rare diseases +MONDO:0012522 gard_rare diseases +MONDO:0012522 nord_rare diseases +MONDO:0012522 rare diseases +MONDO:0012523 gard_rare diseases +MONDO:0012523 nord_rare diseases +MONDO:0012523 rare diseases +MONDO:0012524 gard_rare diseases +MONDO:0012524 nord_rare diseases +MONDO:0012524 otar diseases +MONDO:0012524 rare diseases +MONDO:0012525 gard_rare diseases +MONDO:0012525 nord_rare diseases +MONDO:0012525 rare diseases +MONDO:0012526 clingen diseases +MONDO:0012526 gard_rare diseases +MONDO:0012526 nord_rare diseases +MONDO:0012526 ordo_etiological_subtype diseases +MONDO:0012526 ordo_subtype_of_a_disorder diseases +MONDO:0012526 otar diseases +MONDO:0012526 rare diseases +MONDO:0012527 gard_rare diseases +MONDO:0012527 nord_rare diseases +MONDO:0012527 rare diseases +MONDO:0012528 clingen diseases +MONDO:0012528 gard_rare diseases +MONDO:0012528 rare diseases +MONDO:0012529 gard_rare diseases +MONDO:0012529 nord_rare diseases +MONDO:0012529 rare diseases +MONDO:0012530 gard_rare diseases +MONDO:0012530 nord_rare diseases +MONDO:0012530 ordo_disorder diseases +MONDO:0012530 orphanet_rare diseases +MONDO:0012530 otar diseases +MONDO:0012530 rare diseases +MONDO:0012531 clingen diseases +MONDO:0012531 gard_rare diseases +MONDO:0012531 nord_rare diseases +MONDO:0012531 otar diseases +MONDO:0012531 rare diseases +MONDO:0012532 gard_rare diseases +MONDO:0012532 nord_rare diseases +MONDO:0012532 rare diseases +MONDO:0012534 gard_rare diseases +MONDO:0012534 nord_rare diseases +MONDO:0012534 ordo_disorder diseases +MONDO:0012534 orphanet_rare diseases +MONDO:0012534 otar diseases +MONDO:0012534 rare diseases +MONDO:0012536 gard_rare diseases +MONDO:0012536 nord_rare diseases +MONDO:0012536 rare diseases +MONDO:0012537 gard_rare diseases +MONDO:0012537 nord_rare diseases +MONDO:0012537 rare diseases +MONDO:0012538 clingen diseases +MONDO:0012538 gard_rare diseases +MONDO:0012538 otar diseases +MONDO:0012538 rare diseases +MONDO:0012539 gard_rare diseases +MONDO:0012539 nord_rare diseases +MONDO:0012539 rare diseases +MONDO:0012540 gard_rare diseases +MONDO:0012540 nord_rare diseases +MONDO:0012540 rare diseases +MONDO:0012541 clingen diseases +MONDO:0012541 gard_rare diseases +MONDO:0012541 nord_rare diseases +MONDO:0012541 ordo_disorder diseases +MONDO:0012541 ordo_malformation_syndrome diseases +MONDO:0012541 orphanet_rare diseases +MONDO:0012541 otar diseases +MONDO:0012541 rare diseases +MONDO:0012543 gard_rare diseases +MONDO:0012543 nord_rare diseases +MONDO:0012543 rare diseases +MONDO:0012544 gard_rare diseases +MONDO:0012544 nord_rare diseases +MONDO:0012544 ordo_disorder diseases +MONDO:0012544 ordo_malformation_syndrome diseases +MONDO:0012544 orphanet_rare diseases +MONDO:0012544 otar diseases +MONDO:0012544 rare diseases +MONDO:0012545 clingen diseases +MONDO:0012545 gard_rare diseases +MONDO:0012545 nord_rare diseases +MONDO:0012545 ordo_disorder diseases +MONDO:0012545 orphanet_rare diseases +MONDO:0012545 otar diseases +MONDO:0012545 rare diseases +MONDO:0012546 gard_rare diseases +MONDO:0012546 rare diseases +MONDO:0012547 gard_rare diseases +MONDO:0012547 nord_rare diseases +MONDO:0012547 rare diseases +MONDO:0012548 gard_rare diseases +MONDO:0012548 nord_rare diseases +MONDO:0012548 ordo_disorder diseases +MONDO:0012548 orphanet_rare diseases +MONDO:0012548 otar diseases +MONDO:0012548 rare diseases +MONDO:0012549 gard_rare diseases +MONDO:0012549 nord_rare diseases +MONDO:0012549 ordo_disorder diseases +MONDO:0012549 orphanet_rare diseases +MONDO:0012549 otar diseases +MONDO:0012549 rare diseases +MONDO:0012551 gard_rare diseases +MONDO:0012551 nord_rare diseases +MONDO:0012551 rare diseases +MONDO:0012552 clingen diseases +MONDO:0012552 gard_rare diseases +MONDO:0012552 nord_rare diseases +MONDO:0012552 ordo_disorder diseases +MONDO:0012552 orphanet_rare diseases +MONDO:0012552 otar diseases +MONDO:0012552 rare diseases +MONDO:0012553 gard_rare diseases +MONDO:0012553 nord_rare diseases +MONDO:0012553 rare diseases +MONDO:0012554 gard_rare diseases +MONDO:0012554 nord_rare diseases +MONDO:0012554 rare diseases +MONDO:0012555 gard_rare diseases +MONDO:0012555 nord_rare diseases +MONDO:0012555 rare diseases +MONDO:0012556 gard_rare diseases +MONDO:0012556 nord_rare diseases +MONDO:0012556 ordo_disorder diseases +MONDO:0012556 orphanet_rare diseases +MONDO:0012556 otar diseases +MONDO:0012556 rare diseases +MONDO:0012557 gard_rare diseases +MONDO:0012557 nord_rare diseases +MONDO:0012557 ordo_disorder diseases +MONDO:0012557 orphanet_rare diseases +MONDO:0012557 otar diseases +MONDO:0012557 rare diseases +MONDO:0012559 gard_rare diseases +MONDO:0012559 nord_rare diseases +MONDO:0012559 ordo_disorder diseases +MONDO:0012559 orphanet_rare diseases +MONDO:0012559 otar diseases +MONDO:0012559 rare diseases +MONDO:0012561 gard_rare diseases +MONDO:0012561 nord_rare diseases +MONDO:0012561 otar diseases +MONDO:0012561 predisposition diseases +MONDO:0012561 rare diseases +MONDO:0012562 gard_rare diseases +MONDO:0012562 nord_rare diseases +MONDO:0012562 rare diseases +MONDO:0012563 gard_rare diseases +MONDO:0012563 nord_rare diseases +MONDO:0012563 rare diseases +MONDO:0012565 clingen diseases +MONDO:0012565 gard_rare diseases +MONDO:0012565 nord_rare diseases +MONDO:0012565 otar diseases +MONDO:0012565 rare diseases +MONDO:0012569 gard_rare diseases +MONDO:0012569 nord_rare diseases +MONDO:0012569 rare diseases +MONDO:0012570 gard_rare diseases +MONDO:0012570 nord_rare diseases +MONDO:0012570 ordo_disorder diseases +MONDO:0012570 orphanet_rare diseases +MONDO:0012570 otar diseases +MONDO:0012570 rare diseases +MONDO:0012571 clingen diseases +MONDO:0012571 gard_rare diseases +MONDO:0012571 nord_rare diseases +MONDO:0012571 rare diseases +MONDO:0012573 gard_rare diseases +MONDO:0012573 nord_rare diseases +MONDO:0012573 rare diseases +MONDO:0012574 gard_rare diseases +MONDO:0012574 nord_rare diseases +MONDO:0012574 ordo_disorder diseases +MONDO:0012574 ordo_malformation_syndrome diseases +MONDO:0012574 orphanet_rare diseases +MONDO:0012574 otar diseases +MONDO:0012574 rare diseases +MONDO:0012575 gard_rare diseases +MONDO:0012575 rare diseases +MONDO:0012576 gard_rare diseases +MONDO:0012576 nord_rare diseases +MONDO:0012576 rare diseases +MONDO:0012579 gard_rare diseases +MONDO:0012579 nord_rare diseases +MONDO:0012579 ordo_disorder diseases +MONDO:0012579 orphanet_rare diseases +MONDO:0012579 rare diseases +MONDO:0012580 gard_rare diseases +MONDO:0012580 nord_rare diseases +MONDO:0012580 ordo_disorder diseases +MONDO:0012580 orphanet_rare diseases +MONDO:0012580 otar diseases +MONDO:0012580 rare diseases +MONDO:0012581 gard_rare diseases +MONDO:0012581 nord_rare diseases +MONDO:0012581 rare diseases +MONDO:0012582 gard_rare diseases +MONDO:0012582 nord_rare diseases +MONDO:0012582 ordo_disorder diseases +MONDO:0012582 orphanet_rare diseases +MONDO:0012582 rare diseases +MONDO:0012583 gard_rare diseases +MONDO:0012583 rare diseases +MONDO:0012586 otar diseases +MONDO:0012588 gard_rare diseases +MONDO:0012588 nord_rare diseases +MONDO:0012588 ordo_etiological_subtype diseases +MONDO:0012588 otar diseases +MONDO:0012588 rare diseases +MONDO:0012589 clingen diseases +MONDO:0012589 gard_rare diseases +MONDO:0012589 nord_rare diseases +MONDO:0012589 ordo_disorder diseases +MONDO:0012589 ordo_malformation_syndrome diseases +MONDO:0012589 orphanet_rare diseases +MONDO:0012589 otar diseases +MONDO:0012589 rare diseases +MONDO:0012590 otar diseases +MONDO:0012591 gard_rare diseases +MONDO:0012591 nord_rare diseases +MONDO:0012591 ordo_subtype_of_a_disorder diseases +MONDO:0012591 otar diseases +MONDO:0012591 rare diseases +MONDO:0012592 gard_rare diseases +MONDO:0012592 nord_rare diseases +MONDO:0012592 rare diseases +MONDO:0012593 gard_rare diseases +MONDO:0012593 nord_rare diseases +MONDO:0012593 ordo_disorder diseases +MONDO:0012593 orphanet_rare diseases +MONDO:0012593 otar diseases +MONDO:0012593 rare diseases +MONDO:0012594 gard_rare diseases +MONDO:0012594 nord_rare diseases +MONDO:0012594 ordo_disorder diseases +MONDO:0012594 orphanet_rare diseases +MONDO:0012594 otar diseases +MONDO:0012594 rare diseases +MONDO:0012596 gard_rare diseases +MONDO:0012596 nord_rare diseases +MONDO:0012596 ordo_subtype_of_a_disorder diseases +MONDO:0012596 otar diseases +MONDO:0012596 rare diseases +MONDO:0012597 gard_rare diseases +MONDO:0012597 rare diseases +MONDO:0012598 gard_rare diseases +MONDO:0012598 nord_rare diseases +MONDO:0012598 rare diseases +MONDO:0012602 gard_rare diseases +MONDO:0012602 nord_rare diseases +MONDO:0012602 rare diseases +MONDO:0012603 gard_rare diseases +MONDO:0012603 nord_rare diseases +MONDO:0012603 rare diseases +MONDO:0012604 gard_rare diseases +MONDO:0012604 nord_rare diseases +MONDO:0012604 rare diseases +MONDO:0012605 gard_rare diseases +MONDO:0012605 nord_rare diseases +MONDO:0012605 ordo_disorder diseases +MONDO:0012605 orphanet_rare diseases +MONDO:0012605 otar diseases +MONDO:0012605 rare diseases +MONDO:0012608 gard_rare diseases +MONDO:0012608 nord_rare diseases +MONDO:0012608 ordo_disorder diseases +MONDO:0012608 orphanet_rare diseases +MONDO:0012608 otar diseases +MONDO:0012608 rare diseases +MONDO:0012609 gard_rare diseases +MONDO:0012609 rare diseases +MONDO:0012611 gard_rare diseases +MONDO:0012611 nord_rare diseases +MONDO:0012611 ordo_disorder diseases +MONDO:0012611 orphanet_rare diseases +MONDO:0012611 otar diseases +MONDO:0012611 rare diseases +MONDO:0012612 gard_rare diseases +MONDO:0012612 nord_rare diseases +MONDO:0012612 rare diseases +MONDO:0012613 gard_rare diseases +MONDO:0012613 nord_rare diseases +MONDO:0012613 rare diseases +MONDO:0012614 gard_rare diseases +MONDO:0012614 nord_rare diseases +MONDO:0012614 rare diseases +MONDO:0012615 gard_rare diseases +MONDO:0012615 nord_rare diseases +MONDO:0012615 rare diseases +MONDO:0012617 gard_rare diseases +MONDO:0012617 nord_rare diseases +MONDO:0012617 rare diseases +MONDO:0012618 gard_rare diseases +MONDO:0012618 nord_rare diseases +MONDO:0012618 rare diseases +MONDO:0012619 gard_rare diseases +MONDO:0012619 nord_rare diseases +MONDO:0012619 rare diseases +MONDO:0012620 gard_rare diseases +MONDO:0012620 rare diseases +MONDO:0012621 gard_rare diseases +MONDO:0012621 nord_rare diseases +MONDO:0012621 ordo_disorder diseases +MONDO:0012621 ordo_malformation_syndrome diseases +MONDO:0012621 orphanet_rare diseases +MONDO:0012621 otar diseases +MONDO:0012621 rare diseases +MONDO:0012622 gard_rare diseases +MONDO:0012622 nord_rare diseases +MONDO:0012622 ordo_disorder diseases +MONDO:0012622 orphanet_rare diseases +MONDO:0012622 otar diseases +MONDO:0012622 rare diseases +MONDO:0012623 gard_rare diseases +MONDO:0012623 nord_rare diseases +MONDO:0012623 rare diseases +MONDO:0012624 clingen diseases +MONDO:0012624 gard_rare diseases +MONDO:0012624 nord_rare diseases +MONDO:0012624 ordo_disorder diseases +MONDO:0012624 orphanet_rare diseases +MONDO:0012624 otar diseases +MONDO:0012624 rare diseases +MONDO:0012625 gard_rare diseases +MONDO:0012625 nord_rare diseases +MONDO:0012625 rare diseases +MONDO:0012626 gard_rare diseases +MONDO:0012626 nord_rare diseases +MONDO:0012626 rare diseases +MONDO:0012629 gard_rare diseases +MONDO:0012629 nord_rare diseases +MONDO:0012629 rare diseases +MONDO:0012630 gard_rare diseases +MONDO:0012630 rare diseases +MONDO:0012631 gard_rare diseases +MONDO:0012631 rare diseases +MONDO:0012634 gard_rare diseases +MONDO:0012634 nord_rare diseases +MONDO:0012634 ordo_disorder diseases +MONDO:0012634 ordo_malformation_syndrome diseases +MONDO:0012634 orphanet_rare diseases +MONDO:0012634 otar diseases +MONDO:0012634 rare diseases +MONDO:0012635 gard_rare diseases +MONDO:0012635 nord_rare diseases +MONDO:0012635 ordo_disorder diseases +MONDO:0012635 orphanet_rare diseases +MONDO:0012635 otar diseases +MONDO:0012635 rare diseases +MONDO:0012637 gard_rare diseases +MONDO:0012637 nord_rare diseases +MONDO:0012637 ordo_disorder diseases +MONDO:0012637 orphanet_rare diseases +MONDO:0012637 otar diseases +MONDO:0012637 rare diseases +MONDO:0012638 gard_rare diseases +MONDO:0012638 ordo_disorder diseases +MONDO:0012638 ordo_malformation_syndrome diseases +MONDO:0012638 orphanet_rare diseases +MONDO:0012638 otar diseases +MONDO:0012638 rare diseases +MONDO:0012639 gard_rare diseases +MONDO:0012639 nord_rare diseases +MONDO:0012639 ordo_disorder diseases +MONDO:0012639 orphanet_rare diseases +MONDO:0012639 otar diseases +MONDO:0012639 rare diseases +MONDO:0012640 gard_rare diseases +MONDO:0012640 nord_rare diseases +MONDO:0012640 ordo_disorder diseases +MONDO:0012640 orphanet_rare diseases +MONDO:0012640 otar diseases +MONDO:0012640 rare diseases +MONDO:0012643 gard_rare diseases +MONDO:0012643 nord_rare diseases +MONDO:0012643 ordo_disorder diseases +MONDO:0012643 orphanet_rare diseases +MONDO:0012643 otar diseases +MONDO:0012643 rare diseases +MONDO:0012644 gard_rare diseases +MONDO:0012644 nord_rare diseases +MONDO:0012644 rare diseases +MONDO:0012645 gard_rare diseases +MONDO:0012645 rare diseases +MONDO:0012648 clingen diseases +MONDO:0012648 gard_rare diseases +MONDO:0012648 nord_rare diseases +MONDO:0012648 ordo_disorder diseases +MONDO:0012648 orphanet_rare diseases +MONDO:0012648 otar diseases +MONDO:0012648 rare diseases +MONDO:0012650 clingen diseases +MONDO:0012650 gard_rare diseases +MONDO:0012650 nord_rare diseases +MONDO:0012650 ordo_disorder diseases +MONDO:0012650 orphanet_rare diseases +MONDO:0012650 otar diseases +MONDO:0012650 rare diseases +MONDO:0012651 gard_rare diseases +MONDO:0012651 nord_rare diseases +MONDO:0012651 ordo_disorder diseases +MONDO:0012651 orphanet_rare diseases +MONDO:0012651 otar diseases +MONDO:0012651 rare diseases +MONDO:0012652 gard_rare diseases +MONDO:0012652 nord_rare diseases +MONDO:0012652 ordo_disorder diseases +MONDO:0012652 orphanet_rare diseases +MONDO:0012652 otar diseases +MONDO:0012652 rare diseases +MONDO:0012653 gard_rare diseases +MONDO:0012653 nord_rare diseases +MONDO:0012653 rare diseases +MONDO:0012654 gard_rare diseases +MONDO:0012654 nord_rare diseases +MONDO:0012654 rare diseases +MONDO:0012656 gard_rare diseases +MONDO:0012656 nord_rare diseases +MONDO:0012656 ordo_disorder diseases +MONDO:0012656 ordo_malformation_syndrome diseases +MONDO:0012656 orphanet_rare diseases +MONDO:0012656 otar diseases +MONDO:0012656 rare diseases +MONDO:0012657 otar diseases +MONDO:0012658 gard_rare diseases +MONDO:0012658 nord_rare diseases +MONDO:0012658 ordo_malformation_syndrome diseases +MONDO:0012658 ordo_subtype_of_a_disorder diseases +MONDO:0012658 otar diseases +MONDO:0012658 rare diseases +MONDO:0012659 gard_rare diseases +MONDO:0012659 nord_rare diseases +MONDO:0012659 rare diseases +MONDO:0012662 clingen diseases +MONDO:0012662 gard_rare diseases +MONDO:0012662 nord_rare diseases +MONDO:0012662 otar diseases +MONDO:0012662 rare diseases +MONDO:0012664 gard_rare diseases +MONDO:0012664 nord_rare diseases +MONDO:0012664 ordo_disorder diseases +MONDO:0012664 orphanet_rare diseases +MONDO:0012664 otar diseases +MONDO:0012664 rare diseases +MONDO:0012665 gard_rare diseases +MONDO:0012665 nord_rare diseases +MONDO:0012665 otar diseases +MONDO:0012665 rare diseases +MONDO:0012667 gard_rare diseases +MONDO:0012667 nord_rare diseases +MONDO:0012667 rare diseases +MONDO:0012669 clingen diseases +MONDO:0012669 gard_rare diseases +MONDO:0012669 nord_rare diseases +MONDO:0012669 ordo_disorder diseases +MONDO:0012669 ordo_malformation_syndrome diseases +MONDO:0012669 orphanet_rare diseases +MONDO:0012669 otar diseases +MONDO:0012669 rare diseases +MONDO:0012670 clingen diseases +MONDO:0012670 gard_rare diseases +MONDO:0012670 nord_rare diseases +MONDO:0012670 otar diseases +MONDO:0012670 rare diseases +MONDO:0012672 otar diseases +MONDO:0012673 gard_rare diseases +MONDO:0012673 predisposition diseases +MONDO:0012673 rare diseases +MONDO:0012674 gard_rare diseases +MONDO:0012674 nord_rare diseases +MONDO:0012674 rare diseases +MONDO:0012675 gard_rare diseases +MONDO:0012675 nord_rare diseases +MONDO:0012675 ordo_disorder diseases +MONDO:0012675 orphanet_rare diseases +MONDO:0012675 otar diseases +MONDO:0012675 rare diseases +MONDO:0012676 clingen diseases +MONDO:0012676 gard_rare diseases +MONDO:0012676 nord_rare diseases +MONDO:0012676 otar diseases +MONDO:0012676 rare diseases +MONDO:0012677 gard_rare diseases +MONDO:0012677 nord_rare diseases +MONDO:0012677 rare diseases +MONDO:0012678 gard_rare diseases +MONDO:0012678 rare diseases +MONDO:0012679 gard_rare diseases +MONDO:0012679 nord_rare diseases +MONDO:0012679 ordo_disorder diseases +MONDO:0012679 ordo_malformation_syndrome diseases +MONDO:0012679 orphanet_rare diseases +MONDO:0012679 otar diseases +MONDO:0012679 rare diseases +MONDO:0012680 clingen diseases +MONDO:0012680 gard_rare diseases +MONDO:0012680 nord_rare diseases +MONDO:0012680 rare diseases +MONDO:0012682 gard_rare diseases +MONDO:0012682 nord_rare diseases +MONDO:0012682 ordo_disorder diseases +MONDO:0012682 orphanet_rare diseases +MONDO:0012682 predisposition diseases +MONDO:0012682 rare diseases +MONDO:0012683 gard_rare diseases +MONDO:0012683 nord_rare diseases +MONDO:0012683 ordo_disorder diseases +MONDO:0012683 ordo_malformation_syndrome diseases +MONDO:0012683 orphanet_rare diseases +MONDO:0012683 otar diseases +MONDO:0012683 rare diseases +MONDO:0012684 gard_rare diseases +MONDO:0012684 nord_rare diseases +MONDO:0012684 rare diseases +MONDO:0012687 gard_rare diseases +MONDO:0012687 nord_rare diseases +MONDO:0012687 ordo_disorder diseases +MONDO:0012687 ordo_morphological_anomaly diseases +MONDO:0012687 orphanet_rare diseases +MONDO:0012687 rare diseases +MONDO:0012688 gard_rare diseases +MONDO:0012688 nord_rare diseases +MONDO:0012688 rare diseases +MONDO:0012689 gard_rare diseases +MONDO:0012689 nord_rare diseases +MONDO:0012689 rare diseases +MONDO:0012690 gard_rare diseases +MONDO:0012690 nord_rare diseases +MONDO:0012690 rare diseases +MONDO:0012691 gard_rare diseases +MONDO:0012691 nord_rare diseases +MONDO:0012691 rare diseases +MONDO:0012693 gard_rare diseases +MONDO:0012693 nord_rare diseases +MONDO:0012693 ordo_disorder diseases +MONDO:0012693 orphanet_rare diseases +MONDO:0012693 otar diseases +MONDO:0012693 rare diseases +MONDO:0012694 gard_rare diseases +MONDO:0012694 nord_rare diseases +MONDO:0012694 rare diseases +MONDO:0012695 gard_rare diseases +MONDO:0012695 nord_rare diseases +MONDO:0012695 rare diseases +MONDO:0012696 gard_rare diseases +MONDO:0012696 rare diseases +MONDO:0012697 gard_rare diseases +MONDO:0012697 rare diseases +MONDO:0012698 gard_rare diseases +MONDO:0012698 rare diseases +MONDO:0012699 gard_rare diseases +MONDO:0012699 nord_rare diseases +MONDO:0012699 ordo_disorder diseases +MONDO:0012699 orphanet_rare diseases +MONDO:0012699 otar diseases +MONDO:0012699 rare diseases +MONDO:0012700 gard_rare diseases +MONDO:0012700 nord_rare diseases +MONDO:0012700 ordo_subtype_of_a_disorder diseases +MONDO:0012700 otar diseases +MONDO:0012700 rare diseases +MONDO:0012701 otar diseases +MONDO:0012703 gard_rare diseases +MONDO:0012703 nord_rare diseases +MONDO:0012703 ordo_disorder diseases +MONDO:0012703 ordo_malformation_syndrome diseases +MONDO:0012703 orphanet_rare diseases +MONDO:0012703 otar diseases +MONDO:0012703 rare diseases +MONDO:0012704 gard_rare diseases +MONDO:0012704 nord_rare diseases +MONDO:0012704 rare diseases +MONDO:0012705 gard_rare diseases +MONDO:0012705 nord_rare diseases +MONDO:0012705 rare diseases +MONDO:0012706 gard_rare diseases +MONDO:0012706 nord_rare diseases +MONDO:0012706 rare diseases +MONDO:0012708 gard_rare diseases +MONDO:0012708 rare diseases +MONDO:0012709 gard_rare diseases +MONDO:0012709 nord_rare diseases +MONDO:0012709 rare diseases +MONDO:0012713 gard_rare diseases +MONDO:0012713 nord_rare diseases +MONDO:0012713 rare diseases +MONDO:0012714 gard_rare diseases +MONDO:0012714 nord_rare diseases +MONDO:0012714 ordo_disorder diseases +MONDO:0012714 orphanet_rare diseases +MONDO:0012714 otar diseases +MONDO:0012714 rare diseases +MONDO:0012716 gard_rare diseases +MONDO:0012716 nord_rare diseases +MONDO:0012716 ordo_disorder diseases +MONDO:0012716 orphanet_rare diseases +MONDO:0012716 otar diseases +MONDO:0012716 rare diseases +MONDO:0012717 gard_rare diseases +MONDO:0012717 nord_rare diseases +MONDO:0012717 rare diseases +MONDO:0012718 gard_rare diseases +MONDO:0012718 nord_rare diseases +MONDO:0012718 ordo_disorder diseases +MONDO:0012718 orphanet_rare diseases +MONDO:0012718 otar diseases +MONDO:0012718 rare diseases +MONDO:0012719 clingen diseases +MONDO:0012719 gard_rare diseases +MONDO:0012719 nord_rare diseases +MONDO:0012719 ordo_disorder diseases +MONDO:0012719 orphanet_rare diseases +MONDO:0012719 otar diseases +MONDO:0012719 rare diseases +MONDO:0012720 gard_rare diseases +MONDO:0012720 nord_rare diseases +MONDO:0012720 otar diseases +MONDO:0012720 rare diseases +MONDO:0012721 gard_rare diseases +MONDO:0012721 nord_rare diseases +MONDO:0012721 ordo_subtype_of_a_disorder diseases +MONDO:0012721 otar diseases +MONDO:0012721 rare diseases +MONDO:0012723 gard_rare diseases +MONDO:0012723 nord_rare diseases +MONDO:0012723 rare diseases +MONDO:0012724 gard_rare diseases +MONDO:0012724 nord_rare diseases +MONDO:0012724 ordo_disorder diseases +MONDO:0012724 orphanet_rare diseases +MONDO:0012724 otar diseases +MONDO:0012724 rare diseases +MONDO:0012725 gard_rare diseases +MONDO:0012725 nord_rare diseases +MONDO:0012725 ordo_disorder diseases +MONDO:0012725 orphanet_rare diseases +MONDO:0012725 otar diseases +MONDO:0012725 rare diseases +MONDO:0012726 gard_rare diseases +MONDO:0012726 nord_rare diseases +MONDO:0012726 ordo_disorder diseases +MONDO:0012726 orphanet_rare diseases +MONDO:0012726 otar diseases +MONDO:0012726 rare diseases +MONDO:0012727 gard_rare diseases +MONDO:0012727 nord_rare diseases +MONDO:0012727 ordo_disorder diseases +MONDO:0012727 orphanet_rare diseases +MONDO:0012727 otar diseases +MONDO:0012727 rare diseases +MONDO:0012728 gard_rare diseases +MONDO:0012728 rare diseases +MONDO:0012729 gard_rare diseases +MONDO:0012729 nord_rare diseases +MONDO:0012729 rare diseases +MONDO:0012730 gard_rare diseases +MONDO:0012730 nord_rare diseases +MONDO:0012730 rare diseases +MONDO:0012731 gard_rare diseases +MONDO:0012731 nord_rare diseases +MONDO:0012731 rare diseases +MONDO:0012733 gard_rare diseases +MONDO:0012733 nord_rare diseases +MONDO:0012733 ordo_disorder diseases +MONDO:0012733 orphanet_rare diseases +MONDO:0012733 otar diseases +MONDO:0012733 rare diseases +MONDO:0012734 gard_rare diseases +MONDO:0012734 nord_rare diseases +MONDO:0012734 ordo_disorder diseases +MONDO:0012734 ordo_malformation_syndrome diseases +MONDO:0012734 orphanet_rare diseases +MONDO:0012734 otar diseases +MONDO:0012734 rare diseases +MONDO:0012735 gard_rare diseases +MONDO:0012735 nord_rare diseases +MONDO:0012735 ordo_disorder diseases +MONDO:0012735 orphanet_rare diseases +MONDO:0012735 rare diseases +MONDO:0012736 gard_rare diseases +MONDO:0012736 rare diseases +MONDO:0012737 gard_rare diseases +MONDO:0012737 otar diseases +MONDO:0012737 rare diseases +MONDO:0012738 gard_rare diseases +MONDO:0012738 otar diseases +MONDO:0012738 rare diseases +MONDO:0012739 gard_rare diseases +MONDO:0012739 nord_rare diseases +MONDO:0012739 ordo_disorder diseases +MONDO:0012739 ordo_malformation_syndrome diseases +MONDO:0012739 orphanet_rare diseases +MONDO:0012739 otar diseases +MONDO:0012739 rare diseases +MONDO:0012740 gard_rare diseases +MONDO:0012740 nord_rare diseases +MONDO:0012740 ordo_disorder diseases +MONDO:0012740 ordo_malformation_syndrome diseases +MONDO:0012740 orphanet_rare diseases +MONDO:0012740 otar diseases +MONDO:0012740 rare diseases +MONDO:0012741 gard_rare diseases +MONDO:0012741 rare diseases +MONDO:0012742 gard_rare diseases +MONDO:0012742 rare diseases +MONDO:0012743 gard_rare diseases +MONDO:0012743 rare diseases +MONDO:0012744 gard_rare diseases +MONDO:0012744 nord_rare diseases +MONDO:0012744 rare diseases +MONDO:0012745 gard_rare diseases +MONDO:0012745 nord_rare diseases +MONDO:0012745 rare diseases +MONDO:0012746 gard_rare diseases +MONDO:0012746 nord_rare diseases +MONDO:0012746 rare diseases +MONDO:0012747 gard_rare diseases +MONDO:0012747 nord_rare diseases +MONDO:0012747 ordo_disorder diseases +MONDO:0012747 orphanet_rare diseases +MONDO:0012747 otar diseases +MONDO:0012747 rare diseases +MONDO:0012748 clingen diseases +MONDO:0012748 gard_rare diseases +MONDO:0012748 nord_rare diseases +MONDO:0012748 rare diseases +MONDO:0012750 gard_rare diseases +MONDO:0012750 nord_rare diseases +MONDO:0012750 ordo_disorder diseases +MONDO:0012750 ordo_malformation_syndrome diseases +MONDO:0012750 orphanet_rare diseases +MONDO:0012750 otar diseases +MONDO:0012750 rare diseases +MONDO:0012751 gard_rare diseases +MONDO:0012751 nord_rare diseases +MONDO:0012751 rare diseases +MONDO:0012752 gard_rare diseases +MONDO:0012752 nord_rare diseases +MONDO:0012752 rare diseases +MONDO:0012753 clingen diseases +MONDO:0012753 gard_rare diseases +MONDO:0012753 nord_rare diseases +MONDO:0012753 rare diseases +MONDO:0012754 gard_rare diseases +MONDO:0012754 nord_rare diseases +MONDO:0012754 rare diseases +MONDO:0012755 gard_rare diseases +MONDO:0012755 nord_rare diseases +MONDO:0012755 ordo_disorder diseases +MONDO:0012755 orphanet_rare diseases +MONDO:0012755 otar diseases +MONDO:0012755 rare diseases +MONDO:0012756 gard_rare diseases +MONDO:0012756 nord_rare diseases +MONDO:0012756 ordo_disorder diseases +MONDO:0012756 ordo_malformation_syndrome diseases +MONDO:0012756 orphanet_rare diseases +MONDO:0012756 otar diseases +MONDO:0012756 predisposition diseases +MONDO:0012756 rare diseases +MONDO:0012757 gard_rare diseases +MONDO:0012757 ordo_disorder diseases +MONDO:0012757 orphanet_rare diseases +MONDO:0012757 otar diseases +MONDO:0012757 rare diseases +MONDO:0012758 gard_rare diseases +MONDO:0012758 rare diseases +MONDO:0012759 gard_rare diseases +MONDO:0012759 nord_rare diseases +MONDO:0012759 ordo_disorder diseases +MONDO:0012759 ordo_malformation_syndrome diseases +MONDO:0012759 orphanet_rare diseases +MONDO:0012759 rare diseases +MONDO:0012761 gard_rare diseases +MONDO:0012761 nord_rare diseases +MONDO:0012761 ordo_disorder diseases +MONDO:0012761 ordo_malformation_syndrome diseases +MONDO:0012761 orphanet_rare diseases +MONDO:0012761 otar diseases +MONDO:0012761 rare diseases +MONDO:0012762 gard_rare diseases +MONDO:0012762 rare diseases +MONDO:0012764 clingen diseases +MONDO:0012764 gard_rare diseases +MONDO:0012764 nord_rare diseases +MONDO:0012764 ordo_disorder diseases +MONDO:0012764 ordo_malformation_syndrome diseases +MONDO:0012764 orphanet_rare diseases +MONDO:0012764 rare diseases +MONDO:0012765 gard_rare diseases +MONDO:0012765 nord_rare diseases +MONDO:0012765 rare diseases +MONDO:0012766 gard_rare diseases +MONDO:0012766 nord_rare diseases +MONDO:0012766 ordo_disorder diseases +MONDO:0012766 orphanet_rare diseases +MONDO:0012766 otar diseases +MONDO:0012766 rare diseases +MONDO:0012767 gard_rare diseases +MONDO:0012767 nord_rare diseases +MONDO:0012767 rare diseases +MONDO:0012768 gard_rare diseases +MONDO:0012768 rare diseases +MONDO:0012769 gard_rare diseases +MONDO:0012769 rare diseases +MONDO:0012770 gard_rare diseases +MONDO:0012770 rare diseases +MONDO:0012774 gard_rare diseases +MONDO:0012774 nord_rare diseases +MONDO:0012774 ordo_disorder diseases +MONDO:0012774 ordo_malformation_syndrome diseases +MONDO:0012774 orphanet_rare diseases +MONDO:0012774 otar diseases +MONDO:0012774 rare diseases +MONDO:0012775 clingen diseases +MONDO:0012775 gard_rare diseases +MONDO:0012775 nord_rare diseases +MONDO:0012775 rare diseases +MONDO:0012783 clingen diseases +MONDO:0012783 gard_rare diseases +MONDO:0012783 nord_rare diseases +MONDO:0012783 ordo_disorder diseases +MONDO:0012783 orphanet_rare diseases +MONDO:0012783 otar diseases +MONDO:0012783 rare diseases +MONDO:0012784 gard_rare diseases +MONDO:0012784 nord_rare diseases +MONDO:0012784 ordo_disorder diseases +MONDO:0012784 orphanet_rare diseases +MONDO:0012784 otar diseases +MONDO:0012784 rare diseases +MONDO:0012786 gard_rare diseases +MONDO:0012786 nord_rare diseases +MONDO:0012786 ordo_disorder diseases +MONDO:0012786 orphanet_rare diseases +MONDO:0012786 otar diseases +MONDO:0012786 rare diseases +MONDO:0012787 gard_rare diseases +MONDO:0012787 nord_rare diseases +MONDO:0012787 ordo_disorder diseases +MONDO:0012787 orphanet_rare diseases +MONDO:0012787 otar diseases +MONDO:0012787 rare diseases +MONDO:0012789 gard_rare diseases +MONDO:0012789 nord_rare diseases +MONDO:0012789 ordo_disorder diseases +MONDO:0012789 orphanet_rare diseases +MONDO:0012789 otar diseases +MONDO:0012789 rare diseases +MONDO:0012790 clingen diseases +MONDO:0012790 gard_rare diseases +MONDO:0012790 nord_rare diseases +MONDO:0012790 rare diseases +MONDO:0012791 gard_rare diseases +MONDO:0012791 nord_rare diseases +MONDO:0012791 ordo_disorder diseases +MONDO:0012791 orphanet_rare diseases +MONDO:0012791 otar diseases +MONDO:0012791 rare diseases +MONDO:0012792 gard_rare diseases +MONDO:0012792 nord_rare diseases +MONDO:0012792 ordo_disorder diseases +MONDO:0012792 orphanet_rare diseases +MONDO:0012792 otar diseases +MONDO:0012792 rare diseases +MONDO:0012793 gard_rare diseases +MONDO:0012793 nord_rare diseases +MONDO:0012793 otar diseases +MONDO:0012793 rare diseases +MONDO:0012794 gard_rare diseases +MONDO:0012794 nord_rare diseases +MONDO:0012794 ordo_disorder diseases +MONDO:0012794 orphanet_rare diseases +MONDO:0012794 otar diseases +MONDO:0012794 rare diseases +MONDO:0012796 gard_rare diseases +MONDO:0012796 nord_rare diseases +MONDO:0012796 rare diseases +MONDO:0012797 gard_rare diseases +MONDO:0012797 rare diseases +MONDO:0012799 gard_rare diseases +MONDO:0012799 nord_rare diseases +MONDO:0012799 otar diseases +MONDO:0012799 rare diseases +MONDO:0012800 gard_rare diseases +MONDO:0012800 nord_rare diseases +MONDO:0012800 rare diseases +MONDO:0012802 clingen diseases +MONDO:0012802 gard_rare diseases +MONDO:0012802 nord_rare diseases +MONDO:0012802 ordo_disorder diseases +MONDO:0012802 ordo_malformation_syndrome diseases +MONDO:0012802 orphanet_rare diseases +MONDO:0012802 otar diseases +MONDO:0012802 rare diseases +MONDO:0012803 gard_rare diseases +MONDO:0012803 nord_rare diseases +MONDO:0012803 ordo_disorder diseases +MONDO:0012803 orphanet_rare diseases +MONDO:0012803 otar diseases +MONDO:0012803 rare diseases +MONDO:0012804 gard_rare diseases +MONDO:0012804 nord_rare diseases +MONDO:0012804 otar diseases +MONDO:0012804 rare diseases +MONDO:0012805 gard_rare diseases +MONDO:0012805 nord_rare diseases +MONDO:0012805 ordo_disorder diseases +MONDO:0012805 orphanet_rare diseases +MONDO:0012805 otar diseases +MONDO:0012805 rare diseases +MONDO:0012806 gard_rare diseases +MONDO:0012806 nord_rare diseases +MONDO:0012806 otar diseases +MONDO:0012806 rare diseases +MONDO:0012807 gard_rare diseases +MONDO:0012807 nord_rare diseases +MONDO:0012807 ordo_disorder diseases +MONDO:0012807 orphanet_rare diseases +MONDO:0012807 otar diseases +MONDO:0012807 rare diseases +MONDO:0012808 gard_rare diseases +MONDO:0012808 nord_rare diseases +MONDO:0012808 rare diseases +MONDO:0012809 gard_rare diseases +MONDO:0012809 nord_rare diseases +MONDO:0012809 ordo_disorder diseases +MONDO:0012809 orphanet_rare diseases +MONDO:0012809 rare diseases +MONDO:0012810 gard_rare diseases +MONDO:0012810 nord_rare diseases +MONDO:0012810 rare diseases +MONDO:0012811 gard_rare diseases +MONDO:0012811 nord_rare diseases +MONDO:0012811 rare diseases +MONDO:0012812 gard_rare diseases +MONDO:0012812 nord_rare diseases +MONDO:0012812 ordo_disorder diseases +MONDO:0012812 orphanet_rare diseases +MONDO:0012812 rare diseases +MONDO:0012813 gard_rare diseases +MONDO:0012813 nord_rare diseases +MONDO:0012813 rare diseases +MONDO:0012815 gard_rare diseases +MONDO:0012815 nord_rare diseases +MONDO:0012815 ordo_disorder diseases +MONDO:0012815 orphanet_rare diseases +MONDO:0012815 otar diseases +MONDO:0012815 rare diseases +MONDO:0012816 gard_rare diseases +MONDO:0012816 rare diseases +MONDO:0012817 gard_rare diseases +MONDO:0012817 ordo_disorder diseases +MONDO:0012817 orphanet_rare diseases +MONDO:0012817 otar diseases +MONDO:0012817 rare diseases +MONDO:0012818 gard_rare diseases +MONDO:0012818 nord_rare diseases +MONDO:0012818 rare diseases +MONDO:0012819 otar diseases +MONDO:0012820 gard_rare diseases +MONDO:0012820 predisposition diseases +MONDO:0012820 rare diseases +MONDO:0012821 gard_rare diseases +MONDO:0012821 predisposition diseases +MONDO:0012821 rare diseases +MONDO:0012822 gard_rare diseases +MONDO:0012822 predisposition diseases +MONDO:0012822 rare diseases +MONDO:0012823 gard_rare diseases +MONDO:0012823 predisposition diseases +MONDO:0012823 rare diseases +MONDO:0012824 gard_rare diseases +MONDO:0012824 nord_rare diseases +MONDO:0012824 ordo_subtype_of_a_disorder diseases +MONDO:0012824 otar diseases +MONDO:0012824 rare diseases +MONDO:0012825 gard_rare diseases +MONDO:0012825 nord_rare diseases +MONDO:0012825 ordo_disorder diseases +MONDO:0012825 orphanet_rare diseases +MONDO:0012825 otar diseases +MONDO:0012825 rare diseases +MONDO:0012828 gard_rare diseases +MONDO:0012828 rare diseases +MONDO:0012830 gard_rare diseases +MONDO:0012830 nord_rare diseases +MONDO:0012830 ordo_disorder diseases +MONDO:0012830 ordo_malformation_syndrome diseases +MONDO:0012830 orphanet_rare diseases +MONDO:0012830 otar diseases +MONDO:0012830 rare diseases +MONDO:0012833 clingen diseases +MONDO:0012833 gard_rare diseases +MONDO:0012833 nord_rare diseases +MONDO:0012833 ordo_disorder diseases +MONDO:0012833 ordo_malformation_syndrome diseases +MONDO:0012833 orphanet_rare diseases +MONDO:0012833 otar diseases +MONDO:0012833 rare diseases +MONDO:0012839 gard_rare diseases +MONDO:0012839 nord_rare diseases +MONDO:0012839 ordo_disorder diseases +MONDO:0012839 orphanet_rare diseases +MONDO:0012839 rare diseases +MONDO:0012842 gard_rare diseases +MONDO:0012842 predisposition diseases +MONDO:0012842 rare diseases +MONDO:0012844 gard_rare diseases +MONDO:0012844 nord_rare diseases +MONDO:0012844 rare diseases +MONDO:0012846 gard_rare diseases +MONDO:0012846 rare diseases +MONDO:0012847 gard_rare diseases +MONDO:0012847 nord_rare diseases +MONDO:0012847 rare diseases +MONDO:0012848 gard_rare diseases +MONDO:0012848 nord_rare diseases +MONDO:0012848 rare diseases +MONDO:0012849 gard_rare diseases +MONDO:0012849 nord_rare diseases +MONDO:0012849 rare diseases +MONDO:0012850 gard_rare diseases +MONDO:0012850 nord_rare diseases +MONDO:0012850 rare diseases +MONDO:0012851 gard_rare diseases +MONDO:0012851 nord_rare diseases +MONDO:0012851 rare diseases +MONDO:0012853 gard_rare diseases +MONDO:0012853 nord_rare diseases +MONDO:0012853 ordo_disorder diseases +MONDO:0012853 ordo_malformation_syndrome diseases +MONDO:0012853 orphanet_rare diseases +MONDO:0012853 otar diseases +MONDO:0012853 rare diseases +MONDO:0012854 gard_rare diseases +MONDO:0012854 ordo_disorder diseases +MONDO:0012854 ordo_malformation_syndrome diseases +MONDO:0012854 orphanet_rare diseases +MONDO:0012854 otar diseases +MONDO:0012854 rare diseases +MONDO:0012855 gard_rare diseases +MONDO:0012855 nord_rare diseases +MONDO:0012855 rare diseases +MONDO:0012856 gard_rare diseases +MONDO:0012856 nord_rare diseases +MONDO:0012856 ordo_disorder diseases +MONDO:0012856 orphanet_rare diseases +MONDO:0012856 otar diseases +MONDO:0012856 rare diseases +MONDO:0012857 gard_rare diseases +MONDO:0012857 nord_rare diseases +MONDO:0012857 rare diseases +MONDO:0012858 gard_rare diseases +MONDO:0012858 nord_rare diseases +MONDO:0012858 ordo_disorder diseases +MONDO:0012858 orphanet_rare diseases +MONDO:0012858 otar diseases +MONDO:0012858 rare diseases +MONDO:0012859 gard_rare diseases +MONDO:0012859 nord_rare diseases +MONDO:0012859 ordo_disorder diseases +MONDO:0012859 orphanet_rare diseases +MONDO:0012859 otar diseases +MONDO:0012859 rare diseases +MONDO:0012860 gard_rare diseases +MONDO:0012860 nord_rare diseases +MONDO:0012860 rare diseases +MONDO:0012861 gard_rare diseases +MONDO:0012861 nord_rare diseases +MONDO:0012861 rare diseases +MONDO:0012864 gard_rare diseases +MONDO:0012864 nord_rare diseases +MONDO:0012864 ordo_disorder diseases +MONDO:0012864 ordo_malformation_syndrome diseases +MONDO:0012864 ordo_subtype_of_a_disorder diseases +MONDO:0012864 orphanet_rare diseases +MONDO:0012864 otar diseases +MONDO:0012864 rare diseases +MONDO:0012866 gard_rare diseases +MONDO:0012866 nord_rare diseases +MONDO:0012866 ordo_disorder diseases +MONDO:0012866 orphanet_rare diseases +MONDO:0012866 otar diseases +MONDO:0012866 rare diseases +MONDO:0012867 gard_rare diseases +MONDO:0012867 nord_rare diseases +MONDO:0012867 ordo_disorder diseases +MONDO:0012867 orphanet_rare diseases +MONDO:0012867 otar diseases +MONDO:0012867 rare diseases +MONDO:0012868 gard_rare diseases +MONDO:0012868 nord_rare diseases +MONDO:0012868 ordo_disorder diseases +MONDO:0012868 orphanet_rare diseases +MONDO:0012868 otar diseases +MONDO:0012868 rare diseases +MONDO:0012869 gard_rare diseases +MONDO:0012869 nord_rare diseases +MONDO:0012869 rare diseases +MONDO:0012870 gard_rare diseases +MONDO:0012870 nord_rare diseases +MONDO:0012870 rare diseases +MONDO:0012871 clingen diseases +MONDO:0012871 gard_rare diseases +MONDO:0012871 nord_rare diseases +MONDO:0012871 rare diseases +MONDO:0012872 clingen diseases +MONDO:0012872 gard_rare diseases +MONDO:0012872 nord_rare diseases +MONDO:0012872 rare diseases +MONDO:0012873 gard_rare diseases +MONDO:0012873 nord_rare diseases +MONDO:0012873 ordo_subtype_of_a_disorder diseases +MONDO:0012873 otar diseases +MONDO:0012873 rare diseases +MONDO:0012874 gard_rare diseases +MONDO:0012874 nord_rare diseases +MONDO:0012874 rare diseases +MONDO:0012876 clingen diseases +MONDO:0012876 gard_rare diseases +MONDO:0012876 nord_rare diseases +MONDO:0012876 otar diseases +MONDO:0012876 rare diseases +MONDO:0012878 gard_rare diseases +MONDO:0012878 rare diseases +MONDO:0012880 gard_rare diseases +MONDO:0012880 otar diseases +MONDO:0012880 rare diseases +MONDO:0012883 gard_rare diseases +MONDO:0012883 nord_rare diseases +MONDO:0012883 ordo_disorder diseases +MONDO:0012883 orphanet_rare diseases +MONDO:0012883 otar diseases +MONDO:0012883 rare diseases +MONDO:0012885 gard_rare diseases +MONDO:0012885 nord_rare diseases +MONDO:0012885 ordo_disorder diseases +MONDO:0012885 orphanet_rare diseases +MONDO:0012885 otar diseases +MONDO:0012885 rare diseases +MONDO:0012890 gard_rare diseases +MONDO:0012890 nord_rare diseases +MONDO:0012890 rare diseases +MONDO:0012891 gard_rare diseases +MONDO:0012891 nord_rare diseases +MONDO:0012891 rare diseases +MONDO:0012892 gard_rare diseases +MONDO:0012892 nord_rare diseases +MONDO:0012892 ordo_disorder diseases +MONDO:0012892 orphanet_rare diseases +MONDO:0012892 otar diseases +MONDO:0012892 rare diseases +MONDO:0012895 gard_rare diseases +MONDO:0012895 nord_rare diseases +MONDO:0012895 ordo_disorder diseases +MONDO:0012895 orphanet_rare diseases +MONDO:0012895 otar diseases +MONDO:0012895 rare diseases +MONDO:0012897 clingen diseases +MONDO:0012897 gard_rare diseases +MONDO:0012897 nord_rare diseases +MONDO:0012897 ordo_disorder diseases +MONDO:0012897 orphanet_rare diseases +MONDO:0012897 otar diseases +MONDO:0012897 rare diseases +MONDO:0012899 gard_rare diseases +MONDO:0012899 nord_rare diseases +MONDO:0012899 rare diseases +MONDO:0012900 gard_rare diseases +MONDO:0012900 nord_rare diseases +MONDO:0012900 rare diseases +MONDO:0012901 clingen diseases +MONDO:0012901 gard_rare diseases +MONDO:0012901 nord_rare diseases +MONDO:0012901 ordo_disorder diseases +MONDO:0012901 orphanet_rare diseases +MONDO:0012901 otar diseases +MONDO:0012901 rare diseases +MONDO:0012902 gard_rare diseases +MONDO:0012902 nord_rare diseases +MONDO:0012902 rare diseases +MONDO:0012903 gard_rare diseases +MONDO:0012903 nord_rare diseases +MONDO:0012903 rare diseases +MONDO:0012904 gard_rare diseases +MONDO:0012904 nord_rare diseases +MONDO:0012904 rare diseases +MONDO:0012905 gard_rare diseases +MONDO:0012905 nord_rare diseases +MONDO:0012905 ordo_disorder diseases +MONDO:0012905 orphanet_rare diseases +MONDO:0012905 otar diseases +MONDO:0012905 rare diseases +MONDO:0012906 clingen diseases +MONDO:0012906 gard_rare diseases +MONDO:0012906 nord_rare diseases +MONDO:0012906 rare diseases +MONDO:0012907 gard_rare diseases +MONDO:0012907 ordo_disorder diseases +MONDO:0012907 ordo_malformation_syndrome diseases +MONDO:0012907 orphanet_rare diseases +MONDO:0012907 rare diseases +MONDO:0012908 gard_rare diseases +MONDO:0012908 rare diseases +MONDO:0012909 otar diseases +MONDO:0012911 gard_rare diseases +MONDO:0012911 nord_rare diseases +MONDO:0012911 ordo_disorder diseases +MONDO:0012911 orphanet_rare diseases +MONDO:0012911 otar diseases +MONDO:0012911 rare diseases +MONDO:0012912 gard_rare diseases +MONDO:0012912 nord_rare diseases +MONDO:0012912 ordo_disorder diseases +MONDO:0012912 orphanet_rare diseases +MONDO:0012912 otar diseases +MONDO:0012912 rare diseases +MONDO:0012913 gard_rare diseases +MONDO:0012913 nord_rare diseases +MONDO:0012913 rare diseases +MONDO:0012914 gard_rare diseases +MONDO:0012914 nord_rare diseases +MONDO:0012914 ordo_disorder diseases +MONDO:0012914 ordo_malformation_syndrome diseases +MONDO:0012914 orphanet_rare diseases +MONDO:0012914 otar diseases +MONDO:0012914 rare diseases +MONDO:0012915 gard_rare diseases +MONDO:0012915 nord_rare diseases +MONDO:0012915 ordo_disorder diseases +MONDO:0012915 ordo_malformation_syndrome diseases +MONDO:0012915 orphanet_rare diseases +MONDO:0012915 otar diseases +MONDO:0012915 rare diseases +MONDO:0012916 gard_rare diseases +MONDO:0012916 nord_rare diseases +MONDO:0012916 ordo_disorder diseases +MONDO:0012916 ordo_malformation_syndrome diseases +MONDO:0012916 orphanet_rare diseases +MONDO:0012916 otar diseases +MONDO:0012916 rare diseases +MONDO:0012918 gard_rare diseases +MONDO:0012918 nord_rare diseases +MONDO:0012918 rare diseases +MONDO:0012923 gard_rare diseases +MONDO:0012923 nord_rare diseases +MONDO:0012923 rare diseases +MONDO:0012924 gard_rare diseases +MONDO:0012924 nord_rare diseases +MONDO:0012924 rare diseases +MONDO:0012925 gard_rare diseases +MONDO:0012925 nord_rare diseases +MONDO:0012925 rare diseases +MONDO:0012926 gard_rare diseases +MONDO:0012926 rare diseases +MONDO:0012927 gard_rare diseases +MONDO:0012927 nord_rare diseases +MONDO:0012927 ordo_disorder diseases +MONDO:0012927 ordo_malformation_syndrome diseases +MONDO:0012927 orphanet_rare diseases +MONDO:0012927 otar diseases +MONDO:0012927 rare diseases +MONDO:0012928 gard_rare diseases +MONDO:0012928 nord_rare diseases +MONDO:0012928 ordo_disorder diseases +MONDO:0012928 orphanet_rare diseases +MONDO:0012928 otar diseases +MONDO:0012928 rare diseases +MONDO:0012929 gard_rare diseases +MONDO:0012929 nord_rare diseases +MONDO:0012929 ordo_disorder diseases +MONDO:0012929 orphanet_rare diseases +MONDO:0012929 otar diseases +MONDO:0012929 rare diseases +MONDO:0012930 gard_rare diseases +MONDO:0012930 nord_rare diseases +MONDO:0012930 ordo_disorder diseases +MONDO:0012930 orphanet_rare diseases +MONDO:0012930 otar diseases +MONDO:0012930 rare diseases +MONDO:0012934 inferred_rare diseases +MONDO:0012934 predisposition diseases +MONDO:0012934 rare diseases +MONDO:0012935 inferred_rare diseases +MONDO:0012935 predisposition diseases +MONDO:0012935 rare diseases +MONDO:0012936 inferred_rare diseases +MONDO:0012936 predisposition diseases +MONDO:0012936 rare diseases +MONDO:0012937 clingen diseases +MONDO:0012937 gard_rare diseases +MONDO:0012937 nord_rare diseases +MONDO:0012937 rare diseases +MONDO:0012938 gard_rare diseases +MONDO:0012938 nord_rare diseases +MONDO:0012938 rare diseases +MONDO:0012939 gard_rare diseases +MONDO:0012939 nord_rare diseases +MONDO:0012939 rare diseases +MONDO:0012941 gard_rare diseases +MONDO:0012941 nord_rare diseases +MONDO:0012941 otar diseases +MONDO:0012941 rare diseases +MONDO:0012942 gard_rare diseases +MONDO:0012942 rare diseases +MONDO:0012943 gard_rare diseases +MONDO:0012943 nord_rare diseases +MONDO:0012943 rare diseases +MONDO:0012944 gard_rare diseases +MONDO:0012944 nord_rare diseases +MONDO:0012944 otar diseases +MONDO:0012944 rare diseases +MONDO:0012945 clingen diseases +MONDO:0012945 gard_rare diseases +MONDO:0012945 nord_rare diseases +MONDO:0012945 rare diseases +MONDO:0012946 gard_rare diseases +MONDO:0012946 rare diseases +MONDO:0012947 gard_rare diseases +MONDO:0012947 rare diseases +MONDO:0012948 gard_rare diseases +MONDO:0012948 nord_rare diseases +MONDO:0012948 ordo_disorder diseases +MONDO:0012948 ordo_malformation_syndrome diseases +MONDO:0012948 orphanet_rare diseases +MONDO:0012948 otar diseases +MONDO:0012948 rare diseases +MONDO:0012949 gard_rare diseases +MONDO:0012949 nord_rare diseases +MONDO:0012949 rare diseases +MONDO:0012950 gard_rare diseases +MONDO:0012950 nord_rare diseases +MONDO:0012950 rare diseases +MONDO:0012951 gard_rare diseases +MONDO:0012951 predisposition diseases +MONDO:0012951 rare diseases +MONDO:0012952 gard_rare diseases +MONDO:0012952 predisposition diseases +MONDO:0012952 rare diseases +MONDO:0012953 inferred_rare diseases +MONDO:0012953 predisposition diseases +MONDO:0012953 rare diseases +MONDO:0012954 gard_rare diseases +MONDO:0012954 predisposition diseases +MONDO:0012954 rare diseases +MONDO:0012955 gard_rare diseases +MONDO:0012955 predisposition diseases +MONDO:0012955 rare diseases +MONDO:0012960 gard_rare diseases +MONDO:0012960 rare diseases +MONDO:0012964 gard_rare diseases +MONDO:0012964 nord_rare diseases +MONDO:0012964 ordo_disorder diseases +MONDO:0012964 ordo_malformation_syndrome diseases +MONDO:0012964 orphanet_rare diseases +MONDO:0012964 otar diseases +MONDO:0012964 rare diseases +MONDO:0012965 gard_rare diseases +MONDO:0012965 nord_rare diseases +MONDO:0012965 rare diseases +MONDO:0012967 gard_rare diseases +MONDO:0012967 nord_rare diseases +MONDO:0012967 ordo_disorder diseases +MONDO:0012967 orphanet_rare diseases +MONDO:0012967 otar diseases +MONDO:0012967 rare diseases +MONDO:0012968 gard_rare diseases +MONDO:0012968 nord_rare diseases +MONDO:0012968 rare diseases +MONDO:0012974 gard_rare diseases +MONDO:0012974 nord_rare diseases +MONDO:0012974 rare diseases +MONDO:0012975 gard_rare diseases +MONDO:0012975 nord_rare diseases +MONDO:0012975 rare diseases +MONDO:0012976 gard_rare diseases +MONDO:0012976 nord_rare diseases +MONDO:0012976 rare diseases +MONDO:0012977 gard_rare diseases +MONDO:0012977 nord_rare diseases +MONDO:0012977 rare diseases +MONDO:0012978 clingen diseases +MONDO:0012978 gard_rare diseases +MONDO:0012978 nord_rare diseases +MONDO:0012978 rare diseases +MONDO:0012979 clingen diseases +MONDO:0012979 gard_rare diseases +MONDO:0012979 nord_rare diseases +MONDO:0012979 rare diseases +MONDO:0012980 gard_rare diseases +MONDO:0012980 nord_rare diseases +MONDO:0012980 ordo_disorder diseases +MONDO:0012980 ordo_malformation_syndrome diseases +MONDO:0012980 orphanet_rare diseases +MONDO:0012980 otar diseases +MONDO:0012980 rare diseases +MONDO:0012981 gard_rare diseases +MONDO:0012981 nord_rare diseases +MONDO:0012981 rare diseases +MONDO:0012982 clingen diseases +MONDO:0012982 gard_rare diseases +MONDO:0012982 nord_rare diseases +MONDO:0012982 ordo_disorder diseases +MONDO:0012982 orphanet_rare diseases +MONDO:0012982 otar diseases +MONDO:0012982 rare diseases +MONDO:0012983 gard_rare diseases +MONDO:0012983 nord_rare diseases +MONDO:0012983 rare diseases +MONDO:0012984 clingen diseases +MONDO:0012984 gard_rare diseases +MONDO:0012984 nord_rare diseases +MONDO:0012984 ordo_disorder diseases +MONDO:0012984 orphanet_rare diseases +MONDO:0012984 otar diseases +MONDO:0012984 rare diseases +MONDO:0012985 gard_rare diseases +MONDO:0012985 nord_rare diseases +MONDO:0012985 rare diseases +MONDO:0012986 gard_rare diseases +MONDO:0012986 nord_rare diseases +MONDO:0012986 ordo_subtype_of_a_disorder diseases +MONDO:0012986 otar diseases +MONDO:0012986 rare diseases +MONDO:0012987 clingen diseases +MONDO:0012987 gard_rare diseases +MONDO:0012987 nord_rare diseases +MONDO:0012987 rare diseases +MONDO:0012988 gard_rare diseases +MONDO:0012988 otar diseases +MONDO:0012988 rare diseases +MONDO:0012989 gard_rare diseases +MONDO:0012989 nord_rare diseases +MONDO:0012989 rare diseases +MONDO:0012990 gard_rare diseases +MONDO:0012990 nord_rare diseases +MONDO:0012990 rare diseases +MONDO:0012991 otar diseases +MONDO:0012992 gard_rare diseases +MONDO:0012992 nord_rare diseases +MONDO:0012992 ordo_disorder diseases +MONDO:0012992 orphanet_rare diseases +MONDO:0012992 otar diseases +MONDO:0012992 rare diseases +MONDO:0012993 gard_rare diseases +MONDO:0012993 rare diseases +MONDO:0012994 clingen diseases +MONDO:0012994 gard_rare diseases +MONDO:0012994 nord_rare diseases +MONDO:0012994 ordo_disorder diseases +MONDO:0012994 orphanet_rare diseases +MONDO:0012994 otar diseases +MONDO:0012994 rare diseases +MONDO:0012996 clingen diseases +MONDO:0012996 gard_rare diseases +MONDO:0012996 ordo_disorder diseases +MONDO:0012996 orphanet_rare diseases +MONDO:0012996 otar diseases +MONDO:0012996 rare diseases +MONDO:0012997 gard_rare diseases +MONDO:0012997 ordo_disorder diseases +MONDO:0012997 ordo_malformation_syndrome diseases +MONDO:0012997 orphanet_rare diseases +MONDO:0012997 rare diseases +MONDO:0012999 clingen diseases +MONDO:0012999 gard_rare diseases +MONDO:0012999 nord_rare diseases +MONDO:0012999 ordo_disorder diseases +MONDO:0012999 orphanet_rare diseases +MONDO:0012999 otar diseases +MONDO:0012999 rare diseases +MONDO:0013000 clingen diseases +MONDO:0013000 gard_rare diseases +MONDO:0013000 nord_rare diseases +MONDO:0013000 ordo_disorder diseases +MONDO:0013000 orphanet_rare diseases +MONDO:0013000 otar diseases +MONDO:0013000 rare diseases +MONDO:0013002 gard_rare diseases +MONDO:0013002 nord_rare diseases +MONDO:0013002 rare diseases +MONDO:0013003 gard_rare diseases +MONDO:0013003 nord_rare diseases +MONDO:0013003 ordo_disorder diseases +MONDO:0013003 ordo_morphological_anomaly diseases +MONDO:0013003 orphanet_rare diseases +MONDO:0013003 otar diseases +MONDO:0013003 rare diseases +MONDO:0013005 clingen diseases +MONDO:0013005 gard_rare diseases +MONDO:0013005 nord_rare diseases +MONDO:0013005 ordo_disorder diseases +MONDO:0013005 orphanet_rare diseases +MONDO:0013005 otar diseases +MONDO:0013005 rare diseases +MONDO:0013006 gard_rare diseases +MONDO:0013006 nord_rare diseases +MONDO:0013006 ordo_subtype_of_a_disorder diseases +MONDO:0013006 otar diseases +MONDO:0013006 rare diseases +MONDO:0013007 gard_rare diseases +MONDO:0013007 nord_rare diseases +MONDO:0013007 ordo_subtype_of_a_disorder diseases +MONDO:0013007 otar diseases +MONDO:0013007 rare diseases +MONDO:0013008 gard_rare diseases +MONDO:0013008 nord_rare diseases +MONDO:0013008 ordo_subtype_of_a_disorder diseases +MONDO:0013008 otar diseases +MONDO:0013008 rare diseases +MONDO:0013010 gard_rare diseases +MONDO:0013010 nord_rare diseases +MONDO:0013010 rare diseases +MONDO:0013011 gard_rare diseases +MONDO:0013011 nord_rare diseases +MONDO:0013011 rare diseases +MONDO:0013013 gard_rare diseases +MONDO:0013013 nord_rare diseases +MONDO:0013013 rare diseases +MONDO:0013014 gard_rare diseases +MONDO:0013014 nord_rare diseases +MONDO:0013014 ordo_disorder diseases +MONDO:0013014 orphanet_rare diseases +MONDO:0013014 otar diseases +MONDO:0013014 rare diseases +MONDO:0013015 gard_rare diseases +MONDO:0013015 rare diseases +MONDO:0013016 clingen diseases +MONDO:0013016 gard_rare diseases +MONDO:0013016 nord_rare diseases +MONDO:0013016 ordo_subtype_of_a_disorder diseases +MONDO:0013016 otar diseases +MONDO:0013016 rare diseases +MONDO:0013017 gard_rare diseases +MONDO:0013017 otar diseases +MONDO:0013017 rare diseases +MONDO:0013018 gard_rare diseases +MONDO:0013018 nord_rare diseases +MONDO:0013018 rare diseases +MONDO:0013021 gard_rare diseases +MONDO:0013021 nord_rare diseases +MONDO:0013021 ordo_disorder diseases +MONDO:0013021 orphanet_rare diseases +MONDO:0013021 otar diseases +MONDO:0013021 rare diseases +MONDO:0013024 gard_rare diseases +MONDO:0013024 nord_rare diseases +MONDO:0013024 ordo_disorder diseases +MONDO:0013024 orphanet_rare diseases +MONDO:0013024 rare diseases +MONDO:0013025 gard_rare diseases +MONDO:0013025 nord_rare diseases +MONDO:0013025 ordo_disorder diseases +MONDO:0013025 ordo_malformation_syndrome diseases +MONDO:0013025 orphanet_rare diseases +MONDO:0013025 otar diseases +MONDO:0013025 rare diseases +MONDO:0013026 gard_rare diseases +MONDO:0013026 nord_rare diseases +MONDO:0013026 ordo_disorder diseases +MONDO:0013026 orphanet_rare diseases +MONDO:0013026 otar diseases +MONDO:0013026 rare diseases +MONDO:0013027 gard_rare diseases +MONDO:0013027 nord_rare diseases +MONDO:0013027 ordo_disorder diseases +MONDO:0013027 orphanet_rare diseases +MONDO:0013027 otar diseases +MONDO:0013027 rare diseases +MONDO:0013028 gard_rare diseases +MONDO:0013028 ordo_disorder diseases +MONDO:0013028 orphanet_rare diseases +MONDO:0013028 otar diseases +MONDO:0013028 rare diseases +MONDO:0013029 gard_rare diseases +MONDO:0013029 nord_rare diseases +MONDO:0013029 rare diseases +MONDO:0013030 gard_rare diseases +MONDO:0013030 nord_rare diseases +MONDO:0013030 rare diseases +MONDO:0013031 gard_rare diseases +MONDO:0013031 nord_rare diseases +MONDO:0013031 rare diseases +MONDO:0013033 gard_rare diseases +MONDO:0013033 rare diseases +MONDO:0013034 gard_rare diseases +MONDO:0013034 nord_rare diseases +MONDO:0013034 otar diseases +MONDO:0013034 rare diseases +MONDO:0013035 gard_rare diseases +MONDO:0013035 nord_rare diseases +MONDO:0013035 ordo_disorder diseases +MONDO:0013035 ordo_malformation_syndrome diseases +MONDO:0013035 orphanet_rare diseases +MONDO:0013035 otar diseases +MONDO:0013035 rare diseases +MONDO:0013036 gard_rare diseases +MONDO:0013036 ordo_disorder diseases +MONDO:0013036 ordo_malformation_syndrome diseases +MONDO:0013036 orphanet_rare diseases +MONDO:0013036 otar diseases +MONDO:0013036 rare diseases +MONDO:0013038 gard_rare diseases +MONDO:0013038 nord_rare diseases +MONDO:0013038 ordo_disorder diseases +MONDO:0013038 ordo_malformation_syndrome diseases +MONDO:0013038 orphanet_rare diseases +MONDO:0013038 otar diseases +MONDO:0013038 rare diseases +MONDO:0013039 gard_rare diseases +MONDO:0013039 nord_rare diseases +MONDO:0013039 rare diseases +MONDO:0013040 gard_rare diseases +MONDO:0013040 nord_rare diseases +MONDO:0013040 ordo_etiological_subtype diseases +MONDO:0013040 otar diseases +MONDO:0013040 predisposition diseases +MONDO:0013040 rare diseases +MONDO:0013041 gard_rare diseases +MONDO:0013041 nord_rare diseases +MONDO:0013041 ordo_etiological_subtype diseases +MONDO:0013041 otar diseases +MONDO:0013041 predisposition diseases +MONDO:0013041 rare diseases +MONDO:0013042 clingen diseases +MONDO:0013042 gard_rare diseases +MONDO:0013042 nord_rare diseases +MONDO:0013042 ordo_etiological_subtype diseases +MONDO:0013042 otar diseases +MONDO:0013042 predisposition diseases +MONDO:0013042 rare diseases +MONDO:0013043 clingen diseases +MONDO:0013043 gard_rare diseases +MONDO:0013043 nord_rare diseases +MONDO:0013043 ordo_etiological_subtype diseases +MONDO:0013043 otar diseases +MONDO:0013043 predisposition diseases +MONDO:0013043 rare diseases +MONDO:0013044 gard_rare diseases +MONDO:0013044 nord_rare diseases +MONDO:0013044 ordo_etiological_subtype diseases +MONDO:0013044 otar diseases +MONDO:0013044 predisposition diseases +MONDO:0013044 rare diseases +MONDO:0013046 gard_rare diseases +MONDO:0013046 nord_rare diseases +MONDO:0013046 ordo_disorder diseases +MONDO:0013046 orphanet_rare diseases +MONDO:0013046 otar diseases +MONDO:0013046 rare diseases +MONDO:0013047 gard_rare diseases +MONDO:0013047 nord_rare diseases +MONDO:0013047 ordo_subtype_of_a_disorder diseases +MONDO:0013047 otar diseases +MONDO:0013047 rare diseases +MONDO:0013048 gard_rare diseases +MONDO:0013048 nord_rare diseases +MONDO:0013048 otar diseases +MONDO:0013048 rare diseases +MONDO:0013049 gard_rare diseases +MONDO:0013049 nord_rare diseases +MONDO:0013049 ordo_disorder diseases +MONDO:0013049 orphanet_rare diseases +MONDO:0013049 otar diseases +MONDO:0013049 rare diseases +MONDO:0013050 gard_rare diseases +MONDO:0013050 nord_rare diseases +MONDO:0013050 ordo_disorder diseases +MONDO:0013050 ordo_malformation_syndrome diseases +MONDO:0013050 orphanet_rare diseases +MONDO:0013050 otar diseases +MONDO:0013050 rare diseases +MONDO:0013051 clingen diseases +MONDO:0013051 gard_rare diseases +MONDO:0013051 nord_rare diseases +MONDO:0013051 ordo_disorder diseases +MONDO:0013051 orphanet_rare diseases +MONDO:0013051 otar diseases +MONDO:0013051 rare diseases +MONDO:0013052 gard_rare diseases +MONDO:0013052 nord_rare diseases +MONDO:0013052 rare diseases +MONDO:0013053 gard_rare diseases +MONDO:0013053 nord_rare diseases +MONDO:0013053 ordo_disorder diseases +MONDO:0013053 ordo_malformation_syndrome diseases +MONDO:0013053 orphanet_rare diseases +MONDO:0013053 otar diseases +MONDO:0013053 rare diseases +MONDO:0013056 gard_rare diseases +MONDO:0013056 nord_rare diseases +MONDO:0013056 ordo_disorder diseases +MONDO:0013056 orphanet_rare diseases +MONDO:0013056 otar diseases +MONDO:0013056 rare diseases +MONDO:0013058 gard_rare diseases +MONDO:0013058 nord_rare diseases +MONDO:0013058 ordo_disorder diseases +MONDO:0013058 orphanet_rare diseases +MONDO:0013058 otar diseases +MONDO:0013058 rare diseases +MONDO:0013059 gard_rare diseases +MONDO:0013059 nord_rare diseases +MONDO:0013059 rare diseases +MONDO:0013060 gard_rare diseases +MONDO:0013060 nord_rare diseases +MONDO:0013060 ordo_disorder diseases +MONDO:0013060 orphanet_rare diseases +MONDO:0013060 otar diseases +MONDO:0013060 rare diseases +MONDO:0013061 gard_rare diseases +MONDO:0013061 nord_rare diseases +MONDO:0013061 ordo_disorder diseases +MONDO:0013061 orphanet_rare diseases +MONDO:0013061 otar diseases +MONDO:0013061 rare diseases +MONDO:0013062 gard_rare diseases +MONDO:0013062 nord_rare diseases +MONDO:0013062 otar diseases +MONDO:0013062 rare diseases +MONDO:0013063 gard_rare diseases +MONDO:0013063 rare diseases +MONDO:0013064 gard_rare diseases +MONDO:0013064 nord_rare diseases +MONDO:0013064 rare diseases +MONDO:0013065 gard_rare diseases +MONDO:0013065 nord_rare diseases +MONDO:0013065 rare diseases +MONDO:0013066 gard_rare diseases +MONDO:0013066 nord_rare diseases +MONDO:0013066 rare diseases +MONDO:0013067 gard_rare diseases +MONDO:0013067 rare diseases +MONDO:0013069 gard_rare diseases +MONDO:0013069 nord_rare diseases +MONDO:0013069 ordo_disorder diseases +MONDO:0013069 orphanet_rare diseases +MONDO:0013069 otar diseases +MONDO:0013069 rare diseases +MONDO:0013070 gard_rare diseases +MONDO:0013070 rare diseases +MONDO:0013071 gard_rare diseases +MONDO:0013071 nord_rare diseases +MONDO:0013071 rare diseases +MONDO:0013072 gard_rare diseases +MONDO:0013072 nord_rare diseases +MONDO:0013072 rare diseases +MONDO:0013073 gard_rare diseases +MONDO:0013073 nord_rare diseases +MONDO:0013073 rare diseases +MONDO:0013074 gard_rare diseases +MONDO:0013074 nord_rare diseases +MONDO:0013074 ordo_disorder diseases +MONDO:0013074 orphanet_rare diseases +MONDO:0013074 otar diseases +MONDO:0013074 rare diseases +MONDO:0013079 gard_rare diseases +MONDO:0013079 nord_rare diseases +MONDO:0013079 rare diseases +MONDO:0013080 gard_rare diseases +MONDO:0013080 nord_rare diseases +MONDO:0013080 rare diseases +MONDO:0013081 clingen diseases +MONDO:0013081 gard_rare diseases +MONDO:0013081 nord_rare diseases +MONDO:0013081 ordo_disorder diseases +MONDO:0013081 orphanet_rare diseases +MONDO:0013081 otar diseases +MONDO:0013081 rare diseases +MONDO:0013082 gard_rare diseases +MONDO:0013082 nord_rare diseases +MONDO:0013082 ordo_disorder diseases +MONDO:0013082 ordo_malformation_syndrome diseases +MONDO:0013082 orphanet_rare diseases +MONDO:0013082 otar diseases +MONDO:0013082 predisposition diseases +MONDO:0013082 rare diseases +MONDO:0013083 clingen diseases +MONDO:0013083 inferred_rare diseases +MONDO:0013083 predisposition diseases +MONDO:0013083 rare diseases +MONDO:0013084 inferred_rare diseases +MONDO:0013084 predisposition diseases +MONDO:0013084 rare diseases +MONDO:0013085 inferred_rare diseases +MONDO:0013085 predisposition diseases +MONDO:0013085 rare diseases +MONDO:0013086 inferred_rare diseases +MONDO:0013086 predisposition diseases +MONDO:0013086 rare diseases +MONDO:0013087 gard_rare diseases +MONDO:0013087 nord_rare diseases +MONDO:0013087 rare diseases +MONDO:0013088 inferred_rare diseases +MONDO:0013088 predisposition diseases +MONDO:0013088 rare diseases +MONDO:0013090 gard_rare diseases +MONDO:0013090 nord_rare diseases +MONDO:0013090 ordo_disorder diseases +MONDO:0013090 ordo_malformation_syndrome diseases +MONDO:0013090 orphanet_rare diseases +MONDO:0013090 otar diseases +MONDO:0013090 rare diseases +MONDO:0013091 gard_rare diseases +MONDO:0013091 nord_rare diseases +MONDO:0013091 rare diseases +MONDO:0013092 gard_rare diseases +MONDO:0013092 predisposition diseases +MONDO:0013092 rare diseases +MONDO:0013093 gard_rare diseases +MONDO:0013093 predisposition diseases +MONDO:0013093 rare diseases +MONDO:0013094 gard_rare diseases +MONDO:0013094 rare diseases +MONDO:0013095 gard_rare diseases +MONDO:0013095 rare diseases +MONDO:0013096 gard_rare diseases +MONDO:0013096 rare diseases +MONDO:0013097 gard_rare diseases +MONDO:0013097 rare diseases +MONDO:0013098 otar diseases +MONDO:0013099 clingen diseases +MONDO:0013099 gard_rare diseases +MONDO:0013099 nord_rare diseases +MONDO:0013099 ordo_disorder diseases +MONDO:0013099 orphanet_rare diseases +MONDO:0013099 otar diseases +MONDO:0013099 rare diseases +MONDO:0013100 gard_rare diseases +MONDO:0013100 rare diseases +MONDO:0013108 gard_rare diseases +MONDO:0013108 predisposition diseases +MONDO:0013108 rare diseases +MONDO:0013109 gard_rare diseases +MONDO:0013109 predisposition diseases +MONDO:0013109 rare diseases +MONDO:0013110 clingen diseases +MONDO:0013110 gard_rare diseases +MONDO:0013110 nord_rare diseases +MONDO:0013110 ordo_disorder diseases +MONDO:0013110 orphanet_rare diseases +MONDO:0013110 otar diseases +MONDO:0013110 rare diseases +MONDO:0013111 gard_rare diseases +MONDO:0013111 nord_rare diseases +MONDO:0013111 ordo_disorder diseases +MONDO:0013111 orphanet_rare diseases +MONDO:0013111 otar diseases +MONDO:0013111 rare diseases +MONDO:0013112 gard_rare diseases +MONDO:0013112 nord_rare diseases +MONDO:0013112 rare diseases +MONDO:0013113 gard_rare diseases +MONDO:0013113 nord_rare diseases +MONDO:0013113 rare diseases +MONDO:0013114 gard_rare diseases +MONDO:0013114 nord_rare diseases +MONDO:0013114 rare diseases +MONDO:0013115 clingen diseases +MONDO:0013115 gard_rare diseases +MONDO:0013115 nord_rare diseases +MONDO:0013115 ordo_disorder diseases +MONDO:0013115 ordo_malformation_syndrome diseases +MONDO:0013115 orphanet_rare diseases +MONDO:0013115 otar diseases +MONDO:0013115 rare diseases +MONDO:0013116 gard_rare diseases +MONDO:0013116 nord_rare diseases +MONDO:0013116 ordo_disorder diseases +MONDO:0013116 orphanet_rare diseases +MONDO:0013116 otar diseases +MONDO:0013116 rare diseases +MONDO:0013117 gard_rare diseases +MONDO:0013117 otar diseases +MONDO:0013117 rare diseases +MONDO:0013118 gard_rare diseases +MONDO:0013118 nord_rare diseases +MONDO:0013118 ordo_disorder diseases +MONDO:0013118 ordo_malformation_syndrome diseases +MONDO:0013118 orphanet_rare diseases +MONDO:0013118 otar diseases +MONDO:0013118 rare diseases +MONDO:0013119 gard_rare diseases +MONDO:0013119 nord_rare diseases +MONDO:0013119 rare diseases +MONDO:0013120 gard_rare diseases +MONDO:0013120 nord_rare diseases +MONDO:0013120 rare diseases +MONDO:0013121 gard_rare diseases +MONDO:0013121 rare diseases +MONDO:0013122 clingen diseases +MONDO:0013122 gard_rare diseases +MONDO:0013122 rare diseases +MONDO:0013123 gard_rare diseases +MONDO:0013123 nord_rare diseases +MONDO:0013123 rare diseases +MONDO:0013125 gard_rare diseases +MONDO:0013125 nord_rare diseases +MONDO:0013125 ordo_disorder diseases +MONDO:0013125 ordo_malformation_syndrome diseases +MONDO:0013125 orphanet_rare diseases +MONDO:0013125 otar diseases +MONDO:0013125 rare diseases +MONDO:0013127 gard_rare diseases +MONDO:0013127 nord_rare diseases +MONDO:0013127 ordo_disorder diseases +MONDO:0013127 ordo_malformation_syndrome diseases +MONDO:0013127 orphanet_rare diseases +MONDO:0013127 otar diseases +MONDO:0013127 rare diseases +MONDO:0013128 clingen diseases +MONDO:0013128 gard_rare diseases +MONDO:0013128 nord_rare diseases +MONDO:0013128 ordo_subtype_of_a_disorder diseases +MONDO:0013128 otar diseases +MONDO:0013128 rare diseases +MONDO:0013129 gard_rare diseases +MONDO:0013129 nord_rare diseases +MONDO:0013129 rare diseases +MONDO:0013130 gard_rare diseases +MONDO:0013130 nord_rare diseases +MONDO:0013130 rare diseases +MONDO:0013131 gard_rare diseases +MONDO:0013131 nord_rare diseases +MONDO:0013131 otar diseases +MONDO:0013131 rare diseases +MONDO:0013132 gard_rare diseases +MONDO:0013132 ordo_disorder diseases +MONDO:0013132 orphanet_rare diseases +MONDO:0013132 otar diseases +MONDO:0013132 rare diseases +MONDO:0013133 inferred_rare diseases +MONDO:0013133 predisposition diseases +MONDO:0013133 rare diseases +MONDO:0013134 clingen diseases +MONDO:0013134 gard_rare diseases +MONDO:0013134 rare diseases +MONDO:0013135 clingen diseases +MONDO:0013135 gard_rare diseases +MONDO:0013135 nord_rare diseases +MONDO:0013135 rare diseases +MONDO:0013136 gard_rare diseases +MONDO:0013136 nord_rare diseases +MONDO:0013136 ordo_disorder diseases +MONDO:0013136 orphanet_rare diseases +MONDO:0013136 otar diseases +MONDO:0013136 rare diseases +MONDO:0013137 gard_rare diseases +MONDO:0013137 rare diseases +MONDO:0013138 gard_rare diseases +MONDO:0013138 rare diseases +MONDO:0013139 gard_rare diseases +MONDO:0013139 nord_rare diseases +MONDO:0013139 otar diseases +MONDO:0013139 rare diseases +MONDO:0013140 gard_rare diseases +MONDO:0013140 nord_rare diseases +MONDO:0013140 rare diseases +MONDO:0013142 gard_rare diseases +MONDO:0013142 nord_rare diseases +MONDO:0013142 rare diseases +MONDO:0013143 clingen diseases +MONDO:0013143 gard_rare diseases +MONDO:0013143 nord_rare diseases +MONDO:0013143 ordo_disorder diseases +MONDO:0013143 orphanet_rare diseases +MONDO:0013143 otar diseases +MONDO:0013143 rare diseases +MONDO:0013144 clingen diseases +MONDO:0013144 gard_rare diseases +MONDO:0013144 nord_rare diseases +MONDO:0013144 ordo_disorder diseases +MONDO:0013144 orphanet_rare diseases +MONDO:0013144 otar diseases +MONDO:0013144 rare diseases +MONDO:0013145 gard_rare diseases +MONDO:0013145 nord_rare diseases +MONDO:0013145 rare diseases +MONDO:0013146 gard_rare diseases +MONDO:0013146 rare diseases +MONDO:0013147 gard_rare diseases +MONDO:0013147 nord_rare diseases +MONDO:0013147 rare diseases +MONDO:0013148 gard_rare diseases +MONDO:0013148 rare diseases +MONDO:0013150 gard_rare diseases +MONDO:0013150 nord_rare diseases +MONDO:0013150 ordo_disorder diseases +MONDO:0013150 orphanet_rare diseases +MONDO:0013150 otar diseases +MONDO:0013150 rare diseases +MONDO:0013151 gard_rare diseases +MONDO:0013151 rare diseases +MONDO:0013153 gard_rare diseases +MONDO:0013153 nord_rare diseases +MONDO:0013153 rare diseases +MONDO:0013154 gard_rare diseases +MONDO:0013154 nord_rare diseases +MONDO:0013154 otar diseases +MONDO:0013154 rare diseases +MONDO:0013155 gard_rare diseases +MONDO:0013155 otar diseases +MONDO:0013155 rare diseases +MONDO:0013156 gard_rare diseases +MONDO:0013156 otar diseases +MONDO:0013156 rare diseases +MONDO:0013157 gard_rare diseases +MONDO:0013157 nord_rare diseases +MONDO:0013157 otar diseases +MONDO:0013157 rare diseases +MONDO:0013158 gard_rare diseases +MONDO:0013158 nord_rare diseases +MONDO:0013158 otar diseases +MONDO:0013158 rare diseases +MONDO:0013159 gard_rare diseases +MONDO:0013159 otar diseases +MONDO:0013159 rare diseases +MONDO:0013160 gard_rare diseases +MONDO:0013160 otar diseases +MONDO:0013160 rare diseases +MONDO:0013161 gard_rare diseases +MONDO:0013161 ordo_disorder diseases +MONDO:0013161 orphanet_rare diseases +MONDO:0013161 otar diseases +MONDO:0013161 rare diseases +MONDO:0013162 gard_rare diseases +MONDO:0013162 nord_rare diseases +MONDO:0013162 ordo_disorder diseases +MONDO:0013162 orphanet_rare diseases +MONDO:0013162 otar diseases +MONDO:0013162 rare diseases +MONDO:0013163 clingen diseases +MONDO:0013163 gard_rare diseases +MONDO:0013163 nord_rare diseases +MONDO:0013163 rare diseases +MONDO:0013164 gard_rare diseases +MONDO:0013164 nord_rare diseases +MONDO:0013164 ordo_disorder diseases +MONDO:0013164 orphanet_rare diseases +MONDO:0013164 otar diseases +MONDO:0013164 rare diseases +MONDO:0013165 gard_rare diseases +MONDO:0013165 nord_rare diseases +MONDO:0013165 ordo_disorder diseases +MONDO:0013165 orphanet_rare diseases +MONDO:0013165 otar diseases +MONDO:0013165 rare diseases +MONDO:0013166 gard_rare diseases +MONDO:0013166 nord_rare diseases +MONDO:0013166 ordo_disorder diseases +MONDO:0013166 orphanet_rare diseases +MONDO:0013166 otar diseases +MONDO:0013166 rare diseases +MONDO:0013168 gard_rare diseases +MONDO:0013168 nord_rare diseases +MONDO:0013168 rare diseases +MONDO:0013169 gard_rare diseases +MONDO:0013169 nord_rare diseases +MONDO:0013169 ordo_disorder diseases +MONDO:0013169 ordo_malformation_syndrome diseases +MONDO:0013169 orphanet_rare diseases +MONDO:0013169 otar diseases +MONDO:0013169 rare diseases +MONDO:0013170 gard_rare diseases +MONDO:0013170 nord_rare diseases +MONDO:0013170 ordo_disorder diseases +MONDO:0013170 ordo_malformation_syndrome diseases +MONDO:0013170 orphanet_rare diseases +MONDO:0013170 otar diseases +MONDO:0013170 rare diseases +MONDO:0013171 gard_rare diseases +MONDO:0013171 nord_rare diseases +MONDO:0013171 ordo_disorder diseases +MONDO:0013171 orphanet_rare diseases +MONDO:0013171 otar diseases +MONDO:0013171 rare diseases +MONDO:0013172 gard_rare diseases +MONDO:0013172 nord_rare diseases +MONDO:0013172 ordo_disorder diseases +MONDO:0013172 ordo_malformation_syndrome diseases +MONDO:0013172 orphanet_rare diseases +MONDO:0013172 otar diseases +MONDO:0013172 rare diseases +MONDO:0013173 gard_rare diseases +MONDO:0013173 nord_rare diseases +MONDO:0013173 otar diseases +MONDO:0013173 rare diseases +MONDO:0013174 clingen diseases +MONDO:0013174 gard_rare diseases +MONDO:0013174 nord_rare diseases +MONDO:0013174 rare diseases +MONDO:0013175 gard_rare diseases +MONDO:0013175 nord_rare diseases +MONDO:0013175 rare diseases +MONDO:0013176 gard_rare diseases +MONDO:0013176 nord_rare diseases +MONDO:0013176 ordo_disorder diseases +MONDO:0013176 orphanet_rare diseases +MONDO:0013176 otar diseases +MONDO:0013176 rare diseases +MONDO:0013177 gard_rare diseases +MONDO:0013177 nord_rare diseases +MONDO:0013177 ordo_disorder diseases +MONDO:0013177 orphanet_rare diseases +MONDO:0013177 otar diseases +MONDO:0013177 rare diseases +MONDO:0013178 gard_rare diseases +MONDO:0013178 nord_rare diseases +MONDO:0013178 ordo_disorder diseases +MONDO:0013178 orphanet_rare diseases +MONDO:0013178 otar diseases +MONDO:0013178 rare diseases +MONDO:0013179 gard_rare diseases +MONDO:0013179 nord_rare diseases +MONDO:0013179 ordo_disorder diseases +MONDO:0013179 orphanet_rare diseases +MONDO:0013179 otar diseases +MONDO:0013179 rare diseases +MONDO:0013181 gard_rare diseases +MONDO:0013181 rare diseases +MONDO:0013182 gard_rare diseases +MONDO:0013182 nord_rare diseases +MONDO:0013182 ordo_disorder diseases +MONDO:0013182 ordo_malformation_syndrome diseases +MONDO:0013182 orphanet_rare diseases +MONDO:0013182 rare diseases +MONDO:0013183 gard_rare diseases +MONDO:0013183 rare diseases +MONDO:0013184 gard_rare diseases +MONDO:0013184 nord_rare diseases +MONDO:0013184 ordo_disorder diseases +MONDO:0013184 orphanet_rare diseases +MONDO:0013184 otar diseases +MONDO:0013184 rare diseases +MONDO:0013186 gard_rare diseases +MONDO:0013186 nord_rare diseases +MONDO:0013186 rare diseases +MONDO:0013187 clingen diseases +MONDO:0013187 gard_rare diseases +MONDO:0013187 nord_rare diseases +MONDO:0013187 otar diseases +MONDO:0013187 rare diseases +MONDO:0013188 gard_rare diseases +MONDO:0013188 nord_rare diseases +MONDO:0013188 rare diseases +MONDO:0013190 clingen diseases +MONDO:0013190 gard_rare diseases +MONDO:0013190 nord_rare diseases +MONDO:0013190 rare diseases +MONDO:0013191 gard_rare diseases +MONDO:0013191 nord_rare diseases +MONDO:0013191 rare diseases +MONDO:0013195 gard_rare diseases +MONDO:0013195 nord_rare diseases +MONDO:0013195 otar diseases +MONDO:0013195 rare diseases +MONDO:0013196 gard_rare diseases +MONDO:0013196 nord_rare diseases +MONDO:0013196 otar diseases +MONDO:0013196 rare diseases +MONDO:0013197 gard_rare diseases +MONDO:0013197 nord_rare diseases +MONDO:0013197 rare diseases +MONDO:0013198 gard_rare diseases +MONDO:0013198 nord_rare diseases +MONDO:0013198 rare diseases +MONDO:0013199 gard_rare diseases +MONDO:0013199 nord_rare diseases +MONDO:0013199 rare diseases +MONDO:0013200 gard_rare diseases +MONDO:0013200 nord_rare diseases +MONDO:0013200 rare diseases +MONDO:0013201 clingen diseases +MONDO:0013201 gard_rare diseases +MONDO:0013201 nord_rare diseases +MONDO:0013201 rare diseases +MONDO:0013202 clingen diseases +MONDO:0013202 gard_rare diseases +MONDO:0013202 nord_rare diseases +MONDO:0013202 rare diseases +MONDO:0013203 gard_rare diseases +MONDO:0013203 nord_rare diseases +MONDO:0013203 rare diseases +MONDO:0013204 gard_rare diseases +MONDO:0013204 nord_rare diseases +MONDO:0013204 rare diseases +MONDO:0013205 gard_rare diseases +MONDO:0013205 nord_rare diseases +MONDO:0013205 rare diseases +MONDO:0013206 gard_rare diseases +MONDO:0013206 nord_rare diseases +MONDO:0013206 rare diseases +MONDO:0013207 gard_rare diseases +MONDO:0013207 nord_rare diseases +MONDO:0013207 rare diseases +MONDO:0013208 gard_rare diseases +MONDO:0013208 nord_rare diseases +MONDO:0013208 ordo_disorder diseases +MONDO:0013208 orphanet_rare diseases +MONDO:0013208 otar diseases +MONDO:0013208 rare diseases +MONDO:0013209 otar diseases +MONDO:0013209 predisposition diseases +MONDO:0013210 gard_rare diseases +MONDO:0013210 nord_rare diseases +MONDO:0013210 rare diseases +MONDO:0013211 gard_rare diseases +MONDO:0013211 nord_rare diseases +MONDO:0013211 rare diseases +MONDO:0013212 gard_rare diseases +MONDO:0013212 nord_rare diseases +MONDO:0013212 ordo_disorder diseases +MONDO:0013212 orphanet_rare diseases +MONDO:0013212 otar diseases +MONDO:0013212 rare diseases +MONDO:0013215 gard_rare diseases +MONDO:0013215 nord_rare diseases +MONDO:0013215 rare diseases +MONDO:0013216 gard_rare diseases +MONDO:0013216 nord_rare diseases +MONDO:0013216 rare diseases +MONDO:0013217 gard_rare diseases +MONDO:0013217 nord_rare diseases +MONDO:0013217 rare diseases +MONDO:0013218 gard_rare diseases +MONDO:0013218 nord_rare diseases +MONDO:0013218 rare diseases +MONDO:0013219 gard_rare diseases +MONDO:0013219 nord_rare diseases +MONDO:0013219 rare diseases +MONDO:0013220 gard_rare diseases +MONDO:0013220 nord_rare diseases +MONDO:0013220 otar diseases +MONDO:0013220 rare diseases +MONDO:0013221 gard_rare diseases +MONDO:0013221 rare diseases +MONDO:0013222 gard_rare diseases +MONDO:0013222 nord_rare diseases +MONDO:0013222 ordo_disorder diseases +MONDO:0013222 orphanet_rare diseases +MONDO:0013222 otar diseases +MONDO:0013222 rare diseases +MONDO:0013223 gard_rare diseases +MONDO:0013223 nord_rare diseases +MONDO:0013223 ordo_disorder diseases +MONDO:0013223 ordo_malformation_syndrome diseases +MONDO:0013223 orphanet_rare diseases +MONDO:0013223 otar diseases +MONDO:0013223 rare diseases +MONDO:0013224 clingen diseases +MONDO:0013224 gard_rare diseases +MONDO:0013224 nord_rare diseases +MONDO:0013224 rare diseases +MONDO:0013225 gard_rare diseases +MONDO:0013225 nord_rare diseases +MONDO:0013225 otar diseases +MONDO:0013225 rare diseases +MONDO:0013226 gard_rare diseases +MONDO:0013226 nord_rare diseases +MONDO:0013226 ordo_disorder diseases +MONDO:0013226 orphanet_rare diseases +MONDO:0013226 otar diseases +MONDO:0013226 rare diseases +MONDO:0013227 clingen diseases +MONDO:0013227 gard_rare diseases +MONDO:0013227 nord_rare diseases +MONDO:0013227 ordo_disorder diseases +MONDO:0013227 orphanet_rare diseases +MONDO:0013227 otar diseases +MONDO:0013227 rare diseases +MONDO:0013228 gard_rare diseases +MONDO:0013228 nord_rare diseases +MONDO:0013228 ordo_disorder diseases +MONDO:0013228 orphanet_rare diseases +MONDO:0013228 otar diseases +MONDO:0013228 rare diseases +MONDO:0013229 gard_rare diseases +MONDO:0013229 ordo_disorder diseases +MONDO:0013229 orphanet_rare diseases +MONDO:0013229 rare diseases +MONDO:0013230 gard_rare diseases +MONDO:0013230 rare diseases +MONDO:0013231 gard_rare diseases +MONDO:0013231 nord_rare diseases +MONDO:0013231 rare diseases +MONDO:0013232 gard_rare diseases +MONDO:0013232 nord_rare diseases +MONDO:0013232 ordo_disorder diseases +MONDO:0013232 orphanet_rare diseases +MONDO:0013232 otar diseases +MONDO:0013232 rare diseases +MONDO:0013233 gard_rare diseases +MONDO:0013233 nord_rare diseases +MONDO:0013233 ordo_disorder diseases +MONDO:0013233 orphanet_rare diseases +MONDO:0013233 otar diseases +MONDO:0013233 rare diseases +MONDO:0013234 gard_rare diseases +MONDO:0013234 rare diseases +MONDO:0013235 inferred_rare diseases +MONDO:0013235 predisposition diseases +MONDO:0013235 rare diseases +MONDO:0013236 inferred_rare diseases +MONDO:0013236 predisposition diseases +MONDO:0013236 rare diseases +MONDO:0013238 gard_rare diseases +MONDO:0013238 nord_rare diseases +MONDO:0013238 ordo_disorder diseases +MONDO:0013238 ordo_malformation_syndrome diseases +MONDO:0013238 orphanet_rare diseases +MONDO:0013238 otar diseases +MONDO:0013238 rare diseases +MONDO:0013239 gard_rare diseases +MONDO:0013239 ordo_disorder diseases +MONDO:0013239 orphanet_rare diseases +MONDO:0013239 otar diseases +MONDO:0013239 rare diseases +MONDO:0013240 gard_rare diseases +MONDO:0013240 nord_rare diseases +MONDO:0013240 rare diseases +MONDO:0013241 gard_rare diseases +MONDO:0013241 nord_rare diseases +MONDO:0013241 ordo_disorder diseases +MONDO:0013241 orphanet_rare diseases +MONDO:0013241 otar diseases +MONDO:0013241 rare diseases +MONDO:0013242 gard_rare diseases +MONDO:0013242 nord_rare diseases +MONDO:0013242 rare diseases +MONDO:0013243 gard_rare diseases +MONDO:0013243 nord_rare diseases +MONDO:0013243 rare diseases +MONDO:0013244 gard_rare diseases +MONDO:0013244 nord_rare diseases +MONDO:0013244 rare diseases +MONDO:0013245 gard_rare diseases +MONDO:0013245 nord_rare diseases +MONDO:0013245 ordo_disorder diseases +MONDO:0013245 orphanet_rare diseases +MONDO:0013245 otar diseases +MONDO:0013245 rare diseases +MONDO:0013247 gard_rare diseases +MONDO:0013247 nord_rare diseases +MONDO:0013247 rare diseases +MONDO:0013248 gard_rare diseases +MONDO:0013248 nord_rare diseases +MONDO:0013248 rare diseases +MONDO:0013249 gard_rare diseases +MONDO:0013249 nord_rare diseases +MONDO:0013249 rare diseases +MONDO:0013250 gard_rare diseases +MONDO:0013250 nord_rare diseases +MONDO:0013250 rare diseases +MONDO:0013251 otar diseases +MONDO:0013252 gard_rare diseases +MONDO:0013252 nord_rare diseases +MONDO:0013252 ordo_disorder diseases +MONDO:0013252 ordo_malformation_syndrome diseases +MONDO:0013252 orphanet_rare diseases +MONDO:0013252 otar diseases +MONDO:0013252 rare diseases +MONDO:0013254 clingen diseases +MONDO:0013254 gard_rare diseases +MONDO:0013254 nord_rare diseases +MONDO:0013254 otar diseases +MONDO:0013254 rare diseases +MONDO:0013255 clingen diseases +MONDO:0013255 gard_rare diseases +MONDO:0013255 nord_rare diseases +MONDO:0013255 rare diseases +MONDO:0013256 gard_rare diseases +MONDO:0013256 nord_rare diseases +MONDO:0013256 ordo_malformation_syndrome diseases +MONDO:0013256 ordo_subtype_of_a_disorder diseases +MONDO:0013256 otar diseases +MONDO:0013256 rare diseases +MONDO:0013259 gard_rare diseases +MONDO:0013259 nord_rare diseases +MONDO:0013259 rare diseases +MONDO:0013260 gard_rare diseases +MONDO:0013260 nord_rare diseases +MONDO:0013260 rare diseases +MONDO:0013261 gard_rare diseases +MONDO:0013261 nord_rare diseases +MONDO:0013261 rare diseases +MONDO:0013262 gard_rare diseases +MONDO:0013262 nord_rare diseases +MONDO:0013262 rare diseases +MONDO:0013263 gard_rare diseases +MONDO:0013263 nord_rare diseases +MONDO:0013263 rare diseases +MONDO:0013264 clingen diseases +MONDO:0013264 gard_rare diseases +MONDO:0013264 nord_rare diseases +MONDO:0013264 rare diseases +MONDO:0013266 gard_rare diseases +MONDO:0013266 nord_rare diseases +MONDO:0013266 rare diseases +MONDO:0013267 gard_rare diseases +MONDO:0013267 nord_rare diseases +MONDO:0013267 ordo_disorder diseases +MONDO:0013267 ordo_malformation_syndrome diseases +MONDO:0013267 orphanet_rare diseases +MONDO:0013267 otar diseases +MONDO:0013267 rare diseases +MONDO:0013268 gard_rare diseases +MONDO:0013268 nord_rare diseases +MONDO:0013268 ordo_disorder diseases +MONDO:0013268 ordo_malformation_syndrome diseases +MONDO:0013268 orphanet_rare diseases +MONDO:0013268 otar diseases +MONDO:0013268 rare diseases +MONDO:0013269 gard_rare diseases +MONDO:0013269 nord_rare diseases +MONDO:0013269 rare diseases +MONDO:0013270 gard_rare diseases +MONDO:0013270 nord_rare diseases +MONDO:0013270 rare diseases +MONDO:0013271 clingen diseases +MONDO:0013271 gard_rare diseases +MONDO:0013271 nord_rare diseases +MONDO:0013271 ordo_disorder diseases +MONDO:0013271 ordo_malformation_syndrome diseases +MONDO:0013271 orphanet_rare diseases +MONDO:0013271 otar diseases +MONDO:0013271 rare diseases +MONDO:0013272 gard_rare diseases +MONDO:0013272 nord_rare diseases +MONDO:0013272 ordo_disorder diseases +MONDO:0013272 ordo_malformation_syndrome diseases +MONDO:0013272 orphanet_rare diseases +MONDO:0013272 otar diseases +MONDO:0013272 rare diseases +MONDO:0013273 gard_rare diseases +MONDO:0013273 nord_rare diseases +MONDO:0013273 ordo_disorder diseases +MONDO:0013273 ordo_malformation_syndrome diseases +MONDO:0013273 orphanet_rare diseases +MONDO:0013273 otar diseases +MONDO:0013273 rare diseases +MONDO:0013274 gard_rare diseases +MONDO:0013274 nord_rare diseases +MONDO:0013274 rare diseases +MONDO:0013275 gard_rare diseases +MONDO:0013275 nord_rare diseases +MONDO:0013275 ordo_disorder diseases +MONDO:0013275 orphanet_rare diseases +MONDO:0013275 otar diseases +MONDO:0013275 rare diseases +MONDO:0013276 gard_rare diseases +MONDO:0013276 nord_rare diseases +MONDO:0013276 ordo_disorder diseases +MONDO:0013276 orphanet_rare diseases +MONDO:0013276 otar diseases +MONDO:0013276 rare diseases +MONDO:0013277 gard_rare diseases +MONDO:0013277 nord_rare diseases +MONDO:0013277 rare diseases +MONDO:0013278 gard_rare diseases +MONDO:0013278 nord_rare diseases +MONDO:0013278 rare diseases +MONDO:0013279 gard_rare diseases +MONDO:0013279 nord_rare diseases +MONDO:0013279 otar diseases +MONDO:0013279 rare diseases +MONDO:0013280 gard_rare diseases +MONDO:0013280 nord_rare diseases +MONDO:0013280 otar diseases +MONDO:0013280 rare diseases +MONDO:0013281 clingen diseases +MONDO:0013281 gard_rare diseases +MONDO:0013281 nord_rare diseases +MONDO:0013281 ordo_disorder diseases +MONDO:0013281 orphanet_rare diseases +MONDO:0013281 otar diseases +MONDO:0013281 rare diseases +MONDO:0013282 gard_rare diseases +MONDO:0013282 nord_rare diseases +MONDO:0013282 ordo_disorder diseases +MONDO:0013282 orphanet_rare diseases +MONDO:0013282 otar diseases +MONDO:0013282 rare diseases +MONDO:0013283 clingen diseases +MONDO:0013283 gard_rare diseases +MONDO:0013283 nord_rare diseases +MONDO:0013283 rare diseases +MONDO:0013284 clingen diseases +MONDO:0013284 gard_rare diseases +MONDO:0013284 nord_rare diseases +MONDO:0013284 otar diseases +MONDO:0013284 rare diseases +MONDO:0013285 clingen diseases +MONDO:0013285 gard_rare diseases +MONDO:0013285 nord_rare diseases +MONDO:0013285 rare diseases +MONDO:0013286 clingen diseases +MONDO:0013286 gard_rare diseases +MONDO:0013286 nord_rare diseases +MONDO:0013286 otar diseases +MONDO:0013286 rare diseases +MONDO:0013287 clingen diseases +MONDO:0013287 gard_rare diseases +MONDO:0013287 nord_rare diseases +MONDO:0013287 rare diseases +MONDO:0013288 clingen diseases +MONDO:0013288 gard_rare diseases +MONDO:0013288 nord_rare diseases +MONDO:0013288 rare diseases +MONDO:0013289 clingen diseases +MONDO:0013289 gard_rare diseases +MONDO:0013289 nord_rare diseases +MONDO:0013289 rare diseases +MONDO:0013290 gard_rare diseases +MONDO:0013290 nord_rare diseases +MONDO:0013290 rare diseases +MONDO:0013291 gard_rare diseases +MONDO:0013291 nord_rare diseases +MONDO:0013291 ordo_disorder diseases +MONDO:0013291 orphanet_rare diseases +MONDO:0013291 otar diseases +MONDO:0013291 rare diseases +MONDO:0013292 gard_rare diseases +MONDO:0013292 nord_rare diseases +MONDO:0013292 ordo_disorder diseases +MONDO:0013292 ordo_malformation_syndrome diseases +MONDO:0013292 orphanet_rare diseases +MONDO:0013292 rare diseases +MONDO:0013293 gard_rare diseases +MONDO:0013293 nord_rare diseases +MONDO:0013293 rare diseases +MONDO:0013296 gard_rare diseases +MONDO:0013296 nord_rare diseases +MONDO:0013296 ordo_disorder diseases +MONDO:0013296 orphanet_rare diseases +MONDO:0013296 rare diseases +MONDO:0013297 gard_rare diseases +MONDO:0013297 nord_rare diseases +MONDO:0013297 otar diseases +MONDO:0013297 rare diseases +MONDO:0013298 gard_rare diseases +MONDO:0013298 nord_rare diseases +MONDO:0013298 ordo_disorder diseases +MONDO:0013298 ordo_malformation_syndrome diseases +MONDO:0013298 orphanet_rare diseases +MONDO:0013298 otar diseases +MONDO:0013298 rare diseases +MONDO:0013299 gard_rare diseases +MONDO:0013299 nord_rare diseases +MONDO:0013299 rare diseases +MONDO:0013300 gard_rare diseases +MONDO:0013300 nord_rare diseases +MONDO:0013300 ordo_disorder diseases +MONDO:0013300 ordo_morphological_anomaly diseases +MONDO:0013300 orphanet_rare diseases +MONDO:0013300 otar diseases +MONDO:0013300 rare diseases +MONDO:0013301 gard_rare diseases +MONDO:0013301 nord_rare diseases +MONDO:0013301 ordo_disorder diseases +MONDO:0013301 orphanet_rare diseases +MONDO:0013301 otar diseases +MONDO:0013301 rare diseases +MONDO:0013302 gard_rare diseases +MONDO:0013302 nord_rare diseases +MONDO:0013302 otar diseases +MONDO:0013302 rare diseases +MONDO:0013304 gard_rare diseases +MONDO:0013304 nord_rare diseases +MONDO:0013304 ordo_subtype_of_a_disorder diseases +MONDO:0013304 otar diseases +MONDO:0013304 rare diseases +MONDO:0013305 gard_rare diseases +MONDO:0013305 nord_rare diseases +MONDO:0013305 rare diseases +MONDO:0013306 gard_rare diseases +MONDO:0013306 nord_rare diseases +MONDO:0013306 ordo_disorder diseases +MONDO:0013306 orphanet_rare diseases +MONDO:0013306 otar diseases +MONDO:0013306 rare diseases +MONDO:0013307 gard_rare diseases +MONDO:0013307 nord_rare diseases +MONDO:0013307 rare diseases +MONDO:0013308 clingen diseases +MONDO:0013308 gard_rare diseases +MONDO:0013308 nord_rare diseases +MONDO:0013308 ordo_disorder diseases +MONDO:0013308 ordo_malformation_syndrome diseases +MONDO:0013308 orphanet_rare diseases +MONDO:0013308 otar diseases +MONDO:0013308 rare diseases +MONDO:0013309 gard_rare diseases +MONDO:0013309 nord_rare diseases +MONDO:0013309 rare diseases +MONDO:0013310 gard_rare diseases +MONDO:0013310 nord_rare diseases +MONDO:0013310 ordo_disorder diseases +MONDO:0013310 orphanet_rare diseases +MONDO:0013310 otar diseases +MONDO:0013310 rare diseases +MONDO:0013311 gard_rare diseases +MONDO:0013311 nord_rare diseases +MONDO:0013311 ordo_disorder diseases +MONDO:0013311 ordo_malformation_syndrome diseases +MONDO:0013311 orphanet_rare diseases +MONDO:0013311 otar diseases +MONDO:0013311 prototype_pattern diseases +MONDO:0013311 rare diseases +MONDO:0013312 gard_rare diseases +MONDO:0013312 nord_rare diseases +MONDO:0013312 rare diseases +MONDO:0013313 gard_rare diseases +MONDO:0013313 nord_rare diseases +MONDO:0013313 ordo_disorder diseases +MONDO:0013313 ordo_malformation_syndrome diseases +MONDO:0013313 orphanet_rare diseases +MONDO:0013313 otar diseases +MONDO:0013313 rare diseases +MONDO:0013314 gard_rare diseases +MONDO:0013314 nord_rare diseases +MONDO:0013314 rare diseases +MONDO:0013315 gard_rare diseases +MONDO:0013315 nord_rare diseases +MONDO:0013315 rare diseases +MONDO:0013316 gard_rare diseases +MONDO:0013316 nord_rare diseases +MONDO:0013316 ordo_disorder diseases +MONDO:0013316 orphanet_rare diseases +MONDO:0013316 otar diseases +MONDO:0013316 rare diseases +MONDO:0013317 gard_rare diseases +MONDO:0013317 nord_rare diseases +MONDO:0013317 ordo_disorder diseases +MONDO:0013317 orphanet_rare diseases +MONDO:0013317 rare diseases +MONDO:0013319 gard_rare diseases +MONDO:0013319 nord_rare diseases +MONDO:0013319 rare diseases +MONDO:0013320 gard_rare diseases +MONDO:0013320 nord_rare diseases +MONDO:0013320 ordo_disorder diseases +MONDO:0013320 ordo_malformation_syndrome diseases +MONDO:0013320 orphanet_rare diseases +MONDO:0013320 otar diseases +MONDO:0013320 rare diseases +MONDO:0013322 gard_rare diseases +MONDO:0013322 nord_rare diseases +MONDO:0013322 rare diseases +MONDO:0013323 clingen diseases +MONDO:0013323 gard_rare diseases +MONDO:0013323 nord_rare diseases +MONDO:0013323 rare diseases +MONDO:0013324 gard_rare diseases +MONDO:0013324 nord_rare diseases +MONDO:0013324 ordo_disorder diseases +MONDO:0013324 ordo_malformation_syndrome diseases +MONDO:0013324 orphanet_rare diseases +MONDO:0013324 otar diseases +MONDO:0013324 rare diseases +MONDO:0013325 gard_rare diseases +MONDO:0013325 nord_rare diseases +MONDO:0013325 ordo_disorder diseases +MONDO:0013325 orphanet_rare diseases +MONDO:0013325 otar diseases +MONDO:0013325 rare diseases +MONDO:0013326 gard_rare diseases +MONDO:0013326 nord_rare diseases +MONDO:0013326 rare diseases +MONDO:0013327 gard_rare diseases +MONDO:0013327 nord_rare diseases +MONDO:0013327 ordo_subtype_of_a_disorder diseases +MONDO:0013327 otar diseases +MONDO:0013327 rare diseases +MONDO:0013328 gard_rare diseases +MONDO:0013328 nord_rare diseases +MONDO:0013328 rare diseases +MONDO:0013329 gard_rare diseases +MONDO:0013329 nord_rare diseases +MONDO:0013329 ordo_etiological_subtype diseases +MONDO:0013329 ordo_subtype_of_a_disorder diseases +MONDO:0013329 otar diseases +MONDO:0013329 rare diseases +MONDO:0013331 clingen diseases +MONDO:0013331 gard_rare diseases +MONDO:0013331 nord_rare diseases +MONDO:0013331 rare diseases +MONDO:0013333 gard_rare diseases +MONDO:0013333 nord_rare diseases +MONDO:0013333 rare diseases +MONDO:0013334 gard_rare diseases +MONDO:0013334 nord_rare diseases +MONDO:0013334 ordo_disorder diseases +MONDO:0013334 ordo_malformation_syndrome diseases +MONDO:0013334 orphanet_rare diseases +MONDO:0013334 otar diseases +MONDO:0013334 rare diseases +MONDO:0013336 gard_rare diseases +MONDO:0013336 nord_rare diseases +MONDO:0013336 ordo_disorder diseases +MONDO:0013336 ordo_malformation_syndrome diseases +MONDO:0013336 orphanet_rare diseases +MONDO:0013336 rare diseases +MONDO:0013337 clingen diseases +MONDO:0013337 gard_rare diseases +MONDO:0013337 nord_rare diseases +MONDO:0013337 rare diseases +MONDO:0013338 gard_rare diseases +MONDO:0013338 nord_rare diseases +MONDO:0013338 ordo_disorder diseases +MONDO:0013338 orphanet_rare diseases +MONDO:0013338 otar diseases +MONDO:0013338 rare diseases +MONDO:0013339 gard_rare diseases +MONDO:0013339 nord_rare diseases +MONDO:0013339 rare diseases +MONDO:0013341 clingen diseases +MONDO:0013341 gard_rare diseases +MONDO:0013341 nord_rare diseases +MONDO:0013341 ordo_biological_anomaly diseases +MONDO:0013341 ordo_disorder diseases +MONDO:0013341 orphanet_rare diseases +MONDO:0013341 otar diseases +MONDO:0013341 rare diseases +MONDO:0013342 gard_rare diseases +MONDO:0013342 nord_rare diseases +MONDO:0013342 ordo_disorder diseases +MONDO:0013342 orphanet_rare diseases +MONDO:0013342 otar diseases +MONDO:0013342 rare diseases +MONDO:0013343 clingen diseases +MONDO:0013343 gard_rare diseases +MONDO:0013343 otar diseases +MONDO:0013343 rare diseases +MONDO:0013345 gard_rare diseases +MONDO:0013345 rare diseases +MONDO:0013348 gard_rare diseases +MONDO:0013348 nord_rare diseases +MONDO:0013348 rare diseases +MONDO:0013349 clingen diseases +MONDO:0013349 gard_rare diseases +MONDO:0013349 nord_rare diseases +MONDO:0013349 ordo_disorder diseases +MONDO:0013349 orphanet_rare diseases +MONDO:0013349 otar diseases +MONDO:0013349 rare diseases +MONDO:0013350 gard_rare diseases +MONDO:0013350 rare diseases +MONDO:0013351 gard_rare diseases +MONDO:0013351 nord_rare diseases +MONDO:0013351 ordo_disorder diseases +MONDO:0013351 ordo_malformation_syndrome diseases +MONDO:0013351 orphanet_rare diseases +MONDO:0013351 otar diseases +MONDO:0013351 rare diseases +MONDO:0013352 clingen diseases +MONDO:0013352 gard_rare diseases +MONDO:0013352 nord_rare diseases +MONDO:0013352 ordo_disorder diseases +MONDO:0013352 ordo_malformation_syndrome diseases +MONDO:0013352 orphanet_rare diseases +MONDO:0013352 otar diseases +MONDO:0013352 rare diseases +MONDO:0013353 gard_rare diseases +MONDO:0013353 nord_rare diseases +MONDO:0013353 ordo_disorder diseases +MONDO:0013353 orphanet_rare diseases +MONDO:0013353 rare diseases +MONDO:0013354 gard_rare diseases +MONDO:0013354 nord_rare diseases +MONDO:0013354 ordo_disorder diseases +MONDO:0013354 orphanet_rare diseases +MONDO:0013354 otar diseases +MONDO:0013354 rare diseases +MONDO:0013355 gard_rare diseases +MONDO:0013355 nord_rare diseases +MONDO:0013355 ordo_disorder diseases +MONDO:0013355 orphanet_rare diseases +MONDO:0013355 otar diseases +MONDO:0013355 rare diseases +MONDO:0013356 gard_rare diseases +MONDO:0013356 nord_rare diseases +MONDO:0013356 rare diseases +MONDO:0013357 gard_rare diseases +MONDO:0013357 nord_rare diseases +MONDO:0013357 ordo_disorder diseases +MONDO:0013357 ordo_malformation_syndrome diseases +MONDO:0013357 ordo_subtype_of_a_disorder diseases +MONDO:0013357 orphanet_rare diseases +MONDO:0013357 otar diseases +MONDO:0013357 rare diseases +MONDO:0013358 gard_rare diseases +MONDO:0013358 nord_rare diseases +MONDO:0013358 rare diseases +MONDO:0013359 gard_rare diseases +MONDO:0013359 nord_rare diseases +MONDO:0013359 ordo_disorder diseases +MONDO:0013359 orphanet_rare diseases +MONDO:0013359 otar diseases +MONDO:0013359 rare diseases +MONDO:0013360 gard_rare diseases +MONDO:0013360 nord_rare diseases +MONDO:0013360 ordo_disorder diseases +MONDO:0013360 ordo_malformation_syndrome diseases +MONDO:0013360 orphanet_rare diseases +MONDO:0013360 otar diseases +MONDO:0013360 rare diseases +MONDO:0013361 clingen diseases +MONDO:0013361 gard_rare diseases +MONDO:0013361 nord_rare diseases +MONDO:0013361 ordo_disorder diseases +MONDO:0013361 orphanet_rare diseases +MONDO:0013361 otar diseases +MONDO:0013361 rare diseases +MONDO:0013362 gard_rare diseases +MONDO:0013362 ordo_disorder diseases +MONDO:0013362 ordo_malformation_syndrome diseases +MONDO:0013362 orphanet_rare diseases +MONDO:0013362 otar diseases +MONDO:0013362 rare diseases +MONDO:0013363 gard_rare diseases +MONDO:0013363 nord_rare diseases +MONDO:0013363 ordo_disorder diseases +MONDO:0013363 ordo_malformation_syndrome diseases +MONDO:0013363 orphanet_rare diseases +MONDO:0013363 rare diseases +MONDO:0013364 clingen diseases +MONDO:0013364 gard_rare diseases +MONDO:0013364 nord_rare diseases +MONDO:0013364 ordo_subtype_of_a_disorder diseases +MONDO:0013364 otar diseases +MONDO:0013364 rare diseases +MONDO:0013365 gard_rare diseases +MONDO:0013365 nord_rare diseases +MONDO:0013365 rare diseases +MONDO:0013366 gard_rare diseases +MONDO:0013366 nord_rare diseases +MONDO:0013366 rare diseases +MONDO:0013367 gard_rare diseases +MONDO:0013367 rare diseases +MONDO:0013368 gard_rare diseases +MONDO:0013368 nord_rare diseases +MONDO:0013368 ordo_disorder diseases +MONDO:0013368 ordo_malformation_syndrome diseases +MONDO:0013368 orphanet_rare diseases +MONDO:0013368 otar diseases +MONDO:0013368 rare diseases +MONDO:0013369 gard_rare diseases +MONDO:0013369 nord_rare diseases +MONDO:0013369 rare diseases +MONDO:0013370 gard_rare diseases +MONDO:0013370 rare diseases +MONDO:0013371 gard_rare diseases +MONDO:0013371 nord_rare diseases +MONDO:0013371 rare diseases +MONDO:0013372 clingen diseases +MONDO:0013372 gard_rare diseases +MONDO:0013372 nord_rare diseases +MONDO:0013372 otar diseases +MONDO:0013372 rare diseases +MONDO:0013373 gard_rare diseases +MONDO:0013373 nord_rare diseases +MONDO:0013373 rare diseases +MONDO:0013375 gard_rare diseases +MONDO:0013375 nord_rare diseases +MONDO:0013375 rare diseases +MONDO:0013376 gard_rare diseases +MONDO:0013376 nord_rare diseases +MONDO:0013376 rare diseases +MONDO:0013377 gard_rare diseases +MONDO:0013377 nord_rare diseases +MONDO:0013377 rare diseases +MONDO:0013378 gard_rare diseases +MONDO:0013378 rare diseases +MONDO:0013379 gard_rare diseases +MONDO:0013379 nord_rare diseases +MONDO:0013379 rare diseases +MONDO:0013380 gard_rare diseases +MONDO:0013380 nord_rare diseases +MONDO:0013380 rare diseases +MONDO:0013381 clingen diseases +MONDO:0013381 gard_rare diseases +MONDO:0013381 nord_rare diseases +MONDO:0013381 rare diseases +MONDO:0013382 gard_rare diseases +MONDO:0013382 nord_rare diseases +MONDO:0013382 ordo_disorder diseases +MONDO:0013382 orphanet_rare diseases +MONDO:0013382 otar diseases +MONDO:0013382 rare diseases +MONDO:0013385 gard_rare diseases +MONDO:0013385 nord_rare diseases +MONDO:0013385 rare diseases +MONDO:0013386 gard_rare diseases +MONDO:0013386 nord_rare diseases +MONDO:0013386 rare diseases +MONDO:0013387 gard_rare diseases +MONDO:0013387 nord_rare diseases +MONDO:0013387 ordo_disorder diseases +MONDO:0013387 orphanet_rare diseases +MONDO:0013387 rare diseases +MONDO:0013388 gard_rare diseases +MONDO:0013388 nord_rare diseases +MONDO:0013388 rare diseases +MONDO:0013389 gard_rare diseases +MONDO:0013389 nord_rare diseases +MONDO:0013389 otar diseases +MONDO:0013389 rare diseases +MONDO:0013390 gard_rare diseases +MONDO:0013390 nord_rare diseases +MONDO:0013390 ordo_disorder diseases +MONDO:0013390 orphanet_rare diseases +MONDO:0013390 otar diseases +MONDO:0013390 rare diseases +MONDO:0013391 clingen diseases +MONDO:0013391 gard_rare diseases +MONDO:0013391 nord_rare diseases +MONDO:0013391 ordo_disorder diseases +MONDO:0013391 orphanet_rare diseases +MONDO:0013391 otar diseases +MONDO:0013391 rare diseases +MONDO:0013392 gard_rare diseases +MONDO:0013392 nord_rare diseases +MONDO:0013392 ordo_disorder diseases +MONDO:0013392 orphanet_rare diseases +MONDO:0013392 otar diseases +MONDO:0013392 rare diseases +MONDO:0013393 gard_rare diseases +MONDO:0013393 nord_rare diseases +MONDO:0013393 ordo_disorder diseases +MONDO:0013393 ordo_malformation_syndrome diseases +MONDO:0013393 orphanet_rare diseases +MONDO:0013393 otar diseases +MONDO:0013393 rare diseases +MONDO:0013394 gard_rare diseases +MONDO:0013394 nord_rare diseases +MONDO:0013394 ordo_disorder diseases +MONDO:0013394 ordo_malformation_syndrome diseases +MONDO:0013394 orphanet_rare diseases +MONDO:0013394 otar diseases +MONDO:0013394 rare diseases +MONDO:0013395 gard_rare diseases +MONDO:0013395 nord_rare diseases +MONDO:0013395 rare diseases +MONDO:0013396 gard_rare diseases +MONDO:0013396 nord_rare diseases +MONDO:0013396 ordo_disorder diseases +MONDO:0013396 ordo_malformation_syndrome diseases +MONDO:0013396 orphanet_rare diseases +MONDO:0013396 otar diseases +MONDO:0013396 rare diseases +MONDO:0013400 gard_rare diseases +MONDO:0013400 nord_rare diseases +MONDO:0013400 ordo_disorder diseases +MONDO:0013400 orphanet_rare diseases +MONDO:0013400 otar diseases +MONDO:0013400 rare diseases +MONDO:0013401 gard_rare diseases +MONDO:0013401 nord_rare diseases +MONDO:0013401 otar diseases +MONDO:0013401 rare diseases +MONDO:0013402 gard_rare diseases +MONDO:0013402 nord_rare diseases +MONDO:0013402 rare diseases +MONDO:0013403 gard_rare diseases +MONDO:0013403 nord_rare diseases +MONDO:0013403 rare diseases +MONDO:0013404 clingen diseases +MONDO:0013404 gard_rare diseases +MONDO:0013404 nord_rare diseases +MONDO:0013404 ordo_disorder diseases +MONDO:0013404 orphanet_rare diseases +MONDO:0013404 otar diseases +MONDO:0013404 rare diseases +MONDO:0013405 gard_rare diseases +MONDO:0013405 nord_rare diseases +MONDO:0013405 rare diseases +MONDO:0013406 gard_rare diseases +MONDO:0013406 nord_rare diseases +MONDO:0013406 rare diseases +MONDO:0013407 gard_rare diseases +MONDO:0013407 nord_rare diseases +MONDO:0013407 rare diseases +MONDO:0013408 gard_rare diseases +MONDO:0013408 nord_rare diseases +MONDO:0013408 ordo_disorder diseases +MONDO:0013408 orphanet_rare diseases +MONDO:0013408 otar diseases +MONDO:0013408 rare diseases +MONDO:0013410 gard_rare diseases +MONDO:0013410 nord_rare diseases +MONDO:0013410 otar diseases +MONDO:0013410 rare diseases +MONDO:0013411 gard_rare diseases +MONDO:0013411 nord_rare diseases +MONDO:0013411 otar diseases +MONDO:0013411 rare diseases +MONDO:0013412 gard_rare diseases +MONDO:0013412 nord_rare diseases +MONDO:0013412 rare diseases +MONDO:0013413 gard_rare diseases +MONDO:0013413 nord_rare diseases +MONDO:0013413 rare diseases +MONDO:0013414 gard_rare diseases +MONDO:0013414 nord_rare diseases +MONDO:0013414 rare diseases +MONDO:0013415 gard_rare diseases +MONDO:0013415 nord_rare diseases +MONDO:0013415 otar diseases +MONDO:0013415 rare diseases +MONDO:0013416 gard_rare diseases +MONDO:0013416 nord_rare diseases +MONDO:0013416 rare diseases +MONDO:0013417 gard_rare diseases +MONDO:0013417 nord_rare diseases +MONDO:0013417 ordo_disorder diseases +MONDO:0013417 orphanet_rare diseases +MONDO:0013417 otar diseases +MONDO:0013417 rare diseases +MONDO:0013418 gard_rare diseases +MONDO:0013418 nord_rare diseases +MONDO:0013418 rare diseases +MONDO:0013419 gard_rare diseases +MONDO:0013419 otar diseases +MONDO:0013419 rare diseases +MONDO:0013420 gard_rare diseases +MONDO:0013420 nord_rare diseases +MONDO:0013420 rare diseases +MONDO:0013421 gard_rare diseases +MONDO:0013421 otar diseases +MONDO:0013421 rare diseases +MONDO:0013422 gard_rare diseases +MONDO:0013422 rare diseases +MONDO:0013423 gard_rare diseases +MONDO:0013423 nord_rare diseases +MONDO:0013423 ordo_disorder diseases +MONDO:0013423 orphanet_rare diseases +MONDO:0013423 otar diseases +MONDO:0013423 rare diseases +MONDO:0013424 gard_rare diseases +MONDO:0013424 nord_rare diseases +MONDO:0013424 ordo_disorder diseases +MONDO:0013424 ordo_malformation_syndrome diseases +MONDO:0013424 orphanet_rare diseases +MONDO:0013424 otar diseases +MONDO:0013424 rare diseases +MONDO:0013425 gard_rare diseases +MONDO:0013425 nord_rare diseases +MONDO:0013425 rare diseases +MONDO:0013426 clingen diseases +MONDO:0013426 gard_rare diseases +MONDO:0013426 nord_rare diseases +MONDO:0013426 ordo_disorder diseases +MONDO:0013426 orphanet_rare diseases +MONDO:0013426 otar diseases +MONDO:0013426 rare diseases +MONDO:0013427 gard_rare diseases +MONDO:0013427 nord_rare diseases +MONDO:0013427 ordo_disorder diseases +MONDO:0013427 orphanet_rare diseases +MONDO:0013427 rare diseases +MONDO:0013428 clingen diseases +MONDO:0013428 gard_rare diseases +MONDO:0013428 nord_rare diseases +MONDO:0013428 rare diseases +MONDO:0013429 gard_rare diseases +MONDO:0013429 nord_rare diseases +MONDO:0013429 rare diseases +MONDO:0013430 gard_rare diseases +MONDO:0013430 nord_rare diseases +MONDO:0013430 rare diseases +MONDO:0013431 clingen diseases +MONDO:0013431 gard_rare diseases +MONDO:0013431 nord_rare diseases +MONDO:0013431 rare diseases +MONDO:0013432 gard_rare diseases +MONDO:0013432 nord_rare diseases +MONDO:0013432 rare diseases +MONDO:0013433 gard_rare diseases +MONDO:0013433 nord_rare diseases +MONDO:0013433 ordo_disorder diseases +MONDO:0013433 orphanet_rare diseases +MONDO:0013433 rare diseases +MONDO:0013434 clingen diseases +MONDO:0013434 gard_rare diseases +MONDO:0013434 nord_rare diseases +MONDO:0013434 rare diseases +MONDO:0013435 clingen diseases +MONDO:0013435 gard_rare diseases +MONDO:0013435 nord_rare diseases +MONDO:0013435 rare diseases +MONDO:0013436 gard_rare diseases +MONDO:0013436 nord_rare diseases +MONDO:0013436 rare diseases +MONDO:0013437 gard_rare diseases +MONDO:0013437 nord_rare diseases +MONDO:0013437 rare diseases +MONDO:0013438 gard_rare diseases +MONDO:0013438 nord_rare diseases +MONDO:0013438 rare diseases +MONDO:0013439 gard_rare diseases +MONDO:0013439 nord_rare diseases +MONDO:0013439 ordo_disorder diseases +MONDO:0013439 orphanet_rare diseases +MONDO:0013439 otar diseases +MONDO:0013439 rare diseases +MONDO:0013440 gard_rare diseases +MONDO:0013440 nord_rare diseases +MONDO:0013440 ordo_disorder diseases +MONDO:0013440 orphanet_rare diseases +MONDO:0013440 otar diseases +MONDO:0013440 rare diseases +MONDO:0013441 gard_rare diseases +MONDO:0013441 nord_rare diseases +MONDO:0013441 rare diseases +MONDO:0013442 clingen diseases +MONDO:0013442 gard_rare diseases +MONDO:0013442 nord_rare diseases +MONDO:0013442 rare diseases +MONDO:0013443 gard_rare diseases +MONDO:0013443 nord_rare diseases +MONDO:0013443 rare diseases +MONDO:0013444 gard_rare diseases +MONDO:0013444 nord_rare diseases +MONDO:0013444 rare diseases +MONDO:0013445 gard_rare diseases +MONDO:0013445 rare diseases +MONDO:0013446 gard_rare diseases +MONDO:0013446 nord_rare diseases +MONDO:0013446 rare diseases +MONDO:0013447 gard_rare diseases +MONDO:0013447 nord_rare diseases +MONDO:0013447 rare diseases +MONDO:0013448 gard_rare diseases +MONDO:0013448 rare diseases +MONDO:0013449 gard_rare diseases +MONDO:0013449 nord_rare diseases +MONDO:0013449 rare diseases +MONDO:0013450 gard_rare diseases +MONDO:0013450 rare diseases +MONDO:0013452 gard_rare diseases +MONDO:0013452 nord_rare diseases +MONDO:0013452 ordo_disorder diseases +MONDO:0013452 orphanet_rare diseases +MONDO:0013452 otar diseases +MONDO:0013452 rare diseases +MONDO:0013453 gard_rare diseases +MONDO:0013453 nord_rare diseases +MONDO:0013453 rare diseases +MONDO:0013454 gard_rare diseases +MONDO:0013454 nord_rare diseases +MONDO:0013454 rare diseases +MONDO:0013455 gard_rare diseases +MONDO:0013455 nord_rare diseases +MONDO:0013455 rare diseases +MONDO:0013456 gard_rare diseases +MONDO:0013456 nord_rare diseases +MONDO:0013456 ordo_disorder diseases +MONDO:0013456 orphanet_rare diseases +MONDO:0013456 otar diseases +MONDO:0013456 rare diseases +MONDO:0013457 gard_rare diseases +MONDO:0013457 nord_rare diseases +MONDO:0013457 rare diseases +MONDO:0013458 gard_rare diseases +MONDO:0013458 nord_rare diseases +MONDO:0013458 ordo_disorder diseases +MONDO:0013458 orphanet_rare diseases +MONDO:0013458 otar diseases +MONDO:0013458 rare diseases +MONDO:0013459 gard_rare diseases +MONDO:0013459 nord_rare diseases +MONDO:0013459 rare diseases +MONDO:0013460 gard_rare diseases +MONDO:0013460 nord_rare diseases +MONDO:0013460 rare diseases +MONDO:0013461 otar diseases +MONDO:0013462 otar diseases +MONDO:0013463 gard_rare diseases +MONDO:0013463 nord_rare diseases +MONDO:0013463 rare diseases +MONDO:0013464 gard_rare diseases +MONDO:0013464 nord_rare diseases +MONDO:0013464 ordo_disorder diseases +MONDO:0013464 orphanet_rare diseases +MONDO:0013464 otar diseases +MONDO:0013464 rare diseases +MONDO:0013465 gard_rare diseases +MONDO:0013465 rare diseases +MONDO:0013467 gard_rare diseases +MONDO:0013467 nord_rare diseases +MONDO:0013467 ordo_disorder diseases +MONDO:0013467 orphanet_rare diseases +MONDO:0013467 otar diseases +MONDO:0013467 rare diseases +MONDO:0013468 gard_rare diseases +MONDO:0013468 nord_rare diseases +MONDO:0013468 rare diseases +MONDO:0013469 gard_rare diseases +MONDO:0013469 nord_rare diseases +MONDO:0013469 rare diseases +MONDO:0013470 gard_rare diseases +MONDO:0013470 rare diseases +MONDO:0013471 gard_rare diseases +MONDO:0013471 nord_rare diseases +MONDO:0013471 rare diseases +MONDO:0013472 gard_rare diseases +MONDO:0013472 nord_rare diseases +MONDO:0013472 ordo_disorder diseases +MONDO:0013472 orphanet_rare diseases +MONDO:0013472 otar diseases +MONDO:0013472 rare diseases +MONDO:0013474 gard_rare diseases +MONDO:0013474 nord_rare diseases +MONDO:0013474 otar diseases +MONDO:0013474 rare diseases +MONDO:0013475 gard_rare diseases +MONDO:0013475 nord_rare diseases +MONDO:0013475 rare diseases +MONDO:0013476 gard_rare diseases +MONDO:0013476 nord_rare diseases +MONDO:0013476 rare diseases +MONDO:0013477 gard_rare diseases +MONDO:0013477 nord_rare diseases +MONDO:0013477 otar diseases +MONDO:0013477 rare diseases +MONDO:0013478 gard_rare diseases +MONDO:0013478 nord_rare diseases +MONDO:0013478 ordo_disorder diseases +MONDO:0013478 orphanet_rare diseases +MONDO:0013478 otar diseases +MONDO:0013478 rare diseases +MONDO:0013479 gard_rare diseases +MONDO:0013479 nord_rare diseases +MONDO:0013479 rare diseases +MONDO:0013480 gard_rare diseases +MONDO:0013480 nord_rare diseases +MONDO:0013480 rare diseases +MONDO:0013481 gard_rare diseases +MONDO:0013481 nord_rare diseases +MONDO:0013481 ordo_disorder diseases +MONDO:0013481 ordo_malformation_syndrome diseases +MONDO:0013481 orphanet_rare diseases +MONDO:0013481 otar diseases +MONDO:0013481 rare diseases +MONDO:0013482 gard_rare diseases +MONDO:0013482 rare diseases +MONDO:0013483 otar diseases +MONDO:0013485 gard_rare diseases +MONDO:0013485 nord_rare diseases +MONDO:0013485 ordo_disorder diseases +MONDO:0013485 orphanet_rare diseases +MONDO:0013485 otar diseases +MONDO:0013485 rare diseases +MONDO:0013486 gard_rare diseases +MONDO:0013486 nord_rare diseases +MONDO:0013486 ordo_disorder diseases +MONDO:0013486 orphanet_rare diseases +MONDO:0013486 otar diseases +MONDO:0013486 rare diseases +MONDO:0013487 gard_rare diseases +MONDO:0013487 nord_rare diseases +MONDO:0013487 ordo_disorder diseases +MONDO:0013487 orphanet_rare diseases +MONDO:0013487 otar diseases +MONDO:0013487 rare diseases +MONDO:0013489 gard_rare diseases +MONDO:0013489 nord_rare diseases +MONDO:0013489 rare diseases +MONDO:0013490 clingen diseases +MONDO:0013490 gard_rare diseases +MONDO:0013490 nord_rare diseases +MONDO:0013490 rare diseases +MONDO:0013491 clingen diseases +MONDO:0013491 gard_rare diseases +MONDO:0013491 nord_rare diseases +MONDO:0013491 rare diseases +MONDO:0013492 gard_rare diseases +MONDO:0013492 nord_rare diseases +MONDO:0013492 rare diseases +MONDO:0013495 gard_rare diseases +MONDO:0013495 nord_rare diseases +MONDO:0013495 rare diseases +MONDO:0013497 otar diseases +MONDO:0013499 gard_rare diseases +MONDO:0013499 nord_rare diseases +MONDO:0013499 otar diseases +MONDO:0013499 rare diseases +MONDO:0013500 gard_rare diseases +MONDO:0013500 nord_rare diseases +MONDO:0013500 otar diseases +MONDO:0013500 rare diseases +MONDO:0013501 gard_rare diseases +MONDO:0013501 nord_rare diseases +MONDO:0013501 rare diseases +MONDO:0013502 gard_rare diseases +MONDO:0013502 rare diseases +MONDO:0013503 gard_rare diseases +MONDO:0013503 nord_rare diseases +MONDO:0013503 rare diseases +MONDO:0013504 gard_rare diseases +MONDO:0013504 rare diseases +MONDO:0013505 gard_rare diseases +MONDO:0013505 rare diseases +MONDO:0013507 gard_rare diseases +MONDO:0013507 nord_rare diseases +MONDO:0013507 rare diseases +MONDO:0013509 gard_rare diseases +MONDO:0013509 rare diseases +MONDO:0013510 inferred_rare diseases +MONDO:0013510 predisposition diseases +MONDO:0013510 rare diseases +MONDO:0013511 otar diseases +MONDO:0013512 gard_rare diseases +MONDO:0013512 nord_rare diseases +MONDO:0013512 ordo_subtype_of_a_disorder diseases +MONDO:0013512 otar diseases +MONDO:0013512 rare diseases +MONDO:0013513 gard_rare diseases +MONDO:0013513 rare diseases +MONDO:0013514 gard_rare diseases +MONDO:0013514 rare diseases +MONDO:0013515 gard_rare diseases +MONDO:0013515 nord_rare diseases +MONDO:0013515 rare diseases +MONDO:0013516 gard_rare diseases +MONDO:0013516 nord_rare diseases +MONDO:0013516 rare diseases +MONDO:0013517 clingen diseases +MONDO:0013517 gard_rare diseases +MONDO:0013517 nord_rare diseases +MONDO:0013517 otar diseases +MONDO:0013517 rare diseases +MONDO:0013518 gard_rare diseases +MONDO:0013518 nord_rare diseases +MONDO:0013518 rare diseases +MONDO:0013519 gard_rare diseases +MONDO:0013519 nord_rare diseases +MONDO:0013519 rare diseases +MONDO:0013520 gard_rare diseases +MONDO:0013520 nord_rare diseases +MONDO:0013520 rare diseases +MONDO:0013521 clingen diseases +MONDO:0013521 gard_rare diseases +MONDO:0013521 nord_rare diseases +MONDO:0013521 otar diseases +MONDO:0013521 rare diseases +MONDO:0013522 gard_rare diseases +MONDO:0013522 nord_rare diseases +MONDO:0013522 otar diseases +MONDO:0013522 rare diseases +MONDO:0013523 gard_rare diseases +MONDO:0013523 nord_rare diseases +MONDO:0013523 ordo_disorder diseases +MONDO:0013523 ordo_malformation_syndrome diseases +MONDO:0013523 orphanet_rare diseases +MONDO:0013523 otar diseases +MONDO:0013523 rare diseases +MONDO:0013525 gard_rare diseases +MONDO:0013525 nord_rare diseases +MONDO:0013525 rare diseases +MONDO:0013526 gard_rare diseases +MONDO:0013526 nord_rare diseases +MONDO:0013526 ordo_disorder diseases +MONDO:0013526 orphanet_rare diseases +MONDO:0013526 otar diseases +MONDO:0013526 rare diseases +MONDO:0013527 gard_rare diseases +MONDO:0013527 nord_rare diseases +MONDO:0013527 rare diseases +MONDO:0013528 gard_rare diseases +MONDO:0013528 nord_rare diseases +MONDO:0013528 rare diseases +MONDO:0013529 gard_rare diseases +MONDO:0013529 nord_rare diseases +MONDO:0013529 rare diseases +MONDO:0013530 gard_rare diseases +MONDO:0013530 nord_rare diseases +MONDO:0013530 rare diseases +MONDO:0013531 gard_rare diseases +MONDO:0013531 nord_rare diseases +MONDO:0013531 ordo_subtype_of_a_disorder diseases +MONDO:0013531 otar diseases +MONDO:0013531 rare diseases +MONDO:0013532 otar diseases +MONDO:0013533 gard_rare diseases +MONDO:0013533 nord_rare diseases +MONDO:0013533 ordo_disorder diseases +MONDO:0013533 orphanet_rare diseases +MONDO:0013533 otar diseases +MONDO:0013533 rare diseases +MONDO:0013534 gard_rare diseases +MONDO:0013534 rare diseases +MONDO:0013536 gard_rare diseases +MONDO:0013536 nord_rare diseases +MONDO:0013536 ordo_disorder diseases +MONDO:0013536 orphanet_rare diseases +MONDO:0013536 otar diseases +MONDO:0013536 rare diseases +MONDO:0013537 gard_rare diseases +MONDO:0013537 nord_rare diseases +MONDO:0013537 rare diseases +MONDO:0013539 gard_rare diseases +MONDO:0013539 nord_rare diseases +MONDO:0013539 ordo_disorder diseases +MONDO:0013539 orphanet_rare diseases +MONDO:0013539 rare diseases +MONDO:0013540 gard_rare diseases +MONDO:0013540 nord_rare diseases +MONDO:0013540 ordo_disorder diseases +MONDO:0013540 ordo_malformation_syndrome diseases +MONDO:0013540 orphanet_rare diseases +MONDO:0013540 otar diseases +MONDO:0013540 rare diseases +MONDO:0013541 gard_rare diseases +MONDO:0013541 nord_rare diseases +MONDO:0013541 ordo_disorder diseases +MONDO:0013541 orphanet_rare diseases +MONDO:0013541 otar diseases +MONDO:0013541 rare diseases +MONDO:0013542 gard_rare diseases +MONDO:0013542 nord_rare diseases +MONDO:0013542 rare diseases +MONDO:0013543 otar diseases +MONDO:0013544 gard_rare diseases +MONDO:0013544 rare diseases +MONDO:0013545 gard_rare diseases +MONDO:0013545 rare diseases +MONDO:0013546 gard_rare diseases +MONDO:0013546 nord_rare diseases +MONDO:0013546 ordo_disorder diseases +MONDO:0013546 orphanet_rare diseases +MONDO:0013546 otar diseases +MONDO:0013546 rare diseases +MONDO:0013547 gard_rare diseases +MONDO:0013547 rare diseases +MONDO:0013548 clingen diseases +MONDO:0013548 otar diseases +MONDO:0013549 clingen diseases +MONDO:0013549 otar diseases +MONDO:0013550 gard_rare diseases +MONDO:0013550 nord_rare diseases +MONDO:0013550 ordo_disorder diseases +MONDO:0013550 orphanet_rare diseases +MONDO:0013550 otar diseases +MONDO:0013550 rare diseases +MONDO:0013551 gard_rare diseases +MONDO:0013551 nord_rare diseases +MONDO:0013551 otar diseases +MONDO:0013551 rare diseases +MONDO:0013552 gard_rare diseases +MONDO:0013552 nord_rare diseases +MONDO:0013552 otar diseases +MONDO:0013552 rare diseases +MONDO:0013553 gard_rare diseases +MONDO:0013553 nord_rare diseases +MONDO:0013553 rare diseases +MONDO:0013555 clingen diseases +MONDO:0013555 gard_rare diseases +MONDO:0013555 nord_rare diseases +MONDO:0013555 otar diseases +MONDO:0013555 rare diseases +MONDO:0013556 clingen diseases +MONDO:0013556 gard_rare diseases +MONDO:0013556 nord_rare diseases +MONDO:0013556 rare diseases +MONDO:0013557 clingen diseases +MONDO:0013557 gard_rare diseases +MONDO:0013557 nord_rare diseases +MONDO:0013557 rare diseases +MONDO:0013558 clingen diseases +MONDO:0013558 gard_rare diseases +MONDO:0013558 nord_rare diseases +MONDO:0013558 rare diseases +MONDO:0013559 clingen diseases +MONDO:0013559 gard_rare diseases +MONDO:0013559 nord_rare diseases +MONDO:0013559 ordo_subtype_of_a_disorder diseases +MONDO:0013559 otar diseases +MONDO:0013559 rare diseases +MONDO:0013560 clingen diseases +MONDO:0013560 gard_rare diseases +MONDO:0013560 nord_rare diseases +MONDO:0013560 otar diseases +MONDO:0013560 rare diseases +MONDO:0013561 gard_rare diseases +MONDO:0013561 nord_rare diseases +MONDO:0013561 ordo_disorder diseases +MONDO:0013561 ordo_malformation_syndrome diseases +MONDO:0013561 orphanet_rare diseases +MONDO:0013561 otar diseases +MONDO:0013561 rare diseases +MONDO:0013563 clingen diseases +MONDO:0013563 gard_rare diseases +MONDO:0013563 nord_rare diseases +MONDO:0013563 ordo_disorder diseases +MONDO:0013563 ordo_malformation_syndrome diseases +MONDO:0013563 orphanet_rare diseases +MONDO:0013563 otar diseases +MONDO:0013563 rare diseases +MONDO:0013564 otar diseases +MONDO:0013565 clingen diseases +MONDO:0013565 gard_rare diseases +MONDO:0013565 nord_rare diseases +MONDO:0013565 rare diseases +MONDO:0013566 clingen diseases +MONDO:0013566 gard_rare diseases +MONDO:0013566 nord_rare diseases +MONDO:0013566 otar diseases +MONDO:0013566 rare diseases +MONDO:0013567 gard_rare diseases +MONDO:0013567 nord_rare diseases +MONDO:0013567 rare diseases +MONDO:0013569 clingen diseases +MONDO:0013569 gard_rare diseases +MONDO:0013569 nord_rare diseases +MONDO:0013569 ordo_disorder diseases +MONDO:0013569 ordo_malformation_syndrome diseases +MONDO:0013569 orphanet_rare diseases +MONDO:0013569 rare diseases +MONDO:0013570 gard_rare diseases +MONDO:0013570 nord_rare diseases +MONDO:0013570 ordo_disorder diseases +MONDO:0013570 orphanet_rare diseases +MONDO:0013570 otar diseases +MONDO:0013570 rare diseases +MONDO:0013571 clingen diseases +MONDO:0013571 gard_rare diseases +MONDO:0013571 ordo_disorder diseases +MONDO:0013571 orphanet_rare diseases +MONDO:0013571 otar diseases +MONDO:0013571 rare diseases +MONDO:0013572 gard_rare diseases +MONDO:0013572 nord_rare diseases +MONDO:0013572 ordo_disorder diseases +MONDO:0013572 ordo_malformation_syndrome diseases +MONDO:0013572 orphanet_rare diseases +MONDO:0013572 otar diseases +MONDO:0013572 rare diseases +MONDO:0013573 gard_rare diseases +MONDO:0013573 nord_rare diseases +MONDO:0013573 rare diseases +MONDO:0013574 gard_rare diseases +MONDO:0013574 nord_rare diseases +MONDO:0013574 ordo_disorder diseases +MONDO:0013574 ordo_malformation_syndrome diseases +MONDO:0013574 orphanet_rare diseases +MONDO:0013574 otar diseases +MONDO:0013574 rare diseases +MONDO:0013576 clingen diseases +MONDO:0013576 gard_rare diseases +MONDO:0013576 nord_rare diseases +MONDO:0013576 ordo_disorder diseases +MONDO:0013576 orphanet_rare diseases +MONDO:0013576 otar diseases +MONDO:0013576 rare diseases +MONDO:0013577 otar diseases +MONDO:0013578 gard_rare diseases +MONDO:0013578 nord_rare diseases +MONDO:0013578 ordo_disorder diseases +MONDO:0013578 ordo_malformation_syndrome diseases +MONDO:0013578 orphanet_rare diseases +MONDO:0013578 otar diseases +MONDO:0013578 rare diseases +MONDO:0013579 clingen diseases +MONDO:0013579 gard_rare diseases +MONDO:0013579 nord_rare diseases +MONDO:0013579 ordo_disorder diseases +MONDO:0013579 orphanet_rare diseases +MONDO:0013579 otar diseases +MONDO:0013579 rare diseases +MONDO:0013580 gard_rare diseases +MONDO:0013580 nord_rare diseases +MONDO:0013580 ordo_subtype_of_a_disorder diseases +MONDO:0013580 otar diseases +MONDO:0013580 rare diseases +MONDO:0013581 gard_rare diseases +MONDO:0013581 rare diseases +MONDO:0013582 clingen diseases +MONDO:0013582 gard_rare diseases +MONDO:0013582 nord_rare diseases +MONDO:0013582 rare diseases +MONDO:0013583 gard_rare diseases +MONDO:0013583 nord_rare diseases +MONDO:0013583 ordo_disorder diseases +MONDO:0013583 ordo_malformation_syndrome diseases +MONDO:0013583 orphanet_rare diseases +MONDO:0013583 otar diseases +MONDO:0013583 rare diseases +MONDO:0013584 gard_rare diseases +MONDO:0013584 nord_rare diseases +MONDO:0013584 ordo_disorder diseases +MONDO:0013584 orphanet_rare diseases +MONDO:0013584 otar diseases +MONDO:0013584 rare diseases +MONDO:0013585 gard_rare diseases +MONDO:0013585 nord_rare diseases +MONDO:0013585 otar diseases +MONDO:0013585 rare diseases +MONDO:0013587 gard_rare diseases +MONDO:0013587 nord_rare diseases +MONDO:0013587 ordo_subtype_of_a_disorder diseases +MONDO:0013587 otar diseases +MONDO:0013587 rare diseases +MONDO:0013588 clingen diseases +MONDO:0013588 gard_rare diseases +MONDO:0013588 nord_rare diseases +MONDO:0013588 rare diseases +MONDO:0013589 gard_rare diseases +MONDO:0013589 nord_rare diseases +MONDO:0013589 rare diseases +MONDO:0013590 gard_rare diseases +MONDO:0013590 nord_rare diseases +MONDO:0013590 rare diseases +MONDO:0013591 gard_rare diseases +MONDO:0013591 nord_rare diseases +MONDO:0013591 rare diseases +MONDO:0013592 gard_rare diseases +MONDO:0013592 rare diseases +MONDO:0013593 gard_rare diseases +MONDO:0013593 nord_rare diseases +MONDO:0013593 rare diseases +MONDO:0013594 gard_rare diseases +MONDO:0013594 nord_rare diseases +MONDO:0013594 ordo_disorder diseases +MONDO:0013594 orphanet_rare diseases +MONDO:0013594 otar diseases +MONDO:0013594 rare diseases +MONDO:0013595 gard_rare diseases +MONDO:0013595 nord_rare diseases +MONDO:0013595 ordo_disorder diseases +MONDO:0013595 orphanet_rare diseases +MONDO:0013595 otar diseases +MONDO:0013595 rare diseases +MONDO:0013597 gard_rare diseases +MONDO:0013597 nord_rare diseases +MONDO:0013597 rare diseases +MONDO:0013598 otar diseases +MONDO:0013599 gard_rare diseases +MONDO:0013599 nord_rare diseases +MONDO:0013599 ordo_disorder diseases +MONDO:0013599 orphanet_rare diseases +MONDO:0013599 otar diseases +MONDO:0013599 predisposition diseases +MONDO:0013599 rare diseases +MONDO:0013600 otar diseases +MONDO:0013601 gard_rare diseases +MONDO:0013601 rare diseases +MONDO:0013602 gard_rare diseases +MONDO:0013602 nord_rare diseases +MONDO:0013602 rare diseases +MONDO:0013605 gard_rare diseases +MONDO:0013605 nord_rare diseases +MONDO:0013605 rare diseases +MONDO:0013606 clingen diseases +MONDO:0013606 gard_rare diseases +MONDO:0013606 nord_rare diseases +MONDO:0013606 otar diseases +MONDO:0013606 rare diseases +MONDO:0013607 gard_rare diseases +MONDO:0013607 nord_rare diseases +MONDO:0013607 ordo_disorder diseases +MONDO:0013607 orphanet_rare diseases +MONDO:0013607 otar diseases +MONDO:0013607 predisposition diseases +MONDO:0013607 rare diseases +MONDO:0013608 gard_rare diseases +MONDO:0013608 nord_rare diseases +MONDO:0013608 rare diseases +MONDO:0013609 gard_rare diseases +MONDO:0013609 rare diseases +MONDO:0013610 gard_rare diseases +MONDO:0013610 nord_rare diseases +MONDO:0013610 rare diseases +MONDO:0013611 gard_rare diseases +MONDO:0013611 nord_rare diseases +MONDO:0013611 rare diseases +MONDO:0013612 gard_rare diseases +MONDO:0013612 nord_rare diseases +MONDO:0013612 rare diseases +MONDO:0013613 gard_rare diseases +MONDO:0013613 nord_rare diseases +MONDO:0013613 rare diseases +MONDO:0013614 gard_rare diseases +MONDO:0013614 ordo_disorder diseases +MONDO:0013614 ordo_malformation_syndrome diseases +MONDO:0013614 orphanet_rare diseases +MONDO:0013614 otar diseases +MONDO:0013614 rare diseases +MONDO:0013615 gard_rare diseases +MONDO:0013615 nord_rare diseases +MONDO:0013615 ordo_disorder diseases +MONDO:0013615 ordo_malformation_syndrome diseases +MONDO:0013615 orphanet_rare diseases +MONDO:0013615 otar diseases +MONDO:0013615 rare diseases +MONDO:0013616 gard_rare diseases +MONDO:0013616 nord_rare diseases +MONDO:0013616 rare diseases +MONDO:0013618 otar diseases +MONDO:0013619 gard_rare diseases +MONDO:0013619 rare diseases +MONDO:0013620 gard_rare diseases +MONDO:0013620 nord_rare diseases +MONDO:0013620 rare diseases +MONDO:0013621 otar diseases +MONDO:0013622 gard_rare diseases +MONDO:0013622 nord_rare diseases +MONDO:0013622 ordo_etiological_subtype diseases +MONDO:0013622 ordo_subtype_of_a_disorder diseases +MONDO:0013622 otar diseases +MONDO:0013622 rare diseases +MONDO:0013623 clingen diseases +MONDO:0013623 gard_rare diseases +MONDO:0013623 nord_rare diseases +MONDO:0013623 ordo_etiological_subtype diseases +MONDO:0013623 ordo_subtype_of_a_disorder diseases +MONDO:0013623 otar diseases +MONDO:0013623 rare diseases +MONDO:0013624 gard_rare diseases +MONDO:0013624 nord_rare diseases +MONDO:0013624 rare diseases +MONDO:0013625 gard_rare diseases +MONDO:0013625 nord_rare diseases +MONDO:0013625 rare diseases +MONDO:0013626 gard_rare diseases +MONDO:0013626 ordo_disorder diseases +MONDO:0013626 orphanet_rare diseases +MONDO:0013626 otar diseases +MONDO:0013626 rare diseases +MONDO:0013627 gard_rare diseases +MONDO:0013627 nord_rare diseases +MONDO:0013627 rare diseases +MONDO:0013628 gard_rare diseases +MONDO:0013628 nord_rare diseases +MONDO:0013628 rare diseases +MONDO:0013629 gard_rare diseases +MONDO:0013629 nord_rare diseases +MONDO:0013629 rare diseases +MONDO:0013630 gard_rare diseases +MONDO:0013630 rare diseases +MONDO:0013631 gard_rare diseases +MONDO:0013631 rare diseases +MONDO:0013632 gard_rare diseases +MONDO:0013632 nord_rare diseases +MONDO:0013632 rare diseases +MONDO:0013634 gard_rare diseases +MONDO:0013634 nord_rare diseases +MONDO:0013634 rare diseases +MONDO:0013635 gard_rare diseases +MONDO:0013635 nord_rare diseases +MONDO:0013635 rare diseases +MONDO:0013636 gard_rare diseases +MONDO:0013636 nord_rare diseases +MONDO:0013636 rare diseases +MONDO:0013637 gard_rare diseases +MONDO:0013637 nord_rare diseases +MONDO:0013637 rare diseases +MONDO:0013638 gard_rare diseases +MONDO:0013638 nord_rare diseases +MONDO:0013638 rare diseases +MONDO:0013640 gard_rare diseases +MONDO:0013640 nord_rare diseases +MONDO:0013640 ordo_disorder diseases +MONDO:0013640 ordo_malformation_syndrome diseases +MONDO:0013640 orphanet_rare diseases +MONDO:0013640 otar diseases +MONDO:0013640 rare diseases +MONDO:0013641 gard_rare diseases +MONDO:0013641 nord_rare diseases +MONDO:0013641 rare diseases +MONDO:0013642 gard_rare diseases +MONDO:0013642 nord_rare diseases +MONDO:0013642 rare diseases +MONDO:0013644 gard_rare diseases +MONDO:0013644 nord_rare diseases +MONDO:0013644 ordo_disorder diseases +MONDO:0013644 orphanet_rare diseases +MONDO:0013644 otar diseases +MONDO:0013644 rare diseases +MONDO:0013645 gard_rare diseases +MONDO:0013645 nord_rare diseases +MONDO:0013645 ordo_disorder diseases +MONDO:0013645 orphanet_rare diseases +MONDO:0013645 otar diseases +MONDO:0013645 rare diseases +MONDO:0013646 gard_rare diseases +MONDO:0013646 nord_rare diseases +MONDO:0013646 ordo_disorder diseases +MONDO:0013646 ordo_malformation_syndrome diseases +MONDO:0013646 orphanet_rare diseases +MONDO:0013646 otar diseases +MONDO:0013646 rare diseases +MONDO:0013648 gard_rare diseases +MONDO:0013648 nord_rare diseases +MONDO:0013648 ordo_disorder diseases +MONDO:0013648 orphanet_rare diseases +MONDO:0013648 otar diseases +MONDO:0013648 rare diseases +MONDO:0013649 gard_rare diseases +MONDO:0013649 nord_rare diseases +MONDO:0013649 rare diseases +MONDO:0013650 gard_rare diseases +MONDO:0013650 nord_rare diseases +MONDO:0013650 rare diseases +MONDO:0013651 gard_rare diseases +MONDO:0013651 nord_rare diseases +MONDO:0013651 rare diseases +MONDO:0013652 gard_rare diseases +MONDO:0013652 nord_rare diseases +MONDO:0013652 rare diseases +MONDO:0013654 gard_rare diseases +MONDO:0013654 nord_rare diseases +MONDO:0013654 rare diseases +MONDO:0013655 gard_rare diseases +MONDO:0013655 otar diseases +MONDO:0013655 rare diseases +MONDO:0013656 gard_rare diseases +MONDO:0013656 otar diseases +MONDO:0013656 rare diseases +MONDO:0013657 gard_rare diseases +MONDO:0013657 rare diseases +MONDO:0013658 gard_rare diseases +MONDO:0013658 rare diseases +MONDO:0013659 gard_rare diseases +MONDO:0013659 nord_rare diseases +MONDO:0013659 ordo_disorder diseases +MONDO:0013659 ordo_malformation_syndrome diseases +MONDO:0013659 orphanet_rare diseases +MONDO:0013659 otar diseases +MONDO:0013659 rare diseases +MONDO:0013660 otar diseases +MONDO:0013661 clingen diseases +MONDO:0013661 gard_rare diseases +MONDO:0013661 nord_rare diseases +MONDO:0013661 ordo_disorder diseases +MONDO:0013661 orphanet_rare diseases +MONDO:0013661 otar diseases +MONDO:0013661 rare diseases +MONDO:0013662 otar diseases +MONDO:0013664 gard_rare diseases +MONDO:0013664 nord_rare diseases +MONDO:0013664 ordo_disorder diseases +MONDO:0013664 orphanet_rare diseases +MONDO:0013664 rare diseases +MONDO:0013666 gard_rare diseases +MONDO:0013666 nord_rare diseases +MONDO:0013666 rare diseases +MONDO:0013668 gard_rare diseases +MONDO:0013668 nord_rare diseases +MONDO:0013668 ordo_disorder diseases +MONDO:0013668 ordo_malformation_syndrome diseases +MONDO:0013668 orphanet_rare diseases +MONDO:0013668 rare diseases +MONDO:0013670 gard_rare diseases +MONDO:0013670 nord_rare diseases +MONDO:0013670 rare diseases +MONDO:0013671 gard_rare diseases +MONDO:0013671 rare diseases +MONDO:0013672 gard_rare diseases +MONDO:0013672 nord_rare diseases +MONDO:0013672 rare diseases +MONDO:0013673 clingen diseases +MONDO:0013673 gard_rare diseases +MONDO:0013673 nord_rare diseases +MONDO:0013673 ordo_disorder diseases +MONDO:0013673 orphanet_rare diseases +MONDO:0013673 rare diseases +MONDO:0013674 gard_rare diseases +MONDO:0013674 nord_rare diseases +MONDO:0013674 ordo_disorder diseases +MONDO:0013674 orphanet_rare diseases +MONDO:0013674 otar diseases +MONDO:0013674 rare diseases +MONDO:0013675 gard_rare diseases +MONDO:0013675 nord_rare diseases +MONDO:0013675 ordo_disorder diseases +MONDO:0013675 orphanet_rare diseases +MONDO:0013675 otar diseases +MONDO:0013675 rare diseases +MONDO:0013677 gard_rare diseases +MONDO:0013677 nord_rare diseases +MONDO:0013677 rare diseases +MONDO:0013678 gard_rare diseases +MONDO:0013678 nord_rare diseases +MONDO:0013678 ordo_disorder diseases +MONDO:0013678 orphanet_rare diseases +MONDO:0013678 otar diseases +MONDO:0013678 rare diseases +MONDO:0013679 gard_rare diseases +MONDO:0013679 nord_rare diseases +MONDO:0013679 rare diseases +MONDO:0013680 otar diseases +MONDO:0013681 clingen diseases +MONDO:0013681 gard_rare diseases +MONDO:0013681 otar diseases +MONDO:0013681 rare diseases +MONDO:0013682 gard_rare diseases +MONDO:0013682 nord_rare diseases +MONDO:0013682 rare diseases +MONDO:0013683 gard_rare diseases +MONDO:0013683 nord_rare diseases +MONDO:0013683 rare diseases +MONDO:0013684 gard_rare diseases +MONDO:0013684 nord_rare diseases +MONDO:0013684 rare diseases +MONDO:0013685 inferred_rare diseases +MONDO:0013685 predisposition diseases +MONDO:0013685 rare diseases +MONDO:0013686 gard_rare diseases +MONDO:0013686 nord_rare diseases +MONDO:0013686 ordo_disorder diseases +MONDO:0013686 orphanet_rare diseases +MONDO:0013686 rare diseases +MONDO:0013687 gard_rare diseases +MONDO:0013687 nord_rare diseases +MONDO:0013687 ordo_disorder diseases +MONDO:0013687 orphanet_rare diseases +MONDO:0013687 otar diseases +MONDO:0013687 rare diseases +MONDO:0013688 gard_rare diseases +MONDO:0013688 nord_rare diseases +MONDO:0013688 ordo_disorder diseases +MONDO:0013688 orphanet_rare diseases +MONDO:0013688 otar diseases +MONDO:0013688 rare diseases +MONDO:0013689 gard_rare diseases +MONDO:0013689 nord_rare diseases +MONDO:0013689 rare diseases +MONDO:0013690 gard_rare diseases +MONDO:0013690 nord_rare diseases +MONDO:0013690 rare diseases +MONDO:0013691 gard_rare diseases +MONDO:0013691 nord_rare diseases +MONDO:0013691 ordo_subtype_of_a_disorder diseases +MONDO:0013691 otar diseases +MONDO:0013691 rare diseases +MONDO:0013692 clingen diseases +MONDO:0013692 gard_rare diseases +MONDO:0013692 nord_rare diseases +MONDO:0013692 ordo_disorder diseases +MONDO:0013692 orphanet_rare diseases +MONDO:0013692 otar diseases +MONDO:0013692 rare diseases +MONDO:0013693 gard_rare diseases +MONDO:0013693 nord_rare diseases +MONDO:0013693 rare diseases +MONDO:0013694 gard_rare diseases +MONDO:0013694 nord_rare diseases +MONDO:0013694 rare diseases +MONDO:0013695 gard_rare diseases +MONDO:0013695 nord_rare diseases +MONDO:0013695 rare diseases +MONDO:0013696 gard_rare diseases +MONDO:0013696 nord_rare diseases +MONDO:0013696 otar diseases +MONDO:0013696 rare diseases +MONDO:0013697 gard_rare diseases +MONDO:0013697 nord_rare diseases +MONDO:0013697 rare diseases +MONDO:0013698 gard_rare diseases +MONDO:0013698 nord_rare diseases +MONDO:0013698 rare diseases +MONDO:0013699 gard_rare diseases +MONDO:0013699 nord_rare diseases +MONDO:0013699 rare diseases +MONDO:0013700 gard_rare diseases +MONDO:0013700 nord_rare diseases +MONDO:0013700 ordo_disorder diseases +MONDO:0013700 orphanet_rare diseases +MONDO:0013700 otar diseases +MONDO:0013700 rare diseases +MONDO:0013702 gard_rare diseases +MONDO:0013702 nord_rare diseases +MONDO:0013702 otar diseases +MONDO:0013702 rare diseases +MONDO:0013703 gard_rare diseases +MONDO:0013703 nord_rare diseases +MONDO:0013703 rare diseases +MONDO:0013704 gard_rare diseases +MONDO:0013704 nord_rare diseases +MONDO:0013704 rare diseases +MONDO:0013705 gard_rare diseases +MONDO:0013705 nord_rare diseases +MONDO:0013705 rare diseases +MONDO:0013706 gard_rare diseases +MONDO:0013706 nord_rare diseases +MONDO:0013706 rare diseases +MONDO:0013707 gard_rare diseases +MONDO:0013707 nord_rare diseases +MONDO:0013707 rare diseases +MONDO:0013708 gard_rare diseases +MONDO:0013708 nord_rare diseases +MONDO:0013708 rare diseases +MONDO:0013709 gard_rare diseases +MONDO:0013709 nord_rare diseases +MONDO:0013709 rare diseases +MONDO:0013710 gard_rare diseases +MONDO:0013710 nord_rare diseases +MONDO:0013710 rare diseases +MONDO:0013711 gard_rare diseases +MONDO:0013711 nord_rare diseases +MONDO:0013711 ordo_disorder diseases +MONDO:0013711 orphanet_rare diseases +MONDO:0013711 otar diseases +MONDO:0013711 rare diseases +MONDO:0013712 gard_rare diseases +MONDO:0013712 nord_rare diseases +MONDO:0013712 rare diseases +MONDO:0013714 gard_rare diseases +MONDO:0013714 nord_rare diseases +MONDO:0013714 otar diseases +MONDO:0013714 rare diseases +MONDO:0013715 gard_rare diseases +MONDO:0013715 nord_rare diseases +MONDO:0013715 rare diseases +MONDO:0013716 gard_rare diseases +MONDO:0013716 nord_rare diseases +MONDO:0013716 rare diseases +MONDO:0013717 gard_rare diseases +MONDO:0013717 nord_rare diseases +MONDO:0013717 rare diseases +MONDO:0013718 gard_rare diseases +MONDO:0013718 nord_rare diseases +MONDO:0013718 rare diseases +MONDO:0013719 gard_rare diseases +MONDO:0013719 nord_rare diseases +MONDO:0013719 rare diseases +MONDO:0013720 gard_rare diseases +MONDO:0013720 rare diseases +MONDO:0013721 gard_rare diseases +MONDO:0013721 rare diseases +MONDO:0013722 gard_rare diseases +MONDO:0013722 nord_rare diseases +MONDO:0013722 ordo_disorder diseases +MONDO:0013722 ordo_malformation_syndrome diseases +MONDO:0013722 orphanet_rare diseases +MONDO:0013722 rare diseases +MONDO:0013725 clingen diseases +MONDO:0013725 gard_rare diseases +MONDO:0013725 nord_rare diseases +MONDO:0013725 rare diseases +MONDO:0013726 gard_rare diseases +MONDO:0013726 nord_rare diseases +MONDO:0013726 ordo_subtype_of_a_disorder diseases +MONDO:0013726 otar diseases +MONDO:0013726 rare diseases +MONDO:0013730 gard_rare diseases +MONDO:0013730 nord_rare diseases +MONDO:0013730 ordo_disorder diseases +MONDO:0013730 orphanet_rare diseases +MONDO:0013730 otar diseases +MONDO:0013730 rare diseases +MONDO:0013731 clingen diseases +MONDO:0013731 gard_rare diseases +MONDO:0013731 nord_rare diseases +MONDO:0013731 ordo_disorder diseases +MONDO:0013731 orphanet_rare diseases +MONDO:0013731 otar diseases +MONDO:0013731 rare diseases +MONDO:0013734 gard_rare diseases +MONDO:0013734 nord_rare diseases +MONDO:0013734 rare diseases +MONDO:0013735 gard_rare diseases +MONDO:0013735 ordo_disorder diseases +MONDO:0013735 ordo_malformation_syndrome diseases +MONDO:0013735 orphanet_rare diseases +MONDO:0013735 otar diseases +MONDO:0013735 rare diseases +MONDO:0013737 gard_rare diseases +MONDO:0013737 nord_rare diseases +MONDO:0013737 ordo_disorder diseases +MONDO:0013737 orphanet_rare diseases +MONDO:0013737 otar diseases +MONDO:0013737 rare diseases +MONDO:0013738 gard_rare diseases +MONDO:0013738 nord_rare diseases +MONDO:0013738 rare diseases +MONDO:0013739 gard_rare diseases +MONDO:0013739 nord_rare diseases +MONDO:0013739 rare diseases +MONDO:0013740 gard_rare diseases +MONDO:0013740 nord_rare diseases +MONDO:0013740 ordo_disorder diseases +MONDO:0013740 ordo_malformation_syndrome diseases +MONDO:0013740 orphanet_rare diseases +MONDO:0013740 otar diseases +MONDO:0013740 rare diseases +MONDO:0013741 gard_rare diseases +MONDO:0013741 nord_rare diseases +MONDO:0013741 rare diseases +MONDO:0013743 gard_rare diseases +MONDO:0013743 nord_rare diseases +MONDO:0013743 ordo_disorder diseases +MONDO:0013743 orphanet_rare diseases +MONDO:0013743 otar diseases +MONDO:0013743 rare diseases +MONDO:0013744 gard_rare diseases +MONDO:0013744 nord_rare diseases +MONDO:0013744 rare diseases +MONDO:0013745 clingen diseases +MONDO:0013745 gard_rare diseases +MONDO:0013745 nord_rare diseases +MONDO:0013745 rare diseases +MONDO:0013746 otar diseases +MONDO:0013747 gard_rare diseases +MONDO:0013747 nord_rare diseases +MONDO:0013747 otar diseases +MONDO:0013747 rare diseases +MONDO:0013748 otar diseases +MONDO:0013749 otar diseases +MONDO:0013750 gard_rare diseases +MONDO:0013750 nord_rare diseases +MONDO:0013750 rare diseases +MONDO:0013751 gard_rare diseases +MONDO:0013751 nord_rare diseases +MONDO:0013751 rare diseases +MONDO:0013752 gard_rare diseases +MONDO:0013752 nord_rare diseases +MONDO:0013752 rare diseases +MONDO:0013753 clingen diseases +MONDO:0013753 gard_rare diseases +MONDO:0013753 nord_rare diseases +MONDO:0013753 ordo_disorder diseases +MONDO:0013753 orphanet_rare diseases +MONDO:0013753 otar diseases +MONDO:0013753 rare diseases +MONDO:0013754 gard_rare diseases +MONDO:0013754 nord_rare diseases +MONDO:0013754 rare diseases +MONDO:0013755 gard_rare diseases +MONDO:0013755 nord_rare diseases +MONDO:0013755 ordo_etiological_subtype diseases +MONDO:0013755 ordo_subtype_of_a_disorder diseases +MONDO:0013755 otar diseases +MONDO:0013755 rare diseases +MONDO:0013756 gard_rare diseases +MONDO:0013756 nord_rare diseases +MONDO:0013756 rare diseases +MONDO:0013757 gard_rare diseases +MONDO:0013757 nord_rare diseases +MONDO:0013757 rare diseases +MONDO:0013758 clingen diseases +MONDO:0013758 gard_rare diseases +MONDO:0013758 nord_rare diseases +MONDO:0013758 ordo_disorder diseases +MONDO:0013758 orphanet_rare diseases +MONDO:0013758 otar diseases +MONDO:0013758 rare diseases +MONDO:0013759 ordo_disorder diseases +MONDO:0013759 orphanet_rare diseases +MONDO:0013759 predisposition diseases +MONDO:0013759 rare diseases +MONDO:0013760 gard_rare diseases +MONDO:0013760 nord_rare diseases +MONDO:0013760 ordo_disorder diseases +MONDO:0013760 orphanet_rare diseases +MONDO:0013760 otar diseases +MONDO:0013760 rare diseases +MONDO:0013761 gard_rare diseases +MONDO:0013761 ordo_disorder diseases +MONDO:0013761 orphanet_rare diseases +MONDO:0013761 otar diseases +MONDO:0013761 rare diseases +MONDO:0013762 gard_rare diseases +MONDO:0013762 nord_rare diseases +MONDO:0013762 ordo_disorder diseases +MONDO:0013762 orphanet_rare diseases +MONDO:0013762 otar diseases +MONDO:0013762 rare diseases +MONDO:0013763 gard_rare diseases +MONDO:0013763 nord_rare diseases +MONDO:0013763 rare diseases +MONDO:0013764 gard_rare diseases +MONDO:0013764 nord_rare diseases +MONDO:0013764 rare diseases +MONDO:0013766 gard_rare diseases +MONDO:0013766 nord_rare diseases +MONDO:0013766 ordo_disorder diseases +MONDO:0013766 orphanet_rare diseases +MONDO:0013766 rare diseases +MONDO:0013767 gard_rare diseases +MONDO:0013767 nord_rare diseases +MONDO:0013767 ordo_disorder diseases +MONDO:0013767 orphanet_rare diseases +MONDO:0013767 otar diseases +MONDO:0013767 rare diseases +MONDO:0013768 gard_rare diseases +MONDO:0013768 nord_rare diseases +MONDO:0013768 rare diseases +MONDO:0013769 gard_rare diseases +MONDO:0013769 nord_rare diseases +MONDO:0013769 rare diseases +MONDO:0013770 gard_rare diseases +MONDO:0013770 nord_rare diseases +MONDO:0013770 rare diseases +MONDO:0013771 gard_rare diseases +MONDO:0013771 nord_rare diseases +MONDO:0013771 ordo_disorder diseases +MONDO:0013771 orphanet_rare diseases +MONDO:0013771 otar diseases +MONDO:0013771 rare diseases +MONDO:0013772 gard_rare diseases +MONDO:0013772 nord_rare diseases +MONDO:0013772 ordo_disorder diseases +MONDO:0013772 orphanet_rare diseases +MONDO:0013772 otar diseases +MONDO:0013772 rare diseases +MONDO:0013773 gard_rare diseases +MONDO:0013773 nord_rare diseases +MONDO:0013773 rare diseases +MONDO:0013774 gard_rare diseases +MONDO:0013774 nord_rare diseases +MONDO:0013774 rare diseases +MONDO:0013775 clingen diseases +MONDO:0013775 gard_rare diseases +MONDO:0013775 nord_rare diseases +MONDO:0013775 ordo_disorder diseases +MONDO:0013775 orphanet_rare diseases +MONDO:0013775 otar diseases +MONDO:0013775 rare diseases +MONDO:0013776 gard_rare diseases +MONDO:0013776 nord_rare diseases +MONDO:0013776 ordo_disorder diseases +MONDO:0013776 orphanet_rare diseases +MONDO:0013776 otar diseases +MONDO:0013776 rare diseases +MONDO:0013777 gard_rare diseases +MONDO:0013777 nord_rare diseases +MONDO:0013777 ordo_etiological_subtype diseases +MONDO:0013777 ordo_subtype_of_a_disorder diseases +MONDO:0013777 otar diseases +MONDO:0013777 rare diseases +MONDO:0013778 gard_rare diseases +MONDO:0013778 nord_rare diseases +MONDO:0013778 ordo_etiological_subtype diseases +MONDO:0013778 ordo_subtype_of_a_disorder diseases +MONDO:0013778 otar diseases +MONDO:0013778 rare diseases +MONDO:0013779 clingen diseases +MONDO:0013779 gard_rare diseases +MONDO:0013779 rare diseases +MONDO:0013780 gard_rare diseases +MONDO:0013780 nord_rare diseases +MONDO:0013780 rare diseases +MONDO:0013781 gard_rare diseases +MONDO:0013781 nord_rare diseases +MONDO:0013781 ordo_etiological_subtype diseases +MONDO:0013781 ordo_subtype_of_a_disorder diseases +MONDO:0013781 otar diseases +MONDO:0013781 rare diseases +MONDO:0013782 clingen diseases +MONDO:0013782 gard_rare diseases +MONDO:0013782 nord_rare diseases +MONDO:0013782 ordo_etiological_subtype diseases +MONDO:0013782 ordo_subtype_of_a_disorder diseases +MONDO:0013782 otar diseases +MONDO:0013782 rare diseases +MONDO:0013783 gard_rare diseases +MONDO:0013783 nord_rare diseases +MONDO:0013783 rare diseases +MONDO:0013784 clingen diseases +MONDO:0013784 gard_rare diseases +MONDO:0013784 nord_rare diseases +MONDO:0013784 ordo_disorder diseases +MONDO:0013784 ordo_malformation_syndrome diseases +MONDO:0013784 orphanet_rare diseases +MONDO:0013784 otar diseases +MONDO:0013784 rare diseases +MONDO:0013785 gard_rare diseases +MONDO:0013785 nord_rare diseases +MONDO:0013785 rare diseases +MONDO:0013786 gard_rare diseases +MONDO:0013786 nord_rare diseases +MONDO:0013786 rare diseases +MONDO:0013788 gard_rare diseases +MONDO:0013788 nord_rare diseases +MONDO:0013788 rare diseases +MONDO:0013789 gard_rare diseases +MONDO:0013789 nord_rare diseases +MONDO:0013789 ordo_disorder diseases +MONDO:0013789 orphanet_rare diseases +MONDO:0013789 otar diseases +MONDO:0013789 rare diseases +MONDO:0013790 gard_rare diseases +MONDO:0013790 nord_rare diseases +MONDO:0013790 rare diseases +MONDO:0013791 gard_rare diseases +MONDO:0013791 nord_rare diseases +MONDO:0013791 rare diseases +MONDO:0013792 otar diseases +MONDO:0013794 gard_rare diseases +MONDO:0013794 nord_rare diseases +MONDO:0013794 rare diseases +MONDO:0013795 gard_rare diseases +MONDO:0013795 nord_rare diseases +MONDO:0013795 rare diseases +MONDO:0013796 gard_rare diseases +MONDO:0013796 nord_rare diseases +MONDO:0013796 ordo_disorder diseases +MONDO:0013796 ordo_malformation_syndrome diseases +MONDO:0013796 orphanet_rare diseases +MONDO:0013796 otar diseases +MONDO:0013796 rare diseases +MONDO:0013797 gard_rare diseases +MONDO:0013797 nord_rare diseases +MONDO:0013797 ordo_disorder diseases +MONDO:0013797 ordo_malformation_syndrome diseases +MONDO:0013797 orphanet_rare diseases +MONDO:0013797 otar diseases +MONDO:0013797 rare diseases +MONDO:0013798 gard_rare diseases +MONDO:0013798 nord_rare diseases +MONDO:0013798 ordo_disorder diseases +MONDO:0013798 orphanet_rare diseases +MONDO:0013798 rare diseases +MONDO:0013800 gard_rare diseases +MONDO:0013800 nord_rare diseases +MONDO:0013800 ordo_subtype_of_a_disorder diseases +MONDO:0013800 otar diseases +MONDO:0013800 rare diseases +MONDO:0013801 gard_rare diseases +MONDO:0013801 nord_rare diseases +MONDO:0013801 rare diseases +MONDO:0013802 gard_rare diseases +MONDO:0013802 nord_rare diseases +MONDO:0013802 ordo_disorder diseases +MONDO:0013802 orphanet_rare diseases +MONDO:0013802 otar diseases +MONDO:0013802 rare diseases +MONDO:0013803 gard_rare diseases +MONDO:0013803 nord_rare diseases +MONDO:0013803 ordo_disorder diseases +MONDO:0013803 orphanet_rare diseases +MONDO:0013803 rare diseases +MONDO:0013805 gard_rare diseases +MONDO:0013805 otar diseases +MONDO:0013805 rare diseases +MONDO:0013806 gard_rare diseases +MONDO:0013806 nord_rare diseases +MONDO:0013806 ordo_disorder diseases +MONDO:0013806 orphanet_rare diseases +MONDO:0013806 otar diseases +MONDO:0013806 rare diseases +MONDO:0013807 gard_rare diseases +MONDO:0013807 rare diseases +MONDO:0013808 gard_rare diseases +MONDO:0013808 nord_rare diseases +MONDO:0013808 ordo_disorder diseases +MONDO:0013808 orphanet_rare diseases +MONDO:0013808 otar diseases +MONDO:0013808 rare diseases +MONDO:0013810 gard_rare diseases +MONDO:0013810 nord_rare diseases +MONDO:0013810 ordo_disorder diseases +MONDO:0013810 orphanet_rare diseases +MONDO:0013810 otar diseases +MONDO:0013810 rare diseases +MONDO:0013811 gard_rare diseases +MONDO:0013811 nord_rare diseases +MONDO:0013811 ordo_disorder diseases +MONDO:0013811 orphanet_rare diseases +MONDO:0013811 otar diseases +MONDO:0013811 rare diseases +MONDO:0013812 clingen diseases +MONDO:0013812 gard_rare diseases +MONDO:0013812 nord_rare diseases +MONDO:0013812 rare diseases +MONDO:0013813 gard_rare diseases +MONDO:0013813 nord_rare diseases +MONDO:0013813 ordo_disorder diseases +MONDO:0013813 orphanet_rare diseases +MONDO:0013813 otar diseases +MONDO:0013813 rare diseases +MONDO:0013815 gard_rare diseases +MONDO:0013815 nord_rare diseases +MONDO:0013815 ordo_disorder diseases +MONDO:0013815 orphanet_rare diseases +MONDO:0013815 otar diseases +MONDO:0013815 rare diseases +MONDO:0013817 gard_rare diseases +MONDO:0013817 nord_rare diseases +MONDO:0013817 rare diseases +MONDO:0013818 gard_rare diseases +MONDO:0013818 nord_rare diseases +MONDO:0013818 rare diseases +MONDO:0013819 gard_rare diseases +MONDO:0013819 nord_rare diseases +MONDO:0013819 rare diseases +MONDO:0013820 gard_rare diseases +MONDO:0013820 nord_rare diseases +MONDO:0013820 rare diseases +MONDO:0013821 gard_rare diseases +MONDO:0013821 nord_rare diseases +MONDO:0013821 rare diseases +MONDO:0013822 gard_rare diseases +MONDO:0013822 nord_rare diseases +MONDO:0013822 rare diseases +MONDO:0013823 gard_rare diseases +MONDO:0013823 nord_rare diseases +MONDO:0013823 rare diseases +MONDO:0013824 clingen diseases +MONDO:0013824 gard_rare diseases +MONDO:0013824 nord_rare diseases +MONDO:0013824 otar diseases +MONDO:0013824 rare diseases +MONDO:0013825 gard_rare diseases +MONDO:0013825 nord_rare diseases +MONDO:0013825 ordo_disorder diseases +MONDO:0013825 orphanet_rare diseases +MONDO:0013825 otar diseases +MONDO:0013825 rare diseases +MONDO:0013826 gard_rare diseases +MONDO:0013826 nord_rare diseases +MONDO:0013826 rare diseases +MONDO:0013827 gard_rare diseases +MONDO:0013827 nord_rare diseases +MONDO:0013827 rare diseases +MONDO:0013828 gard_rare diseases +MONDO:0013828 nord_rare diseases +MONDO:0013828 rare diseases +MONDO:0013829 gard_rare diseases +MONDO:0013829 nord_rare diseases +MONDO:0013829 rare diseases +MONDO:0013830 gard_rare diseases +MONDO:0013830 nord_rare diseases +MONDO:0013830 rare diseases +MONDO:0013831 gard_rare diseases +MONDO:0013831 nord_rare diseases +MONDO:0013831 rare diseases +MONDO:0013832 gard_rare diseases +MONDO:0013832 nord_rare diseases +MONDO:0013832 rare diseases +MONDO:0013833 gard_rare diseases +MONDO:0013833 nord_rare diseases +MONDO:0013833 rare diseases +MONDO:0013834 gard_rare diseases +MONDO:0013834 nord_rare diseases +MONDO:0013834 rare diseases +MONDO:0013835 gard_rare diseases +MONDO:0013835 nord_rare diseases +MONDO:0013835 otar diseases +MONDO:0013835 rare diseases +MONDO:0013836 gard_rare diseases +MONDO:0013836 nord_rare diseases +MONDO:0013836 ordo_disorder diseases +MONDO:0013836 orphanet_rare diseases +MONDO:0013836 otar diseases +MONDO:0013836 rare diseases +MONDO:0013837 gard_rare diseases +MONDO:0013837 nord_rare diseases +MONDO:0013837 ordo_disorder diseases +MONDO:0013837 orphanet_rare diseases +MONDO:0013837 otar diseases +MONDO:0013837 rare diseases +MONDO:0013838 gard_rare diseases +MONDO:0013838 nord_rare diseases +MONDO:0013838 rare diseases +MONDO:0013839 clingen diseases +MONDO:0013839 gard_rare diseases +MONDO:0013839 nord_rare diseases +MONDO:0013839 ordo_disorder diseases +MONDO:0013839 orphanet_rare diseases +MONDO:0013839 otar diseases +MONDO:0013839 rare diseases +MONDO:0013840 gard_rare diseases +MONDO:0013840 nord_rare diseases +MONDO:0013840 ordo_disorder diseases +MONDO:0013840 orphanet_rare diseases +MONDO:0013840 otar diseases +MONDO:0013840 rare diseases +MONDO:0013842 gard_rare diseases +MONDO:0013842 nord_rare diseases +MONDO:0013842 rare diseases +MONDO:0013843 gard_rare diseases +MONDO:0013843 nord_rare diseases +MONDO:0013843 ordo_disorder diseases +MONDO:0013843 orphanet_rare diseases +MONDO:0013843 otar diseases +MONDO:0013843 rare diseases +MONDO:0013845 gard_rare diseases +MONDO:0013845 rare diseases +MONDO:0013847 gard_rare diseases +MONDO:0013847 nord_rare diseases +MONDO:0013847 ordo_disorder diseases +MONDO:0013847 ordo_malformation_syndrome diseases +MONDO:0013847 orphanet_rare diseases +MONDO:0013847 predisposition diseases +MONDO:0013847 rare diseases +MONDO:0013848 gard_rare diseases +MONDO:0013848 nord_rare diseases +MONDO:0013848 rare diseases +MONDO:0013849 gard_rare diseases +MONDO:0013849 nord_rare diseases +MONDO:0013849 rare diseases +MONDO:0013851 gard_rare diseases +MONDO:0013851 nord_rare diseases +MONDO:0013851 ordo_disorder diseases +MONDO:0013851 orphanet_rare diseases +MONDO:0013851 otar diseases +MONDO:0013851 rare diseases +MONDO:0013852 gard_rare diseases +MONDO:0013852 nord_rare diseases +MONDO:0013852 rare diseases +MONDO:0013853 gard_rare diseases +MONDO:0013853 nord_rare diseases +MONDO:0013853 rare diseases +MONDO:0013854 clingen diseases +MONDO:0013854 gard_rare diseases +MONDO:0013854 nord_rare diseases +MONDO:0013854 rare diseases +MONDO:0013858 gard_rare diseases +MONDO:0013858 nord_rare diseases +MONDO:0013858 ordo_disorder diseases +MONDO:0013858 ordo_morphological_anomaly diseases +MONDO:0013858 orphanet_rare diseases +MONDO:0013858 rare diseases +MONDO:0013859 gard_rare diseases +MONDO:0013859 nord_rare diseases +MONDO:0013859 rare diseases +MONDO:0013860 gard_rare diseases +MONDO:0013860 nord_rare diseases +MONDO:0013860 ordo_disorder diseases +MONDO:0013860 orphanet_rare diseases +MONDO:0013860 otar diseases +MONDO:0013860 rare diseases +MONDO:0013862 clingen diseases +MONDO:0013862 gard_rare diseases +MONDO:0013862 nord_rare diseases +MONDO:0013862 otar diseases +MONDO:0013862 rare diseases +MONDO:0013863 clingen diseases +MONDO:0013863 gard_rare diseases +MONDO:0013863 nord_rare diseases +MONDO:0013863 ordo_disorder diseases +MONDO:0013863 orphanet_rare diseases +MONDO:0013863 otar diseases +MONDO:0013863 rare diseases +MONDO:0013864 gard_rare diseases +MONDO:0013864 nord_rare diseases +MONDO:0013864 rare diseases +MONDO:0013865 gard_rare diseases +MONDO:0013865 nord_rare diseases +MONDO:0013865 ordo_disorder diseases +MONDO:0013865 orphanet_rare diseases +MONDO:0013865 otar diseases +MONDO:0013865 rare diseases +MONDO:0013866 gard_rare diseases +MONDO:0013866 nord_rare diseases +MONDO:0013866 ordo_etiological_subtype diseases +MONDO:0013866 otar diseases +MONDO:0013866 rare diseases +MONDO:0013867 clingen diseases +MONDO:0013867 gard_rare diseases +MONDO:0013867 nord_rare diseases +MONDO:0013867 ordo_subtype_of_a_disorder diseases +MONDO:0013867 rare diseases +MONDO:0013868 gard_rare diseases +MONDO:0013868 nord_rare diseases +MONDO:0013868 rare diseases +MONDO:0013869 gard_rare diseases +MONDO:0013869 nord_rare diseases +MONDO:0013869 ordo_disorder diseases +MONDO:0013869 orphanet_rare diseases +MONDO:0013869 otar diseases +MONDO:0013869 rare diseases +MONDO:0013870 gard_rare diseases +MONDO:0013870 nord_rare diseases +MONDO:0013870 ordo_disorder diseases +MONDO:0013870 orphanet_rare diseases +MONDO:0013870 otar diseases +MONDO:0013870 rare diseases +MONDO:0013871 gard_rare diseases +MONDO:0013871 nord_rare diseases +MONDO:0013871 rare diseases +MONDO:0013872 gard_rare diseases +MONDO:0013872 rare diseases +MONDO:0013873 gard_rare diseases +MONDO:0013873 nord_rare diseases +MONDO:0013873 ordo_disorder diseases +MONDO:0013873 ordo_malformation_syndrome diseases +MONDO:0013873 orphanet_rare diseases +MONDO:0013873 otar diseases +MONDO:0013873 rare diseases +MONDO:0013874 gard_rare diseases +MONDO:0013874 nord_rare diseases +MONDO:0013874 rare diseases +MONDO:0013875 gard_rare diseases +MONDO:0013875 nord_rare diseases +MONDO:0013875 ordo_disorder diseases +MONDO:0013875 orphanet_rare diseases +MONDO:0013875 otar diseases +MONDO:0013875 rare diseases +MONDO:0013876 gard_rare diseases +MONDO:0013876 predisposition diseases +MONDO:0013876 rare diseases +MONDO:0013877 gard_rare diseases +MONDO:0013877 nord_rare diseases +MONDO:0013877 ordo_disorder diseases +MONDO:0013877 orphanet_rare diseases +MONDO:0013877 otar diseases +MONDO:0013877 rare diseases +MONDO:0013878 gard_rare diseases +MONDO:0013878 nord_rare diseases +MONDO:0013878 otar diseases +MONDO:0013878 rare diseases +MONDO:0013879 gard_rare diseases +MONDO:0013879 nord_rare diseases +MONDO:0013879 rare diseases +MONDO:0013880 gard_rare diseases +MONDO:0013880 nord_rare diseases +MONDO:0013880 rare diseases +MONDO:0013881 gard_rare diseases +MONDO:0013881 nord_rare diseases +MONDO:0013881 ordo_disorder diseases +MONDO:0013881 orphanet_rare diseases +MONDO:0013881 otar diseases +MONDO:0013881 rare diseases +MONDO:0013882 gard_rare diseases +MONDO:0013882 nord_rare diseases +MONDO:0013882 rare diseases +MONDO:0013883 gard_rare diseases +MONDO:0013883 nord_rare diseases +MONDO:0013883 rare diseases +MONDO:0013884 gard_rare diseases +MONDO:0013884 rare diseases +MONDO:0013885 clingen diseases +MONDO:0013885 gard_rare diseases +MONDO:0013885 nord_rare diseases +MONDO:0013885 ordo_disorder diseases +MONDO:0013885 ordo_malformation_syndrome diseases +MONDO:0013885 orphanet_rare diseases +MONDO:0013885 otar diseases +MONDO:0013885 rare diseases +MONDO:0013886 clingen diseases +MONDO:0013886 gard_rare diseases +MONDO:0013886 nord_rare diseases +MONDO:0013886 ordo_disorder diseases +MONDO:0013886 orphanet_rare diseases +MONDO:0013886 otar diseases +MONDO:0013886 rare diseases +MONDO:0013887 gard_rare diseases +MONDO:0013887 nord_rare diseases +MONDO:0013887 rare diseases +MONDO:0013889 gard_rare diseases +MONDO:0013889 nord_rare diseases +MONDO:0013889 ordo_disorder diseases +MONDO:0013889 ordo_malformation_syndrome diseases +MONDO:0013889 orphanet_rare diseases +MONDO:0013889 otar diseases +MONDO:0013889 rare diseases +MONDO:0013890 gard_rare diseases +MONDO:0013890 nord_rare diseases +MONDO:0013890 ordo_disorder diseases +MONDO:0013890 orphanet_rare diseases +MONDO:0013890 otar diseases +MONDO:0013890 rare diseases +MONDO:0013891 clingen diseases +MONDO:0013891 gard_rare diseases +MONDO:0013891 nord_rare diseases +MONDO:0013891 otar diseases +MONDO:0013891 rare diseases +MONDO:0013892 gard_rare diseases +MONDO:0013892 nord_rare diseases +MONDO:0013892 ordo_histopathological_subtype diseases +MONDO:0013892 ordo_subtype_of_a_disorder diseases +MONDO:0013892 otar diseases +MONDO:0013892 rare diseases +MONDO:0013894 gard_rare diseases +MONDO:0013894 nord_rare diseases +MONDO:0013894 ordo_disorder diseases +MONDO:0013894 orphanet_rare diseases +MONDO:0013894 otar diseases +MONDO:0013894 rare diseases +MONDO:0013895 gard_rare diseases +MONDO:0013895 nord_rare diseases +MONDO:0013895 rare diseases +MONDO:0013896 gard_rare diseases +MONDO:0013896 nord_rare diseases +MONDO:0013896 rare diseases +MONDO:0013897 gard_rare diseases +MONDO:0013897 nord_rare diseases +MONDO:0013897 rare diseases +MONDO:0013898 gard_rare diseases +MONDO:0013898 nord_rare diseases +MONDO:0013898 ordo_disorder diseases +MONDO:0013898 orphanet_rare diseases +MONDO:0013898 otar diseases +MONDO:0013898 rare diseases +MONDO:0013899 gard_rare diseases +MONDO:0013899 nord_rare diseases +MONDO:0013899 rare diseases +MONDO:0013900 gard_rare diseases +MONDO:0013900 rare diseases +MONDO:0013901 gard_rare diseases +MONDO:0013901 rare diseases +MONDO:0013902 gard_rare diseases +MONDO:0013902 nord_rare diseases +MONDO:0013902 rare diseases +MONDO:0013904 gard_rare diseases +MONDO:0013904 nord_rare diseases +MONDO:0013904 otar diseases +MONDO:0013904 rare diseases +MONDO:0013905 gard_rare diseases +MONDO:0013905 nord_rare diseases +MONDO:0013905 ordo_subtype_of_a_disorder diseases +MONDO:0013905 otar diseases +MONDO:0013905 rare diseases +MONDO:0013906 gard_rare diseases +MONDO:0013906 otar diseases +MONDO:0013906 rare diseases +MONDO:0013907 gard_rare diseases +MONDO:0013907 nord_rare diseases +MONDO:0013907 ordo_subtype_of_a_disorder diseases +MONDO:0013907 otar diseases +MONDO:0013907 rare diseases +MONDO:0013910 gard_rare diseases +MONDO:0013910 rare diseases +MONDO:0013911 gard_rare diseases +MONDO:0013911 rare diseases +MONDO:0013912 gard_rare diseases +MONDO:0013912 rare diseases +MONDO:0013913 gard_rare diseases +MONDO:0013913 rare diseases +MONDO:0013914 gard_rare diseases +MONDO:0013914 rare diseases +MONDO:0013915 gard_rare diseases +MONDO:0013915 rare diseases +MONDO:0013916 gard_rare diseases +MONDO:0013916 nord_rare diseases +MONDO:0013916 rare diseases +MONDO:0013917 gard_rare diseases +MONDO:0013917 nord_rare diseases +MONDO:0013917 rare diseases +MONDO:0013918 gard_rare diseases +MONDO:0013918 nord_rare diseases +MONDO:0013918 ordo_etiological_subtype diseases +MONDO:0013918 ordo_subtype_of_a_disorder diseases +MONDO:0013918 otar diseases +MONDO:0013918 rare diseases +MONDO:0013922 gard_rare diseases +MONDO:0013922 nord_rare diseases +MONDO:0013922 ordo_disorder diseases +MONDO:0013922 ordo_malformation_syndrome diseases +MONDO:0013922 orphanet_rare diseases +MONDO:0013922 otar diseases +MONDO:0013922 rare diseases +MONDO:0013923 gard_rare diseases +MONDO:0013923 nord_rare diseases +MONDO:0013923 rare diseases +MONDO:0013924 gard_rare diseases +MONDO:0013924 rare diseases +MONDO:0013925 gard_rare diseases +MONDO:0013925 nord_rare diseases +MONDO:0013925 ordo_subtype_of_a_disorder diseases +MONDO:0013925 otar diseases +MONDO:0013925 rare diseases +MONDO:0013926 gard_rare diseases +MONDO:0013926 nord_rare diseases +MONDO:0013926 rare diseases +MONDO:0013927 gard_rare diseases +MONDO:0013927 nord_rare diseases +MONDO:0013927 otar diseases +MONDO:0013927 rare diseases +MONDO:0013928 gard_rare diseases +MONDO:0013928 nord_rare diseases +MONDO:0013928 ordo_disorder diseases +MONDO:0013928 orphanet_rare diseases +MONDO:0013928 otar diseases +MONDO:0013928 rare diseases +MONDO:0013929 gard_rare diseases +MONDO:0013929 nord_rare diseases +MONDO:0013929 rare diseases +MONDO:0013930 gard_rare diseases +MONDO:0013930 nord_rare diseases +MONDO:0013930 otar diseases +MONDO:0013930 rare diseases +MONDO:0013931 gard_rare diseases +MONDO:0013931 nord_rare diseases +MONDO:0013931 otar diseases +MONDO:0013931 rare diseases +MONDO:0013932 gard_rare diseases +MONDO:0013932 nord_rare diseases +MONDO:0013932 otar diseases +MONDO:0013932 rare diseases +MONDO:0013933 gard_rare diseases +MONDO:0013933 nord_rare diseases +MONDO:0013933 rare diseases +MONDO:0013934 clingen diseases +MONDO:0013934 gard_rare diseases +MONDO:0013934 nord_rare diseases +MONDO:0013934 ordo_disorder diseases +MONDO:0013934 orphanet_rare diseases +MONDO:0013934 otar diseases +MONDO:0013934 rare diseases +MONDO:0013935 gard_rare diseases +MONDO:0013935 nord_rare diseases +MONDO:0013935 rare diseases +MONDO:0013936 gard_rare diseases +MONDO:0013936 nord_rare diseases +MONDO:0013936 otar diseases +MONDO:0013936 rare diseases +MONDO:0013937 gard_rare diseases +MONDO:0013937 nord_rare diseases +MONDO:0013937 otar diseases +MONDO:0013937 rare diseases +MONDO:0013938 gard_rare diseases +MONDO:0013938 nord_rare diseases +MONDO:0013938 otar diseases +MONDO:0013938 rare diseases +MONDO:0013939 gard_rare diseases +MONDO:0013939 nord_rare diseases +MONDO:0013939 rare diseases +MONDO:0013940 gard_rare diseases +MONDO:0013940 nord_rare diseases +MONDO:0013940 rare diseases +MONDO:0013941 gard_rare diseases +MONDO:0013941 nord_rare diseases +MONDO:0013941 ordo_disorder diseases +MONDO:0013941 orphanet_rare diseases +MONDO:0013941 otar diseases +MONDO:0013941 rare diseases +MONDO:0013942 gard_rare diseases +MONDO:0013942 nord_rare diseases +MONDO:0013942 otar diseases +MONDO:0013942 rare diseases +MONDO:0013943 gard_rare diseases +MONDO:0013943 nord_rare diseases +MONDO:0013943 rare diseases +MONDO:0013944 gard_rare diseases +MONDO:0013944 nord_rare diseases +MONDO:0013944 ordo_disorder diseases +MONDO:0013944 orphanet_rare diseases +MONDO:0013944 otar diseases +MONDO:0013944 rare diseases +MONDO:0013945 gard_rare diseases +MONDO:0013945 nord_rare diseases +MONDO:0013945 rare diseases +MONDO:0013946 gard_rare diseases +MONDO:0013946 rare diseases +MONDO:0013947 gard_rare diseases +MONDO:0013947 nord_rare diseases +MONDO:0013947 ordo_disorder diseases +MONDO:0013947 orphanet_rare diseases +MONDO:0013947 otar diseases +MONDO:0013947 rare diseases +MONDO:0013948 gard_rare diseases +MONDO:0013948 nord_rare diseases +MONDO:0013948 otar diseases +MONDO:0013948 rare diseases +MONDO:0013949 gard_rare diseases +MONDO:0013949 nord_rare diseases +MONDO:0013949 otar diseases +MONDO:0013949 rare diseases +MONDO:0013950 gard_rare diseases +MONDO:0013950 nord_rare diseases +MONDO:0013950 otar diseases +MONDO:0013950 rare diseases +MONDO:0013951 gard_rare diseases +MONDO:0013951 nord_rare diseases +MONDO:0013951 otar diseases +MONDO:0013951 rare diseases +MONDO:0013952 gard_rare diseases +MONDO:0013952 nord_rare diseases +MONDO:0013952 otar diseases +MONDO:0013952 rare diseases +MONDO:0013953 gard_rare diseases +MONDO:0013953 rare diseases +MONDO:0013959 gard_rare diseases +MONDO:0013959 nord_rare diseases +MONDO:0013959 ordo_disorder diseases +MONDO:0013959 orphanet_rare diseases +MONDO:0013959 otar diseases +MONDO:0013959 rare diseases +MONDO:0013960 clingen diseases +MONDO:0013960 gard_rare diseases +MONDO:0013960 nord_rare diseases +MONDO:0013960 ordo_disorder diseases +MONDO:0013960 orphanet_rare diseases +MONDO:0013960 otar diseases +MONDO:0013960 rare diseases +MONDO:0013961 gard_rare diseases +MONDO:0013961 rare diseases +MONDO:0013962 gard_rare diseases +MONDO:0013962 nord_rare diseases +MONDO:0013962 ordo_disorder diseases +MONDO:0013962 orphanet_rare diseases +MONDO:0013962 otar diseases +MONDO:0013962 rare diseases +MONDO:0013963 gard_rare diseases +MONDO:0013963 nord_rare diseases +MONDO:0013963 rare diseases +MONDO:0013964 gard_rare diseases +MONDO:0013964 nord_rare diseases +MONDO:0013964 rare diseases +MONDO:0013965 gard_rare diseases +MONDO:0013965 nord_rare diseases +MONDO:0013965 rare diseases +MONDO:0013966 gard_rare diseases +MONDO:0013966 rare diseases +MONDO:0013967 gard_rare diseases +MONDO:0013967 nord_rare diseases +MONDO:0013967 otar diseases +MONDO:0013967 rare diseases +MONDO:0013968 gard_rare diseases +MONDO:0013968 nord_rare diseases +MONDO:0013968 ordo_disorder diseases +MONDO:0013968 orphanet_rare diseases +MONDO:0013968 otar diseases +MONDO:0013968 rare diseases +MONDO:0013969 gard_rare diseases +MONDO:0013969 nord_rare diseases +MONDO:0013969 ordo_disorder diseases +MONDO:0013969 orphanet_rare diseases +MONDO:0013969 otar diseases +MONDO:0013969 rare diseases +MONDO:0013970 clingen diseases +MONDO:0013970 gard_rare diseases +MONDO:0013970 nord_rare diseases +MONDO:0013970 ordo_disorder diseases +MONDO:0013970 orphanet_rare diseases +MONDO:0013970 otar diseases +MONDO:0013970 rare diseases +MONDO:0013971 gard_rare diseases +MONDO:0013971 nord_rare diseases +MONDO:0013971 ordo_disorder diseases +MONDO:0013971 orphanet_rare diseases +MONDO:0013971 otar diseases +MONDO:0013971 rare diseases +MONDO:0013972 clingen diseases +MONDO:0013972 gard_rare diseases +MONDO:0013972 nord_rare diseases +MONDO:0013972 ordo_subtype_of_a_disorder diseases +MONDO:0013972 otar diseases +MONDO:0013972 rare diseases +MONDO:0013973 gard_rare diseases +MONDO:0013973 nord_rare diseases +MONDO:0013973 rare diseases +MONDO:0013974 gard_rare diseases +MONDO:0013974 nord_rare diseases +MONDO:0013974 rare diseases +MONDO:0013975 gard_rare diseases +MONDO:0013975 nord_rare diseases +MONDO:0013975 rare diseases +MONDO:0013976 gard_rare diseases +MONDO:0013976 nord_rare diseases +MONDO:0013976 rare diseases +MONDO:0013977 gard_rare diseases +MONDO:0013977 nord_rare diseases +MONDO:0013977 ordo_disorder diseases +MONDO:0013977 orphanet_rare diseases +MONDO:0013977 otar diseases +MONDO:0013977 rare diseases +MONDO:0013978 gard_rare diseases +MONDO:0013978 nord_rare diseases +MONDO:0013978 rare diseases +MONDO:0013979 clingen diseases +MONDO:0013979 gard_rare diseases +MONDO:0013979 nord_rare diseases +MONDO:0013979 rare diseases +MONDO:0013980 gard_rare diseases +MONDO:0013980 nord_rare diseases +MONDO:0013980 rare diseases +MONDO:0013981 gard_rare diseases +MONDO:0013981 nord_rare diseases +MONDO:0013981 ordo_disorder diseases +MONDO:0013981 orphanet_rare diseases +MONDO:0013981 otar diseases +MONDO:0013981 rare diseases +MONDO:0013982 gard_rare diseases +MONDO:0013982 nord_rare diseases +MONDO:0013982 rare diseases +MONDO:0013983 gard_rare diseases +MONDO:0013983 nord_rare diseases +MONDO:0013983 rare diseases +MONDO:0013984 gard_rare diseases +MONDO:0013984 nord_rare diseases +MONDO:0013984 rare diseases +MONDO:0013985 gard_rare diseases +MONDO:0013985 nord_rare diseases +MONDO:0013985 rare diseases +MONDO:0013986 gard_rare diseases +MONDO:0013986 nord_rare diseases +MONDO:0013986 ordo_disorder diseases +MONDO:0013986 orphanet_rare diseases +MONDO:0013986 otar diseases +MONDO:0013986 rare diseases +MONDO:0013987 gard_rare diseases +MONDO:0013987 nord_rare diseases +MONDO:0013987 ordo_disorder diseases +MONDO:0013987 orphanet_rare diseases +MONDO:0013987 otar diseases +MONDO:0013987 rare diseases +MONDO:0013989 gard_rare diseases +MONDO:0013989 nord_rare diseases +MONDO:0013989 otar diseases +MONDO:0013989 rare diseases +MONDO:0013990 gard_rare diseases +MONDO:0013990 nord_rare diseases +MONDO:0013990 ordo_disorder diseases +MONDO:0013990 ordo_malformation_syndrome diseases +MONDO:0013990 orphanet_rare diseases +MONDO:0013990 otar diseases +MONDO:0013990 rare diseases +MONDO:0013991 gard_rare diseases +MONDO:0013991 nord_rare diseases +MONDO:0013991 ordo_subtype_of_a_disorder diseases +MONDO:0013991 otar diseases +MONDO:0013991 rare diseases +MONDO:0013992 gard_rare diseases +MONDO:0013992 nord_rare diseases +MONDO:0013992 ordo_subtype_of_a_disorder diseases +MONDO:0013992 otar diseases +MONDO:0013992 rare diseases +MONDO:0013993 gard_rare diseases +MONDO:0013993 nord_rare diseases +MONDO:0013993 ordo_disorder diseases +MONDO:0013993 ordo_malformation_syndrome diseases +MONDO:0013993 orphanet_rare diseases +MONDO:0013993 otar diseases +MONDO:0013993 rare diseases +MONDO:0013994 gard_rare diseases +MONDO:0013994 nord_rare diseases +MONDO:0013994 rare diseases +MONDO:0013995 gard_rare diseases +MONDO:0013995 nord_rare diseases +MONDO:0013995 rare diseases +MONDO:0013996 gard_rare diseases +MONDO:0013996 nord_rare diseases +MONDO:0013996 ordo_subtype_of_a_disorder diseases +MONDO:0013996 otar diseases +MONDO:0013996 rare diseases +MONDO:0013997 gard_rare diseases +MONDO:0013997 nord_rare diseases +MONDO:0013997 ordo_subtype_of_a_disorder diseases +MONDO:0013997 otar diseases +MONDO:0013997 rare diseases +MONDO:0013998 clingen diseases +MONDO:0013998 gard_rare diseases +MONDO:0013998 nord_rare diseases +MONDO:0013998 rare diseases +MONDO:0013999 gard_rare diseases +MONDO:0013999 nord_rare diseases +MONDO:0013999 ordo_disorder diseases +MONDO:0013999 orphanet_rare diseases +MONDO:0013999 otar diseases +MONDO:0013999 rare diseases +MONDO:0014000 gard_rare diseases +MONDO:0014000 nord_rare diseases +MONDO:0014000 rare diseases +MONDO:0014001 gard_rare diseases +MONDO:0014001 nord_rare diseases +MONDO:0014001 rare diseases +MONDO:0014002 gard_rare diseases +MONDO:0014002 nord_rare diseases +MONDO:0014002 otar diseases +MONDO:0014002 rare diseases +MONDO:0014003 gard_rare diseases +MONDO:0014003 nord_rare diseases +MONDO:0014003 rare diseases +MONDO:0014004 gard_rare diseases +MONDO:0014004 rare diseases +MONDO:0014005 gard_rare diseases +MONDO:0014005 nord_rare diseases +MONDO:0014005 ordo_subtype_of_a_disorder diseases +MONDO:0014005 otar diseases +MONDO:0014005 predisposition diseases +MONDO:0014005 rare diseases +MONDO:0014006 clingen diseases +MONDO:0014006 gard_rare diseases +MONDO:0014006 nord_rare diseases +MONDO:0014006 ordo_disorder diseases +MONDO:0014006 ordo_malformation_syndrome diseases +MONDO:0014006 orphanet_rare diseases +MONDO:0014006 otar diseases +MONDO:0014006 rare diseases +MONDO:0014007 gard_rare diseases +MONDO:0014007 nord_rare diseases +MONDO:0014007 rare diseases +MONDO:0014008 clingen diseases +MONDO:0014008 otar diseases +MONDO:0014009 gard_rare diseases +MONDO:0014009 nord_rare diseases +MONDO:0014009 rare diseases +MONDO:0014010 gard_rare diseases +MONDO:0014010 nord_rare diseases +MONDO:0014010 rare diseases +MONDO:0014011 gard_rare diseases +MONDO:0014011 nord_rare diseases +MONDO:0014011 rare diseases +MONDO:0014012 gard_rare diseases +MONDO:0014012 nord_rare diseases +MONDO:0014012 ordo_disorder diseases +MONDO:0014012 orphanet_rare diseases +MONDO:0014012 otar diseases +MONDO:0014012 rare diseases +MONDO:0014013 clingen diseases +MONDO:0014013 gard_rare diseases +MONDO:0014013 nord_rare diseases +MONDO:0014013 ordo_disorder diseases +MONDO:0014013 orphanet_rare diseases +MONDO:0014013 otar diseases +MONDO:0014013 rare diseases +MONDO:0014014 gard_rare diseases +MONDO:0014014 nord_rare diseases +MONDO:0014014 ordo_disorder diseases +MONDO:0014014 orphanet_rare diseases +MONDO:0014014 rare diseases +MONDO:0014015 gard_rare diseases +MONDO:0014015 nord_rare diseases +MONDO:0014015 ordo_disorder diseases +MONDO:0014015 orphanet_rare diseases +MONDO:0014015 otar diseases +MONDO:0014015 rare diseases +MONDO:0014016 gard_rare diseases +MONDO:0014016 nord_rare diseases +MONDO:0014016 ordo_disorder diseases +MONDO:0014016 orphanet_rare diseases +MONDO:0014016 otar diseases +MONDO:0014016 rare diseases +MONDO:0014018 gard_rare diseases +MONDO:0014018 nord_rare diseases +MONDO:0014018 ordo_disorder diseases +MONDO:0014018 orphanet_rare diseases +MONDO:0014018 otar diseases +MONDO:0014018 rare diseases +MONDO:0014019 gard_rare diseases +MONDO:0014019 nord_rare diseases +MONDO:0014019 ordo_disorder diseases +MONDO:0014019 orphanet_rare diseases +MONDO:0014019 rare diseases +MONDO:0014020 gard_rare diseases +MONDO:0014020 nord_rare diseases +MONDO:0014020 ordo_disorder diseases +MONDO:0014020 orphanet_rare diseases +MONDO:0014020 otar diseases +MONDO:0014020 rare diseases +MONDO:0014021 gard_rare diseases +MONDO:0014021 nord_rare diseases +MONDO:0014021 ordo_subtype_of_a_disorder diseases +MONDO:0014021 otar diseases +MONDO:0014021 rare diseases +MONDO:0014022 gard_rare diseases +MONDO:0014022 nord_rare diseases +MONDO:0014022 otar diseases +MONDO:0014022 rare diseases +MONDO:0014023 gard_rare diseases +MONDO:0014023 nord_rare diseases +MONDO:0014023 ordo_disorder diseases +MONDO:0014023 orphanet_rare diseases +MONDO:0014023 otar diseases +MONDO:0014023 rare diseases +MONDO:0014024 gard_rare diseases +MONDO:0014024 nord_rare diseases +MONDO:0014024 ordo_disorder diseases +MONDO:0014024 orphanet_rare diseases +MONDO:0014024 otar diseases +MONDO:0014024 rare diseases +MONDO:0014025 gard_rare diseases +MONDO:0014025 nord_rare diseases +MONDO:0014025 ordo_disorder diseases +MONDO:0014025 orphanet_rare diseases +MONDO:0014025 otar diseases +MONDO:0014025 rare diseases +MONDO:0014026 gard_rare diseases +MONDO:0014026 rare diseases +MONDO:0014027 gard_rare diseases +MONDO:0014027 nord_rare diseases +MONDO:0014027 rare diseases +MONDO:0014028 gard_rare diseases +MONDO:0014028 nord_rare diseases +MONDO:0014028 ordo_disorder diseases +MONDO:0014028 orphanet_rare diseases +MONDO:0014028 otar diseases +MONDO:0014028 rare diseases +MONDO:0014029 gard_rare diseases +MONDO:0014029 nord_rare diseases +MONDO:0014029 rare diseases +MONDO:0014030 clingen diseases +MONDO:0014030 gard_rare diseases +MONDO:0014030 nord_rare diseases +MONDO:0014030 rare diseases +MONDO:0014031 gard_rare diseases +MONDO:0014031 nord_rare diseases +MONDO:0014031 ordo_disorder diseases +MONDO:0014031 ordo_malformation_syndrome diseases +MONDO:0014031 orphanet_rare diseases +MONDO:0014031 otar diseases +MONDO:0014031 rare diseases +MONDO:0014032 gard_rare diseases +MONDO:0014032 nord_rare diseases +MONDO:0014032 rare diseases +MONDO:0014033 gard_rare diseases +MONDO:0014033 nord_rare diseases +MONDO:0014033 ordo_disorder diseases +MONDO:0014033 orphanet_rare diseases +MONDO:0014033 otar diseases +MONDO:0014033 rare diseases +MONDO:0014034 clingen diseases +MONDO:0014034 gard_rare diseases +MONDO:0014034 nord_rare diseases +MONDO:0014034 ordo_disorder diseases +MONDO:0014034 orphanet_rare diseases +MONDO:0014034 otar diseases +MONDO:0014034 rare diseases +MONDO:0014035 clingen diseases +MONDO:0014035 gard_rare diseases +MONDO:0014035 nord_rare diseases +MONDO:0014035 ordo_disorder diseases +MONDO:0014035 ordo_malformation_syndrome diseases +MONDO:0014035 orphanet_rare diseases +MONDO:0014035 otar diseases +MONDO:0014035 rare diseases +MONDO:0014037 gard_rare diseases +MONDO:0014037 otar diseases +MONDO:0014037 rare diseases +MONDO:0014038 inferred_rare diseases +MONDO:0014038 predisposition diseases +MONDO:0014038 rare diseases +MONDO:0014039 gard_rare diseases +MONDO:0014039 nord_rare diseases +MONDO:0014039 ordo_disorder diseases +MONDO:0014039 orphanet_rare diseases +MONDO:0014039 otar diseases +MONDO:0014039 rare diseases +MONDO:0014040 gard_rare diseases +MONDO:0014040 nord_rare diseases +MONDO:0014040 rare diseases +MONDO:0014042 gard_rare diseases +MONDO:0014042 nord_rare diseases +MONDO:0014042 rare diseases +MONDO:0014043 gard_rare diseases +MONDO:0014043 nord_rare diseases +MONDO:0014043 ordo_disorder diseases +MONDO:0014043 ordo_malformation_syndrome diseases +MONDO:0014043 orphanet_rare diseases +MONDO:0014043 otar diseases +MONDO:0014043 rare diseases +MONDO:0014044 gard_rare diseases +MONDO:0014044 nord_rare diseases +MONDO:0014044 ordo_disorder diseases +MONDO:0014044 ordo_malformation_syndrome diseases +MONDO:0014044 orphanet_rare diseases +MONDO:0014044 otar diseases +MONDO:0014044 rare diseases +MONDO:0014045 gard_rare diseases +MONDO:0014045 rare diseases +MONDO:0014046 gard_rare diseases +MONDO:0014046 rare diseases +MONDO:0014047 gard_rare diseases +MONDO:0014047 rare diseases +MONDO:0014048 gard_rare diseases +MONDO:0014048 rare diseases +MONDO:0014049 gard_rare diseases +MONDO:0014049 rare diseases +MONDO:0014050 gard_rare diseases +MONDO:0014050 nord_rare diseases +MONDO:0014050 rare diseases +MONDO:0014051 gard_rare diseases +MONDO:0014051 nord_rare diseases +MONDO:0014051 rare diseases +MONDO:0014052 gard_rare diseases +MONDO:0014052 nord_rare diseases +MONDO:0014052 otar diseases +MONDO:0014052 rare diseases +MONDO:0014054 gard_rare diseases +MONDO:0014054 rare diseases +MONDO:0014055 gard_rare diseases +MONDO:0014055 nord_rare diseases +MONDO:0014055 rare diseases +MONDO:0014056 inferred_rare diseases +MONDO:0014056 predisposition diseases +MONDO:0014056 rare diseases +MONDO:0014057 clingen diseases +MONDO:0014057 gard_rare diseases +MONDO:0014057 rare diseases +MONDO:0014058 gard_rare diseases +MONDO:0014058 nord_rare diseases +MONDO:0014058 ordo_disorder diseases +MONDO:0014058 orphanet_rare diseases +MONDO:0014058 otar diseases +MONDO:0014058 rare diseases +MONDO:0014059 gard_rare diseases +MONDO:0014059 nord_rare diseases +MONDO:0014059 rare diseases +MONDO:0014060 gard_rare diseases +MONDO:0014060 nord_rare diseases +MONDO:0014060 ordo_disorder diseases +MONDO:0014060 orphanet_rare diseases +MONDO:0014060 otar diseases +MONDO:0014060 rare diseases +MONDO:0014061 gard_rare diseases +MONDO:0014061 nord_rare diseases +MONDO:0014061 ordo_disorder diseases +MONDO:0014061 orphanet_rare diseases +MONDO:0014061 otar diseases +MONDO:0014061 rare diseases +MONDO:0014062 gard_rare diseases +MONDO:0014062 nord_rare diseases +MONDO:0014062 ordo_disorder diseases +MONDO:0014062 orphanet_rare diseases +MONDO:0014062 otar diseases +MONDO:0014062 rare diseases +MONDO:0014063 gard_rare diseases +MONDO:0014063 rare diseases +MONDO:0014064 gard_rare diseases +MONDO:0014064 rare diseases +MONDO:0014065 gard_rare diseases +MONDO:0014065 rare diseases +MONDO:0014066 gard_rare diseases +MONDO:0014066 rare diseases +MONDO:0014067 gard_rare diseases +MONDO:0014067 nord_rare diseases +MONDO:0014067 ordo_disorder diseases +MONDO:0014067 ordo_malformation_syndrome diseases +MONDO:0014067 orphanet_rare diseases +MONDO:0014067 otar diseases +MONDO:0014067 rare diseases +MONDO:0014068 gard_rare diseases +MONDO:0014068 nord_rare diseases +MONDO:0014068 rare diseases +MONDO:0014069 gard_rare diseases +MONDO:0014069 nord_rare diseases +MONDO:0014069 ordo_disorder diseases +MONDO:0014069 ordo_malformation_syndrome diseases +MONDO:0014069 orphanet_rare diseases +MONDO:0014069 otar diseases +MONDO:0014069 rare diseases +MONDO:0014070 gard_rare diseases +MONDO:0014070 nord_rare diseases +MONDO:0014070 ordo_disorder diseases +MONDO:0014070 orphanet_rare diseases +MONDO:0014070 otar diseases +MONDO:0014070 rare diseases +MONDO:0014071 gard_rare diseases +MONDO:0014071 nord_rare diseases +MONDO:0014071 otar diseases +MONDO:0014071 rare diseases +MONDO:0014072 gard_rare diseases +MONDO:0014072 nord_rare diseases +MONDO:0014072 ordo_disorder diseases +MONDO:0014072 orphanet_rare diseases +MONDO:0014072 otar diseases +MONDO:0014072 rare diseases +MONDO:0014073 gard_rare diseases +MONDO:0014073 nord_rare diseases +MONDO:0014073 rare diseases +MONDO:0014074 gard_rare diseases +MONDO:0014074 nord_rare diseases +MONDO:0014074 ordo_disorder diseases +MONDO:0014074 orphanet_rare diseases +MONDO:0014074 otar diseases +MONDO:0014074 rare diseases +MONDO:0014075 gard_rare diseases +MONDO:0014075 nord_rare diseases +MONDO:0014075 rare diseases +MONDO:0014076 gard_rare diseases +MONDO:0014076 nord_rare diseases +MONDO:0014076 otar diseases +MONDO:0014076 rare diseases +MONDO:0014077 clingen diseases +MONDO:0014077 gard_rare diseases +MONDO:0014077 nord_rare diseases +MONDO:0014077 ordo_disorder diseases +MONDO:0014077 orphanet_rare diseases +MONDO:0014077 otar diseases +MONDO:0014077 rare diseases +MONDO:0014078 clingen diseases +MONDO:0014078 gard_rare diseases +MONDO:0014078 nord_rare diseases +MONDO:0014078 otar diseases +MONDO:0014078 rare diseases +MONDO:0014080 gard_rare diseases +MONDO:0014080 nord_rare diseases +MONDO:0014080 ordo_disorder diseases +MONDO:0014080 ordo_malformation_syndrome diseases +MONDO:0014080 orphanet_rare diseases +MONDO:0014080 otar diseases +MONDO:0014080 rare diseases +MONDO:0014081 clingen diseases +MONDO:0014081 gard_rare diseases +MONDO:0014081 nord_rare diseases +MONDO:0014081 ordo_disorder diseases +MONDO:0014081 orphanet_rare diseases +MONDO:0014081 otar diseases +MONDO:0014081 rare diseases +MONDO:0014082 gard_rare diseases +MONDO:0014082 nord_rare diseases +MONDO:0014082 ordo_disorder diseases +MONDO:0014082 orphanet_rare diseases +MONDO:0014082 otar diseases +MONDO:0014082 rare diseases +MONDO:0014083 clingen diseases +MONDO:0014083 gard_rare diseases +MONDO:0014083 nord_rare diseases +MONDO:0014083 rare diseases +MONDO:0014084 gard_rare diseases +MONDO:0014084 nord_rare diseases +MONDO:0014084 rare diseases +MONDO:0014085 gard_rare diseases +MONDO:0014085 nord_rare diseases +MONDO:0014085 rare diseases +MONDO:0014086 gard_rare diseases +MONDO:0014086 nord_rare diseases +MONDO:0014086 rare diseases +MONDO:0014087 gard_rare diseases +MONDO:0014087 nord_rare diseases +MONDO:0014087 rare diseases +MONDO:0014088 gard_rare diseases +MONDO:0014088 nord_rare diseases +MONDO:0014088 rare diseases +MONDO:0014089 gard_rare diseases +MONDO:0014089 nord_rare diseases +MONDO:0014089 ordo_disorder diseases +MONDO:0014089 orphanet_rare diseases +MONDO:0014089 otar diseases +MONDO:0014089 rare diseases +MONDO:0014090 gard_rare diseases +MONDO:0014090 nord_rare diseases +MONDO:0014090 rare diseases +MONDO:0014091 gard_rare diseases +MONDO:0014091 rare diseases +MONDO:0014093 gard_rare diseases +MONDO:0014093 nord_rare diseases +MONDO:0014093 rare diseases +MONDO:0014094 gard_rare diseases +MONDO:0014094 nord_rare diseases +MONDO:0014094 ordo_disorder diseases +MONDO:0014094 orphanet_rare diseases +MONDO:0014094 otar diseases +MONDO:0014094 rare diseases +MONDO:0014095 gard_rare diseases +MONDO:0014095 nord_rare diseases +MONDO:0014095 rare diseases +MONDO:0014096 gard_rare diseases +MONDO:0014096 ordo_malformation_syndrome diseases +MONDO:0014096 otar diseases +MONDO:0014096 rare diseases +MONDO:0014097 gard_rare diseases +MONDO:0014097 nord_rare diseases +MONDO:0014097 ordo_disorder diseases +MONDO:0014097 ordo_morphological_anomaly diseases +MONDO:0014097 orphanet_rare diseases +MONDO:0014097 otar diseases +MONDO:0014097 rare diseases +MONDO:0014098 gard_rare diseases +MONDO:0014098 nord_rare diseases +MONDO:0014098 ordo_disorder diseases +MONDO:0014098 orphanet_rare diseases +MONDO:0014098 rare diseases +MONDO:0014099 gard_rare diseases +MONDO:0014099 rare diseases +MONDO:0014100 gard_rare diseases +MONDO:0014100 nord_rare diseases +MONDO:0014100 rare diseases +MONDO:0014101 gard_rare diseases +MONDO:0014101 nord_rare diseases +MONDO:0014101 otar diseases +MONDO:0014101 rare diseases +MONDO:0014102 gard_rare diseases +MONDO:0014102 nord_rare diseases +MONDO:0014102 rare diseases +MONDO:0014103 gard_rare diseases +MONDO:0014103 nord_rare diseases +MONDO:0014103 rare diseases +MONDO:0014104 gard_rare diseases +MONDO:0014104 nord_rare diseases +MONDO:0014104 rare diseases +MONDO:0014105 gard_rare diseases +MONDO:0014105 nord_rare diseases +MONDO:0014105 rare diseases +MONDO:0014106 gard_rare diseases +MONDO:0014106 nord_rare diseases +MONDO:0014106 rare diseases +MONDO:0014107 gard_rare diseases +MONDO:0014107 nord_rare diseases +MONDO:0014107 rare diseases +MONDO:0014108 gard_rare diseases +MONDO:0014108 nord_rare diseases +MONDO:0014108 rare diseases +MONDO:0014110 gard_rare diseases +MONDO:0014110 nord_rare diseases +MONDO:0014110 rare diseases +MONDO:0014111 gard_rare diseases +MONDO:0014111 nord_rare diseases +MONDO:0014111 rare diseases +MONDO:0014112 gard_rare diseases +MONDO:0014112 nord_rare diseases +MONDO:0014112 rare diseases +MONDO:0014113 gard_rare diseases +MONDO:0014113 nord_rare diseases +MONDO:0014113 rare diseases +MONDO:0014114 gard_rare diseases +MONDO:0014114 nord_rare diseases +MONDO:0014114 rare diseases +MONDO:0014115 gard_rare diseases +MONDO:0014115 nord_rare diseases +MONDO:0014115 ordo_disorder diseases +MONDO:0014115 orphanet_rare diseases +MONDO:0014115 otar diseases +MONDO:0014115 rare diseases +MONDO:0014116 clingen diseases +MONDO:0014117 clingen diseases +MONDO:0014117 gard_rare diseases +MONDO:0014117 nord_rare diseases +MONDO:0014117 ordo_disorder diseases +MONDO:0014117 orphanet_rare diseases +MONDO:0014117 otar diseases +MONDO:0014117 rare diseases +MONDO:0014118 gard_rare diseases +MONDO:0014118 nord_rare diseases +MONDO:0014118 ordo_disorder diseases +MONDO:0014118 orphanet_rare diseases +MONDO:0014118 otar diseases +MONDO:0014118 rare diseases +MONDO:0014119 gard_rare diseases +MONDO:0014119 nord_rare diseases +MONDO:0014119 ordo_disorder diseases +MONDO:0014119 orphanet_rare diseases +MONDO:0014119 otar diseases +MONDO:0014119 rare diseases +MONDO:0014120 clingen diseases +MONDO:0014120 gard_rare diseases +MONDO:0014120 nord_rare diseases +MONDO:0014120 otar diseases +MONDO:0014120 rare diseases +MONDO:0014121 gard_rare diseases +MONDO:0014121 nord_rare diseases +MONDO:0014121 ordo_subtype_of_a_disorder diseases +MONDO:0014121 otar diseases +MONDO:0014121 rare diseases +MONDO:0014122 gard_rare diseases +MONDO:0014122 nord_rare diseases +MONDO:0014122 rare diseases +MONDO:0014123 gard_rare diseases +MONDO:0014123 nord_rare diseases +MONDO:0014123 rare diseases +MONDO:0014124 gard_rare diseases +MONDO:0014124 nord_rare diseases +MONDO:0014124 rare diseases +MONDO:0014125 gard_rare diseases +MONDO:0014125 nord_rare diseases +MONDO:0014125 rare diseases +MONDO:0014126 gard_rare diseases +MONDO:0014126 nord_rare diseases +MONDO:0014126 rare diseases +MONDO:0014127 gard_rare diseases +MONDO:0014127 nord_rare diseases +MONDO:0014127 ordo_disorder diseases +MONDO:0014127 orphanet_rare diseases +MONDO:0014127 otar diseases +MONDO:0014127 rare diseases +MONDO:0014128 clingen diseases +MONDO:0014128 gard_rare diseases +MONDO:0014128 nord_rare diseases +MONDO:0014128 otar diseases +MONDO:0014128 rare diseases +MONDO:0014130 gard_rare diseases +MONDO:0014130 nord_rare diseases +MONDO:0014130 rare diseases +MONDO:0014131 gard_rare diseases +MONDO:0014131 nord_rare diseases +MONDO:0014131 ordo_disorder diseases +MONDO:0014131 orphanet_rare diseases +MONDO:0014131 otar diseases +MONDO:0014131 rare diseases +MONDO:0014132 gard_rare diseases +MONDO:0014132 nord_rare diseases +MONDO:0014132 ordo_disorder diseases +MONDO:0014132 orphanet_rare diseases +MONDO:0014132 otar diseases +MONDO:0014132 rare diseases +MONDO:0014133 gard_rare diseases +MONDO:0014133 nord_rare diseases +MONDO:0014133 rare diseases +MONDO:0014134 gard_rare diseases +MONDO:0014134 nord_rare diseases +MONDO:0014134 rare diseases +MONDO:0014135 gard_rare diseases +MONDO:0014135 nord_rare diseases +MONDO:0014135 rare diseases +MONDO:0014136 gard_rare diseases +MONDO:0014136 nord_rare diseases +MONDO:0014136 rare diseases +MONDO:0014137 gard_rare diseases +MONDO:0014137 otar diseases +MONDO:0014137 rare diseases +MONDO:0014138 clingen diseases +MONDO:0014138 gard_rare diseases +MONDO:0014138 otar diseases +MONDO:0014138 rare diseases +MONDO:0014139 gard_rare diseases +MONDO:0014139 nord_rare diseases +MONDO:0014139 ordo_subtype_of_a_disorder diseases +MONDO:0014139 rare diseases +MONDO:0014140 gard_rare diseases +MONDO:0014140 nord_rare diseases +MONDO:0014140 otar diseases +MONDO:0014140 rare diseases +MONDO:0014141 gard_rare diseases +MONDO:0014141 otar diseases +MONDO:0014141 rare diseases +MONDO:0014142 gard_rare diseases +MONDO:0014142 nord_rare diseases +MONDO:0014142 ordo_disorder diseases +MONDO:0014142 orphanet_rare diseases +MONDO:0014142 otar diseases +MONDO:0014142 rare diseases +MONDO:0014143 gard_rare diseases +MONDO:0014143 nord_rare diseases +MONDO:0014143 rare diseases +MONDO:0014144 gard_rare diseases +MONDO:0014144 nord_rare diseases +MONDO:0014144 ordo_disorder diseases +MONDO:0014144 orphanet_rare diseases +MONDO:0014144 otar diseases +MONDO:0014144 rare diseases +MONDO:0014145 gard_rare diseases +MONDO:0014145 nord_rare diseases +MONDO:0014145 rare diseases +MONDO:0014146 gard_rare diseases +MONDO:0014146 rare diseases +MONDO:0014147 gard_rare diseases +MONDO:0014147 nord_rare diseases +MONDO:0014147 ordo_etiological_subtype diseases +MONDO:0014147 otar diseases +MONDO:0014147 rare diseases +MONDO:0014148 gard_rare diseases +MONDO:0014148 nord_rare diseases +MONDO:0014148 ordo_disorder diseases +MONDO:0014148 orphanet_rare diseases +MONDO:0014148 rare diseases +MONDO:0014149 gard_rare diseases +MONDO:0014149 nord_rare diseases +MONDO:0014149 ordo_disorder diseases +MONDO:0014149 orphanet_rare diseases +MONDO:0014149 otar diseases +MONDO:0014149 rare diseases +MONDO:0014150 gard_rare diseases +MONDO:0014150 nord_rare diseases +MONDO:0014150 rare diseases +MONDO:0014152 gard_rare diseases +MONDO:0014152 nord_rare diseases +MONDO:0014152 rare diseases +MONDO:0014153 gard_rare diseases +MONDO:0014153 nord_rare diseases +MONDO:0014153 rare diseases +MONDO:0014154 gard_rare diseases +MONDO:0014154 nord_rare diseases +MONDO:0014154 ordo_disorder diseases +MONDO:0014154 orphanet_rare diseases +MONDO:0014154 otar diseases +MONDO:0014154 rare diseases +MONDO:0014155 gard_rare diseases +MONDO:0014155 rare diseases +MONDO:0014156 gard_rare diseases +MONDO:0014156 rare diseases +MONDO:0014157 gard_rare diseases +MONDO:0014157 nord_rare diseases +MONDO:0014157 ordo_disorder diseases +MONDO:0014157 orphanet_rare diseases +MONDO:0014157 otar diseases +MONDO:0014157 rare diseases +MONDO:0014158 clingen diseases +MONDO:0014158 gard_rare diseases +MONDO:0014158 nord_rare diseases +MONDO:0014158 otar diseases +MONDO:0014158 rare diseases +MONDO:0014159 gard_rare diseases +MONDO:0014159 nord_rare diseases +MONDO:0014159 ordo_disorder diseases +MONDO:0014159 orphanet_rare diseases +MONDO:0014159 otar diseases +MONDO:0014159 rare diseases +MONDO:0014160 clingen diseases +MONDO:0014160 gard_rare diseases +MONDO:0014160 nord_rare diseases +MONDO:0014160 ordo_disorder diseases +MONDO:0014160 orphanet_rare diseases +MONDO:0014160 otar diseases +MONDO:0014160 rare diseases +MONDO:0014161 gard_rare diseases +MONDO:0014161 nord_rare diseases +MONDO:0014161 rare diseases +MONDO:0014162 gard_rare diseases +MONDO:0014162 nord_rare diseases +MONDO:0014162 ordo_disorder diseases +MONDO:0014162 orphanet_rare diseases +MONDO:0014162 otar diseases +MONDO:0014162 rare diseases +MONDO:0014163 gard_rare diseases +MONDO:0014163 nord_rare diseases +MONDO:0014163 rare diseases +MONDO:0014164 gard_rare diseases +MONDO:0014164 rare diseases +MONDO:0014165 gard_rare diseases +MONDO:0014165 nord_rare diseases +MONDO:0014165 ordo_disorder diseases +MONDO:0014165 ordo_malformation_syndrome diseases +MONDO:0014165 orphanet_rare diseases +MONDO:0014165 otar diseases +MONDO:0014165 rare diseases +MONDO:0014166 gard_rare diseases +MONDO:0014166 nord_rare diseases +MONDO:0014166 otar diseases +MONDO:0014166 rare diseases +MONDO:0014167 gard_rare diseases +MONDO:0014167 nord_rare diseases +MONDO:0014167 rare diseases +MONDO:0014168 clingen diseases +MONDO:0014168 gard_rare diseases +MONDO:0014168 nord_rare diseases +MONDO:0014168 ordo_disorder diseases +MONDO:0014168 orphanet_rare diseases +MONDO:0014168 otar diseases +MONDO:0014168 rare diseases +MONDO:0014169 gard_rare diseases +MONDO:0014169 rare diseases +MONDO:0014172 gard_rare diseases +MONDO:0014172 rare diseases +MONDO:0014173 gard_rare diseases +MONDO:0014173 nord_rare diseases +MONDO:0014173 rare diseases +MONDO:0014174 clingen diseases +MONDO:0014174 gard_rare diseases +MONDO:0014174 rare diseases +MONDO:0014175 clingen diseases +MONDO:0014175 gard_rare diseases +MONDO:0014175 otar diseases +MONDO:0014175 rare diseases +MONDO:0014176 gard_rare diseases +MONDO:0014176 nord_rare diseases +MONDO:0014176 ordo_disorder diseases +MONDO:0014176 orphanet_rare diseases +MONDO:0014176 otar diseases +MONDO:0014176 prototype_pattern diseases +MONDO:0014176 rare diseases +MONDO:0014178 gard_rare diseases +MONDO:0014178 rare diseases +MONDO:0014179 gard_rare diseases +MONDO:0014179 rare diseases +MONDO:0014180 gard_rare diseases +MONDO:0014180 nord_rare diseases +MONDO:0014180 ordo_disorder diseases +MONDO:0014180 orphanet_rare diseases +MONDO:0014180 otar diseases +MONDO:0014180 rare diseases +MONDO:0014181 gard_rare diseases +MONDO:0014181 nord_rare diseases +MONDO:0014181 rare diseases +MONDO:0014182 gard_rare diseases +MONDO:0014182 nord_rare diseases +MONDO:0014182 rare diseases +MONDO:0014183 gard_rare diseases +MONDO:0014183 nord_rare diseases +MONDO:0014183 rare diseases +MONDO:0014184 otar diseases +MONDO:0014185 gard_rare diseases +MONDO:0014185 nord_rare diseases +MONDO:0014185 ordo_disorder diseases +MONDO:0014185 ordo_malformation_syndrome diseases +MONDO:0014185 orphanet_rare diseases +MONDO:0014185 otar diseases +MONDO:0014185 rare diseases +MONDO:0014186 clingen diseases +MONDO:0014186 gard_rare diseases +MONDO:0014186 nord_rare diseases +MONDO:0014186 rare diseases +MONDO:0014187 gard_rare diseases +MONDO:0014187 nord_rare diseases +MONDO:0014187 rare diseases +MONDO:0014190 gard_rare diseases +MONDO:0014190 nord_rare diseases +MONDO:0014190 ordo_disorder diseases +MONDO:0014190 orphanet_rare diseases +MONDO:0014190 otar diseases +MONDO:0014190 rare diseases +MONDO:0014191 gard_rare diseases +MONDO:0014191 nord_rare diseases +MONDO:0014191 rare diseases +MONDO:0014192 clingen diseases +MONDO:0014192 gard_rare diseases +MONDO:0014192 nord_rare diseases +MONDO:0014192 rare diseases +MONDO:0014193 clingen diseases +MONDO:0014193 gard_rare diseases +MONDO:0014193 nord_rare diseases +MONDO:0014193 rare diseases +MONDO:0014194 gard_rare diseases +MONDO:0014194 rare diseases +MONDO:0014195 clingen diseases +MONDO:0014195 gard_rare diseases +MONDO:0014195 nord_rare diseases +MONDO:0014195 ordo_disorder diseases +MONDO:0014195 orphanet_rare diseases +MONDO:0014195 otar diseases +MONDO:0014195 rare diseases +MONDO:0014196 clingen diseases +MONDO:0014196 gard_rare diseases +MONDO:0014196 nord_rare diseases +MONDO:0014196 ordo_disorder diseases +MONDO:0014196 ordo_malformation_syndrome diseases +MONDO:0014196 orphanet_rare diseases +MONDO:0014196 otar diseases +MONDO:0014196 rare diseases +MONDO:0014197 clingen diseases +MONDO:0014197 gard_rare diseases +MONDO:0014197 nord_rare diseases +MONDO:0014197 ordo_disorder diseases +MONDO:0014197 orphanet_rare diseases +MONDO:0014197 otar diseases +MONDO:0014197 rare diseases +MONDO:0014198 gard_rare diseases +MONDO:0014198 nord_rare diseases +MONDO:0014198 ordo_disorder diseases +MONDO:0014198 orphanet_rare diseases +MONDO:0014198 otar diseases +MONDO:0014198 rare diseases +MONDO:0014199 gard_rare diseases +MONDO:0014199 nord_rare diseases +MONDO:0014199 rare diseases +MONDO:0014200 gard_rare diseases +MONDO:0014200 nord_rare diseases +MONDO:0014200 ordo_disorder diseases +MONDO:0014200 orphanet_rare diseases +MONDO:0014200 otar diseases +MONDO:0014200 rare diseases +MONDO:0014201 gard_rare diseases +MONDO:0014201 nord_rare diseases +MONDO:0014201 otar diseases +MONDO:0014201 rare diseases +MONDO:0014202 clingen diseases +MONDO:0014202 gard_rare diseases +MONDO:0014202 nord_rare diseases +MONDO:0014202 rare diseases +MONDO:0014203 gard_rare diseases +MONDO:0014203 nord_rare diseases +MONDO:0014203 rare diseases +MONDO:0014204 gard_rare diseases +MONDO:0014204 rare diseases +MONDO:0014205 gard_rare diseases +MONDO:0014205 nord_rare diseases +MONDO:0014205 ordo_disorder diseases +MONDO:0014205 orphanet_rare diseases +MONDO:0014205 otar diseases +MONDO:0014205 rare diseases +MONDO:0014206 gard_rare diseases +MONDO:0014206 nord_rare diseases +MONDO:0014206 ordo_disorder diseases +MONDO:0014206 orphanet_rare diseases +MONDO:0014206 otar diseases +MONDO:0014206 rare diseases +MONDO:0014207 gard_rare diseases +MONDO:0014207 nord_rare diseases +MONDO:0014207 rare diseases +MONDO:0014208 gard_rare diseases +MONDO:0014208 nord_rare diseases +MONDO:0014208 ordo_disorder diseases +MONDO:0014208 orphanet_rare diseases +MONDO:0014208 otar diseases +MONDO:0014208 rare diseases +MONDO:0014209 gard_rare diseases +MONDO:0014209 nord_rare diseases +MONDO:0014209 ordo_disorder diseases +MONDO:0014209 orphanet_rare diseases +MONDO:0014209 otar diseases +MONDO:0014209 rare diseases +MONDO:0014210 gard_rare diseases +MONDO:0014210 nord_rare diseases +MONDO:0014210 ordo_disorder diseases +MONDO:0014210 orphanet_rare diseases +MONDO:0014210 otar diseases +MONDO:0014210 rare diseases +MONDO:0014211 clingen diseases +MONDO:0014211 gard_rare diseases +MONDO:0014211 nord_rare diseases +MONDO:0014211 rare diseases +MONDO:0014212 clingen diseases +MONDO:0014212 gard_rare diseases +MONDO:0014212 nord_rare diseases +MONDO:0014212 ordo_etiological_subtype diseases +MONDO:0014212 ordo_subtype_of_a_disorder diseases +MONDO:0014212 otar diseases +MONDO:0014212 rare diseases +MONDO:0014213 gard_rare diseases +MONDO:0014213 nord_rare diseases +MONDO:0014213 ordo_disorder diseases +MONDO:0014213 orphanet_rare diseases +MONDO:0014213 otar diseases +MONDO:0014213 rare diseases +MONDO:0014214 gard_rare diseases +MONDO:0014214 nord_rare diseases +MONDO:0014214 rare diseases +MONDO:0014215 gard_rare diseases +MONDO:0014215 nord_rare diseases +MONDO:0014215 rare diseases +MONDO:0014216 clingen diseases +MONDO:0014216 gard_rare diseases +MONDO:0014216 nord_rare diseases +MONDO:0014216 rare diseases +MONDO:0014217 clingen diseases +MONDO:0014217 gard_rare diseases +MONDO:0014217 nord_rare diseases +MONDO:0014217 rare diseases +MONDO:0014218 gard_rare diseases +MONDO:0014218 nord_rare diseases +MONDO:0014218 ordo_disorder diseases +MONDO:0014218 orphanet_rare diseases +MONDO:0014218 otar diseases +MONDO:0014218 rare diseases +MONDO:0014219 gard_rare diseases +MONDO:0014219 nord_rare diseases +MONDO:0014219 rare diseases +MONDO:0014220 gard_rare diseases +MONDO:0014220 prototype_pattern diseases +MONDO:0014220 rare diseases +MONDO:0014221 gard_rare diseases +MONDO:0014221 nord_rare diseases +MONDO:0014221 ordo_disorder diseases +MONDO:0014221 orphanet_rare diseases +MONDO:0014221 otar diseases +MONDO:0014221 rare diseases +MONDO:0014222 clingen diseases +MONDO:0014222 gard_rare diseases +MONDO:0014222 nord_rare diseases +MONDO:0014222 rare diseases +MONDO:0014223 clingen diseases +MONDO:0014223 gard_rare diseases +MONDO:0014223 nord_rare diseases +MONDO:0014223 rare diseases +MONDO:0014224 gard_rare diseases +MONDO:0014224 nord_rare diseases +MONDO:0014224 ordo_disorder diseases +MONDO:0014224 orphanet_rare diseases +MONDO:0014224 otar diseases +MONDO:0014224 rare diseases +MONDO:0014225 gard_rare diseases +MONDO:0014225 merged_class diseases +MONDO:0014225 nord_rare diseases +MONDO:0014225 ordo_disorder diseases +MONDO:0014225 orphanet_rare diseases +MONDO:0014225 otar diseases +MONDO:0014225 rare diseases +MONDO:0014226 gard_rare diseases +MONDO:0014226 nord_rare diseases +MONDO:0014226 ordo_disorder diseases +MONDO:0014226 orphanet_rare diseases +MONDO:0014226 otar diseases +MONDO:0014226 rare diseases +MONDO:0014227 gard_rare diseases +MONDO:0014227 nord_rare diseases +MONDO:0014227 ordo_disorder diseases +MONDO:0014227 orphanet_rare diseases +MONDO:0014227 otar diseases +MONDO:0014227 rare diseases +MONDO:0014228 gard_rare diseases +MONDO:0014228 nord_rare diseases +MONDO:0014228 rare diseases +MONDO:0014229 gard_rare diseases +MONDO:0014229 nord_rare diseases +MONDO:0014229 rare diseases +MONDO:0014230 gard_rare diseases +MONDO:0014230 nord_rare diseases +MONDO:0014230 rare diseases +MONDO:0014231 gard_rare diseases +MONDO:0014231 rare diseases +MONDO:0014233 gard_rare diseases +MONDO:0014233 rare diseases +MONDO:0014234 gard_rare diseases +MONDO:0014234 nord_rare diseases +MONDO:0014234 ordo_disorder diseases +MONDO:0014234 orphanet_rare diseases +MONDO:0014234 otar diseases +MONDO:0014234 rare diseases +MONDO:0014235 gard_rare diseases +MONDO:0014235 nord_rare diseases +MONDO:0014235 rare diseases +MONDO:0014236 gard_rare diseases +MONDO:0014236 nord_rare diseases +MONDO:0014236 rare diseases +MONDO:0014237 gard_rare diseases +MONDO:0014237 nord_rare diseases +MONDO:0014237 rare diseases +MONDO:0014238 gard_rare diseases +MONDO:0014238 nord_rare diseases +MONDO:0014238 ordo_disorder diseases +MONDO:0014238 ordo_malformation_syndrome diseases +MONDO:0014238 orphanet_rare diseases +MONDO:0014238 otar diseases +MONDO:0014238 rare diseases +MONDO:0014239 gard_rare diseases +MONDO:0014239 nord_rare diseases +MONDO:0014239 rare diseases +MONDO:0014240 gard_rare diseases +MONDO:0014240 nord_rare diseases +MONDO:0014240 rare diseases +MONDO:0014241 gard_rare diseases +MONDO:0014241 predisposition diseases +MONDO:0014241 rare diseases +MONDO:0014242 gard_rare diseases +MONDO:0014242 nord_rare diseases +MONDO:0014242 rare diseases +MONDO:0014243 clingen diseases +MONDO:0014243 gard_rare diseases +MONDO:0014243 nord_rare diseases +MONDO:0014243 ordo_disorder diseases +MONDO:0014243 ordo_etiological_subtype diseases +MONDO:0014243 orphanet_rare diseases +MONDO:0014243 otar diseases +MONDO:0014243 rare diseases +MONDO:0014244 gard_rare diseases +MONDO:0014244 nord_rare diseases +MONDO:0014244 ordo_disorder diseases +MONDO:0014244 orphanet_rare diseases +MONDO:0014244 otar diseases +MONDO:0014244 rare diseases +MONDO:0014245 gard_rare diseases +MONDO:0014245 nord_rare diseases +MONDO:0014245 rare diseases +MONDO:0014246 gard_rare diseases +MONDO:0014246 nord_rare diseases +MONDO:0014246 rare diseases +MONDO:0014247 gard_rare diseases +MONDO:0014247 nord_rare diseases +MONDO:0014247 ordo_subtype_of_a_disorder diseases +MONDO:0014247 otar diseases +MONDO:0014247 rare diseases +MONDO:0014248 gard_rare diseases +MONDO:0014248 nord_rare diseases +MONDO:0014248 ordo_disorder diseases +MONDO:0014248 orphanet_rare diseases +MONDO:0014248 otar diseases +MONDO:0014248 rare diseases +MONDO:0014249 gard_rare diseases +MONDO:0014249 nord_rare diseases +MONDO:0014249 rare diseases +MONDO:0014250 gard_rare diseases +MONDO:0014250 nord_rare diseases +MONDO:0014250 ordo_disorder diseases +MONDO:0014250 orphanet_rare diseases +MONDO:0014250 otar diseases +MONDO:0014250 rare diseases +MONDO:0014252 clingen diseases +MONDO:0014252 gard_rare diseases +MONDO:0014252 nord_rare diseases +MONDO:0014252 otar diseases +MONDO:0014252 rare diseases +MONDO:0014254 gard_rare diseases +MONDO:0014254 nord_rare diseases +MONDO:0014254 rare diseases +MONDO:0014256 gard_rare diseases +MONDO:0014256 nord_rare diseases +MONDO:0014256 rare diseases +MONDO:0014257 gard_rare diseases +MONDO:0014257 rare diseases +MONDO:0014258 clingen diseases +MONDO:0014258 gard_rare diseases +MONDO:0014258 nord_rare diseases +MONDO:0014258 ordo_disorder diseases +MONDO:0014258 orphanet_rare diseases +MONDO:0014258 otar diseases +MONDO:0014258 rare diseases +MONDO:0014259 gard_rare diseases +MONDO:0014259 nord_rare diseases +MONDO:0014259 rare diseases +MONDO:0014260 clingen diseases +MONDO:0014260 gard_rare diseases +MONDO:0014260 nord_rare diseases +MONDO:0014260 otar diseases +MONDO:0014260 rare diseases +MONDO:0014261 gard_rare diseases +MONDO:0014261 nord_rare diseases +MONDO:0014261 ordo_disorder diseases +MONDO:0014261 orphanet_rare diseases +MONDO:0014261 otar diseases +MONDO:0014261 rare diseases +MONDO:0014262 gard_rare diseases +MONDO:0014262 nord_rare diseases +MONDO:0014262 otar diseases +MONDO:0014262 rare diseases +MONDO:0014263 gard_rare diseases +MONDO:0014263 nord_rare diseases +MONDO:0014263 ordo_disorder diseases +MONDO:0014263 ordo_malformation_syndrome diseases +MONDO:0014263 orphanet_rare diseases +MONDO:0014263 otar diseases +MONDO:0014263 rare diseases +MONDO:0014264 gard_rare diseases +MONDO:0014264 rare diseases +MONDO:0014265 gard_rare diseases +MONDO:0014265 rare diseases +MONDO:0014267 clingen diseases +MONDO:0014267 gard_rare diseases +MONDO:0014267 nord_rare diseases +MONDO:0014267 ordo_disorder diseases +MONDO:0014267 orphanet_rare diseases +MONDO:0014267 otar diseases +MONDO:0014267 rare diseases +MONDO:0014268 clingen diseases +MONDO:0014268 gard_rare diseases +MONDO:0014268 nord_rare diseases +MONDO:0014268 ordo_disorder diseases +MONDO:0014268 orphanet_rare diseases +MONDO:0014268 otar diseases +MONDO:0014268 rare diseases +MONDO:0014269 gard_rare diseases +MONDO:0014269 rare diseases +MONDO:0014270 gard_rare diseases +MONDO:0014270 nord_rare diseases +MONDO:0014270 ordo_disorder diseases +MONDO:0014270 orphanet_rare diseases +MONDO:0014270 otar diseases +MONDO:0014270 rare diseases +MONDO:0014271 gard_rare diseases +MONDO:0014271 nord_rare diseases +MONDO:0014271 ordo_disorder diseases +MONDO:0014271 orphanet_rare diseases +MONDO:0014271 otar diseases +MONDO:0014271 rare diseases +MONDO:0014272 gard_rare diseases +MONDO:0014272 nord_rare diseases +MONDO:0014272 ordo_disorder diseases +MONDO:0014272 orphanet_rare diseases +MONDO:0014272 otar diseases +MONDO:0014272 rare diseases +MONDO:0014273 gard_rare diseases +MONDO:0014273 nord_rare diseases +MONDO:0014273 ordo_disorder diseases +MONDO:0014273 orphanet_rare diseases +MONDO:0014273 otar diseases +MONDO:0014273 rare diseases +MONDO:0014274 gard_rare diseases +MONDO:0014274 nord_rare diseases +MONDO:0014274 ordo_biological_anomaly diseases +MONDO:0014274 ordo_disorder diseases +MONDO:0014274 orphanet_rare diseases +MONDO:0014274 otar diseases +MONDO:0014274 rare diseases +MONDO:0014275 clingen diseases +MONDO:0014275 gard_rare diseases +MONDO:0014275 nord_rare diseases +MONDO:0014275 rare diseases +MONDO:0014276 clingen diseases +MONDO:0014276 gard_rare diseases +MONDO:0014276 nord_rare diseases +MONDO:0014276 ordo_disorder diseases +MONDO:0014276 orphanet_rare diseases +MONDO:0014276 otar diseases +MONDO:0014276 rare diseases +MONDO:0014278 clingen diseases +MONDO:0014278 gard_rare diseases +MONDO:0014278 nord_rare diseases +MONDO:0014278 otar diseases +MONDO:0014278 rare diseases +MONDO:0014280 clingen diseases +MONDO:0014280 gard_rare diseases +MONDO:0014280 nord_rare diseases +MONDO:0014280 rare diseases +MONDO:0014281 inferred_rare diseases +MONDO:0014281 predisposition diseases +MONDO:0014281 rare diseases +MONDO:0014282 gard_rare diseases +MONDO:0014282 nord_rare diseases +MONDO:0014282 ordo_disorder diseases +MONDO:0014282 ordo_inheritance_inconsistent diseases +MONDO:0014282 orphanet_rare diseases +MONDO:0014282 otar diseases +MONDO:0014282 rare diseases +MONDO:0014283 gard_rare diseases +MONDO:0014283 nord_rare diseases +MONDO:0014283 rare diseases +MONDO:0014284 gard_rare diseases +MONDO:0014284 nord_rare diseases +MONDO:0014284 otar diseases +MONDO:0014284 rare diseases +MONDO:0014285 gard_rare diseases +MONDO:0014285 nord_rare diseases +MONDO:0014285 rare diseases +MONDO:0014286 clingen diseases +MONDO:0014286 gard_rare diseases +MONDO:0014286 nord_rare diseases +MONDO:0014286 otar diseases +MONDO:0014286 rare diseases +MONDO:0014287 gard_rare diseases +MONDO:0014287 nord_rare diseases +MONDO:0014287 rare diseases +MONDO:0014288 clingen diseases +MONDO:0014288 gard_rare diseases +MONDO:0014288 nord_rare diseases +MONDO:0014288 rare diseases +MONDO:0014289 gard_rare diseases +MONDO:0014289 nord_rare diseases +MONDO:0014289 ordo_disorder diseases +MONDO:0014289 ordo_malformation_syndrome diseases +MONDO:0014289 orphanet_rare diseases +MONDO:0014289 otar diseases +MONDO:0014289 rare diseases +MONDO:0014290 gard_rare diseases +MONDO:0014290 nord_rare diseases +MONDO:0014290 ordo_disorder diseases +MONDO:0014290 orphanet_rare diseases +MONDO:0014290 otar diseases +MONDO:0014290 rare diseases +MONDO:0014291 gard_rare diseases +MONDO:0014291 nord_rare diseases +MONDO:0014291 rare diseases +MONDO:0014292 gard_rare diseases +MONDO:0014292 nord_rare diseases +MONDO:0014292 ordo_disorder diseases +MONDO:0014292 orphanet_rare diseases +MONDO:0014292 otar diseases +MONDO:0014292 rare diseases +MONDO:0014293 gard_rare diseases +MONDO:0014293 nord_rare diseases +MONDO:0014293 rare diseases +MONDO:0014294 gard_rare diseases +MONDO:0014294 nord_rare diseases +MONDO:0014294 ordo_disorder diseases +MONDO:0014294 ordo_malformation_syndrome diseases +MONDO:0014294 orphanet_rare diseases +MONDO:0014294 otar diseases +MONDO:0014294 rare diseases +MONDO:0014295 gard_rare diseases +MONDO:0014295 nord_rare diseases +MONDO:0014295 ordo_disorder diseases +MONDO:0014295 orphanet_rare diseases +MONDO:0014295 rare diseases +MONDO:0014296 gard_rare diseases +MONDO:0014296 nord_rare diseases +MONDO:0014296 rare diseases +MONDO:0014297 gard_rare diseases +MONDO:0014297 nord_rare diseases +MONDO:0014297 rare diseases +MONDO:0014298 gard_rare diseases +MONDO:0014298 nord_rare diseases +MONDO:0014298 ordo_disorder diseases +MONDO:0014298 ordo_malformation_syndrome diseases +MONDO:0014298 orphanet_rare diseases +MONDO:0014298 rare diseases +MONDO:0014299 gard_rare diseases +MONDO:0014299 nord_rare diseases +MONDO:0014299 rare diseases +MONDO:0014300 gard_rare diseases +MONDO:0014300 nord_rare diseases +MONDO:0014300 ordo_disorder diseases +MONDO:0014300 orphanet_rare diseases +MONDO:0014300 otar diseases +MONDO:0014300 rare diseases +MONDO:0014301 gard_rare diseases +MONDO:0014301 nord_rare diseases +MONDO:0014301 rare diseases +MONDO:0014302 gard_rare diseases +MONDO:0014302 nord_rare diseases +MONDO:0014302 ordo_disorder diseases +MONDO:0014302 orphanet_rare diseases +MONDO:0014302 otar diseases +MONDO:0014302 rare diseases +MONDO:0014303 gard_rare diseases +MONDO:0014303 nord_rare diseases +MONDO:0014303 ordo_disorder diseases +MONDO:0014303 orphanet_rare diseases +MONDO:0014303 otar diseases +MONDO:0014303 rare diseases +MONDO:0014304 gard_rare diseases +MONDO:0014304 nord_rare diseases +MONDO:0014304 ordo_disorder diseases +MONDO:0014304 orphanet_rare diseases +MONDO:0014304 otar diseases +MONDO:0014304 rare diseases +MONDO:0014305 gard_rare diseases +MONDO:0014305 nord_rare diseases +MONDO:0014305 ordo_disorder diseases +MONDO:0014305 orphanet_rare diseases +MONDO:0014305 otar diseases +MONDO:0014305 rare diseases +MONDO:0014306 gard_rare diseases +MONDO:0014306 nord_rare diseases +MONDO:0014306 ordo_disorder diseases +MONDO:0014306 orphanet_rare diseases +MONDO:0014306 otar diseases +MONDO:0014306 rare diseases +MONDO:0014307 gard_rare diseases +MONDO:0014307 nord_rare diseases +MONDO:0014307 rare diseases +MONDO:0014308 gard_rare diseases +MONDO:0014308 nord_rare diseases +MONDO:0014308 rare diseases +MONDO:0014309 gard_rare diseases +MONDO:0014309 nord_rare diseases +MONDO:0014309 ordo_subtype_of_a_disorder diseases +MONDO:0014309 otar diseases +MONDO:0014309 rare diseases +MONDO:0014310 gard_rare diseases +MONDO:0014310 nord_rare diseases +MONDO:0014310 ordo_disorder diseases +MONDO:0014310 orphanet_rare diseases +MONDO:0014310 otar diseases +MONDO:0014310 rare diseases +MONDO:0014311 gard_rare diseases +MONDO:0014311 nord_rare diseases +MONDO:0014311 ordo_disorder diseases +MONDO:0014311 orphanet_rare diseases +MONDO:0014311 otar diseases +MONDO:0014311 rare diseases +MONDO:0014312 gard_rare diseases +MONDO:0014312 nord_rare diseases +MONDO:0014312 rare diseases +MONDO:0014313 gard_rare diseases +MONDO:0014313 nord_rare diseases +MONDO:0014313 ordo_disorder diseases +MONDO:0014313 orphanet_rare diseases +MONDO:0014313 otar diseases +MONDO:0014313 rare diseases +MONDO:0014314 gard_rare diseases +MONDO:0014314 nord_rare diseases +MONDO:0014314 ordo_disorder diseases +MONDO:0014314 ordo_malformation_syndrome diseases +MONDO:0014314 orphanet_rare diseases +MONDO:0014314 otar diseases +MONDO:0014314 rare diseases +MONDO:0014316 gard_rare diseases +MONDO:0014316 rare diseases +MONDO:0014317 gard_rare diseases +MONDO:0014317 nord_rare diseases +MONDO:0014317 ordo_disorder diseases +MONDO:0014317 orphanet_rare diseases +MONDO:0014317 otar diseases +MONDO:0014317 rare diseases +MONDO:0014318 clingen diseases +MONDO:0014318 gard_rare diseases +MONDO:0014318 nord_rare diseases +MONDO:0014318 rare diseases +MONDO:0014319 gard_rare diseases +MONDO:0014319 nord_rare diseases +MONDO:0014319 rare diseases +MONDO:0014320 clingen diseases +MONDO:0014320 gard_rare diseases +MONDO:0014320 nord_rare diseases +MONDO:0014320 ordo_disorder diseases +MONDO:0014320 orphanet_rare diseases +MONDO:0014320 otar diseases +MONDO:0014320 rare diseases +MONDO:0014321 gard_rare diseases +MONDO:0014321 nord_rare diseases +MONDO:0014321 rare diseases +MONDO:0014322 gard_rare diseases +MONDO:0014322 nord_rare diseases +MONDO:0014322 rare diseases +MONDO:0014323 gard_rare diseases +MONDO:0014323 nord_rare diseases +MONDO:0014323 rare diseases +MONDO:0014324 gard_rare diseases +MONDO:0014324 nord_rare diseases +MONDO:0014324 rare diseases +MONDO:0014325 gard_rare diseases +MONDO:0014325 nord_rare diseases +MONDO:0014325 rare diseases +MONDO:0014326 clingen diseases +MONDO:0014326 gard_rare diseases +MONDO:0014326 otar diseases +MONDO:0014326 rare diseases +MONDO:0014327 gard_rare diseases +MONDO:0014327 nord_rare diseases +MONDO:0014327 ordo_disorder diseases +MONDO:0014327 orphanet_rare diseases +MONDO:0014327 otar diseases +MONDO:0014327 rare diseases +MONDO:0014328 gard_rare diseases +MONDO:0014328 nord_rare diseases +MONDO:0014328 rare diseases +MONDO:0014329 gard_rare diseases +MONDO:0014329 nord_rare diseases +MONDO:0014329 rare diseases +MONDO:0014331 gard_rare diseases +MONDO:0014331 nord_rare diseases +MONDO:0014331 ordo_disorder diseases +MONDO:0014331 orphanet_rare diseases +MONDO:0014331 otar diseases +MONDO:0014331 rare diseases +MONDO:0014332 clingen diseases +MONDO:0014332 gard_rare diseases +MONDO:0014332 nord_rare diseases +MONDO:0014332 ordo_disorder diseases +MONDO:0014332 orphanet_rare diseases +MONDO:0014332 otar diseases +MONDO:0014332 rare diseases +MONDO:0014333 gard_rare diseases +MONDO:0014333 nord_rare diseases +MONDO:0014333 rare diseases +MONDO:0014334 clingen diseases +MONDO:0014334 gard_rare diseases +MONDO:0014334 nord_rare diseases +MONDO:0014334 ordo_disorder diseases +MONDO:0014334 orphanet_rare diseases +MONDO:0014334 otar diseases +MONDO:0014334 rare diseases +MONDO:0014335 clingen diseases +MONDO:0014335 gard_rare diseases +MONDO:0014335 nord_rare diseases +MONDO:0014335 ordo_disorder diseases +MONDO:0014335 ordo_malformation_syndrome diseases +MONDO:0014335 orphanet_rare diseases +MONDO:0014335 otar diseases +MONDO:0014335 rare diseases +MONDO:0014336 gard_rare diseases +MONDO:0014336 nord_rare diseases +MONDO:0014336 ordo_disorder diseases +MONDO:0014336 ordo_malformation_syndrome diseases +MONDO:0014336 orphanet_rare diseases +MONDO:0014336 otar diseases +MONDO:0014336 rare diseases +MONDO:0014338 gard_rare diseases +MONDO:0014338 nord_rare diseases +MONDO:0014338 ordo_disorder diseases +MONDO:0014338 orphanet_rare diseases +MONDO:0014338 rare diseases +MONDO:0014339 gard_rare diseases +MONDO:0014339 nord_rare diseases +MONDO:0014339 ordo_disorder diseases +MONDO:0014339 orphanet_rare diseases +MONDO:0014339 otar diseases +MONDO:0014339 rare diseases +MONDO:0014340 gard_rare diseases +MONDO:0014340 rare diseases +MONDO:0014342 gard_rare diseases +MONDO:0014342 nord_rare diseases +MONDO:0014342 ordo_disorder diseases +MONDO:0014342 orphanet_rare diseases +MONDO:0014342 otar diseases +MONDO:0014342 rare diseases +MONDO:0014343 gard_rare diseases +MONDO:0014343 nord_rare diseases +MONDO:0014343 otar diseases +MONDO:0014343 rare diseases +MONDO:0014344 gard_rare diseases +MONDO:0014344 nord_rare diseases +MONDO:0014344 rare diseases +MONDO:0014345 gard_rare diseases +MONDO:0014345 nord_rare diseases +MONDO:0014345 rare diseases +MONDO:0014346 gard_rare diseases +MONDO:0014346 nord_rare diseases +MONDO:0014346 rare diseases +MONDO:0014347 gard_rare diseases +MONDO:0014347 nord_rare diseases +MONDO:0014347 otar diseases +MONDO:0014347 rare diseases +MONDO:0014348 gard_rare diseases +MONDO:0014348 nord_rare diseases +MONDO:0014348 rare diseases +MONDO:0014349 gard_rare diseases +MONDO:0014349 nord_rare diseases +MONDO:0014349 ordo_disorder diseases +MONDO:0014349 ordo_malformation_syndrome diseases +MONDO:0014349 orphanet_rare diseases +MONDO:0014349 otar diseases +MONDO:0014349 rare diseases +MONDO:0014350 gard_rare diseases +MONDO:0014350 nord_rare diseases +MONDO:0014350 rare diseases +MONDO:0014351 gard_rare diseases +MONDO:0014351 nord_rare diseases +MONDO:0014351 ordo_disorder diseases +MONDO:0014351 ordo_malformation_syndrome diseases +MONDO:0014351 orphanet_rare diseases +MONDO:0014351 otar diseases +MONDO:0014351 rare diseases +MONDO:0014352 gard_rare diseases +MONDO:0014352 rare diseases +MONDO:0014353 gard_rare diseases +MONDO:0014353 nord_rare diseases +MONDO:0014353 ordo_disorder diseases +MONDO:0014353 orphanet_rare diseases +MONDO:0014353 otar diseases +MONDO:0014353 rare diseases +MONDO:0014354 gard_rare diseases +MONDO:0014354 nord_rare diseases +MONDO:0014354 rare diseases +MONDO:0014355 gard_rare diseases +MONDO:0014355 rare diseases +MONDO:0014356 gard_rare diseases +MONDO:0014356 rare diseases +MONDO:0014357 gard_rare diseases +MONDO:0014357 rare diseases +MONDO:0014358 clingen diseases +MONDO:0014358 gard_rare diseases +MONDO:0014358 nord_rare diseases +MONDO:0014358 ordo_disorder diseases +MONDO:0014358 ordo_malformation_syndrome diseases +MONDO:0014358 orphanet_rare diseases +MONDO:0014358 rare diseases +MONDO:0014359 gard_rare diseases +MONDO:0014359 nord_rare diseases +MONDO:0014359 rare diseases +MONDO:0014360 gard_rare diseases +MONDO:0014360 nord_rare diseases +MONDO:0014360 rare diseases +MONDO:0014361 gard_rare diseases +MONDO:0014361 nord_rare diseases +MONDO:0014361 ordo_disorder diseases +MONDO:0014361 orphanet_rare diseases +MONDO:0014361 otar diseases +MONDO:0014361 rare diseases +MONDO:0014362 gard_rare diseases +MONDO:0014362 nord_rare diseases +MONDO:0014362 rare diseases +MONDO:0014363 gard_rare diseases +MONDO:0014363 nord_rare diseases +MONDO:0014363 rare diseases +MONDO:0014364 gard_rare diseases +MONDO:0014364 rare diseases +MONDO:0014365 gard_rare diseases +MONDO:0014365 otar diseases +MONDO:0014365 rare diseases +MONDO:0014366 gard_rare diseases +MONDO:0014366 otar diseases +MONDO:0014366 rare diseases +MONDO:0014367 gard_rare diseases +MONDO:0014367 nord_rare diseases +MONDO:0014367 otar diseases +MONDO:0014367 rare diseases +MONDO:0014368 gard_rare diseases +MONDO:0014368 predisposition diseases +MONDO:0014368 rare diseases +MONDO:0014369 gard_rare diseases +MONDO:0014369 nord_rare diseases +MONDO:0014369 ordo_disorder diseases +MONDO:0014369 ordo_malformation_syndrome diseases +MONDO:0014369 orphanet_rare diseases +MONDO:0014369 otar diseases +MONDO:0014369 rare diseases +MONDO:0014370 gard_rare diseases +MONDO:0014370 nord_rare diseases +MONDO:0014370 rare diseases +MONDO:0014371 gard_rare diseases +MONDO:0014371 nord_rare diseases +MONDO:0014371 ordo_disorder diseases +MONDO:0014371 ordo_malformation_syndrome diseases +MONDO:0014371 orphanet_rare diseases +MONDO:0014371 rare diseases +MONDO:0014372 gard_rare diseases +MONDO:0014372 nord_rare diseases +MONDO:0014372 rare diseases +MONDO:0014373 gard_rare diseases +MONDO:0014373 rare diseases +MONDO:0014374 gard_rare diseases +MONDO:0014374 nord_rare diseases +MONDO:0014374 rare diseases +MONDO:0014375 gard_rare diseases +MONDO:0014375 nord_rare diseases +MONDO:0014375 ordo_disorder diseases +MONDO:0014375 orphanet_rare diseases +MONDO:0014375 otar diseases +MONDO:0014375 rare diseases +MONDO:0014376 gard_rare diseases +MONDO:0014376 nord_rare diseases +MONDO:0014376 rare diseases +MONDO:0014377 gard_rare diseases +MONDO:0014377 nord_rare diseases +MONDO:0014377 rare diseases +MONDO:0014378 clingen diseases +MONDO:0014378 gard_rare diseases +MONDO:0014378 nord_rare diseases +MONDO:0014378 rare diseases +MONDO:0014379 clingen diseases +MONDO:0014379 gard_rare diseases +MONDO:0014379 nord_rare diseases +MONDO:0014379 ordo_disorder diseases +MONDO:0014379 ordo_malformation_syndrome diseases +MONDO:0014379 orphanet_rare diseases +MONDO:0014379 otar diseases +MONDO:0014379 rare diseases +MONDO:0014380 gard_rare diseases +MONDO:0014380 nord_rare diseases +MONDO:0014380 ordo_disorder diseases +MONDO:0014380 ordo_malformation_syndrome diseases +MONDO:0014380 orphanet_rare diseases +MONDO:0014380 rare diseases +MONDO:0014381 gard_rare diseases +MONDO:0014381 nord_rare diseases +MONDO:0014381 ordo_subtype_of_a_disorder diseases +MONDO:0014381 rare diseases +MONDO:0014382 clingen diseases +MONDO:0014382 gard_rare diseases +MONDO:0014382 nord_rare diseases +MONDO:0014382 ordo_disorder diseases +MONDO:0014382 ordo_malformation_syndrome diseases +MONDO:0014382 orphanet_rare diseases +MONDO:0014382 otar diseases +MONDO:0014382 rare diseases +MONDO:0014383 gard_rare diseases +MONDO:0014383 rare diseases +MONDO:0014384 gard_rare diseases +MONDO:0014384 nord_rare diseases +MONDO:0014384 rare diseases +MONDO:0014385 gard_rare diseases +MONDO:0014385 rare diseases +MONDO:0014386 clingen diseases +MONDO:0014386 gard_rare diseases +MONDO:0014386 nord_rare diseases +MONDO:0014386 ordo_disorder diseases +MONDO:0014386 orphanet_rare diseases +MONDO:0014386 otar diseases +MONDO:0014386 rare diseases +MONDO:0014387 gard_rare diseases +MONDO:0014387 nord_rare diseases +MONDO:0014387 rare diseases +MONDO:0014388 gard_rare diseases +MONDO:0014388 nord_rare diseases +MONDO:0014388 ordo_disorder diseases +MONDO:0014388 ordo_malformation_syndrome diseases +MONDO:0014388 orphanet_rare diseases +MONDO:0014388 otar diseases +MONDO:0014388 rare diseases +MONDO:0014389 gard_rare diseases +MONDO:0014389 nord_rare diseases +MONDO:0014389 ordo_disorder diseases +MONDO:0014389 orphanet_rare diseases +MONDO:0014389 otar diseases +MONDO:0014389 rare diseases +MONDO:0014390 gard_rare diseases +MONDO:0014390 nord_rare diseases +MONDO:0014390 rare diseases +MONDO:0014391 gard_rare diseases +MONDO:0014391 nord_rare diseases +MONDO:0014391 ordo_disorder diseases +MONDO:0014391 orphanet_rare diseases +MONDO:0014391 otar diseases +MONDO:0014391 rare diseases +MONDO:0014392 gard_rare diseases +MONDO:0014392 nord_rare diseases +MONDO:0014392 rare diseases +MONDO:0014393 gard_rare diseases +MONDO:0014393 nord_rare diseases +MONDO:0014393 rare diseases +MONDO:0014394 gard_rare diseases +MONDO:0014394 nord_rare diseases +MONDO:0014394 rare diseases +MONDO:0014395 clingen diseases +MONDO:0014395 gard_rare diseases +MONDO:0014395 nord_rare diseases +MONDO:0014395 rare diseases +MONDO:0014396 gard_rare diseases +MONDO:0014396 nord_rare diseases +MONDO:0014396 rare diseases +MONDO:0014397 gard_rare diseases +MONDO:0014397 nord_rare diseases +MONDO:0014397 ordo_disorder diseases +MONDO:0014397 orphanet_rare diseases +MONDO:0014397 otar diseases +MONDO:0014397 rare diseases +MONDO:0014398 gard_rare diseases +MONDO:0014398 nord_rare diseases +MONDO:0014398 ordo_disorder diseases +MONDO:0014398 orphanet_rare diseases +MONDO:0014398 rare diseases +MONDO:0014399 gard_rare diseases +MONDO:0014399 nord_rare diseases +MONDO:0014399 ordo_disorder diseases +MONDO:0014399 orphanet_rare diseases +MONDO:0014399 rare diseases +MONDO:0014400 gard_rare diseases +MONDO:0014400 nord_rare diseases +MONDO:0014400 rare diseases +MONDO:0014401 gard_rare diseases +MONDO:0014401 nord_rare diseases +MONDO:0014401 ordo_disorder diseases +MONDO:0014401 orphanet_rare diseases +MONDO:0014401 otar diseases +MONDO:0014401 rare diseases +MONDO:0014402 gard_rare diseases +MONDO:0014402 nord_rare diseases +MONDO:0014402 ordo_disorder diseases +MONDO:0014402 orphanet_rare diseases +MONDO:0014402 otar diseases +MONDO:0014402 rare diseases +MONDO:0014403 gard_rare diseases +MONDO:0014403 nord_rare diseases +MONDO:0014403 ordo_disorder diseases +MONDO:0014403 orphanet_rare diseases +MONDO:0014403 otar diseases +MONDO:0014403 rare diseases +MONDO:0014404 otar diseases +MONDO:0014405 gard_rare diseases +MONDO:0014405 nord_rare diseases +MONDO:0014405 ordo_disorder diseases +MONDO:0014405 orphanet_rare diseases +MONDO:0014405 otar diseases +MONDO:0014405 rare diseases +MONDO:0014406 gard_rare diseases +MONDO:0014406 nord_rare diseases +MONDO:0014406 rare diseases +MONDO:0014407 gard_rare diseases +MONDO:0014407 nord_rare diseases +MONDO:0014407 otar diseases +MONDO:0014407 rare diseases +MONDO:0014408 gard_rare diseases +MONDO:0014408 nord_rare diseases +MONDO:0014408 otar diseases +MONDO:0014408 rare diseases +MONDO:0014409 gard_rare diseases +MONDO:0014409 nord_rare diseases +MONDO:0014409 rare diseases +MONDO:0014410 gard_rare diseases +MONDO:0014410 nord_rare diseases +MONDO:0014410 ordo_disorder diseases +MONDO:0014410 orphanet_rare diseases +MONDO:0014410 otar diseases +MONDO:0014410 rare diseases +MONDO:0014412 gard_rare diseases +MONDO:0014412 nord_rare diseases +MONDO:0014412 ordo_etiological_subtype diseases +MONDO:0014412 ordo_subtype_of_a_disorder diseases +MONDO:0014412 rare diseases +MONDO:0014413 clingen diseases +MONDO:0014413 gard_rare diseases +MONDO:0014413 nord_rare diseases +MONDO:0014413 ordo_disorder diseases +MONDO:0014413 ordo_malformation_syndrome diseases +MONDO:0014413 orphanet_rare diseases +MONDO:0014413 otar diseases +MONDO:0014413 rare diseases +MONDO:0014414 clingen diseases +MONDO:0014414 gard_rare diseases +MONDO:0014414 nord_rare diseases +MONDO:0014414 ordo_disorder diseases +MONDO:0014414 orphanet_rare diseases +MONDO:0014414 rare diseases +MONDO:0014415 otar diseases +MONDO:0014416 gard_rare diseases +MONDO:0014416 nord_rare diseases +MONDO:0014416 rare diseases +MONDO:0014417 gard_rare diseases +MONDO:0014417 nord_rare diseases +MONDO:0014417 ordo_disorder diseases +MONDO:0014417 orphanet_rare diseases +MONDO:0014417 rare diseases +MONDO:0014418 clingen diseases +MONDO:0014418 gard_rare diseases +MONDO:0014418 otar diseases +MONDO:0014418 rare diseases +MONDO:0014419 gard_rare diseases +MONDO:0014419 nord_rare diseases +MONDO:0014419 ordo_disorder diseases +MONDO:0014419 orphanet_rare diseases +MONDO:0014419 otar diseases +MONDO:0014419 rare diseases +MONDO:0014420 gard_rare diseases +MONDO:0014420 nord_rare diseases +MONDO:0014420 ordo_disorder diseases +MONDO:0014420 orphanet_rare diseases +MONDO:0014420 otar diseases +MONDO:0014420 rare diseases +MONDO:0014421 gard_rare diseases +MONDO:0014421 nord_rare diseases +MONDO:0014421 ordo_disorder diseases +MONDO:0014421 orphanet_rare diseases +MONDO:0014421 otar diseases +MONDO:0014421 rare diseases +MONDO:0014422 gard_rare diseases +MONDO:0014422 nord_rare diseases +MONDO:0014422 rare diseases +MONDO:0014423 clingen diseases +MONDO:0014423 gard_rare diseases +MONDO:0014423 nord_rare diseases +MONDO:0014423 ordo_disorder diseases +MONDO:0014423 orphanet_rare diseases +MONDO:0014423 otar diseases +MONDO:0014423 rare diseases +MONDO:0014426 gard_rare diseases +MONDO:0014426 nord_rare diseases +MONDO:0014426 rare diseases +MONDO:0014427 gard_rare diseases +MONDO:0014427 nord_rare diseases +MONDO:0014427 rare diseases +MONDO:0014428 clingen diseases +MONDO:0014428 gard_rare diseases +MONDO:0014428 nord_rare diseases +MONDO:0014428 otar diseases +MONDO:0014428 rare diseases +MONDO:0014430 gard_rare diseases +MONDO:0014430 nord_rare diseases +MONDO:0014430 rare diseases +MONDO:0014431 gard_rare diseases +MONDO:0014431 nord_rare diseases +MONDO:0014431 ordo_disorder diseases +MONDO:0014431 orphanet_rare diseases +MONDO:0014431 otar diseases +MONDO:0014431 rare diseases +MONDO:0014432 gard_rare diseases +MONDO:0014432 nord_rare diseases +MONDO:0014432 rare diseases +MONDO:0014433 gard_rare diseases +MONDO:0014433 nord_rare diseases +MONDO:0014433 rare diseases +MONDO:0014434 gard_rare diseases +MONDO:0014434 nord_rare diseases +MONDO:0014434 rare diseases +MONDO:0014435 gard_rare diseases +MONDO:0014435 nord_rare diseases +MONDO:0014435 rare diseases +MONDO:0014436 gard_rare diseases +MONDO:0014436 nord_rare diseases +MONDO:0014436 rare diseases +MONDO:0014437 gard_rare diseases +MONDO:0014437 nord_rare diseases +MONDO:0014437 rare diseases +MONDO:0014438 gard_rare diseases +MONDO:0014438 nord_rare diseases +MONDO:0014438 rare diseases +MONDO:0014439 gard_rare diseases +MONDO:0014439 nord_rare diseases +MONDO:0014439 rare diseases +MONDO:0014440 gard_rare diseases +MONDO:0014440 nord_rare diseases +MONDO:0014440 rare diseases +MONDO:0014441 gard_rare diseases +MONDO:0014441 nord_rare diseases +MONDO:0014441 rare diseases +MONDO:0014442 gard_rare diseases +MONDO:0014442 nord_rare diseases +MONDO:0014442 rare diseases +MONDO:0014443 gard_rare diseases +MONDO:0014443 nord_rare diseases +MONDO:0014443 rare diseases +MONDO:0014444 gard_rare diseases +MONDO:0014444 nord_rare diseases +MONDO:0014444 otar diseases +MONDO:0014444 rare diseases +MONDO:0014445 gard_rare diseases +MONDO:0014445 nord_rare diseases +MONDO:0014445 rare diseases +MONDO:0014446 gard_rare diseases +MONDO:0014446 nord_rare diseases +MONDO:0014446 rare diseases +MONDO:0014447 gard_rare diseases +MONDO:0014447 nord_rare diseases +MONDO:0014447 rare diseases +MONDO:0014449 gard_rare diseases +MONDO:0014449 nord_rare diseases +MONDO:0014449 ordo_disorder diseases +MONDO:0014449 orphanet_rare diseases +MONDO:0014449 otar diseases +MONDO:0014449 rare diseases +MONDO:0014450 gard_rare diseases +MONDO:0014450 nord_rare diseases +MONDO:0014450 otar diseases +MONDO:0014450 rare diseases +MONDO:0014451 clingen diseases +MONDO:0014451 gard_rare diseases +MONDO:0014451 nord_rare diseases +MONDO:0014451 rare diseases +MONDO:0014452 gard_rare diseases +MONDO:0014452 nord_rare diseases +MONDO:0014452 ordo_subtype_of_a_disorder diseases +MONDO:0014452 otar diseases +MONDO:0014452 rare diseases +MONDO:0014453 clingen diseases +MONDO:0014453 gard_rare diseases +MONDO:0014453 nord_rare diseases +MONDO:0014453 otar diseases +MONDO:0014453 rare diseases +MONDO:0014454 gard_rare diseases +MONDO:0014454 nord_rare diseases +MONDO:0014454 otar diseases +MONDO:0014454 rare diseases +MONDO:0014455 gard_rare diseases +MONDO:0014455 nord_rare diseases +MONDO:0014455 ordo_disorder diseases +MONDO:0014455 orphanet_rare diseases +MONDO:0014455 otar diseases +MONDO:0014455 rare diseases +MONDO:0014456 gard_rare diseases +MONDO:0014456 nord_rare diseases +MONDO:0014456 ordo_disorder diseases +MONDO:0014456 orphanet_rare diseases +MONDO:0014456 otar diseases +MONDO:0014456 rare diseases +MONDO:0014457 gard_rare diseases +MONDO:0014457 nord_rare diseases +MONDO:0014457 rare diseases +MONDO:0014458 gard_rare diseases +MONDO:0014458 nord_rare diseases +MONDO:0014458 rare diseases +MONDO:0014459 gard_rare diseases +MONDO:0014459 nord_rare diseases +MONDO:0014459 rare diseases +MONDO:0014460 gard_rare diseases +MONDO:0014460 nord_rare diseases +MONDO:0014460 ordo_disorder diseases +MONDO:0014460 orphanet_rare diseases +MONDO:0014460 rare diseases +MONDO:0014461 gard_rare diseases +MONDO:0014461 nord_rare diseases +MONDO:0014461 rare diseases +MONDO:0014462 gard_rare diseases +MONDO:0014462 nord_rare diseases +MONDO:0014462 rare diseases +MONDO:0014464 clingen diseases +MONDO:0014464 gard_rare diseases +MONDO:0014464 nord_rare diseases +MONDO:0014464 ordo_disorder diseases +MONDO:0014464 orphanet_rare diseases +MONDO:0014464 otar diseases +MONDO:0014464 rare diseases +MONDO:0014465 clingen diseases +MONDO:0014465 gard_rare diseases +MONDO:0014465 nord_rare diseases +MONDO:0014465 rare diseases +MONDO:0014466 gard_rare diseases +MONDO:0014466 nord_rare diseases +MONDO:0014466 ordo_subtype_of_a_disorder diseases +MONDO:0014466 rare diseases +MONDO:0014467 gard_rare diseases +MONDO:0014467 nord_rare diseases +MONDO:0014467 ordo_disorder diseases +MONDO:0014467 orphanet_rare diseases +MONDO:0014467 rare diseases +MONDO:0014468 clingen diseases +MONDO:0014468 gard_rare diseases +MONDO:0014468 nord_rare diseases +MONDO:0014468 rare diseases +MONDO:0014469 gard_rare diseases +MONDO:0014469 nord_rare diseases +MONDO:0014469 rare diseases +MONDO:0014470 gard_rare diseases +MONDO:0014470 nord_rare diseases +MONDO:0014470 otar diseases +MONDO:0014470 rare diseases +MONDO:0014471 gard_rare diseases +MONDO:0014471 nord_rare diseases +MONDO:0014471 ordo_disorder diseases +MONDO:0014471 orphanet_rare diseases +MONDO:0014471 otar diseases +MONDO:0014471 rare diseases +MONDO:0014472 gard_rare diseases +MONDO:0014472 nord_rare diseases +MONDO:0014472 ordo_disorder diseases +MONDO:0014472 orphanet_rare diseases +MONDO:0014472 otar diseases +MONDO:0014472 rare diseases +MONDO:0014473 gard_rare diseases +MONDO:0014473 nord_rare diseases +MONDO:0014473 rare diseases +MONDO:0014474 gard_rare diseases +MONDO:0014474 nord_rare diseases +MONDO:0014474 ordo_disorder diseases +MONDO:0014474 orphanet_rare diseases +MONDO:0014474 otar diseases +MONDO:0014474 rare diseases +MONDO:0014475 gard_rare diseases +MONDO:0014475 nord_rare diseases +MONDO:0014475 ordo_disorder diseases +MONDO:0014475 orphanet_rare diseases +MONDO:0014475 rare diseases +MONDO:0014476 gard_rare diseases +MONDO:0014476 nord_rare diseases +MONDO:0014476 ordo_disorder diseases +MONDO:0014476 orphanet_rare diseases +MONDO:0014476 otar diseases +MONDO:0014476 rare diseases +MONDO:0014477 gard_rare diseases +MONDO:0014477 nord_rare diseases +MONDO:0014477 rare diseases +MONDO:0014478 gard_rare diseases +MONDO:0014478 nord_rare diseases +MONDO:0014478 otar diseases +MONDO:0014478 rare diseases +MONDO:0014479 gard_rare diseases +MONDO:0014479 nord_rare diseases +MONDO:0014479 rare diseases +MONDO:0014480 gard_rare diseases +MONDO:0014480 nord_rare diseases +MONDO:0014480 rare diseases +MONDO:0014481 gard_rare diseases +MONDO:0014481 nord_rare diseases +MONDO:0014481 otar diseases +MONDO:0014481 rare diseases +MONDO:0014482 gard_rare diseases +MONDO:0014482 nord_rare diseases +MONDO:0014482 otar diseases +MONDO:0014482 rare diseases +MONDO:0014483 gard_rare diseases +MONDO:0014483 nord_rare diseases +MONDO:0014483 ordo_disorder diseases +MONDO:0014483 orphanet_rare diseases +MONDO:0014483 otar diseases +MONDO:0014483 rare diseases +MONDO:0014484 gard_rare diseases +MONDO:0014484 nord_rare diseases +MONDO:0014484 rare diseases +MONDO:0014485 gard_rare diseases +MONDO:0014485 nord_rare diseases +MONDO:0014485 rare diseases +MONDO:0014486 gard_rare diseases +MONDO:0014486 nord_rare diseases +MONDO:0014486 rare diseases +MONDO:0014487 clingen diseases +MONDO:0014487 gard_rare diseases +MONDO:0014487 nord_rare diseases +MONDO:0014487 ordo_disorder diseases +MONDO:0014487 orphanet_rare diseases +MONDO:0014487 otar diseases +MONDO:0014487 rare diseases +MONDO:0014488 gard_rare diseases +MONDO:0014488 rare diseases +MONDO:0014489 gard_rare diseases +MONDO:0014489 nord_rare diseases +MONDO:0014489 ordo_disorder diseases +MONDO:0014489 orphanet_rare diseases +MONDO:0014489 otar diseases +MONDO:0014489 rare diseases +MONDO:0014490 gard_rare diseases +MONDO:0014490 nord_rare diseases +MONDO:0014490 ordo_disorder diseases +MONDO:0014490 orphanet_rare diseases +MONDO:0014490 rare diseases +MONDO:0014491 clingen diseases +MONDO:0014491 gard_rare diseases +MONDO:0014491 rare diseases +MONDO:0014492 gard_rare diseases +MONDO:0014492 nord_rare diseases +MONDO:0014492 ordo_disorder diseases +MONDO:0014492 orphanet_rare diseases +MONDO:0014492 rare diseases +MONDO:0014493 clingen diseases +MONDO:0014493 gard_rare diseases +MONDO:0014493 nord_rare diseases +MONDO:0014493 ordo_disorder diseases +MONDO:0014493 orphanet_rare diseases +MONDO:0014493 otar diseases +MONDO:0014493 rare diseases +MONDO:0014495 gard_rare diseases +MONDO:0014495 nord_rare diseases +MONDO:0014495 ordo_disorder diseases +MONDO:0014495 orphanet_rare diseases +MONDO:0014495 rare diseases +MONDO:0014496 gard_rare diseases +MONDO:0014496 rare diseases +MONDO:0014497 gard_rare diseases +MONDO:0014497 nord_rare diseases +MONDO:0014497 ordo_disorder diseases +MONDO:0014497 orphanet_rare diseases +MONDO:0014497 otar diseases +MONDO:0014497 rare diseases +MONDO:0014498 gard_rare diseases +MONDO:0014498 nord_rare diseases +MONDO:0014498 ordo_disorder diseases +MONDO:0014498 orphanet_rare diseases +MONDO:0014498 otar diseases +MONDO:0014498 rare diseases +MONDO:0014499 gard_rare diseases +MONDO:0014499 nord_rare diseases +MONDO:0014499 rare diseases +MONDO:0014500 gard_rare diseases +MONDO:0014500 nord_rare diseases +MONDO:0014500 ordo_disorder diseases +MONDO:0014500 orphanet_rare diseases +MONDO:0014500 otar diseases +MONDO:0014500 rare diseases +MONDO:0014501 gard_rare diseases +MONDO:0014501 nord_rare diseases +MONDO:0014501 rare diseases +MONDO:0014503 gard_rare diseases +MONDO:0014503 nord_rare diseases +MONDO:0014503 ordo_disorder diseases +MONDO:0014503 orphanet_rare diseases +MONDO:0014503 rare diseases +MONDO:0014504 gard_rare diseases +MONDO:0014504 nord_rare diseases +MONDO:0014504 rare diseases +MONDO:0014505 gard_rare diseases +MONDO:0014505 nord_rare diseases +MONDO:0014505 rare diseases +MONDO:0014506 gard_rare diseases +MONDO:0014506 nord_rare diseases +MONDO:0014506 ordo_disorder diseases +MONDO:0014506 orphanet_rare diseases +MONDO:0014506 otar diseases +MONDO:0014506 rare diseases +MONDO:0014507 gard_rare diseases +MONDO:0014507 nord_rare diseases +MONDO:0014507 ordo_disorder diseases +MONDO:0014507 ordo_malformation_syndrome diseases +MONDO:0014507 orphanet_rare diseases +MONDO:0014507 otar diseases +MONDO:0014507 rare diseases +MONDO:0014508 gard_rare diseases +MONDO:0014508 nord_rare diseases +MONDO:0014508 rare diseases +MONDO:0014509 gard_rare diseases +MONDO:0014509 nord_rare diseases +MONDO:0014509 rare diseases +MONDO:0014510 clingen diseases +MONDO:0014510 gard_rare diseases +MONDO:0014510 nord_rare diseases +MONDO:0014510 ordo_disorder diseases +MONDO:0014510 orphanet_rare diseases +MONDO:0014510 otar diseases +MONDO:0014510 rare diseases +MONDO:0014511 gard_rare diseases +MONDO:0014511 nord_rare diseases +MONDO:0014511 ordo_disorder diseases +MONDO:0014511 orphanet_rare diseases +MONDO:0014511 otar diseases +MONDO:0014511 rare diseases +MONDO:0014512 gard_rare diseases +MONDO:0014512 nord_rare diseases +MONDO:0014512 ordo_subtype_of_a_disorder diseases +MONDO:0014512 otar diseases +MONDO:0014512 rare diseases +MONDO:0014513 clingen diseases +MONDO:0014513 gard_rare diseases +MONDO:0014513 rare diseases +MONDO:0014514 gard_rare diseases +MONDO:0014514 nord_rare diseases +MONDO:0014514 rare diseases +MONDO:0014515 gard_rare diseases +MONDO:0014515 nord_rare diseases +MONDO:0014515 otar diseases +MONDO:0014515 rare diseases +MONDO:0014516 gard_rare diseases +MONDO:0014516 nord_rare diseases +MONDO:0014516 rare diseases +MONDO:0014517 gard_rare diseases +MONDO:0014517 rare diseases +MONDO:0014518 gard_rare diseases +MONDO:0014518 nord_rare diseases +MONDO:0014518 ordo_disorder diseases +MONDO:0014518 orphanet_rare diseases +MONDO:0014518 otar diseases +MONDO:0014518 rare diseases +MONDO:0014520 gard_rare diseases +MONDO:0014520 nord_rare diseases +MONDO:0014520 ordo_disorder diseases +MONDO:0014520 orphanet_rare diseases +MONDO:0014520 rare diseases +MONDO:0014521 gard_rare diseases +MONDO:0014521 nord_rare diseases +MONDO:0014521 ordo_disorder diseases +MONDO:0014521 orphanet_rare diseases +MONDO:0014521 rare diseases +MONDO:0014522 gard_rare diseases +MONDO:0014522 nord_rare diseases +MONDO:0014522 rare diseases +MONDO:0014523 gard_rare diseases +MONDO:0014523 nord_rare diseases +MONDO:0014523 ordo_disorder diseases +MONDO:0014523 orphanet_rare diseases +MONDO:0014523 rare diseases +MONDO:0014524 gard_rare diseases +MONDO:0014524 nord_rare diseases +MONDO:0014524 rare diseases +MONDO:0014525 gard_rare diseases +MONDO:0014525 nord_rare diseases +MONDO:0014525 ordo_disorder diseases +MONDO:0014525 orphanet_rare diseases +MONDO:0014525 rare diseases +MONDO:0014526 clingen diseases +MONDO:0014526 gard_rare diseases +MONDO:0014526 nord_rare diseases +MONDO:0014526 ordo_disorder diseases +MONDO:0014526 orphanet_rare diseases +MONDO:0014526 otar diseases +MONDO:0014526 rare diseases +MONDO:0014527 gard_rare diseases +MONDO:0014527 nord_rare diseases +MONDO:0014527 ordo_disorder diseases +MONDO:0014527 orphanet_rare diseases +MONDO:0014527 otar diseases +MONDO:0014527 rare diseases +MONDO:0014528 gard_rare diseases +MONDO:0014528 nord_rare diseases +MONDO:0014528 ordo_disorder diseases +MONDO:0014528 orphanet_rare diseases +MONDO:0014528 otar diseases +MONDO:0014528 rare diseases +MONDO:0014529 gard_rare diseases +MONDO:0014529 nord_rare diseases +MONDO:0014529 ordo_disorder diseases +MONDO:0014529 ordo_malformation_syndrome diseases +MONDO:0014529 orphanet_rare diseases +MONDO:0014529 rare diseases +MONDO:0014530 gard_rare diseases +MONDO:0014530 nord_rare diseases +MONDO:0014530 ordo_subtype_of_a_disorder diseases +MONDO:0014530 otar diseases +MONDO:0014530 rare diseases +MONDO:0014531 clingen diseases +MONDO:0014531 gard_rare diseases +MONDO:0014531 nord_rare diseases +MONDO:0014531 rare diseases +MONDO:0014532 gard_rare diseases +MONDO:0014532 nord_rare diseases +MONDO:0014532 ordo_disorder diseases +MONDO:0014532 orphanet_rare diseases +MONDO:0014532 otar diseases +MONDO:0014532 rare diseases +MONDO:0014533 gard_rare diseases +MONDO:0014533 nord_rare diseases +MONDO:0014533 rare diseases +MONDO:0014534 gard_rare diseases +MONDO:0014534 nord_rare diseases +MONDO:0014534 rare diseases +MONDO:0014535 otar diseases +MONDO:0014536 clingen diseases +MONDO:0014536 gard_rare diseases +MONDO:0014536 nord_rare diseases +MONDO:0014536 otar diseases +MONDO:0014536 rare diseases +MONDO:0014537 gard_rare diseases +MONDO:0014537 nord_rare diseases +MONDO:0014537 rare diseases +MONDO:0014538 gard_rare diseases +MONDO:0014538 nord_rare diseases +MONDO:0014538 rare diseases +MONDO:0014539 clingen diseases +MONDO:0014539 gard_rare diseases +MONDO:0014539 nord_rare diseases +MONDO:0014539 rare diseases +MONDO:0014540 gard_rare diseases +MONDO:0014540 rare diseases +MONDO:0014541 gard_rare diseases +MONDO:0014541 nord_rare diseases +MONDO:0014541 ordo_disorder diseases +MONDO:0014541 ordo_malformation_syndrome diseases +MONDO:0014541 orphanet_rare diseases +MONDO:0014541 otar diseases +MONDO:0014541 rare diseases +MONDO:0014542 gard_rare diseases +MONDO:0014542 nord_rare diseases +MONDO:0014542 rare diseases +MONDO:0014543 gard_rare diseases +MONDO:0014543 nord_rare diseases +MONDO:0014543 rare diseases +MONDO:0014544 gard_rare diseases +MONDO:0014544 nord_rare diseases +MONDO:0014544 rare diseases +MONDO:0014545 gard_rare diseases +MONDO:0014545 nord_rare diseases +MONDO:0014545 ordo_disorder diseases +MONDO:0014545 orphanet_rare diseases +MONDO:0014545 rare diseases +MONDO:0014546 gard_rare diseases +MONDO:0014546 nord_rare diseases +MONDO:0014546 ordo_disorder diseases +MONDO:0014546 orphanet_rare diseases +MONDO:0014546 otar diseases +MONDO:0014546 rare diseases +MONDO:0014547 gard_rare diseases +MONDO:0014547 nord_rare diseases +MONDO:0014547 ordo_disorder diseases +MONDO:0014547 orphanet_rare diseases +MONDO:0014547 rare diseases +MONDO:0014548 gard_rare diseases +MONDO:0014548 otar diseases +MONDO:0014548 rare diseases +MONDO:0014549 gard_rare diseases +MONDO:0014549 nord_rare diseases +MONDO:0014549 rare diseases +MONDO:0014550 gard_rare diseases +MONDO:0014550 otar diseases +MONDO:0014550 rare diseases +MONDO:0014552 gard_rare diseases +MONDO:0014552 nord_rare diseases +MONDO:0014552 ordo_disorder diseases +MONDO:0014552 ordo_malformation_syndrome diseases +MONDO:0014552 orphanet_rare diseases +MONDO:0014552 rare diseases +MONDO:0014553 otar diseases +MONDO:0014555 gard_rare diseases +MONDO:0014555 nord_rare diseases +MONDO:0014555 ordo_subtype_of_a_disorder diseases +MONDO:0014555 otar diseases +MONDO:0014555 rare diseases +MONDO:0014556 gard_rare diseases +MONDO:0014556 nord_rare diseases +MONDO:0014556 ordo_disorder diseases +MONDO:0014556 orphanet_rare diseases +MONDO:0014556 otar diseases +MONDO:0014556 rare diseases +MONDO:0014557 gard_rare diseases +MONDO:0014557 nord_rare diseases +MONDO:0014557 ordo_disorder diseases +MONDO:0014557 orphanet_rare diseases +MONDO:0014557 rare diseases +MONDO:0014558 gard_rare diseases +MONDO:0014558 nord_rare diseases +MONDO:0014558 ordo_disorder diseases +MONDO:0014558 ordo_malformation_syndrome diseases +MONDO:0014558 orphanet_rare diseases +MONDO:0014558 otar diseases +MONDO:0014558 rare diseases +MONDO:0014559 gard_rare diseases +MONDO:0014559 nord_rare diseases +MONDO:0014559 ordo_disorder diseases +MONDO:0014559 orphanet_rare diseases +MONDO:0014559 rare diseases +MONDO:0014560 gard_rare diseases +MONDO:0014560 rare diseases +MONDO:0014561 gard_rare diseases +MONDO:0014561 nord_rare diseases +MONDO:0014561 ordo_disorder diseases +MONDO:0014561 orphanet_rare diseases +MONDO:0014561 otar diseases +MONDO:0014561 rare diseases +MONDO:0014562 gard_rare diseases +MONDO:0014562 nord_rare diseases +MONDO:0014562 ordo_disorder diseases +MONDO:0014562 orphanet_rare diseases +MONDO:0014562 otar diseases +MONDO:0014562 rare diseases +MONDO:0014563 clingen diseases +MONDO:0014563 gard_rare diseases +MONDO:0014563 nord_rare diseases +MONDO:0014563 ordo_disorder diseases +MONDO:0014563 orphanet_rare diseases +MONDO:0014563 otar diseases +MONDO:0014563 rare diseases +MONDO:0014564 clingen diseases +MONDO:0014564 gard_rare diseases +MONDO:0014564 otar diseases +MONDO:0014564 rare diseases +MONDO:0014565 gard_rare diseases +MONDO:0014565 nord_rare diseases +MONDO:0014565 rare diseases +MONDO:0014566 gard_rare diseases +MONDO:0014566 nord_rare diseases +MONDO:0014566 ordo_disorder diseases +MONDO:0014566 orphanet_rare diseases +MONDO:0014566 otar diseases +MONDO:0014566 rare diseases +MONDO:0014567 clingen diseases +MONDO:0014567 gard_rare diseases +MONDO:0014567 nord_rare diseases +MONDO:0014567 ordo_disorder diseases +MONDO:0014567 orphanet_rare diseases +MONDO:0014567 otar diseases +MONDO:0014567 rare diseases +MONDO:0014568 gard_rare diseases +MONDO:0014568 nord_rare diseases +MONDO:0014568 ordo_disorder diseases +MONDO:0014568 orphanet_rare diseases +MONDO:0014568 otar diseases +MONDO:0014568 rare diseases +MONDO:0014569 gard_rare diseases +MONDO:0014569 nord_rare diseases +MONDO:0014569 rare diseases +MONDO:0014570 gard_rare diseases +MONDO:0014570 nord_rare diseases +MONDO:0014570 rare diseases +MONDO:0014571 gard_rare diseases +MONDO:0014571 nord_rare diseases +MONDO:0014571 rare diseases +MONDO:0014572 gard_rare diseases +MONDO:0014572 nord_rare diseases +MONDO:0014572 ordo_disorder diseases +MONDO:0014572 orphanet_rare diseases +MONDO:0014572 otar diseases +MONDO:0014572 rare diseases +MONDO:0014573 gard_rare diseases +MONDO:0014573 nord_rare diseases +MONDO:0014573 rare diseases +MONDO:0014574 gard_rare diseases +MONDO:0014574 nord_rare diseases +MONDO:0014574 ordo_disorder diseases +MONDO:0014574 orphanet_rare diseases +MONDO:0014574 rare diseases +MONDO:0014575 gard_rare diseases +MONDO:0014575 nord_rare diseases +MONDO:0014575 rare diseases +MONDO:0014576 gard_rare diseases +MONDO:0014576 nord_rare diseases +MONDO:0014576 ordo_disorder diseases +MONDO:0014576 orphanet_rare diseases +MONDO:0014576 otar diseases +MONDO:0014576 rare diseases +MONDO:0014577 gard_rare diseases +MONDO:0014577 nord_rare diseases +MONDO:0014577 rare diseases +MONDO:0014578 gard_rare diseases +MONDO:0014578 nord_rare diseases +MONDO:0014578 rare diseases +MONDO:0014579 gard_rare diseases +MONDO:0014579 nord_rare diseases +MONDO:0014579 rare diseases +MONDO:0014580 gard_rare diseases +MONDO:0014580 nord_rare diseases +MONDO:0014580 rare diseases +MONDO:0014581 gard_rare diseases +MONDO:0014581 nord_rare diseases +MONDO:0014581 rare diseases +MONDO:0014582 gard_rare diseases +MONDO:0014582 nord_rare diseases +MONDO:0014582 rare diseases +MONDO:0014583 gard_rare diseases +MONDO:0014583 nord_rare diseases +MONDO:0014583 rare diseases +MONDO:0014584 gard_rare diseases +MONDO:0014584 nord_rare diseases +MONDO:0014584 rare diseases +MONDO:0014585 gard_rare diseases +MONDO:0014585 nord_rare diseases +MONDO:0014585 rare diseases +MONDO:0014586 gard_rare diseases +MONDO:0014586 nord_rare diseases +MONDO:0014586 rare diseases +MONDO:0014587 gard_rare diseases +MONDO:0014587 nord_rare diseases +MONDO:0014587 rare diseases +MONDO:0014588 gard_rare diseases +MONDO:0014588 nord_rare diseases +MONDO:0014588 rare diseases +MONDO:0014589 gard_rare diseases +MONDO:0014589 nord_rare diseases +MONDO:0014589 rare diseases +MONDO:0014590 gard_rare diseases +MONDO:0014590 nord_rare diseases +MONDO:0014590 rare diseases +MONDO:0014591 gard_rare diseases +MONDO:0014591 nord_rare diseases +MONDO:0014591 rare diseases +MONDO:0014592 gard_rare diseases +MONDO:0014592 nord_rare diseases +MONDO:0014592 rare diseases +MONDO:0014593 gard_rare diseases +MONDO:0014593 nord_rare diseases +MONDO:0014593 otar diseases +MONDO:0014593 rare diseases +MONDO:0014594 gard_rare diseases +MONDO:0014594 nord_rare diseases +MONDO:0014594 rare diseases +MONDO:0014595 gard_rare diseases +MONDO:0014595 nord_rare diseases +MONDO:0014595 rare diseases +MONDO:0014596 gard_rare diseases +MONDO:0014596 nord_rare diseases +MONDO:0014596 rare diseases +MONDO:0014597 gard_rare diseases +MONDO:0014597 rare diseases +MONDO:0014598 gard_rare diseases +MONDO:0014598 nord_rare diseases +MONDO:0014598 rare diseases +MONDO:0014599 gard_rare diseases +MONDO:0014599 nord_rare diseases +MONDO:0014599 rare diseases +MONDO:0014600 gard_rare diseases +MONDO:0014600 nord_rare diseases +MONDO:0014600 rare diseases +MONDO:0014601 gard_rare diseases +MONDO:0014601 nord_rare diseases +MONDO:0014601 ordo_disorder diseases +MONDO:0014601 ordo_malformation_syndrome diseases +MONDO:0014601 orphanet_rare diseases +MONDO:0014601 otar diseases +MONDO:0014601 rare diseases +MONDO:0014602 gard_rare diseases +MONDO:0014602 nord_rare diseases +MONDO:0014602 ordo_disorder diseases +MONDO:0014602 ordo_malformation_syndrome diseases +MONDO:0014602 orphanet_rare diseases +MONDO:0014602 rare diseases +MONDO:0014603 gard_rare diseases +MONDO:0014603 nord_rare diseases +MONDO:0014603 otar diseases +MONDO:0014603 rare diseases +MONDO:0014604 gard_rare diseases +MONDO:0014604 nord_rare diseases +MONDO:0014604 rare diseases +MONDO:0014605 gard_rare diseases +MONDO:0014605 nord_rare diseases +MONDO:0014605 ordo_disorder diseases +MONDO:0014605 ordo_malformation_syndrome diseases +MONDO:0014605 orphanet_rare diseases +MONDO:0014605 rare diseases +MONDO:0014606 clingen diseases +MONDO:0014606 gard_rare diseases +MONDO:0014606 nord_rare diseases +MONDO:0014606 ordo_disorder diseases +MONDO:0014606 orphanet_rare diseases +MONDO:0014606 otar diseases +MONDO:0014606 rare diseases +MONDO:0014607 gard_rare diseases +MONDO:0014607 nord_rare diseases +MONDO:0014607 rare diseases +MONDO:0014608 gard_rare diseases +MONDO:0014608 nord_rare diseases +MONDO:0014608 ordo_disorder diseases +MONDO:0014608 ordo_malformation_syndrome diseases +MONDO:0014608 orphanet_rare diseases +MONDO:0014608 otar diseases +MONDO:0014608 rare diseases +MONDO:0014609 gard_rare diseases +MONDO:0014609 nord_rare diseases +MONDO:0014609 ordo_disorder diseases +MONDO:0014609 ordo_malformation_syndrome diseases +MONDO:0014609 orphanet_rare diseases +MONDO:0014609 rare diseases +MONDO:0014611 gard_rare diseases +MONDO:0014611 nord_rare diseases +MONDO:0014611 ordo_disorder diseases +MONDO:0014611 orphanet_rare diseases +MONDO:0014611 otar diseases +MONDO:0014611 rare diseases +MONDO:0014612 gard_rare diseases +MONDO:0014612 nord_rare diseases +MONDO:0014612 rare diseases +MONDO:0014613 gard_rare diseases +MONDO:0014613 nord_rare diseases +MONDO:0014613 rare diseases +MONDO:0014614 gard_rare diseases +MONDO:0014614 rare diseases +MONDO:0014615 gard_rare diseases +MONDO:0014615 nord_rare diseases +MONDO:0014615 rare diseases +MONDO:0014617 gard_rare diseases +MONDO:0014617 rare diseases +MONDO:0014618 gard_rare diseases +MONDO:0014618 nord_rare diseases +MONDO:0014618 otar diseases +MONDO:0014618 rare diseases +MONDO:0014619 gard_rare diseases +MONDO:0014619 nord_rare diseases +MONDO:0014619 otar diseases +MONDO:0014619 rare diseases +MONDO:0014620 gard_rare diseases +MONDO:0014620 nord_rare diseases +MONDO:0014620 otar diseases +MONDO:0014620 rare diseases +MONDO:0014621 gard_rare diseases +MONDO:0014621 rare diseases +MONDO:0014622 gard_rare diseases +MONDO:0014622 nord_rare diseases +MONDO:0014622 ordo_disorder diseases +MONDO:0014622 orphanet_rare diseases +MONDO:0014622 rare diseases +MONDO:0014623 gard_rare diseases +MONDO:0014623 nord_rare diseases +MONDO:0014623 rare diseases +MONDO:0014625 gard_rare diseases +MONDO:0014625 nord_rare diseases +MONDO:0014625 rare diseases +MONDO:0014626 gard_rare diseases +MONDO:0014626 nord_rare diseases +MONDO:0014626 ordo_disorder diseases +MONDO:0014626 orphanet_rare diseases +MONDO:0014626 rare diseases +MONDO:0014627 clingen diseases +MONDO:0014627 gard_rare diseases +MONDO:0014627 nord_rare diseases +MONDO:0014627 ordo_disorder diseases +MONDO:0014627 orphanet_rare diseases +MONDO:0014627 rare diseases +MONDO:0014628 gard_rare diseases +MONDO:0014628 otar diseases +MONDO:0014628 rare diseases +MONDO:0014629 gard_rare diseases +MONDO:0014629 nord_rare diseases +MONDO:0014629 ordo_disorder diseases +MONDO:0014629 orphanet_rare diseases +MONDO:0014629 otar diseases +MONDO:0014629 rare diseases +MONDO:0014630 gard_rare diseases +MONDO:0014630 nord_rare diseases +MONDO:0014630 ordo_subtype_of_a_disorder diseases +MONDO:0014630 rare diseases +MONDO:0014631 gard_rare diseases +MONDO:0014631 rare diseases +MONDO:0014632 gard_rare diseases +MONDO:0014632 nord_rare diseases +MONDO:0014632 otar diseases +MONDO:0014632 rare diseases +MONDO:0014633 gard_rare diseases +MONDO:0014633 nord_rare diseases +MONDO:0014633 rare diseases +MONDO:0014634 gard_rare diseases +MONDO:0014634 nord_rare diseases +MONDO:0014634 rare diseases +MONDO:0014635 gard_rare diseases +MONDO:0014635 nord_rare diseases +MONDO:0014635 rare diseases +MONDO:0014636 gard_rare diseases +MONDO:0014636 nord_rare diseases +MONDO:0014636 ordo_disorder diseases +MONDO:0014636 orphanet_rare diseases +MONDO:0014636 rare diseases +MONDO:0014637 clingen diseases +MONDO:0014637 gard_rare diseases +MONDO:0014637 nord_rare diseases +MONDO:0014637 ordo_disorder diseases +MONDO:0014637 orphanet_rare diseases +MONDO:0014637 otar diseases +MONDO:0014637 rare diseases +MONDO:0014638 gard_rare diseases +MONDO:0014638 nord_rare diseases +MONDO:0014638 rare diseases +MONDO:0014639 gard_rare diseases +MONDO:0014639 nord_rare diseases +MONDO:0014639 otar diseases +MONDO:0014639 rare diseases +MONDO:0014640 clingen diseases +MONDO:0014640 gard_rare diseases +MONDO:0014640 nord_rare diseases +MONDO:0014640 rare diseases +MONDO:0014641 clingen diseases +MONDO:0014641 gard_rare diseases +MONDO:0014641 nord_rare diseases +MONDO:0014641 otar diseases +MONDO:0014641 rare diseases +MONDO:0014642 gard_rare diseases +MONDO:0014642 nord_rare diseases +MONDO:0014642 rare diseases +MONDO:0014643 gard_rare diseases +MONDO:0014643 nord_rare diseases +MONDO:0014643 ordo_disorder diseases +MONDO:0014643 ordo_malformation_syndrome diseases +MONDO:0014643 orphanet_rare diseases +MONDO:0014643 otar diseases +MONDO:0014643 rare diseases +MONDO:0014644 gard_rare diseases +MONDO:0014644 nord_rare diseases +MONDO:0014644 ordo_disorder diseases +MONDO:0014644 orphanet_rare diseases +MONDO:0014644 otar diseases +MONDO:0014644 rare diseases +MONDO:0014645 clingen diseases +MONDO:0014645 gard_rare diseases +MONDO:0014645 nord_rare diseases +MONDO:0014645 ordo_disorder diseases +MONDO:0014645 orphanet_rare diseases +MONDO:0014645 otar diseases +MONDO:0014645 rare diseases +MONDO:0014646 gard_rare diseases +MONDO:0014646 nord_rare diseases +MONDO:0014646 rare diseases +MONDO:0014647 gard_rare diseases +MONDO:0014647 nord_rare diseases +MONDO:0014647 ordo_disorder diseases +MONDO:0014647 orphanet_rare diseases +MONDO:0014647 rare diseases +MONDO:0014648 gard_rare diseases +MONDO:0014648 nord_rare diseases +MONDO:0014648 rare diseases +MONDO:0014649 gard_rare diseases +MONDO:0014649 nord_rare diseases +MONDO:0014649 rare diseases +MONDO:0014650 gard_rare diseases +MONDO:0014650 nord_rare diseases +MONDO:0014650 rare diseases +MONDO:0014651 gard_rare diseases +MONDO:0014651 nord_rare diseases +MONDO:0014651 rare diseases +MONDO:0014652 gard_rare diseases +MONDO:0014652 nord_rare diseases +MONDO:0014652 rare diseases +MONDO:0014653 gard_rare diseases +MONDO:0014653 nord_rare diseases +MONDO:0014653 rare diseases +MONDO:0014654 gard_rare diseases +MONDO:0014654 otar diseases +MONDO:0014654 rare diseases +MONDO:0014656 gard_rare diseases +MONDO:0014656 otar diseases +MONDO:0014656 rare diseases +MONDO:0014657 gard_rare diseases +MONDO:0014657 nord_rare diseases +MONDO:0014657 rare diseases +MONDO:0014658 clingen diseases +MONDO:0014658 gard_rare diseases +MONDO:0014658 nord_rare diseases +MONDO:0014658 ordo_disorder diseases +MONDO:0014658 orphanet_rare diseases +MONDO:0014658 otar diseases +MONDO:0014658 rare diseases +MONDO:0014659 gard_rare diseases +MONDO:0014659 nord_rare diseases +MONDO:0014659 otar diseases +MONDO:0014659 rare diseases +MONDO:0014660 gard_rare diseases +MONDO:0014660 nord_rare diseases +MONDO:0014660 rare diseases +MONDO:0014661 gard_rare diseases +MONDO:0014661 nord_rare diseases +MONDO:0014661 otar diseases +MONDO:0014661 rare diseases +MONDO:0014662 gard_rare diseases +MONDO:0014662 nord_rare diseases +MONDO:0014662 ordo_disorder diseases +MONDO:0014662 orphanet_rare diseases +MONDO:0014662 otar diseases +MONDO:0014662 rare diseases +MONDO:0014663 gard_rare diseases +MONDO:0014663 nord_rare diseases +MONDO:0014663 rare diseases +MONDO:0014664 gard_rare diseases +MONDO:0014664 nord_rare diseases +MONDO:0014664 rare diseases +MONDO:0014665 gard_rare diseases +MONDO:0014665 nord_rare diseases +MONDO:0014665 ordo_disorder diseases +MONDO:0014665 orphanet_rare diseases +MONDO:0014665 otar diseases +MONDO:0014665 rare diseases +MONDO:0014666 gard_rare diseases +MONDO:0014666 nord_rare diseases +MONDO:0014666 rare diseases +MONDO:0014667 gard_rare diseases +MONDO:0014667 nord_rare diseases +MONDO:0014667 rare diseases +MONDO:0014668 gard_rare diseases +MONDO:0014668 nord_rare diseases +MONDO:0014668 rare diseases +MONDO:0014669 gard_rare diseases +MONDO:0014669 nord_rare diseases +MONDO:0014669 rare diseases +MONDO:0014670 gard_rare diseases +MONDO:0014670 nord_rare diseases +MONDO:0014670 rare diseases +MONDO:0014671 clingen diseases +MONDO:0014671 gard_rare diseases +MONDO:0014671 nord_rare diseases +MONDO:0014671 otar diseases +MONDO:0014671 rare diseases +MONDO:0014672 gard_rare diseases +MONDO:0014672 nord_rare diseases +MONDO:0014672 rare diseases +MONDO:0014673 gard_rare diseases +MONDO:0014673 nord_rare diseases +MONDO:0014673 rare diseases +MONDO:0014674 gard_rare diseases +MONDO:0014674 nord_rare diseases +MONDO:0014674 rare diseases +MONDO:0014675 gard_rare diseases +MONDO:0014675 nord_rare diseases +MONDO:0014675 rare diseases +MONDO:0014676 gard_rare diseases +MONDO:0014676 nord_rare diseases +MONDO:0014676 rare diseases +MONDO:0014677 gard_rare diseases +MONDO:0014677 nord_rare diseases +MONDO:0014677 rare diseases +MONDO:0014678 otar diseases +MONDO:0014679 gard_rare diseases +MONDO:0014679 nord_rare diseases +MONDO:0014679 rare diseases +MONDO:0014681 gard_rare diseases +MONDO:0014681 nord_rare diseases +MONDO:0014681 rare diseases +MONDO:0014682 gard_rare diseases +MONDO:0014682 nord_rare diseases +MONDO:0014682 rare diseases +MONDO:0014683 gard_rare diseases +MONDO:0014683 nord_rare diseases +MONDO:0014683 otar diseases +MONDO:0014683 rare diseases +MONDO:0014684 gard_rare diseases +MONDO:0014684 nord_rare diseases +MONDO:0014684 ordo_disorder diseases +MONDO:0014684 orphanet_rare diseases +MONDO:0014684 rare diseases +MONDO:0014685 gard_rare diseases +MONDO:0014685 nord_rare diseases +MONDO:0014685 ordo_disorder diseases +MONDO:0014685 orphanet_rare diseases +MONDO:0014685 rare diseases +MONDO:0014686 gard_rare diseases +MONDO:0014686 nord_rare diseases +MONDO:0014686 rare diseases +MONDO:0014687 gard_rare diseases +MONDO:0014687 nord_rare diseases +MONDO:0014687 rare diseases +MONDO:0014688 gard_rare diseases +MONDO:0014688 nord_rare diseases +MONDO:0014688 otar diseases +MONDO:0014688 rare diseases +MONDO:0014689 clingen diseases +MONDO:0014689 gard_rare diseases +MONDO:0014689 nord_rare diseases +MONDO:0014689 ordo_disorder diseases +MONDO:0014689 ordo_malformation_syndrome diseases +MONDO:0014689 orphanet_rare diseases +MONDO:0014689 otar diseases +MONDO:0014689 rare diseases +MONDO:0014690 gard_rare diseases +MONDO:0014690 nord_rare diseases +MONDO:0014690 rare diseases +MONDO:0014691 gard_rare diseases +MONDO:0014691 nord_rare diseases +MONDO:0014691 rare diseases +MONDO:0014692 gard_rare diseases +MONDO:0014692 nord_rare diseases +MONDO:0014692 rare diseases +MONDO:0014693 gard_rare diseases +MONDO:0014693 nord_rare diseases +MONDO:0014693 rare diseases +MONDO:0014694 gard_rare diseases +MONDO:0014694 nord_rare diseases +MONDO:0014694 rare diseases +MONDO:0014696 gard_rare diseases +MONDO:0014696 nord_rare diseases +MONDO:0014696 rare diseases +MONDO:0014697 clingen diseases +MONDO:0014697 gard_rare diseases +MONDO:0014697 nord_rare diseases +MONDO:0014697 rare diseases +MONDO:0014698 gard_rare diseases +MONDO:0014698 nord_rare diseases +MONDO:0014698 ordo_disorder diseases +MONDO:0014698 ordo_malformation_syndrome diseases +MONDO:0014698 orphanet_rare diseases +MONDO:0014698 rare diseases +MONDO:0014699 gard_rare diseases +MONDO:0014699 rare diseases +MONDO:0014700 gard_rare diseases +MONDO:0014700 nord_rare diseases +MONDO:0014700 ordo_disorder diseases +MONDO:0014700 ordo_etiological_subtype diseases +MONDO:0014700 ordo_malformation_syndrome diseases +MONDO:0014700 ordo_subtype_of_a_disorder diseases +MONDO:0014700 orphanet_rare diseases +MONDO:0014700 otar diseases +MONDO:0014700 rare diseases +MONDO:0014701 clingen diseases +MONDO:0014701 gard_rare diseases +MONDO:0014701 nord_rare diseases +MONDO:0014701 ordo_disorder diseases +MONDO:0014701 orphanet_rare diseases +MONDO:0014701 otar diseases +MONDO:0014701 rare diseases +MONDO:0014702 gard_rare diseases +MONDO:0014702 nord_rare diseases +MONDO:0014702 ordo_disorder diseases +MONDO:0014702 orphanet_rare diseases +MONDO:0014702 rare diseases +MONDO:0014703 gard_rare diseases +MONDO:0014703 nord_rare diseases +MONDO:0014703 rare diseases +MONDO:0014704 gard_rare diseases +MONDO:0014704 nord_rare diseases +MONDO:0014704 ordo_disorder diseases +MONDO:0014704 ordo_malformation_syndrome diseases +MONDO:0014704 orphanet_rare diseases +MONDO:0014704 otar diseases +MONDO:0014704 rare diseases +MONDO:0014705 gard_rare diseases +MONDO:0014705 nord_rare diseases +MONDO:0014705 rare diseases +MONDO:0014706 gard_rare diseases +MONDO:0014706 nord_rare diseases +MONDO:0014706 rare diseases +MONDO:0014707 gard_rare diseases +MONDO:0014707 nord_rare diseases +MONDO:0014707 ordo_disorder diseases +MONDO:0014707 orphanet_rare diseases +MONDO:0014707 rare diseases +MONDO:0014708 gard_rare diseases +MONDO:0014708 nord_rare diseases +MONDO:0014708 ordo_disorder diseases +MONDO:0014708 ordo_malformation_syndrome diseases +MONDO:0014708 orphanet_rare diseases +MONDO:0014708 rare diseases +MONDO:0014711 gard_rare diseases +MONDO:0014711 nord_rare diseases +MONDO:0014711 ordo_disorder diseases +MONDO:0014711 orphanet_rare diseases +MONDO:0014711 otar diseases +MONDO:0014711 rare diseases +MONDO:0014712 gard_rare diseases +MONDO:0014712 nord_rare diseases +MONDO:0014712 rare diseases +MONDO:0014713 gard_rare diseases +MONDO:0014713 nord_rare diseases +MONDO:0014713 rare diseases +MONDO:0014714 gard_rare diseases +MONDO:0014714 nord_rare diseases +MONDO:0014714 ordo_disorder diseases +MONDO:0014714 ordo_malformation_syndrome diseases +MONDO:0014714 orphanet_rare diseases +MONDO:0014714 otar diseases +MONDO:0014714 rare diseases +MONDO:0014715 gard_rare diseases +MONDO:0014715 nord_rare diseases +MONDO:0014715 ordo_disorder diseases +MONDO:0014715 orphanet_rare diseases +MONDO:0014715 otar diseases +MONDO:0014715 rare diseases +MONDO:0014716 gard_rare diseases +MONDO:0014716 nord_rare diseases +MONDO:0014716 ordo_disorder diseases +MONDO:0014716 ordo_malformation_syndrome diseases +MONDO:0014716 orphanet_rare diseases +MONDO:0014716 rare diseases +MONDO:0014717 gard_rare diseases +MONDO:0014717 nord_rare diseases +MONDO:0014717 ordo_disorder diseases +MONDO:0014717 orphanet_rare diseases +MONDO:0014717 otar diseases +MONDO:0014717 rare diseases +MONDO:0014718 gard_rare diseases +MONDO:0014718 nord_rare diseases +MONDO:0014718 rare diseases +MONDO:0014719 gard_rare diseases +MONDO:0014719 nord_rare diseases +MONDO:0014719 ordo_disorder diseases +MONDO:0014719 orphanet_rare diseases +MONDO:0014719 rare diseases +MONDO:0014720 gard_rare diseases +MONDO:0014720 nord_rare diseases +MONDO:0014720 ordo_disorder diseases +MONDO:0014720 orphanet_rare diseases +MONDO:0014720 otar diseases +MONDO:0014720 rare diseases +MONDO:0014722 gard_rare diseases +MONDO:0014722 nord_rare diseases +MONDO:0014722 ordo_disorder diseases +MONDO:0014722 orphanet_rare diseases +MONDO:0014722 otar diseases +MONDO:0014722 rare diseases +MONDO:0014723 gard_rare diseases +MONDO:0014723 nord_rare diseases +MONDO:0014723 ordo_disorder diseases +MONDO:0014723 ordo_malformation_syndrome diseases +MONDO:0014723 orphanet_rare diseases +MONDO:0014723 rare diseases +MONDO:0014724 clingen diseases +MONDO:0014724 gard_rare diseases +MONDO:0014724 nord_rare diseases +MONDO:0014724 rare diseases +MONDO:0014725 clingen diseases +MONDO:0014725 gard_rare diseases +MONDO:0014725 nord_rare diseases +MONDO:0014725 ordo_disorder diseases +MONDO:0014725 orphanet_rare diseases +MONDO:0014725 otar diseases +MONDO:0014725 rare diseases +MONDO:0014726 gard_rare diseases +MONDO:0014726 nord_rare diseases +MONDO:0014726 ordo_disorder diseases +MONDO:0014726 orphanet_rare diseases +MONDO:0014726 otar diseases +MONDO:0014726 rare diseases +MONDO:0014728 gard_rare diseases +MONDO:0014728 nord_rare diseases +MONDO:0014728 ordo_disorder diseases +MONDO:0014728 orphanet_rare diseases +MONDO:0014728 rare diseases +MONDO:0014729 gard_rare diseases +MONDO:0014729 nord_rare diseases +MONDO:0014729 ordo_disorder diseases +MONDO:0014729 orphanet_rare diseases +MONDO:0014729 rare diseases +MONDO:0014730 gard_rare diseases +MONDO:0014730 nord_rare diseases +MONDO:0014730 rare diseases +MONDO:0014731 gard_rare diseases +MONDO:0014731 nord_rare diseases +MONDO:0014731 ordo_disorder diseases +MONDO:0014731 orphanet_rare diseases +MONDO:0014731 otar diseases +MONDO:0014731 rare diseases +MONDO:0014732 gard_rare diseases +MONDO:0014732 nord_rare diseases +MONDO:0014732 ordo_disorder diseases +MONDO:0014732 orphanet_rare diseases +MONDO:0014732 otar diseases +MONDO:0014732 rare diseases +MONDO:0014733 gard_rare diseases +MONDO:0014733 nord_rare diseases +MONDO:0014733 ordo_disorder diseases +MONDO:0014733 orphanet_rare diseases +MONDO:0014733 otar diseases +MONDO:0014733 rare diseases +MONDO:0014735 gard_rare diseases +MONDO:0014735 nord_rare diseases +MONDO:0014735 ordo_disorder diseases +MONDO:0014735 orphanet_rare diseases +MONDO:0014735 rare diseases +MONDO:0014736 clingen diseases +MONDO:0014736 gard_rare diseases +MONDO:0014736 nord_rare diseases +MONDO:0014736 ordo_disorder diseases +MONDO:0014736 orphanet_rare diseases +MONDO:0014736 otar diseases +MONDO:0014736 rare diseases +MONDO:0014737 gard_rare diseases +MONDO:0014737 nord_rare diseases +MONDO:0014737 rare diseases +MONDO:0014738 gard_rare diseases +MONDO:0014738 nord_rare diseases +MONDO:0014738 rare diseases +MONDO:0014739 gard_rare diseases +MONDO:0014739 nord_rare diseases +MONDO:0014739 rare diseases +MONDO:0014740 gard_rare diseases +MONDO:0014740 nord_rare diseases +MONDO:0014740 rare diseases +MONDO:0014741 gard_rare diseases +MONDO:0014741 nord_rare diseases +MONDO:0014741 ordo_subtype_of_a_disorder diseases +MONDO:0014741 otar diseases +MONDO:0014741 rare diseases +MONDO:0014742 gard_rare diseases +MONDO:0014742 nord_rare diseases +MONDO:0014742 rare diseases +MONDO:0014743 gard_rare diseases +MONDO:0014743 nord_rare diseases +MONDO:0014743 ordo_malformation_syndrome diseases +MONDO:0014743 ordo_subtype_of_a_disorder diseases +MONDO:0014743 otar diseases +MONDO:0014743 rare diseases +MONDO:0014744 gard_rare diseases +MONDO:0014744 nord_rare diseases +MONDO:0014744 ordo_disorder diseases +MONDO:0014744 orphanet_rare diseases +MONDO:0014744 rare diseases +MONDO:0014745 gard_rare diseases +MONDO:0014745 nord_rare diseases +MONDO:0014745 rare diseases +MONDO:0014746 gard_rare diseases +MONDO:0014746 nord_rare diseases +MONDO:0014746 ordo_disorder diseases +MONDO:0014746 orphanet_rare diseases +MONDO:0014746 otar diseases +MONDO:0014746 rare diseases +MONDO:0014747 gard_rare diseases +MONDO:0014747 nord_rare diseases +MONDO:0014747 ordo_disorder diseases +MONDO:0014747 orphanet_rare diseases +MONDO:0014747 rare diseases +MONDO:0014748 gard_rare diseases +MONDO:0014748 nord_rare diseases +MONDO:0014748 ordo_disorder diseases +MONDO:0014748 ordo_malformation_syndrome diseases +MONDO:0014748 orphanet_rare diseases +MONDO:0014748 rare diseases +MONDO:0014749 gard_rare diseases +MONDO:0014749 rare diseases +MONDO:0014750 gard_rare diseases +MONDO:0014750 nord_rare diseases +MONDO:0014750 rare diseases +MONDO:0014751 gard_rare diseases +MONDO:0014751 nord_rare diseases +MONDO:0014751 ordo_disorder diseases +MONDO:0014751 ordo_malformation_syndrome diseases +MONDO:0014751 orphanet_rare diseases +MONDO:0014751 otar diseases +MONDO:0014751 rare diseases +MONDO:0014752 gard_rare diseases +MONDO:0014752 rare diseases +MONDO:0014754 gard_rare diseases +MONDO:0014754 nord_rare diseases +MONDO:0014754 rare diseases +MONDO:0014755 gard_rare diseases +MONDO:0014755 rare diseases +MONDO:0014757 clingen diseases +MONDO:0014757 gard_rare diseases +MONDO:0014757 nord_rare diseases +MONDO:0014757 ordo_disorder diseases +MONDO:0014757 ordo_malformation_syndrome diseases +MONDO:0014757 orphanet_rare diseases +MONDO:0014757 otar diseases +MONDO:0014757 rare diseases +MONDO:0014758 gard_rare diseases +MONDO:0014758 nord_rare diseases +MONDO:0014758 rare diseases +MONDO:0014759 gard_rare diseases +MONDO:0014759 nord_rare diseases +MONDO:0014759 rare diseases +MONDO:0014760 clingen diseases +MONDO:0014760 gard_rare diseases +MONDO:0014760 nord_rare diseases +MONDO:0014760 ordo_disorder diseases +MONDO:0014760 orphanet_rare diseases +MONDO:0014760 rare diseases +MONDO:0014762 gard_rare diseases +MONDO:0014762 nord_rare diseases +MONDO:0014762 rare diseases +MONDO:0014764 gard_rare diseases +MONDO:0014764 nord_rare diseases +MONDO:0014764 ordo_disorder diseases +MONDO:0014764 orphanet_rare diseases +MONDO:0014764 otar diseases +MONDO:0014764 rare diseases +MONDO:0014765 gard_rare diseases +MONDO:0014765 nord_rare diseases +MONDO:0014765 rare diseases +MONDO:0014766 otar diseases +MONDO:0014767 gard_rare diseases +MONDO:0014767 nord_rare diseases +MONDO:0014767 rare diseases +MONDO:0014768 gard_rare diseases +MONDO:0014768 nord_rare diseases +MONDO:0014768 otar diseases +MONDO:0014768 rare diseases +MONDO:0014769 otar diseases +MONDO:0014769 prototype_pattern diseases +MONDO:0014770 gard_rare diseases +MONDO:0014770 nord_rare diseases +MONDO:0014770 rare diseases +MONDO:0014771 gard_rare diseases +MONDO:0014771 nord_rare diseases +MONDO:0014771 rare diseases +MONDO:0014772 gard_rare diseases +MONDO:0014772 rare diseases +MONDO:0014773 gard_rare diseases +MONDO:0014773 nord_rare diseases +MONDO:0014773 ordo_disorder diseases +MONDO:0014773 ordo_malformation_syndrome diseases +MONDO:0014773 orphanet_rare diseases +MONDO:0014773 otar diseases +MONDO:0014773 rare diseases +MONDO:0014774 inferred_rare diseases +MONDO:0014774 predisposition diseases +MONDO:0014774 rare diseases +MONDO:0014775 gard_rare diseases +MONDO:0014775 nord_rare diseases +MONDO:0014775 ordo_disorder diseases +MONDO:0014775 orphanet_rare diseases +MONDO:0014775 rare diseases +MONDO:0014776 gard_rare diseases +MONDO:0014776 nord_rare diseases +MONDO:0014776 ordo_disorder diseases +MONDO:0014776 orphanet_rare diseases +MONDO:0014776 otar diseases +MONDO:0014776 rare diseases +MONDO:0014777 clingen diseases +MONDO:0014777 gard_rare diseases +MONDO:0014777 nord_rare diseases +MONDO:0014777 rare diseases +MONDO:0014778 clingen diseases +MONDO:0014778 gard_rare diseases +MONDO:0014778 nord_rare diseases +MONDO:0014778 ordo_disorder diseases +MONDO:0014778 orphanet_rare diseases +MONDO:0014778 rare diseases +MONDO:0014779 gard_rare diseases +MONDO:0014779 nord_rare diseases +MONDO:0014779 rare diseases +MONDO:0014780 gard_rare diseases +MONDO:0014780 nord_rare diseases +MONDO:0014780 rare diseases +MONDO:0014781 gard_rare diseases +MONDO:0014781 nord_rare diseases +MONDO:0014781 ordo_disorder diseases +MONDO:0014781 orphanet_rare diseases +MONDO:0014781 rare diseases +MONDO:0014782 gard_rare diseases +MONDO:0014782 nord_rare diseases +MONDO:0014782 ordo_disorder diseases +MONDO:0014782 orphanet_rare diseases +MONDO:0014782 otar diseases +MONDO:0014782 rare diseases +MONDO:0014784 gard_rare diseases +MONDO:0014784 nord_rare diseases +MONDO:0014784 ordo_disorder diseases +MONDO:0014784 orphanet_rare diseases +MONDO:0014784 rare diseases +MONDO:0014785 gard_rare diseases +MONDO:0014785 nord_rare diseases +MONDO:0014785 rare diseases +MONDO:0014787 gard_rare diseases +MONDO:0014787 nord_rare diseases +MONDO:0014787 ordo_disorder diseases +MONDO:0014787 ordo_malformation_syndrome diseases +MONDO:0014787 orphanet_rare diseases +MONDO:0014787 rare diseases +MONDO:0014788 gard_rare diseases +MONDO:0014788 nord_rare diseases +MONDO:0014788 otar diseases +MONDO:0014788 rare diseases +MONDO:0014789 gard_rare diseases +MONDO:0014789 nord_rare diseases +MONDO:0014789 ordo_disorder diseases +MONDO:0014789 orphanet_rare diseases +MONDO:0014789 otar diseases +MONDO:0014789 rare diseases +MONDO:0014790 gard_rare diseases +MONDO:0014790 nord_rare diseases +MONDO:0014790 ordo_disorder diseases +MONDO:0014790 orphanet_rare diseases +MONDO:0014790 otar diseases +MONDO:0014790 rare diseases +MONDO:0014791 gard_rare diseases +MONDO:0014791 nord_rare diseases +MONDO:0014791 ordo_disorder diseases +MONDO:0014791 orphanet_rare diseases +MONDO:0014791 otar diseases +MONDO:0014791 rare diseases +MONDO:0014793 gard_rare diseases +MONDO:0014793 nord_rare diseases +MONDO:0014793 ordo_disorder diseases +MONDO:0014793 ordo_malformation_syndrome diseases +MONDO:0014793 orphanet_rare diseases +MONDO:0014793 rare diseases +MONDO:0014794 gard_rare diseases +MONDO:0014794 nord_rare diseases +MONDO:0014794 rare diseases +MONDO:0014795 otar diseases +MONDO:0014796 gard_rare diseases +MONDO:0014796 nord_rare diseases +MONDO:0014796 rare diseases +MONDO:0014797 gard_rare diseases +MONDO:0014797 nord_rare diseases +MONDO:0014797 rare diseases +MONDO:0014798 gard_rare diseases +MONDO:0014798 nord_rare diseases +MONDO:0014798 rare diseases +MONDO:0014799 gard_rare diseases +MONDO:0014799 nord_rare diseases +MONDO:0014799 rare diseases +MONDO:0014800 gard_rare diseases +MONDO:0014800 nord_rare diseases +MONDO:0014800 ordo_disorder diseases +MONDO:0014800 orphanet_rare diseases +MONDO:0014800 rare diseases +MONDO:0014801 gard_rare diseases +MONDO:0014801 nord_rare diseases +MONDO:0014801 ordo_disorder diseases +MONDO:0014801 ordo_malformation_syndrome diseases +MONDO:0014801 orphanet_rare diseases +MONDO:0014801 otar diseases +MONDO:0014801 rare diseases +MONDO:0014802 gard_rare diseases +MONDO:0014802 rare diseases +MONDO:0014803 gard_rare diseases +MONDO:0014803 nord_rare diseases +MONDO:0014803 ordo_disorder diseases +MONDO:0014803 orphanet_rare diseases +MONDO:0014803 otar diseases +MONDO:0014803 rare diseases +MONDO:0014804 gard_rare diseases +MONDO:0014804 nord_rare diseases +MONDO:0014804 ordo_disorder diseases +MONDO:0014804 orphanet_rare diseases +MONDO:0014804 otar diseases +MONDO:0014804 rare diseases +MONDO:0014805 clingen diseases +MONDO:0014805 gard_rare diseases +MONDO:0014805 nord_rare diseases +MONDO:0014805 ordo_disorder diseases +MONDO:0014805 ordo_malformation_syndrome diseases +MONDO:0014805 orphanet_rare diseases +MONDO:0014805 otar diseases +MONDO:0014805 rare diseases +MONDO:0014806 gard_rare diseases +MONDO:0014806 nord_rare diseases +MONDO:0014806 otar diseases +MONDO:0014806 rare diseases +MONDO:0014807 gard_rare diseases +MONDO:0014807 nord_rare diseases +MONDO:0014807 otar diseases +MONDO:0014807 rare diseases +MONDO:0014808 gard_rare diseases +MONDO:0014808 nord_rare diseases +MONDO:0014808 rare diseases +MONDO:0014809 clingen diseases +MONDO:0014809 gard_rare diseases +MONDO:0014809 nord_rare diseases +MONDO:0014809 ordo_disorder diseases +MONDO:0014809 orphanet_rare diseases +MONDO:0014809 otar diseases +MONDO:0014809 rare diseases +MONDO:0014810 clingen diseases +MONDO:0014810 gard_rare diseases +MONDO:0014810 nord_rare diseases +MONDO:0014810 ordo_disorder diseases +MONDO:0014810 orphanet_rare diseases +MONDO:0014810 otar diseases +MONDO:0014810 rare diseases +MONDO:0014811 inferred_rare diseases +MONDO:0014811 rare diseases +MONDO:0014813 gard_rare diseases +MONDO:0014813 nord_rare diseases +MONDO:0014813 otar diseases +MONDO:0014813 rare diseases +MONDO:0014814 gard_rare diseases +MONDO:0014814 nord_rare diseases +MONDO:0014814 rare diseases +MONDO:0014815 gard_rare diseases +MONDO:0014815 nord_rare diseases +MONDO:0014815 rare diseases +MONDO:0014816 gard_rare diseases +MONDO:0014816 nord_rare diseases +MONDO:0014816 ordo_disorder diseases +MONDO:0014816 ordo_malformation_syndrome diseases +MONDO:0014816 orphanet_rare diseases +MONDO:0014816 rare diseases +MONDO:0014817 gard_rare diseases +MONDO:0014817 rare diseases +MONDO:0014818 gard_rare diseases +MONDO:0014818 rare diseases +MONDO:0014819 gard_rare diseases +MONDO:0014819 nord_rare diseases +MONDO:0014819 rare diseases +MONDO:0014820 gard_rare diseases +MONDO:0014820 otar diseases +MONDO:0014820 rare diseases +MONDO:0014821 gard_rare diseases +MONDO:0014821 nord_rare diseases +MONDO:0014821 ordo_disorder diseases +MONDO:0014821 ordo_malformation_syndrome diseases +MONDO:0014821 orphanet_rare diseases +MONDO:0014821 otar diseases +MONDO:0014821 rare diseases +MONDO:0014822 gard_rare diseases +MONDO:0014822 nord_rare diseases +MONDO:0014822 ordo_malformation_syndrome diseases +MONDO:0014822 ordo_subtype_of_a_disorder diseases +MONDO:0014822 otar diseases +MONDO:0014822 rare diseases +MONDO:0014823 gard_rare diseases +MONDO:0014823 nord_rare diseases +MONDO:0014823 ordo_disorder diseases +MONDO:0014823 ordo_malformation_syndrome diseases +MONDO:0014823 orphanet_rare diseases +MONDO:0014823 rare diseases +MONDO:0014825 gard_rare diseases +MONDO:0014825 nord_rare diseases +MONDO:0014825 rare diseases +MONDO:0014827 gard_rare diseases +MONDO:0014827 nord_rare diseases +MONDO:0014827 ordo_disorder diseases +MONDO:0014827 orphanet_rare diseases +MONDO:0014827 rare diseases +MONDO:0014828 clingen diseases +MONDO:0014828 gard_rare diseases +MONDO:0014828 nord_rare diseases +MONDO:0014828 rare diseases +MONDO:0014829 clingen diseases +MONDO:0014829 gard_rare diseases +MONDO:0014829 nord_rare diseases +MONDO:0014829 rare diseases +MONDO:0014830 clingen diseases +MONDO:0014830 gard_rare diseases +MONDO:0014830 nord_rare diseases +MONDO:0014830 ordo_disorder diseases +MONDO:0014830 orphanet_rare diseases +MONDO:0014830 rare diseases +MONDO:0014831 gard_rare diseases +MONDO:0014831 nord_rare diseases +MONDO:0014831 ordo_disorder diseases +MONDO:0014831 orphanet_rare diseases +MONDO:0014831 otar diseases +MONDO:0014831 rare diseases +MONDO:0014832 gard_rare diseases +MONDO:0014832 nord_rare diseases +MONDO:0014832 ordo_disorder diseases +MONDO:0014832 orphanet_rare diseases +MONDO:0014832 otar diseases +MONDO:0014832 rare diseases +MONDO:0014835 gard_rare diseases +MONDO:0014835 nord_rare diseases +MONDO:0014835 rare diseases +MONDO:0014836 clingen diseases +MONDO:0014836 gard_rare diseases +MONDO:0014836 nord_rare diseases +MONDO:0014836 otar diseases +MONDO:0014836 rare diseases +MONDO:0014837 clingen diseases +MONDO:0014837 gard_rare diseases +MONDO:0014837 nord_rare diseases +MONDO:0014837 ordo_disorder diseases +MONDO:0014837 orphanet_rare diseases +MONDO:0014837 rare diseases +MONDO:0014838 gard_rare diseases +MONDO:0014838 nord_rare diseases +MONDO:0014838 rare diseases +MONDO:0014839 otar diseases +MONDO:0014840 gard_rare diseases +MONDO:0014840 nord_rare diseases +MONDO:0014840 rare diseases +MONDO:0014841 gard_rare diseases +MONDO:0014841 nord_rare diseases +MONDO:0014841 rare diseases +MONDO:0014842 gard_rare diseases +MONDO:0014842 nord_rare diseases +MONDO:0014842 otar diseases +MONDO:0014842 rare diseases +MONDO:0014843 gard_rare diseases +MONDO:0014843 nord_rare diseases +MONDO:0014843 rare diseases +MONDO:0014844 gard_rare diseases +MONDO:0014844 nord_rare diseases +MONDO:0014844 rare diseases +MONDO:0014845 gard_rare diseases +MONDO:0014845 nord_rare diseases +MONDO:0014845 rare diseases +MONDO:0014846 gard_rare diseases +MONDO:0014846 nord_rare diseases +MONDO:0014846 ordo_disorder diseases +MONDO:0014846 orphanet_rare diseases +MONDO:0014846 otar diseases +MONDO:0014846 rare diseases +MONDO:0014847 gard_rare diseases +MONDO:0014847 otar diseases +MONDO:0014847 rare diseases +MONDO:0014848 clingen diseases +MONDO:0014848 gard_rare diseases +MONDO:0014848 nord_rare diseases +MONDO:0014848 ordo_disorder diseases +MONDO:0014848 ordo_malformation_syndrome diseases +MONDO:0014848 orphanet_rare diseases +MONDO:0014848 rare diseases +MONDO:0014850 otar diseases +MONDO:0014851 gard_rare diseases +MONDO:0014851 nord_rare diseases +MONDO:0014851 rare diseases +MONDO:0014853 gard_rare diseases +MONDO:0014853 nord_rare diseases +MONDO:0014853 otar diseases +MONDO:0014853 rare diseases +MONDO:0014854 gard_rare diseases +MONDO:0014854 nord_rare diseases +MONDO:0014854 rare diseases +MONDO:0014855 gard_rare diseases +MONDO:0014855 nord_rare diseases +MONDO:0014855 rare diseases +MONDO:0014856 gard_rare diseases +MONDO:0014856 nord_rare diseases +MONDO:0014856 ordo_disorder diseases +MONDO:0014856 orphanet_rare diseases +MONDO:0014856 rare diseases +MONDO:0014857 gard_rare diseases +MONDO:0014857 nord_rare diseases +MONDO:0014857 ordo_disorder diseases +MONDO:0014857 orphanet_rare diseases +MONDO:0014857 otar diseases +MONDO:0014857 rare diseases +MONDO:0014858 gard_rare diseases +MONDO:0014858 nord_rare diseases +MONDO:0014858 otar diseases +MONDO:0014858 rare diseases +MONDO:0014859 gard_rare diseases +MONDO:0014859 nord_rare diseases +MONDO:0014859 rare diseases +MONDO:0014860 clingen diseases +MONDO:0014860 gard_rare diseases +MONDO:0014860 rare diseases +MONDO:0014862 gard_rare diseases +MONDO:0014862 rare diseases +MONDO:0014863 otar diseases +MONDO:0014864 gard_rare diseases +MONDO:0014864 nord_rare diseases +MONDO:0014864 ordo_disorder diseases +MONDO:0014864 orphanet_rare diseases +MONDO:0014864 rare diseases +MONDO:0014865 gard_rare diseases +MONDO:0014865 nord_rare diseases +MONDO:0014865 ordo_disorder diseases +MONDO:0014865 orphanet_rare diseases +MONDO:0014865 otar diseases +MONDO:0014865 rare diseases +MONDO:0014866 clingen diseases +MONDO:0014866 gard_rare diseases +MONDO:0014866 nord_rare diseases +MONDO:0014866 ordo_disorder diseases +MONDO:0014866 orphanet_rare diseases +MONDO:0014866 rare diseases +MONDO:0014867 gard_rare diseases +MONDO:0014867 nord_rare diseases +MONDO:0014867 ordo_disorder diseases +MONDO:0014867 orphanet_rare diseases +MONDO:0014867 rare diseases +MONDO:0014868 gard_rare diseases +MONDO:0014868 nord_rare diseases +MONDO:0014868 rare diseases +MONDO:0014869 gard_rare diseases +MONDO:0014869 nord_rare diseases +MONDO:0014869 ordo_disorder diseases +MONDO:0014869 orphanet_rare diseases +MONDO:0014869 rare diseases +MONDO:0014870 gard_rare diseases +MONDO:0014870 nord_rare diseases +MONDO:0014870 ordo_disorder diseases +MONDO:0014870 ordo_malformation_syndrome diseases +MONDO:0014870 orphanet_rare diseases +MONDO:0014870 rare diseases +MONDO:0014871 gard_rare diseases +MONDO:0014871 nord_rare diseases +MONDO:0014871 rare diseases +MONDO:0014872 gard_rare diseases +MONDO:0014872 rare diseases +MONDO:0014873 gard_rare diseases +MONDO:0014873 nord_rare diseases +MONDO:0014873 ordo_disorder diseases +MONDO:0014873 orphanet_rare diseases +MONDO:0014873 otar diseases +MONDO:0014873 rare diseases +MONDO:0014874 gard_rare diseases +MONDO:0014874 nord_rare diseases +MONDO:0014874 rare diseases +MONDO:0014875 gard_rare diseases +MONDO:0014875 nord_rare diseases +MONDO:0014875 ordo_disorder diseases +MONDO:0014875 orphanet_rare diseases +MONDO:0014875 rare diseases +MONDO:0014876 gard_rare diseases +MONDO:0014876 nord_rare diseases +MONDO:0014876 rare diseases +MONDO:0014877 gard_rare diseases +MONDO:0014877 nord_rare diseases +MONDO:0014877 ordo_disorder diseases +MONDO:0014877 orphanet_rare diseases +MONDO:0014877 rare diseases +MONDO:0014878 gard_rare diseases +MONDO:0014878 nord_rare diseases +MONDO:0014878 otar diseases +MONDO:0014878 rare diseases +MONDO:0014880 gard_rare diseases +MONDO:0014880 nord_rare diseases +MONDO:0014880 rare diseases +MONDO:0014881 gard_rare diseases +MONDO:0014881 nord_rare diseases +MONDO:0014881 ordo_disorder diseases +MONDO:0014881 ordo_malformation_syndrome diseases +MONDO:0014881 orphanet_rare diseases +MONDO:0014881 rare diseases +MONDO:0014882 gard_rare diseases +MONDO:0014882 nord_rare diseases +MONDO:0014882 ordo_disorder diseases +MONDO:0014882 orphanet_rare diseases +MONDO:0014882 otar diseases +MONDO:0014882 rare diseases +MONDO:0014883 gard_rare diseases +MONDO:0014883 nord_rare diseases +MONDO:0014883 otar diseases +MONDO:0014883 rare diseases +MONDO:0014884 gard_rare diseases +MONDO:0014884 nord_rare diseases +MONDO:0014884 ordo_subtype_of_a_disorder diseases +MONDO:0014884 rare diseases +MONDO:0014885 clingen diseases +MONDO:0014885 gard_rare diseases +MONDO:0014885 nord_rare diseases +MONDO:0014885 otar diseases +MONDO:0014885 rare diseases +MONDO:0014886 gard_rare diseases +MONDO:0014886 nord_rare diseases +MONDO:0014886 ordo_disorder diseases +MONDO:0014886 ordo_malformation_syndrome diseases +MONDO:0014886 orphanet_rare diseases +MONDO:0014886 rare diseases +MONDO:0014887 gard_rare diseases +MONDO:0014887 nord_rare diseases +MONDO:0014887 rare diseases +MONDO:0014888 gard_rare diseases +MONDO:0014888 nord_rare diseases +MONDO:0014888 ordo_disorder diseases +MONDO:0014888 orphanet_rare diseases +MONDO:0014888 otar diseases +MONDO:0014888 rare diseases +MONDO:0014889 gard_rare diseases +MONDO:0014889 nord_rare diseases +MONDO:0014889 ordo_disorder diseases +MONDO:0014889 orphanet_rare diseases +MONDO:0014889 otar diseases +MONDO:0014889 rare diseases +MONDO:0014890 gard_rare diseases +MONDO:0014890 nord_rare diseases +MONDO:0014890 ordo_disorder diseases +MONDO:0014890 orphanet_rare diseases +MONDO:0014890 rare diseases +MONDO:0014892 gard_rare diseases +MONDO:0014892 nord_rare diseases +MONDO:0014892 ordo_disorder diseases +MONDO:0014892 ordo_malformation_syndrome diseases +MONDO:0014892 orphanet_rare diseases +MONDO:0014892 otar diseases +MONDO:0014892 rare diseases +MONDO:0014893 otar diseases +MONDO:0014894 clingen diseases +MONDO:0014894 gard_rare diseases +MONDO:0014894 nord_rare diseases +MONDO:0014894 rare diseases +MONDO:0014895 gard_rare diseases +MONDO:0014895 nord_rare diseases +MONDO:0014895 rare diseases +MONDO:0014896 gard_rare diseases +MONDO:0014896 ordo_disorder diseases +MONDO:0014896 orphanet_rare diseases +MONDO:0014896 rare diseases +MONDO:0014898 gard_rare diseases +MONDO:0014898 rare diseases +MONDO:0014899 gard_rare diseases +MONDO:0014899 nord_rare diseases +MONDO:0014899 ordo_disorder diseases +MONDO:0014899 orphanet_rare diseases +MONDO:0014899 otar diseases +MONDO:0014899 rare diseases +MONDO:0014900 gard_rare diseases +MONDO:0014900 nord_rare diseases +MONDO:0014900 ordo_disorder diseases +MONDO:0014900 orphanet_rare diseases +MONDO:0014900 otar diseases +MONDO:0014900 rare diseases +MONDO:0014901 gard_rare diseases +MONDO:0014901 rare diseases +MONDO:0014902 inferred_rare diseases +MONDO:0014902 predisposition diseases +MONDO:0014902 rare diseases +MONDO:0014903 gard_rare diseases +MONDO:0014903 nord_rare diseases +MONDO:0014903 rare diseases +MONDO:0014904 gard_rare diseases +MONDO:0014904 rare diseases +MONDO:0014905 gard_rare diseases +MONDO:0014905 nord_rare diseases +MONDO:0014905 ordo_malformation_syndrome diseases +MONDO:0014905 ordo_subtype_of_a_disorder diseases +MONDO:0014905 rare diseases +MONDO:0014906 gard_rare diseases +MONDO:0014906 nord_rare diseases +MONDO:0014906 rare diseases +MONDO:0014907 gard_rare diseases +MONDO:0014907 nord_rare diseases +MONDO:0014907 rare diseases +MONDO:0014908 gard_rare diseases +MONDO:0014908 nord_rare diseases +MONDO:0014908 rare diseases +MONDO:0014909 gard_rare diseases +MONDO:0014909 nord_rare diseases +MONDO:0014909 rare diseases +MONDO:0014910 clingen diseases +MONDO:0014910 gard_rare diseases +MONDO:0014910 nord_rare diseases +MONDO:0014910 rare diseases +MONDO:0014911 gard_rare diseases +MONDO:0014911 nord_rare diseases +MONDO:0014911 ordo_disorder diseases +MONDO:0014911 orphanet_rare diseases +MONDO:0014911 rare diseases +MONDO:0014912 gard_rare diseases +MONDO:0014912 nord_rare diseases +MONDO:0014912 ordo_disorder diseases +MONDO:0014912 orphanet_rare diseases +MONDO:0014912 otar diseases +MONDO:0014912 rare diseases +MONDO:0014914 clingen diseases +MONDO:0014914 otar diseases +MONDO:0014915 gard_rare diseases +MONDO:0014915 nord_rare diseases +MONDO:0014915 rare diseases +MONDO:0014916 clingen diseases +MONDO:0014916 gard_rare diseases +MONDO:0014916 nord_rare diseases +MONDO:0014916 otar diseases +MONDO:0014916 rare diseases +MONDO:0014917 gard_rare diseases +MONDO:0014917 nord_rare diseases +MONDO:0014917 rare diseases +MONDO:0014918 gard_rare diseases +MONDO:0014918 nord_rare diseases +MONDO:0014918 ordo_disorder diseases +MONDO:0014918 ordo_malformation_syndrome diseases +MONDO:0014918 orphanet_rare diseases +MONDO:0014918 rare diseases +MONDO:0014919 clingen diseases +MONDO:0014919 gard_rare diseases +MONDO:0014919 nord_rare diseases +MONDO:0014919 otar diseases +MONDO:0014919 rare diseases +MONDO:0014920 gard_rare diseases +MONDO:0014920 nord_rare diseases +MONDO:0014920 ordo_disorder diseases +MONDO:0014920 orphanet_rare diseases +MONDO:0014920 rare diseases +MONDO:0014921 gard_rare diseases +MONDO:0014921 nord_rare diseases +MONDO:0014921 rare diseases +MONDO:0014922 gard_rare diseases +MONDO:0014922 rare diseases +MONDO:0014923 gard_rare diseases +MONDO:0014923 nord_rare diseases +MONDO:0014923 rare diseases +MONDO:0014924 gard_rare diseases +MONDO:0014924 nord_rare diseases +MONDO:0014924 rare diseases +MONDO:0014925 gard_rare diseases +MONDO:0014925 nord_rare diseases +MONDO:0014925 rare diseases +MONDO:0014926 gard_rare diseases +MONDO:0014926 nord_rare diseases +MONDO:0014926 rare diseases +MONDO:0014927 gard_rare diseases +MONDO:0014927 nord_rare diseases +MONDO:0014927 rare diseases +MONDO:0014928 gard_rare diseases +MONDO:0014928 nord_rare diseases +MONDO:0014928 rare diseases +MONDO:0014929 gard_rare diseases +MONDO:0014929 nord_rare diseases +MONDO:0014929 rare diseases +MONDO:0014930 gard_rare diseases +MONDO:0014930 nord_rare diseases +MONDO:0014930 otar diseases +MONDO:0014930 rare diseases +MONDO:0014931 otar diseases +MONDO:0014932 gard_rare diseases +MONDO:0014932 nord_rare diseases +MONDO:0014932 rare diseases +MONDO:0014933 gard_rare diseases +MONDO:0014933 nord_rare diseases +MONDO:0014933 rare diseases +MONDO:0014934 gard_rare diseases +MONDO:0014934 nord_rare diseases +MONDO:0014934 rare diseases +MONDO:0014935 gard_rare diseases +MONDO:0014935 nord_rare diseases +MONDO:0014935 rare diseases +MONDO:0014936 clingen diseases +MONDO:0014936 gard_rare diseases +MONDO:0014936 nord_rare diseases +MONDO:0014936 ordo_disorder diseases +MONDO:0014936 ordo_malformation_syndrome diseases +MONDO:0014936 orphanet_rare diseases +MONDO:0014936 rare diseases +MONDO:0014937 gard_rare diseases +MONDO:0014937 nord_rare diseases +MONDO:0014937 rare diseases +MONDO:0014938 gard_rare diseases +MONDO:0014938 nord_rare diseases +MONDO:0014938 rare diseases +MONDO:0014939 gard_rare diseases +MONDO:0014939 nord_rare diseases +MONDO:0014939 rare diseases +MONDO:0014940 otar diseases +MONDO:0014941 gard_rare diseases +MONDO:0014941 nord_rare diseases +MONDO:0014941 rare diseases +MONDO:0014942 gard_rare diseases +MONDO:0014942 nord_rare diseases +MONDO:0014942 rare diseases +MONDO:0014943 gard_rare diseases +MONDO:0014943 otar diseases +MONDO:0014943 rare diseases +MONDO:0014944 gard_rare diseases +MONDO:0014944 nord_rare diseases +MONDO:0014944 ordo_disorder diseases +MONDO:0014944 ordo_malformation_syndrome diseases +MONDO:0014944 orphanet_rare diseases +MONDO:0014944 otar diseases +MONDO:0014944 rare diseases +MONDO:0014945 gard_rare diseases +MONDO:0014945 rare diseases +MONDO:0014946 gard_rare diseases +MONDO:0014946 ordo_disorder diseases +MONDO:0014946 orphanet_rare diseases +MONDO:0014946 otar diseases +MONDO:0014946 rare diseases +MONDO:0014947 gard_rare diseases +MONDO:0014947 nord_rare diseases +MONDO:0014947 rare diseases +MONDO:0014948 otar diseases +MONDO:0014949 gard_rare diseases +MONDO:0014949 nord_rare diseases +MONDO:0014949 rare diseases +MONDO:0014950 gard_rare diseases +MONDO:0014950 nord_rare diseases +MONDO:0014950 rare diseases +MONDO:0014951 gard_rare diseases +MONDO:0014951 nord_rare diseases +MONDO:0014951 rare diseases +MONDO:0014952 gard_rare diseases +MONDO:0014952 nord_rare diseases +MONDO:0014952 ordo_disorder diseases +MONDO:0014952 orphanet_rare diseases +MONDO:0014952 rare diseases +MONDO:0014953 gard_rare diseases +MONDO:0014953 nord_rare diseases +MONDO:0014953 ordo_disorder diseases +MONDO:0014953 orphanet_rare diseases +MONDO:0014953 otar diseases +MONDO:0014953 rare diseases +MONDO:0014954 gard_rare diseases +MONDO:0014954 otar diseases +MONDO:0014954 rare diseases +MONDO:0014955 clingen diseases +MONDO:0014955 gard_rare diseases +MONDO:0014955 nord_rare diseases +MONDO:0014955 rare diseases +MONDO:0014956 otar diseases +MONDO:0014957 otar diseases +MONDO:0014958 gard_rare diseases +MONDO:0014958 nord_rare diseases +MONDO:0014958 ordo_disorder diseases +MONDO:0014958 orphanet_rare diseases +MONDO:0014958 otar diseases +MONDO:0014958 rare diseases +MONDO:0014959 gard_rare diseases +MONDO:0014959 otar diseases +MONDO:0014959 rare diseases +MONDO:0014960 gard_rare diseases +MONDO:0014960 otar diseases +MONDO:0014960 rare diseases +MONDO:0014962 gard_rare diseases +MONDO:0014962 nord_rare diseases +MONDO:0014962 otar diseases +MONDO:0014962 rare diseases +MONDO:0014963 otar diseases +MONDO:0014965 gard_rare diseases +MONDO:0014965 nord_rare diseases +MONDO:0014965 rare diseases +MONDO:0014966 clingen diseases +MONDO:0014966 gard_rare diseases +MONDO:0014966 nord_rare diseases +MONDO:0014966 rare diseases +MONDO:0014967 gard_rare diseases +MONDO:0014967 nord_rare diseases +MONDO:0014967 rare diseases +MONDO:0014968 otar diseases +MONDO:0014969 gard_rare diseases +MONDO:0014969 nord_rare diseases +MONDO:0014969 ordo_disorder diseases +MONDO:0014969 orphanet_rare diseases +MONDO:0014969 rare diseases +MONDO:0014971 gard_rare diseases +MONDO:0014971 rare diseases +MONDO:0014972 gard_rare diseases +MONDO:0014972 nord_rare diseases +MONDO:0014972 rare diseases +MONDO:0014975 gard_rare diseases +MONDO:0014975 nord_rare diseases +MONDO:0014975 ordo_disorder diseases +MONDO:0014975 orphanet_rare diseases +MONDO:0014975 otar diseases +MONDO:0014975 rare diseases +MONDO:0014976 gard_rare diseases +MONDO:0014976 nord_rare diseases +MONDO:0014976 ordo_disorder diseases +MONDO:0014976 orphanet_rare diseases +MONDO:0014976 rare diseases +MONDO:0014977 gard_rare diseases +MONDO:0014977 nord_rare diseases +MONDO:0014977 ordo_disorder diseases +MONDO:0014977 orphanet_rare diseases +MONDO:0014977 rare diseases +MONDO:0014980 clingen diseases +MONDO:0014981 gard_rare diseases +MONDO:0014981 nord_rare diseases +MONDO:0014981 rare diseases +MONDO:0014983 gard_rare diseases +MONDO:0014983 nord_rare diseases +MONDO:0014983 rare diseases +MONDO:0014985 gard_rare diseases +MONDO:0014985 nord_rare diseases +MONDO:0014985 rare diseases +MONDO:0014986 gard_rare diseases +MONDO:0014986 nord_rare diseases +MONDO:0014986 rare diseases +MONDO:0014987 gard_rare diseases +MONDO:0014987 nord_rare diseases +MONDO:0014987 rare diseases +MONDO:0014989 gard_rare diseases +MONDO:0014989 nord_rare diseases +MONDO:0014989 rare diseases +MONDO:0014990 gard_rare diseases +MONDO:0014990 nord_rare diseases +MONDO:0014990 rare diseases +MONDO:0014991 gard_rare diseases +MONDO:0014991 nord_rare diseases +MONDO:0014991 rare diseases +MONDO:0014992 gard_rare diseases +MONDO:0014992 nord_rare diseases +MONDO:0014992 rare diseases +MONDO:0014993 clingen diseases +MONDO:0014993 gard_rare diseases +MONDO:0014993 otar diseases +MONDO:0014993 rare diseases +MONDO:0014994 otar diseases +MONDO:0014995 otar diseases +MONDO:0014996 gard_rare diseases +MONDO:0014996 nord_rare diseases +MONDO:0014996 otar diseases +MONDO:0014996 rare diseases +MONDO:0014997 clingen diseases +MONDO:0014997 gard_rare diseases +MONDO:0014997 nord_rare diseases +MONDO:0014997 rare diseases +MONDO:0014998 gard_rare diseases +MONDO:0014998 rare diseases +MONDO:0014999 gard_rare diseases +MONDO:0014999 rare diseases +MONDO:0015000 gard_rare diseases +MONDO:0015000 nord_rare diseases +MONDO:0015000 rare diseases +MONDO:0015001 gard_rare diseases +MONDO:0015001 rare diseases +MONDO:0015002 gard_rare diseases +MONDO:0015002 nord_rare diseases +MONDO:0015002 rare diseases +MONDO:0015003 gard_rare diseases +MONDO:0015003 nord_rare diseases +MONDO:0015003 ordo_disorder diseases +MONDO:0015003 ordo_malformation_syndrome diseases +MONDO:0015003 orphanet_rare diseases +MONDO:0015003 otar diseases +MONDO:0015003 rare diseases +MONDO:0015004 gard_rare diseases +MONDO:0015004 nord_rare diseases +MONDO:0015004 ordo_disorder diseases +MONDO:0015004 orphanet_rare diseases +MONDO:0015004 otar diseases +MONDO:0015004 rare diseases +MONDO:0015005 gard_rare diseases +MONDO:0015005 rare diseases +MONDO:0015006 gard_rare diseases +MONDO:0015006 nord_rare diseases +MONDO:0015006 ordo_disorder diseases +MONDO:0015006 orphanet_rare diseases +MONDO:0015006 otar diseases +MONDO:0015006 rare diseases +MONDO:0015007 gard_rare diseases +MONDO:0015007 nord_rare diseases +MONDO:0015007 ordo_disorder diseases +MONDO:0015007 ordo_malformation_syndrome diseases +MONDO:0015007 orphanet_rare diseases +MONDO:0015007 otar diseases +MONDO:0015007 rare diseases +MONDO:0015008 gard_rare diseases +MONDO:0015008 otar diseases +MONDO:0015008 rare diseases +MONDO:0015009 gard_rare diseases +MONDO:0015009 nord_rare diseases +MONDO:0015009 otar diseases +MONDO:0015009 predisposition diseases +MONDO:0015009 rare diseases +MONDO:0015010 gard_rare diseases +MONDO:0015010 nord_rare diseases +MONDO:0015010 ordo_subtype_of_a_disorder diseases +MONDO:0015010 otar diseases +MONDO:0015010 rare diseases +MONDO:0015011 gard_rare diseases +MONDO:0015011 nord_rare diseases +MONDO:0015011 rare diseases +MONDO:0015012 gard_rare diseases +MONDO:0015012 nord_rare diseases +MONDO:0015012 ordo_disorder diseases +MONDO:0015012 ordo_malformation_syndrome diseases +MONDO:0015012 orphanet_rare diseases +MONDO:0015012 rare diseases +MONDO:0015013 gard_rare diseases +MONDO:0015013 nord_rare diseases +MONDO:0015013 rare diseases +MONDO:0015014 gard_rare diseases +MONDO:0015014 nord_rare diseases +MONDO:0015014 ordo_disorder diseases +MONDO:0015014 orphanet_rare diseases +MONDO:0015014 otar diseases +MONDO:0015014 rare diseases +MONDO:0015015 clingen diseases +MONDO:0015015 gard_rare diseases +MONDO:0015015 rare diseases +MONDO:0015016 gard_rare diseases +MONDO:0015016 nord_rare diseases +MONDO:0015016 rare diseases +MONDO:0015017 clingen diseases +MONDO:0015017 gard_rare diseases +MONDO:0015017 nord_rare diseases +MONDO:0015017 ordo_disorder diseases +MONDO:0015017 orphanet_rare diseases +MONDO:0015017 rare diseases +MONDO:0015018 gard_rare diseases +MONDO:0015018 nord_rare diseases +MONDO:0015018 rare diseases +MONDO:0015019 otar diseases +MONDO:0015019 predisposition diseases +MONDO:0015020 gard_rare diseases +MONDO:0015020 nord_rare diseases +MONDO:0015020 rare diseases +MONDO:0015021 clingen diseases +MONDO:0015021 gard_rare diseases +MONDO:0015021 ordo_disorder diseases +MONDO:0015021 orphanet_rare diseases +MONDO:0015021 rare diseases +MONDO:0015023 clingen diseases +MONDO:0015023 gard_rare diseases +MONDO:0015023 otar diseases +MONDO:0015023 rare diseases +MONDO:0015024 gard_rare diseases +MONDO:0015024 nord_rare diseases +MONDO:0015024 rare diseases +MONDO:0015025 gard_rare diseases +MONDO:0015025 nord_rare diseases +MONDO:0015025 rare diseases +MONDO:0015026 gard_rare diseases +MONDO:0015026 nord_rare diseases +MONDO:0015026 rare diseases +MONDO:0015027 gard_rare diseases +MONDO:0015027 nord_rare diseases +MONDO:0015027 ordo_disorder diseases +MONDO:0015027 orphanet_rare diseases +MONDO:0015027 otar diseases +MONDO:0015027 rare diseases +MONDO:0015028 gard_rare diseases +MONDO:0015028 nord_rare diseases +MONDO:0015028 ordo_disorder diseases +MONDO:0015028 ordo_malformation_syndrome diseases +MONDO:0015028 orphanet_rare diseases +MONDO:0015028 otar diseases +MONDO:0015028 rare diseases +MONDO:0015029 gard_rare diseases +MONDO:0015029 nord_rare diseases +MONDO:0015029 ordo_subtype_of_a_disorder diseases +MONDO:0015029 rare diseases +MONDO:0015030 gard_rare diseases +MONDO:0015030 nord_rare diseases +MONDO:0015030 ordo_subtype_of_a_disorder diseases +MONDO:0015030 rare diseases +MONDO:0015031 gard_rare diseases +MONDO:0015031 nord_rare diseases +MONDO:0015031 ordo_disorder diseases +MONDO:0015031 orphanet_rare diseases +MONDO:0015031 rare diseases +MONDO:0015032 gard_rare diseases +MONDO:0015032 nord_rare diseases +MONDO:0015032 ordo_disorder diseases +MONDO:0015032 orphanet_rare diseases +MONDO:0015032 otar diseases +MONDO:0015032 rare diseases +MONDO:0015033 gard_rare diseases +MONDO:0015033 nord_rare diseases +MONDO:0015033 ordo_subtype_of_a_disorder diseases +MONDO:0015033 otar diseases +MONDO:0015033 rare diseases +MONDO:0015034 gard_rare diseases +MONDO:0015034 nord_rare diseases +MONDO:0015034 ordo_disorder diseases +MONDO:0015034 ordo_malformation_syndrome diseases +MONDO:0015034 orphanet_rare diseases +MONDO:0015034 rare diseases +MONDO:0015035 gard_rare diseases +MONDO:0015035 nord_rare diseases +MONDO:0015035 ordo_disorder diseases +MONDO:0015035 ordo_malformation_syndrome diseases +MONDO:0015035 orphanet_rare diseases +MONDO:0015035 rare diseases +MONDO:0015036 gard_rare diseases +MONDO:0015036 nord_rare diseases +MONDO:0015036 ordo_disorder diseases +MONDO:0015036 ordo_malformation_syndrome diseases +MONDO:0015036 orphanet_rare diseases +MONDO:0015036 rare diseases +MONDO:0015037 gard_rare diseases +MONDO:0015037 nord_rare diseases +MONDO:0015037 ordo_disorder diseases +MONDO:0015037 ordo_malformation_syndrome diseases +MONDO:0015037 orphanet_rare diseases +MONDO:0015037 rare diseases +MONDO:0015038 gard_rare diseases +MONDO:0015038 nord_rare diseases +MONDO:0015038 ordo_disorder diseases +MONDO:0015038 ordo_malformation_syndrome diseases +MONDO:0015038 orphanet_rare diseases +MONDO:0015038 rare diseases +MONDO:0015039 gard_rare diseases +MONDO:0015039 nord_rare diseases +MONDO:0015039 ordo_disorder diseases +MONDO:0015039 ordo_malformation_syndrome diseases +MONDO:0015039 orphanet_rare diseases +MONDO:0015039 rare diseases +MONDO:0015040 gard_rare diseases +MONDO:0015040 nord_rare diseases +MONDO:0015040 ordo_subtype_of_a_disorder diseases +MONDO:0015040 rare diseases +MONDO:0015041 gard_rare diseases +MONDO:0015041 nord_rare diseases +MONDO:0015041 ordo_subtype_of_a_disorder diseases +MONDO:0015041 rare diseases +MONDO:0015042 gard_rare diseases +MONDO:0015042 nord_rare diseases +MONDO:0015042 ordo_subtype_of_a_disorder diseases +MONDO:0015042 rare diseases +MONDO:0015043 gard_rare diseases +MONDO:0015043 nord_rare diseases +MONDO:0015043 ordo_subtype_of_a_disorder diseases +MONDO:0015043 rare diseases +MONDO:0015044 gard_rare diseases +MONDO:0015044 nord_rare diseases +MONDO:0015044 ordo_subtype_of_a_disorder diseases +MONDO:0015044 rare diseases +MONDO:0015045 gard_rare diseases +MONDO:0015045 nord_rare diseases +MONDO:0015045 ordo_subtype_of_a_disorder diseases +MONDO:0015045 rare diseases +MONDO:0015046 gard_rare diseases +MONDO:0015046 nord_rare diseases +MONDO:0015046 ordo_subtype_of_a_disorder diseases +MONDO:0015046 rare diseases +MONDO:0015047 gard_rare diseases +MONDO:0015047 ordo_subtype_of_a_disorder diseases +MONDO:0015047 otar diseases +MONDO:0015047 rare diseases +MONDO:0015048 gard_rare diseases +MONDO:0015048 ordo_subtype_of_a_disorder diseases +MONDO:0015048 rare diseases +MONDO:0015049 gard_rare diseases +MONDO:0015049 nord_rare diseases +MONDO:0015049 ordo_disorder diseases +MONDO:0015049 orphanet_rare diseases +MONDO:0015049 rare diseases +MONDO:0015050 gard_rare diseases +MONDO:0015050 nord_rare diseases +MONDO:0015050 ordo_disorder diseases +MONDO:0015050 ordo_morphological_anomaly diseases +MONDO:0015050 orphanet_rare diseases +MONDO:0015050 rare diseases +MONDO:0015051 gard_rare diseases +MONDO:0015051 nord_rare diseases +MONDO:0015051 ordo_disorder diseases +MONDO:0015051 ordo_morphological_anomaly diseases +MONDO:0015051 orphanet_rare diseases +MONDO:0015051 rare diseases +MONDO:0015053 gard_rare diseases +MONDO:0015053 nord_rare diseases +MONDO:0015053 ordo_etiological_subtype diseases +MONDO:0015053 ordo_subtype_of_a_disorder diseases +MONDO:0015053 otar diseases +MONDO:0015053 rare diseases +MONDO:0015054 gard_rare diseases +MONDO:0015054 nord_rare diseases +MONDO:0015054 ordo_etiological_subtype diseases +MONDO:0015054 ordo_subtype_of_a_disorder diseases +MONDO:0015054 otar diseases +MONDO:0015054 rare diseases +MONDO:0015055 gard_rare diseases +MONDO:0015055 nord_rare diseases +MONDO:0015055 ordo_subtype_of_a_disorder diseases +MONDO:0015055 rare diseases +MONDO:0015056 gard_rare diseases +MONDO:0015056 nord_rare diseases +MONDO:0015056 ordo_subtype_of_a_disorder diseases +MONDO:0015056 rare diseases +MONDO:0015057 gard_rare diseases +MONDO:0015057 ordo_disorder diseases +MONDO:0015057 orphanet_rare diseases +MONDO:0015057 rare diseases +MONDO:0015059 gard_rare diseases +MONDO:0015059 nord_rare diseases +MONDO:0015059 ordo_disorder diseases +MONDO:0015059 orphanet_rare diseases +MONDO:0015059 otar diseases +MONDO:0015059 rare diseases +MONDO:0015060 gard_rare diseases +MONDO:0015060 nord_rare diseases +MONDO:0015060 ordo_disorder diseases +MONDO:0015060 ordo_malformation_syndrome diseases +MONDO:0015060 orphanet_rare diseases +MONDO:0015060 rare diseases +MONDO:0015061 gard_rare diseases +MONDO:0015061 nord_rare diseases +MONDO:0015061 ordo_subtype_of_a_disorder diseases +MONDO:0015061 rare diseases +MONDO:0015062 gard_rare diseases +MONDO:0015062 otar diseases +MONDO:0015062 rare diseases +MONDO:0015063 disease_grouping diseases +MONDO:0015063 gard_rare diseases +MONDO:0015063 ordo_group_of_disorders diseases +MONDO:0015063 otar diseases +MONDO:0015063 rare diseases +MONDO:0015064 gard_rare diseases +MONDO:0015064 ordo_group_of_disorders diseases +MONDO:0015064 otar diseases +MONDO:0015064 rare diseases +MONDO:0015065 gard_rare diseases +MONDO:0015065 nord_rare diseases +MONDO:0015065 ordo_disorder diseases +MONDO:0015065 orphanet_rare diseases +MONDO:0015065 otar diseases +MONDO:0015065 rare diseases +MONDO:0015066 gard_rare diseases +MONDO:0015066 nord_rare diseases +MONDO:0015066 ordo_disorder diseases +MONDO:0015066 orphanet_rare diseases +MONDO:0015066 otar diseases +MONDO:0015066 rare diseases +MONDO:0015067 gard_rare diseases +MONDO:0015067 rare diseases +MONDO:0015068 gard_rare diseases +MONDO:0015068 rare diseases +MONDO:0015069 gard_rare diseases +MONDO:0015069 nord_rare diseases +MONDO:0015069 ordo_disorder diseases +MONDO:0015069 orphanet_rare diseases +MONDO:0015069 rare diseases +MONDO:0015070 gard_rare diseases +MONDO:0015070 nord_rare diseases +MONDO:0015070 ordo_disorder diseases +MONDO:0015070 orphanet_rare diseases +MONDO:0015070 otar diseases +MONDO:0015070 rare diseases +MONDO:0015071 gard_rare diseases +MONDO:0015071 nord_rare diseases +MONDO:0015071 ordo_disorder diseases +MONDO:0015071 orphanet_rare diseases +MONDO:0015071 rare diseases +MONDO:0015072 gard_rare diseases +MONDO:0015072 nord_rare diseases +MONDO:0015072 ordo_disorder diseases +MONDO:0015072 orphanet_rare diseases +MONDO:0015072 rare diseases +MONDO:0015073 gard_rare diseases +MONDO:0015073 nord_rare diseases +MONDO:0015073 ordo_disorder diseases +MONDO:0015073 orphanet_rare diseases +MONDO:0015073 otar diseases +MONDO:0015073 rare diseases +MONDO:0015074 disease_grouping diseases +MONDO:0015074 gard_rare diseases +MONDO:0015074 ordo_group_of_disorders diseases +MONDO:0015074 otar diseases +MONDO:0015074 rare diseases +MONDO:0015075 disease_grouping diseases +MONDO:0015075 gard_rare diseases +MONDO:0015075 ordo_group_of_disorders diseases +MONDO:0015075 otar diseases +MONDO:0015075 rare diseases +MONDO:0015079 disease_grouping diseases +MONDO:0015079 gard_rare diseases +MONDO:0015079 nord_rare diseases +MONDO:0015079 ordo_group_of_disorders diseases +MONDO:0015079 rare diseases +MONDO:0015082 gard_rare diseases +MONDO:0015082 nord_rare diseases +MONDO:0015082 ordo_disorder diseases +MONDO:0015082 orphanet_rare diseases +MONDO:0015082 otar diseases +MONDO:0015082 rare diseases +MONDO:0015083 disease_grouping diseases +MONDO:0015083 gard_rare diseases +MONDO:0015083 rare diseases +MONDO:0015084 gard_rare diseases +MONDO:0015084 ordo_disorder diseases +MONDO:0015084 orphanet_rare diseases +MONDO:0015084 otar diseases +MONDO:0015084 rare diseases +MONDO:0015085 gard_rare diseases +MONDO:0015085 nord_rare diseases +MONDO:0015085 ordo_disorder diseases +MONDO:0015085 orphanet_rare diseases +MONDO:0015085 otar diseases +MONDO:0015085 rare diseases +MONDO:0015086 gard_rare diseases +MONDO:0015086 nord_rare diseases +MONDO:0015086 ordo_disorder diseases +MONDO:0015086 ordo_malformation_syndrome diseases +MONDO:0015086 orphanet_rare diseases +MONDO:0015086 rare diseases +MONDO:0015087 disease_grouping diseases +MONDO:0015087 gard_rare diseases +MONDO:0015087 ordo_group_of_disorders diseases +MONDO:0015087 rare diseases +MONDO:0015091 gard_rare diseases +MONDO:0015091 otar diseases +MONDO:0015091 rare diseases +MONDO:0015092 gard_rare diseases +MONDO:0015092 nord_rare diseases +MONDO:0015092 ordo_disorder diseases +MONDO:0015092 ordo_morphological_anomaly diseases +MONDO:0015092 orphanet_rare diseases +MONDO:0015092 rare diseases +MONDO:0015093 gard_rare diseases +MONDO:0015093 nord_rare diseases +MONDO:0015093 ordo_subtype_of_a_disorder diseases +MONDO:0015093 otar diseases +MONDO:0015093 rare diseases +MONDO:0015094 gard_rare diseases +MONDO:0015094 nord_rare diseases +MONDO:0015094 ordo_subtype_of_a_disorder diseases +MONDO:0015094 otar diseases +MONDO:0015094 rare diseases +MONDO:0015095 gard_rare diseases +MONDO:0015095 rare diseases +MONDO:0015096 gard_rare diseases +MONDO:0015096 nord_rare diseases +MONDO:0015096 ordo_subtype_of_a_disorder diseases +MONDO:0015096 otar diseases +MONDO:0015096 rare diseases +MONDO:0015097 gard_rare diseases +MONDO:0015097 nord_rare diseases +MONDO:0015097 ordo_subtype_of_a_disorder diseases +MONDO:0015097 rare diseases +MONDO:0015099 gard_rare diseases +MONDO:0015099 nord_rare diseases +MONDO:0015099 ordo_subtype_of_a_disorder diseases +MONDO:0015099 otar diseases +MONDO:0015099 rare diseases +MONDO:0015100 gard_rare diseases +MONDO:0015100 nord_rare diseases +MONDO:0015100 ordo_disorder diseases +MONDO:0015100 orphanet_rare diseases +MONDO:0015100 rare diseases +MONDO:0015101 gard_rare diseases +MONDO:0015101 ordo_subtype_of_a_disorder diseases +MONDO:0015101 rare diseases +MONDO:0015102 gard_rare diseases +MONDO:0015102 rare diseases +MONDO:0015103 gard_rare diseases +MONDO:0015103 nord_rare diseases +MONDO:0015103 ordo_disorder diseases +MONDO:0015103 ordo_malformation_syndrome diseases +MONDO:0015103 orphanet_rare diseases +MONDO:0015103 rare diseases +MONDO:0015104 gard_rare diseases +MONDO:0015104 ordo_disorder diseases +MONDO:0015104 orphanet_rare diseases +MONDO:0015104 otar diseases +MONDO:0015104 rare diseases +MONDO:0015109 gard_rare diseases +MONDO:0015109 nord_rare diseases +MONDO:0015109 ordo_disorder diseases +MONDO:0015109 ordo_morphological_anomaly diseases +MONDO:0015109 orphanet_rare diseases +MONDO:0015109 rare diseases +MONDO:0015126 disease_grouping diseases +MONDO:0015126 gard_rare diseases +MONDO:0015126 ordo_group_of_disorders diseases +MONDO:0015126 otar diseases +MONDO:0015126 rare diseases +MONDO:0015127 disease_grouping diseases +MONDO:0015127 gard_rare diseases +MONDO:0015127 ordo_group_of_disorders diseases +MONDO:0015127 otar diseases +MONDO:0015127 rare diseases +MONDO:0015128 disease_grouping diseases +MONDO:0015128 gard_rare diseases +MONDO:0015128 ordo_group_of_disorders diseases +MONDO:0015128 otar diseases +MONDO:0015128 rare diseases +MONDO:0015129 disease_grouping diseases +MONDO:0015129 gard_rare diseases +MONDO:0015129 ordo_group_of_disorders diseases +MONDO:0015129 otar diseases +MONDO:0015129 rare diseases +MONDO:0015131 clingen diseases +MONDO:0015131 disease_grouping diseases +MONDO:0015131 gard_rare diseases +MONDO:0015131 ordo_group_of_disorders diseases +MONDO:0015131 otar diseases +MONDO:0015131 rare diseases +MONDO:0015134 disease_grouping diseases +MONDO:0015134 gard_rare diseases +MONDO:0015134 ordo_group_of_disorders diseases +MONDO:0015134 otar diseases +MONDO:0015134 rare diseases +MONDO:0015137 disease_grouping diseases +MONDO:0015137 gard_rare diseases +MONDO:0015137 nord_rare diseases +MONDO:0015137 ordo_group_of_disorders diseases +MONDO:0015137 otar diseases +MONDO:0015137 rare diseases +MONDO:0015140 gard_rare diseases +MONDO:0015140 nord_rare diseases +MONDO:0015140 ordo_disorder diseases +MONDO:0015140 orphanet_rare diseases +MONDO:0015140 otar diseases +MONDO:0015140 rare diseases +MONDO:0015146 disease_grouping diseases +MONDO:0015146 gard_rare diseases +MONDO:0015146 nord_rare diseases +MONDO:0015146 ordo_group_of_disorders diseases +MONDO:0015146 otar diseases +MONDO:0015146 rare diseases +MONDO:0015148 disease_grouping diseases +MONDO:0015148 gard_rare diseases +MONDO:0015148 nord_rare diseases +MONDO:0015148 ordo_group_of_disorders diseases +MONDO:0015148 otar diseases +MONDO:0015148 rare diseases +MONDO:0015149 disease_grouping diseases +MONDO:0015149 gard_rare diseases +MONDO:0015149 ordo_group_of_disorders diseases +MONDO:0015149 otar diseases +MONDO:0015149 rare diseases +MONDO:0015150 clingen diseases +MONDO:0015150 disease_grouping diseases +MONDO:0015150 gard_rare diseases +MONDO:0015150 ordo_group_of_disorders diseases +MONDO:0015150 otar diseases +MONDO:0015150 rare diseases +MONDO:0015151 clingen diseases +MONDO:0015151 disease_grouping diseases +MONDO:0015151 gard_rare diseases +MONDO:0015151 ordo_group_of_disorders diseases +MONDO:0015151 otar diseases +MONDO:0015151 rare diseases +MONDO:0015152 clingen diseases +MONDO:0015152 disease_grouping diseases +MONDO:0015152 gard_rare diseases +MONDO:0015152 ordo_group_of_disorders diseases +MONDO:0015152 otar diseases +MONDO:0015152 rare diseases +MONDO:0015157 disease_grouping diseases +MONDO:0015157 gard_rare diseases +MONDO:0015157 nord_rare diseases +MONDO:0015157 ordo_group_of_disorders diseases +MONDO:0015157 rare diseases +MONDO:0015158 disease_grouping diseases +MONDO:0015158 gard_rare diseases +MONDO:0015158 nord_rare diseases +MONDO:0015158 ordo_group_of_disorders diseases +MONDO:0015158 rare diseases +MONDO:0015159 disease_grouping diseases +MONDO:0015159 gard_rare diseases +MONDO:0015159 ordo_group_of_disorders diseases +MONDO:0015159 otar diseases +MONDO:0015159 rare diseases +MONDO:0015160 disease_grouping diseases +MONDO:0015160 gard_rare diseases +MONDO:0015160 rare diseases +MONDO:0015161 disease_grouping diseases +MONDO:0015161 gard_rare diseases +MONDO:0015161 ordo_group_of_disorders diseases +MONDO:0015161 rare diseases +MONDO:0015164 gard_rare diseases +MONDO:0015164 nord_rare diseases +MONDO:0015164 ordo_disorder diseases +MONDO:0015164 orphanet_rare diseases +MONDO:0015164 rare diseases +MONDO:0015165 gard_rare diseases +MONDO:0015165 nord_rare diseases +MONDO:0015165 ordo_disorder diseases +MONDO:0015165 orphanet_rare diseases +MONDO:0015165 rare diseases +MONDO:0015166 gard_rare diseases +MONDO:0015166 nord_rare diseases +MONDO:0015166 ordo_disorder diseases +MONDO:0015166 orphanet_rare diseases +MONDO:0015166 rare diseases +MONDO:0015167 disease_grouping diseases +MONDO:0015167 gard_rare diseases +MONDO:0015167 nord_rare diseases +MONDO:0015167 ordo_disorder diseases +MONDO:0015167 ordo_malformation_syndrome diseases +MONDO:0015167 orphanet_rare diseases +MONDO:0015167 otar diseases +MONDO:0015167 rare diseases +MONDO:0015168 clingen diseases +MONDO:0015168 disease_grouping diseases +MONDO:0015168 gard_rare diseases +MONDO:0015168 nord_rare diseases +MONDO:0015168 ordo_group_of_disorders diseases +MONDO:0015168 otar diseases +MONDO:0015168 rare diseases +MONDO:0015169 gard_rare diseases +MONDO:0015169 nord_rare diseases +MONDO:0015169 ordo_disorder diseases +MONDO:0015169 orphanet_rare diseases +MONDO:0015169 otar diseases +MONDO:0015169 rare diseases +MONDO:0015170 gard_rare diseases +MONDO:0015170 nord_rare diseases +MONDO:0015170 ordo_disorder diseases +MONDO:0015170 orphanet_rare diseases +MONDO:0015170 otar diseases +MONDO:0015170 rare diseases +MONDO:0015171 gard_rare diseases +MONDO:0015171 nord_rare diseases +MONDO:0015171 ordo_disorder diseases +MONDO:0015171 orphanet_rare diseases +MONDO:0015171 otar diseases +MONDO:0015171 rare diseases +MONDO:0015174 gard_rare diseases +MONDO:0015174 rare diseases +MONDO:0015175 gard_rare diseases +MONDO:0015175 nord_rare diseases +MONDO:0015175 ordo_group_of_disorders diseases +MONDO:0015175 otar diseases +MONDO:0015175 rare diseases +MONDO:0015176 gard_rare diseases +MONDO:0015176 nord_rare diseases +MONDO:0015176 ordo_disorder diseases +MONDO:0015176 orphanet_rare diseases +MONDO:0015176 rare diseases +MONDO:0015177 gard_rare diseases +MONDO:0015177 ordo_disorder diseases +MONDO:0015177 orphanet_rare diseases +MONDO:0015177 otar diseases +MONDO:0015177 rare diseases +MONDO:0015183 disease_grouping diseases +MONDO:0015183 gard_rare diseases +MONDO:0015183 nord_rare diseases +MONDO:0015183 ordo_group_of_disorders diseases +MONDO:0015183 otar diseases +MONDO:0015183 rare diseases +MONDO:0015185 disease_grouping diseases +MONDO:0015185 gard_rare diseases +MONDO:0015185 ordo_group_of_disorders diseases +MONDO:0015185 otar diseases +MONDO:0015185 rare diseases +MONDO:0015191 gard_rare diseases +MONDO:0015191 nord_rare diseases +MONDO:0015191 ordo_etiological_subtype diseases +MONDO:0015191 ordo_subtype_of_a_disorder diseases +MONDO:0015191 otar diseases +MONDO:0015191 rare diseases +MONDO:0015193 gard_rare diseases +MONDO:0015193 nord_rare diseases +MONDO:0015193 ordo_disorder diseases +MONDO:0015193 ordo_malformation_syndrome diseases +MONDO:0015193 orphanet_rare diseases +MONDO:0015193 otar diseases +MONDO:0015193 rare diseases +MONDO:0015194 disease_grouping diseases +MONDO:0015194 gard_rare diseases +MONDO:0015194 nord_rare diseases +MONDO:0015194 ordo_group_of_disorders diseases +MONDO:0015194 otar diseases +MONDO:0015194 rare diseases +MONDO:0015195 gard_rare diseases +MONDO:0015195 nord_rare diseases +MONDO:0015195 ordo_disorder diseases +MONDO:0015195 ordo_morphological_anomaly diseases +MONDO:0015195 orphanet_rare diseases +MONDO:0015195 otar diseases +MONDO:0015195 rare diseases +MONDO:0015196 gard_rare diseases +MONDO:0015196 nord_rare diseases +MONDO:0015196 ordo_disorder diseases +MONDO:0015196 ordo_morphological_anomaly diseases +MONDO:0015196 orphanet_rare diseases +MONDO:0015196 rare diseases +MONDO:0015197 gard_rare diseases +MONDO:0015197 nord_rare diseases +MONDO:0015197 ordo_disorder diseases +MONDO:0015197 ordo_morphological_anomaly diseases +MONDO:0015197 orphanet_rare diseases +MONDO:0015197 rare diseases +MONDO:0015198 gard_rare diseases +MONDO:0015198 nord_rare diseases +MONDO:0015198 ordo_disorder diseases +MONDO:0015198 ordo_malformation_syndrome diseases +MONDO:0015198 orphanet_rare diseases +MONDO:0015198 otar diseases +MONDO:0015198 rare diseases +MONDO:0015199 gard_rare diseases +MONDO:0015199 nord_rare diseases +MONDO:0015199 ordo_disorder diseases +MONDO:0015199 ordo_malformation_syndrome diseases +MONDO:0015199 orphanet_rare diseases +MONDO:0015199 rare diseases +MONDO:0015200 gard_rare diseases +MONDO:0015200 nord_rare diseases +MONDO:0015200 ordo_disorder diseases +MONDO:0015200 orphanet_rare diseases +MONDO:0015200 otar diseases +MONDO:0015200 rare diseases +MONDO:0015201 gard_rare diseases +MONDO:0015201 nord_rare diseases +MONDO:0015201 ordo_malformation_syndrome diseases +MONDO:0015201 ordo_subtype_of_a_disorder diseases +MONDO:0015201 rare diseases +MONDO:0015203 disease_grouping diseases +MONDO:0015203 gard_rare diseases +MONDO:0015203 nord_rare diseases +MONDO:0015203 ordo_group_of_disorders diseases +MONDO:0015203 rare diseases +MONDO:0015204 gard_rare diseases +MONDO:0015204 nord_rare diseases +MONDO:0015204 ordo_disorder diseases +MONDO:0015204 ordo_morphological_anomaly diseases +MONDO:0015204 orphanet_rare diseases +MONDO:0015204 otar diseases +MONDO:0015204 rare diseases +MONDO:0015205 gard_rare diseases +MONDO:0015205 nord_rare diseases +MONDO:0015205 ordo_disorder diseases +MONDO:0015205 orphanet_rare diseases +MONDO:0015205 otar diseases +MONDO:0015205 rare diseases +MONDO:0015206 gard_rare diseases +MONDO:0015206 ordo_malformation_syndrome diseases +MONDO:0015206 rare diseases +MONDO:0015225 clingen diseases +MONDO:0015225 disease_grouping diseases +MONDO:0015225 gard_rare diseases +MONDO:0015225 ordo_group_of_disorders diseases +MONDO:0015225 otar diseases +MONDO:0015225 rare diseases +MONDO:0015228 gard_rare diseases +MONDO:0015228 nord_rare diseases +MONDO:0015228 ordo_disorder diseases +MONDO:0015228 ordo_malformation_syndrome diseases +MONDO:0015228 orphanet_rare diseases +MONDO:0015228 otar diseases +MONDO:0015228 rare diseases +MONDO:0015229 gard_rare diseases +MONDO:0015229 nord_rare diseases +MONDO:0015229 ordo_disorder diseases +MONDO:0015229 orphanet_rare diseases +MONDO:0015229 otar diseases +MONDO:0015229 rare diseases +MONDO:0015230 gard_rare diseases +MONDO:0015230 ordo_disorder diseases +MONDO:0015230 ordo_malformation_syndrome diseases +MONDO:0015230 orphanet_rare diseases +MONDO:0015230 otar diseases +MONDO:0015230 rare diseases +MONDO:0015231 gard_rare diseases +MONDO:0015231 nord_rare diseases +MONDO:0015231 ordo_disorder diseases +MONDO:0015231 orphanet_rare diseases +MONDO:0015231 otar diseases +MONDO:0015231 rare diseases +MONDO:0015232 gard_rare diseases +MONDO:0015232 nord_rare diseases +MONDO:0015232 ordo_disorder diseases +MONDO:0015232 ordo_malformation_syndrome diseases +MONDO:0015232 orphanet_rare diseases +MONDO:0015232 rare diseases +MONDO:0015233 gard_rare diseases +MONDO:0015233 ordo_disorder diseases +MONDO:0015233 ordo_malformation_syndrome diseases +MONDO:0015233 orphanet_rare diseases +MONDO:0015233 otar diseases +MONDO:0015233 rare diseases +MONDO:0015234 gard_rare diseases +MONDO:0015234 nord_rare diseases +MONDO:0015234 ordo_disorder diseases +MONDO:0015234 ordo_malformation_syndrome diseases +MONDO:0015234 orphanet_rare diseases +MONDO:0015234 otar diseases +MONDO:0015234 rare diseases +MONDO:0015235 gard_rare diseases +MONDO:0015235 nord_rare diseases +MONDO:0015235 ordo_disorder diseases +MONDO:0015235 ordo_malformation_syndrome diseases +MONDO:0015235 orphanet_rare diseases +MONDO:0015235 rare diseases +MONDO:0015236 disease_grouping diseases +MONDO:0015236 gard_rare diseases +MONDO:0015236 ordo_group_of_disorders diseases +MONDO:0015236 rare diseases +MONDO:0015237 gard_rare diseases +MONDO:0015237 nord_rare diseases +MONDO:0015237 ordo_disorder diseases +MONDO:0015237 ordo_malformation_syndrome diseases +MONDO:0015237 orphanet_rare diseases +MONDO:0015237 rare diseases +MONDO:0015238 gard_rare diseases +MONDO:0015238 nord_rare diseases +MONDO:0015238 ordo_disorder diseases +MONDO:0015238 ordo_malformation_syndrome diseases +MONDO:0015238 orphanet_rare diseases +MONDO:0015238 otar diseases +MONDO:0015238 rare diseases +MONDO:0015239 disease_grouping diseases +MONDO:0015239 gard_rare diseases +MONDO:0015239 ordo_group_of_disorders diseases +MONDO:0015239 rare diseases +MONDO:0015240 gard_rare diseases +MONDO:0015240 nord_rare diseases +MONDO:0015240 ordo_disorder diseases +MONDO:0015240 ordo_malformation_syndrome diseases +MONDO:0015240 orphanet_rare diseases +MONDO:0015240 otar diseases +MONDO:0015240 rare diseases +MONDO:0015241 gard_rare diseases +MONDO:0015241 nord_rare diseases +MONDO:0015241 ordo_disorder diseases +MONDO:0015241 ordo_malformation_syndrome diseases +MONDO:0015241 orphanet_rare diseases +MONDO:0015241 otar diseases +MONDO:0015241 rare diseases +MONDO:0015243 gard_rare diseases +MONDO:0015243 nord_rare diseases +MONDO:0015243 ordo_disorder diseases +MONDO:0015243 orphanet_rare diseases +MONDO:0015243 otar diseases +MONDO:0015243 rare diseases +MONDO:0015244 disease_grouping diseases +MONDO:0015244 gard_rare diseases +MONDO:0015244 nord_rare diseases +MONDO:0015244 ordo_group_of_disorders diseases +MONDO:0015244 otar diseases +MONDO:0015244 rare diseases +MONDO:0015247 gard_rare diseases +MONDO:0015247 nord_rare diseases +MONDO:0015247 ordo_disorder diseases +MONDO:0015247 orphanet_rare diseases +MONDO:0015247 otar diseases +MONDO:0015247 rare diseases +MONDO:0015248 gard_rare diseases +MONDO:0015248 nord_rare diseases +MONDO:0015248 ordo_disorder diseases +MONDO:0015248 ordo_malformation_syndrome diseases +MONDO:0015248 orphanet_rare diseases +MONDO:0015248 rare diseases +MONDO:0015249 gard_rare diseases +MONDO:0015249 nord_rare diseases +MONDO:0015249 ordo_disorder diseases +MONDO:0015249 ordo_morphological_anomaly diseases +MONDO:0015249 orphanet_rare diseases +MONDO:0015249 rare diseases +MONDO:0015250 gard_rare diseases +MONDO:0015250 ordo_disorder diseases +MONDO:0015250 orphanet_rare diseases +MONDO:0015250 rare diseases +MONDO:0015252 gard_rare diseases +MONDO:0015252 nord_rare diseases +MONDO:0015252 ordo_disorder diseases +MONDO:0015252 ordo_malformation_syndrome diseases +MONDO:0015252 orphanet_rare diseases +MONDO:0015252 rare diseases +MONDO:0015253 clingen diseases +MONDO:0015253 gard_rare diseases +MONDO:0015253 nord_rare diseases +MONDO:0015253 ordo_disorder diseases +MONDO:0015253 orphanet_rare diseases +MONDO:0015253 otar diseases +MONDO:0015253 rare diseases +MONDO:0015254 gard_rare diseases +MONDO:0015254 nord_rare diseases +MONDO:0015254 ordo_disorder diseases +MONDO:0015254 orphanet_rare diseases +MONDO:0015254 otar diseases +MONDO:0015254 rare diseases +MONDO:0015256 ordo_malformation_syndrome diseases +MONDO:0015257 gard_rare diseases +MONDO:0015257 nord_rare diseases +MONDO:0015257 rare diseases +MONDO:0015259 gard_rare diseases +MONDO:0015259 nord_rare diseases +MONDO:0015259 ordo_disorder diseases +MONDO:0015259 ordo_malformation_syndrome diseases +MONDO:0015259 orphanet_rare diseases +MONDO:0015259 otar diseases +MONDO:0015259 rare diseases +MONDO:0015260 gard_rare diseases +MONDO:0015260 nord_rare diseases +MONDO:0015260 ordo_disorder diseases +MONDO:0015260 orphanet_rare diseases +MONDO:0015260 otar diseases +MONDO:0015260 rare diseases +MONDO:0015261 gard_rare diseases +MONDO:0015261 nord_rare diseases +MONDO:0015261 ordo_disorder diseases +MONDO:0015261 orphanet_rare diseases +MONDO:0015261 rare diseases +MONDO:0015262 disease_grouping diseases +MONDO:0015262 gard_rare diseases +MONDO:0015262 nord_rare diseases +MONDO:0015262 ordo_group_of_disorders diseases +MONDO:0015262 otar diseases +MONDO:0015262 rare diseases +MONDO:0015263 clingen diseases +MONDO:0015263 gard_rare diseases +MONDO:0015263 nord_rare diseases +MONDO:0015263 ordo_disorder diseases +MONDO:0015263 orphanet_rare diseases +MONDO:0015263 otar diseases +MONDO:0015263 rare diseases +MONDO:0015264 gard_rare diseases +MONDO:0015264 nord_rare diseases +MONDO:0015264 ordo_disorder diseases +MONDO:0015264 orphanet_rare diseases +MONDO:0015264 otar diseases +MONDO:0015264 rare diseases +MONDO:0015265 gard_rare diseases +MONDO:0015265 nord_rare diseases +MONDO:0015265 ordo_group_of_disorders diseases +MONDO:0015265 otar diseases +MONDO:0015265 rare diseases +MONDO:0015267 gard_rare diseases +MONDO:0015267 nord_rare diseases +MONDO:0015267 ordo_disorder diseases +MONDO:0015267 ordo_malformation_syndrome diseases +MONDO:0015267 orphanet_rare diseases +MONDO:0015267 otar diseases +MONDO:0015267 rare diseases +MONDO:0015268 gard_rare diseases +MONDO:0015268 nord_rare diseases +MONDO:0015268 ordo_disorder diseases +MONDO:0015268 ordo_morphological_anomaly diseases +MONDO:0015268 orphanet_rare diseases +MONDO:0015268 otar diseases +MONDO:0015268 rare diseases +MONDO:0015269 gard_rare diseases +MONDO:0015269 nord_rare diseases +MONDO:0015269 ordo_disorder diseases +MONDO:0015269 orphanet_rare diseases +MONDO:0015269 rare diseases +MONDO:0015270 gard_rare diseases +MONDO:0015270 ordo_disorder diseases +MONDO:0015270 orphanet_rare diseases +MONDO:0015270 otar diseases +MONDO:0015270 rare diseases +MONDO:0015271 gard_rare diseases +MONDO:0015271 ordo_disorder diseases +MONDO:0015271 ordo_morphological_anomaly diseases +MONDO:0015271 orphanet_rare diseases +MONDO:0015271 rare diseases +MONDO:0015272 gard_rare diseases +MONDO:0015272 nord_rare diseases +MONDO:0015272 ordo_disorder diseases +MONDO:0015272 ordo_malformation_syndrome diseases +MONDO:0015272 orphanet_rare diseases +MONDO:0015272 otar diseases +MONDO:0015272 rare diseases +MONDO:0015273 gard_rare diseases +MONDO:0015273 nord_rare diseases +MONDO:0015273 ordo_disorder diseases +MONDO:0015273 ordo_morphological_anomaly diseases +MONDO:0015273 orphanet_rare diseases +MONDO:0015273 rare diseases +MONDO:0015274 gard_rare diseases +MONDO:0015274 ordo_disorder diseases +MONDO:0015274 orphanet_rare diseases +MONDO:0015274 otar diseases +MONDO:0015274 rare diseases +MONDO:0015275 gard_rare diseases +MONDO:0015275 nord_rare diseases +MONDO:0015275 ordo_disorder diseases +MONDO:0015275 ordo_morphological_anomaly diseases +MONDO:0015275 orphanet_rare diseases +MONDO:0015275 rare diseases +MONDO:0015277 gard_rare diseases +MONDO:0015277 ordo_disorder diseases +MONDO:0015277 orphanet_rare diseases +MONDO:0015277 otar diseases +MONDO:0015277 rare diseases +MONDO:0015278 gard_rare diseases +MONDO:0015278 nord_rare diseases +MONDO:0015278 ordo_disorder diseases +MONDO:0015278 orphanet_rare diseases +MONDO:0015278 otar diseases +MONDO:0015278 rare diseases +MONDO:0015279 gard_rare diseases +MONDO:0015279 nord_rare diseases +MONDO:0015279 ordo_disorder diseases +MONDO:0015279 orphanet_rare diseases +MONDO:0015279 otar diseases +MONDO:0015279 rare diseases +MONDO:0015280 clingen diseases +MONDO:0015280 gard_rare diseases +MONDO:0015280 nord_rare diseases +MONDO:0015280 ordo_disorder diseases +MONDO:0015280 ordo_malformation_syndrome diseases +MONDO:0015280 orphanet_rare diseases +MONDO:0015280 otar diseases +MONDO:0015280 rare diseases +MONDO:0015281 gard_rare diseases +MONDO:0015281 nord_rare diseases +MONDO:0015281 ordo_disorder diseases +MONDO:0015281 orphanet_rare diseases +MONDO:0015281 otar diseases +MONDO:0015281 rare diseases +MONDO:0015282 gard_rare diseases +MONDO:0015282 ordo_disorder diseases +MONDO:0015282 orphanet_rare diseases +MONDO:0015282 otar diseases +MONDO:0015282 rare diseases +MONDO:0015283 gard_rare diseases +MONDO:0015283 nord_rare diseases +MONDO:0015283 ordo_disorder diseases +MONDO:0015283 ordo_malformation_syndrome diseases +MONDO:0015283 orphanet_rare diseases +MONDO:0015283 otar diseases +MONDO:0015283 rare diseases +MONDO:0015284 gard_rare diseases +MONDO:0015284 nord_rare diseases +MONDO:0015284 ordo_disorder diseases +MONDO:0015284 ordo_malformation_syndrome diseases +MONDO:0015284 orphanet_rare diseases +MONDO:0015284 otar diseases +MONDO:0015284 rare diseases +MONDO:0015285 gard_rare diseases +MONDO:0015285 nord_rare diseases +MONDO:0015285 ordo_disorder diseases +MONDO:0015285 orphanet_rare diseases +MONDO:0015285 otar diseases +MONDO:0015285 rare diseases +MONDO:0015286 disease_grouping diseases +MONDO:0015286 gard_rare diseases +MONDO:0015286 ordo_group_of_disorders diseases +MONDO:0015286 otar diseases +MONDO:0015286 rare diseases +MONDO:0015288 disease_grouping diseases +MONDO:0015288 gard_rare diseases +MONDO:0015288 otar diseases +MONDO:0015288 rare diseases +MONDO:0015289 gard_rare diseases +MONDO:0015289 nord_rare diseases +MONDO:0015289 ordo_disorder diseases +MONDO:0015289 orphanet_rare diseases +MONDO:0015289 rare diseases +MONDO:0015290 gard_rare diseases +MONDO:0015290 nord_rare diseases +MONDO:0015290 ordo_disorder diseases +MONDO:0015290 orphanet_rare diseases +MONDO:0015290 rare diseases +MONDO:0015291 gard_rare diseases +MONDO:0015291 nord_rare diseases +MONDO:0015291 ordo_disorder diseases +MONDO:0015291 orphanet_rare diseases +MONDO:0015291 rare diseases +MONDO:0015292 gard_rare diseases +MONDO:0015292 nord_rare diseases +MONDO:0015292 ordo_disorder diseases +MONDO:0015292 orphanet_rare diseases +MONDO:0015292 rare diseases +MONDO:0015293 gard_rare diseases +MONDO:0015293 nord_rare diseases +MONDO:0015293 ordo_disorder diseases +MONDO:0015293 ordo_malformation_syndrome diseases +MONDO:0015293 orphanet_rare diseases +MONDO:0015293 otar diseases +MONDO:0015293 rare diseases +MONDO:0015294 gard_rare diseases +MONDO:0015294 nord_rare diseases +MONDO:0015294 ordo_disorder diseases +MONDO:0015294 orphanet_rare diseases +MONDO:0015294 rare diseases +MONDO:0015295 gard_rare diseases +MONDO:0015295 nord_rare diseases +MONDO:0015295 ordo_disorder diseases +MONDO:0015295 ordo_malformation_syndrome diseases +MONDO:0015295 orphanet_rare diseases +MONDO:0015295 rare diseases +MONDO:0015296 gard_rare diseases +MONDO:0015296 ordo_disorder diseases +MONDO:0015296 ordo_malformation_syndrome diseases +MONDO:0015296 orphanet_rare diseases +MONDO:0015296 rare diseases +MONDO:0015298 gard_rare diseases +MONDO:0015298 nord_rare diseases +MONDO:0015298 ordo_disorder diseases +MONDO:0015298 orphanet_rare diseases +MONDO:0015298 rare diseases +MONDO:0015299 gard_rare diseases +MONDO:0015299 nord_rare diseases +MONDO:0015299 ordo_disorder diseases +MONDO:0015299 orphanet_rare diseases +MONDO:0015299 rare diseases +MONDO:0015300 gard_rare diseases +MONDO:0015300 nord_rare diseases +MONDO:0015300 ordo_disorder diseases +MONDO:0015300 ordo_malformation_syndrome diseases +MONDO:0015300 orphanet_rare diseases +MONDO:0015300 otar diseases +MONDO:0015300 rare diseases +MONDO:0015301 disease_grouping diseases +MONDO:0015301 gard_rare diseases +MONDO:0015301 nord_rare diseases +MONDO:0015301 ordo_group_of_disorders diseases +MONDO:0015301 otar diseases +MONDO:0015301 rare diseases +MONDO:0015302 gard_rare diseases +MONDO:0015302 nord_rare diseases +MONDO:0015302 ordo_disorder diseases +MONDO:0015302 orphanet_rare diseases +MONDO:0015302 otar diseases +MONDO:0015302 rare diseases +MONDO:0015303 gard_rare diseases +MONDO:0015303 nord_rare diseases +MONDO:0015303 ordo_disorder diseases +MONDO:0015303 orphanet_rare diseases +MONDO:0015303 rare diseases +MONDO:0015304 gard_rare diseases +MONDO:0015304 nord_rare diseases +MONDO:0015304 ordo_disorder diseases +MONDO:0015304 orphanet_rare diseases +MONDO:0015304 rare diseases +MONDO:0015306 gard_rare diseases +MONDO:0015306 nord_rare diseases +MONDO:0015306 ordo_disorder diseases +MONDO:0015306 orphanet_rare diseases +MONDO:0015306 rare diseases +MONDO:0015307 gard_rare diseases +MONDO:0015307 nord_rare diseases +MONDO:0015307 ordo_disorder diseases +MONDO:0015307 orphanet_rare diseases +MONDO:0015307 otar diseases +MONDO:0015307 rare diseases +MONDO:0015311 gard_rare diseases +MONDO:0015311 nord_rare diseases +MONDO:0015311 ordo_malformation_syndrome diseases +MONDO:0015311 rare diseases +MONDO:0015312 gard_rare diseases +MONDO:0015312 nord_rare diseases +MONDO:0015312 ordo_subtype_of_a_disorder diseases +MONDO:0015312 rare diseases +MONDO:0015313 gard_rare diseases +MONDO:0015313 nord_rare diseases +MONDO:0015313 ordo_subtype_of_a_disorder diseases +MONDO:0015313 rare diseases +MONDO:0015314 gard_rare diseases +MONDO:0015314 nord_rare diseases +MONDO:0015314 ordo_disorder diseases +MONDO:0015314 ordo_malformation_syndrome diseases +MONDO:0015314 orphanet_rare diseases +MONDO:0015314 rare diseases +MONDO:0015315 gard_rare diseases +MONDO:0015315 nord_rare diseases +MONDO:0015315 ordo_disorder diseases +MONDO:0015315 orphanet_rare diseases +MONDO:0015315 rare diseases +MONDO:0015316 gard_rare diseases +MONDO:0015316 nord_rare diseases +MONDO:0015316 ordo_disorder diseases +MONDO:0015316 ordo_malformation_syndrome diseases +MONDO:0015316 orphanet_rare diseases +MONDO:0015316 rare diseases +MONDO:0015317 gard_rare diseases +MONDO:0015317 nord_rare diseases +MONDO:0015317 ordo_disorder diseases +MONDO:0015317 orphanet_rare diseases +MONDO:0015317 rare diseases +MONDO:0015324 gard_rare diseases +MONDO:0015324 ordo_disorder diseases +MONDO:0015324 ordo_malformation_syndrome diseases +MONDO:0015324 orphanet_rare diseases +MONDO:0015324 otar diseases +MONDO:0015324 rare diseases +MONDO:0015325 gard_rare diseases +MONDO:0015325 ordo_disorder diseases +MONDO:0015325 ordo_malformation_syndrome diseases +MONDO:0015325 orphanet_rare diseases +MONDO:0015325 otar diseases +MONDO:0015325 rare diseases +MONDO:0015326 gard_rare diseases +MONDO:0015326 ordo_disorder diseases +MONDO:0015326 ordo_malformation_syndrome diseases +MONDO:0015326 orphanet_rare diseases +MONDO:0015326 otar diseases +MONDO:0015326 rare diseases +MONDO:0015327 disease_grouping diseases +MONDO:0015327 gard_rare diseases +MONDO:0015327 ordo_group_of_disorders diseases +MONDO:0015327 rare diseases +MONDO:0015333 disease_grouping diseases +MONDO:0015333 gard_rare diseases +MONDO:0015333 ordo_group_of_disorders diseases +MONDO:0015333 otar diseases +MONDO:0015333 rare diseases +MONDO:0015337 disease_grouping diseases +MONDO:0015337 inferred_rare diseases +MONDO:0015337 ordo_group_of_disorders diseases +MONDO:0015337 otar diseases +MONDO:0015337 rare diseases +MONDO:0015338 disease_grouping diseases +MONDO:0015338 gard_rare diseases +MONDO:0015338 ordo_group_of_disorders diseases +MONDO:0015338 otar diseases +MONDO:0015338 rare diseases +MONDO:0015339 gard_rare diseases +MONDO:0015339 nord_rare diseases +MONDO:0015339 ordo_subtype_of_a_disorder diseases +MONDO:0015339 otar diseases +MONDO:0015339 rare diseases +MONDO:0015340 gard_rare diseases +MONDO:0015340 nord_rare diseases +MONDO:0015340 ordo_disorder diseases +MONDO:0015340 orphanet_rare diseases +MONDO:0015340 rare diseases +MONDO:0015341 gard_rare diseases +MONDO:0015341 nord_rare diseases +MONDO:0015341 ordo_disorder diseases +MONDO:0015341 orphanet_rare diseases +MONDO:0015341 rare diseases +MONDO:0015342 gard_rare diseases +MONDO:0015342 nord_rare diseases +MONDO:0015342 ordo_disorder diseases +MONDO:0015342 orphanet_rare diseases +MONDO:0015342 otar diseases +MONDO:0015342 rare diseases +MONDO:0015344 gard_rare diseases +MONDO:0015344 nord_rare diseases +MONDO:0015344 ordo_subtype_of_a_disorder diseases +MONDO:0015344 rare diseases +MONDO:0015345 gard_rare diseases +MONDO:0015345 nord_rare diseases +MONDO:0015345 ordo_disorder diseases +MONDO:0015345 orphanet_rare diseases +MONDO:0015345 rare diseases +MONDO:0015346 gard_rare diseases +MONDO:0015346 nord_rare diseases +MONDO:0015346 ordo_disorder diseases +MONDO:0015346 orphanet_rare diseases +MONDO:0015346 otar diseases +MONDO:0015346 rare diseases +MONDO:0015347 gard_rare diseases +MONDO:0015347 nord_rare diseases +MONDO:0015347 ordo_disorder diseases +MONDO:0015347 orphanet_rare diseases +MONDO:0015347 rare diseases +MONDO:0015348 gard_rare diseases +MONDO:0015348 nord_rare diseases +MONDO:0015348 ordo_disorder diseases +MONDO:0015348 orphanet_rare diseases +MONDO:0015348 rare diseases +MONDO:0015349 gard_rare diseases +MONDO:0015349 nord_rare diseases +MONDO:0015349 ordo_disorder diseases +MONDO:0015349 orphanet_rare diseases +MONDO:0015349 otar diseases +MONDO:0015349 rare diseases +MONDO:0015350 gard_rare diseases +MONDO:0015350 nord_rare diseases +MONDO:0015350 ordo_disorder diseases +MONDO:0015350 ordo_malformation_syndrome diseases +MONDO:0015350 orphanet_rare diseases +MONDO:0015350 otar diseases +MONDO:0015350 rare diseases +MONDO:0015351 gard_rare diseases +MONDO:0015351 nord_rare diseases +MONDO:0015351 ordo_disorder diseases +MONDO:0015351 orphanet_rare diseases +MONDO:0015351 otar diseases +MONDO:0015351 rare diseases +MONDO:0015352 gard_rare diseases +MONDO:0015352 nord_rare diseases +MONDO:0015352 ordo_disorder diseases +MONDO:0015352 orphanet_rare diseases +MONDO:0015352 otar diseases +MONDO:0015352 rare diseases +MONDO:0015353 gard_rare diseases +MONDO:0015353 nord_rare diseases +MONDO:0015353 otar diseases +MONDO:0015353 rare diseases +MONDO:0015354 gard_rare diseases +MONDO:0015354 nord_rare diseases +MONDO:0015354 ordo_disorder diseases +MONDO:0015354 orphanet_rare diseases +MONDO:0015354 rare diseases +MONDO:0015355 gard_rare diseases +MONDO:0015355 nord_rare diseases +MONDO:0015355 ordo_disorder diseases +MONDO:0015355 orphanet_rare diseases +MONDO:0015355 otar diseases +MONDO:0015355 rare diseases +MONDO:0015356 disease_grouping diseases +MONDO:0015356 gard_rare diseases +MONDO:0015356 ordo_group_of_disorders diseases +MONDO:0015356 otar diseases +MONDO:0015356 predisposition diseases +MONDO:0015356 rare diseases +MONDO:0015357 gard_rare diseases +MONDO:0015357 nord_rare diseases +MONDO:0015357 ordo_disorder diseases +MONDO:0015357 orphanet_rare diseases +MONDO:0015357 rare diseases +MONDO:0015358 disease_grouping diseases +MONDO:0015358 gard_rare diseases +MONDO:0015358 otar diseases +MONDO:0015358 rare diseases +MONDO:0015362 clingen diseases +MONDO:0015362 disease_grouping diseases +MONDO:0015362 gard_rare diseases +MONDO:0015362 ordo_group_of_disorders diseases +MONDO:0015362 otar diseases +MONDO:0015362 rare diseases +MONDO:0015363 disease_grouping diseases +MONDO:0015363 gard_rare diseases +MONDO:0015363 nord_rare diseases +MONDO:0015363 ordo_group_of_disorders diseases +MONDO:0015363 otar diseases +MONDO:0015363 rare diseases +MONDO:0015364 clingen diseases +MONDO:0015364 disease_grouping diseases +MONDO:0015364 gard_rare diseases +MONDO:0015364 ordo_group_of_disorders diseases +MONDO:0015364 otar diseases +MONDO:0015364 rare diseases +MONDO:0015367 gard_rare diseases +MONDO:0015367 nord_rare diseases +MONDO:0015367 ordo_disorder diseases +MONDO:0015367 ordo_malformation_syndrome diseases +MONDO:0015367 orphanet_rare diseases +MONDO:0015367 otar diseases +MONDO:0015367 rare diseases +MONDO:0015369 disease_grouping diseases +MONDO:0015369 gard_rare diseases +MONDO:0015369 nord_rare diseases +MONDO:0015369 ordo_group_of_disorders diseases +MONDO:0015369 otar diseases +MONDO:0015369 rare diseases +MONDO:0015371 gard_rare diseases +MONDO:0015371 nord_rare diseases +MONDO:0015371 ordo_disorder diseases +MONDO:0015371 orphanet_rare diseases +MONDO:0015371 otar diseases +MONDO:0015371 rare diseases +MONDO:0015372 clingen diseases +MONDO:0015372 gard_rare diseases +MONDO:0015372 nord_rare diseases +MONDO:0015372 ordo_disorder diseases +MONDO:0015372 orphanet_rare diseases +MONDO:0015372 otar diseases +MONDO:0015372 rare diseases +MONDO:0015374 gard_rare diseases +MONDO:0015374 nord_rare diseases +MONDO:0015374 ordo_disorder diseases +MONDO:0015374 orphanet_rare diseases +MONDO:0015374 otar diseases +MONDO:0015374 rare diseases +MONDO:0015375 disease_grouping diseases +MONDO:0015375 gard_rare diseases +MONDO:0015375 nord_rare diseases +MONDO:0015375 ordo_group_of_disorders diseases +MONDO:0015375 otar diseases +MONDO:0015375 rare diseases +MONDO:0015376 gard_rare diseases +MONDO:0015376 nord_rare diseases +MONDO:0015376 ordo_disorder diseases +MONDO:0015376 ordo_morphological_anomaly diseases +MONDO:0015376 orphanet_rare diseases +MONDO:0015376 rare diseases +MONDO:0015377 gard_rare diseases +MONDO:0015377 nord_rare diseases +MONDO:0015377 ordo_disorder diseases +MONDO:0015377 ordo_morphological_anomaly diseases +MONDO:0015377 orphanet_rare diseases +MONDO:0015377 rare diseases +MONDO:0015378 gard_rare diseases +MONDO:0015378 nord_rare diseases +MONDO:0015378 ordo_disorder diseases +MONDO:0015378 ordo_morphological_anomaly diseases +MONDO:0015378 orphanet_rare diseases +MONDO:0015378 rare diseases +MONDO:0015379 gard_rare diseases +MONDO:0015379 nord_rare diseases +MONDO:0015379 ordo_disorder diseases +MONDO:0015379 ordo_morphological_anomaly diseases +MONDO:0015379 orphanet_rare diseases +MONDO:0015379 rare diseases +MONDO:0015380 gard_rare diseases +MONDO:0015380 nord_rare diseases +MONDO:0015380 ordo_disorder diseases +MONDO:0015380 ordo_morphological_anomaly diseases +MONDO:0015380 orphanet_rare diseases +MONDO:0015380 rare diseases +MONDO:0015381 gard_rare diseases +MONDO:0015381 nord_rare diseases +MONDO:0015381 ordo_disorder diseases +MONDO:0015381 ordo_morphological_anomaly diseases +MONDO:0015381 orphanet_rare diseases +MONDO:0015381 rare diseases +MONDO:0015382 gard_rare diseases +MONDO:0015382 nord_rare diseases +MONDO:0015382 ordo_disorder diseases +MONDO:0015382 ordo_morphological_anomaly diseases +MONDO:0015382 orphanet_rare diseases +MONDO:0015382 rare diseases +MONDO:0015383 gard_rare diseases +MONDO:0015383 nord_rare diseases +MONDO:0015383 ordo_disorder diseases +MONDO:0015383 ordo_morphological_anomaly diseases +MONDO:0015383 orphanet_rare diseases +MONDO:0015383 rare diseases +MONDO:0015384 gard_rare diseases +MONDO:0015384 nord_rare diseases +MONDO:0015384 ordo_disorder diseases +MONDO:0015384 ordo_morphological_anomaly diseases +MONDO:0015384 orphanet_rare diseases +MONDO:0015384 rare diseases +MONDO:0015386 gard_rare diseases +MONDO:0015386 nord_rare diseases +MONDO:0015386 ordo_subtype_of_a_disorder diseases +MONDO:0015386 rare diseases +MONDO:0015387 gard_rare diseases +MONDO:0015387 nord_rare diseases +MONDO:0015387 ordo_disorder diseases +MONDO:0015387 ordo_morphological_anomaly diseases +MONDO:0015387 orphanet_rare diseases +MONDO:0015387 rare diseases +MONDO:0015388 gard_rare diseases +MONDO:0015388 nord_rare diseases +MONDO:0015388 ordo_disorder diseases +MONDO:0015388 ordo_malformation_syndrome diseases +MONDO:0015388 orphanet_rare diseases +MONDO:0015388 rare diseases +MONDO:0015389 gard_rare diseases +MONDO:0015389 nord_rare diseases +MONDO:0015389 ordo_disorder diseases +MONDO:0015389 ordo_malformation_syndrome diseases +MONDO:0015389 orphanet_rare diseases +MONDO:0015389 rare diseases +MONDO:0015390 gard_rare diseases +MONDO:0015390 nord_rare diseases +MONDO:0015390 ordo_disorder diseases +MONDO:0015390 ordo_malformation_syndrome diseases +MONDO:0015390 orphanet_rare diseases +MONDO:0015390 rare diseases +MONDO:0015391 gard_rare diseases +MONDO:0015391 nord_rare diseases +MONDO:0015391 ordo_subtype_of_a_disorder diseases +MONDO:0015391 rare diseases +MONDO:0015392 gard_rare diseases +MONDO:0015392 nord_rare diseases +MONDO:0015392 ordo_disorder diseases +MONDO:0015392 orphanet_rare diseases +MONDO:0015392 rare diseases +MONDO:0015393 gard_rare diseases +MONDO:0015393 nord_rare diseases +MONDO:0015393 ordo_subtype_of_a_disorder diseases +MONDO:0015393 rare diseases +MONDO:0015394 gard_rare diseases +MONDO:0015394 nord_rare diseases +MONDO:0015394 ordo_subtype_of_a_disorder diseases +MONDO:0015394 rare diseases +MONDO:0015395 gard_rare diseases +MONDO:0015395 nord_rare diseases +MONDO:0015395 ordo_disorder diseases +MONDO:0015395 ordo_malformation_syndrome diseases +MONDO:0015395 orphanet_rare diseases +MONDO:0015395 rare diseases +MONDO:0015396 gard_rare diseases +MONDO:0015396 nord_rare diseases +MONDO:0015396 ordo_disorder diseases +MONDO:0015396 ordo_malformation_syndrome diseases +MONDO:0015396 orphanet_rare diseases +MONDO:0015396 rare diseases +MONDO:0015397 disease_grouping diseases +MONDO:0015397 gard_rare diseases +MONDO:0015397 nord_rare diseases +MONDO:0015397 ordo_disorder diseases +MONDO:0015397 ordo_malformation_syndrome diseases +MONDO:0015397 orphanet_rare diseases +MONDO:0015397 otar diseases +MONDO:0015397 rare diseases +MONDO:0015399 gard_rare diseases +MONDO:0015399 nord_rare diseases +MONDO:0015399 ordo_disorder diseases +MONDO:0015399 ordo_malformation_syndrome diseases +MONDO:0015399 orphanet_rare diseases +MONDO:0015399 rare diseases +MONDO:0015400 gard_rare diseases +MONDO:0015400 nord_rare diseases +MONDO:0015400 ordo_disorder diseases +MONDO:0015400 ordo_malformation_syndrome diseases +MONDO:0015400 orphanet_rare diseases +MONDO:0015400 rare diseases +MONDO:0015401 gard_rare diseases +MONDO:0015401 nord_rare diseases +MONDO:0015401 ordo_disorder diseases +MONDO:0015401 ordo_malformation_syndrome diseases +MONDO:0015401 orphanet_rare diseases +MONDO:0015401 rare diseases +MONDO:0015402 gard_rare diseases +MONDO:0015402 nord_rare diseases +MONDO:0015402 ordo_disorder diseases +MONDO:0015402 ordo_malformation_syndrome diseases +MONDO:0015402 orphanet_rare diseases +MONDO:0015402 rare diseases +MONDO:0015403 gard_rare diseases +MONDO:0015403 nord_rare diseases +MONDO:0015403 ordo_disorder diseases +MONDO:0015403 orphanet_rare diseases +MONDO:0015403 rare diseases +MONDO:0015404 gard_rare diseases +MONDO:0015404 nord_rare diseases +MONDO:0015404 ordo_disorder diseases +MONDO:0015404 orphanet_rare diseases +MONDO:0015404 rare diseases +MONDO:0015405 disease_grouping diseases +MONDO:0015405 gard_rare diseases +MONDO:0015405 nord_rare diseases +MONDO:0015405 ordo_group_of_disorders diseases +MONDO:0015405 otar diseases +MONDO:0015405 rare diseases +MONDO:0015406 gard_rare diseases +MONDO:0015406 nord_rare diseases +MONDO:0015406 ordo_disorder diseases +MONDO:0015406 ordo_malformation_syndrome diseases +MONDO:0015406 orphanet_rare diseases +MONDO:0015406 rare diseases +MONDO:0015407 gard_rare diseases +MONDO:0015407 nord_rare diseases +MONDO:0015407 ordo_disorder diseases +MONDO:0015407 ordo_malformation_syndrome diseases +MONDO:0015407 orphanet_rare diseases +MONDO:0015407 rare diseases +MONDO:0015408 gard_rare diseases +MONDO:0015408 nord_rare diseases +MONDO:0015408 ordo_disorder diseases +MONDO:0015408 orphanet_rare diseases +MONDO:0015408 rare diseases +MONDO:0015409 gard_rare diseases +MONDO:0015409 nord_rare diseases +MONDO:0015409 ordo_disorder diseases +MONDO:0015409 ordo_malformation_syndrome diseases +MONDO:0015409 orphanet_rare diseases +MONDO:0015409 rare diseases +MONDO:0015410 gard_rare diseases +MONDO:0015410 nord_rare diseases +MONDO:0015410 ordo_disorder diseases +MONDO:0015410 ordo_morphological_anomaly diseases +MONDO:0015410 orphanet_rare diseases +MONDO:0015410 rare diseases +MONDO:0015411 disease_grouping diseases +MONDO:0015411 gard_rare diseases +MONDO:0015411 ordo_group_of_disorders diseases +MONDO:0015411 otar diseases +MONDO:0015411 rare diseases +MONDO:0015413 gard_rare diseases +MONDO:0015413 nord_rare diseases +MONDO:0015413 ordo_disorder diseases +MONDO:0015413 ordo_morphological_anomaly diseases +MONDO:0015413 orphanet_rare diseases +MONDO:0015413 rare diseases +MONDO:0015414 gard_rare diseases +MONDO:0015414 nord_rare diseases +MONDO:0015414 ordo_disorder diseases +MONDO:0015414 ordo_morphological_anomaly diseases +MONDO:0015414 orphanet_rare diseases +MONDO:0015414 rare diseases +MONDO:0015416 gard_rare diseases +MONDO:0015416 nord_rare diseases +MONDO:0015416 ordo_disorder diseases +MONDO:0015416 ordo_morphological_anomaly diseases +MONDO:0015416 orphanet_rare diseases +MONDO:0015416 rare diseases +MONDO:0015417 gard_rare diseases +MONDO:0015417 nord_rare diseases +MONDO:0015417 ordo_disorder diseases +MONDO:0015417 ordo_morphological_anomaly diseases +MONDO:0015417 orphanet_rare diseases +MONDO:0015417 rare diseases +MONDO:0015419 gard_rare diseases +MONDO:0015419 nord_rare diseases +MONDO:0015419 ordo_disorder diseases +MONDO:0015419 ordo_morphological_anomaly diseases +MONDO:0015419 orphanet_rare diseases +MONDO:0015419 rare diseases +MONDO:0015420 gard_rare diseases +MONDO:0015420 nord_rare diseases +MONDO:0015420 ordo_disorder diseases +MONDO:0015420 ordo_morphological_anomaly diseases +MONDO:0015420 orphanet_rare diseases +MONDO:0015420 rare diseases +MONDO:0015421 gard_rare diseases +MONDO:0015421 nord_rare diseases +MONDO:0015421 ordo_disorder diseases +MONDO:0015421 ordo_malformation_syndrome diseases +MONDO:0015421 orphanet_rare diseases +MONDO:0015421 rare diseases +MONDO:0015422 gard_rare diseases +MONDO:0015422 nord_rare diseases +MONDO:0015422 ordo_disorder diseases +MONDO:0015422 ordo_malformation_syndrome diseases +MONDO:0015422 orphanet_rare diseases +MONDO:0015422 rare diseases +MONDO:0015424 gard_rare diseases +MONDO:0015424 ordo_malformation_syndrome diseases +MONDO:0015424 rare diseases +MONDO:0015425 gard_rare diseases +MONDO:0015425 nord_rare diseases +MONDO:0015425 ordo_disorder diseases +MONDO:0015425 ordo_malformation_syndrome diseases +MONDO:0015425 orphanet_rare diseases +MONDO:0015425 otar diseases +MONDO:0015425 rare diseases +MONDO:0015426 gard_rare diseases +MONDO:0015426 ordo_disorder diseases +MONDO:0015426 orphanet_rare diseases +MONDO:0015426 otar diseases +MONDO:0015426 rare diseases +MONDO:0015427 disease_grouping diseases +MONDO:0015427 gard_rare diseases +MONDO:0015427 nord_rare diseases +MONDO:0015427 ordo_group_of_disorders diseases +MONDO:0015427 otar diseases +MONDO:0015427 rare diseases +MONDO:0015428 gard_rare diseases +MONDO:0015428 nord_rare diseases +MONDO:0015428 ordo_disorder diseases +MONDO:0015428 ordo_malformation_syndrome diseases +MONDO:0015428 orphanet_rare diseases +MONDO:0015428 otar diseases +MONDO:0015428 rare diseases +MONDO:0015429 gard_rare diseases +MONDO:0015429 obsoletion_candidate diseases +MONDO:0015429 rare diseases +MONDO:0015430 gard_rare diseases +MONDO:0015430 nord_rare diseases +MONDO:0015430 ordo_disorder diseases +MONDO:0015430 ordo_malformation_syndrome diseases +MONDO:0015430 orphanet_rare diseases +MONDO:0015430 otar diseases +MONDO:0015430 rare diseases +MONDO:0015431 gard_rare diseases +MONDO:0015431 nord_rare diseases +MONDO:0015431 ordo_disorder diseases +MONDO:0015431 ordo_malformation_syndrome diseases +MONDO:0015431 orphanet_rare diseases +MONDO:0015431 rare diseases +MONDO:0015432 gard_rare diseases +MONDO:0015432 nord_rare diseases +MONDO:0015432 ordo_disorder diseases +MONDO:0015432 ordo_malformation_syndrome diseases +MONDO:0015432 orphanet_rare diseases +MONDO:0015432 otar diseases +MONDO:0015432 rare diseases +MONDO:0015433 gard_rare diseases +MONDO:0015433 nord_rare diseases +MONDO:0015433 ordo_disorder diseases +MONDO:0015433 ordo_malformation_syndrome diseases +MONDO:0015433 orphanet_rare diseases +MONDO:0015433 rare diseases +MONDO:0015434 gard_rare diseases +MONDO:0015434 nord_rare diseases +MONDO:0015434 ordo_disorder diseases +MONDO:0015434 ordo_malformation_syndrome diseases +MONDO:0015434 orphanet_rare diseases +MONDO:0015434 rare diseases +MONDO:0015435 gard_rare diseases +MONDO:0015435 nord_rare diseases +MONDO:0015435 ordo_disorder diseases +MONDO:0015435 ordo_malformation_syndrome diseases +MONDO:0015435 orphanet_rare diseases +MONDO:0015435 rare diseases +MONDO:0015436 gard_rare diseases +MONDO:0015436 nord_rare diseases +MONDO:0015436 ordo_disorder diseases +MONDO:0015436 ordo_malformation_syndrome diseases +MONDO:0015436 orphanet_rare diseases +MONDO:0015436 otar diseases +MONDO:0015436 rare diseases +MONDO:0015437 gard_rare diseases +MONDO:0015437 nord_rare diseases +MONDO:0015437 ordo_disorder diseases +MONDO:0015437 ordo_malformation_syndrome diseases +MONDO:0015437 orphanet_rare diseases +MONDO:0015437 otar diseases +MONDO:0015437 rare diseases +MONDO:0015438 gard_rare diseases +MONDO:0015438 nord_rare diseases +MONDO:0015438 ordo_disorder diseases +MONDO:0015438 ordo_malformation_syndrome diseases +MONDO:0015438 orphanet_rare diseases +MONDO:0015438 otar diseases +MONDO:0015438 rare diseases +MONDO:0015439 gard_rare diseases +MONDO:0015439 nord_rare diseases +MONDO:0015439 ordo_disorder diseases +MONDO:0015439 ordo_malformation_syndrome diseases +MONDO:0015439 orphanet_rare diseases +MONDO:0015439 otar diseases +MONDO:0015439 rare diseases +MONDO:0015440 gard_rare diseases +MONDO:0015440 nord_rare diseases +MONDO:0015440 ordo_disorder diseases +MONDO:0015440 ordo_malformation_syndrome diseases +MONDO:0015440 orphanet_rare diseases +MONDO:0015440 otar diseases +MONDO:0015440 rare diseases +MONDO:0015441 gard_rare diseases +MONDO:0015441 nord_rare diseases +MONDO:0015441 ordo_disorder diseases +MONDO:0015441 ordo_malformation_syndrome diseases +MONDO:0015441 orphanet_rare diseases +MONDO:0015441 otar diseases +MONDO:0015441 rare diseases +MONDO:0015443 gard_rare diseases +MONDO:0015443 nord_rare diseases +MONDO:0015443 ordo_disorder diseases +MONDO:0015443 ordo_malformation_syndrome diseases +MONDO:0015443 orphanet_rare diseases +MONDO:0015443 otar diseases +MONDO:0015443 rare diseases +MONDO:0015445 gard_rare diseases +MONDO:0015445 nord_rare diseases +MONDO:0015445 ordo_subtype_of_a_disorder diseases +MONDO:0015445 rare diseases +MONDO:0015446 gard_rare diseases +MONDO:0015446 nord_rare diseases +MONDO:0015446 ordo_subtype_of_a_disorder diseases +MONDO:0015446 otar diseases +MONDO:0015446 rare diseases +MONDO:0015447 gard_rare diseases +MONDO:0015447 nord_rare diseases +MONDO:0015447 ordo_disorder diseases +MONDO:0015447 orphanet_rare diseases +MONDO:0015447 otar diseases +MONDO:0015447 rare diseases +MONDO:0015448 gard_rare diseases +MONDO:0015448 ordo_disorder diseases +MONDO:0015448 orphanet_rare diseases +MONDO:0015448 otar diseases +MONDO:0015448 rare diseases +MONDO:0015449 gard_rare diseases +MONDO:0015449 nord_rare diseases +MONDO:0015449 ordo_disorder diseases +MONDO:0015449 ordo_morphological_anomaly diseases +MONDO:0015449 orphanet_rare diseases +MONDO:0015449 rare diseases +MONDO:0015450 disease_grouping diseases +MONDO:0015450 gard_rare diseases +MONDO:0015450 nord_rare diseases +MONDO:0015450 ordo_group_of_disorders diseases +MONDO:0015450 rare diseases +MONDO:0015451 gard_rare diseases +MONDO:0015451 nord_rare diseases +MONDO:0015451 ordo_disorder diseases +MONDO:0015451 ordo_morphological_anomaly diseases +MONDO:0015451 orphanet_rare diseases +MONDO:0015451 rare diseases +MONDO:0015452 clingen diseases +MONDO:0015452 gard_rare diseases +MONDO:0015452 nord_rare diseases +MONDO:0015452 ordo_disorder diseases +MONDO:0015452 ordo_malformation_syndrome diseases +MONDO:0015452 orphanet_rare diseases +MONDO:0015452 otar diseases +MONDO:0015452 rare diseases +MONDO:0015453 gard_rare diseases +MONDO:0015453 nord_rare diseases +MONDO:0015453 ordo_disorder diseases +MONDO:0015453 orphanet_rare diseases +MONDO:0015453 rare diseases +MONDO:0015454 disease_grouping diseases +MONDO:0015454 gard_rare diseases +MONDO:0015454 nord_rare diseases +MONDO:0015454 ordo_group_of_disorders diseases +MONDO:0015454 otar diseases +MONDO:0015454 rare diseases +MONDO:0015455 gard_rare diseases +MONDO:0015455 nord_rare diseases +MONDO:0015455 ordo_disorder diseases +MONDO:0015455 orphanet_rare diseases +MONDO:0015455 rare diseases +MONDO:0015457 ordo_malformation_syndrome diseases +MONDO:0015458 gard_rare diseases +MONDO:0015458 nord_rare diseases +MONDO:0015458 ordo_disorder diseases +MONDO:0015458 ordo_malformation_syndrome diseases +MONDO:0015458 orphanet_rare diseases +MONDO:0015458 otar diseases +MONDO:0015458 rare diseases +MONDO:0015459 gard_rare diseases +MONDO:0015459 nord_rare diseases +MONDO:0015459 ordo_disorder diseases +MONDO:0015459 orphanet_rare diseases +MONDO:0015459 rare diseases +MONDO:0015461 disease_grouping diseases +MONDO:0015461 gard_rare diseases +MONDO:0015461 nord_rare diseases +MONDO:0015461 ordo_group_of_disorders diseases +MONDO:0015461 otar diseases +MONDO:0015461 rare diseases +MONDO:0015462 gard_rare diseases +MONDO:0015462 ordo_disorder diseases +MONDO:0015462 ordo_malformation_syndrome diseases +MONDO:0015462 orphanet_rare diseases +MONDO:0015462 otar diseases +MONDO:0015462 rare diseases +MONDO:0015463 gard_rare diseases +MONDO:0015463 ordo_disorder diseases +MONDO:0015463 ordo_malformation_syndrome diseases +MONDO:0015463 orphanet_rare diseases +MONDO:0015463 otar diseases +MONDO:0015463 rare diseases +MONDO:0015464 gard_rare diseases +MONDO:0015464 nord_rare diseases +MONDO:0015464 ordo_disorder diseases +MONDO:0015464 ordo_malformation_syndrome diseases +MONDO:0015464 orphanet_rare diseases +MONDO:0015464 otar diseases +MONDO:0015464 rare diseases +MONDO:0015465 gard_rare diseases +MONDO:0015465 nord_rare diseases +MONDO:0015465 ordo_disorder diseases +MONDO:0015465 ordo_malformation_syndrome diseases +MONDO:0015465 orphanet_rare diseases +MONDO:0015465 otar diseases +MONDO:0015465 rare diseases +MONDO:0015466 gard_rare diseases +MONDO:0015466 nord_rare diseases +MONDO:0015466 ordo_disorder diseases +MONDO:0015466 ordo_malformation_syndrome diseases +MONDO:0015466 orphanet_rare diseases +MONDO:0015466 otar diseases +MONDO:0015466 rare diseases +MONDO:0015467 gard_rare diseases +MONDO:0015467 nord_rare diseases +MONDO:0015467 ordo_disorder diseases +MONDO:0015467 ordo_malformation_syndrome diseases +MONDO:0015467 orphanet_rare diseases +MONDO:0015467 otar diseases +MONDO:0015467 rare diseases +MONDO:0015468 gard_rare diseases +MONDO:0015468 ordo_malformation_syndrome diseases +MONDO:0015468 rare diseases +MONDO:0015469 disease_grouping diseases +MONDO:0015469 gard_rare diseases +MONDO:0015469 ordo_group_of_disorders diseases +MONDO:0015469 otar diseases +MONDO:0015469 rare diseases +MONDO:0015471 gard_rare diseases +MONDO:0015471 nord_rare diseases +MONDO:0015471 ordo_disorder diseases +MONDO:0015471 orphanet_rare diseases +MONDO:0015471 rare diseases +MONDO:0015473 gard_rare diseases +MONDO:0015473 nord_rare diseases +MONDO:0015473 ordo_disorder diseases +MONDO:0015473 ordo_malformation_syndrome diseases +MONDO:0015473 orphanet_rare diseases +MONDO:0015473 otar diseases +MONDO:0015473 rare diseases +MONDO:0015474 otar diseases +MONDO:0015476 disease_grouping diseases +MONDO:0015476 gard_rare diseases +MONDO:0015476 ordo_group_of_disorders diseases +MONDO:0015476 rare diseases +MONDO:0015477 gard_rare diseases +MONDO:0015477 nord_rare diseases +MONDO:0015477 ordo_disorder diseases +MONDO:0015477 ordo_morphological_anomaly diseases +MONDO:0015477 orphanet_rare diseases +MONDO:0015477 rare diseases +MONDO:0015479 gard_rare diseases +MONDO:0015479 nord_rare diseases +MONDO:0015479 ordo_disorder diseases +MONDO:0015479 ordo_morphological_anomaly diseases +MONDO:0015479 orphanet_rare diseases +MONDO:0015479 rare diseases +MONDO:0015480 gard_rare diseases +MONDO:0015480 nord_rare diseases +MONDO:0015480 ordo_disorder diseases +MONDO:0015480 ordo_morphological_anomaly diseases +MONDO:0015480 orphanet_rare diseases +MONDO:0015480 rare diseases +MONDO:0015481 gard_rare diseases +MONDO:0015481 nord_rare diseases +MONDO:0015481 ordo_disorder diseases +MONDO:0015481 ordo_morphological_anomaly diseases +MONDO:0015481 orphanet_rare diseases +MONDO:0015481 rare diseases +MONDO:0015483 disease_grouping diseases +MONDO:0015483 gard_rare diseases +MONDO:0015483 nord_rare diseases +MONDO:0015483 ordo_group_of_disorders diseases +MONDO:0015483 otar diseases +MONDO:0015483 rare diseases +MONDO:0015484 gard_rare diseases +MONDO:0015484 nord_rare diseases +MONDO:0015484 ordo_disorder diseases +MONDO:0015484 orphanet_rare diseases +MONDO:0015484 otar diseases +MONDO:0015484 rare diseases +MONDO:0015486 disease_grouping diseases +MONDO:0015486 gard_rare diseases +MONDO:0015486 nord_rare diseases +MONDO:0015486 otar diseases +MONDO:0015486 rare diseases +MONDO:0015487 gard_rare diseases +MONDO:0015487 nord_rare diseases +MONDO:0015487 ordo_disorder diseases +MONDO:0015487 orphanet_rare diseases +MONDO:0015487 otar diseases +MONDO:0015487 rare diseases +MONDO:0015491 disease_grouping diseases +MONDO:0015491 gard_rare diseases +MONDO:0015491 ordo_group_of_disorders diseases +MONDO:0015491 rare diseases +MONDO:0015492 disease_grouping diseases +MONDO:0015492 gard_rare diseases +MONDO:0015492 ordo_group_of_disorders diseases +MONDO:0015492 otar diseases +MONDO:0015492 rare diseases +MONDO:0015493 gard_rare diseases +MONDO:0015493 nord_rare diseases +MONDO:0015493 otar diseases +MONDO:0015493 rare diseases +MONDO:0015494 disease_grouping diseases +MONDO:0015494 gard_rare diseases +MONDO:0015494 nord_rare diseases +MONDO:0015494 ordo_group_of_disorders diseases +MONDO:0015494 otar diseases +MONDO:0015494 rare diseases +MONDO:0015496 disease_grouping diseases +MONDO:0015496 gard_rare diseases +MONDO:0015496 ordo_group_of_disorders diseases +MONDO:0015496 otar diseases +MONDO:0015496 rare diseases +MONDO:0015498 disease_grouping diseases +MONDO:0015498 gard_rare diseases +MONDO:0015498 ordo_group_of_disorders diseases +MONDO:0015498 rare diseases +MONDO:0015500 disease_grouping diseases +MONDO:0015500 gard_rare diseases +MONDO:0015500 nord_rare diseases +MONDO:0015500 ordo_group_of_disorders diseases +MONDO:0015500 rare diseases +MONDO:0015514 disease_grouping diseases +MONDO:0015514 gard_rare diseases +MONDO:0015514 ordo_group_of_disorders diseases +MONDO:0015514 otar diseases +MONDO:0015514 rare diseases +MONDO:0015515 clingen diseases +MONDO:0015515 gard_rare diseases +MONDO:0015515 nord_rare diseases +MONDO:0015515 ordo_disorder diseases +MONDO:0015515 orphanet_rare diseases +MONDO:0015515 otar diseases +MONDO:0015515 rare diseases +MONDO:0015516 gard_rare diseases +MONDO:0015516 nord_rare diseases +MONDO:0015516 ordo_disorder diseases +MONDO:0015516 ordo_malformation_syndrome diseases +MONDO:0015516 orphanet_rare diseases +MONDO:0015516 otar diseases +MONDO:0015516 rare diseases +MONDO:0015517 clingen diseases +MONDO:0015517 gard_rare diseases +MONDO:0015517 nord_rare diseases +MONDO:0015517 ordo_disorder diseases +MONDO:0015517 orphanet_rare diseases +MONDO:0015517 otar diseases +MONDO:0015517 rare diseases +MONDO:0015518 gard_rare diseases +MONDO:0015518 nord_rare diseases +MONDO:0015518 ordo_group_of_disorders diseases +MONDO:0015518 otar diseases +MONDO:0015518 rare diseases +MONDO:0015519 gard_rare diseases +MONDO:0015519 nord_rare diseases +MONDO:0015519 ordo_subtype_of_a_disorder diseases +MONDO:0015519 otar diseases +MONDO:0015519 rare diseases +MONDO:0015520 gard_rare diseases +MONDO:0015520 nord_rare diseases +MONDO:0015520 ordo_subtype_of_a_disorder diseases +MONDO:0015520 otar diseases +MONDO:0015520 rare diseases +MONDO:0015521 gard_rare diseases +MONDO:0015521 nord_rare diseases +MONDO:0015521 ordo_subtype_of_a_disorder diseases +MONDO:0015521 otar diseases +MONDO:0015521 rare diseases +MONDO:0015523 gard_rare diseases +MONDO:0015523 nord_rare diseases +MONDO:0015523 ordo_disorder diseases +MONDO:0015523 orphanet_rare diseases +MONDO:0015523 otar diseases +MONDO:0015523 rare diseases +MONDO:0015524 gard_rare diseases +MONDO:0015524 ordo_disorder diseases +MONDO:0015524 orphanet_rare diseases +MONDO:0015524 otar diseases +MONDO:0015524 rare diseases +MONDO:0015525 gard_rare diseases +MONDO:0015525 nord_rare diseases +MONDO:0015525 ordo_disorder diseases +MONDO:0015525 ordo_morphological_anomaly diseases +MONDO:0015525 orphanet_rare diseases +MONDO:0015525 otar diseases +MONDO:0015525 rare diseases +MONDO:0015526 gard_rare diseases +MONDO:0015526 nord_rare diseases +MONDO:0015526 ordo_disorder diseases +MONDO:0015526 orphanet_rare diseases +MONDO:0015526 otar diseases +MONDO:0015526 rare diseases +MONDO:0015528 gard_rare diseases +MONDO:0015528 nord_rare diseases +MONDO:0015528 ordo_disorder diseases +MONDO:0015528 orphanet_rare diseases +MONDO:0015528 rare diseases +MONDO:0015529 gard_rare diseases +MONDO:0015529 nord_rare diseases +MONDO:0015529 ordo_disorder diseases +MONDO:0015529 orphanet_rare diseases +MONDO:0015529 otar diseases +MONDO:0015529 rare diseases +MONDO:0015530 disease_grouping diseases +MONDO:0015530 gard_rare diseases +MONDO:0015530 ordo_group_of_disorders diseases +MONDO:0015530 otar diseases +MONDO:0015530 rare diseases +MONDO:0015531 disease_grouping diseases +MONDO:0015531 gard_rare diseases +MONDO:0015531 ordo_group_of_disorders diseases +MONDO:0015531 otar diseases +MONDO:0015531 rare diseases +MONDO:0015532 gard_rare diseases +MONDO:0015532 nord_rare diseases +MONDO:0015532 ordo_disorder diseases +MONDO:0015532 orphanet_rare diseases +MONDO:0015532 rare diseases +MONDO:0015533 gard_rare diseases +MONDO:0015533 nord_rare diseases +MONDO:0015533 ordo_disorder diseases +MONDO:0015533 orphanet_rare diseases +MONDO:0015533 rare diseases +MONDO:0015534 gard_rare diseases +MONDO:0015534 nord_rare diseases +MONDO:0015534 ordo_disorder diseases +MONDO:0015534 orphanet_rare diseases +MONDO:0015534 otar diseases +MONDO:0015534 rare diseases +MONDO:0015535 gard_rare diseases +MONDO:0015535 nord_rare diseases +MONDO:0015535 ordo_disorder diseases +MONDO:0015535 orphanet_rare diseases +MONDO:0015535 rare diseases +MONDO:0015536 gard_rare diseases +MONDO:0015536 nord_rare diseases +MONDO:0015536 ordo_disorder diseases +MONDO:0015536 orphanet_rare diseases +MONDO:0015536 rare diseases +MONDO:0015537 gard_rare diseases +MONDO:0015537 nord_rare diseases +MONDO:0015537 ordo_disorder diseases +MONDO:0015537 orphanet_rare diseases +MONDO:0015537 otar diseases +MONDO:0015537 rare diseases +MONDO:0015538 gard_rare diseases +MONDO:0015538 nord_rare diseases +MONDO:0015538 ordo_disorder diseases +MONDO:0015538 orphanet_rare diseases +MONDO:0015538 rare diseases +MONDO:0015539 gard_rare diseases +MONDO:0015539 nord_rare diseases +MONDO:0015539 ordo_disorder diseases +MONDO:0015539 orphanet_rare diseases +MONDO:0015539 rare diseases +MONDO:0015540 disease_grouping diseases +MONDO:0015540 gard_rare diseases +MONDO:0015540 nord_rare diseases +MONDO:0015540 ordo_group_of_disorders diseases +MONDO:0015540 otar diseases +MONDO:0015540 rare diseases +MONDO:0015541 disease_grouping diseases +MONDO:0015541 gard_rare diseases +MONDO:0015541 nord_rare diseases +MONDO:0015541 ordo_disorder diseases +MONDO:0015541 orphanet_rare diseases +MONDO:0015541 otar diseases +MONDO:0015541 rare diseases +MONDO:0015542 disease_grouping diseases +MONDO:0015542 gard_rare diseases +MONDO:0015542 ordo_group_of_disorders diseases +MONDO:0015542 otar diseases +MONDO:0015542 rare diseases +MONDO:0015544 gard_rare diseases +MONDO:0015544 nord_rare diseases +MONDO:0015544 ordo_clinical_situation diseases +MONDO:0015544 ordo_disorder diseases +MONDO:0015544 orphanet_rare diseases +MONDO:0015544 rare diseases +MONDO:0015545 gard_rare diseases +MONDO:0015545 nord_rare diseases +MONDO:0015545 ordo_clinical_syndrome diseases +MONDO:0015545 ordo_disorder diseases +MONDO:0015545 orphanet_rare diseases +MONDO:0015545 otar diseases +MONDO:0015545 rare diseases +MONDO:0015546 gard_rare diseases +MONDO:0015546 nord_rare diseases +MONDO:0015546 ordo_disorder diseases +MONDO:0015546 ordo_malformation_syndrome diseases +MONDO:0015546 orphanet_rare diseases +MONDO:0015546 otar diseases +MONDO:0015546 rare diseases +MONDO:0015547 disease_grouping diseases +MONDO:0015547 gard_rare diseases +MONDO:0015547 ordo_group_of_disorders diseases +MONDO:0015547 otar diseases +MONDO:0015547 rare diseases +MONDO:0015548 disease_grouping diseases +MONDO:0015548 gard_rare diseases +MONDO:0015548 ordo_group_of_disorders diseases +MONDO:0015548 otar diseases +MONDO:0015548 rare diseases +MONDO:0015550 disease_grouping diseases +MONDO:0015550 gard_rare diseases +MONDO:0015550 rare diseases +MONDO:0015552 gard_rare diseases +MONDO:0015552 nord_rare diseases +MONDO:0015552 ordo_subtype_of_a_disorder diseases +MONDO:0015552 otar diseases +MONDO:0015552 rare diseases +MONDO:0015553 gard_rare diseases +MONDO:0015553 nord_rare diseases +MONDO:0015553 ordo_subtype_of_a_disorder diseases +MONDO:0015553 otar diseases +MONDO:0015553 rare diseases +MONDO:0015554 gard_rare diseases +MONDO:0015554 nord_rare diseases +MONDO:0015554 ordo_subtype_of_a_disorder diseases +MONDO:0015554 rare diseases +MONDO:0015555 gard_rare diseases +MONDO:0015555 nord_rare diseases +MONDO:0015555 ordo_subtype_of_a_disorder diseases +MONDO:0015555 rare diseases +MONDO:0015556 gard_rare diseases +MONDO:0015556 nord_rare diseases +MONDO:0015556 ordo_subtype_of_a_disorder diseases +MONDO:0015556 rare diseases +MONDO:0015557 gard_rare diseases +MONDO:0015557 nord_rare diseases +MONDO:0015557 ordo_disorder diseases +MONDO:0015557 orphanet_rare diseases +MONDO:0015557 rare diseases +MONDO:0015558 gard_rare diseases +MONDO:0015558 nord_rare diseases +MONDO:0015558 ordo_disorder diseases +MONDO:0015558 orphanet_rare diseases +MONDO:0015558 rare diseases +MONDO:0015559 gard_rare diseases +MONDO:0015559 rare diseases +MONDO:0015562 gard_rare diseases +MONDO:0015562 nord_rare diseases +MONDO:0015562 ordo_disorder diseases +MONDO:0015562 ordo_malformation_syndrome diseases +MONDO:0015562 orphanet_rare diseases +MONDO:0015562 otar diseases +MONDO:0015562 rare diseases +MONDO:0015564 gard_rare diseases +MONDO:0015564 nord_rare diseases +MONDO:0015564 ordo_disorder diseases +MONDO:0015564 orphanet_rare diseases +MONDO:0015564 otar diseases +MONDO:0015564 rare diseases +MONDO:0015565 gard_rare diseases +MONDO:0015565 nord_rare diseases +MONDO:0015565 ordo_disorder diseases +MONDO:0015565 orphanet_rare diseases +MONDO:0015565 rare diseases +MONDO:0015566 gard_rare diseases +MONDO:0015566 nord_rare diseases +MONDO:0015566 ordo_disorder diseases +MONDO:0015566 ordo_malformation_syndrome diseases +MONDO:0015566 orphanet_rare diseases +MONDO:0015566 otar diseases +MONDO:0015566 rare diseases +MONDO:0015567 gard_rare diseases +MONDO:0015567 nord_rare diseases +MONDO:0015567 ordo_disorder diseases +MONDO:0015567 ordo_malformation_syndrome diseases +MONDO:0015567 orphanet_rare diseases +MONDO:0015567 otar diseases +MONDO:0015567 rare diseases +MONDO:0015568 gard_rare diseases +MONDO:0015568 nord_rare diseases +MONDO:0015568 ordo_disorder diseases +MONDO:0015568 ordo_malformation_syndrome diseases +MONDO:0015568 orphanet_rare diseases +MONDO:0015568 rare diseases +MONDO:0015569 ordo_malformation_syndrome diseases +MONDO:0015570 gard_rare diseases +MONDO:0015570 nord_rare diseases +MONDO:0015570 ordo_disorder diseases +MONDO:0015570 ordo_morphological_anomaly diseases +MONDO:0015570 orphanet_rare diseases +MONDO:0015570 rare diseases +MONDO:0015571 gard_rare diseases +MONDO:0015571 nord_rare diseases +MONDO:0015571 ordo_disorder diseases +MONDO:0015571 ordo_malformation_syndrome diseases +MONDO:0015571 orphanet_rare diseases +MONDO:0015571 rare diseases +MONDO:0015573 gard_rare diseases +MONDO:0015573 nord_rare diseases +MONDO:0015573 ordo_disorder diseases +MONDO:0015573 orphanet_rare diseases +MONDO:0015573 rare diseases +MONDO:0015574 disease_grouping diseases +MONDO:0015574 gard_rare diseases +MONDO:0015574 nord_rare diseases +MONDO:0015574 ordo_group_of_disorders diseases +MONDO:0015574 otar diseases +MONDO:0015574 rare diseases +MONDO:0015579 gard_rare diseases +MONDO:0015579 nord_rare diseases +MONDO:0015579 ordo_subtype_of_a_disorder diseases +MONDO:0015579 otar diseases +MONDO:0015579 rare diseases +MONDO:0015580 gard_rare diseases +MONDO:0015580 nord_rare diseases +MONDO:0015580 ordo_disorder diseases +MONDO:0015580 ordo_malformation_syndrome diseases +MONDO:0015580 orphanet_rare diseases +MONDO:0015580 otar diseases +MONDO:0015580 rare diseases +MONDO:0015583 gard_rare diseases +MONDO:0015583 nord_rare diseases +MONDO:0015583 ordo_disorder diseases +MONDO:0015583 orphanet_rare diseases +MONDO:0015583 otar diseases +MONDO:0015583 rare diseases +MONDO:0015584 gard_rare diseases +MONDO:0015584 nord_rare diseases +MONDO:0015584 ordo_disorder diseases +MONDO:0015584 orphanet_rare diseases +MONDO:0015584 rare diseases +MONDO:0015585 gard_rare diseases +MONDO:0015585 nord_rare diseases +MONDO:0015585 ordo_disorder diseases +MONDO:0015585 orphanet_rare diseases +MONDO:0015585 rare diseases +MONDO:0015587 gard_rare diseases +MONDO:0015587 nord_rare diseases +MONDO:0015587 ordo_disorder diseases +MONDO:0015587 orphanet_rare diseases +MONDO:0015587 otar diseases +MONDO:0015587 rare diseases +MONDO:0015588 disease_grouping diseases +MONDO:0015588 gard_rare diseases +MONDO:0015588 nord_rare diseases +MONDO:0015588 rare diseases +MONDO:0015589 disease_grouping diseases +MONDO:0015589 gard_rare diseases +MONDO:0015589 rare diseases +MONDO:0015590 gard_rare diseases +MONDO:0015590 rare diseases +MONDO:0015592 gard_rare diseases +MONDO:0015592 rare diseases +MONDO:0015595 gard_rare diseases +MONDO:0015595 nord_rare diseases +MONDO:0015595 ordo_clinical_situation diseases +MONDO:0015595 ordo_disorder diseases +MONDO:0015595 orphanet_rare diseases +MONDO:0015595 rare diseases +MONDO:0015596 gard_rare diseases +MONDO:0015596 rare diseases +MONDO:0015597 gard_rare diseases +MONDO:0015597 nord_rare diseases +MONDO:0015597 ordo_disorder diseases +MONDO:0015597 orphanet_rare diseases +MONDO:0015597 otar diseases +MONDO:0015597 rare diseases +MONDO:0015599 gard_rare diseases +MONDO:0015599 nord_rare diseases +MONDO:0015599 ordo_disorder diseases +MONDO:0015599 orphanet_rare diseases +MONDO:0015599 rare diseases +MONDO:0015600 gard_rare diseases +MONDO:0015600 nord_rare diseases +MONDO:0015600 ordo_disorder diseases +MONDO:0015600 orphanet_rare diseases +MONDO:0015600 otar diseases +MONDO:0015600 rare diseases +MONDO:0015601 gard_rare diseases +MONDO:0015601 nord_rare diseases +MONDO:0015601 ordo_disorder diseases +MONDO:0015601 ordo_malformation_syndrome diseases +MONDO:0015601 orphanet_rare diseases +MONDO:0015601 otar diseases +MONDO:0015601 rare diseases +MONDO:0015604 disease_grouping diseases +MONDO:0015604 gard_rare diseases +MONDO:0015604 ordo_group_of_disorders diseases +MONDO:0015604 rare diseases +MONDO:0015605 gard_rare diseases +MONDO:0015605 nord_rare diseases +MONDO:0015605 ordo_disorder diseases +MONDO:0015605 ordo_malformation_syndrome diseases +MONDO:0015605 orphanet_rare diseases +MONDO:0015605 otar diseases +MONDO:0015605 rare diseases +MONDO:0015606 gard_rare diseases +MONDO:0015606 nord_rare diseases +MONDO:0015606 ordo_disorder diseases +MONDO:0015606 ordo_malformation_syndrome diseases +MONDO:0015606 orphanet_rare diseases +MONDO:0015606 otar diseases +MONDO:0015606 rare diseases +MONDO:0015607 gard_rare diseases +MONDO:0015607 nord_rare diseases +MONDO:0015607 ordo_disorder diseases +MONDO:0015607 ordo_malformation_syndrome diseases +MONDO:0015607 orphanet_rare diseases +MONDO:0015607 otar diseases +MONDO:0015607 rare diseases +MONDO:0015608 gard_rare diseases +MONDO:0015608 nord_rare diseases +MONDO:0015608 ordo_disorder diseases +MONDO:0015608 orphanet_rare diseases +MONDO:0015608 rare diseases +MONDO:0015609 gard_rare diseases +MONDO:0015609 nord_rare diseases +MONDO:0015609 ordo_disorder diseases +MONDO:0015609 orphanet_rare diseases +MONDO:0015609 otar diseases +MONDO:0015609 rare diseases +MONDO:0015610 disease_grouping diseases +MONDO:0015610 gard_rare diseases +MONDO:0015610 ordo_group_of_disorders diseases +MONDO:0015610 rare diseases +MONDO:0015611 disease_grouping diseases +MONDO:0015611 gard_rare diseases +MONDO:0015611 ordo_group_of_disorders diseases +MONDO:0015611 otar diseases +MONDO:0015611 rare diseases +MONDO:0015612 gard_rare diseases +MONDO:0015612 nord_rare diseases +MONDO:0015612 ordo_disorder diseases +MONDO:0015612 orphanet_rare diseases +MONDO:0015612 otar diseases +MONDO:0015612 rare diseases +MONDO:0015613 gard_rare diseases +MONDO:0015613 ordo_disorder diseases +MONDO:0015613 orphanet_rare diseases +MONDO:0015613 otar diseases +MONDO:0015613 rare diseases +MONDO:0015614 gard_rare diseases +MONDO:0015614 ordo_disorder diseases +MONDO:0015614 orphanet_rare diseases +MONDO:0015614 otar diseases +MONDO:0015614 rare diseases +MONDO:0015622 gard_rare diseases +MONDO:0015622 nord_rare diseases +MONDO:0015622 ordo_disorder diseases +MONDO:0015622 orphanet_rare diseases +MONDO:0015622 rare diseases +MONDO:0015623 gard_rare diseases +MONDO:0015623 nord_rare diseases +MONDO:0015623 ordo_disorder diseases +MONDO:0015623 orphanet_rare diseases +MONDO:0015623 rare diseases +MONDO:0015624 disease_grouping diseases +MONDO:0015624 gard_rare diseases +MONDO:0015624 ordo_group_of_disorders diseases +MONDO:0015624 rare diseases +MONDO:0015625 disease_grouping diseases +MONDO:0015625 gard_rare diseases +MONDO:0015625 nord_rare diseases +MONDO:0015625 ordo_group_of_disorders diseases +MONDO:0015625 rare diseases +MONDO:0015626 clingen diseases +MONDO:0015626 disease_grouping diseases +MONDO:0015626 gard_rare diseases +MONDO:0015626 nord_rare diseases +MONDO:0015626 ordo_group_of_disorders diseases +MONDO:0015626 otar diseases +MONDO:0015626 rare diseases +MONDO:0015627 gard_rare diseases +MONDO:0015627 nord_rare diseases +MONDO:0015627 ordo_disorder diseases +MONDO:0015627 orphanet_rare diseases +MONDO:0015627 otar diseases +MONDO:0015627 rare diseases +MONDO:0015628 gard_rare diseases +MONDO:0015628 nord_rare diseases +MONDO:0015628 ordo_subtype_of_a_disorder diseases +MONDO:0015628 otar diseases +MONDO:0015628 rare diseases +MONDO:0015629 clingen diseases +MONDO:0015629 gard_rare diseases +MONDO:0015629 nord_rare diseases +MONDO:0015629 ordo_subtype_of_a_disorder diseases +MONDO:0015629 otar diseases +MONDO:0015629 rare diseases +MONDO:0015630 gard_rare diseases +MONDO:0015630 nord_rare diseases +MONDO:0015630 ordo_subtype_of_a_disorder diseases +MONDO:0015630 otar diseases +MONDO:0015630 rare diseases +MONDO:0015631 gard_rare diseases +MONDO:0015631 nord_rare diseases +MONDO:0015631 ordo_subtype_of_a_disorder diseases +MONDO:0015631 otar diseases +MONDO:0015631 rare diseases +MONDO:0015632 gard_rare diseases +MONDO:0015632 nord_rare diseases +MONDO:0015632 ordo_disorder diseases +MONDO:0015632 orphanet_rare diseases +MONDO:0015632 otar diseases +MONDO:0015632 rare diseases +MONDO:0015634 gard_rare diseases +MONDO:0015634 nord_rare diseases +MONDO:0015634 ordo_disorder diseases +MONDO:0015634 orphanet_rare diseases +MONDO:0015634 otar diseases +MONDO:0015634 rare diseases +MONDO:0015635 gard_rare diseases +MONDO:0015635 nord_rare diseases +MONDO:0015635 ordo_disorder diseases +MONDO:0015635 orphanet_rare diseases +MONDO:0015635 otar diseases +MONDO:0015635 rare diseases +MONDO:0015636 gard_rare diseases +MONDO:0015636 nord_rare diseases +MONDO:0015636 ordo_disorder diseases +MONDO:0015636 orphanet_rare diseases +MONDO:0015636 otar diseases +MONDO:0015636 rare diseases +MONDO:0015637 disease_grouping diseases +MONDO:0015637 gard_rare diseases +MONDO:0015637 nord_rare diseases +MONDO:0015637 ordo_group_of_disorders diseases +MONDO:0015637 rare diseases +MONDO:0015638 gard_rare diseases +MONDO:0015638 nord_rare diseases +MONDO:0015638 ordo_disorder diseases +MONDO:0015638 orphanet_rare diseases +MONDO:0015638 rare diseases +MONDO:0015639 gard_rare diseases +MONDO:0015639 nord_rare diseases +MONDO:0015639 ordo_disorder diseases +MONDO:0015639 orphanet_rare diseases +MONDO:0015639 rare diseases +MONDO:0015640 gard_rare diseases +MONDO:0015640 nord_rare diseases +MONDO:0015640 ordo_disorder diseases +MONDO:0015640 orphanet_rare diseases +MONDO:0015640 rare diseases +MONDO:0015641 gard_rare diseases +MONDO:0015641 nord_rare diseases +MONDO:0015641 ordo_disorder diseases +MONDO:0015641 orphanet_rare diseases +MONDO:0015641 rare diseases +MONDO:0015642 disease_grouping diseases +MONDO:0015642 gard_rare diseases +MONDO:0015642 nord_rare diseases +MONDO:0015642 ordo_group_of_disorders diseases +MONDO:0015642 rare diseases +MONDO:0015643 gard_rare diseases +MONDO:0015643 nord_rare diseases +MONDO:0015643 ordo_disorder diseases +MONDO:0015643 orphanet_rare diseases +MONDO:0015643 otar diseases +MONDO:0015643 rare diseases +MONDO:0015644 gard_rare diseases +MONDO:0015644 nord_rare diseases +MONDO:0015644 ordo_disorder diseases +MONDO:0015644 orphanet_rare diseases +MONDO:0015644 rare diseases +MONDO:0015645 gard_rare diseases +MONDO:0015645 nord_rare diseases +MONDO:0015645 ordo_disorder diseases +MONDO:0015645 orphanet_rare diseases +MONDO:0015645 rare diseases +MONDO:0015646 gard_rare diseases +MONDO:0015646 nord_rare diseases +MONDO:0015646 ordo_disorder diseases +MONDO:0015646 orphanet_rare diseases +MONDO:0015646 rare diseases +MONDO:0015647 gard_rare diseases +MONDO:0015647 nord_rare diseases +MONDO:0015647 ordo_disorder diseases +MONDO:0015647 orphanet_rare diseases +MONDO:0015647 rare diseases +MONDO:0015648 gard_rare diseases +MONDO:0015648 nord_rare diseases +MONDO:0015648 ordo_disorder diseases +MONDO:0015648 orphanet_rare diseases +MONDO:0015648 rare diseases +MONDO:0015649 gard_rare diseases +MONDO:0015649 nord_rare diseases +MONDO:0015649 ordo_disorder diseases +MONDO:0015649 orphanet_rare diseases +MONDO:0015649 rare diseases +MONDO:0015650 disease_grouping diseases +MONDO:0015650 gard_rare diseases +MONDO:0015650 ordo_group_of_disorders diseases +MONDO:0015650 otar diseases +MONDO:0015650 rare diseases +MONDO:0015653 disease_grouping diseases +MONDO:0015653 gard_rare diseases +MONDO:0015653 ordo_group_of_disorders diseases +MONDO:0015653 rare diseases +MONDO:0015660 gard_rare diseases +MONDO:0015660 nord_rare diseases +MONDO:0015660 ordo_disorder diseases +MONDO:0015660 ordo_malformation_syndrome diseases +MONDO:0015660 orphanet_rare diseases +MONDO:0015660 otar diseases +MONDO:0015660 rare diseases +MONDO:0015661 gard_rare diseases +MONDO:0015661 nord_rare diseases +MONDO:0015661 ordo_disorder diseases +MONDO:0015661 ordo_morphological_anomaly diseases +MONDO:0015661 orphanet_rare diseases +MONDO:0015661 rare diseases +MONDO:0015663 gard_rare diseases +MONDO:0015663 nord_rare diseases +MONDO:0015663 ordo_disorder diseases +MONDO:0015663 orphanet_rare diseases +MONDO:0015663 rare diseases +MONDO:0015664 gard_rare diseases +MONDO:0015664 nord_rare diseases +MONDO:0015664 ordo_disorder diseases +MONDO:0015664 orphanet_rare diseases +MONDO:0015664 rare diseases +MONDO:0015665 gard_rare diseases +MONDO:0015665 nord_rare diseases +MONDO:0015665 ordo_disorder diseases +MONDO:0015665 orphanet_rare diseases +MONDO:0015665 rare diseases +MONDO:0015666 gard_rare diseases +MONDO:0015666 nord_rare diseases +MONDO:0015666 ordo_disorder diseases +MONDO:0015666 ordo_morphological_anomaly diseases +MONDO:0015666 orphanet_rare diseases +MONDO:0015666 otar diseases +MONDO:0015666 rare diseases +MONDO:0015667 disease_grouping diseases +MONDO:0015667 gard_rare diseases +MONDO:0015667 ordo_group_of_disorders diseases +MONDO:0015667 otar diseases +MONDO:0015667 rare diseases +MONDO:0015672 gard_rare diseases +MONDO:0015672 ordo_disorder diseases +MONDO:0015672 ordo_morphological_anomaly diseases +MONDO:0015672 orphanet_rare diseases +MONDO:0015672 rare diseases +MONDO:0015674 gard_rare diseases +MONDO:0015674 nord_rare diseases +MONDO:0015674 ordo_disorder diseases +MONDO:0015674 orphanet_rare diseases +MONDO:0015674 otar diseases +MONDO:0015674 rare diseases +MONDO:0015675 gard_rare diseases +MONDO:0015675 nord_rare diseases +MONDO:0015675 ordo_group_of_disorders diseases +MONDO:0015675 rare diseases +MONDO:0015677 gard_rare diseases +MONDO:0015677 nord_rare diseases +MONDO:0015677 ordo_disorder diseases +MONDO:0015677 ordo_morphological_anomaly diseases +MONDO:0015677 orphanet_rare diseases +MONDO:0015677 rare diseases +MONDO:0015678 gard_rare diseases +MONDO:0015678 nord_rare diseases +MONDO:0015678 ordo_disorder diseases +MONDO:0015678 orphanet_rare diseases +MONDO:0015678 otar diseases +MONDO:0015678 rare diseases +MONDO:0015681 gard_rare diseases +MONDO:0015681 nord_rare diseases +MONDO:0015681 ordo_disorder diseases +MONDO:0015681 orphanet_rare diseases +MONDO:0015681 otar diseases +MONDO:0015681 rare diseases +MONDO:0015686 gard_rare diseases +MONDO:0015686 nord_rare diseases +MONDO:0015686 ordo_disorder diseases +MONDO:0015686 orphanet_rare diseases +MONDO:0015686 otar diseases +MONDO:0015686 rare diseases +MONDO:0015687 gard_rare diseases +MONDO:0015687 nord_rare diseases +MONDO:0015687 ordo_disorder diseases +MONDO:0015687 orphanet_rare diseases +MONDO:0015687 rare diseases +MONDO:0015688 disease_grouping diseases +MONDO:0015688 gard_rare diseases +MONDO:0015688 nord_rare diseases +MONDO:0015688 ordo_group_of_disorders diseases +MONDO:0015688 rare diseases +MONDO:0015689 gard_rare diseases +MONDO:0015689 ordo_disorder diseases +MONDO:0015689 orphanet_rare diseases +MONDO:0015689 rare diseases +MONDO:0015690 gard_rare diseases +MONDO:0015690 nord_rare diseases +MONDO:0015690 ordo_disorder diseases +MONDO:0015690 orphanet_rare diseases +MONDO:0015690 rare diseases +MONDO:0015691 disease_grouping diseases +MONDO:0015691 gard_rare diseases +MONDO:0015691 nord_rare diseases +MONDO:0015691 ordo_group_of_disorders diseases +MONDO:0015691 otar diseases +MONDO:0015691 rare diseases +MONDO:0015692 gard_rare diseases +MONDO:0015692 nord_rare diseases +MONDO:0015692 ordo_disorder diseases +MONDO:0015692 orphanet_rare diseases +MONDO:0015692 rare diseases +MONDO:0015694 gard_rare diseases +MONDO:0015694 nord_rare diseases +MONDO:0015694 ordo_disorder diseases +MONDO:0015694 orphanet_rare diseases +MONDO:0015694 rare diseases +MONDO:0015695 gard_rare diseases +MONDO:0015695 nord_rare diseases +MONDO:0015695 ordo_disorder diseases +MONDO:0015695 orphanet_rare diseases +MONDO:0015695 otar diseases +MONDO:0015695 rare diseases +MONDO:0015696 gard_rare diseases +MONDO:0015696 nord_rare diseases +MONDO:0015696 ordo_disorder diseases +MONDO:0015696 orphanet_rare diseases +MONDO:0015696 rare diseases +MONDO:0015697 gard_rare diseases +MONDO:0015697 nord_rare diseases +MONDO:0015697 ordo_disorder diseases +MONDO:0015697 orphanet_rare diseases +MONDO:0015697 rare diseases +MONDO:0015698 gard_rare diseases +MONDO:0015698 nord_rare diseases +MONDO:0015698 ordo_disorder diseases +MONDO:0015698 orphanet_rare diseases +MONDO:0015698 rare diseases +MONDO:0015699 gard_rare diseases +MONDO:0015699 ordo_disorder diseases +MONDO:0015699 orphanet_rare diseases +MONDO:0015699 otar diseases +MONDO:0015699 rare diseases +MONDO:0015700 gard_rare diseases +MONDO:0015700 nord_rare diseases +MONDO:0015700 ordo_disorder diseases +MONDO:0015700 orphanet_rare diseases +MONDO:0015700 otar diseases +MONDO:0015700 rare diseases +MONDO:0015701 gard_rare diseases +MONDO:0015701 nord_rare diseases +MONDO:0015701 ordo_disorder diseases +MONDO:0015701 orphanet_rare diseases +MONDO:0015701 otar diseases +MONDO:0015701 rare diseases +MONDO:0015702 gard_rare diseases +MONDO:0015702 nord_rare diseases +MONDO:0015702 ordo_disorder diseases +MONDO:0015702 orphanet_rare diseases +MONDO:0015702 otar diseases +MONDO:0015702 rare diseases +MONDO:0015703 gard_rare diseases +MONDO:0015703 nord_rare diseases +MONDO:0015703 ordo_disorder diseases +MONDO:0015703 orphanet_rare diseases +MONDO:0015703 otar diseases +MONDO:0015703 rare diseases +MONDO:0015704 disease_grouping diseases +MONDO:0015704 gard_rare diseases +MONDO:0015704 nord_rare diseases +MONDO:0015704 ordo_group_of_disorders diseases +MONDO:0015704 otar diseases +MONDO:0015704 rare diseases +MONDO:0015705 gard_rare diseases +MONDO:0015705 nord_rare diseases +MONDO:0015705 ordo_disorder diseases +MONDO:0015705 orphanet_rare diseases +MONDO:0015705 otar diseases +MONDO:0015705 rare diseases +MONDO:0015706 gard_rare diseases +MONDO:0015706 nord_rare diseases +MONDO:0015706 ordo_disorder diseases +MONDO:0015706 ordo_malformation_syndrome diseases +MONDO:0015706 orphanet_rare diseases +MONDO:0015706 otar diseases +MONDO:0015706 rare diseases +MONDO:0015708 disease_grouping diseases +MONDO:0015708 gard_rare diseases +MONDO:0015708 ordo_group_of_disorders diseases +MONDO:0015708 otar diseases +MONDO:0015708 rare diseases +MONDO:0015712 gard_rare diseases +MONDO:0015712 nord_rare diseases +MONDO:0015712 ordo_disorder diseases +MONDO:0015712 ordo_malformation_syndrome diseases +MONDO:0015712 orphanet_rare diseases +MONDO:0015712 otar diseases +MONDO:0015712 rare diseases +MONDO:0015713 inferred_rare diseases +MONDO:0015713 ordo_etiological_subtype diseases +MONDO:0015713 otar diseases +MONDO:0015713 rare diseases +MONDO:0015714 inferred_rare diseases +MONDO:0015714 ordo_etiological_subtype diseases +MONDO:0015714 rare diseases +MONDO:0015715 gard_rare diseases +MONDO:0015715 nord_rare diseases +MONDO:0015715 ordo_subtype_of_a_disorder diseases +MONDO:0015715 otar diseases +MONDO:0015715 rare diseases +MONDO:0015716 gard_rare diseases +MONDO:0015716 nord_rare diseases +MONDO:0015716 ordo_subtype_of_a_disorder diseases +MONDO:0015716 otar diseases +MONDO:0015716 rare diseases +MONDO:0015717 gard_rare diseases +MONDO:0015717 nord_rare diseases +MONDO:0015717 ordo_subtype_of_a_disorder diseases +MONDO:0015717 otar diseases +MONDO:0015717 rare diseases +MONDO:0015718 gard_rare diseases +MONDO:0015718 nord_rare diseases +MONDO:0015718 ordo_disorder diseases +MONDO:0015718 ordo_malformation_syndrome diseases +MONDO:0015718 orphanet_rare diseases +MONDO:0015718 rare diseases +MONDO:0015719 gard_rare diseases +MONDO:0015719 nord_rare diseases +MONDO:0015719 ordo_subtype_of_a_disorder diseases +MONDO:0015719 otar diseases +MONDO:0015719 rare diseases +MONDO:0015720 gard_rare diseases +MONDO:0015720 nord_rare diseases +MONDO:0015720 ordo_subtype_of_a_disorder diseases +MONDO:0015720 otar diseases +MONDO:0015720 rare diseases +MONDO:0015721 gard_rare diseases +MONDO:0015721 nord_rare diseases +MONDO:0015721 ordo_subtype_of_a_disorder diseases +MONDO:0015721 otar diseases +MONDO:0015721 rare diseases +MONDO:0015722 disease_grouping diseases +MONDO:0015722 gard_rare diseases +MONDO:0015722 ordo_disorder diseases +MONDO:0015722 ordo_group_of_disorders diseases +MONDO:0015722 orphanet_rare diseases +MONDO:0015722 rare diseases +MONDO:0015723 gard_rare diseases +MONDO:0015723 nord_rare diseases +MONDO:0015723 ordo_disorder diseases +MONDO:0015723 ordo_malformation_syndrome diseases +MONDO:0015723 orphanet_rare diseases +MONDO:0015723 otar diseases +MONDO:0015723 rare diseases +MONDO:0015724 gard_rare diseases +MONDO:0015724 nord_rare diseases +MONDO:0015724 ordo_disorder diseases +MONDO:0015724 ordo_malformation_syndrome diseases +MONDO:0015724 orphanet_rare diseases +MONDO:0015724 otar diseases +MONDO:0015724 rare diseases +MONDO:0015725 gard_rare diseases +MONDO:0015725 nord_rare diseases +MONDO:0015725 ordo_disorder diseases +MONDO:0015725 ordo_malformation_syndrome diseases +MONDO:0015725 orphanet_rare diseases +MONDO:0015725 otar diseases +MONDO:0015725 rare diseases +MONDO:0015726 gard_rare diseases +MONDO:0015726 nord_rare diseases +MONDO:0015726 ordo_disorder diseases +MONDO:0015726 ordo_malformation_syndrome diseases +MONDO:0015726 orphanet_rare diseases +MONDO:0015726 otar diseases +MONDO:0015726 rare diseases +MONDO:0015727 gard_rare diseases +MONDO:0015727 nord_rare diseases +MONDO:0015727 ordo_disorder diseases +MONDO:0015727 ordo_malformation_syndrome diseases +MONDO:0015727 orphanet_rare diseases +MONDO:0015727 otar diseases +MONDO:0015727 rare diseases +MONDO:0015728 gard_rare diseases +MONDO:0015728 nord_rare diseases +MONDO:0015728 ordo_etiological_subtype diseases +MONDO:0015728 ordo_subtype_of_a_disorder diseases +MONDO:0015728 otar diseases +MONDO:0015728 rare diseases +MONDO:0015729 gard_rare diseases +MONDO:0015729 nord_rare diseases +MONDO:0015729 ordo_disorder diseases +MONDO:0015729 ordo_malformation_syndrome diseases +MONDO:0015729 orphanet_rare diseases +MONDO:0015729 otar diseases +MONDO:0015729 rare diseases +MONDO:0015730 gard_rare diseases +MONDO:0015730 nord_rare diseases +MONDO:0015730 ordo_disorder diseases +MONDO:0015730 ordo_malformation_syndrome diseases +MONDO:0015730 orphanet_rare diseases +MONDO:0015730 otar diseases +MONDO:0015730 rare diseases +MONDO:0015734 gard_rare diseases +MONDO:0015734 nord_rare diseases +MONDO:0015734 ordo_disorder diseases +MONDO:0015734 ordo_morphological_anomaly diseases +MONDO:0015734 orphanet_rare diseases +MONDO:0015734 rare diseases +MONDO:0015735 gard_rare diseases +MONDO:0015735 nord_rare diseases +MONDO:0015735 ordo_disorder diseases +MONDO:0015735 orphanet_rare diseases +MONDO:0015735 otar diseases +MONDO:0015735 rare diseases +MONDO:0015736 gard_rare diseases +MONDO:0015736 nord_rare diseases +MONDO:0015736 ordo_disorder diseases +MONDO:0015736 orphanet_rare diseases +MONDO:0015736 otar diseases +MONDO:0015736 rare diseases +MONDO:0015737 gard_rare diseases +MONDO:0015737 nord_rare diseases +MONDO:0015737 ordo_disorder diseases +MONDO:0015737 orphanet_rare diseases +MONDO:0015737 otar diseases +MONDO:0015737 rare diseases +MONDO:0015738 gard_rare diseases +MONDO:0015738 nord_rare diseases +MONDO:0015738 ordo_disorder diseases +MONDO:0015738 orphanet_rare diseases +MONDO:0015738 otar diseases +MONDO:0015738 rare diseases +MONDO:0015739 gard_rare diseases +MONDO:0015739 nord_rare diseases +MONDO:0015739 ordo_disorder diseases +MONDO:0015739 orphanet_rare diseases +MONDO:0015739 otar diseases +MONDO:0015739 rare diseases +MONDO:0015740 gard_rare diseases +MONDO:0015740 nord_rare diseases +MONDO:0015740 ordo_disorder diseases +MONDO:0015740 ordo_malformation_syndrome diseases +MONDO:0015740 orphanet_rare diseases +MONDO:0015740 otar diseases +MONDO:0015740 rare diseases +MONDO:0015741 gard_rare diseases +MONDO:0015741 nord_rare diseases +MONDO:0015741 ordo_disorder diseases +MONDO:0015741 ordo_malformation_syndrome diseases +MONDO:0015741 orphanet_rare diseases +MONDO:0015741 otar diseases +MONDO:0015741 rare diseases +MONDO:0015742 otar diseases +MONDO:0015743 gard_rare diseases +MONDO:0015743 nord_rare diseases +MONDO:0015743 ordo_disorder diseases +MONDO:0015743 orphanet_rare diseases +MONDO:0015743 rare diseases +MONDO:0015744 gard_rare diseases +MONDO:0015744 nord_rare diseases +MONDO:0015744 ordo_disorder diseases +MONDO:0015744 ordo_malformation_syndrome diseases +MONDO:0015744 orphanet_rare diseases +MONDO:0015744 rare diseases +MONDO:0015745 gard_rare diseases +MONDO:0015745 nord_rare diseases +MONDO:0015745 ordo_disorder diseases +MONDO:0015745 ordo_malformation_syndrome diseases +MONDO:0015745 orphanet_rare diseases +MONDO:0015745 otar diseases +MONDO:0015745 rare diseases +MONDO:0015746 gard_rare diseases +MONDO:0015746 nord_rare diseases +MONDO:0015746 ordo_subtype_of_a_disorder diseases +MONDO:0015746 otar diseases +MONDO:0015746 rare diseases +MONDO:0015748 gard_rare diseases +MONDO:0015748 nord_rare diseases +MONDO:0015748 ordo_disorder diseases +MONDO:0015748 orphanet_rare diseases +MONDO:0015748 rare diseases +MONDO:0015749 gard_rare diseases +MONDO:0015749 nord_rare diseases +MONDO:0015749 ordo_disorder diseases +MONDO:0015749 orphanet_rare diseases +MONDO:0015749 otar diseases +MONDO:0015749 rare diseases +MONDO:0015751 gard_rare diseases +MONDO:0015751 nord_rare diseases +MONDO:0015751 ordo_disorder diseases +MONDO:0015751 ordo_malformation_syndrome diseases +MONDO:0015751 orphanet_rare diseases +MONDO:0015751 otar diseases +MONDO:0015751 rare diseases +MONDO:0015753 gard_rare diseases +MONDO:0015753 nord_rare diseases +MONDO:0015753 ordo_disorder diseases +MONDO:0015753 orphanet_rare diseases +MONDO:0015753 otar diseases +MONDO:0015753 rare diseases +MONDO:0015755 gard_rare diseases +MONDO:0015755 nord_rare diseases +MONDO:0015755 ordo_disorder diseases +MONDO:0015755 orphanet_rare diseases +MONDO:0015755 rare diseases +MONDO:0015756 disease_grouping diseases +MONDO:0015756 gard_rare diseases +MONDO:0015756 ordo_group_of_disorders diseases +MONDO:0015756 otar diseases +MONDO:0015756 rare diseases +MONDO:0015757 disease_grouping diseases +MONDO:0015757 gard_rare diseases +MONDO:0015757 ordo_group_of_disorders diseases +MONDO:0015757 rare diseases +MONDO:0015758 disease_grouping diseases +MONDO:0015758 gard_rare diseases +MONDO:0015758 nord_rare diseases +MONDO:0015758 ordo_group_of_disorders diseases +MONDO:0015758 otar diseases +MONDO:0015758 rare diseases +MONDO:0015759 disease_grouping diseases +MONDO:0015759 gard_rare diseases +MONDO:0015759 nord_rare diseases +MONDO:0015759 ordo_group_of_disorders diseases +MONDO:0015759 otar diseases +MONDO:0015759 rare diseases +MONDO:0015760 disease_grouping diseases +MONDO:0015760 gard_rare diseases +MONDO:0015760 nord_rare diseases +MONDO:0015760 ordo_group_of_disorders diseases +MONDO:0015760 otar diseases +MONDO:0015760 rare diseases +MONDO:0015761 gard_rare diseases +MONDO:0015761 nord_rare diseases +MONDO:0015761 ordo_disorder diseases +MONDO:0015761 ordo_malformation_syndrome diseases +MONDO:0015761 orphanet_rare diseases +MONDO:0015761 otar diseases +MONDO:0015761 rare diseases +MONDO:0015762 gard_rare diseases +MONDO:0015762 nord_rare diseases +MONDO:0015762 ordo_disorder diseases +MONDO:0015762 orphanet_rare diseases +MONDO:0015762 otar diseases +MONDO:0015762 rare diseases +MONDO:0015763 gard_rare diseases +MONDO:0015763 nord_rare diseases +MONDO:0015763 ordo_disorder diseases +MONDO:0015763 ordo_malformation_syndrome diseases +MONDO:0015763 orphanet_rare diseases +MONDO:0015763 rare diseases +MONDO:0015764 gard_rare diseases +MONDO:0015764 nord_rare diseases +MONDO:0015764 ordo_disorder diseases +MONDO:0015764 ordo_malformation_syndrome diseases +MONDO:0015764 orphanet_rare diseases +MONDO:0015764 otar diseases +MONDO:0015764 rare diseases +MONDO:0015766 gard_rare diseases +MONDO:0015766 nord_rare diseases +MONDO:0015766 ordo_disorder diseases +MONDO:0015766 orphanet_rare diseases +MONDO:0015766 rare diseases +MONDO:0015767 gard_rare diseases +MONDO:0015767 nord_rare diseases +MONDO:0015767 ordo_disorder diseases +MONDO:0015767 ordo_malformation_syndrome diseases +MONDO:0015767 orphanet_rare diseases +MONDO:0015767 otar diseases +MONDO:0015767 rare diseases +MONDO:0015768 gard_rare diseases +MONDO:0015768 nord_rare diseases +MONDO:0015768 ordo_disorder diseases +MONDO:0015768 ordo_malformation_syndrome diseases +MONDO:0015768 orphanet_rare diseases +MONDO:0015768 rare diseases +MONDO:0015769 gard_rare diseases +MONDO:0015769 nord_rare diseases +MONDO:0015769 ordo_disorder diseases +MONDO:0015769 ordo_malformation_syndrome diseases +MONDO:0015769 orphanet_rare diseases +MONDO:0015769 otar diseases +MONDO:0015769 rare diseases +MONDO:0015770 disease_grouping diseases +MONDO:0015770 gard_rare diseases +MONDO:0015770 ordo_group_of_disorders diseases +MONDO:0015770 otar diseases +MONDO:0015770 rare diseases +MONDO:0015771 gard_rare diseases +MONDO:0015771 nord_rare diseases +MONDO:0015771 ordo_disorder diseases +MONDO:0015771 ordo_malformation_syndrome diseases +MONDO:0015771 orphanet_rare diseases +MONDO:0015771 rare diseases +MONDO:0015772 gard_rare diseases +MONDO:0015772 nord_rare diseases +MONDO:0015772 ordo_disorder diseases +MONDO:0015772 ordo_malformation_syndrome diseases +MONDO:0015772 orphanet_rare diseases +MONDO:0015772 otar diseases +MONDO:0015772 rare diseases +MONDO:0015773 gard_rare diseases +MONDO:0015773 nord_rare diseases +MONDO:0015773 ordo_disorder diseases +MONDO:0015773 ordo_malformation_syndrome diseases +MONDO:0015773 orphanet_rare diseases +MONDO:0015773 otar diseases +MONDO:0015773 rare diseases +MONDO:0015774 gard_rare diseases +MONDO:0015774 nord_rare diseases +MONDO:0015774 ordo_disorder diseases +MONDO:0015774 ordo_malformation_syndrome diseases +MONDO:0015774 orphanet_rare diseases +MONDO:0015774 otar diseases +MONDO:0015774 rare diseases +MONDO:0015775 disease_grouping diseases +MONDO:0015775 gard_rare diseases +MONDO:0015775 ordo_group_of_disorders diseases +MONDO:0015775 rare diseases +MONDO:0015776 gard_rare diseases +MONDO:0015776 nord_rare diseases +MONDO:0015776 ordo_disorder diseases +MONDO:0015776 orphanet_rare diseases +MONDO:0015776 otar diseases +MONDO:0015776 rare diseases +MONDO:0015779 gard_rare diseases +MONDO:0015779 nord_rare diseases +MONDO:0015779 ordo_disorder diseases +MONDO:0015779 ordo_malformation_syndrome diseases +MONDO:0015779 orphanet_rare diseases +MONDO:0015779 otar diseases +MONDO:0015779 rare diseases +MONDO:0015780 clingen diseases +MONDO:0015780 gard_rare diseases +MONDO:0015780 nord_rare diseases +MONDO:0015780 ordo_disorder diseases +MONDO:0015780 orphanet_rare diseases +MONDO:0015780 otar diseases +MONDO:0015780 rare diseases +MONDO:0015781 gard_rare diseases +MONDO:0015781 nord_rare diseases +MONDO:0015781 ordo_disorder diseases +MONDO:0015781 ordo_malformation_syndrome diseases +MONDO:0015781 orphanet_rare diseases +MONDO:0015781 otar diseases +MONDO:0015781 rare diseases +MONDO:0015782 gard_rare diseases +MONDO:0015782 ordo_disorder diseases +MONDO:0015782 ordo_malformation_syndrome diseases +MONDO:0015782 orphanet_rare diseases +MONDO:0015782 otar diseases +MONDO:0015782 rare diseases +MONDO:0015783 gard_rare diseases +MONDO:0015783 nord_rare diseases +MONDO:0015783 ordo_etiological_subtype diseases +MONDO:0015783 ordo_subtype_of_a_disorder diseases +MONDO:0015783 otar diseases +MONDO:0015783 rare diseases +MONDO:0015784 gard_rare diseases +MONDO:0015784 nord_rare diseases +MONDO:0015784 ordo_etiological_subtype diseases +MONDO:0015784 ordo_subtype_of_a_disorder diseases +MONDO:0015784 otar diseases +MONDO:0015784 rare diseases +MONDO:0015785 gard_rare diseases +MONDO:0015785 nord_rare diseases +MONDO:0015785 ordo_etiological_subtype diseases +MONDO:0015785 ordo_subtype_of_a_disorder diseases +MONDO:0015785 otar diseases +MONDO:0015785 rare diseases +MONDO:0015786 gard_rare diseases +MONDO:0015786 nord_rare diseases +MONDO:0015786 ordo_etiological_subtype diseases +MONDO:0015786 ordo_subtype_of_a_disorder diseases +MONDO:0015786 otar diseases +MONDO:0015786 rare diseases +MONDO:0015787 gard_rare diseases +MONDO:0015787 nord_rare diseases +MONDO:0015787 ordo_subtype_of_a_disorder diseases +MONDO:0015787 otar diseases +MONDO:0015787 rare diseases +MONDO:0015788 gard_rare diseases +MONDO:0015788 nord_rare diseases +MONDO:0015788 ordo_subtype_of_a_disorder diseases +MONDO:0015788 otar diseases +MONDO:0015788 rare diseases +MONDO:0015790 gard_rare diseases +MONDO:0015790 nord_rare diseases +MONDO:0015790 ordo_disorder diseases +MONDO:0015790 orphanet_rare diseases +MONDO:0015790 rare diseases +MONDO:0015791 disease_grouping diseases +MONDO:0015791 gard_rare diseases +MONDO:0015791 ordo_group_of_disorders diseases +MONDO:0015791 otar diseases +MONDO:0015791 rare diseases +MONDO:0015792 disease_grouping diseases +MONDO:0015792 gard_rare diseases +MONDO:0015792 nord_rare diseases +MONDO:0015792 ordo_group_of_disorders diseases +MONDO:0015792 rare diseases +MONDO:0015793 gard_rare diseases +MONDO:0015793 nord_rare diseases +MONDO:0015793 ordo_subtype_of_a_disorder diseases +MONDO:0015793 otar diseases +MONDO:0015793 rare diseases +MONDO:0015794 gard_rare diseases +MONDO:0015794 nord_rare diseases +MONDO:0015794 ordo_subtype_of_a_disorder diseases +MONDO:0015794 otar diseases +MONDO:0015794 rare diseases +MONDO:0015795 gard_rare diseases +MONDO:0015795 nord_rare diseases +MONDO:0015795 ordo_disorder diseases +MONDO:0015795 orphanet_rare diseases +MONDO:0015795 rare diseases +MONDO:0015796 gard_rare diseases +MONDO:0015796 ordo_clinical_situation diseases +MONDO:0015796 ordo_disorder diseases +MONDO:0015796 orphanet_rare diseases +MONDO:0015796 otar diseases +MONDO:0015796 rare diseases +MONDO:0015797 gard_rare diseases +MONDO:0015797 nord_rare diseases +MONDO:0015797 ordo_disorder diseases +MONDO:0015797 orphanet_rare diseases +MONDO:0015797 otar diseases +MONDO:0015797 rare diseases +MONDO:0015798 gard_rare diseases +MONDO:0015798 nord_rare diseases +MONDO:0015798 ordo_disorder diseases +MONDO:0015798 orphanet_rare diseases +MONDO:0015798 otar diseases +MONDO:0015798 rare diseases +MONDO:0015799 gard_rare diseases +MONDO:0015799 nord_rare diseases +MONDO:0015799 ordo_disorder diseases +MONDO:0015799 orphanet_rare diseases +MONDO:0015799 otar diseases +MONDO:0015799 rare diseases +MONDO:0015800 gard_rare diseases +MONDO:0015800 nord_rare diseases +MONDO:0015800 ordo_disorder diseases +MONDO:0015800 ordo_malformation_syndrome diseases +MONDO:0015800 orphanet_rare diseases +MONDO:0015800 otar diseases +MONDO:0015800 rare diseases +MONDO:0015801 gard_rare diseases +MONDO:0015801 nord_rare diseases +MONDO:0015801 ordo_disorder diseases +MONDO:0015801 orphanet_rare diseases +MONDO:0015801 otar diseases +MONDO:0015801 rare diseases +MONDO:0015802 gard_rare diseases +MONDO:0015802 ordo_subtype_of_a_disorder diseases +MONDO:0015802 otar diseases +MONDO:0015802 rare diseases +MONDO:0015803 gard_rare diseases +MONDO:0015803 nord_rare diseases +MONDO:0015803 ordo_etiological_subtype diseases +MONDO:0015803 ordo_subtype_of_a_disorder diseases +MONDO:0015803 rare diseases +MONDO:0015804 gard_rare diseases +MONDO:0015804 nord_rare diseases +MONDO:0015804 ordo_subtype_of_a_disorder diseases +MONDO:0015804 rare diseases +MONDO:0015805 gard_rare diseases +MONDO:0015805 nord_rare diseases +MONDO:0015805 ordo_subtype_of_a_disorder diseases +MONDO:0015805 rare diseases +MONDO:0015806 gard_rare diseases +MONDO:0015806 nord_rare diseases +MONDO:0015806 ordo_subtype_of_a_disorder diseases +MONDO:0015806 rare diseases +MONDO:0015807 gard_rare diseases +MONDO:0015807 nord_rare diseases +MONDO:0015807 ordo_disorder diseases +MONDO:0015807 orphanet_rare diseases +MONDO:0015807 otar diseases +MONDO:0015807 rare diseases +MONDO:0015808 gard_rare diseases +MONDO:0015808 nord_rare diseases +MONDO:0015808 ordo_disorder diseases +MONDO:0015808 orphanet_rare diseases +MONDO:0015808 rare diseases +MONDO:0015809 gard_rare diseases +MONDO:0015809 nord_rare diseases +MONDO:0015809 ordo_disorder diseases +MONDO:0015809 orphanet_rare diseases +MONDO:0015809 rare diseases +MONDO:0015810 gard_rare diseases +MONDO:0015810 nord_rare diseases +MONDO:0015810 ordo_disorder diseases +MONDO:0015810 orphanet_rare diseases +MONDO:0015810 rare diseases +MONDO:0015811 gard_rare diseases +MONDO:0015811 nord_rare diseases +MONDO:0015811 ordo_disorder diseases +MONDO:0015811 orphanet_rare diseases +MONDO:0015811 rare diseases +MONDO:0015812 gard_rare diseases +MONDO:0015812 nord_rare diseases +MONDO:0015812 ordo_disorder diseases +MONDO:0015812 orphanet_rare diseases +MONDO:0015812 rare diseases +MONDO:0015813 gard_rare diseases +MONDO:0015813 nord_rare diseases +MONDO:0015813 ordo_disorder diseases +MONDO:0015813 orphanet_rare diseases +MONDO:0015813 otar diseases +MONDO:0015813 rare diseases +MONDO:0015814 gard_rare diseases +MONDO:0015814 nord_rare diseases +MONDO:0015814 ordo_disorder diseases +MONDO:0015814 orphanet_rare diseases +MONDO:0015814 rare diseases +MONDO:0015816 disease_grouping diseases +MONDO:0015816 gard_rare diseases +MONDO:0015816 ordo_group_of_disorders diseases +MONDO:0015816 rare diseases +MONDO:0015819 disease_grouping diseases +MONDO:0015819 gard_rare diseases +MONDO:0015819 ordo_group_of_disorders diseases +MONDO:0015819 rare diseases +MONDO:0015820 disease_grouping diseases +MONDO:0015820 gard_rare diseases +MONDO:0015820 ordo_group_of_disorders diseases +MONDO:0015820 otar diseases +MONDO:0015820 rare diseases +MONDO:0015821 disease_grouping diseases +MONDO:0015821 gard_rare diseases +MONDO:0015821 nord_rare diseases +MONDO:0015821 ordo_group_of_disorders diseases +MONDO:0015821 rare diseases +MONDO:0015824 gard_rare diseases +MONDO:0015824 nord_rare diseases +MONDO:0015824 ordo_disorder diseases +MONDO:0015824 ordo_malformation_syndrome diseases +MONDO:0015824 orphanet_rare diseases +MONDO:0015824 otar diseases +MONDO:0015824 rare diseases +MONDO:0015826 gard_rare diseases +MONDO:0015826 nord_rare diseases +MONDO:0015826 ordo_disorder diseases +MONDO:0015826 ordo_malformation_syndrome diseases +MONDO:0015826 orphanet_rare diseases +MONDO:0015826 otar diseases +MONDO:0015826 rare diseases +MONDO:0015827 gard_rare diseases +MONDO:0015827 nord_rare diseases +MONDO:0015827 ordo_disorder diseases +MONDO:0015827 orphanet_rare diseases +MONDO:0015827 otar diseases +MONDO:0015827 rare diseases +MONDO:0015830 disease_grouping diseases +MONDO:0015830 gard_rare diseases +MONDO:0015830 ordo_group_of_disorders diseases +MONDO:0015830 rare diseases +MONDO:0015831 disease_grouping diseases +MONDO:0015831 gard_rare diseases +MONDO:0015831 ordo_group_of_disorders diseases +MONDO:0015831 rare diseases +MONDO:0015832 gard_rare diseases +MONDO:0015832 nord_rare diseases +MONDO:0015832 ordo_disorder diseases +MONDO:0015832 ordo_morphological_anomaly diseases +MONDO:0015832 orphanet_rare diseases +MONDO:0015832 rare diseases +MONDO:0015833 gard_rare diseases +MONDO:0015833 nord_rare diseases +MONDO:0015833 ordo_disorder diseases +MONDO:0015833 ordo_morphological_anomaly diseases +MONDO:0015833 orphanet_rare diseases +MONDO:0015833 rare diseases +MONDO:0015834 gard_rare diseases +MONDO:0015834 nord_rare diseases +MONDO:0015834 ordo_disorder diseases +MONDO:0015834 ordo_morphological_anomaly diseases +MONDO:0015834 orphanet_rare diseases +MONDO:0015834 rare diseases +MONDO:0015835 gard_rare diseases +MONDO:0015835 nord_rare diseases +MONDO:0015835 ordo_subtype_of_a_disorder diseases +MONDO:0015835 rare diseases +MONDO:0015836 gard_rare diseases +MONDO:0015836 nord_rare diseases +MONDO:0015836 ordo_subtype_of_a_disorder diseases +MONDO:0015836 rare diseases +MONDO:0015838 ordo_morphological_anomaly diseases +MONDO:0015839 disease_grouping diseases +MONDO:0015839 gard_rare diseases +MONDO:0015839 nord_rare diseases +MONDO:0015839 ordo_group_of_disorders diseases +MONDO:0015839 rare diseases +MONDO:0015840 gard_rare diseases +MONDO:0015840 nord_rare diseases +MONDO:0015840 ordo_disorder diseases +MONDO:0015840 ordo_morphological_anomaly diseases +MONDO:0015840 orphanet_rare diseases +MONDO:0015840 rare diseases +MONDO:0015841 gard_rare diseases +MONDO:0015841 nord_rare diseases +MONDO:0015841 ordo_disorder diseases +MONDO:0015841 ordo_morphological_anomaly diseases +MONDO:0015841 orphanet_rare diseases +MONDO:0015841 rare diseases +MONDO:0015842 disease_grouping diseases +MONDO:0015842 gard_rare diseases +MONDO:0015842 nord_rare diseases +MONDO:0015842 ordo_group_of_disorders diseases +MONDO:0015842 rare diseases +MONDO:0015843 gard_rare diseases +MONDO:0015843 nord_rare diseases +MONDO:0015843 ordo_disorder diseases +MONDO:0015843 ordo_morphological_anomaly diseases +MONDO:0015843 orphanet_rare diseases +MONDO:0015843 rare diseases +MONDO:0015844 gard_rare diseases +MONDO:0015844 nord_rare diseases +MONDO:0015844 ordo_disorder diseases +MONDO:0015844 ordo_morphological_anomaly diseases +MONDO:0015844 orphanet_rare diseases +MONDO:0015844 rare diseases +MONDO:0015845 gard_rare diseases +MONDO:0015845 nord_rare diseases +MONDO:0015845 ordo_disorder diseases +MONDO:0015845 ordo_morphological_anomaly diseases +MONDO:0015845 orphanet_rare diseases +MONDO:0015845 rare diseases +MONDO:0015849 gard_rare diseases +MONDO:0015849 nord_rare diseases +MONDO:0015849 ordo_subtype_of_a_disorder diseases +MONDO:0015849 rare diseases +MONDO:0015850 gard_rare diseases +MONDO:0015850 nord_rare diseases +MONDO:0015850 ordo_subtype_of_a_disorder diseases +MONDO:0015850 rare diseases +MONDO:0015854 gard_rare diseases +MONDO:0015854 nord_rare diseases +MONDO:0015854 ordo_disorder diseases +MONDO:0015854 ordo_morphological_anomaly diseases +MONDO:0015854 orphanet_rare diseases +MONDO:0015854 rare diseases +MONDO:0015855 gard_rare diseases +MONDO:0015855 nord_rare diseases +MONDO:0015855 ordo_disorder diseases +MONDO:0015855 ordo_morphological_anomaly diseases +MONDO:0015855 orphanet_rare diseases +MONDO:0015855 otar diseases +MONDO:0015855 rare diseases +MONDO:0015856 disease_grouping diseases +MONDO:0015856 gard_rare diseases +MONDO:0015856 ordo_group_of_disorders diseases +MONDO:0015856 rare diseases +MONDO:0015863 gard_rare diseases +MONDO:0015863 nord_rare diseases +MONDO:0015863 ordo_disorder diseases +MONDO:0015863 orphanet_rare diseases +MONDO:0015863 rare diseases +MONDO:0015864 gard_rare diseases +MONDO:0015864 ordo_disorder diseases +MONDO:0015864 orphanet_rare diseases +MONDO:0015864 otar diseases +MONDO:0015864 rare diseases +MONDO:0015867 gard_rare diseases +MONDO:0015867 ordo_disorder diseases +MONDO:0015867 orphanet_rare diseases +MONDO:0015867 otar diseases +MONDO:0015867 rare diseases +MONDO:0015871 nord_rare diseases +MONDO:0015871 ordo_disorder diseases +MONDO:0015871 orphanet_rare diseases +MONDO:0015871 rare diseases +MONDO:0015873 gard_rare diseases +MONDO:0015873 nord_rare diseases +MONDO:0015873 ordo_disorder diseases +MONDO:0015873 orphanet_rare diseases +MONDO:0015873 rare diseases +MONDO:0015883 gard_rare diseases +MONDO:0015883 nord_rare diseases +MONDO:0015883 ordo_disorder diseases +MONDO:0015883 ordo_malformation_syndrome diseases +MONDO:0015883 orphanet_rare diseases +MONDO:0015883 otar diseases +MONDO:0015883 rare diseases +MONDO:0015884 gard_rare diseases +MONDO:0015884 nord_rare diseases +MONDO:0015884 ordo_etiological_subtype diseases +MONDO:0015884 ordo_subtype_of_a_disorder diseases +MONDO:0015884 otar diseases +MONDO:0015884 rare diseases +MONDO:0015892 disease_grouping diseases +MONDO:0015892 gard_rare diseases +MONDO:0015892 nord_rare diseases +MONDO:0015892 ordo_group_of_disorders diseases +MONDO:0015892 otar diseases +MONDO:0015892 rare diseases +MONDO:0015898 disease_grouping diseases +MONDO:0015898 gard_rare diseases +MONDO:0015898 ordo_group_of_disorders diseases +MONDO:0015898 otar diseases +MONDO:0015898 rare diseases +MONDO:0015900 disease_grouping diseases +MONDO:0015900 gard_rare diseases +MONDO:0015900 ordo_group_of_disorders diseases +MONDO:0015900 otar diseases +MONDO:0015900 rare diseases +MONDO:0015903 disease_grouping diseases +MONDO:0015903 gard_rare diseases +MONDO:0015903 nord_rare diseases +MONDO:0015903 ordo_group_of_disorders diseases +MONDO:0015903 otar diseases +MONDO:0015903 rare diseases +MONDO:0015905 disease_grouping diseases +MONDO:0015905 gard_rare diseases +MONDO:0015905 ordo_group_of_disorders diseases +MONDO:0015905 rare diseases +MONDO:0015907 gard_rare diseases +MONDO:0015907 ordo_malformation_syndrome diseases +MONDO:0015907 rare diseases +MONDO:0015908 gard_rare diseases +MONDO:0015908 nord_rare diseases +MONDO:0015908 ordo_disorder diseases +MONDO:0015908 orphanet_rare diseases +MONDO:0015908 otar diseases +MONDO:0015908 rare diseases +MONDO:0015909 disease_grouping diseases +MONDO:0015909 gard_rare diseases +MONDO:0015909 nord_rare diseases +MONDO:0015909 ordo_group_of_disorders diseases +MONDO:0015909 otar diseases +MONDO:0015909 rare diseases +MONDO:0015912 clingen diseases +MONDO:0015912 gard_rare diseases +MONDO:0015912 nord_rare diseases +MONDO:0015912 ordo_disorder diseases +MONDO:0015912 orphanet_rare diseases +MONDO:0015912 otar diseases +MONDO:0015912 rare diseases +MONDO:0015914 disease_grouping diseases +MONDO:0015914 ordo_group_of_disorders diseases +MONDO:0015914 otar diseases +MONDO:0015923 disease_grouping diseases +MONDO:0015923 gard_rare diseases +MONDO:0015923 nord_rare diseases +MONDO:0015923 ordo_group_of_disorders diseases +MONDO:0015923 otar diseases +MONDO:0015923 rare diseases +MONDO:0015924 clingen diseases +MONDO:0015924 disease_grouping diseases +MONDO:0015924 gard_rare diseases +MONDO:0015924 nord_rare diseases +MONDO:0015924 ordo_group_of_disorders diseases +MONDO:0015924 otar diseases +MONDO:0015924 rare diseases +MONDO:0015925 disease_grouping diseases +MONDO:0015925 ordo_group_of_disorders diseases +MONDO:0015925 otar diseases +MONDO:0015926 disease_grouping diseases +MONDO:0015926 gard_rare diseases +MONDO:0015926 ordo_group_of_disorders diseases +MONDO:0015926 otar diseases +MONDO:0015926 rare diseases +MONDO:0015927 disease_grouping diseases +MONDO:0015927 gard_rare diseases +MONDO:0015927 ordo_group_of_disorders diseases +MONDO:0015927 rare diseases +MONDO:0015929 disease_grouping diseases +MONDO:0015929 gard_rare diseases +MONDO:0015929 ordo_group_of_disorders diseases +MONDO:0015929 rare diseases +MONDO:0015935 gard_rare diseases +MONDO:0015935 nord_rare diseases +MONDO:0015935 ordo_disorder diseases +MONDO:0015935 orphanet_rare diseases +MONDO:0015935 otar diseases +MONDO:0015935 rare diseases +MONDO:0015941 gard_rare diseases +MONDO:0015941 nord_rare diseases +MONDO:0015941 ordo_disorder diseases +MONDO:0015941 ordo_malformation_syndrome diseases +MONDO:0015941 orphanet_rare diseases +MONDO:0015941 otar diseases +MONDO:0015941 rare diseases +MONDO:0015942 gard_rare diseases +MONDO:0015942 nord_rare diseases +MONDO:0015942 ordo_disorder diseases +MONDO:0015942 orphanet_rare diseases +MONDO:0015942 otar diseases +MONDO:0015942 prototype_pattern diseases +MONDO:0015942 rare diseases +MONDO:0015943 gard_rare diseases +MONDO:0015943 nord_rare diseases +MONDO:0015943 ordo_disorder diseases +MONDO:0015943 orphanet_rare diseases +MONDO:0015943 otar diseases +MONDO:0015943 rare diseases +MONDO:0015944 gard_rare diseases +MONDO:0015944 nord_rare diseases +MONDO:0015944 ordo_disorder diseases +MONDO:0015944 ordo_malformation_syndrome diseases +MONDO:0015944 orphanet_rare diseases +MONDO:0015944 otar diseases +MONDO:0015944 rare diseases +MONDO:0015947 disease_grouping diseases +MONDO:0015947 gard_rare diseases +MONDO:0015947 ordo_group_of_disorders diseases +MONDO:0015947 otar diseases +MONDO:0015947 rare diseases +MONDO:0015951 disease_grouping diseases +MONDO:0015951 gard_rare diseases +MONDO:0015951 mondo_rare diseases +MONDO:0015951 ordo_group_of_disorders diseases +MONDO:0015951 otar diseases +MONDO:0015951 rare diseases +MONDO:0015962 disease_grouping diseases +MONDO:0015962 gard_rare diseases +MONDO:0015962 ordo_group_of_disorders diseases +MONDO:0015962 rare diseases +MONDO:0015967 clingen diseases +MONDO:0015967 disease_grouping diseases +MONDO:0015967 inferred_rare diseases +MONDO:0015967 ordo_group_of_disorders diseases +MONDO:0015967 otar diseases +MONDO:0015967 rare diseases +MONDO:0015974 disease_grouping diseases +MONDO:0015974 gard_rare diseases +MONDO:0015974 nord_rare diseases +MONDO:0015974 ordo_group_of_disorders diseases +MONDO:0015974 otar diseases +MONDO:0015974 rare diseases +MONDO:0015977 clingen diseases +MONDO:0015977 disease_grouping diseases +MONDO:0015977 gard_rare diseases +MONDO:0015977 ordo_group_of_disorders diseases +MONDO:0015977 otar diseases +MONDO:0015977 rare diseases +MONDO:0015978 disease_grouping diseases +MONDO:0015978 gard_rare diseases +MONDO:0015978 ordo_group_of_disorders diseases +MONDO:0015978 otar diseases +MONDO:0015978 rare diseases +MONDO:0015985 gard_rare diseases +MONDO:0015985 ordo_malformation_syndrome diseases +MONDO:0015985 rare diseases +MONDO:0015986 gard_rare diseases +MONDO:0015986 nord_rare diseases +MONDO:0015986 ordo_subtype_of_a_disorder diseases +MONDO:0015986 otar diseases +MONDO:0015986 rare diseases +MONDO:0015987 gard_rare diseases +MONDO:0015987 nord_rare diseases +MONDO:0015987 ordo_disorder diseases +MONDO:0015987 ordo_malformation_syndrome diseases +MONDO:0015987 orphanet_rare diseases +MONDO:0015987 otar diseases +MONDO:0015987 rare diseases +MONDO:0015988 gard_rare diseases +MONDO:0015988 nord_rare diseases +MONDO:0015988 ordo_disorder diseases +MONDO:0015988 ordo_morphological_anomaly diseases +MONDO:0015988 orphanet_rare diseases +MONDO:0015988 otar diseases +MONDO:0015988 rare diseases +MONDO:0015990 disease_grouping diseases +MONDO:0015990 gard_rare diseases +MONDO:0015990 nord_rare diseases +MONDO:0015990 ordo_group_of_disorders diseases +MONDO:0015990 otar diseases +MONDO:0015990 rare diseases +MONDO:0015991 disease_grouping diseases +MONDO:0015991 gard_rare diseases +MONDO:0015991 ordo_group_of_disorders diseases +MONDO:0015991 otar diseases +MONDO:0015991 rare diseases +MONDO:0015993 gard_rare diseases +MONDO:0015993 nord_rare diseases +MONDO:0015993 ordo_disorder diseases +MONDO:0015993 orphanet_rare diseases +MONDO:0015993 otar diseases +MONDO:0015993 rare diseases +MONDO:0015994 gard_rare diseases +MONDO:0015994 rare diseases +MONDO:0015995 gard_rare diseases +MONDO:0015995 nord_rare diseases +MONDO:0015995 ordo_disorder diseases +MONDO:0015995 ordo_malformation_syndrome diseases +MONDO:0015995 orphanet_rare diseases +MONDO:0015995 otar diseases +MONDO:0015995 rare diseases +MONDO:0015997 gard_rare diseases +MONDO:0015997 ordo_disorder diseases +MONDO:0015997 orphanet_rare diseases +MONDO:0015997 rare diseases +MONDO:0015998 gard_rare diseases +MONDO:0015998 nord_rare diseases +MONDO:0015998 ordo_disorder diseases +MONDO:0015998 ordo_malformation_syndrome diseases +MONDO:0015998 orphanet_rare diseases +MONDO:0015998 otar diseases +MONDO:0015998 rare diseases +MONDO:0015999 gard_rare diseases +MONDO:0015999 nord_rare diseases +MONDO:0015999 otar diseases +MONDO:0015999 rare diseases +MONDO:0016000 gard_rare diseases +MONDO:0016000 ordo_subtype_of_a_disorder diseases +MONDO:0016000 otar diseases +MONDO:0016000 rare diseases +MONDO:0016001 disease_grouping diseases +MONDO:0016001 gard_rare diseases +MONDO:0016001 nord_rare diseases +MONDO:0016001 ordo_group_of_disorders diseases +MONDO:0016001 otar diseases +MONDO:0016001 rare diseases +MONDO:0016002 gard_rare diseases +MONDO:0016002 nord_rare diseases +MONDO:0016002 ordo_subtype_of_a_disorder diseases +MONDO:0016002 otar diseases +MONDO:0016002 rare diseases +MONDO:0016003 gard_rare diseases +MONDO:0016003 nord_rare diseases +MONDO:0016003 ordo_disorder diseases +MONDO:0016003 orphanet_rare diseases +MONDO:0016003 rare diseases +MONDO:0016004 nord_rare diseases +MONDO:0016004 ordo_disorder diseases +MONDO:0016004 ordo_malformation_syndrome diseases +MONDO:0016004 orphanet_rare diseases +MONDO:0016004 rare diseases +MONDO:0016005 nord_rare diseases +MONDO:0016005 ordo_disorder diseases +MONDO:0016005 ordo_malformation_syndrome diseases +MONDO:0016005 orphanet_rare diseases +MONDO:0016005 rare diseases +MONDO:0016006 gard_rare diseases +MONDO:0016006 nord_rare diseases +MONDO:0016006 ordo_disorder diseases +MONDO:0016006 orphanet_rare diseases +MONDO:0016006 otar diseases +MONDO:0016006 rare diseases +MONDO:0016007 gard_rare diseases +MONDO:0016007 nord_rare diseases +MONDO:0016007 ordo_disorder diseases +MONDO:0016007 ordo_malformation_syndrome diseases +MONDO:0016007 orphanet_rare diseases +MONDO:0016007 rare diseases +MONDO:0016008 gard_rare diseases +MONDO:0016008 nord_rare diseases +MONDO:0016008 ordo_disorder diseases +MONDO:0016008 ordo_malformation_syndrome diseases +MONDO:0016008 orphanet_rare diseases +MONDO:0016008 rare diseases +MONDO:0016009 gard_rare diseases +MONDO:0016009 nord_rare diseases +MONDO:0016009 ordo_disorder diseases +MONDO:0016009 ordo_malformation_syndrome diseases +MONDO:0016009 orphanet_rare diseases +MONDO:0016009 otar diseases +MONDO:0016009 rare diseases +MONDO:0016010 nord_rare diseases +MONDO:0016010 ordo_disorder diseases +MONDO:0016010 ordo_malformation_syndrome diseases +MONDO:0016010 orphanet_rare diseases +MONDO:0016010 rare diseases +MONDO:0016011 gard_rare diseases +MONDO:0016011 ordo_disorder diseases +MONDO:0016011 ordo_malformation_syndrome diseases +MONDO:0016011 orphanet_rare diseases +MONDO:0016011 rare diseases +MONDO:0016012 gard_rare diseases +MONDO:0016012 nord_rare diseases +MONDO:0016012 ordo_disorder diseases +MONDO:0016012 orphanet_rare diseases +MONDO:0016012 rare diseases +MONDO:0016013 gard_rare diseases +MONDO:0016013 nord_rare diseases +MONDO:0016013 ordo_disorder diseases +MONDO:0016013 ordo_malformation_syndrome diseases +MONDO:0016013 orphanet_rare diseases +MONDO:0016013 rare diseases +MONDO:0016014 gard_rare diseases +MONDO:0016014 nord_rare diseases +MONDO:0016014 ordo_disorder diseases +MONDO:0016014 ordo_malformation_syndrome diseases +MONDO:0016014 orphanet_rare diseases +MONDO:0016014 rare diseases +MONDO:0016015 gard_rare diseases +MONDO:0016015 nord_rare diseases +MONDO:0016015 ordo_disorder diseases +MONDO:0016015 ordo_malformation_syndrome diseases +MONDO:0016015 orphanet_rare diseases +MONDO:0016015 rare diseases +MONDO:0016016 gard_rare diseases +MONDO:0016016 nord_rare diseases +MONDO:0016016 ordo_disorder diseases +MONDO:0016016 ordo_malformation_syndrome diseases +MONDO:0016016 orphanet_rare diseases +MONDO:0016016 rare diseases +MONDO:0016017 nord_rare diseases +MONDO:0016017 ordo_disorder diseases +MONDO:0016017 ordo_malformation_syndrome diseases +MONDO:0016017 orphanet_rare diseases +MONDO:0016017 rare diseases +MONDO:0016018 gard_rare diseases +MONDO:0016018 nord_rare diseases +MONDO:0016018 ordo_disorder diseases +MONDO:0016018 ordo_malformation_syndrome diseases +MONDO:0016018 orphanet_rare diseases +MONDO:0016018 rare diseases +MONDO:0016019 gard_rare diseases +MONDO:0016019 nord_rare diseases +MONDO:0016019 ordo_disorder diseases +MONDO:0016019 orphanet_rare diseases +MONDO:0016019 rare diseases +MONDO:0016020 gard_rare diseases +MONDO:0016020 nord_rare diseases +MONDO:0016020 ordo_subtype_of_a_disorder diseases +MONDO:0016020 otar diseases +MONDO:0016020 rare diseases +MONDO:0016022 gard_rare diseases +MONDO:0016022 nord_rare diseases +MONDO:0016022 ordo_clinical_syndrome diseases +MONDO:0016022 ordo_disorder diseases +MONDO:0016022 orphanet_rare diseases +MONDO:0016022 otar diseases +MONDO:0016022 rare diseases +MONDO:0016024 gard_rare diseases +MONDO:0016024 ordo_malformation_syndrome diseases +MONDO:0016024 rare diseases +MONDO:0016025 gard_rare diseases +MONDO:0016025 nord_rare diseases +MONDO:0016025 ordo_disorder diseases +MONDO:0016025 orphanet_rare diseases +MONDO:0016025 otar diseases +MONDO:0016025 rare diseases +MONDO:0016026 gard_rare diseases +MONDO:0016026 nord_rare diseases +MONDO:0016026 ordo_disorder diseases +MONDO:0016026 orphanet_rare diseases +MONDO:0016026 rare diseases +MONDO:0016027 gard_rare diseases +MONDO:0016027 nord_rare diseases +MONDO:0016027 ordo_disorder diseases +MONDO:0016027 orphanet_rare diseases +MONDO:0016027 otar diseases +MONDO:0016027 rare diseases +MONDO:0016028 otar diseases +MONDO:0016029 gard_rare diseases +MONDO:0016029 nord_rare diseases +MONDO:0016029 ordo_disorder diseases +MONDO:0016029 orphanet_rare diseases +MONDO:0016029 rare diseases +MONDO:0016030 gard_rare diseases +MONDO:0016030 nord_rare diseases +MONDO:0016030 ordo_disorder diseases +MONDO:0016030 orphanet_rare diseases +MONDO:0016030 otar diseases +MONDO:0016030 rare diseases +MONDO:0016031 gard_rare diseases +MONDO:0016031 ordo_disorder diseases +MONDO:0016031 ordo_malformation_syndrome diseases +MONDO:0016031 orphanet_rare diseases +MONDO:0016031 rare diseases +MONDO:0016032 gard_rare diseases +MONDO:0016032 nord_rare diseases +MONDO:0016032 ordo_disorder diseases +MONDO:0016032 ordo_malformation_syndrome diseases +MONDO:0016032 orphanet_rare diseases +MONDO:0016032 otar diseases +MONDO:0016032 rare diseases +MONDO:0016033 clingen diseases +MONDO:0016033 gard_rare diseases +MONDO:0016033 nord_rare diseases +MONDO:0016033 ordo_disorder diseases +MONDO:0016033 ordo_malformation_syndrome diseases +MONDO:0016033 orphanet_rare diseases +MONDO:0016033 otar diseases +MONDO:0016033 rare diseases +MONDO:0016035 gard_rare diseases +MONDO:0016035 nord_rare diseases +MONDO:0016035 ordo_disorder diseases +MONDO:0016035 orphanet_rare diseases +MONDO:0016035 rare diseases +MONDO:0016037 disease_grouping diseases +MONDO:0016037 ordo_group_of_disorders diseases +MONDO:0016037 otar diseases +MONDO:0016038 gard_rare diseases +MONDO:0016038 nord_rare diseases +MONDO:0016038 ordo_disorder diseases +MONDO:0016038 orphanet_rare diseases +MONDO:0016038 rare diseases +MONDO:0016039 gard_rare diseases +MONDO:0016039 nord_rare diseases +MONDO:0016039 ordo_disorder diseases +MONDO:0016039 orphanet_rare diseases +MONDO:0016039 rare diseases +MONDO:0016040 gard_rare diseases +MONDO:0016040 nord_rare diseases +MONDO:0016040 ordo_disorder diseases +MONDO:0016040 orphanet_rare diseases +MONDO:0016040 otar diseases +MONDO:0016040 rare diseases +MONDO:0016041 gard_rare diseases +MONDO:0016041 nord_rare diseases +MONDO:0016041 ordo_disorder diseases +MONDO:0016041 ordo_morphological_anomaly diseases +MONDO:0016041 orphanet_rare diseases +MONDO:0016041 rare diseases +MONDO:0016042 gard_rare diseases +MONDO:0016042 nord_rare diseases +MONDO:0016042 ordo_disorder diseases +MONDO:0016042 orphanet_rare diseases +MONDO:0016042 rare diseases +MONDO:0016043 gard_rare diseases +MONDO:0016043 nord_rare diseases +MONDO:0016043 ordo_disorder diseases +MONDO:0016043 ordo_morphological_anomaly diseases +MONDO:0016043 orphanet_rare diseases +MONDO:0016043 rare diseases +MONDO:0016044 gard_rare diseases +MONDO:0016044 nord_rare diseases +MONDO:0016044 ordo_disorder diseases +MONDO:0016044 ordo_morphological_anomaly diseases +MONDO:0016044 orphanet_rare diseases +MONDO:0016044 rare diseases +MONDO:0016045 gard_rare diseases +MONDO:0016045 nord_rare diseases +MONDO:0016045 ordo_disorder diseases +MONDO:0016045 ordo_malformation_syndrome diseases +MONDO:0016045 orphanet_rare diseases +MONDO:0016045 otar diseases +MONDO:0016045 rare diseases +MONDO:0016046 gard_rare diseases +MONDO:0016046 nord_rare diseases +MONDO:0016046 ordo_disorder diseases +MONDO:0016046 ordo_malformation_syndrome diseases +MONDO:0016046 orphanet_rare diseases +MONDO:0016046 rare diseases +MONDO:0016047 gard_rare diseases +MONDO:0016047 nord_rare diseases +MONDO:0016047 ordo_disorder diseases +MONDO:0016047 orphanet_rare diseases +MONDO:0016047 otar diseases +MONDO:0016047 rare diseases +MONDO:0016048 gard_rare diseases +MONDO:0016048 nord_rare diseases +MONDO:0016048 ordo_disorder diseases +MONDO:0016048 orphanet_rare diseases +MONDO:0016048 otar diseases +MONDO:0016048 rare diseases +MONDO:0016049 gard_rare diseases +MONDO:0016049 nord_rare diseases +MONDO:0016049 ordo_disorder diseases +MONDO:0016049 orphanet_rare diseases +MONDO:0016049 otar diseases +MONDO:0016049 rare diseases +MONDO:0016051 gard_rare diseases +MONDO:0016051 nord_rare diseases +MONDO:0016051 ordo_disorder diseases +MONDO:0016051 ordo_malformation_syndrome diseases +MONDO:0016051 orphanet_rare diseases +MONDO:0016051 otar diseases +MONDO:0016051 rare diseases +MONDO:0016052 gard_rare diseases +MONDO:0016052 nord_rare diseases +MONDO:0016052 ordo_disorder diseases +MONDO:0016052 orphanet_rare diseases +MONDO:0016052 otar diseases +MONDO:0016052 rare diseases +MONDO:0016053 gard_rare diseases +MONDO:0016053 nord_rare diseases +MONDO:0016053 ordo_disorder diseases +MONDO:0016053 ordo_morphological_anomaly diseases +MONDO:0016053 orphanet_rare diseases +MONDO:0016053 rare diseases +MONDO:0016056 gard_rare diseases +MONDO:0016056 nord_rare diseases +MONDO:0016056 ordo_disorder diseases +MONDO:0016056 ordo_malformation_syndrome diseases +MONDO:0016056 orphanet_rare diseases +MONDO:0016056 rare diseases +MONDO:0016057 gard_rare diseases +MONDO:0016057 nord_rare diseases +MONDO:0016057 ordo_disorder diseases +MONDO:0016057 ordo_morphological_anomaly diseases +MONDO:0016057 orphanet_rare diseases +MONDO:0016057 rare diseases +MONDO:0016058 disease_grouping diseases +MONDO:0016058 gard_rare diseases +MONDO:0016058 nord_rare diseases +MONDO:0016058 ordo_group_of_disorders diseases +MONDO:0016058 otar diseases +MONDO:0016058 rare diseases +MONDO:0016059 gard_rare diseases +MONDO:0016059 ordo_disorder diseases +MONDO:0016059 ordo_malformation_syndrome diseases +MONDO:0016059 orphanet_rare diseases +MONDO:0016059 otar diseases +MONDO:0016059 rare diseases +MONDO:0016060 gard_rare diseases +MONDO:0016060 nord_rare diseases +MONDO:0016060 ordo_disorder diseases +MONDO:0016060 ordo_morphological_anomaly diseases +MONDO:0016060 orphanet_rare diseases +MONDO:0016060 otar diseases +MONDO:0016060 rare diseases +MONDO:0016061 gard_rare diseases +MONDO:0016061 nord_rare diseases +MONDO:0016061 ordo_disorder diseases +MONDO:0016061 orphanet_rare diseases +MONDO:0016061 otar diseases +MONDO:0016061 rare diseases +MONDO:0016062 gard_rare diseases +MONDO:0016062 nord_rare diseases +MONDO:0016062 ordo_disorder diseases +MONDO:0016062 ordo_morphological_anomaly diseases +MONDO:0016062 orphanet_rare diseases +MONDO:0016062 rare diseases +MONDO:0016063 gard_rare diseases +MONDO:0016063 nord_rare diseases +MONDO:0016063 ordo_disorder diseases +MONDO:0016063 orphanet_rare diseases +MONDO:0016063 otar diseases +MONDO:0016063 rare diseases +MONDO:0016064 disease_grouping diseases +MONDO:0016064 ordo_group_of_disorders diseases +MONDO:0016064 otar diseases +MONDO:0016065 gard_rare diseases +MONDO:0016065 ordo_disorder diseases +MONDO:0016065 ordo_malformation_syndrome diseases +MONDO:0016065 orphanet_rare diseases +MONDO:0016065 otar diseases +MONDO:0016065 rare diseases +MONDO:0016066 disease_grouping diseases +MONDO:0016066 gard_rare diseases +MONDO:0016066 nord_rare diseases +MONDO:0016066 ordo_disorder diseases +MONDO:0016066 orphanet_rare diseases +MONDO:0016066 rare diseases +MONDO:0016067 gard_rare diseases +MONDO:0016067 nord_rare diseases +MONDO:0016067 ordo_disorder diseases +MONDO:0016067 orphanet_rare diseases +MONDO:0016067 otar diseases +MONDO:0016067 rare diseases +MONDO:0016068 gard_rare diseases +MONDO:0016068 nord_rare diseases +MONDO:0016068 ordo_disorder diseases +MONDO:0016068 orphanet_rare diseases +MONDO:0016068 otar diseases +MONDO:0016068 rare diseases +MONDO:0016070 gard_rare diseases +MONDO:0016070 nord_rare diseases +MONDO:0016070 ordo_disorder diseases +MONDO:0016070 ordo_malformation_syndrome diseases +MONDO:0016070 orphanet_rare diseases +MONDO:0016070 otar diseases +MONDO:0016070 rare diseases +MONDO:0016071 gard_rare diseases +MONDO:0016071 nord_rare diseases +MONDO:0016071 ordo_subtype_of_a_disorder diseases +MONDO:0016071 otar diseases +MONDO:0016071 rare diseases +MONDO:0016073 disease_grouping diseases +MONDO:0016073 gard_rare diseases +MONDO:0016073 ordo_group_of_disorders diseases +MONDO:0016073 otar diseases +MONDO:0016073 rare diseases +MONDO:0016075 disease_grouping diseases +MONDO:0016075 gard_rare diseases +MONDO:0016075 nord_rare diseases +MONDO:0016075 ordo_group_of_disorders diseases +MONDO:0016075 otar diseases +MONDO:0016075 rare diseases +MONDO:0016077 gard_rare diseases +MONDO:0016077 nord_rare diseases +MONDO:0016077 ordo_disorder diseases +MONDO:0016077 ordo_morphological_anomaly diseases +MONDO:0016077 orphanet_rare diseases +MONDO:0016077 rare diseases +MONDO:0016078 gard_rare diseases +MONDO:0016078 nord_rare diseases +MONDO:0016078 ordo_disorder diseases +MONDO:0016078 ordo_morphological_anomaly diseases +MONDO:0016078 orphanet_rare diseases +MONDO:0016078 rare diseases +MONDO:0016079 gard_rare diseases +MONDO:0016079 nord_rare diseases +MONDO:0016079 ordo_disorder diseases +MONDO:0016079 orphanet_rare diseases +MONDO:0016079 rare diseases +MONDO:0016080 gard_rare diseases +MONDO:0016080 nord_rare diseases +MONDO:0016080 ordo_disorder diseases +MONDO:0016080 ordo_morphological_anomaly diseases +MONDO:0016080 orphanet_rare diseases +MONDO:0016080 rare diseases +MONDO:0016081 gard_rare diseases +MONDO:0016081 nord_rare diseases +MONDO:0016081 ordo_disorder diseases +MONDO:0016081 ordo_morphological_anomaly diseases +MONDO:0016081 orphanet_rare diseases +MONDO:0016081 rare diseases +MONDO:0016083 gard_rare diseases +MONDO:0016083 nord_rare diseases +MONDO:0016083 ordo_disorder diseases +MONDO:0016083 orphanet_rare diseases +MONDO:0016083 otar diseases +MONDO:0016083 rare diseases +MONDO:0016085 gard_rare diseases +MONDO:0016085 nord_rare diseases +MONDO:0016085 ordo_disorder diseases +MONDO:0016085 ordo_malformation_syndrome diseases +MONDO:0016085 orphanet_rare diseases +MONDO:0016085 otar diseases +MONDO:0016085 rare diseases +MONDO:0016086 gard_rare diseases +MONDO:0016086 ordo_disorder diseases +MONDO:0016086 orphanet_rare diseases +MONDO:0016086 rare diseases +MONDO:0016087 gard_rare diseases +MONDO:0016087 nord_rare diseases +MONDO:0016087 ordo_disorder diseases +MONDO:0016087 ordo_malformation_syndrome diseases +MONDO:0016087 orphanet_rare diseases +MONDO:0016087 otar diseases +MONDO:0016087 rare diseases +MONDO:0016088 disease_grouping diseases +MONDO:0016088 gard_rare diseases +MONDO:0016088 nord_rare diseases +MONDO:0016088 ordo_group_of_disorders diseases +MONDO:0016088 otar diseases +MONDO:0016088 rare diseases +MONDO:0016089 gard_rare diseases +MONDO:0016089 nord_rare diseases +MONDO:0016089 ordo_subtype_of_a_disorder diseases +MONDO:0016089 otar diseases +MONDO:0016089 rare diseases +MONDO:0016090 gard_rare diseases +MONDO:0016090 nord_rare diseases +MONDO:0016090 ordo_subtype_of_a_disorder diseases +MONDO:0016090 otar diseases +MONDO:0016090 rare diseases +MONDO:0016091 gard_rare diseases +MONDO:0016091 nord_rare diseases +MONDO:0016091 ordo_subtype_of_a_disorder diseases +MONDO:0016091 otar diseases +MONDO:0016091 rare diseases +MONDO:0016092 gard_rare diseases +MONDO:0016092 nord_rare diseases +MONDO:0016092 ordo_disorder diseases +MONDO:0016092 orphanet_rare diseases +MONDO:0016092 rare diseases +MONDO:0016093 gard_rare diseases +MONDO:0016093 nord_rare diseases +MONDO:0016093 otar diseases +MONDO:0016093 rare diseases +MONDO:0016094 gard_rare diseases +MONDO:0016094 nord_rare diseases +MONDO:0016094 ordo_disorder diseases +MONDO:0016094 orphanet_rare diseases +MONDO:0016094 rare diseases +MONDO:0016095 gard_rare diseases +MONDO:0016095 nord_rare diseases +MONDO:0016095 ordo_disorder diseases +MONDO:0016095 orphanet_rare diseases +MONDO:0016095 rare diseases +MONDO:0016096 gard_rare diseases +MONDO:0016096 nord_rare diseases +MONDO:0016096 ordo_disorder diseases +MONDO:0016096 orphanet_rare diseases +MONDO:0016096 rare diseases +MONDO:0016097 gard_rare diseases +MONDO:0016097 nord_rare diseases +MONDO:0016097 ordo_disorder diseases +MONDO:0016097 orphanet_rare diseases +MONDO:0016097 otar diseases +MONDO:0016097 rare diseases +MONDO:0016098 gard_rare diseases +MONDO:0016098 nord_rare diseases +MONDO:0016098 ordo_disorder diseases +MONDO:0016098 orphanet_rare diseases +MONDO:0016098 rare diseases +MONDO:0016099 gard_rare diseases +MONDO:0016099 nord_rare diseases +MONDO:0016099 ordo_disorder diseases +MONDO:0016099 orphanet_rare diseases +MONDO:0016099 rare diseases +MONDO:0016100 gard_rare diseases +MONDO:0016100 nord_rare diseases +MONDO:0016100 ordo_disorder diseases +MONDO:0016100 orphanet_rare diseases +MONDO:0016100 rare diseases +MONDO:0016101 gard_rare diseases +MONDO:0016101 nord_rare diseases +MONDO:0016101 ordo_disorder diseases +MONDO:0016101 orphanet_rare diseases +MONDO:0016101 rare diseases +MONDO:0016102 gard_rare diseases +MONDO:0016102 nord_rare diseases +MONDO:0016102 ordo_disorder diseases +MONDO:0016102 orphanet_rare diseases +MONDO:0016102 rare diseases +MONDO:0016103 nord_rare diseases +MONDO:0016103 ordo_biological_anomaly diseases +MONDO:0016103 ordo_disorder diseases +MONDO:0016103 orphanet_rare diseases +MONDO:0016103 otar diseases +MONDO:0016103 rare diseases +MONDO:0016105 disease_grouping diseases +MONDO:0016105 ordo_group_of_disorders diseases +MONDO:0016106 clingen diseases +MONDO:0016106 disease_grouping diseases +MONDO:0016106 gard_rare diseases +MONDO:0016106 ordo_group_of_disorders diseases +MONDO:0016106 otar diseases +MONDO:0016106 rare diseases +MONDO:0016107 disease_grouping diseases +MONDO:0016107 gard_rare diseases +MONDO:0016107 ordo_group_of_disorders diseases +MONDO:0016107 otar diseases +MONDO:0016107 rare diseases +MONDO:0016108 disease_grouping diseases +MONDO:0016108 gard_rare diseases +MONDO:0016108 ordo_group_of_disorders diseases +MONDO:0016108 otar diseases +MONDO:0016108 rare diseases +MONDO:0016112 disease_grouping diseases +MONDO:0016112 gard_rare diseases +MONDO:0016112 nord_rare diseases +MONDO:0016112 ordo_group_of_disorders diseases +MONDO:0016112 otar diseases +MONDO:0016112 rare diseases +MONDO:0016113 disease_grouping diseases +MONDO:0016113 gard_rare diseases +MONDO:0016113 nord_rare diseases +MONDO:0016113 ordo_group_of_disorders diseases +MONDO:0016113 otar diseases +MONDO:0016113 rare diseases +MONDO:0016120 disease_grouping diseases +MONDO:0016120 gard_rare diseases +MONDO:0016120 nord_rare diseases +MONDO:0016120 ordo_group_of_disorders diseases +MONDO:0016120 otar diseases +MONDO:0016120 rare diseases +MONDO:0016122 disease_grouping diseases +MONDO:0016122 gard_rare diseases +MONDO:0016122 nord_rare diseases +MONDO:0016122 ordo_group_of_disorders diseases +MONDO:0016122 otar diseases +MONDO:0016122 rare diseases +MONDO:0016126 gard_rare diseases +MONDO:0016126 ordo_disorder diseases +MONDO:0016126 orphanet_rare diseases +MONDO:0016126 rare diseases +MONDO:0016127 gard_rare diseases +MONDO:0016127 nord_rare diseases +MONDO:0016127 ordo_disorder diseases +MONDO:0016127 orphanet_rare diseases +MONDO:0016127 rare diseases +MONDO:0016128 disease_grouping diseases +MONDO:0016128 gard_rare diseases +MONDO:0016128 nord_rare diseases +MONDO:0016128 ordo_group_of_disorders diseases +MONDO:0016128 rare diseases +MONDO:0016129 gard_rare diseases +MONDO:0016129 nord_rare diseases +MONDO:0016129 ordo_disorder diseases +MONDO:0016129 orphanet_rare diseases +MONDO:0016129 rare diseases +MONDO:0016130 gard_rare diseases +MONDO:0016130 nord_rare diseases +MONDO:0016130 ordo_disorder diseases +MONDO:0016130 orphanet_rare diseases +MONDO:0016130 rare diseases +MONDO:0016139 disease_grouping diseases +MONDO:0016139 gard_rare diseases +MONDO:0016139 nord_rare diseases +MONDO:0016139 ordo_group_of_disorders diseases +MONDO:0016139 rare diseases +MONDO:0016140 disease_grouping diseases +MONDO:0016140 gard_rare diseases +MONDO:0016140 nord_rare diseases +MONDO:0016140 ordo_group_of_disorders diseases +MONDO:0016140 otar diseases +MONDO:0016140 rare diseases +MONDO:0016141 disease_grouping diseases +MONDO:0016141 gard_rare diseases +MONDO:0016141 nord_rare diseases +MONDO:0016141 ordo_group_of_disorders diseases +MONDO:0016141 otar diseases +MONDO:0016141 rare diseases +MONDO:0016142 disease_grouping diseases +MONDO:0016142 gard_rare diseases +MONDO:0016142 nord_rare diseases +MONDO:0016142 ordo_group_of_disorders diseases +MONDO:0016142 otar diseases +MONDO:0016142 rare diseases +MONDO:0016143 disease_grouping diseases +MONDO:0016143 gard_rare diseases +MONDO:0016143 nord_rare diseases +MONDO:0016143 ordo_group_of_disorders diseases +MONDO:0016143 rare diseases +MONDO:0016144 disease_grouping diseases +MONDO:0016144 gard_rare diseases +MONDO:0016144 nord_rare diseases +MONDO:0016144 ordo_group_of_disorders diseases +MONDO:0016144 otar diseases +MONDO:0016144 rare diseases +MONDO:0016145 disease_grouping diseases +MONDO:0016145 gard_rare diseases +MONDO:0016145 nord_rare diseases +MONDO:0016145 ordo_group_of_disorders diseases +MONDO:0016145 otar diseases +MONDO:0016145 rare diseases +MONDO:0016146 clingen diseases +MONDO:0016146 disease_grouping diseases +MONDO:0016146 gard_rare diseases +MONDO:0016146 ordo_group_of_disorders diseases +MONDO:0016146 otar diseases +MONDO:0016146 rare diseases +MONDO:0016147 disease_grouping diseases +MONDO:0016147 gard_rare diseases +MONDO:0016147 nord_rare diseases +MONDO:0016147 ordo_group_of_disorders diseases +MONDO:0016147 otar diseases +MONDO:0016147 rare diseases +MONDO:0016151 disease_grouping diseases +MONDO:0016151 gard_rare diseases +MONDO:0016151 nord_rare diseases +MONDO:0016151 ordo_group_of_disorders diseases +MONDO:0016151 otar diseases +MONDO:0016151 rare diseases +MONDO:0016153 disease_grouping diseases +MONDO:0016153 gard_rare diseases +MONDO:0016153 nord_rare diseases +MONDO:0016153 ordo_group_of_disorders diseases +MONDO:0016153 rare diseases +MONDO:0016155 disease_grouping diseases +MONDO:0016155 gard_rare diseases +MONDO:0016155 nord_rare diseases +MONDO:0016155 ordo_group_of_disorders diseases +MONDO:0016155 otar diseases +MONDO:0016155 rare diseases +MONDO:0016156 disease_grouping diseases +MONDO:0016156 gard_rare diseases +MONDO:0016156 nord_rare diseases +MONDO:0016156 ordo_group_of_disorders diseases +MONDO:0016156 rare diseases +MONDO:0016158 gard_rare diseases +MONDO:0016158 nord_rare diseases +MONDO:0016158 ordo_disorder diseases +MONDO:0016158 orphanet_rare diseases +MONDO:0016158 otar diseases +MONDO:0016158 rare diseases +MONDO:0016159 gard_rare diseases +MONDO:0016159 nord_rare diseases +MONDO:0016159 ordo_disorder diseases +MONDO:0016159 ordo_malformation_syndrome diseases +MONDO:0016159 orphanet_rare diseases +MONDO:0016159 rare diseases +MONDO:0016160 disease_grouping diseases +MONDO:0016160 gard_rare diseases +MONDO:0016160 nord_rare diseases +MONDO:0016160 ordo_group_of_disorders diseases +MONDO:0016160 rare diseases +MONDO:0016161 gard_rare diseases +MONDO:0016161 nord_rare diseases +MONDO:0016161 ordo_malformation_syndrome diseases +MONDO:0016161 rare diseases +MONDO:0016162 gard_rare diseases +MONDO:0016162 nord_rare diseases +MONDO:0016162 ordo_subtype_of_a_disorder diseases +MONDO:0016162 otar diseases +MONDO:0016162 rare diseases +MONDO:0016163 disease_grouping diseases +MONDO:0016163 gard_rare diseases +MONDO:0016163 nord_rare diseases +MONDO:0016163 ordo_disorder diseases +MONDO:0016163 ordo_group_of_disorders diseases +MONDO:0016163 orphanet_rare diseases +MONDO:0016163 otar diseases +MONDO:0016163 rare diseases +MONDO:0016164 gard_rare diseases +MONDO:0016164 nord_rare diseases +MONDO:0016164 ordo_disorder diseases +MONDO:0016164 orphanet_rare diseases +MONDO:0016164 rare diseases +MONDO:0016165 disease_grouping diseases +MONDO:0016165 gard_rare diseases +MONDO:0016165 ordo_group_of_disorders diseases +MONDO:0016165 otar diseases +MONDO:0016165 rare diseases +MONDO:0016166 disease_grouping diseases +MONDO:0016166 gard_rare diseases +MONDO:0016166 ordo_group_of_disorders diseases +MONDO:0016166 otar diseases +MONDO:0016166 rare diseases +MONDO:0016167 gard_rare diseases +MONDO:0016167 nord_rare diseases +MONDO:0016167 ordo_disorder diseases +MONDO:0016167 orphanet_rare diseases +MONDO:0016167 otar diseases +MONDO:0016167 rare diseases +MONDO:0016168 disease_grouping diseases +MONDO:0016168 gard_rare diseases +MONDO:0016168 nord_rare diseases +MONDO:0016168 ordo_group_of_disorders diseases +MONDO:0016168 otar diseases +MONDO:0016168 rare diseases +MONDO:0016171 gard_rare diseases +MONDO:0016171 nord_rare diseases +MONDO:0016171 rare diseases +MONDO:0016175 disease_grouping diseases +MONDO:0016175 gard_rare diseases +MONDO:0016175 nord_rare diseases +MONDO:0016175 ordo_group_of_disorders diseases +MONDO:0016175 otar diseases +MONDO:0016175 rare diseases +MONDO:0016176 gard_rare diseases +MONDO:0016176 nord_rare diseases +MONDO:0016176 ordo_disorder diseases +MONDO:0016176 orphanet_rare diseases +MONDO:0016176 rare diseases +MONDO:0016184 disease_grouping diseases +MONDO:0016184 gard_rare diseases +MONDO:0016184 nord_rare diseases +MONDO:0016184 ordo_group_of_disorders diseases +MONDO:0016184 rare diseases +MONDO:0016185 disease_grouping diseases +MONDO:0016185 gard_rare diseases +MONDO:0016185 nord_rare diseases +MONDO:0016185 ordo_group_of_disorders diseases +MONDO:0016185 rare diseases +MONDO:0016186 disease_grouping diseases +MONDO:0016186 gard_rare diseases +MONDO:0016186 nord_rare diseases +MONDO:0016186 ordo_group_of_disorders diseases +MONDO:0016186 rare diseases +MONDO:0016187 disease_grouping diseases +MONDO:0016187 gard_rare diseases +MONDO:0016187 nord_rare diseases +MONDO:0016187 ordo_group_of_disorders diseases +MONDO:0016187 rare diseases +MONDO:0016188 disease_grouping diseases +MONDO:0016188 gard_rare diseases +MONDO:0016188 nord_rare diseases +MONDO:0016188 ordo_group_of_disorders diseases +MONDO:0016188 rare diseases +MONDO:0016189 disease_grouping diseases +MONDO:0016189 gard_rare diseases +MONDO:0016189 ordo_group_of_disorders diseases +MONDO:0016189 rare diseases +MONDO:0016190 disease_grouping diseases +MONDO:0016190 gard_rare diseases +MONDO:0016190 ordo_group_of_disorders diseases +MONDO:0016190 rare diseases +MONDO:0016191 disease_grouping diseases +MONDO:0016191 gard_rare diseases +MONDO:0016191 nord_rare diseases +MONDO:0016191 ordo_group_of_disorders diseases +MONDO:0016191 rare diseases +MONDO:0016192 disease_grouping diseases +MONDO:0016192 gard_rare diseases +MONDO:0016192 nord_rare diseases +MONDO:0016192 ordo_group_of_disorders diseases +MONDO:0016192 rare diseases +MONDO:0016193 disease_grouping diseases +MONDO:0016193 gard_rare diseases +MONDO:0016193 nord_rare diseases +MONDO:0016193 ordo_group_of_disorders diseases +MONDO:0016193 rare diseases +MONDO:0016194 disease_grouping diseases +MONDO:0016194 gard_rare diseases +MONDO:0016194 nord_rare diseases +MONDO:0016194 ordo_group_of_disorders diseases +MONDO:0016194 rare diseases +MONDO:0016195 disease_grouping diseases +MONDO:0016195 gard_rare diseases +MONDO:0016195 nord_rare diseases +MONDO:0016195 ordo_group_of_disorders diseases +MONDO:0016195 otar diseases +MONDO:0016195 rare diseases +MONDO:0016197 disease_grouping diseases +MONDO:0016197 gard_rare diseases +MONDO:0016197 ordo_group_of_disorders diseases +MONDO:0016197 rare diseases +MONDO:0016198 disease_grouping diseases +MONDO:0016198 gard_rare diseases +MONDO:0016198 nord_rare diseases +MONDO:0016198 ordo_group_of_disorders diseases +MONDO:0016198 otar diseases +MONDO:0016198 rare diseases +MONDO:0016199 disease_grouping diseases +MONDO:0016199 gard_rare diseases +MONDO:0016199 nord_rare diseases +MONDO:0016199 ordo_group_of_disorders diseases +MONDO:0016199 rare diseases +MONDO:0016202 gard_rare diseases +MONDO:0016202 ordo_disorder diseases +MONDO:0016202 orphanet_rare diseases +MONDO:0016202 otar diseases +MONDO:0016202 rare diseases +MONDO:0016203 gard_rare diseases +MONDO:0016203 nord_rare diseases +MONDO:0016203 ordo_disorder diseases +MONDO:0016203 orphanet_rare diseases +MONDO:0016203 otar diseases +MONDO:0016203 rare diseases +MONDO:0016204 gard_rare diseases +MONDO:0016204 nord_rare diseases +MONDO:0016204 ordo_disorder diseases +MONDO:0016204 orphanet_rare diseases +MONDO:0016204 rare diseases +MONDO:0016205 gard_rare diseases +MONDO:0016205 nord_rare diseases +MONDO:0016205 ordo_disorder diseases +MONDO:0016205 orphanet_rare diseases +MONDO:0016205 otar diseases +MONDO:0016205 rare diseases +MONDO:0016206 gard_rare diseases +MONDO:0016206 ordo_disorder diseases +MONDO:0016206 orphanet_rare diseases +MONDO:0016206 rare diseases +MONDO:0016207 gard_rare diseases +MONDO:0016207 ordo_disorder diseases +MONDO:0016207 orphanet_rare diseases +MONDO:0016207 rare diseases +MONDO:0016208 gard_rare diseases +MONDO:0016208 nord_rare diseases +MONDO:0016208 ordo_disorder diseases +MONDO:0016208 orphanet_rare diseases +MONDO:0016208 rare diseases +MONDO:0016209 gard_rare diseases +MONDO:0016209 nord_rare diseases +MONDO:0016209 ordo_disorder diseases +MONDO:0016209 orphanet_rare diseases +MONDO:0016209 rare diseases +MONDO:0016210 disease_grouping diseases +MONDO:0016210 gard_rare diseases +MONDO:0016210 nord_rare diseases +MONDO:0016210 ordo_group_of_disorders diseases +MONDO:0016210 otar diseases +MONDO:0016210 rare diseases +MONDO:0016211 gard_rare diseases +MONDO:0016211 nord_rare diseases +MONDO:0016211 ordo_disorder diseases +MONDO:0016211 orphanet_rare diseases +MONDO:0016211 rare diseases +MONDO:0016213 gard_rare diseases +MONDO:0016213 nord_rare diseases +MONDO:0016213 ordo_disorder diseases +MONDO:0016213 orphanet_rare diseases +MONDO:0016213 rare diseases +MONDO:0016214 gard_rare diseases +MONDO:0016214 nord_rare diseases +MONDO:0016214 ordo_disorder diseases +MONDO:0016214 orphanet_rare diseases +MONDO:0016214 rare diseases +MONDO:0016215 gard_rare diseases +MONDO:0016215 nord_rare diseases +MONDO:0016215 ordo_disorder diseases +MONDO:0016215 orphanet_rare diseases +MONDO:0016215 otar diseases +MONDO:0016215 rare diseases +MONDO:0016216 gard_rare diseases +MONDO:0016216 nord_rare diseases +MONDO:0016216 ordo_disorder diseases +MONDO:0016216 orphanet_rare diseases +MONDO:0016216 rare diseases +MONDO:0016217 gard_rare diseases +MONDO:0016217 nord_rare diseases +MONDO:0016217 ordo_clinical_syndrome diseases +MONDO:0016217 ordo_disorder diseases +MONDO:0016217 orphanet_rare diseases +MONDO:0016217 rare diseases +MONDO:0016218 disease_grouping diseases +MONDO:0016218 gard_rare diseases +MONDO:0016218 nord_rare diseases +MONDO:0016218 ordo_group_of_disorders diseases +MONDO:0016218 otar diseases +MONDO:0016218 rare diseases +MONDO:0016219 gard_rare diseases +MONDO:0016219 nord_rare diseases +MONDO:0016219 ordo_disorder diseases +MONDO:0016219 ordo_malformation_syndrome diseases +MONDO:0016219 orphanet_rare diseases +MONDO:0016219 rare diseases +MONDO:0016220 gard_rare diseases +MONDO:0016220 nord_rare diseases +MONDO:0016220 ordo_disorder diseases +MONDO:0016220 orphanet_rare diseases +MONDO:0016220 rare diseases +MONDO:0016222 gard_rare diseases +MONDO:0016222 nord_rare diseases +MONDO:0016222 ordo_disorder diseases +MONDO:0016222 orphanet_rare diseases +MONDO:0016222 otar diseases +MONDO:0016222 rare diseases +MONDO:0016223 disease_grouping diseases +MONDO:0016223 gard_rare diseases +MONDO:0016223 nord_rare diseases +MONDO:0016223 ordo_group_of_disorders diseases +MONDO:0016223 rare diseases +MONDO:0016225 disease_grouping diseases +MONDO:0016225 nord_rare diseases +MONDO:0016225 ordo_group_of_disorders diseases +MONDO:0016225 rare diseases +MONDO:0016226 clingen diseases +MONDO:0016226 disease_grouping diseases +MONDO:0016226 nord_rare diseases +MONDO:0016226 ordo_group_of_disorders diseases +MONDO:0016226 otar diseases +MONDO:0016226 rare diseases +MONDO:0016227 disease_grouping diseases +MONDO:0016227 gard_rare diseases +MONDO:0016227 nord_rare diseases +MONDO:0016227 ordo_group_of_disorders diseases +MONDO:0016227 otar diseases +MONDO:0016227 rare diseases +MONDO:0016231 disease_grouping diseases +MONDO:0016231 ordo_group_of_disorders diseases +MONDO:0016231 otar diseases +MONDO:0016236 gard_rare diseases +MONDO:0016236 nord_rare diseases +MONDO:0016236 ordo_disorder diseases +MONDO:0016236 orphanet_rare diseases +MONDO:0016236 otar diseases +MONDO:0016236 rare diseases +MONDO:0016237 gard_rare diseases +MONDO:0016237 nord_rare diseases +MONDO:0016237 ordo_disorder diseases +MONDO:0016237 ordo_malformation_syndrome diseases +MONDO:0016237 orphanet_rare diseases +MONDO:0016237 rare diseases +MONDO:0016238 gard_rare diseases +MONDO:0016238 nord_rare diseases +MONDO:0016238 ordo_disorder diseases +MONDO:0016238 orphanet_rare diseases +MONDO:0016238 otar diseases +MONDO:0016238 rare diseases +MONDO:0016239 gard_rare diseases +MONDO:0016239 nord_rare diseases +MONDO:0016239 ordo_disorder diseases +MONDO:0016239 orphanet_rare diseases +MONDO:0016239 otar diseases +MONDO:0016239 rare diseases +MONDO:0016240 disease_grouping diseases +MONDO:0016240 gard_rare diseases +MONDO:0016240 ordo_group_of_disorders diseases +MONDO:0016240 rare diseases +MONDO:0016241 gard_rare diseases +MONDO:0016241 nord_rare diseases +MONDO:0016241 ordo_disorder diseases +MONDO:0016241 orphanet_rare diseases +MONDO:0016241 otar diseases +MONDO:0016241 rare diseases +MONDO:0016242 nord_rare diseases +MONDO:0016242 ordo_disorder diseases +MONDO:0016242 orphanet_rare diseases +MONDO:0016242 otar diseases +MONDO:0016242 rare diseases +MONDO:0016243 gard_rare diseases +MONDO:0016243 nord_rare diseases +MONDO:0016243 ordo_disorder diseases +MONDO:0016243 orphanet_rare diseases +MONDO:0016243 otar diseases +MONDO:0016243 rare diseases +MONDO:0016244 clingen diseases +MONDO:0016244 gard_rare diseases +MONDO:0016244 nord_rare diseases +MONDO:0016244 ordo_disorder diseases +MONDO:0016244 orphanet_rare diseases +MONDO:0016244 otar diseases +MONDO:0016244 rare diseases +MONDO:0016248 clingen diseases +MONDO:0016248 disease_grouping diseases +MONDO:0016248 gard_rare diseases +MONDO:0016248 otar diseases +MONDO:0016248 rare diseases +MONDO:0016249 gard_rare diseases +MONDO:0016249 otar diseases +MONDO:0016249 rare diseases +MONDO:0016255 disease_grouping diseases +MONDO:0016255 gard_rare diseases +MONDO:0016255 ordo_group_of_disorders diseases +MONDO:0016255 rare diseases +MONDO:0016256 gard_rare diseases +MONDO:0016256 nord_rare diseases +MONDO:0016256 ordo_disorder diseases +MONDO:0016256 ordo_malformation_syndrome diseases +MONDO:0016256 orphanet_rare diseases +MONDO:0016256 otar diseases +MONDO:0016256 rare diseases +MONDO:0016258 gard_rare diseases +MONDO:0016258 nord_rare diseases +MONDO:0016258 ordo_disorder diseases +MONDO:0016258 orphanet_rare diseases +MONDO:0016258 rare diseases +MONDO:0016259 gard_rare diseases +MONDO:0016259 nord_rare diseases +MONDO:0016259 ordo_disorder diseases +MONDO:0016259 orphanet_rare diseases +MONDO:0016259 otar diseases +MONDO:0016259 rare diseases +MONDO:0016260 gard_rare diseases +MONDO:0016260 nord_rare diseases +MONDO:0016260 ordo_disorder diseases +MONDO:0016260 orphanet_rare diseases +MONDO:0016260 otar diseases +MONDO:0016260 rare diseases +MONDO:0016262 gard_rare diseases +MONDO:0016262 nord_rare diseases +MONDO:0016262 ordo_disorder diseases +MONDO:0016262 orphanet_rare diseases +MONDO:0016262 otar diseases +MONDO:0016262 rare diseases +MONDO:0016263 gard_rare diseases +MONDO:0016263 nord_rare diseases +MONDO:0016263 ordo_disorder diseases +MONDO:0016263 orphanet_rare diseases +MONDO:0016263 rare diseases +MONDO:0016264 gard_rare diseases +MONDO:0016264 nord_rare diseases +MONDO:0016264 ordo_disorder diseases +MONDO:0016264 orphanet_rare diseases +MONDO:0016264 otar diseases +MONDO:0016264 rare diseases +MONDO:0016266 gard_rare diseases +MONDO:0016266 nord_rare diseases +MONDO:0016266 ordo_disorder diseases +MONDO:0016266 orphanet_rare diseases +MONDO:0016266 rare diseases +MONDO:0016267 gard_rare diseases +MONDO:0016267 nord_rare diseases +MONDO:0016267 ordo_disorder diseases +MONDO:0016267 orphanet_rare diseases +MONDO:0016267 rare diseases +MONDO:0016268 gard_rare diseases +MONDO:0016268 nord_rare diseases +MONDO:0016268 ordo_disorder diseases +MONDO:0016268 orphanet_rare diseases +MONDO:0016268 rare diseases +MONDO:0016269 gard_rare diseases +MONDO:0016269 nord_rare diseases +MONDO:0016269 ordo_disorder diseases +MONDO:0016269 orphanet_rare diseases +MONDO:0016269 rare diseases +MONDO:0016270 gard_rare diseases +MONDO:0016270 nord_rare diseases +MONDO:0016270 ordo_disorder diseases +MONDO:0016270 orphanet_rare diseases +MONDO:0016270 rare diseases +MONDO:0016271 gard_rare diseases +MONDO:0016271 rare diseases +MONDO:0016272 gard_rare diseases +MONDO:0016272 nord_rare diseases +MONDO:0016272 ordo_disorder diseases +MONDO:0016272 orphanet_rare diseases +MONDO:0016272 rare diseases +MONDO:0016273 gard_rare diseases +MONDO:0016273 nord_rare diseases +MONDO:0016273 ordo_disorder diseases +MONDO:0016273 orphanet_rare diseases +MONDO:0016273 rare diseases +MONDO:0016276 gard_rare diseases +MONDO:0016276 nord_rare diseases +MONDO:0016276 ordo_disorder diseases +MONDO:0016276 orphanet_rare diseases +MONDO:0016276 rare diseases +MONDO:0016277 disease_grouping diseases +MONDO:0016277 gard_rare diseases +MONDO:0016277 nord_rare diseases +MONDO:0016277 ordo_group_of_disorders diseases +MONDO:0016277 rare diseases +MONDO:0016280 disease_grouping diseases +MONDO:0016280 gard_rare diseases +MONDO:0016280 nord_rare diseases +MONDO:0016280 ordo_group_of_disorders diseases +MONDO:0016280 rare diseases +MONDO:0016281 gard_rare diseases +MONDO:0016281 ordo_disorder diseases +MONDO:0016281 ordo_malformation_syndrome diseases +MONDO:0016281 orphanet_rare diseases +MONDO:0016281 otar diseases +MONDO:0016281 rare diseases +MONDO:0016282 gard_rare diseases +MONDO:0016282 nord_rare diseases +MONDO:0016282 ordo_disorder diseases +MONDO:0016282 orphanet_rare diseases +MONDO:0016282 rare diseases +MONDO:0016283 gard_rare diseases +MONDO:0016283 nord_rare diseases +MONDO:0016283 ordo_disorder diseases +MONDO:0016283 orphanet_rare diseases +MONDO:0016283 rare diseases +MONDO:0016284 gard_rare diseases +MONDO:0016284 nord_rare diseases +MONDO:0016284 ordo_disorder diseases +MONDO:0016284 orphanet_rare diseases +MONDO:0016284 rare diseases +MONDO:0016285 gard_rare diseases +MONDO:0016285 nord_rare diseases +MONDO:0016285 rare diseases +MONDO:0016289 gard_rare diseases +MONDO:0016289 nord_rare diseases +MONDO:0016289 ordo_disorder diseases +MONDO:0016289 orphanet_rare diseases +MONDO:0016289 rare diseases +MONDO:0016290 gard_rare diseases +MONDO:0016290 nord_rare diseases +MONDO:0016290 ordo_disorder diseases +MONDO:0016290 ordo_malformation_syndrome diseases +MONDO:0016290 orphanet_rare diseases +MONDO:0016290 otar diseases +MONDO:0016290 rare diseases +MONDO:0016291 gard_rare diseases +MONDO:0016291 nord_rare diseases +MONDO:0016291 ordo_disorder diseases +MONDO:0016291 ordo_malformation_syndrome diseases +MONDO:0016291 orphanet_rare diseases +MONDO:0016291 otar diseases +MONDO:0016291 rare diseases +MONDO:0016292 gard_rare diseases +MONDO:0016292 nord_rare diseases +MONDO:0016292 ordo_disorder diseases +MONDO:0016292 ordo_morphological_anomaly diseases +MONDO:0016292 orphanet_rare diseases +MONDO:0016292 otar diseases +MONDO:0016292 rare diseases +MONDO:0016293 gard_rare diseases +MONDO:0016293 ordo_disorder diseases +MONDO:0016293 orphanet_rare diseases +MONDO:0016293 otar diseases +MONDO:0016293 rare diseases +MONDO:0016294 gard_rare diseases +MONDO:0016294 ordo_disorder diseases +MONDO:0016294 ordo_malformation_syndrome diseases +MONDO:0016294 orphanet_rare diseases +MONDO:0016294 otar diseases +MONDO:0016294 rare diseases +MONDO:0016295 clingen diseases +MONDO:0016295 disease_grouping diseases +MONDO:0016295 gard_rare diseases +MONDO:0016295 ordo_group_of_disorders diseases +MONDO:0016295 otar diseases +MONDO:0016295 rare diseases +MONDO:0016296 clingen diseases +MONDO:0016296 gard_rare diseases +MONDO:0016296 nord_rare diseases +MONDO:0016296 ordo_disorder diseases +MONDO:0016296 ordo_malformation_syndrome diseases +MONDO:0016296 orphanet_rare diseases +MONDO:0016296 otar diseases +MONDO:0016296 rare diseases +MONDO:0016297 gard_rare diseases +MONDO:0016297 rare diseases +MONDO:0016298 gard_rare diseases +MONDO:0016298 rare diseases +MONDO:0016299 gard_rare diseases +MONDO:0016299 nord_rare diseases +MONDO:0016299 ordo_disorder diseases +MONDO:0016299 ordo_malformation_syndrome diseases +MONDO:0016299 orphanet_rare diseases +MONDO:0016299 rare diseases +MONDO:0016301 gard_rare diseases +MONDO:0016301 nord_rare diseases +MONDO:0016301 ordo_disorder diseases +MONDO:0016301 ordo_morphological_anomaly diseases +MONDO:0016301 orphanet_rare diseases +MONDO:0016301 rare diseases +MONDO:0016302 gard_rare diseases +MONDO:0016302 nord_rare diseases +MONDO:0016302 ordo_subtype_of_a_disorder diseases +MONDO:0016302 rare diseases +MONDO:0016303 gard_rare diseases +MONDO:0016303 nord_rare diseases +MONDO:0016303 ordo_subtype_of_a_disorder diseases +MONDO:0016303 rare diseases +MONDO:0016304 gard_rare diseases +MONDO:0016304 nord_rare diseases +MONDO:0016304 ordo_subtype_of_a_disorder diseases +MONDO:0016304 otar diseases +MONDO:0016304 rare diseases +MONDO:0016305 gard_rare diseases +MONDO:0016305 nord_rare diseases +MONDO:0016305 ordo_subtype_of_a_disorder diseases +MONDO:0016305 otar diseases +MONDO:0016305 rare diseases +MONDO:0016306 gard_rare diseases +MONDO:0016306 nord_rare diseases +MONDO:0016306 ordo_subtype_of_a_disorder diseases +MONDO:0016306 otar diseases +MONDO:0016306 rare diseases +MONDO:0016307 gard_rare diseases +MONDO:0016307 nord_rare diseases +MONDO:0016307 ordo_subtype_of_a_disorder diseases +MONDO:0016307 otar diseases +MONDO:0016307 rare diseases +MONDO:0016308 gard_rare diseases +MONDO:0016308 nord_rare diseases +MONDO:0016308 ordo_subtype_of_a_disorder diseases +MONDO:0016308 otar diseases +MONDO:0016308 rare diseases +MONDO:0016309 gard_rare diseases +MONDO:0016309 nord_rare diseases +MONDO:0016309 ordo_subtype_of_a_disorder diseases +MONDO:0016309 otar diseases +MONDO:0016309 rare diseases +MONDO:0016310 gard_rare diseases +MONDO:0016310 nord_rare diseases +MONDO:0016310 ordo_subtype_of_a_disorder diseases +MONDO:0016310 otar diseases +MONDO:0016310 rare diseases +MONDO:0016311 gard_rare diseases +MONDO:0016311 nord_rare diseases +MONDO:0016311 ordo_disorder diseases +MONDO:0016311 ordo_malformation_syndrome diseases +MONDO:0016311 orphanet_rare diseases +MONDO:0016311 rare diseases +MONDO:0016312 nord_rare diseases +MONDO:0016312 ordo_clinical_situation diseases +MONDO:0016312 ordo_disorder diseases +MONDO:0016312 orphanet_rare diseases +MONDO:0016312 rare diseases +MONDO:0016315 gard_rare diseases +MONDO:0016315 nord_rare diseases +MONDO:0016315 ordo_subtype_of_a_disorder diseases +MONDO:0016315 otar diseases +MONDO:0016315 rare diseases +MONDO:0016316 gard_rare diseases +MONDO:0016316 nord_rare diseases +MONDO:0016316 ordo_subtype_of_a_disorder diseases +MONDO:0016316 otar diseases +MONDO:0016316 rare diseases +MONDO:0016318 gard_rare diseases +MONDO:0016318 nord_rare diseases +MONDO:0016318 ordo_disorder diseases +MONDO:0016318 orphanet_rare diseases +MONDO:0016318 otar diseases +MONDO:0016318 rare diseases +MONDO:0016319 gard_rare diseases +MONDO:0016319 nord_rare diseases +MONDO:0016319 ordo_disorder diseases +MONDO:0016319 orphanet_rare diseases +MONDO:0016319 rare diseases +MONDO:0016321 gard_rare diseases +MONDO:0016321 nord_rare diseases +MONDO:0016321 ordo_disorder diseases +MONDO:0016321 orphanet_rare diseases +MONDO:0016321 rare diseases +MONDO:0016322 gard_rare diseases +MONDO:0016322 nord_rare diseases +MONDO:0016322 ordo_disorder diseases +MONDO:0016322 orphanet_rare diseases +MONDO:0016322 otar diseases +MONDO:0016322 rare diseases +MONDO:0016323 gard_rare diseases +MONDO:0016323 nord_rare diseases +MONDO:0016323 ordo_disorder diseases +MONDO:0016323 orphanet_rare diseases +MONDO:0016323 otar diseases +MONDO:0016323 rare diseases +MONDO:0016330 disease_grouping diseases +MONDO:0016330 inferred_rare diseases +MONDO:0016330 ordo_group_of_disorders diseases +MONDO:0016330 rare diseases +MONDO:0016331 gard_rare diseases +MONDO:0016331 ordo_subtype_of_a_disorder diseases +MONDO:0016331 otar diseases +MONDO:0016331 rare diseases +MONDO:0016332 gard_rare diseases +MONDO:0016332 rare diseases +MONDO:0016333 disease_grouping diseases +MONDO:0016333 gard_rare diseases +MONDO:0016333 ordo_group_of_disorders diseases +MONDO:0016333 otar diseases +MONDO:0016333 rare diseases +MONDO:0016338 disease_grouping diseases +MONDO:0016338 gard_rare diseases +MONDO:0016338 nord_rare diseases +MONDO:0016338 ordo_group_of_disorders diseases +MONDO:0016338 rare diseases +MONDO:0016340 disease_grouping diseases +MONDO:0016340 gard_rare diseases +MONDO:0016340 nord_rare diseases +MONDO:0016340 ordo_group_of_disorders diseases +MONDO:0016340 otar diseases +MONDO:0016340 rare diseases +MONDO:0016342 clingen diseases +MONDO:0016342 gard_rare diseases +MONDO:0016342 nord_rare diseases +MONDO:0016342 ordo_disorder diseases +MONDO:0016342 orphanet_rare diseases +MONDO:0016342 otar diseases +MONDO:0016342 rare diseases +MONDO:0016344 gard_rare diseases +MONDO:0016344 nord_rare diseases +MONDO:0016344 ordo_disorder diseases +MONDO:0016344 ordo_malformation_syndrome diseases +MONDO:0016344 orphanet_rare diseases +MONDO:0016344 otar diseases +MONDO:0016344 rare diseases +MONDO:0016345 disease_grouping diseases +MONDO:0016345 gard_rare diseases +MONDO:0016345 ordo_group_of_disorders diseases +MONDO:0016345 rare diseases +MONDO:0016346 gard_rare diseases +MONDO:0016346 ordo_disorder diseases +MONDO:0016346 ordo_malformation_syndrome diseases +MONDO:0016346 orphanet_rare diseases +MONDO:0016346 otar diseases +MONDO:0016346 rare diseases +MONDO:0016349 gard_rare diseases +MONDO:0016349 nord_rare diseases +MONDO:0016349 ordo_disorder diseases +MONDO:0016349 ordo_malformation_syndrome diseases +MONDO:0016349 orphanet_rare diseases +MONDO:0016349 otar diseases +MONDO:0016349 rare diseases +MONDO:0016350 gard_rare diseases +MONDO:0016350 nord_rare diseases +MONDO:0016350 ordo_disorder diseases +MONDO:0016350 ordo_malformation_syndrome diseases +MONDO:0016350 orphanet_rare diseases +MONDO:0016350 rare diseases +MONDO:0016351 gard_rare diseases +MONDO:0016351 nord_rare diseases +MONDO:0016351 rare diseases +MONDO:0016353 gard_rare diseases +MONDO:0016353 nord_rare diseases +MONDO:0016353 ordo_disorder diseases +MONDO:0016353 orphanet_rare diseases +MONDO:0016353 rare diseases +MONDO:0016354 gard_rare diseases +MONDO:0016354 nord_rare diseases +MONDO:0016354 ordo_disorder diseases +MONDO:0016354 orphanet_rare diseases +MONDO:0016354 otar diseases +MONDO:0016354 rare diseases +MONDO:0016356 gard_rare diseases +MONDO:0016356 nord_rare diseases +MONDO:0016356 ordo_subtype_of_a_disorder diseases +MONDO:0016356 rare diseases +MONDO:0016357 gard_rare diseases +MONDO:0016357 nord_rare diseases +MONDO:0016357 ordo_disorder diseases +MONDO:0016357 ordo_malformation_syndrome diseases +MONDO:0016357 orphanet_rare diseases +MONDO:0016357 rare diseases +MONDO:0016358 gard_rare diseases +MONDO:0016358 nord_rare diseases +MONDO:0016358 ordo_subtype_of_a_disorder diseases +MONDO:0016358 rare diseases +MONDO:0016359 gard_rare diseases +MONDO:0016359 nord_rare diseases +MONDO:0016359 ordo_subtype_of_a_disorder diseases +MONDO:0016359 rare diseases +MONDO:0016360 gard_rare diseases +MONDO:0016360 nord_rare diseases +MONDO:0016360 ordo_disorder diseases +MONDO:0016360 orphanet_rare diseases +MONDO:0016360 rare diseases +MONDO:0016362 gard_rare diseases +MONDO:0016362 nord_rare diseases +MONDO:0016362 ordo_disorder diseases +MONDO:0016362 orphanet_rare diseases +MONDO:0016362 otar diseases +MONDO:0016362 rare diseases +MONDO:0016364 gard_rare diseases +MONDO:0016364 nord_rare diseases +MONDO:0016364 ordo_disorder diseases +MONDO:0016364 orphanet_rare diseases +MONDO:0016364 otar diseases +MONDO:0016364 rare diseases +MONDO:0016365 disease_grouping diseases +MONDO:0016365 gard_rare diseases +MONDO:0016365 ordo_group_of_disorders diseases +MONDO:0016365 rare diseases +MONDO:0016366 gard_rare diseases +MONDO:0016366 nord_rare diseases +MONDO:0016366 ordo_disorder diseases +MONDO:0016366 ordo_malformation_syndrome diseases +MONDO:0016366 orphanet_rare diseases +MONDO:0016366 otar diseases +MONDO:0016366 rare diseases +MONDO:0016367 gard_rare diseases +MONDO:0016367 nord_rare diseases +MONDO:0016367 ordo_disorder diseases +MONDO:0016367 orphanet_rare diseases +MONDO:0016367 otar diseases +MONDO:0016367 rare diseases +MONDO:0016368 gard_rare diseases +MONDO:0016368 nord_rare diseases +MONDO:0016368 ordo_subtype_of_a_disorder diseases +MONDO:0016368 otar diseases +MONDO:0016368 rare diseases +MONDO:0016369 gard_rare diseases +MONDO:0016369 nord_rare diseases +MONDO:0016369 ordo_subtype_of_a_disorder diseases +MONDO:0016369 otar diseases +MONDO:0016369 rare diseases +MONDO:0016370 gard_rare diseases +MONDO:0016370 nord_rare diseases +MONDO:0016370 ordo_disorder diseases +MONDO:0016370 orphanet_rare diseases +MONDO:0016370 otar diseases +MONDO:0016370 rare diseases +MONDO:0016371 gard_rare diseases +MONDO:0016371 nord_rare diseases +MONDO:0016371 ordo_disorder diseases +MONDO:0016371 orphanet_rare diseases +MONDO:0016371 rare diseases +MONDO:0016372 gard_rare diseases +MONDO:0016372 nord_rare diseases +MONDO:0016372 ordo_disorder diseases +MONDO:0016372 orphanet_rare diseases +MONDO:0016372 rare diseases +MONDO:0016374 disease_grouping diseases +MONDO:0016374 gard_rare diseases +MONDO:0016374 nord_rare diseases +MONDO:0016374 ordo_group_of_disorders diseases +MONDO:0016374 rare diseases +MONDO:0016376 gard_rare diseases +MONDO:0016376 nord_rare diseases +MONDO:0016376 ordo_disorder diseases +MONDO:0016376 orphanet_rare diseases +MONDO:0016376 rare diseases +MONDO:0016377 gard_rare diseases +MONDO:0016377 otar diseases +MONDO:0016377 rare diseases +MONDO:0016378 gard_rare diseases +MONDO:0016378 nord_rare diseases +MONDO:0016378 ordo_disorder diseases +MONDO:0016378 ordo_malformation_syndrome diseases +MONDO:0016378 orphanet_rare diseases +MONDO:0016378 rare diseases +MONDO:0016379 gard_rare diseases +MONDO:0016379 nord_rare diseases +MONDO:0016379 ordo_disorder diseases +MONDO:0016379 orphanet_rare diseases +MONDO:0016379 rare diseases +MONDO:0016380 gard_rare diseases +MONDO:0016380 nord_rare diseases +MONDO:0016380 ordo_disorder diseases +MONDO:0016380 orphanet_rare diseases +MONDO:0016380 rare diseases +MONDO:0016381 gard_rare diseases +MONDO:0016381 nord_rare diseases +MONDO:0016381 ordo_disorder diseases +MONDO:0016381 orphanet_rare diseases +MONDO:0016381 otar diseases +MONDO:0016381 rare diseases +MONDO:0016382 disease_grouping diseases +MONDO:0016382 gard_rare diseases +MONDO:0016382 ordo_group_of_disorders diseases +MONDO:0016382 rare diseases +MONDO:0016383 gard_rare diseases +MONDO:0016383 nord_rare diseases +MONDO:0016383 ordo_disorder diseases +MONDO:0016383 orphanet_rare diseases +MONDO:0016383 otar diseases +MONDO:0016383 rare diseases +MONDO:0016384 gard_rare diseases +MONDO:0016384 nord_rare diseases +MONDO:0016384 ordo_disorder diseases +MONDO:0016384 orphanet_rare diseases +MONDO:0016384 rare diseases +MONDO:0016385 gard_rare diseases +MONDO:0016385 ordo_disorder diseases +MONDO:0016385 orphanet_rare diseases +MONDO:0016385 otar diseases +MONDO:0016385 rare diseases +MONDO:0016386 gard_rare diseases +MONDO:0016386 nord_rare diseases +MONDO:0016386 ordo_disorder diseases +MONDO:0016386 orphanet_rare diseases +MONDO:0016386 otar diseases +MONDO:0016386 rare diseases +MONDO:0016387 disease_grouping diseases +MONDO:0016387 gard_rare diseases +MONDO:0016387 ordo_group_of_disorders diseases +MONDO:0016387 otar diseases +MONDO:0016387 rare diseases +MONDO:0016390 gard_rare diseases +MONDO:0016390 nord_rare diseases +MONDO:0016390 ordo_disorder diseases +MONDO:0016390 orphanet_rare diseases +MONDO:0016390 otar diseases +MONDO:0016390 rare diseases +MONDO:0016391 disease_grouping diseases +MONDO:0016391 gard_rare diseases +MONDO:0016391 nord_rare diseases +MONDO:0016391 ordo_group_of_disorders diseases +MONDO:0016391 otar diseases +MONDO:0016391 rare diseases +MONDO:0016392 gard_rare diseases +MONDO:0016392 nord_rare diseases +MONDO:0016392 ordo_disorder diseases +MONDO:0016392 ordo_malformation_syndrome diseases +MONDO:0016392 orphanet_rare diseases +MONDO:0016392 rare diseases +MONDO:0016393 gard_rare diseases +MONDO:0016393 nord_rare diseases +MONDO:0016393 ordo_disorder diseases +MONDO:0016393 orphanet_rare diseases +MONDO:0016393 otar diseases +MONDO:0016393 rare diseases +MONDO:0016394 gard_rare diseases +MONDO:0016394 nord_rare diseases +MONDO:0016394 ordo_disorder diseases +MONDO:0016394 orphanet_rare diseases +MONDO:0016394 otar diseases +MONDO:0016394 rare diseases +MONDO:0016395 gard_rare diseases +MONDO:0016395 nord_rare diseases +MONDO:0016395 ordo_disorder diseases +MONDO:0016395 orphanet_rare diseases +MONDO:0016395 otar diseases +MONDO:0016395 rare diseases +MONDO:0016396 gard_rare diseases +MONDO:0016396 nord_rare diseases +MONDO:0016396 ordo_disorder diseases +MONDO:0016396 ordo_malformation_syndrome diseases +MONDO:0016396 orphanet_rare diseases +MONDO:0016396 otar diseases +MONDO:0016396 rare diseases +MONDO:0016407 gard_rare diseases +MONDO:0016407 nord_rare diseases +MONDO:0016407 ordo_disorder diseases +MONDO:0016407 ordo_morphological_anomaly diseases +MONDO:0016407 orphanet_rare diseases +MONDO:0016407 rare diseases +MONDO:0016408 disease_grouping diseases +MONDO:0016408 gard_rare diseases +MONDO:0016408 nord_rare diseases +MONDO:0016408 ordo_group_of_disorders diseases +MONDO:0016408 otar diseases +MONDO:0016408 rare diseases +MONDO:0016410 disease_grouping diseases +MONDO:0016410 gard_rare diseases +MONDO:0016410 nord_rare diseases +MONDO:0016410 ordo_group_of_disorders diseases +MONDO:0016410 otar diseases +MONDO:0016410 rare diseases +MONDO:0016411 gard_rare diseases +MONDO:0016411 nord_rare diseases +MONDO:0016411 ordo_disorder diseases +MONDO:0016411 orphanet_rare diseases +MONDO:0016411 otar diseases +MONDO:0016411 rare diseases +MONDO:0016412 disease_grouping diseases +MONDO:0016412 gard_rare diseases +MONDO:0016412 otar diseases +MONDO:0016412 rare diseases +MONDO:0016413 gard_rare diseases +MONDO:0016413 nord_rare diseases +MONDO:0016413 ordo_disorder diseases +MONDO:0016413 orphanet_rare diseases +MONDO:0016413 rare diseases +MONDO:0016414 gard_rare diseases +MONDO:0016414 ordo_disorder diseases +MONDO:0016414 orphanet_rare diseases +MONDO:0016414 otar diseases +MONDO:0016414 rare diseases +MONDO:0016416 gard_rare diseases +MONDO:0016416 nord_rare diseases +MONDO:0016416 ordo_disorder diseases +MONDO:0016416 ordo_morphological_anomaly diseases +MONDO:0016416 orphanet_rare diseases +MONDO:0016416 rare diseases +MONDO:0016417 gard_rare diseases +MONDO:0016417 ordo_disorder diseases +MONDO:0016417 orphanet_rare diseases +MONDO:0016417 otar diseases +MONDO:0016417 rare diseases +MONDO:0016418 gard_rare diseases +MONDO:0016418 nord_rare diseases +MONDO:0016418 ordo_subtype_of_a_disorder diseases +MONDO:0016418 rare diseases +MONDO:0016419 clingen diseases +MONDO:0016419 gard_rare diseases +MONDO:0016419 nord_rare diseases +MONDO:0016419 ordo_disorder diseases +MONDO:0016419 orphanet_rare diseases +MONDO:0016419 otar diseases +MONDO:0016419 rare diseases +MONDO:0016420 disease_grouping diseases +MONDO:0016420 gard_rare diseases +MONDO:0016420 rare diseases +MONDO:0016421 gard_rare diseases +MONDO:0016421 nord_rare diseases +MONDO:0016421 ordo_disorder diseases +MONDO:0016421 orphanet_rare diseases +MONDO:0016421 rare diseases +MONDO:0016422 gard_rare diseases +MONDO:0016422 nord_rare diseases +MONDO:0016422 ordo_disorder diseases +MONDO:0016422 orphanet_rare diseases +MONDO:0016422 rare diseases +MONDO:0016423 gard_rare diseases +MONDO:0016423 nord_rare diseases +MONDO:0016423 ordo_disorder diseases +MONDO:0016423 orphanet_rare diseases +MONDO:0016423 rare diseases +MONDO:0016424 gard_rare diseases +MONDO:0016424 nord_rare diseases +MONDO:0016424 ordo_disorder diseases +MONDO:0016424 orphanet_rare diseases +MONDO:0016424 otar diseases +MONDO:0016424 rare diseases +MONDO:0016425 gard_rare diseases +MONDO:0016425 nord_rare diseases +MONDO:0016425 ordo_disorder diseases +MONDO:0016425 orphanet_rare diseases +MONDO:0016425 rare diseases +MONDO:0016426 gard_rare diseases +MONDO:0016426 nord_rare diseases +MONDO:0016426 ordo_disorder diseases +MONDO:0016426 orphanet_rare diseases +MONDO:0016426 otar diseases +MONDO:0016426 rare diseases +MONDO:0016429 gard_rare diseases +MONDO:0016429 nord_rare diseases +MONDO:0016429 ordo_disorder diseases +MONDO:0016429 orphanet_rare diseases +MONDO:0016429 rare diseases +MONDO:0016430 gard_rare diseases +MONDO:0016430 nord_rare diseases +MONDO:0016430 ordo_disorder diseases +MONDO:0016430 orphanet_rare diseases +MONDO:0016430 rare diseases +MONDO:0016431 gard_rare diseases +MONDO:0016431 nord_rare diseases +MONDO:0016431 ordo_disorder diseases +MONDO:0016431 orphanet_rare diseases +MONDO:0016431 otar diseases +MONDO:0016431 rare diseases +MONDO:0016432 disease_grouping diseases +MONDO:0016432 gard_rare diseases +MONDO:0016432 nord_rare diseases +MONDO:0016432 ordo_group_of_disorders diseases +MONDO:0016432 otar diseases +MONDO:0016432 rare diseases +MONDO:0016433 gard_rare diseases +MONDO:0016433 nord_rare diseases +MONDO:0016433 ordo_disorder diseases +MONDO:0016433 ordo_malformation_syndrome diseases +MONDO:0016433 orphanet_rare diseases +MONDO:0016433 rare diseases +MONDO:0016437 gard_rare diseases +MONDO:0016437 nord_rare diseases +MONDO:0016437 ordo_disorder diseases +MONDO:0016437 orphanet_rare diseases +MONDO:0016437 rare diseases +MONDO:0016438 gard_rare diseases +MONDO:0016438 nord_rare diseases +MONDO:0016438 ordo_disorder diseases +MONDO:0016438 orphanet_rare diseases +MONDO:0016438 rare diseases +MONDO:0016439 gard_rare diseases +MONDO:0016439 nord_rare diseases +MONDO:0016439 ordo_disorder diseases +MONDO:0016439 orphanet_rare diseases +MONDO:0016439 rare diseases +MONDO:0016440 gard_rare diseases +MONDO:0016440 nord_rare diseases +MONDO:0016440 ordo_disorder diseases +MONDO:0016440 orphanet_rare diseases +MONDO:0016440 rare diseases +MONDO:0016441 gard_rare diseases +MONDO:0016441 nord_rare diseases +MONDO:0016441 ordo_disorder diseases +MONDO:0016441 orphanet_rare diseases +MONDO:0016441 rare diseases +MONDO:0016442 gard_rare diseases +MONDO:0016442 nord_rare diseases +MONDO:0016442 ordo_disorder diseases +MONDO:0016442 orphanet_rare diseases +MONDO:0016442 rare diseases +MONDO:0016443 gard_rare diseases +MONDO:0016443 nord_rare diseases +MONDO:0016443 ordo_disorder diseases +MONDO:0016443 orphanet_rare diseases +MONDO:0016443 rare diseases +MONDO:0016444 gard_rare diseases +MONDO:0016444 nord_rare diseases +MONDO:0016444 ordo_disorder diseases +MONDO:0016444 orphanet_rare diseases +MONDO:0016444 rare diseases +MONDO:0016445 gard_rare diseases +MONDO:0016445 nord_rare diseases +MONDO:0016445 ordo_disorder diseases +MONDO:0016445 orphanet_rare diseases +MONDO:0016445 otar diseases +MONDO:0016445 rare diseases +MONDO:0016446 gard_rare diseases +MONDO:0016446 nord_rare diseases +MONDO:0016446 ordo_disorder diseases +MONDO:0016446 orphanet_rare diseases +MONDO:0016446 otar diseases +MONDO:0016446 rare diseases +MONDO:0016447 gard_rare diseases +MONDO:0016447 nord_rare diseases +MONDO:0016447 ordo_disorder diseases +MONDO:0016447 orphanet_rare diseases +MONDO:0016447 rare diseases +MONDO:0016448 gard_rare diseases +MONDO:0016448 nord_rare diseases +MONDO:0016448 ordo_disorder diseases +MONDO:0016448 orphanet_rare diseases +MONDO:0016448 rare diseases +MONDO:0016449 gard_rare diseases +MONDO:0016449 nord_rare diseases +MONDO:0016449 ordo_disorder diseases +MONDO:0016449 orphanet_rare diseases +MONDO:0016449 rare diseases +MONDO:0016450 disease_grouping diseases +MONDO:0016450 gard_rare diseases +MONDO:0016450 nord_rare diseases +MONDO:0016450 ordo_group_of_disorders diseases +MONDO:0016450 otar diseases +MONDO:0016450 rare diseases +MONDO:0016451 gard_rare diseases +MONDO:0016451 nord_rare diseases +MONDO:0016451 rare diseases +MONDO:0016452 gard_rare diseases +MONDO:0016452 rare diseases +MONDO:0016453 gard_rare diseases +MONDO:0016453 nord_rare diseases +MONDO:0016453 ordo_subtype_of_a_disorder diseases +MONDO:0016453 rare diseases +MONDO:0016454 gard_rare diseases +MONDO:0016454 nord_rare diseases +MONDO:0016454 ordo_disorder diseases +MONDO:0016454 orphanet_rare diseases +MONDO:0016454 otar diseases +MONDO:0016454 rare diseases +MONDO:0016455 gard_rare diseases +MONDO:0016455 nord_rare diseases +MONDO:0016455 ordo_disorder diseases +MONDO:0016455 orphanet_rare diseases +MONDO:0016455 rare diseases +MONDO:0016456 gard_rare diseases +MONDO:0016456 nord_rare diseases +MONDO:0016456 ordo_disorder diseases +MONDO:0016456 ordo_malformation_syndrome diseases +MONDO:0016456 orphanet_rare diseases +MONDO:0016456 otar diseases +MONDO:0016456 rare diseases +MONDO:0016457 gard_rare diseases +MONDO:0016457 ordo_disorder diseases +MONDO:0016457 ordo_malformation_syndrome diseases +MONDO:0016457 orphanet_rare diseases +MONDO:0016457 otar diseases +MONDO:0016457 rare diseases +MONDO:0016458 gard_rare diseases +MONDO:0016458 nord_rare diseases +MONDO:0016458 ordo_disorder diseases +MONDO:0016458 ordo_malformation_syndrome diseases +MONDO:0016458 orphanet_rare diseases +MONDO:0016458 rare diseases +MONDO:0016459 gard_rare diseases +MONDO:0016459 nord_rare diseases +MONDO:0016459 ordo_disorder diseases +MONDO:0016459 ordo_malformation_syndrome diseases +MONDO:0016459 orphanet_rare diseases +MONDO:0016459 otar diseases +MONDO:0016459 rare diseases +MONDO:0016460 gard_rare diseases +MONDO:0016460 nord_rare diseases +MONDO:0016460 ordo_disorder diseases +MONDO:0016460 ordo_malformation_syndrome diseases +MONDO:0016460 orphanet_rare diseases +MONDO:0016460 otar diseases +MONDO:0016460 rare diseases +MONDO:0016461 gard_rare diseases +MONDO:0016461 nord_rare diseases +MONDO:0016461 ordo_disorder diseases +MONDO:0016461 ordo_malformation_syndrome diseases +MONDO:0016461 orphanet_rare diseases +MONDO:0016461 rare diseases +MONDO:0016462 gard_rare diseases +MONDO:0016462 nord_rare diseases +MONDO:0016462 ordo_disorder diseases +MONDO:0016462 orphanet_rare diseases +MONDO:0016462 otar diseases +MONDO:0016462 rare diseases +MONDO:0016463 disease_grouping diseases +MONDO:0016463 gard_rare diseases +MONDO:0016463 ordo_group_of_disorders diseases +MONDO:0016463 rare diseases +MONDO:0016464 gard_rare diseases +MONDO:0016464 nord_rare diseases +MONDO:0016464 ordo_disorder diseases +MONDO:0016464 orphanet_rare diseases +MONDO:0016464 otar diseases +MONDO:0016464 rare diseases +MONDO:0016466 gard_rare diseases +MONDO:0016466 nord_rare diseases +MONDO:0016466 ordo_disorder diseases +MONDO:0016466 orphanet_rare diseases +MONDO:0016466 otar diseases +MONDO:0016466 rare diseases +MONDO:0016467 gard_rare diseases +MONDO:0016467 nord_rare diseases +MONDO:0016467 ordo_disorder diseases +MONDO:0016467 ordo_malformation_syndrome diseases +MONDO:0016467 orphanet_rare diseases +MONDO:0016467 rare diseases +MONDO:0016468 gard_rare diseases +MONDO:0016468 nord_rare diseases +MONDO:0016468 ordo_subtype_of_a_disorder diseases +MONDO:0016468 rare diseases +MONDO:0016469 gard_rare diseases +MONDO:0016469 rare diseases +MONDO:0016470 gard_rare diseases +MONDO:0016470 nord_rare diseases +MONDO:0016470 ordo_disorder diseases +MONDO:0016470 orphanet_rare diseases +MONDO:0016470 otar diseases +MONDO:0016470 rare diseases +MONDO:0016471 gard_rare diseases +MONDO:0016471 nord_rare diseases +MONDO:0016471 ordo_disorder diseases +MONDO:0016471 orphanet_rare diseases +MONDO:0016471 otar diseases +MONDO:0016471 rare diseases +MONDO:0016472 gard_rare diseases +MONDO:0016472 nord_rare diseases +MONDO:0016472 ordo_disorder diseases +MONDO:0016472 orphanet_rare diseases +MONDO:0016472 otar diseases +MONDO:0016472 rare diseases +MONDO:0016473 gard_rare diseases +MONDO:0016473 nord_rare diseases +MONDO:0016473 ordo_disorder diseases +MONDO:0016473 orphanet_rare diseases +MONDO:0016473 otar diseases +MONDO:0016473 rare diseases +MONDO:0016474 gard_rare diseases +MONDO:0016474 nord_rare diseases +MONDO:0016474 ordo_disorder diseases +MONDO:0016474 orphanet_rare diseases +MONDO:0016474 otar diseases +MONDO:0016474 rare diseases +MONDO:0016475 gard_rare diseases +MONDO:0016475 nord_rare diseases +MONDO:0016475 ordo_etiological_subtype diseases +MONDO:0016475 ordo_subtype_of_a_disorder diseases +MONDO:0016475 otar diseases +MONDO:0016475 rare diseases +MONDO:0016476 gard_rare diseases +MONDO:0016476 nord_rare diseases +MONDO:0016476 ordo_etiological_subtype diseases +MONDO:0016476 ordo_subtype_of_a_disorder diseases +MONDO:0016476 otar diseases +MONDO:0016476 rare diseases +MONDO:0016477 gard_rare diseases +MONDO:0016477 nord_rare diseases +MONDO:0016477 ordo_etiological_subtype diseases +MONDO:0016477 ordo_subtype_of_a_disorder diseases +MONDO:0016477 rare diseases +MONDO:0016478 gard_rare diseases +MONDO:0016478 nord_rare diseases +MONDO:0016478 ordo_etiological_subtype diseases +MONDO:0016478 ordo_subtype_of_a_disorder diseases +MONDO:0016478 rare diseases +MONDO:0016479 gard_rare diseases +MONDO:0016479 nord_rare diseases +MONDO:0016479 ordo_etiological_subtype diseases +MONDO:0016479 ordo_subtype_of_a_disorder diseases +MONDO:0016479 otar diseases +MONDO:0016479 rare diseases +MONDO:0016480 gard_rare diseases +MONDO:0016480 nord_rare diseases +MONDO:0016480 ordo_etiological_subtype diseases +MONDO:0016480 ordo_subtype_of_a_disorder diseases +MONDO:0016480 otar diseases +MONDO:0016480 rare diseases +MONDO:0016481 gard_rare diseases +MONDO:0016481 nord_rare diseases +MONDO:0016481 ordo_etiological_subtype diseases +MONDO:0016481 ordo_subtype_of_a_disorder diseases +MONDO:0016481 otar diseases +MONDO:0016481 rare diseases +MONDO:0016482 gard_rare diseases +MONDO:0016482 nord_rare diseases +MONDO:0016482 ordo_etiological_subtype diseases +MONDO:0016482 ordo_subtype_of_a_disorder diseases +MONDO:0016482 rare diseases +MONDO:0016483 gard_rare diseases +MONDO:0016483 nord_rare diseases +MONDO:0016483 ordo_disorder diseases +MONDO:0016483 orphanet_rare diseases +MONDO:0016483 otar diseases +MONDO:0016483 rare diseases +MONDO:0016484 clingen diseases +MONDO:0016484 gard_rare diseases +MONDO:0016484 nord_rare diseases +MONDO:0016484 ordo_subtype_of_a_disorder diseases +MONDO:0016484 otar diseases +MONDO:0016484 rare diseases +MONDO:0016485 clingen diseases +MONDO:0016485 gard_rare diseases +MONDO:0016485 nord_rare diseases +MONDO:0016485 ordo_subtype_of_a_disorder diseases +MONDO:0016485 otar diseases +MONDO:0016485 rare diseases +MONDO:0016486 gard_rare diseases +MONDO:0016486 nord_rare diseases +MONDO:0016486 ordo_subtype_of_a_disorder diseases +MONDO:0016486 otar diseases +MONDO:0016486 rare diseases +MONDO:0016487 gard_rare diseases +MONDO:0016487 nord_rare diseases +MONDO:0016487 ordo_subtype_of_a_disorder diseases +MONDO:0016487 otar diseases +MONDO:0016487 rare diseases +MONDO:0016489 gard_rare diseases +MONDO:0016489 nord_rare diseases +MONDO:0016489 ordo_disorder diseases +MONDO:0016489 orphanet_rare diseases +MONDO:0016489 otar diseases +MONDO:0016489 rare diseases +MONDO:0016490 gard_rare diseases +MONDO:0016490 nord_rare diseases +MONDO:0016490 ordo_disorder diseases +MONDO:0016490 orphanet_rare diseases +MONDO:0016490 otar diseases +MONDO:0016490 rare diseases +MONDO:0016491 gard_rare diseases +MONDO:0016491 nord_rare diseases +MONDO:0016491 ordo_disorder diseases +MONDO:0016491 orphanet_rare diseases +MONDO:0016491 otar diseases +MONDO:0016491 rare diseases +MONDO:0016496 gard_rare diseases +MONDO:0016496 nord_rare diseases +MONDO:0016496 ordo_disorder diseases +MONDO:0016496 orphanet_rare diseases +MONDO:0016496 rare diseases +MONDO:0016497 gard_rare diseases +MONDO:0016497 nord_rare diseases +MONDO:0016497 ordo_disorder diseases +MONDO:0016497 orphanet_rare diseases +MONDO:0016497 rare diseases +MONDO:0016498 gard_rare diseases +MONDO:0016498 nord_rare diseases +MONDO:0016498 ordo_disorder diseases +MONDO:0016498 orphanet_rare diseases +MONDO:0016498 rare diseases +MONDO:0016499 gard_rare diseases +MONDO:0016499 nord_rare diseases +MONDO:0016499 ordo_disorder diseases +MONDO:0016499 orphanet_rare diseases +MONDO:0016499 rare diseases +MONDO:0016500 gard_rare diseases +MONDO:0016500 nord_rare diseases +MONDO:0016500 ordo_disorder diseases +MONDO:0016500 orphanet_rare diseases +MONDO:0016500 rare diseases +MONDO:0016501 gard_rare diseases +MONDO:0016501 nord_rare diseases +MONDO:0016501 ordo_subtype_of_a_disorder diseases +MONDO:0016501 otar diseases +MONDO:0016501 rare diseases +MONDO:0016502 gard_rare diseases +MONDO:0016502 nord_rare diseases +MONDO:0016502 ordo_subtype_of_a_disorder diseases +MONDO:0016502 otar diseases +MONDO:0016502 rare diseases +MONDO:0016503 gard_rare diseases +MONDO:0016503 nord_rare diseases +MONDO:0016503 ordo_disorder diseases +MONDO:0016503 orphanet_rare diseases +MONDO:0016503 rare diseases +MONDO:0016504 gard_rare diseases +MONDO:0016504 nord_rare diseases +MONDO:0016504 ordo_disorder diseases +MONDO:0016504 orphanet_rare diseases +MONDO:0016504 rare diseases +MONDO:0016505 gard_rare diseases +MONDO:0016505 nord_rare diseases +MONDO:0016505 ordo_disorder diseases +MONDO:0016505 orphanet_rare diseases +MONDO:0016505 otar diseases +MONDO:0016505 rare diseases +MONDO:0016506 gard_rare diseases +MONDO:0016506 nord_rare diseases +MONDO:0016506 ordo_disorder diseases +MONDO:0016506 orphanet_rare diseases +MONDO:0016506 rare diseases +MONDO:0016509 gard_rare diseases +MONDO:0016509 nord_rare diseases +MONDO:0016509 ordo_disorder diseases +MONDO:0016509 ordo_malformation_syndrome diseases +MONDO:0016509 orphanet_rare diseases +MONDO:0016509 rare diseases +MONDO:0016510 gard_rare diseases +MONDO:0016510 ordo_disorder diseases +MONDO:0016510 ordo_malformation_syndrome diseases +MONDO:0016510 orphanet_rare diseases +MONDO:0016510 rare diseases +MONDO:0016511 disease_grouping diseases +MONDO:0016511 ordo_group_of_disorders diseases +MONDO:0016512 gard_rare diseases +MONDO:0016512 nord_rare diseases +MONDO:0016512 ordo_disorder diseases +MONDO:0016512 ordo_malformation_syndrome diseases +MONDO:0016512 orphanet_rare diseases +MONDO:0016512 otar diseases +MONDO:0016512 rare diseases +MONDO:0016514 gard_rare diseases +MONDO:0016514 nord_rare diseases +MONDO:0016514 ordo_disorder diseases +MONDO:0016514 ordo_malformation_syndrome diseases +MONDO:0016514 orphanet_rare diseases +MONDO:0016514 otar diseases +MONDO:0016514 rare diseases +MONDO:0016515 gard_rare diseases +MONDO:0016515 nord_rare diseases +MONDO:0016515 ordo_disorder diseases +MONDO:0016515 ordo_malformation_syndrome diseases +MONDO:0016515 orphanet_rare diseases +MONDO:0016515 otar diseases +MONDO:0016515 rare diseases +MONDO:0016516 gard_rare diseases +MONDO:0016516 nord_rare diseases +MONDO:0016516 ordo_disorder diseases +MONDO:0016516 ordo_malformation_syndrome diseases +MONDO:0016516 orphanet_rare diseases +MONDO:0016516 otar diseases +MONDO:0016516 rare diseases +MONDO:0016521 gard_rare diseases +MONDO:0016521 nord_rare diseases +MONDO:0016521 ordo_disorder diseases +MONDO:0016521 orphanet_rare diseases +MONDO:0016521 otar diseases +MONDO:0016521 rare diseases +MONDO:0016522 gard_rare diseases +MONDO:0016522 nord_rare diseases +MONDO:0016522 ordo_disorder diseases +MONDO:0016522 ordo_malformation_syndrome diseases +MONDO:0016522 orphanet_rare diseases +MONDO:0016522 rare diseases +MONDO:0016523 gard_rare diseases +MONDO:0016523 nord_rare diseases +MONDO:0016523 ordo_disorder diseases +MONDO:0016523 ordo_morphological_anomaly diseases +MONDO:0016523 orphanet_rare diseases +MONDO:0016523 rare diseases +MONDO:0016525 disease_grouping diseases +MONDO:0016525 gard_rare diseases +MONDO:0016525 nord_rare diseases +MONDO:0016525 ordo_group_of_disorders diseases +MONDO:0016525 otar diseases +MONDO:0016525 rare diseases +MONDO:0016526 disease_grouping diseases +MONDO:0016526 gard_rare diseases +MONDO:0016526 nord_rare diseases +MONDO:0016526 ordo_disorder diseases +MONDO:0016526 ordo_group_of_disorders diseases +MONDO:0016526 ordo_malformation_syndrome diseases +MONDO:0016526 orphanet_rare diseases +MONDO:0016526 otar diseases +MONDO:0016526 rare diseases +MONDO:0016527 gard_rare diseases +MONDO:0016527 ordo_disorder diseases +MONDO:0016527 orphanet_rare diseases +MONDO:0016527 otar diseases +MONDO:0016527 rare diseases +MONDO:0016528 gard_rare diseases +MONDO:0016528 nord_rare diseases +MONDO:0016528 ordo_disorder diseases +MONDO:0016528 ordo_malformation_syndrome diseases +MONDO:0016528 orphanet_rare diseases +MONDO:0016528 rare diseases +MONDO:0016529 gard_rare diseases +MONDO:0016529 nord_rare diseases +MONDO:0016529 ordo_disorder diseases +MONDO:0016529 ordo_morphological_anomaly diseases +MONDO:0016529 orphanet_rare diseases +MONDO:0016529 otar diseases +MONDO:0016529 rare diseases +MONDO:0016530 gard_rare diseases +MONDO:0016530 nord_rare diseases +MONDO:0016530 ordo_disorder diseases +MONDO:0016530 ordo_malformation_syndrome diseases +MONDO:0016530 orphanet_rare diseases +MONDO:0016530 rare diseases +MONDO:0016531 gard_rare diseases +MONDO:0016531 nord_rare diseases +MONDO:0016531 ordo_disorder diseases +MONDO:0016531 ordo_morphological_anomaly diseases +MONDO:0016531 orphanet_rare diseases +MONDO:0016531 rare diseases +MONDO:0016532 gard_rare diseases +MONDO:0016532 nord_rare diseases +MONDO:0016532 ordo_disorder diseases +MONDO:0016532 orphanet_rare diseases +MONDO:0016532 otar diseases +MONDO:0016532 rare diseases +MONDO:0016533 gard_rare diseases +MONDO:0016533 nord_rare diseases +MONDO:0016533 ordo_subtype_of_a_disorder diseases +MONDO:0016533 otar diseases +MONDO:0016533 rare diseases +MONDO:0016534 gard_rare diseases +MONDO:0016534 nord_rare diseases +MONDO:0016534 ordo_disorder diseases +MONDO:0016534 orphanet_rare diseases +MONDO:0016534 rare diseases +MONDO:0016535 gard_rare diseases +MONDO:0016535 nord_rare diseases +MONDO:0016535 ordo_disorder diseases +MONDO:0016535 orphanet_rare diseases +MONDO:0016535 otar diseases +MONDO:0016535 rare diseases +MONDO:0016537 disease_grouping diseases +MONDO:0016537 gard_rare diseases +MONDO:0016537 ordo_group_of_disorders diseases +MONDO:0016537 otar diseases +MONDO:0016537 rare diseases +MONDO:0016539 gard_rare diseases +MONDO:0016539 nord_rare diseases +MONDO:0016539 ordo_disorder diseases +MONDO:0016539 orphanet_rare diseases +MONDO:0016539 otar diseases +MONDO:0016539 rare diseases +MONDO:0016540 disease_grouping diseases +MONDO:0016540 gard_rare diseases +MONDO:0016540 ordo_group_of_disorders diseases +MONDO:0016540 rare diseases +MONDO:0016541 disease_grouping diseases +MONDO:0016541 gard_rare diseases +MONDO:0016541 ordo_group_of_disorders diseases +MONDO:0016541 rare diseases +MONDO:0016542 gard_rare diseases +MONDO:0016542 nord_rare diseases +MONDO:0016542 ordo_disorder diseases +MONDO:0016542 orphanet_rare diseases +MONDO:0016542 otar diseases +MONDO:0016542 rare diseases +MONDO:0016543 gard_rare diseases +MONDO:0016543 nord_rare diseases +MONDO:0016543 ordo_disorder diseases +MONDO:0016543 orphanet_rare diseases +MONDO:0016543 otar diseases +MONDO:0016543 rare diseases +MONDO:0016544 gard_rare diseases +MONDO:0016544 nord_rare diseases +MONDO:0016544 ordo_subtype_of_a_disorder diseases +MONDO:0016544 rare diseases +MONDO:0016545 gard_rare diseases +MONDO:0016545 nord_rare diseases +MONDO:0016545 ordo_disorder diseases +MONDO:0016545 orphanet_rare diseases +MONDO:0016545 otar diseases +MONDO:0016545 rare diseases +MONDO:0016546 gard_rare diseases +MONDO:0016546 nord_rare diseases +MONDO:0016546 ordo_disorder diseases +MONDO:0016546 orphanet_rare diseases +MONDO:0016546 rare diseases +MONDO:0016547 gard_rare diseases +MONDO:0016547 nord_rare diseases +MONDO:0016547 ordo_etiological_subtype diseases +MONDO:0016547 ordo_subtype_of_a_disorder diseases +MONDO:0016547 otar diseases +MONDO:0016547 rare diseases +MONDO:0016548 gard_rare diseases +MONDO:0016548 nord_rare diseases +MONDO:0016548 ordo_disorder diseases +MONDO:0016548 orphanet_rare diseases +MONDO:0016548 rare diseases +MONDO:0016549 gard_rare diseases +MONDO:0016549 nord_rare diseases +MONDO:0016549 ordo_subtype_of_a_disorder diseases +MONDO:0016549 rare diseases +MONDO:0016550 gard_rare diseases +MONDO:0016550 nord_rare diseases +MONDO:0016550 ordo_subtype_of_a_disorder diseases +MONDO:0016550 rare diseases +MONDO:0016551 gard_rare diseases +MONDO:0016551 nord_rare diseases +MONDO:0016551 ordo_subtype_of_a_disorder diseases +MONDO:0016551 rare diseases +MONDO:0016552 gard_rare diseases +MONDO:0016552 nord_rare diseases +MONDO:0016552 ordo_subtype_of_a_disorder diseases +MONDO:0016552 rare diseases +MONDO:0016553 disease_grouping diseases +MONDO:0016553 gard_rare diseases +MONDO:0016553 nord_rare diseases +MONDO:0016553 ordo_disorder diseases +MONDO:0016553 orphanet_rare diseases +MONDO:0016553 otar diseases +MONDO:0016553 rare diseases +MONDO:0016554 gard_rare diseases +MONDO:0016554 nord_rare diseases +MONDO:0016554 ordo_disorder diseases +MONDO:0016554 orphanet_rare diseases +MONDO:0016554 rare diseases +MONDO:0016555 disease_grouping diseases +MONDO:0016555 gard_rare diseases +MONDO:0016555 nord_rare diseases +MONDO:0016555 ordo_group_of_disorders diseases +MONDO:0016555 rare diseases +MONDO:0016556 disease_grouping diseases +MONDO:0016556 gard_rare diseases +MONDO:0016556 ordo_group_of_disorders diseases +MONDO:0016556 rare diseases +MONDO:0016557 gard_rare diseases +MONDO:0016557 nord_rare diseases +MONDO:0016557 ordo_disorder diseases +MONDO:0016557 orphanet_rare diseases +MONDO:0016557 otar diseases +MONDO:0016557 rare diseases +MONDO:0016558 gard_rare diseases +MONDO:0016558 nord_rare diseases +MONDO:0016558 ordo_disorder diseases +MONDO:0016558 orphanet_rare diseases +MONDO:0016558 otar diseases +MONDO:0016558 rare diseases +MONDO:0016559 gard_rare diseases +MONDO:0016559 nord_rare diseases +MONDO:0016559 ordo_disorder diseases +MONDO:0016559 ordo_malformation_syndrome diseases +MONDO:0016559 orphanet_rare diseases +MONDO:0016559 otar diseases +MONDO:0016559 rare diseases +MONDO:0016560 gard_rare diseases +MONDO:0016560 ordo_malformation_syndrome diseases +MONDO:0016560 rare diseases +MONDO:0016561 gard_rare diseases +MONDO:0016561 nord_rare diseases +MONDO:0016561 ordo_disorder diseases +MONDO:0016561 ordo_malformation_syndrome diseases +MONDO:0016561 orphanet_rare diseases +MONDO:0016561 otar diseases +MONDO:0016561 rare diseases +MONDO:0016562 gard_rare diseases +MONDO:0016562 nord_rare diseases +MONDO:0016562 ordo_subtype_of_a_disorder diseases +MONDO:0016562 otar diseases +MONDO:0016562 rare diseases +MONDO:0016563 gard_rare diseases +MONDO:0016563 nord_rare diseases +MONDO:0016563 ordo_subtype_of_a_disorder diseases +MONDO:0016563 otar diseases +MONDO:0016563 rare diseases +MONDO:0016564 gard_rare diseases +MONDO:0016564 nord_rare diseases +MONDO:0016564 ordo_subtype_of_a_disorder diseases +MONDO:0016564 otar diseases +MONDO:0016564 rare diseases +MONDO:0016566 gard_rare diseases +MONDO:0016566 nord_rare diseases +MONDO:0016566 ordo_disorder diseases +MONDO:0016566 orphanet_rare diseases +MONDO:0016566 otar diseases +MONDO:0016566 rare diseases +MONDO:0016567 gard_rare diseases +MONDO:0016567 nord_rare diseases +MONDO:0016567 ordo_disorder diseases +MONDO:0016567 orphanet_rare diseases +MONDO:0016567 rare diseases +MONDO:0016568 gard_rare diseases +MONDO:0016568 nord_rare diseases +MONDO:0016568 ordo_disorder diseases +MONDO:0016568 ordo_malformation_syndrome diseases +MONDO:0016568 orphanet_rare diseases +MONDO:0016568 otar diseases +MONDO:0016568 rare diseases +MONDO:0016570 gard_rare diseases +MONDO:0016570 nord_rare diseases +MONDO:0016570 ordo_disorder diseases +MONDO:0016570 orphanet_rare diseases +MONDO:0016570 rare diseases +MONDO:0016571 gard_rare diseases +MONDO:0016571 nord_rare diseases +MONDO:0016571 ordo_disorder diseases +MONDO:0016571 ordo_malformation_syndrome diseases +MONDO:0016571 orphanet_rare diseases +MONDO:0016571 rare diseases +MONDO:0016572 gard_rare diseases +MONDO:0016572 nord_rare diseases +MONDO:0016572 rare diseases +MONDO:0016573 gard_rare diseases +MONDO:0016573 nord_rare diseases +MONDO:0016573 ordo_disorder diseases +MONDO:0016573 orphanet_rare diseases +MONDO:0016573 rare diseases +MONDO:0016574 gard_rare diseases +MONDO:0016574 ordo_disorder diseases +MONDO:0016574 orphanet_rare diseases +MONDO:0016574 otar diseases +MONDO:0016574 rare diseases +MONDO:0016575 clingen diseases +MONDO:0016575 gard_rare diseases +MONDO:0016575 nord_rare diseases +MONDO:0016575 ordo_disorder diseases +MONDO:0016575 orphanet_rare diseases +MONDO:0016575 otar diseases +MONDO:0016575 rare diseases +MONDO:0016576 gard_rare diseases +MONDO:0016576 nord_rare diseases +MONDO:0016576 ordo_disorder diseases +MONDO:0016576 ordo_malformation_syndrome diseases +MONDO:0016576 orphanet_rare diseases +MONDO:0016576 otar diseases +MONDO:0016576 rare diseases +MONDO:0016577 gard_rare diseases +MONDO:0016577 nord_rare diseases +MONDO:0016577 ordo_disorder diseases +MONDO:0016577 ordo_malformation_syndrome diseases +MONDO:0016577 orphanet_rare diseases +MONDO:0016577 rare diseases +MONDO:0016580 gard_rare diseases +MONDO:0016580 nord_rare diseases +MONDO:0016580 ordo_disorder diseases +MONDO:0016580 ordo_malformation_syndrome diseases +MONDO:0016580 orphanet_rare diseases +MONDO:0016580 rare diseases +MONDO:0016581 disease_grouping diseases +MONDO:0016581 gard_rare diseases +MONDO:0016581 ordo_group_of_disorders diseases +MONDO:0016581 otar diseases +MONDO:0016581 rare diseases +MONDO:0016582 disease_grouping diseases +MONDO:0016582 gard_rare diseases +MONDO:0016582 ordo_group_of_disorders diseases +MONDO:0016582 rare diseases +MONDO:0016583 ordo_malformation_syndrome diseases +MONDO:0016584 gard_rare diseases +MONDO:0016584 nord_rare diseases +MONDO:0016584 ordo_disorder diseases +MONDO:0016584 ordo_malformation_syndrome diseases +MONDO:0016584 orphanet_rare diseases +MONDO:0016584 otar diseases +MONDO:0016584 rare diseases +MONDO:0016586 disease_grouping diseases +MONDO:0016586 gard_rare diseases +MONDO:0016586 nord_rare diseases +MONDO:0016586 ordo_group_of_disorders diseases +MONDO:0016586 otar diseases +MONDO:0016586 rare diseases +MONDO:0016587 clingen diseases +MONDO:0016587 disease_grouping diseases +MONDO:0016587 gard_rare diseases +MONDO:0016587 ordo_group_of_disorders diseases +MONDO:0016587 otar diseases +MONDO:0016587 rare diseases +MONDO:0016588 gard_rare diseases +MONDO:0016588 nord_rare diseases +MONDO:0016588 ordo_disorder diseases +MONDO:0016588 orphanet_rare diseases +MONDO:0016588 rare diseases +MONDO:0016591 gard_rare diseases +MONDO:0016591 nord_rare diseases +MONDO:0016591 ordo_disorder diseases +MONDO:0016591 orphanet_rare diseases +MONDO:0016591 rare diseases +MONDO:0016593 disease_grouping diseases +MONDO:0016593 gard_rare diseases +MONDO:0016593 ordo_group_of_disorders diseases +MONDO:0016593 otar diseases +MONDO:0016593 rare diseases +MONDO:0016594 gard_rare diseases +MONDO:0016594 nord_rare diseases +MONDO:0016594 ordo_disorder diseases +MONDO:0016594 orphanet_rare diseases +MONDO:0016594 rare diseases +MONDO:0016595 gard_rare diseases +MONDO:0016595 nord_rare diseases +MONDO:0016595 ordo_disorder diseases +MONDO:0016595 orphanet_rare diseases +MONDO:0016595 rare diseases +MONDO:0016596 gard_rare diseases +MONDO:0016596 nord_rare diseases +MONDO:0016596 ordo_disorder diseases +MONDO:0016596 orphanet_rare diseases +MONDO:0016596 otar diseases +MONDO:0016596 rare diseases +MONDO:0016598 gard_rare diseases +MONDO:0016598 nord_rare diseases +MONDO:0016598 ordo_disorder diseases +MONDO:0016598 orphanet_rare diseases +MONDO:0016598 otar diseases +MONDO:0016598 rare diseases +MONDO:0016600 gard_rare diseases +MONDO:0016600 nord_rare diseases +MONDO:0016600 ordo_subtype_of_a_disorder diseases +MONDO:0016600 otar diseases +MONDO:0016600 rare diseases +MONDO:0016601 gard_rare diseases +MONDO:0016601 nord_rare diseases +MONDO:0016601 ordo_subtype_of_a_disorder diseases +MONDO:0016601 otar diseases +MONDO:0016601 rare diseases +MONDO:0016602 clingen diseases +MONDO:0016602 disease_grouping diseases +MONDO:0016602 gard_rare diseases +MONDO:0016602 ordo_group_of_disorders diseases +MONDO:0016602 otar diseases +MONDO:0016602 rare diseases +MONDO:0016603 gard_rare diseases +MONDO:0016603 ordo_disorder diseases +MONDO:0016603 orphanet_rare diseases +MONDO:0016603 otar diseases +MONDO:0016603 rare diseases +MONDO:0016604 gard_rare diseases +MONDO:0016604 ordo_disorder diseases +MONDO:0016604 ordo_malformation_syndrome diseases +MONDO:0016604 orphanet_rare diseases +MONDO:0016604 otar diseases +MONDO:0016604 rare diseases +MONDO:0016605 gard_rare diseases +MONDO:0016605 nord_rare diseases +MONDO:0016605 ordo_subtype_of_a_disorder diseases +MONDO:0016605 otar diseases +MONDO:0016605 rare diseases +MONDO:0016607 gard_rare diseases +MONDO:0016607 nord_rare diseases +MONDO:0016607 ordo_subtype_of_a_disorder diseases +MONDO:0016607 otar diseases +MONDO:0016607 rare diseases +MONDO:0016608 gard_rare diseases +MONDO:0016608 nord_rare diseases +MONDO:0016608 ordo_disorder diseases +MONDO:0016608 ordo_malformation_syndrome diseases +MONDO:0016608 orphanet_rare diseases +MONDO:0016608 otar diseases +MONDO:0016608 rare diseases +MONDO:0016609 gard_rare diseases +MONDO:0016609 nord_rare diseases +MONDO:0016609 ordo_disorder diseases +MONDO:0016609 orphanet_rare diseases +MONDO:0016609 rare diseases +MONDO:0016610 gard_rare diseases +MONDO:0016610 nord_rare diseases +MONDO:0016610 ordo_disorder diseases +MONDO:0016610 orphanet_rare diseases +MONDO:0016610 rare diseases +MONDO:0016611 gard_rare diseases +MONDO:0016611 nord_rare diseases +MONDO:0016611 ordo_disorder diseases +MONDO:0016611 orphanet_rare diseases +MONDO:0016611 otar diseases +MONDO:0016611 rare diseases +MONDO:0016612 disease_grouping diseases +MONDO:0016612 gard_rare diseases +MONDO:0016612 nord_rare diseases +MONDO:0016612 ordo_group_of_disorders diseases +MONDO:0016612 otar diseases +MONDO:0016612 rare diseases +MONDO:0016613 gard_rare diseases +MONDO:0016613 nord_rare diseases +MONDO:0016613 ordo_subtype_of_a_disorder diseases +MONDO:0016613 otar diseases +MONDO:0016613 rare diseases +MONDO:0016614 gard_rare diseases +MONDO:0016614 nord_rare diseases +MONDO:0016614 ordo_disorder diseases +MONDO:0016614 orphanet_rare diseases +MONDO:0016614 otar diseases +MONDO:0016614 rare diseases +MONDO:0016615 gard_rare diseases +MONDO:0016615 ordo_etiological_subtype diseases +MONDO:0016615 rare diseases +MONDO:0016616 gard_rare diseases +MONDO:0016616 ordo_etiological_subtype diseases +MONDO:0016616 rare diseases +MONDO:0016617 gard_rare diseases +MONDO:0016617 ordo_etiological_subtype diseases +MONDO:0016617 rare diseases +MONDO:0016618 gard_rare diseases +MONDO:0016618 ordo_etiological_subtype diseases +MONDO:0016618 rare diseases +MONDO:0016619 gard_rare diseases +MONDO:0016619 nord_rare diseases +MONDO:0016619 ordo_etiological_subtype diseases +MONDO:0016619 ordo_subtype_of_a_disorder diseases +MONDO:0016619 otar diseases +MONDO:0016619 rare diseases +MONDO:0016620 disease_grouping diseases +MONDO:0016620 gard_rare diseases +MONDO:0016620 nord_rare diseases +MONDO:0016620 ordo_disorder diseases +MONDO:0016620 ordo_group_of_disorders diseases +MONDO:0016620 ordo_malformation_syndrome diseases +MONDO:0016620 orphanet_rare diseases +MONDO:0016620 otar diseases +MONDO:0016620 rare diseases +MONDO:0016621 gard_rare diseases +MONDO:0016621 nord_rare diseases +MONDO:0016621 ordo_disorder diseases +MONDO:0016621 orphanet_rare diseases +MONDO:0016621 otar diseases +MONDO:0016621 rare diseases +MONDO:0016622 gard_rare diseases +MONDO:0016622 n_of_one diseases +MONDO:0016622 ordo_disorder diseases +MONDO:0016622 ordo_malformation_syndrome diseases +MONDO:0016622 orphanet_rare diseases +MONDO:0016622 rare diseases +MONDO:0016624 disease_grouping diseases +MONDO:0016624 gard_rare diseases +MONDO:0016624 ordo_group_of_disorders diseases +MONDO:0016624 rare diseases +MONDO:0016625 disease_grouping diseases +MONDO:0016625 inferred_rare diseases +MONDO:0016625 ordo_group_of_disorders diseases +MONDO:0016625 rare diseases +MONDO:0016630 gard_rare diseases +MONDO:0016630 nord_rare diseases +MONDO:0016630 ordo_disorder diseases +MONDO:0016630 orphanet_rare diseases +MONDO:0016630 otar diseases +MONDO:0016630 rare diseases +MONDO:0016638 gard_rare diseases +MONDO:0016638 nord_rare diseases +MONDO:0016638 ordo_subtype_of_a_disorder diseases +MONDO:0016638 otar diseases +MONDO:0016638 rare diseases +MONDO:0016639 gard_rare diseases +MONDO:0016639 ordo_disorder diseases +MONDO:0016639 ordo_malformation_syndrome diseases +MONDO:0016639 orphanet_rare diseases +MONDO:0016639 rare diseases +MONDO:0016641 gard_rare diseases +MONDO:0016641 nord_rare diseases +MONDO:0016641 ordo_disorder diseases +MONDO:0016641 ordo_malformation_syndrome diseases +MONDO:0016641 orphanet_rare diseases +MONDO:0016641 otar diseases +MONDO:0016641 rare diseases +MONDO:0016642 gard_rare diseases +MONDO:0016642 nord_rare diseases +MONDO:0016642 ordo_disorder diseases +MONDO:0016642 orphanet_rare diseases +MONDO:0016642 otar diseases +MONDO:0016642 rare diseases +MONDO:0016643 disease_grouping diseases +MONDO:0016643 gard_rare diseases +MONDO:0016643 nord_rare diseases +MONDO:0016643 ordo_group_of_disorders diseases +MONDO:0016643 otar diseases +MONDO:0016643 rare diseases +MONDO:0016644 gard_rare diseases +MONDO:0016644 nord_rare diseases +MONDO:0016644 ordo_disorder diseases +MONDO:0016644 orphanet_rare diseases +MONDO:0016644 rare diseases +MONDO:0016646 gard_rare diseases +MONDO:0016646 nord_rare diseases +MONDO:0016646 ordo_disorder diseases +MONDO:0016646 orphanet_rare diseases +MONDO:0016646 rare diseases +MONDO:0016648 clingen diseases +MONDO:0016648 disease_grouping diseases +MONDO:0016648 gard_rare diseases +MONDO:0016648 nord_rare diseases +MONDO:0016648 ordo_group_of_disorders diseases +MONDO:0016648 otar diseases +MONDO:0016648 rare diseases +MONDO:0016649 clingen diseases +MONDO:0016649 gard_rare diseases +MONDO:0016649 nord_rare diseases +MONDO:0016649 ordo_disorder diseases +MONDO:0016649 ordo_malformation_syndrome diseases +MONDO:0016649 orphanet_rare diseases +MONDO:0016649 otar diseases +MONDO:0016649 rare diseases +MONDO:0016650 gard_rare diseases +MONDO:0016650 nord_rare diseases +MONDO:0016650 ordo_disorder diseases +MONDO:0016650 ordo_malformation_syndrome diseases +MONDO:0016650 orphanet_rare diseases +MONDO:0016650 otar diseases +MONDO:0016650 rare diseases +MONDO:0016651 gard_rare diseases +MONDO:0016651 nord_rare diseases +MONDO:0016651 ordo_disorder diseases +MONDO:0016651 ordo_malformation_syndrome diseases +MONDO:0016651 orphanet_rare diseases +MONDO:0016651 otar diseases +MONDO:0016651 rare diseases +MONDO:0016652 gard_rare diseases +MONDO:0016652 nord_rare diseases +MONDO:0016652 ordo_disorder diseases +MONDO:0016652 ordo_malformation_syndrome diseases +MONDO:0016652 orphanet_rare diseases +MONDO:0016652 otar diseases +MONDO:0016652 rare diseases +MONDO:0016653 gard_rare diseases +MONDO:0016653 nord_rare diseases +MONDO:0016653 ordo_malformation_syndrome diseases +MONDO:0016653 ordo_subtype_of_a_disorder diseases +MONDO:0016653 otar diseases +MONDO:0016653 rare diseases +MONDO:0016654 gard_rare diseases +MONDO:0016654 nord_rare diseases +MONDO:0016654 ordo_disorder diseases +MONDO:0016654 ordo_malformation_syndrome diseases +MONDO:0016654 orphanet_rare diseases +MONDO:0016654 otar diseases +MONDO:0016654 rare diseases +MONDO:0016655 gard_rare diseases +MONDO:0016655 nord_rare diseases +MONDO:0016655 ordo_disorder diseases +MONDO:0016655 ordo_malformation_syndrome diseases +MONDO:0016655 orphanet_rare diseases +MONDO:0016655 rare diseases +MONDO:0016656 gard_rare diseases +MONDO:0016656 nord_rare diseases +MONDO:0016656 ordo_disorder diseases +MONDO:0016656 ordo_malformation_syndrome diseases +MONDO:0016656 orphanet_rare diseases +MONDO:0016656 rare diseases +MONDO:0016657 gard_rare diseases +MONDO:0016657 nord_rare diseases +MONDO:0016657 ordo_disorder diseases +MONDO:0016657 ordo_malformation_syndrome diseases +MONDO:0016657 orphanet_rare diseases +MONDO:0016657 otar diseases +MONDO:0016657 rare diseases +MONDO:0016658 gard_rare diseases +MONDO:0016658 nord_rare diseases +MONDO:0016658 ordo_disorder diseases +MONDO:0016658 ordo_malformation_syndrome diseases +MONDO:0016658 orphanet_rare diseases +MONDO:0016658 otar diseases +MONDO:0016658 rare diseases +MONDO:0016659 gard_rare diseases +MONDO:0016659 nord_rare diseases +MONDO:0016659 ordo_disorder diseases +MONDO:0016659 ordo_malformation_syndrome diseases +MONDO:0016659 orphanet_rare diseases +MONDO:0016659 otar diseases +MONDO:0016659 rare diseases +MONDO:0016660 clingen diseases +MONDO:0016660 gard_rare diseases +MONDO:0016660 nord_rare diseases +MONDO:0016660 ordo_etiological_subtype diseases +MONDO:0016660 ordo_subtype_of_a_disorder diseases +MONDO:0016660 otar diseases +MONDO:0016660 rare diseases +MONDO:0016661 gard_rare diseases +MONDO:0016661 nord_rare diseases +MONDO:0016661 ordo_disorder diseases +MONDO:0016661 orphanet_rare diseases +MONDO:0016661 rare diseases +MONDO:0016662 gard_rare diseases +MONDO:0016662 nord_rare diseases +MONDO:0016662 ordo_disorder diseases +MONDO:0016662 orphanet_rare diseases +MONDO:0016662 rare diseases +MONDO:0016663 disease_grouping diseases +MONDO:0016663 gard_rare diseases +MONDO:0016663 ordo_group_of_disorders diseases +MONDO:0016663 otar diseases +MONDO:0016663 rare diseases +MONDO:0016664 gard_rare diseases +MONDO:0016664 nord_rare diseases +MONDO:0016664 ordo_disorder diseases +MONDO:0016664 orphanet_rare diseases +MONDO:0016664 rare diseases +MONDO:0016666 gard_rare diseases +MONDO:0016666 nord_rare diseases +MONDO:0016666 ordo_disorder diseases +MONDO:0016666 orphanet_rare diseases +MONDO:0016666 rare diseases +MONDO:0016668 gard_rare diseases +MONDO:0016668 nord_rare diseases +MONDO:0016668 ordo_disorder diseases +MONDO:0016668 orphanet_rare diseases +MONDO:0016668 otar diseases +MONDO:0016668 rare diseases +MONDO:0016669 gard_rare diseases +MONDO:0016669 nord_rare diseases +MONDO:0016669 ordo_disorder diseases +MONDO:0016669 orphanet_rare diseases +MONDO:0016669 otar diseases +MONDO:0016669 rare diseases +MONDO:0016670 gard_rare diseases +MONDO:0016670 nord_rare diseases +MONDO:0016670 ordo_disorder diseases +MONDO:0016670 orphanet_rare diseases +MONDO:0016670 otar diseases +MONDO:0016670 rare diseases +MONDO:0016671 gard_rare diseases +MONDO:0016671 nord_rare diseases +MONDO:0016671 ordo_disorder diseases +MONDO:0016671 orphanet_rare diseases +MONDO:0016671 otar diseases +MONDO:0016671 rare diseases +MONDO:0016672 gard_rare diseases +MONDO:0016672 nord_rare diseases +MONDO:0016672 ordo_disorder diseases +MONDO:0016672 orphanet_rare diseases +MONDO:0016672 otar diseases +MONDO:0016672 rare diseases +MONDO:0016673 gard_rare diseases +MONDO:0016673 nord_rare diseases +MONDO:0016673 ordo_disorder diseases +MONDO:0016673 orphanet_rare diseases +MONDO:0016673 otar diseases +MONDO:0016673 rare diseases +MONDO:0016674 gard_rare diseases +MONDO:0016674 nord_rare diseases +MONDO:0016674 ordo_disorder diseases +MONDO:0016674 ordo_malformation_syndrome diseases +MONDO:0016674 orphanet_rare diseases +MONDO:0016674 otar diseases +MONDO:0016674 rare diseases +MONDO:0016675 gard_rare diseases +MONDO:0016675 nord_rare diseases +MONDO:0016675 ordo_disorder diseases +MONDO:0016675 ordo_malformation_syndrome diseases +MONDO:0016675 orphanet_rare diseases +MONDO:0016675 otar diseases +MONDO:0016675 rare diseases +MONDO:0016676 gard_rare diseases +MONDO:0016676 nord_rare diseases +MONDO:0016676 ordo_disorder diseases +MONDO:0016676 orphanet_rare diseases +MONDO:0016676 otar diseases +MONDO:0016676 rare diseases +MONDO:0016677 disease_grouping diseases +MONDO:0016677 ordo_group_of_disorders diseases +MONDO:0016680 disease_grouping diseases +MONDO:0016680 gard_rare diseases +MONDO:0016680 nord_rare diseases +MONDO:0016680 ordo_group_of_disorders diseases +MONDO:0016680 otar diseases +MONDO:0016680 rare diseases +MONDO:0016681 gard_rare diseases +MONDO:0016681 nord_rare diseases +MONDO:0016681 ordo_histopathological_subtype diseases +MONDO:0016681 ordo_subtype_of_a_disorder diseases +MONDO:0016681 otar diseases +MONDO:0016681 rare diseases +MONDO:0016682 gard_rare diseases +MONDO:0016682 nord_rare diseases +MONDO:0016682 ordo_histopathological_subtype diseases +MONDO:0016682 ordo_subtype_of_a_disorder diseases +MONDO:0016682 rare diseases +MONDO:0016683 gard_rare diseases +MONDO:0016683 nord_rare diseases +MONDO:0016683 ordo_disorder diseases +MONDO:0016683 orphanet_rare diseases +MONDO:0016683 otar diseases +MONDO:0016683 rare diseases +MONDO:0016684 gard_rare diseases +MONDO:0016684 nord_rare diseases +MONDO:0016684 ordo_disorder diseases +MONDO:0016684 orphanet_rare diseases +MONDO:0016684 otar diseases +MONDO:0016684 rare diseases +MONDO:0016685 disease_grouping diseases +MONDO:0016685 gard_rare diseases +MONDO:0016685 ordo_group_of_disorders diseases +MONDO:0016685 otar diseases +MONDO:0016685 rare diseases +MONDO:0016686 gard_rare diseases +MONDO:0016686 nord_rare diseases +MONDO:0016686 ordo_disorder diseases +MONDO:0016686 orphanet_rare diseases +MONDO:0016686 rare diseases +MONDO:0016687 gard_rare diseases +MONDO:0016687 nord_rare diseases +MONDO:0016687 ordo_histopathological_subtype diseases +MONDO:0016687 ordo_subtype_of_a_disorder diseases +MONDO:0016687 rare diseases +MONDO:0016688 gard_rare diseases +MONDO:0016688 nord_rare diseases +MONDO:0016688 ordo_histopathological_subtype diseases +MONDO:0016688 ordo_subtype_of_a_disorder diseases +MONDO:0016688 rare diseases +MONDO:0016689 gard_rare diseases +MONDO:0016689 nord_rare diseases +MONDO:0016689 ordo_histopathological_subtype diseases +MONDO:0016689 ordo_subtype_of_a_disorder diseases +MONDO:0016689 rare diseases +MONDO:0016690 gard_rare diseases +MONDO:0016690 nord_rare diseases +MONDO:0016690 ordo_disorder diseases +MONDO:0016690 orphanet_rare diseases +MONDO:0016690 otar diseases +MONDO:0016690 rare diseases +MONDO:0016691 gard_rare diseases +MONDO:0016691 nord_rare diseases +MONDO:0016691 ordo_disorder diseases +MONDO:0016691 orphanet_rare diseases +MONDO:0016691 otar diseases +MONDO:0016691 rare diseases +MONDO:0016692 gard_rare diseases +MONDO:0016692 ordo_histopathological_subtype diseases +MONDO:0016692 ordo_subtype_of_a_disorder diseases +MONDO:0016692 otar diseases +MONDO:0016692 rare diseases +MONDO:0016693 gard_rare diseases +MONDO:0016693 nord_rare diseases +MONDO:0016693 ordo_disorder diseases +MONDO:0016693 orphanet_rare diseases +MONDO:0016693 otar diseases +MONDO:0016693 rare diseases +MONDO:0016695 gard_rare diseases +MONDO:0016695 nord_rare diseases +MONDO:0016695 ordo_disorder diseases +MONDO:0016695 orphanet_rare diseases +MONDO:0016695 otar diseases +MONDO:0016695 rare diseases +MONDO:0016696 gard_rare diseases +MONDO:0016696 nord_rare diseases +MONDO:0016696 ordo_disorder diseases +MONDO:0016696 orphanet_rare diseases +MONDO:0016696 otar diseases +MONDO:0016696 rare diseases +MONDO:0016697 gard_rare diseases +MONDO:0016697 otar diseases +MONDO:0016697 rare diseases +MONDO:0016698 gard_rare diseases +MONDO:0016698 nord_rare diseases +MONDO:0016698 ordo_disorder diseases +MONDO:0016698 ordo_histopathological_subtype diseases +MONDO:0016698 orphanet_rare diseases +MONDO:0016698 otar diseases +MONDO:0016698 rare diseases +MONDO:0016699 gard_rare diseases +MONDO:0016699 ordo_disorder diseases +MONDO:0016699 ordo_histopathological_subtype diseases +MONDO:0016699 orphanet_rare diseases +MONDO:0016699 rare diseases +MONDO:0016700 gard_rare diseases +MONDO:0016700 nord_rare diseases +MONDO:0016700 ordo_disorder diseases +MONDO:0016700 orphanet_rare diseases +MONDO:0016700 otar diseases +MONDO:0016700 rare diseases +MONDO:0016702 gard_rare diseases +MONDO:0016702 nord_rare diseases +MONDO:0016702 ordo_disorder diseases +MONDO:0016702 orphanet_rare diseases +MONDO:0016702 otar diseases +MONDO:0016702 rare diseases +MONDO:0016703 gard_rare diseases +MONDO:0016703 nord_rare diseases +MONDO:0016703 ordo_disorder diseases +MONDO:0016703 orphanet_rare diseases +MONDO:0016703 otar diseases +MONDO:0016703 rare diseases +MONDO:0016705 gard_rare diseases +MONDO:0016705 nord_rare diseases +MONDO:0016705 ordo_disorder diseases +MONDO:0016705 orphanet_rare diseases +MONDO:0016705 rare diseases +MONDO:0016706 gard_rare diseases +MONDO:0016706 nord_rare diseases +MONDO:0016706 ordo_disorder diseases +MONDO:0016706 orphanet_rare diseases +MONDO:0016706 rare diseases +MONDO:0016707 gard_rare diseases +MONDO:0016707 nord_rare diseases +MONDO:0016707 ordo_disorder diseases +MONDO:0016707 orphanet_rare diseases +MONDO:0016707 otar diseases +MONDO:0016707 rare diseases +MONDO:0016709 gard_rare diseases +MONDO:0016709 nord_rare diseases +MONDO:0016709 ordo_histopathological_subtype diseases +MONDO:0016709 ordo_subtype_of_a_disorder diseases +MONDO:0016709 rare diseases +MONDO:0016710 gard_rare diseases +MONDO:0016710 nord_rare diseases +MONDO:0016710 ordo_histopathological_subtype diseases +MONDO:0016710 ordo_subtype_of_a_disorder diseases +MONDO:0016710 otar diseases +MONDO:0016710 rare diseases +MONDO:0016711 gard_rare diseases +MONDO:0016711 nord_rare diseases +MONDO:0016711 ordo_histopathological_subtype diseases +MONDO:0016711 ordo_subtype_of_a_disorder diseases +MONDO:0016711 rare diseases +MONDO:0016712 gard_rare diseases +MONDO:0016712 nord_rare diseases +MONDO:0016712 ordo_histopathological_subtype diseases +MONDO:0016712 ordo_subtype_of_a_disorder diseases +MONDO:0016712 otar diseases +MONDO:0016712 rare diseases +MONDO:0016713 disease_grouping diseases +MONDO:0016713 gard_rare diseases +MONDO:0016713 nord_rare diseases +MONDO:0016713 ordo_group_of_disorders diseases +MONDO:0016713 rare diseases +MONDO:0016715 gard_rare diseases +MONDO:0016715 nord_rare diseases +MONDO:0016715 otar diseases +MONDO:0016715 rare diseases +MONDO:0016717 disease_grouping diseases +MONDO:0016717 gard_rare diseases +MONDO:0016717 ordo_group_of_disorders diseases +MONDO:0016717 otar diseases +MONDO:0016717 rare diseases +MONDO:0016718 gard_rare diseases +MONDO:0016718 nord_rare diseases +MONDO:0016718 ordo_disorder diseases +MONDO:0016718 orphanet_rare diseases +MONDO:0016718 otar diseases +MONDO:0016718 rare diseases +MONDO:0016719 gard_rare diseases +MONDO:0016719 ordo_disorder diseases +MONDO:0016719 ordo_malformation_syndrome diseases +MONDO:0016719 orphanet_rare diseases +MONDO:0016719 otar diseases +MONDO:0016719 rare diseases +MONDO:0016722 gard_rare diseases +MONDO:0016722 nord_rare diseases +MONDO:0016722 ordo_disorder diseases +MONDO:0016722 orphanet_rare diseases +MONDO:0016722 otar diseases +MONDO:0016722 rare diseases +MONDO:0016723 gard_rare diseases +MONDO:0016723 nord_rare diseases +MONDO:0016723 ordo_disorder diseases +MONDO:0016723 orphanet_rare diseases +MONDO:0016723 otar diseases +MONDO:0016723 rare diseases +MONDO:0016724 gard_rare diseases +MONDO:0016724 nord_rare diseases +MONDO:0016724 ordo_disorder diseases +MONDO:0016724 orphanet_rare diseases +MONDO:0016724 rare diseases +MONDO:0016727 gard_rare diseases +MONDO:0016727 nord_rare diseases +MONDO:0016727 ordo_disorder diseases +MONDO:0016727 orphanet_rare diseases +MONDO:0016727 otar diseases +MONDO:0016727 rare diseases +MONDO:0016729 disease_grouping diseases +MONDO:0016729 gard_rare diseases +MONDO:0016729 nord_rare diseases +MONDO:0016729 ordo_group_of_disorders diseases +MONDO:0016729 otar diseases +MONDO:0016729 rare diseases +MONDO:0016730 gard_rare diseases +MONDO:0016730 nord_rare diseases +MONDO:0016730 ordo_disorder diseases +MONDO:0016730 orphanet_rare diseases +MONDO:0016730 otar diseases +MONDO:0016730 rare diseases +MONDO:0016731 gard_rare diseases +MONDO:0016731 nord_rare diseases +MONDO:0016731 ordo_disorder diseases +MONDO:0016731 orphanet_rare diseases +MONDO:0016731 rare diseases +MONDO:0016733 gard_rare diseases +MONDO:0016733 nord_rare diseases +MONDO:0016733 ordo_disorder diseases +MONDO:0016733 orphanet_rare diseases +MONDO:0016733 otar diseases +MONDO:0016733 rare diseases +MONDO:0016734 gard_rare diseases +MONDO:0016734 nord_rare diseases +MONDO:0016734 ordo_disorder diseases +MONDO:0016734 orphanet_rare diseases +MONDO:0016734 rare diseases +MONDO:0016735 gard_rare diseases +MONDO:0016735 nord_rare diseases +MONDO:0016735 ordo_disorder diseases +MONDO:0016735 orphanet_rare diseases +MONDO:0016735 otar diseases +MONDO:0016735 rare diseases +MONDO:0016736 gard_rare diseases +MONDO:0016736 nord_rare diseases +MONDO:0016736 ordo_disorder diseases +MONDO:0016736 orphanet_rare diseases +MONDO:0016736 otar diseases +MONDO:0016736 rare diseases +MONDO:0016739 gard_rare diseases +MONDO:0016739 nord_rare diseases +MONDO:0016739 ordo_subtype_of_a_disorder diseases +MONDO:0016739 rare diseases +MONDO:0016740 gard_rare diseases +MONDO:0016740 nord_rare diseases +MONDO:0016740 ordo_disorder diseases +MONDO:0016740 orphanet_rare diseases +MONDO:0016740 rare diseases +MONDO:0016742 gard_rare diseases +MONDO:0016742 nord_rare diseases +MONDO:0016742 ordo_subtype_of_a_disorder diseases +MONDO:0016742 otar diseases +MONDO:0016742 rare diseases +MONDO:0016743 disease_grouping diseases +MONDO:0016743 gard_rare diseases +MONDO:0016743 ordo_group_of_disorders diseases +MONDO:0016743 otar diseases +MONDO:0016743 rare diseases +MONDO:0016745 gard_rare diseases +MONDO:0016745 nord_rare diseases +MONDO:0016745 ordo_disorder diseases +MONDO:0016745 orphanet_rare diseases +MONDO:0016745 rare diseases +MONDO:0016746 gard_rare diseases +MONDO:0016746 nord_rare diseases +MONDO:0016746 ordo_disorder diseases +MONDO:0016746 orphanet_rare diseases +MONDO:0016746 rare diseases +MONDO:0016747 gard_rare diseases +MONDO:0016747 nord_rare diseases +MONDO:0016747 ordo_disorder diseases +MONDO:0016747 orphanet_rare diseases +MONDO:0016747 otar diseases +MONDO:0016747 rare diseases +MONDO:0016748 gard_rare diseases +MONDO:0016748 nord_rare diseases +MONDO:0016748 ordo_disorder diseases +MONDO:0016748 orphanet_rare diseases +MONDO:0016748 otar diseases +MONDO:0016748 rare diseases +MONDO:0016749 disease_grouping diseases +MONDO:0016749 gard_rare diseases +MONDO:0016749 ordo_group_of_disorders diseases +MONDO:0016749 rare diseases +MONDO:0016750 gard_rare diseases +MONDO:0016750 ordo_disorder diseases +MONDO:0016750 ordo_malformation_syndrome diseases +MONDO:0016750 orphanet_rare diseases +MONDO:0016750 rare diseases +MONDO:0016751 gard_rare diseases +MONDO:0016751 nord_rare diseases +MONDO:0016751 ordo_subtype_of_a_disorder diseases +MONDO:0016751 rare diseases +MONDO:0016752 disease_grouping diseases +MONDO:0016752 inferred_rare diseases +MONDO:0016752 ordo_group_of_disorders diseases +MONDO:0016752 otar diseases +MONDO:0016752 rare diseases +MONDO:0016755 gard_rare diseases +MONDO:0016755 nord_rare diseases +MONDO:0016755 ordo_disorder diseases +MONDO:0016755 orphanet_rare diseases +MONDO:0016755 rare diseases +MONDO:0016757 gard_rare diseases +MONDO:0016757 nord_rare diseases +MONDO:0016757 ordo_subtype_of_a_disorder diseases +MONDO:0016757 otar diseases +MONDO:0016757 rare diseases +MONDO:0016758 gard_rare diseases +MONDO:0016758 nord_rare diseases +MONDO:0016758 ordo_disorder diseases +MONDO:0016758 ordo_malformation_syndrome diseases +MONDO:0016758 orphanet_rare diseases +MONDO:0016758 otar diseases +MONDO:0016758 rare diseases +MONDO:0016759 gard_rare diseases +MONDO:0016759 nord_rare diseases +MONDO:0016759 ordo_disorder diseases +MONDO:0016759 ordo_malformation_syndrome diseases +MONDO:0016759 orphanet_rare diseases +MONDO:0016759 otar diseases +MONDO:0016759 rare diseases +MONDO:0016760 gard_rare diseases +MONDO:0016760 ordo_disorder diseases +MONDO:0016760 ordo_malformation_syndrome diseases +MONDO:0016760 orphanet_rare diseases +MONDO:0016760 otar diseases +MONDO:0016760 rare diseases +MONDO:0016761 disease_grouping diseases +MONDO:0016761 gard_rare diseases +MONDO:0016761 nord_rare diseases +MONDO:0016761 otar diseases +MONDO:0016761 rare diseases +MONDO:0016762 ordo_malformation_syndrome diseases +MONDO:0016763 clingen diseases +MONDO:0016763 disease_grouping diseases +MONDO:0016763 gard_rare diseases +MONDO:0016763 nord_rare diseases +MONDO:0016763 ordo_group_of_disorders diseases +MONDO:0016763 otar diseases +MONDO:0016763 rare diseases +MONDO:0016764 disease_grouping diseases +MONDO:0016764 gard_rare diseases +MONDO:0016764 nord_rare diseases +MONDO:0016764 ordo_group_of_disorders diseases +MONDO:0016764 otar diseases +MONDO:0016764 rare diseases +MONDO:0016765 gard_rare diseases +MONDO:0016765 nord_rare diseases +MONDO:0016765 ordo_disorder diseases +MONDO:0016765 ordo_malformation_syndrome diseases +MONDO:0016765 orphanet_rare diseases +MONDO:0016765 rare diseases +MONDO:0016769 gard_rare diseases +MONDO:0016769 nord_rare diseases +MONDO:0016769 ordo_disorder diseases +MONDO:0016769 orphanet_rare diseases +MONDO:0016769 rare diseases +MONDO:0016770 gard_rare diseases +MONDO:0016770 nord_rare diseases +MONDO:0016770 ordo_disorder diseases +MONDO:0016770 orphanet_rare diseases +MONDO:0016770 rare diseases +MONDO:0016771 gard_rare diseases +MONDO:0016771 nord_rare diseases +MONDO:0016771 ordo_disorder diseases +MONDO:0016771 orphanet_rare diseases +MONDO:0016771 rare diseases +MONDO:0016772 gard_rare diseases +MONDO:0016772 nord_rare diseases +MONDO:0016772 ordo_disorder diseases +MONDO:0016772 orphanet_rare diseases +MONDO:0016772 rare diseases +MONDO:0016773 gard_rare diseases +MONDO:0016773 nord_rare diseases +MONDO:0016773 ordo_disorder diseases +MONDO:0016773 orphanet_rare diseases +MONDO:0016773 rare diseases +MONDO:0016774 gard_rare diseases +MONDO:0016774 nord_rare diseases +MONDO:0016774 ordo_disorder diseases +MONDO:0016774 orphanet_rare diseases +MONDO:0016774 rare diseases +MONDO:0016775 gard_rare diseases +MONDO:0016775 nord_rare diseases +MONDO:0016775 ordo_disorder diseases +MONDO:0016775 orphanet_rare diseases +MONDO:0016775 rare diseases +MONDO:0016776 gard_rare diseases +MONDO:0016776 nord_rare diseases +MONDO:0016776 ordo_disorder diseases +MONDO:0016776 orphanet_rare diseases +MONDO:0016776 rare diseases +MONDO:0016777 gard_rare diseases +MONDO:0016777 nord_rare diseases +MONDO:0016777 ordo_subtype_of_a_disorder diseases +MONDO:0016777 rare diseases +MONDO:0016778 gard_rare diseases +MONDO:0016778 nord_rare diseases +MONDO:0016778 ordo_subtype_of_a_disorder diseases +MONDO:0016778 otar diseases +MONDO:0016778 rare diseases +MONDO:0016779 gard_rare diseases +MONDO:0016779 nord_rare diseases +MONDO:0016779 ordo_disorder diseases +MONDO:0016779 ordo_malformation_syndrome diseases +MONDO:0016779 orphanet_rare diseases +MONDO:0016779 otar diseases +MONDO:0016779 rare diseases +MONDO:0016780 gard_rare diseases +MONDO:0016780 nord_rare diseases +MONDO:0016780 ordo_etiological_subtype diseases +MONDO:0016780 ordo_subtype_of_a_disorder diseases +MONDO:0016780 otar diseases +MONDO:0016780 rare diseases +MONDO:0016781 gard_rare diseases +MONDO:0016781 nord_rare diseases +MONDO:0016781 ordo_etiological_subtype diseases +MONDO:0016781 ordo_subtype_of_a_disorder diseases +MONDO:0016781 otar diseases +MONDO:0016781 rare diseases +MONDO:0016782 gard_rare diseases +MONDO:0016782 nord_rare diseases +MONDO:0016782 ordo_etiological_subtype diseases +MONDO:0016782 ordo_subtype_of_a_disorder diseases +MONDO:0016782 otar diseases +MONDO:0016782 rare diseases +MONDO:0016783 gard_rare diseases +MONDO:0016783 nord_rare diseases +MONDO:0016783 ordo_etiological_subtype diseases +MONDO:0016783 ordo_subtype_of_a_disorder diseases +MONDO:0016783 otar diseases +MONDO:0016783 rare diseases +MONDO:0016785 gard_rare diseases +MONDO:0016785 nord_rare diseases +MONDO:0016785 ordo_subtype_of_a_disorder diseases +MONDO:0016785 otar diseases +MONDO:0016785 rare diseases +MONDO:0016786 gard_rare diseases +MONDO:0016786 nord_rare diseases +MONDO:0016786 ordo_subtype_of_a_disorder diseases +MONDO:0016786 rare diseases +MONDO:0016787 gard_rare diseases +MONDO:0016787 nord_rare diseases +MONDO:0016787 ordo_disorder diseases +MONDO:0016787 orphanet_rare diseases +MONDO:0016787 rare diseases +MONDO:0016789 disease_grouping diseases +MONDO:0016789 gard_rare diseases +MONDO:0016789 ordo_group_of_disorders diseases +MONDO:0016789 rare diseases +MONDO:0016790 disease_grouping diseases +MONDO:0016790 gard_rare diseases +MONDO:0016790 ordo_group_of_disorders diseases +MONDO:0016790 otar diseases +MONDO:0016790 rare diseases +MONDO:0016796 disease_grouping diseases +MONDO:0016796 gard_rare diseases +MONDO:0016796 ordo_group_of_disorders diseases +MONDO:0016796 otar diseases +MONDO:0016796 rare diseases +MONDO:0016798 disease_grouping diseases +MONDO:0016798 gard_rare diseases +MONDO:0016798 ordo_group_of_disorders diseases +MONDO:0016798 otar diseases +MONDO:0016798 rare diseases +MONDO:0016800 disease_grouping diseases +MONDO:0016800 gard_rare diseases +MONDO:0016800 ordo_group_of_disorders diseases +MONDO:0016800 rare diseases +MONDO:0016801 disease_grouping diseases +MONDO:0016801 gard_rare diseases +MONDO:0016801 ordo_group_of_disorders diseases +MONDO:0016801 rare diseases +MONDO:0016802 disease_grouping diseases +MONDO:0016802 gard_rare diseases +MONDO:0016802 ordo_group_of_disorders diseases +MONDO:0016802 otar diseases +MONDO:0016802 rare diseases +MONDO:0016806 gard_rare diseases +MONDO:0016806 nord_rare diseases +MONDO:0016806 ordo_disorder diseases +MONDO:0016806 orphanet_rare diseases +MONDO:0016806 rare diseases +MONDO:0016807 gard_rare diseases +MONDO:0016807 nord_rare diseases +MONDO:0016807 ordo_disorder diseases +MONDO:0016807 orphanet_rare diseases +MONDO:0016807 otar diseases +MONDO:0016807 rare diseases +MONDO:0016809 gard_rare diseases +MONDO:0016809 nord_rare diseases +MONDO:0016809 ordo_disorder diseases +MONDO:0016809 orphanet_rare diseases +MONDO:0016809 otar diseases +MONDO:0016809 rare diseases +MONDO:0016810 gard_rare diseases +MONDO:0016810 nord_rare diseases +MONDO:0016810 ordo_disorder diseases +MONDO:0016810 orphanet_rare diseases +MONDO:0016810 otar diseases +MONDO:0016810 rare diseases +MONDO:0016811 gard_rare diseases +MONDO:0016811 ordo_disorder diseases +MONDO:0016811 orphanet_rare diseases +MONDO:0016811 otar diseases +MONDO:0016811 rare diseases +MONDO:0016812 disease_grouping diseases +MONDO:0016812 gard_rare diseases +MONDO:0016812 nord_rare diseases +MONDO:0016812 ordo_group_of_disorders diseases +MONDO:0016812 otar diseases +MONDO:0016812 rare diseases +MONDO:0016814 gard_rare diseases +MONDO:0016814 nord_rare diseases +MONDO:0016814 ordo_disorder diseases +MONDO:0016814 orphanet_rare diseases +MONDO:0016814 otar diseases +MONDO:0016814 rare diseases +MONDO:0016817 gard_rare diseases +MONDO:0016817 nord_rare diseases +MONDO:0016817 ordo_disorder diseases +MONDO:0016817 ordo_malformation_syndrome diseases +MONDO:0016817 orphanet_rare diseases +MONDO:0016817 otar diseases +MONDO:0016817 rare diseases +MONDO:0016818 gard_rare diseases +MONDO:0016818 nord_rare diseases +MONDO:0016818 ordo_disorder diseases +MONDO:0016818 ordo_malformation_syndrome diseases +MONDO:0016818 orphanet_rare diseases +MONDO:0016818 rare diseases +MONDO:0016819 gard_rare diseases +MONDO:0016819 nord_rare diseases +MONDO:0016819 ordo_disorder diseases +MONDO:0016819 ordo_malformation_syndrome diseases +MONDO:0016819 orphanet_rare diseases +MONDO:0016819 otar diseases +MONDO:0016819 rare diseases +MONDO:0016820 gard_rare diseases +MONDO:0016820 nord_rare diseases +MONDO:0016820 ordo_disorder diseases +MONDO:0016820 orphanet_rare diseases +MONDO:0016820 otar diseases +MONDO:0016820 rare diseases +MONDO:0016821 ordo_malformation_syndrome diseases +MONDO:0016822 gard_rare diseases +MONDO:0016822 nord_rare diseases +MONDO:0016822 ordo_disorder diseases +MONDO:0016822 ordo_malformation_syndrome diseases +MONDO:0016822 orphanet_rare diseases +MONDO:0016822 rare diseases +MONDO:0016823 gard_rare diseases +MONDO:0016823 nord_rare diseases +MONDO:0016823 ordo_disorder diseases +MONDO:0016823 orphanet_rare diseases +MONDO:0016823 rare diseases +MONDO:0016824 gard_rare diseases +MONDO:0016824 nord_rare diseases +MONDO:0016824 ordo_disorder diseases +MONDO:0016824 orphanet_rare diseases +MONDO:0016824 otar diseases +MONDO:0016824 rare diseases +MONDO:0016825 gard_rare diseases +MONDO:0016825 nord_rare diseases +MONDO:0016825 ordo_disorder diseases +MONDO:0016825 orphanet_rare diseases +MONDO:0016825 otar diseases +MONDO:0016825 rare diseases +MONDO:0016826 gard_rare diseases +MONDO:0016826 nord_rare diseases +MONDO:0016826 ordo_disorder diseases +MONDO:0016826 orphanet_rare diseases +MONDO:0016826 rare diseases +MONDO:0016827 ordo_malformation_syndrome diseases +MONDO:0016828 gard_rare diseases +MONDO:0016828 nord_rare diseases +MONDO:0016828 ordo_disorder diseases +MONDO:0016828 orphanet_rare diseases +MONDO:0016828 otar diseases +MONDO:0016828 rare diseases +MONDO:0016829 gard_rare diseases +MONDO:0016829 nord_rare diseases +MONDO:0016829 ordo_disorder diseases +MONDO:0016829 orphanet_rare diseases +MONDO:0016829 otar diseases +MONDO:0016829 rare diseases +MONDO:0016830 gard_rare diseases +MONDO:0016830 nord_rare diseases +MONDO:0016830 ordo_disorder diseases +MONDO:0016830 orphanet_rare diseases +MONDO:0016830 otar diseases +MONDO:0016830 rare diseases +MONDO:0016831 gard_rare diseases +MONDO:0016831 nord_rare diseases +MONDO:0016831 ordo_disorder diseases +MONDO:0016831 orphanet_rare diseases +MONDO:0016831 rare diseases +MONDO:0016832 gard_rare diseases +MONDO:0016832 ordo_disorder diseases +MONDO:0016832 ordo_malformation_syndrome diseases +MONDO:0016832 orphanet_rare diseases +MONDO:0016832 otar diseases +MONDO:0016832 rare diseases +MONDO:0016833 gard_rare diseases +MONDO:0016833 nord_rare diseases +MONDO:0016833 ordo_malformation_syndrome diseases +MONDO:0016833 ordo_subtype_of_a_disorder diseases +MONDO:0016833 otar diseases +MONDO:0016833 rare diseases +MONDO:0016834 gard_rare diseases +MONDO:0016834 nord_rare diseases +MONDO:0016834 ordo_disorder diseases +MONDO:0016834 ordo_malformation_syndrome diseases +MONDO:0016834 orphanet_rare diseases +MONDO:0016834 otar diseases +MONDO:0016834 rare diseases +MONDO:0016835 gard_rare diseases +MONDO:0016835 nord_rare diseases +MONDO:0016835 ordo_disorder diseases +MONDO:0016835 ordo_malformation_syndrome diseases +MONDO:0016835 orphanet_rare diseases +MONDO:0016835 rare diseases +MONDO:0016836 gard_rare diseases +MONDO:0016836 nord_rare diseases +MONDO:0016836 ordo_disorder diseases +MONDO:0016836 ordo_malformation_syndrome diseases +MONDO:0016836 orphanet_rare diseases +MONDO:0016836 otar diseases +MONDO:0016836 rare diseases +MONDO:0016837 gard_rare diseases +MONDO:0016837 nord_rare diseases +MONDO:0016837 ordo_disorder diseases +MONDO:0016837 ordo_malformation_syndrome diseases +MONDO:0016837 orphanet_rare diseases +MONDO:0016837 otar diseases +MONDO:0016837 rare diseases +MONDO:0016838 gard_rare diseases +MONDO:0016838 nord_rare diseases +MONDO:0016838 ordo_disorder diseases +MONDO:0016838 ordo_malformation_syndrome diseases +MONDO:0016838 orphanet_rare diseases +MONDO:0016838 otar diseases +MONDO:0016838 rare diseases +MONDO:0016839 gard_rare diseases +MONDO:0016839 nord_rare diseases +MONDO:0016839 ordo_disorder diseases +MONDO:0016839 ordo_malformation_syndrome diseases +MONDO:0016839 orphanet_rare diseases +MONDO:0016839 rare diseases +MONDO:0016840 gard_rare diseases +MONDO:0016840 nord_rare diseases +MONDO:0016840 ordo_disorder diseases +MONDO:0016840 ordo_malformation_syndrome diseases +MONDO:0016840 orphanet_rare diseases +MONDO:0016840 otar diseases +MONDO:0016840 rare diseases +MONDO:0016841 gard_rare diseases +MONDO:0016841 nord_rare diseases +MONDO:0016841 ordo_disorder diseases +MONDO:0016841 ordo_malformation_syndrome diseases +MONDO:0016841 orphanet_rare diseases +MONDO:0016841 otar diseases +MONDO:0016841 rare diseases +MONDO:0016842 gard_rare diseases +MONDO:0016842 nord_rare diseases +MONDO:0016842 ordo_disorder diseases +MONDO:0016842 ordo_malformation_syndrome diseases +MONDO:0016842 orphanet_rare diseases +MONDO:0016842 otar diseases +MONDO:0016842 rare diseases +MONDO:0016843 gard_rare diseases +MONDO:0016843 nord_rare diseases +MONDO:0016843 ordo_disorder diseases +MONDO:0016843 ordo_malformation_syndrome diseases +MONDO:0016843 orphanet_rare diseases +MONDO:0016843 otar diseases +MONDO:0016843 rare diseases +MONDO:0016844 gard_rare diseases +MONDO:0016844 nord_rare diseases +MONDO:0016844 ordo_disorder diseases +MONDO:0016844 ordo_malformation_syndrome diseases +MONDO:0016844 orphanet_rare diseases +MONDO:0016844 otar diseases +MONDO:0016844 rare diseases +MONDO:0016845 gard_rare diseases +MONDO:0016845 nord_rare diseases +MONDO:0016845 ordo_disorder diseases +MONDO:0016845 ordo_malformation_syndrome diseases +MONDO:0016845 orphanet_rare diseases +MONDO:0016845 otar diseases +MONDO:0016845 rare diseases +MONDO:0016846 gard_rare diseases +MONDO:0016846 nord_rare diseases +MONDO:0016846 ordo_disorder diseases +MONDO:0016846 ordo_malformation_syndrome diseases +MONDO:0016846 orphanet_rare diseases +MONDO:0016846 otar diseases +MONDO:0016846 rare diseases +MONDO:0016847 gard_rare diseases +MONDO:0016847 nord_rare diseases +MONDO:0016847 ordo_disorder diseases +MONDO:0016847 ordo_malformation_syndrome diseases +MONDO:0016847 orphanet_rare diseases +MONDO:0016847 otar diseases +MONDO:0016847 rare diseases +MONDO:0016848 gard_rare diseases +MONDO:0016848 nord_rare diseases +MONDO:0016848 ordo_disorder diseases +MONDO:0016848 orphanet_rare diseases +MONDO:0016848 rare diseases +MONDO:0016850 gard_rare diseases +MONDO:0016850 nord_rare diseases +MONDO:0016850 ordo_disorder diseases +MONDO:0016850 ordo_malformation_syndrome diseases +MONDO:0016850 orphanet_rare diseases +MONDO:0016850 rare diseases +MONDO:0016851 gard_rare diseases +MONDO:0016851 nord_rare diseases +MONDO:0016851 ordo_disorder diseases +MONDO:0016851 ordo_malformation_syndrome diseases +MONDO:0016851 orphanet_rare diseases +MONDO:0016851 otar diseases +MONDO:0016851 rare diseases +MONDO:0016852 gard_rare diseases +MONDO:0016852 nord_rare diseases +MONDO:0016852 ordo_disorder diseases +MONDO:0016852 ordo_malformation_syndrome diseases +MONDO:0016852 orphanet_rare diseases +MONDO:0016852 otar diseases +MONDO:0016852 rare diseases +MONDO:0016853 gard_rare diseases +MONDO:0016853 nord_rare diseases +MONDO:0016853 ordo_disorder diseases +MONDO:0016853 ordo_malformation_syndrome diseases +MONDO:0016853 orphanet_rare diseases +MONDO:0016853 otar diseases +MONDO:0016853 rare diseases +MONDO:0016854 gard_rare diseases +MONDO:0016854 nord_rare diseases +MONDO:0016854 ordo_disorder diseases +MONDO:0016854 ordo_malformation_syndrome diseases +MONDO:0016854 orphanet_rare diseases +MONDO:0016854 otar diseases +MONDO:0016854 rare diseases +MONDO:0016855 gard_rare diseases +MONDO:0016855 nord_rare diseases +MONDO:0016855 ordo_etiological_subtype diseases +MONDO:0016855 ordo_subtype_of_a_disorder diseases +MONDO:0016855 otar diseases +MONDO:0016855 rare diseases +MONDO:0016856 gard_rare diseases +MONDO:0016856 nord_rare diseases +MONDO:0016856 ordo_etiological_subtype diseases +MONDO:0016856 ordo_subtype_of_a_disorder diseases +MONDO:0016856 otar diseases +MONDO:0016856 rare diseases +MONDO:0016857 gard_rare diseases +MONDO:0016857 nord_rare diseases +MONDO:0016857 ordo_etiological_subtype diseases +MONDO:0016857 rare diseases +MONDO:0016858 gard_rare diseases +MONDO:0016858 ordo_etiological_subtype diseases +MONDO:0016858 rare diseases +MONDO:0016859 gard_rare diseases +MONDO:0016859 ordo_etiological_subtype diseases +MONDO:0016859 rare diseases +MONDO:0016860 gard_rare diseases +MONDO:0016860 nord_rare diseases +MONDO:0016860 ordo_etiological_subtype diseases +MONDO:0016860 ordo_subtype_of_a_disorder diseases +MONDO:0016860 otar diseases +MONDO:0016860 rare diseases +MONDO:0016861 gard_rare diseases +MONDO:0016861 nord_rare diseases +MONDO:0016861 ordo_etiological_subtype diseases +MONDO:0016861 ordo_subtype_of_a_disorder diseases +MONDO:0016861 otar diseases +MONDO:0016861 rare diseases +MONDO:0016862 gard_rare diseases +MONDO:0016862 nord_rare diseases +MONDO:0016862 ordo_etiological_subtype diseases +MONDO:0016862 ordo_subtype_of_a_disorder diseases +MONDO:0016862 otar diseases +MONDO:0016862 rare diseases +MONDO:0016863 gard_rare diseases +MONDO:0016863 nord_rare diseases +MONDO:0016863 ordo_etiological_subtype diseases +MONDO:0016863 ordo_subtype_of_a_disorder diseases +MONDO:0016863 rare diseases +MONDO:0016864 gard_rare diseases +MONDO:0016864 nord_rare diseases +MONDO:0016864 ordo_etiological_subtype diseases +MONDO:0016864 ordo_subtype_of_a_disorder diseases +MONDO:0016864 otar diseases +MONDO:0016864 rare diseases +MONDO:0016865 gard_rare diseases +MONDO:0016865 nord_rare diseases +MONDO:0016865 ordo_etiological_subtype diseases +MONDO:0016865 ordo_subtype_of_a_disorder diseases +MONDO:0016865 otar diseases +MONDO:0016865 rare diseases +MONDO:0016866 disease_grouping diseases +MONDO:0016866 gard_rare diseases +MONDO:0016866 ordo_group_of_disorders diseases +MONDO:0016866 rare diseases +MONDO:0016867 disease_grouping diseases +MONDO:0016867 gard_rare diseases +MONDO:0016867 ordo_group_of_disorders diseases +MONDO:0016867 rare diseases +MONDO:0016868 disease_grouping diseases +MONDO:0016868 gard_rare diseases +MONDO:0016868 ordo_group_of_disorders diseases +MONDO:0016868 rare diseases +MONDO:0016869 disease_grouping diseases +MONDO:0016869 gard_rare diseases +MONDO:0016869 ordo_group_of_disorders diseases +MONDO:0016869 rare diseases +MONDO:0016870 disease_grouping diseases +MONDO:0016870 gard_rare diseases +MONDO:0016870 ordo_group_of_disorders diseases +MONDO:0016870 rare diseases +MONDO:0016871 disease_grouping diseases +MONDO:0016871 gard_rare diseases +MONDO:0016871 ordo_group_of_disorders diseases +MONDO:0016871 rare diseases +MONDO:0016872 disease_grouping diseases +MONDO:0016872 gard_rare diseases +MONDO:0016872 ordo_group_of_disorders diseases +MONDO:0016872 rare diseases +MONDO:0016873 disease_grouping diseases +MONDO:0016873 gard_rare diseases +MONDO:0016873 ordo_group_of_disorders diseases +MONDO:0016873 rare diseases +MONDO:0016874 disease_grouping diseases +MONDO:0016874 gard_rare diseases +MONDO:0016874 ordo_group_of_disorders diseases +MONDO:0016874 rare diseases +MONDO:0016875 disease_grouping diseases +MONDO:0016875 gard_rare diseases +MONDO:0016875 ordo_group_of_disorders diseases +MONDO:0016875 rare diseases +MONDO:0016876 disease_grouping diseases +MONDO:0016876 gard_rare diseases +MONDO:0016876 ordo_group_of_disorders diseases +MONDO:0016876 rare diseases +MONDO:0016877 disease_grouping diseases +MONDO:0016877 gard_rare diseases +MONDO:0016877 ordo_group_of_disorders diseases +MONDO:0016877 rare diseases +MONDO:0016878 disease_grouping diseases +MONDO:0016878 gard_rare diseases +MONDO:0016878 ordo_group_of_disorders diseases +MONDO:0016878 rare diseases +MONDO:0016879 disease_grouping diseases +MONDO:0016879 gard_rare diseases +MONDO:0016879 ordo_group_of_disorders diseases +MONDO:0016879 rare diseases +MONDO:0016880 disease_grouping diseases +MONDO:0016880 gard_rare diseases +MONDO:0016880 ordo_group_of_disorders diseases +MONDO:0016880 rare diseases +MONDO:0016881 disease_grouping diseases +MONDO:0016881 gard_rare diseases +MONDO:0016881 ordo_group_of_disorders diseases +MONDO:0016881 rare diseases +MONDO:0016882 disease_grouping diseases +MONDO:0016882 gard_rare diseases +MONDO:0016882 ordo_group_of_disorders diseases +MONDO:0016882 rare diseases +MONDO:0016883 disease_grouping diseases +MONDO:0016883 gard_rare diseases +MONDO:0016883 ordo_group_of_disorders diseases +MONDO:0016883 rare diseases +MONDO:0016884 disease_grouping diseases +MONDO:0016884 gard_rare diseases +MONDO:0016884 ordo_group_of_disorders diseases +MONDO:0016884 rare diseases +MONDO:0016885 disease_grouping diseases +MONDO:0016885 gard_rare diseases +MONDO:0016885 ordo_group_of_disorders diseases +MONDO:0016885 rare diseases +MONDO:0016887 disease_grouping diseases +MONDO:0016887 gard_rare diseases +MONDO:0016887 ordo_group_of_disorders diseases +MONDO:0016887 rare diseases +MONDO:0016888 disease_grouping diseases +MONDO:0016888 gard_rare diseases +MONDO:0016888 nord_rare diseases +MONDO:0016888 ordo_group_of_disorders diseases +MONDO:0016888 rare diseases +MONDO:0016889 disease_grouping diseases +MONDO:0016889 gard_rare diseases +MONDO:0016889 ordo_group_of_disorders diseases +MONDO:0016889 otar diseases +MONDO:0016889 rare diseases +MONDO:0016890 disease_grouping diseases +MONDO:0016890 gard_rare diseases +MONDO:0016890 ordo_group_of_disorders diseases +MONDO:0016890 rare diseases +MONDO:0016892 disease_grouping diseases +MONDO:0016892 gard_rare diseases +MONDO:0016892 ordo_group_of_disorders diseases +MONDO:0016892 rare diseases +MONDO:0016893 disease_grouping diseases +MONDO:0016893 gard_rare diseases +MONDO:0016893 ordo_group_of_disorders diseases +MONDO:0016893 rare diseases +MONDO:0016894 disease_grouping diseases +MONDO:0016894 gard_rare diseases +MONDO:0016894 ordo_group_of_disorders diseases +MONDO:0016894 rare diseases +MONDO:0016897 disease_grouping diseases +MONDO:0016897 gard_rare diseases +MONDO:0016897 ordo_group_of_disorders diseases +MONDO:0016897 rare diseases +MONDO:0016898 disease_grouping diseases +MONDO:0016898 gard_rare diseases +MONDO:0016898 ordo_group_of_disorders diseases +MONDO:0016898 rare diseases +MONDO:0016901 disease_grouping diseases +MONDO:0016901 gard_rare diseases +MONDO:0016901 ordo_group_of_disorders diseases +MONDO:0016901 rare diseases +MONDO:0016902 disease_grouping diseases +MONDO:0016902 gard_rare diseases +MONDO:0016902 ordo_group_of_disorders diseases +MONDO:0016902 rare diseases +MONDO:0016903 disease_grouping diseases +MONDO:0016903 gard_rare diseases +MONDO:0016903 ordo_group_of_disorders diseases +MONDO:0016903 rare diseases +MONDO:0016904 disease_grouping diseases +MONDO:0016904 gard_rare diseases +MONDO:0016904 ordo_group_of_disorders diseases +MONDO:0016904 rare diseases +MONDO:0016905 disease_grouping diseases +MONDO:0016905 gard_rare diseases +MONDO:0016905 ordo_group_of_disorders diseases +MONDO:0016905 rare diseases +MONDO:0016906 disease_grouping diseases +MONDO:0016906 gard_rare diseases +MONDO:0016906 ordo_group_of_disorders diseases +MONDO:0016906 rare diseases +MONDO:0016907 disease_grouping diseases +MONDO:0016907 gard_rare diseases +MONDO:0016907 ordo_group_of_disorders diseases +MONDO:0016907 rare diseases +MONDO:0016908 disease_grouping diseases +MONDO:0016908 gard_rare diseases +MONDO:0016908 ordo_group_of_disorders diseases +MONDO:0016908 rare diseases +MONDO:0016909 disease_grouping diseases +MONDO:0016909 gard_rare diseases +MONDO:0016909 ordo_group_of_disorders diseases +MONDO:0016909 rare diseases +MONDO:0016910 disease_grouping diseases +MONDO:0016910 gard_rare diseases +MONDO:0016910 ordo_group_of_disorders diseases +MONDO:0016910 rare diseases +MONDO:0016911 disease_grouping diseases +MONDO:0016911 gard_rare diseases +MONDO:0016911 ordo_group_of_disorders diseases +MONDO:0016911 rare diseases +MONDO:0016912 disease_grouping diseases +MONDO:0016912 gard_rare diseases +MONDO:0016912 ordo_group_of_disorders diseases +MONDO:0016912 rare diseases +MONDO:0016913 disease_grouping diseases +MONDO:0016913 gard_rare diseases +MONDO:0016913 ordo_group_of_disorders diseases +MONDO:0016913 rare diseases +MONDO:0016914 disease_grouping diseases +MONDO:0016914 gard_rare diseases +MONDO:0016914 ordo_group_of_disorders diseases +MONDO:0016914 rare diseases +MONDO:0016915 disease_grouping diseases +MONDO:0016915 gard_rare diseases +MONDO:0016915 ordo_group_of_disorders diseases +MONDO:0016915 rare diseases +MONDO:0016917 disease_grouping diseases +MONDO:0016917 gard_rare diseases +MONDO:0016917 ordo_group_of_disorders diseases +MONDO:0016917 rare diseases +MONDO:0016918 disease_grouping diseases +MONDO:0016918 gard_rare diseases +MONDO:0016918 ordo_group_of_disorders diseases +MONDO:0016918 rare diseases +MONDO:0016919 disease_grouping diseases +MONDO:0016919 gard_rare diseases +MONDO:0016919 ordo_group_of_disorders diseases +MONDO:0016919 rare diseases +MONDO:0016921 disease_grouping diseases +MONDO:0016921 gard_rare diseases +MONDO:0016921 ordo_group_of_disorders diseases +MONDO:0016921 rare diseases +MONDO:0016922 disease_grouping diseases +MONDO:0016922 gard_rare diseases +MONDO:0016922 ordo_group_of_disorders diseases +MONDO:0016922 rare diseases +MONDO:0016923 disease_grouping diseases +MONDO:0016923 gard_rare diseases +MONDO:0016923 ordo_group_of_disorders diseases +MONDO:0016923 rare diseases +MONDO:0016924 disease_grouping diseases +MONDO:0016924 gard_rare diseases +MONDO:0016924 ordo_group_of_disorders diseases +MONDO:0016924 rare diseases +MONDO:0016925 disease_grouping diseases +MONDO:0016925 gard_rare diseases +MONDO:0016925 ordo_group_of_disorders diseases +MONDO:0016925 rare diseases +MONDO:0016927 disease_grouping diseases +MONDO:0016927 gard_rare diseases +MONDO:0016927 ordo_group_of_disorders diseases +MONDO:0016927 rare diseases +MONDO:0016928 disease_grouping diseases +MONDO:0016928 gard_rare diseases +MONDO:0016928 ordo_group_of_disorders diseases +MONDO:0016928 rare diseases +MONDO:0016929 disease_grouping diseases +MONDO:0016929 gard_rare diseases +MONDO:0016929 nord_rare diseases +MONDO:0016929 ordo_group_of_disorders diseases +MONDO:0016929 rare diseases +MONDO:0016930 disease_grouping diseases +MONDO:0016930 gard_rare diseases +MONDO:0016930 nord_rare diseases +MONDO:0016930 ordo_group_of_disorders diseases +MONDO:0016930 rare diseases +MONDO:0016931 disease_grouping diseases +MONDO:0016931 gard_rare diseases +MONDO:0016931 ordo_group_of_disorders diseases +MONDO:0016931 rare diseases +MONDO:0016932 disease_grouping diseases +MONDO:0016932 gard_rare diseases +MONDO:0016932 ordo_group_of_disorders diseases +MONDO:0016932 rare diseases +MONDO:0016933 disease_grouping diseases +MONDO:0016933 gard_rare diseases +MONDO:0016933 ordo_group_of_disorders diseases +MONDO:0016933 rare diseases +MONDO:0016934 disease_grouping diseases +MONDO:0016934 gard_rare diseases +MONDO:0016934 ordo_group_of_disorders diseases +MONDO:0016934 rare diseases +MONDO:0016935 disease_grouping diseases +MONDO:0016935 gard_rare diseases +MONDO:0016935 ordo_group_of_disorders diseases +MONDO:0016935 rare diseases +MONDO:0016936 disease_grouping diseases +MONDO:0016936 gard_rare diseases +MONDO:0016936 ordo_group_of_disorders diseases +MONDO:0016936 rare diseases +MONDO:0016937 disease_grouping diseases +MONDO:0016937 gard_rare diseases +MONDO:0016937 ordo_group_of_disorders diseases +MONDO:0016937 rare diseases +MONDO:0016938 disease_grouping diseases +MONDO:0016938 gard_rare diseases +MONDO:0016938 ordo_group_of_disorders diseases +MONDO:0016938 rare diseases +MONDO:0016939 disease_grouping diseases +MONDO:0016939 gard_rare diseases +MONDO:0016939 ordo_group_of_disorders diseases +MONDO:0016939 rare diseases +MONDO:0016940 disease_grouping diseases +MONDO:0016940 gard_rare diseases +MONDO:0016940 ordo_group_of_disorders diseases +MONDO:0016940 rare diseases +MONDO:0016941 disease_grouping diseases +MONDO:0016941 gard_rare diseases +MONDO:0016941 ordo_group_of_disorders diseases +MONDO:0016941 rare diseases +MONDO:0016942 disease_grouping diseases +MONDO:0016942 gard_rare diseases +MONDO:0016942 ordo_group_of_disorders diseases +MONDO:0016942 rare diseases +MONDO:0016943 disease_grouping diseases +MONDO:0016943 gard_rare diseases +MONDO:0016943 ordo_group_of_disorders diseases +MONDO:0016943 rare diseases +MONDO:0016944 disease_grouping diseases +MONDO:0016944 gard_rare diseases +MONDO:0016944 ordo_group_of_disorders diseases +MONDO:0016944 rare diseases +MONDO:0016945 disease_grouping diseases +MONDO:0016945 gard_rare diseases +MONDO:0016945 ordo_group_of_disorders diseases +MONDO:0016945 rare diseases +MONDO:0016947 disease_grouping diseases +MONDO:0016947 gard_rare diseases +MONDO:0016947 ordo_group_of_disorders diseases +MONDO:0016947 rare diseases +MONDO:0016948 disease_grouping diseases +MONDO:0016948 gard_rare diseases +MONDO:0016948 ordo_group_of_disorders diseases +MONDO:0016948 rare diseases +MONDO:0016949 disease_grouping diseases +MONDO:0016949 gard_rare diseases +MONDO:0016949 ordo_group_of_disorders diseases +MONDO:0016949 rare diseases +MONDO:0016950 disease_grouping diseases +MONDO:0016950 gard_rare diseases +MONDO:0016950 ordo_group_of_disorders diseases +MONDO:0016950 rare diseases +MONDO:0016951 disease_grouping diseases +MONDO:0016951 gard_rare diseases +MONDO:0016951 ordo_group_of_disorders diseases +MONDO:0016951 rare diseases +MONDO:0016952 disease_grouping diseases +MONDO:0016952 gard_rare diseases +MONDO:0016952 ordo_group_of_disorders diseases +MONDO:0016952 rare diseases +MONDO:0016953 disease_grouping diseases +MONDO:0016953 gard_rare diseases +MONDO:0016953 ordo_group_of_disorders diseases +MONDO:0016953 rare diseases +MONDO:0016954 disease_grouping diseases +MONDO:0016954 gard_rare diseases +MONDO:0016954 ordo_group_of_disorders diseases +MONDO:0016954 rare diseases +MONDO:0016955 disease_grouping diseases +MONDO:0016955 gard_rare diseases +MONDO:0016955 ordo_group_of_disorders diseases +MONDO:0016955 rare diseases +MONDO:0016956 disease_grouping diseases +MONDO:0016956 gard_rare diseases +MONDO:0016956 ordo_group_of_disorders diseases +MONDO:0016956 rare diseases +MONDO:0016957 disease_grouping diseases +MONDO:0016957 gard_rare diseases +MONDO:0016957 ordo_group_of_disorders diseases +MONDO:0016957 rare diseases +MONDO:0016958 disease_grouping diseases +MONDO:0016958 gard_rare diseases +MONDO:0016958 ordo_group_of_disorders diseases +MONDO:0016958 rare diseases +MONDO:0016959 disease_grouping diseases +MONDO:0016959 gard_rare diseases +MONDO:0016959 ordo_group_of_disorders diseases +MONDO:0016959 rare diseases +MONDO:0016960 disease_grouping diseases +MONDO:0016960 gard_rare diseases +MONDO:0016960 ordo_group_of_disorders diseases +MONDO:0016960 rare diseases +MONDO:0016961 disease_grouping diseases +MONDO:0016961 gard_rare diseases +MONDO:0016961 ordo_group_of_disorders diseases +MONDO:0016961 rare diseases +MONDO:0016964 disease_grouping diseases +MONDO:0016964 gard_rare diseases +MONDO:0016964 ordo_group_of_disorders diseases +MONDO:0016964 rare diseases +MONDO:0016965 disease_grouping diseases +MONDO:0016965 gard_rare diseases +MONDO:0016965 ordo_group_of_disorders diseases +MONDO:0016965 otar diseases +MONDO:0016965 rare diseases +MONDO:0016966 disease_grouping diseases +MONDO:0016966 gard_rare diseases +MONDO:0016966 ordo_group_of_disorders diseases +MONDO:0016966 rare diseases +MONDO:0016967 disease_grouping diseases +MONDO:0016967 gard_rare diseases +MONDO:0016967 ordo_group_of_disorders diseases +MONDO:0016967 rare diseases +MONDO:0016968 disease_grouping diseases +MONDO:0016968 gard_rare diseases +MONDO:0016968 ordo_group_of_disorders diseases +MONDO:0016968 rare diseases +MONDO:0016969 disease_grouping diseases +MONDO:0016969 gard_rare diseases +MONDO:0016969 ordo_group_of_disorders diseases +MONDO:0016969 rare diseases +MONDO:0016970 disease_grouping diseases +MONDO:0016970 gard_rare diseases +MONDO:0016970 ordo_group_of_disorders diseases +MONDO:0016970 rare diseases +MONDO:0016971 disease_grouping diseases +MONDO:0016971 gard_rare diseases +MONDO:0016971 nord_rare diseases +MONDO:0016971 ordo_group_of_disorders diseases +MONDO:0016971 otar diseases +MONDO:0016971 rare diseases +MONDO:0016972 disease_grouping diseases +MONDO:0016972 gard_rare diseases +MONDO:0016972 ordo_group_of_disorders diseases +MONDO:0016972 rare diseases +MONDO:0016974 gard_rare diseases +MONDO:0016974 nord_rare diseases +MONDO:0016974 ordo_histopathological_subtype diseases +MONDO:0016974 ordo_subtype_of_a_disorder diseases +MONDO:0016974 otar diseases +MONDO:0016974 rare diseases +MONDO:0016975 gard_rare diseases +MONDO:0016975 nord_rare diseases +MONDO:0016975 ordo_histopathological_subtype diseases +MONDO:0016975 ordo_subtype_of_a_disorder diseases +MONDO:0016975 otar diseases +MONDO:0016975 rare diseases +MONDO:0016976 gard_rare diseases +MONDO:0016976 nord_rare diseases +MONDO:0016976 ordo_histopathological_subtype diseases +MONDO:0016976 ordo_subtype_of_a_disorder diseases +MONDO:0016976 rare diseases +MONDO:0016977 gard_rare diseases +MONDO:0016977 nord_rare diseases +MONDO:0016977 ordo_histopathological_subtype diseases +MONDO:0016977 ordo_subtype_of_a_disorder diseases +MONDO:0016977 rare diseases +MONDO:0016978 gard_rare diseases +MONDO:0016978 nord_rare diseases +MONDO:0016978 ordo_histopathological_subtype diseases +MONDO:0016978 ordo_subtype_of_a_disorder diseases +MONDO:0016978 rare diseases +MONDO:0016979 gard_rare diseases +MONDO:0016979 nord_rare diseases +MONDO:0016979 ordo_disorder diseases +MONDO:0016979 orphanet_rare diseases +MONDO:0016979 otar diseases +MONDO:0016979 rare diseases +MONDO:0016980 clingen diseases +MONDO:0016980 disease_grouping diseases +MONDO:0016980 otar diseases +MONDO:0016981 gard_rare diseases +MONDO:0016981 nord_rare diseases +MONDO:0016981 ordo_disorder diseases +MONDO:0016981 orphanet_rare diseases +MONDO:0016981 rare diseases +MONDO:0016982 gard_rare diseases +MONDO:0016982 nord_rare diseases +MONDO:0016982 ordo_disorder diseases +MONDO:0016982 orphanet_rare diseases +MONDO:0016982 otar diseases +MONDO:0016982 rare diseases +MONDO:0016983 gard_rare diseases +MONDO:0016983 nord_rare diseases +MONDO:0016983 otar diseases +MONDO:0016983 rare diseases +MONDO:0016984 gard_rare diseases +MONDO:0016984 nord_rare diseases +MONDO:0016984 ordo_disorder diseases +MONDO:0016984 orphanet_rare diseases +MONDO:0016984 otar diseases +MONDO:0016984 rare diseases +MONDO:0016985 gard_rare diseases +MONDO:0016985 nord_rare diseases +MONDO:0016985 ordo_disorder diseases +MONDO:0016985 orphanet_rare diseases +MONDO:0016985 otar diseases +MONDO:0016985 rare diseases +MONDO:0016986 gard_rare diseases +MONDO:0016986 nord_rare diseases +MONDO:0016986 ordo_disorder diseases +MONDO:0016986 orphanet_rare diseases +MONDO:0016986 rare diseases +MONDO:0016987 disease_grouping diseases +MONDO:0016987 gard_rare diseases +MONDO:0016987 nord_rare diseases +MONDO:0016987 ordo_group_of_disorders diseases +MONDO:0016987 otar diseases +MONDO:0016987 rare diseases +MONDO:0016988 gard_rare diseases +MONDO:0016988 nord_rare diseases +MONDO:0016988 ordo_disorder diseases +MONDO:0016988 orphanet_rare diseases +MONDO:0016988 otar diseases +MONDO:0016988 rare diseases +MONDO:0016989 gard_rare diseases +MONDO:0016989 nord_rare diseases +MONDO:0016989 ordo_disorder diseases +MONDO:0016989 orphanet_rare diseases +MONDO:0016989 rare diseases +MONDO:0016990 gard_rare diseases +MONDO:0016990 nord_rare diseases +MONDO:0016990 ordo_disorder diseases +MONDO:0016990 orphanet_rare diseases +MONDO:0016990 rare diseases +MONDO:0016991 gard_rare diseases +MONDO:0016991 nord_rare diseases +MONDO:0016991 ordo_disorder diseases +MONDO:0016991 orphanet_rare diseases +MONDO:0016991 rare diseases +MONDO:0016993 gard_rare diseases +MONDO:0016993 nord_rare diseases +MONDO:0016993 rare diseases +MONDO:0016994 gard_rare diseases +MONDO:0016994 nord_rare diseases +MONDO:0016994 ordo_disorder diseases +MONDO:0016994 ordo_malformation_syndrome diseases +MONDO:0016994 orphanet_rare diseases +MONDO:0016994 otar diseases +MONDO:0016994 rare diseases +MONDO:0016995 gard_rare diseases +MONDO:0016995 nord_rare diseases +MONDO:0016995 ordo_disorder diseases +MONDO:0016995 orphanet_rare diseases +MONDO:0016995 rare diseases +MONDO:0016996 gard_rare diseases +MONDO:0016996 nord_rare diseases +MONDO:0016996 ordo_disorder diseases +MONDO:0016996 orphanet_rare diseases +MONDO:0016996 otar diseases +MONDO:0016996 rare diseases +MONDO:0017003 disease_grouping diseases +MONDO:0017003 gard_rare diseases +MONDO:0017003 ordo_group_of_disorders diseases +MONDO:0017003 rare diseases +MONDO:0017004 disease_grouping diseases +MONDO:0017004 gard_rare diseases +MONDO:0017004 ordo_group_of_disorders diseases +MONDO:0017004 rare diseases +MONDO:0017007 disease_grouping diseases +MONDO:0017007 gard_rare diseases +MONDO:0017007 ordo_group_of_disorders diseases +MONDO:0017007 rare diseases +MONDO:0017008 disease_grouping diseases +MONDO:0017008 gard_rare diseases +MONDO:0017008 ordo_group_of_disorders diseases +MONDO:0017008 rare diseases +MONDO:0017009 disease_grouping diseases +MONDO:0017009 gard_rare diseases +MONDO:0017009 ordo_group_of_disorders diseases +MONDO:0017009 rare diseases +MONDO:0017010 disease_grouping diseases +MONDO:0017010 gard_rare diseases +MONDO:0017010 nord_rare diseases +MONDO:0017010 ordo_group_of_disorders diseases +MONDO:0017010 rare diseases +MONDO:0017012 disease_grouping diseases +MONDO:0017012 gard_rare diseases +MONDO:0017012 ordo_group_of_disorders diseases +MONDO:0017012 rare diseases +MONDO:0017013 gard_rare diseases +MONDO:0017013 nord_rare diseases +MONDO:0017013 ordo_disorder diseases +MONDO:0017013 ordo_malformation_syndrome diseases +MONDO:0017013 orphanet_rare diseases +MONDO:0017013 otar diseases +MONDO:0017013 rare diseases +MONDO:0017014 disease_grouping diseases +MONDO:0017014 ordo_group_of_disorders diseases +MONDO:0017014 otar diseases +MONDO:0017015 disease_grouping diseases +MONDO:0017015 gard_rare diseases +MONDO:0017015 ordo_group_of_disorders diseases +MONDO:0017015 otar diseases +MONDO:0017015 rare diseases +MONDO:0017018 gard_rare diseases +MONDO:0017018 nord_rare diseases +MONDO:0017018 ordo_disorder diseases +MONDO:0017018 orphanet_rare diseases +MONDO:0017018 rare diseases +MONDO:0017019 disease_grouping diseases +MONDO:0017019 inferred_rare diseases +MONDO:0017019 ordo_group_of_disorders diseases +MONDO:0017019 rare diseases +MONDO:0017025 disease_grouping diseases +MONDO:0017025 gard_rare diseases +MONDO:0017025 rare diseases +MONDO:0017026 disease_grouping diseases +MONDO:0017026 ordo_group_of_disorders diseases +MONDO:0017029 disease_grouping diseases +MONDO:0017029 gard_rare diseases +MONDO:0017029 rare diseases +MONDO:0017039 gard_rare diseases +MONDO:0017039 nord_rare diseases +MONDO:0017039 ordo_clinical_situation diseases +MONDO:0017039 ordo_disorder diseases +MONDO:0017039 orphanet_rare diseases +MONDO:0017039 rare diseases +MONDO:0017041 gard_rare diseases +MONDO:0017041 ordo_disorder diseases +MONDO:0017041 ordo_malformation_syndrome diseases +MONDO:0017041 orphanet_rare diseases +MONDO:0017041 rare diseases +MONDO:0017042 gard_rare diseases +MONDO:0017042 nord_rare diseases +MONDO:0017042 ordo_disorder diseases +MONDO:0017042 orphanet_rare diseases +MONDO:0017042 otar diseases +MONDO:0017042 rare diseases +MONDO:0017043 gard_rare diseases +MONDO:0017043 nord_rare diseases +MONDO:0017043 ordo_disorder diseases +MONDO:0017043 orphanet_rare diseases +MONDO:0017043 otar diseases +MONDO:0017043 rare diseases +MONDO:0017044 gard_rare diseases +MONDO:0017044 ordo_disorder diseases +MONDO:0017044 orphanet_rare diseases +MONDO:0017044 rare diseases +MONDO:0017045 gard_rare diseases +MONDO:0017045 ordo_malformation_syndrome diseases +MONDO:0017045 rare diseases +MONDO:0017046 gard_rare diseases +MONDO:0017046 nord_rare diseases +MONDO:0017046 rare diseases +MONDO:0017047 gard_rare diseases +MONDO:0017047 otar diseases +MONDO:0017047 rare diseases +MONDO:0017048 gard_rare diseases +MONDO:0017048 nord_rare diseases +MONDO:0017048 ordo_disorder diseases +MONDO:0017048 orphanet_rare diseases +MONDO:0017048 rare diseases +MONDO:0017050 gard_rare diseases +MONDO:0017050 nord_rare diseases +MONDO:0017050 ordo_disorder diseases +MONDO:0017050 orphanet_rare diseases +MONDO:0017050 otar diseases +MONDO:0017050 rare diseases +MONDO:0017051 gard_rare diseases +MONDO:0017051 nord_rare diseases +MONDO:0017051 ordo_subtype_of_a_disorder diseases +MONDO:0017051 otar diseases +MONDO:0017051 rare diseases +MONDO:0017052 gard_rare diseases +MONDO:0017052 nord_rare diseases +MONDO:0017052 ordo_subtype_of_a_disorder diseases +MONDO:0017052 otar diseases +MONDO:0017052 rare diseases +MONDO:0017053 gard_rare diseases +MONDO:0017053 nord_rare diseases +MONDO:0017053 ordo_subtype_of_a_disorder diseases +MONDO:0017053 otar diseases +MONDO:0017053 rare diseases +MONDO:0017054 gard_rare diseases +MONDO:0017054 nord_rare diseases +MONDO:0017054 ordo_subtype_of_a_disorder diseases +MONDO:0017054 otar diseases +MONDO:0017054 rare diseases +MONDO:0017055 gard_rare diseases +MONDO:0017055 nord_rare diseases +MONDO:0017055 ordo_disorder diseases +MONDO:0017055 orphanet_rare diseases +MONDO:0017055 rare diseases +MONDO:0017056 gard_rare diseases +MONDO:0017056 nord_rare diseases +MONDO:0017056 ordo_subtype_of_a_disorder diseases +MONDO:0017056 rare diseases +MONDO:0017058 disease_grouping diseases +MONDO:0017058 gard_rare diseases +MONDO:0017058 ordo_group_of_disorders diseases +MONDO:0017058 rare diseases +MONDO:0017060 gard_rare diseases +MONDO:0017060 nord_rare diseases +MONDO:0017060 ordo_subtype_of_a_disorder diseases +MONDO:0017060 rare diseases +MONDO:0017061 gard_rare diseases +MONDO:0017061 nord_rare diseases +MONDO:0017061 ordo_subtype_of_a_disorder diseases +MONDO:0017061 rare diseases +MONDO:0017062 gard_rare diseases +MONDO:0017062 nord_rare diseases +MONDO:0017062 ordo_group_of_disorders diseases +MONDO:0017062 ordo_morphological_anomaly diseases +MONDO:0017062 otar diseases +MONDO:0017062 rare diseases +MONDO:0017063 gard_rare diseases +MONDO:0017063 nord_rare diseases +MONDO:0017063 rare diseases +MONDO:0017064 gard_rare diseases +MONDO:0017064 nord_rare diseases +MONDO:0017064 rare diseases +MONDO:0017065 gard_rare diseases +MONDO:0017065 nord_rare diseases +MONDO:0017065 rare diseases +MONDO:0017066 gard_rare diseases +MONDO:0017066 nord_rare diseases +MONDO:0017066 rare diseases +MONDO:0017067 gard_rare diseases +MONDO:0017067 nord_rare diseases +MONDO:0017067 rare diseases +MONDO:0017068 gard_rare diseases +MONDO:0017068 nord_rare diseases +MONDO:0017068 rare diseases +MONDO:0017069 disease_grouping diseases +MONDO:0017069 gard_rare diseases +MONDO:0017069 nord_rare diseases +MONDO:0017069 ordo_group_of_disorders diseases +MONDO:0017069 otar diseases +MONDO:0017069 rare diseases +MONDO:0017070 gard_rare diseases +MONDO:0017070 nord_rare diseases +MONDO:0017070 rare diseases +MONDO:0017071 gard_rare diseases +MONDO:0017071 nord_rare diseases +MONDO:0017071 rare diseases +MONDO:0017072 gard_rare diseases +MONDO:0017072 nord_rare diseases +MONDO:0017072 rare diseases +MONDO:0017073 gard_rare diseases +MONDO:0017073 nord_rare diseases +MONDO:0017073 rare diseases +MONDO:0017074 gard_rare diseases +MONDO:0017074 nord_rare diseases +MONDO:0017074 rare diseases +MONDO:0017075 gard_rare diseases +MONDO:0017075 nord_rare diseases +MONDO:0017075 rare diseases +MONDO:0017076 gard_rare diseases +MONDO:0017076 nord_rare diseases +MONDO:0017076 ordo_disorder diseases +MONDO:0017076 ordo_morphological_anomaly diseases +MONDO:0017076 orphanet_rare diseases +MONDO:0017076 otar diseases +MONDO:0017076 rare diseases +MONDO:0017077 gard_rare diseases +MONDO:0017077 nord_rare diseases +MONDO:0017077 ordo_group_of_disorders diseases +MONDO:0017077 ordo_morphological_anomaly diseases +MONDO:0017077 rare diseases +MONDO:0017078 disease_grouping diseases +MONDO:0017078 gard_rare diseases +MONDO:0017078 ordo_group_of_disorders diseases +MONDO:0017078 otar diseases +MONDO:0017078 rare diseases +MONDO:0017079 gard_rare diseases +MONDO:0017079 nord_rare diseases +MONDO:0017079 ordo_disorder diseases +MONDO:0017079 ordo_morphological_anomaly diseases +MONDO:0017079 orphanet_rare diseases +MONDO:0017079 otar diseases +MONDO:0017079 rare diseases +MONDO:0017080 gard_rare diseases +MONDO:0017080 nord_rare diseases +MONDO:0017080 ordo_subtype_of_a_disorder diseases +MONDO:0017080 otar diseases +MONDO:0017080 rare diseases +MONDO:0017081 gard_rare diseases +MONDO:0017081 nord_rare diseases +MONDO:0017081 ordo_subtype_of_a_disorder diseases +MONDO:0017081 rare diseases +MONDO:0017082 gard_rare diseases +MONDO:0017082 nord_rare diseases +MONDO:0017082 ordo_subtype_of_a_disorder diseases +MONDO:0017082 rare diseases +MONDO:0017084 gard_rare diseases +MONDO:0017084 nord_rare diseases +MONDO:0017084 ordo_morphological_anomaly diseases +MONDO:0017084 rare diseases +MONDO:0017086 gard_rare diseases +MONDO:0017086 nord_rare diseases +MONDO:0017086 ordo_disorder diseases +MONDO:0017086 ordo_morphological_anomaly diseases +MONDO:0017086 orphanet_rare diseases +MONDO:0017086 otar diseases +MONDO:0017086 rare diseases +MONDO:0017087 gard_rare diseases +MONDO:0017087 nord_rare diseases +MONDO:0017087 ordo_disorder diseases +MONDO:0017087 ordo_morphological_anomaly diseases +MONDO:0017087 orphanet_rare diseases +MONDO:0017087 otar diseases +MONDO:0017087 rare diseases +MONDO:0017088 gard_rare diseases +MONDO:0017088 nord_rare diseases +MONDO:0017088 ordo_disorder diseases +MONDO:0017088 ordo_morphological_anomaly diseases +MONDO:0017088 orphanet_rare diseases +MONDO:0017088 rare diseases +MONDO:0017089 gard_rare diseases +MONDO:0017089 nord_rare diseases +MONDO:0017089 ordo_subtype_of_a_disorder diseases +MONDO:0017089 otar diseases +MONDO:0017089 rare diseases +MONDO:0017091 gard_rare diseases +MONDO:0017091 nord_rare diseases +MONDO:0017091 ordo_disorder diseases +MONDO:0017091 ordo_morphological_anomaly diseases +MONDO:0017091 orphanet_rare diseases +MONDO:0017091 otar diseases +MONDO:0017091 rare diseases +MONDO:0017092 gard_rare diseases +MONDO:0017092 nord_rare diseases +MONDO:0017092 ordo_disorder diseases +MONDO:0017092 ordo_morphological_anomaly diseases +MONDO:0017092 orphanet_rare diseases +MONDO:0017092 otar diseases +MONDO:0017092 rare diseases +MONDO:0017093 gard_rare diseases +MONDO:0017093 nord_rare diseases +MONDO:0017093 ordo_subtype_of_a_disorder diseases +MONDO:0017093 otar diseases +MONDO:0017093 rare diseases +MONDO:0017094 disease_grouping diseases +MONDO:0017094 gard_rare diseases +MONDO:0017094 nord_rare diseases +MONDO:0017094 ordo_group_of_disorders diseases +MONDO:0017094 otar diseases +MONDO:0017094 rare diseases +MONDO:0017095 gard_rare diseases +MONDO:0017095 nord_rare diseases +MONDO:0017095 ordo_subtype_of_a_disorder diseases +MONDO:0017095 otar diseases +MONDO:0017095 rare diseases +MONDO:0017096 gard_rare diseases +MONDO:0017096 nord_rare diseases +MONDO:0017096 ordo_histopathological_subtype diseases +MONDO:0017096 ordo_subtype_of_a_disorder diseases +MONDO:0017096 otar diseases +MONDO:0017096 rare diseases +MONDO:0017097 gard_rare diseases +MONDO:0017097 nord_rare diseases +MONDO:0017097 ordo_histopathological_subtype diseases +MONDO:0017097 ordo_subtype_of_a_disorder diseases +MONDO:0017097 rare diseases +MONDO:0017098 gard_rare diseases +MONDO:0017098 nord_rare diseases +MONDO:0017098 ordo_histopathological_subtype diseases +MONDO:0017098 ordo_subtype_of_a_disorder diseases +MONDO:0017098 rare diseases +MONDO:0017100 gard_rare diseases +MONDO:0017100 ordo_disorder diseases +MONDO:0017100 orphanet_rare diseases +MONDO:0017100 otar diseases +MONDO:0017100 rare diseases +MONDO:0017101 gard_rare diseases +MONDO:0017101 nord_rare diseases +MONDO:0017101 ordo_histopathological_subtype diseases +MONDO:0017101 ordo_subtype_of_a_disorder diseases +MONDO:0017101 otar diseases +MONDO:0017101 rare diseases +MONDO:0017102 gard_rare diseases +MONDO:0017102 nord_rare diseases +MONDO:0017102 ordo_histopathological_subtype diseases +MONDO:0017102 ordo_subtype_of_a_disorder diseases +MONDO:0017102 otar diseases +MONDO:0017102 rare diseases +MONDO:0017103 disease_grouping diseases +MONDO:0017103 gard_rare diseases +MONDO:0017103 ordo_group_of_disorders diseases +MONDO:0017103 rare diseases +MONDO:0017105 gard_rare diseases +MONDO:0017105 nord_rare diseases +MONDO:0017105 ordo_disorder diseases +MONDO:0017105 ordo_morphological_anomaly diseases +MONDO:0017105 orphanet_rare diseases +MONDO:0017105 rare diseases +MONDO:0017106 gard_rare diseases +MONDO:0017106 nord_rare diseases +MONDO:0017106 ordo_morphological_anomaly diseases +MONDO:0017106 rare diseases +MONDO:0017107 gard_rare diseases +MONDO:0017107 nord_rare diseases +MONDO:0017107 ordo_disorder diseases +MONDO:0017107 ordo_morphological_anomaly diseases +MONDO:0017107 orphanet_rare diseases +MONDO:0017107 rare diseases +MONDO:0017108 gard_rare diseases +MONDO:0017108 nord_rare diseases +MONDO:0017108 ordo_subtype_of_a_disorder diseases +MONDO:0017108 rare diseases +MONDO:0017109 gard_rare diseases +MONDO:0017109 nord_rare diseases +MONDO:0017109 ordo_subtype_of_a_disorder diseases +MONDO:0017109 rare diseases +MONDO:0017110 gard_rare diseases +MONDO:0017110 nord_rare diseases +MONDO:0017110 ordo_subtype_of_a_disorder diseases +MONDO:0017110 rare diseases +MONDO:0017111 gard_rare diseases +MONDO:0017111 nord_rare diseases +MONDO:0017111 ordo_subtype_of_a_disorder diseases +MONDO:0017111 otar diseases +MONDO:0017111 rare diseases +MONDO:0017112 gard_rare diseases +MONDO:0017112 nord_rare diseases +MONDO:0017112 ordo_disorder diseases +MONDO:0017112 ordo_morphological_anomaly diseases +MONDO:0017112 orphanet_rare diseases +MONDO:0017112 rare diseases +MONDO:0017113 gard_rare diseases +MONDO:0017113 nord_rare diseases +MONDO:0017113 ordo_disorder diseases +MONDO:0017113 ordo_morphological_anomaly diseases +MONDO:0017113 orphanet_rare diseases +MONDO:0017113 rare diseases +MONDO:0017116 gard_rare diseases +MONDO:0017116 nord_rare diseases +MONDO:0017116 ordo_subtype_of_a_disorder diseases +MONDO:0017116 otar diseases +MONDO:0017116 rare diseases +MONDO:0017117 gard_rare diseases +MONDO:0017117 nord_rare diseases +MONDO:0017117 ordo_subtype_of_a_disorder diseases +MONDO:0017117 otar diseases +MONDO:0017117 rare diseases +MONDO:0017123 gard_rare diseases +MONDO:0017123 nord_rare diseases +MONDO:0017123 ordo_disorder diseases +MONDO:0017123 ordo_malformation_syndrome diseases +MONDO:0017123 orphanet_rare diseases +MONDO:0017123 otar diseases +MONDO:0017123 rare diseases +MONDO:0017124 gard_rare diseases +MONDO:0017124 nord_rare diseases +MONDO:0017124 ordo_disorder diseases +MONDO:0017124 orphanet_rare diseases +MONDO:0017124 otar diseases +MONDO:0017124 rare diseases +MONDO:0017126 ordo_malformation_syndrome diseases +MONDO:0017134 gard_rare diseases +MONDO:0017134 nord_rare diseases +MONDO:0017134 ordo_disorder diseases +MONDO:0017134 ordo_malformation_syndrome diseases +MONDO:0017134 orphanet_rare diseases +MONDO:0017134 otar diseases +MONDO:0017134 rare diseases +MONDO:0017135 gard_rare diseases +MONDO:0017135 nord_rare diseases +MONDO:0017135 ordo_disorder diseases +MONDO:0017135 ordo_malformation_syndrome diseases +MONDO:0017135 orphanet_rare diseases +MONDO:0017135 otar diseases +MONDO:0017135 rare diseases +MONDO:0017136 gard_rare diseases +MONDO:0017136 nord_rare diseases +MONDO:0017136 ordo_disorder diseases +MONDO:0017136 ordo_malformation_syndrome diseases +MONDO:0017136 orphanet_rare diseases +MONDO:0017136 otar diseases +MONDO:0017136 rare diseases +MONDO:0017137 gard_rare diseases +MONDO:0017137 nord_rare diseases +MONDO:0017137 ordo_disorder diseases +MONDO:0017137 orphanet_rare diseases +MONDO:0017137 otar diseases +MONDO:0017137 rare diseases +MONDO:0017138 gard_rare diseases +MONDO:0017138 nord_rare diseases +MONDO:0017138 ordo_disorder diseases +MONDO:0017138 ordo_inheritance_inconsistent diseases +MONDO:0017138 ordo_malformation_syndrome diseases +MONDO:0017138 orphanet_rare diseases +MONDO:0017138 otar diseases +MONDO:0017138 rare diseases +MONDO:0017139 disease_grouping diseases +MONDO:0017139 gard_rare diseases +MONDO:0017139 nord_rare diseases +MONDO:0017139 ordo_group_of_disorders diseases +MONDO:0017139 rare diseases +MONDO:0017140 clingen diseases +MONDO:0017140 gard_rare diseases +MONDO:0017140 nord_rare diseases +MONDO:0017140 ordo_disorder diseases +MONDO:0017140 ordo_malformation_syndrome diseases +MONDO:0017140 orphanet_rare diseases +MONDO:0017140 otar diseases +MONDO:0017140 rare diseases +MONDO:0017145 disease_grouping diseases +MONDO:0017145 gard_rare diseases +MONDO:0017145 ordo_group_of_disorders diseases +MONDO:0017145 rare diseases +MONDO:0017147 gard_rare diseases +MONDO:0017147 nord_rare diseases +MONDO:0017147 ordo_etiological_subtype diseases +MONDO:0017147 ordo_subtype_of_a_disorder diseases +MONDO:0017147 otar diseases +MONDO:0017147 rare diseases +MONDO:0017148 gard_rare diseases +MONDO:0017148 nord_rare diseases +MONDO:0017148 ordo_etiological_subtype diseases +MONDO:0017148 ordo_subtype_of_a_disorder diseases +MONDO:0017148 otar diseases +MONDO:0017148 rare diseases +MONDO:0017149 disease_grouping diseases +MONDO:0017149 gard_rare diseases +MONDO:0017149 nord_rare diseases +MONDO:0017149 ordo_group_of_disorders diseases +MONDO:0017149 otar diseases +MONDO:0017149 rare diseases +MONDO:0017157 disease_grouping diseases +MONDO:0017157 gard_rare diseases +MONDO:0017157 ordo_group_of_disorders diseases +MONDO:0017157 rare diseases +MONDO:0017160 gard_rare diseases +MONDO:0017160 nord_rare diseases +MONDO:0017160 ordo_disorder diseases +MONDO:0017160 orphanet_rare diseases +MONDO:0017160 otar diseases +MONDO:0017160 rare diseases +MONDO:0017161 gard_rare diseases +MONDO:0017161 nord_rare diseases +MONDO:0017161 ordo_disorder diseases +MONDO:0017161 orphanet_rare diseases +MONDO:0017161 otar diseases +MONDO:0017161 rare diseases +MONDO:0017162 gard_rare diseases +MONDO:0017162 nord_rare diseases +MONDO:0017162 ordo_disorder diseases +MONDO:0017162 ordo_malformation_syndrome diseases +MONDO:0017162 orphanet_rare diseases +MONDO:0017162 rare diseases +MONDO:0017164 gard_rare diseases +MONDO:0017164 nord_rare diseases +MONDO:0017164 ordo_disorder diseases +MONDO:0017164 orphanet_rare diseases +MONDO:0017164 rare diseases +MONDO:0017165 gard_rare diseases +MONDO:0017165 nord_rare diseases +MONDO:0017165 ordo_disorder diseases +MONDO:0017165 orphanet_rare diseases +MONDO:0017165 rare diseases +MONDO:0017167 gard_rare diseases +MONDO:0017167 nord_rare diseases +MONDO:0017167 ordo_disorder diseases +MONDO:0017167 orphanet_rare diseases +MONDO:0017167 otar diseases +MONDO:0017167 rare diseases +MONDO:0017168 nord_rare diseases +MONDO:0017168 ordo_disorder diseases +MONDO:0017168 orphanet_rare diseases +MONDO:0017168 rare diseases +MONDO:0017169 disease_grouping diseases +MONDO:0017169 gard_rare diseases +MONDO:0017169 nord_rare diseases +MONDO:0017169 ordo_group_of_disorders diseases +MONDO:0017169 otar diseases +MONDO:0017169 rare diseases +MONDO:0017170 gard_rare diseases +MONDO:0017170 nord_rare diseases +MONDO:0017170 ordo_disorder diseases +MONDO:0017170 orphanet_rare diseases +MONDO:0017170 rare diseases +MONDO:0017171 gard_rare diseases +MONDO:0017171 nord_rare diseases +MONDO:0017171 ordo_subtype_of_a_disorder diseases +MONDO:0017171 otar diseases +MONDO:0017171 rare diseases +MONDO:0017172 gard_rare diseases +MONDO:0017172 nord_rare diseases +MONDO:0017172 ordo_subtype_of_a_disorder diseases +MONDO:0017172 otar diseases +MONDO:0017172 rare diseases +MONDO:0017174 gard_rare diseases +MONDO:0017174 nord_rare diseases +MONDO:0017174 ordo_subtype_of_a_disorder diseases +MONDO:0017174 otar diseases +MONDO:0017174 rare diseases +MONDO:0017175 gard_rare diseases +MONDO:0017175 nord_rare diseases +MONDO:0017175 ordo_subtype_of_a_disorder diseases +MONDO:0017175 otar diseases +MONDO:0017175 rare diseases +MONDO:0017176 gard_rare diseases +MONDO:0017176 nord_rare diseases +MONDO:0017176 ordo_subtype_of_a_disorder diseases +MONDO:0017176 otar diseases +MONDO:0017176 rare diseases +MONDO:0017177 gard_rare diseases +MONDO:0017177 nord_rare diseases +MONDO:0017177 ordo_disorder diseases +MONDO:0017177 ordo_malformation_syndrome diseases +MONDO:0017177 orphanet_rare diseases +MONDO:0017177 otar diseases +MONDO:0017177 rare diseases +MONDO:0017178 gard_rare diseases +MONDO:0017178 nord_rare diseases +MONDO:0017178 ordo_disorder diseases +MONDO:0017178 orphanet_rare diseases +MONDO:0017178 otar diseases +MONDO:0017178 rare diseases +MONDO:0017179 gard_rare diseases +MONDO:0017179 rare diseases +MONDO:0017180 gard_rare diseases +MONDO:0017180 nord_rare diseases +MONDO:0017180 ordo_disorder diseases +MONDO:0017180 ordo_malformation_syndrome diseases +MONDO:0017180 orphanet_rare diseases +MONDO:0017180 otar diseases +MONDO:0017180 rare diseases +MONDO:0017181 gard_rare diseases +MONDO:0017181 nord_rare diseases +MONDO:0017181 ordo_disorder diseases +MONDO:0017181 orphanet_rare diseases +MONDO:0017181 rare diseases +MONDO:0017182 disease_grouping diseases +MONDO:0017182 gard_rare diseases +MONDO:0017182 ordo_group_of_disorders diseases +MONDO:0017182 otar diseases +MONDO:0017182 rare diseases +MONDO:0017183 gard_rare diseases +MONDO:0017183 nord_rare diseases +MONDO:0017183 ordo_disorder diseases +MONDO:0017183 orphanet_rare diseases +MONDO:0017183 otar diseases +MONDO:0017183 rare diseases +MONDO:0017184 gard_rare diseases +MONDO:0017184 nord_rare diseases +MONDO:0017184 ordo_disorder diseases +MONDO:0017184 orphanet_rare diseases +MONDO:0017184 otar diseases +MONDO:0017184 rare diseases +MONDO:0017185 gard_rare diseases +MONDO:0017185 nord_rare diseases +MONDO:0017185 ordo_disorder diseases +MONDO:0017185 orphanet_rare diseases +MONDO:0017185 otar diseases +MONDO:0017185 rare diseases +MONDO:0017186 disease_grouping diseases +MONDO:0017186 gard_rare diseases +MONDO:0017186 nord_rare diseases +MONDO:0017186 ordo_group_of_disorders diseases +MONDO:0017186 rare diseases +MONDO:0017187 gard_rare diseases +MONDO:0017187 nord_rare diseases +MONDO:0017187 ordo_disorder diseases +MONDO:0017187 orphanet_rare diseases +MONDO:0017187 otar diseases +MONDO:0017187 rare diseases +MONDO:0017188 gard_rare diseases +MONDO:0017188 nord_rare diseases +MONDO:0017188 ordo_disorder diseases +MONDO:0017188 orphanet_rare diseases +MONDO:0017188 otar diseases +MONDO:0017188 rare diseases +MONDO:0017189 gard_rare diseases +MONDO:0017189 nord_rare diseases +MONDO:0017189 ordo_disorder diseases +MONDO:0017189 orphanet_rare diseases +MONDO:0017189 otar diseases +MONDO:0017189 rare diseases +MONDO:0017190 gard_rare diseases +MONDO:0017190 nord_rare diseases +MONDO:0017190 ordo_disorder diseases +MONDO:0017190 orphanet_rare diseases +MONDO:0017190 rare diseases +MONDO:0017191 gard_rare diseases +MONDO:0017191 nord_rare diseases +MONDO:0017191 rare diseases +MONDO:0017192 gard_rare diseases +MONDO:0017192 rare diseases +MONDO:0017193 gard_rare diseases +MONDO:0017193 nord_rare diseases +MONDO:0017193 ordo_disorder diseases +MONDO:0017193 ordo_malformation_syndrome diseases +MONDO:0017193 orphanet_rare diseases +MONDO:0017193 otar diseases +MONDO:0017193 rare diseases +MONDO:0017194 gard_rare diseases +MONDO:0017194 nord_rare diseases +MONDO:0017194 ordo_disorder diseases +MONDO:0017194 ordo_malformation_syndrome diseases +MONDO:0017194 orphanet_rare diseases +MONDO:0017194 otar diseases +MONDO:0017194 rare diseases +MONDO:0017195 gard_rare diseases +MONDO:0017195 nord_rare diseases +MONDO:0017195 ordo_disorder diseases +MONDO:0017195 ordo_malformation_syndrome diseases +MONDO:0017195 orphanet_rare diseases +MONDO:0017195 otar diseases +MONDO:0017195 rare diseases +MONDO:0017196 gard_rare diseases +MONDO:0017196 nord_rare diseases +MONDO:0017196 ordo_disorder diseases +MONDO:0017196 ordo_malformation_syndrome diseases +MONDO:0017196 orphanet_rare diseases +MONDO:0017196 otar diseases +MONDO:0017196 rare diseases +MONDO:0017197 gard_rare diseases +MONDO:0017197 ordo_disorder diseases +MONDO:0017197 ordo_malformation_syndrome diseases +MONDO:0017197 orphanet_rare diseases +MONDO:0017197 otar diseases +MONDO:0017197 rare diseases +MONDO:0017198 disease_grouping diseases +MONDO:0017198 gard_rare diseases +MONDO:0017198 nord_rare diseases +MONDO:0017198 ordo_group_of_disorders diseases +MONDO:0017198 otar diseases +MONDO:0017198 rare diseases +MONDO:0017199 gard_rare diseases +MONDO:0017199 ordo_disorder diseases +MONDO:0017199 ordo_malformation_syndrome diseases +MONDO:0017199 orphanet_rare diseases +MONDO:0017199 otar diseases +MONDO:0017199 rare diseases +MONDO:0017200 gard_rare diseases +MONDO:0017200 nord_rare diseases +MONDO:0017200 ordo_disorder diseases +MONDO:0017200 orphanet_rare diseases +MONDO:0017200 rare diseases +MONDO:0017201 gard_rare diseases +MONDO:0017201 nord_rare diseases +MONDO:0017201 ordo_clinical_syndrome diseases +MONDO:0017201 ordo_disorder diseases +MONDO:0017201 orphanet_rare diseases +MONDO:0017201 rare diseases +MONDO:0017202 gard_rare diseases +MONDO:0017202 nord_rare diseases +MONDO:0017202 ordo_subtype_of_a_disorder diseases +MONDO:0017202 rare diseases +MONDO:0017203 gard_rare diseases +MONDO:0017203 nord_rare diseases +MONDO:0017203 ordo_subtype_of_a_disorder diseases +MONDO:0017203 rare diseases +MONDO:0017204 nord_rare diseases +MONDO:0017204 ordo_disorder diseases +MONDO:0017204 orphanet_rare diseases +MONDO:0017204 rare diseases +MONDO:0017205 gard_rare diseases +MONDO:0017205 nord_rare diseases +MONDO:0017205 ordo_disorder diseases +MONDO:0017205 orphanet_rare diseases +MONDO:0017205 rare diseases +MONDO:0017207 disease_grouping diseases +MONDO:0017207 gard_rare diseases +MONDO:0017207 ordo_group_of_disorders diseases +MONDO:0017207 rare diseases +MONDO:0017209 gard_rare diseases +MONDO:0017209 nord_rare diseases +MONDO:0017209 ordo_disorder diseases +MONDO:0017209 orphanet_rare diseases +MONDO:0017209 rare diseases +MONDO:0017210 gard_rare diseases +MONDO:0017210 nord_rare diseases +MONDO:0017210 ordo_disorder diseases +MONDO:0017210 orphanet_rare diseases +MONDO:0017210 rare diseases +MONDO:0017211 gard_rare diseases +MONDO:0017211 nord_rare diseases +MONDO:0017211 ordo_disorder diseases +MONDO:0017211 orphanet_rare diseases +MONDO:0017211 rare diseases +MONDO:0017212 gard_rare diseases +MONDO:0017212 nord_rare diseases +MONDO:0017212 ordo_disorder diseases +MONDO:0017212 orphanet_rare diseases +MONDO:0017212 rare diseases +MONDO:0017213 gard_rare diseases +MONDO:0017213 nord_rare diseases +MONDO:0017213 ordo_clinical_syndrome diseases +MONDO:0017213 ordo_disorder diseases +MONDO:0017213 orphanet_rare diseases +MONDO:0017213 rare diseases +MONDO:0017214 gard_rare diseases +MONDO:0017214 nord_rare diseases +MONDO:0017214 ordo_disorder diseases +MONDO:0017214 orphanet_rare diseases +MONDO:0017214 otar diseases +MONDO:0017214 rare diseases +MONDO:0017215 gard_rare diseases +MONDO:0017215 nord_rare diseases +MONDO:0017215 ordo_disorder diseases +MONDO:0017215 orphanet_rare diseases +MONDO:0017215 rare diseases +MONDO:0017216 gard_rare diseases +MONDO:0017216 nord_rare diseases +MONDO:0017216 ordo_subtype_of_a_disorder diseases +MONDO:0017216 rare diseases +MONDO:0017217 gard_rare diseases +MONDO:0017217 nord_rare diseases +MONDO:0017217 ordo_subtype_of_a_disorder diseases +MONDO:0017217 rare diseases +MONDO:0017219 gard_rare diseases +MONDO:0017219 nord_rare diseases +MONDO:0017219 ordo_disorder diseases +MONDO:0017219 ordo_malformation_syndrome diseases +MONDO:0017219 orphanet_rare diseases +MONDO:0017219 otar diseases +MONDO:0017219 rare diseases +MONDO:0017220 gard_rare diseases +MONDO:0017220 nord_rare diseases +MONDO:0017220 ordo_subtype_of_a_disorder diseases +MONDO:0017220 rare diseases +MONDO:0017221 gard_rare diseases +MONDO:0017221 nord_rare diseases +MONDO:0017221 ordo_subtype_of_a_disorder diseases +MONDO:0017221 otar diseases +MONDO:0017221 rare diseases +MONDO:0017222 gard_rare diseases +MONDO:0017222 nord_rare diseases +MONDO:0017222 ordo_subtype_of_a_disorder diseases +MONDO:0017222 otar diseases +MONDO:0017222 rare diseases +MONDO:0017223 gard_rare diseases +MONDO:0017223 nord_rare diseases +MONDO:0017223 ordo_subtype_of_a_disorder diseases +MONDO:0017223 otar diseases +MONDO:0017223 rare diseases +MONDO:0017224 gard_rare diseases +MONDO:0017224 nord_rare diseases +MONDO:0017224 ordo_subtype_of_a_disorder diseases +MONDO:0017224 otar diseases +MONDO:0017224 rare diseases +MONDO:0017225 gard_rare diseases +MONDO:0017225 nord_rare diseases +MONDO:0017225 ordo_subtype_of_a_disorder diseases +MONDO:0017225 otar diseases +MONDO:0017225 rare diseases +MONDO:0017226 gard_rare diseases +MONDO:0017226 nord_rare diseases +MONDO:0017226 ordo_disorder diseases +MONDO:0017226 orphanet_rare diseases +MONDO:0017226 otar diseases +MONDO:0017226 rare diseases +MONDO:0017227 gard_rare diseases +MONDO:0017227 nord_rare diseases +MONDO:0017227 ordo_subtype_of_a_disorder diseases +MONDO:0017227 otar diseases +MONDO:0017227 rare diseases +MONDO:0017228 gard_rare diseases +MONDO:0017228 nord_rare diseases +MONDO:0017228 ordo_disorder diseases +MONDO:0017228 orphanet_rare diseases +MONDO:0017228 rare diseases +MONDO:0017229 gard_rare diseases +MONDO:0017229 nord_rare diseases +MONDO:0017229 ordo_disorder diseases +MONDO:0017229 ordo_malformation_syndrome diseases +MONDO:0017229 orphanet_rare diseases +MONDO:0017229 rare diseases +MONDO:0017230 gard_rare diseases +MONDO:0017230 nord_rare diseases +MONDO:0017230 ordo_disorder diseases +MONDO:0017230 orphanet_rare diseases +MONDO:0017230 otar diseases +MONDO:0017230 rare diseases +MONDO:0017231 gard_rare diseases +MONDO:0017231 nord_rare diseases +MONDO:0017231 ordo_disorder diseases +MONDO:0017231 orphanet_rare diseases +MONDO:0017231 rare diseases +MONDO:0017232 gard_rare diseases +MONDO:0017232 nord_rare diseases +MONDO:0017232 ordo_disorder diseases +MONDO:0017232 orphanet_rare diseases +MONDO:0017232 otar diseases +MONDO:0017232 rare diseases +MONDO:0017233 gard_rare diseases +MONDO:0017233 nord_rare diseases +MONDO:0017233 ordo_disorder diseases +MONDO:0017233 orphanet_rare diseases +MONDO:0017233 rare diseases +MONDO:0017235 gard_rare diseases +MONDO:0017235 nord_rare diseases +MONDO:0017235 ordo_disorder diseases +MONDO:0017235 ordo_malformation_syndrome diseases +MONDO:0017235 orphanet_rare diseases +MONDO:0017235 rare diseases +MONDO:0017236 gard_rare diseases +MONDO:0017236 otar diseases +MONDO:0017236 rare diseases +MONDO:0017237 gard_rare diseases +MONDO:0017237 nord_rare diseases +MONDO:0017237 ordo_disorder diseases +MONDO:0017237 orphanet_rare diseases +MONDO:0017237 otar diseases +MONDO:0017237 rare diseases +MONDO:0017238 gard_rare diseases +MONDO:0017238 nord_rare diseases +MONDO:0017238 ordo_disorder diseases +MONDO:0017238 orphanet_rare diseases +MONDO:0017238 otar diseases +MONDO:0017238 rare diseases +MONDO:0017239 gard_rare diseases +MONDO:0017239 nord_rare diseases +MONDO:0017239 ordo_disorder diseases +MONDO:0017239 orphanet_rare diseases +MONDO:0017239 otar diseases +MONDO:0017239 rare diseases +MONDO:0017242 gard_rare diseases +MONDO:0017242 ordo_disorder diseases +MONDO:0017242 orphanet_rare diseases +MONDO:0017242 rare diseases +MONDO:0017243 gard_rare diseases +MONDO:0017243 nord_rare diseases +MONDO:0017243 ordo_subtype_of_a_disorder diseases +MONDO:0017243 rare diseases +MONDO:0017244 gard_rare diseases +MONDO:0017244 nord_rare diseases +MONDO:0017244 ordo_subtype_of_a_disorder diseases +MONDO:0017244 rare diseases +MONDO:0017245 gard_rare diseases +MONDO:0017245 nord_rare diseases +MONDO:0017245 ordo_subtype_of_a_disorder diseases +MONDO:0017245 rare diseases +MONDO:0017246 gard_rare diseases +MONDO:0017246 nord_rare diseases +MONDO:0017246 ordo_subtype_of_a_disorder diseases +MONDO:0017246 rare diseases +MONDO:0017247 gard_rare diseases +MONDO:0017247 nord_rare diseases +MONDO:0017247 ordo_subtype_of_a_disorder diseases +MONDO:0017247 rare diseases +MONDO:0017248 gard_rare diseases +MONDO:0017248 nord_rare diseases +MONDO:0017248 ordo_subtype_of_a_disorder diseases +MONDO:0017248 rare diseases +MONDO:0017249 gard_rare diseases +MONDO:0017249 nord_rare diseases +MONDO:0017249 ordo_subtype_of_a_disorder diseases +MONDO:0017249 rare diseases +MONDO:0017250 gard_rare diseases +MONDO:0017250 nord_rare diseases +MONDO:0017250 ordo_subtype_of_a_disorder diseases +MONDO:0017250 rare diseases +MONDO:0017251 gard_rare diseases +MONDO:0017251 nord_rare diseases +MONDO:0017251 ordo_subtype_of_a_disorder diseases +MONDO:0017251 rare diseases +MONDO:0017252 gard_rare diseases +MONDO:0017252 nord_rare diseases +MONDO:0017252 ordo_subtype_of_a_disorder diseases +MONDO:0017252 rare diseases +MONDO:0017255 disease_grouping diseases +MONDO:0017255 gard_rare diseases +MONDO:0017255 ordo_group_of_disorders diseases +MONDO:0017255 otar diseases +MONDO:0017255 rare diseases +MONDO:0017256 inferred_rare diseases +MONDO:0017256 otar diseases +MONDO:0017256 rare diseases +MONDO:0017257 gard_rare diseases +MONDO:0017257 nord_rare diseases +MONDO:0017257 ordo_disorder diseases +MONDO:0017257 orphanet_rare diseases +MONDO:0017257 rare diseases +MONDO:0017258 gard_rare diseases +MONDO:0017258 nord_rare diseases +MONDO:0017258 ordo_disorder diseases +MONDO:0017258 orphanet_rare diseases +MONDO:0017258 otar diseases +MONDO:0017258 rare diseases +MONDO:0017264 gard_rare diseases +MONDO:0017264 nord_rare diseases +MONDO:0017264 ordo_disorder diseases +MONDO:0017264 orphanet_rare diseases +MONDO:0017264 otar diseases +MONDO:0017264 rare diseases +MONDO:0017265 disease_grouping diseases +MONDO:0017265 gard_rare diseases +MONDO:0017265 nord_rare diseases +MONDO:0017265 ordo_group_of_disorders diseases +MONDO:0017265 otar diseases +MONDO:0017265 rare diseases +MONDO:0017266 disease_grouping diseases +MONDO:0017266 gard_rare diseases +MONDO:0017266 nord_rare diseases +MONDO:0017266 ordo_group_of_disorders diseases +MONDO:0017266 otar diseases +MONDO:0017266 rare diseases +MONDO:0017267 gard_rare diseases +MONDO:0017267 nord_rare diseases +MONDO:0017267 ordo_disorder diseases +MONDO:0017267 orphanet_rare diseases +MONDO:0017267 otar diseases +MONDO:0017267 rare diseases +MONDO:0017268 gard_rare diseases +MONDO:0017268 nord_rare diseases +MONDO:0017268 ordo_disorder diseases +MONDO:0017268 orphanet_rare diseases +MONDO:0017268 otar diseases +MONDO:0017268 rare diseases +MONDO:0017269 disease_grouping diseases +MONDO:0017269 gard_rare diseases +MONDO:0017269 nord_rare diseases +MONDO:0017269 ordo_group_of_disorders diseases +MONDO:0017269 rare diseases +MONDO:0017275 gard_rare diseases +MONDO:0017275 ordo_disorder diseases +MONDO:0017275 ordo_malformation_syndrome diseases +MONDO:0017275 orphanet_rare diseases +MONDO:0017275 otar diseases +MONDO:0017275 rare diseases +MONDO:0017276 disease_grouping diseases +MONDO:0017276 gard_rare diseases +MONDO:0017276 ordo_group_of_disorders diseases +MONDO:0017276 otar diseases +MONDO:0017276 rare diseases +MONDO:0017277 disease_grouping diseases +MONDO:0017277 gard_rare diseases +MONDO:0017277 ordo_group_of_disorders diseases +MONDO:0017277 rare diseases +MONDO:0017278 disease_grouping diseases +MONDO:0017278 gard_rare diseases +MONDO:0017278 nord_rare diseases +MONDO:0017278 ordo_group_of_disorders diseases +MONDO:0017278 otar diseases +MONDO:0017278 rare diseases +MONDO:0017279 gard_rare diseases +MONDO:0017279 nord_rare diseases +MONDO:0017279 ordo_disorder diseases +MONDO:0017279 orphanet_rare diseases +MONDO:0017279 otar diseases +MONDO:0017279 rare diseases +MONDO:0017280 gard_rare diseases +MONDO:0017280 nord_rare diseases +MONDO:0017280 ordo_disorder diseases +MONDO:0017280 orphanet_rare diseases +MONDO:0017280 rare diseases +MONDO:0017281 gard_rare diseases +MONDO:0017281 ordo_disorder diseases +MONDO:0017281 ordo_malformation_syndrome diseases +MONDO:0017281 orphanet_rare diseases +MONDO:0017281 rare diseases +MONDO:0017282 gard_rare diseases +MONDO:0017282 nord_rare diseases +MONDO:0017282 ordo_disorder diseases +MONDO:0017282 orphanet_rare diseases +MONDO:0017282 rare diseases +MONDO:0017283 gard_rare diseases +MONDO:0017283 nord_rare diseases +MONDO:0017283 ordo_subtype_of_a_disorder diseases +MONDO:0017283 otar diseases +MONDO:0017283 rare diseases +MONDO:0017284 gard_rare diseases +MONDO:0017284 nord_rare diseases +MONDO:0017284 ordo_disorder diseases +MONDO:0017284 ordo_malformation_syndrome diseases +MONDO:0017284 orphanet_rare diseases +MONDO:0017284 otar diseases +MONDO:0017284 rare diseases +MONDO:0017285 gard_rare diseases +MONDO:0017285 nord_rare diseases +MONDO:0017285 ordo_disorder diseases +MONDO:0017285 ordo_morphological_anomaly diseases +MONDO:0017285 orphanet_rare diseases +MONDO:0017285 rare diseases +MONDO:0017286 gard_rare diseases +MONDO:0017286 nord_rare diseases +MONDO:0017286 ordo_clinical_syndrome diseases +MONDO:0017286 ordo_disorder diseases +MONDO:0017286 orphanet_rare diseases +MONDO:0017286 rare diseases +MONDO:0017287 disease_grouping diseases +MONDO:0017287 gard_rare diseases +MONDO:0017287 ordo_disorder diseases +MONDO:0017287 ordo_group_of_disorders diseases +MONDO:0017287 orphanet_rare diseases +MONDO:0017287 otar diseases +MONDO:0017287 rare diseases +MONDO:0017289 gard_rare diseases +MONDO:0017289 nord_rare diseases +MONDO:0017289 ordo_subtype_of_a_disorder diseases +MONDO:0017289 rare diseases +MONDO:0017290 disease_grouping diseases +MONDO:0017290 gard_rare diseases +MONDO:0017290 ordo_group_of_disorders diseases +MONDO:0017290 otar diseases +MONDO:0017290 rare diseases +MONDO:0017291 gard_rare diseases +MONDO:0017291 nord_rare diseases +MONDO:0017291 ordo_clinical_syndrome diseases +MONDO:0017291 ordo_disorder diseases +MONDO:0017291 orphanet_rare diseases +MONDO:0017291 rare diseases +MONDO:0017292 gard_rare diseases +MONDO:0017292 nord_rare diseases +MONDO:0017292 ordo_disorder diseases +MONDO:0017292 orphanet_rare diseases +MONDO:0017292 otar diseases +MONDO:0017292 rare diseases +MONDO:0017294 gard_rare diseases +MONDO:0017294 rare diseases +MONDO:0017295 gard_rare diseases +MONDO:0017295 nord_rare diseases +MONDO:0017295 ordo_subtype_of_a_disorder diseases +MONDO:0017295 otar diseases +MONDO:0017295 rare diseases +MONDO:0017296 gard_rare diseases +MONDO:0017296 nord_rare diseases +MONDO:0017296 ordo_subtype_of_a_disorder diseases +MONDO:0017296 otar diseases +MONDO:0017296 rare diseases +MONDO:0017297 gard_rare diseases +MONDO:0017297 nord_rare diseases +MONDO:0017297 ordo_disorder diseases +MONDO:0017297 orphanet_rare diseases +MONDO:0017297 rare diseases +MONDO:0017298 gard_rare diseases +MONDO:0017298 nord_rare diseases +MONDO:0017298 ordo_disorder diseases +MONDO:0017298 orphanet_rare diseases +MONDO:0017298 rare diseases +MONDO:0017299 gard_rare diseases +MONDO:0017299 nord_rare diseases +MONDO:0017299 ordo_disorder diseases +MONDO:0017299 orphanet_rare diseases +MONDO:0017299 rare diseases +MONDO:0017300 disease_grouping diseases +MONDO:0017300 gard_rare diseases +MONDO:0017300 nord_rare diseases +MONDO:0017300 ordo_group_of_disorders diseases +MONDO:0017300 rare diseases +MONDO:0017301 gard_rare diseases +MONDO:0017301 nord_rare diseases +MONDO:0017301 ordo_disorder diseases +MONDO:0017301 ordo_malformation_syndrome diseases +MONDO:0017301 orphanet_rare diseases +MONDO:0017301 otar diseases +MONDO:0017301 rare diseases +MONDO:0017303 disease_grouping diseases +MONDO:0017303 gard_rare diseases +MONDO:0017303 ordo_group_of_disorders diseases +MONDO:0017303 rare diseases +MONDO:0017304 disease_grouping diseases +MONDO:0017304 gard_rare diseases +MONDO:0017304 nord_rare diseases +MONDO:0017304 ordo_group_of_disorders diseases +MONDO:0017304 otar diseases +MONDO:0017304 rare diseases +MONDO:0017305 disease_grouping diseases +MONDO:0017305 gard_rare diseases +MONDO:0017305 ordo_group_of_disorders diseases +MONDO:0017305 rare diseases +MONDO:0017306 disease_grouping diseases +MONDO:0017306 gard_rare diseases +MONDO:0017306 ordo_group_of_disorders diseases +MONDO:0017306 otar diseases +MONDO:0017306 rare diseases +MONDO:0017307 disease_grouping diseases +MONDO:0017307 gard_rare diseases +MONDO:0017307 ordo_group_of_disorders diseases +MONDO:0017307 rare diseases +MONDO:0017309 gard_rare diseases +MONDO:0017309 nord_rare diseases +MONDO:0017309 ordo_disorder diseases +MONDO:0017309 orphanet_rare diseases +MONDO:0017309 otar diseases +MONDO:0017309 rare diseases +MONDO:0017310 disease_grouping diseases +MONDO:0017310 gard_rare diseases +MONDO:0017310 ordo_group_of_disorders diseases +MONDO:0017310 otar diseases +MONDO:0017310 rare diseases +MONDO:0017312 clingen diseases +MONDO:0017312 gard_rare diseases +MONDO:0017312 nord_rare diseases +MONDO:0017312 ordo_disorder diseases +MONDO:0017312 orphanet_rare diseases +MONDO:0017312 otar diseases +MONDO:0017312 rare diseases +MONDO:0017313 disease_grouping diseases +MONDO:0017313 gard_rare diseases +MONDO:0017313 ordo_group_of_disorders diseases +MONDO:0017313 rare diseases +MONDO:0017314 clingen diseases +MONDO:0017314 gard_rare diseases +MONDO:0017314 nord_rare diseases +MONDO:0017314 ordo_disorder diseases +MONDO:0017314 orphanet_rare diseases +MONDO:0017314 otar diseases +MONDO:0017314 rare diseases +MONDO:0017315 gard_rare diseases +MONDO:0017315 nord_rare diseases +MONDO:0017315 ordo_disorder diseases +MONDO:0017315 ordo_malformation_syndrome diseases +MONDO:0017315 orphanet_rare diseases +MONDO:0017315 rare diseases +MONDO:0017316 gard_rare diseases +MONDO:0017316 ordo_disorder diseases +MONDO:0017316 ordo_malformation_syndrome diseases +MONDO:0017316 orphanet_rare diseases +MONDO:0017316 otar diseases +MONDO:0017316 rare diseases +MONDO:0017317 gard_rare diseases +MONDO:0017317 nord_rare diseases +MONDO:0017317 ordo_disorder diseases +MONDO:0017317 ordo_malformation_syndrome diseases +MONDO:0017317 orphanet_rare diseases +MONDO:0017317 otar diseases +MONDO:0017317 rare diseases +MONDO:0017318 gard_rare diseases +MONDO:0017318 nord_rare diseases +MONDO:0017318 ordo_disorder diseases +MONDO:0017318 orphanet_rare diseases +MONDO:0017318 otar diseases +MONDO:0017318 rare diseases +MONDO:0017319 gard_rare diseases +MONDO:0017319 nord_rare diseases +MONDO:0017319 ordo_disorder diseases +MONDO:0017319 orphanet_rare diseases +MONDO:0017319 otar diseases +MONDO:0017319 rare diseases +MONDO:0017320 gard_rare diseases +MONDO:0017320 ordo_disorder diseases +MONDO:0017320 orphanet_rare diseases +MONDO:0017320 otar diseases +MONDO:0017320 rare diseases +MONDO:0017321 gard_rare diseases +MONDO:0017321 nord_rare diseases +MONDO:0017321 ordo_disorder diseases +MONDO:0017321 ordo_malformation_syndrome diseases +MONDO:0017321 orphanet_rare diseases +MONDO:0017321 otar diseases +MONDO:0017321 rare diseases +MONDO:0017322 disease_grouping diseases +MONDO:0017322 gard_rare diseases +MONDO:0017322 ordo_group_of_disorders diseases +MONDO:0017322 otar diseases +MONDO:0017322 rare diseases +MONDO:0017323 disease_grouping diseases +MONDO:0017323 gard_rare diseases +MONDO:0017323 ordo_group_of_disorders diseases +MONDO:0017323 otar diseases +MONDO:0017323 rare diseases +MONDO:0017324 gard_rare diseases +MONDO:0017324 nord_rare diseases +MONDO:0017324 ordo_disorder diseases +MONDO:0017324 orphanet_rare diseases +MONDO:0017324 otar diseases +MONDO:0017324 rare diseases +MONDO:0017325 gard_rare diseases +MONDO:0017325 nord_rare diseases +MONDO:0017325 ordo_disorder diseases +MONDO:0017325 orphanet_rare diseases +MONDO:0017325 otar diseases +MONDO:0017325 rare diseases +MONDO:0017326 gard_rare diseases +MONDO:0017326 nord_rare diseases +MONDO:0017326 ordo_disorder diseases +MONDO:0017326 orphanet_rare diseases +MONDO:0017326 rare diseases +MONDO:0017327 gard_rare diseases +MONDO:0017327 nord_rare diseases +MONDO:0017327 ordo_disorder diseases +MONDO:0017327 orphanet_rare diseases +MONDO:0017327 rare diseases +MONDO:0017328 gard_rare diseases +MONDO:0017328 nord_rare diseases +MONDO:0017328 ordo_subtype_of_a_disorder diseases +MONDO:0017328 rare diseases +MONDO:0017329 gard_rare diseases +MONDO:0017329 nord_rare diseases +MONDO:0017329 ordo_disorder diseases +MONDO:0017329 ordo_malformation_syndrome diseases +MONDO:0017329 orphanet_rare diseases +MONDO:0017329 otar diseases +MONDO:0017329 rare diseases +MONDO:0017330 gard_rare diseases +MONDO:0017330 nord_rare diseases +MONDO:0017330 ordo_clinical_situation diseases +MONDO:0017330 ordo_disorder diseases +MONDO:0017330 orphanet_rare diseases +MONDO:0017330 rare diseases +MONDO:0017331 ordo_malformation_syndrome diseases +MONDO:0017332 gard_rare diseases +MONDO:0017332 nord_rare diseases +MONDO:0017332 ordo_disorder diseases +MONDO:0017332 orphanet_rare diseases +MONDO:0017332 rare diseases +MONDO:0017334 gard_rare diseases +MONDO:0017334 nord_rare diseases +MONDO:0017334 ordo_disorder diseases +MONDO:0017334 ordo_malformation_syndrome diseases +MONDO:0017334 orphanet_rare diseases +MONDO:0017334 rare diseases +MONDO:0017335 gard_rare diseases +MONDO:0017335 nord_rare diseases +MONDO:0017335 ordo_disorder diseases +MONDO:0017335 ordo_malformation_syndrome diseases +MONDO:0017335 orphanet_rare diseases +MONDO:0017335 otar diseases +MONDO:0017335 rare diseases +MONDO:0017337 gard_rare diseases +MONDO:0017337 nord_rare diseases +MONDO:0017337 ordo_disorder diseases +MONDO:0017337 orphanet_rare diseases +MONDO:0017337 otar diseases +MONDO:0017337 rare diseases +MONDO:0017338 disease_grouping diseases +MONDO:0017338 gard_rare diseases +MONDO:0017338 ordo_group_of_disorders diseases +MONDO:0017338 otar diseases +MONDO:0017338 rare diseases +MONDO:0017339 clingen diseases +MONDO:0017339 gard_rare diseases +MONDO:0017339 nord_rare diseases +MONDO:0017339 ordo_disorder diseases +MONDO:0017339 orphanet_rare diseases +MONDO:0017339 otar diseases +MONDO:0017339 rare diseases +MONDO:0017340 gard_rare diseases +MONDO:0017340 nord_rare diseases +MONDO:0017340 ordo_disorder diseases +MONDO:0017340 orphanet_rare diseases +MONDO:0017340 rare diseases +MONDO:0017341 disease_grouping diseases +MONDO:0017341 gard_rare diseases +MONDO:0017341 ordo_group_of_disorders diseases +MONDO:0017341 otar diseases +MONDO:0017341 rare diseases +MONDO:0017342 disease_grouping diseases +MONDO:0017342 gard_rare diseases +MONDO:0017342 ordo_group_of_disorders diseases +MONDO:0017342 rare diseases +MONDO:0017343 disease_grouping diseases +MONDO:0017343 gard_rare diseases +MONDO:0017343 ordo_group_of_disorders diseases +MONDO:0017343 rare diseases +MONDO:0017344 disease_grouping diseases +MONDO:0017344 gard_rare diseases +MONDO:0017344 ordo_group_of_disorders diseases +MONDO:0017344 rare diseases +MONDO:0017345 disease_grouping diseases +MONDO:0017345 gard_rare diseases +MONDO:0017345 ordo_group_of_disorders diseases +MONDO:0017345 rare diseases +MONDO:0017346 gard_rare diseases +MONDO:0017346 nord_rare diseases +MONDO:0017346 ordo_disorder diseases +MONDO:0017346 orphanet_rare diseases +MONDO:0017346 otar diseases +MONDO:0017346 rare diseases +MONDO:0017347 gard_rare diseases +MONDO:0017347 nord_rare diseases +MONDO:0017347 ordo_disorder diseases +MONDO:0017347 orphanet_rare diseases +MONDO:0017347 rare diseases +MONDO:0017348 gard_rare diseases +MONDO:0017348 nord_rare diseases +MONDO:0017348 ordo_disorder diseases +MONDO:0017348 orphanet_rare diseases +MONDO:0017348 rare diseases +MONDO:0017349 gard_rare diseases +MONDO:0017349 nord_rare diseases +MONDO:0017349 ordo_disorder diseases +MONDO:0017349 orphanet_rare diseases +MONDO:0017349 otar diseases +MONDO:0017349 rare diseases +MONDO:0017350 disease_grouping diseases +MONDO:0017350 gard_rare diseases +MONDO:0017350 ordo_group_of_disorders diseases +MONDO:0017350 rare diseases +MONDO:0017351 clingen diseases +MONDO:0017351 disease_grouping diseases +MONDO:0017351 gard_rare diseases +MONDO:0017351 ordo_group_of_disorders diseases +MONDO:0017351 otar diseases +MONDO:0017351 rare diseases +MONDO:0017352 disease_grouping diseases +MONDO:0017352 gard_rare diseases +MONDO:0017352 ordo_group_of_disorders diseases +MONDO:0017352 otar diseases +MONDO:0017352 rare diseases +MONDO:0017353 gard_rare diseases +MONDO:0017353 ordo_subtype_of_a_disorder diseases +MONDO:0017353 otar diseases +MONDO:0017353 rare diseases +MONDO:0017354 gard_rare diseases +MONDO:0017354 nord_rare diseases +MONDO:0017354 ordo_subtype_of_a_disorder diseases +MONDO:0017354 otar diseases +MONDO:0017354 rare diseases +MONDO:0017355 disease_grouping diseases +MONDO:0017355 gard_rare diseases +MONDO:0017355 ordo_group_of_disorders diseases +MONDO:0017355 rare diseases +MONDO:0017356 disease_grouping diseases +MONDO:0017356 gard_rare diseases +MONDO:0017356 ordo_group_of_disorders diseases +MONDO:0017356 rare diseases +MONDO:0017357 gard_rare diseases +MONDO:0017357 nord_rare diseases +MONDO:0017357 ordo_clinical_situation diseases +MONDO:0017357 ordo_disorder diseases +MONDO:0017357 orphanet_rare diseases +MONDO:0017357 rare diseases +MONDO:0017359 disease_grouping diseases +MONDO:0017359 gard_rare diseases +MONDO:0017359 ordo_group_of_disorders diseases +MONDO:0017359 otar diseases +MONDO:0017359 rare diseases +MONDO:0017360 gard_rare diseases +MONDO:0017360 nord_rare diseases +MONDO:0017360 ordo_subtype_of_a_disorder diseases +MONDO:0017360 otar diseases +MONDO:0017360 rare diseases +MONDO:0017361 gard_rare diseases +MONDO:0017361 nord_rare diseases +MONDO:0017361 ordo_disorder diseases +MONDO:0017361 orphanet_rare diseases +MONDO:0017361 otar diseases +MONDO:0017361 rare diseases +MONDO:0017362 clingen diseases +MONDO:0017362 gard_rare diseases +MONDO:0017362 nord_rare diseases +MONDO:0017362 ordo_disorder diseases +MONDO:0017362 orphanet_rare diseases +MONDO:0017362 otar diseases +MONDO:0017362 rare diseases +MONDO:0017363 gard_rare diseases +MONDO:0017363 nord_rare diseases +MONDO:0017363 ordo_disorder diseases +MONDO:0017363 orphanet_rare diseases +MONDO:0017363 rare diseases +MONDO:0017364 gard_rare diseases +MONDO:0017364 nord_rare diseases +MONDO:0017364 ordo_disorder diseases +MONDO:0017364 orphanet_rare diseases +MONDO:0017364 otar diseases +MONDO:0017364 rare diseases +MONDO:0017365 gard_rare diseases +MONDO:0017365 ordo_disorder diseases +MONDO:0017365 orphanet_rare diseases +MONDO:0017365 otar diseases +MONDO:0017365 rare diseases +MONDO:0017366 clingen diseases +MONDO:0017366 gard_rare diseases +MONDO:0017366 nord_rare diseases +MONDO:0017366 ordo_disorder diseases +MONDO:0017366 orphanet_rare diseases +MONDO:0017366 otar diseases +MONDO:0017366 rare diseases +MONDO:0017372 gard_rare diseases +MONDO:0017372 nord_rare diseases +MONDO:0017372 ordo_disorder diseases +MONDO:0017372 orphanet_rare diseases +MONDO:0017372 rare diseases +MONDO:0017373 gard_rare diseases +MONDO:0017373 nord_rare diseases +MONDO:0017373 ordo_disorder diseases +MONDO:0017373 orphanet_rare diseases +MONDO:0017373 otar diseases +MONDO:0017373 rare diseases +MONDO:0017375 gard_rare diseases +MONDO:0017375 nord_rare diseases +MONDO:0017375 ordo_disorder diseases +MONDO:0017375 orphanet_rare diseases +MONDO:0017375 otar diseases +MONDO:0017375 rare diseases +MONDO:0017376 gard_rare diseases +MONDO:0017376 nord_rare diseases +MONDO:0017376 ordo_disorder diseases +MONDO:0017376 orphanet_rare diseases +MONDO:0017376 otar diseases +MONDO:0017376 rare diseases +MONDO:0017377 gard_rare diseases +MONDO:0017377 nord_rare diseases +MONDO:0017377 ordo_disorder diseases +MONDO:0017377 ordo_malformation_syndrome diseases +MONDO:0017377 orphanet_rare diseases +MONDO:0017377 otar diseases +MONDO:0017377 rare diseases +MONDO:0017379 gard_rare diseases +MONDO:0017379 ordo_disorder diseases +MONDO:0017379 ordo_malformation_syndrome diseases +MONDO:0017379 orphanet_rare diseases +MONDO:0017379 otar diseases +MONDO:0017379 rare diseases +MONDO:0017380 clingen diseases +MONDO:0017380 gard_rare diseases +MONDO:0017380 nord_rare diseases +MONDO:0017380 ordo_disorder diseases +MONDO:0017380 orphanet_rare diseases +MONDO:0017380 otar diseases +MONDO:0017380 rare diseases +MONDO:0017381 gard_rare diseases +MONDO:0017381 nord_rare diseases +MONDO:0017381 ordo_disorder diseases +MONDO:0017381 orphanet_rare diseases +MONDO:0017381 rare diseases +MONDO:0017382 gard_rare diseases +MONDO:0017382 nord_rare diseases +MONDO:0017382 ordo_etiological_subtype diseases +MONDO:0017382 ordo_subtype_of_a_disorder diseases +MONDO:0017382 rare diseases +MONDO:0017383 gard_rare diseases +MONDO:0017383 ordo_etiological_subtype diseases +MONDO:0017383 ordo_subtype_of_a_disorder diseases +MONDO:0017383 otar diseases +MONDO:0017383 rare diseases +MONDO:0017384 gard_rare diseases +MONDO:0017384 nord_rare diseases +MONDO:0017384 ordo_disorder diseases +MONDO:0017384 orphanet_rare diseases +MONDO:0017384 rare diseases +MONDO:0017385 gard_rare diseases +MONDO:0017385 nord_rare diseases +MONDO:0017385 ordo_disorder diseases +MONDO:0017385 orphanet_rare diseases +MONDO:0017385 otar diseases +MONDO:0017385 rare diseases +MONDO:0017386 gard_rare diseases +MONDO:0017386 nord_rare diseases +MONDO:0017386 ordo_subtype_of_a_disorder diseases +MONDO:0017386 otar diseases +MONDO:0017386 rare diseases +MONDO:0017387 gard_rare diseases +MONDO:0017387 nord_rare diseases +MONDO:0017387 ordo_disorder diseases +MONDO:0017387 orphanet_rare diseases +MONDO:0017387 otar diseases +MONDO:0017387 rare diseases +MONDO:0017388 gard_rare diseases +MONDO:0017388 nord_rare diseases +MONDO:0017388 ordo_disorder diseases +MONDO:0017388 orphanet_rare diseases +MONDO:0017388 rare diseases +MONDO:0017389 gard_rare diseases +MONDO:0017389 nord_rare diseases +MONDO:0017389 ordo_subtype_of_a_disorder diseases +MONDO:0017389 otar diseases +MONDO:0017389 rare diseases +MONDO:0017391 gard_rare diseases +MONDO:0017391 nord_rare diseases +MONDO:0017391 ordo_disorder diseases +MONDO:0017391 orphanet_rare diseases +MONDO:0017391 rare diseases +MONDO:0017392 gard_rare diseases +MONDO:0017392 nord_rare diseases +MONDO:0017392 ordo_disorder diseases +MONDO:0017392 orphanet_rare diseases +MONDO:0017392 otar diseases +MONDO:0017392 rare diseases +MONDO:0017393 disease_grouping diseases +MONDO:0017393 gard_rare diseases +MONDO:0017393 nord_rare diseases +MONDO:0017393 ordo_group_of_disorders diseases +MONDO:0017393 otar diseases +MONDO:0017393 rare diseases +MONDO:0017394 nord_rare diseases +MONDO:0017394 ordo_clinical_situation diseases +MONDO:0017394 ordo_disorder diseases +MONDO:0017394 orphanet_rare diseases +MONDO:0017394 rare diseases +MONDO:0017395 gard_rare diseases +MONDO:0017395 nord_rare diseases +MONDO:0017395 ordo_disorder diseases +MONDO:0017395 orphanet_rare diseases +MONDO:0017395 rare diseases +MONDO:0017396 disease_grouping diseases +MONDO:0017396 gard_rare diseases +MONDO:0017396 nord_rare diseases +MONDO:0017396 ordo_group_of_disorders diseases +MONDO:0017396 rare diseases +MONDO:0017398 gard_rare diseases +MONDO:0017398 nord_rare diseases +MONDO:0017398 ordo_disorder diseases +MONDO:0017398 ordo_malformation_syndrome diseases +MONDO:0017398 orphanet_rare diseases +MONDO:0017398 otar diseases +MONDO:0017398 rare diseases +MONDO:0017399 gard_rare diseases +MONDO:0017399 nord_rare diseases +MONDO:0017399 rare diseases +MONDO:0017400 gard_rare diseases +MONDO:0017400 nord_rare diseases +MONDO:0017400 ordo_disorder diseases +MONDO:0017400 ordo_malformation_syndrome diseases +MONDO:0017400 orphanet_rare diseases +MONDO:0017400 otar diseases +MONDO:0017400 rare diseases +MONDO:0017401 gard_rare diseases +MONDO:0017401 nord_rare diseases +MONDO:0017401 ordo_subtype_of_a_disorder diseases +MONDO:0017401 otar diseases +MONDO:0017401 rare diseases +MONDO:0017402 gard_rare diseases +MONDO:0017402 nord_rare diseases +MONDO:0017402 ordo_subtype_of_a_disorder diseases +MONDO:0017402 otar diseases +MONDO:0017402 rare diseases +MONDO:0017403 gard_rare diseases +MONDO:0017403 nord_rare diseases +MONDO:0017403 ordo_subtype_of_a_disorder diseases +MONDO:0017403 otar diseases +MONDO:0017403 rare diseases +MONDO:0017404 gard_rare diseases +MONDO:0017404 nord_rare diseases +MONDO:0017404 ordo_disorder diseases +MONDO:0017404 ordo_malformation_syndrome diseases +MONDO:0017404 orphanet_rare diseases +MONDO:0017404 otar diseases +MONDO:0017404 rare diseases +MONDO:0017405 gard_rare diseases +MONDO:0017405 nord_rare diseases +MONDO:0017405 ordo_disorder diseases +MONDO:0017405 ordo_malformation_syndrome diseases +MONDO:0017405 orphanet_rare diseases +MONDO:0017405 rare diseases +MONDO:0017406 gard_rare diseases +MONDO:0017406 ordo_disorder diseases +MONDO:0017406 ordo_malformation_syndrome diseases +MONDO:0017406 orphanet_rare diseases +MONDO:0017406 otar diseases +MONDO:0017406 rare diseases +MONDO:0017407 gard_rare diseases +MONDO:0017407 nord_rare diseases +MONDO:0017407 ordo_disorder diseases +MONDO:0017407 orphanet_rare diseases +MONDO:0017407 otar diseases +MONDO:0017407 rare diseases +MONDO:0017408 gard_rare diseases +MONDO:0017408 nord_rare diseases +MONDO:0017408 ordo_disorder diseases +MONDO:0017408 orphanet_rare diseases +MONDO:0017408 otar diseases +MONDO:0017408 rare diseases +MONDO:0017409 gard_rare diseases +MONDO:0017409 nord_rare diseases +MONDO:0017409 ordo_disorder diseases +MONDO:0017409 orphanet_rare diseases +MONDO:0017409 rare diseases +MONDO:0017410 gard_rare diseases +MONDO:0017410 nord_rare diseases +MONDO:0017410 ordo_disorder diseases +MONDO:0017410 orphanet_rare diseases +MONDO:0017410 otar diseases +MONDO:0017410 rare diseases +MONDO:0017411 gard_rare diseases +MONDO:0017411 nord_rare diseases +MONDO:0017411 ordo_disorder diseases +MONDO:0017411 orphanet_rare diseases +MONDO:0017411 otar diseases +MONDO:0017411 rare diseases +MONDO:0017413 gard_rare diseases +MONDO:0017413 otar diseases +MONDO:0017413 rare diseases +MONDO:0017415 disease_grouping diseases +MONDO:0017415 gard_rare diseases +MONDO:0017415 nord_rare diseases +MONDO:0017415 ordo_group_of_disorders diseases +MONDO:0017415 otar diseases +MONDO:0017415 rare diseases +MONDO:0017416 gard_rare diseases +MONDO:0017416 nord_rare diseases +MONDO:0017416 ordo_disorder diseases +MONDO:0017416 orphanet_rare diseases +MONDO:0017416 otar diseases +MONDO:0017416 rare diseases +MONDO:0017417 gard_rare diseases +MONDO:0017417 nord_rare diseases +MONDO:0017417 ordo_disorder diseases +MONDO:0017417 ordo_malformation_syndrome diseases +MONDO:0017417 orphanet_rare diseases +MONDO:0017417 otar diseases +MONDO:0017417 rare diseases +MONDO:0017418 gard_rare diseases +MONDO:0017418 nord_rare diseases +MONDO:0017418 ordo_clinical_syndrome diseases +MONDO:0017418 ordo_disorder diseases +MONDO:0017418 orphanet_rare diseases +MONDO:0017418 rare diseases +MONDO:0017419 disease_grouping diseases +MONDO:0017419 gard_rare diseases +MONDO:0017419 nord_rare diseases +MONDO:0017419 ordo_group_of_disorders diseases +MONDO:0017419 rare diseases +MONDO:0017424 disease_grouping diseases +MONDO:0017424 otar diseases +MONDO:0017425 disease_grouping diseases +MONDO:0017425 gard_rare diseases +MONDO:0017425 otar diseases +MONDO:0017425 rare diseases +MONDO:0017426 disease_grouping diseases +MONDO:0017426 gard_rare diseases +MONDO:0017426 nord_rare diseases +MONDO:0017426 otar diseases +MONDO:0017426 rare diseases +MONDO:0017427 disease_grouping diseases +MONDO:0017427 gard_rare diseases +MONDO:0017427 ordo_group_of_disorders diseases +MONDO:0017427 rare diseases +MONDO:0017435 disease_grouping diseases +MONDO:0017435 gard_rare diseases +MONDO:0017435 nord_rare diseases +MONDO:0017435 ordo_group_of_disorders diseases +MONDO:0017435 otar diseases +MONDO:0017435 rare diseases +MONDO:0017436 disease_grouping diseases +MONDO:0017436 gard_rare diseases +MONDO:0017436 nord_rare diseases +MONDO:0017436 ordo_group_of_disorders diseases +MONDO:0017436 otar diseases +MONDO:0017436 rare diseases +MONDO:0017437 gard_rare diseases +MONDO:0017437 nord_rare diseases +MONDO:0017437 ordo_disorder diseases +MONDO:0017437 ordo_morphological_anomaly diseases +MONDO:0017437 orphanet_rare diseases +MONDO:0017437 rare diseases +MONDO:0017438 gard_rare diseases +MONDO:0017438 nord_rare diseases +MONDO:0017438 ordo_disorder diseases +MONDO:0017438 ordo_morphological_anomaly diseases +MONDO:0017438 orphanet_rare diseases +MONDO:0017438 rare diseases +MONDO:0017439 gard_rare diseases +MONDO:0017439 nord_rare diseases +MONDO:0017439 ordo_disorder diseases +MONDO:0017439 ordo_morphological_anomaly diseases +MONDO:0017439 orphanet_rare diseases +MONDO:0017439 otar diseases +MONDO:0017439 rare diseases +MONDO:0017440 gard_rare diseases +MONDO:0017440 nord_rare diseases +MONDO:0017440 ordo_disorder diseases +MONDO:0017440 ordo_morphological_anomaly diseases +MONDO:0017440 orphanet_rare diseases +MONDO:0017440 rare diseases +MONDO:0017441 gard_rare diseases +MONDO:0017441 nord_rare diseases +MONDO:0017441 ordo_disorder diseases +MONDO:0017441 ordo_morphological_anomaly diseases +MONDO:0017441 orphanet_rare diseases +MONDO:0017441 otar diseases +MONDO:0017441 rare diseases +MONDO:0017442 gard_rare diseases +MONDO:0017442 nord_rare diseases +MONDO:0017442 ordo_disorder diseases +MONDO:0017442 ordo_morphological_anomaly diseases +MONDO:0017442 orphanet_rare diseases +MONDO:0017442 rare diseases +MONDO:0017443 gard_rare diseases +MONDO:0017443 nord_rare diseases +MONDO:0017443 ordo_disorder diseases +MONDO:0017443 ordo_morphological_anomaly diseases +MONDO:0017443 orphanet_rare diseases +MONDO:0017443 rare diseases +MONDO:0017444 gard_rare diseases +MONDO:0017444 nord_rare diseases +MONDO:0017444 ordo_disorder diseases +MONDO:0017444 ordo_morphological_anomaly diseases +MONDO:0017444 orphanet_rare diseases +MONDO:0017444 rare diseases +MONDO:0017445 gard_rare diseases +MONDO:0017445 nord_rare diseases +MONDO:0017445 ordo_disorder diseases +MONDO:0017445 ordo_morphological_anomaly diseases +MONDO:0017445 orphanet_rare diseases +MONDO:0017445 rare diseases +MONDO:0017446 gard_rare diseases +MONDO:0017446 nord_rare diseases +MONDO:0017446 ordo_disorder diseases +MONDO:0017446 ordo_morphological_anomaly diseases +MONDO:0017446 orphanet_rare diseases +MONDO:0017446 rare diseases +MONDO:0017449 gard_rare diseases +MONDO:0017449 ordo_morphological_anomaly diseases +MONDO:0017449 otar diseases +MONDO:0017449 rare diseases +MONDO:0017450 gard_rare diseases +MONDO:0017450 ordo_morphological_anomaly diseases +MONDO:0017450 otar diseases +MONDO:0017450 rare diseases +MONDO:0017451 ordo_morphological_anomaly diseases +MONDO:0017452 ordo_morphological_anomaly diseases +MONDO:0017453 gard_rare diseases +MONDO:0017453 nord_rare diseases +MONDO:0017453 ordo_disorder diseases +MONDO:0017453 ordo_malformation_syndrome diseases +MONDO:0017453 orphanet_rare diseases +MONDO:0017453 rare diseases +MONDO:0017454 gard_rare diseases +MONDO:0017454 ordo_malformation_syndrome diseases +MONDO:0017454 otar diseases +MONDO:0017454 rare diseases +MONDO:0017455 gard_rare diseases +MONDO:0017455 nord_rare diseases +MONDO:0017455 ordo_disorder diseases +MONDO:0017455 ordo_morphological_anomaly diseases +MONDO:0017455 orphanet_rare diseases +MONDO:0017455 otar diseases +MONDO:0017455 rare diseases +MONDO:0017456 gard_rare diseases +MONDO:0017456 ordo_disorder diseases +MONDO:0017456 ordo_morphological_anomaly diseases +MONDO:0017456 orphanet_rare diseases +MONDO:0017456 rare diseases +MONDO:0017457 gard_rare diseases +MONDO:0017457 ordo_morphological_anomaly diseases +MONDO:0017457 rare diseases +MONDO:0017460 gard_rare diseases +MONDO:0017460 nord_rare diseases +MONDO:0017460 ordo_disorder diseases +MONDO:0017460 ordo_morphological_anomaly diseases +MONDO:0017460 orphanet_rare diseases +MONDO:0017460 rare diseases +MONDO:0017461 gard_rare diseases +MONDO:0017461 nord_rare diseases +MONDO:0017461 ordo_disorder diseases +MONDO:0017461 ordo_morphological_anomaly diseases +MONDO:0017461 orphanet_rare diseases +MONDO:0017461 rare diseases +MONDO:0017462 gard_rare diseases +MONDO:0017462 nord_rare diseases +MONDO:0017462 ordo_subtype_of_a_disorder diseases +MONDO:0017462 rare diseases +MONDO:0017463 gard_rare diseases +MONDO:0017463 nord_rare diseases +MONDO:0017463 ordo_subtype_of_a_disorder diseases +MONDO:0017463 rare diseases +MONDO:0017464 gard_rare diseases +MONDO:0017464 nord_rare diseases +MONDO:0017464 ordo_subtype_of_a_disorder diseases +MONDO:0017464 rare diseases +MONDO:0017465 gard_rare diseases +MONDO:0017465 nord_rare diseases +MONDO:0017465 ordo_subtype_of_a_disorder diseases +MONDO:0017465 rare diseases +MONDO:0017466 gard_rare diseases +MONDO:0017466 nord_rare diseases +MONDO:0017466 ordo_subtype_of_a_disorder diseases +MONDO:0017466 rare diseases +MONDO:0017467 gard_rare diseases +MONDO:0017467 nord_rare diseases +MONDO:0017467 ordo_disorder diseases +MONDO:0017467 ordo_morphological_anomaly diseases +MONDO:0017467 orphanet_rare diseases +MONDO:0017467 rare diseases +MONDO:0017468 gard_rare diseases +MONDO:0017468 nord_rare diseases +MONDO:0017468 ordo_disorder diseases +MONDO:0017468 ordo_morphological_anomaly diseases +MONDO:0017468 orphanet_rare diseases +MONDO:0017468 rare diseases +MONDO:0017469 gard_rare diseases +MONDO:0017469 nord_rare diseases +MONDO:0017469 ordo_disorder diseases +MONDO:0017469 ordo_morphological_anomaly diseases +MONDO:0017469 orphanet_rare diseases +MONDO:0017469 rare diseases +MONDO:0017470 gard_rare diseases +MONDO:0017470 nord_rare diseases +MONDO:0017470 ordo_disorder diseases +MONDO:0017470 ordo_morphological_anomaly diseases +MONDO:0017470 orphanet_rare diseases +MONDO:0017470 rare diseases +MONDO:0017471 gard_rare diseases +MONDO:0017471 nord_rare diseases +MONDO:0017471 ordo_disorder diseases +MONDO:0017471 ordo_morphological_anomaly diseases +MONDO:0017471 orphanet_rare diseases +MONDO:0017471 otar diseases +MONDO:0017471 rare diseases +MONDO:0017472 gard_rare diseases +MONDO:0017472 nord_rare diseases +MONDO:0017472 rare diseases +MONDO:0017473 gard_rare diseases +MONDO:0017473 rare diseases +MONDO:0017474 gard_rare diseases +MONDO:0017474 nord_rare diseases +MONDO:0017474 ordo_disorder diseases +MONDO:0017474 ordo_morphological_anomaly diseases +MONDO:0017474 orphanet_rare diseases +MONDO:0017474 rare diseases +MONDO:0017475 gard_rare diseases +MONDO:0017475 nord_rare diseases +MONDO:0017475 ordo_disorder diseases +MONDO:0017475 ordo_morphological_anomaly diseases +MONDO:0017475 orphanet_rare diseases +MONDO:0017475 otar diseases +MONDO:0017475 rare diseases +MONDO:0017476 gard_rare diseases +MONDO:0017476 nord_rare diseases +MONDO:0017476 ordo_disorder diseases +MONDO:0017476 ordo_morphological_anomaly diseases +MONDO:0017476 orphanet_rare diseases +MONDO:0017476 rare diseases +MONDO:0017477 gard_rare diseases +MONDO:0017477 nord_rare diseases +MONDO:0017477 ordo_disorder diseases +MONDO:0017477 ordo_morphological_anomaly diseases +MONDO:0017477 orphanet_rare diseases +MONDO:0017477 rare diseases +MONDO:0017478 gard_rare diseases +MONDO:0017478 nord_rare diseases +MONDO:0017478 rare diseases +MONDO:0017479 gard_rare diseases +MONDO:0017479 rare diseases +MONDO:0017480 gard_rare diseases +MONDO:0017480 rare diseases +MONDO:0017481 gard_rare diseases +MONDO:0017481 rare diseases +MONDO:0017482 gard_rare diseases +MONDO:0017482 rare diseases +MONDO:0017483 gard_rare diseases +MONDO:0017483 rare diseases +MONDO:0017484 gard_rare diseases +MONDO:0017484 rare diseases +MONDO:0017485 gard_rare diseases +MONDO:0017485 nord_rare diseases +MONDO:0017485 rare diseases +MONDO:0017486 gard_rare diseases +MONDO:0017486 rare diseases +MONDO:0017487 gard_rare diseases +MONDO:0017487 rare diseases +MONDO:0017488 gard_rare diseases +MONDO:0017488 rare diseases +MONDO:0017489 gard_rare diseases +MONDO:0017489 rare diseases +MONDO:0017490 gard_rare diseases +MONDO:0017490 rare diseases +MONDO:0017491 gard_rare diseases +MONDO:0017491 rare diseases +MONDO:0017492 gard_rare diseases +MONDO:0017492 rare diseases +MONDO:0017493 gard_rare diseases +MONDO:0017493 rare diseases +MONDO:0017496 gard_rare diseases +MONDO:0017496 rare diseases +MONDO:0017497 gard_rare diseases +MONDO:0017497 rare diseases +MONDO:0017498 gard_rare diseases +MONDO:0017498 nord_rare diseases +MONDO:0017498 rare diseases +MONDO:0017499 gard_rare diseases +MONDO:0017499 nord_rare diseases +MONDO:0017499 rare diseases +MONDO:0017500 gard_rare diseases +MONDO:0017500 rare diseases +MONDO:0017501 gard_rare diseases +MONDO:0017501 rare diseases +MONDO:0017502 gard_rare diseases +MONDO:0017502 rare diseases +MONDO:0017503 gard_rare diseases +MONDO:0017503 nord_rare diseases +MONDO:0017503 rare diseases +MONDO:0017504 gard_rare diseases +MONDO:0017504 rare diseases +MONDO:0017505 gard_rare diseases +MONDO:0017505 rare diseases +MONDO:0017509 gard_rare diseases +MONDO:0017509 rare diseases +MONDO:0017510 gard_rare diseases +MONDO:0017510 rare diseases +MONDO:0017511 gard_rare diseases +MONDO:0017511 rare diseases +MONDO:0017512 gard_rare diseases +MONDO:0017512 nord_rare diseases +MONDO:0017512 rare diseases +MONDO:0017513 gard_rare diseases +MONDO:0017513 rare diseases +MONDO:0017514 gard_rare diseases +MONDO:0017514 rare diseases +MONDO:0017515 gard_rare diseases +MONDO:0017515 nord_rare diseases +MONDO:0017515 rare diseases +MONDO:0017519 gard_rare diseases +MONDO:0017519 nord_rare diseases +MONDO:0017519 rare diseases +MONDO:0017520 gard_rare diseases +MONDO:0017520 nord_rare diseases +MONDO:0017520 rare diseases +MONDO:0017521 gard_rare diseases +MONDO:0017521 rare diseases +MONDO:0017522 gard_rare diseases +MONDO:0017522 nord_rare diseases +MONDO:0017522 rare diseases +MONDO:0017523 gard_rare diseases +MONDO:0017523 nord_rare diseases +MONDO:0017523 rare diseases +MONDO:0017524 gard_rare diseases +MONDO:0017524 rare diseases +MONDO:0017525 gard_rare diseases +MONDO:0017525 nord_rare diseases +MONDO:0017525 rare diseases +MONDO:0017526 gard_rare diseases +MONDO:0017526 nord_rare diseases +MONDO:0017526 rare diseases +MONDO:0017527 gard_rare diseases +MONDO:0017527 nord_rare diseases +MONDO:0017527 rare diseases +MONDO:0017528 gard_rare diseases +MONDO:0017528 rare diseases +MONDO:0017529 gard_rare diseases +MONDO:0017529 rare diseases +MONDO:0017530 gard_rare diseases +MONDO:0017530 rare diseases +MONDO:0017531 gard_rare diseases +MONDO:0017531 rare diseases +MONDO:0017532 gard_rare diseases +MONDO:0017532 rare diseases +MONDO:0017533 gard_rare diseases +MONDO:0017533 rare diseases +MONDO:0017534 gard_rare diseases +MONDO:0017534 rare diseases +MONDO:0017535 gard_rare diseases +MONDO:0017535 nord_rare diseases +MONDO:0017535 rare diseases +MONDO:0017536 gard_rare diseases +MONDO:0017536 rare diseases +MONDO:0017537 gard_rare diseases +MONDO:0017537 rare diseases +MONDO:0017538 gard_rare diseases +MONDO:0017538 rare diseases +MONDO:0017543 gard_rare diseases +MONDO:0017543 nord_rare diseases +MONDO:0017543 ordo_subtype_of_a_disorder diseases +MONDO:0017543 otar diseases +MONDO:0017543 rare diseases +MONDO:0017544 gard_rare diseases +MONDO:0017544 nord_rare diseases +MONDO:0017544 ordo_subtype_of_a_disorder diseases +MONDO:0017544 otar diseases +MONDO:0017544 rare diseases +MONDO:0017545 gard_rare diseases +MONDO:0017545 nord_rare diseases +MONDO:0017545 ordo_subtype_of_a_disorder diseases +MONDO:0017545 rare diseases +MONDO:0017546 gard_rare diseases +MONDO:0017546 nord_rare diseases +MONDO:0017546 ordo_subtype_of_a_disorder diseases +MONDO:0017546 otar diseases +MONDO:0017546 rare diseases +MONDO:0017547 gard_rare diseases +MONDO:0017547 nord_rare diseases +MONDO:0017547 ordo_subtype_of_a_disorder diseases +MONDO:0017547 otar diseases +MONDO:0017547 rare diseases +MONDO:0017548 gard_rare diseases +MONDO:0017548 rare diseases +MONDO:0017549 gard_rare diseases +MONDO:0017549 rare diseases +MONDO:0017550 gard_rare diseases +MONDO:0017550 rare diseases +MONDO:0017551 gard_rare diseases +MONDO:0017551 rare diseases +MONDO:0017552 gard_rare diseases +MONDO:0017552 nord_rare diseases +MONDO:0017552 ordo_subtype_of_a_disorder diseases +MONDO:0017552 rare diseases +MONDO:0017553 gard_rare diseases +MONDO:0017553 nord_rare diseases +MONDO:0017553 ordo_subtype_of_a_disorder diseases +MONDO:0017553 rare diseases +MONDO:0017554 gard_rare diseases +MONDO:0017554 nord_rare diseases +MONDO:0017554 ordo_subtype_of_a_disorder diseases +MONDO:0017554 rare diseases +MONDO:0017555 gard_rare diseases +MONDO:0017555 nord_rare diseases +MONDO:0017555 ordo_subtype_of_a_disorder diseases +MONDO:0017555 rare diseases +MONDO:0017556 gard_rare diseases +MONDO:0017556 rare diseases +MONDO:0017557 gard_rare diseases +MONDO:0017557 rare diseases +MONDO:0017558 gard_rare diseases +MONDO:0017558 nord_rare diseases +MONDO:0017558 ordo_subtype_of_a_disorder diseases +MONDO:0017558 rare diseases +MONDO:0017559 gard_rare diseases +MONDO:0017559 nord_rare diseases +MONDO:0017559 ordo_subtype_of_a_disorder diseases +MONDO:0017559 rare diseases +MONDO:0017560 gard_rare diseases +MONDO:0017560 nord_rare diseases +MONDO:0017560 ordo_subtype_of_a_disorder diseases +MONDO:0017560 rare diseases +MONDO:0017561 gard_rare diseases +MONDO:0017561 nord_rare diseases +MONDO:0017561 ordo_subtype_of_a_disorder diseases +MONDO:0017561 rare diseases +MONDO:0017562 gard_rare diseases +MONDO:0017562 rare diseases +MONDO:0017563 gard_rare diseases +MONDO:0017563 rare diseases +MONDO:0017564 gard_rare diseases +MONDO:0017564 nord_rare diseases +MONDO:0017564 ordo_subtype_of_a_disorder diseases +MONDO:0017564 rare diseases +MONDO:0017565 gard_rare diseases +MONDO:0017565 nord_rare diseases +MONDO:0017565 ordo_subtype_of_a_disorder diseases +MONDO:0017565 rare diseases +MONDO:0017566 gard_rare diseases +MONDO:0017566 nord_rare diseases +MONDO:0017566 ordo_subtype_of_a_disorder diseases +MONDO:0017566 rare diseases +MONDO:0017567 gard_rare diseases +MONDO:0017567 nord_rare diseases +MONDO:0017567 ordo_subtype_of_a_disorder diseases +MONDO:0017567 rare diseases +MONDO:0017568 gard_rare diseases +MONDO:0017568 ordo_disorder diseases +MONDO:0017568 ordo_malformation_syndrome diseases +MONDO:0017568 orphanet_rare diseases +MONDO:0017568 otar diseases +MONDO:0017568 rare diseases +MONDO:0017569 gard_rare diseases +MONDO:0017569 nord_rare diseases +MONDO:0017569 ordo_disorder diseases +MONDO:0017569 orphanet_rare diseases +MONDO:0017569 otar diseases +MONDO:0017569 rare diseases +MONDO:0017570 gard_rare diseases +MONDO:0017570 nord_rare diseases +MONDO:0017570 ordo_disorder diseases +MONDO:0017570 orphanet_rare diseases +MONDO:0017570 otar diseases +MONDO:0017570 rare diseases +MONDO:0017571 gard_rare diseases +MONDO:0017571 nord_rare diseases +MONDO:0017571 ordo_disorder diseases +MONDO:0017571 orphanet_rare diseases +MONDO:0017571 otar diseases +MONDO:0017571 rare diseases +MONDO:0017572 gard_rare diseases +MONDO:0017572 nord_rare diseases +MONDO:0017572 ordo_disorder diseases +MONDO:0017572 orphanet_rare diseases +MONDO:0017572 otar diseases +MONDO:0017572 rare diseases +MONDO:0017573 gard_rare diseases +MONDO:0017573 nord_rare diseases +MONDO:0017573 ordo_disorder diseases +MONDO:0017573 ordo_malformation_syndrome diseases +MONDO:0017573 orphanet_rare diseases +MONDO:0017573 rare diseases +MONDO:0017574 gard_rare diseases +MONDO:0017574 nord_rare diseases +MONDO:0017574 ordo_clinical_syndrome diseases +MONDO:0017574 ordo_disorder diseases +MONDO:0017574 orphanet_rare diseases +MONDO:0017574 otar diseases +MONDO:0017574 rare diseases +MONDO:0017575 gard_rare diseases +MONDO:0017575 nord_rare diseases +MONDO:0017575 ordo_disorder diseases +MONDO:0017575 orphanet_rare diseases +MONDO:0017575 otar diseases +MONDO:0017575 rare diseases +MONDO:0017576 disease_grouping diseases +MONDO:0017576 gard_rare diseases +MONDO:0017576 ordo_group_of_disorders diseases +MONDO:0017576 otar diseases +MONDO:0017576 rare diseases +MONDO:0017577 gard_rare diseases +MONDO:0017577 nord_rare diseases +MONDO:0017577 ordo_disorder diseases +MONDO:0017577 orphanet_rare diseases +MONDO:0017577 rare diseases +MONDO:0017578 disease_grouping diseases +MONDO:0017578 gard_rare diseases +MONDO:0017578 ordo_group_of_disorders diseases +MONDO:0017578 rare diseases +MONDO:0017579 clingen diseases +MONDO:0017579 gard_rare diseases +MONDO:0017579 nord_rare diseases +MONDO:0017579 ordo_disorder diseases +MONDO:0017579 ordo_malformation_syndrome diseases +MONDO:0017579 orphanet_rare diseases +MONDO:0017579 otar diseases +MONDO:0017579 rare diseases +MONDO:0017580 gard_rare diseases +MONDO:0017580 nord_rare diseases +MONDO:0017580 ordo_disorder diseases +MONDO:0017580 ordo_malformation_syndrome diseases +MONDO:0017580 orphanet_rare diseases +MONDO:0017580 rare diseases +MONDO:0017582 gard_rare diseases +MONDO:0017582 nord_rare diseases +MONDO:0017582 ordo_disorder diseases +MONDO:0017582 orphanet_rare diseases +MONDO:0017582 otar diseases +MONDO:0017582 rare diseases +MONDO:0017583 gard_rare diseases +MONDO:0017583 nord_rare diseases +MONDO:0017583 ordo_disorder diseases +MONDO:0017583 ordo_malformation_syndrome diseases +MONDO:0017583 orphanet_rare diseases +MONDO:0017583 otar diseases +MONDO:0017583 rare diseases +MONDO:0017584 gard_rare diseases +MONDO:0017584 nord_rare diseases +MONDO:0017584 ordo_clinical_situation diseases +MONDO:0017584 ordo_disorder diseases +MONDO:0017584 orphanet_rare diseases +MONDO:0017584 rare diseases +MONDO:0017585 gard_rare diseases +MONDO:0017585 nord_rare diseases +MONDO:0017585 ordo_disorder diseases +MONDO:0017585 orphanet_rare diseases +MONDO:0017585 rare diseases +MONDO:0017586 gard_rare diseases +MONDO:0017586 nord_rare diseases +MONDO:0017586 ordo_disorder diseases +MONDO:0017586 orphanet_rare diseases +MONDO:0017586 rare diseases +MONDO:0017587 gard_rare diseases +MONDO:0017587 nord_rare diseases +MONDO:0017587 ordo_disorder diseases +MONDO:0017587 orphanet_rare diseases +MONDO:0017587 rare diseases +MONDO:0017588 disease_grouping diseases +MONDO:0017588 gard_rare diseases +MONDO:0017588 ordo_group_of_disorders diseases +MONDO:0017588 rare diseases +MONDO:0017589 gard_rare diseases +MONDO:0017589 nord_rare diseases +MONDO:0017589 ordo_disorder diseases +MONDO:0017589 orphanet_rare diseases +MONDO:0017589 rare diseases +MONDO:0017590 gard_rare diseases +MONDO:0017590 nord_rare diseases +MONDO:0017590 ordo_disorder diseases +MONDO:0017590 orphanet_rare diseases +MONDO:0017590 otar diseases +MONDO:0017590 rare diseases +MONDO:0017591 gard_rare diseases +MONDO:0017591 nord_rare diseases +MONDO:0017591 ordo_disorder diseases +MONDO:0017591 orphanet_rare diseases +MONDO:0017591 rare diseases +MONDO:0017592 disease_grouping diseases +MONDO:0017592 gard_rare diseases +MONDO:0017592 ordo_group_of_disorders diseases +MONDO:0017592 otar diseases +MONDO:0017592 rare diseases +MONDO:0017593 gard_rare diseases +MONDO:0017593 nord_rare diseases +MONDO:0017593 ordo_disorder diseases +MONDO:0017593 orphanet_rare diseases +MONDO:0017593 otar diseases +MONDO:0017593 rare diseases +MONDO:0017594 disease_grouping diseases +MONDO:0017594 gard_rare diseases +MONDO:0017594 ordo_group_of_disorders diseases +MONDO:0017594 otar diseases +MONDO:0017594 rare diseases +MONDO:0017595 disease_grouping diseases +MONDO:0017595 gard_rare diseases +MONDO:0017595 nord_rare diseases +MONDO:0017595 ordo_group_of_disorders diseases +MONDO:0017595 rare diseases +MONDO:0017596 gard_rare diseases +MONDO:0017596 nord_rare diseases +MONDO:0017596 ordo_disorder diseases +MONDO:0017596 orphanet_rare diseases +MONDO:0017596 otar diseases +MONDO:0017596 rare diseases +MONDO:0017597 gard_rare diseases +MONDO:0017597 nord_rare diseases +MONDO:0017597 ordo_disorder diseases +MONDO:0017597 orphanet_rare diseases +MONDO:0017597 rare diseases +MONDO:0017598 gard_rare diseases +MONDO:0017598 nord_rare diseases +MONDO:0017598 ordo_disorder diseases +MONDO:0017598 orphanet_rare diseases +MONDO:0017598 rare diseases +MONDO:0017599 gard_rare diseases +MONDO:0017599 nord_rare diseases +MONDO:0017599 ordo_disorder diseases +MONDO:0017599 orphanet_rare diseases +MONDO:0017599 otar diseases +MONDO:0017599 rare diseases +MONDO:0017600 gard_rare diseases +MONDO:0017600 nord_rare diseases +MONDO:0017600 ordo_disorder diseases +MONDO:0017600 orphanet_rare diseases +MONDO:0017600 rare diseases +MONDO:0017601 gard_rare diseases +MONDO:0017601 nord_rare diseases +MONDO:0017601 ordo_disorder diseases +MONDO:0017601 orphanet_rare diseases +MONDO:0017601 rare diseases +MONDO:0017602 gard_rare diseases +MONDO:0017602 nord_rare diseases +MONDO:0017602 ordo_histopathological_subtype diseases +MONDO:0017602 ordo_subtype_of_a_disorder diseases +MONDO:0017602 rare diseases +MONDO:0017603 gard_rare diseases +MONDO:0017603 nord_rare diseases +MONDO:0017603 ordo_histopathological_subtype diseases +MONDO:0017603 ordo_subtype_of_a_disorder diseases +MONDO:0017603 otar diseases +MONDO:0017603 rare diseases +MONDO:0017604 disease_grouping diseases +MONDO:0017604 gard_rare diseases +MONDO:0017604 nord_rare diseases +MONDO:0017604 ordo_group_of_disorders diseases +MONDO:0017604 otar diseases +MONDO:0017604 rare diseases +MONDO:0017607 gard_rare diseases +MONDO:0017607 nord_rare diseases +MONDO:0017607 ordo_disorder diseases +MONDO:0017607 ordo_malformation_syndrome diseases +MONDO:0017607 orphanet_rare diseases +MONDO:0017607 otar diseases +MONDO:0017607 rare diseases +MONDO:0017609 gard_rare diseases +MONDO:0017609 nord_rare diseases +MONDO:0017609 ordo_disorder diseases +MONDO:0017609 ordo_malformation_syndrome diseases +MONDO:0017609 orphanet_rare diseases +MONDO:0017609 otar diseases +MONDO:0017609 rare diseases +MONDO:0017610 disease_grouping diseases +MONDO:0017610 gard_rare diseases +MONDO:0017610 nord_rare diseases +MONDO:0017610 ordo_group_of_disorders diseases +MONDO:0017610 otar diseases +MONDO:0017610 rare diseases +MONDO:0017611 disease_grouping diseases +MONDO:0017611 gard_rare diseases +MONDO:0017611 nord_rare diseases +MONDO:0017611 ordo_group_of_disorders diseases +MONDO:0017611 otar diseases +MONDO:0017611 rare diseases +MONDO:0017612 disease_grouping diseases +MONDO:0017612 gard_rare diseases +MONDO:0017612 nord_rare diseases +MONDO:0017612 ordo_group_of_disorders diseases +MONDO:0017612 otar diseases +MONDO:0017612 rare diseases +MONDO:0017614 gard_rare diseases +MONDO:0017614 ordo_disorder diseases +MONDO:0017614 ordo_malformation_syndrome diseases +MONDO:0017614 orphanet_rare diseases +MONDO:0017614 otar diseases +MONDO:0017614 rare diseases +MONDO:0017615 clingen diseases +MONDO:0017615 gard_rare diseases +MONDO:0017615 nord_rare diseases +MONDO:0017615 ordo_disorder diseases +MONDO:0017615 orphanet_rare diseases +MONDO:0017615 otar diseases +MONDO:0017615 rare diseases +MONDO:0017616 gard_rare diseases +MONDO:0017616 nord_rare diseases +MONDO:0017616 rare diseases +MONDO:0017617 gard_rare diseases +MONDO:0017617 nord_rare diseases +MONDO:0017617 ordo_disorder diseases +MONDO:0017617 orphanet_rare diseases +MONDO:0017617 rare diseases +MONDO:0017618 gard_rare diseases +MONDO:0017618 rare diseases +MONDO:0017619 gard_rare diseases +MONDO:0017619 rare diseases +MONDO:0017620 gard_rare diseases +MONDO:0017620 rare diseases +MONDO:0017621 gard_rare diseases +MONDO:0017621 rare diseases +MONDO:0017622 gard_rare diseases +MONDO:0017622 rare diseases +MONDO:0017623 clingen diseases +MONDO:0017623 disease_grouping diseases +MONDO:0017623 gard_rare diseases +MONDO:0017623 nord_rare diseases +MONDO:0017623 ordo_group_of_disorders diseases +MONDO:0017623 otar diseases +MONDO:0017623 rare diseases +MONDO:0017624 disease_grouping diseases +MONDO:0017624 gard_rare diseases +MONDO:0017624 nord_rare diseases +MONDO:0017624 ordo_disorder diseases +MONDO:0017624 orphanet_rare diseases +MONDO:0017624 otar diseases +MONDO:0017624 rare diseases +MONDO:0017625 disease_grouping diseases +MONDO:0017625 gard_rare diseases +MONDO:0017625 nord_rare diseases +MONDO:0017625 rare diseases +MONDO:0017626 disease_grouping diseases +MONDO:0017626 gard_rare diseases +MONDO:0017626 rare diseases +MONDO:0017627 gard_rare diseases +MONDO:0017627 nord_rare diseases +MONDO:0017627 ordo_disorder diseases +MONDO:0017627 ordo_morphological_anomaly diseases +MONDO:0017627 orphanet_rare diseases +MONDO:0017627 otar diseases +MONDO:0017627 rare diseases +MONDO:0017628 gard_rare diseases +MONDO:0017628 nord_rare diseases +MONDO:0017628 ordo_disorder diseases +MONDO:0017628 orphanet_rare diseases +MONDO:0017628 rare diseases +MONDO:0017630 gard_rare diseases +MONDO:0017630 nord_rare diseases +MONDO:0017630 ordo_subtype_of_a_disorder diseases +MONDO:0017630 otar diseases +MONDO:0017630 rare diseases +MONDO:0017634 disease_grouping diseases +MONDO:0017634 gard_rare diseases +MONDO:0017634 ordo_group_of_disorders diseases +MONDO:0017634 otar diseases +MONDO:0017634 rare diseases +MONDO:0017636 gard_rare diseases +MONDO:0017636 nord_rare diseases +MONDO:0017636 ordo_disorder diseases +MONDO:0017636 orphanet_rare diseases +MONDO:0017636 otar diseases +MONDO:0017636 rare diseases +MONDO:0017638 gard_rare diseases +MONDO:0017638 nord_rare diseases +MONDO:0017638 ordo_disorder diseases +MONDO:0017638 orphanet_rare diseases +MONDO:0017638 otar diseases +MONDO:0017638 rare diseases +MONDO:0017639 gard_rare diseases +MONDO:0017639 nord_rare diseases +MONDO:0017639 ordo_disorder diseases +MONDO:0017639 orphanet_rare diseases +MONDO:0017639 rare diseases +MONDO:0017640 gard_rare diseases +MONDO:0017640 nord_rare diseases +MONDO:0017640 ordo_disorder diseases +MONDO:0017640 orphanet_rare diseases +MONDO:0017640 rare diseases +MONDO:0017642 ordo_malformation_syndrome diseases +MONDO:0017648 gard_rare diseases +MONDO:0017648 nord_rare diseases +MONDO:0017648 ordo_clinical_situation diseases +MONDO:0017648 ordo_disorder diseases +MONDO:0017648 orphanet_rare diseases +MONDO:0017648 rare diseases +MONDO:0017649 gard_rare diseases +MONDO:0017649 nord_rare diseases +MONDO:0017649 ordo_disorder diseases +MONDO:0017649 orphanet_rare diseases +MONDO:0017649 rare diseases +MONDO:0017658 disease_grouping diseases +MONDO:0017658 gard_rare diseases +MONDO:0017658 ordo_group_of_disorders diseases +MONDO:0017658 otar diseases +MONDO:0017658 rare diseases +MONDO:0017659 gard_rare diseases +MONDO:0017659 nord_rare diseases +MONDO:0017659 ordo_disorder diseases +MONDO:0017659 orphanet_rare diseases +MONDO:0017659 rare diseases +MONDO:0017666 disease_grouping diseases +MONDO:0017666 gard_rare diseases +MONDO:0017666 ordo_group_of_disorders diseases +MONDO:0017666 otar diseases +MONDO:0017666 rare diseases +MONDO:0017668 gard_rare diseases +MONDO:0017668 ordo_disorder diseases +MONDO:0017668 ordo_malformation_syndrome diseases +MONDO:0017668 orphanet_rare diseases +MONDO:0017668 otar diseases +MONDO:0017668 rare diseases +MONDO:0017672 disease_grouping diseases +MONDO:0017672 gard_rare diseases +MONDO:0017672 ordo_group_of_disorders diseases +MONDO:0017672 otar diseases +MONDO:0017672 rare diseases +MONDO:0017675 disease_grouping diseases +MONDO:0017675 gard_rare diseases +MONDO:0017675 nord_rare diseases +MONDO:0017675 ordo_group_of_disorders diseases +MONDO:0017675 otar diseases +MONDO:0017675 rare diseases +MONDO:0017677 gard_rare diseases +MONDO:0017677 nord_rare diseases +MONDO:0017677 ordo_disorder diseases +MONDO:0017677 orphanet_rare diseases +MONDO:0017677 rare diseases +MONDO:0017682 gard_rare diseases +MONDO:0017682 ordo_disorder diseases +MONDO:0017682 ordo_malformation_syndrome diseases +MONDO:0017682 orphanet_rare diseases +MONDO:0017682 otar diseases +MONDO:0017682 rare diseases +MONDO:0017683 gard_rare diseases +MONDO:0017683 nord_rare diseases +MONDO:0017683 ordo_subtype_of_a_disorder diseases +MONDO:0017683 otar diseases +MONDO:0017683 rare diseases +MONDO:0017684 disease_grouping diseases +MONDO:0017684 gard_rare diseases +MONDO:0017684 ordo_group_of_disorders diseases +MONDO:0017684 rare diseases +MONDO:0017685 gard_rare diseases +MONDO:0017685 nord_rare diseases +MONDO:0017685 ordo_subtype_of_a_disorder diseases +MONDO:0017685 otar diseases +MONDO:0017685 rare diseases +MONDO:0017686 disease_grouping diseases +MONDO:0017686 gard_rare diseases +MONDO:0017686 ordo_group_of_disorders diseases +MONDO:0017686 rare diseases +MONDO:0017687 disease_grouping diseases +MONDO:0017687 gard_rare diseases +MONDO:0017687 ordo_group_of_disorders diseases +MONDO:0017687 rare diseases +MONDO:0017688 disease_grouping diseases +MONDO:0017688 gard_rare diseases +MONDO:0017688 ordo_group_of_disorders diseases +MONDO:0017688 rare diseases +MONDO:0017689 disease_grouping diseases +MONDO:0017689 gard_rare diseases +MONDO:0017689 ordo_group_of_disorders diseases +MONDO:0017689 otar diseases +MONDO:0017689 rare diseases +MONDO:0017690 disease_grouping diseases +MONDO:0017690 gard_rare diseases +MONDO:0017690 ordo_group_of_disorders diseases +MONDO:0017690 otar diseases +MONDO:0017690 rare diseases +MONDO:0017691 gard_rare diseases +MONDO:0017691 nord_rare diseases +MONDO:0017691 ordo_subtype_of_a_disorder diseases +MONDO:0017691 otar diseases +MONDO:0017691 rare diseases +MONDO:0017692 gard_rare diseases +MONDO:0017692 nord_rare diseases +MONDO:0017692 ordo_subtype_of_a_disorder diseases +MONDO:0017692 otar diseases +MONDO:0017692 rare diseases +MONDO:0017694 gard_rare diseases +MONDO:0017694 nord_rare diseases +MONDO:0017694 ordo_subtype_of_a_disorder diseases +MONDO:0017694 otar diseases +MONDO:0017694 rare diseases +MONDO:0017695 gard_rare diseases +MONDO:0017695 nord_rare diseases +MONDO:0017695 ordo_subtype_of_a_disorder diseases +MONDO:0017695 otar diseases +MONDO:0017695 rare diseases +MONDO:0017696 gard_rare diseases +MONDO:0017696 nord_rare diseases +MONDO:0017696 ordo_subtype_of_a_disorder diseases +MONDO:0017696 otar diseases +MONDO:0017696 rare diseases +MONDO:0017697 gard_rare diseases +MONDO:0017697 nord_rare diseases +MONDO:0017697 ordo_subtype_of_a_disorder diseases +MONDO:0017697 otar diseases +MONDO:0017697 rare diseases +MONDO:0017698 gard_rare diseases +MONDO:0017698 nord_rare diseases +MONDO:0017698 ordo_subtype_of_a_disorder diseases +MONDO:0017698 otar diseases +MONDO:0017698 rare diseases +MONDO:0017699 gard_rare diseases +MONDO:0017699 nord_rare diseases +MONDO:0017699 ordo_subtype_of_a_disorder diseases +MONDO:0017699 otar diseases +MONDO:0017699 rare diseases +MONDO:0017700 gard_rare diseases +MONDO:0017700 nord_rare diseases +MONDO:0017700 ordo_subtype_of_a_disorder diseases +MONDO:0017700 otar diseases +MONDO:0017700 rare diseases +MONDO:0017701 gard_rare diseases +MONDO:0017701 nord_rare diseases +MONDO:0017701 ordo_subtype_of_a_disorder diseases +MONDO:0017701 otar diseases +MONDO:0017701 rare diseases +MONDO:0017703 disease_grouping diseases +MONDO:0017703 gard_rare diseases +MONDO:0017703 ordo_group_of_disorders diseases +MONDO:0017703 rare diseases +MONDO:0017704 disease_grouping diseases +MONDO:0017704 gard_rare diseases +MONDO:0017704 ordo_group_of_disorders diseases +MONDO:0017704 otar diseases +MONDO:0017704 rare diseases +MONDO:0017705 disease_grouping diseases +MONDO:0017705 gard_rare diseases +MONDO:0017705 nord_rare diseases +MONDO:0017705 ordo_group_of_disorders diseases +MONDO:0017705 otar diseases +MONDO:0017705 rare diseases +MONDO:0017706 disease_grouping diseases +MONDO:0017706 gard_rare diseases +MONDO:0017706 ordo_group_of_disorders diseases +MONDO:0017706 rare diseases +MONDO:0017708 disease_grouping diseases +MONDO:0017708 gard_rare diseases +MONDO:0017708 nord_rare diseases +MONDO:0017708 ordo_disorder diseases +MONDO:0017708 orphanet_rare diseases +MONDO:0017708 otar diseases +MONDO:0017708 rare diseases +MONDO:0017711 gard_rare diseases +MONDO:0017711 nord_rare diseases +MONDO:0017711 ordo_disorder diseases +MONDO:0017711 orphanet_rare diseases +MONDO:0017711 otar diseases +MONDO:0017711 rare diseases +MONDO:0017712 gard_rare diseases +MONDO:0017712 nord_rare diseases +MONDO:0017712 ordo_disorder diseases +MONDO:0017712 orphanet_rare diseases +MONDO:0017712 rare diseases +MONDO:0017713 disease_grouping diseases +MONDO:0017713 gard_rare diseases +MONDO:0017713 ordo_group_of_disorders diseases +MONDO:0017713 rare diseases +MONDO:0017714 disease_grouping diseases +MONDO:0017714 gard_rare diseases +MONDO:0017714 ordo_group_of_disorders diseases +MONDO:0017714 otar diseases +MONDO:0017714 rare diseases +MONDO:0017715 disease_grouping diseases +MONDO:0017715 gard_rare diseases +MONDO:0017715 ordo_group_of_disorders diseases +MONDO:0017715 otar diseases +MONDO:0017715 rare diseases +MONDO:0017716 disease_grouping diseases +MONDO:0017716 gard_rare diseases +MONDO:0017716 ordo_group_of_disorders diseases +MONDO:0017716 rare diseases +MONDO:0017719 disease_grouping diseases +MONDO:0017719 gard_rare diseases +MONDO:0017719 ordo_group_of_disorders diseases +MONDO:0017719 otar diseases +MONDO:0017719 rare diseases +MONDO:0017720 disease_grouping diseases +MONDO:0017720 gard_rare diseases +MONDO:0017720 nord_rare diseases +MONDO:0017720 ordo_group_of_disorders diseases +MONDO:0017720 otar diseases +MONDO:0017720 rare diseases +MONDO:0017721 gard_rare diseases +MONDO:0017721 nord_rare diseases +MONDO:0017721 ordo_subtype_of_a_disorder diseases +MONDO:0017721 otar diseases +MONDO:0017721 rare diseases +MONDO:0017722 gard_rare diseases +MONDO:0017722 nord_rare diseases +MONDO:0017722 ordo_subtype_of_a_disorder diseases +MONDO:0017722 otar diseases +MONDO:0017722 rare diseases +MONDO:0017723 gard_rare diseases +MONDO:0017723 nord_rare diseases +MONDO:0017723 ordo_subtype_of_a_disorder diseases +MONDO:0017723 otar diseases +MONDO:0017723 rare diseases +MONDO:0017724 gard_rare diseases +MONDO:0017724 nord_rare diseases +MONDO:0017724 ordo_subtype_of_a_disorder diseases +MONDO:0017724 otar diseases +MONDO:0017724 rare diseases +MONDO:0017725 gard_rare diseases +MONDO:0017725 nord_rare diseases +MONDO:0017725 ordo_subtype_of_a_disorder diseases +MONDO:0017725 otar diseases +MONDO:0017725 rare diseases +MONDO:0017726 gard_rare diseases +MONDO:0017726 nord_rare diseases +MONDO:0017726 ordo_subtype_of_a_disorder diseases +MONDO:0017726 otar diseases +MONDO:0017726 rare diseases +MONDO:0017727 gard_rare diseases +MONDO:0017727 nord_rare diseases +MONDO:0017727 ordo_disorder diseases +MONDO:0017727 ordo_morphological_anomaly diseases +MONDO:0017727 orphanet_rare diseases +MONDO:0017727 rare diseases +MONDO:0017728 gard_rare diseases +MONDO:0017728 nord_rare diseases +MONDO:0017728 otar diseases +MONDO:0017728 rare diseases +MONDO:0017729 gard_rare diseases +MONDO:0017729 nord_rare diseases +MONDO:0017729 ordo_subtype_of_a_disorder diseases +MONDO:0017729 otar diseases +MONDO:0017729 rare diseases +MONDO:0017730 gard_rare diseases +MONDO:0017730 nord_rare diseases +MONDO:0017730 ordo_subtype_of_a_disorder diseases +MONDO:0017730 otar diseases +MONDO:0017730 rare diseases +MONDO:0017731 disease_grouping diseases +MONDO:0017731 gard_rare diseases +MONDO:0017731 ordo_group_of_disorders diseases +MONDO:0017731 rare diseases +MONDO:0017732 gard_rare diseases +MONDO:0017732 nord_rare diseases +MONDO:0017732 ordo_subtype_of_a_disorder diseases +MONDO:0017732 otar diseases +MONDO:0017732 rare diseases +MONDO:0017733 gard_rare diseases +MONDO:0017733 nord_rare diseases +MONDO:0017733 ordo_subtype_of_a_disorder diseases +MONDO:0017733 otar diseases +MONDO:0017733 rare diseases +MONDO:0017734 clingen diseases +MONDO:0017734 disease_grouping diseases +MONDO:0017734 gard_rare diseases +MONDO:0017734 ordo_group_of_disorders diseases +MONDO:0017734 otar diseases +MONDO:0017734 rare diseases +MONDO:0017735 gard_rare diseases +MONDO:0017735 nord_rare diseases +MONDO:0017735 ordo_disorder diseases +MONDO:0017735 ordo_morphological_anomaly diseases +MONDO:0017735 orphanet_rare diseases +MONDO:0017735 rare diseases +MONDO:0017736 disease_grouping diseases +MONDO:0017736 gard_rare diseases +MONDO:0017736 ordo_group_of_disorders diseases +MONDO:0017736 rare diseases +MONDO:0017737 gard_rare diseases +MONDO:0017737 nord_rare diseases +MONDO:0017737 ordo_subtype_of_a_disorder diseases +MONDO:0017737 otar diseases +MONDO:0017737 rare diseases +MONDO:0017738 disease_grouping diseases +MONDO:0017738 gard_rare diseases +MONDO:0017738 ordo_group_of_disorders diseases +MONDO:0017738 otar diseases +MONDO:0017738 rare diseases +MONDO:0017739 disease_grouping diseases +MONDO:0017739 gard_rare diseases +MONDO:0017739 ordo_group_of_disorders diseases +MONDO:0017739 rare diseases +MONDO:0017740 disease_grouping diseases +MONDO:0017740 gard_rare diseases +MONDO:0017740 ordo_group_of_disorders diseases +MONDO:0017740 rare diseases +MONDO:0017741 disease_grouping diseases +MONDO:0017741 gard_rare diseases +MONDO:0017741 ordo_group_of_disorders diseases +MONDO:0017741 rare diseases +MONDO:0017746 gard_rare diseases +MONDO:0017746 nord_rare diseases +MONDO:0017746 ordo_disorder diseases +MONDO:0017746 orphanet_rare diseases +MONDO:0017746 otar diseases +MONDO:0017746 rare diseases +MONDO:0017747 disease_grouping diseases +MONDO:0017747 gard_rare diseases +MONDO:0017747 ordo_group_of_disorders diseases +MONDO:0017747 rare diseases +MONDO:0017748 disease_grouping diseases +MONDO:0017748 gard_rare diseases +MONDO:0017748 ordo_group_of_disorders diseases +MONDO:0017748 rare diseases +MONDO:0017749 disease_grouping diseases +MONDO:0017749 gard_rare diseases +MONDO:0017749 ordo_group_of_disorders diseases +MONDO:0017749 rare diseases +MONDO:0017750 disease_grouping diseases +MONDO:0017750 gard_rare diseases +MONDO:0017750 ordo_group_of_disorders diseases +MONDO:0017750 rare diseases +MONDO:0017752 disease_grouping diseases +MONDO:0017752 gard_rare diseases +MONDO:0017752 ordo_group_of_disorders diseases +MONDO:0017752 rare diseases +MONDO:0017754 disease_grouping diseases +MONDO:0017754 gard_rare diseases +MONDO:0017754 ordo_group_of_disorders diseases +MONDO:0017754 rare diseases +MONDO:0017755 disease_grouping diseases +MONDO:0017755 gard_rare diseases +MONDO:0017755 ordo_group_of_disorders diseases +MONDO:0017755 rare diseases +MONDO:0017757 disease_grouping diseases +MONDO:0017757 gard_rare diseases +MONDO:0017757 ordo_group_of_disorders diseases +MONDO:0017757 otar diseases +MONDO:0017757 rare diseases +MONDO:0017758 disease_grouping diseases +MONDO:0017758 gard_rare diseases +MONDO:0017758 ordo_group_of_disorders diseases +MONDO:0017758 rare diseases +MONDO:0017759 disease_grouping diseases +MONDO:0017759 gard_rare diseases +MONDO:0017759 ordo_group_of_disorders diseases +MONDO:0017759 rare diseases +MONDO:0017761 disease_grouping diseases +MONDO:0017761 gard_rare diseases +MONDO:0017761 ordo_group_of_disorders diseases +MONDO:0017761 rare diseases +MONDO:0017762 disease_grouping diseases +MONDO:0017762 gard_rare diseases +MONDO:0017762 ordo_group_of_disorders diseases +MONDO:0017762 otar diseases +MONDO:0017762 rare diseases +MONDO:0017763 disease_grouping diseases +MONDO:0017763 gard_rare diseases +MONDO:0017763 ordo_group_of_disorders diseases +MONDO:0017763 rare diseases +MONDO:0017764 disease_grouping diseases +MONDO:0017764 gard_rare diseases +MONDO:0017764 ordo_group_of_disorders diseases +MONDO:0017764 otar diseases +MONDO:0017764 rare diseases +MONDO:0017765 disease_grouping diseases +MONDO:0017765 gard_rare diseases +MONDO:0017765 ordo_group_of_disorders diseases +MONDO:0017765 rare diseases +MONDO:0017766 disease_grouping diseases +MONDO:0017766 gard_rare diseases +MONDO:0017766 ordo_group_of_disorders diseases +MONDO:0017766 otar diseases +MONDO:0017766 rare diseases +MONDO:0017767 gard_rare diseases +MONDO:0017767 nord_rare diseases +MONDO:0017767 ordo_disorder diseases +MONDO:0017767 orphanet_rare diseases +MONDO:0017767 otar diseases +MONDO:0017767 rare diseases +MONDO:0017768 disease_grouping diseases +MONDO:0017768 gard_rare diseases +MONDO:0017768 ordo_group_of_disorders diseases +MONDO:0017768 otar diseases +MONDO:0017768 rare diseases +MONDO:0017769 disease_grouping diseases +MONDO:0017769 gard_rare diseases +MONDO:0017769 ordo_group_of_disorders diseases +MONDO:0017769 otar diseases +MONDO:0017769 rare diseases +MONDO:0017770 gard_rare diseases +MONDO:0017770 ordo_malformation_syndrome diseases +MONDO:0017770 otar diseases +MONDO:0017770 rare diseases +MONDO:0017771 gard_rare diseases +MONDO:0017771 nord_rare diseases +MONDO:0017771 ordo_disorder diseases +MONDO:0017771 ordo_malformation_syndrome diseases +MONDO:0017771 orphanet_rare diseases +MONDO:0017771 otar diseases +MONDO:0017771 rare diseases +MONDO:0017773 disease_grouping diseases +MONDO:0017773 gard_rare diseases +MONDO:0017773 ordo_group_of_disorders diseases +MONDO:0017773 otar diseases +MONDO:0017773 rare diseases +MONDO:0017774 disease_grouping diseases +MONDO:0017774 gard_rare diseases +MONDO:0017774 nord_rare diseases +MONDO:0017774 ordo_group_of_disorders diseases +MONDO:0017774 otar diseases +MONDO:0017774 rare diseases +MONDO:0017775 gard_rare diseases +MONDO:0017775 nord_rare diseases +MONDO:0017775 ordo_disorder diseases +MONDO:0017775 orphanet_rare diseases +MONDO:0017775 rare diseases +MONDO:0017776 gard_rare diseases +MONDO:0017776 nord_rare diseases +MONDO:0017776 ordo_disorder diseases +MONDO:0017776 orphanet_rare diseases +MONDO:0017776 otar diseases +MONDO:0017776 rare diseases +MONDO:0017778 gard_rare diseases +MONDO:0017778 nord_rare diseases +MONDO:0017778 ordo_disorder diseases +MONDO:0017778 orphanet_rare diseases +MONDO:0017778 otar diseases +MONDO:0017778 rare diseases +MONDO:0017779 clingen diseases +MONDO:0017779 gard_rare diseases +MONDO:0017779 nord_rare diseases +MONDO:0017779 ordo_disorder diseases +MONDO:0017779 orphanet_rare diseases +MONDO:0017779 otar diseases +MONDO:0017779 rare diseases +MONDO:0017780 gard_rare diseases +MONDO:0017780 nord_rare diseases +MONDO:0017780 ordo_disorder diseases +MONDO:0017780 ordo_malformation_syndrome diseases +MONDO:0017780 orphanet_rare diseases +MONDO:0017780 otar diseases +MONDO:0017780 rare diseases +MONDO:0017781 gard_rare diseases +MONDO:0017781 nord_rare diseases +MONDO:0017781 ordo_malformation_syndrome diseases +MONDO:0017781 ordo_subtype_of_a_disorder diseases +MONDO:0017781 rare diseases +MONDO:0017782 gard_rare diseases +MONDO:0017782 nord_rare diseases +MONDO:0017782 ordo_subtype_of_a_disorder diseases +MONDO:0017782 otar diseases +MONDO:0017782 rare diseases +MONDO:0017783 gard_rare diseases +MONDO:0017783 nord_rare diseases +MONDO:0017783 ordo_disorder diseases +MONDO:0017783 ordo_morphological_anomaly diseases +MONDO:0017783 orphanet_rare diseases +MONDO:0017783 rare diseases +MONDO:0017784 gard_rare diseases +MONDO:0017784 nord_rare diseases +MONDO:0017784 ordo_disorder diseases +MONDO:0017784 orphanet_rare diseases +MONDO:0017784 rare diseases +MONDO:0017785 gard_rare diseases +MONDO:0017785 nord_rare diseases +MONDO:0017785 ordo_disorder diseases +MONDO:0017785 orphanet_rare diseases +MONDO:0017785 rare diseases +MONDO:0017786 gard_rare diseases +MONDO:0017786 nord_rare diseases +MONDO:0017786 ordo_disorder diseases +MONDO:0017786 ordo_malformation_syndrome diseases +MONDO:0017786 orphanet_rare diseases +MONDO:0017786 rare diseases +MONDO:0017787 gard_rare diseases +MONDO:0017787 nord_rare diseases +MONDO:0017787 ordo_disorder diseases +MONDO:0017787 orphanet_rare diseases +MONDO:0017787 otar diseases +MONDO:0017787 rare diseases +MONDO:0017788 gard_rare diseases +MONDO:0017788 nord_rare diseases +MONDO:0017788 ordo_disorder diseases +MONDO:0017788 ordo_malformation_syndrome diseases +MONDO:0017788 orphanet_rare diseases +MONDO:0017788 rare diseases +MONDO:0017789 gard_rare diseases +MONDO:0017789 nord_rare diseases +MONDO:0017789 ordo_disorder diseases +MONDO:0017789 orphanet_rare diseases +MONDO:0017789 rare diseases +MONDO:0017790 clingen diseases +MONDO:0017790 gard_rare diseases +MONDO:0017790 n_of_one diseases +MONDO:0017790 nord_rare diseases +MONDO:0017790 ordo_disorder diseases +MONDO:0017790 orphanet_rare diseases +MONDO:0017790 rare diseases +MONDO:0017791 gard_rare diseases +MONDO:0017791 nord_rare diseases +MONDO:0017791 ordo_disorder diseases +MONDO:0017791 orphanet_rare diseases +MONDO:0017791 otar diseases +MONDO:0017791 rare diseases +MONDO:0017792 gard_rare diseases +MONDO:0017792 nord_rare diseases +MONDO:0017792 ordo_disorder diseases +MONDO:0017792 ordo_malformation_syndrome diseases +MONDO:0017792 orphanet_rare diseases +MONDO:0017792 otar diseases +MONDO:0017792 rare diseases +MONDO:0017793 gard_rare diseases +MONDO:0017793 nord_rare diseases +MONDO:0017793 ordo_disorder diseases +MONDO:0017793 ordo_malformation_syndrome diseases +MONDO:0017793 orphanet_rare diseases +MONDO:0017793 rare diseases +MONDO:0017794 gard_rare diseases +MONDO:0017794 nord_rare diseases +MONDO:0017794 ordo_disorder diseases +MONDO:0017794 ordo_malformation_syndrome diseases +MONDO:0017794 orphanet_rare diseases +MONDO:0017794 rare diseases +MONDO:0017795 gard_rare diseases +MONDO:0017795 nord_rare diseases +MONDO:0017795 ordo_disorder diseases +MONDO:0017795 orphanet_rare diseases +MONDO:0017795 otar diseases +MONDO:0017795 rare diseases +MONDO:0017798 gard_rare diseases +MONDO:0017798 nord_rare diseases +MONDO:0017798 ordo_disorder diseases +MONDO:0017798 ordo_malformation_syndrome diseases +MONDO:0017798 orphanet_rare diseases +MONDO:0017798 rare diseases +MONDO:0017799 gard_rare diseases +MONDO:0017799 nord_rare diseases +MONDO:0017799 ordo_clinical_syndrome diseases +MONDO:0017799 ordo_disorder diseases +MONDO:0017799 orphanet_rare diseases +MONDO:0017799 rare diseases +MONDO:0017800 gard_rare diseases +MONDO:0017800 nord_rare diseases +MONDO:0017800 ordo_clinical_syndrome diseases +MONDO:0017800 ordo_disorder diseases +MONDO:0017800 orphanet_rare diseases +MONDO:0017800 rare diseases +MONDO:0017801 gard_rare diseases +MONDO:0017801 nord_rare diseases +MONDO:0017801 ordo_clinical_syndrome diseases +MONDO:0017801 ordo_disorder diseases +MONDO:0017801 orphanet_rare diseases +MONDO:0017801 rare diseases +MONDO:0017802 gard_rare diseases +MONDO:0017802 nord_rare diseases +MONDO:0017802 ordo_disorder diseases +MONDO:0017802 orphanet_rare diseases +MONDO:0017802 rare diseases +MONDO:0017803 gard_rare diseases +MONDO:0017803 nord_rare diseases +MONDO:0017803 ordo_disorder diseases +MONDO:0017803 orphanet_rare diseases +MONDO:0017803 rare diseases +MONDO:0017804 gard_rare diseases +MONDO:0017804 nord_rare diseases +MONDO:0017804 ordo_disorder diseases +MONDO:0017804 orphanet_rare diseases +MONDO:0017804 rare diseases +MONDO:0017805 gard_rare diseases +MONDO:0017805 nord_rare diseases +MONDO:0017805 ordo_disorder diseases +MONDO:0017805 ordo_malformation_syndrome diseases +MONDO:0017805 orphanet_rare diseases +MONDO:0017805 otar diseases +MONDO:0017805 rare diseases +MONDO:0017806 gard_rare diseases +MONDO:0017806 nord_rare diseases +MONDO:0017806 ordo_disorder diseases +MONDO:0017806 ordo_malformation_syndrome diseases +MONDO:0017806 orphanet_rare diseases +MONDO:0017806 otar diseases +MONDO:0017806 rare diseases +MONDO:0017807 gard_rare diseases +MONDO:0017807 nord_rare diseases +MONDO:0017807 ordo_clinical_situation diseases +MONDO:0017807 ordo_disorder diseases +MONDO:0017807 orphanet_rare diseases +MONDO:0017807 rare diseases +MONDO:0017808 gard_rare diseases +MONDO:0017808 nord_rare diseases +MONDO:0017808 ordo_disorder diseases +MONDO:0017808 ordo_morphological_anomaly diseases +MONDO:0017808 orphanet_rare diseases +MONDO:0017808 otar diseases +MONDO:0017808 rare diseases +MONDO:0017809 gard_rare diseases +MONDO:0017809 nord_rare diseases +MONDO:0017809 ordo_disorder diseases +MONDO:0017809 orphanet_rare diseases +MONDO:0017809 otar diseases +MONDO:0017809 rare diseases +MONDO:0017810 gard_rare diseases +MONDO:0017810 nord_rare diseases +MONDO:0017810 ordo_disorder diseases +MONDO:0017810 orphanet_rare diseases +MONDO:0017810 otar diseases +MONDO:0017810 rare diseases +MONDO:0017811 gard_rare diseases +MONDO:0017811 nord_rare diseases +MONDO:0017811 ordo_subtype_of_a_disorder diseases +MONDO:0017811 otar diseases +MONDO:0017811 rare diseases +MONDO:0017812 gard_rare diseases +MONDO:0017812 nord_rare diseases +MONDO:0017812 ordo_disorder diseases +MONDO:0017812 orphanet_rare diseases +MONDO:0017812 rare diseases +MONDO:0017813 gard_rare diseases +MONDO:0017813 nord_rare diseases +MONDO:0017813 ordo_disorder diseases +MONDO:0017813 ordo_malformation_syndrome diseases +MONDO:0017813 orphanet_rare diseases +MONDO:0017813 otar diseases +MONDO:0017813 rare diseases +MONDO:0017814 gard_rare diseases +MONDO:0017814 nord_rare diseases +MONDO:0017814 ordo_disorder diseases +MONDO:0017814 orphanet_rare diseases +MONDO:0017814 otar diseases +MONDO:0017814 rare diseases +MONDO:0017815 gard_rare diseases +MONDO:0017815 nord_rare diseases +MONDO:0017815 ordo_etiological_subtype diseases +MONDO:0017815 ordo_subtype_of_a_disorder diseases +MONDO:0017815 rare diseases +MONDO:0017816 gard_rare diseases +MONDO:0017816 nord_rare diseases +MONDO:0017816 ordo_subtype_of_a_disorder diseases +MONDO:0017816 otar diseases +MONDO:0017816 rare diseases +MONDO:0017817 gard_rare diseases +MONDO:0017817 nord_rare diseases +MONDO:0017817 ordo_subtype_of_a_disorder diseases +MONDO:0017817 rare diseases +MONDO:0017818 gard_rare diseases +MONDO:0017818 nord_rare diseases +MONDO:0017818 ordo_disorder diseases +MONDO:0017818 orphanet_rare diseases +MONDO:0017818 otar diseases +MONDO:0017818 rare diseases +MONDO:0017819 gard_rare diseases +MONDO:0017819 ordo_subtype_of_a_disorder diseases +MONDO:0017819 otar diseases +MONDO:0017819 rare diseases +MONDO:0017822 disease_grouping diseases +MONDO:0017822 gard_rare diseases +MONDO:0017822 ordo_group_of_disorders diseases +MONDO:0017822 rare diseases +MONDO:0017823 gard_rare diseases +MONDO:0017823 nord_rare diseases +MONDO:0017823 ordo_disorder diseases +MONDO:0017823 orphanet_rare diseases +MONDO:0017823 rare diseases +MONDO:0017824 gard_rare diseases +MONDO:0017824 nord_rare diseases +MONDO:0017824 ordo_disorder diseases +MONDO:0017824 orphanet_rare diseases +MONDO:0017824 otar diseases +MONDO:0017824 rare diseases +MONDO:0017825 gard_rare diseases +MONDO:0017825 nord_rare diseases +MONDO:0017825 ordo_histopathological_subtype diseases +MONDO:0017825 ordo_subtype_of_a_disorder diseases +MONDO:0017825 rare diseases +MONDO:0017826 gard_rare diseases +MONDO:0017826 nord_rare diseases +MONDO:0017826 ordo_histopathological_subtype diseases +MONDO:0017826 ordo_subtype_of_a_disorder diseases +MONDO:0017826 rare diseases +MONDO:0017827 gard_rare diseases +MONDO:0017827 nord_rare diseases +MONDO:0017827 ordo_disorder diseases +MONDO:0017827 orphanet_rare diseases +MONDO:0017827 otar diseases +MONDO:0017827 rare diseases +MONDO:0017829 gard_rare diseases +MONDO:0017829 nord_rare diseases +MONDO:0017829 ordo_subtype_of_a_disorder diseases +MONDO:0017829 rare diseases +MONDO:0017830 gard_rare diseases +MONDO:0017830 nord_rare diseases +MONDO:0017830 ordo_subtype_of_a_disorder diseases +MONDO:0017830 otar diseases +MONDO:0017830 rare diseases +MONDO:0017831 gard_rare diseases +MONDO:0017831 nord_rare diseases +MONDO:0017831 ordo_subtype_of_a_disorder diseases +MONDO:0017831 otar diseases +MONDO:0017831 rare diseases +MONDO:0017832 gard_rare diseases +MONDO:0017832 nord_rare diseases +MONDO:0017832 rare diseases +MONDO:0017833 gard_rare diseases +MONDO:0017833 nord_rare diseases +MONDO:0017833 ordo_disorder diseases +MONDO:0017833 orphanet_rare diseases +MONDO:0017833 rare diseases +MONDO:0017834 gard_rare diseases +MONDO:0017834 nord_rare diseases +MONDO:0017834 ordo_disorder diseases +MONDO:0017834 orphanet_rare diseases +MONDO:0017834 rare diseases +MONDO:0017835 gard_rare diseases +MONDO:0017835 nord_rare diseases +MONDO:0017835 ordo_subtype_of_a_disorder diseases +MONDO:0017835 rare diseases +MONDO:0017836 gard_rare diseases +MONDO:0017836 nord_rare diseases +MONDO:0017836 ordo_disorder diseases +MONDO:0017836 orphanet_rare diseases +MONDO:0017836 rare diseases +MONDO:0017837 gard_rare diseases +MONDO:0017837 ordo_disorder diseases +MONDO:0017837 orphanet_rare diseases +MONDO:0017837 otar diseases +MONDO:0017837 rare diseases +MONDO:0017838 gard_rare diseases +MONDO:0017838 ordo_disorder diseases +MONDO:0017838 ordo_malformation_syndrome diseases +MONDO:0017838 orphanet_rare diseases +MONDO:0017838 otar diseases +MONDO:0017838 rare diseases +MONDO:0017839 gard_rare diseases +MONDO:0017839 nord_rare diseases +MONDO:0017839 ordo_subtype_of_a_disorder diseases +MONDO:0017839 otar diseases +MONDO:0017839 rare diseases +MONDO:0017840 gard_rare diseases +MONDO:0017840 nord_rare diseases +MONDO:0017840 ordo_subtype_of_a_disorder diseases +MONDO:0017840 otar diseases +MONDO:0017840 rare diseases +MONDO:0017842 gard_rare diseases +MONDO:0017842 nord_rare diseases +MONDO:0017842 ordo_disorder diseases +MONDO:0017842 orphanet_rare diseases +MONDO:0017842 otar diseases +MONDO:0017842 rare diseases +MONDO:0017843 gard_rare diseases +MONDO:0017843 nord_rare diseases +MONDO:0017843 ordo_disorder diseases +MONDO:0017843 ordo_malformation_syndrome diseases +MONDO:0017843 orphanet_rare diseases +MONDO:0017843 rare diseases +MONDO:0017844 gard_rare diseases +MONDO:0017844 nord_rare diseases +MONDO:0017844 ordo_disorder diseases +MONDO:0017844 orphanet_rare diseases +MONDO:0017844 otar diseases +MONDO:0017844 rare diseases +MONDO:0017845 disease_grouping diseases +MONDO:0017845 gard_rare diseases +MONDO:0017845 ordo_group_of_disorders diseases +MONDO:0017845 otar diseases +MONDO:0017845 rare diseases +MONDO:0017846 disease_grouping diseases +MONDO:0017846 gard_rare diseases +MONDO:0017846 ordo_group_of_disorders diseases +MONDO:0017846 otar diseases +MONDO:0017846 rare diseases +MONDO:0017847 disease_grouping diseases +MONDO:0017847 gard_rare diseases +MONDO:0017847 ordo_group_of_disorders diseases +MONDO:0017847 otar diseases +MONDO:0017847 rare diseases +MONDO:0017849 gard_rare diseases +MONDO:0017849 ordo_disorder diseases +MONDO:0017849 ordo_malformation_syndrome diseases +MONDO:0017849 orphanet_rare diseases +MONDO:0017849 rare diseases +MONDO:0017850 gard_rare diseases +MONDO:0017850 nord_rare diseases +MONDO:0017850 ordo_disorder diseases +MONDO:0017850 ordo_malformation_syndrome diseases +MONDO:0017850 orphanet_rare diseases +MONDO:0017850 otar diseases +MONDO:0017850 rare diseases +MONDO:0017851 clingen diseases +MONDO:0017851 disease_grouping diseases +MONDO:0017851 gard_rare diseases +MONDO:0017851 nord_rare diseases +MONDO:0017851 ordo_disorder diseases +MONDO:0017851 ordo_group_of_disorders diseases +MONDO:0017851 orphanet_rare diseases +MONDO:0017851 otar diseases +MONDO:0017851 rare diseases +MONDO:0017852 gard_rare diseases +MONDO:0017852 nord_rare diseases +MONDO:0017852 ordo_disorder diseases +MONDO:0017852 orphanet_rare diseases +MONDO:0017852 otar diseases +MONDO:0017852 rare diseases +MONDO:0017853 disease_grouping diseases +MONDO:0017853 gard_rare diseases +MONDO:0017853 nord_rare diseases +MONDO:0017853 ordo_group_of_disorders diseases +MONDO:0017853 otar diseases +MONDO:0017853 rare diseases +MONDO:0017855 disease_grouping diseases +MONDO:0017855 gard_rare diseases +MONDO:0017855 nord_rare diseases +MONDO:0017855 ordo_group_of_disorders diseases +MONDO:0017855 otar diseases +MONDO:0017855 rare diseases +MONDO:0017856 gard_rare diseases +MONDO:0017856 nord_rare diseases +MONDO:0017856 ordo_disorder diseases +MONDO:0017856 orphanet_rare diseases +MONDO:0017856 otar diseases +MONDO:0017856 rare diseases +MONDO:0017857 gard_rare diseases +MONDO:0017857 ordo_disorder diseases +MONDO:0017857 ordo_malformation_syndrome diseases +MONDO:0017857 orphanet_rare diseases +MONDO:0017857 otar diseases +MONDO:0017857 rare diseases +MONDO:0017858 gard_rare diseases +MONDO:0017858 nord_rare diseases +MONDO:0017858 ordo_disorder diseases +MONDO:0017858 orphanet_rare diseases +MONDO:0017858 otar diseases +MONDO:0017858 rare diseases +MONDO:0017859 nord_rare diseases +MONDO:0017859 ordo_clinical_situation diseases +MONDO:0017859 ordo_disorder diseases +MONDO:0017859 orphanet_rare diseases +MONDO:0017859 rare diseases +MONDO:0017860 gard_rare diseases +MONDO:0017860 nord_rare diseases +MONDO:0017860 ordo_disorder diseases +MONDO:0017860 orphanet_rare diseases +MONDO:0017860 rare diseases +MONDO:0017861 gard_rare diseases +MONDO:0017861 nord_rare diseases +MONDO:0017861 ordo_disorder diseases +MONDO:0017861 orphanet_rare diseases +MONDO:0017861 rare diseases +MONDO:0017862 gard_rare diseases +MONDO:0017862 nord_rare diseases +MONDO:0017862 ordo_disorder diseases +MONDO:0017862 orphanet_rare diseases +MONDO:0017862 rare diseases +MONDO:0017863 nord_rare diseases +MONDO:0017863 ordo_clinical_situation diseases +MONDO:0017863 ordo_disorder diseases +MONDO:0017863 orphanet_rare diseases +MONDO:0017863 rare diseases +MONDO:0017864 gard_rare diseases +MONDO:0017864 nord_rare diseases +MONDO:0017864 ordo_group_of_disorders diseases +MONDO:0017864 ordo_morphological_anomaly diseases +MONDO:0017864 rare diseases +MONDO:0017865 gard_rare diseases +MONDO:0017865 nord_rare diseases +MONDO:0017865 ordo_disorder diseases +MONDO:0017865 ordo_morphological_anomaly diseases +MONDO:0017865 orphanet_rare diseases +MONDO:0017865 rare diseases +MONDO:0017866 gard_rare diseases +MONDO:0017866 nord_rare diseases +MONDO:0017866 ordo_subtype_of_a_disorder diseases +MONDO:0017866 rare diseases +MONDO:0017867 gard_rare diseases +MONDO:0017867 nord_rare diseases +MONDO:0017867 ordo_disorder diseases +MONDO:0017867 ordo_malformation_syndrome diseases +MONDO:0017867 orphanet_rare diseases +MONDO:0017867 otar diseases +MONDO:0017867 rare diseases +MONDO:0017868 gard_rare diseases +MONDO:0017868 nord_rare diseases +MONDO:0017868 ordo_disorder diseases +MONDO:0017868 ordo_morphological_anomaly diseases +MONDO:0017868 orphanet_rare diseases +MONDO:0017868 otar diseases +MONDO:0017868 rare diseases +MONDO:0017869 gard_rare diseases +MONDO:0017869 nord_rare diseases +MONDO:0017869 ordo_disorder diseases +MONDO:0017869 orphanet_rare diseases +MONDO:0017869 otar diseases +MONDO:0017869 rare diseases +MONDO:0017870 gard_rare diseases +MONDO:0017870 nord_rare diseases +MONDO:0017870 ordo_subtype_of_a_disorder diseases +MONDO:0017870 rare diseases +MONDO:0017871 gard_rare diseases +MONDO:0017871 nord_rare diseases +MONDO:0017871 ordo_etiological_subtype diseases +MONDO:0017871 ordo_subtype_of_a_disorder diseases +MONDO:0017871 rare diseases +MONDO:0017872 gard_rare diseases +MONDO:0017872 nord_rare diseases +MONDO:0017872 ordo_disorder diseases +MONDO:0017872 orphanet_rare diseases +MONDO:0017872 rare diseases +MONDO:0017874 gard_rare diseases +MONDO:0017874 nord_rare diseases +MONDO:0017874 ordo_disorder diseases +MONDO:0017874 orphanet_rare diseases +MONDO:0017874 rare diseases +MONDO:0017875 gard_rare diseases +MONDO:0017875 nord_rare diseases +MONDO:0017875 ordo_disorder diseases +MONDO:0017875 orphanet_rare diseases +MONDO:0017875 rare diseases +MONDO:0017876 gard_rare diseases +MONDO:0017876 nord_rare diseases +MONDO:0017876 ordo_disorder diseases +MONDO:0017876 orphanet_rare diseases +MONDO:0017876 rare diseases +MONDO:0017877 gard_rare diseases +MONDO:0017877 nord_rare diseases +MONDO:0017877 ordo_disorder diseases +MONDO:0017877 orphanet_rare diseases +MONDO:0017877 rare diseases +MONDO:0017878 gard_rare diseases +MONDO:0017878 nord_rare diseases +MONDO:0017878 ordo_disorder diseases +MONDO:0017878 orphanet_rare diseases +MONDO:0017878 rare diseases +MONDO:0017879 gard_rare diseases +MONDO:0017879 nord_rare diseases +MONDO:0017879 ordo_disorder diseases +MONDO:0017879 orphanet_rare diseases +MONDO:0017879 otar diseases +MONDO:0017879 rare diseases +MONDO:0017880 gard_rare diseases +MONDO:0017880 nord_rare diseases +MONDO:0017880 ordo_disorder diseases +MONDO:0017880 orphanet_rare diseases +MONDO:0017880 rare diseases +MONDO:0017881 gard_rare diseases +MONDO:0017881 nord_rare diseases +MONDO:0017881 ordo_disorder diseases +MONDO:0017881 orphanet_rare diseases +MONDO:0017881 rare diseases +MONDO:0017882 gard_rare diseases +MONDO:0017882 nord_rare diseases +MONDO:0017882 ordo_disorder diseases +MONDO:0017882 orphanet_rare diseases +MONDO:0017882 rare diseases +MONDO:0017884 clingen diseases +MONDO:0017884 gard_rare diseases +MONDO:0017884 nord_rare diseases +MONDO:0017884 ordo_disorder diseases +MONDO:0017884 orphanet_rare diseases +MONDO:0017884 otar diseases +MONDO:0017884 rare diseases +MONDO:0017885 gard_rare diseases +MONDO:0017885 nord_rare diseases +MONDO:0017885 ordo_disorder diseases +MONDO:0017885 orphanet_rare diseases +MONDO:0017885 otar diseases +MONDO:0017885 rare diseases +MONDO:0017886 gard_rare diseases +MONDO:0017886 nord_rare diseases +MONDO:0017886 ordo_disorder diseases +MONDO:0017886 orphanet_rare diseases +MONDO:0017886 rare diseases +MONDO:0017887 gard_rare diseases +MONDO:0017887 ordo_histopathological_subtype diseases +MONDO:0017887 rare diseases +MONDO:0017890 gard_rare diseases +MONDO:0017890 nord_rare diseases +MONDO:0017890 ordo_disorder diseases +MONDO:0017890 orphanet_rare diseases +MONDO:0017890 rare diseases +MONDO:0017892 gard_rare diseases +MONDO:0017892 nord_rare diseases +MONDO:0017892 ordo_disorder diseases +MONDO:0017892 orphanet_rare diseases +MONDO:0017892 otar diseases +MONDO:0017892 rare diseases +MONDO:0017893 gard_rare diseases +MONDO:0017893 nord_rare diseases +MONDO:0017893 ordo_disorder diseases +MONDO:0017893 orphanet_rare diseases +MONDO:0017893 otar diseases +MONDO:0017893 rare diseases +MONDO:0017894 gard_rare diseases +MONDO:0017894 nord_rare diseases +MONDO:0017894 ordo_disorder diseases +MONDO:0017894 orphanet_rare diseases +MONDO:0017894 rare diseases +MONDO:0017895 gard_rare diseases +MONDO:0017895 nord_rare diseases +MONDO:0017895 ordo_disorder diseases +MONDO:0017895 orphanet_rare diseases +MONDO:0017895 otar diseases +MONDO:0017895 rare diseases +MONDO:0017896 disease_grouping diseases +MONDO:0017896 gard_rare diseases +MONDO:0017896 nord_rare diseases +MONDO:0017896 ordo_group_of_disorders diseases +MONDO:0017896 otar diseases +MONDO:0017896 rare diseases +MONDO:0017904 gard_rare diseases +MONDO:0017904 nord_rare diseases +MONDO:0017904 ordo_disorder diseases +MONDO:0017904 orphanet_rare diseases +MONDO:0017904 otar diseases +MONDO:0017904 rare diseases +MONDO:0017906 gard_rare diseases +MONDO:0017906 nord_rare diseases +MONDO:0017906 ordo_disorder diseases +MONDO:0017906 orphanet_rare diseases +MONDO:0017906 otar diseases +MONDO:0017906 rare diseases +MONDO:0017907 gard_rare diseases +MONDO:0017907 nord_rare diseases +MONDO:0017907 ordo_disorder diseases +MONDO:0017907 orphanet_rare diseases +MONDO:0017907 rare diseases +MONDO:0017909 clingen diseases +MONDO:0017909 gard_rare diseases +MONDO:0017909 nord_rare diseases +MONDO:0017909 ordo_disorder diseases +MONDO:0017909 orphanet_rare diseases +MONDO:0017909 otar diseases +MONDO:0017909 rare diseases +MONDO:0017910 gard_rare diseases +MONDO:0017910 nord_rare diseases +MONDO:0017910 ordo_disorder diseases +MONDO:0017910 orphanet_rare diseases +MONDO:0017910 otar diseases +MONDO:0017910 rare diseases +MONDO:0017913 disease_grouping diseases +MONDO:0017913 gard_rare diseases +MONDO:0017913 ordo_group_of_disorders diseases +MONDO:0017913 rare diseases +MONDO:0017917 gard_rare diseases +MONDO:0017917 nord_rare diseases +MONDO:0017917 ordo_disorder diseases +MONDO:0017917 orphanet_rare diseases +MONDO:0017917 otar diseases +MONDO:0017917 rare diseases +MONDO:0017918 gard_rare diseases +MONDO:0017918 nord_rare diseases +MONDO:0017918 ordo_disorder diseases +MONDO:0017918 ordo_malformation_syndrome diseases +MONDO:0017918 orphanet_rare diseases +MONDO:0017918 otar diseases +MONDO:0017918 rare diseases +MONDO:0017919 gard_rare diseases +MONDO:0017919 nord_rare diseases +MONDO:0017919 ordo_disorder diseases +MONDO:0017919 ordo_malformation_syndrome diseases +MONDO:0017919 orphanet_rare diseases +MONDO:0017919 otar diseases +MONDO:0017919 rare diseases +MONDO:0017920 gard_rare diseases +MONDO:0017920 nord_rare diseases +MONDO:0017920 ordo_disorder diseases +MONDO:0017920 ordo_malformation_syndrome diseases +MONDO:0017920 orphanet_rare diseases +MONDO:0017920 otar diseases +MONDO:0017920 rare diseases +MONDO:0017921 gard_rare diseases +MONDO:0017921 nord_rare diseases +MONDO:0017921 ordo_disorder diseases +MONDO:0017921 ordo_malformation_syndrome diseases +MONDO:0017921 orphanet_rare diseases +MONDO:0017921 otar diseases +MONDO:0017921 rare diseases +MONDO:0017923 gard_rare diseases +MONDO:0017923 nord_rare diseases +MONDO:0017923 ordo_disorder diseases +MONDO:0017923 ordo_malformation_syndrome diseases +MONDO:0017923 orphanet_rare diseases +MONDO:0017923 otar diseases +MONDO:0017923 rare diseases +MONDO:0017924 gard_rare diseases +MONDO:0017924 nord_rare diseases +MONDO:0017924 ordo_disorder diseases +MONDO:0017924 orphanet_rare diseases +MONDO:0017924 otar diseases +MONDO:0017924 rare diseases +MONDO:0017925 gard_rare diseases +MONDO:0017925 nord_rare diseases +MONDO:0017925 ordo_disorder diseases +MONDO:0017925 orphanet_rare diseases +MONDO:0017925 otar diseases +MONDO:0017925 rare diseases +MONDO:0017926 gard_rare diseases +MONDO:0017926 nord_rare diseases +MONDO:0017926 ordo_disorder diseases +MONDO:0017926 orphanet_rare diseases +MONDO:0017926 rare diseases +MONDO:0017927 gard_rare diseases +MONDO:0017927 nord_rare diseases +MONDO:0017927 ordo_disorder diseases +MONDO:0017927 orphanet_rare diseases +MONDO:0017927 rare diseases +MONDO:0017928 gard_rare diseases +MONDO:0017928 nord_rare diseases +MONDO:0017928 ordo_disorder diseases +MONDO:0017928 ordo_malformation_syndrome diseases +MONDO:0017928 orphanet_rare diseases +MONDO:0017928 otar diseases +MONDO:0017928 rare diseases +MONDO:0017929 gard_rare diseases +MONDO:0017929 nord_rare diseases +MONDO:0017929 ordo_disorder diseases +MONDO:0017929 ordo_morphological_anomaly diseases +MONDO:0017929 orphanet_rare diseases +MONDO:0017929 rare diseases +MONDO:0017930 gard_rare diseases +MONDO:0017930 ordo_disorder diseases +MONDO:0017930 orphanet_rare diseases +MONDO:0017930 rare diseases +MONDO:0017931 gard_rare diseases +MONDO:0017931 nord_rare diseases +MONDO:0017931 ordo_disorder diseases +MONDO:0017931 orphanet_rare diseases +MONDO:0017931 otar diseases +MONDO:0017931 rare diseases +MONDO:0017932 gard_rare diseases +MONDO:0017932 nord_rare diseases +MONDO:0017932 ordo_disorder diseases +MONDO:0017932 ordo_malformation_syndrome diseases +MONDO:0017932 orphanet_rare diseases +MONDO:0017932 otar diseases +MONDO:0017932 rare diseases +MONDO:0017933 gard_rare diseases +MONDO:0017933 nord_rare diseases +MONDO:0017933 ordo_disorder diseases +MONDO:0017933 orphanet_rare diseases +MONDO:0017933 otar diseases +MONDO:0017933 rare diseases +MONDO:0017934 gard_rare diseases +MONDO:0017934 ordo_disorder diseases +MONDO:0017934 ordo_malformation_syndrome diseases +MONDO:0017934 orphanet_rare diseases +MONDO:0017934 otar diseases +MONDO:0017934 rare diseases +MONDO:0017935 gard_rare diseases +MONDO:0017935 nord_rare diseases +MONDO:0017935 ordo_disorder diseases +MONDO:0017935 orphanet_rare diseases +MONDO:0017935 otar diseases +MONDO:0017935 rare diseases +MONDO:0017936 gard_rare diseases +MONDO:0017936 nord_rare diseases +MONDO:0017936 ordo_disorder diseases +MONDO:0017936 orphanet_rare diseases +MONDO:0017936 otar diseases +MONDO:0017936 rare diseases +MONDO:0017937 gard_rare diseases +MONDO:0017937 nord_rare diseases +MONDO:0017937 ordo_disorder diseases +MONDO:0017937 orphanet_rare diseases +MONDO:0017937 otar diseases +MONDO:0017937 rare diseases +MONDO:0017939 gard_rare diseases +MONDO:0017939 ordo_subtype_of_a_disorder diseases +MONDO:0017939 otar diseases +MONDO:0017939 rare diseases +MONDO:0017940 gard_rare diseases +MONDO:0017940 nord_rare diseases +MONDO:0017940 ordo_disorder diseases +MONDO:0017940 orphanet_rare diseases +MONDO:0017940 otar diseases +MONDO:0017940 rare diseases +MONDO:0017941 gard_rare diseases +MONDO:0017941 nord_rare diseases +MONDO:0017941 ordo_disorder diseases +MONDO:0017941 orphanet_rare diseases +MONDO:0017941 rare diseases +MONDO:0017942 gard_rare diseases +MONDO:0017942 nord_rare diseases +MONDO:0017942 ordo_disorder diseases +MONDO:0017942 orphanet_rare diseases +MONDO:0017942 rare diseases +MONDO:0017943 gard_rare diseases +MONDO:0017943 nord_rare diseases +MONDO:0017943 ordo_disorder diseases +MONDO:0017943 orphanet_rare diseases +MONDO:0017943 rare diseases +MONDO:0017944 gard_rare diseases +MONDO:0017944 nord_rare diseases +MONDO:0017944 ordo_disorder diseases +MONDO:0017944 orphanet_rare diseases +MONDO:0017944 rare diseases +MONDO:0017945 gard_rare diseases +MONDO:0017945 nord_rare diseases +MONDO:0017945 ordo_subtype_of_a_disorder diseases +MONDO:0017945 otar diseases +MONDO:0017945 rare diseases +MONDO:0017946 gard_rare diseases +MONDO:0017946 nord_rare diseases +MONDO:0017946 ordo_subtype_of_a_disorder diseases +MONDO:0017946 otar diseases +MONDO:0017946 rare diseases +MONDO:0017947 gard_rare diseases +MONDO:0017947 nord_rare diseases +MONDO:0017947 ordo_subtype_of_a_disorder diseases +MONDO:0017947 otar diseases +MONDO:0017947 rare diseases +MONDO:0017948 gard_rare diseases +MONDO:0017948 nord_rare diseases +MONDO:0017948 ordo_subtype_of_a_disorder diseases +MONDO:0017948 otar diseases +MONDO:0017948 rare diseases +MONDO:0017949 gard_rare diseases +MONDO:0017949 nord_rare diseases +MONDO:0017949 ordo_subtype_of_a_disorder diseases +MONDO:0017949 otar diseases +MONDO:0017949 rare diseases +MONDO:0017951 disease_grouping diseases +MONDO:0017951 gard_rare diseases +MONDO:0017951 nord_rare diseases +MONDO:0017951 ordo_group_of_disorders diseases +MONDO:0017951 otar diseases +MONDO:0017951 rare diseases +MONDO:0017953 disease_grouping diseases +MONDO:0017953 gard_rare diseases +MONDO:0017953 nord_rare diseases +MONDO:0017953 ordo_group_of_disorders diseases +MONDO:0017953 otar diseases +MONDO:0017953 rare diseases +MONDO:0017958 gard_rare diseases +MONDO:0017958 nord_rare diseases +MONDO:0017958 ordo_disorder diseases +MONDO:0017958 orphanet_rare diseases +MONDO:0017958 rare diseases +MONDO:0017967 gard_rare diseases +MONDO:0017967 nord_rare diseases +MONDO:0017967 ordo_disorder diseases +MONDO:0017967 ordo_morphological_anomaly diseases +MONDO:0017967 orphanet_rare diseases +MONDO:0017967 otar diseases +MONDO:0017967 rare diseases +MONDO:0017968 gard_rare diseases +MONDO:0017968 nord_rare diseases +MONDO:0017968 ordo_disorder diseases +MONDO:0017968 orphanet_rare diseases +MONDO:0017968 otar diseases +MONDO:0017968 rare diseases +MONDO:0017972 gard_rare diseases +MONDO:0017972 nord_rare diseases +MONDO:0017972 ordo_subtype_of_a_disorder diseases +MONDO:0017972 otar diseases +MONDO:0017972 rare diseases +MONDO:0017973 gard_rare diseases +MONDO:0017973 nord_rare diseases +MONDO:0017973 ordo_subtype_of_a_disorder diseases +MONDO:0017973 otar diseases +MONDO:0017973 rare diseases +MONDO:0017975 disease_grouping diseases +MONDO:0017975 ordo_group_of_disorders diseases +MONDO:0017975 otar diseases +MONDO:0017979 gard_rare diseases +MONDO:0017979 nord_rare diseases +MONDO:0017979 ordo_disorder diseases +MONDO:0017979 orphanet_rare diseases +MONDO:0017979 otar diseases +MONDO:0017979 rare diseases +MONDO:0017980 gard_rare diseases +MONDO:0017980 nord_rare diseases +MONDO:0017980 ordo_disorder diseases +MONDO:0017980 ordo_malformation_syndrome diseases +MONDO:0017980 orphanet_rare diseases +MONDO:0017980 rare diseases +MONDO:0017981 gard_rare diseases +MONDO:0017981 ordo_disorder diseases +MONDO:0017981 ordo_malformation_syndrome diseases +MONDO:0017981 orphanet_rare diseases +MONDO:0017981 rare diseases +MONDO:0017983 gard_rare diseases +MONDO:0017983 nord_rare diseases +MONDO:0017983 ordo_disorder diseases +MONDO:0017983 ordo_morphological_anomaly diseases +MONDO:0017983 orphanet_rare diseases +MONDO:0017983 otar diseases +MONDO:0017983 rare diseases +MONDO:0017985 gard_rare diseases +MONDO:0017985 nord_rare diseases +MONDO:0017985 ordo_disorder diseases +MONDO:0017985 ordo_morphological_anomaly diseases +MONDO:0017985 orphanet_rare diseases +MONDO:0017985 otar diseases +MONDO:0017985 rare diseases +MONDO:0017986 disease_grouping diseases +MONDO:0017986 gard_rare diseases +MONDO:0017986 ordo_group_of_disorders diseases +MONDO:0017986 rare diseases +MONDO:0017987 disease_grouping diseases +MONDO:0017987 gard_rare diseases +MONDO:0017987 nord_rare diseases +MONDO:0017987 ordo_group_of_disorders diseases +MONDO:0017987 otar diseases +MONDO:0017987 rare diseases +MONDO:0017988 gard_rare diseases +MONDO:0017988 nord_rare diseases +MONDO:0017988 ordo_disorder diseases +MONDO:0017988 orphanet_rare diseases +MONDO:0017988 rare diseases +MONDO:0017989 gard_rare diseases +MONDO:0017989 nord_rare diseases +MONDO:0017989 ordo_disorder diseases +MONDO:0017989 orphanet_rare diseases +MONDO:0017989 otar diseases +MONDO:0017989 rare diseases +MONDO:0017990 clingen diseases +MONDO:0017990 gard_rare diseases +MONDO:0017990 nord_rare diseases +MONDO:0017990 ordo_disorder diseases +MONDO:0017990 orphanet_rare diseases +MONDO:0017990 otar diseases +MONDO:0017990 rare diseases +MONDO:0017991 gard_rare diseases +MONDO:0017991 nord_rare diseases +MONDO:0017991 ordo_disorder diseases +MONDO:0017991 orphanet_rare diseases +MONDO:0017991 otar diseases +MONDO:0017991 rare diseases +MONDO:0017992 gard_rare diseases +MONDO:0017992 nord_rare diseases +MONDO:0017992 ordo_disorder diseases +MONDO:0017992 orphanet_rare diseases +MONDO:0017992 otar diseases +MONDO:0017992 rare diseases +MONDO:0017993 gard_rare diseases +MONDO:0017993 nord_rare diseases +MONDO:0017993 ordo_disorder diseases +MONDO:0017993 orphanet_rare diseases +MONDO:0017993 rare diseases +MONDO:0017994 gard_rare diseases +MONDO:0017994 nord_rare diseases +MONDO:0017994 ordo_subtype_of_a_disorder diseases +MONDO:0017994 otar diseases +MONDO:0017994 rare diseases +MONDO:0017995 gard_rare diseases +MONDO:0017995 rare diseases +MONDO:0017997 gard_rare diseases +MONDO:0017997 ordo_disorder diseases +MONDO:0017997 ordo_malformation_syndrome diseases +MONDO:0017997 orphanet_rare diseases +MONDO:0017997 rare diseases +MONDO:0017998 disease_grouping diseases +MONDO:0017998 gard_rare diseases +MONDO:0017998 nord_rare diseases +MONDO:0017998 ordo_group_of_disorders diseases +MONDO:0017998 otar diseases +MONDO:0017998 rare diseases +MONDO:0017999 gard_rare diseases +MONDO:0017999 nord_rare diseases +MONDO:0017999 ordo_disorder diseases +MONDO:0017999 orphanet_rare diseases +MONDO:0017999 otar diseases +MONDO:0017999 rare diseases +MONDO:0018000 gard_rare diseases +MONDO:0018000 nord_rare diseases +MONDO:0018000 ordo_disorder diseases +MONDO:0018000 orphanet_rare diseases +MONDO:0018000 otar diseases +MONDO:0018000 rare diseases +MONDO:0018001 gard_rare diseases +MONDO:0018001 nord_rare diseases +MONDO:0018001 ordo_disorder diseases +MONDO:0018001 orphanet_rare diseases +MONDO:0018001 rare diseases +MONDO:0018002 gard_rare diseases +MONDO:0018002 nord_rare diseases +MONDO:0018002 ordo_disorder diseases +MONDO:0018002 orphanet_rare diseases +MONDO:0018002 otar diseases +MONDO:0018002 rare diseases +MONDO:0018003 gard_rare diseases +MONDO:0018003 rare diseases +MONDO:0018004 gard_rare diseases +MONDO:0018004 nord_rare diseases +MONDO:0018004 ordo_subtype_of_a_disorder diseases +MONDO:0018004 rare diseases +MONDO:0018005 gard_rare diseases +MONDO:0018005 nord_rare diseases +MONDO:0018005 ordo_disorder diseases +MONDO:0018005 orphanet_rare diseases +MONDO:0018005 otar diseases +MONDO:0018005 rare diseases +MONDO:0018006 gard_rare diseases +MONDO:0018006 nord_rare diseases +MONDO:0018006 ordo_disorder diseases +MONDO:0018006 orphanet_rare diseases +MONDO:0018006 otar diseases +MONDO:0018006 rare diseases +MONDO:0018007 gard_rare diseases +MONDO:0018007 nord_rare diseases +MONDO:0018007 ordo_disorder diseases +MONDO:0018007 ordo_malformation_syndrome diseases +MONDO:0018007 orphanet_rare diseases +MONDO:0018007 rare diseases +MONDO:0018008 gard_rare diseases +MONDO:0018008 nord_rare diseases +MONDO:0018008 ordo_disorder diseases +MONDO:0018008 orphanet_rare diseases +MONDO:0018008 rare diseases +MONDO:0018009 gard_rare diseases +MONDO:0018009 nord_rare diseases +MONDO:0018009 ordo_disorder diseases +MONDO:0018009 orphanet_rare diseases +MONDO:0018009 rare diseases +MONDO:0018010 disease_grouping diseases +MONDO:0018010 gard_rare diseases +MONDO:0018010 ordo_group_of_disorders diseases +MONDO:0018010 otar diseases +MONDO:0018010 rare diseases +MONDO:0018011 gard_rare diseases +MONDO:0018011 nord_rare diseases +MONDO:0018011 ordo_disorder diseases +MONDO:0018011 orphanet_rare diseases +MONDO:0018011 rare diseases +MONDO:0018013 gard_rare diseases +MONDO:0018013 nord_rare diseases +MONDO:0018013 ordo_subtype_of_a_disorder diseases +MONDO:0018013 otar diseases +MONDO:0018013 rare diseases +MONDO:0018014 gard_rare diseases +MONDO:0018014 nord_rare diseases +MONDO:0018014 ordo_disorder diseases +MONDO:0018014 orphanet_rare diseases +MONDO:0018014 rare diseases +MONDO:0018015 gard_rare diseases +MONDO:0018015 nord_rare diseases +MONDO:0018015 ordo_disorder diseases +MONDO:0018015 orphanet_rare diseases +MONDO:0018015 otar diseases +MONDO:0018015 rare diseases +MONDO:0018016 gard_rare diseases +MONDO:0018016 nord_rare diseases +MONDO:0018016 ordo_subtype_of_a_disorder diseases +MONDO:0018016 rare diseases +MONDO:0018017 gard_rare diseases +MONDO:0018017 nord_rare diseases +MONDO:0018017 ordo_subtype_of_a_disorder diseases +MONDO:0018017 rare diseases +MONDO:0018018 gard_rare diseases +MONDO:0018018 nord_rare diseases +MONDO:0018018 ordo_disorder diseases +MONDO:0018018 orphanet_rare diseases +MONDO:0018018 rare diseases +MONDO:0018019 gard_rare diseases +MONDO:0018019 nord_rare diseases +MONDO:0018019 ordo_disorder diseases +MONDO:0018019 orphanet_rare diseases +MONDO:0018019 rare diseases +MONDO:0018020 gard_rare diseases +MONDO:0018020 nord_rare diseases +MONDO:0018020 ordo_disorder diseases +MONDO:0018020 orphanet_rare diseases +MONDO:0018020 otar diseases +MONDO:0018020 rare diseases +MONDO:0018021 gard_rare diseases +MONDO:0018021 nord_rare diseases +MONDO:0018021 ordo_disorder diseases +MONDO:0018021 orphanet_rare diseases +MONDO:0018021 rare diseases +MONDO:0018022 gard_rare diseases +MONDO:0018022 nord_rare diseases +MONDO:0018022 ordo_disorder diseases +MONDO:0018022 orphanet_rare diseases +MONDO:0018022 rare diseases +MONDO:0018023 gard_rare diseases +MONDO:0018023 nord_rare diseases +MONDO:0018023 ordo_disorder diseases +MONDO:0018023 orphanet_rare diseases +MONDO:0018023 otar diseases +MONDO:0018023 rare diseases +MONDO:0018024 gard_rare diseases +MONDO:0018024 nord_rare diseases +MONDO:0018024 ordo_disorder diseases +MONDO:0018024 orphanet_rare diseases +MONDO:0018024 rare diseases +MONDO:0018025 gard_rare diseases +MONDO:0018025 nord_rare diseases +MONDO:0018025 ordo_disorder diseases +MONDO:0018025 orphanet_rare diseases +MONDO:0018025 rare diseases +MONDO:0018026 gard_rare diseases +MONDO:0018026 nord_rare diseases +MONDO:0018026 ordo_disorder diseases +MONDO:0018026 ordo_malformation_syndrome diseases +MONDO:0018026 orphanet_rare diseases +MONDO:0018026 rare diseases +MONDO:0018027 gard_rare diseases +MONDO:0018027 nord_rare diseases +MONDO:0018027 ordo_disorder diseases +MONDO:0018027 ordo_malformation_syndrome diseases +MONDO:0018027 orphanet_rare diseases +MONDO:0018027 otar diseases +MONDO:0018027 rare diseases +MONDO:0018028 gard_rare diseases +MONDO:0018028 nord_rare diseases +MONDO:0018028 ordo_disorder diseases +MONDO:0018028 ordo_malformation_syndrome diseases +MONDO:0018028 orphanet_rare diseases +MONDO:0018028 otar diseases +MONDO:0018028 rare diseases +MONDO:0018029 gard_rare diseases +MONDO:0018029 nord_rare diseases +MONDO:0018029 ordo_disorder diseases +MONDO:0018029 orphanet_rare diseases +MONDO:0018029 otar diseases +MONDO:0018029 rare diseases +MONDO:0018030 gard_rare diseases +MONDO:0018030 nord_rare diseases +MONDO:0018030 ordo_disorder diseases +MONDO:0018030 ordo_malformation_syndrome diseases +MONDO:0018030 orphanet_rare diseases +MONDO:0018030 otar diseases +MONDO:0018030 rare diseases +MONDO:0018031 gard_rare diseases +MONDO:0018031 nord_rare diseases +MONDO:0018031 ordo_disorder diseases +MONDO:0018031 orphanet_rare diseases +MONDO:0018031 rare diseases +MONDO:0018034 gard_rare diseases +MONDO:0018034 nord_rare diseases +MONDO:0018034 ordo_disorder diseases +MONDO:0018034 orphanet_rare diseases +MONDO:0018034 rare diseases +MONDO:0018037 disease_grouping diseases +MONDO:0018037 gard_rare diseases +MONDO:0018037 ordo_group_of_disorders diseases +MONDO:0018037 otar diseases +MONDO:0018037 rare diseases +MONDO:0018039 gard_rare diseases +MONDO:0018039 nord_rare diseases +MONDO:0018039 ordo_disorder diseases +MONDO:0018039 orphanet_rare diseases +MONDO:0018039 otar diseases +MONDO:0018039 rare diseases +MONDO:0018043 gard_rare diseases +MONDO:0018043 ordo_disorder diseases +MONDO:0018043 ordo_malformation_syndrome diseases +MONDO:0018043 orphanet_rare diseases +MONDO:0018043 otar diseases +MONDO:0018043 rare diseases +MONDO:0018044 gard_rare diseases +MONDO:0018044 nord_rare diseases +MONDO:0018044 ordo_disorder diseases +MONDO:0018044 orphanet_rare diseases +MONDO:0018044 otar diseases +MONDO:0018044 rare diseases +MONDO:0018045 gard_rare diseases +MONDO:0018045 nord_rare diseases +MONDO:0018045 ordo_disorder diseases +MONDO:0018045 orphanet_rare diseases +MONDO:0018045 otar diseases +MONDO:0018045 rare diseases +MONDO:0018046 ordo_malformation_syndrome diseases +MONDO:0018047 gard_rare diseases +MONDO:0018047 nord_rare diseases +MONDO:0018047 ordo_disorder diseases +MONDO:0018047 orphanet_rare diseases +MONDO:0018047 rare diseases +MONDO:0018048 gard_rare diseases +MONDO:0018048 nord_rare diseases +MONDO:0018048 ordo_disorder diseases +MONDO:0018048 orphanet_rare diseases +MONDO:0018048 rare diseases +MONDO:0018050 gard_rare diseases +MONDO:0018050 nord_rare diseases +MONDO:0018050 ordo_disorder diseases +MONDO:0018050 ordo_malformation_syndrome diseases +MONDO:0018050 orphanet_rare diseases +MONDO:0018050 otar diseases +MONDO:0018050 rare diseases +MONDO:0018051 gard_rare diseases +MONDO:0018051 nord_rare diseases +MONDO:0018051 ordo_disorder diseases +MONDO:0018051 orphanet_rare diseases +MONDO:0018051 rare diseases +MONDO:0018053 gard_rare diseases +MONDO:0018053 nord_rare diseases +MONDO:0018053 ordo_disorder diseases +MONDO:0018053 orphanet_rare diseases +MONDO:0018053 otar diseases +MONDO:0018053 rare diseases +MONDO:0018054 gard_rare diseases +MONDO:0018054 nord_rare diseases +MONDO:0018054 ordo_disorder diseases +MONDO:0018054 orphanet_rare diseases +MONDO:0018054 otar diseases +MONDO:0018054 rare diseases +MONDO:0018055 gard_rare diseases +MONDO:0018055 nord_rare diseases +MONDO:0018055 ordo_disorder diseases +MONDO:0018055 orphanet_rare diseases +MONDO:0018055 rare diseases +MONDO:0018056 gard_rare diseases +MONDO:0018056 nord_rare diseases +MONDO:0018056 ordo_disorder diseases +MONDO:0018056 orphanet_rare diseases +MONDO:0018056 rare diseases +MONDO:0018058 gard_rare diseases +MONDO:0018058 nord_rare diseases +MONDO:0018058 ordo_disorder diseases +MONDO:0018058 ordo_morphological_anomaly diseases +MONDO:0018058 orphanet_rare diseases +MONDO:0018058 rare diseases +MONDO:0018059 gard_rare diseases +MONDO:0018059 nord_rare diseases +MONDO:0018059 ordo_disorder diseases +MONDO:0018059 orphanet_rare diseases +MONDO:0018059 otar diseases +MONDO:0018059 rare diseases +MONDO:0018060 clingen diseases +MONDO:0018060 gard_rare diseases +MONDO:0018060 nord_rare diseases +MONDO:0018060 ordo_disorder diseases +MONDO:0018060 orphanet_rare diseases +MONDO:0018060 otar diseases +MONDO:0018060 rare diseases +MONDO:0018061 gard_rare diseases +MONDO:0018061 nord_rare diseases +MONDO:0018061 ordo_disorder diseases +MONDO:0018061 ordo_malformation_syndrome diseases +MONDO:0018061 orphanet_rare diseases +MONDO:0018061 otar diseases +MONDO:0018061 rare diseases +MONDO:0018062 gard_rare diseases +MONDO:0018062 nord_rare diseases +MONDO:0018062 ordo_malformation_syndrome diseases +MONDO:0018062 rare diseases +MONDO:0018063 gard_rare diseases +MONDO:0018063 nord_rare diseases +MONDO:0018063 ordo_disorder diseases +MONDO:0018063 orphanet_rare diseases +MONDO:0018063 otar diseases +MONDO:0018063 rare diseases +MONDO:0018064 gard_rare diseases +MONDO:0018064 nord_rare diseases +MONDO:0018064 ordo_disorder diseases +MONDO:0018064 ordo_malformation_syndrome diseases +MONDO:0018064 orphanet_rare diseases +MONDO:0018064 rare diseases +MONDO:0018065 gard_rare diseases +MONDO:0018065 nord_rare diseases +MONDO:0018065 ordo_disorder diseases +MONDO:0018065 ordo_morphological_anomaly diseases +MONDO:0018065 orphanet_rare diseases +MONDO:0018065 otar diseases +MONDO:0018065 rare diseases +MONDO:0018066 gard_rare diseases +MONDO:0018066 nord_rare diseases +MONDO:0018066 ordo_disorder diseases +MONDO:0018066 ordo_malformation_syndrome diseases +MONDO:0018066 orphanet_rare diseases +MONDO:0018066 otar diseases +MONDO:0018066 rare diseases +MONDO:0018067 gard_rare diseases +MONDO:0018067 nord_rare diseases +MONDO:0018067 ordo_disorder diseases +MONDO:0018067 ordo_malformation_syndrome diseases +MONDO:0018067 orphanet_rare diseases +MONDO:0018067 otar diseases +MONDO:0018067 rare diseases +MONDO:0018068 gard_rare diseases +MONDO:0018068 nord_rare diseases +MONDO:0018068 ordo_disorder diseases +MONDO:0018068 ordo_malformation_syndrome diseases +MONDO:0018068 orphanet_rare diseases +MONDO:0018068 otar diseases +MONDO:0018068 rare diseases +MONDO:0018069 gard_rare diseases +MONDO:0018069 nord_rare diseases +MONDO:0018069 ordo_disorder diseases +MONDO:0018069 ordo_malformation_syndrome diseases +MONDO:0018069 orphanet_rare diseases +MONDO:0018069 otar diseases +MONDO:0018069 rare diseases +MONDO:0018070 gard_rare diseases +MONDO:0018070 nord_rare diseases +MONDO:0018070 rare diseases +MONDO:0018071 gard_rare diseases +MONDO:0018071 nord_rare diseases +MONDO:0018071 ordo_disorder diseases +MONDO:0018071 ordo_malformation_syndrome diseases +MONDO:0018071 orphanet_rare diseases +MONDO:0018071 otar diseases +MONDO:0018071 rare diseases +MONDO:0018072 gard_rare diseases +MONDO:0018072 nord_rare diseases +MONDO:0018072 ordo_disorder diseases +MONDO:0018072 ordo_morphological_anomaly diseases +MONDO:0018072 orphanet_rare diseases +MONDO:0018072 otar diseases +MONDO:0018072 rare diseases +MONDO:0018075 disease_grouping diseases +MONDO:0018075 gard_rare diseases +MONDO:0018075 ordo_group_of_disorders diseases +MONDO:0018075 otar diseases +MONDO:0018075 rare diseases +MONDO:0018076 gard_rare diseases +MONDO:0018076 nord_rare diseases +MONDO:0018076 ordo_group_of_disorders diseases +MONDO:0018076 otar diseases +MONDO:0018076 rare diseases +MONDO:0018077 gard_rare diseases +MONDO:0018077 nord_rare diseases +MONDO:0018077 ordo_disorder diseases +MONDO:0018077 orphanet_rare diseases +MONDO:0018077 otar diseases +MONDO:0018077 rare diseases +MONDO:0018078 disease_grouping diseases +MONDO:0018078 gard_rare diseases +MONDO:0018078 nord_rare diseases +MONDO:0018078 ordo_group_of_disorders diseases +MONDO:0018078 otar diseases +MONDO:0018078 rare diseases +MONDO:0018079 disease_grouping diseases +MONDO:0018079 gard_rare diseases +MONDO:0018079 nord_rare diseases +MONDO:0018079 ordo_group_of_disorders diseases +MONDO:0018079 otar diseases +MONDO:0018079 rare diseases +MONDO:0018081 gard_rare diseases +MONDO:0018081 nord_rare diseases +MONDO:0018081 ordo_disorder diseases +MONDO:0018081 orphanet_rare diseases +MONDO:0018081 rare diseases +MONDO:0018082 gard_rare diseases +MONDO:0018082 nord_rare diseases +MONDO:0018082 ordo_disorder diseases +MONDO:0018082 ordo_morphological_anomaly diseases +MONDO:0018082 orphanet_rare diseases +MONDO:0018082 rare diseases +MONDO:0018083 gard_rare diseases +MONDO:0018083 nord_rare diseases +MONDO:0018083 ordo_disorder diseases +MONDO:0018083 orphanet_rare diseases +MONDO:0018083 rare diseases +MONDO:0018084 gard_rare diseases +MONDO:0018084 nord_rare diseases +MONDO:0018084 ordo_disorder diseases +MONDO:0018084 ordo_morphological_anomaly diseases +MONDO:0018084 orphanet_rare diseases +MONDO:0018084 rare diseases +MONDO:0018085 gard_rare diseases +MONDO:0018085 nord_rare diseases +MONDO:0018085 ordo_disorder diseases +MONDO:0018085 ordo_malformation_syndrome diseases +MONDO:0018085 orphanet_rare diseases +MONDO:0018085 otar diseases +MONDO:0018085 rare diseases +MONDO:0018086 gard_rare diseases +MONDO:0018086 nord_rare diseases +MONDO:0018086 ordo_disorder diseases +MONDO:0018086 orphanet_rare diseases +MONDO:0018086 otar diseases +MONDO:0018086 rare diseases +MONDO:0018087 disease_grouping diseases +MONDO:0018087 gard_rare diseases +MONDO:0018087 nord_rare diseases +MONDO:0018087 ordo_group_of_disorders diseases +MONDO:0018087 otar diseases +MONDO:0018087 rare diseases +MONDO:0018088 clingen diseases +MONDO:0018088 gard_rare diseases +MONDO:0018088 nord_rare diseases +MONDO:0018088 ordo_disorder diseases +MONDO:0018088 orphanet_rare diseases +MONDO:0018088 otar diseases +MONDO:0018088 rare diseases +MONDO:0018089 gard_rare diseases +MONDO:0018089 nord_rare diseases +MONDO:0018089 ordo_disorder diseases +MONDO:0018089 ordo_morphological_anomaly diseases +MONDO:0018089 orphanet_rare diseases +MONDO:0018089 otar diseases +MONDO:0018089 rare diseases +MONDO:0018090 gard_rare diseases +MONDO:0018090 nord_rare diseases +MONDO:0018090 ordo_disorder diseases +MONDO:0018090 ordo_morphological_anomaly diseases +MONDO:0018090 orphanet_rare diseases +MONDO:0018090 rare diseases +MONDO:0018091 gard_rare diseases +MONDO:0018091 ordo_disorder diseases +MONDO:0018091 ordo_malformation_syndrome diseases +MONDO:0018091 orphanet_rare diseases +MONDO:0018091 otar diseases +MONDO:0018091 rare diseases +MONDO:0018092 gard_rare diseases +MONDO:0018092 nord_rare diseases +MONDO:0018092 ordo_disorder diseases +MONDO:0018092 orphanet_rare diseases +MONDO:0018092 otar diseases +MONDO:0018092 rare diseases +MONDO:0018093 disease_grouping diseases +MONDO:0018093 gard_rare diseases +MONDO:0018093 nord_rare diseases +MONDO:0018093 ordo_group_of_disorders diseases +MONDO:0018093 rare diseases +MONDO:0018094 clingen diseases +MONDO:0018094 gard_rare diseases +MONDO:0018094 nord_rare diseases +MONDO:0018094 ordo_disorder diseases +MONDO:0018094 orphanet_rare diseases +MONDO:0018094 otar diseases +MONDO:0018094 rare diseases +MONDO:0018095 gard_rare diseases +MONDO:0018095 nord_rare diseases +MONDO:0018095 ordo_disorder diseases +MONDO:0018095 ordo_malformation_syndrome diseases +MONDO:0018095 orphanet_rare diseases +MONDO:0018095 otar diseases +MONDO:0018095 rare diseases +MONDO:0018096 gard_rare diseases +MONDO:0018096 nord_rare diseases +MONDO:0018096 ordo_disorder diseases +MONDO:0018096 ordo_malformation_syndrome diseases +MONDO:0018096 orphanet_rare diseases +MONDO:0018096 otar diseases +MONDO:0018096 rare diseases +MONDO:0018097 gard_rare diseases +MONDO:0018097 nord_rare diseases +MONDO:0018097 ordo_clinical_syndrome diseases +MONDO:0018097 ordo_disorder diseases +MONDO:0018097 orphanet_rare diseases +MONDO:0018097 otar diseases +MONDO:0018097 rare diseases +MONDO:0018098 gard_rare diseases +MONDO:0018098 otar diseases +MONDO:0018098 rare diseases +MONDO:0018100 disease_grouping diseases +MONDO:0018100 gard_rare diseases +MONDO:0018100 otar diseases +MONDO:0018100 rare diseases +MONDO:0018101 gard_rare diseases +MONDO:0018101 otar diseases +MONDO:0018101 rare diseases +MONDO:0018102 disease_grouping diseases +MONDO:0018102 nord_rare diseases +MONDO:0018102 ordo_group_of_disorders diseases +MONDO:0018102 otar diseases +MONDO:0018102 rare diseases +MONDO:0018103 gard_rare diseases +MONDO:0018103 nord_rare diseases +MONDO:0018103 ordo_disorder diseases +MONDO:0018103 orphanet_rare diseases +MONDO:0018103 rare diseases +MONDO:0018105 clingen diseases +MONDO:0018105 gard_rare diseases +MONDO:0018105 ordo_disorder diseases +MONDO:0018105 orphanet_rare diseases +MONDO:0018105 otar diseases +MONDO:0018105 rare diseases +MONDO:0018106 gard_rare diseases +MONDO:0018106 nord_rare diseases +MONDO:0018106 ordo_disorder diseases +MONDO:0018106 orphanet_rare diseases +MONDO:0018106 otar diseases +MONDO:0018106 rare diseases +MONDO:0018108 gard_rare diseases +MONDO:0018108 nord_rare diseases +MONDO:0018108 ordo_disorder diseases +MONDO:0018108 orphanet_rare diseases +MONDO:0018108 rare diseases +MONDO:0018109 gard_rare diseases +MONDO:0018109 nord_rare diseases +MONDO:0018109 ordo_disorder diseases +MONDO:0018109 orphanet_rare diseases +MONDO:0018109 otar diseases +MONDO:0018109 rare diseases +MONDO:0018115 gard_rare diseases +MONDO:0018115 nord_rare diseases +MONDO:0018115 ordo_disorder diseases +MONDO:0018115 orphanet_rare diseases +MONDO:0018115 otar diseases +MONDO:0018115 rare diseases +MONDO:0018116 clingen diseases +MONDO:0018116 disease_grouping diseases +MONDO:0018116 gard_rare diseases +MONDO:0018116 nord_rare diseases +MONDO:0018116 ordo_group_of_disorders diseases +MONDO:0018116 otar diseases +MONDO:0018116 rare diseases +MONDO:0018117 disease_grouping diseases +MONDO:0018117 gard_rare diseases +MONDO:0018117 ordo_group_of_disorders diseases +MONDO:0018117 rare diseases +MONDO:0018121 disease_grouping diseases +MONDO:0018121 gard_rare diseases +MONDO:0018121 ordo_group_of_disorders diseases +MONDO:0018121 otar diseases +MONDO:0018121 rare diseases +MONDO:0018123 clingen diseases +MONDO:0018123 gard_rare diseases +MONDO:0018123 nord_rare diseases +MONDO:0018123 ordo_disorder diseases +MONDO:0018123 orphanet_rare diseases +MONDO:0018123 otar diseases +MONDO:0018123 rare diseases +MONDO:0018124 gard_rare diseases +MONDO:0018124 nord_rare diseases +MONDO:0018124 ordo_disorder diseases +MONDO:0018124 orphanet_rare diseases +MONDO:0018124 rare diseases +MONDO:0018125 gard_rare diseases +MONDO:0018125 nord_rare diseases +MONDO:0018125 ordo_disorder diseases +MONDO:0018125 orphanet_rare diseases +MONDO:0018125 otar diseases +MONDO:0018125 rare diseases +MONDO:0018126 gard_rare diseases +MONDO:0018126 nord_rare diseases +MONDO:0018126 ordo_disorder diseases +MONDO:0018126 orphanet_rare diseases +MONDO:0018126 otar diseases +MONDO:0018126 rare diseases +MONDO:0018127 gard_rare diseases +MONDO:0018127 nord_rare diseases +MONDO:0018127 ordo_disorder diseases +MONDO:0018127 orphanet_rare diseases +MONDO:0018127 rare diseases +MONDO:0018128 gard_rare diseases +MONDO:0018128 nord_rare diseases +MONDO:0018128 ordo_disorder diseases +MONDO:0018128 orphanet_rare diseases +MONDO:0018128 rare diseases +MONDO:0018129 gard_rare diseases +MONDO:0018129 nord_rare diseases +MONDO:0018129 ordo_disorder diseases +MONDO:0018129 orphanet_rare diseases +MONDO:0018129 otar diseases +MONDO:0018129 rare diseases +MONDO:0018130 gard_rare diseases +MONDO:0018130 nord_rare diseases +MONDO:0018130 ordo_disorder diseases +MONDO:0018130 orphanet_rare diseases +MONDO:0018130 otar diseases +MONDO:0018130 rare diseases +MONDO:0018131 gard_rare diseases +MONDO:0018131 nord_rare diseases +MONDO:0018131 ordo_etiological_subtype diseases +MONDO:0018131 ordo_subtype_of_a_disorder diseases +MONDO:0018131 otar diseases +MONDO:0018131 rare diseases +MONDO:0018133 gard_rare diseases +MONDO:0018133 nord_rare diseases +MONDO:0018133 ordo_disorder diseases +MONDO:0018133 orphanet_rare diseases +MONDO:0018133 otar diseases +MONDO:0018133 rare diseases +MONDO:0018134 disease_grouping diseases +MONDO:0018134 gard_rare diseases +MONDO:0018134 ordo_group_of_disorders diseases +MONDO:0018134 otar diseases +MONDO:0018134 rare diseases +MONDO:0018135 clingen diseases +MONDO:0018135 gard_rare diseases +MONDO:0018135 nord_rare diseases +MONDO:0018135 ordo_disorder diseases +MONDO:0018135 orphanet_rare diseases +MONDO:0018135 otar diseases +MONDO:0018135 rare diseases +MONDO:0018136 gard_rare diseases +MONDO:0018136 nord_rare diseases +MONDO:0018136 ordo_subtype_of_a_disorder diseases +MONDO:0018136 otar diseases +MONDO:0018136 rare diseases +MONDO:0018137 gard_rare diseases +MONDO:0018137 nord_rare diseases +MONDO:0018137 ordo_subtype_of_a_disorder diseases +MONDO:0018137 otar diseases +MONDO:0018137 rare diseases +MONDO:0018141 gard_rare diseases +MONDO:0018141 nord_rare diseases +MONDO:0018141 ordo_subtype_of_a_disorder diseases +MONDO:0018141 otar diseases +MONDO:0018141 rare diseases +MONDO:0018142 gard_rare diseases +MONDO:0018142 nord_rare diseases +MONDO:0018142 ordo_subtype_of_a_disorder diseases +MONDO:0018142 otar diseases +MONDO:0018142 rare diseases +MONDO:0018143 gard_rare diseases +MONDO:0018143 nord_rare diseases +MONDO:0018143 ordo_subtype_of_a_disorder diseases +MONDO:0018143 otar diseases +MONDO:0018143 rare diseases +MONDO:0018145 gard_rare diseases +MONDO:0018145 nord_rare diseases +MONDO:0018145 ordo_disorder diseases +MONDO:0018145 ordo_morphological_anomaly diseases +MONDO:0018145 orphanet_rare diseases +MONDO:0018145 rare diseases +MONDO:0018146 gard_rare diseases +MONDO:0018146 nord_rare diseases +MONDO:0018146 ordo_disorder diseases +MONDO:0018146 orphanet_rare diseases +MONDO:0018146 rare diseases +MONDO:0018147 gard_rare diseases +MONDO:0018147 nord_rare diseases +MONDO:0018147 ordo_disorder diseases +MONDO:0018147 orphanet_rare diseases +MONDO:0018147 rare diseases +MONDO:0018148 gard_rare diseases +MONDO:0018148 nord_rare diseases +MONDO:0018148 ordo_disorder diseases +MONDO:0018148 orphanet_rare diseases +MONDO:0018148 rare diseases +MONDO:0018149 gard_rare diseases +MONDO:0018149 nord_rare diseases +MONDO:0018149 ordo_disorder diseases +MONDO:0018149 orphanet_rare diseases +MONDO:0018149 otar diseases +MONDO:0018149 rare diseases +MONDO:0018150 clingen diseases +MONDO:0018150 gard_rare diseases +MONDO:0018150 nord_rare diseases +MONDO:0018150 ordo_disorder diseases +MONDO:0018150 orphanet_rare diseases +MONDO:0018150 otar diseases +MONDO:0018150 rare diseases +MONDO:0018151 disease_grouping diseases +MONDO:0018151 gard_rare diseases +MONDO:0018151 ordo_group_of_disorders diseases +MONDO:0018151 otar diseases +MONDO:0018151 rare diseases +MONDO:0018152 gard_rare diseases +MONDO:0018152 nord_rare diseases +MONDO:0018152 ordo_disorder diseases +MONDO:0018152 orphanet_rare diseases +MONDO:0018152 rare diseases +MONDO:0018153 gard_rare diseases +MONDO:0018153 nord_rare diseases +MONDO:0018153 ordo_disorder diseases +MONDO:0018153 orphanet_rare diseases +MONDO:0018153 otar diseases +MONDO:0018153 rare diseases +MONDO:0018154 gard_rare diseases +MONDO:0018154 ordo_morphological_anomaly diseases +MONDO:0018154 rare diseases +MONDO:0018155 gard_rare diseases +MONDO:0018155 ordo_disorder diseases +MONDO:0018155 orphanet_rare diseases +MONDO:0018155 otar diseases +MONDO:0018155 rare diseases +MONDO:0018156 gard_rare diseases +MONDO:0018156 nord_rare diseases +MONDO:0018156 ordo_disorder diseases +MONDO:0018156 ordo_malformation_syndrome diseases +MONDO:0018156 orphanet_rare diseases +MONDO:0018156 rare diseases +MONDO:0018158 disease_grouping diseases +MONDO:0018158 gard_rare diseases +MONDO:0018158 ordo_group_of_disorders diseases +MONDO:0018158 otar diseases +MONDO:0018158 rare diseases +MONDO:0018159 gard_rare diseases +MONDO:0018159 nord_rare diseases +MONDO:0018159 ordo_disorder diseases +MONDO:0018159 ordo_etiological_subtype diseases +MONDO:0018159 orphanet_rare diseases +MONDO:0018159 otar diseases +MONDO:0018159 rare diseases +MONDO:0018160 gard_rare diseases +MONDO:0018160 nord_rare diseases +MONDO:0018160 ordo_subtype_of_a_disorder diseases +MONDO:0018160 otar diseases +MONDO:0018160 rare diseases +MONDO:0018161 gard_rare diseases +MONDO:0018161 nord_rare diseases +MONDO:0018161 ordo_subtype_of_a_disorder diseases +MONDO:0018161 otar diseases +MONDO:0018161 rare diseases +MONDO:0018162 clingen diseases +MONDO:0018162 disease_grouping diseases +MONDO:0018162 gard_rare diseases +MONDO:0018162 ordo_group_of_disorders diseases +MONDO:0018162 otar diseases +MONDO:0018162 rare diseases +MONDO:0018163 gard_rare diseases +MONDO:0018163 nord_rare diseases +MONDO:0018163 ordo_disorder diseases +MONDO:0018163 orphanet_rare diseases +MONDO:0018163 otar diseases +MONDO:0018163 rare diseases +MONDO:0018164 gard_rare diseases +MONDO:0018164 nord_rare diseases +MONDO:0018164 ordo_subtype_of_a_disorder diseases +MONDO:0018164 rare diseases +MONDO:0018165 gard_rare diseases +MONDO:0018165 nord_rare diseases +MONDO:0018165 ordo_subtype_of_a_disorder diseases +MONDO:0018165 rare diseases +MONDO:0018166 gard_rare diseases +MONDO:0018166 nord_rare diseases +MONDO:0018166 ordo_disorder diseases +MONDO:0018166 orphanet_rare diseases +MONDO:0018166 otar diseases +MONDO:0018166 rare diseases +MONDO:0018167 gard_rare diseases +MONDO:0018167 nord_rare diseases +MONDO:0018167 ordo_disorder diseases +MONDO:0018167 orphanet_rare diseases +MONDO:0018167 rare diseases +MONDO:0018168 gard_rare diseases +MONDO:0018168 nord_rare diseases +MONDO:0018168 ordo_disorder diseases +MONDO:0018168 orphanet_rare diseases +MONDO:0018168 otar diseases +MONDO:0018168 rare diseases +MONDO:0018169 gard_rare diseases +MONDO:0018169 nord_rare diseases +MONDO:0018169 ordo_disorder diseases +MONDO:0018169 ordo_morphological_anomaly diseases +MONDO:0018169 orphanet_rare diseases +MONDO:0018169 otar diseases +MONDO:0018169 rare diseases +MONDO:0018170 disease_grouping diseases +MONDO:0018170 gard_rare diseases +MONDO:0018170 ordo_group_of_disorders diseases +MONDO:0018170 otar diseases +MONDO:0018170 rare diseases +MONDO:0018171 disease_grouping diseases +MONDO:0018171 gard_rare diseases +MONDO:0018171 nord_rare diseases +MONDO:0018171 ordo_group_of_disorders diseases +MONDO:0018171 otar diseases +MONDO:0018171 rare diseases +MONDO:0018172 disease_grouping diseases +MONDO:0018172 gard_rare diseases +MONDO:0018172 ordo_group_of_disorders diseases +MONDO:0018172 rare diseases +MONDO:0018173 nord_rare diseases +MONDO:0018173 ordo_disorder diseases +MONDO:0018173 orphanet_rare diseases +MONDO:0018173 rare diseases +MONDO:0018174 disease_grouping diseases +MONDO:0018174 gard_rare diseases +MONDO:0018174 ordo_group_of_disorders diseases +MONDO:0018174 otar diseases +MONDO:0018174 rare diseases +MONDO:0018175 gard_rare diseases +MONDO:0018175 nord_rare diseases +MONDO:0018175 ordo_disorder diseases +MONDO:0018175 orphanet_rare diseases +MONDO:0018175 otar diseases +MONDO:0018175 rare diseases +MONDO:0018177 gard_rare diseases +MONDO:0018177 nord_rare diseases +MONDO:0018177 ordo_disorder diseases +MONDO:0018177 orphanet_rare diseases +MONDO:0018177 otar diseases +MONDO:0018177 rare diseases +MONDO:0018178 disease_grouping diseases +MONDO:0018178 gard_rare diseases +MONDO:0018178 nord_rare diseases +MONDO:0018178 ordo_group_of_disorders diseases +MONDO:0018178 otar diseases +MONDO:0018178 rare diseases +MONDO:0018180 gard_rare diseases +MONDO:0018180 nord_rare diseases +MONDO:0018180 ordo_disorder diseases +MONDO:0018180 orphanet_rare diseases +MONDO:0018180 rare diseases +MONDO:0018181 gard_rare diseases +MONDO:0018181 nord_rare diseases +MONDO:0018181 ordo_disorder diseases +MONDO:0018181 orphanet_rare diseases +MONDO:0018181 otar diseases +MONDO:0018181 rare diseases +MONDO:0018182 gard_rare diseases +MONDO:0018182 nord_rare diseases +MONDO:0018182 ordo_disorder diseases +MONDO:0018182 orphanet_rare diseases +MONDO:0018182 rare diseases +MONDO:0018183 gard_rare diseases +MONDO:0018183 nord_rare diseases +MONDO:0018183 ordo_disorder diseases +MONDO:0018183 orphanet_rare diseases +MONDO:0018183 rare diseases +MONDO:0018184 gard_rare diseases +MONDO:0018184 nord_rare diseases +MONDO:0018184 ordo_clinical_situation diseases +MONDO:0018184 ordo_disorder diseases +MONDO:0018184 orphanet_rare diseases +MONDO:0018184 rare diseases +MONDO:0018189 gard_rare diseases +MONDO:0018189 nord_rare diseases +MONDO:0018189 ordo_disorder diseases +MONDO:0018189 orphanet_rare diseases +MONDO:0018189 rare diseases +MONDO:0018190 gard_rare diseases +MONDO:0018190 nord_rare diseases +MONDO:0018190 ordo_disorder diseases +MONDO:0018190 orphanet_rare diseases +MONDO:0018190 otar diseases +MONDO:0018190 rare diseases +MONDO:0018192 gard_rare diseases +MONDO:0018192 nord_rare diseases +MONDO:0018192 ordo_disorder diseases +MONDO:0018192 orphanet_rare diseases +MONDO:0018192 rare diseases +MONDO:0018193 gard_rare diseases +MONDO:0018193 nord_rare diseases +MONDO:0018193 ordo_disorder diseases +MONDO:0018193 orphanet_rare diseases +MONDO:0018193 otar diseases +MONDO:0018193 rare diseases +MONDO:0018197 gard_rare diseases +MONDO:0018197 nord_rare diseases +MONDO:0018197 ordo_disorder diseases +MONDO:0018197 orphanet_rare diseases +MONDO:0018197 otar diseases +MONDO:0018197 rare diseases +MONDO:0018198 gard_rare diseases +MONDO:0018198 nord_rare diseases +MONDO:0018198 ordo_disorder diseases +MONDO:0018198 orphanet_rare diseases +MONDO:0018198 rare diseases +MONDO:0018199 gard_rare diseases +MONDO:0018199 nord_rare diseases +MONDO:0018199 ordo_disorder diseases +MONDO:0018199 orphanet_rare diseases +MONDO:0018199 rare diseases +MONDO:0018201 disease_grouping diseases +MONDO:0018201 gard_rare diseases +MONDO:0018201 ordo_group_of_disorders diseases +MONDO:0018201 otar diseases +MONDO:0018201 rare diseases +MONDO:0018202 disease_grouping diseases +MONDO:0018202 gard_rare diseases +MONDO:0018202 ordo_group_of_disorders diseases +MONDO:0018202 otar diseases +MONDO:0018202 rare diseases +MONDO:0018203 gard_rare diseases +MONDO:0018203 nord_rare diseases +MONDO:0018203 ordo_disorder diseases +MONDO:0018203 orphanet_rare diseases +MONDO:0018203 otar diseases +MONDO:0018203 rare diseases +MONDO:0018204 gard_rare diseases +MONDO:0018204 nord_rare diseases +MONDO:0018204 ordo_disorder diseases +MONDO:0018204 ordo_malformation_syndrome diseases +MONDO:0018204 orphanet_rare diseases +MONDO:0018204 otar diseases +MONDO:0018204 rare diseases +MONDO:0018205 gard_rare diseases +MONDO:0018205 nord_rare diseases +MONDO:0018205 ordo_disorder diseases +MONDO:0018205 ordo_malformation_syndrome diseases +MONDO:0018205 orphanet_rare diseases +MONDO:0018205 otar diseases +MONDO:0018205 rare diseases +MONDO:0018206 gard_rare diseases +MONDO:0018206 nord_rare diseases +MONDO:0018206 ordo_disorder diseases +MONDO:0018206 orphanet_rare diseases +MONDO:0018206 otar diseases +MONDO:0018206 rare diseases +MONDO:0018207 gard_rare diseases +MONDO:0018207 nord_rare diseases +MONDO:0018207 ordo_disorder diseases +MONDO:0018207 ordo_malformation_syndrome diseases +MONDO:0018207 orphanet_rare diseases +MONDO:0018207 rare diseases +MONDO:0018208 gard_rare diseases +MONDO:0018208 nord_rare diseases +MONDO:0018208 ordo_etiological_subtype diseases +MONDO:0018208 ordo_subtype_of_a_disorder diseases +MONDO:0018208 otar diseases +MONDO:0018208 rare diseases +MONDO:0018209 gard_rare diseases +MONDO:0018209 nord_rare diseases +MONDO:0018209 ordo_subtype_of_a_disorder diseases +MONDO:0018209 otar diseases +MONDO:0018209 rare diseases +MONDO:0018210 gard_rare diseases +MONDO:0018210 nord_rare diseases +MONDO:0018210 ordo_subtype_of_a_disorder diseases +MONDO:0018210 otar diseases +MONDO:0018210 rare diseases +MONDO:0018211 gard_rare diseases +MONDO:0018211 nord_rare diseases +MONDO:0018211 ordo_disorder diseases +MONDO:0018211 orphanet_rare diseases +MONDO:0018211 rare diseases +MONDO:0018212 gard_rare diseases +MONDO:0018212 nord_rare diseases +MONDO:0018212 ordo_disorder diseases +MONDO:0018212 orphanet_rare diseases +MONDO:0018212 otar diseases +MONDO:0018212 rare diseases +MONDO:0018213 gard_rare diseases +MONDO:0018213 nord_rare diseases +MONDO:0018213 ordo_disorder diseases +MONDO:0018213 orphanet_rare diseases +MONDO:0018213 otar diseases +MONDO:0018213 rare diseases +MONDO:0018214 clingen diseases +MONDO:0018214 gard_rare diseases +MONDO:0018214 ordo_disorder diseases +MONDO:0018214 orphanet_rare diseases +MONDO:0018214 otar diseases +MONDO:0018214 rare diseases +MONDO:0018215 disease_grouping diseases +MONDO:0018215 gard_rare diseases +MONDO:0018215 nord_rare diseases +MONDO:0018215 ordo_group_of_disorders diseases +MONDO:0018215 otar diseases +MONDO:0018215 rare diseases +MONDO:0018216 gard_rare diseases +MONDO:0018216 nord_rare diseases +MONDO:0018216 ordo_etiological_subtype diseases +MONDO:0018216 ordo_subtype_of_a_disorder diseases +MONDO:0018216 rare diseases +MONDO:0018217 gard_rare diseases +MONDO:0018217 nord_rare diseases +MONDO:0018217 ordo_etiological_subtype diseases +MONDO:0018217 ordo_subtype_of_a_disorder diseases +MONDO:0018217 otar diseases +MONDO:0018217 rare diseases +MONDO:0018218 gard_rare diseases +MONDO:0018218 nord_rare diseases +MONDO:0018218 ordo_disorder diseases +MONDO:0018218 orphanet_rare diseases +MONDO:0018218 otar diseases +MONDO:0018218 rare diseases +MONDO:0018221 gard_rare diseases +MONDO:0018221 nord_rare diseases +MONDO:0018221 ordo_subtype_of_a_disorder diseases +MONDO:0018221 rare diseases +MONDO:0018223 gard_rare diseases +MONDO:0018223 nord_rare diseases +MONDO:0018223 ordo_disorder diseases +MONDO:0018223 orphanet_rare diseases +MONDO:0018223 rare diseases +MONDO:0018224 gard_rare diseases +MONDO:0018224 nord_rare diseases +MONDO:0018224 ordo_disorder diseases +MONDO:0018224 orphanet_rare diseases +MONDO:0018224 rare diseases +MONDO:0018225 gard_rare diseases +MONDO:0018225 nord_rare diseases +MONDO:0018225 ordo_disorder diseases +MONDO:0018225 orphanet_rare diseases +MONDO:0018225 rare diseases +MONDO:0018226 gard_rare diseases +MONDO:0018226 nord_rare diseases +MONDO:0018226 ordo_disorder diseases +MONDO:0018226 orphanet_rare diseases +MONDO:0018226 otar diseases +MONDO:0018226 rare diseases +MONDO:0018227 gard_rare diseases +MONDO:0018227 nord_rare diseases +MONDO:0018227 ordo_disorder diseases +MONDO:0018227 orphanet_rare diseases +MONDO:0018227 rare diseases +MONDO:0018228 gard_rare diseases +MONDO:0018228 nord_rare diseases +MONDO:0018228 ordo_disorder diseases +MONDO:0018228 ordo_morphological_anomaly diseases +MONDO:0018228 orphanet_rare diseases +MONDO:0018228 rare diseases +MONDO:0018229 gard_rare diseases +MONDO:0018229 nord_rare diseases +MONDO:0018229 ordo_subtype_of_a_disorder diseases +MONDO:0018229 otar diseases +MONDO:0018229 rare diseases +MONDO:0018230 disease_grouping diseases +MONDO:0018230 ordo_group_of_disorders diseases +MONDO:0018230 otar diseases +MONDO:0018233 disease_grouping diseases +MONDO:0018233 gard_rare diseases +MONDO:0018233 nord_rare diseases +MONDO:0018233 ordo_group_of_disorders diseases +MONDO:0018233 otar diseases +MONDO:0018233 rare diseases +MONDO:0018234 disease_grouping diseases +MONDO:0018234 gard_rare diseases +MONDO:0018234 ordo_group_of_disorders diseases +MONDO:0018234 otar diseases +MONDO:0018234 rare diseases +MONDO:0018237 disease_grouping diseases +MONDO:0018237 gard_rare diseases +MONDO:0018237 ordo_group_of_disorders diseases +MONDO:0018237 otar diseases +MONDO:0018237 rare diseases +MONDO:0018240 clingen diseases +MONDO:0018240 disease_grouping diseases +MONDO:0018240 gard_rare diseases +MONDO:0018240 nord_rare diseases +MONDO:0018240 ordo_group_of_disorders diseases +MONDO:0018240 otar diseases +MONDO:0018240 rare diseases +MONDO:0018242 gard_rare diseases +MONDO:0018242 nord_rare diseases +MONDO:0018242 ordo_disorder diseases +MONDO:0018242 orphanet_rare diseases +MONDO:0018242 otar diseases +MONDO:0018242 rare diseases +MONDO:0018243 gard_rare diseases +MONDO:0018243 nord_rare diseases +MONDO:0018243 ordo_disorder diseases +MONDO:0018243 orphanet_rare diseases +MONDO:0018243 otar diseases +MONDO:0018243 rare diseases +MONDO:0018244 gard_rare diseases +MONDO:0018244 nord_rare diseases +MONDO:0018244 ordo_subtype_of_a_disorder diseases +MONDO:0018244 otar diseases +MONDO:0018244 rare diseases +MONDO:0018245 gard_rare diseases +MONDO:0018245 nord_rare diseases +MONDO:0018245 ordo_disorder diseases +MONDO:0018245 ordo_malformation_syndrome diseases +MONDO:0018245 orphanet_rare diseases +MONDO:0018245 rare diseases +MONDO:0018247 gard_rare diseases +MONDO:0018247 nord_rare diseases +MONDO:0018247 ordo_disorder diseases +MONDO:0018247 orphanet_rare diseases +MONDO:0018247 otar diseases +MONDO:0018247 rare diseases +MONDO:0018248 gard_rare diseases +MONDO:0018248 nord_rare diseases +MONDO:0018248 ordo_disorder diseases +MONDO:0018248 orphanet_rare diseases +MONDO:0018248 rare diseases +MONDO:0018249 gard_rare diseases +MONDO:0018249 nord_rare diseases +MONDO:0018249 ordo_disorder diseases +MONDO:0018249 ordo_malformation_syndrome diseases +MONDO:0018249 orphanet_rare diseases +MONDO:0018249 rare diseases +MONDO:0018250 gard_rare diseases +MONDO:0018250 nord_rare diseases +MONDO:0018250 ordo_disorder diseases +MONDO:0018250 orphanet_rare diseases +MONDO:0018250 otar diseases +MONDO:0018250 rare diseases +MONDO:0018252 gard_rare diseases +MONDO:0018252 nord_rare diseases +MONDO:0018252 ordo_disorder diseases +MONDO:0018252 orphanet_rare diseases +MONDO:0018252 otar diseases +MONDO:0018252 rare diseases +MONDO:0018253 gard_rare diseases +MONDO:0018253 nord_rare diseases +MONDO:0018253 ordo_disorder diseases +MONDO:0018253 ordo_malformation_syndrome diseases +MONDO:0018253 orphanet_rare diseases +MONDO:0018253 otar diseases +MONDO:0018253 rare diseases +MONDO:0018254 gard_rare diseases +MONDO:0018254 nord_rare diseases +MONDO:0018254 ordo_disorder diseases +MONDO:0018254 orphanet_rare diseases +MONDO:0018254 rare diseases +MONDO:0018255 gard_rare diseases +MONDO:0018255 nord_rare diseases +MONDO:0018255 rare diseases +MONDO:0018256 gard_rare diseases +MONDO:0018256 nord_rare diseases +MONDO:0018256 ordo_disorder diseases +MONDO:0018256 orphanet_rare diseases +MONDO:0018256 rare diseases +MONDO:0018257 gard_rare diseases +MONDO:0018257 nord_rare diseases +MONDO:0018257 ordo_subtype_of_a_disorder diseases +MONDO:0018257 rare diseases +MONDO:0018258 gard_rare diseases +MONDO:0018258 nord_rare diseases +MONDO:0018258 ordo_disorder diseases +MONDO:0018258 orphanet_rare diseases +MONDO:0018258 rare diseases +MONDO:0018259 gard_rare diseases +MONDO:0018259 nord_rare diseases +MONDO:0018259 ordo_disorder diseases +MONDO:0018259 orphanet_rare diseases +MONDO:0018259 rare diseases +MONDO:0018260 gard_rare diseases +MONDO:0018260 nord_rare diseases +MONDO:0018260 ordo_disorder diseases +MONDO:0018260 orphanet_rare diseases +MONDO:0018260 rare diseases +MONDO:0018261 gard_rare diseases +MONDO:0018261 nord_rare diseases +MONDO:0018261 ordo_disorder diseases +MONDO:0018261 orphanet_rare diseases +MONDO:0018261 rare diseases +MONDO:0018263 gard_rare diseases +MONDO:0018263 nord_rare diseases +MONDO:0018263 ordo_disorder diseases +MONDO:0018263 orphanet_rare diseases +MONDO:0018263 rare diseases +MONDO:0018264 gard_rare diseases +MONDO:0018264 nord_rare diseases +MONDO:0018264 ordo_disorder diseases +MONDO:0018264 orphanet_rare diseases +MONDO:0018264 otar diseases +MONDO:0018264 rare diseases +MONDO:0018266 gard_rare diseases +MONDO:0018266 nord_rare diseases +MONDO:0018266 ordo_disorder diseases +MONDO:0018266 orphanet_rare diseases +MONDO:0018266 otar diseases +MONDO:0018266 rare diseases +MONDO:0018267 gard_rare diseases +MONDO:0018267 nord_rare diseases +MONDO:0018267 rare diseases +MONDO:0018268 gard_rare diseases +MONDO:0018268 nord_rare diseases +MONDO:0018268 ordo_disorder diseases +MONDO:0018268 orphanet_rare diseases +MONDO:0018268 rare diseases +MONDO:0018269 gard_rare diseases +MONDO:0018269 nord_rare diseases +MONDO:0018269 ordo_disorder diseases +MONDO:0018269 orphanet_rare diseases +MONDO:0018269 rare diseases +MONDO:0018270 gard_rare diseases +MONDO:0018270 nord_rare diseases +MONDO:0018270 ordo_disorder diseases +MONDO:0018270 orphanet_rare diseases +MONDO:0018270 rare diseases +MONDO:0018271 gard_rare diseases +MONDO:0018271 nord_rare diseases +MONDO:0018271 ordo_disorder diseases +MONDO:0018271 orphanet_rare diseases +MONDO:0018271 otar diseases +MONDO:0018271 rare diseases +MONDO:0018273 gard_rare diseases +MONDO:0018273 nord_rare diseases +MONDO:0018273 ordo_disorder diseases +MONDO:0018273 orphanet_rare diseases +MONDO:0018273 otar diseases +MONDO:0018273 rare diseases +MONDO:0018274 clingen diseases +MONDO:0018274 disease_grouping diseases +MONDO:0018274 gard_rare diseases +MONDO:0018274 nord_rare diseases +MONDO:0018274 ordo_disorder diseases +MONDO:0018274 orphanet_rare diseases +MONDO:0018274 otar diseases +MONDO:0018274 rare diseases +MONDO:0018276 disease_grouping diseases +MONDO:0018276 gard_rare diseases +MONDO:0018276 ordo_group_of_disorders diseases +MONDO:0018276 otar diseases +MONDO:0018276 rare diseases +MONDO:0018278 gard_rare diseases +MONDO:0018278 nord_rare diseases +MONDO:0018278 ordo_disorder diseases +MONDO:0018278 orphanet_rare diseases +MONDO:0018278 otar diseases +MONDO:0018278 rare diseases +MONDO:0018280 gard_rare diseases +MONDO:0018280 nord_rare diseases +MONDO:0018280 ordo_disorder diseases +MONDO:0018280 orphanet_rare diseases +MONDO:0018280 otar diseases +MONDO:0018280 rare diseases +MONDO:0018281 gard_rare diseases +MONDO:0018281 nord_rare diseases +MONDO:0018281 ordo_disorder diseases +MONDO:0018281 orphanet_rare diseases +MONDO:0018281 rare diseases +MONDO:0018282 disease_grouping diseases +MONDO:0018282 gard_rare diseases +MONDO:0018282 ordo_group_of_disorders diseases +MONDO:0018282 otar diseases +MONDO:0018282 rare diseases +MONDO:0018298 gard_rare diseases +MONDO:0018298 nord_rare diseases +MONDO:0018298 ordo_disorder diseases +MONDO:0018298 orphanet_rare diseases +MONDO:0018298 otar diseases +MONDO:0018298 rare diseases +MONDO:0018301 gard_rare diseases +MONDO:0018301 nord_rare diseases +MONDO:0018301 ordo_disorder diseases +MONDO:0018301 orphanet_rare diseases +MONDO:0018301 otar diseases +MONDO:0018301 rare diseases +MONDO:0018302 gard_rare diseases +MONDO:0018302 nord_rare diseases +MONDO:0018302 ordo_disorder diseases +MONDO:0018302 orphanet_rare diseases +MONDO:0018302 rare diseases +MONDO:0018304 gard_rare diseases +MONDO:0018304 nord_rare diseases +MONDO:0018304 ordo_disorder diseases +MONDO:0018304 ordo_malformation_syndrome diseases +MONDO:0018304 orphanet_rare diseases +MONDO:0018304 otar diseases +MONDO:0018304 rare diseases +MONDO:0018305 gard_rare diseases +MONDO:0018305 nord_rare diseases +MONDO:0018305 ordo_disorder diseases +MONDO:0018305 orphanet_rare diseases +MONDO:0018305 otar diseases +MONDO:0018305 rare diseases +MONDO:0018306 gard_rare diseases +MONDO:0018306 nord_rare diseases +MONDO:0018306 ordo_disorder diseases +MONDO:0018306 orphanet_rare diseases +MONDO:0018306 otar diseases +MONDO:0018306 rare diseases +MONDO:0018307 disease_grouping diseases +MONDO:0018307 gard_rare diseases +MONDO:0018307 nord_rare diseases +MONDO:0018307 ordo_group_of_disorders diseases +MONDO:0018307 otar diseases +MONDO:0018307 rare diseases +MONDO:0018308 gard_rare diseases +MONDO:0018308 nord_rare diseases +MONDO:0018308 ordo_disorder diseases +MONDO:0018308 orphanet_rare diseases +MONDO:0018308 rare diseases +MONDO:0018309 gard_rare diseases +MONDO:0018309 nord_rare diseases +MONDO:0018309 ordo_disorder diseases +MONDO:0018309 orphanet_rare diseases +MONDO:0018309 otar diseases +MONDO:0018309 rare diseases +MONDO:0018310 disease_grouping diseases +MONDO:0018310 gard_rare diseases +MONDO:0018310 nord_rare diseases +MONDO:0018310 ordo_disorder diseases +MONDO:0018310 orphanet_rare diseases +MONDO:0018310 otar diseases +MONDO:0018310 rare diseases +MONDO:0018311 gard_rare diseases +MONDO:0018311 nord_rare diseases +MONDO:0018311 ordo_disorder diseases +MONDO:0018311 orphanet_rare diseases +MONDO:0018311 rare diseases +MONDO:0018312 gard_rare diseases +MONDO:0018312 nord_rare diseases +MONDO:0018312 ordo_disorder diseases +MONDO:0018312 orphanet_rare diseases +MONDO:0018312 otar diseases +MONDO:0018312 rare diseases +MONDO:0018314 gard_rare diseases +MONDO:0018314 nord_rare diseases +MONDO:0018314 ordo_disorder diseases +MONDO:0018314 orphanet_rare diseases +MONDO:0018314 otar diseases +MONDO:0018314 rare diseases +MONDO:0018315 gard_rare diseases +MONDO:0018315 nord_rare diseases +MONDO:0018315 ordo_disorder diseases +MONDO:0018315 orphanet_rare diseases +MONDO:0018315 otar diseases +MONDO:0018315 rare diseases +MONDO:0018316 gard_rare diseases +MONDO:0018316 nord_rare diseases +MONDO:0018316 ordo_disorder diseases +MONDO:0018316 orphanet_rare diseases +MONDO:0018316 otar diseases +MONDO:0018316 rare diseases +MONDO:0018317 gard_rare diseases +MONDO:0018317 nord_rare diseases +MONDO:0018317 ordo_disorder diseases +MONDO:0018317 orphanet_rare diseases +MONDO:0018317 otar diseases +MONDO:0018317 rare diseases +MONDO:0018319 gard_rare diseases +MONDO:0018319 nord_rare diseases +MONDO:0018319 ordo_disorder diseases +MONDO:0018319 orphanet_rare diseases +MONDO:0018319 otar diseases +MONDO:0018319 rare diseases +MONDO:0018320 gard_rare diseases +MONDO:0018320 nord_rare diseases +MONDO:0018320 ordo_disorder diseases +MONDO:0018320 orphanet_rare diseases +MONDO:0018320 otar diseases +MONDO:0018320 rare diseases +MONDO:0018321 gard_rare diseases +MONDO:0018321 nord_rare diseases +MONDO:0018321 ordo_disorder diseases +MONDO:0018321 orphanet_rare diseases +MONDO:0018321 otar diseases +MONDO:0018321 rare diseases +MONDO:0018322 gard_rare diseases +MONDO:0018322 nord_rare diseases +MONDO:0018322 ordo_subtype_of_a_disorder diseases +MONDO:0018322 otar diseases +MONDO:0018322 rare diseases +MONDO:0018323 gard_rare diseases +MONDO:0018323 nord_rare diseases +MONDO:0018323 ordo_subtype_of_a_disorder diseases +MONDO:0018323 otar diseases +MONDO:0018323 rare diseases +MONDO:0018324 gard_rare diseases +MONDO:0018324 nord_rare diseases +MONDO:0018324 ordo_subtype_of_a_disorder diseases +MONDO:0018324 otar diseases +MONDO:0018324 rare diseases +MONDO:0018325 gard_rare diseases +MONDO:0018325 nord_rare diseases +MONDO:0018325 ordo_subtype_of_a_disorder diseases +MONDO:0018325 rare diseases +MONDO:0018326 gard_rare diseases +MONDO:0018326 nord_rare diseases +MONDO:0018326 ordo_subtype_of_a_disorder diseases +MONDO:0018326 rare diseases +MONDO:0018327 gard_rare diseases +MONDO:0018327 nord_rare diseases +MONDO:0018327 ordo_disorder diseases +MONDO:0018327 orphanet_rare diseases +MONDO:0018327 otar diseases +MONDO:0018327 rare diseases +MONDO:0018328 gard_rare diseases +MONDO:0018328 nord_rare diseases +MONDO:0018328 ordo_disorder diseases +MONDO:0018328 orphanet_rare diseases +MONDO:0018328 otar diseases +MONDO:0018328 rare diseases +MONDO:0018330 gard_rare diseases +MONDO:0018330 nord_rare diseases +MONDO:0018330 ordo_disorder diseases +MONDO:0018330 orphanet_rare diseases +MONDO:0018330 otar diseases +MONDO:0018330 rare diseases +MONDO:0018332 gard_rare diseases +MONDO:0018332 nord_rare diseases +MONDO:0018332 ordo_subtype_of_a_disorder diseases +MONDO:0018332 otar diseases +MONDO:0018332 rare diseases +MONDO:0018333 gard_rare diseases +MONDO:0018333 nord_rare diseases +MONDO:0018333 ordo_subtype_of_a_disorder diseases +MONDO:0018333 otar diseases +MONDO:0018333 rare diseases +MONDO:0018334 gard_rare diseases +MONDO:0018334 nord_rare diseases +MONDO:0018334 ordo_disorder diseases +MONDO:0018334 orphanet_rare diseases +MONDO:0018334 rare diseases +MONDO:0018338 gard_rare diseases +MONDO:0018338 nord_rare diseases +MONDO:0018338 ordo_disorder diseases +MONDO:0018338 orphanet_rare diseases +MONDO:0018338 otar diseases +MONDO:0018338 rare diseases +MONDO:0018339 gard_rare diseases +MONDO:0018339 nord_rare diseases +MONDO:0018339 ordo_disorder diseases +MONDO:0018339 orphanet_rare diseases +MONDO:0018339 otar diseases +MONDO:0018339 rare diseases +MONDO:0018341 gard_rare diseases +MONDO:0018341 nord_rare diseases +MONDO:0018341 ordo_disorder diseases +MONDO:0018341 orphanet_rare diseases +MONDO:0018341 otar diseases +MONDO:0018341 rare diseases +MONDO:0018342 gard_rare diseases +MONDO:0018342 nord_rare diseases +MONDO:0018342 ordo_disorder diseases +MONDO:0018342 ordo_malformation_syndrome diseases +MONDO:0018342 orphanet_rare diseases +MONDO:0018342 otar diseases +MONDO:0018342 rare diseases +MONDO:0018343 gard_rare diseases +MONDO:0018343 nord_rare diseases +MONDO:0018343 ordo_disorder diseases +MONDO:0018343 orphanet_rare diseases +MONDO:0018343 otar diseases +MONDO:0018343 rare diseases +MONDO:0018346 gard_rare diseases +MONDO:0018346 nord_rare diseases +MONDO:0018346 ordo_disorder diseases +MONDO:0018346 orphanet_rare diseases +MONDO:0018346 otar diseases +MONDO:0018346 rare diseases +MONDO:0018349 clingen diseases +MONDO:0018349 gard_rare diseases +MONDO:0018349 nord_rare diseases +MONDO:0018349 ordo_disorder diseases +MONDO:0018349 orphanet_rare diseases +MONDO:0018349 otar diseases +MONDO:0018349 rare diseases +MONDO:0018352 gard_rare diseases +MONDO:0018352 nord_rare diseases +MONDO:0018352 ordo_disorder diseases +MONDO:0018352 orphanet_rare diseases +MONDO:0018352 otar diseases +MONDO:0018352 rare diseases +MONDO:0018353 gard_rare diseases +MONDO:0018353 nord_rare diseases +MONDO:0018353 ordo_disorder diseases +MONDO:0018353 orphanet_rare diseases +MONDO:0018353 otar diseases +MONDO:0018353 rare diseases +MONDO:0018354 gard_rare diseases +MONDO:0018354 nord_rare diseases +MONDO:0018354 ordo_group_of_disorders diseases +MONDO:0018354 otar diseases +MONDO:0018354 rare diseases +MONDO:0018355 gard_rare diseases +MONDO:0018355 nord_rare diseases +MONDO:0018355 ordo_disorder diseases +MONDO:0018355 orphanet_rare diseases +MONDO:0018355 otar diseases +MONDO:0018355 rare diseases +MONDO:0018356 disease_grouping diseases +MONDO:0018356 gard_rare diseases +MONDO:0018356 ordo_group_of_disorders diseases +MONDO:0018356 rare diseases +MONDO:0018357 gard_rare diseases +MONDO:0018357 nord_rare diseases +MONDO:0018357 ordo_disorder diseases +MONDO:0018357 orphanet_rare diseases +MONDO:0018357 rare diseases +MONDO:0018358 gard_rare diseases +MONDO:0018358 nord_rare diseases +MONDO:0018358 ordo_disorder diseases +MONDO:0018358 orphanet_rare diseases +MONDO:0018358 rare diseases +MONDO:0018359 gard_rare diseases +MONDO:0018359 nord_rare diseases +MONDO:0018359 ordo_disorder diseases +MONDO:0018359 orphanet_rare diseases +MONDO:0018359 rare diseases +MONDO:0018360 gard_rare diseases +MONDO:0018360 nord_rare diseases +MONDO:0018360 ordo_disorder diseases +MONDO:0018360 orphanet_rare diseases +MONDO:0018360 otar diseases +MONDO:0018360 rare diseases +MONDO:0018361 gard_rare diseases +MONDO:0018361 nord_rare diseases +MONDO:0018361 ordo_disorder diseases +MONDO:0018361 orphanet_rare diseases +MONDO:0018361 rare diseases +MONDO:0018362 gard_rare diseases +MONDO:0018362 nord_rare diseases +MONDO:0018362 ordo_disorder diseases +MONDO:0018362 orphanet_rare diseases +MONDO:0018362 rare diseases +MONDO:0018363 gard_rare diseases +MONDO:0018363 nord_rare diseases +MONDO:0018363 ordo_disorder diseases +MONDO:0018363 ordo_malformation_syndrome diseases +MONDO:0018363 orphanet_rare diseases +MONDO:0018363 otar diseases +MONDO:0018363 rare diseases +MONDO:0018364 disease_grouping diseases +MONDO:0018364 gard_rare diseases +MONDO:0018364 ordo_group_of_disorders diseases +MONDO:0018364 otar diseases +MONDO:0018364 rare diseases +MONDO:0018365 disease_grouping diseases +MONDO:0018365 gard_rare diseases +MONDO:0018365 ordo_group_of_disorders diseases +MONDO:0018365 otar diseases +MONDO:0018365 rare diseases +MONDO:0018368 gard_rare diseases +MONDO:0018368 nord_rare diseases +MONDO:0018368 rare diseases +MONDO:0018369 gard_rare diseases +MONDO:0018369 nord_rare diseases +MONDO:0018369 ordo_disorder diseases +MONDO:0018369 orphanet_rare diseases +MONDO:0018369 rare diseases +MONDO:0018370 gard_rare diseases +MONDO:0018370 nord_rare diseases +MONDO:0018370 ordo_disorder diseases +MONDO:0018370 orphanet_rare diseases +MONDO:0018370 otar diseases +MONDO:0018370 rare diseases +MONDO:0018371 gard_rare diseases +MONDO:0018371 nord_rare diseases +MONDO:0018371 ordo_disorder diseases +MONDO:0018371 orphanet_rare diseases +MONDO:0018371 otar diseases +MONDO:0018371 rare diseases +MONDO:0018373 disease_grouping diseases +MONDO:0018373 gard_rare diseases +MONDO:0018373 nord_rare diseases +MONDO:0018373 ordo_group_of_disorders diseases +MONDO:0018373 otar diseases +MONDO:0018373 rare diseases +MONDO:0018374 disease_grouping diseases +MONDO:0018374 gard_rare diseases +MONDO:0018374 ordo_group_of_disorders diseases +MONDO:0018374 rare diseases +MONDO:0018375 gard_rare diseases +MONDO:0018375 nord_rare diseases +MONDO:0018375 ordo_disorder diseases +MONDO:0018375 orphanet_rare diseases +MONDO:0018375 rare diseases +MONDO:0018376 gard_rare diseases +MONDO:0018376 nord_rare diseases +MONDO:0018376 ordo_disorder diseases +MONDO:0018376 orphanet_rare diseases +MONDO:0018376 rare diseases +MONDO:0018378 gard_rare diseases +MONDO:0018378 nord_rare diseases +MONDO:0018378 ordo_disorder diseases +MONDO:0018378 orphanet_rare diseases +MONDO:0018378 rare diseases +MONDO:0018379 disease_grouping diseases +MONDO:0018379 gard_rare diseases +MONDO:0018379 ordo_group_of_disorders diseases +MONDO:0018379 rare diseases +MONDO:0018380 gard_rare diseases +MONDO:0018380 nord_rare diseases +MONDO:0018380 ordo_disorder diseases +MONDO:0018380 orphanet_rare diseases +MONDO:0018380 rare diseases +MONDO:0018381 disease_grouping diseases +MONDO:0018381 gard_rare diseases +MONDO:0018381 nord_rare diseases +MONDO:0018381 ordo_group_of_disorders diseases +MONDO:0018381 rare diseases +MONDO:0018382 gard_rare diseases +MONDO:0018382 nord_rare diseases +MONDO:0018382 ordo_disorder diseases +MONDO:0018382 orphanet_rare diseases +MONDO:0018382 rare diseases +MONDO:0018383 disease_grouping diseases +MONDO:0018383 gard_rare diseases +MONDO:0018383 ordo_group_of_disorders diseases +MONDO:0018383 rare diseases +MONDO:0018394 gard_rare diseases +MONDO:0018394 nord_rare diseases +MONDO:0018394 ordo_disorder diseases +MONDO:0018394 orphanet_rare diseases +MONDO:0018394 otar diseases +MONDO:0018394 rare diseases +MONDO:0018408 gard_rare diseases +MONDO:0018408 nord_rare diseases +MONDO:0018408 ordo_disorder diseases +MONDO:0018408 orphanet_rare diseases +MONDO:0018408 rare diseases +MONDO:0018416 gard_rare diseases +MONDO:0018416 nord_rare diseases +MONDO:0018416 ordo_disorder diseases +MONDO:0018416 orphanet_rare diseases +MONDO:0018416 otar diseases +MONDO:0018416 rare diseases +MONDO:0018417 gard_rare diseases +MONDO:0018417 nord_rare diseases +MONDO:0018417 ordo_disorder diseases +MONDO:0018417 orphanet_rare diseases +MONDO:0018417 otar diseases +MONDO:0018417 rare diseases +MONDO:0018418 gard_rare diseases +MONDO:0018418 nord_rare diseases +MONDO:0018418 ordo_disorder diseases +MONDO:0018418 orphanet_rare diseases +MONDO:0018418 otar diseases +MONDO:0018418 rare diseases +MONDO:0018419 gard_rare diseases +MONDO:0018419 nord_rare diseases +MONDO:0018419 ordo_disorder diseases +MONDO:0018419 orphanet_rare diseases +MONDO:0018419 otar diseases +MONDO:0018419 rare diseases +MONDO:0018420 gard_rare diseases +MONDO:0018420 rare diseases +MONDO:0018421 gard_rare diseases +MONDO:0018421 nord_rare diseases +MONDO:0018421 ordo_disorder diseases +MONDO:0018421 orphanet_rare diseases +MONDO:0018421 otar diseases +MONDO:0018421 rare diseases +MONDO:0018422 gard_rare diseases +MONDO:0018422 nord_rare diseases +MONDO:0018422 ordo_disorder diseases +MONDO:0018422 orphanet_rare diseases +MONDO:0018422 otar diseases +MONDO:0018422 rare diseases +MONDO:0018423 gard_rare diseases +MONDO:0018423 nord_rare diseases +MONDO:0018423 ordo_disorder diseases +MONDO:0018423 orphanet_rare diseases +MONDO:0018423 otar diseases +MONDO:0018423 rare diseases +MONDO:0018424 disease_grouping diseases +MONDO:0018424 gard_rare diseases +MONDO:0018424 ordo_group_of_disorders diseases +MONDO:0018424 rare diseases +MONDO:0018425 gard_rare diseases +MONDO:0018425 nord_rare diseases +MONDO:0018425 ordo_disorder diseases +MONDO:0018425 orphanet_rare diseases +MONDO:0018425 otar diseases +MONDO:0018425 rare diseases +MONDO:0018426 gard_rare diseases +MONDO:0018426 nord_rare diseases +MONDO:0018426 ordo_subtype_of_a_disorder diseases +MONDO:0018426 otar diseases +MONDO:0018426 rare diseases +MONDO:0018428 gard_rare diseases +MONDO:0018428 nord_rare diseases +MONDO:0018428 ordo_disorder diseases +MONDO:0018428 ordo_malformation_syndrome diseases +MONDO:0018428 orphanet_rare diseases +MONDO:0018428 otar diseases +MONDO:0018428 rare diseases +MONDO:0018429 gard_rare diseases +MONDO:0018429 nord_rare diseases +MONDO:0018429 ordo_disorder diseases +MONDO:0018429 ordo_malformation_syndrome diseases +MONDO:0018429 orphanet_rare diseases +MONDO:0018429 otar diseases +MONDO:0018429 rare diseases +MONDO:0018430 gard_rare diseases +MONDO:0018430 nord_rare diseases +MONDO:0018430 ordo_disorder diseases +MONDO:0018430 ordo_malformation_syndrome diseases +MONDO:0018430 orphanet_rare diseases +MONDO:0018430 otar diseases +MONDO:0018430 rare diseases +MONDO:0018431 disease_grouping diseases +MONDO:0018431 gard_rare diseases +MONDO:0018431 ordo_group_of_disorders diseases +MONDO:0018431 ordo_inheritance_inconsistent diseases +MONDO:0018431 rare diseases +MONDO:0018432 disease_grouping diseases +MONDO:0018432 gard_rare diseases +MONDO:0018432 ordo_group_of_disorders diseases +MONDO:0018432 rare diseases +MONDO:0018433 gard_rare diseases +MONDO:0018433 nord_rare diseases +MONDO:0018433 ordo_disorder diseases +MONDO:0018433 orphanet_rare diseases +MONDO:0018433 rare diseases +MONDO:0018434 gard_rare diseases +MONDO:0018434 nord_rare diseases +MONDO:0018434 ordo_disorder diseases +MONDO:0018434 orphanet_rare diseases +MONDO:0018434 rare diseases +MONDO:0018435 gard_rare diseases +MONDO:0018435 nord_rare diseases +MONDO:0018435 ordo_disorder diseases +MONDO:0018435 orphanet_rare diseases +MONDO:0018435 rare diseases +MONDO:0018436 gard_rare diseases +MONDO:0018436 nord_rare diseases +MONDO:0018436 ordo_disorder diseases +MONDO:0018436 orphanet_rare diseases +MONDO:0018436 rare diseases +MONDO:0018437 gard_rare diseases +MONDO:0018437 nord_rare diseases +MONDO:0018437 ordo_disorder diseases +MONDO:0018437 orphanet_rare diseases +MONDO:0018437 rare diseases +MONDO:0018438 disease_grouping diseases +MONDO:0018438 gard_rare diseases +MONDO:0018438 ordo_group_of_disorders diseases +MONDO:0018438 otar diseases +MONDO:0018438 rare diseases +MONDO:0018439 gard_rare diseases +MONDO:0018439 nord_rare diseases +MONDO:0018439 ordo_disorder diseases +MONDO:0018439 orphanet_rare diseases +MONDO:0018439 rare diseases +MONDO:0018440 gard_rare diseases +MONDO:0018440 nord_rare diseases +MONDO:0018440 ordo_subtype_of_a_disorder diseases +MONDO:0018440 otar diseases +MONDO:0018440 rare diseases +MONDO:0018442 gard_rare diseases +MONDO:0018442 nord_rare diseases +MONDO:0018442 ordo_disorder diseases +MONDO:0018442 orphanet_rare diseases +MONDO:0018442 rare diseases +MONDO:0018443 gard_rare diseases +MONDO:0018443 nord_rare diseases +MONDO:0018443 ordo_disorder diseases +MONDO:0018443 ordo_malformation_syndrome diseases +MONDO:0018443 orphanet_rare diseases +MONDO:0018443 otar diseases +MONDO:0018443 rare diseases +MONDO:0018445 gard_rare diseases +MONDO:0018445 nord_rare diseases +MONDO:0018445 ordo_disorder diseases +MONDO:0018445 ordo_malformation_syndrome diseases +MONDO:0018445 orphanet_rare diseases +MONDO:0018445 otar diseases +MONDO:0018445 rare diseases +MONDO:0018446 disease_grouping diseases +MONDO:0018446 gard_rare diseases +MONDO:0018446 ordo_group_of_disorders diseases +MONDO:0018446 rare diseases +MONDO:0018447 gard_rare diseases +MONDO:0018447 nord_rare diseases +MONDO:0018447 ordo_disorder diseases +MONDO:0018447 orphanet_rare diseases +MONDO:0018447 otar diseases +MONDO:0018447 rare diseases +MONDO:0018448 gard_rare diseases +MONDO:0018448 nord_rare diseases +MONDO:0018448 ordo_histopathological_subtype diseases +MONDO:0018448 ordo_subtype_of_a_disorder diseases +MONDO:0018448 rare diseases +MONDO:0018449 gard_rare diseases +MONDO:0018449 nord_rare diseases +MONDO:0018449 ordo_disorder diseases +MONDO:0018449 orphanet_rare diseases +MONDO:0018449 rare diseases +MONDO:0018450 gard_rare diseases +MONDO:0018450 nord_rare diseases +MONDO:0018450 ordo_disorder diseases +MONDO:0018450 orphanet_rare diseases +MONDO:0018450 otar diseases +MONDO:0018450 rare diseases +MONDO:0018453 gard_rare diseases +MONDO:0018453 nord_rare diseases +MONDO:0018453 ordo_disorder diseases +MONDO:0018453 orphanet_rare diseases +MONDO:0018453 otar diseases +MONDO:0018453 rare diseases +MONDO:0018456 disease_grouping diseases +MONDO:0018456 gard_rare diseases +MONDO:0018456 nord_rare diseases +MONDO:0018456 ordo_group_of_disorders diseases +MONDO:0018456 otar diseases +MONDO:0018456 rare diseases +MONDO:0018458 gard_rare diseases +MONDO:0018458 ordo_disorder diseases +MONDO:0018458 orphanet_rare diseases +MONDO:0018458 otar diseases +MONDO:0018458 rare diseases +MONDO:0018459 gard_rare diseases +MONDO:0018459 nord_rare diseases +MONDO:0018459 ordo_disorder diseases +MONDO:0018459 orphanet_rare diseases +MONDO:0018459 otar diseases +MONDO:0018459 rare diseases +MONDO:0018460 gard_rare diseases +MONDO:0018460 nord_rare diseases +MONDO:0018460 ordo_disorder diseases +MONDO:0018460 orphanet_rare diseases +MONDO:0018460 rare diseases +MONDO:0018461 gard_rare diseases +MONDO:0018461 nord_rare diseases +MONDO:0018461 ordo_etiological_subtype diseases +MONDO:0018461 ordo_subtype_of_a_disorder diseases +MONDO:0018461 rare diseases +MONDO:0018462 gard_rare diseases +MONDO:0018462 nord_rare diseases +MONDO:0018462 ordo_etiological_subtype diseases +MONDO:0018462 ordo_subtype_of_a_disorder diseases +MONDO:0018462 rare diseases +MONDO:0018463 gard_rare diseases +MONDO:0018463 nord_rare diseases +MONDO:0018463 ordo_subtype_of_a_disorder diseases +MONDO:0018463 rare diseases +MONDO:0018464 gard_rare diseases +MONDO:0018464 nord_rare diseases +MONDO:0018464 ordo_subtype_of_a_disorder diseases +MONDO:0018464 rare diseases +MONDO:0018465 gard_rare diseases +MONDO:0018465 nord_rare diseases +MONDO:0018465 ordo_disorder diseases +MONDO:0018465 orphanet_rare diseases +MONDO:0018465 rare diseases +MONDO:0018467 gard_rare diseases +MONDO:0018467 nord_rare diseases +MONDO:0018467 ordo_subtype_of_a_disorder diseases +MONDO:0018467 rare diseases +MONDO:0018468 gard_rare diseases +MONDO:0018468 nord_rare diseases +MONDO:0018468 ordo_disorder diseases +MONDO:0018468 orphanet_rare diseases +MONDO:0018468 rare diseases +MONDO:0018469 gard_rare diseases +MONDO:0018469 nord_rare diseases +MONDO:0018469 ordo_disorder diseases +MONDO:0018469 orphanet_rare diseases +MONDO:0018469 otar diseases +MONDO:0018469 rare diseases +MONDO:0018470 gard_rare diseases +MONDO:0018470 nord_rare diseases +MONDO:0018470 ordo_disorder diseases +MONDO:0018470 ordo_morphological_anomaly diseases +MONDO:0018470 orphanet_rare diseases +MONDO:0018470 otar diseases +MONDO:0018470 rare diseases +MONDO:0018471 gard_rare diseases +MONDO:0018471 nord_rare diseases +MONDO:0018471 ordo_disorder diseases +MONDO:0018471 orphanet_rare diseases +MONDO:0018471 rare diseases +MONDO:0018472 gard_rare diseases +MONDO:0018472 nord_rare diseases +MONDO:0018472 ordo_disorder diseases +MONDO:0018472 orphanet_rare diseases +MONDO:0018472 rare diseases +MONDO:0018473 gard_rare diseases +MONDO:0018473 nord_rare diseases +MONDO:0018473 ordo_disorder diseases +MONDO:0018473 orphanet_rare diseases +MONDO:0018473 otar diseases +MONDO:0018473 rare diseases +MONDO:0018474 gard_rare diseases +MONDO:0018474 nord_rare diseases +MONDO:0018474 ordo_disorder diseases +MONDO:0018474 ordo_malformation_syndrome diseases +MONDO:0018474 orphanet_rare diseases +MONDO:0018474 rare diseases +MONDO:0018475 gard_rare diseases +MONDO:0018475 nord_rare diseases +MONDO:0018475 ordo_disorder diseases +MONDO:0018475 orphanet_rare diseases +MONDO:0018475 rare diseases +MONDO:0018476 gard_rare diseases +MONDO:0018476 nord_rare diseases +MONDO:0018476 ordo_disorder diseases +MONDO:0018476 orphanet_rare diseases +MONDO:0018476 rare diseases +MONDO:0018477 gard_rare diseases +MONDO:0018477 ordo_clinical_syndrome diseases +MONDO:0018477 ordo_group_of_disorders diseases +MONDO:0018477 otar diseases +MONDO:0018477 rare diseases +MONDO:0018479 disease_grouping diseases +MONDO:0018479 gard_rare diseases +MONDO:0018479 nord_rare diseases +MONDO:0018479 ordo_group_of_disorders diseases +MONDO:0018479 otar diseases +MONDO:0018479 rare diseases +MONDO:0018480 gard_rare diseases +MONDO:0018480 nord_rare diseases +MONDO:0018480 ordo_disorder diseases +MONDO:0018480 orphanet_rare diseases +MONDO:0018480 rare diseases +MONDO:0018481 gard_rare diseases +MONDO:0018481 nord_rare diseases +MONDO:0018481 ordo_disorder diseases +MONDO:0018481 orphanet_rare diseases +MONDO:0018481 rare diseases +MONDO:0018483 gard_rare diseases +MONDO:0018483 nord_rare diseases +MONDO:0018483 ordo_disorder diseases +MONDO:0018483 orphanet_rare diseases +MONDO:0018483 rare diseases +MONDO:0018484 gard_rare diseases +MONDO:0018484 nord_rare diseases +MONDO:0018484 ordo_clinical_syndrome diseases +MONDO:0018484 ordo_disorder diseases +MONDO:0018484 orphanet_rare diseases +MONDO:0018484 rare diseases +MONDO:0018485 gard_rare diseases +MONDO:0018485 nord_rare diseases +MONDO:0018485 ordo_subtype_of_a_disorder diseases +MONDO:0018485 otar diseases +MONDO:0018485 rare diseases +MONDO:0018486 gard_rare diseases +MONDO:0018486 nord_rare diseases +MONDO:0018486 ordo_disorder diseases +MONDO:0018486 orphanet_rare diseases +MONDO:0018486 rare diseases +MONDO:0018487 gard_rare diseases +MONDO:0018487 nord_rare diseases +MONDO:0018487 ordo_disorder diseases +MONDO:0018487 orphanet_rare diseases +MONDO:0018487 rare diseases +MONDO:0018489 gard_rare diseases +MONDO:0018489 nord_rare diseases +MONDO:0018489 ordo_disorder diseases +MONDO:0018489 orphanet_rare diseases +MONDO:0018489 rare diseases +MONDO:0018490 gard_rare diseases +MONDO:0018490 nord_rare diseases +MONDO:0018490 ordo_disorder diseases +MONDO:0018490 ordo_malformation_syndrome diseases +MONDO:0018490 orphanet_rare diseases +MONDO:0018490 rare diseases +MONDO:0018491 disease_grouping diseases +MONDO:0018491 gard_rare diseases +MONDO:0018491 rare diseases +MONDO:0018492 gard_rare diseases +MONDO:0018492 nord_rare diseases +MONDO:0018492 ordo_disorder diseases +MONDO:0018492 orphanet_rare diseases +MONDO:0018492 otar diseases +MONDO:0018492 rare diseases +MONDO:0018493 gard_rare diseases +MONDO:0018493 nord_rare diseases +MONDO:0018493 ordo_disorder diseases +MONDO:0018493 orphanet_rare diseases +MONDO:0018493 otar diseases +MONDO:0018493 rare diseases +MONDO:0018494 gard_rare diseases +MONDO:0018494 nord_rare diseases +MONDO:0018494 ordo_disorder diseases +MONDO:0018494 ordo_malformation_syndrome diseases +MONDO:0018494 orphanet_rare diseases +MONDO:0018494 rare diseases +MONDO:0018495 gard_rare diseases +MONDO:0018495 nord_rare diseases +MONDO:0018495 ordo_disorder diseases +MONDO:0018495 orphanet_rare diseases +MONDO:0018495 rare diseases +MONDO:0018498 gard_rare diseases +MONDO:0018498 nord_rare diseases +MONDO:0018498 ordo_subtype_of_a_disorder diseases +MONDO:0018498 rare diseases +MONDO:0018499 gard_rare diseases +MONDO:0018499 nord_rare diseases +MONDO:0018499 ordo_subtype_of_a_disorder diseases +MONDO:0018499 rare diseases +MONDO:0018500 gard_rare diseases +MONDO:0018500 nord_rare diseases +MONDO:0018500 ordo_disorder diseases +MONDO:0018500 orphanet_rare diseases +MONDO:0018500 rare diseases +MONDO:0018502 disease_grouping diseases +MONDO:0018502 gard_rare diseases +MONDO:0018502 nord_rare diseases +MONDO:0018502 ordo_group_of_disorders diseases +MONDO:0018502 otar diseases +MONDO:0018502 rare diseases +MONDO:0018504 gard_rare diseases +MONDO:0018504 nord_rare diseases +MONDO:0018504 ordo_disorder diseases +MONDO:0018504 orphanet_rare diseases +MONDO:0018504 rare diseases +MONDO:0018506 disease_grouping diseases +MONDO:0018506 gard_rare diseases +MONDO:0018506 ordo_group_of_disorders diseases +MONDO:0018506 rare diseases +MONDO:0018507 gard_rare diseases +MONDO:0018507 nord_rare diseases +MONDO:0018507 ordo_disorder diseases +MONDO:0018507 orphanet_rare diseases +MONDO:0018507 rare diseases +MONDO:0018509 gard_rare diseases +MONDO:0018509 nord_rare diseases +MONDO:0018509 ordo_disorder diseases +MONDO:0018509 orphanet_rare diseases +MONDO:0018509 rare diseases +MONDO:0018510 disease_grouping diseases +MONDO:0018510 gard_rare diseases +MONDO:0018510 ordo_group_of_disorders diseases +MONDO:0018510 otar diseases +MONDO:0018510 rare diseases +MONDO:0018511 disease_grouping diseases +MONDO:0018511 gard_rare diseases +MONDO:0018511 nord_rare diseases +MONDO:0018511 ordo_group_of_disorders diseases +MONDO:0018511 rare diseases +MONDO:0018513 gard_rare diseases +MONDO:0018513 nord_rare diseases +MONDO:0018513 ordo_disorder diseases +MONDO:0018513 orphanet_rare diseases +MONDO:0018513 otar diseases +MONDO:0018513 rare diseases +MONDO:0018515 gard_rare diseases +MONDO:0018515 nord_rare diseases +MONDO:0018515 ordo_disorder diseases +MONDO:0018515 orphanet_rare diseases +MONDO:0018515 otar diseases +MONDO:0018515 rare diseases +MONDO:0018516 disease_grouping diseases +MONDO:0018516 gard_rare diseases +MONDO:0018516 nord_rare diseases +MONDO:0018516 ordo_group_of_disorders diseases +MONDO:0018516 rare diseases +MONDO:0018521 gard_rare diseases +MONDO:0018521 nord_rare diseases +MONDO:0018521 ordo_disorder diseases +MONDO:0018521 orphanet_rare diseases +MONDO:0018521 otar diseases +MONDO:0018521 rare diseases +MONDO:0018523 gard_rare diseases +MONDO:0018523 nord_rare diseases +MONDO:0018523 ordo_disorder diseases +MONDO:0018523 orphanet_rare diseases +MONDO:0018523 rare diseases +MONDO:0018525 gard_rare diseases +MONDO:0018525 nord_rare diseases +MONDO:0018525 ordo_disorder diseases +MONDO:0018525 orphanet_rare diseases +MONDO:0018525 rare diseases +MONDO:0018528 clingen diseases +MONDO:0018528 gard_rare diseases +MONDO:0018528 nord_rare diseases +MONDO:0018528 ordo_disorder diseases +MONDO:0018528 orphanet_rare diseases +MONDO:0018528 otar diseases +MONDO:0018528 rare diseases +MONDO:0018531 disease_grouping diseases +MONDO:0018531 gard_rare diseases +MONDO:0018531 ordo_group_of_disorders diseases +MONDO:0018531 otar diseases +MONDO:0018531 rare diseases +MONDO:0018533 gard_rare diseases +MONDO:0018533 nord_rare diseases +MONDO:0018533 ordo_disorder diseases +MONDO:0018533 orphanet_rare diseases +MONDO:0018533 rare diseases +MONDO:0018534 gard_rare diseases +MONDO:0018534 nord_rare diseases +MONDO:0018534 ordo_disorder diseases +MONDO:0018534 orphanet_rare diseases +MONDO:0018534 rare diseases +MONDO:0018535 gard_rare diseases +MONDO:0018535 nord_rare diseases +MONDO:0018535 ordo_disorder diseases +MONDO:0018535 orphanet_rare diseases +MONDO:0018535 rare diseases +MONDO:0018536 gard_rare diseases +MONDO:0018536 nord_rare diseases +MONDO:0018536 ordo_disorder diseases +MONDO:0018536 orphanet_rare diseases +MONDO:0018536 rare diseases +MONDO:0018537 gard_rare diseases +MONDO:0018537 nord_rare diseases +MONDO:0018537 ordo_disorder diseases +MONDO:0018537 orphanet_rare diseases +MONDO:0018537 rare diseases +MONDO:0018540 gard_rare diseases +MONDO:0018540 nord_rare diseases +MONDO:0018540 ordo_disorder diseases +MONDO:0018540 orphanet_rare diseases +MONDO:0018540 otar diseases +MONDO:0018540 rare diseases +MONDO:0018541 gard_rare diseases +MONDO:0018541 nord_rare diseases +MONDO:0018541 ordo_disorder diseases +MONDO:0018541 orphanet_rare diseases +MONDO:0018541 otar diseases +MONDO:0018541 rare diseases +MONDO:0018542 disease_grouping diseases +MONDO:0018542 gard_rare diseases +MONDO:0018542 nord_rare diseases +MONDO:0018542 ordo_group_of_disorders diseases +MONDO:0018542 otar diseases +MONDO:0018542 rare diseases +MONDO:0018543 gard_rare diseases +MONDO:0018543 nord_rare diseases +MONDO:0018543 ordo_subtype_of_a_disorder diseases +MONDO:0018543 otar diseases +MONDO:0018543 rare diseases +MONDO:0018544 clingen diseases +MONDO:0018544 gard_rare diseases +MONDO:0018544 nord_rare diseases +MONDO:0018544 ordo_disorder diseases +MONDO:0018544 orphanet_rare diseases +MONDO:0018544 otar diseases +MONDO:0018544 rare diseases +MONDO:0018546 gard_rare diseases +MONDO:0018546 nord_rare diseases +MONDO:0018546 ordo_disorder diseases +MONDO:0018546 orphanet_rare diseases +MONDO:0018546 otar diseases +MONDO:0018546 rare diseases +MONDO:0018547 nord_rare diseases +MONDO:0018547 ordo_clinical_situation diseases +MONDO:0018547 ordo_disorder diseases +MONDO:0018547 orphanet_rare diseases +MONDO:0018547 rare diseases +MONDO:0018548 nord_rare diseases +MONDO:0018548 ordo_clinical_situation diseases +MONDO:0018548 ordo_disorder diseases +MONDO:0018548 orphanet_rare diseases +MONDO:0018548 rare diseases +MONDO:0018551 gard_rare diseases +MONDO:0018551 nord_rare diseases +MONDO:0018551 ordo_disorder diseases +MONDO:0018551 ordo_morphological_anomaly diseases +MONDO:0018551 orphanet_rare diseases +MONDO:0018551 rare diseases +MONDO:0018552 gard_rare diseases +MONDO:0018552 nord_rare diseases +MONDO:0018552 ordo_disorder diseases +MONDO:0018552 ordo_morphological_anomaly diseases +MONDO:0018552 orphanet_rare diseases +MONDO:0018552 rare diseases +MONDO:0018553 gard_rare diseases +MONDO:0018553 nord_rare diseases +MONDO:0018553 ordo_disorder diseases +MONDO:0018553 ordo_morphological_anomaly diseases +MONDO:0018553 orphanet_rare diseases +MONDO:0018553 rare diseases +MONDO:0018554 clingen diseases +MONDO:0018554 disease_grouping diseases +MONDO:0018554 gard_rare diseases +MONDO:0018554 nord_rare diseases +MONDO:0018554 ordo_group_of_disorders diseases +MONDO:0018554 otar diseases +MONDO:0018554 rare diseases +MONDO:0018555 gard_rare diseases +MONDO:0018555 ordo_subtype_of_a_disorder diseases +MONDO:0018555 otar diseases +MONDO:0018555 rare diseases +MONDO:0018556 gard_rare diseases +MONDO:0018556 nord_rare diseases +MONDO:0018556 ordo_disorder diseases +MONDO:0018556 orphanet_rare diseases +MONDO:0018556 rare diseases +MONDO:0018559 disease_grouping diseases +MONDO:0018559 gard_rare diseases +MONDO:0018559 ordo_group_of_disorders diseases +MONDO:0018559 otar diseases +MONDO:0018559 rare diseases +MONDO:0018561 disease_grouping diseases +MONDO:0018561 gard_rare diseases +MONDO:0018561 ordo_group_of_disorders diseases +MONDO:0018561 rare diseases +MONDO:0018563 gard_rare diseases +MONDO:0018563 ordo_morphological_anomaly diseases +MONDO:0018563 rare diseases +MONDO:0018564 gard_rare diseases +MONDO:0018564 nord_rare diseases +MONDO:0018564 ordo_disorder diseases +MONDO:0018564 ordo_malformation_syndrome diseases +MONDO:0018564 orphanet_rare diseases +MONDO:0018564 rare diseases +MONDO:0018565 disease_grouping diseases +MONDO:0018565 gard_rare diseases +MONDO:0018565 nord_rare diseases +MONDO:0018565 ordo_group_of_disorders diseases +MONDO:0018565 rare diseases +MONDO:0018566 gard_rare diseases +MONDO:0018566 nord_rare diseases +MONDO:0018566 ordo_disorder diseases +MONDO:0018566 orphanet_rare diseases +MONDO:0018566 rare diseases +MONDO:0018567 gard_rare diseases +MONDO:0018567 nord_rare diseases +MONDO:0018567 ordo_disorder diseases +MONDO:0018567 orphanet_rare diseases +MONDO:0018567 rare diseases +MONDO:0018569 gard_rare diseases +MONDO:0018569 nord_rare diseases +MONDO:0018569 ordo_disorder diseases +MONDO:0018569 ordo_malformation_syndrome diseases +MONDO:0018569 orphanet_rare diseases +MONDO:0018569 rare diseases +MONDO:0018570 gard_rare diseases +MONDO:0018570 nord_rare diseases +MONDO:0018570 ordo_disorder diseases +MONDO:0018570 orphanet_rare diseases +MONDO:0018570 otar diseases +MONDO:0018570 rare diseases +MONDO:0018571 gard_rare diseases +MONDO:0018571 ordo_disorder diseases +MONDO:0018571 ordo_malformation_syndrome diseases +MONDO:0018571 orphanet_rare diseases +MONDO:0018571 rare diseases +MONDO:0018572 gard_rare diseases +MONDO:0018572 nord_rare diseases +MONDO:0018572 ordo_disorder diseases +MONDO:0018572 ordo_malformation_syndrome diseases +MONDO:0018572 orphanet_rare diseases +MONDO:0018572 rare diseases +MONDO:0018573 gard_rare diseases +MONDO:0018573 nord_rare diseases +MONDO:0018573 ordo_disorder diseases +MONDO:0018573 orphanet_rare diseases +MONDO:0018573 rare diseases +MONDO:0018576 gard_rare diseases +MONDO:0018576 nord_rare diseases +MONDO:0018576 ordo_disorder diseases +MONDO:0018576 orphanet_rare diseases +MONDO:0018576 rare diseases +MONDO:0018577 gard_rare diseases +MONDO:0018577 nord_rare diseases +MONDO:0018577 ordo_disorder diseases +MONDO:0018577 orphanet_rare diseases +MONDO:0018577 rare diseases +MONDO:0018581 gard_rare diseases +MONDO:0018581 nord_rare diseases +MONDO:0018581 ordo_subtype_of_a_disorder diseases +MONDO:0018581 rare diseases +MONDO:0018582 gard_rare diseases +MONDO:0018582 nord_rare diseases +MONDO:0018582 ordo_disorder diseases +MONDO:0018582 orphanet_rare diseases +MONDO:0018582 otar diseases +MONDO:0018582 rare diseases +MONDO:0018583 gard_rare diseases +MONDO:0018583 nord_rare diseases +MONDO:0018583 ordo_disorder diseases +MONDO:0018583 orphanet_rare diseases +MONDO:0018583 rare diseases +MONDO:0018585 gard_rare diseases +MONDO:0018585 nord_rare diseases +MONDO:0018585 ordo_clinical_syndrome diseases +MONDO:0018585 ordo_disorder diseases +MONDO:0018585 orphanet_rare diseases +MONDO:0018585 rare diseases +MONDO:0018586 gard_rare diseases +MONDO:0018586 nord_rare diseases +MONDO:0018586 ordo_clinical_situation diseases +MONDO:0018586 ordo_disorder diseases +MONDO:0018586 orphanet_rare diseases +MONDO:0018586 rare diseases +MONDO:0018587 gard_rare diseases +MONDO:0018587 nord_rare diseases +MONDO:0018587 ordo_disorder diseases +MONDO:0018587 orphanet_rare diseases +MONDO:0018587 rare diseases +MONDO:0018588 gard_rare diseases +MONDO:0018588 nord_rare diseases +MONDO:0018588 ordo_disorder diseases +MONDO:0018588 orphanet_rare diseases +MONDO:0018588 otar diseases +MONDO:0018588 rare diseases +MONDO:0018589 gard_rare diseases +MONDO:0018589 nord_rare diseases +MONDO:0018589 ordo_disorder diseases +MONDO:0018589 orphanet_rare diseases +MONDO:0018589 rare diseases +MONDO:0018590 disease_grouping diseases +MONDO:0018590 gard_rare diseases +MONDO:0018590 ordo_group_of_disorders diseases +MONDO:0018590 rare diseases +MONDO:0018591 gard_rare diseases +MONDO:0018591 nord_rare diseases +MONDO:0018591 ordo_disorder diseases +MONDO:0018591 orphanet_rare diseases +MONDO:0018591 otar diseases +MONDO:0018591 rare diseases +MONDO:0018592 gard_rare diseases +MONDO:0018592 nord_rare diseases +MONDO:0018592 ordo_subtype_of_a_disorder diseases +MONDO:0018592 rare diseases +MONDO:0018593 gard_rare diseases +MONDO:0018593 nord_rare diseases +MONDO:0018593 ordo_subtype_of_a_disorder diseases +MONDO:0018593 rare diseases +MONDO:0018594 gard_rare diseases +MONDO:0018594 nord_rare diseases +MONDO:0018594 ordo_subtype_of_a_disorder diseases +MONDO:0018594 rare diseases +MONDO:0018595 gard_rare diseases +MONDO:0018595 nord_rare diseases +MONDO:0018595 ordo_subtype_of_a_disorder diseases +MONDO:0018595 rare diseases +MONDO:0018596 gard_rare diseases +MONDO:0018596 nord_rare diseases +MONDO:0018596 ordo_subtype_of_a_disorder diseases +MONDO:0018596 rare diseases +MONDO:0018597 gard_rare diseases +MONDO:0018597 nord_rare diseases +MONDO:0018597 ordo_clinical_situation diseases +MONDO:0018597 ordo_disorder diseases +MONDO:0018597 orphanet_rare diseases +MONDO:0018597 rare diseases +MONDO:0018599 gard_rare diseases +MONDO:0018599 nord_rare diseases +MONDO:0018599 ordo_disorder diseases +MONDO:0018599 orphanet_rare diseases +MONDO:0018599 rare diseases +MONDO:0018600 gard_rare diseases +MONDO:0018600 nord_rare diseases +MONDO:0018600 ordo_disorder diseases +MONDO:0018600 orphanet_rare diseases +MONDO:0018600 rare diseases +MONDO:0018601 gard_rare diseases +MONDO:0018601 nord_rare diseases +MONDO:0018601 ordo_disorder diseases +MONDO:0018601 ordo_malformation_syndrome diseases +MONDO:0018601 orphanet_rare diseases +MONDO:0018601 rare diseases +MONDO:0018602 gard_rare diseases +MONDO:0018602 nord_rare diseases +MONDO:0018602 ordo_disorder diseases +MONDO:0018602 orphanet_rare diseases +MONDO:0018602 rare diseases +MONDO:0018603 gard_rare diseases +MONDO:0018603 nord_rare diseases +MONDO:0018603 ordo_disorder diseases +MONDO:0018603 orphanet_rare diseases +MONDO:0018603 rare diseases +MONDO:0018604 gard_rare diseases +MONDO:0018604 nord_rare diseases +MONDO:0018604 ordo_disorder diseases +MONDO:0018604 orphanet_rare diseases +MONDO:0018604 rare diseases +MONDO:0018605 disease_grouping diseases +MONDO:0018605 gard_rare diseases +MONDO:0018605 ordo_group_of_disorders diseases +MONDO:0018605 rare diseases +MONDO:0018606 gard_rare diseases +MONDO:0018606 nord_rare diseases +MONDO:0018606 ordo_disorder diseases +MONDO:0018606 orphanet_rare diseases +MONDO:0018606 rare diseases +MONDO:0018607 gard_rare diseases +MONDO:0018607 nord_rare diseases +MONDO:0018607 ordo_disorder diseases +MONDO:0018607 orphanet_rare diseases +MONDO:0018607 rare diseases +MONDO:0018608 gard_rare diseases +MONDO:0018608 nord_rare diseases +MONDO:0018608 ordo_disorder diseases +MONDO:0018608 orphanet_rare diseases +MONDO:0018608 rare diseases +MONDO:0018610 gard_rare diseases +MONDO:0018610 nord_rare diseases +MONDO:0018610 ordo_subtype_of_a_disorder diseases +MONDO:0018610 rare diseases +MONDO:0018611 gard_rare diseases +MONDO:0018611 nord_rare diseases +MONDO:0018611 ordo_subtype_of_a_disorder diseases +MONDO:0018611 rare diseases +MONDO:0018612 disease_grouping diseases +MONDO:0018612 gard_rare diseases +MONDO:0018612 nord_rare diseases +MONDO:0018612 ordo_group_of_disorders diseases +MONDO:0018612 otar diseases +MONDO:0018612 rare diseases +MONDO:0018613 gard_rare diseases +MONDO:0018613 nord_rare diseases +MONDO:0018613 ordo_disorder diseases +MONDO:0018613 orphanet_rare diseases +MONDO:0018613 rare diseases +MONDO:0018614 clingen diseases +MONDO:0018614 gard_rare diseases +MONDO:0018614 nord_rare diseases +MONDO:0018614 ordo_disorder diseases +MONDO:0018614 orphanet_rare diseases +MONDO:0018614 otar diseases +MONDO:0018614 rare diseases +MONDO:0018615 gard_rare diseases +MONDO:0018615 nord_rare diseases +MONDO:0018615 ordo_disorder diseases +MONDO:0018615 orphanet_rare diseases +MONDO:0018615 rare diseases +MONDO:0018616 gard_rare diseases +MONDO:0018616 nord_rare diseases +MONDO:0018616 ordo_disorder diseases +MONDO:0018616 orphanet_rare diseases +MONDO:0018616 rare diseases +MONDO:0018617 gard_rare diseases +MONDO:0018617 nord_rare diseases +MONDO:0018617 ordo_clinical_syndrome diseases +MONDO:0018617 ordo_disorder diseases +MONDO:0018617 orphanet_rare diseases +MONDO:0018617 rare diseases +MONDO:0018620 gard_rare diseases +MONDO:0018620 nord_rare diseases +MONDO:0018620 ordo_disorder diseases +MONDO:0018620 orphanet_rare diseases +MONDO:0018620 rare diseases +MONDO:0018621 gard_rare diseases +MONDO:0018621 nord_rare diseases +MONDO:0018621 ordo_disorder diseases +MONDO:0018621 orphanet_rare diseases +MONDO:0018621 rare diseases +MONDO:0018623 gard_rare diseases +MONDO:0018623 nord_rare diseases +MONDO:0018623 ordo_disorder diseases +MONDO:0018623 orphanet_rare diseases +MONDO:0018623 rare diseases +MONDO:0018624 gard_rare diseases +MONDO:0018624 nord_rare diseases +MONDO:0018624 ordo_disorder diseases +MONDO:0018624 orphanet_rare diseases +MONDO:0018624 rare diseases +MONDO:0018625 gard_rare diseases +MONDO:0018625 nord_rare diseases +MONDO:0018625 ordo_subtype_of_a_disorder diseases +MONDO:0018625 rare diseases +MONDO:0018626 gard_rare diseases +MONDO:0018626 nord_rare diseases +MONDO:0018626 ordo_disorder diseases +MONDO:0018626 orphanet_rare diseases +MONDO:0018626 otar diseases +MONDO:0018626 rare diseases +MONDO:0018628 gard_rare diseases +MONDO:0018628 nord_rare diseases +MONDO:0018628 ordo_clinical_situation diseases +MONDO:0018628 ordo_disorder diseases +MONDO:0018628 orphanet_rare diseases +MONDO:0018628 rare diseases +MONDO:0018629 gard_rare diseases +MONDO:0018629 nord_rare diseases +MONDO:0018629 ordo_subtype_of_a_disorder diseases +MONDO:0018629 rare diseases +MONDO:0018630 clingen diseases +MONDO:0018630 disease_grouping diseases +MONDO:0018630 gard_rare diseases +MONDO:0018630 nord_rare diseases +MONDO:0018630 ordo_group_of_disorders diseases +MONDO:0018630 otar diseases +MONDO:0018630 rare diseases +MONDO:0018631 gard_rare diseases +MONDO:0018631 nord_rare diseases +MONDO:0018631 ordo_disorder diseases +MONDO:0018631 orphanet_rare diseases +MONDO:0018631 otar diseases +MONDO:0018631 rare diseases +MONDO:0018632 gard_rare diseases +MONDO:0018632 nord_rare diseases +MONDO:0018632 ordo_disorder diseases +MONDO:0018632 ordo_malformation_syndrome diseases +MONDO:0018632 orphanet_rare diseases +MONDO:0018632 rare diseases +MONDO:0018633 gard_rare diseases +MONDO:0018633 nord_rare diseases +MONDO:0018633 ordo_disorder diseases +MONDO:0018633 ordo_malformation_syndrome diseases +MONDO:0018633 orphanet_rare diseases +MONDO:0018633 rare diseases +MONDO:0018634 disease_grouping diseases +MONDO:0018634 gard_rare diseases +MONDO:0018634 nord_rare diseases +MONDO:0018634 ordo_group_of_disorders diseases +MONDO:0018634 otar diseases +MONDO:0018634 rare diseases +MONDO:0018635 gard_rare diseases +MONDO:0018635 nord_rare diseases +MONDO:0018635 ordo_disorder diseases +MONDO:0018635 orphanet_rare diseases +MONDO:0018635 rare diseases +MONDO:0018636 gard_rare diseases +MONDO:0018636 nord_rare diseases +MONDO:0018636 ordo_disorder diseases +MONDO:0018636 orphanet_rare diseases +MONDO:0018636 rare diseases +MONDO:0018637 gard_rare diseases +MONDO:0018637 nord_rare diseases +MONDO:0018637 ordo_disorder diseases +MONDO:0018637 orphanet_rare diseases +MONDO:0018637 otar diseases +MONDO:0018637 rare diseases +MONDO:0018638 disease_grouping diseases +MONDO:0018638 gard_rare diseases +MONDO:0018638 ordo_group_of_disorders diseases +MONDO:0018638 otar diseases +MONDO:0018638 rare diseases +MONDO:0018639 disease_grouping diseases +MONDO:0018639 gard_rare diseases +MONDO:0018639 nord_rare diseases +MONDO:0018639 ordo_group_of_disorders diseases +MONDO:0018639 rare diseases +MONDO:0018640 disease_grouping diseases +MONDO:0018640 gard_rare diseases +MONDO:0018640 ordo_group_of_disorders diseases +MONDO:0018640 otar diseases +MONDO:0018640 rare diseases +MONDO:0018642 gard_rare diseases +MONDO:0018642 nord_rare diseases +MONDO:0018642 ordo_disorder diseases +MONDO:0018642 orphanet_rare diseases +MONDO:0018642 otar diseases +MONDO:0018642 rare diseases +MONDO:0018644 gard_rare diseases +MONDO:0018644 ordo_disorder diseases +MONDO:0018644 orphanet_rare diseases +MONDO:0018644 rare diseases +MONDO:0018645 gard_rare diseases +MONDO:0018645 nord_rare diseases +MONDO:0018645 ordo_subtype_of_a_disorder diseases +MONDO:0018645 rare diseases +MONDO:0018646 disease_grouping diseases +MONDO:0018646 gard_rare diseases +MONDO:0018646 ordo_group_of_disorders diseases +MONDO:0018646 otar diseases +MONDO:0018646 rare diseases +MONDO:0018647 gard_rare diseases +MONDO:0018647 nord_rare diseases +MONDO:0018647 ordo_disorder diseases +MONDO:0018647 orphanet_rare diseases +MONDO:0018647 rare diseases +MONDO:0018648 gard_rare diseases +MONDO:0018648 nord_rare diseases +MONDO:0018648 ordo_disorder diseases +MONDO:0018648 orphanet_rare diseases +MONDO:0018648 otar diseases +MONDO:0018648 rare diseases +MONDO:0018653 gard_rare diseases +MONDO:0018653 nord_rare diseases +MONDO:0018653 ordo_subtype_of_a_disorder diseases +MONDO:0018653 otar diseases +MONDO:0018653 rare diseases +MONDO:0018654 gard_rare diseases +MONDO:0018654 nord_rare diseases +MONDO:0018654 ordo_clinical_syndrome diseases +MONDO:0018654 ordo_disorder diseases +MONDO:0018654 orphanet_rare diseases +MONDO:0018654 otar diseases +MONDO:0018654 rare diseases +MONDO:0018655 gard_rare diseases +MONDO:0018655 ordo_subtype_of_a_disorder diseases +MONDO:0018655 rare diseases +MONDO:0018656 gard_rare diseases +MONDO:0018656 nord_rare diseases +MONDO:0018656 ordo_subtype_of_a_disorder diseases +MONDO:0018656 otar diseases +MONDO:0018656 rare diseases +MONDO:0018657 gard_rare diseases +MONDO:0018657 nord_rare diseases +MONDO:0018657 ordo_disorder diseases +MONDO:0018657 orphanet_rare diseases +MONDO:0018657 rare diseases +MONDO:0018658 gard_rare diseases +MONDO:0018658 nord_rare diseases +MONDO:0018658 ordo_disorder diseases +MONDO:0018658 ordo_malformation_syndrome diseases +MONDO:0018658 orphanet_rare diseases +MONDO:0018658 rare diseases +MONDO:0018659 disease_grouping diseases +MONDO:0018659 gard_rare diseases +MONDO:0018659 ordo_group_of_disorders diseases +MONDO:0018659 rare diseases +MONDO:0018660 disease_grouping diseases +MONDO:0018660 gard_rare diseases +MONDO:0018660 nord_rare diseases +MONDO:0018660 ordo_group_of_disorders diseases +MONDO:0018660 otar diseases +MONDO:0018660 rare diseases +MONDO:0018661 gard_rare diseases +MONDO:0018661 nord_rare diseases +MONDO:0018661 ordo_disorder diseases +MONDO:0018661 orphanet_rare diseases +MONDO:0018661 otar diseases +MONDO:0018661 rare diseases +MONDO:0018662 gard_rare diseases +MONDO:0018662 nord_rare diseases +MONDO:0018662 ordo_disorder diseases +MONDO:0018662 ordo_malformation_syndrome diseases +MONDO:0018662 orphanet_rare diseases +MONDO:0018662 otar diseases +MONDO:0018662 rare diseases +MONDO:0018663 clingen diseases +MONDO:0018663 gard_rare diseases +MONDO:0018663 nord_rare diseases +MONDO:0018663 ordo_disorder diseases +MONDO:0018663 ordo_malformation_syndrome diseases +MONDO:0018663 orphanet_rare diseases +MONDO:0018663 otar diseases +MONDO:0018663 rare diseases +MONDO:0018664 gard_rare diseases +MONDO:0018664 nord_rare diseases +MONDO:0018664 ordo_disorder diseases +MONDO:0018664 ordo_morphological_anomaly diseases +MONDO:0018664 orphanet_rare diseases +MONDO:0018664 rare diseases +MONDO:0018666 gard_rare diseases +MONDO:0018666 nord_rare diseases +MONDO:0018666 ordo_disorder diseases +MONDO:0018666 orphanet_rare diseases +MONDO:0018666 otar diseases +MONDO:0018666 rare diseases +MONDO:0018667 gard_rare diseases +MONDO:0018667 nord_rare diseases +MONDO:0018667 ordo_clinical_situation diseases +MONDO:0018667 ordo_disorder diseases +MONDO:0018667 orphanet_rare diseases +MONDO:0018667 otar diseases +MONDO:0018667 rare diseases +MONDO:0018668 gard_rare diseases +MONDO:0018668 nord_rare diseases +MONDO:0018668 ordo_disorder diseases +MONDO:0018668 orphanet_rare diseases +MONDO:0018668 rare diseases +MONDO:0018669 gard_rare diseases +MONDO:0018669 nord_rare diseases +MONDO:0018669 ordo_clinical_situation diseases +MONDO:0018669 ordo_disorder diseases +MONDO:0018669 orphanet_rare diseases +MONDO:0018669 rare diseases +MONDO:0018670 gard_rare diseases +MONDO:0018670 nord_rare diseases +MONDO:0018670 ordo_disorder diseases +MONDO:0018670 orphanet_rare diseases +MONDO:0018670 rare diseases +MONDO:0018671 gard_rare diseases +MONDO:0018671 nord_rare diseases +MONDO:0018671 ordo_subtype_of_a_disorder diseases +MONDO:0018671 rare diseases +MONDO:0018672 gard_rare diseases +MONDO:0018672 nord_rare diseases +MONDO:0018672 ordo_subtype_of_a_disorder diseases +MONDO:0018672 rare diseases +MONDO:0018673 gard_rare diseases +MONDO:0018673 nord_rare diseases +MONDO:0018673 ordo_subtype_of_a_disorder diseases +MONDO:0018673 rare diseases +MONDO:0018674 gard_rare diseases +MONDO:0018674 nord_rare diseases +MONDO:0018674 ordo_subtype_of_a_disorder diseases +MONDO:0018674 rare diseases +MONDO:0018675 gard_rare diseases +MONDO:0018675 nord_rare diseases +MONDO:0018675 ordo_subtype_of_a_disorder diseases +MONDO:0018675 otar diseases +MONDO:0018675 rare diseases +MONDO:0018676 gard_rare diseases +MONDO:0018676 nord_rare diseases +MONDO:0018676 ordo_disorder diseases +MONDO:0018676 orphanet_rare diseases +MONDO:0018676 rare diseases +MONDO:0018677 disease_grouping diseases +MONDO:0018677 gard_rare diseases +MONDO:0018677 nord_rare diseases +MONDO:0018677 ordo_disorder diseases +MONDO:0018677 ordo_group_of_disorders diseases +MONDO:0018677 ordo_morphological_anomaly diseases +MONDO:0018677 orphanet_rare diseases +MONDO:0018677 otar diseases +MONDO:0018677 rare diseases +MONDO:0018678 gard_rare diseases +MONDO:0018678 nord_rare diseases +MONDO:0018678 ordo_clinical_syndrome diseases +MONDO:0018678 ordo_disorder diseases +MONDO:0018678 orphanet_rare diseases +MONDO:0018678 rare diseases +MONDO:0018679 gard_rare diseases +MONDO:0018679 nord_rare diseases +MONDO:0018679 ordo_disorder diseases +MONDO:0018679 orphanet_rare diseases +MONDO:0018679 rare diseases +MONDO:0018680 gard_rare diseases +MONDO:0018680 nord_rare diseases +MONDO:0018680 ordo_disorder diseases +MONDO:0018680 orphanet_rare diseases +MONDO:0018680 rare diseases +MONDO:0018681 clingen diseases +MONDO:0018681 gard_rare diseases +MONDO:0018681 nord_rare diseases +MONDO:0018681 ordo_disorder diseases +MONDO:0018681 ordo_malformation_syndrome diseases +MONDO:0018681 orphanet_rare diseases +MONDO:0018681 otar diseases +MONDO:0018681 rare diseases +MONDO:0018682 gard_rare diseases +MONDO:0018682 nord_rare diseases +MONDO:0018682 ordo_disorder diseases +MONDO:0018682 orphanet_rare diseases +MONDO:0018682 rare diseases +MONDO:0018683 gard_rare diseases +MONDO:0018683 nord_rare diseases +MONDO:0018683 ordo_disorder diseases +MONDO:0018683 orphanet_rare diseases +MONDO:0018683 otar diseases +MONDO:0018683 rare diseases +MONDO:0018684 gard_rare diseases +MONDO:0018684 nord_rare diseases +MONDO:0018684 ordo_disorder diseases +MONDO:0018684 orphanet_rare diseases +MONDO:0018684 rare diseases +MONDO:0018685 gard_rare diseases +MONDO:0018685 nord_rare diseases +MONDO:0018685 ordo_disorder diseases +MONDO:0018685 orphanet_rare diseases +MONDO:0018685 rare diseases +MONDO:0018686 gard_rare diseases +MONDO:0018686 nord_rare diseases +MONDO:0018686 ordo_group_of_disorders diseases +MONDO:0018686 otar diseases +MONDO:0018686 rare diseases +MONDO:0018687 gard_rare diseases +MONDO:0018687 nord_rare diseases +MONDO:0018687 ordo_disorder diseases +MONDO:0018687 orphanet_rare diseases +MONDO:0018687 rare diseases +MONDO:0018688 gard_rare diseases +MONDO:0018688 nord_rare diseases +MONDO:0018688 ordo_disorder diseases +MONDO:0018688 orphanet_rare diseases +MONDO:0018688 rare diseases +MONDO:0018689 gard_rare diseases +MONDO:0018689 nord_rare diseases +MONDO:0018689 ordo_disorder diseases +MONDO:0018689 orphanet_rare diseases +MONDO:0018689 otar diseases +MONDO:0018689 rare diseases +MONDO:0018690 gard_rare diseases +MONDO:0018690 nord_rare diseases +MONDO:0018690 ordo_disorder diseases +MONDO:0018690 orphanet_rare diseases +MONDO:0018690 otar diseases +MONDO:0018690 rare diseases +MONDO:0018692 gard_rare diseases +MONDO:0018692 nord_rare diseases +MONDO:0018692 ordo_disorder diseases +MONDO:0018692 orphanet_rare diseases +MONDO:0018692 rare diseases +MONDO:0018694 gard_rare diseases +MONDO:0018694 nord_rare diseases +MONDO:0018694 ordo_disorder diseases +MONDO:0018694 ordo_morphological_anomaly diseases +MONDO:0018694 orphanet_rare diseases +MONDO:0018694 rare diseases +MONDO:0018695 gard_rare diseases +MONDO:0018695 nord_rare diseases +MONDO:0018695 ordo_disorder diseases +MONDO:0018695 orphanet_rare diseases +MONDO:0018695 otar diseases +MONDO:0018695 rare diseases +MONDO:0018696 gard_rare diseases +MONDO:0018696 nord_rare diseases +MONDO:0018696 ordo_disorder diseases +MONDO:0018696 orphanet_rare diseases +MONDO:0018696 otar diseases +MONDO:0018696 rare diseases +MONDO:0018697 gard_rare diseases +MONDO:0018697 nord_rare diseases +MONDO:0018697 ordo_disorder diseases +MONDO:0018697 ordo_malformation_syndrome diseases +MONDO:0018697 orphanet_rare diseases +MONDO:0018697 rare diseases +MONDO:0018698 gard_rare diseases +MONDO:0018698 nord_rare diseases +MONDO:0018698 ordo_disorder diseases +MONDO:0018698 orphanet_rare diseases +MONDO:0018698 otar diseases +MONDO:0018698 rare diseases +MONDO:0018702 gard_rare diseases +MONDO:0018702 nord_rare diseases +MONDO:0018702 ordo_disorder diseases +MONDO:0018702 orphanet_rare diseases +MONDO:0018702 rare diseases +MONDO:0018703 gard_rare diseases +MONDO:0018703 nord_rare diseases +MONDO:0018703 ordo_disorder diseases +MONDO:0018703 ordo_morphological_anomaly diseases +MONDO:0018703 orphanet_rare diseases +MONDO:0018703 rare diseases +MONDO:0018705 gard_rare diseases +MONDO:0018705 nord_rare diseases +MONDO:0018705 ordo_disorder diseases +MONDO:0018705 orphanet_rare diseases +MONDO:0018705 rare diseases +MONDO:0018708 gard_rare diseases +MONDO:0018708 rare diseases +MONDO:0018709 gard_rare diseases +MONDO:0018709 nord_rare diseases +MONDO:0018709 ordo_disorder diseases +MONDO:0018709 orphanet_rare diseases +MONDO:0018709 rare diseases +MONDO:0018710 gard_rare diseases +MONDO:0018710 nord_rare diseases +MONDO:0018710 ordo_disorder diseases +MONDO:0018710 ordo_malformation_syndrome diseases +MONDO:0018710 orphanet_rare diseases +MONDO:0018710 rare diseases +MONDO:0018711 gard_rare diseases +MONDO:0018711 nord_rare diseases +MONDO:0018711 ordo_disorder diseases +MONDO:0018711 ordo_malformation_syndrome diseases +MONDO:0018711 orphanet_rare diseases +MONDO:0018711 rare diseases +MONDO:0018712 gard_rare diseases +MONDO:0018712 nord_rare diseases +MONDO:0018712 ordo_disorder diseases +MONDO:0018712 orphanet_rare diseases +MONDO:0018712 rare diseases +MONDO:0018713 gard_rare diseases +MONDO:0018713 nord_rare diseases +MONDO:0018713 ordo_disorder diseases +MONDO:0018713 orphanet_rare diseases +MONDO:0018713 rare diseases +MONDO:0018714 gard_rare diseases +MONDO:0018714 nord_rare diseases +MONDO:0018714 ordo_disorder diseases +MONDO:0018714 orphanet_rare diseases +MONDO:0018714 rare diseases +MONDO:0018715 disease_grouping diseases +MONDO:0018715 gard_rare diseases +MONDO:0018715 ordo_group_of_disorders diseases +MONDO:0018715 otar diseases +MONDO:0018715 rare diseases +MONDO:0018716 gard_rare diseases +MONDO:0018716 nord_rare diseases +MONDO:0018716 ordo_disorder diseases +MONDO:0018716 orphanet_rare diseases +MONDO:0018716 rare diseases +MONDO:0018717 gard_rare diseases +MONDO:0018717 nord_rare diseases +MONDO:0018717 ordo_disorder diseases +MONDO:0018717 ordo_malformation_syndrome diseases +MONDO:0018717 orphanet_rare diseases +MONDO:0018717 rare diseases +MONDO:0018724 gard_rare diseases +MONDO:0018724 nord_rare diseases +MONDO:0018724 ordo_disorder diseases +MONDO:0018724 ordo_malformation_syndrome diseases +MONDO:0018724 orphanet_rare diseases +MONDO:0018724 rare diseases +MONDO:0018725 gard_rare diseases +MONDO:0018725 nord_rare diseases +MONDO:0018725 ordo_disorder diseases +MONDO:0018725 ordo_malformation_syndrome diseases +MONDO:0018725 orphanet_rare diseases +MONDO:0018725 rare diseases +MONDO:0018733 gard_rare diseases +MONDO:0018733 nord_rare diseases +MONDO:0018733 ordo_subtype_of_a_disorder diseases +MONDO:0018733 rare diseases +MONDO:0018734 gard_rare diseases +MONDO:0018734 nord_rare diseases +MONDO:0018734 ordo_disorder diseases +MONDO:0018734 orphanet_rare diseases +MONDO:0018734 rare diseases +MONDO:0018735 gard_rare diseases +MONDO:0018735 nord_rare diseases +MONDO:0018735 ordo_disorder diseases +MONDO:0018735 orphanet_rare diseases +MONDO:0018735 rare diseases +MONDO:0018736 gard_rare diseases +MONDO:0018736 nord_rare diseases +MONDO:0018736 ordo_disorder diseases +MONDO:0018736 orphanet_rare diseases +MONDO:0018736 rare diseases +MONDO:0018737 gard_rare diseases +MONDO:0018737 nord_rare diseases +MONDO:0018737 ordo_disorder diseases +MONDO:0018737 orphanet_rare diseases +MONDO:0018737 rare diseases +MONDO:0018738 nord_rare diseases +MONDO:0018738 ordo_disorder diseases +MONDO:0018738 orphanet_rare diseases +MONDO:0018738 rare diseases +MONDO:0018739 gard_rare diseases +MONDO:0018739 nord_rare diseases +MONDO:0018739 ordo_disorder diseases +MONDO:0018739 orphanet_rare diseases +MONDO:0018739 rare diseases +MONDO:0018740 gard_rare diseases +MONDO:0018740 nord_rare diseases +MONDO:0018740 ordo_disorder diseases +MONDO:0018740 orphanet_rare diseases +MONDO:0018740 otar diseases +MONDO:0018740 rare diseases +MONDO:0018741 nord_rare diseases +MONDO:0018741 ordo_clinical_situation diseases +MONDO:0018741 ordo_disorder diseases +MONDO:0018741 orphanet_rare diseases +MONDO:0018741 rare diseases +MONDO:0018742 gard_rare diseases +MONDO:0018742 nord_rare diseases +MONDO:0018742 ordo_disorder diseases +MONDO:0018742 orphanet_rare diseases +MONDO:0018742 rare diseases +MONDO:0018744 disease_grouping diseases +MONDO:0018744 gard_rare diseases +MONDO:0018744 nord_rare diseases +MONDO:0018744 ordo_group_of_disorders diseases +MONDO:0018744 otar diseases +MONDO:0018744 rare diseases +MONDO:0018746 gard_rare diseases +MONDO:0018746 ordo_disorder diseases +MONDO:0018746 orphanet_rare diseases +MONDO:0018746 otar diseases +MONDO:0018746 rare diseases +MONDO:0018747 gard_rare diseases +MONDO:0018747 nord_rare diseases +MONDO:0018747 ordo_disorder diseases +MONDO:0018747 orphanet_rare diseases +MONDO:0018747 otar diseases +MONDO:0018747 rare diseases +MONDO:0018748 gard_rare diseases +MONDO:0018748 nord_rare diseases +MONDO:0018748 ordo_disorder diseases +MONDO:0018748 orphanet_rare diseases +MONDO:0018748 otar diseases +MONDO:0018748 rare diseases +MONDO:0018749 gard_rare diseases +MONDO:0018749 nord_rare diseases +MONDO:0018749 ordo_disorder diseases +MONDO:0018749 orphanet_rare diseases +MONDO:0018749 otar diseases +MONDO:0018749 rare diseases +MONDO:0018751 disease_grouping diseases +MONDO:0018751 gard_rare diseases +MONDO:0018751 ordo_group_of_disorders diseases +MONDO:0018751 rare diseases +MONDO:0018752 gard_rare diseases +MONDO:0018752 nord_rare diseases +MONDO:0018752 ordo_disorder diseases +MONDO:0018752 orphanet_rare diseases +MONDO:0018752 rare diseases +MONDO:0018754 nord_rare diseases +MONDO:0018754 ordo_clinical_situation diseases +MONDO:0018754 ordo_disorder diseases +MONDO:0018754 orphanet_rare diseases +MONDO:0018754 rare diseases +MONDO:0018755 gard_rare diseases +MONDO:0018755 nord_rare diseases +MONDO:0018755 ordo_disorder diseases +MONDO:0018755 orphanet_rare diseases +MONDO:0018755 rare diseases +MONDO:0018756 gard_rare diseases +MONDO:0018756 nord_rare diseases +MONDO:0018756 ordo_disorder diseases +MONDO:0018756 orphanet_rare diseases +MONDO:0018756 rare diseases +MONDO:0018757 gard_rare diseases +MONDO:0018757 nord_rare diseases +MONDO:0018757 ordo_disorder diseases +MONDO:0018757 ordo_morphological_anomaly diseases +MONDO:0018757 orphanet_rare diseases +MONDO:0018757 rare diseases +MONDO:0018759 gard_rare diseases +MONDO:0018759 nord_rare diseases +MONDO:0018759 ordo_disorder diseases +MONDO:0018759 orphanet_rare diseases +MONDO:0018759 rare diseases +MONDO:0018760 clingen diseases +MONDO:0018760 gard_rare diseases +MONDO:0018760 nord_rare diseases +MONDO:0018760 ordo_disorder diseases +MONDO:0018760 ordo_malformation_syndrome diseases +MONDO:0018760 orphanet_rare diseases +MONDO:0018760 otar diseases +MONDO:0018760 rare diseases +MONDO:0018761 gard_rare diseases +MONDO:0018761 nord_rare diseases +MONDO:0018761 ordo_disorder diseases +MONDO:0018761 orphanet_rare diseases +MONDO:0018761 rare diseases +MONDO:0018762 disease_grouping diseases +MONDO:0018762 gard_rare diseases +MONDO:0018762 nord_rare diseases +MONDO:0018762 ordo_group_of_disorders diseases +MONDO:0018762 otar diseases +MONDO:0018762 rare diseases +MONDO:0018763 gard_rare diseases +MONDO:0018763 nord_rare diseases +MONDO:0018763 ordo_disorder diseases +MONDO:0018763 orphanet_rare diseases +MONDO:0018763 rare diseases +MONDO:0018764 gard_rare diseases +MONDO:0018764 nord_rare diseases +MONDO:0018764 ordo_disorder diseases +MONDO:0018764 ordo_malformation_syndrome diseases +MONDO:0018764 orphanet_rare diseases +MONDO:0018764 otar diseases +MONDO:0018764 rare diseases +MONDO:0018765 gard_rare diseases +MONDO:0018765 nord_rare diseases +MONDO:0018765 ordo_disorder diseases +MONDO:0018765 orphanet_rare diseases +MONDO:0018765 rare diseases +MONDO:0018766 gard_rare diseases +MONDO:0018766 nord_rare diseases +MONDO:0018766 ordo_disorder diseases +MONDO:0018766 orphanet_rare diseases +MONDO:0018766 rare diseases +MONDO:0018767 gard_rare diseases +MONDO:0018767 nord_rare diseases +MONDO:0018767 ordo_disorder diseases +MONDO:0018767 orphanet_rare diseases +MONDO:0018767 rare diseases +MONDO:0018768 gard_rare diseases +MONDO:0018768 nord_rare diseases +MONDO:0018768 ordo_disorder diseases +MONDO:0018768 orphanet_rare diseases +MONDO:0018768 otar diseases +MONDO:0018768 rare diseases +MONDO:0018769 gard_rare diseases +MONDO:0018769 nord_rare diseases +MONDO:0018769 ordo_disorder diseases +MONDO:0018769 orphanet_rare diseases +MONDO:0018769 otar diseases +MONDO:0018769 rare diseases +MONDO:0018770 gard_rare diseases +MONDO:0018770 nord_rare diseases +MONDO:0018770 ordo_disorder diseases +MONDO:0018770 ordo_malformation_syndrome diseases +MONDO:0018770 orphanet_rare diseases +MONDO:0018770 otar diseases +MONDO:0018770 rare diseases +MONDO:0018772 clingen diseases +MONDO:0018772 gard_rare diseases +MONDO:0018772 nord_rare diseases +MONDO:0018772 ordo_disorder diseases +MONDO:0018772 orphanet_rare diseases +MONDO:0018772 otar diseases +MONDO:0018772 rare diseases +MONDO:0018773 gard_rare diseases +MONDO:0018773 nord_rare diseases +MONDO:0018773 ordo_disorder diseases +MONDO:0018773 orphanet_rare diseases +MONDO:0018773 rare diseases +MONDO:0018774 gard_rare diseases +MONDO:0018774 nord_rare diseases +MONDO:0018774 obsoletion_candidate diseases +MONDO:0018774 ordo_disorder diseases +MONDO:0018774 orphanet_rare diseases +MONDO:0018774 rare diseases +MONDO:0018776 clingen diseases +MONDO:0018776 disease_grouping diseases +MONDO:0018776 gard_rare diseases +MONDO:0018776 ordo_group_of_disorders diseases +MONDO:0018776 otar diseases +MONDO:0018776 rare diseases +MONDO:0018777 gard_rare diseases +MONDO:0018777 nord_rare diseases +MONDO:0018777 ordo_disorder diseases +MONDO:0018777 ordo_malformation_syndrome diseases +MONDO:0018777 orphanet_rare diseases +MONDO:0018777 rare diseases +MONDO:0018778 disease_grouping diseases +MONDO:0018778 gard_rare diseases +MONDO:0018778 nord_rare diseases +MONDO:0018778 ordo_group_of_disorders diseases +MONDO:0018778 otar diseases +MONDO:0018778 rare diseases +MONDO:0018780 gard_rare diseases +MONDO:0018780 nord_rare diseases +MONDO:0018780 ordo_disorder diseases +MONDO:0018780 orphanet_rare diseases +MONDO:0018780 rare diseases +MONDO:0018781 gard_rare diseases +MONDO:0018781 nord_rare diseases +MONDO:0018781 ordo_disorder diseases +MONDO:0018781 ordo_inheritance_inconsistent diseases +MONDO:0018781 orphanet_rare diseases +MONDO:0018781 otar diseases +MONDO:0018781 rare diseases +MONDO:0018783 gard_rare diseases +MONDO:0018783 nord_rare diseases +MONDO:0018783 ordo_disorder diseases +MONDO:0018783 orphanet_rare diseases +MONDO:0018783 rare diseases +MONDO:0018784 gard_rare diseases +MONDO:0018784 nord_rare diseases +MONDO:0018784 ordo_disorder diseases +MONDO:0018784 orphanet_rare diseases +MONDO:0018784 rare diseases +MONDO:0018793 gard_rare diseases +MONDO:0018793 nord_rare diseases +MONDO:0018793 ordo_disorder diseases +MONDO:0018793 orphanet_rare diseases +MONDO:0018793 rare diseases +MONDO:0018794 clingen diseases +MONDO:0018794 gard_rare diseases +MONDO:0018794 nord_rare diseases +MONDO:0018794 ordo_disorder diseases +MONDO:0018794 orphanet_rare diseases +MONDO:0018794 otar diseases +MONDO:0018794 rare diseases +MONDO:0018795 clingen diseases +MONDO:0018795 disease_grouping diseases +MONDO:0018795 gard_rare diseases +MONDO:0018795 ordo_group_of_disorders diseases +MONDO:0018795 otar diseases +MONDO:0018795 rare diseases +MONDO:0018800 gard_rare diseases +MONDO:0018800 nord_rare diseases +MONDO:0018800 ordo_subtype_of_a_disorder diseases +MONDO:0018800 otar diseases +MONDO:0018800 rare diseases +MONDO:0018801 gard_rare diseases +MONDO:0018801 nord_rare diseases +MONDO:0018801 ordo_disorder diseases +MONDO:0018801 ordo_morphological_anomaly diseases +MONDO:0018801 orphanet_rare diseases +MONDO:0018801 otar diseases +MONDO:0018801 rare diseases +MONDO:0018804 gard_rare diseases +MONDO:0018804 nord_rare diseases +MONDO:0018804 ordo_subtype_of_a_disorder diseases +MONDO:0018804 rare diseases +MONDO:0018805 gard_rare diseases +MONDO:0018805 nord_rare diseases +MONDO:0018805 ordo_disorder diseases +MONDO:0018805 ordo_morphological_anomaly diseases +MONDO:0018805 orphanet_rare diseases +MONDO:0018805 rare diseases +MONDO:0018806 gard_rare diseases +MONDO:0018806 nord_rare diseases +MONDO:0018806 ordo_disorder diseases +MONDO:0018806 orphanet_rare diseases +MONDO:0018806 rare diseases +MONDO:0018807 gard_rare diseases +MONDO:0018807 nord_rare diseases +MONDO:0018807 ordo_disorder diseases +MONDO:0018807 orphanet_rare diseases +MONDO:0018807 rare diseases +MONDO:0018808 gard_rare diseases +MONDO:0018808 nord_rare diseases +MONDO:0018808 ordo_disorder diseases +MONDO:0018808 ordo_malformation_syndrome diseases +MONDO:0018808 orphanet_rare diseases +MONDO:0018808 rare diseases +MONDO:0018809 gard_rare diseases +MONDO:0018809 nord_rare diseases +MONDO:0018809 ordo_disorder diseases +MONDO:0018809 orphanet_rare diseases +MONDO:0018809 rare diseases +MONDO:0018810 gard_rare diseases +MONDO:0018810 nord_rare diseases +MONDO:0018810 ordo_disorder diseases +MONDO:0018810 ordo_malformation_syndrome diseases +MONDO:0018810 orphanet_rare diseases +MONDO:0018810 rare diseases +MONDO:0018811 gard_rare diseases +MONDO:0018811 nord_rare diseases +MONDO:0018811 ordo_disorder diseases +MONDO:0018811 ordo_morphological_anomaly diseases +MONDO:0018811 orphanet_rare diseases +MONDO:0018811 rare diseases +MONDO:0018813 gard_rare diseases +MONDO:0018813 nord_rare diseases +MONDO:0018813 ordo_disorder diseases +MONDO:0018813 orphanet_rare diseases +MONDO:0018813 rare diseases +MONDO:0018814 disease_grouping diseases +MONDO:0018814 gard_rare diseases +MONDO:0018814 obsoletion_candidate diseases +MONDO:0018814 ordo_group_of_disorders diseases +MONDO:0018814 rare diseases +MONDO:0018815 gard_rare diseases +MONDO:0018815 nord_rare diseases +MONDO:0018815 ordo_disorder diseases +MONDO:0018815 orphanet_rare diseases +MONDO:0018815 otar diseases +MONDO:0018815 rare diseases +MONDO:0018816 gard_rare diseases +MONDO:0018816 nord_rare diseases +MONDO:0018816 ordo_disorder diseases +MONDO:0018816 orphanet_rare diseases +MONDO:0018816 rare diseases +MONDO:0018818 gard_rare diseases +MONDO:0018818 nord_rare diseases +MONDO:0018818 ordo_disorder diseases +MONDO:0018818 orphanet_rare diseases +MONDO:0018818 rare diseases +MONDO:0018820 gard_rare diseases +MONDO:0018820 nord_rare diseases +MONDO:0018820 ordo_disorder diseases +MONDO:0018820 orphanet_rare diseases +MONDO:0018820 otar diseases +MONDO:0018820 rare diseases +MONDO:0018821 gard_rare diseases +MONDO:0018821 nord_rare diseases +MONDO:0018821 ordo_disorder diseases +MONDO:0018821 ordo_malformation_syndrome diseases +MONDO:0018821 orphanet_rare diseases +MONDO:0018821 rare diseases +MONDO:0018822 gard_rare diseases +MONDO:0018822 nord_rare diseases +MONDO:0018822 ordo_disorder diseases +MONDO:0018822 orphanet_rare diseases +MONDO:0018822 rare diseases +MONDO:0018823 gard_rare diseases +MONDO:0018823 nord_rare diseases +MONDO:0018823 ordo_disorder diseases +MONDO:0018823 ordo_malformation_syndrome diseases +MONDO:0018823 orphanet_rare diseases +MONDO:0018823 rare diseases +MONDO:0018824 gard_rare diseases +MONDO:0018824 nord_rare diseases +MONDO:0018824 ordo_disorder diseases +MONDO:0018824 orphanet_rare diseases +MONDO:0018824 rare diseases +MONDO:0018825 gard_rare diseases +MONDO:0018825 nord_rare diseases +MONDO:0018825 ordo_disorder diseases +MONDO:0018825 ordo_malformation_syndrome diseases +MONDO:0018825 orphanet_rare diseases +MONDO:0018825 rare diseases +MONDO:0018826 gard_rare diseases +MONDO:0018826 nord_rare diseases +MONDO:0018826 ordo_subtype_of_a_disorder diseases +MONDO:0018826 rare diseases +MONDO:0018827 gard_rare diseases +MONDO:0018827 nord_rare diseases +MONDO:0018827 ordo_disorder diseases +MONDO:0018827 orphanet_rare diseases +MONDO:0018827 otar diseases +MONDO:0018827 rare diseases +MONDO:0018828 gard_rare diseases +MONDO:0018828 nord_rare diseases +MONDO:0018828 ordo_disorder diseases +MONDO:0018828 orphanet_rare diseases +MONDO:0018828 rare diseases +MONDO:0018829 gard_rare diseases +MONDO:0018829 nord_rare diseases +MONDO:0018829 ordo_etiological_subtype diseases +MONDO:0018829 ordo_subtype_of_a_disorder diseases +MONDO:0018829 otar diseases +MONDO:0018829 rare diseases +MONDO:0018830 gard_rare diseases +MONDO:0018830 nord_rare diseases +MONDO:0018830 ordo_disorder diseases +MONDO:0018830 orphanet_rare diseases +MONDO:0018830 otar diseases +MONDO:0018830 rare diseases +MONDO:0018832 gard_rare diseases +MONDO:0018832 ordo_disorder diseases +MONDO:0018832 orphanet_rare diseases +MONDO:0018832 rare diseases +MONDO:0018835 gard_rare diseases +MONDO:0018835 nord_rare diseases +MONDO:0018835 ordo_subtype_of_a_disorder diseases +MONDO:0018835 rare diseases +MONDO:0018837 gard_rare diseases +MONDO:0018837 nord_rare diseases +MONDO:0018837 ordo_disorder diseases +MONDO:0018837 orphanet_rare diseases +MONDO:0018837 otar diseases +MONDO:0018837 rare diseases +MONDO:0018838 clingen diseases +MONDO:0018838 disease_grouping diseases +MONDO:0018838 gard_rare diseases +MONDO:0018838 nord_rare diseases +MONDO:0018838 ordo_group_of_disorders diseases +MONDO:0018838 otar diseases +MONDO:0018838 rare diseases +MONDO:0018839 gard_rare diseases +MONDO:0018839 nord_rare diseases +MONDO:0018839 ordo_etiological_subtype diseases +MONDO:0018839 ordo_subtype_of_a_disorder diseases +MONDO:0018839 rare diseases +MONDO:0018840 gard_rare diseases +MONDO:0018840 nord_rare diseases +MONDO:0018840 ordo_disorder diseases +MONDO:0018840 orphanet_rare diseases +MONDO:0018840 rare diseases +MONDO:0018841 disease_grouping diseases +MONDO:0018841 gard_rare diseases +MONDO:0018841 ordo_group_of_disorders diseases +MONDO:0018841 otar diseases +MONDO:0018841 rare diseases +MONDO:0018842 gard_rare diseases +MONDO:0018842 nord_rare diseases +MONDO:0018842 ordo_disorder diseases +MONDO:0018842 orphanet_rare diseases +MONDO:0018842 otar diseases +MONDO:0018842 rare diseases +MONDO:0018843 gard_rare diseases +MONDO:0018843 nord_rare diseases +MONDO:0018843 ordo_subtype_of_a_disorder diseases +MONDO:0018843 otar diseases +MONDO:0018843 rare diseases +MONDO:0018844 gard_rare diseases +MONDO:0018844 nord_rare diseases +MONDO:0018844 ordo_disorder diseases +MONDO:0018844 ordo_morphological_anomaly diseases +MONDO:0018844 orphanet_rare diseases +MONDO:0018844 otar diseases +MONDO:0018844 rare diseases +MONDO:0018845 gard_rare diseases +MONDO:0018845 nord_rare diseases +MONDO:0018845 ordo_disorder diseases +MONDO:0018845 orphanet_rare diseases +MONDO:0018845 rare diseases +MONDO:0018846 gard_rare diseases +MONDO:0018846 nord_rare diseases +MONDO:0018846 ordo_disorder diseases +MONDO:0018846 ordo_morphological_anomaly diseases +MONDO:0018846 orphanet_rare diseases +MONDO:0018846 rare diseases +MONDO:0018847 gard_rare diseases +MONDO:0018847 nord_rare diseases +MONDO:0018847 ordo_disorder diseases +MONDO:0018847 ordo_morphological_anomaly diseases +MONDO:0018847 orphanet_rare diseases +MONDO:0018847 rare diseases +MONDO:0018848 gard_rare diseases +MONDO:0018848 nord_rare diseases +MONDO:0018848 ordo_subtype_of_a_disorder diseases +MONDO:0018848 otar diseases +MONDO:0018848 rare diseases +MONDO:0018849 clingen diseases +MONDO:0018849 gard_rare diseases +MONDO:0018849 nord_rare diseases +MONDO:0018849 ordo_disorder diseases +MONDO:0018849 orphanet_rare diseases +MONDO:0018849 otar diseases +MONDO:0018849 rare diseases +MONDO:0018850 gard_rare diseases +MONDO:0018850 nord_rare diseases +MONDO:0018850 ordo_disorder diseases +MONDO:0018850 orphanet_rare diseases +MONDO:0018850 rare diseases +MONDO:0018851 gard_rare diseases +MONDO:0018851 nord_rare diseases +MONDO:0018851 ordo_disorder diseases +MONDO:0018851 orphanet_rare diseases +MONDO:0018851 otar diseases +MONDO:0018851 rare diseases +MONDO:0018852 clingen diseases +MONDO:0018852 gard_rare diseases +MONDO:0018852 nord_rare diseases +MONDO:0018852 ordo_disorder diseases +MONDO:0018852 orphanet_rare diseases +MONDO:0018852 otar diseases +MONDO:0018852 rare diseases +MONDO:0018853 gard_rare diseases +MONDO:0018853 nord_rare diseases +MONDO:0018853 ordo_disorder diseases +MONDO:0018853 orphanet_rare diseases +MONDO:0018853 otar diseases +MONDO:0018853 rare diseases +MONDO:0018854 gard_rare diseases +MONDO:0018854 nord_rare diseases +MONDO:0018854 ordo_disorder diseases +MONDO:0018854 orphanet_rare diseases +MONDO:0018854 rare diseases +MONDO:0018855 disease_grouping diseases +MONDO:0018855 gard_rare diseases +MONDO:0018855 nord_rare diseases +MONDO:0018855 ordo_group_of_disorders diseases +MONDO:0018855 otar diseases +MONDO:0018855 rare diseases +MONDO:0018856 gard_rare diseases +MONDO:0018856 nord_rare diseases +MONDO:0018856 ordo_disorder diseases +MONDO:0018856 orphanet_rare diseases +MONDO:0018856 rare diseases +MONDO:0018857 gard_rare diseases +MONDO:0018857 nord_rare diseases +MONDO:0018857 ordo_disorder diseases +MONDO:0018857 orphanet_rare diseases +MONDO:0018857 rare diseases +MONDO:0018858 gard_rare diseases +MONDO:0018858 nord_rare diseases +MONDO:0018858 ordo_disorder diseases +MONDO:0018858 orphanet_rare diseases +MONDO:0018858 otar diseases +MONDO:0018858 rare diseases +MONDO:0018860 gard_rare diseases +MONDO:0018860 nord_rare diseases +MONDO:0018860 ordo_disorder diseases +MONDO:0018860 ordo_malformation_syndrome diseases +MONDO:0018860 orphanet_rare diseases +MONDO:0018860 rare diseases +MONDO:0018861 gard_rare diseases +MONDO:0018861 nord_rare diseases +MONDO:0018861 ordo_disorder diseases +MONDO:0018861 orphanet_rare diseases +MONDO:0018861 otar diseases +MONDO:0018861 rare diseases +MONDO:0018864 gard_rare diseases +MONDO:0018864 nord_rare diseases +MONDO:0018864 ordo_disorder diseases +MONDO:0018864 orphanet_rare diseases +MONDO:0018864 rare diseases +MONDO:0018865 gard_rare diseases +MONDO:0018865 nord_rare diseases +MONDO:0018865 ordo_disorder diseases +MONDO:0018865 orphanet_rare diseases +MONDO:0018865 otar diseases +MONDO:0018865 rare diseases +MONDO:0018866 gard_rare diseases +MONDO:0018866 nord_rare diseases +MONDO:0018866 ordo_disorder diseases +MONDO:0018866 orphanet_rare diseases +MONDO:0018866 otar diseases +MONDO:0018866 rare diseases +MONDO:0018868 clingen diseases +MONDO:0018868 gard_rare diseases +MONDO:0018868 nord_rare diseases +MONDO:0018868 ordo_disorder diseases +MONDO:0018868 orphanet_rare diseases +MONDO:0018868 otar diseases +MONDO:0018868 rare diseases +MONDO:0018869 disease_grouping diseases +MONDO:0018869 gard_rare diseases +MONDO:0018869 nord_rare diseases +MONDO:0018869 ordo_group_of_disorders diseases +MONDO:0018869 otar diseases +MONDO:0018869 rare diseases +MONDO:0018870 gard_rare diseases +MONDO:0018870 nord_rare diseases +MONDO:0018870 ordo_disorder diseases +MONDO:0018870 orphanet_rare diseases +MONDO:0018870 otar diseases +MONDO:0018870 rare diseases +MONDO:0018871 gard_rare diseases +MONDO:0018871 nord_rare diseases +MONDO:0018871 ordo_disorder diseases +MONDO:0018871 orphanet_rare diseases +MONDO:0018871 otar diseases +MONDO:0018871 rare diseases +MONDO:0018872 gard_rare diseases +MONDO:0018872 nord_rare diseases +MONDO:0018872 ordo_disorder diseases +MONDO:0018872 orphanet_rare diseases +MONDO:0018872 otar diseases +MONDO:0018872 rare diseases +MONDO:0018873 gard_rare diseases +MONDO:0018873 nord_rare diseases +MONDO:0018873 ordo_disorder diseases +MONDO:0018873 orphanet_rare diseases +MONDO:0018873 rare diseases +MONDO:0018874 clingen diseases +MONDO:0018874 disease_grouping diseases +MONDO:0018874 gard_rare diseases +MONDO:0018874 nord_rare diseases +MONDO:0018874 ordo_group_of_disorders diseases +MONDO:0018874 otar diseases +MONDO:0018874 rare diseases +MONDO:0018875 gard_rare diseases +MONDO:0018875 nord_rare diseases +MONDO:0018875 ordo_disorder diseases +MONDO:0018875 orphanet_rare diseases +MONDO:0018875 otar diseases +MONDO:0018875 rare diseases +MONDO:0018876 gard_rare diseases +MONDO:0018876 nord_rare diseases +MONDO:0018876 ordo_disorder diseases +MONDO:0018876 orphanet_rare diseases +MONDO:0018876 otar diseases +MONDO:0018876 rare diseases +MONDO:0018877 gard_rare diseases +MONDO:0018877 nord_rare diseases +MONDO:0018877 ordo_disorder diseases +MONDO:0018877 orphanet_rare diseases +MONDO:0018877 otar diseases +MONDO:0018877 rare diseases +MONDO:0018878 gard_rare diseases +MONDO:0018878 nord_rare diseases +MONDO:0018878 ordo_disorder diseases +MONDO:0018878 ordo_malformation_syndrome diseases +MONDO:0018878 orphanet_rare diseases +MONDO:0018878 otar diseases +MONDO:0018878 rare diseases +MONDO:0018879 gard_rare diseases +MONDO:0018879 nord_rare diseases +MONDO:0018879 ordo_disorder diseases +MONDO:0018879 orphanet_rare diseases +MONDO:0018879 rare diseases +MONDO:0018881 disease_grouping diseases +MONDO:0018881 gard_rare diseases +MONDO:0018881 nord_rare diseases +MONDO:0018881 ordo_group_of_disorders diseases +MONDO:0018881 otar diseases +MONDO:0018881 rare diseases +MONDO:0018882 disease_grouping diseases +MONDO:0018882 gard_rare diseases +MONDO:0018882 ordo_group_of_disorders diseases +MONDO:0018882 otar diseases +MONDO:0018882 rare diseases +MONDO:0018883 gard_rare diseases +MONDO:0018883 nord_rare diseases +MONDO:0018883 ordo_disorder diseases +MONDO:0018883 orphanet_rare diseases +MONDO:0018883 otar diseases +MONDO:0018883 rare diseases +MONDO:0018884 gard_rare diseases +MONDO:0018884 nord_rare diseases +MONDO:0018884 ordo_disorder diseases +MONDO:0018884 orphanet_rare diseases +MONDO:0018884 otar diseases +MONDO:0018884 rare diseases +MONDO:0018885 gard_rare diseases +MONDO:0018885 nord_rare diseases +MONDO:0018885 ordo_disorder diseases +MONDO:0018885 orphanet_rare diseases +MONDO:0018885 rare diseases +MONDO:0018889 gard_rare diseases +MONDO:0018889 nord_rare diseases +MONDO:0018889 ordo_disorder diseases +MONDO:0018889 orphanet_rare diseases +MONDO:0018889 otar diseases +MONDO:0018889 rare diseases +MONDO:0018890 gard_rare diseases +MONDO:0018890 nord_rare diseases +MONDO:0018890 ordo_subtype_of_a_disorder diseases +MONDO:0018890 rare diseases +MONDO:0018891 gard_rare diseases +MONDO:0018891 nord_rare diseases +MONDO:0018891 ordo_disorder diseases +MONDO:0018891 orphanet_rare diseases +MONDO:0018891 otar diseases +MONDO:0018891 rare diseases +MONDO:0018892 gard_rare diseases +MONDO:0018892 nord_rare diseases +MONDO:0018892 ordo_disorder diseases +MONDO:0018892 ordo_malformation_syndrome diseases +MONDO:0018892 orphanet_rare diseases +MONDO:0018892 otar diseases +MONDO:0018892 rare diseases +MONDO:0018893 gard_rare diseases +MONDO:0018893 nord_rare diseases +MONDO:0018893 ordo_disorder diseases +MONDO:0018893 ordo_malformation_syndrome diseases +MONDO:0018893 orphanet_rare diseases +MONDO:0018893 rare diseases +MONDO:0018894 clingen diseases +MONDO:0018894 disease_grouping diseases +MONDO:0018894 gard_rare diseases +MONDO:0018894 ordo_group_of_disorders diseases +MONDO:0018894 otar diseases +MONDO:0018894 rare diseases +MONDO:0018895 gard_rare diseases +MONDO:0018895 nord_rare diseases +MONDO:0018895 ordo_disorder diseases +MONDO:0018895 orphanet_rare diseases +MONDO:0018895 rare diseases +MONDO:0018896 gard_rare diseases +MONDO:0018896 nord_rare diseases +MONDO:0018896 ordo_disorder diseases +MONDO:0018896 orphanet_rare diseases +MONDO:0018896 otar diseases +MONDO:0018896 rare diseases +MONDO:0018897 disease_grouping diseases +MONDO:0018897 gard_rare diseases +MONDO:0018897 nord_rare diseases +MONDO:0018897 ordo_group_of_disorders diseases +MONDO:0018897 rare diseases +MONDO:0018898 disease_grouping diseases +MONDO:0018898 gard_rare diseases +MONDO:0018898 nord_rare diseases +MONDO:0018898 ordo_group_of_disorders diseases +MONDO:0018898 otar diseases +MONDO:0018898 rare diseases +MONDO:0018899 gard_rare diseases +MONDO:0018899 nord_rare diseases +MONDO:0018899 ordo_disorder diseases +MONDO:0018899 orphanet_rare diseases +MONDO:0018899 otar diseases +MONDO:0018899 rare diseases +MONDO:0018900 gard_rare diseases +MONDO:0018900 nord_rare diseases +MONDO:0018900 ordo_disorder diseases +MONDO:0018900 orphanet_rare diseases +MONDO:0018900 rare diseases +MONDO:0018901 gard_rare diseases +MONDO:0018901 nord_rare diseases +MONDO:0018901 ordo_disorder diseases +MONDO:0018901 orphanet_rare diseases +MONDO:0018901 otar diseases +MONDO:0018901 rare diseases +MONDO:0018902 gard_rare diseases +MONDO:0018902 nord_rare diseases +MONDO:0018902 ordo_disorder diseases +MONDO:0018902 orphanet_rare diseases +MONDO:0018902 otar diseases +MONDO:0018902 rare diseases +MONDO:0018903 gard_rare diseases +MONDO:0018903 nord_rare diseases +MONDO:0018903 ordo_disorder diseases +MONDO:0018903 orphanet_rare diseases +MONDO:0018903 otar diseases +MONDO:0018903 rare diseases +MONDO:0018904 gard_rare diseases +MONDO:0018904 nord_rare diseases +MONDO:0018904 ordo_disorder diseases +MONDO:0018904 orphanet_rare diseases +MONDO:0018904 otar diseases +MONDO:0018904 rare diseases +MONDO:0018905 disease_grouping diseases +MONDO:0018905 gard_rare diseases +MONDO:0018905 nord_rare diseases +MONDO:0018905 ordo_group_of_disorders diseases +MONDO:0018905 otar diseases +MONDO:0018905 rare diseases +MONDO:0018906 gard_rare diseases +MONDO:0018906 nord_rare diseases +MONDO:0018906 ordo_disorder diseases +MONDO:0018906 orphanet_rare diseases +MONDO:0018906 otar diseases +MONDO:0018906 rare diseases +MONDO:0018907 gard_rare diseases +MONDO:0018907 nord_rare diseases +MONDO:0018907 ordo_disorder diseases +MONDO:0018907 orphanet_rare diseases +MONDO:0018907 otar diseases +MONDO:0018907 rare diseases +MONDO:0018908 disease_grouping diseases +MONDO:0018908 nord_rare diseases +MONDO:0018908 ordo_group_of_disorders diseases +MONDO:0018908 otar diseases +MONDO:0018908 rare diseases +MONDO:0018910 disease_grouping diseases +MONDO:0018910 gard_rare diseases +MONDO:0018910 nord_rare diseases +MONDO:0018910 ordo_group_of_disorders diseases +MONDO:0018910 otar diseases +MONDO:0018910 rare diseases +MONDO:0018911 gard_rare diseases +MONDO:0018911 nord_rare diseases +MONDO:0018911 ordo_disorder diseases +MONDO:0018911 orphanet_rare diseases +MONDO:0018911 otar diseases +MONDO:0018911 rare diseases +MONDO:0018912 disease_grouping diseases +MONDO:0018912 gard_rare diseases +MONDO:0018912 otar diseases +MONDO:0018912 rare diseases +MONDO:0018913 gard_rare diseases +MONDO:0018913 nord_rare diseases +MONDO:0018913 ordo_disorder diseases +MONDO:0018913 orphanet_rare diseases +MONDO:0018913 otar diseases +MONDO:0018913 rare diseases +MONDO:0018914 gard_rare diseases +MONDO:0018914 nord_rare diseases +MONDO:0018914 ordo_disorder diseases +MONDO:0018914 orphanet_rare diseases +MONDO:0018914 otar diseases +MONDO:0018914 rare diseases +MONDO:0018918 disease_grouping diseases +MONDO:0018918 gard_rare diseases +MONDO:0018918 ordo_group_of_disorders diseases +MONDO:0018918 rare diseases +MONDO:0018919 gard_rare diseases +MONDO:0018919 nord_rare diseases +MONDO:0018919 ordo_disorder diseases +MONDO:0018919 orphanet_rare diseases +MONDO:0018919 otar diseases +MONDO:0018919 rare diseases +MONDO:0018920 gard_rare diseases +MONDO:0018920 nord_rare diseases +MONDO:0018920 ordo_disorder diseases +MONDO:0018920 orphanet_rare diseases +MONDO:0018920 otar diseases +MONDO:0018920 rare diseases +MONDO:0018921 gard_rare diseases +MONDO:0018921 ordo_disorder diseases +MONDO:0018921 ordo_malformation_syndrome diseases +MONDO:0018921 orphanet_rare diseases +MONDO:0018921 otar diseases +MONDO:0018921 rare diseases +MONDO:0018922 gard_rare diseases +MONDO:0018922 nord_rare diseases +MONDO:0018922 ordo_disorder diseases +MONDO:0018922 orphanet_rare diseases +MONDO:0018922 otar diseases +MONDO:0018922 rare diseases +MONDO:0018923 gard_rare diseases +MONDO:0018923 nord_rare diseases +MONDO:0018923 ordo_disorder diseases +MONDO:0018923 ordo_malformation_syndrome diseases +MONDO:0018923 orphanet_rare diseases +MONDO:0018923 otar diseases +MONDO:0018923 rare diseases +MONDO:0018924 gard_rare diseases +MONDO:0018924 nord_rare diseases +MONDO:0018924 ordo_disorder diseases +MONDO:0018924 ordo_malformation_syndrome diseases +MONDO:0018924 orphanet_rare diseases +MONDO:0018924 otar diseases +MONDO:0018924 rare diseases +MONDO:0018925 clingen diseases +MONDO:0018925 gard_rare diseases +MONDO:0018925 nord_rare diseases +MONDO:0018925 ordo_disorder diseases +MONDO:0018925 orphanet_rare diseases +MONDO:0018925 otar diseases +MONDO:0018925 rare diseases +MONDO:0018926 disease_grouping diseases +MONDO:0018926 gard_rare diseases +MONDO:0018926 nord_rare diseases +MONDO:0018926 ordo_group_of_disorders diseases +MONDO:0018926 otar diseases +MONDO:0018926 rare diseases +MONDO:0018927 gard_rare diseases +MONDO:0018927 nord_rare diseases +MONDO:0018927 ordo_disorder diseases +MONDO:0018927 orphanet_rare diseases +MONDO:0018927 rare diseases +MONDO:0018929 gard_rare diseases +MONDO:0018929 nord_rare diseases +MONDO:0018929 ordo_disorder diseases +MONDO:0018929 orphanet_rare diseases +MONDO:0018929 rare diseases +MONDO:0018930 gard_rare diseases +MONDO:0018930 nord_rare diseases +MONDO:0018930 ordo_disorder diseases +MONDO:0018930 ordo_malformation_syndrome diseases +MONDO:0018930 orphanet_rare diseases +MONDO:0018930 rare diseases +MONDO:0018931 gard_rare diseases +MONDO:0018931 nord_rare diseases +MONDO:0018931 ordo_disorder diseases +MONDO:0018931 ordo_subtype_of_a_disorder diseases +MONDO:0018931 orphanet_rare diseases +MONDO:0018931 otar diseases +MONDO:0018931 rare diseases +MONDO:0018932 gard_rare diseases +MONDO:0018932 nord_rare diseases +MONDO:0018932 ordo_disorder diseases +MONDO:0018932 orphanet_rare diseases +MONDO:0018932 rare diseases +MONDO:0018933 gard_rare diseases +MONDO:0018933 nord_rare diseases +MONDO:0018933 ordo_disorder diseases +MONDO:0018933 ordo_malformation_syndrome diseases +MONDO:0018933 orphanet_rare diseases +MONDO:0018933 otar diseases +MONDO:0018933 rare diseases +MONDO:0018935 gard_rare diseases +MONDO:0018935 nord_rare diseases +MONDO:0018935 ordo_disorder diseases +MONDO:0018935 orphanet_rare diseases +MONDO:0018935 otar diseases +MONDO:0018935 rare diseases +MONDO:0018936 gard_rare diseases +MONDO:0018936 nord_rare diseases +MONDO:0018936 ordo_disorder diseases +MONDO:0018936 orphanet_rare diseases +MONDO:0018936 rare diseases +MONDO:0018937 clingen diseases +MONDO:0018937 gard_rare diseases +MONDO:0018937 nord_rare diseases +MONDO:0018937 ordo_disorder diseases +MONDO:0018937 orphanet_rare diseases +MONDO:0018937 otar diseases +MONDO:0018937 rare diseases +MONDO:0018938 gard_rare diseases +MONDO:0018938 nord_rare diseases +MONDO:0018938 ordo_disorder diseases +MONDO:0018938 orphanet_rare diseases +MONDO:0018938 otar diseases +MONDO:0018938 rare diseases +MONDO:0018939 clingen diseases +MONDO:0018939 gard_rare diseases +MONDO:0018939 nord_rare diseases +MONDO:0018939 ordo_disorder diseases +MONDO:0018939 orphanet_rare diseases +MONDO:0018939 otar diseases +MONDO:0018939 rare diseases +MONDO:0018940 gard_rare diseases +MONDO:0018940 nord_rare diseases +MONDO:0018940 ordo_disorder diseases +MONDO:0018940 orphanet_rare diseases +MONDO:0018940 otar diseases +MONDO:0018940 rare diseases +MONDO:0018941 gard_rare diseases +MONDO:0018941 nord_rare diseases +MONDO:0018941 ordo_disorder diseases +MONDO:0018941 orphanet_rare diseases +MONDO:0018941 rare diseases +MONDO:0018942 gard_rare diseases +MONDO:0018942 nord_rare diseases +MONDO:0018942 ordo_disorder diseases +MONDO:0018942 orphanet_rare diseases +MONDO:0018942 rare diseases +MONDO:0018943 clingen diseases +MONDO:0018943 disease_grouping diseases +MONDO:0018943 gard_rare diseases +MONDO:0018943 ordo_group_of_disorders diseases +MONDO:0018943 otar diseases +MONDO:0018943 rare diseases +MONDO:0018944 disease_grouping diseases +MONDO:0018944 gard_rare diseases +MONDO:0018944 nord_rare diseases +MONDO:0018944 ordo_group_of_disorders diseases +MONDO:0018944 otar diseases +MONDO:0018944 rare diseases +MONDO:0018945 gard_rare diseases +MONDO:0018945 nord_rare diseases +MONDO:0018945 ordo_disorder diseases +MONDO:0018945 orphanet_rare diseases +MONDO:0018945 otar diseases +MONDO:0018945 rare diseases +MONDO:0018946 gard_rare diseases +MONDO:0018946 nord_rare diseases +MONDO:0018946 ordo_disorder diseases +MONDO:0018946 ordo_malformation_syndrome diseases +MONDO:0018946 orphanet_rare diseases +MONDO:0018946 rare diseases +MONDO:0018947 clingen diseases +MONDO:0018947 disease_grouping diseases +MONDO:0018947 gard_rare diseases +MONDO:0018947 nord_rare diseases +MONDO:0018947 ordo_group_of_disorders diseases +MONDO:0018947 otar diseases +MONDO:0018947 rare diseases +MONDO:0018948 gard_rare diseases +MONDO:0018948 nord_rare diseases +MONDO:0018948 ordo_disorder diseases +MONDO:0018948 orphanet_rare diseases +MONDO:0018948 otar diseases +MONDO:0018948 rare diseases +MONDO:0018949 disease_grouping diseases +MONDO:0018949 gard_rare diseases +MONDO:0018949 ordo_group_of_disorders diseases +MONDO:0018949 otar diseases +MONDO:0018949 rare diseases +MONDO:0018950 clingen diseases +MONDO:0018950 gard_rare diseases +MONDO:0018950 nord_rare diseases +MONDO:0018950 ordo_disorder diseases +MONDO:0018950 orphanet_rare diseases +MONDO:0018950 otar diseases +MONDO:0018950 rare diseases +MONDO:0018951 gard_rare diseases +MONDO:0018951 nord_rare diseases +MONDO:0018951 ordo_disorder diseases +MONDO:0018951 orphanet_rare diseases +MONDO:0018951 otar diseases +MONDO:0018951 rare diseases +MONDO:0018952 gard_rare diseases +MONDO:0018952 nord_rare diseases +MONDO:0018952 ordo_disorder diseases +MONDO:0018952 orphanet_rare diseases +MONDO:0018952 rare diseases +MONDO:0018953 clingen diseases +MONDO:0018953 gard_rare diseases +MONDO:0018953 nord_rare diseases +MONDO:0018953 ordo_disorder diseases +MONDO:0018953 ordo_malformation_syndrome diseases +MONDO:0018953 orphanet_rare diseases +MONDO:0018953 otar diseases +MONDO:0018953 rare diseases +MONDO:0018954 clingen diseases +MONDO:0018954 gard_rare diseases +MONDO:0018954 nord_rare diseases +MONDO:0018954 ordo_disorder diseases +MONDO:0018954 ordo_malformation_syndrome diseases +MONDO:0018954 orphanet_rare diseases +MONDO:0018954 otar diseases +MONDO:0018954 rare diseases +MONDO:0018955 gard_rare diseases +MONDO:0018955 nord_rare diseases +MONDO:0018955 ordo_disorder diseases +MONDO:0018955 orphanet_rare diseases +MONDO:0018955 rare diseases +MONDO:0018956 gard_rare diseases +MONDO:0018956 nord_rare diseases +MONDO:0018956 ordo_disorder diseases +MONDO:0018956 orphanet_rare diseases +MONDO:0018956 otar diseases +MONDO:0018956 rare diseases +MONDO:0018957 gard_rare diseases +MONDO:0018957 nord_rare diseases +MONDO:0018957 ordo_disorder diseases +MONDO:0018957 orphanet_rare diseases +MONDO:0018957 rare diseases +MONDO:0018958 clingen diseases +MONDO:0018958 disease_grouping diseases +MONDO:0018958 gard_rare diseases +MONDO:0018958 ordo_group_of_disorders diseases +MONDO:0018958 otar diseases +MONDO:0018958 rare diseases +MONDO:0018959 disease_grouping diseases +MONDO:0018959 gard_rare diseases +MONDO:0018959 ordo_group_of_disorders diseases +MONDO:0018959 otar diseases +MONDO:0018959 rare diseases +MONDO:0018960 gard_rare diseases +MONDO:0018960 nord_rare diseases +MONDO:0018960 ordo_disorder diseases +MONDO:0018960 ordo_morphological_anomaly diseases +MONDO:0018960 orphanet_rare diseases +MONDO:0018960 otar diseases +MONDO:0018960 rare diseases +MONDO:0018961 gard_rare diseases +MONDO:0018961 nord_rare diseases +MONDO:0018961 ordo_disorder diseases +MONDO:0018961 orphanet_rare diseases +MONDO:0018961 otar diseases +MONDO:0018961 rare diseases +MONDO:0018962 ordo_morphological_anomaly diseases +MONDO:0018963 gard_rare diseases +MONDO:0018963 nord_rare diseases +MONDO:0018963 ordo_disorder diseases +MONDO:0018963 orphanet_rare diseases +MONDO:0018963 otar diseases +MONDO:0018963 rare diseases +MONDO:0018964 gard_rare diseases +MONDO:0018964 nord_rare diseases +MONDO:0018964 ordo_disorder diseases +MONDO:0018964 orphanet_rare diseases +MONDO:0018964 otar diseases +MONDO:0018964 rare diseases +MONDO:0018965 clingen diseases +MONDO:0018965 gard_rare diseases +MONDO:0018965 nord_rare diseases +MONDO:0018965 ordo_disorder diseases +MONDO:0018965 orphanet_rare diseases +MONDO:0018965 otar diseases +MONDO:0018965 rare diseases +MONDO:0018967 gard_rare diseases +MONDO:0018967 nord_rare diseases +MONDO:0018967 ordo_subtype_of_a_disorder diseases +MONDO:0018967 otar diseases +MONDO:0018967 rare diseases +MONDO:0018968 gard_rare diseases +MONDO:0018968 nord_rare diseases +MONDO:0018968 ordo_disorder diseases +MONDO:0018968 ordo_morphological_anomaly diseases +MONDO:0018968 orphanet_rare diseases +MONDO:0018968 otar diseases +MONDO:0018968 rare diseases +MONDO:0018969 gard_rare diseases +MONDO:0018969 nord_rare diseases +MONDO:0018969 ordo_disorder diseases +MONDO:0018969 ordo_morphological_anomaly diseases +MONDO:0018969 orphanet_rare diseases +MONDO:0018969 otar diseases +MONDO:0018969 rare diseases +MONDO:0018971 gard_rare diseases +MONDO:0018971 ordo_morphological_anomaly diseases +MONDO:0018971 otar diseases +MONDO:0018971 rare diseases +MONDO:0018973 disease_grouping diseases +MONDO:0018973 gard_rare diseases +MONDO:0018973 ordo_group_of_disorders diseases +MONDO:0018973 otar diseases +MONDO:0018973 rare diseases +MONDO:0018974 gard_rare diseases +MONDO:0018974 nord_rare diseases +MONDO:0018974 ordo_disorder diseases +MONDO:0018974 orphanet_rare diseases +MONDO:0018974 otar diseases +MONDO:0018974 rare diseases +MONDO:0018975 clingen diseases +MONDO:0018975 gard_rare diseases +MONDO:0018975 nord_rare diseases +MONDO:0018975 ordo_disorder diseases +MONDO:0018975 orphanet_rare diseases +MONDO:0018975 otar diseases +MONDO:0018975 rare diseases +MONDO:0018976 gard_rare diseases +MONDO:0018976 nord_rare diseases +MONDO:0018976 ordo_disorder diseases +MONDO:0018976 ordo_malformation_syndrome diseases +MONDO:0018976 orphanet_rare diseases +MONDO:0018976 rare diseases +MONDO:0018977 gard_rare diseases +MONDO:0018977 nord_rare diseases +MONDO:0018977 ordo_disorder diseases +MONDO:0018977 orphanet_rare diseases +MONDO:0018977 rare diseases +MONDO:0018978 gard_rare diseases +MONDO:0018978 nord_rare diseases +MONDO:0018978 ordo_subtype_of_a_disorder diseases +MONDO:0018978 rare diseases +MONDO:0018979 gard_rare diseases +MONDO:0018979 nord_rare diseases +MONDO:0018979 ordo_disorder diseases +MONDO:0018979 orphanet_rare diseases +MONDO:0018979 rare diseases +MONDO:0018980 gard_rare diseases +MONDO:0018980 nord_rare diseases +MONDO:0018980 ordo_disorder diseases +MONDO:0018980 ordo_malformation_syndrome diseases +MONDO:0018980 orphanet_rare diseases +MONDO:0018980 rare diseases +MONDO:0018981 gard_rare diseases +MONDO:0018981 nord_rare diseases +MONDO:0018981 ordo_disorder diseases +MONDO:0018981 orphanet_rare diseases +MONDO:0018981 rare diseases +MONDO:0018982 gard_rare diseases +MONDO:0018982 nord_rare diseases +MONDO:0018982 ordo_disorder diseases +MONDO:0018982 orphanet_rare diseases +MONDO:0018982 otar diseases +MONDO:0018982 rare diseases +MONDO:0018983 gard_rare diseases +MONDO:0018983 nord_rare diseases +MONDO:0018983 ordo_disorder diseases +MONDO:0018983 orphanet_rare diseases +MONDO:0018983 otar diseases +MONDO:0018983 rare diseases +MONDO:0018984 gard_rare diseases +MONDO:0018984 nord_rare diseases +MONDO:0018984 ordo_disorder diseases +MONDO:0018984 orphanet_rare diseases +MONDO:0018984 rare diseases +MONDO:0018987 gard_rare diseases +MONDO:0018987 nord_rare diseases +MONDO:0018987 ordo_disorder diseases +MONDO:0018987 orphanet_rare diseases +MONDO:0018987 rare diseases +MONDO:0018988 gard_rare diseases +MONDO:0018988 nord_rare diseases +MONDO:0018988 ordo_disorder diseases +MONDO:0018988 orphanet_rare diseases +MONDO:0018988 otar diseases +MONDO:0018988 rare diseases +MONDO:0018991 gard_rare diseases +MONDO:0018991 nord_rare diseases +MONDO:0018991 ordo_subtype_of_a_disorder diseases +MONDO:0018991 rare diseases +MONDO:0018992 gard_rare diseases +MONDO:0018992 nord_rare diseases +MONDO:0018992 ordo_subtype_of_a_disorder diseases +MONDO:0018992 rare diseases +MONDO:0018993 clingen diseases +MONDO:0018993 disease_grouping diseases +MONDO:0018993 gard_rare diseases +MONDO:0018993 nord_rare diseases +MONDO:0018993 ordo_group_of_disorders diseases +MONDO:0018993 otar diseases +MONDO:0018993 rare diseases +MONDO:0018994 disease_grouping diseases +MONDO:0018994 gard_rare diseases +MONDO:0018994 nord_rare diseases +MONDO:0018994 ordo_group_of_disorders diseases +MONDO:0018994 otar diseases +MONDO:0018994 rare diseases +MONDO:0018995 clingen diseases +MONDO:0018995 disease_grouping diseases +MONDO:0018995 gard_rare diseases +MONDO:0018995 nord_rare diseases +MONDO:0018995 ordo_group_of_disorders diseases +MONDO:0018995 otar diseases +MONDO:0018995 rare diseases +MONDO:0018996 gard_rare diseases +MONDO:0018996 nord_rare diseases +MONDO:0018996 ordo_disorder diseases +MONDO:0018996 orphanet_rare diseases +MONDO:0018996 otar diseases +MONDO:0018996 rare diseases +MONDO:0018997 clingen diseases +MONDO:0018997 gard_rare diseases +MONDO:0018997 nord_rare diseases +MONDO:0018997 ordo_disorder diseases +MONDO:0018997 ordo_malformation_syndrome diseases +MONDO:0018997 orphanet_rare diseases +MONDO:0018997 otar diseases +MONDO:0018997 rare diseases +MONDO:0018998 gard_rare diseases +MONDO:0018998 nord_rare diseases +MONDO:0018998 ordo_disorder diseases +MONDO:0018998 orphanet_rare diseases +MONDO:0018998 otar diseases +MONDO:0018998 rare diseases +MONDO:0018999 gard_rare diseases +MONDO:0018999 nord_rare diseases +MONDO:0018999 ordo_disorder diseases +MONDO:0018999 orphanet_rare diseases +MONDO:0018999 otar diseases +MONDO:0018999 rare diseases +MONDO:0019000 gard_rare diseases +MONDO:0019000 ordo_disorder diseases +MONDO:0019000 orphanet_rare diseases +MONDO:0019000 rare diseases +MONDO:0019002 gard_rare diseases +MONDO:0019002 nord_rare diseases +MONDO:0019002 ordo_disorder diseases +MONDO:0019002 orphanet_rare diseases +MONDO:0019002 otar diseases +MONDO:0019002 rare diseases +MONDO:0019003 gard_rare diseases +MONDO:0019003 nord_rare diseases +MONDO:0019003 ordo_disorder diseases +MONDO:0019003 orphanet_rare diseases +MONDO:0019003 otar diseases +MONDO:0019003 rare diseases +MONDO:0019004 gard_rare diseases +MONDO:0019004 nord_rare diseases +MONDO:0019004 ordo_disorder diseases +MONDO:0019004 orphanet_rare diseases +MONDO:0019004 otar diseases +MONDO:0019004 rare diseases +MONDO:0019005 clingen diseases +MONDO:0019005 gard_rare diseases +MONDO:0019005 nord_rare diseases +MONDO:0019005 ordo_disorder diseases +MONDO:0019005 orphanet_rare diseases +MONDO:0019005 otar diseases +MONDO:0019005 rare diseases +MONDO:0019006 gard_rare diseases +MONDO:0019006 ordo_disorder diseases +MONDO:0019006 orphanet_rare diseases +MONDO:0019006 otar diseases +MONDO:0019006 rare diseases +MONDO:0019007 gard_rare diseases +MONDO:0019007 nord_rare diseases +MONDO:0019007 ordo_disorder diseases +MONDO:0019007 ordo_morphological_anomaly diseases +MONDO:0019007 orphanet_rare diseases +MONDO:0019007 rare diseases +MONDO:0019008 gard_rare diseases +MONDO:0019008 nord_rare diseases +MONDO:0019008 ordo_disorder diseases +MONDO:0019008 orphanet_rare diseases +MONDO:0019008 otar diseases +MONDO:0019008 rare diseases +MONDO:0019009 gard_rare diseases +MONDO:0019009 nord_rare diseases +MONDO:0019009 ordo_disorder diseases +MONDO:0019009 orphanet_rare diseases +MONDO:0019009 otar diseases +MONDO:0019009 rare diseases +MONDO:0019010 disease_grouping diseases +MONDO:0019010 gard_rare diseases +MONDO:0019010 nord_rare diseases +MONDO:0019010 ordo_group_of_disorders diseases +MONDO:0019010 otar diseases +MONDO:0019010 rare diseases +MONDO:0019011 disease_grouping diseases +MONDO:0019011 gard_rare diseases +MONDO:0019011 nord_rare diseases +MONDO:0019011 ordo_group_of_disorders diseases +MONDO:0019011 otar diseases +MONDO:0019011 rare diseases +MONDO:0019012 gard_rare diseases +MONDO:0019012 nord_rare diseases +MONDO:0019012 ordo_disorder diseases +MONDO:0019012 ordo_malformation_syndrome diseases +MONDO:0019012 orphanet_rare diseases +MONDO:0019012 otar diseases +MONDO:0019012 rare diseases +MONDO:0019013 disease_grouping diseases +MONDO:0019013 gard_rare diseases +MONDO:0019013 nord_rare diseases +MONDO:0019013 ordo_group_of_disorders diseases +MONDO:0019013 rare diseases +MONDO:0019015 gard_rare diseases +MONDO:0019015 nord_rare diseases +MONDO:0019015 ordo_disorder diseases +MONDO:0019015 ordo_morphological_anomaly diseases +MONDO:0019015 orphanet_rare diseases +MONDO:0019015 rare diseases +MONDO:0019016 gard_rare diseases +MONDO:0019016 nord_rare diseases +MONDO:0019016 ordo_disorder diseases +MONDO:0019016 orphanet_rare diseases +MONDO:0019016 otar diseases +MONDO:0019016 rare diseases +MONDO:0019017 gard_rare diseases +MONDO:0019017 nord_rare diseases +MONDO:0019017 ordo_disorder diseases +MONDO:0019017 orphanet_rare diseases +MONDO:0019017 otar diseases +MONDO:0019017 rare diseases +MONDO:0019018 gard_rare diseases +MONDO:0019018 nord_rare diseases +MONDO:0019018 ordo_disorder diseases +MONDO:0019018 orphanet_rare diseases +MONDO:0019018 otar diseases +MONDO:0019018 rare diseases +MONDO:0019019 gard_rare diseases +MONDO:0019019 nord_rare diseases +MONDO:0019019 ordo_disorder diseases +MONDO:0019019 orphanet_rare diseases +MONDO:0019019 otar diseases +MONDO:0019019 rare diseases +MONDO:0019020 gard_rare diseases +MONDO:0019020 nord_rare diseases +MONDO:0019020 ordo_disorder diseases +MONDO:0019020 orphanet_rare diseases +MONDO:0019020 rare diseases +MONDO:0019022 gard_rare diseases +MONDO:0019022 nord_rare diseases +MONDO:0019022 ordo_disorder diseases +MONDO:0019022 ordo_malformation_syndrome diseases +MONDO:0019022 orphanet_rare diseases +MONDO:0019022 otar diseases +MONDO:0019022 rare diseases +MONDO:0019023 disease_grouping diseases +MONDO:0019023 gard_rare diseases +MONDO:0019023 nord_rare diseases +MONDO:0019023 ordo_group_of_disorders diseases +MONDO:0019023 otar diseases +MONDO:0019023 rare diseases +MONDO:0019024 gard_rare diseases +MONDO:0019024 nord_rare diseases +MONDO:0019024 ordo_disorder diseases +MONDO:0019024 orphanet_rare diseases +MONDO:0019024 otar diseases +MONDO:0019024 rare diseases +MONDO:0019025 gard_rare diseases +MONDO:0019025 nord_rare diseases +MONDO:0019025 ordo_disorder diseases +MONDO:0019025 orphanet_rare diseases +MONDO:0019025 rare diseases +MONDO:0019026 gard_rare diseases +MONDO:0019026 nord_rare diseases +MONDO:0019026 ordo_disorder diseases +MONDO:0019026 ordo_malformation_syndrome diseases +MONDO:0019026 orphanet_rare diseases +MONDO:0019026 otar diseases +MONDO:0019026 rare diseases +MONDO:0019027 gard_rare diseases +MONDO:0019027 ordo_malformation_syndrome diseases +MONDO:0019027 otar diseases +MONDO:0019027 rare diseases +MONDO:0019028 gard_rare diseases +MONDO:0019028 nord_rare diseases +MONDO:0019028 ordo_disorder diseases +MONDO:0019028 orphanet_rare diseases +MONDO:0019028 rare diseases +MONDO:0019029 gard_rare diseases +MONDO:0019029 nord_rare diseases +MONDO:0019029 ordo_disorder diseases +MONDO:0019029 orphanet_rare diseases +MONDO:0019029 rare diseases +MONDO:0019031 gard_rare diseases +MONDO:0019031 nord_rare diseases +MONDO:0019031 ordo_disorder diseases +MONDO:0019031 orphanet_rare diseases +MONDO:0019031 otar diseases +MONDO:0019031 rare diseases +MONDO:0019032 gard_rare diseases +MONDO:0019032 nord_rare diseases +MONDO:0019032 ordo_subtype_of_a_disorder diseases +MONDO:0019032 otar diseases +MONDO:0019032 rare diseases +MONDO:0019033 disease_grouping diseases +MONDO:0019033 gard_rare diseases +MONDO:0019033 nord_rare diseases +MONDO:0019033 ordo_group_of_disorders diseases +MONDO:0019033 otar diseases +MONDO:0019033 rare diseases +MONDO:0019034 gard_rare diseases +MONDO:0019034 nord_rare diseases +MONDO:0019034 ordo_disorder diseases +MONDO:0019034 ordo_morphological_anomaly diseases +MONDO:0019034 orphanet_rare diseases +MONDO:0019034 rare diseases +MONDO:0019035 gard_rare diseases +MONDO:0019035 nord_rare diseases +MONDO:0019035 ordo_disorder diseases +MONDO:0019035 orphanet_rare diseases +MONDO:0019035 rare diseases +MONDO:0019036 gard_rare diseases +MONDO:0019036 nord_rare diseases +MONDO:0019036 ordo_disorder diseases +MONDO:0019036 orphanet_rare diseases +MONDO:0019036 rare diseases +MONDO:0019037 gard_rare diseases +MONDO:0019037 nord_rare diseases +MONDO:0019037 ordo_disorder diseases +MONDO:0019037 orphanet_rare diseases +MONDO:0019037 otar diseases +MONDO:0019037 rare diseases +MONDO:0019040 disease_grouping diseases +MONDO:0019040 ordo_group_of_disorders diseases +MONDO:0019040 otar diseases +MONDO:0019040 rare_grouping diseases +MONDO:0019042 disease_grouping diseases +MONDO:0019042 gard_rare diseases +MONDO:0019042 ordo_group_of_disorders diseases +MONDO:0019042 otar diseases +MONDO:0019042 rare diseases +MONDO:0019046 disease_grouping diseases +MONDO:0019046 gard_rare diseases +MONDO:0019046 merged_class diseases +MONDO:0019046 nord_rare diseases +MONDO:0019046 ordo_group_of_disorders diseases +MONDO:0019046 otar diseases +MONDO:0019046 rare diseases +MONDO:0019050 disease_grouping diseases +MONDO:0019050 gard_rare diseases +MONDO:0019050 ordo_group_of_disorders diseases +MONDO:0019050 rare diseases +MONDO:0019052 disease_grouping diseases +MONDO:0019052 gard_rare diseases +MONDO:0019052 ordo_group_of_disorders diseases +MONDO:0019052 otar diseases +MONDO:0019052 rare diseases +MONDO:0019053 disease_grouping diseases +MONDO:0019053 gard_rare diseases +MONDO:0019053 ordo_group_of_disorders diseases +MONDO:0019053 otar diseases +MONDO:0019053 rare diseases +MONDO:0019054 disease_grouping diseases +MONDO:0019054 ordo_group_of_disorders diseases +MONDO:0019056 clingen diseases +MONDO:0019056 disease_grouping diseases +MONDO:0019056 ordo_group_of_disorders diseases +MONDO:0019056 otar diseases +MONDO:0019060 disease_grouping diseases +MONDO:0019060 gard_rare diseases +MONDO:0019060 ordo_group_of_disorders diseases +MONDO:0019060 otar diseases +MONDO:0019060 rare diseases +MONDO:0019064 clingen diseases +MONDO:0019064 disease_grouping diseases +MONDO:0019064 gard_rare diseases +MONDO:0019064 nord_rare diseases +MONDO:0019064 ordo_group_of_disorders diseases +MONDO:0019064 otar diseases +MONDO:0019064 rare diseases +MONDO:0019065 disease_grouping diseases +MONDO:0019065 gard_rare diseases +MONDO:0019065 ordo_group_of_disorders diseases +MONDO:0019065 otar diseases +MONDO:0019065 rare diseases +MONDO:0019067 gard_rare diseases +MONDO:0019067 nord_rare diseases +MONDO:0019067 ordo_clinical_syndrome diseases +MONDO:0019067 ordo_disorder diseases +MONDO:0019067 orphanet_rare diseases +MONDO:0019067 rare diseases +MONDO:0019068 gard_rare diseases +MONDO:0019068 nord_rare diseases +MONDO:0019068 ordo_disorder diseases +MONDO:0019068 orphanet_rare diseases +MONDO:0019068 rare diseases +MONDO:0019071 gard_rare diseases +MONDO:0019071 nord_rare diseases +MONDO:0019071 ordo_disorder diseases +MONDO:0019071 ordo_malformation_syndrome diseases +MONDO:0019071 orphanet_rare diseases +MONDO:0019071 otar diseases +MONDO:0019071 rare diseases +MONDO:0019072 otar diseases +MONDO:0019073 gard_rare diseases +MONDO:0019073 nord_rare diseases +MONDO:0019073 rare diseases +MONDO:0019074 gard_rare diseases +MONDO:0019074 nord_rare diseases +MONDO:0019074 ordo_disorder diseases +MONDO:0019074 orphanet_rare diseases +MONDO:0019074 rare diseases +MONDO:0019075 gard_rare diseases +MONDO:0019075 nord_rare diseases +MONDO:0019075 ordo_disorder diseases +MONDO:0019075 ordo_malformation_syndrome diseases +MONDO:0019075 orphanet_rare diseases +MONDO:0019075 otar diseases +MONDO:0019075 rare diseases +MONDO:0019076 gard_rare diseases +MONDO:0019076 nord_rare diseases +MONDO:0019076 ordo_disorder diseases +MONDO:0019076 orphanet_rare diseases +MONDO:0019076 rare diseases +MONDO:0019077 gard_rare diseases +MONDO:0019077 nord_rare diseases +MONDO:0019077 ordo_disorder diseases +MONDO:0019077 orphanet_rare diseases +MONDO:0019077 rare diseases +MONDO:0019078 gard_rare diseases +MONDO:0019078 nord_rare diseases +MONDO:0019078 ordo_disorder diseases +MONDO:0019078 ordo_malformation_syndrome diseases +MONDO:0019078 orphanet_rare diseases +MONDO:0019078 otar diseases +MONDO:0019078 rare diseases +MONDO:0019079 gard_rare diseases +MONDO:0019079 nord_rare diseases +MONDO:0019079 ordo_disorder diseases +MONDO:0019079 orphanet_rare diseases +MONDO:0019079 otar diseases +MONDO:0019079 rare diseases +MONDO:0019080 gard_rare diseases +MONDO:0019080 nord_rare diseases +MONDO:0019080 ordo_disorder diseases +MONDO:0019080 orphanet_rare diseases +MONDO:0019080 otar diseases +MONDO:0019080 rare diseases +MONDO:0019082 gard_rare diseases +MONDO:0019082 nord_rare diseases +MONDO:0019082 ordo_disorder diseases +MONDO:0019082 orphanet_rare diseases +MONDO:0019082 otar diseases +MONDO:0019082 rare diseases +MONDO:0019083 gard_rare diseases +MONDO:0019083 nord_rare diseases +MONDO:0019083 otar diseases +MONDO:0019083 rare diseases +MONDO:0019084 gard_rare diseases +MONDO:0019084 nord_rare diseases +MONDO:0019084 ordo_disorder diseases +MONDO:0019084 orphanet_rare diseases +MONDO:0019084 rare diseases +MONDO:0019085 gard_rare diseases +MONDO:0019085 nord_rare diseases +MONDO:0019085 ordo_disorder diseases +MONDO:0019085 orphanet_rare diseases +MONDO:0019085 rare diseases +MONDO:0019086 disease_grouping diseases +MONDO:0019086 gard_rare diseases +MONDO:0019086 ordo_group_of_disorders diseases +MONDO:0019086 otar diseases +MONDO:0019086 rare diseases +MONDO:0019087 gard_rare diseases +MONDO:0019087 nord_rare diseases +MONDO:0019087 ordo_disorder diseases +MONDO:0019087 orphanet_rare diseases +MONDO:0019087 otar diseases +MONDO:0019087 rare diseases +MONDO:0019088 gard_rare diseases +MONDO:0019088 nord_rare diseases +MONDO:0019088 ordo_disorder diseases +MONDO:0019088 orphanet_rare diseases +MONDO:0019088 otar diseases +MONDO:0019088 rare diseases +MONDO:0019091 gard_rare diseases +MONDO:0019091 nord_rare diseases +MONDO:0019091 ordo_disorder diseases +MONDO:0019091 ordo_malformation_syndrome diseases +MONDO:0019091 orphanet_rare diseases +MONDO:0019091 otar diseases +MONDO:0019091 rare diseases +MONDO:0019092 gard_rare diseases +MONDO:0019092 nord_rare diseases +MONDO:0019092 ordo_disorder diseases +MONDO:0019092 orphanet_rare diseases +MONDO:0019092 rare diseases +MONDO:0019093 gard_rare diseases +MONDO:0019093 nord_rare diseases +MONDO:0019093 ordo_disorder diseases +MONDO:0019093 orphanet_rare diseases +MONDO:0019093 otar diseases +MONDO:0019093 rare diseases +MONDO:0019094 gard_rare diseases +MONDO:0019094 nord_rare diseases +MONDO:0019094 ordo_disorder diseases +MONDO:0019094 orphanet_rare diseases +MONDO:0019094 rare diseases +MONDO:0019095 gard_rare diseases +MONDO:0019095 nord_rare diseases +MONDO:0019095 ordo_disorder diseases +MONDO:0019095 orphanet_rare diseases +MONDO:0019095 otar diseases +MONDO:0019095 rare diseases +MONDO:0019098 disease_grouping diseases +MONDO:0019098 gard_rare diseases +MONDO:0019098 nord_rare diseases +MONDO:0019098 ordo_group_of_disorders diseases +MONDO:0019098 otar diseases +MONDO:0019098 rare diseases +MONDO:0019100 gard_rare diseases +MONDO:0019100 nord_rare diseases +MONDO:0019100 ordo_disorder diseases +MONDO:0019100 orphanet_rare diseases +MONDO:0019100 otar diseases +MONDO:0019100 rare diseases +MONDO:0019101 gard_rare diseases +MONDO:0019101 nord_rare diseases +MONDO:0019101 ordo_disorder diseases +MONDO:0019101 orphanet_rare diseases +MONDO:0019101 otar diseases +MONDO:0019101 rare diseases +MONDO:0019102 gard_rare diseases +MONDO:0019102 nord_rare diseases +MONDO:0019102 ordo_disorder diseases +MONDO:0019102 ordo_malformation_syndrome diseases +MONDO:0019102 orphanet_rare diseases +MONDO:0019102 otar diseases +MONDO:0019102 rare diseases +MONDO:0019104 gard_rare diseases +MONDO:0019104 nord_rare diseases +MONDO:0019104 ordo_disorder diseases +MONDO:0019104 orphanet_rare diseases +MONDO:0019104 rare diseases +MONDO:0019105 gard_rare diseases +MONDO:0019105 nord_rare diseases +MONDO:0019105 ordo_disorder diseases +MONDO:0019105 orphanet_rare diseases +MONDO:0019105 otar diseases +MONDO:0019105 rare diseases +MONDO:0019107 gard_rare diseases +MONDO:0019107 nord_rare diseases +MONDO:0019107 ordo_disorder diseases +MONDO:0019107 orphanet_rare diseases +MONDO:0019107 otar diseases +MONDO:0019107 rare diseases +MONDO:0019108 gard_rare diseases +MONDO:0019108 nord_rare diseases +MONDO:0019108 ordo_disorder diseases +MONDO:0019108 orphanet_rare diseases +MONDO:0019108 rare diseases +MONDO:0019109 gard_rare diseases +MONDO:0019109 nord_rare diseases +MONDO:0019109 ordo_disorder diseases +MONDO:0019109 orphanet_rare diseases +MONDO:0019109 rare diseases +MONDO:0019111 gard_rare diseases +MONDO:0019111 nord_rare diseases +MONDO:0019111 ordo_disorder diseases +MONDO:0019111 orphanet_rare diseases +MONDO:0019111 otar diseases +MONDO:0019111 rare diseases +MONDO:0019112 gard_rare diseases +MONDO:0019112 nord_rare diseases +MONDO:0019112 ordo_disorder diseases +MONDO:0019112 orphanet_rare diseases +MONDO:0019112 otar diseases +MONDO:0019112 rare diseases +MONDO:0019113 gard_rare diseases +MONDO:0019113 nord_rare diseases +MONDO:0019113 ordo_disorder diseases +MONDO:0019113 orphanet_rare diseases +MONDO:0019113 otar diseases +MONDO:0019113 rare diseases +MONDO:0019114 gard_rare diseases +MONDO:0019114 nord_rare diseases +MONDO:0019114 ordo_clinical_syndrome diseases +MONDO:0019114 ordo_disorder diseases +MONDO:0019114 orphanet_rare diseases +MONDO:0019114 rare diseases +MONDO:0019115 gard_rare diseases +MONDO:0019115 nord_rare diseases +MONDO:0019115 ordo_malformation_syndrome diseases +MONDO:0019115 ordo_subtype_of_a_disorder diseases +MONDO:0019115 otar diseases +MONDO:0019115 rare diseases +MONDO:0019118 clingen diseases +MONDO:0019118 disease_grouping diseases +MONDO:0019118 gard_rare diseases +MONDO:0019118 ordo_group_of_disorders diseases +MONDO:0019118 otar diseases +MONDO:0019118 rare diseases +MONDO:0019119 disease_grouping diseases +MONDO:0019119 gard_rare diseases +MONDO:0019119 ordo_group_of_disorders diseases +MONDO:0019119 rare diseases +MONDO:0019120 gard_rare diseases +MONDO:0019120 nord_rare diseases +MONDO:0019120 ordo_disorder diseases +MONDO:0019120 orphanet_rare diseases +MONDO:0019120 otar diseases +MONDO:0019120 rare diseases +MONDO:0019121 gard_rare diseases +MONDO:0019121 nord_rare diseases +MONDO:0019121 ordo_disorder diseases +MONDO:0019121 orphanet_rare diseases +MONDO:0019121 otar diseases +MONDO:0019121 rare diseases +MONDO:0019122 gard_rare diseases +MONDO:0019122 nord_rare diseases +MONDO:0019122 ordo_disorder diseases +MONDO:0019122 orphanet_rare diseases +MONDO:0019122 rare diseases +MONDO:0019123 gard_rare diseases +MONDO:0019123 nord_rare diseases +MONDO:0019123 ordo_disorder diseases +MONDO:0019123 orphanet_rare diseases +MONDO:0019123 otar diseases +MONDO:0019123 rare diseases +MONDO:0019124 gard_rare diseases +MONDO:0019124 nord_rare diseases +MONDO:0019124 ordo_disorder diseases +MONDO:0019124 orphanet_rare diseases +MONDO:0019124 otar diseases +MONDO:0019124 rare diseases +MONDO:0019125 gard_rare diseases +MONDO:0019125 nord_rare diseases +MONDO:0019125 ordo_disorder diseases +MONDO:0019125 orphanet_rare diseases +MONDO:0019125 otar diseases +MONDO:0019125 rare diseases +MONDO:0019127 gard_rare diseases +MONDO:0019127 nord_rare diseases +MONDO:0019127 ordo_disorder diseases +MONDO:0019127 orphanet_rare diseases +MONDO:0019127 otar diseases +MONDO:0019127 rare diseases +MONDO:0019128 disease_grouping diseases +MONDO:0019128 gard_rare diseases +MONDO:0019128 ordo_group_of_disorders diseases +MONDO:0019128 otar diseases +MONDO:0019128 rare diseases +MONDO:0019129 gard_rare diseases +MONDO:0019129 ordo_disorder diseases +MONDO:0019129 ordo_malformation_syndrome diseases +MONDO:0019129 orphanet_rare diseases +MONDO:0019129 otar diseases +MONDO:0019129 rare diseases +MONDO:0019130 gard_rare diseases +MONDO:0019130 nord_rare diseases +MONDO:0019130 ordo_disorder diseases +MONDO:0019130 orphanet_rare diseases +MONDO:0019130 otar diseases +MONDO:0019130 rare diseases +MONDO:0019131 gard_rare diseases +MONDO:0019131 nord_rare diseases +MONDO:0019131 ordo_disorder diseases +MONDO:0019131 orphanet_rare diseases +MONDO:0019131 otar diseases +MONDO:0019131 rare diseases +MONDO:0019132 gard_rare diseases +MONDO:0019132 ordo_disorder diseases +MONDO:0019132 ordo_malformation_syndrome diseases +MONDO:0019132 orphanet_rare diseases +MONDO:0019132 otar diseases +MONDO:0019132 rare diseases +MONDO:0019133 gard_rare diseases +MONDO:0019133 ordo_disorder diseases +MONDO:0019133 ordo_malformation_syndrome diseases +MONDO:0019133 orphanet_rare diseases +MONDO:0019133 otar diseases +MONDO:0019133 rare diseases +MONDO:0019134 gard_rare diseases +MONDO:0019134 nord_rare diseases +MONDO:0019134 ordo_disorder diseases +MONDO:0019134 orphanet_rare diseases +MONDO:0019134 rare diseases +MONDO:0019136 gard_rare diseases +MONDO:0019136 nord_rare diseases +MONDO:0019136 ordo_disorder diseases +MONDO:0019136 orphanet_rare diseases +MONDO:0019136 otar diseases +MONDO:0019136 rare diseases +MONDO:0019137 gard_rare diseases +MONDO:0019137 nord_rare diseases +MONDO:0019137 ordo_disorder diseases +MONDO:0019137 orphanet_rare diseases +MONDO:0019137 rare diseases +MONDO:0019139 gard_rare diseases +MONDO:0019139 otar diseases +MONDO:0019139 rare diseases +MONDO:0019140 gard_rare diseases +MONDO:0019140 nord_rare diseases +MONDO:0019140 ordo_disorder diseases +MONDO:0019140 orphanet_rare diseases +MONDO:0019140 rare diseases +MONDO:0019141 gard_rare diseases +MONDO:0019141 nord_rare diseases +MONDO:0019141 ordo_disorder diseases +MONDO:0019141 orphanet_rare diseases +MONDO:0019141 otar diseases +MONDO:0019141 rare diseases +MONDO:0019142 disease_grouping diseases +MONDO:0019142 gard_rare diseases +MONDO:0019142 nord_rare diseases +MONDO:0019142 ordo_group_of_disorders diseases +MONDO:0019142 rare diseases +MONDO:0019143 gard_rare diseases +MONDO:0019143 nord_rare diseases +MONDO:0019143 ordo_disorder diseases +MONDO:0019143 orphanet_rare diseases +MONDO:0019143 rare diseases +MONDO:0019144 clingen diseases +MONDO:0019144 gard_rare diseases +MONDO:0019144 nord_rare diseases +MONDO:0019144 ordo_disorder diseases +MONDO:0019144 orphanet_rare diseases +MONDO:0019144 otar diseases +MONDO:0019144 rare diseases +MONDO:0019145 clingen diseases +MONDO:0019145 gard_rare diseases +MONDO:0019145 nord_rare diseases +MONDO:0019145 ordo_disorder diseases +MONDO:0019145 orphanet_rare diseases +MONDO:0019145 otar diseases +MONDO:0019145 rare diseases +MONDO:0019147 disease_grouping diseases +MONDO:0019147 gard_rare diseases +MONDO:0019147 ordo_group_of_disorders diseases +MONDO:0019147 otar diseases +MONDO:0019147 rare diseases +MONDO:0019148 gard_rare diseases +MONDO:0019148 nord_rare diseases +MONDO:0019148 ordo_subtype_of_a_disorder diseases +MONDO:0019148 otar diseases +MONDO:0019148 rare diseases +MONDO:0019149 gard_rare diseases +MONDO:0019149 nord_rare diseases +MONDO:0019149 ordo_subtype_of_a_disorder diseases +MONDO:0019149 otar diseases +MONDO:0019149 rare diseases +MONDO:0019151 gard_rare diseases +MONDO:0019151 nord_rare diseases +MONDO:0019151 ordo_disorder diseases +MONDO:0019151 orphanet_rare diseases +MONDO:0019151 otar diseases +MONDO:0019151 rare diseases +MONDO:0019152 clingen diseases +MONDO:0019152 gard_rare diseases +MONDO:0019152 nord_rare diseases +MONDO:0019152 ordo_disorder diseases +MONDO:0019152 ordo_malformation_syndrome diseases +MONDO:0019152 orphanet_rare diseases +MONDO:0019152 otar diseases +MONDO:0019152 rare diseases +MONDO:0019153 gard_rare diseases +MONDO:0019153 nord_rare diseases +MONDO:0019153 ordo_disorder diseases +MONDO:0019153 ordo_malformation_syndrome diseases +MONDO:0019153 orphanet_rare diseases +MONDO:0019153 otar diseases +MONDO:0019153 rare diseases +MONDO:0019154 disease_grouping diseases +MONDO:0019154 gard_rare diseases +MONDO:0019154 nord_rare diseases +MONDO:0019154 ordo_group_of_disorders diseases +MONDO:0019154 otar diseases +MONDO:0019154 rare diseases +MONDO:0019155 gard_rare diseases +MONDO:0019155 nord_rare diseases +MONDO:0019155 ordo_disorder diseases +MONDO:0019155 orphanet_rare diseases +MONDO:0019155 otar diseases +MONDO:0019155 rare diseases +MONDO:0019156 gard_rare diseases +MONDO:0019156 nord_rare diseases +MONDO:0019156 ordo_disorder diseases +MONDO:0019156 ordo_malformation_syndrome diseases +MONDO:0019156 orphanet_rare diseases +MONDO:0019156 otar diseases +MONDO:0019156 rare diseases +MONDO:0019157 gard_rare diseases +MONDO:0019157 nord_rare diseases +MONDO:0019157 ordo_disorder diseases +MONDO:0019157 orphanet_rare diseases +MONDO:0019157 otar diseases +MONDO:0019157 rare diseases +MONDO:0019158 gard_rare diseases +MONDO:0019158 nord_rare diseases +MONDO:0019158 ordo_disorder diseases +MONDO:0019158 orphanet_rare diseases +MONDO:0019158 rare diseases +MONDO:0019159 gard_rare diseases +MONDO:0019159 nord_rare diseases +MONDO:0019159 ordo_disorder diseases +MONDO:0019159 orphanet_rare diseases +MONDO:0019159 rare diseases +MONDO:0019160 gard_rare diseases +MONDO:0019160 nord_rare diseases +MONDO:0019160 ordo_clinical_syndrome diseases +MONDO:0019160 ordo_disorder diseases +MONDO:0019160 orphanet_rare diseases +MONDO:0019160 rare diseases +MONDO:0019161 gard_rare diseases +MONDO:0019161 nord_rare diseases +MONDO:0019161 ordo_disorder diseases +MONDO:0019161 orphanet_rare diseases +MONDO:0019161 otar diseases +MONDO:0019161 rare diseases +MONDO:0019162 gard_rare diseases +MONDO:0019162 nord_rare diseases +MONDO:0019162 ordo_disorder diseases +MONDO:0019162 orphanet_rare diseases +MONDO:0019162 otar diseases +MONDO:0019162 rare diseases +MONDO:0019164 gard_rare diseases +MONDO:0019164 nord_rare diseases +MONDO:0019164 ordo_disorder diseases +MONDO:0019164 ordo_malformation_syndrome diseases +MONDO:0019164 orphanet_rare diseases +MONDO:0019164 rare diseases +MONDO:0019165 gard_rare diseases +MONDO:0019165 ordo_group_of_disorders diseases +MONDO:0019165 otar diseases +MONDO:0019165 rare diseases +MONDO:0019167 gard_rare diseases +MONDO:0019167 nord_rare diseases +MONDO:0019167 ordo_disorder diseases +MONDO:0019167 orphanet_rare diseases +MONDO:0019167 rare diseases +MONDO:0019168 gard_rare diseases +MONDO:0019168 nord_rare diseases +MONDO:0019168 ordo_disorder diseases +MONDO:0019168 orphanet_rare diseases +MONDO:0019168 otar diseases +MONDO:0019168 rare diseases +MONDO:0019169 gard_rare diseases +MONDO:0019169 nord_rare diseases +MONDO:0019169 ordo_disorder diseases +MONDO:0019169 orphanet_rare diseases +MONDO:0019169 otar diseases +MONDO:0019169 rare diseases +MONDO:0019170 gard_rare diseases +MONDO:0019170 nord_rare diseases +MONDO:0019170 ordo_disorder diseases +MONDO:0019170 orphanet_rare diseases +MONDO:0019170 rare diseases +MONDO:0019171 clingen diseases +MONDO:0019171 gard_rare diseases +MONDO:0019171 nord_rare diseases +MONDO:0019171 ordo_disorder diseases +MONDO:0019171 ordo_group_of_disorders diseases +MONDO:0019171 orphanet_rare diseases +MONDO:0019171 otar diseases +MONDO:0019171 rare diseases +MONDO:0019172 clingen diseases +MONDO:0019172 disease_grouping diseases +MONDO:0019172 otar diseases +MONDO:0019173 gard_rare diseases +MONDO:0019173 nord_rare diseases +MONDO:0019173 ordo_disorder diseases +MONDO:0019173 orphanet_rare diseases +MONDO:0019173 rare diseases +MONDO:0019175 disease_grouping diseases +MONDO:0019175 gard_rare diseases +MONDO:0019175 ordo_group_of_disorders diseases +MONDO:0019175 otar diseases +MONDO:0019175 rare diseases +MONDO:0019177 gard_rare diseases +MONDO:0019177 nord_rare diseases +MONDO:0019177 ordo_subtype_of_a_disorder diseases +MONDO:0019177 otar diseases +MONDO:0019177 rare diseases +MONDO:0019178 gard_rare diseases +MONDO:0019178 ordo_disorder diseases +MONDO:0019178 ordo_malformation_syndrome diseases +MONDO:0019178 orphanet_rare diseases +MONDO:0019178 otar diseases +MONDO:0019178 rare diseases +MONDO:0019179 gard_rare diseases +MONDO:0019179 nord_rare diseases +MONDO:0019179 ordo_disorder diseases +MONDO:0019179 ordo_malformation_syndrome diseases +MONDO:0019179 orphanet_rare diseases +MONDO:0019179 otar diseases +MONDO:0019179 rare diseases +MONDO:0019180 gard_rare diseases +MONDO:0019180 nord_rare diseases +MONDO:0019180 ordo_disorder diseases +MONDO:0019180 orphanet_rare diseases +MONDO:0019180 otar diseases +MONDO:0019180 rare diseases +MONDO:0019181 clingen diseases +MONDO:0019181 gard_rare diseases +MONDO:0019181 nord_rare diseases +MONDO:0019181 ordo_etiological_subtype diseases +MONDO:0019181 ordo_subtype_of_a_disorder diseases +MONDO:0019181 otar diseases +MONDO:0019181 rare diseases +MONDO:0019182 disease_grouping diseases +MONDO:0019182 gard_rare diseases +MONDO:0019182 ordo_group_of_disorders diseases +MONDO:0019182 otar diseases +MONDO:0019182 rare diseases +MONDO:0019186 gard_rare diseases +MONDO:0019186 nord_rare diseases +MONDO:0019186 ordo_disorder diseases +MONDO:0019186 orphanet_rare diseases +MONDO:0019186 otar diseases +MONDO:0019186 rare diseases +MONDO:0019187 gard_rare diseases +MONDO:0019187 nord_rare diseases +MONDO:0019187 ordo_disorder diseases +MONDO:0019187 ordo_malformation_syndrome diseases +MONDO:0019187 orphanet_rare diseases +MONDO:0019187 otar diseases +MONDO:0019187 rare diseases +MONDO:0019188 clingen diseases +MONDO:0019188 gard_rare diseases +MONDO:0019188 nord_rare diseases +MONDO:0019188 ordo_disorder diseases +MONDO:0019188 ordo_malformation_syndrome diseases +MONDO:0019188 orphanet_rare diseases +MONDO:0019188 otar diseases +MONDO:0019188 rare diseases +MONDO:0019189 disease_grouping diseases +MONDO:0019189 gard_rare diseases +MONDO:0019189 ordo_group_of_disorders diseases +MONDO:0019189 rare diseases +MONDO:0019190 gard_rare diseases +MONDO:0019190 nord_rare diseases +MONDO:0019190 ordo_subtype_of_a_disorder diseases +MONDO:0019190 otar diseases +MONDO:0019190 rare diseases +MONDO:0019191 gard_rare diseases +MONDO:0019191 nord_rare diseases +MONDO:0019191 ordo_subtype_of_a_disorder diseases +MONDO:0019191 otar diseases +MONDO:0019191 rare diseases +MONDO:0019192 gard_rare diseases +MONDO:0019192 nord_rare diseases +MONDO:0019192 ordo_disorder diseases +MONDO:0019192 orphanet_rare diseases +MONDO:0019192 otar diseases +MONDO:0019192 rare diseases +MONDO:0019193 gard_rare diseases +MONDO:0019193 nord_rare diseases +MONDO:0019193 ordo_disorder diseases +MONDO:0019193 orphanet_rare diseases +MONDO:0019193 otar diseases +MONDO:0019193 rare diseases +MONDO:0019194 disease_grouping diseases +MONDO:0019194 gard_rare diseases +MONDO:0019194 nord_rare diseases +MONDO:0019194 ordo_group_of_disorders diseases +MONDO:0019194 rare diseases +MONDO:0019195 gard_rare diseases +MONDO:0019195 nord_rare diseases +MONDO:0019195 ordo_disorder diseases +MONDO:0019195 orphanet_rare diseases +MONDO:0019195 otar diseases +MONDO:0019195 rare diseases +MONDO:0019196 gard_rare diseases +MONDO:0019196 nord_rare diseases +MONDO:0019196 ordo_disorder diseases +MONDO:0019196 ordo_malformation_syndrome diseases +MONDO:0019196 orphanet_rare diseases +MONDO:0019196 rare diseases +MONDO:0019197 gard_rare diseases +MONDO:0019197 ordo_disorder diseases +MONDO:0019197 orphanet_rare diseases +MONDO:0019197 otar diseases +MONDO:0019197 rare diseases +MONDO:0019198 gard_rare diseases +MONDO:0019198 nord_rare diseases +MONDO:0019198 ordo_disorder diseases +MONDO:0019198 orphanet_rare diseases +MONDO:0019198 otar diseases +MONDO:0019198 rare diseases +MONDO:0019199 gard_rare diseases +MONDO:0019199 nord_rare diseases +MONDO:0019199 ordo_disorder diseases +MONDO:0019199 orphanet_rare diseases +MONDO:0019199 rare diseases +MONDO:0019200 gard_rare diseases +MONDO:0019200 nord_rare diseases +MONDO:0019200 ordo_disorder diseases +MONDO:0019200 orphanet_rare diseases +MONDO:0019200 otar diseases +MONDO:0019200 prototype_pattern diseases +MONDO:0019200 rare diseases +MONDO:0019201 gard_rare diseases +MONDO:0019201 nord_rare diseases +MONDO:0019201 ordo_disorder diseases +MONDO:0019201 orphanet_rare diseases +MONDO:0019201 otar diseases +MONDO:0019201 rare diseases +MONDO:0019202 gard_rare diseases +MONDO:0019202 nord_rare diseases +MONDO:0019202 ordo_disorder diseases +MONDO:0019202 orphanet_rare diseases +MONDO:0019202 otar diseases +MONDO:0019202 rare diseases +MONDO:0019203 gard_rare diseases +MONDO:0019203 nord_rare diseases +MONDO:0019203 ordo_disorder diseases +MONDO:0019203 orphanet_rare diseases +MONDO:0019203 rare diseases +MONDO:0019204 gard_rare diseases +MONDO:0019204 nord_rare diseases +MONDO:0019204 ordo_disorder diseases +MONDO:0019204 orphanet_rare diseases +MONDO:0019204 rare diseases +MONDO:0019205 gard_rare diseases +MONDO:0019205 nord_rare diseases +MONDO:0019205 ordo_disorder diseases +MONDO:0019205 ordo_malformation_syndrome diseases +MONDO:0019205 orphanet_rare diseases +MONDO:0019205 otar diseases +MONDO:0019205 rare diseases +MONDO:0019207 gard_rare diseases +MONDO:0019207 nord_rare diseases +MONDO:0019207 ordo_disorder diseases +MONDO:0019207 orphanet_rare diseases +MONDO:0019207 otar diseases +MONDO:0019207 rare diseases +MONDO:0019208 gard_rare diseases +MONDO:0019208 nord_rare diseases +MONDO:0019208 ordo_disorder diseases +MONDO:0019208 orphanet_rare diseases +MONDO:0019208 rare diseases +MONDO:0019209 gard_rare diseases +MONDO:0019209 nord_rare diseases +MONDO:0019209 ordo_disorder diseases +MONDO:0019209 orphanet_rare diseases +MONDO:0019209 otar diseases +MONDO:0019209 rare diseases +MONDO:0019210 gard_rare diseases +MONDO:0019210 nord_rare diseases +MONDO:0019210 ordo_disorder diseases +MONDO:0019210 orphanet_rare diseases +MONDO:0019210 rare diseases +MONDO:0019211 gard_rare diseases +MONDO:0019211 nord_rare diseases +MONDO:0019211 ordo_disorder diseases +MONDO:0019211 orphanet_rare diseases +MONDO:0019211 rare diseases +MONDO:0019212 gard_rare diseases +MONDO:0019212 nord_rare diseases +MONDO:0019212 ordo_disorder diseases +MONDO:0019212 orphanet_rare diseases +MONDO:0019212 otar diseases +MONDO:0019212 rare diseases +MONDO:0019214 disease_grouping diseases +MONDO:0019214 gard_rare diseases +MONDO:0019214 ordo_group_of_disorders diseases +MONDO:0019214 rare diseases +MONDO:0019215 disease_grouping diseases +MONDO:0019215 gard_rare diseases +MONDO:0019215 ordo_group_of_disorders diseases +MONDO:0019215 rare diseases +MONDO:0019216 disease_grouping diseases +MONDO:0019216 gard_rare diseases +MONDO:0019216 ordo_group_of_disorders diseases +MONDO:0019216 rare diseases +MONDO:0019218 disease_grouping diseases +MONDO:0019218 gard_rare diseases +MONDO:0019218 ordo_group_of_disorders diseases +MONDO:0019218 rare diseases +MONDO:0019219 disease_grouping diseases +MONDO:0019219 gard_rare diseases +MONDO:0019219 ordo_group_of_disorders diseases +MONDO:0019219 rare diseases +MONDO:0019220 clingen diseases +MONDO:0019220 disease_grouping diseases +MONDO:0019220 gard_rare diseases +MONDO:0019220 ordo_group_of_disorders diseases +MONDO:0019220 otar diseases +MONDO:0019220 rare diseases +MONDO:0019222 disease_grouping diseases +MONDO:0019222 gard_rare diseases +MONDO:0019222 ordo_group_of_disorders diseases +MONDO:0019222 rare diseases +MONDO:0019223 disease_grouping diseases +MONDO:0019223 gard_rare diseases +MONDO:0019223 ordo_group_of_disorders diseases +MONDO:0019223 rare diseases +MONDO:0019225 disease_grouping diseases +MONDO:0019225 gard_rare diseases +MONDO:0019225 ordo_group_of_disorders diseases +MONDO:0019225 otar diseases +MONDO:0019225 rare diseases +MONDO:0019226 disease_grouping diseases +MONDO:0019226 gard_rare diseases +MONDO:0019226 ordo_group_of_disorders diseases +MONDO:0019226 otar diseases +MONDO:0019226 rare diseases +MONDO:0019228 disease_grouping diseases +MONDO:0019228 gard_rare diseases +MONDO:0019228 ordo_group_of_disorders diseases +MONDO:0019228 rare diseases +MONDO:0019229 disease_grouping diseases +MONDO:0019229 gard_rare diseases +MONDO:0019229 ordo_group_of_disorders diseases +MONDO:0019229 rare diseases +MONDO:0019230 disease_grouping diseases +MONDO:0019230 gard_rare diseases +MONDO:0019230 ordo_group_of_disorders diseases +MONDO:0019230 rare diseases +MONDO:0019231 disease_grouping diseases +MONDO:0019231 gard_rare diseases +MONDO:0019231 ordo_group_of_disorders diseases +MONDO:0019231 rare diseases +MONDO:0019232 disease_grouping diseases +MONDO:0019232 gard_rare diseases +MONDO:0019232 ordo_group_of_disorders diseases +MONDO:0019232 rare diseases +MONDO:0019233 disease_grouping diseases +MONDO:0019233 gard_rare diseases +MONDO:0019233 nord_rare diseases +MONDO:0019233 ordo_group_of_disorders diseases +MONDO:0019233 rare diseases +MONDO:0019234 clingen diseases +MONDO:0019234 disease_grouping diseases +MONDO:0019234 gard_rare diseases +MONDO:0019234 nord_rare diseases +MONDO:0019234 ordo_group_of_disorders diseases +MONDO:0019234 otar diseases +MONDO:0019234 rare diseases +MONDO:0019235 disease_grouping diseases +MONDO:0019235 gard_rare diseases +MONDO:0019235 ordo_group_of_disorders diseases +MONDO:0019235 rare diseases +MONDO:0019236 disease_grouping diseases +MONDO:0019236 gard_rare diseases +MONDO:0019236 ordo_group_of_disorders diseases +MONDO:0019236 rare diseases +MONDO:0019237 disease_grouping diseases +MONDO:0019237 gard_rare diseases +MONDO:0019237 ordo_group_of_disorders diseases +MONDO:0019237 rare diseases +MONDO:0019238 disease_grouping diseases +MONDO:0019238 gard_rare diseases +MONDO:0019238 ordo_group_of_disorders diseases +MONDO:0019238 rare diseases +MONDO:0019239 disease_grouping diseases +MONDO:0019239 gard_rare diseases +MONDO:0019239 ordo_group_of_disorders diseases +MONDO:0019239 rare diseases +MONDO:0019240 disease_grouping diseases +MONDO:0019240 gard_rare diseases +MONDO:0019240 ordo_group_of_disorders diseases +MONDO:0019240 rare diseases +MONDO:0019241 disease_grouping diseases +MONDO:0019241 gard_rare diseases +MONDO:0019241 ordo_group_of_disorders diseases +MONDO:0019241 rare diseases +MONDO:0019242 disease_grouping diseases +MONDO:0019242 gard_rare diseases +MONDO:0019242 ordo_group_of_disorders diseases +MONDO:0019242 rare diseases +MONDO:0019243 disease_grouping diseases +MONDO:0019243 gard_rare diseases +MONDO:0019243 ordo_group_of_disorders diseases +MONDO:0019243 rare diseases +MONDO:0019245 disease_grouping diseases +MONDO:0019245 gard_rare diseases +MONDO:0019245 ordo_group_of_disorders diseases +MONDO:0019245 otar diseases +MONDO:0019245 rare diseases +MONDO:0019246 disease_grouping diseases +MONDO:0019246 gard_rare diseases +MONDO:0019246 ordo_group_of_disorders diseases +MONDO:0019246 rare diseases +MONDO:0019248 disease_grouping diseases +MONDO:0019248 gard_rare diseases +MONDO:0019248 ordo_group_of_disorders diseases +MONDO:0019248 otar diseases +MONDO:0019248 rare diseases +MONDO:0019249 disease_grouping diseases +MONDO:0019249 gard_rare diseases +MONDO:0019249 nord_rare diseases +MONDO:0019249 ordo_group_of_disorders diseases +MONDO:0019249 otar diseases +MONDO:0019249 rare diseases +MONDO:0019250 disease_grouping diseases +MONDO:0019250 gard_rare diseases +MONDO:0019250 ordo_group_of_disorders diseases +MONDO:0019250 rare diseases +MONDO:0019251 disease_grouping diseases +MONDO:0019251 gard_rare diseases +MONDO:0019251 ordo_group_of_disorders diseases +MONDO:0019251 rare diseases +MONDO:0019253 disease_grouping diseases +MONDO:0019253 gard_rare diseases +MONDO:0019253 ordo_group_of_disorders diseases +MONDO:0019253 rare diseases +MONDO:0019254 disease_grouping diseases +MONDO:0019254 gard_rare diseases +MONDO:0019254 ordo_group_of_disorders diseases +MONDO:0019254 rare diseases +MONDO:0019255 disease_grouping diseases +MONDO:0019255 gard_rare diseases +MONDO:0019255 nord_rare diseases +MONDO:0019255 ordo_group_of_disorders diseases +MONDO:0019255 otar diseases +MONDO:0019255 rare diseases +MONDO:0019256 disease_grouping diseases +MONDO:0019256 gard_rare diseases +MONDO:0019256 ordo_group_of_disorders diseases +MONDO:0019256 rare diseases +MONDO:0019257 gard_rare diseases +MONDO:0019257 nord_rare diseases +MONDO:0019257 ordo_disorder diseases +MONDO:0019257 orphanet_rare diseases +MONDO:0019257 otar diseases +MONDO:0019257 rare diseases +MONDO:0019258 gard_rare diseases +MONDO:0019258 nord_rare diseases +MONDO:0019258 ordo_subtype_of_a_disorder diseases +MONDO:0019258 otar diseases +MONDO:0019258 rare diseases +MONDO:0019259 gard_rare diseases +MONDO:0019259 nord_rare diseases +MONDO:0019259 ordo_subtype_of_a_disorder diseases +MONDO:0019259 otar diseases +MONDO:0019259 rare diseases +MONDO:0019260 clingen diseases +MONDO:0019260 gard_rare diseases +MONDO:0019260 nord_rare diseases +MONDO:0019260 ordo_disorder diseases +MONDO:0019260 orphanet_rare diseases +MONDO:0019260 otar diseases +MONDO:0019260 rare diseases +MONDO:0019261 gard_rare diseases +MONDO:0019261 nord_rare diseases +MONDO:0019261 ordo_disorder diseases +MONDO:0019261 orphanet_rare diseases +MONDO:0019261 otar diseases +MONDO:0019261 rare diseases +MONDO:0019262 gard_rare diseases +MONDO:0019262 nord_rare diseases +MONDO:0019262 ordo_disorder diseases +MONDO:0019262 orphanet_rare diseases +MONDO:0019262 otar diseases +MONDO:0019262 rare diseases +MONDO:0019263 gard_rare diseases +MONDO:0019263 nord_rare diseases +MONDO:0019263 ordo_disorder diseases +MONDO:0019263 orphanet_rare diseases +MONDO:0019263 otar diseases +MONDO:0019263 rare diseases +MONDO:0019264 gard_rare diseases +MONDO:0019264 ordo_subtype_of_a_disorder diseases +MONDO:0019264 otar diseases +MONDO:0019264 rare diseases +MONDO:0019265 disease_grouping diseases +MONDO:0019265 gard_rare diseases +MONDO:0019265 nord_rare diseases +MONDO:0019265 ordo_group_of_disorders diseases +MONDO:0019265 rare diseases +MONDO:0019266 gard_rare diseases +MONDO:0019266 nord_rare diseases +MONDO:0019266 ordo_disorder diseases +MONDO:0019266 orphanet_rare diseases +MONDO:0019266 otar diseases +MONDO:0019266 rare diseases +MONDO:0019267 gard_rare diseases +MONDO:0019267 nord_rare diseases +MONDO:0019267 ordo_subtype_of_a_disorder diseases +MONDO:0019267 otar diseases +MONDO:0019267 rare diseases +MONDO:0019268 disease_grouping diseases +MONDO:0019268 ordo_group_of_disorders diseases +MONDO:0019268 otar diseases +MONDO:0019269 disease_grouping diseases +MONDO:0019269 gard_rare diseases +MONDO:0019269 ordo_group_of_disorders diseases +MONDO:0019269 otar diseases +MONDO:0019269 rare diseases +MONDO:0019270 disease_grouping diseases +MONDO:0019270 gard_rare diseases +MONDO:0019270 ordo_group_of_disorders diseases +MONDO:0019270 otar diseases +MONDO:0019270 rare diseases +MONDO:0019272 disease_grouping diseases +MONDO:0019272 gard_rare diseases +MONDO:0019272 ordo_group_of_disorders diseases +MONDO:0019272 otar diseases +MONDO:0019272 rare diseases +MONDO:0019276 disease_grouping diseases +MONDO:0019276 gard_rare diseases +MONDO:0019276 nord_rare diseases +MONDO:0019276 ordo_group_of_disorders diseases +MONDO:0019276 otar diseases +MONDO:0019276 rare diseases +MONDO:0019278 disease_grouping diseases +MONDO:0019278 ordo_group_of_disorders diseases +MONDO:0019280 disease_grouping diseases +MONDO:0019280 gard_rare diseases +MONDO:0019280 ordo_group_of_disorders diseases +MONDO:0019280 otar diseases +MONDO:0019280 rare diseases +MONDO:0019283 disease_grouping diseases +MONDO:0019283 nord_rare diseases +MONDO:0019283 ordo_group_of_disorders diseases +MONDO:0019283 otar diseases +MONDO:0019283 rare diseases +MONDO:0019284 disease_grouping diseases +MONDO:0019284 gard_rare diseases +MONDO:0019284 ordo_group_of_disorders diseases +MONDO:0019284 otar diseases +MONDO:0019284 rare diseases +MONDO:0019287 disease_grouping diseases +MONDO:0019287 gard_rare diseases +MONDO:0019287 nord_rare diseases +MONDO:0019287 ordo_group_of_disorders diseases +MONDO:0019287 otar diseases +MONDO:0019287 rare diseases +MONDO:0019288 disease_grouping diseases +MONDO:0019288 ordo_group_of_disorders diseases +MONDO:0019288 otar diseases +MONDO:0019289 disease_grouping diseases +MONDO:0019289 ordo_group_of_disorders diseases +MONDO:0019289 otar diseases +MONDO:0019290 disease_grouping diseases +MONDO:0019290 ordo_group_of_disorders diseases +MONDO:0019290 otar diseases +MONDO:0019293 disease_grouping diseases +MONDO:0019293 ordo_group_of_disorders diseases +MONDO:0019293 otar diseases +MONDO:0019294 disease_grouping diseases +MONDO:0019294 ordo_group_of_disorders diseases +MONDO:0019296 disease_grouping diseases +MONDO:0019296 ordo_group_of_disorders diseases +MONDO:0019296 otar diseases +MONDO:0019296 rare_grouping diseases +MONDO:0019297 disease_grouping diseases +MONDO:0019297 otar diseases +MONDO:0019303 disease_grouping diseases +MONDO:0019303 gard_rare diseases +MONDO:0019303 ordo_group_of_disorders diseases +MONDO:0019303 otar diseases +MONDO:0019303 rare diseases +MONDO:0019306 gard_rare diseases +MONDO:0019306 nord_rare diseases +MONDO:0019306 ordo_disorder diseases +MONDO:0019306 orphanet_rare diseases +MONDO:0019306 otar diseases +MONDO:0019306 rare diseases +MONDO:0019307 gard_rare diseases +MONDO:0019307 nord_rare diseases +MONDO:0019307 ordo_disorder diseases +MONDO:0019307 orphanet_rare diseases +MONDO:0019307 otar diseases +MONDO:0019307 rare diseases +MONDO:0019308 gard_rare diseases +MONDO:0019308 nord_rare diseases +MONDO:0019308 ordo_disorder diseases +MONDO:0019308 orphanet_rare diseases +MONDO:0019308 otar diseases +MONDO:0019308 rare diseases +MONDO:0019309 gard_rare diseases +MONDO:0019309 nord_rare diseases +MONDO:0019309 ordo_disorder diseases +MONDO:0019309 orphanet_rare diseases +MONDO:0019309 otar diseases +MONDO:0019309 rare diseases +MONDO:0019310 gard_rare diseases +MONDO:0019310 nord_rare diseases +MONDO:0019310 ordo_disorder diseases +MONDO:0019310 orphanet_rare diseases +MONDO:0019310 otar diseases +MONDO:0019310 rare diseases +MONDO:0019311 gard_rare diseases +MONDO:0019311 nord_rare diseases +MONDO:0019311 ordo_disorder diseases +MONDO:0019311 orphanet_rare diseases +MONDO:0019311 otar diseases +MONDO:0019311 rare diseases +MONDO:0019312 gard_rare diseases +MONDO:0019312 nord_rare diseases +MONDO:0019312 ordo_disorder diseases +MONDO:0019312 orphanet_rare diseases +MONDO:0019312 otar diseases +MONDO:0019312 rare diseases +MONDO:0019313 gard_rare diseases +MONDO:0019313 otar diseases +MONDO:0019313 rare diseases +MONDO:0019314 gard_rare diseases +MONDO:0019314 nord_rare diseases +MONDO:0019314 ordo_disorder diseases +MONDO:0019314 orphanet_rare diseases +MONDO:0019314 rare diseases +MONDO:0019315 gard_rare diseases +MONDO:0019315 nord_rare diseases +MONDO:0019315 ordo_disorder diseases +MONDO:0019315 orphanet_rare diseases +MONDO:0019315 rare diseases +MONDO:0019316 gard_rare diseases +MONDO:0019316 nord_rare diseases +MONDO:0019316 ordo_disorder diseases +MONDO:0019316 orphanet_rare diseases +MONDO:0019316 otar diseases +MONDO:0019316 rare diseases +MONDO:0019317 gard_rare diseases +MONDO:0019317 rare diseases +MONDO:0019318 gard_rare diseases +MONDO:0019318 nord_rare diseases +MONDO:0019318 ordo_subtype_of_a_disorder diseases +MONDO:0019318 rare diseases +MONDO:0019319 gard_rare diseases +MONDO:0019319 nord_rare diseases +MONDO:0019319 ordo_subtype_of_a_disorder diseases +MONDO:0019319 rare diseases +MONDO:0019320 gard_rare diseases +MONDO:0019320 nord_rare diseases +MONDO:0019320 ordo_subtype_of_a_disorder diseases +MONDO:0019320 rare diseases +MONDO:0019321 gard_rare diseases +MONDO:0019321 nord_rare diseases +MONDO:0019321 ordo_disorder diseases +MONDO:0019321 orphanet_rare diseases +MONDO:0019321 otar diseases +MONDO:0019321 rare diseases +MONDO:0019322 gard_rare diseases +MONDO:0019322 nord_rare diseases +MONDO:0019322 ordo_disorder diseases +MONDO:0019322 orphanet_rare diseases +MONDO:0019322 otar diseases +MONDO:0019322 rare diseases +MONDO:0019323 gard_rare diseases +MONDO:0019323 nord_rare diseases +MONDO:0019323 ordo_disorder diseases +MONDO:0019323 orphanet_rare diseases +MONDO:0019323 otar diseases +MONDO:0019323 rare diseases +MONDO:0019324 gard_rare diseases +MONDO:0019324 nord_rare diseases +MONDO:0019324 ordo_disorder diseases +MONDO:0019324 orphanet_rare diseases +MONDO:0019324 otar diseases +MONDO:0019324 rare diseases +MONDO:0019325 gard_rare diseases +MONDO:0019325 nord_rare diseases +MONDO:0019325 ordo_subtype_of_a_disorder diseases +MONDO:0019325 rare diseases +MONDO:0019326 gard_rare diseases +MONDO:0019326 nord_rare diseases +MONDO:0019326 ordo_subtype_of_a_disorder diseases +MONDO:0019326 rare diseases +MONDO:0019327 gard_rare diseases +MONDO:0019327 nord_rare diseases +MONDO:0019327 ordo_subtype_of_a_disorder diseases +MONDO:0019327 rare diseases +MONDO:0019328 gard_rare diseases +MONDO:0019328 nord_rare diseases +MONDO:0019328 ordo_disorder diseases +MONDO:0019328 ordo_malformation_syndrome diseases +MONDO:0019328 orphanet_rare diseases +MONDO:0019328 rare diseases +MONDO:0019329 gard_rare diseases +MONDO:0019329 nord_rare diseases +MONDO:0019329 ordo_disorder diseases +MONDO:0019329 ordo_malformation_syndrome diseases +MONDO:0019329 orphanet_rare diseases +MONDO:0019329 rare diseases +MONDO:0019330 gard_rare diseases +MONDO:0019330 nord_rare diseases +MONDO:0019330 ordo_disorder diseases +MONDO:0019330 orphanet_rare diseases +MONDO:0019330 otar diseases +MONDO:0019330 rare diseases +MONDO:0019332 gard_rare diseases +MONDO:0019332 nord_rare diseases +MONDO:0019332 ordo_disorder diseases +MONDO:0019332 orphanet_rare diseases +MONDO:0019332 otar diseases +MONDO:0019332 rare diseases +MONDO:0019333 gard_rare diseases +MONDO:0019333 nord_rare diseases +MONDO:0019333 ordo_disorder diseases +MONDO:0019333 orphanet_rare diseases +MONDO:0019333 otar diseases +MONDO:0019333 rare diseases +MONDO:0019334 gard_rare diseases +MONDO:0019334 nord_rare diseases +MONDO:0019334 ordo_disorder diseases +MONDO:0019334 orphanet_rare diseases +MONDO:0019334 otar diseases +MONDO:0019334 rare diseases +MONDO:0019335 gard_rare diseases +MONDO:0019335 nord_rare diseases +MONDO:0019335 ordo_subtype_of_a_disorder diseases +MONDO:0019335 otar diseases +MONDO:0019335 rare diseases +MONDO:0019336 gard_rare diseases +MONDO:0019336 nord_rare diseases +MONDO:0019336 ordo_subtype_of_a_disorder diseases +MONDO:0019336 otar diseases +MONDO:0019336 rare diseases +MONDO:0019337 disease_grouping diseases +MONDO:0019337 gard_rare diseases +MONDO:0019337 ordo_group_of_disorders diseases +MONDO:0019337 otar diseases +MONDO:0019337 rare diseases +MONDO:0019338 gard_rare diseases +MONDO:0019338 nord_rare diseases +MONDO:0019338 ordo_disorder diseases +MONDO:0019338 orphanet_rare diseases +MONDO:0019338 otar diseases +MONDO:0019338 rare diseases +MONDO:0019339 gard_rare diseases +MONDO:0019339 nord_rare diseases +MONDO:0019339 ordo_disorder diseases +MONDO:0019339 ordo_malformation_syndrome diseases +MONDO:0019339 orphanet_rare diseases +MONDO:0019339 otar diseases +MONDO:0019339 rare diseases +MONDO:0019340 disease_grouping diseases +MONDO:0019340 gard_rare diseases +MONDO:0019340 ordo_group_of_disorders diseases +MONDO:0019340 otar diseases +MONDO:0019340 rare diseases +MONDO:0019342 gard_rare diseases +MONDO:0019342 nord_rare diseases +MONDO:0019342 ordo_disorder diseases +MONDO:0019342 ordo_malformation_syndrome diseases +MONDO:0019342 orphanet_rare diseases +MONDO:0019342 otar diseases +MONDO:0019342 rare diseases +MONDO:0019344 gard_rare diseases +MONDO:0019344 nord_rare diseases +MONDO:0019344 ordo_disorder diseases +MONDO:0019344 orphanet_rare diseases +MONDO:0019344 otar diseases +MONDO:0019344 rare diseases +MONDO:0019345 gard_rare diseases +MONDO:0019345 nord_rare diseases +MONDO:0019345 ordo_disorder diseases +MONDO:0019345 orphanet_rare diseases +MONDO:0019345 otar diseases +MONDO:0019345 rare diseases +MONDO:0019346 gard_rare diseases +MONDO:0019346 nord_rare diseases +MONDO:0019346 ordo_disorder diseases +MONDO:0019346 orphanet_rare diseases +MONDO:0019346 otar diseases +MONDO:0019346 rare diseases +MONDO:0019347 disease_grouping diseases +MONDO:0019347 gard_rare diseases +MONDO:0019347 nord_rare diseases +MONDO:0019347 ordo_group_of_disorders diseases +MONDO:0019347 otar diseases +MONDO:0019347 rare diseases +MONDO:0019349 clingen diseases +MONDO:0019349 gard_rare diseases +MONDO:0019349 nord_rare diseases +MONDO:0019349 ordo_disorder diseases +MONDO:0019349 orphanet_rare diseases +MONDO:0019349 otar diseases +MONDO:0019349 rare diseases +MONDO:0019350 clingen diseases +MONDO:0019350 gard_rare diseases +MONDO:0019350 nord_rare diseases +MONDO:0019350 ordo_disorder diseases +MONDO:0019350 orphanet_rare diseases +MONDO:0019350 otar diseases +MONDO:0019350 rare diseases +MONDO:0019351 disease_grouping diseases +MONDO:0019351 gard_rare diseases +MONDO:0019351 nord_rare diseases +MONDO:0019351 ordo_group_of_disorders diseases +MONDO:0019351 otar diseases +MONDO:0019351 rare diseases +MONDO:0019353 gard_rare diseases +MONDO:0019353 nord_rare diseases +MONDO:0019353 ordo_disorder diseases +MONDO:0019353 orphanet_rare diseases +MONDO:0019353 otar diseases +MONDO:0019353 rare diseases +MONDO:0019354 clingen diseases +MONDO:0019354 gard_rare diseases +MONDO:0019354 nord_rare diseases +MONDO:0019354 ordo_disorder diseases +MONDO:0019354 orphanet_rare diseases +MONDO:0019354 otar diseases +MONDO:0019354 rare diseases +MONDO:0019355 gard_rare diseases +MONDO:0019355 nord_rare diseases +MONDO:0019355 ordo_disorder diseases +MONDO:0019355 orphanet_rare diseases +MONDO:0019355 otar diseases +MONDO:0019355 rare diseases +MONDO:0019356 disease_grouping diseases +MONDO:0019356 gard_rare diseases +MONDO:0019356 ordo_group_of_disorders diseases +MONDO:0019356 rare diseases +MONDO:0019357 gard_rare diseases +MONDO:0019357 nord_rare diseases +MONDO:0019357 ordo_disorder diseases +MONDO:0019357 orphanet_rare diseases +MONDO:0019357 rare diseases +MONDO:0019358 gard_rare diseases +MONDO:0019358 nord_rare diseases +MONDO:0019358 ordo_disorder diseases +MONDO:0019358 orphanet_rare diseases +MONDO:0019358 otar diseases +MONDO:0019358 rare diseases +MONDO:0019359 gard_rare diseases +MONDO:0019359 nord_rare diseases +MONDO:0019359 ordo_disorder diseases +MONDO:0019359 orphanet_rare diseases +MONDO:0019359 rare diseases +MONDO:0019360 gard_rare diseases +MONDO:0019360 nord_rare diseases +MONDO:0019360 ordo_disorder diseases +MONDO:0019360 orphanet_rare diseases +MONDO:0019360 rare diseases +MONDO:0019362 gard_rare diseases +MONDO:0019362 nord_rare diseases +MONDO:0019362 ordo_disorder diseases +MONDO:0019362 orphanet_rare diseases +MONDO:0019362 otar diseases +MONDO:0019362 rare diseases +MONDO:0019364 gard_rare diseases +MONDO:0019364 nord_rare diseases +MONDO:0019364 ordo_disorder diseases +MONDO:0019364 orphanet_rare diseases +MONDO:0019364 rare diseases +MONDO:0019365 gard_rare diseases +MONDO:0019365 nord_rare diseases +MONDO:0019365 ordo_disorder diseases +MONDO:0019365 orphanet_rare diseases +MONDO:0019365 otar diseases +MONDO:0019365 rare diseases +MONDO:0019366 gard_rare diseases +MONDO:0019366 ordo_disorder diseases +MONDO:0019366 orphanet_rare diseases +MONDO:0019366 otar diseases +MONDO:0019366 rare diseases +MONDO:0019367 gard_rare diseases +MONDO:0019367 nord_rare diseases +MONDO:0019367 ordo_disorder diseases +MONDO:0019367 orphanet_rare diseases +MONDO:0019367 rare diseases +MONDO:0019368 gard_rare diseases +MONDO:0019368 nord_rare diseases +MONDO:0019368 ordo_disorder diseases +MONDO:0019368 orphanet_rare diseases +MONDO:0019368 rare diseases +MONDO:0019369 gard_rare diseases +MONDO:0019369 nord_rare diseases +MONDO:0019369 ordo_disorder diseases +MONDO:0019369 orphanet_rare diseases +MONDO:0019369 otar diseases +MONDO:0019369 rare diseases +MONDO:0019370 gard_rare diseases +MONDO:0019370 nord_rare diseases +MONDO:0019370 ordo_disorder diseases +MONDO:0019370 orphanet_rare diseases +MONDO:0019370 rare diseases +MONDO:0019371 gard_rare diseases +MONDO:0019371 nord_rare diseases +MONDO:0019371 ordo_disorder diseases +MONDO:0019371 orphanet_rare diseases +MONDO:0019371 otar diseases +MONDO:0019371 rare diseases +MONDO:0019372 gard_rare diseases +MONDO:0019372 nord_rare diseases +MONDO:0019372 ordo_disorder diseases +MONDO:0019372 orphanet_rare diseases +MONDO:0019372 rare diseases +MONDO:0019373 gard_rare diseases +MONDO:0019373 nord_rare diseases +MONDO:0019373 ordo_disorder diseases +MONDO:0019373 orphanet_rare diseases +MONDO:0019373 otar diseases +MONDO:0019373 rare diseases +MONDO:0019374 gard_rare diseases +MONDO:0019374 ordo_disorder diseases +MONDO:0019374 ordo_malformation_syndrome diseases +MONDO:0019374 orphanet_rare diseases +MONDO:0019374 otar diseases +MONDO:0019374 rare diseases +MONDO:0019375 gard_rare diseases +MONDO:0019375 nord_rare diseases +MONDO:0019375 ordo_disorder diseases +MONDO:0019375 ordo_malformation_syndrome diseases +MONDO:0019375 orphanet_rare diseases +MONDO:0019375 otar diseases +MONDO:0019375 rare diseases +MONDO:0019376 gard_rare diseases +MONDO:0019376 nord_rare diseases +MONDO:0019376 ordo_disorder diseases +MONDO:0019376 orphanet_rare diseases +MONDO:0019376 otar diseases +MONDO:0019376 rare diseases +MONDO:0019377 gard_rare diseases +MONDO:0019377 nord_rare diseases +MONDO:0019377 ordo_disorder diseases +MONDO:0019377 orphanet_rare diseases +MONDO:0019377 rare diseases +MONDO:0019378 gard_rare diseases +MONDO:0019378 nord_rare diseases +MONDO:0019378 ordo_disorder diseases +MONDO:0019378 orphanet_rare diseases +MONDO:0019378 rare diseases +MONDO:0019380 gard_rare diseases +MONDO:0019380 nord_rare diseases +MONDO:0019380 ordo_disorder diseases +MONDO:0019380 orphanet_rare diseases +MONDO:0019380 otar diseases +MONDO:0019380 rare diseases +MONDO:0019383 gard_rare diseases +MONDO:0019383 nord_rare diseases +MONDO:0019383 ordo_disorder diseases +MONDO:0019383 orphanet_rare diseases +MONDO:0019383 otar diseases +MONDO:0019383 rare diseases +MONDO:0019384 gard_rare diseases +MONDO:0019384 historic_epidemic diseases +MONDO:0019384 nord_rare diseases +MONDO:0019384 ordo_disorder diseases +MONDO:0019384 orphanet_rare diseases +MONDO:0019384 rare diseases +MONDO:0019385 gard_rare diseases +MONDO:0019385 nord_rare diseases +MONDO:0019385 ordo_disorder diseases +MONDO:0019385 orphanet_rare diseases +MONDO:0019385 rare diseases +MONDO:0019386 gard_rare diseases +MONDO:0019386 nord_rare diseases +MONDO:0019386 ordo_disorder diseases +MONDO:0019386 orphanet_rare diseases +MONDO:0019386 rare diseases +MONDO:0019387 gard_rare diseases +MONDO:0019387 nord_rare diseases +MONDO:0019387 ordo_disorder diseases +MONDO:0019387 ordo_malformation_syndrome diseases +MONDO:0019387 orphanet_rare diseases +MONDO:0019387 rare diseases +MONDO:0019388 gard_rare diseases +MONDO:0019388 nord_rare diseases +MONDO:0019388 ordo_disorder diseases +MONDO:0019388 ordo_malformation_syndrome diseases +MONDO:0019388 orphanet_rare diseases +MONDO:0019388 otar diseases +MONDO:0019388 rare diseases +MONDO:0019390 gard_rare diseases +MONDO:0019390 nord_rare diseases +MONDO:0019390 ordo_disorder diseases +MONDO:0019390 orphanet_rare diseases +MONDO:0019390 otar diseases +MONDO:0019390 rare diseases +MONDO:0019391 clingen diseases +MONDO:0019391 gard_rare diseases +MONDO:0019391 nord_rare diseases +MONDO:0019391 ordo_disorder diseases +MONDO:0019391 ordo_malformation_syndrome diseases +MONDO:0019391 orphanet_rare diseases +MONDO:0019391 otar diseases +MONDO:0019391 rare diseases +MONDO:0019392 gard_rare diseases +MONDO:0019392 nord_rare diseases +MONDO:0019392 ordo_disorder diseases +MONDO:0019392 orphanet_rare diseases +MONDO:0019392 otar diseases +MONDO:0019392 rare diseases +MONDO:0019393 gard_rare diseases +MONDO:0019393 nord_rare diseases +MONDO:0019393 ordo_disorder diseases +MONDO:0019393 orphanet_rare diseases +MONDO:0019393 rare diseases +MONDO:0019394 gard_rare diseases +MONDO:0019394 nord_rare diseases +MONDO:0019394 ordo_disorder diseases +MONDO:0019394 orphanet_rare diseases +MONDO:0019394 otar diseases +MONDO:0019394 rare diseases +MONDO:0019395 gard_rare diseases +MONDO:0019395 nord_rare diseases +MONDO:0019395 ordo_disorder diseases +MONDO:0019395 orphanet_rare diseases +MONDO:0019395 rare diseases +MONDO:0019396 gard_rare diseases +MONDO:0019396 nord_rare diseases +MONDO:0019396 ordo_disorder diseases +MONDO:0019396 orphanet_rare diseases +MONDO:0019396 rare diseases +MONDO:0019397 gard_rare diseases +MONDO:0019397 rare diseases +MONDO:0019398 gard_rare diseases +MONDO:0019398 nord_rare diseases +MONDO:0019398 ordo_disorder diseases +MONDO:0019398 orphanet_rare diseases +MONDO:0019398 otar diseases +MONDO:0019398 rare diseases +MONDO:0019399 gard_rare diseases +MONDO:0019399 nord_rare diseases +MONDO:0019399 ordo_disorder diseases +MONDO:0019399 orphanet_rare diseases +MONDO:0019399 rare diseases +MONDO:0019401 gard_rare diseases +MONDO:0019401 ordo_clinical_syndrome diseases +MONDO:0019401 otar diseases +MONDO:0019401 rare diseases +MONDO:0019402 gard_rare diseases +MONDO:0019402 nord_rare diseases +MONDO:0019402 ordo_disorder diseases +MONDO:0019402 orphanet_rare diseases +MONDO:0019402 otar diseases +MONDO:0019402 rare diseases +MONDO:0019403 disease_grouping diseases +MONDO:0019403 gard_rare diseases +MONDO:0019403 nord_rare diseases +MONDO:0019403 ordo_group_of_disorders diseases +MONDO:0019403 otar diseases +MONDO:0019403 rare diseases +MONDO:0019404 disease_grouping diseases +MONDO:0019404 gard_rare diseases +MONDO:0019404 nord_rare diseases +MONDO:0019404 ordo_group_of_disorders diseases +MONDO:0019404 otar diseases +MONDO:0019404 rare diseases +MONDO:0019405 gard_rare diseases +MONDO:0019405 nord_rare diseases +MONDO:0019405 ordo_disorder diseases +MONDO:0019405 orphanet_rare diseases +MONDO:0019405 otar diseases +MONDO:0019405 rare diseases +MONDO:0019406 gard_rare diseases +MONDO:0019406 nord_rare diseases +MONDO:0019406 ordo_disorder diseases +MONDO:0019406 ordo_malformation_syndrome diseases +MONDO:0019406 orphanet_rare diseases +MONDO:0019406 otar diseases +MONDO:0019406 rare diseases +MONDO:0019407 gard_rare diseases +MONDO:0019407 nord_rare diseases +MONDO:0019407 ordo_disorder diseases +MONDO:0019407 orphanet_rare diseases +MONDO:0019407 otar diseases +MONDO:0019407 rare diseases +MONDO:0019408 gard_rare diseases +MONDO:0019408 nord_rare diseases +MONDO:0019408 ordo_disorder diseases +MONDO:0019408 ordo_malformation_syndrome diseases +MONDO:0019408 orphanet_rare diseases +MONDO:0019408 otar diseases +MONDO:0019408 rare diseases +MONDO:0019409 gard_rare diseases +MONDO:0019409 nord_rare diseases +MONDO:0019409 ordo_disorder diseases +MONDO:0019409 ordo_malformation_syndrome diseases +MONDO:0019409 orphanet_rare diseases +MONDO:0019409 otar diseases +MONDO:0019409 rare diseases +MONDO:0019411 gard_rare diseases +MONDO:0019411 nord_rare diseases +MONDO:0019411 ordo_disorder diseases +MONDO:0019411 orphanet_rare diseases +MONDO:0019411 otar diseases +MONDO:0019411 rare diseases +MONDO:0019412 gard_rare diseases +MONDO:0019412 nord_rare diseases +MONDO:0019412 ordo_disorder diseases +MONDO:0019412 ordo_malformation_syndrome diseases +MONDO:0019412 orphanet_rare diseases +MONDO:0019412 otar diseases +MONDO:0019412 rare diseases +MONDO:0019413 gard_rare diseases +MONDO:0019413 nord_rare diseases +MONDO:0019413 ordo_disorder diseases +MONDO:0019413 ordo_malformation_syndrome diseases +MONDO:0019413 orphanet_rare diseases +MONDO:0019413 otar diseases +MONDO:0019413 rare diseases +MONDO:0019414 gard_rare diseases +MONDO:0019414 ordo_disorder diseases +MONDO:0019414 ordo_malformation_syndrome diseases +MONDO:0019414 orphanet_rare diseases +MONDO:0019414 otar diseases +MONDO:0019414 rare diseases +MONDO:0019415 gard_rare diseases +MONDO:0019415 nord_rare diseases +MONDO:0019415 ordo_disorder diseases +MONDO:0019415 orphanet_rare diseases +MONDO:0019415 rare diseases +MONDO:0019416 gard_rare diseases +MONDO:0019416 nord_rare diseases +MONDO:0019416 ordo_disorder diseases +MONDO:0019416 ordo_malformation_syndrome diseases +MONDO:0019416 orphanet_rare diseases +MONDO:0019416 otar diseases +MONDO:0019416 rare diseases +MONDO:0019417 ordo_malformation_syndrome diseases +MONDO:0019418 gard_rare diseases +MONDO:0019418 nord_rare diseases +MONDO:0019418 ordo_disorder diseases +MONDO:0019418 ordo_malformation_syndrome diseases +MONDO:0019418 orphanet_rare diseases +MONDO:0019418 rare diseases +MONDO:0019419 gard_rare diseases +MONDO:0019419 nord_rare diseases +MONDO:0019419 ordo_disorder diseases +MONDO:0019419 ordo_malformation_syndrome diseases +MONDO:0019419 orphanet_rare diseases +MONDO:0019419 otar diseases +MONDO:0019419 rare diseases +MONDO:0019420 gard_rare diseases +MONDO:0019420 nord_rare diseases +MONDO:0019420 ordo_disorder diseases +MONDO:0019420 ordo_malformation_syndrome diseases +MONDO:0019420 orphanet_rare diseases +MONDO:0019420 otar diseases +MONDO:0019420 rare diseases +MONDO:0019421 gard_rare diseases +MONDO:0019421 nord_rare diseases +MONDO:0019421 ordo_disorder diseases +MONDO:0019421 orphanet_rare diseases +MONDO:0019421 otar diseases +MONDO:0019421 rare diseases +MONDO:0019422 gard_rare diseases +MONDO:0019422 nord_rare diseases +MONDO:0019422 ordo_disorder diseases +MONDO:0019422 ordo_malformation_syndrome diseases +MONDO:0019422 orphanet_rare diseases +MONDO:0019422 otar diseases +MONDO:0019422 rare diseases +MONDO:0019423 gard_rare diseases +MONDO:0019423 nord_rare diseases +MONDO:0019423 ordo_disorder diseases +MONDO:0019423 ordo_malformation_syndrome diseases +MONDO:0019423 orphanet_rare diseases +MONDO:0019423 otar diseases +MONDO:0019423 rare diseases +MONDO:0019424 gard_rare diseases +MONDO:0019424 ordo_disorder diseases +MONDO:0019424 orphanet_rare diseases +MONDO:0019424 otar diseases +MONDO:0019424 rare diseases +MONDO:0019427 gard_rare diseases +MONDO:0019427 nord_rare diseases +MONDO:0019427 ordo_disorder diseases +MONDO:0019427 orphanet_rare diseases +MONDO:0019427 otar diseases +MONDO:0019427 rare diseases +MONDO:0019428 gard_rare diseases +MONDO:0019428 ordo_disorder diseases +MONDO:0019428 ordo_malformation_syndrome diseases +MONDO:0019428 orphanet_rare diseases +MONDO:0019428 otar diseases +MONDO:0019428 rare diseases +MONDO:0019429 gard_rare diseases +MONDO:0019429 nord_rare diseases +MONDO:0019429 ordo_disorder diseases +MONDO:0019429 orphanet_rare diseases +MONDO:0019429 rare diseases +MONDO:0019430 gard_rare diseases +MONDO:0019430 ordo_disorder diseases +MONDO:0019430 orphanet_rare diseases +MONDO:0019430 otar diseases +MONDO:0019430 rare diseases +MONDO:0019431 gard_rare diseases +MONDO:0019431 nord_rare diseases +MONDO:0019431 ordo_clinical_syndrome diseases +MONDO:0019431 ordo_disorder diseases +MONDO:0019431 orphanet_rare diseases +MONDO:0019431 rare diseases +MONDO:0019432 gard_rare diseases +MONDO:0019432 nord_rare diseases +MONDO:0019432 ordo_disorder diseases +MONDO:0019432 orphanet_rare diseases +MONDO:0019432 otar diseases +MONDO:0019432 rare diseases +MONDO:0019433 gard_rare diseases +MONDO:0019433 nord_rare diseases +MONDO:0019433 ordo_disorder diseases +MONDO:0019433 orphanet_rare diseases +MONDO:0019433 otar diseases +MONDO:0019433 rare diseases +MONDO:0019434 gard_rare diseases +MONDO:0019434 nord_rare diseases +MONDO:0019434 ordo_disorder diseases +MONDO:0019434 orphanet_rare diseases +MONDO:0019434 otar diseases +MONDO:0019434 rare diseases +MONDO:0019435 gard_rare diseases +MONDO:0019435 nord_rare diseases +MONDO:0019435 ordo_disorder diseases +MONDO:0019435 orphanet_rare diseases +MONDO:0019435 otar diseases +MONDO:0019435 rare diseases +MONDO:0019436 gard_rare diseases +MONDO:0019436 nord_rare diseases +MONDO:0019436 ordo_disorder diseases +MONDO:0019436 orphanet_rare diseases +MONDO:0019436 otar diseases +MONDO:0019436 rare diseases +MONDO:0019437 gard_rare diseases +MONDO:0019437 nord_rare diseases +MONDO:0019437 ordo_disorder diseases +MONDO:0019437 ordo_malformation_syndrome diseases +MONDO:0019437 orphanet_rare diseases +MONDO:0019437 otar diseases +MONDO:0019437 rare diseases +MONDO:0019438 gard_rare diseases +MONDO:0019438 nord_rare diseases +MONDO:0019438 ordo_disorder diseases +MONDO:0019438 orphanet_rare diseases +MONDO:0019438 otar diseases +MONDO:0019438 rare diseases +MONDO:0019439 gard_rare diseases +MONDO:0019439 nord_rare diseases +MONDO:0019439 ordo_disorder diseases +MONDO:0019439 orphanet_rare diseases +MONDO:0019439 otar diseases +MONDO:0019439 rare diseases +MONDO:0019440 gard_rare diseases +MONDO:0019440 nord_rare diseases +MONDO:0019440 ordo_disorder diseases +MONDO:0019440 orphanet_rare diseases +MONDO:0019440 rare diseases +MONDO:0019441 gard_rare diseases +MONDO:0019441 nord_rare diseases +MONDO:0019441 ordo_disorder diseases +MONDO:0019441 orphanet_rare diseases +MONDO:0019441 otar diseases +MONDO:0019441 rare diseases +MONDO:0019443 gard_rare diseases +MONDO:0019443 nord_rare diseases +MONDO:0019443 ordo_disorder diseases +MONDO:0019443 ordo_morphological_anomaly diseases +MONDO:0019443 orphanet_rare diseases +MONDO:0019443 otar diseases +MONDO:0019443 rare diseases +MONDO:0019444 gard_rare diseases +MONDO:0019444 nord_rare diseases +MONDO:0019444 ordo_disorder diseases +MONDO:0019444 orphanet_rare diseases +MONDO:0019444 rare diseases +MONDO:0019445 gard_rare diseases +MONDO:0019445 nord_rare diseases +MONDO:0019445 ordo_disorder diseases +MONDO:0019445 orphanet_rare diseases +MONDO:0019445 rare diseases +MONDO:0019446 disease_grouping diseases +MONDO:0019446 gard_rare diseases +MONDO:0019446 ordo_group_of_disorders diseases +MONDO:0019446 rare diseases +MONDO:0019447 gard_rare diseases +MONDO:0019447 nord_rare diseases +MONDO:0019447 ordo_disorder diseases +MONDO:0019447 orphanet_rare diseases +MONDO:0019447 rare diseases +MONDO:0019448 gard_rare diseases +MONDO:0019448 nord_rare diseases +MONDO:0019448 ordo_disorder diseases +MONDO:0019448 orphanet_rare diseases +MONDO:0019448 otar diseases +MONDO:0019448 rare diseases +MONDO:0019449 gard_rare diseases +MONDO:0019449 nord_rare diseases +MONDO:0019449 ordo_disorder diseases +MONDO:0019449 ordo_malformation_syndrome diseases +MONDO:0019449 orphanet_rare diseases +MONDO:0019449 rare diseases +MONDO:0019450 clingen diseases +MONDO:0019450 disease_grouping diseases +MONDO:0019450 gard_rare diseases +MONDO:0019450 nord_rare diseases +MONDO:0019450 ordo_group_of_disorders diseases +MONDO:0019450 otar diseases +MONDO:0019450 rare diseases +MONDO:0019451 gard_rare diseases +MONDO:0019451 nord_rare diseases +MONDO:0019451 ordo_disorder diseases +MONDO:0019451 orphanet_rare diseases +MONDO:0019451 otar diseases +MONDO:0019451 rare diseases +MONDO:0019452 gard_rare diseases +MONDO:0019452 nord_rare diseases +MONDO:0019452 ordo_disorder diseases +MONDO:0019452 orphanet_rare diseases +MONDO:0019452 otar diseases +MONDO:0019452 rare diseases +MONDO:0019453 disease_grouping diseases +MONDO:0019453 gard_rare diseases +MONDO:0019453 nord_rare diseases +MONDO:0019453 ordo_group_of_disorders diseases +MONDO:0019453 otar diseases +MONDO:0019453 rare diseases +MONDO:0019454 gard_rare diseases +MONDO:0019454 nord_rare diseases +MONDO:0019454 ordo_disorder diseases +MONDO:0019454 orphanet_rare diseases +MONDO:0019454 otar diseases +MONDO:0019454 rare diseases +MONDO:0019455 gard_rare diseases +MONDO:0019455 nord_rare diseases +MONDO:0019455 ordo_disorder diseases +MONDO:0019455 orphanet_rare diseases +MONDO:0019455 otar diseases +MONDO:0019455 rare diseases +MONDO:0019456 gard_rare diseases +MONDO:0019456 nord_rare diseases +MONDO:0019456 ordo_disorder diseases +MONDO:0019456 orphanet_rare diseases +MONDO:0019456 rare diseases +MONDO:0019457 disease_grouping diseases +MONDO:0019457 gard_rare diseases +MONDO:0019457 ordo_group_of_disorders diseases +MONDO:0019457 otar diseases +MONDO:0019457 rare diseases +MONDO:0019458 gard_rare diseases +MONDO:0019458 nord_rare diseases +MONDO:0019458 ordo_disorder diseases +MONDO:0019458 orphanet_rare diseases +MONDO:0019458 otar diseases +MONDO:0019458 rare diseases +MONDO:0019460 disease_grouping diseases +MONDO:0019460 gard_rare diseases +MONDO:0019460 nord_rare diseases +MONDO:0019460 ordo_group_of_disorders diseases +MONDO:0019460 otar diseases +MONDO:0019460 rare diseases +MONDO:0019461 gard_rare diseases +MONDO:0019461 nord_rare diseases +MONDO:0019461 ordo_disorder diseases +MONDO:0019461 orphanet_rare diseases +MONDO:0019461 otar diseases +MONDO:0019461 rare diseases +MONDO:0019462 gard_rare diseases +MONDO:0019462 nord_rare diseases +MONDO:0019462 ordo_disorder diseases +MONDO:0019462 orphanet_rare diseases +MONDO:0019462 otar diseases +MONDO:0019462 rare diseases +MONDO:0019463 gard_rare diseases +MONDO:0019463 nord_rare diseases +MONDO:0019463 ordo_disorder diseases +MONDO:0019463 orphanet_rare diseases +MONDO:0019463 rare diseases +MONDO:0019464 gard_rare diseases +MONDO:0019464 nord_rare diseases +MONDO:0019464 ordo_disorder diseases +MONDO:0019464 orphanet_rare diseases +MONDO:0019464 otar diseases +MONDO:0019464 rare diseases +MONDO:0019465 gard_rare diseases +MONDO:0019465 nord_rare diseases +MONDO:0019465 ordo_disorder diseases +MONDO:0019465 orphanet_rare diseases +MONDO:0019465 otar diseases +MONDO:0019465 rare diseases +MONDO:0019466 gard_rare diseases +MONDO:0019466 nord_rare diseases +MONDO:0019466 ordo_disorder diseases +MONDO:0019466 orphanet_rare diseases +MONDO:0019466 rare diseases +MONDO:0019467 gard_rare diseases +MONDO:0019467 nord_rare diseases +MONDO:0019467 ordo_disorder diseases +MONDO:0019467 orphanet_rare diseases +MONDO:0019467 otar diseases +MONDO:0019467 rare diseases +MONDO:0019468 gard_rare diseases +MONDO:0019468 nord_rare diseases +MONDO:0019468 ordo_disorder diseases +MONDO:0019468 orphanet_rare diseases +MONDO:0019468 otar diseases +MONDO:0019468 rare diseases +MONDO:0019469 gard_rare diseases +MONDO:0019469 nord_rare diseases +MONDO:0019469 ordo_disorder diseases +MONDO:0019469 orphanet_rare diseases +MONDO:0019469 otar diseases +MONDO:0019469 rare diseases +MONDO:0019470 gard_rare diseases +MONDO:0019470 nord_rare diseases +MONDO:0019470 ordo_disorder diseases +MONDO:0019470 orphanet_rare diseases +MONDO:0019470 otar diseases +MONDO:0019470 rare diseases +MONDO:0019471 gard_rare diseases +MONDO:0019471 nord_rare diseases +MONDO:0019471 ordo_disorder diseases +MONDO:0019471 orphanet_rare diseases +MONDO:0019471 otar diseases +MONDO:0019471 rare diseases +MONDO:0019472 gard_rare diseases +MONDO:0019472 nord_rare diseases +MONDO:0019472 ordo_disorder diseases +MONDO:0019472 orphanet_rare diseases +MONDO:0019472 otar diseases +MONDO:0019472 rare diseases +MONDO:0019473 gard_rare diseases +MONDO:0019473 nord_rare diseases +MONDO:0019473 ordo_disorder diseases +MONDO:0019473 orphanet_rare diseases +MONDO:0019473 otar diseases +MONDO:0019473 rare diseases +MONDO:0019474 gard_rare diseases +MONDO:0019474 nord_rare diseases +MONDO:0019474 ordo_disorder diseases +MONDO:0019474 orphanet_rare diseases +MONDO:0019474 otar diseases +MONDO:0019474 rare diseases +MONDO:0019475 gard_rare diseases +MONDO:0019475 nord_rare diseases +MONDO:0019475 ordo_disorder diseases +MONDO:0019475 orphanet_rare diseases +MONDO:0019475 otar diseases +MONDO:0019475 rare diseases +MONDO:0019476 gard_rare diseases +MONDO:0019476 nord_rare diseases +MONDO:0019476 ordo_disorder diseases +MONDO:0019476 orphanet_rare diseases +MONDO:0019476 rare diseases +MONDO:0019478 gard_rare diseases +MONDO:0019478 rare diseases +MONDO:0019479 gard_rare diseases +MONDO:0019479 nord_rare diseases +MONDO:0019479 ordo_disorder diseases +MONDO:0019479 orphanet_rare diseases +MONDO:0019479 otar diseases +MONDO:0019479 rare diseases +MONDO:0019480 gard_rare diseases +MONDO:0019480 nord_rare diseases +MONDO:0019480 ordo_disorder diseases +MONDO:0019480 orphanet_rare diseases +MONDO:0019480 otar diseases +MONDO:0019480 rare diseases +MONDO:0019483 gard_rare diseases +MONDO:0019483 nord_rare diseases +MONDO:0019483 ordo_disorder diseases +MONDO:0019483 orphanet_rare diseases +MONDO:0019483 rare diseases +MONDO:0019484 gard_rare diseases +MONDO:0019484 nord_rare diseases +MONDO:0019484 ordo_disorder diseases +MONDO:0019484 orphanet_rare diseases +MONDO:0019484 rare diseases +MONDO:0019485 gard_rare diseases +MONDO:0019485 nord_rare diseases +MONDO:0019485 ordo_disorder diseases +MONDO:0019485 orphanet_rare diseases +MONDO:0019485 rare diseases +MONDO:0019487 gard_rare diseases +MONDO:0019487 nord_rare diseases +MONDO:0019487 ordo_disorder diseases +MONDO:0019487 orphanet_rare diseases +MONDO:0019487 otar diseases +MONDO:0019487 rare diseases +MONDO:0019488 gard_rare diseases +MONDO:0019488 nord_rare diseases +MONDO:0019488 ordo_disorder diseases +MONDO:0019488 ordo_malformation_syndrome diseases +MONDO:0019488 orphanet_rare diseases +MONDO:0019488 rare diseases +MONDO:0019489 gard_rare diseases +MONDO:0019489 nord_rare diseases +MONDO:0019489 ordo_disorder diseases +MONDO:0019489 orphanet_rare diseases +MONDO:0019489 rare diseases +MONDO:0019490 gard_rare diseases +MONDO:0019490 nord_rare diseases +MONDO:0019490 ordo_disorder diseases +MONDO:0019490 orphanet_rare diseases +MONDO:0019490 otar diseases +MONDO:0019490 rare diseases +MONDO:0019493 gard_rare diseases +MONDO:0019493 ordo_disorder diseases +MONDO:0019493 orphanet_rare diseases +MONDO:0019493 rare diseases +MONDO:0019494 gard_rare diseases +MONDO:0019494 ordo_disorder diseases +MONDO:0019494 orphanet_rare diseases +MONDO:0019494 rare diseases +MONDO:0019496 disease_grouping diseases +MONDO:0019496 gard_rare diseases +MONDO:0019496 ordo_group_of_disorders diseases +MONDO:0019496 otar diseases +MONDO:0019496 rare diseases +MONDO:0019497 clingen diseases +MONDO:0019497 disease_grouping diseases +MONDO:0019497 gard_rare diseases +MONDO:0019497 nord_rare diseases +MONDO:0019497 ordo_disorder diseases +MONDO:0019497 orphanet_rare diseases +MONDO:0019497 otar diseases +MONDO:0019497 rare diseases +MONDO:0019498 gard_rare diseases +MONDO:0019498 nord_rare diseases +MONDO:0019498 ordo_disorder diseases +MONDO:0019498 orphanet_rare diseases +MONDO:0019498 otar diseases +MONDO:0019498 rare diseases +MONDO:0019499 gard_rare diseases +MONDO:0019499 nord_rare diseases +MONDO:0019499 ordo_disorder diseases +MONDO:0019499 ordo_malformation_syndrome diseases +MONDO:0019499 orphanet_rare diseases +MONDO:0019499 otar diseases +MONDO:0019499 rare diseases +MONDO:0019500 gard_rare diseases +MONDO:0019500 nord_rare diseases +MONDO:0019500 ordo_disorder diseases +MONDO:0019500 orphanet_rare diseases +MONDO:0019500 otar diseases +MONDO:0019500 rare diseases +MONDO:0019501 gard_rare diseases +MONDO:0019501 nord_rare diseases +MONDO:0019501 ordo_disorder diseases +MONDO:0019501 orphanet_rare diseases +MONDO:0019501 otar diseases +MONDO:0019501 rare diseases +MONDO:0019502 gard_rare diseases +MONDO:0019502 nord_rare diseases +MONDO:0019502 ordo_subtype_of_a_disorder diseases +MONDO:0019502 otar diseases +MONDO:0019502 rare diseases +MONDO:0019503 disease_grouping diseases +MONDO:0019503 gard_rare diseases +MONDO:0019503 ordo_group_of_disorders diseases +MONDO:0019503 otar diseases +MONDO:0019503 rare diseases +MONDO:0019504 gard_rare diseases +MONDO:0019504 nord_rare diseases +MONDO:0019504 ordo_disorder diseases +MONDO:0019504 orphanet_rare diseases +MONDO:0019504 rare diseases +MONDO:0019506 gard_rare diseases +MONDO:0019506 ordo_disorder diseases +MONDO:0019506 orphanet_rare diseases +MONDO:0019506 otar diseases +MONDO:0019506 rare diseases +MONDO:0019507 clingen diseases +MONDO:0019507 gard_rare diseases +MONDO:0019507 nord_rare diseases +MONDO:0019507 ordo_disorder diseases +MONDO:0019507 orphanet_rare diseases +MONDO:0019507 otar diseases +MONDO:0019507 rare diseases +MONDO:0019508 gard_rare diseases +MONDO:0019508 nord_rare diseases +MONDO:0019508 ordo_disorder diseases +MONDO:0019508 ordo_malformation_syndrome diseases +MONDO:0019508 orphanet_rare diseases +MONDO:0019508 otar diseases +MONDO:0019508 rare diseases +MONDO:0019509 gard_rare diseases +MONDO:0019509 nord_rare diseases +MONDO:0019509 ordo_disorder diseases +MONDO:0019509 orphanet_rare diseases +MONDO:0019509 rare diseases +MONDO:0019512 disease_grouping diseases +MONDO:0019512 ordo_group_of_disorders diseases +MONDO:0019512 otar diseases +MONDO:0019514 gard_rare diseases +MONDO:0019514 nord_rare diseases +MONDO:0019514 ordo_disorder diseases +MONDO:0019514 orphanet_rare diseases +MONDO:0019514 otar diseases +MONDO:0019514 rare diseases +MONDO:0019516 gard_rare diseases +MONDO:0019516 nord_rare diseases +MONDO:0019516 ordo_disorder diseases +MONDO:0019516 orphanet_rare diseases +MONDO:0019516 otar diseases +MONDO:0019516 rare diseases +MONDO:0019517 clingen diseases +MONDO:0019517 gard_rare diseases +MONDO:0019517 nord_rare diseases +MONDO:0019517 ordo_subtype_of_a_disorder diseases +MONDO:0019517 otar diseases +MONDO:0019517 rare diseases +MONDO:0019518 gard_rare diseases +MONDO:0019518 nord_rare diseases +MONDO:0019518 ordo_disorder diseases +MONDO:0019518 orphanet_rare diseases +MONDO:0019518 otar diseases +MONDO:0019518 rare diseases +MONDO:0019521 gard_rare diseases +MONDO:0019521 nord_rare diseases +MONDO:0019521 rare diseases +MONDO:0019522 gard_rare diseases +MONDO:0019522 nord_rare diseases +MONDO:0019522 ordo_disorder diseases +MONDO:0019522 orphanet_rare diseases +MONDO:0019522 otar diseases +MONDO:0019522 rare diseases +MONDO:0019524 gard_rare diseases +MONDO:0019524 nord_rare diseases +MONDO:0019524 ordo_subtype_of_a_disorder diseases +MONDO:0019524 otar diseases +MONDO:0019524 rare diseases +MONDO:0019525 gard_rare diseases +MONDO:0019525 nord_rare diseases +MONDO:0019525 ordo_disorder diseases +MONDO:0019525 ordo_malformation_syndrome diseases +MONDO:0019525 orphanet_rare diseases +MONDO:0019525 otar diseases +MONDO:0019525 rare diseases +MONDO:0019526 gard_rare diseases +MONDO:0019526 nord_rare diseases +MONDO:0019526 ordo_disorder diseases +MONDO:0019526 orphanet_rare diseases +MONDO:0019526 rare diseases +MONDO:0019527 gard_rare diseases +MONDO:0019527 nord_rare diseases +MONDO:0019527 ordo_disorder diseases +MONDO:0019527 orphanet_rare diseases +MONDO:0019527 rare diseases +MONDO:0019528 gard_rare diseases +MONDO:0019528 nord_rare diseases +MONDO:0019528 ordo_disorder diseases +MONDO:0019528 orphanet_rare diseases +MONDO:0019528 rare diseases +MONDO:0019529 gard_rare diseases +MONDO:0019529 nord_rare diseases +MONDO:0019529 ordo_disorder diseases +MONDO:0019529 orphanet_rare diseases +MONDO:0019529 rare diseases +MONDO:0019530 disease_grouping diseases +MONDO:0019530 ordo_group_of_disorders diseases +MONDO:0019530 otar diseases +MONDO:0019531 gard_rare diseases +MONDO:0019531 nord_rare diseases +MONDO:0019531 ordo_disorder diseases +MONDO:0019531 orphanet_rare diseases +MONDO:0019531 otar diseases +MONDO:0019531 rare diseases +MONDO:0019532 gard_rare diseases +MONDO:0019532 nord_rare diseases +MONDO:0019532 ordo_disorder diseases +MONDO:0019532 orphanet_rare diseases +MONDO:0019532 rare diseases +MONDO:0019533 gard_rare diseases +MONDO:0019533 nord_rare diseases +MONDO:0019533 ordo_disorder diseases +MONDO:0019533 orphanet_rare diseases +MONDO:0019533 rare diseases +MONDO:0019534 gard_rare diseases +MONDO:0019534 nord_rare diseases +MONDO:0019534 ordo_disorder diseases +MONDO:0019534 orphanet_rare diseases +MONDO:0019534 rare diseases +MONDO:0019535 gard_rare diseases +MONDO:0019535 nord_rare diseases +MONDO:0019535 ordo_disorder diseases +MONDO:0019535 orphanet_rare diseases +MONDO:0019535 rare diseases +MONDO:0019536 gard_rare diseases +MONDO:0019536 nord_rare diseases +MONDO:0019536 ordo_subtype_of_a_disorder diseases +MONDO:0019536 rare diseases +MONDO:0019537 gard_rare diseases +MONDO:0019537 nord_rare diseases +MONDO:0019537 ordo_disorder diseases +MONDO:0019537 orphanet_rare diseases +MONDO:0019537 otar diseases +MONDO:0019537 rare diseases +MONDO:0019538 gard_rare diseases +MONDO:0019538 nord_rare diseases +MONDO:0019538 ordo_disorder diseases +MONDO:0019538 orphanet_rare diseases +MONDO:0019538 rare diseases +MONDO:0019540 gard_rare diseases +MONDO:0019540 nord_rare diseases +MONDO:0019540 ordo_clinical_situation diseases +MONDO:0019540 ordo_disorder diseases +MONDO:0019540 orphanet_rare diseases +MONDO:0019540 rare diseases +MONDO:0019542 gard_rare diseases +MONDO:0019542 nord_rare diseases +MONDO:0019542 ordo_clinical_situation diseases +MONDO:0019542 ordo_disorder diseases +MONDO:0019542 orphanet_rare diseases +MONDO:0019542 rare diseases +MONDO:0019543 gard_rare diseases +MONDO:0019543 nord_rare diseases +MONDO:0019543 ordo_clinical_situation diseases +MONDO:0019543 ordo_disorder diseases +MONDO:0019543 orphanet_rare diseases +MONDO:0019543 rare diseases +MONDO:0019544 nord_rare diseases +MONDO:0019544 ordo_disorder diseases +MONDO:0019544 orphanet_rare diseases +MONDO:0019544 rare diseases +MONDO:0019545 nord_rare diseases +MONDO:0019545 ordo_disorder diseases +MONDO:0019545 orphanet_rare diseases +MONDO:0019545 rare diseases +MONDO:0019547 gard_rare diseases +MONDO:0019547 nord_rare diseases +MONDO:0019547 ordo_disorder diseases +MONDO:0019547 orphanet_rare diseases +MONDO:0019547 rare diseases +MONDO:0019548 disease_grouping diseases +MONDO:0019548 gard_rare diseases +MONDO:0019548 nord_rare diseases +MONDO:0019548 ordo_group_of_disorders diseases +MONDO:0019548 otar diseases +MONDO:0019548 rare diseases +MONDO:0019549 gard_rare diseases +MONDO:0019549 nord_rare diseases +MONDO:0019549 ordo_disorder diseases +MONDO:0019549 orphanet_rare diseases +MONDO:0019549 otar diseases +MONDO:0019549 rare diseases +MONDO:0019550 gard_rare diseases +MONDO:0019550 nord_rare diseases +MONDO:0019550 ordo_disorder diseases +MONDO:0019550 orphanet_rare diseases +MONDO:0019550 rare diseases +MONDO:0019551 gard_rare diseases +MONDO:0019551 nord_rare diseases +MONDO:0019551 ordo_disorder diseases +MONDO:0019551 orphanet_rare diseases +MONDO:0019551 otar diseases +MONDO:0019551 rare diseases +MONDO:0019552 gard_rare diseases +MONDO:0019552 nord_rare diseases +MONDO:0019552 ordo_disorder diseases +MONDO:0019552 orphanet_rare diseases +MONDO:0019552 rare diseases +MONDO:0019553 gard_rare diseases +MONDO:0019553 nord_rare diseases +MONDO:0019553 ordo_disorder diseases +MONDO:0019553 orphanet_rare diseases +MONDO:0019553 rare diseases +MONDO:0019554 gard_rare diseases +MONDO:0019554 nord_rare diseases +MONDO:0019554 ordo_disorder diseases +MONDO:0019554 orphanet_rare diseases +MONDO:0019554 rare diseases +MONDO:0019555 gard_rare diseases +MONDO:0019555 nord_rare diseases +MONDO:0019555 ordo_disorder diseases +MONDO:0019555 orphanet_rare diseases +MONDO:0019555 rare diseases +MONDO:0019556 gard_rare diseases +MONDO:0019556 nord_rare diseases +MONDO:0019556 ordo_disorder diseases +MONDO:0019556 orphanet_rare diseases +MONDO:0019556 rare diseases +MONDO:0019557 gard_rare diseases +MONDO:0019557 nord_rare diseases +MONDO:0019557 ordo_disorder diseases +MONDO:0019557 orphanet_rare diseases +MONDO:0019557 otar diseases +MONDO:0019557 rare diseases +MONDO:0019558 gard_rare diseases +MONDO:0019558 nord_rare diseases +MONDO:0019558 ordo_disorder diseases +MONDO:0019558 orphanet_rare diseases +MONDO:0019558 otar diseases +MONDO:0019558 rare diseases +MONDO:0019559 gard_rare diseases +MONDO:0019559 nord_rare diseases +MONDO:0019559 ordo_disorder diseases +MONDO:0019559 orphanet_rare diseases +MONDO:0019559 rare diseases +MONDO:0019560 gard_rare diseases +MONDO:0019560 nord_rare diseases +MONDO:0019560 ordo_disorder diseases +MONDO:0019560 orphanet_rare diseases +MONDO:0019560 rare diseases +MONDO:0019561 gard_rare diseases +MONDO:0019561 nord_rare diseases +MONDO:0019561 ordo_disorder diseases +MONDO:0019561 orphanet_rare diseases +MONDO:0019561 rare diseases +MONDO:0019562 gard_rare diseases +MONDO:0019562 ordo_disorder diseases +MONDO:0019562 orphanet_rare diseases +MONDO:0019562 otar diseases +MONDO:0019562 rare diseases +MONDO:0019563 gard_rare diseases +MONDO:0019563 rare diseases +MONDO:0019565 clingen diseases +MONDO:0019565 gard_rare diseases +MONDO:0019565 nord_rare diseases +MONDO:0019565 ordo_disorder diseases +MONDO:0019565 orphanet_rare diseases +MONDO:0019565 otar diseases +MONDO:0019565 rare diseases +MONDO:0019567 clingen diseases +MONDO:0019567 gard_rare diseases +MONDO:0019567 nord_rare diseases +MONDO:0019567 ordo_etiological_subtype diseases +MONDO:0019567 otar diseases +MONDO:0019567 rare diseases +MONDO:0019568 gard_rare diseases +MONDO:0019568 nord_rare diseases +MONDO:0019568 ordo_etiological_subtype diseases +MONDO:0019568 otar diseases +MONDO:0019568 rare diseases +MONDO:0019569 clingen diseases +MONDO:0019569 gard_rare diseases +MONDO:0019569 nord_rare diseases +MONDO:0019569 ordo_subtype_of_a_disorder diseases +MONDO:0019569 otar diseases +MONDO:0019569 rare diseases +MONDO:0019570 gard_rare diseases +MONDO:0019570 nord_rare diseases +MONDO:0019570 ordo_subtype_of_a_disorder diseases +MONDO:0019570 otar diseases +MONDO:0019570 rare diseases +MONDO:0019571 gard_rare diseases +MONDO:0019571 nord_rare diseases +MONDO:0019571 ordo_disorder diseases +MONDO:0019571 orphanet_rare diseases +MONDO:0019571 otar diseases +MONDO:0019571 rare diseases +MONDO:0019572 gard_rare diseases +MONDO:0019572 nord_rare diseases +MONDO:0019572 ordo_disorder diseases +MONDO:0019572 orphanet_rare diseases +MONDO:0019572 otar diseases +MONDO:0019572 rare diseases +MONDO:0019573 disease_grouping diseases +MONDO:0019573 gard_rare diseases +MONDO:0019573 nord_rare diseases +MONDO:0019573 ordo_group_of_disorders diseases +MONDO:0019573 otar diseases +MONDO:0019573 rare diseases +MONDO:0019574 gard_rare diseases +MONDO:0019574 nord_rare diseases +MONDO:0019574 ordo_disorder diseases +MONDO:0019574 orphanet_rare diseases +MONDO:0019574 rare diseases +MONDO:0019575 gard_rare diseases +MONDO:0019575 nord_rare diseases +MONDO:0019575 ordo_disorder diseases +MONDO:0019575 orphanet_rare diseases +MONDO:0019575 otar diseases +MONDO:0019575 rare diseases +MONDO:0019576 gard_rare diseases +MONDO:0019576 nord_rare diseases +MONDO:0019576 ordo_subtype_of_a_disorder diseases +MONDO:0019576 rare diseases +MONDO:0019577 gard_rare diseases +MONDO:0019577 ordo_subtype_of_a_disorder diseases +MONDO:0019577 rare diseases +MONDO:0019578 gard_rare diseases +MONDO:0019578 nord_rare diseases +MONDO:0019578 ordo_disorder diseases +MONDO:0019578 orphanet_rare diseases +MONDO:0019578 rare diseases +MONDO:0019579 gard_rare diseases +MONDO:0019579 nord_rare diseases +MONDO:0019579 ordo_disorder diseases +MONDO:0019579 orphanet_rare diseases +MONDO:0019579 rare diseases +MONDO:0019580 gard_rare diseases +MONDO:0019580 nord_rare diseases +MONDO:0019580 ordo_disorder diseases +MONDO:0019580 orphanet_rare diseases +MONDO:0019580 rare diseases +MONDO:0019581 gard_rare diseases +MONDO:0019581 nord_rare diseases +MONDO:0019581 ordo_disorder diseases +MONDO:0019581 orphanet_rare diseases +MONDO:0019581 rare diseases +MONDO:0019582 gard_rare diseases +MONDO:0019582 nord_rare diseases +MONDO:0019582 ordo_disorder diseases +MONDO:0019582 orphanet_rare diseases +MONDO:0019582 rare diseases +MONDO:0019583 gard_rare diseases +MONDO:0019583 nord_rare diseases +MONDO:0019583 ordo_subtype_of_a_disorder diseases +MONDO:0019583 rare diseases +MONDO:0019584 gard_rare diseases +MONDO:0019584 ordo_subtype_of_a_disorder diseases +MONDO:0019584 rare diseases +MONDO:0019585 gard_rare diseases +MONDO:0019585 nord_rare diseases +MONDO:0019585 ordo_subtype_of_a_disorder diseases +MONDO:0019585 rare diseases +MONDO:0019586 gard_rare diseases +MONDO:0019586 nord_rare diseases +MONDO:0019586 ordo_subtype_of_a_disorder diseases +MONDO:0019586 otar diseases +MONDO:0019586 rare diseases +MONDO:0019587 clingen diseases +MONDO:0019587 gard_rare diseases +MONDO:0019587 nord_rare diseases +MONDO:0019587 ordo_etiological_subtype diseases +MONDO:0019587 ordo_subtype_of_a_disorder diseases +MONDO:0019587 otar diseases +MONDO:0019587 rare diseases +MONDO:0019588 clingen diseases +MONDO:0019588 gard_rare diseases +MONDO:0019588 nord_rare diseases +MONDO:0019588 ordo_etiological_subtype diseases +MONDO:0019588 ordo_subtype_of_a_disorder diseases +MONDO:0019588 otar diseases +MONDO:0019588 prototype_pattern diseases +MONDO:0019588 rare diseases +MONDO:0019591 gard_rare diseases +MONDO:0019591 nord_rare diseases +MONDO:0019591 ordo_disorder diseases +MONDO:0019591 orphanet_rare diseases +MONDO:0019591 otar diseases +MONDO:0019591 rare diseases +MONDO:0019600 gard_rare diseases +MONDO:0019600 nord_rare diseases +MONDO:0019600 ordo_disorder diseases +MONDO:0019600 orphanet_rare diseases +MONDO:0019600 otar diseases +MONDO:0019600 rare diseases +MONDO:0019603 gard_rare diseases +MONDO:0019603 ordo_malformation_syndrome diseases +MONDO:0019603 rare diseases +MONDO:0019604 gard_rare diseases +MONDO:0019604 ordo_disorder diseases +MONDO:0019604 orphanet_rare diseases +MONDO:0019604 rare diseases +MONDO:0019605 disease_grouping diseases +MONDO:0019605 gard_rare diseases +MONDO:0019605 nord_rare diseases +MONDO:0019605 ordo_group_of_disorders diseases +MONDO:0019605 rare diseases +MONDO:0019606 gard_rare diseases +MONDO:0019606 nord_rare diseases +MONDO:0019606 ordo_disorder diseases +MONDO:0019606 orphanet_rare diseases +MONDO:0019606 rare diseases +MONDO:0019607 gard_rare diseases +MONDO:0019607 nord_rare diseases +MONDO:0019607 ordo_disorder diseases +MONDO:0019607 orphanet_rare diseases +MONDO:0019607 otar diseases +MONDO:0019607 rare diseases +MONDO:0019609 gard_rare diseases +MONDO:0019609 nord_rare diseases +MONDO:0019609 ordo_disorder diseases +MONDO:0019609 orphanet_rare diseases +MONDO:0019609 otar diseases +MONDO:0019609 rare diseases +MONDO:0019610 gard_rare diseases +MONDO:0019610 nord_rare diseases +MONDO:0019610 ordo_disorder diseases +MONDO:0019610 orphanet_rare diseases +MONDO:0019610 otar diseases +MONDO:0019610 rare diseases +MONDO:0019611 gard_rare diseases +MONDO:0019611 nord_rare diseases +MONDO:0019611 ordo_disorder diseases +MONDO:0019611 orphanet_rare diseases +MONDO:0019611 otar diseases +MONDO:0019611 rare diseases +MONDO:0019612 gard_rare diseases +MONDO:0019612 nord_rare diseases +MONDO:0019612 ordo_disorder diseases +MONDO:0019612 orphanet_rare diseases +MONDO:0019612 rare diseases +MONDO:0019613 gard_rare diseases +MONDO:0019613 nord_rare diseases +MONDO:0019613 ordo_disorder diseases +MONDO:0019613 orphanet_rare diseases +MONDO:0019613 otar diseases +MONDO:0019613 rare diseases +MONDO:0019614 gard_rare diseases +MONDO:0019614 nord_rare diseases +MONDO:0019614 ordo_disorder diseases +MONDO:0019614 orphanet_rare diseases +MONDO:0019614 rare diseases +MONDO:0019615 gard_rare diseases +MONDO:0019615 nord_rare diseases +MONDO:0019615 ordo_disorder diseases +MONDO:0019615 orphanet_rare diseases +MONDO:0019615 rare diseases +MONDO:0019617 gard_rare diseases +MONDO:0019617 nord_rare diseases +MONDO:0019617 ordo_disorder diseases +MONDO:0019617 orphanet_rare diseases +MONDO:0019617 rare diseases +MONDO:0019618 gard_rare diseases +MONDO:0019618 nord_rare diseases +MONDO:0019618 ordo_disorder diseases +MONDO:0019618 ordo_malformation_syndrome diseases +MONDO:0019618 orphanet_rare diseases +MONDO:0019618 rare diseases +MONDO:0019620 gard_rare diseases +MONDO:0019620 nord_rare diseases +MONDO:0019620 ordo_disorder diseases +MONDO:0019620 ordo_morphological_anomaly diseases +MONDO:0019620 orphanet_rare diseases +MONDO:0019620 rare diseases +MONDO:0019621 gard_rare diseases +MONDO:0019621 nord_rare diseases +MONDO:0019621 ordo_disorder diseases +MONDO:0019621 orphanet_rare diseases +MONDO:0019621 rare diseases +MONDO:0019622 gard_rare diseases +MONDO:0019622 nord_rare diseases +MONDO:0019622 ordo_disorder diseases +MONDO:0019622 orphanet_rare diseases +MONDO:0019622 rare diseases +MONDO:0019623 gard_rare diseases +MONDO:0019623 ordo_group_of_disorders diseases +MONDO:0019623 otar diseases +MONDO:0019623 rare diseases +MONDO:0019624 gard_rare diseases +MONDO:0019624 nord_rare diseases +MONDO:0019624 ordo_group_of_disorders diseases +MONDO:0019624 otar diseases +MONDO:0019624 rare diseases +MONDO:0019625 clingen diseases +MONDO:0019625 gard_rare diseases +MONDO:0019625 nord_rare diseases +MONDO:0019625 ordo_disorder diseases +MONDO:0019625 orphanet_rare diseases +MONDO:0019625 otar diseases +MONDO:0019625 prototype_pattern diseases +MONDO:0019625 rare diseases +MONDO:0019626 gard_rare diseases +MONDO:0019626 nord_rare diseases +MONDO:0019626 ordo_disorder diseases +MONDO:0019626 ordo_morphological_anomaly diseases +MONDO:0019626 orphanet_rare diseases +MONDO:0019626 rare diseases +MONDO:0019627 gard_rare diseases +MONDO:0019627 nord_rare diseases +MONDO:0019627 ordo_disorder diseases +MONDO:0019627 orphanet_rare diseases +MONDO:0019627 otar diseases +MONDO:0019627 rare diseases +MONDO:0019628 gard_rare diseases +MONDO:0019628 nord_rare diseases +MONDO:0019628 ordo_disorder diseases +MONDO:0019628 ordo_morphological_anomaly diseases +MONDO:0019628 orphanet_rare diseases +MONDO:0019628 otar diseases +MONDO:0019628 rare diseases +MONDO:0019629 gard_rare diseases +MONDO:0019629 nord_rare diseases +MONDO:0019629 ordo_disorder diseases +MONDO:0019629 ordo_morphological_anomaly diseases +MONDO:0019629 orphanet_rare diseases +MONDO:0019629 otar diseases +MONDO:0019629 rare diseases +MONDO:0019630 gard_rare diseases +MONDO:0019630 nord_rare diseases +MONDO:0019630 ordo_disorder diseases +MONDO:0019630 ordo_malformation_syndrome diseases +MONDO:0019630 orphanet_rare diseases +MONDO:0019630 rare diseases +MONDO:0019631 gard_rare diseases +MONDO:0019631 nord_rare diseases +MONDO:0019631 ordo_disorder diseases +MONDO:0019631 orphanet_rare diseases +MONDO:0019631 otar diseases +MONDO:0019631 rare diseases +MONDO:0019632 ordo_disorder diseases +MONDO:0019632 orphanet_rare diseases +MONDO:0019632 otar diseases +MONDO:0019632 rare diseases +MONDO:0019633 gard_rare diseases +MONDO:0019633 nord_rare diseases +MONDO:0019633 ordo_disorder diseases +MONDO:0019633 orphanet_rare diseases +MONDO:0019633 rare diseases +MONDO:0019634 gard_rare diseases +MONDO:0019634 nord_rare diseases +MONDO:0019634 ordo_disorder diseases +MONDO:0019634 orphanet_rare diseases +MONDO:0019634 rare diseases +MONDO:0019635 gard_rare diseases +MONDO:0019635 nord_rare diseases +MONDO:0019635 ordo_disorder diseases +MONDO:0019635 orphanet_rare diseases +MONDO:0019635 rare diseases +MONDO:0019636 gard_rare diseases +MONDO:0019636 nord_rare diseases +MONDO:0019636 ordo_subtype_of_a_disorder diseases +MONDO:0019636 otar diseases +MONDO:0019636 rare diseases +MONDO:0019637 gard_rare diseases +MONDO:0019637 nord_rare diseases +MONDO:0019637 ordo_disorder diseases +MONDO:0019637 ordo_morphological_anomaly diseases +MONDO:0019637 orphanet_rare diseases +MONDO:0019637 otar diseases +MONDO:0019637 rare diseases +MONDO:0019638 gard_rare diseases +MONDO:0019638 nord_rare diseases +MONDO:0019638 ordo_disorder diseases +MONDO:0019638 ordo_morphological_anomaly diseases +MONDO:0019638 orphanet_rare diseases +MONDO:0019638 otar diseases +MONDO:0019638 rare diseases +MONDO:0019639 gard_rare diseases +MONDO:0019639 nord_rare diseases +MONDO:0019639 ordo_disorder diseases +MONDO:0019639 ordo_morphological_anomaly diseases +MONDO:0019639 orphanet_rare diseases +MONDO:0019639 rare diseases +MONDO:0019640 gard_rare diseases +MONDO:0019640 nord_rare diseases +MONDO:0019640 ordo_disorder diseases +MONDO:0019640 ordo_morphological_anomaly diseases +MONDO:0019640 orphanet_rare diseases +MONDO:0019640 otar diseases +MONDO:0019640 rare diseases +MONDO:0019641 gard_rare diseases +MONDO:0019641 nord_rare diseases +MONDO:0019641 ordo_disorder diseases +MONDO:0019641 orphanet_rare diseases +MONDO:0019641 rare diseases +MONDO:0019642 gard_rare diseases +MONDO:0019642 ordo_disorder diseases +MONDO:0019642 orphanet_rare diseases +MONDO:0019642 otar diseases +MONDO:0019642 rare diseases +MONDO:0019643 gard_rare diseases +MONDO:0019643 nord_rare diseases +MONDO:0019643 ordo_disorder diseases +MONDO:0019643 ordo_malformation_syndrome diseases +MONDO:0019643 orphanet_rare diseases +MONDO:0019643 rare diseases +MONDO:0019644 gard_rare diseases +MONDO:0019644 nord_rare diseases +MONDO:0019644 ordo_subtype_of_a_disorder diseases +MONDO:0019644 otar diseases +MONDO:0019644 rare diseases +MONDO:0019645 gard_rare diseases +MONDO:0019645 nord_rare diseases +MONDO:0019645 ordo_subtype_of_a_disorder diseases +MONDO:0019645 otar diseases +MONDO:0019645 rare diseases +MONDO:0019646 gard_rare diseases +MONDO:0019646 nord_rare diseases +MONDO:0019646 ordo_subtype_of_a_disorder diseases +MONDO:0019646 rare diseases +MONDO:0019647 gard_rare diseases +MONDO:0019647 nord_rare diseases +MONDO:0019647 ordo_subtype_of_a_disorder diseases +MONDO:0019647 rare diseases +MONDO:0019648 gard_rare diseases +MONDO:0019648 nord_rare diseases +MONDO:0019648 ordo_disorder diseases +MONDO:0019648 orphanet_rare diseases +MONDO:0019648 otar diseases +MONDO:0019648 rare diseases +MONDO:0019649 gard_rare diseases +MONDO:0019649 ordo_histopathological_subtype diseases +MONDO:0019649 rare diseases +MONDO:0019650 gard_rare diseases +MONDO:0019650 ordo_histopathological_subtype diseases +MONDO:0019650 rare diseases +MONDO:0019651 gard_rare diseases +MONDO:0019651 ordo_histopathological_subtype diseases +MONDO:0019651 rare diseases +MONDO:0019652 gard_rare diseases +MONDO:0019652 ordo_histopathological_subtype diseases +MONDO:0019652 rare diseases +MONDO:0019653 gard_rare diseases +MONDO:0019653 ordo_histopathological_subtype diseases +MONDO:0019653 rare diseases +MONDO:0019654 gard_rare diseases +MONDO:0019654 ordo_histopathological_subtype diseases +MONDO:0019654 rare diseases +MONDO:0019655 gard_rare diseases +MONDO:0019655 ordo_histopathological_subtype diseases +MONDO:0019655 rare diseases +MONDO:0019656 gard_rare diseases +MONDO:0019656 ordo_histopathological_subtype diseases +MONDO:0019656 rare diseases +MONDO:0019659 clingen diseases +MONDO:0019659 gard_rare diseases +MONDO:0019659 nord_rare diseases +MONDO:0019659 ordo_subtype_of_a_disorder diseases +MONDO:0019659 otar diseases +MONDO:0019659 rare diseases +MONDO:0019660 gard_rare diseases +MONDO:0019660 nord_rare diseases +MONDO:0019660 ordo_subtype_of_a_disorder diseases +MONDO:0019660 otar diseases +MONDO:0019660 rare diseases +MONDO:0019661 gard_rare diseases +MONDO:0019661 nord_rare diseases +MONDO:0019661 ordo_subtype_of_a_disorder diseases +MONDO:0019661 otar diseases +MONDO:0019661 rare diseases +MONDO:0019662 gard_rare diseases +MONDO:0019662 nord_rare diseases +MONDO:0019662 ordo_disorder diseases +MONDO:0019662 ordo_malformation_syndrome diseases +MONDO:0019662 orphanet_rare diseases +MONDO:0019662 otar diseases +MONDO:0019662 rare diseases +MONDO:0019665 gard_rare diseases +MONDO:0019665 nord_rare diseases +MONDO:0019665 ordo_subtype_of_a_disorder diseases +MONDO:0019665 otar diseases +MONDO:0019665 rare diseases +MONDO:0019666 gard_rare diseases +MONDO:0019666 nord_rare diseases +MONDO:0019666 ordo_disorder diseases +MONDO:0019666 orphanet_rare diseases +MONDO:0019666 otar diseases +MONDO:0019666 rare diseases +MONDO:0019667 gard_rare diseases +MONDO:0019667 nord_rare diseases +MONDO:0019667 ordo_disorder diseases +MONDO:0019667 orphanet_rare diseases +MONDO:0019667 otar diseases +MONDO:0019667 rare diseases +MONDO:0019668 gard_rare diseases +MONDO:0019668 nord_rare diseases +MONDO:0019668 ordo_disorder diseases +MONDO:0019668 orphanet_rare diseases +MONDO:0019668 rare diseases +MONDO:0019669 gard_rare diseases +MONDO:0019669 nord_rare diseases +MONDO:0019669 ordo_subtype_of_a_disorder diseases +MONDO:0019669 otar diseases +MONDO:0019669 rare diseases +MONDO:0019670 gard_rare diseases +MONDO:0019670 nord_rare diseases +MONDO:0019670 ordo_disorder diseases +MONDO:0019670 ordo_morphological_anomaly diseases +MONDO:0019670 orphanet_rare diseases +MONDO:0019670 otar diseases +MONDO:0019670 rare diseases +MONDO:0019671 gard_rare diseases +MONDO:0019671 nord_rare diseases +MONDO:0019671 ordo_disorder diseases +MONDO:0019671 ordo_morphological_anomaly diseases +MONDO:0019671 orphanet_rare diseases +MONDO:0019671 otar diseases +MONDO:0019671 rare diseases +MONDO:0019672 gard_rare diseases +MONDO:0019672 nord_rare diseases +MONDO:0019672 ordo_disorder diseases +MONDO:0019672 ordo_morphological_anomaly diseases +MONDO:0019672 orphanet_rare diseases +MONDO:0019672 otar diseases +MONDO:0019672 rare diseases +MONDO:0019673 gard_rare diseases +MONDO:0019673 nord_rare diseases +MONDO:0019673 ordo_disorder diseases +MONDO:0019673 ordo_morphological_anomaly diseases +MONDO:0019673 orphanet_rare diseases +MONDO:0019673 otar diseases +MONDO:0019673 rare diseases +MONDO:0019674 gard_rare diseases +MONDO:0019674 nord_rare diseases +MONDO:0019674 ordo_disorder diseases +MONDO:0019674 ordo_morphological_anomaly diseases +MONDO:0019674 orphanet_rare diseases +MONDO:0019674 otar diseases +MONDO:0019674 rare diseases +MONDO:0019675 gard_rare diseases +MONDO:0019675 nord_rare diseases +MONDO:0019675 otar diseases +MONDO:0019675 rare diseases +MONDO:0019676 gard_rare diseases +MONDO:0019676 nord_rare diseases +MONDO:0019676 ordo_disorder diseases +MONDO:0019676 ordo_malformation_syndrome diseases +MONDO:0019676 orphanet_rare diseases +MONDO:0019676 otar diseases +MONDO:0019676 rare diseases +MONDO:0019677 gard_rare diseases +MONDO:0019677 nord_rare diseases +MONDO:0019677 ordo_disorder diseases +MONDO:0019677 ordo_malformation_syndrome diseases +MONDO:0019677 orphanet_rare diseases +MONDO:0019677 otar diseases +MONDO:0019677 rare diseases +MONDO:0019678 gard_rare diseases +MONDO:0019678 nord_rare diseases +MONDO:0019678 ordo_malformation_syndrome diseases +MONDO:0019678 rare diseases +MONDO:0019679 gard_rare diseases +MONDO:0019679 nord_rare diseases +MONDO:0019679 ordo_disorder diseases +MONDO:0019679 ordo_malformation_syndrome diseases +MONDO:0019679 orphanet_rare diseases +MONDO:0019679 otar diseases +MONDO:0019679 rare diseases +MONDO:0019680 gard_rare diseases +MONDO:0019680 nord_rare diseases +MONDO:0019680 ordo_disorder diseases +MONDO:0019680 orphanet_rare diseases +MONDO:0019680 rare diseases +MONDO:0019681 gard_rare diseases +MONDO:0019681 nord_rare diseases +MONDO:0019681 ordo_subtype_of_a_disorder diseases +MONDO:0019681 otar diseases +MONDO:0019681 rare diseases +MONDO:0019682 gard_rare diseases +MONDO:0019682 nord_rare diseases +MONDO:0019682 ordo_subtype_of_a_disorder diseases +MONDO:0019682 otar diseases +MONDO:0019682 rare diseases +MONDO:0019685 disease_grouping diseases +MONDO:0019685 gard_rare diseases +MONDO:0019685 nord_rare diseases +MONDO:0019685 ordo_group_of_disorders diseases +MONDO:0019685 otar diseases +MONDO:0019685 rare diseases +MONDO:0019690 disease_grouping diseases +MONDO:0019690 gard_rare diseases +MONDO:0019690 ordo_group_of_disorders diseases +MONDO:0019690 rare diseases +MONDO:0019691 disease_grouping diseases +MONDO:0019691 gard_rare diseases +MONDO:0019691 ordo_group_of_disorders diseases +MONDO:0019691 otar diseases +MONDO:0019691 rare diseases +MONDO:0019694 disease_grouping diseases +MONDO:0019694 gard_rare diseases +MONDO:0019694 ordo_group_of_disorders diseases +MONDO:0019694 otar diseases +MONDO:0019694 rare diseases +MONDO:0019695 disease_grouping diseases +MONDO:0019695 gard_rare diseases +MONDO:0019695 nord_rare diseases +MONDO:0019695 ordo_group_of_disorders diseases +MONDO:0019695 otar diseases +MONDO:0019695 rare diseases +MONDO:0019696 disease_grouping diseases +MONDO:0019696 gard_rare diseases +MONDO:0019696 nord_rare diseases +MONDO:0019696 ordo_group_of_disorders diseases +MONDO:0019696 otar diseases +MONDO:0019696 rare diseases +MONDO:0019698 disease_grouping diseases +MONDO:0019698 gard_rare diseases +MONDO:0019698 nord_rare diseases +MONDO:0019698 ordo_group_of_disorders diseases +MONDO:0019698 otar diseases +MONDO:0019698 rare diseases +MONDO:0019701 disease_grouping diseases +MONDO:0019701 gard_rare diseases +MONDO:0019701 nord_rare diseases +MONDO:0019701 ordo_group_of_disorders diseases +MONDO:0019701 otar diseases +MONDO:0019701 rare diseases +MONDO:0019702 disease_grouping diseases +MONDO:0019702 gard_rare diseases +MONDO:0019702 ordo_group_of_disorders diseases +MONDO:0019702 rare diseases +MONDO:0019707 disease_grouping diseases +MONDO:0019707 gard_rare diseases +MONDO:0019707 ordo_group_of_disorders diseases +MONDO:0019707 rare diseases +MONDO:0019713 disease_grouping diseases +MONDO:0019713 gard_rare diseases +MONDO:0019713 ordo_group_of_disorders diseases +MONDO:0019713 rare diseases +MONDO:0019716 disease_grouping diseases +MONDO:0019716 gard_rare diseases +MONDO:0019716 ordo_group_of_disorders diseases +MONDO:0019716 otar diseases +MONDO:0019716 rare diseases +MONDO:0019719 clingen diseases +MONDO:0019719 disease_grouping diseases +MONDO:0019719 gard_rare diseases +MONDO:0019719 ordo_group_of_disorders diseases +MONDO:0019719 otar diseases +MONDO:0019719 rare diseases +MONDO:0019722 disease_grouping diseases +MONDO:0019722 ordo_group_of_disorders diseases +MONDO:0019722 otar diseases +MONDO:0019725 gard_rare diseases +MONDO:0019725 nord_rare diseases +MONDO:0019725 ordo_disorder diseases +MONDO:0019725 orphanet_rare diseases +MONDO:0019725 rare diseases +MONDO:0019726 gard_rare diseases +MONDO:0019726 nord_rare diseases +MONDO:0019726 ordo_etiological_subtype diseases +MONDO:0019726 ordo_subtype_of_a_disorder diseases +MONDO:0019726 rare diseases +MONDO:0019727 gard_rare diseases +MONDO:0019727 nord_rare diseases +MONDO:0019727 ordo_etiological_subtype diseases +MONDO:0019727 ordo_subtype_of_a_disorder diseases +MONDO:0019727 rare diseases +MONDO:0019728 gard_rare diseases +MONDO:0019728 nord_rare diseases +MONDO:0019728 ordo_subtype_of_a_disorder diseases +MONDO:0019728 rare diseases +MONDO:0019729 gard_rare diseases +MONDO:0019729 nord_rare diseases +MONDO:0019729 ordo_subtype_of_a_disorder diseases +MONDO:0019729 rare diseases +MONDO:0019730 gard_rare diseases +MONDO:0019730 nord_rare diseases +MONDO:0019730 ordo_subtype_of_a_disorder diseases +MONDO:0019730 rare diseases +MONDO:0019731 gard_rare diseases +MONDO:0019731 nord_rare diseases +MONDO:0019731 ordo_subtype_of_a_disorder diseases +MONDO:0019731 otar diseases +MONDO:0019731 rare diseases +MONDO:0019732 gard_rare diseases +MONDO:0019732 nord_rare diseases +MONDO:0019732 ordo_subtype_of_a_disorder diseases +MONDO:0019732 otar diseases +MONDO:0019732 rare diseases +MONDO:0019733 gard_rare diseases +MONDO:0019733 nord_rare diseases +MONDO:0019733 ordo_subtype_of_a_disorder diseases +MONDO:0019733 otar diseases +MONDO:0019733 rare diseases +MONDO:0019734 gard_rare diseases +MONDO:0019734 nord_rare diseases +MONDO:0019734 ordo_disorder diseases +MONDO:0019734 orphanet_rare diseases +MONDO:0019734 otar diseases +MONDO:0019734 rare diseases +MONDO:0019735 gard_rare diseases +MONDO:0019735 nord_rare diseases +MONDO:0019735 ordo_disorder diseases +MONDO:0019735 orphanet_rare diseases +MONDO:0019735 otar diseases +MONDO:0019735 rare diseases +MONDO:0019736 gard_rare diseases +MONDO:0019736 nord_rare diseases +MONDO:0019736 ordo_histopathological_subtype diseases +MONDO:0019736 ordo_subtype_of_a_disorder diseases +MONDO:0019736 otar diseases +MONDO:0019736 rare diseases +MONDO:0019737 disease_grouping diseases +MONDO:0019737 gard_rare diseases +MONDO:0019737 nord_rare diseases +MONDO:0019737 ordo_group_of_disorders diseases +MONDO:0019737 otar diseases +MONDO:0019737 rare diseases +MONDO:0019738 gard_rare diseases +MONDO:0019738 ordo_etiological_subtype diseases +MONDO:0019738 otar diseases +MONDO:0019738 rare diseases +MONDO:0019739 gard_rare diseases +MONDO:0019739 nord_rare diseases +MONDO:0019739 ordo_etiological_subtype diseases +MONDO:0019739 ordo_subtype_of_a_disorder diseases +MONDO:0019739 otar diseases +MONDO:0019739 rare diseases +MONDO:0019740 gard_rare diseases +MONDO:0019740 nord_rare diseases +MONDO:0019740 ordo_subtype_of_a_disorder diseases +MONDO:0019740 otar diseases +MONDO:0019740 rare diseases +MONDO:0019741 disease_grouping diseases +MONDO:0019741 gard_rare diseases +MONDO:0019741 nord_rare diseases +MONDO:0019741 ordo_group_of_disorders diseases +MONDO:0019741 rare diseases +MONDO:0019742 gard_rare diseases +MONDO:0019742 nord_rare diseases +MONDO:0019742 ordo_subtype_of_a_disorder diseases +MONDO:0019742 otar diseases +MONDO:0019742 rare diseases +MONDO:0019745 gard_rare diseases +MONDO:0019745 nord_rare diseases +MONDO:0019745 ordo_etiological_subtype diseases +MONDO:0019745 ordo_subtype_of_a_disorder diseases +MONDO:0019745 otar diseases +MONDO:0019745 rare diseases +MONDO:0019746 gard_rare diseases +MONDO:0019746 nord_rare diseases +MONDO:0019746 ordo_etiological_subtype diseases +MONDO:0019746 ordo_subtype_of_a_disorder diseases +MONDO:0019746 otar diseases +MONDO:0019746 rare diseases +MONDO:0019751 disease_grouping diseases +MONDO:0019751 gard_rare diseases +MONDO:0019751 ordo_group_of_disorders diseases +MONDO:0019751 otar diseases +MONDO:0019751 rare diseases +MONDO:0019752 gard_rare diseases +MONDO:0019752 nord_rare diseases +MONDO:0019752 rare diseases +MONDO:0019753 gard_rare diseases +MONDO:0019753 nord_rare diseases +MONDO:0019753 ordo_subtype_of_a_disorder diseases +MONDO:0019753 rare diseases +MONDO:0019754 gard_rare diseases +MONDO:0019754 ordo_subtype_of_a_disorder diseases +MONDO:0019754 rare diseases +MONDO:0019755 disease_grouping diseases +MONDO:0019755 ordo_group_of_disorders diseases +MONDO:0019755 otar diseases +MONDO:0019756 gard_rare diseases +MONDO:0019756 nord_rare diseases +MONDO:0019756 ordo_subtype_of_a_disorder diseases +MONDO:0019756 otar diseases +MONDO:0019756 rare diseases +MONDO:0019757 gard_rare diseases +MONDO:0019757 nord_rare diseases +MONDO:0019757 ordo_subtype_of_a_disorder diseases +MONDO:0019757 otar diseases +MONDO:0019757 rare diseases +MONDO:0019759 gard_rare diseases +MONDO:0019759 nord_rare diseases +MONDO:0019759 ordo_subtype_of_a_disorder diseases +MONDO:0019759 otar diseases +MONDO:0019759 rare diseases +MONDO:0019760 gard_rare diseases +MONDO:0019760 ordo_morphological_anomaly diseases +MONDO:0019760 rare diseases +MONDO:0019761 gard_rare diseases +MONDO:0019761 nord_rare diseases +MONDO:0019761 ordo_subtype_of_a_disorder diseases +MONDO:0019761 rare diseases +MONDO:0019762 gard_rare diseases +MONDO:0019762 nord_rare diseases +MONDO:0019762 ordo_subtype_of_a_disorder diseases +MONDO:0019762 rare diseases +MONDO:0019763 gard_rare diseases +MONDO:0019763 nord_rare diseases +MONDO:0019763 ordo_subtype_of_a_disorder diseases +MONDO:0019763 rare diseases +MONDO:0019764 gard_rare diseases +MONDO:0019764 nord_rare diseases +MONDO:0019764 ordo_subtype_of_a_disorder diseases +MONDO:0019764 rare diseases +MONDO:0019766 gard_rare diseases +MONDO:0019766 ordo_subtype_of_a_disorder diseases +MONDO:0019766 otar diseases +MONDO:0019766 rare diseases +MONDO:0019767 gard_rare diseases +MONDO:0019767 ordo_subtype_of_a_disorder diseases +MONDO:0019767 otar diseases +MONDO:0019767 rare diseases +MONDO:0019768 gard_rare diseases +MONDO:0019768 ordo_subtype_of_a_disorder diseases +MONDO:0019768 otar diseases +MONDO:0019768 rare diseases +MONDO:0019769 gard_rare diseases +MONDO:0019769 ordo_subtype_of_a_disorder diseases +MONDO:0019769 otar diseases +MONDO:0019769 rare diseases +MONDO:0019770 gard_rare diseases +MONDO:0019770 rare diseases +MONDO:0019771 gard_rare diseases +MONDO:0019771 nord_rare diseases +MONDO:0019771 ordo_disorder diseases +MONDO:0019771 orphanet_rare diseases +MONDO:0019771 otar diseases +MONDO:0019771 rare diseases +MONDO:0019772 gard_rare diseases +MONDO:0019772 nord_rare diseases +MONDO:0019772 ordo_disorder diseases +MONDO:0019772 orphanet_rare diseases +MONDO:0019772 otar diseases +MONDO:0019772 rare diseases +MONDO:0019773 gard_rare diseases +MONDO:0019773 nord_rare diseases +MONDO:0019773 ordo_disorder diseases +MONDO:0019773 ordo_morphological_anomaly diseases +MONDO:0019773 orphanet_rare diseases +MONDO:0019773 otar diseases +MONDO:0019773 rare diseases +MONDO:0019780 gard_rare diseases +MONDO:0019780 nord_rare diseases +MONDO:0019780 ordo_disorder diseases +MONDO:0019780 ordo_morphological_anomaly diseases +MONDO:0019780 orphanet_rare diseases +MONDO:0019780 rare diseases +MONDO:0019781 gard_rare diseases +MONDO:0019781 otar diseases +MONDO:0019781 rare diseases +MONDO:0019782 gard_rare diseases +MONDO:0019782 nord_rare diseases +MONDO:0019782 ordo_disorder diseases +MONDO:0019782 ordo_morphological_anomaly diseases +MONDO:0019782 orphanet_rare diseases +MONDO:0019782 rare diseases +MONDO:0019783 gard_rare diseases +MONDO:0019783 nord_rare diseases +MONDO:0019783 ordo_clinical_situation diseases +MONDO:0019783 ordo_disorder diseases +MONDO:0019783 orphanet_rare diseases +MONDO:0019783 otar diseases +MONDO:0019783 rare diseases +MONDO:0019784 gard_rare diseases +MONDO:0019784 nord_rare diseases +MONDO:0019784 ordo_disorder diseases +MONDO:0019784 ordo_malformation_syndrome diseases +MONDO:0019784 orphanet_rare diseases +MONDO:0019784 otar diseases +MONDO:0019784 rare diseases +MONDO:0019786 gard_rare diseases +MONDO:0019786 nord_rare diseases +MONDO:0019786 ordo_disorder diseases +MONDO:0019786 ordo_malformation_syndrome diseases +MONDO:0019786 orphanet_rare diseases +MONDO:0019786 otar diseases +MONDO:0019786 rare diseases +MONDO:0019787 disease_grouping diseases +MONDO:0019787 gard_rare diseases +MONDO:0019787 nord_rare diseases +MONDO:0019787 ordo_group_of_disorders diseases +MONDO:0019787 otar diseases +MONDO:0019787 rare diseases +MONDO:0019788 gard_rare diseases +MONDO:0019788 nord_rare diseases +MONDO:0019788 ordo_disorder diseases +MONDO:0019788 orphanet_rare diseases +MONDO:0019788 rare diseases +MONDO:0019789 gard_rare diseases +MONDO:0019789 nord_rare diseases +MONDO:0019789 ordo_disorder diseases +MONDO:0019789 orphanet_rare diseases +MONDO:0019789 rare diseases +MONDO:0019790 gard_rare diseases +MONDO:0019790 nord_rare diseases +MONDO:0019790 ordo_disorder diseases +MONDO:0019790 orphanet_rare diseases +MONDO:0019790 otar diseases +MONDO:0019790 rare diseases +MONDO:0019791 gard_rare diseases +MONDO:0019791 nord_rare diseases +MONDO:0019791 ordo_disorder diseases +MONDO:0019791 orphanet_rare diseases +MONDO:0019791 otar diseases +MONDO:0019791 rare diseases +MONDO:0019792 disease_grouping diseases +MONDO:0019792 gard_rare diseases +MONDO:0019792 nord_rare diseases +MONDO:0019792 ordo_group_of_disorders diseases +MONDO:0019792 otar diseases +MONDO:0019792 rare diseases +MONDO:0019793 disease_grouping diseases +MONDO:0019793 gard_rare diseases +MONDO:0019793 nord_rare diseases +MONDO:0019793 ordo_group_of_disorders diseases +MONDO:0019793 rare diseases +MONDO:0019794 disease_grouping diseases +MONDO:0019794 gard_rare diseases +MONDO:0019794 ordo_group_of_disorders diseases +MONDO:0019794 rare diseases +MONDO:0019795 gard_rare diseases +MONDO:0019795 nord_rare diseases +MONDO:0019795 ordo_disorder diseases +MONDO:0019795 ordo_malformation_syndrome diseases +MONDO:0019795 orphanet_rare diseases +MONDO:0019795 rare diseases +MONDO:0019796 disease_grouping diseases +MONDO:0019796 gard_rare diseases +MONDO:0019796 otar diseases +MONDO:0019796 rare diseases +MONDO:0019797 gard_rare diseases +MONDO:0019797 nord_rare diseases +MONDO:0019797 ordo_disorder diseases +MONDO:0019797 ordo_malformation_syndrome diseases +MONDO:0019797 orphanet_rare diseases +MONDO:0019797 otar diseases +MONDO:0019797 rare diseases +MONDO:0019799 gard_rare diseases +MONDO:0019799 nord_rare diseases +MONDO:0019799 ordo_disorder diseases +MONDO:0019799 orphanet_rare diseases +MONDO:0019799 otar diseases +MONDO:0019799 rare diseases +MONDO:0019801 gard_rare diseases +MONDO:0019801 nord_rare diseases +MONDO:0019801 ordo_clinical_syndrome diseases +MONDO:0019801 ordo_disorder diseases +MONDO:0019801 orphanet_rare diseases +MONDO:0019801 otar diseases +MONDO:0019801 rare diseases +MONDO:0019802 gard_rare diseases +MONDO:0019802 nord_rare diseases +MONDO:0019802 ordo_disorder diseases +MONDO:0019802 orphanet_rare diseases +MONDO:0019802 rare diseases +MONDO:0019803 gard_rare diseases +MONDO:0019803 nord_rare diseases +MONDO:0019803 ordo_disorder diseases +MONDO:0019803 orphanet_rare diseases +MONDO:0019803 otar diseases +MONDO:0019803 rare diseases +MONDO:0019804 gard_rare diseases +MONDO:0019804 nord_rare diseases +MONDO:0019804 ordo_disorder diseases +MONDO:0019804 ordo_morphological_anomaly diseases +MONDO:0019804 orphanet_rare diseases +MONDO:0019804 otar diseases +MONDO:0019804 rare diseases +MONDO:0019805 gard_rare diseases +MONDO:0019805 nord_rare diseases +MONDO:0019805 ordo_disorder diseases +MONDO:0019805 orphanet_rare diseases +MONDO:0019805 otar diseases +MONDO:0019805 rare diseases +MONDO:0019806 disease_grouping diseases +MONDO:0019806 gard_rare diseases +MONDO:0019806 ordo_group_of_disorders diseases +MONDO:0019806 otar diseases +MONDO:0019806 rare diseases +MONDO:0019807 gard_rare diseases +MONDO:0019807 nord_rare diseases +MONDO:0019807 ordo_disorder diseases +MONDO:0019807 ordo_morphological_anomaly diseases +MONDO:0019807 orphanet_rare diseases +MONDO:0019807 rare diseases +MONDO:0019808 gard_rare diseases +MONDO:0019808 nord_rare diseases +MONDO:0019808 ordo_subtype_of_a_disorder diseases +MONDO:0019808 rare diseases +MONDO:0019809 gard_rare diseases +MONDO:0019809 nord_rare diseases +MONDO:0019809 rare diseases +MONDO:0019810 gard_rare diseases +MONDO:0019810 nord_rare diseases +MONDO:0019810 ordo_disorder diseases +MONDO:0019810 orphanet_rare diseases +MONDO:0019810 otar diseases +MONDO:0019810 rare diseases +MONDO:0019811 gard_rare diseases +MONDO:0019811 nord_rare diseases +MONDO:0019811 ordo_disorder diseases +MONDO:0019811 ordo_morphological_anomaly diseases +MONDO:0019811 orphanet_rare diseases +MONDO:0019811 rare diseases +MONDO:0019813 gard_rare diseases +MONDO:0019813 nord_rare diseases +MONDO:0019813 ordo_disorder diseases +MONDO:0019813 ordo_morphological_anomaly diseases +MONDO:0019813 orphanet_rare diseases +MONDO:0019813 rare diseases +MONDO:0019814 gard_rare diseases +MONDO:0019814 nord_rare diseases +MONDO:0019814 ordo_disorder diseases +MONDO:0019814 ordo_morphological_anomaly diseases +MONDO:0019814 orphanet_rare diseases +MONDO:0019814 rare diseases +MONDO:0019815 gard_rare diseases +MONDO:0019815 nord_rare diseases +MONDO:0019815 ordo_disorder diseases +MONDO:0019815 ordo_morphological_anomaly diseases +MONDO:0019815 orphanet_rare diseases +MONDO:0019815 rare diseases +MONDO:0019817 disease_grouping diseases +MONDO:0019817 gard_rare diseases +MONDO:0019817 ordo_group_of_disorders diseases +MONDO:0019817 rare diseases +MONDO:0019818 gard_rare diseases +MONDO:0019818 nord_rare diseases +MONDO:0019818 ordo_disorder diseases +MONDO:0019818 ordo_morphological_anomaly diseases +MONDO:0019818 orphanet_rare diseases +MONDO:0019818 rare diseases +MONDO:0019819 gard_rare diseases +MONDO:0019819 nord_rare diseases +MONDO:0019819 ordo_subtype_of_a_disorder diseases +MONDO:0019819 rare diseases +MONDO:0019820 disease_grouping diseases +MONDO:0019820 gard_rare diseases +MONDO:0019820 ordo_group_of_disorders diseases +MONDO:0019820 rare diseases +MONDO:0019821 gard_rare diseases +MONDO:0019821 ordo_morphological_anomaly diseases +MONDO:0019821 otar diseases +MONDO:0019821 rare diseases +MONDO:0019823 gard_rare diseases +MONDO:0019823 nord_rare diseases +MONDO:0019823 ordo_disorder diseases +MONDO:0019823 ordo_morphological_anomaly diseases +MONDO:0019823 orphanet_rare diseases +MONDO:0019823 rare diseases +MONDO:0019824 disease_grouping diseases +MONDO:0019824 gard_rare diseases +MONDO:0019824 ordo_group_of_disorders diseases +MONDO:0019824 rare diseases +MONDO:0019825 gard_rare diseases +MONDO:0019825 nord_rare diseases +MONDO:0019825 ordo_disorder diseases +MONDO:0019825 ordo_morphological_anomaly diseases +MONDO:0019825 orphanet_rare diseases +MONDO:0019825 rare diseases +MONDO:0019828 gard_rare diseases +MONDO:0019828 nord_rare diseases +MONDO:0019828 ordo_disorder diseases +MONDO:0019828 ordo_morphological_anomaly diseases +MONDO:0019828 orphanet_rare diseases +MONDO:0019828 otar diseases +MONDO:0019828 rare diseases +MONDO:0019829 disease_grouping diseases +MONDO:0019829 gard_rare diseases +MONDO:0019829 ordo_group_of_disorders diseases +MONDO:0019829 rare diseases +MONDO:0019830 disease_grouping diseases +MONDO:0019830 gard_rare diseases +MONDO:0019830 nord_rare diseases +MONDO:0019830 ordo_group_of_disorders diseases +MONDO:0019830 rare diseases +MONDO:0019832 disease_grouping diseases +MONDO:0019832 gard_rare diseases +MONDO:0019832 ordo_group_of_disorders diseases +MONDO:0019832 otar diseases +MONDO:0019832 rare diseases +MONDO:0019835 disease_grouping diseases +MONDO:0019835 gard_rare diseases +MONDO:0019835 ordo_group_of_disorders diseases +MONDO:0019835 rare diseases +MONDO:0019836 gard_rare diseases +MONDO:0019836 nord_rare diseases +MONDO:0019836 ordo_disorder diseases +MONDO:0019836 ordo_morphological_anomaly diseases +MONDO:0019836 orphanet_rare diseases +MONDO:0019836 rare diseases +MONDO:0019838 gard_rare diseases +MONDO:0019838 nord_rare diseases +MONDO:0019838 ordo_disorder diseases +MONDO:0019838 orphanet_rare diseases +MONDO:0019838 rare diseases +MONDO:0019839 gard_rare diseases +MONDO:0019839 nord_rare diseases +MONDO:0019839 ordo_disorder diseases +MONDO:0019839 orphanet_rare diseases +MONDO:0019839 rare diseases +MONDO:0019840 gard_rare diseases +MONDO:0019840 ordo_malformation_syndrome diseases +MONDO:0019840 rare diseases +MONDO:0019845 gard_rare diseases +MONDO:0019845 ordo_disorder diseases +MONDO:0019845 orphanet_rare diseases +MONDO:0019845 rare diseases +MONDO:0019846 gard_rare diseases +MONDO:0019846 nord_rare diseases +MONDO:0019846 ordo_subtype_of_a_disorder diseases +MONDO:0019846 otar diseases +MONDO:0019846 rare diseases +MONDO:0019848 gard_rare diseases +MONDO:0019848 nord_rare diseases +MONDO:0019848 ordo_disorder diseases +MONDO:0019848 ordo_morphological_anomaly diseases +MONDO:0019848 orphanet_rare diseases +MONDO:0019848 rare diseases +MONDO:0019849 gard_rare diseases +MONDO:0019849 nord_rare diseases +MONDO:0019849 ordo_disorder diseases +MONDO:0019849 ordo_morphological_anomaly diseases +MONDO:0019849 orphanet_rare diseases +MONDO:0019849 rare diseases +MONDO:0019851 disease_grouping diseases +MONDO:0019851 gard_rare diseases +MONDO:0019851 ordo_group_of_disorders diseases +MONDO:0019851 rare diseases +MONDO:0019852 disease_grouping diseases +MONDO:0019852 gard_rare diseases +MONDO:0019852 ordo_group_of_disorders diseases +MONDO:0019852 otar diseases +MONDO:0019852 rare diseases +MONDO:0019854 gard_rare diseases +MONDO:0019854 nord_rare diseases +MONDO:0019854 ordo_disorder diseases +MONDO:0019854 ordo_morphological_anomaly diseases +MONDO:0019854 orphanet_rare diseases +MONDO:0019854 otar diseases +MONDO:0019854 rare diseases +MONDO:0019855 gard_rare diseases +MONDO:0019855 nord_rare diseases +MONDO:0019855 ordo_disorder diseases +MONDO:0019855 ordo_morphological_anomaly diseases +MONDO:0019855 orphanet_rare diseases +MONDO:0019855 otar diseases +MONDO:0019855 rare diseases +MONDO:0019857 gard_rare diseases +MONDO:0019857 nord_rare diseases +MONDO:0019857 ordo_disorder diseases +MONDO:0019857 orphanet_rare diseases +MONDO:0019857 rare diseases +MONDO:0019858 gard_rare diseases +MONDO:0019858 nord_rare diseases +MONDO:0019858 ordo_disorder diseases +MONDO:0019858 orphanet_rare diseases +MONDO:0019858 rare diseases +MONDO:0019860 gard_rare diseases +MONDO:0019860 nord_rare diseases +MONDO:0019860 ordo_disorder diseases +MONDO:0019860 ordo_morphological_anomaly diseases +MONDO:0019860 orphanet_rare diseases +MONDO:0019860 otar diseases +MONDO:0019860 rare diseases +MONDO:0019861 gard_rare diseases +MONDO:0019861 nord_rare diseases +MONDO:0019861 ordo_disorder diseases +MONDO:0019861 ordo_morphological_anomaly diseases +MONDO:0019861 orphanet_rare diseases +MONDO:0019861 otar diseases +MONDO:0019861 rare diseases +MONDO:0019862 gard_rare diseases +MONDO:0019862 nord_rare diseases +MONDO:0019862 ordo_disorder diseases +MONDO:0019862 ordo_morphological_anomaly diseases +MONDO:0019862 orphanet_rare diseases +MONDO:0019862 rare diseases +MONDO:0019864 gard_rare diseases +MONDO:0019864 nord_rare diseases +MONDO:0019864 ordo_disorder diseases +MONDO:0019864 ordo_malformation_syndrome diseases +MONDO:0019864 orphanet_rare diseases +MONDO:0019864 rare diseases +MONDO:0019865 gard_rare diseases +MONDO:0019865 nord_rare diseases +MONDO:0019865 ordo_disorder diseases +MONDO:0019865 ordo_malformation_syndrome diseases +MONDO:0019865 orphanet_rare diseases +MONDO:0019865 rare diseases +MONDO:0019866 gard_rare diseases +MONDO:0019866 nord_rare diseases +MONDO:0019866 ordo_disorder diseases +MONDO:0019866 ordo_malformation_syndrome diseases +MONDO:0019866 orphanet_rare diseases +MONDO:0019866 rare diseases +MONDO:0019867 gard_rare diseases +MONDO:0019867 nord_rare diseases +MONDO:0019867 ordo_disorder diseases +MONDO:0019867 ordo_malformation_syndrome diseases +MONDO:0019867 orphanet_rare diseases +MONDO:0019867 otar diseases +MONDO:0019867 rare diseases +MONDO:0019868 gard_rare diseases +MONDO:0019868 nord_rare diseases +MONDO:0019868 ordo_disorder diseases +MONDO:0019868 ordo_malformation_syndrome diseases +MONDO:0019868 orphanet_rare diseases +MONDO:0019868 rare diseases +MONDO:0019869 gard_rare diseases +MONDO:0019869 nord_rare diseases +MONDO:0019869 ordo_disorder diseases +MONDO:0019869 ordo_malformation_syndrome diseases +MONDO:0019869 orphanet_rare diseases +MONDO:0019869 rare diseases +MONDO:0019870 gard_rare diseases +MONDO:0019870 nord_rare diseases +MONDO:0019870 ordo_disorder diseases +MONDO:0019870 ordo_malformation_syndrome diseases +MONDO:0019870 orphanet_rare diseases +MONDO:0019870 rare diseases +MONDO:0019871 gard_rare diseases +MONDO:0019871 nord_rare diseases +MONDO:0019871 ordo_disorder diseases +MONDO:0019871 ordo_malformation_syndrome diseases +MONDO:0019871 orphanet_rare diseases +MONDO:0019871 rare diseases +MONDO:0019872 gard_rare diseases +MONDO:0019872 nord_rare diseases +MONDO:0019872 ordo_disorder diseases +MONDO:0019872 ordo_malformation_syndrome diseases +MONDO:0019872 orphanet_rare diseases +MONDO:0019872 rare diseases +MONDO:0019873 gard_rare diseases +MONDO:0019873 nord_rare diseases +MONDO:0019873 ordo_disorder diseases +MONDO:0019873 ordo_malformation_syndrome diseases +MONDO:0019873 orphanet_rare diseases +MONDO:0019873 rare diseases +MONDO:0019874 gard_rare diseases +MONDO:0019874 nord_rare diseases +MONDO:0019874 ordo_disorder diseases +MONDO:0019874 ordo_malformation_syndrome diseases +MONDO:0019874 orphanet_rare diseases +MONDO:0019874 rare diseases +MONDO:0019875 gard_rare diseases +MONDO:0019875 nord_rare diseases +MONDO:0019875 ordo_etiological_subtype diseases +MONDO:0019875 ordo_subtype_of_a_disorder diseases +MONDO:0019875 rare diseases +MONDO:0019876 gard_rare diseases +MONDO:0019876 nord_rare diseases +MONDO:0019876 ordo_disorder diseases +MONDO:0019876 ordo_malformation_syndrome diseases +MONDO:0019876 orphanet_rare diseases +MONDO:0019876 otar diseases +MONDO:0019876 rare diseases +MONDO:0019877 gard_rare diseases +MONDO:0019877 nord_rare diseases +MONDO:0019877 ordo_disorder diseases +MONDO:0019877 ordo_malformation_syndrome diseases +MONDO:0019877 orphanet_rare diseases +MONDO:0019877 rare diseases +MONDO:0019878 gard_rare diseases +MONDO:0019878 nord_rare diseases +MONDO:0019878 ordo_disorder diseases +MONDO:0019878 ordo_malformation_syndrome diseases +MONDO:0019878 orphanet_rare diseases +MONDO:0019878 otar diseases +MONDO:0019878 rare diseases +MONDO:0019879 gard_rare diseases +MONDO:0019879 nord_rare diseases +MONDO:0019879 ordo_disorder diseases +MONDO:0019879 ordo_malformation_syndrome diseases +MONDO:0019879 orphanet_rare diseases +MONDO:0019879 rare diseases +MONDO:0019880 gard_rare diseases +MONDO:0019880 nord_rare diseases +MONDO:0019880 ordo_disorder diseases +MONDO:0019880 ordo_malformation_syndrome diseases +MONDO:0019880 orphanet_rare diseases +MONDO:0019880 otar diseases +MONDO:0019880 rare diseases +MONDO:0019881 gard_rare diseases +MONDO:0019881 nord_rare diseases +MONDO:0019881 ordo_disorder diseases +MONDO:0019881 ordo_malformation_syndrome diseases +MONDO:0019881 orphanet_rare diseases +MONDO:0019881 rare diseases +MONDO:0019882 gard_rare diseases +MONDO:0019882 nord_rare diseases +MONDO:0019882 ordo_disorder diseases +MONDO:0019882 ordo_malformation_syndrome diseases +MONDO:0019882 orphanet_rare diseases +MONDO:0019882 rare diseases +MONDO:0019883 gard_rare diseases +MONDO:0019883 nord_rare diseases +MONDO:0019883 ordo_disorder diseases +MONDO:0019883 ordo_malformation_syndrome diseases +MONDO:0019883 orphanet_rare diseases +MONDO:0019883 rare diseases +MONDO:0019884 gard_rare diseases +MONDO:0019884 nord_rare diseases +MONDO:0019884 ordo_disorder diseases +MONDO:0019884 ordo_malformation_syndrome diseases +MONDO:0019884 orphanet_rare diseases +MONDO:0019884 rare diseases +MONDO:0019885 gard_rare diseases +MONDO:0019885 nord_rare diseases +MONDO:0019885 ordo_disorder diseases +MONDO:0019885 ordo_malformation_syndrome diseases +MONDO:0019885 orphanet_rare diseases +MONDO:0019885 rare diseases +MONDO:0019886 gard_rare diseases +MONDO:0019886 nord_rare diseases +MONDO:0019886 ordo_disorder diseases +MONDO:0019886 ordo_malformation_syndrome diseases +MONDO:0019886 orphanet_rare diseases +MONDO:0019886 rare diseases +MONDO:0019887 gard_rare diseases +MONDO:0019887 nord_rare diseases +MONDO:0019887 ordo_disorder diseases +MONDO:0019887 ordo_malformation_syndrome diseases +MONDO:0019887 orphanet_rare diseases +MONDO:0019887 rare diseases +MONDO:0019888 gard_rare diseases +MONDO:0019888 nord_rare diseases +MONDO:0019888 ordo_disorder diseases +MONDO:0019888 ordo_malformation_syndrome diseases +MONDO:0019888 orphanet_rare diseases +MONDO:0019888 rare diseases +MONDO:0019889 gard_rare diseases +MONDO:0019889 nord_rare diseases +MONDO:0019889 ordo_disorder diseases +MONDO:0019889 ordo_malformation_syndrome diseases +MONDO:0019889 orphanet_rare diseases +MONDO:0019889 rare diseases +MONDO:0019890 gard_rare diseases +MONDO:0019890 nord_rare diseases +MONDO:0019890 ordo_disorder diseases +MONDO:0019890 ordo_malformation_syndrome diseases +MONDO:0019890 orphanet_rare diseases +MONDO:0019890 rare diseases +MONDO:0019891 gard_rare diseases +MONDO:0019891 nord_rare diseases +MONDO:0019891 ordo_disorder diseases +MONDO:0019891 ordo_malformation_syndrome diseases +MONDO:0019891 orphanet_rare diseases +MONDO:0019891 otar diseases +MONDO:0019891 rare diseases +MONDO:0019892 gard_rare diseases +MONDO:0019892 nord_rare diseases +MONDO:0019892 ordo_disorder diseases +MONDO:0019892 ordo_malformation_syndrome diseases +MONDO:0019892 orphanet_rare diseases +MONDO:0019892 rare diseases +MONDO:0019893 gard_rare diseases +MONDO:0019893 nord_rare diseases +MONDO:0019893 ordo_disorder diseases +MONDO:0019893 ordo_malformation_syndrome diseases +MONDO:0019893 orphanet_rare diseases +MONDO:0019893 otar diseases +MONDO:0019893 rare diseases +MONDO:0019895 gard_rare diseases +MONDO:0019895 nord_rare diseases +MONDO:0019895 ordo_disorder diseases +MONDO:0019895 ordo_malformation_syndrome diseases +MONDO:0019895 orphanet_rare diseases +MONDO:0019895 rare diseases +MONDO:0019896 gard_rare diseases +MONDO:0019896 nord_rare diseases +MONDO:0019896 ordo_etiological_subtype diseases +MONDO:0019896 ordo_subtype_of_a_disorder diseases +MONDO:0019896 otar diseases +MONDO:0019896 rare diseases +MONDO:0019897 gard_rare diseases +MONDO:0019897 nord_rare diseases +MONDO:0019897 ordo_disorder diseases +MONDO:0019897 ordo_malformation_syndrome diseases +MONDO:0019897 orphanet_rare diseases +MONDO:0019897 otar diseases +MONDO:0019897 rare diseases +MONDO:0019898 gard_rare diseases +MONDO:0019898 nord_rare diseases +MONDO:0019898 ordo_disorder diseases +MONDO:0019898 ordo_malformation_syndrome diseases +MONDO:0019898 orphanet_rare diseases +MONDO:0019898 rare diseases +MONDO:0019900 gard_rare diseases +MONDO:0019900 nord_rare diseases +MONDO:0019900 ordo_disorder diseases +MONDO:0019900 ordo_malformation_syndrome diseases +MONDO:0019900 orphanet_rare diseases +MONDO:0019900 rare diseases +MONDO:0019901 gard_rare diseases +MONDO:0019901 ordo_malformation_syndrome diseases +MONDO:0019901 rare diseases +MONDO:0019902 gard_rare diseases +MONDO:0019902 nord_rare diseases +MONDO:0019902 ordo_disorder diseases +MONDO:0019902 ordo_malformation_syndrome diseases +MONDO:0019902 orphanet_rare diseases +MONDO:0019902 rare diseases +MONDO:0019903 gard_rare diseases +MONDO:0019903 nord_rare diseases +MONDO:0019903 ordo_disorder diseases +MONDO:0019903 ordo_malformation_syndrome diseases +MONDO:0019903 orphanet_rare diseases +MONDO:0019903 rare diseases +MONDO:0019904 gard_rare diseases +MONDO:0019904 nord_rare diseases +MONDO:0019904 ordo_disorder diseases +MONDO:0019904 ordo_malformation_syndrome diseases +MONDO:0019904 orphanet_rare diseases +MONDO:0019904 rare diseases +MONDO:0019905 gard_rare diseases +MONDO:0019905 nord_rare diseases +MONDO:0019905 ordo_disorder diseases +MONDO:0019905 ordo_malformation_syndrome diseases +MONDO:0019905 orphanet_rare diseases +MONDO:0019905 rare diseases +MONDO:0019906 gard_rare diseases +MONDO:0019906 nord_rare diseases +MONDO:0019906 ordo_disorder diseases +MONDO:0019906 ordo_malformation_syndrome diseases +MONDO:0019906 orphanet_rare diseases +MONDO:0019906 rare diseases +MONDO:0019907 gard_rare diseases +MONDO:0019907 nord_rare diseases +MONDO:0019907 ordo_disorder diseases +MONDO:0019907 ordo_malformation_syndrome diseases +MONDO:0019907 orphanet_rare diseases +MONDO:0019907 otar diseases +MONDO:0019907 rare diseases +MONDO:0019908 gard_rare diseases +MONDO:0019908 nord_rare diseases +MONDO:0019908 ordo_disorder diseases +MONDO:0019908 ordo_malformation_syndrome diseases +MONDO:0019908 orphanet_rare diseases +MONDO:0019908 otar diseases +MONDO:0019908 rare diseases +MONDO:0019909 gard_rare diseases +MONDO:0019909 nord_rare diseases +MONDO:0019909 ordo_disorder diseases +MONDO:0019909 ordo_malformation_syndrome diseases +MONDO:0019909 orphanet_rare diseases +MONDO:0019909 rare diseases +MONDO:0019910 gard_rare diseases +MONDO:0019910 nord_rare diseases +MONDO:0019910 ordo_disorder diseases +MONDO:0019910 ordo_malformation_syndrome diseases +MONDO:0019910 orphanet_rare diseases +MONDO:0019910 otar diseases +MONDO:0019910 rare diseases +MONDO:0019911 gard_rare diseases +MONDO:0019911 nord_rare diseases +MONDO:0019911 ordo_disorder diseases +MONDO:0019911 ordo_malformation_syndrome diseases +MONDO:0019911 orphanet_rare diseases +MONDO:0019911 otar diseases +MONDO:0019911 rare diseases +MONDO:0019912 gard_rare diseases +MONDO:0019912 nord_rare diseases +MONDO:0019912 ordo_disorder diseases +MONDO:0019912 ordo_malformation_syndrome diseases +MONDO:0019912 orphanet_rare diseases +MONDO:0019912 otar diseases +MONDO:0019912 rare diseases +MONDO:0019913 gard_rare diseases +MONDO:0019913 nord_rare diseases +MONDO:0019913 ordo_etiological_subtype diseases +MONDO:0019913 ordo_subtype_of_a_disorder diseases +MONDO:0019913 otar diseases +MONDO:0019913 rare diseases +MONDO:0019914 gard_rare diseases +MONDO:0019914 nord_rare diseases +MONDO:0019914 ordo_disorder diseases +MONDO:0019914 ordo_malformation_syndrome diseases +MONDO:0019914 orphanet_rare diseases +MONDO:0019914 otar diseases +MONDO:0019914 rare diseases +MONDO:0019915 gard_rare diseases +MONDO:0019915 nord_rare diseases +MONDO:0019915 ordo_etiological_subtype diseases +MONDO:0019915 ordo_subtype_of_a_disorder diseases +MONDO:0019915 otar diseases +MONDO:0019915 rare diseases +MONDO:0019916 gard_rare diseases +MONDO:0019916 nord_rare diseases +MONDO:0019916 ordo_disorder diseases +MONDO:0019916 ordo_malformation_syndrome diseases +MONDO:0019916 orphanet_rare diseases +MONDO:0019916 rare diseases +MONDO:0019917 gard_rare diseases +MONDO:0019917 nord_rare diseases +MONDO:0019917 ordo_disorder diseases +MONDO:0019917 ordo_malformation_syndrome diseases +MONDO:0019917 orphanet_rare diseases +MONDO:0019917 otar diseases +MONDO:0019917 rare diseases +MONDO:0019918 gard_rare diseases +MONDO:0019918 nord_rare diseases +MONDO:0019918 ordo_disorder diseases +MONDO:0019918 ordo_malformation_syndrome diseases +MONDO:0019918 orphanet_rare diseases +MONDO:0019918 rare diseases +MONDO:0019919 gard_rare diseases +MONDO:0019919 nord_rare diseases +MONDO:0019919 ordo_disorder diseases +MONDO:0019919 ordo_malformation_syndrome diseases +MONDO:0019919 orphanet_rare diseases +MONDO:0019919 rare diseases +MONDO:0019920 gard_rare diseases +MONDO:0019920 nord_rare diseases +MONDO:0019920 ordo_disorder diseases +MONDO:0019920 ordo_malformation_syndrome diseases +MONDO:0019920 orphanet_rare diseases +MONDO:0019920 otar diseases +MONDO:0019920 rare diseases +MONDO:0019921 gard_rare diseases +MONDO:0019921 nord_rare diseases +MONDO:0019921 ordo_disorder diseases +MONDO:0019921 ordo_malformation_syndrome diseases +MONDO:0019921 orphanet_rare diseases +MONDO:0019921 otar diseases +MONDO:0019921 rare diseases +MONDO:0019922 gard_rare diseases +MONDO:0019922 nord_rare diseases +MONDO:0019922 ordo_disorder diseases +MONDO:0019922 ordo_malformation_syndrome diseases +MONDO:0019922 orphanet_rare diseases +MONDO:0019922 rare diseases +MONDO:0019923 gard_rare diseases +MONDO:0019923 nord_rare diseases +MONDO:0019923 ordo_etiological_subtype diseases +MONDO:0019923 ordo_subtype_of_a_disorder diseases +MONDO:0019923 rare diseases +MONDO:0019924 gard_rare diseases +MONDO:0019924 nord_rare diseases +MONDO:0019924 ordo_disorder diseases +MONDO:0019924 ordo_malformation_syndrome diseases +MONDO:0019924 orphanet_rare diseases +MONDO:0019924 rare diseases +MONDO:0019925 gard_rare diseases +MONDO:0019925 nord_rare diseases +MONDO:0019925 ordo_disorder diseases +MONDO:0019925 ordo_malformation_syndrome diseases +MONDO:0019925 orphanet_rare diseases +MONDO:0019925 rare diseases +MONDO:0019926 gard_rare diseases +MONDO:0019926 nord_rare diseases +MONDO:0019926 ordo_disorder diseases +MONDO:0019926 ordo_malformation_syndrome diseases +MONDO:0019926 orphanet_rare diseases +MONDO:0019926 rare diseases +MONDO:0019927 gard_rare diseases +MONDO:0019927 otar diseases +MONDO:0019927 rare diseases +MONDO:0019928 gard_rare diseases +MONDO:0019928 nord_rare diseases +MONDO:0019928 ordo_disorder diseases +MONDO:0019928 ordo_malformation_syndrome diseases +MONDO:0019928 orphanet_rare diseases +MONDO:0019928 otar diseases +MONDO:0019928 rare diseases +MONDO:0019929 gard_rare diseases +MONDO:0019929 nord_rare diseases +MONDO:0019929 ordo_disorder diseases +MONDO:0019929 ordo_malformation_syndrome diseases +MONDO:0019929 orphanet_rare diseases +MONDO:0019929 otar diseases +MONDO:0019929 rare diseases +MONDO:0019930 gard_rare diseases +MONDO:0019930 nord_rare diseases +MONDO:0019930 ordo_subtype_of_a_disorder diseases +MONDO:0019930 otar diseases +MONDO:0019930 rare diseases +MONDO:0019931 gard_rare diseases +MONDO:0019931 nord_rare diseases +MONDO:0019931 ordo_subtype_of_a_disorder diseases +MONDO:0019931 otar diseases +MONDO:0019931 rare diseases +MONDO:0019932 gard_rare diseases +MONDO:0019932 nord_rare diseases +MONDO:0019932 ordo_disorder diseases +MONDO:0019932 ordo_morphological_anomaly diseases +MONDO:0019932 orphanet_rare diseases +MONDO:0019932 rare diseases +MONDO:0019933 gard_rare diseases +MONDO:0019933 nord_rare diseases +MONDO:0019933 ordo_disorder diseases +MONDO:0019933 orphanet_rare diseases +MONDO:0019933 otar diseases +MONDO:0019933 rare diseases +MONDO:0019934 disease_grouping diseases +MONDO:0019934 gard_rare diseases +MONDO:0019934 nord_rare diseases +MONDO:0019934 ordo_group_of_disorders diseases +MONDO:0019934 rare diseases +MONDO:0019935 disease_grouping diseases +MONDO:0019935 gard_rare diseases +MONDO:0019935 nord_rare diseases +MONDO:0019935 ordo_group_of_disorders diseases +MONDO:0019935 rare diseases +MONDO:0019938 disease_grouping diseases +MONDO:0019938 gard_rare diseases +MONDO:0019938 ordo_group_of_disorders diseases +MONDO:0019938 otar diseases +MONDO:0019938 rare diseases +MONDO:0019939 gard_rare diseases +MONDO:0019939 rare diseases +MONDO:0019940 gard_rare diseases +MONDO:0019940 ordo_malformation_syndrome diseases +MONDO:0019940 rare diseases +MONDO:0019941 gard_rare diseases +MONDO:0019941 nord_rare diseases +MONDO:0019941 ordo_disorder diseases +MONDO:0019941 orphanet_rare diseases +MONDO:0019941 otar diseases +MONDO:0019941 rare diseases +MONDO:0019942 disease_grouping diseases +MONDO:0019942 gard_rare diseases +MONDO:0019942 nord_rare diseases +MONDO:0019942 ordo_group_of_disorders diseases +MONDO:0019942 otar diseases +MONDO:0019942 rare diseases +MONDO:0019943 gard_rare diseases +MONDO:0019943 nord_rare diseases +MONDO:0019943 ordo_disorder diseases +MONDO:0019943 orphanet_rare diseases +MONDO:0019943 otar diseases +MONDO:0019943 rare diseases +MONDO:0019944 gard_rare diseases +MONDO:0019944 nord_rare diseases +MONDO:0019944 ordo_disorder diseases +MONDO:0019944 ordo_malformation_syndrome diseases +MONDO:0019944 orphanet_rare diseases +MONDO:0019944 otar diseases +MONDO:0019944 rare diseases +MONDO:0019945 gard_rare diseases +MONDO:0019945 nord_rare diseases +MONDO:0019945 ordo_disorder diseases +MONDO:0019945 orphanet_rare diseases +MONDO:0019945 rare diseases +MONDO:0019947 gard_rare diseases +MONDO:0019947 ordo_disorder diseases +MONDO:0019947 orphanet_rare diseases +MONDO:0019947 otar diseases +MONDO:0019947 rare diseases +MONDO:0019948 gard_rare diseases +MONDO:0019948 nord_rare diseases +MONDO:0019948 ordo_disorder diseases +MONDO:0019948 orphanet_rare diseases +MONDO:0019948 otar diseases +MONDO:0019948 rare diseases +MONDO:0019949 gard_rare diseases +MONDO:0019949 nord_rare diseases +MONDO:0019949 ordo_disorder diseases +MONDO:0019949 orphanet_rare diseases +MONDO:0019949 otar diseases +MONDO:0019949 rare diseases +MONDO:0019950 disease_grouping diseases +MONDO:0019950 gard_rare diseases +MONDO:0019950 ordo_group_of_disorders diseases +MONDO:0019950 otar diseases +MONDO:0019950 rare diseases +MONDO:0019951 gard_rare diseases +MONDO:0019951 nord_rare diseases +MONDO:0019951 ordo_disorder diseases +MONDO:0019951 orphanet_rare diseases +MONDO:0019951 otar diseases +MONDO:0019951 rare diseases +MONDO:0019952 clingen diseases +MONDO:0019952 disease_grouping diseases +MONDO:0019952 gard_rare diseases +MONDO:0019952 ordo_group_of_disorders diseases +MONDO:0019952 otar diseases +MONDO:0019952 rare diseases +MONDO:0019953 gard_rare diseases +MONDO:0019953 nord_rare diseases +MONDO:0019953 ordo_disorder diseases +MONDO:0019953 ordo_morphological_anomaly diseases +MONDO:0019953 orphanet_rare diseases +MONDO:0019953 rare diseases +MONDO:0019954 disease_grouping diseases +MONDO:0019954 gard_rare diseases +MONDO:0019954 ordo_group_of_disorders diseases +MONDO:0019954 otar diseases +MONDO:0019954 rare diseases +MONDO:0019955 gard_rare diseases +MONDO:0019955 nord_rare diseases +MONDO:0019955 ordo_disorder diseases +MONDO:0019955 orphanet_rare diseases +MONDO:0019955 rare diseases +MONDO:0019956 disease_grouping diseases +MONDO:0019956 ordo_group_of_disorders diseases +MONDO:0019956 otar diseases +MONDO:0019957 gard_rare diseases +MONDO:0019957 nord_rare diseases +MONDO:0019957 ordo_disorder diseases +MONDO:0019957 orphanet_rare diseases +MONDO:0019957 rare diseases +MONDO:0019959 gard_rare diseases +MONDO:0019959 nord_rare diseases +MONDO:0019959 ordo_disorder diseases +MONDO:0019959 orphanet_rare diseases +MONDO:0019959 rare diseases +MONDO:0019960 gard_rare diseases +MONDO:0019960 nord_rare diseases +MONDO:0019960 ordo_disorder diseases +MONDO:0019960 orphanet_rare diseases +MONDO:0019960 rare diseases +MONDO:0019962 gard_rare diseases +MONDO:0019962 nord_rare diseases +MONDO:0019962 ordo_disorder diseases +MONDO:0019962 orphanet_rare diseases +MONDO:0019962 otar diseases +MONDO:0019962 rare diseases +MONDO:0019963 gard_rare diseases +MONDO:0019963 nord_rare diseases +MONDO:0019963 ordo_disorder diseases +MONDO:0019963 orphanet_rare diseases +MONDO:0019963 rare diseases +MONDO:0019964 gard_rare diseases +MONDO:0019964 nord_rare diseases +MONDO:0019964 ordo_disorder diseases +MONDO:0019964 orphanet_rare diseases +MONDO:0019964 otar diseases +MONDO:0019964 rare diseases +MONDO:0019967 gard_rare diseases +MONDO:0019967 nord_rare diseases +MONDO:0019967 ordo_disorder diseases +MONDO:0019967 orphanet_rare diseases +MONDO:0019967 rare diseases +MONDO:0019969 gard_rare diseases +MONDO:0019969 nord_rare diseases +MONDO:0019969 ordo_disorder diseases +MONDO:0019969 orphanet_rare diseases +MONDO:0019969 rare diseases +MONDO:0019970 gard_rare diseases +MONDO:0019970 nord_rare diseases +MONDO:0019970 ordo_disorder diseases +MONDO:0019970 orphanet_rare diseases +MONDO:0019970 rare diseases +MONDO:0019971 gard_rare diseases +MONDO:0019971 nord_rare diseases +MONDO:0019971 ordo_disorder diseases +MONDO:0019971 orphanet_rare diseases +MONDO:0019971 rare diseases +MONDO:0019972 gard_rare diseases +MONDO:0019972 nord_rare diseases +MONDO:0019972 ordo_disorder diseases +MONDO:0019972 ordo_morphological_anomaly diseases +MONDO:0019972 orphanet_rare diseases +MONDO:0019972 rare diseases +MONDO:0019973 gard_rare diseases +MONDO:0019973 nord_rare diseases +MONDO:0019973 ordo_disorder diseases +MONDO:0019973 orphanet_rare diseases +MONDO:0019973 rare diseases +MONDO:0019975 clingen diseases +MONDO:0019975 gard_rare diseases +MONDO:0019975 nord_rare diseases +MONDO:0019975 ordo_disorder diseases +MONDO:0019975 orphanet_rare diseases +MONDO:0019975 rare diseases +MONDO:0019976 gard_rare diseases +MONDO:0019976 nord_rare diseases +MONDO:0019976 ordo_disorder diseases +MONDO:0019976 orphanet_rare diseases +MONDO:0019976 rare diseases +MONDO:0019977 gard_rare diseases +MONDO:0019977 nord_rare diseases +MONDO:0019977 ordo_disorder diseases +MONDO:0019977 orphanet_rare diseases +MONDO:0019977 rare diseases +MONDO:0019978 gard_rare diseases +MONDO:0019978 nord_rare diseases +MONDO:0019978 ordo_disorder diseases +MONDO:0019978 ordo_malformation_syndrome diseases +MONDO:0019978 orphanet_rare diseases +MONDO:0019978 otar diseases +MONDO:0019978 rare diseases +MONDO:0019979 gard_rare diseases +MONDO:0019979 nord_rare diseases +MONDO:0019979 ordo_subtype_of_a_disorder diseases +MONDO:0019979 rare diseases +MONDO:0019980 gard_rare diseases +MONDO:0019980 nord_rare diseases +MONDO:0019980 ordo_subtype_of_a_disorder diseases +MONDO:0019980 otar diseases +MONDO:0019980 rare diseases +MONDO:0019981 gard_rare diseases +MONDO:0019981 nord_rare diseases +MONDO:0019981 ordo_subtype_of_a_disorder diseases +MONDO:0019981 otar diseases +MONDO:0019981 rare diseases +MONDO:0019982 gard_rare diseases +MONDO:0019982 nord_rare diseases +MONDO:0019982 ordo_subtype_of_a_disorder diseases +MONDO:0019982 otar diseases +MONDO:0019982 rare diseases +MONDO:0019983 gard_rare diseases +MONDO:0019983 nord_rare diseases +MONDO:0019983 ordo_disorder diseases +MONDO:0019983 ordo_morphological_anomaly diseases +MONDO:0019983 orphanet_rare diseases +MONDO:0019983 rare diseases +MONDO:0019984 gard_rare diseases +MONDO:0019984 nord_rare diseases +MONDO:0019984 ordo_etiological_subtype diseases +MONDO:0019984 ordo_subtype_of_a_disorder diseases +MONDO:0019984 rare diseases +MONDO:0019985 gard_rare diseases +MONDO:0019985 nord_rare diseases +MONDO:0019985 ordo_etiological_subtype diseases +MONDO:0019985 ordo_subtype_of_a_disorder diseases +MONDO:0019985 rare diseases +MONDO:0019986 gard_rare diseases +MONDO:0019986 ordo_histopathological_subtype diseases +MONDO:0019986 rare diseases +MONDO:0019988 gard_rare diseases +MONDO:0019988 nord_rare diseases +MONDO:0019988 ordo_subtype_of_a_disorder diseases +MONDO:0019988 rare diseases +MONDO:0019989 gard_rare diseases +MONDO:0019989 nord_rare diseases +MONDO:0019989 ordo_subtype_of_a_disorder diseases +MONDO:0019989 rare diseases +MONDO:0019990 gard_rare diseases +MONDO:0019990 nord_rare diseases +MONDO:0019990 ordo_disorder diseases +MONDO:0019990 orphanet_rare diseases +MONDO:0019990 rare diseases +MONDO:0019991 gard_rare diseases +MONDO:0019991 nord_rare diseases +MONDO:0019991 ordo_disorder diseases +MONDO:0019991 orphanet_rare diseases +MONDO:0019991 rare diseases +MONDO:0019992 disease_grouping diseases +MONDO:0019992 gard_rare diseases +MONDO:0019992 nord_rare diseases +MONDO:0019992 ordo_group_of_disorders diseases +MONDO:0019992 otar diseases +MONDO:0019992 rare diseases +MONDO:0019993 gard_rare diseases +MONDO:0019993 nord_rare diseases +MONDO:0019993 ordo_disorder diseases +MONDO:0019993 orphanet_rare diseases +MONDO:0019993 rare diseases +MONDO:0019994 gard_rare diseases +MONDO:0019994 nord_rare diseases +MONDO:0019994 ordo_disorder diseases +MONDO:0019994 ordo_malformation_syndrome diseases +MONDO:0019994 orphanet_rare diseases +MONDO:0019994 rare diseases +MONDO:0019995 gard_rare diseases +MONDO:0019995 otar diseases +MONDO:0019995 rare diseases +MONDO:0020001 disease_grouping diseases +MONDO:0020001 gard_rare diseases +MONDO:0020001 ordo_group_of_disorders diseases +MONDO:0020001 rare diseases +MONDO:0020007 gard_rare diseases +MONDO:0020007 nord_rare diseases +MONDO:0020007 ordo_disorder diseases +MONDO:0020007 ordo_morphological_anomaly diseases +MONDO:0020007 orphanet_rare diseases +MONDO:0020007 rare diseases +MONDO:0020010 disease_grouping diseases +MONDO:0020010 ordo_group_of_disorders diseases +MONDO:0020010 otar diseases +MONDO:0020022 disease_grouping diseases +MONDO:0020022 gard_rare diseases +MONDO:0020022 ordo_group_of_disorders diseases +MONDO:0020022 otar diseases +MONDO:0020022 rare diseases +MONDO:0020040 disease_grouping diseases +MONDO:0020040 gard_rare diseases +MONDO:0020040 ordo_group_of_disorders diseases +MONDO:0020040 otar diseases +MONDO:0020040 rare diseases +MONDO:0020043 disease_grouping diseases +MONDO:0020043 gard_rare diseases +MONDO:0020043 nord_rare diseases +MONDO:0020043 ordo_group_of_disorders diseases +MONDO:0020043 otar diseases +MONDO:0020043 rare diseases +MONDO:0020044 disease_grouping diseases +MONDO:0020044 gard_rare diseases +MONDO:0020044 ordo_group_of_disorders diseases +MONDO:0020044 rare diseases +MONDO:0020046 disease_grouping diseases +MONDO:0020046 gard_rare diseases +MONDO:0020046 ordo_group_of_disorders diseases +MONDO:0020046 rare diseases +MONDO:0020047 disease_grouping diseases +MONDO:0020047 gard_rare diseases +MONDO:0020047 ordo_group_of_disorders diseases +MONDO:0020047 otar diseases +MONDO:0020047 rare diseases +MONDO:0020048 gard_rare diseases +MONDO:0020048 nord_rare diseases +MONDO:0020048 ordo_disorder diseases +MONDO:0020048 ordo_morphological_anomaly diseases +MONDO:0020048 orphanet_rare diseases +MONDO:0020048 rare diseases +MONDO:0020049 disease_grouping diseases +MONDO:0020049 gard_rare diseases +MONDO:0020049 ordo_group_of_disorders diseases +MONDO:0020049 rare diseases +MONDO:0020058 disease_grouping diseases +MONDO:0020058 ordo_group_of_disorders diseases +MONDO:0020064 disease_grouping diseases +MONDO:0020064 gard_rare diseases +MONDO:0020064 nord_rare diseases +MONDO:0020064 ordo_group_of_disorders diseases +MONDO:0020064 rare diseases +MONDO:0020065 disease_grouping diseases +MONDO:0020065 gard_rare diseases +MONDO:0020065 ordo_group_of_disorders diseases +MONDO:0020065 rare diseases +MONDO:0020066 disease_grouping diseases +MONDO:0020066 gard_rare diseases +MONDO:0020066 nord_rare diseases +MONDO:0020066 ordo_group_of_disorders diseases +MONDO:0020066 otar diseases +MONDO:0020066 rare diseases +MONDO:0020067 disease_grouping diseases +MONDO:0020067 gard_rare diseases +MONDO:0020067 otar diseases +MONDO:0020067 rare diseases +MONDO:0020068 disease_grouping diseases +MONDO:0020068 gard_rare diseases +MONDO:0020068 rare diseases +MONDO:0020070 disease_grouping diseases +MONDO:0020070 gard_rare diseases +MONDO:0020070 ordo_group_of_disorders diseases +MONDO:0020070 otar diseases +MONDO:0020070 rare diseases +MONDO:0020071 disease_grouping diseases +MONDO:0020071 gard_rare diseases +MONDO:0020071 ordo_group_of_disorders diseases +MONDO:0020071 otar diseases +MONDO:0020071 rare diseases +MONDO:0020072 clingen diseases +MONDO:0020072 disease_grouping diseases +MONDO:0020072 gard_rare diseases +MONDO:0020072 nord_rare diseases +MONDO:0020072 ordo_group_of_disorders diseases +MONDO:0020072 otar diseases +MONDO:0020072 rare diseases +MONDO:0020073 disease_grouping diseases +MONDO:0020073 gard_rare diseases +MONDO:0020073 ordo_group_of_disorders diseases +MONDO:0020073 rare diseases +MONDO:0020074 clingen diseases +MONDO:0020074 disease_grouping diseases +MONDO:0020074 gard_rare diseases +MONDO:0020074 nord_rare diseases +MONDO:0020074 ordo_group_of_disorders diseases +MONDO:0020074 otar diseases +MONDO:0020074 rare diseases +MONDO:0020076 disease_grouping diseases +MONDO:0020076 gard_rare diseases +MONDO:0020076 ordo_group_of_disorders diseases +MONDO:0020076 otar diseases +MONDO:0020076 rare diseases +MONDO:0020077 disease_grouping diseases +MONDO:0020077 gard_rare diseases +MONDO:0020077 ordo_group_of_disorders diseases +MONDO:0020077 otar diseases +MONDO:0020077 rare diseases +MONDO:0020082 disease_grouping diseases +MONDO:0020082 gard_rare diseases +MONDO:0020082 nord_rare diseases +MONDO:0020082 ordo_group_of_disorders diseases +MONDO:0020082 otar diseases +MONDO:0020082 rare diseases +MONDO:0020083 disease_grouping diseases +MONDO:0020083 gard_rare diseases +MONDO:0020083 ordo_group_of_disorders diseases +MONDO:0020083 rare diseases +MONDO:0020087 disease_grouping diseases +MONDO:0020087 gard_rare diseases +MONDO:0020087 ordo_group_of_disorders diseases +MONDO:0020087 otar diseases +MONDO:0020087 rare diseases +MONDO:0020088 disease_grouping diseases +MONDO:0020088 gard_rare diseases +MONDO:0020088 nord_rare diseases +MONDO:0020088 ordo_group_of_disorders diseases +MONDO:0020088 otar diseases +MONDO:0020088 rare diseases +MONDO:0020089 disease_grouping diseases +MONDO:0020089 gard_rare diseases +MONDO:0020089 ordo_group_of_disorders diseases +MONDO:0020089 otar diseases +MONDO:0020089 rare diseases +MONDO:0020099 disease_grouping diseases +MONDO:0020099 gard_rare diseases +MONDO:0020099 nord_rare diseases +MONDO:0020099 ordo_group_of_disorders diseases +MONDO:0020099 rare diseases +MONDO:0020102 disease_grouping diseases +MONDO:0020102 gard_rare diseases +MONDO:0020102 nord_rare diseases +MONDO:0020102 ordo_group_of_disorders diseases +MONDO:0020102 otar diseases +MONDO:0020102 rare diseases +MONDO:0020108 disease_grouping diseases +MONDO:0020108 gard_rare diseases +MONDO:0020108 nord_rare diseases +MONDO:0020108 ordo_group_of_disorders diseases +MONDO:0020108 otar diseases +MONDO:0020108 rare diseases +MONDO:0020110 gard_rare diseases +MONDO:0020110 nord_rare diseases +MONDO:0020110 ordo_disorder diseases +MONDO:0020110 ordo_morphological_anomaly diseases +MONDO:0020110 orphanet_rare diseases +MONDO:0020110 rare diseases +MONDO:0020112 disease_grouping diseases +MONDO:0020112 gard_rare diseases +MONDO:0020112 nord_rare diseases +MONDO:0020112 ordo_group_of_disorders diseases +MONDO:0020112 rare diseases +MONDO:0020113 disease_grouping diseases +MONDO:0020113 gard_rare diseases +MONDO:0020113 ordo_group_of_disorders diseases +MONDO:0020113 rare diseases +MONDO:0020115 disease_grouping diseases +MONDO:0020115 gard_rare diseases +MONDO:0020115 nord_rare diseases +MONDO:0020115 ordo_group_of_disorders diseases +MONDO:0020115 otar diseases +MONDO:0020115 rare diseases +MONDO:0020117 disease_grouping diseases +MONDO:0020117 gard_rare diseases +MONDO:0020117 ordo_group_of_disorders diseases +MONDO:0020117 rare diseases +MONDO:0020119 clingen diseases +MONDO:0020119 disease_grouping diseases +MONDO:0020119 otar diseases +MONDO:0020120 disease_grouping diseases +MONDO:0020120 ordo_group_of_disorders diseases +MONDO:0020120 otar diseases +MONDO:0020121 disease_grouping diseases +MONDO:0020121 gard_rare diseases +MONDO:0020121 ordo_group_of_disorders diseases +MONDO:0020121 otar diseases +MONDO:0020121 rare diseases +MONDO:0020122 disease_grouping diseases +MONDO:0020122 gard_rare diseases +MONDO:0020122 ordo_group_of_disorders diseases +MONDO:0020122 otar diseases +MONDO:0020122 rare diseases +MONDO:0020123 disease_grouping diseases +MONDO:0020123 gard_rare diseases +MONDO:0020123 ordo_group_of_disorders diseases +MONDO:0020123 otar diseases +MONDO:0020123 rare diseases +MONDO:0020124 disease_grouping diseases +MONDO:0020124 gard_rare diseases +MONDO:0020124 ordo_group_of_disorders diseases +MONDO:0020124 otar diseases +MONDO:0020124 rare diseases +MONDO:0020127 clingen diseases +MONDO:0020127 disease_grouping diseases +MONDO:0020127 gard_rare diseases +MONDO:0020127 ordo_group_of_disorders diseases +MONDO:0020127 otar diseases +MONDO:0020127 rare diseases +MONDO:0020128 disease_grouping diseases +MONDO:0020128 gard_rare diseases +MONDO:0020128 ordo_group_of_disorders diseases +MONDO:0020128 otar diseases +MONDO:0020128 rare diseases +MONDO:0020129 disease_grouping diseases +MONDO:0020129 gard_rare diseases +MONDO:0020129 ordo_group_of_disorders diseases +MONDO:0020129 rare diseases +MONDO:0020134 disease_grouping diseases +MONDO:0020134 gard_rare diseases +MONDO:0020134 rare diseases +MONDO:0020135 disease_grouping diseases +MONDO:0020135 gard_rare diseases +MONDO:0020135 nord_rare diseases +MONDO:0020135 ordo_group_of_disorders diseases +MONDO:0020135 otar diseases +MONDO:0020135 rare diseases +MONDO:0020143 disease_grouping diseases +MONDO:0020143 gard_rare diseases +MONDO:0020143 ordo_group_of_disorders diseases +MONDO:0020143 otar diseases +MONDO:0020143 rare diseases +MONDO:0020153 disease_grouping diseases +MONDO:0020153 gard_rare diseases +MONDO:0020153 ordo_group_of_disorders diseases +MONDO:0020153 otar diseases +MONDO:0020153 rare diseases +MONDO:0020159 disease_grouping diseases +MONDO:0020161 disease_grouping diseases +MONDO:0020161 gard_rare diseases +MONDO:0020161 nord_rare diseases +MONDO:0020161 ordo_group_of_disorders diseases +MONDO:0020161 rare diseases +MONDO:0020172 disease_grouping diseases +MONDO:0020173 disease_grouping diseases +MONDO:0020175 disease_grouping diseases +MONDO:0020175 obsoletion_candidate diseases +MONDO:0020179 disease_grouping diseases +MONDO:0020179 otar diseases +MONDO:0020204 disease_grouping diseases +MONDO:0020204 otar diseases +MONDO:0020212 disease_grouping diseases +MONDO:0020212 nord_rare diseases +MONDO:0020212 ordo_group_of_disorders diseases +MONDO:0020212 otar diseases +MONDO:0020212 rare diseases +MONDO:0020213 disease_grouping diseases +MONDO:0020213 gard_rare diseases +MONDO:0020213 nord_rare diseases +MONDO:0020213 ordo_group_of_disorders diseases +MONDO:0020213 otar diseases +MONDO:0020213 rare diseases +MONDO:0020214 disease_grouping diseases +MONDO:0020214 gard_rare diseases +MONDO:0020214 nord_rare diseases +MONDO:0020214 ordo_group_of_disorders diseases +MONDO:0020214 otar diseases +MONDO:0020214 rare diseases +MONDO:0020242 disease_grouping diseases +MONDO:0020242 gard_rare diseases +MONDO:0020242 otar diseases +MONDO:0020242 rare diseases +MONDO:0020246 disease_grouping diseases +MONDO:0020246 gard_rare diseases +MONDO:0020246 ordo_group_of_disorders diseases +MONDO:0020246 rare diseases +MONDO:0020247 disease_grouping diseases +MONDO:0020247 gard_rare diseases +MONDO:0020247 otar diseases +MONDO:0020247 rare diseases +MONDO:0020248 disease_grouping diseases +MONDO:0020248 gard_rare diseases +MONDO:0020248 otar diseases +MONDO:0020248 rare diseases +MONDO:0020249 disease_grouping diseases +MONDO:0020249 gard_rare diseases +MONDO:0020249 ordo_group_of_disorders diseases +MONDO:0020249 otar diseases +MONDO:0020249 rare diseases +MONDO:0020250 disease_grouping diseases +MONDO:0020250 gard_rare diseases +MONDO:0020250 ordo_group_of_disorders diseases +MONDO:0020250 otar diseases +MONDO:0020250 rare diseases +MONDO:0020257 disease_grouping diseases +MONDO:0020257 gard_rare diseases +MONDO:0020257 ordo_group_of_disorders diseases +MONDO:0020257 otar diseases +MONDO:0020257 rare diseases +MONDO:0020283 disease_grouping diseases +MONDO:0020283 gard_rare diseases +MONDO:0020283 ordo_group_of_disorders diseases +MONDO:0020283 otar diseases +MONDO:0020283 rare diseases +MONDO:0020289 disease_grouping diseases +MONDO:0020289 gard_rare diseases +MONDO:0020289 nord_rare diseases +MONDO:0020289 ordo_group_of_disorders diseases +MONDO:0020289 rare diseases +MONDO:0020290 disease_grouping diseases +MONDO:0020290 gard_rare diseases +MONDO:0020290 nord_rare diseases +MONDO:0020290 ordo_group_of_disorders diseases +MONDO:0020290 otar diseases +MONDO:0020290 rare diseases +MONDO:0020291 disease_grouping diseases +MONDO:0020291 gard_rare diseases +MONDO:0020291 nord_rare diseases +MONDO:0020291 ordo_group_of_disorders diseases +MONDO:0020291 rare diseases +MONDO:0020292 disease_grouping diseases +MONDO:0020292 gard_rare diseases +MONDO:0020292 ordo_group_of_disorders diseases +MONDO:0020292 otar diseases +MONDO:0020292 rare diseases +MONDO:0020295 disease_grouping diseases +MONDO:0020295 gard_rare diseases +MONDO:0020295 ordo_group_of_disorders diseases +MONDO:0020295 rare diseases +MONDO:0020296 disease_grouping diseases +MONDO:0020296 gard_rare diseases +MONDO:0020296 ordo_group_of_disorders diseases +MONDO:0020296 rare diseases +MONDO:0020297 disease_grouping diseases +MONDO:0020297 gard_rare diseases +MONDO:0020297 ordo_group_of_disorders diseases +MONDO:0020297 otar diseases +MONDO:0020297 rare diseases +MONDO:0020298 gard_rare diseases +MONDO:0020298 nord_rare diseases +MONDO:0020298 ordo_etiological_subtype diseases +MONDO:0020298 ordo_subtype_of_a_disorder diseases +MONDO:0020298 otar diseases +MONDO:0020298 rare diseases +MONDO:0020300 gard_rare diseases +MONDO:0020300 nord_rare diseases +MONDO:0020300 ordo_disorder diseases +MONDO:0020300 orphanet_rare diseases +MONDO:0020300 otar diseases +MONDO:0020300 rare diseases +MONDO:0020301 gard_rare diseases +MONDO:0020301 nord_rare diseases +MONDO:0020301 ordo_etiological_subtype diseases +MONDO:0020301 ordo_subtype_of_a_disorder diseases +MONDO:0020301 otar diseases +MONDO:0020301 rare diseases +MONDO:0020302 gard_rare diseases +MONDO:0020302 nord_rare diseases +MONDO:0020302 ordo_etiological_subtype diseases +MONDO:0020302 ordo_subtype_of_a_disorder diseases +MONDO:0020302 otar diseases +MONDO:0020302 rare diseases +MONDO:0020303 gard_rare diseases +MONDO:0020303 nord_rare diseases +MONDO:0020303 ordo_etiological_subtype diseases +MONDO:0020303 ordo_subtype_of_a_disorder diseases +MONDO:0020303 otar diseases +MONDO:0020303 rare diseases +MONDO:0020304 gard_rare diseases +MONDO:0020304 nord_rare diseases +MONDO:0020304 ordo_disorder diseases +MONDO:0020304 ordo_malformation_syndrome diseases +MONDO:0020304 orphanet_rare diseases +MONDO:0020304 otar diseases +MONDO:0020304 rare diseases +MONDO:0020305 gard_rare diseases +MONDO:0020305 nord_rare diseases +MONDO:0020305 ordo_disorder diseases +MONDO:0020305 ordo_malformation_syndrome diseases +MONDO:0020305 orphanet_rare diseases +MONDO:0020305 otar diseases +MONDO:0020305 rare diseases +MONDO:0020307 gard_rare diseases +MONDO:0020307 nord_rare diseases +MONDO:0020307 ordo_subtype_of_a_disorder diseases +MONDO:0020307 otar diseases +MONDO:0020307 rare diseases +MONDO:0020308 gard_rare diseases +MONDO:0020308 nord_rare diseases +MONDO:0020308 ordo_subtype_of_a_disorder diseases +MONDO:0020308 rare diseases +MONDO:0020310 gard_rare diseases +MONDO:0020310 nord_rare diseases +MONDO:0020310 ordo_disorder diseases +MONDO:0020310 orphanet_rare diseases +MONDO:0020310 otar diseases +MONDO:0020310 prototype_pattern diseases +MONDO:0020310 rare diseases +MONDO:0020311 gard_rare diseases +MONDO:0020311 nord_rare diseases +MONDO:0020311 ordo_disorder diseases +MONDO:0020311 orphanet_rare diseases +MONDO:0020311 otar diseases +MONDO:0020311 rare diseases +MONDO:0020316 gard_rare diseases +MONDO:0020316 nord_rare diseases +MONDO:0020316 ordo_disorder diseases +MONDO:0020316 orphanet_rare diseases +MONDO:0020316 rare diseases +MONDO:0020317 gard_rare diseases +MONDO:0020317 nord_rare diseases +MONDO:0020317 ordo_disorder diseases +MONDO:0020317 orphanet_rare diseases +MONDO:0020317 rare diseases +MONDO:0020320 gard_rare diseases +MONDO:0020320 nord_rare diseases +MONDO:0020320 ordo_disorder diseases +MONDO:0020320 orphanet_rare diseases +MONDO:0020320 otar diseases +MONDO:0020320 rare diseases +MONDO:0020321 gard_rare diseases +MONDO:0020321 nord_rare diseases +MONDO:0020321 ordo_disorder diseases +MONDO:0020321 orphanet_rare diseases +MONDO:0020321 rare diseases +MONDO:0020322 gard_rare diseases +MONDO:0020322 nord_rare diseases +MONDO:0020322 otar diseases +MONDO:0020322 rare diseases +MONDO:0020323 gard_rare diseases +MONDO:0020323 nord_rare diseases +MONDO:0020323 ordo_disorder diseases +MONDO:0020323 orphanet_rare diseases +MONDO:0020323 rare diseases +MONDO:0020324 gard_rare diseases +MONDO:0020324 nord_rare diseases +MONDO:0020324 ordo_disorder diseases +MONDO:0020324 orphanet_rare diseases +MONDO:0020324 rare diseases +MONDO:0020325 gard_rare diseases +MONDO:0020325 nord_rare diseases +MONDO:0020325 ordo_disorder diseases +MONDO:0020325 orphanet_rare diseases +MONDO:0020325 otar diseases +MONDO:0020325 rare diseases +MONDO:0020326 gard_rare diseases +MONDO:0020326 nord_rare diseases +MONDO:0020326 ordo_disorder diseases +MONDO:0020326 orphanet_rare diseases +MONDO:0020326 rare diseases +MONDO:0020331 gard_rare diseases +MONDO:0020331 nord_rare diseases +MONDO:0020331 ordo_disorder diseases +MONDO:0020331 orphanet_rare diseases +MONDO:0020331 rare diseases +MONDO:0020332 gard_rare diseases +MONDO:0020332 nord_rare diseases +MONDO:0020332 ordo_disorder diseases +MONDO:0020332 orphanet_rare diseases +MONDO:0020332 otar diseases +MONDO:0020332 rare diseases +MONDO:0020333 gard_rare diseases +MONDO:0020333 nord_rare diseases +MONDO:0020333 ordo_disorder diseases +MONDO:0020333 orphanet_rare diseases +MONDO:0020333 rare diseases +MONDO:0020334 disease_grouping diseases +MONDO:0020334 gard_rare diseases +MONDO:0020334 nord_rare diseases +MONDO:0020334 ordo_disorder diseases +MONDO:0020334 orphanet_rare diseases +MONDO:0020334 otar diseases +MONDO:0020334 rare diseases +MONDO:0020336 gard_rare diseases +MONDO:0020336 nord_rare diseases +MONDO:0020336 ordo_etiological_subtype diseases +MONDO:0020336 ordo_subtype_of_a_disorder diseases +MONDO:0020336 otar diseases +MONDO:0020336 rare diseases +MONDO:0020337 gard_rare diseases +MONDO:0020337 nord_rare diseases +MONDO:0020337 ordo_disorder diseases +MONDO:0020337 orphanet_rare diseases +MONDO:0020337 otar diseases +MONDO:0020337 rare diseases +MONDO:0020338 gard_rare diseases +MONDO:0020338 nord_rare diseases +MONDO:0020338 ordo_disorder diseases +MONDO:0020338 orphanet_rare diseases +MONDO:0020338 rare diseases +MONDO:0020340 gard_rare diseases +MONDO:0020340 nord_rare diseases +MONDO:0020340 ordo_subtype_of_a_disorder diseases +MONDO:0020340 otar diseases +MONDO:0020340 rare diseases +MONDO:0020341 clingen diseases +MONDO:0020341 gard_rare diseases +MONDO:0020341 nord_rare diseases +MONDO:0020341 ordo_subtype_of_a_disorder diseases +MONDO:0020341 otar diseases +MONDO:0020341 rare diseases +MONDO:0020344 gard_rare diseases +MONDO:0020344 nord_rare diseases +MONDO:0020344 ordo_etiological_subtype diseases +MONDO:0020344 ordo_subtype_of_a_disorder diseases +MONDO:0020344 otar diseases +MONDO:0020344 rare diseases +MONDO:0020347 gard_rare diseases +MONDO:0020347 nord_rare diseases +MONDO:0020347 ordo_disorder diseases +MONDO:0020347 orphanet_rare diseases +MONDO:0020347 rare diseases +MONDO:0020348 gard_rare diseases +MONDO:0020348 nord_rare diseases +MONDO:0020348 ordo_disorder diseases +MONDO:0020348 orphanet_rare diseases +MONDO:0020348 rare diseases +MONDO:0020349 gard_rare diseases +MONDO:0020349 nord_rare diseases +MONDO:0020349 ordo_disorder diseases +MONDO:0020349 orphanet_rare diseases +MONDO:0020349 rare diseases +MONDO:0020351 gard_rare diseases +MONDO:0020351 nord_rare diseases +MONDO:0020351 ordo_disorder diseases +MONDO:0020351 ordo_morphological_anomaly diseases +MONDO:0020351 orphanet_rare diseases +MONDO:0020351 rare diseases +MONDO:0020352 gard_rare diseases +MONDO:0020352 nord_rare diseases +MONDO:0020352 ordo_subtype_of_a_disorder diseases +MONDO:0020352 rare diseases +MONDO:0020353 gard_rare diseases +MONDO:0020353 ordo_malformation_syndrome diseases +MONDO:0020353 rare diseases +MONDO:0020354 gard_rare diseases +MONDO:0020354 nord_rare diseases +MONDO:0020354 ordo_disorder diseases +MONDO:0020354 ordo_morphological_anomaly diseases +MONDO:0020354 orphanet_rare diseases +MONDO:0020354 otar diseases +MONDO:0020354 rare diseases +MONDO:0020355 gard_rare diseases +MONDO:0020355 nord_rare diseases +MONDO:0020355 ordo_disorder diseases +MONDO:0020355 ordo_morphological_anomaly diseases +MONDO:0020355 orphanet_rare diseases +MONDO:0020355 otar diseases +MONDO:0020355 rare diseases +MONDO:0020356 gard_rare diseases +MONDO:0020356 ordo_disorder diseases +MONDO:0020356 ordo_morphological_anomaly diseases +MONDO:0020356 orphanet_rare diseases +MONDO:0020356 otar diseases +MONDO:0020356 rare diseases +MONDO:0020357 gard_rare diseases +MONDO:0020357 nord_rare diseases +MONDO:0020357 ordo_disorder diseases +MONDO:0020357 ordo_morphological_anomaly diseases +MONDO:0020357 orphanet_rare diseases +MONDO:0020357 otar diseases +MONDO:0020357 rare diseases +MONDO:0020359 gard_rare diseases +MONDO:0020359 nord_rare diseases +MONDO:0020359 ordo_subtype_of_a_disorder diseases +MONDO:0020359 rare diseases +MONDO:0020360 gard_rare diseases +MONDO:0020360 nord_rare diseases +MONDO:0020360 ordo_subtype_of_a_disorder diseases +MONDO:0020360 otar diseases +MONDO:0020360 rare diseases +MONDO:0020361 gard_rare diseases +MONDO:0020361 nord_rare diseases +MONDO:0020361 ordo_subtype_of_a_disorder diseases +MONDO:0020361 rare diseases +MONDO:0020362 gard_rare diseases +MONDO:0020362 nord_rare diseases +MONDO:0020362 ordo_subtype_of_a_disorder diseases +MONDO:0020362 rare diseases +MONDO:0020363 gard_rare diseases +MONDO:0020363 nord_rare diseases +MONDO:0020363 ordo_disorder diseases +MONDO:0020363 orphanet_rare diseases +MONDO:0020363 rare diseases +MONDO:0020364 gard_rare diseases +MONDO:0020364 nord_rare diseases +MONDO:0020364 ordo_disorder diseases +MONDO:0020364 orphanet_rare diseases +MONDO:0020364 otar diseases +MONDO:0020364 rare diseases +MONDO:0020365 gard_rare diseases +MONDO:0020365 nord_rare diseases +MONDO:0020365 ordo_disorder diseases +MONDO:0020365 orphanet_rare diseases +MONDO:0020365 otar diseases +MONDO:0020365 rare diseases +MONDO:0020366 gard_rare diseases +MONDO:0020366 nord_rare diseases +MONDO:0020366 otar diseases +MONDO:0020366 rare diseases +MONDO:0020367 gard_rare diseases +MONDO:0020367 nord_rare diseases +MONDO:0020367 ordo_disorder diseases +MONDO:0020367 orphanet_rare diseases +MONDO:0020367 otar diseases +MONDO:0020367 rare diseases +MONDO:0020368 gard_rare diseases +MONDO:0020368 ordo_disorder diseases +MONDO:0020368 ordo_morphological_anomaly diseases +MONDO:0020368 orphanet_rare diseases +MONDO:0020368 otar diseases +MONDO:0020368 rare diseases +MONDO:0020369 gard_rare diseases +MONDO:0020369 nord_rare diseases +MONDO:0020369 ordo_subtype_of_a_disorder diseases +MONDO:0020369 otar diseases +MONDO:0020369 rare diseases +MONDO:0020370 gard_rare diseases +MONDO:0020370 nord_rare diseases +MONDO:0020370 ordo_subtype_of_a_disorder diseases +MONDO:0020370 rare diseases +MONDO:0020371 gard_rare diseases +MONDO:0020371 nord_rare diseases +MONDO:0020371 ordo_subtype_of_a_disorder diseases +MONDO:0020371 rare diseases +MONDO:0020372 gard_rare diseases +MONDO:0020372 nord_rare diseases +MONDO:0020372 ordo_subtype_of_a_disorder diseases +MONDO:0020372 otar diseases +MONDO:0020372 rare diseases +MONDO:0020373 gard_rare diseases +MONDO:0020373 nord_rare diseases +MONDO:0020373 ordo_subtype_of_a_disorder diseases +MONDO:0020373 otar diseases +MONDO:0020373 rare diseases +MONDO:0020374 gard_rare diseases +MONDO:0020374 nord_rare diseases +MONDO:0020374 ordo_subtype_of_a_disorder diseases +MONDO:0020374 otar diseases +MONDO:0020374 rare diseases +MONDO:0020376 gard_rare diseases +MONDO:0020376 nord_rare diseases +MONDO:0020376 ordo_subtype_of_a_disorder diseases +MONDO:0020376 otar diseases +MONDO:0020376 rare diseases +MONDO:0020377 gard_rare diseases +MONDO:0020377 nord_rare diseases +MONDO:0020377 ordo_subtype_of_a_disorder diseases +MONDO:0020377 rare diseases +MONDO:0020378 gard_rare diseases +MONDO:0020378 nord_rare diseases +MONDO:0020378 ordo_subtype_of_a_disorder diseases +MONDO:0020378 otar diseases +MONDO:0020378 rare diseases +MONDO:0020379 gard_rare diseases +MONDO:0020379 nord_rare diseases +MONDO:0020379 ordo_subtype_of_a_disorder diseases +MONDO:0020379 otar diseases +MONDO:0020379 rare diseases +MONDO:0020380 disease_grouping diseases +MONDO:0020380 gard_rare diseases +MONDO:0020380 nord_rare diseases +MONDO:0020380 ordo_group_of_disorders diseases +MONDO:0020380 otar diseases +MONDO:0020380 rare diseases +MONDO:0020381 gard_rare diseases +MONDO:0020381 otar diseases +MONDO:0020381 rare diseases +MONDO:0020382 gard_rare diseases +MONDO:0020382 nord_rare diseases +MONDO:0020382 ordo_disorder diseases +MONDO:0020382 orphanet_rare diseases +MONDO:0020382 otar diseases +MONDO:0020382 rare diseases +MONDO:0020383 gard_rare diseases +MONDO:0020383 nord_rare diseases +MONDO:0020383 ordo_disorder diseases +MONDO:0020383 orphanet_rare diseases +MONDO:0020383 rare diseases +MONDO:0020384 gard_rare diseases +MONDO:0020384 otar diseases +MONDO:0020384 rare diseases +MONDO:0020385 gard_rare diseases +MONDO:0020385 ordo_subtype_of_a_disorder diseases +MONDO:0020385 rare diseases +MONDO:0020386 gard_rare diseases +MONDO:0020386 nord_rare diseases +MONDO:0020386 ordo_subtype_of_a_disorder diseases +MONDO:0020386 rare diseases +MONDO:0020387 gard_rare diseases +MONDO:0020387 nord_rare diseases +MONDO:0020387 ordo_subtype_of_a_disorder diseases +MONDO:0020387 rare diseases +MONDO:0020388 gard_rare diseases +MONDO:0020388 nord_rare diseases +MONDO:0020388 ordo_subtype_of_a_disorder diseases +MONDO:0020388 rare diseases +MONDO:0020389 gard_rare diseases +MONDO:0020389 nord_rare diseases +MONDO:0020389 ordo_disorder diseases +MONDO:0020389 ordo_malformation_syndrome diseases +MONDO:0020389 orphanet_rare diseases +MONDO:0020389 rare diseases +MONDO:0020390 gard_rare diseases +MONDO:0020390 nord_rare diseases +MONDO:0020390 ordo_disorder diseases +MONDO:0020390 ordo_morphological_anomaly diseases +MONDO:0020390 orphanet_rare diseases +MONDO:0020390 rare diseases +MONDO:0020391 gard_rare diseases +MONDO:0020391 nord_rare diseases +MONDO:0020391 ordo_disorder diseases +MONDO:0020391 ordo_morphological_anomaly diseases +MONDO:0020391 orphanet_rare diseases +MONDO:0020391 rare diseases +MONDO:0020393 gard_rare diseases +MONDO:0020393 nord_rare diseases +MONDO:0020393 ordo_subtype_of_a_disorder diseases +MONDO:0020393 rare diseases +MONDO:0020394 gard_rare diseases +MONDO:0020394 nord_rare diseases +MONDO:0020394 ordo_subtype_of_a_disorder diseases +MONDO:0020394 rare diseases +MONDO:0020395 gard_rare diseases +MONDO:0020395 nord_rare diseases +MONDO:0020395 ordo_subtype_of_a_disorder diseases +MONDO:0020395 rare diseases +MONDO:0020396 gard_rare diseases +MONDO:0020396 nord_rare diseases +MONDO:0020396 ordo_disorder diseases +MONDO:0020396 ordo_morphological_anomaly diseases +MONDO:0020396 orphanet_rare diseases +MONDO:0020396 rare diseases +MONDO:0020397 gard_rare diseases +MONDO:0020397 nord_rare diseases +MONDO:0020397 ordo_disorder diseases +MONDO:0020397 ordo_morphological_anomaly diseases +MONDO:0020397 orphanet_rare diseases +MONDO:0020397 rare diseases +MONDO:0020398 gard_rare diseases +MONDO:0020398 nord_rare diseases +MONDO:0020398 ordo_disorder diseases +MONDO:0020398 ordo_morphological_anomaly diseases +MONDO:0020398 orphanet_rare diseases +MONDO:0020398 rare diseases +MONDO:0020399 gard_rare diseases +MONDO:0020399 nord_rare diseases +MONDO:0020399 ordo_disorder diseases +MONDO:0020399 ordo_morphological_anomaly diseases +MONDO:0020399 orphanet_rare diseases +MONDO:0020399 rare diseases +MONDO:0020400 gard_rare diseases +MONDO:0020400 nord_rare diseases +MONDO:0020400 ordo_disorder diseases +MONDO:0020400 ordo_morphological_anomaly diseases +MONDO:0020400 orphanet_rare diseases +MONDO:0020400 rare diseases +MONDO:0020401 gard_rare diseases +MONDO:0020401 nord_rare diseases +MONDO:0020401 ordo_disorder diseases +MONDO:0020401 ordo_morphological_anomaly diseases +MONDO:0020401 orphanet_rare diseases +MONDO:0020401 rare diseases +MONDO:0020402 gard_rare diseases +MONDO:0020402 nord_rare diseases +MONDO:0020402 ordo_disorder diseases +MONDO:0020402 ordo_morphological_anomaly diseases +MONDO:0020402 orphanet_rare diseases +MONDO:0020402 rare diseases +MONDO:0020403 gard_rare diseases +MONDO:0020403 nord_rare diseases +MONDO:0020403 ordo_disorder diseases +MONDO:0020403 ordo_morphological_anomaly diseases +MONDO:0020403 orphanet_rare diseases +MONDO:0020403 rare diseases +MONDO:0020404 gard_rare diseases +MONDO:0020404 nord_rare diseases +MONDO:0020404 ordo_disorder diseases +MONDO:0020404 ordo_malformation_syndrome diseases +MONDO:0020404 orphanet_rare diseases +MONDO:0020404 otar diseases +MONDO:0020404 rare diseases +MONDO:0020405 gard_rare diseases +MONDO:0020405 nord_rare diseases +MONDO:0020405 ordo_subtype_of_a_disorder diseases +MONDO:0020405 rare diseases +MONDO:0020406 gard_rare diseases +MONDO:0020406 rare diseases +MONDO:0020407 gard_rare diseases +MONDO:0020407 nord_rare diseases +MONDO:0020407 ordo_subtype_of_a_disorder diseases +MONDO:0020407 rare diseases +MONDO:0020408 gard_rare diseases +MONDO:0020408 nord_rare diseases +MONDO:0020408 ordo_subtype_of_a_disorder diseases +MONDO:0020408 rare diseases +MONDO:0020409 gard_rare diseases +MONDO:0020409 nord_rare diseases +MONDO:0020409 rare diseases +MONDO:0020410 gard_rare diseases +MONDO:0020410 nord_rare diseases +MONDO:0020410 ordo_subtype_of_a_disorder diseases +MONDO:0020410 rare diseases +MONDO:0020411 gard_rare diseases +MONDO:0020411 nord_rare diseases +MONDO:0020411 ordo_subtype_of_a_disorder diseases +MONDO:0020411 rare diseases +MONDO:0020412 gard_rare diseases +MONDO:0020412 nord_rare diseases +MONDO:0020412 ordo_disorder diseases +MONDO:0020412 ordo_morphological_anomaly diseases +MONDO:0020412 orphanet_rare diseases +MONDO:0020412 rare diseases +MONDO:0020413 gard_rare diseases +MONDO:0020413 nord_rare diseases +MONDO:0020413 ordo_disorder diseases +MONDO:0020413 ordo_morphological_anomaly diseases +MONDO:0020413 orphanet_rare diseases +MONDO:0020413 rare diseases +MONDO:0020414 gard_rare diseases +MONDO:0020414 nord_rare diseases +MONDO:0020414 ordo_disorder diseases +MONDO:0020414 ordo_morphological_anomaly diseases +MONDO:0020414 orphanet_rare diseases +MONDO:0020414 rare diseases +MONDO:0020415 gard_rare diseases +MONDO:0020415 nord_rare diseases +MONDO:0020415 ordo_disorder diseases +MONDO:0020415 ordo_morphological_anomaly diseases +MONDO:0020415 orphanet_rare diseases +MONDO:0020415 rare diseases +MONDO:0020416 gard_rare diseases +MONDO:0020416 nord_rare diseases +MONDO:0020416 ordo_disorder diseases +MONDO:0020416 ordo_morphological_anomaly diseases +MONDO:0020416 orphanet_rare diseases +MONDO:0020416 rare diseases +MONDO:0020417 gard_rare diseases +MONDO:0020417 nord_rare diseases +MONDO:0020417 ordo_disorder diseases +MONDO:0020417 ordo_morphological_anomaly diseases +MONDO:0020417 orphanet_rare diseases +MONDO:0020417 rare diseases +MONDO:0020418 gard_rare diseases +MONDO:0020418 nord_rare diseases +MONDO:0020418 ordo_disorder diseases +MONDO:0020418 ordo_morphological_anomaly diseases +MONDO:0020418 orphanet_rare diseases +MONDO:0020418 rare diseases +MONDO:0020419 gard_rare diseases +MONDO:0020419 nord_rare diseases +MONDO:0020419 ordo_disorder diseases +MONDO:0020419 ordo_morphological_anomaly diseases +MONDO:0020419 orphanet_rare diseases +MONDO:0020419 rare diseases +MONDO:0020420 gard_rare diseases +MONDO:0020420 nord_rare diseases +MONDO:0020420 ordo_disorder diseases +MONDO:0020420 ordo_morphological_anomaly diseases +MONDO:0020420 orphanet_rare diseases +MONDO:0020420 rare diseases +MONDO:0020421 gard_rare diseases +MONDO:0020421 ordo_morphological_anomaly diseases +MONDO:0020421 rare diseases +MONDO:0020422 gard_rare diseases +MONDO:0020422 ordo_morphological_anomaly diseases +MONDO:0020422 rare diseases +MONDO:0020423 gard_rare diseases +MONDO:0020423 nord_rare diseases +MONDO:0020423 ordo_disorder diseases +MONDO:0020423 ordo_morphological_anomaly diseases +MONDO:0020423 orphanet_rare diseases +MONDO:0020423 rare diseases +MONDO:0020424 gard_rare diseases +MONDO:0020424 ordo_morphological_anomaly diseases +MONDO:0020424 rare diseases +MONDO:0020425 gard_rare diseases +MONDO:0020425 nord_rare diseases +MONDO:0020425 ordo_disorder diseases +MONDO:0020425 ordo_morphological_anomaly diseases +MONDO:0020425 orphanet_rare diseases +MONDO:0020425 rare diseases +MONDO:0020426 gard_rare diseases +MONDO:0020426 nord_rare diseases +MONDO:0020426 ordo_disorder diseases +MONDO:0020426 ordo_morphological_anomaly diseases +MONDO:0020426 orphanet_rare diseases +MONDO:0020426 rare diseases +MONDO:0020427 gard_rare diseases +MONDO:0020427 nord_rare diseases +MONDO:0020427 ordo_disorder diseases +MONDO:0020427 ordo_morphological_anomaly diseases +MONDO:0020427 orphanet_rare diseases +MONDO:0020427 otar diseases +MONDO:0020427 rare diseases +MONDO:0020428 gard_rare diseases +MONDO:0020428 nord_rare diseases +MONDO:0020428 ordo_disorder diseases +MONDO:0020428 ordo_morphological_anomaly diseases +MONDO:0020428 orphanet_rare diseases +MONDO:0020428 otar diseases +MONDO:0020428 rare diseases +MONDO:0020429 gard_rare diseases +MONDO:0020429 nord_rare diseases +MONDO:0020429 ordo_disorder diseases +MONDO:0020429 ordo_morphological_anomaly diseases +MONDO:0020429 orphanet_rare diseases +MONDO:0020429 rare diseases +MONDO:0020430 gard_rare diseases +MONDO:0020430 nord_rare diseases +MONDO:0020430 ordo_disorder diseases +MONDO:0020430 ordo_morphological_anomaly diseases +MONDO:0020430 orphanet_rare diseases +MONDO:0020430 rare diseases +MONDO:0020431 gard_rare diseases +MONDO:0020431 nord_rare diseases +MONDO:0020431 ordo_disorder diseases +MONDO:0020431 ordo_morphological_anomaly diseases +MONDO:0020431 orphanet_rare diseases +MONDO:0020431 rare diseases +MONDO:0020432 gard_rare diseases +MONDO:0020432 nord_rare diseases +MONDO:0020432 ordo_disorder diseases +MONDO:0020432 ordo_morphological_anomaly diseases +MONDO:0020432 orphanet_rare diseases +MONDO:0020432 rare diseases +MONDO:0020433 gard_rare diseases +MONDO:0020433 nord_rare diseases +MONDO:0020433 ordo_disorder diseases +MONDO:0020433 ordo_morphological_anomaly diseases +MONDO:0020433 orphanet_rare diseases +MONDO:0020433 rare diseases +MONDO:0020434 gard_rare diseases +MONDO:0020434 nord_rare diseases +MONDO:0020434 ordo_subtype_of_a_disorder diseases +MONDO:0020434 otar diseases +MONDO:0020434 rare diseases +MONDO:0020435 gard_rare diseases +MONDO:0020435 nord_rare diseases +MONDO:0020435 ordo_subtype_of_a_disorder diseases +MONDO:0020435 otar diseases +MONDO:0020435 rare diseases +MONDO:0020436 gard_rare diseases +MONDO:0020436 nord_rare diseases +MONDO:0020436 ordo_subtype_of_a_disorder diseases +MONDO:0020436 otar diseases +MONDO:0020436 rare diseases +MONDO:0020437 gard_rare diseases +MONDO:0020437 nord_rare diseases +MONDO:0020437 ordo_subtype_of_a_disorder diseases +MONDO:0020437 otar diseases +MONDO:0020437 rare diseases +MONDO:0020438 gard_rare diseases +MONDO:0020438 nord_rare diseases +MONDO:0020438 ordo_disorder diseases +MONDO:0020438 ordo_morphological_anomaly diseases +MONDO:0020438 orphanet_rare diseases +MONDO:0020438 rare diseases +MONDO:0020439 inferred_rare diseases +MONDO:0020439 ordo_morphological_anomaly diseases +MONDO:0020439 rare diseases +MONDO:0020440 gard_rare diseases +MONDO:0020440 nord_rare diseases +MONDO:0020440 ordo_disorder diseases +MONDO:0020440 ordo_morphological_anomaly diseases +MONDO:0020440 orphanet_rare diseases +MONDO:0020440 rare diseases +MONDO:0020441 gard_rare diseases +MONDO:0020441 nord_rare diseases +MONDO:0020441 ordo_disorder diseases +MONDO:0020441 ordo_morphological_anomaly diseases +MONDO:0020441 orphanet_rare diseases +MONDO:0020441 rare diseases +MONDO:0020442 gard_rare diseases +MONDO:0020442 nord_rare diseases +MONDO:0020442 ordo_disorder diseases +MONDO:0020442 ordo_morphological_anomaly diseases +MONDO:0020442 orphanet_rare diseases +MONDO:0020442 rare diseases +MONDO:0020443 gard_rare diseases +MONDO:0020443 nord_rare diseases +MONDO:0020443 ordo_disorder diseases +MONDO:0020443 ordo_morphological_anomaly diseases +MONDO:0020443 orphanet_rare diseases +MONDO:0020443 rare diseases +MONDO:0020444 gard_rare diseases +MONDO:0020444 nord_rare diseases +MONDO:0020444 ordo_disorder diseases +MONDO:0020444 ordo_morphological_anomaly diseases +MONDO:0020444 orphanet_rare diseases +MONDO:0020444 rare diseases +MONDO:0020445 gard_rare diseases +MONDO:0020445 nord_rare diseases +MONDO:0020445 ordo_disorder diseases +MONDO:0020445 ordo_morphological_anomaly diseases +MONDO:0020445 orphanet_rare diseases +MONDO:0020445 rare diseases +MONDO:0020446 gard_rare diseases +MONDO:0020446 nord_rare diseases +MONDO:0020446 ordo_disorder diseases +MONDO:0020446 ordo_morphological_anomaly diseases +MONDO:0020446 orphanet_rare diseases +MONDO:0020446 rare diseases +MONDO:0020447 gard_rare diseases +MONDO:0020447 nord_rare diseases +MONDO:0020447 ordo_disorder diseases +MONDO:0020447 ordo_morphological_anomaly diseases +MONDO:0020447 orphanet_rare diseases +MONDO:0020447 rare diseases +MONDO:0020448 gard_rare diseases +MONDO:0020448 nord_rare diseases +MONDO:0020448 ordo_disorder diseases +MONDO:0020448 ordo_morphological_anomaly diseases +MONDO:0020448 orphanet_rare diseases +MONDO:0020448 rare diseases +MONDO:0020449 gard_rare diseases +MONDO:0020449 nord_rare diseases +MONDO:0020449 ordo_disorder diseases +MONDO:0020449 ordo_morphological_anomaly diseases +MONDO:0020449 orphanet_rare diseases +MONDO:0020449 rare diseases +MONDO:0020450 gard_rare diseases +MONDO:0020450 nord_rare diseases +MONDO:0020450 ordo_disorder diseases +MONDO:0020450 ordo_morphological_anomaly diseases +MONDO:0020450 orphanet_rare diseases +MONDO:0020450 rare diseases +MONDO:0020451 gard_rare diseases +MONDO:0020451 nord_rare diseases +MONDO:0020451 ordo_disorder diseases +MONDO:0020451 ordo_morphological_anomaly diseases +MONDO:0020451 orphanet_rare diseases +MONDO:0020451 rare diseases +MONDO:0020452 gard_rare diseases +MONDO:0020452 nord_rare diseases +MONDO:0020452 ordo_disorder diseases +MONDO:0020452 ordo_morphological_anomaly diseases +MONDO:0020452 orphanet_rare diseases +MONDO:0020452 rare diseases +MONDO:0020453 gard_rare diseases +MONDO:0020453 nord_rare diseases +MONDO:0020453 ordo_disorder diseases +MONDO:0020453 ordo_morphological_anomaly diseases +MONDO:0020453 orphanet_rare diseases +MONDO:0020453 rare diseases +MONDO:0020454 gard_rare diseases +MONDO:0020454 nord_rare diseases +MONDO:0020454 ordo_disorder diseases +MONDO:0020454 ordo_morphological_anomaly diseases +MONDO:0020454 orphanet_rare diseases +MONDO:0020454 rare diseases +MONDO:0020455 gard_rare diseases +MONDO:0020455 nord_rare diseases +MONDO:0020455 ordo_disorder diseases +MONDO:0020455 ordo_morphological_anomaly diseases +MONDO:0020455 orphanet_rare diseases +MONDO:0020455 rare diseases +MONDO:0020456 gard_rare diseases +MONDO:0020456 nord_rare diseases +MONDO:0020456 ordo_disorder diseases +MONDO:0020456 ordo_morphological_anomaly diseases +MONDO:0020456 orphanet_rare diseases +MONDO:0020456 rare diseases +MONDO:0020457 gard_rare diseases +MONDO:0020457 nord_rare diseases +MONDO:0020457 ordo_disorder diseases +MONDO:0020457 orphanet_rare diseases +MONDO:0020457 rare diseases +MONDO:0020458 gard_rare diseases +MONDO:0020458 nord_rare diseases +MONDO:0020458 ordo_disorder diseases +MONDO:0020458 orphanet_rare diseases +MONDO:0020458 otar diseases +MONDO:0020458 rare diseases +MONDO:0020459 gard_rare diseases +MONDO:0020459 nord_rare diseases +MONDO:0020459 ordo_disorder diseases +MONDO:0020459 orphanet_rare diseases +MONDO:0020459 rare diseases +MONDO:0020460 gard_rare diseases +MONDO:0020460 nord_rare diseases +MONDO:0020460 ordo_disorder diseases +MONDO:0020460 orphanet_rare diseases +MONDO:0020460 otar diseases +MONDO:0020460 rare diseases +MONDO:0020461 gard_rare diseases +MONDO:0020461 nord_rare diseases +MONDO:0020461 ordo_disorder diseases +MONDO:0020461 ordo_morphological_anomaly diseases +MONDO:0020461 orphanet_rare diseases +MONDO:0020461 rare diseases +MONDO:0020462 gard_rare diseases +MONDO:0020462 nord_rare diseases +MONDO:0020462 ordo_disorder diseases +MONDO:0020462 ordo_morphological_anomaly diseases +MONDO:0020462 orphanet_rare diseases +MONDO:0020462 rare diseases +MONDO:0020463 gard_rare diseases +MONDO:0020463 nord_rare diseases +MONDO:0020463 ordo_disorder diseases +MONDO:0020463 ordo_morphological_anomaly diseases +MONDO:0020463 orphanet_rare diseases +MONDO:0020463 rare diseases +MONDO:0020464 gard_rare diseases +MONDO:0020464 nord_rare diseases +MONDO:0020464 ordo_disorder diseases +MONDO:0020464 ordo_morphological_anomaly diseases +MONDO:0020464 orphanet_rare diseases +MONDO:0020464 rare diseases +MONDO:0020465 gard_rare diseases +MONDO:0020465 nord_rare diseases +MONDO:0020465 ordo_disorder diseases +MONDO:0020465 ordo_morphological_anomaly diseases +MONDO:0020465 orphanet_rare diseases +MONDO:0020465 rare diseases +MONDO:0020466 gard_rare diseases +MONDO:0020466 nord_rare diseases +MONDO:0020466 ordo_etiological_subtype diseases +MONDO:0020466 ordo_subtype_of_a_disorder diseases +MONDO:0020466 otar diseases +MONDO:0020466 rare diseases +MONDO:0020467 gard_rare diseases +MONDO:0020467 nord_rare diseases +MONDO:0020467 ordo_etiological_subtype diseases +MONDO:0020467 ordo_subtype_of_a_disorder diseases +MONDO:0020467 otar diseases +MONDO:0020467 rare diseases +MONDO:0020468 gard_rare diseases +MONDO:0020468 nord_rare diseases +MONDO:0020468 ordo_disorder diseases +MONDO:0020468 ordo_malformation_syndrome diseases +MONDO:0020468 orphanet_rare diseases +MONDO:0020468 rare diseases +MONDO:0020469 gard_rare diseases +MONDO:0020469 nord_rare diseases +MONDO:0020469 ordo_disorder diseases +MONDO:0020469 ordo_malformation_syndrome diseases +MONDO:0020469 orphanet_rare diseases +MONDO:0020469 otar diseases +MONDO:0020469 rare diseases +MONDO:0020470 gard_rare diseases +MONDO:0020470 nord_rare diseases +MONDO:0020470 ordo_disorder diseases +MONDO:0020470 ordo_malformation_syndrome diseases +MONDO:0020470 orphanet_rare diseases +MONDO:0020470 otar diseases +MONDO:0020470 rare diseases +MONDO:0020472 gard_rare diseases +MONDO:0020472 nord_rare diseases +MONDO:0020472 ordo_etiological_subtype diseases +MONDO:0020472 ordo_subtype_of_a_disorder diseases +MONDO:0020472 otar diseases +MONDO:0020472 rare diseases +MONDO:0020473 gard_rare diseases +MONDO:0020473 rare diseases +MONDO:0020474 gard_rare diseases +MONDO:0020474 nord_rare diseases +MONDO:0020474 ordo_disorder diseases +MONDO:0020474 orphanet_rare diseases +MONDO:0020474 rare diseases +MONDO:0020475 gard_rare diseases +MONDO:0020475 nord_rare diseases +MONDO:0020475 ordo_disorder diseases +MONDO:0020475 ordo_malformation_syndrome diseases +MONDO:0020475 orphanet_rare diseases +MONDO:0020475 otar diseases +MONDO:0020475 rare diseases +MONDO:0020476 gard_rare diseases +MONDO:0020476 nord_rare diseases +MONDO:0020476 ordo_disorder diseases +MONDO:0020476 orphanet_rare diseases +MONDO:0020476 otar diseases +MONDO:0020476 rare diseases +MONDO:0020478 gard_rare diseases +MONDO:0020478 nord_rare diseases +MONDO:0020478 ordo_disorder diseases +MONDO:0020478 orphanet_rare diseases +MONDO:0020478 otar diseases +MONDO:0020478 rare diseases +MONDO:0020479 gard_rare diseases +MONDO:0020479 nord_rare diseases +MONDO:0020479 ordo_disorder diseases +MONDO:0020479 orphanet_rare diseases +MONDO:0020479 rare diseases +MONDO:0020480 gard_rare diseases +MONDO:0020480 nord_rare diseases +MONDO:0020480 ordo_subtype_of_a_disorder diseases +MONDO:0020480 otar diseases +MONDO:0020480 rare diseases +MONDO:0020481 gard_rare diseases +MONDO:0020481 nord_rare diseases +MONDO:0020481 ordo_disorder diseases +MONDO:0020481 orphanet_rare diseases +MONDO:0020481 otar diseases +MONDO:0020481 rare diseases +MONDO:0020482 gard_rare diseases +MONDO:0020482 nord_rare diseases +MONDO:0020482 ordo_disorder diseases +MONDO:0020482 orphanet_rare diseases +MONDO:0020482 otar diseases +MONDO:0020482 rare diseases +MONDO:0020483 gard_rare diseases +MONDO:0020483 nord_rare diseases +MONDO:0020483 ordo_disorder diseases +MONDO:0020483 orphanet_rare diseases +MONDO:0020483 otar diseases +MONDO:0020483 rare diseases +MONDO:0020485 gard_rare diseases +MONDO:0020485 nord_rare diseases +MONDO:0020485 ordo_disorder diseases +MONDO:0020485 ordo_malformation_syndrome diseases +MONDO:0020485 orphanet_rare diseases +MONDO:0020485 otar diseases +MONDO:0020485 rare diseases +MONDO:0020487 gard_rare diseases +MONDO:0020487 nord_rare diseases +MONDO:0020487 ordo_disorder diseases +MONDO:0020487 orphanet_rare diseases +MONDO:0020487 rare diseases +MONDO:0020488 gard_rare diseases +MONDO:0020488 nord_rare diseases +MONDO:0020488 ordo_subtype_of_a_disorder diseases +MONDO:0020488 otar diseases +MONDO:0020488 rare diseases +MONDO:0020490 gard_rare diseases +MONDO:0020490 nord_rare diseases +MONDO:0020490 ordo_disorder diseases +MONDO:0020490 ordo_malformation_syndrome diseases +MONDO:0020490 orphanet_rare diseases +MONDO:0020490 otar diseases +MONDO:0020490 rare diseases +MONDO:0020491 gard_rare diseases +MONDO:0020491 nord_rare diseases +MONDO:0020491 ordo_disorder diseases +MONDO:0020491 ordo_morphological_anomaly diseases +MONDO:0020491 orphanet_rare diseases +MONDO:0020491 otar diseases +MONDO:0020491 rare diseases +MONDO:0020492 gard_rare diseases +MONDO:0020492 nord_rare diseases +MONDO:0020492 ordo_disorder diseases +MONDO:0020492 ordo_malformation_syndrome diseases +MONDO:0020492 orphanet_rare diseases +MONDO:0020492 otar diseases +MONDO:0020492 rare diseases +MONDO:0020493 clingen diseases +MONDO:0020493 gard_rare diseases +MONDO:0020493 nord_rare diseases +MONDO:0020493 ordo_disorder diseases +MONDO:0020493 ordo_malformation_syndrome diseases +MONDO:0020493 orphanet_rare diseases +MONDO:0020493 otar diseases +MONDO:0020493 rare diseases +MONDO:0020494 gard_rare diseases +MONDO:0020494 nord_rare diseases +MONDO:0020494 ordo_disorder diseases +MONDO:0020494 ordo_malformation_syndrome diseases +MONDO:0020494 orphanet_rare diseases +MONDO:0020494 otar diseases +MONDO:0020494 rare diseases +MONDO:0020495 gard_rare diseases +MONDO:0020495 ordo_disorder diseases +MONDO:0020495 orphanet_rare diseases +MONDO:0020495 rare diseases +MONDO:0020496 gard_rare diseases +MONDO:0020496 ordo_etiological_subtype diseases +MONDO:0020496 ordo_subtype_of_a_disorder diseases +MONDO:0020496 otar diseases +MONDO:0020496 rare diseases +MONDO:0020497 gard_rare diseases +MONDO:0020497 nord_rare diseases +MONDO:0020497 ordo_subtype_of_a_disorder diseases +MONDO:0020497 otar diseases +MONDO:0020497 rare diseases +MONDO:0020499 gard_rare diseases +MONDO:0020499 nord_rare diseases +MONDO:0020499 ordo_disorder diseases +MONDO:0020499 orphanet_rare diseases +MONDO:0020499 rare diseases +MONDO:0020500 gard_rare diseases +MONDO:0020500 nord_rare diseases +MONDO:0020500 ordo_disorder diseases +MONDO:0020500 orphanet_rare diseases +MONDO:0020500 otar diseases +MONDO:0020500 rare diseases +MONDO:0020501 gard_rare diseases +MONDO:0020501 nord_rare diseases +MONDO:0020501 ordo_disorder diseases +MONDO:0020501 orphanet_rare diseases +MONDO:0020501 rare diseases +MONDO:0020502 gard_rare diseases +MONDO:0020502 nord_rare diseases +MONDO:0020502 ordo_disorder diseases +MONDO:0020502 orphanet_rare diseases +MONDO:0020502 rare diseases +MONDO:0020504 gard_rare diseases +MONDO:0020504 ordo_disorder diseases +MONDO:0020504 orphanet_rare diseases +MONDO:0020504 otar diseases +MONDO:0020504 rare diseases +MONDO:0020505 gard_rare diseases +MONDO:0020505 nord_rare diseases +MONDO:0020505 ordo_disorder diseases +MONDO:0020505 orphanet_rare diseases +MONDO:0020505 otar diseases +MONDO:0020505 rare diseases +MONDO:0020507 gard_rare diseases +MONDO:0020507 nord_rare diseases +MONDO:0020507 ordo_subtype_of_a_disorder diseases +MONDO:0020507 otar diseases +MONDO:0020507 rare diseases +MONDO:0020508 gard_rare diseases +MONDO:0020508 nord_rare diseases +MONDO:0020508 ordo_disorder diseases +MONDO:0020508 ordo_morphological_anomaly diseases +MONDO:0020508 orphanet_rare diseases +MONDO:0020508 rare diseases +MONDO:0020509 gard_rare diseases +MONDO:0020509 nord_rare diseases +MONDO:0020509 ordo_disorder diseases +MONDO:0020509 orphanet_rare diseases +MONDO:0020509 rare diseases +MONDO:0020510 gard_rare diseases +MONDO:0020510 mondo_rare diseases +MONDO:0020510 nord_rare diseases +MONDO:0020510 ordo_subtype_of_a_disorder diseases +MONDO:0020510 rare diseases +MONDO:0020511 gard_rare diseases +MONDO:0020511 nord_rare diseases +MONDO:0020511 ordo_disorder diseases +MONDO:0020511 orphanet_rare diseases +MONDO:0020511 otar diseases +MONDO:0020511 rare diseases +MONDO:0020512 gard_rare diseases +MONDO:0020512 nord_rare diseases +MONDO:0020512 ordo_disorder diseases +MONDO:0020512 orphanet_rare diseases +MONDO:0020512 otar diseases +MONDO:0020512 rare diseases +MONDO:0020513 gard_rare diseases +MONDO:0020513 nord_rare diseases +MONDO:0020513 ordo_disorder diseases +MONDO:0020513 orphanet_rare diseases +MONDO:0020513 otar diseases +MONDO:0020513 rare diseases +MONDO:0020516 gard_rare diseases +MONDO:0020516 nord_rare diseases +MONDO:0020516 ordo_disorder diseases +MONDO:0020516 orphanet_rare diseases +MONDO:0020516 otar diseases +MONDO:0020516 rare diseases +MONDO:0020517 gard_rare diseases +MONDO:0020517 nord_rare diseases +MONDO:0020517 rare diseases +MONDO:0020518 gard_rare diseases +MONDO:0020518 rare diseases +MONDO:0020519 gard_rare diseases +MONDO:0020519 rare diseases +MONDO:0020520 gard_rare diseases +MONDO:0020520 rare diseases +MONDO:0020521 gard_rare diseases +MONDO:0020521 ordo_etiological_subtype diseases +MONDO:0020521 otar diseases +MONDO:0020521 rare diseases +MONDO:0020522 gard_rare diseases +MONDO:0020522 ordo_etiological_subtype diseases +MONDO:0020522 rare diseases +MONDO:0020523 otar diseases +MONDO:0020525 gard_rare diseases +MONDO:0020525 nord_rare diseases +MONDO:0020525 otar diseases +MONDO:0020525 rare diseases +MONDO:0020526 gard_rare diseases +MONDO:0020526 nord_rare diseases +MONDO:0020526 ordo_subtype_of_a_disorder diseases +MONDO:0020526 otar diseases +MONDO:0020526 rare diseases +MONDO:0020527 gard_rare diseases +MONDO:0020527 ordo_disorder diseases +MONDO:0020527 orphanet_rare diseases +MONDO:0020527 rare diseases +MONDO:0020528 disease_grouping diseases +MONDO:0020528 gard_rare diseases +MONDO:0020528 ordo_group_of_disorders diseases +MONDO:0020528 otar diseases +MONDO:0020528 rare diseases +MONDO:0020529 disease_grouping diseases +MONDO:0020529 gard_rare diseases +MONDO:0020529 ordo_group_of_disorders diseases +MONDO:0020529 rare diseases +MONDO:0020531 clingen diseases +MONDO:0020531 gard_rare diseases +MONDO:0020531 otar diseases +MONDO:0020531 rare diseases +MONDO:0020532 gard_rare diseases +MONDO:0020532 nord_rare diseases +MONDO:0020532 ordo_etiological_subtype diseases +MONDO:0020532 ordo_subtype_of_a_disorder diseases +MONDO:0020532 rare diseases +MONDO:0020533 gard_rare diseases +MONDO:0020533 nord_rare diseases +MONDO:0020533 ordo_etiological_subtype diseases +MONDO:0020533 ordo_subtype_of_a_disorder diseases +MONDO:0020533 rare diseases +MONDO:0020535 gard_rare diseases +MONDO:0020535 nord_rare diseases +MONDO:0020535 ordo_disorder diseases +MONDO:0020535 orphanet_rare diseases +MONDO:0020535 rare diseases +MONDO:0020538 gard_rare diseases +MONDO:0020538 nord_rare diseases +MONDO:0020538 ordo_disorder diseases +MONDO:0020538 orphanet_rare diseases +MONDO:0020538 rare diseases +MONDO:0020539 disease_grouping diseases +MONDO:0020539 gard_rare diseases +MONDO:0020539 ordo_group_of_disorders diseases +MONDO:0020539 rare diseases +MONDO:0020540 gard_rare diseases +MONDO:0020540 nord_rare diseases +MONDO:0020540 ordo_disorder diseases +MONDO:0020540 orphanet_rare diseases +MONDO:0020540 rare diseases +MONDO:0020541 gard_rare diseases +MONDO:0020541 nord_rare diseases +MONDO:0020541 ordo_disorder diseases +MONDO:0020541 orphanet_rare diseases +MONDO:0020541 rare diseases +MONDO:0020542 gard_rare diseases +MONDO:0020542 ordo_disorder diseases +MONDO:0020542 orphanet_rare diseases +MONDO:0020542 rare diseases +MONDO:0020543 gard_rare diseases +MONDO:0020543 nord_rare diseases +MONDO:0020543 ordo_disorder diseases +MONDO:0020543 orphanet_rare diseases +MONDO:0020543 rare diseases +MONDO:0020544 gard_rare diseases +MONDO:0020544 nord_rare diseases +MONDO:0020544 ordo_etiological_subtype diseases +MONDO:0020544 ordo_subtype_of_a_disorder diseases +MONDO:0020544 rare diseases +MONDO:0020545 gard_rare diseases +MONDO:0020545 nord_rare diseases +MONDO:0020545 ordo_etiological_subtype diseases +MONDO:0020545 ordo_subtype_of_a_disorder diseases +MONDO:0020545 rare diseases +MONDO:0020546 gard_rare diseases +MONDO:0020546 nord_rare diseases +MONDO:0020546 ordo_subtype_of_a_disorder diseases +MONDO:0020546 rare diseases +MONDO:0020547 gard_rare diseases +MONDO:0020547 nord_rare diseases +MONDO:0020547 ordo_subtype_of_a_disorder diseases +MONDO:0020547 otar diseases +MONDO:0020547 rare diseases +MONDO:0020549 gard_rare diseases +MONDO:0020549 nord_rare diseases +MONDO:0020549 ordo_disorder diseases +MONDO:0020549 orphanet_rare diseases +MONDO:0020549 rare diseases +MONDO:0020550 gard_rare diseases +MONDO:0020550 nord_rare diseases +MONDO:0020550 ordo_disorder diseases +MONDO:0020550 orphanet_rare diseases +MONDO:0020550 otar diseases +MONDO:0020550 rare diseases +MONDO:0020552 gard_rare diseases +MONDO:0020552 nord_rare diseases +MONDO:0020552 ordo_disorder diseases +MONDO:0020552 orphanet_rare diseases +MONDO:0020552 otar diseases +MONDO:0020552 rare diseases +MONDO:0020553 gard_rare diseases +MONDO:0020553 nord_rare diseases +MONDO:0020553 ordo_disorder diseases +MONDO:0020553 orphanet_rare diseases +MONDO:0020553 rare diseases +MONDO:0020554 gard_rare diseases +MONDO:0020554 nord_rare diseases +MONDO:0020554 ordo_subtype_of_a_disorder diseases +MONDO:0020554 rare diseases +MONDO:0020555 gard_rare diseases +MONDO:0020555 nord_rare diseases +MONDO:0020555 ordo_subtype_of_a_disorder diseases +MONDO:0020555 rare diseases +MONDO:0020556 gard_rare diseases +MONDO:0020556 nord_rare diseases +MONDO:0020556 ordo_subtype_of_a_disorder diseases +MONDO:0020556 rare diseases +MONDO:0020557 gard_rare diseases +MONDO:0020557 nord_rare diseases +MONDO:0020557 ordo_subtype_of_a_disorder diseases +MONDO:0020557 rare diseases +MONDO:0020558 gard_rare diseases +MONDO:0020558 nord_rare diseases +MONDO:0020558 ordo_disorder diseases +MONDO:0020558 orphanet_rare diseases +MONDO:0020558 otar diseases +MONDO:0020558 rare diseases +MONDO:0020559 gard_rare diseases +MONDO:0020559 nord_rare diseases +MONDO:0020559 ordo_disorder diseases +MONDO:0020559 orphanet_rare diseases +MONDO:0020559 rare diseases +MONDO:0020560 gard_rare diseases +MONDO:0020560 nord_rare diseases +MONDO:0020560 ordo_disorder diseases +MONDO:0020560 orphanet_rare diseases +MONDO:0020560 otar diseases +MONDO:0020560 rare diseases +MONDO:0020561 gard_rare diseases +MONDO:0020561 nord_rare diseases +MONDO:0020561 ordo_histopathological_subtype diseases +MONDO:0020561 ordo_subtype_of_a_disorder diseases +MONDO:0020561 otar diseases +MONDO:0020561 rare diseases +MONDO:0020562 gard_rare diseases +MONDO:0020562 nord_rare diseases +MONDO:0020562 ordo_histopathological_subtype diseases +MONDO:0020562 ordo_subtype_of_a_disorder diseases +MONDO:0020562 otar diseases +MONDO:0020562 rare diseases +MONDO:0020563 gard_rare diseases +MONDO:0020563 nord_rare diseases +MONDO:0020563 ordo_histopathological_subtype diseases +MONDO:0020563 ordo_subtype_of_a_disorder diseases +MONDO:0020563 otar diseases +MONDO:0020563 rare diseases +MONDO:0020567 gard_rare diseases +MONDO:0020567 nord_rare diseases +MONDO:0020567 ordo_disorder diseases +MONDO:0020567 orphanet_rare diseases +MONDO:0020567 rare diseases +MONDO:0020568 disease_grouping diseases +MONDO:0020568 gard_rare diseases +MONDO:0020568 nord_rare diseases +MONDO:0020568 ordo_group_of_disorders diseases +MONDO:0020568 rare diseases +MONDO:0020569 gard_rare diseases +MONDO:0020569 nord_rare diseases +MONDO:0020569 ordo_disorder diseases +MONDO:0020569 orphanet_rare diseases +MONDO:0020569 otar diseases +MONDO:0020569 rare diseases +MONDO:0020571 gard_rare diseases +MONDO:0020571 nord_rare diseases +MONDO:0020571 ordo_subtype_of_a_disorder diseases +MONDO:0020571 rare diseases +MONDO:0020572 gard_rare diseases +MONDO:0020572 nord_rare diseases +MONDO:0020572 ordo_subtype_of_a_disorder diseases +MONDO:0020572 otar diseases +MONDO:0020572 rare diseases +MONDO:0020574 gard_rare diseases +MONDO:0020574 nord_rare diseases +MONDO:0020574 otar diseases +MONDO:0020574 rare diseases +MONDO:0020575 otar diseases +MONDO:0020576 gard_rare diseases +MONDO:0020576 rare diseases +MONDO:0020577 gard_rare diseases +MONDO:0020577 rare diseases +MONDO:0020580 gard_rare diseases +MONDO:0020580 otar diseases +MONDO:0020580 rare diseases +MONDO:0020581 inferred_rare diseases +MONDO:0020581 rare diseases +MONDO:0020583 gard_rare diseases +MONDO:0020583 rare diseases +MONDO:0020584 gard_rare diseases +MONDO:0020584 rare diseases +MONDO:0020585 gard_rare diseases +MONDO:0020585 rare diseases +MONDO:0020586 gard_rare diseases +MONDO:0020586 nord_rare diseases +MONDO:0020586 otar diseases +MONDO:0020586 rare diseases +MONDO:0020587 gard_rare diseases +MONDO:0020587 otar diseases +MONDO:0020587 rare diseases +MONDO:0020588 gard_rare diseases +MONDO:0020588 otar diseases +MONDO:0020588 rare diseases +MONDO:0020589 gard_rare diseases +MONDO:0020589 rare diseases +MONDO:0020590 otar diseases +MONDO:0020592 otar diseases +MONDO:0020593 otar diseases +MONDO:0020596 otar diseases +MONDO:0020598 otar diseases +MONDO:0020599 gard_rare diseases +MONDO:0020599 rare diseases +MONDO:0020600 otar diseases +MONDO:0020601 gard_rare diseases +MONDO:0020601 rare diseases +MONDO:0020602 gard_rare diseases +MONDO:0020602 nord_rare diseases +MONDO:0020602 rare diseases +MONDO:0020603 gard_rare diseases +MONDO:0020603 nord_rare diseases +MONDO:0020603 ordo_disorder diseases +MONDO:0020603 orphanet_rare diseases +MONDO:0020603 rare diseases +MONDO:0020604 otar diseases +MONDO:0020605 otar diseases +MONDO:0020607 gard_rare diseases +MONDO:0020607 rare diseases +MONDO:0020627 gard_rare diseases +MONDO:0020627 rare diseases +MONDO:0020628 gard_rare diseases +MONDO:0020628 nord_rare diseases +MONDO:0020628 otar diseases +MONDO:0020628 rare diseases +MONDO:0020629 gard_rare diseases +MONDO:0020629 nord_rare diseases +MONDO:0020629 rare diseases +MONDO:0020630 gard_rare diseases +MONDO:0020630 nord_rare diseases +MONDO:0020630 otar diseases +MONDO:0020630 rare diseases +MONDO:0020631 gard_rare diseases +MONDO:0020631 nord_rare diseases +MONDO:0020631 rare diseases +MONDO:0020632 gard_rare diseases +MONDO:0020632 nord_rare diseases +MONDO:0020632 rare diseases +MONDO:0020633 otar diseases +MONDO:0020634 gard_rare diseases +MONDO:0020634 otar diseases +MONDO:0020634 rare diseases +MONDO:0020635 gard_rare diseases +MONDO:0020635 rare diseases +MONDO:0020638 otar diseases +MONDO:0020639 gard_rare diseases +MONDO:0020639 otar diseases +MONDO:0020639 rare diseases +MONDO:0020640 gard_rare diseases +MONDO:0020640 nord_rare diseases +MONDO:0020640 ordo_group_of_disorders diseases +MONDO:0020640 rare diseases +MONDO:0020641 otar diseases +MONDO:0020642 clingen diseases +MONDO:0020642 gard_rare diseases +MONDO:0020642 otar diseases +MONDO:0020642 rare diseases +MONDO:0020644 gard_rare diseases +MONDO:0020644 rare diseases +MONDO:0020645 gard_rare diseases +MONDO:0020645 otar diseases +MONDO:0020645 rare diseases +MONDO:0020646 gard_rare diseases +MONDO:0020646 nord_rare diseases +MONDO:0020646 rare diseases +MONDO:0020647 otar diseases +MONDO:0020648 gard_rare diseases +MONDO:0020648 otar diseases +MONDO:0020648 rare diseases +MONDO:0020649 gard_rare diseases +MONDO:0020649 rare diseases +MONDO:0020650 gard_rare diseases +MONDO:0020650 rare diseases +MONDO:0020651 gard_rare diseases +MONDO:0020651 rare diseases +MONDO:0020652 gard_rare diseases +MONDO:0020652 rare diseases +MONDO:0020653 gard_rare diseases +MONDO:0020653 rare diseases +MONDO:0020654 gard_rare diseases +MONDO:0020654 otar diseases +MONDO:0020654 rare diseases +MONDO:0020656 gard_rare diseases +MONDO:0020656 rare diseases +MONDO:0020657 gard_rare diseases +MONDO:0020657 nord_rare diseases +MONDO:0020657 otar diseases +MONDO:0020657 rare diseases +MONDO:0020658 gard_rare diseases +MONDO:0020658 rare diseases +MONDO:0020659 gard_rare diseases +MONDO:0020659 nord_rare diseases +MONDO:0020659 obsoletion_candidate diseases +MONDO:0020659 ordo_disorder diseases +MONDO:0020659 orphanet_rare diseases +MONDO:0020659 rare diseases +MONDO:0020660 gard_rare diseases +MONDO:0020660 nord_rare diseases +MONDO:0020660 rare diseases +MONDO:0020661 gard_rare diseases +MONDO:0020661 rare diseases +MONDO:0020662 gard_rare diseases +MONDO:0020662 otar diseases +MONDO:0020662 rare diseases +MONDO:0020663 otar diseases +MONDO:0020664 otar diseases +MONDO:0020666 gard_rare diseases +MONDO:0020666 rare diseases +MONDO:0020667 gard_rare diseases +MONDO:0020667 nord_rare diseases +MONDO:0020667 ordo_subtype_of_a_disorder diseases +MONDO:0020667 rare diseases +MONDO:0020669 gard_rare diseases +MONDO:0020669 otar diseases +MONDO:0020669 rare diseases +MONDO:0020672 otar diseases +MONDO:0020673 otar diseases +MONDO:0020674 otar diseases +MONDO:0020677 otar diseases +MONDO:0020678 otar diseases +MONDO:0020681 gard_rare diseases +MONDO:0020681 nord_rare diseases +MONDO:0020681 rare diseases +MONDO:0020682 gard_rare diseases +MONDO:0020682 nord_rare diseases +MONDO:0020682 rare diseases +MONDO:0020684 gard_rare diseases +MONDO:0020684 rare diseases +MONDO:0020685 gard_rare diseases +MONDO:0020685 nord_rare diseases +MONDO:0020685 rare diseases +MONDO:0020687 gard_rare diseases +MONDO:0020687 rare diseases +MONDO:0020688 otar diseases +MONDO:0020689 gard_rare diseases +MONDO:0020689 nord_rare diseases +MONDO:0020689 otar diseases +MONDO:0020689 rare diseases +MONDO:0020690 gard_rare diseases +MONDO:0020690 rare diseases +MONDO:0020692 gard_rare diseases +MONDO:0020692 nord_rare diseases +MONDO:0020692 rare diseases +MONDO:0020693 gard_rare diseases +MONDO:0020693 nord_rare diseases +MONDO:0020693 ordo_disorder diseases +MONDO:0020693 orphanet_rare diseases +MONDO:0020693 otar diseases +MONDO:0020693 rare diseases +MONDO:0020696 otar diseases +MONDO:0020698 gard_rare diseases +MONDO:0020698 rare diseases +MONDO:0020701 gard_rare diseases +MONDO:0020701 nord_rare diseases +MONDO:0020701 rare diseases +MONDO:0020702 gard_rare diseases +MONDO:0020702 ordo_disorder diseases +MONDO:0020702 orphanet_rare diseases +MONDO:0020702 otar diseases +MONDO:0020702 rare diseases +MONDO:0020703 gard_rare diseases +MONDO:0020703 otar diseases +MONDO:0020703 rare diseases +MONDO:0020704 gard_rare diseases +MONDO:0020704 nord_rare diseases +MONDO:0020704 otar diseases +MONDO:0020704 rare diseases +MONDO:0020711 gard_rare diseases +MONDO:0020711 mondo_rare diseases +MONDO:0020711 nord_rare diseases +MONDO:0020711 rare diseases +MONDO:0020712 gard_rare diseases +MONDO:0020712 nord_rare diseases +MONDO:0020712 rare diseases +MONDO:0020713 gard_rare diseases +MONDO:0020713 rare diseases +MONDO:0020714 gard_rare diseases +MONDO:0020714 rare diseases +MONDO:0020716 gard_rare diseases +MONDO:0020716 nord_rare diseases +MONDO:0020716 rare diseases +MONDO:0020717 gard_rare diseases +MONDO:0020717 nord_rare diseases +MONDO:0020717 rare diseases +MONDO:0020718 gard_rare diseases +MONDO:0020718 nord_rare diseases +MONDO:0020718 rare diseases +MONDO:0020720 gard_rare diseases +MONDO:0020720 otar diseases +MONDO:0020720 rare diseases +MONDO:0020721 gard_rare diseases +MONDO:0020721 nord_rare diseases +MONDO:0020721 ordo_disorder diseases +MONDO:0020721 orphanet_rare diseases +MONDO:0020721 otar diseases +MONDO:0020721 rare diseases +MONDO:0020723 gard_rare diseases +MONDO:0020723 nord_rare diseases +MONDO:0020723 otar diseases +MONDO:0020723 rare diseases +MONDO:0020724 gard_rare diseases +MONDO:0020724 nord_rare diseases +MONDO:0020724 rare diseases +MONDO:0020726 clingen diseases +MONDO:0020726 gard_rare diseases +MONDO:0020726 nord_rare diseases +MONDO:0020726 ordo_subtype_of_a_disorder diseases +MONDO:0020726 otar diseases +MONDO:0020726 rare diseases +MONDO:0020727 gard_rare diseases +MONDO:0020727 n_of_one diseases +MONDO:0020727 rare diseases +MONDO:0020728 gard_rare diseases +MONDO:0020728 nord_rare diseases +MONDO:0020728 rare diseases +MONDO:0020729 clingen diseases +MONDO:0020729 gard_rare diseases +MONDO:0020729 nord_rare diseases +MONDO:0020729 rare diseases +MONDO:0020730 gard_rare diseases +MONDO:0020730 nord_rare diseases +MONDO:0020730 rare diseases +MONDO:0020731 otar diseases +MONDO:0020732 gard_rare diseases +MONDO:0020732 obsoletion_candidate diseases +MONDO:0020732 otar diseases +MONDO:0020732 rare diseases +MONDO:0020733 gard_rare diseases +MONDO:0020733 nord_rare diseases +MONDO:0020733 rare diseases +MONDO:0020735 gard_rare diseases +MONDO:0020735 nord_rare diseases +MONDO:0020735 rare diseases +MONDO:0020736 gard_rare diseases +MONDO:0020736 nord_rare diseases +MONDO:0020736 rare diseases +MONDO:0020737 gard_rare diseases +MONDO:0020737 nord_rare diseases +MONDO:0020737 rare diseases +MONDO:0020738 gard_rare diseases +MONDO:0020738 rare diseases +MONDO:0020739 gard_rare diseases +MONDO:0020739 rare diseases +MONDO:0020740 gard_rare diseases +MONDO:0020740 nord_rare diseases +MONDO:0020740 otar diseases +MONDO:0020740 rare diseases +MONDO:0020741 gard_rare diseases +MONDO:0020741 rare diseases +MONDO:0020743 gard_rare diseases +MONDO:0020743 nord_rare diseases +MONDO:0020743 ordo_disorder diseases +MONDO:0020743 orphanet_rare diseases +MONDO:0020743 otar diseases +MONDO:0020743 rare diseases +MONDO:0020745 n_of_one diseases +MONDO:0020745 otar diseases +MONDO:0020746 gard_rare diseases +MONDO:0020746 nord_rare diseases +MONDO:0020746 rare diseases +MONDO:0020747 gard_rare diseases +MONDO:0020747 nord_rare diseases +MONDO:0020747 rare diseases +MONDO:0020748 gard_rare diseases +MONDO:0020748 nord_rare diseases +MONDO:0020748 rare diseases +MONDO:0020749 gard_rare diseases +MONDO:0020749 nord_rare diseases +MONDO:0020749 rare diseases +MONDO:0020750 gard_rare diseases +MONDO:0020750 nord_rare diseases +MONDO:0020750 rare diseases +MONDO:0020751 gard_rare diseases +MONDO:0020751 nord_rare diseases +MONDO:0020751 rare diseases +MONDO:0020754 otar diseases +MONDO:0020756 gard_rare diseases +MONDO:0020756 nord_rare diseases +MONDO:0020756 rare diseases +MONDO:0020757 gard_rare diseases +MONDO:0020757 rare diseases +MONDO:0020760 otar diseases +MONDO:0020761 gard_rare diseases +MONDO:0020761 nord_rare diseases +MONDO:0020761 otar diseases +MONDO:0020761 rare diseases +MONDO:0020762 clingen diseases +MONDO:0020762 gard_rare diseases +MONDO:0020762 rare diseases +MONDO:0020763 gard_rare diseases +MONDO:0020763 rare diseases +MONDO:0020764 otar diseases +MONDO:0020765 gard_rare diseases +MONDO:0020765 nord_rare diseases +MONDO:0020765 rare diseases +MONDO:0020766 gard_rare diseases +MONDO:0020766 nord_rare diseases +MONDO:0020766 rare diseases +MONDO:0020768 otar diseases +MONDO:0020769 gard_rare diseases +MONDO:0020769 rare diseases +MONDO:0020770 gard_rare diseases +MONDO:0020770 nord_rare diseases +MONDO:0020770 rare diseases +MONDO:0020771 gard_rare diseases +MONDO:0020771 otar diseases +MONDO:0020771 rare diseases +MONDO:0020774 gard_rare diseases +MONDO:0020774 nord_rare diseases +MONDO:0020774 ordo_disorder diseases +MONDO:0020774 orphanet_rare diseases +MONDO:0020774 rare diseases +MONDO:0020775 gard_rare diseases +MONDO:0020775 rare diseases +MONDO:0020776 otar diseases +MONDO:0020777 gard_rare diseases +MONDO:0020777 rare diseases +MONDO:0020781 gard_rare diseases +MONDO:0020781 nord_rare diseases +MONDO:0020781 ordo_disorder diseases +MONDO:0020781 orphanet_rare diseases +MONDO:0020781 rare diseases +MONDO:0020782 otar diseases +MONDO:0020783 gard_rare diseases +MONDO:0020783 nord_rare diseases +MONDO:0020783 ordo_disorder diseases +MONDO:0020783 orphanet_rare diseases +MONDO:0020783 rare diseases +MONDO:0020785 gard_rare diseases +MONDO:0020785 nord_rare diseases +MONDO:0020785 rare diseases +MONDO:0020787 gard_rare diseases +MONDO:0020787 nord_rare diseases +MONDO:0020787 rare diseases +MONDO:0020788 gard_rare diseases +MONDO:0020788 nord_rare diseases +MONDO:0020788 rare diseases +MONDO:0020789 gard_rare diseases +MONDO:0020789 rare diseases +MONDO:0020790 clingen diseases +MONDO:0020790 gard_rare diseases +MONDO:0020790 nord_rare diseases +MONDO:0020790 rare diseases +MONDO:0020791 gard_rare diseases +MONDO:0020791 nord_rare diseases +MONDO:0020791 rare diseases +MONDO:0020792 n_of_one diseases +MONDO:0020793 gard_rare diseases +MONDO:0020793 nord_rare diseases +MONDO:0020793 rare diseases +MONDO:0020794 otar diseases +MONDO:0020795 gard_rare diseases +MONDO:0020795 nord_rare diseases +MONDO:0020795 otar diseases +MONDO:0020795 rare diseases +MONDO:0020796 gard_rare diseases +MONDO:0020796 nord_rare diseases +MONDO:0020796 rare diseases +MONDO:0020798 gard_rare diseases +MONDO:0020798 otar diseases +MONDO:0020798 rare diseases +MONDO:0020799 otar diseases +MONDO:0020804 otar diseases +MONDO:0020808 gard_rare diseases +MONDO:0020808 nord_rare diseases +MONDO:0020808 rare diseases +MONDO:0020811 gard_rare diseases +MONDO:0020811 rare diseases +MONDO:0020813 inferred_rare diseases +MONDO:0020813 rare diseases +MONDO:0020820 gard_rare diseases +MONDO:0020820 nord_rare diseases +MONDO:0020820 otar diseases +MONDO:0020820 rare diseases +MONDO:0020830 gard_rare diseases +MONDO:0020830 rare diseases +MONDO:0020831 gard_rare diseases +MONDO:0020831 nord_rare diseases +MONDO:0020831 ordo_disorder diseases +MONDO:0020831 ordo_malformation_syndrome diseases +MONDO:0020831 orphanet_rare diseases +MONDO:0020831 otar diseases +MONDO:0020831 rare diseases +MONDO:0020835 gard_rare diseases +MONDO:0020835 nord_rare diseases +MONDO:0020835 rare diseases +MONDO:0020838 gard_rare diseases +MONDO:0020838 rare diseases +MONDO:0020841 clingen diseases +MONDO:0020841 otar diseases +MONDO:0020843 gard_rare diseases +MONDO:0020843 rare diseases +MONDO:0020845 gard_rare diseases +MONDO:0020845 otar diseases +MONDO:0020845 rare diseases +MONDO:0020846 gard_rare diseases +MONDO:0020846 nord_rare diseases +MONDO:0020846 otar diseases +MONDO:0020846 rare diseases +MONDO:0020847 gard_rare diseases +MONDO:0020847 nord_rare diseases +MONDO:0020847 otar diseases +MONDO:0020847 rare diseases +MONDO:0020848 gard_rare diseases +MONDO:0020848 nord_rare diseases +MONDO:0020848 rare diseases +MONDO:0020850 gard_rare diseases +MONDO:0020850 nord_rare diseases +MONDO:0020850 otar diseases +MONDO:0020850 rare diseases +MONDO:0020851 gard_rare diseases +MONDO:0020851 rare diseases +MONDO:0020852 otar diseases +MONDO:0020853 otar diseases +MONDO:0020854 gard_rare diseases +MONDO:0020854 otar diseases +MONDO:0020854 rare diseases +MONDO:0020855 gard_rare diseases +MONDO:0020855 rare diseases +MONDO:0020856 gard_rare diseases +MONDO:0020856 nord_rare diseases +MONDO:0020856 rare diseases +MONDO:0020857 gard_rare diseases +MONDO:0020857 nord_rare diseases +MONDO:0020857 rare diseases +MONDO:0020858 gard_rare diseases +MONDO:0020858 otar diseases +MONDO:0020858 rare diseases +MONDO:0020860 gard_rare diseases +MONDO:0020860 rare diseases +MONDO:0020863 gard_rare diseases +MONDO:0020863 rare diseases +MONDO:0020866 gard_rare diseases +MONDO:0020866 rare diseases +MONDO:0020920 otar diseases +MONDO:0020927 gard_rare diseases +MONDO:0020927 otar diseases +MONDO:0020927 rare diseases +MONDO:0020937 gard_rare diseases +MONDO:0020937 nord_rare diseases +MONDO:0020937 otar diseases +MONDO:0020937 rare diseases +MONDO:0020947 otar diseases +MONDO:0020950 otar diseases +MONDO:0020959 gard_rare diseases +MONDO:0020959 rare diseases +MONDO:0020983 gard_rare diseases +MONDO:0020983 nord_rare diseases +MONDO:0020983 rare diseases +MONDO:0020989 gard_rare diseases +MONDO:0020989 nord_rare diseases +MONDO:0020989 rare diseases +MONDO:0021001 inferred_rare diseases +MONDO:0021001 otar diseases +MONDO:0021001 rare diseases +MONDO:0021002 otar diseases +MONDO:0021003 otar diseases +MONDO:0021004 otar diseases +MONDO:0021005 gard_rare diseases +MONDO:0021005 ordo_disorder diseases +MONDO:0021005 orphanet_rare diseases +MONDO:0021005 otar diseases +MONDO:0021005 rare diseases +MONDO:0021008 gard_rare diseases +MONDO:0021008 rare diseases +MONDO:0021009 gard_rare diseases +MONDO:0021009 otar diseases +MONDO:0021009 rare diseases +MONDO:0021010 gard_rare diseases +MONDO:0021010 rare diseases +MONDO:0021011 gard_rare diseases +MONDO:0021011 nord_rare diseases +MONDO:0021011 rare diseases +MONDO:0021013 gard_rare diseases +MONDO:0021013 nord_rare diseases +MONDO:0021013 rare diseases +MONDO:0021018 gard_rare diseases +MONDO:0021018 nord_rare diseases +MONDO:0021018 ordo_disorder diseases +MONDO:0021018 orphanet_rare diseases +MONDO:0021018 otar diseases +MONDO:0021018 rare diseases +MONDO:0021019 gard_rare diseases +MONDO:0021019 nord_rare diseases +MONDO:0021019 ordo_disorder diseases +MONDO:0021019 orphanet_rare diseases +MONDO:0021019 otar diseases +MONDO:0021019 rare diseases +MONDO:0021020 gard_rare diseases +MONDO:0021020 nord_rare diseases +MONDO:0021020 ordo_subtype_of_a_disorder diseases +MONDO:0021020 otar diseases +MONDO:0021020 rare diseases +MONDO:0021021 gard_rare diseases +MONDO:0021021 nord_rare diseases +MONDO:0021021 rare diseases +MONDO:0021022 gard_rare diseases +MONDO:0021022 nord_rare diseases +MONDO:0021022 ordo_disorder diseases +MONDO:0021022 orphanet_rare diseases +MONDO:0021022 otar diseases +MONDO:0021022 rare diseases +MONDO:0021023 gard_rare diseases +MONDO:0021023 nord_rare diseases +MONDO:0021023 ordo_disorder diseases +MONDO:0021023 orphanet_rare diseases +MONDO:0021023 otar diseases +MONDO:0021023 rare diseases +MONDO:0021025 gard_rare diseases +MONDO:0021025 nord_rare diseases +MONDO:0021025 rare diseases +MONDO:0021026 gard_rare diseases +MONDO:0021026 ordo_group_of_disorders diseases +MONDO:0021026 rare diseases +MONDO:0021029 gard_rare diseases +MONDO:0021029 ordo_group_of_disorders diseases +MONDO:0021029 rare diseases +MONDO:0021035 gard_rare diseases +MONDO:0021035 nord_rare diseases +MONDO:0021035 rare diseases +MONDO:0021036 otar diseases +MONDO:0021038 otar diseases +MONDO:0021039 otar diseases +MONDO:0021040 otar diseases +MONDO:0021041 gard_rare diseases +MONDO:0021041 otar diseases +MONDO:0021041 rare diseases +MONDO:0021042 gard_rare diseases +MONDO:0021042 ordo_group_of_disorders diseases +MONDO:0021042 otar diseases +MONDO:0021042 rare diseases +MONDO:0021043 otar diseases +MONDO:0021045 otar diseases +MONDO:0021046 otar diseases +MONDO:0021047 gard_rare diseases +MONDO:0021047 nord_rare diseases +MONDO:0021047 otar diseases +MONDO:0021047 rare diseases +MONDO:0021048 inferred_rare diseases +MONDO:0021048 rare diseases +MONDO:0021049 otar diseases +MONDO:0021050 otar diseases +MONDO:0021052 gard_rare diseases +MONDO:0021052 otar diseases +MONDO:0021052 rare diseases +MONDO:0021053 gard_rare diseases +MONDO:0021053 nord_rare diseases +MONDO:0021053 otar diseases +MONDO:0021053 rare diseases +MONDO:0021054 disease_grouping diseases +MONDO:0021054 gard_rare diseases +MONDO:0021054 ordo_group_of_disorders diseases +MONDO:0021054 otar diseases +MONDO:0021054 rare diseases +MONDO:0021055 gard_rare diseases +MONDO:0021055 nord_rare diseases +MONDO:0021055 ordo_disorder diseases +MONDO:0021055 orphanet_rare diseases +MONDO:0021055 otar diseases +MONDO:0021055 rare diseases +MONDO:0021056 gard_rare diseases +MONDO:0021056 nord_rare diseases +MONDO:0021056 otar diseases +MONDO:0021056 rare diseases +MONDO:0021057 clingen diseases +MONDO:0021057 gard_rare diseases +MONDO:0021057 otar diseases +MONDO:0021057 rare diseases +MONDO:0021058 otar diseases +MONDO:0021060 clingen diseases +MONDO:0021060 disease_grouping diseases +MONDO:0021060 gard_rare diseases +MONDO:0021060 ordo_group_of_disorders diseases +MONDO:0021060 otar diseases +MONDO:0021060 rare diseases +MONDO:0021061 gard_rare diseases +MONDO:0021061 nord_rare diseases +MONDO:0021061 otar diseases +MONDO:0021061 rare diseases +MONDO:0021063 otar diseases +MONDO:0021064 gard_rare diseases +MONDO:0021064 otar diseases +MONDO:0021064 rare diseases +MONDO:0021065 otar diseases +MONDO:0021066 otar diseases +MONDO:0021067 gard_rare diseases +MONDO:0021067 otar diseases +MONDO:0021067 rare diseases +MONDO:0021068 otar diseases +MONDO:0021069 otar diseases +MONDO:0021071 otar diseases +MONDO:0021072 gard_rare diseases +MONDO:0021072 otar diseases +MONDO:0021072 rare diseases +MONDO:0021074 otar diseases +MONDO:0021075 otar diseases +MONDO:0021076 otar diseases +MONDO:0021077 otar diseases +MONDO:0021078 otar diseases +MONDO:0021079 otar diseases +MONDO:0021080 otar diseases +MONDO:0021081 gard_rare diseases +MONDO:0021081 nord_rare diseases +MONDO:0021081 ordo_disorder diseases +MONDO:0021081 orphanet_rare diseases +MONDO:0021081 rare diseases +MONDO:0021083 gard_rare diseases +MONDO:0021083 nord_rare diseases +MONDO:0021083 rare diseases +MONDO:0021084 otar diseases +MONDO:0021085 otar diseases +MONDO:0021086 otar diseases +MONDO:0021088 gard_rare diseases +MONDO:0021088 rare diseases +MONDO:0021089 otar diseases +MONDO:0021091 otar diseases +MONDO:0021093 clingen diseases +MONDO:0021093 gard_rare diseases +MONDO:0021093 nord_rare diseases +MONDO:0021093 rare diseases +MONDO:0021094 clingen diseases +MONDO:0021094 otar diseases +MONDO:0021095 otar diseases +MONDO:0021096 otar diseases +MONDO:0021100 otar diseases +MONDO:0021101 gard_rare diseases +MONDO:0021101 rare diseases +MONDO:0021102 gard_rare diseases +MONDO:0021102 nord_rare diseases +MONDO:0021102 ordo_disorder diseases +MONDO:0021102 orphanet_rare diseases +MONDO:0021102 rare diseases +MONDO:0021105 predisposition diseases +MONDO:0021106 disease_grouping diseases +MONDO:0021106 gard_rare diseases +MONDO:0021106 ordo_group_of_disorders diseases +MONDO:0021106 otar diseases +MONDO:0021106 rare diseases +MONDO:0021107 gard_rare diseases +MONDO:0021107 ordo_group_of_disorders diseases +MONDO:0021107 otar diseases +MONDO:0021107 rare diseases +MONDO:0021108 otar diseases +MONDO:0021109 otar diseases +MONDO:0021110 otar diseases +MONDO:0021111 otar diseases +MONDO:0021113 otar diseases +MONDO:0021115 otar diseases +MONDO:0021116 otar diseases +MONDO:0021117 otar diseases +MONDO:0021118 otar diseases +MONDO:0021121 otar diseases +MONDO:0021123 gard_rare diseases +MONDO:0021123 nord_rare diseases +MONDO:0021123 otar diseases +MONDO:0021123 rare diseases +MONDO:0021124 otar diseases +MONDO:0021129 otar diseases +MONDO:0021130 gard_rare diseases +MONDO:0021130 rare diseases +MONDO:0021131 gard_rare diseases +MONDO:0021131 nord_rare diseases +MONDO:0021131 rare diseases +MONDO:0021133 gard_rare diseases +MONDO:0021133 nord_rare diseases +MONDO:0021133 ordo_disorder diseases +MONDO:0021133 orphanet_rare diseases +MONDO:0021133 rare diseases +MONDO:0021134 gard_rare diseases +MONDO:0021134 nord_rare diseases +MONDO:0021134 ordo_disorder diseases +MONDO:0021134 orphanet_rare diseases +MONDO:0021134 otar diseases +MONDO:0021134 rare diseases +MONDO:0021138 gard_rare diseases +MONDO:0021138 otar diseases +MONDO:0021138 rare diseases +MONDO:0021142 gard_rare diseases +MONDO:0021142 rare diseases +MONDO:0021143 otar diseases +MONDO:0021144 otar diseases +MONDO:0021146 otar diseases +MONDO:0021147 harrisons_view diseases +MONDO:0021147 rare_grouping diseases +MONDO:0021148 otar diseases +MONDO:0021154 disease_grouping diseases +MONDO:0021154 ordo_group_of_disorders diseases +MONDO:0021155 gard_rare diseases +MONDO:0021155 otar diseases +MONDO:0021155 rare diseases +MONDO:0021163 otar diseases +MONDO:0021164 otar diseases +MONDO:0021165 otar diseases +MONDO:0021166 harrisons_view diseases +MONDO:0021166 rare_grouping diseases +MONDO:0021167 gard_rare diseases +MONDO:0021167 otar diseases +MONDO:0021167 rare diseases +MONDO:0021169 otar diseases +MONDO:0021171 gard_rare diseases +MONDO:0021171 rare diseases +MONDO:0021172 gard_rare diseases +MONDO:0021172 nord_rare diseases +MONDO:0021172 ordo_subtype_of_a_disorder diseases +MONDO:0021172 rare diseases +MONDO:0021176 gard_rare diseases +MONDO:0021176 nord_rare diseases +MONDO:0021176 ordo_subtype_of_a_disorder diseases +MONDO:0021176 rare diseases +MONDO:0021177 gard_rare diseases +MONDO:0021177 rare diseases +MONDO:0021179 otar diseases +MONDO:0021181 disease_grouping diseases +MONDO:0021181 gard_rare diseases +MONDO:0021181 ordo_group_of_disorders diseases +MONDO:0021181 rare diseases +MONDO:0021183 otar diseases +MONDO:0021184 otar diseases +MONDO:0021187 otar diseases +MONDO:0021189 otar diseases +MONDO:0021190 gard_rare diseases +MONDO:0021190 otar diseases +MONDO:0021190 rare diseases +MONDO:0021192 otar diseases +MONDO:0021193 otar diseases +MONDO:0021201 otar diseases +MONDO:0021204 otar diseases +MONDO:0021205 otar diseases +MONDO:0021208 gard_rare diseases +MONDO:0021208 rare diseases +MONDO:0021209 otar diseases +MONDO:0021210 otar diseases +MONDO:0021211 otar diseases +MONDO:0021218 otar diseases +MONDO:0021220 otar diseases +MONDO:0021222 otar diseases +MONDO:0021223 otar diseases +MONDO:0021224 otar diseases +MONDO:0021225 otar diseases +MONDO:0021227 disease_grouping diseases +MONDO:0021227 gard_rare diseases +MONDO:0021227 ordo_group_of_disorders diseases +MONDO:0021227 otar diseases +MONDO:0021227 rare diseases +MONDO:0021228 otar diseases +MONDO:0021229 otar diseases +MONDO:0021230 otar diseases +MONDO:0021231 otar diseases +MONDO:0021232 otar diseases +MONDO:0021233 otar diseases +MONDO:0021234 otar diseases +MONDO:0021237 gard_rare diseases +MONDO:0021237 otar diseases +MONDO:0021237 rare diseases +MONDO:0021238 otar diseases +MONDO:0021239 otar diseases +MONDO:0021240 otar diseases +MONDO:0021243 otar diseases +MONDO:0021244 otar diseases +MONDO:0021245 otar diseases +MONDO:0021246 otar diseases +MONDO:0021248 otar diseases +MONDO:0021249 otar diseases +MONDO:0021250 otar diseases +MONDO:0021251 otar diseases +MONDO:0021253 otar diseases +MONDO:0021254 otar diseases +MONDO:0021258 otar diseases +MONDO:0021259 otar diseases +MONDO:0021271 otar diseases +MONDO:0021272 gard_rare diseases +MONDO:0021272 nord_rare diseases +MONDO:0021272 ordo_group_of_disorders diseases +MONDO:0021272 rare diseases +MONDO:0021279 gard_rare diseases +MONDO:0021279 otar diseases +MONDO:0021279 rare diseases +MONDO:0021280 gard_rare diseases +MONDO:0021280 otar diseases +MONDO:0021280 rare diseases +MONDO:0021281 gard_rare diseases +MONDO:0021281 rare diseases +MONDO:0021282 gard_rare diseases +MONDO:0021282 rare diseases +MONDO:0021283 gard_rare diseases +MONDO:0021283 rare diseases +MONDO:0021289 otar diseases +MONDO:0021290 gard_rare diseases +MONDO:0021290 rare diseases +MONDO:0021297 gard_rare diseases +MONDO:0021297 nord_rare diseases +MONDO:0021297 rare diseases +MONDO:0021299 gard_rare diseases +MONDO:0021299 rare diseases +MONDO:0021300 gard_rare diseases +MONDO:0021300 otar diseases +MONDO:0021300 rare diseases +MONDO:0021301 otar diseases +MONDO:0021303 otar diseases +MONDO:0021310 otar diseases +MONDO:0021311 otar diseases +MONDO:0021312 gard_rare diseases +MONDO:0021312 otar diseases +MONDO:0021312 rare diseases +MONDO:0021313 otar diseases +MONDO:0021320 otar diseases +MONDO:0021321 gard_rare diseases +MONDO:0021321 otar diseases +MONDO:0021321 rare diseases +MONDO:0021322 gard_rare diseases +MONDO:0021322 otar diseases +MONDO:0021322 rare diseases +MONDO:0021327 otar diseases +MONDO:0021331 otar diseases +MONDO:0021334 otar diseases +MONDO:0021335 gard_rare diseases +MONDO:0021335 otar diseases +MONDO:0021335 rare diseases +MONDO:0021337 otar diseases +MONDO:0021340 otar diseases +MONDO:0021343 otar diseases +MONDO:0021345 otar diseases +MONDO:0021348 otar diseases +MONDO:0021350 otar diseases +MONDO:0021351 otar diseases +MONDO:0021353 otar diseases +MONDO:0021354 otar diseases +MONDO:0021355 otar diseases +MONDO:0021357 otar diseases +MONDO:0021358 otar diseases +MONDO:0021360 otar diseases +MONDO:0021364 otar diseases +MONDO:0021366 otar diseases +MONDO:0021367 gard_rare diseases +MONDO:0021367 rare diseases +MONDO:0021370 otar diseases +MONDO:0021374 otar diseases +MONDO:0021375 otar diseases +MONDO:0021381 otar diseases +MONDO:0021383 otar diseases +MONDO:0021385 otar diseases +MONDO:0021386 otar diseases +MONDO:0021389 gard_rare diseases +MONDO:0021389 rare diseases +MONDO:0021392 otar diseases +MONDO:0021398 otar diseases +MONDO:0021400 otar diseases +MONDO:0021416 otar diseases +MONDO:0021420 otar diseases +MONDO:0021427 gard_rare diseases +MONDO:0021427 nord_rare diseases +MONDO:0021427 ordo_disorder diseases +MONDO:0021427 orphanet_rare diseases +MONDO:0021427 rare diseases +MONDO:0021429 gard_rare diseases +MONDO:0021429 rare diseases +MONDO:0021431 gard_rare diseases +MONDO:0021431 rare diseases +MONDO:0021439 inferred_rare diseases +MONDO:0021439 otar diseases +MONDO:0021439 rare diseases +MONDO:0021440 otar diseases +MONDO:0021443 inferred_rare diseases +MONDO:0021443 rare diseases +MONDO:0021444 otar diseases +MONDO:0021445 otar diseases +MONDO:0021449 otar diseases +MONDO:0021451 otar diseases +MONDO:0021454 otar diseases +MONDO:0021460 otar diseases +MONDO:0021462 otar diseases +MONDO:0021463 otar diseases +MONDO:0021468 inferred_rare diseases +MONDO:0021468 rare diseases +MONDO:0021469 otar diseases +MONDO:0021470 otar diseases +MONDO:0021477 inferred_rare diseases +MONDO:0021477 rare diseases +MONDO:0021483 inferred_rare diseases +MONDO:0021483 rare diseases +MONDO:0021484 inferred_rare diseases +MONDO:0021484 rare diseases +MONDO:0021489 otar diseases +MONDO:0021498 otar diseases +MONDO:0021500 inferred_rare diseases +MONDO:0021500 rare diseases +MONDO:0021501 otar diseases +MONDO:0021510 otar diseases +MONDO:0021511 inferred_rare diseases +MONDO:0021511 otar diseases +MONDO:0021511 rare diseases +MONDO:0021512 inferred_rare diseases +MONDO:0021512 rare diseases +MONDO:0021515 inferred_rare diseases +MONDO:0021515 rare diseases +MONDO:0021522 inferred_rare diseases +MONDO:0021522 rare diseases +MONDO:0021527 inferred_rare diseases +MONDO:0021527 rare diseases +MONDO:0021533 gard_rare diseases +MONDO:0021533 otar diseases +MONDO:0021533 rare diseases +MONDO:0021534 gard_rare diseases +MONDO:0021534 rare diseases +MONDO:0021535 gard_rare diseases +MONDO:0021535 rare diseases +MONDO:0021537 gard_rare diseases +MONDO:0021537 nord_rare diseases +MONDO:0021537 rare diseases +MONDO:0021538 gard_rare diseases +MONDO:0021538 rare diseases +MONDO:0021545 otar diseases +MONDO:0021546 gard_rare diseases +MONDO:0021546 rare diseases +MONDO:0021547 gard_rare diseases +MONDO:0021547 rare diseases +MONDO:0021548 gard_rare diseases +MONDO:0021548 nord_rare diseases +MONDO:0021548 ordo_subtype_of_a_disorder diseases +MONDO:0021548 otar diseases +MONDO:0021548 rare diseases +MONDO:0021553 otar diseases +MONDO:0021559 gard_rare diseases +MONDO:0021559 otar diseases +MONDO:0021559 rare diseases +MONDO:0021568 otar diseases +MONDO:0021569 gard_rare diseases +MONDO:0021569 nord_rare diseases +MONDO:0021569 otar diseases +MONDO:0021569 rare diseases +MONDO:0021573 gard_rare diseases +MONDO:0021573 rare diseases +MONDO:0021575 gard_rare diseases +MONDO:0021575 rare diseases +MONDO:0021579 gard_rare diseases +MONDO:0021579 rare diseases +MONDO:0021580 gard_rare diseases +MONDO:0021580 rare diseases +MONDO:0021581 otar diseases +MONDO:0021582 otar diseases +MONDO:0021583 otar diseases +MONDO:0021588 gard_rare diseases +MONDO:0021588 ordo_disorder diseases +MONDO:0021588 orphanet_rare diseases +MONDO:0021588 rare diseases +MONDO:0021605 otar diseases +MONDO:0021631 gard_rare diseases +MONDO:0021631 otar diseases +MONDO:0021631 rare diseases +MONDO:0021632 otar diseases +MONDO:0021633 gard_rare diseases +MONDO:0021633 otar diseases +MONDO:0021633 rare diseases +MONDO:0021634 otar diseases +MONDO:0021636 disease_grouping diseases +MONDO:0021636 gard_rare diseases +MONDO:0021636 ordo_group_of_disorders diseases +MONDO:0021636 otar diseases +MONDO:0021636 rare diseases +MONDO:0021637 gard_rare diseases +MONDO:0021637 otar diseases +MONDO:0021637 rare diseases +MONDO:0021638 gard_rare diseases +MONDO:0021638 rare diseases +MONDO:0021639 gard_rare diseases +MONDO:0021639 otar diseases +MONDO:0021639 rare diseases +MONDO:0021640 gard_rare diseases +MONDO:0021640 otar diseases +MONDO:0021640 rare diseases +MONDO:0021641 otar diseases +MONDO:0021650 gard_rare diseases +MONDO:0021650 rare diseases +MONDO:0021651 gard_rare diseases +MONDO:0021651 nord_rare diseases +MONDO:0021651 ordo_disorder diseases +MONDO:0021651 ordo_morphological_anomaly diseases +MONDO:0021651 orphanet_rare diseases +MONDO:0021651 otar diseases +MONDO:0021651 rare diseases +MONDO:0021652 otar diseases +MONDO:0021653 otar diseases +MONDO:0021656 gard_rare diseases +MONDO:0021656 otar diseases +MONDO:0021656 rare diseases +MONDO:0021657 otar diseases +MONDO:0021658 otar diseases +MONDO:0021660 gard_rare diseases +MONDO:0021660 nord_rare diseases +MONDO:0021660 ordo_disorder diseases +MONDO:0021660 orphanet_rare diseases +MONDO:0021660 rare diseases +MONDO:0021661 otar diseases +MONDO:0021662 otar diseases +MONDO:0021663 otar diseases +MONDO:0021666 otar diseases +MONDO:0021667 gard_rare diseases +MONDO:0021667 otar diseases +MONDO:0021667 rare diseases +MONDO:0021669 otar diseases +MONDO:0021677 gard_rare diseases +MONDO:0021677 rare diseases +MONDO:0021678 otar diseases +MONDO:0021679 otar diseases +MONDO:0021680 otar diseases +MONDO:0021681 otar diseases +MONDO:0021697 otar diseases +MONDO:0021698 otar diseases +MONDO:0021699 otar diseases +MONDO:0021702 otar diseases +MONDO:0021718 gard_rare diseases +MONDO:0021718 otar diseases +MONDO:0021718 rare diseases +MONDO:0021726 gard_rare diseases +MONDO:0021726 rare diseases +MONDO:0021739 otar diseases +MONDO:0021742 otar diseases +MONDO:0021747 otar diseases +MONDO:0021758 gard_rare diseases +MONDO:0021758 nord_rare diseases +MONDO:0021758 rare diseases +MONDO:0021759 inferred_rare diseases +MONDO:0021759 rare diseases +MONDO:0021762 gard_rare diseases +MONDO:0021762 rare diseases +MONDO:0021764 gard_rare diseases +MONDO:0021764 n_of_one diseases +MONDO:0021764 rare diseases +MONDO:0021765 otar diseases +MONDO:0021804 gard_rare diseases +MONDO:0021804 nord_rare diseases +MONDO:0021804 otar diseases +MONDO:0021804 rare diseases +MONDO:0021805 gard_rare diseases +MONDO:0021805 nord_rare diseases +MONDO:0021805 rare diseases +MONDO:0021812 otar diseases +MONDO:0021824 gard_rare diseases +MONDO:0021824 nord_rare diseases +MONDO:0021824 rare diseases +MONDO:0021826 gard_rare diseases +MONDO:0021826 rare diseases +MONDO:0021836 n_of_one diseases +MONDO:0021838 gard_rare diseases +MONDO:0021838 n_of_one diseases +MONDO:0021838 rare diseases +MONDO:0021839 otar diseases +MONDO:0021845 gard_rare diseases +MONDO:0021845 n_of_one diseases +MONDO:0021845 rare diseases +MONDO:0021851 gard_rare diseases +MONDO:0021851 rare diseases +MONDO:0021879 gard_rare diseases +MONDO:0021879 nord_rare diseases +MONDO:0021879 rare diseases +MONDO:0021895 gard_rare diseases +MONDO:0021895 rare diseases +MONDO:0021907 gard_rare diseases +MONDO:0021907 nord_rare diseases +MONDO:0021907 rare diseases +MONDO:0021908 gard_rare diseases +MONDO:0021908 rare diseases +MONDO:0021915 gard_rare diseases +MONDO:0021915 rare diseases +MONDO:0021921 gard_rare diseases +MONDO:0021921 rare diseases +MONDO:0021923 n_of_one diseases +MONDO:0021925 otar diseases +MONDO:0021929 gard_rare diseases +MONDO:0021929 rare diseases +MONDO:0021932 gard_rare diseases +MONDO:0021932 rare diseases +MONDO:0021935 gard_rare diseases +MONDO:0021935 rare diseases +MONDO:0021941 gard_rare diseases +MONDO:0021941 rare diseases +MONDO:0021943 gard_rare diseases +MONDO:0021943 rare diseases +MONDO:0021944 clingen diseases +MONDO:0021944 gard_rare diseases +MONDO:0021944 nord_rare diseases +MONDO:0021944 otar diseases +MONDO:0021944 rare diseases +MONDO:0021945 otar diseases +MONDO:0021948 gard_rare diseases +MONDO:0021948 rare diseases +MONDO:0021953 gard_rare diseases +MONDO:0021953 rare diseases +MONDO:0021957 gard_rare diseases +MONDO:0021957 nord_rare diseases +MONDO:0021957 rare diseases +MONDO:0021964 gard_rare diseases +MONDO:0021964 nord_rare diseases +MONDO:0021964 rare diseases +MONDO:0021966 n_of_one diseases +MONDO:0021994 gard_rare diseases +MONDO:0021994 nord_rare diseases +MONDO:0021994 rare diseases +MONDO:0022022 gard_rare diseases +MONDO:0022022 nord_rare diseases +MONDO:0022022 rare diseases +MONDO:0022025 gard_rare diseases +MONDO:0022025 rare diseases +MONDO:0022034 otar diseases +MONDO:0022037 gard_rare diseases +MONDO:0022037 nord_rare diseases +MONDO:0022037 rare diseases +MONDO:0022055 gard_rare diseases +MONDO:0022055 rare diseases +MONDO:0022057 otar diseases +MONDO:0022096 otar diseases +MONDO:0022113 gard_rare diseases +MONDO:0022113 nord_rare diseases +MONDO:0022113 otar diseases +MONDO:0022113 rare diseases +MONDO:0022173 disease_grouping diseases +MONDO:0022173 gard_rare diseases +MONDO:0022173 ordo_group_of_disorders diseases +MONDO:0022173 rare diseases +MONDO:0022174 disease_grouping diseases +MONDO:0022174 gard_rare diseases +MONDO:0022174 ordo_group_of_disorders diseases +MONDO:0022174 rare diseases +MONDO:0022177 disease_grouping diseases +MONDO:0022177 gard_rare diseases +MONDO:0022177 nord_rare diseases +MONDO:0022177 ordo_group_of_disorders diseases +MONDO:0022177 rare diseases +MONDO:0022178 gard_rare diseases +MONDO:0022178 nord_rare diseases +MONDO:0022178 rare diseases +MONDO:0022180 gard_rare diseases +MONDO:0022180 nord_rare diseases +MONDO:0022180 otar diseases +MONDO:0022180 rare diseases +MONDO:0022208 otar diseases +MONDO:0022311 gard_rare diseases +MONDO:0022311 rare diseases +MONDO:0022316 ordo_malformation_syndrome diseases +MONDO:0022321 gard_rare diseases +MONDO:0022321 rare diseases +MONDO:0022330 gard_rare diseases +MONDO:0022330 rare diseases +MONDO:0022333 gard_rare diseases +MONDO:0022333 rare diseases +MONDO:0022349 gard_rare diseases +MONDO:0022349 nord_rare diseases +MONDO:0022349 rare diseases +MONDO:0022357 gard_rare diseases +MONDO:0022357 nord_rare diseases +MONDO:0022357 rare diseases +MONDO:0022394 gard_rare diseases +MONDO:0022394 nord_rare diseases +MONDO:0022394 otar diseases +MONDO:0022394 rare diseases +MONDO:0022410 disease_grouping diseases +MONDO:0022410 gard_rare diseases +MONDO:0022410 ordo_group_of_disorders diseases +MONDO:0022410 otar diseases +MONDO:0022410 rare diseases +MONDO:0022417 gard_rare diseases +MONDO:0022417 rare diseases +MONDO:0022424 gard_rare diseases +MONDO:0022424 nord_rare diseases +MONDO:0022424 rare diseases +MONDO:0022430 otar diseases +MONDO:0022432 gard_rare diseases +MONDO:0022432 rare diseases +MONDO:0022444 gard_rare diseases +MONDO:0022444 rare diseases +MONDO:0022454 nord_rare diseases +MONDO:0022454 rare diseases +MONDO:0022462 n_of_one diseases +MONDO:0022468 gard_rare diseases +MONDO:0022468 rare diseases +MONDO:0022471 gard_rare diseases +MONDO:0022471 rare diseases +MONDO:0022481 gard_rare diseases +MONDO:0022481 rare diseases +MONDO:0022513 gard_rare diseases +MONDO:0022513 ordo_disorder diseases +MONDO:0022513 orphanet_rare diseases +MONDO:0022513 rare diseases +MONDO:0022519 gard_rare diseases +MONDO:0022519 nord_rare diseases +MONDO:0022519 rare diseases +MONDO:0022529 otar diseases +MONDO:0022552 gard_rare diseases +MONDO:0022552 rare diseases +MONDO:0022557 gard_rare diseases +MONDO:0022557 rare diseases +MONDO:0022559 gard_rare diseases +MONDO:0022559 nord_rare diseases +MONDO:0022559 rare diseases +MONDO:0022572 gard_rare diseases +MONDO:0022572 rare diseases +MONDO:0022573 gard_rare diseases +MONDO:0022573 rare diseases +MONDO:0022574 gard_rare diseases +MONDO:0022574 rare diseases +MONDO:0022575 obsoletion_candidate diseases +MONDO:0022577 obsoletion_candidate diseases +MONDO:0022586 gard_rare diseases +MONDO:0022586 rare diseases +MONDO:0022587 gard_rare diseases +MONDO:0022587 rare diseases +MONDO:0022608 gard_rare diseases +MONDO:0022608 rare diseases +MONDO:0022611 gard_rare diseases +MONDO:0022611 rare diseases +MONDO:0022618 gard_rare diseases +MONDO:0022618 rare diseases +MONDO:0022622 gard_rare diseases +MONDO:0022622 rare diseases +MONDO:0022642 gard_rare diseases +MONDO:0022642 rare diseases +MONDO:0022653 gard_rare diseases +MONDO:0022653 nord_rare diseases +MONDO:0022653 rare diseases +MONDO:0022655 gard_rare diseases +MONDO:0022655 rare diseases +MONDO:0022687 otar diseases +MONDO:0022714 nord_rare diseases +MONDO:0022714 rare diseases +MONDO:0022723 otar diseases +MONDO:0022736 otar diseases +MONDO:0022737 gard_rare diseases +MONDO:0022737 rare diseases +MONDO:0022745 gard_rare diseases +MONDO:0022745 nord_rare diseases +MONDO:0022745 rare diseases +MONDO:0022746 gard_rare diseases +MONDO:0022746 rare diseases +MONDO:0022749 otar diseases +MONDO:0022752 gard_rare diseases +MONDO:0022752 rare diseases +MONDO:0022754 disease_grouping diseases +MONDO:0022754 gard_rare diseases +MONDO:0022754 ordo_group_of_disorders diseases +MONDO:0022754 otar diseases +MONDO:0022754 rare diseases +MONDO:0022755 gard_rare diseases +MONDO:0022755 nord_rare diseases +MONDO:0022755 rare diseases +MONDO:0022756 disease_grouping diseases +MONDO:0022756 gard_rare diseases +MONDO:0022756 ordo_group_of_disorders diseases +MONDO:0022756 rare diseases +MONDO:0022757 gard_rare diseases +MONDO:0022757 rare diseases +MONDO:0022758 gard_rare diseases +MONDO:0022758 rare diseases +MONDO:0022759 gard_rare diseases +MONDO:0022759 nord_rare diseases +MONDO:0022759 rare diseases +MONDO:0022760 disease_grouping diseases +MONDO:0022760 gard_rare diseases +MONDO:0022760 ordo_group_of_disorders diseases +MONDO:0022760 rare diseases +MONDO:0022761 gard_rare diseases +MONDO:0022761 rare diseases +MONDO:0022762 disease_grouping diseases +MONDO:0022762 gard_rare diseases +MONDO:0022762 ordo_group_of_disorders diseases +MONDO:0022762 rare diseases +MONDO:0022768 gard_rare diseases +MONDO:0022768 rare diseases +MONDO:0022772 gard_rare diseases +MONDO:0022772 rare diseases +MONDO:0022795 gard_rare diseases +MONDO:0022795 rare diseases +MONDO:0022799 otar diseases +MONDO:0022800 disease_grouping diseases +MONDO:0022800 gard_rare diseases +MONDO:0022800 nord_rare diseases +MONDO:0022800 ordo_group_of_disorders diseases +MONDO:0022800 otar diseases +MONDO:0022800 rare diseases +MONDO:0022812 gard_rare diseases +MONDO:0022812 rare diseases +MONDO:0022825 gard_rare diseases +MONDO:0022825 nord_rare diseases +MONDO:0022825 ordo_disorder diseases +MONDO:0022825 ordo_morphological_anomaly diseases +MONDO:0022825 orphanet_rare diseases +MONDO:0022825 rare diseases +MONDO:0022826 gard_rare diseases +MONDO:0022826 rare diseases +MONDO:0022851 gard_rare diseases +MONDO:0022851 n_of_one diseases +MONDO:0022851 ordo_disorder diseases +MONDO:0022851 orphanet_rare diseases +MONDO:0022851 rare diseases +MONDO:0022858 obsoletion_candidate diseases +MONDO:0022869 obsoletion_candidate diseases +MONDO:0022890 gard_rare diseases +MONDO:0022890 nord_rare diseases +MONDO:0022890 rare diseases +MONDO:0022891 gard_rare diseases +MONDO:0022891 rare diseases +MONDO:0022892 gard_rare diseases +MONDO:0022892 rare diseases +MONDO:0022893 gard_rare diseases +MONDO:0022893 rare diseases +MONDO:0022894 gard_rare diseases +MONDO:0022894 rare diseases +MONDO:0022895 gard_rare diseases +MONDO:0022895 rare diseases +MONDO:0022896 gard_rare diseases +MONDO:0022896 rare diseases +MONDO:0022897 gard_rare diseases +MONDO:0022897 rare diseases +MONDO:0022898 gard_rare diseases +MONDO:0022898 rare diseases +MONDO:0022900 gard_rare diseases +MONDO:0022900 obsoletion_candidate diseases +MONDO:0022900 rare diseases +MONDO:0022912 gard_rare diseases +MONDO:0022912 rare diseases +MONDO:0022930 gard_rare diseases +MONDO:0022930 nord_rare diseases +MONDO:0022930 rare diseases +MONDO:0022932 n_of_one diseases +MONDO:0022948 gard_rare diseases +MONDO:0022948 rare diseases +MONDO:0022949 gard_rare diseases +MONDO:0022949 rare diseases +MONDO:0022963 gard_rare diseases +MONDO:0022963 nord_rare diseases +MONDO:0022963 otar diseases +MONDO:0022963 rare diseases +MONDO:0022965 gard_rare diseases +MONDO:0022965 nord_rare diseases +MONDO:0022965 otar diseases +MONDO:0022965 rare diseases +MONDO:0022982 obsoletion_candidate diseases +MONDO:0022983 gard_rare diseases +MONDO:0022983 nord_rare diseases +MONDO:0022983 rare diseases +MONDO:0022986 gard_rare diseases +MONDO:0022986 nord_rare diseases +MONDO:0022986 ordo_disorder diseases +MONDO:0022986 orphanet_rare diseases +MONDO:0022986 rare diseases +MONDO:0022991 gard_rare diseases +MONDO:0022991 nord_rare diseases +MONDO:0022991 rare diseases +MONDO:0022998 gard_rare diseases +MONDO:0022998 rare diseases +MONDO:0023006 gard_rare diseases +MONDO:0023006 nord_rare diseases +MONDO:0023006 rare diseases +MONDO:0023007 gard_rare diseases +MONDO:0023007 nord_rare diseases +MONDO:0023007 rare diseases +MONDO:0023011 gard_rare diseases +MONDO:0023011 nord_rare diseases +MONDO:0023011 rare diseases +MONDO:0023040 gard_rare diseases +MONDO:0023040 nord_rare diseases +MONDO:0023040 rare diseases +MONDO:0023042 gard_rare diseases +MONDO:0023042 nord_rare diseases +MONDO:0023042 rare diseases +MONDO:0023043 gard_rare diseases +MONDO:0023043 rare diseases +MONDO:0023045 gard_rare diseases +MONDO:0023045 nord_rare diseases +MONDO:0023045 rare diseases +MONDO:0023046 gard_rare diseases +MONDO:0023046 rare diseases +MONDO:0023048 gard_rare diseases +MONDO:0023048 rare diseases +MONDO:0023054 gard_rare diseases +MONDO:0023054 nord_rare diseases +MONDO:0023054 rare diseases +MONDO:0023067 gard_rare diseases +MONDO:0023067 nord_rare diseases +MONDO:0023067 rare diseases +MONDO:0023069 clingen diseases +MONDO:0023069 otar diseases +MONDO:0023076 gard_rare diseases +MONDO:0023076 nord_rare diseases +MONDO:0023076 rare diseases +MONDO:0023099 gard_rare diseases +MONDO:0023099 rare diseases +MONDO:0023113 gard_rare diseases +MONDO:0023113 nord_rare diseases +MONDO:0023113 otar diseases +MONDO:0023113 rare diseases +MONDO:0023119 gard_rare diseases +MONDO:0023119 rare diseases +MONDO:0023122 gard_rare diseases +MONDO:0023122 nord_rare diseases +MONDO:0023122 ordo_disorder diseases +MONDO:0023122 orphanet_rare diseases +MONDO:0023122 otar diseases +MONDO:0023122 rare diseases +MONDO:0023134 gard_rare diseases +MONDO:0023134 rare diseases +MONDO:0023143 gard_rare diseases +MONDO:0023143 rare diseases +MONDO:0023147 gard_rare diseases +MONDO:0023147 nord_rare diseases +MONDO:0023147 rare diseases +MONDO:0023148 gard_rare diseases +MONDO:0023148 rare diseases +MONDO:0023149 gard_rare diseases +MONDO:0023149 nord_rare diseases +MONDO:0023149 otar diseases +MONDO:0023149 rare diseases +MONDO:0023153 gard_rare diseases +MONDO:0023153 rare diseases +MONDO:0023161 gard_rare diseases +MONDO:0023161 nord_rare diseases +MONDO:0023161 rare diseases +MONDO:0023171 gard_rare diseases +MONDO:0023171 nord_rare diseases +MONDO:0023171 ordo_disorder diseases +MONDO:0023171 orphanet_rare diseases +MONDO:0023171 rare diseases +MONDO:0023175 gard_rare diseases +MONDO:0023175 nord_rare diseases +MONDO:0023175 rare diseases +MONDO:0023176 gard_rare diseases +MONDO:0023176 nord_rare diseases +MONDO:0023176 rare diseases +MONDO:0023178 inferred_rare diseases +MONDO:0023178 rare diseases +MONDO:0023179 inferred_rare diseases +MONDO:0023179 rare diseases +MONDO:0023180 inferred_rare diseases +MONDO:0023180 rare diseases +MONDO:0023182 gard_rare diseases +MONDO:0023182 rare diseases +MONDO:0023188 gard_rare diseases +MONDO:0023188 nord_rare diseases +MONDO:0023188 ordo_disorder diseases +MONDO:0023188 orphanet_rare diseases +MONDO:0023188 rare diseases +MONDO:0023193 obsoletion_candidate diseases +MONDO:0023201 gard_rare diseases +MONDO:0023201 ordo_disorder diseases +MONDO:0023201 orphanet_rare diseases +MONDO:0023201 rare diseases +MONDO:0023204 gard_rare diseases +MONDO:0023204 nord_rare diseases +MONDO:0023204 rare diseases +MONDO:0023206 disease_grouping diseases +MONDO:0023206 gard_rare diseases +MONDO:0023206 ordo_group_of_disorders diseases +MONDO:0023206 otar diseases +MONDO:0023206 rare diseases +MONDO:0023209 gard_rare diseases +MONDO:0023209 rare diseases +MONDO:0023224 gard_rare diseases +MONDO:0023224 nord_rare diseases +MONDO:0023224 rare diseases +MONDO:0023232 gard_rare diseases +MONDO:0023232 nord_rare diseases +MONDO:0023232 rare diseases +MONDO:0023243 inferred_rare diseases +MONDO:0023243 n_of_one diseases +MONDO:0023243 rare diseases +MONDO:0023246 gard_rare diseases +MONDO:0023246 nord_rare diseases +MONDO:0023246 rare diseases +MONDO:0023249 gard_rare diseases +MONDO:0023249 nord_rare diseases +MONDO:0023249 rare diseases +MONDO:0023250 gard_rare diseases +MONDO:0023250 rare diseases +MONDO:0023258 gard_rare diseases +MONDO:0023258 otar diseases +MONDO:0023258 rare diseases +MONDO:0023273 gard_rare diseases +MONDO:0023273 nord_rare diseases +MONDO:0023273 rare diseases +MONDO:0023275 gard_rare diseases +MONDO:0023275 nord_rare diseases +MONDO:0023275 ordo_disorder diseases +MONDO:0023275 orphanet_rare diseases +MONDO:0023275 rare diseases +MONDO:0023286 gard_rare diseases +MONDO:0023286 rare diseases +MONDO:0023297 otar diseases +MONDO:0023305 gard_rare diseases +MONDO:0023305 nord_rare diseases +MONDO:0023305 otar diseases +MONDO:0023305 rare diseases +MONDO:0023370 otar diseases +MONDO:0023388 gard_rare diseases +MONDO:0023388 nord_rare diseases +MONDO:0023388 rare diseases +MONDO:0023419 gard_rare diseases +MONDO:0023419 otar diseases +MONDO:0023419 rare diseases +MONDO:0023483 gard_rare diseases +MONDO:0023483 rare diseases +MONDO:0023513 gard_rare diseases +MONDO:0023513 n_of_one diseases +MONDO:0023513 rare diseases +MONDO:0023521 gard_rare diseases +MONDO:0023521 rare diseases +MONDO:0023551 gard_rare diseases +MONDO:0023551 nord_rare diseases +MONDO:0023551 rare diseases +MONDO:0023557 otar diseases +MONDO:0023558 gard_rare diseases +MONDO:0023558 nord_rare diseases +MONDO:0023558 rare diseases +MONDO:0023563 gard_rare diseases +MONDO:0023563 rare diseases +MONDO:0023573 gard_rare diseases +MONDO:0023573 nord_rare diseases +MONDO:0023573 rare diseases +MONDO:0023581 gard_rare diseases +MONDO:0023581 rare diseases +MONDO:0023595 gard_rare diseases +MONDO:0023595 nord_rare diseases +MONDO:0023595 rare diseases +MONDO:0023597 gard_rare diseases +MONDO:0023597 nord_rare diseases +MONDO:0023597 rare diseases +MONDO:0023601 gard_rare diseases +MONDO:0023601 rare diseases +MONDO:0023603 otar diseases +MONDO:0023619 otar diseases +MONDO:0023642 gard_rare diseases +MONDO:0023642 nord_rare diseases +MONDO:0023642 rare diseases +MONDO:0023644 otar diseases +MONDO:0023646 gard_rare diseases +MONDO:0023646 rare diseases +MONDO:0023650 gard_rare diseases +MONDO:0023650 nord_rare diseases +MONDO:0023650 rare diseases +MONDO:0023655 clingen diseases +MONDO:0023657 gard_rare diseases +MONDO:0023657 rare diseases +MONDO:0023659 gard_rare diseases +MONDO:0023659 nord_rare diseases +MONDO:0023659 rare diseases +MONDO:0023660 gard_rare diseases +MONDO:0023660 rare diseases +MONDO:0023662 gard_rare diseases +MONDO:0023662 nord_rare diseases +MONDO:0023662 rare diseases +MONDO:0023670 gard_rare diseases +MONDO:0023670 nord_rare diseases +MONDO:0023670 otar diseases +MONDO:0023670 rare diseases +MONDO:0023671 gard_rare diseases +MONDO:0023671 nord_rare diseases +MONDO:0023671 rare diseases +MONDO:0023679 gard_rare diseases +MONDO:0023679 nord_rare diseases +MONDO:0023679 rare diseases +MONDO:0023682 gard_rare diseases +MONDO:0023682 rare diseases +MONDO:0023691 clingen diseases +MONDO:0023691 gard_rare diseases +MONDO:0023691 otar diseases +MONDO:0023691 rare diseases +MONDO:0023692 clingen diseases +MONDO:0023692 gard_rare diseases +MONDO:0023692 otar diseases +MONDO:0023692 rare diseases +MONDO:0023693 gard_rare diseases +MONDO:0023693 rare diseases +MONDO:0023699 gard_rare diseases +MONDO:0023699 nord_rare diseases +MONDO:0023699 rare diseases +MONDO:0023704 gard_rare diseases +MONDO:0023704 n_of_one diseases +MONDO:0023704 rare diseases +MONDO:0023726 gard_rare diseases +MONDO:0023726 otar diseases +MONDO:0023726 rare diseases +MONDO:0023757 gard_rare diseases +MONDO:0023757 nord_rare diseases +MONDO:0023757 otar diseases +MONDO:0023757 rare diseases +MONDO:0023833 gard_rare diseases +MONDO:0023833 nord_rare diseases +MONDO:0023833 rare diseases +MONDO:0023865 disease_grouping diseases +MONDO:0023865 inferred_rare diseases +MONDO:0023865 ordo_group_of_disorders diseases +MONDO:0023865 otar diseases +MONDO:0023865 rare diseases +MONDO:0023868 gard_rare diseases +MONDO:0023868 nord_rare diseases +MONDO:0023868 otar diseases +MONDO:0023868 rare diseases +MONDO:0023880 clingen diseases +MONDO:0023910 gard_rare diseases +MONDO:0023910 rare diseases +MONDO:0024237 clingen diseases +MONDO:0024237 disease_grouping diseases +MONDO:0024237 gard_rare diseases +MONDO:0024237 ordo_group_of_disorders diseases +MONDO:0024237 otar diseases +MONDO:0024237 rare diseases +MONDO:0024239 otar diseases +MONDO:0024240 otar diseases +MONDO:0024247 otar diseases +MONDO:0024249 gard_rare diseases +MONDO:0024249 rare diseases +MONDO:0024250 gard_rare diseases +MONDO:0024250 rare diseases +MONDO:0024252 gard_rare diseases +MONDO:0024252 nord_rare diseases +MONDO:0024252 obsoletion_candidate diseases +MONDO:0024252 ordo_disorder diseases +MONDO:0024252 ordo_malformation_syndrome diseases +MONDO:0024252 orphanet_rare diseases +MONDO:0024252 otar diseases +MONDO:0024252 rare diseases +MONDO:0024257 disease_grouping diseases +MONDO:0024257 gard_rare diseases +MONDO:0024257 ordo_group_of_disorders diseases +MONDO:0024257 otar diseases +MONDO:0024257 rare diseases +MONDO:0024264 gard_rare diseases +MONDO:0024264 nord_rare diseases +MONDO:0024264 rare diseases +MONDO:0024265 gard_rare diseases +MONDO:0024265 nord_rare diseases +MONDO:0024265 rare diseases +MONDO:0024266 gard_rare diseases +MONDO:0024266 nord_rare diseases +MONDO:0024266 rare diseases +MONDO:0024268 otar diseases +MONDO:0024270 otar diseases +MONDO:0024271 otar diseases +MONDO:0024275 otar diseases +MONDO:0024276 otar diseases +MONDO:0024277 gard_rare diseases +MONDO:0024277 nord_rare diseases +MONDO:0024277 rare diseases +MONDO:0024280 otar diseases +MONDO:0024282 gard_rare diseases +MONDO:0024282 otar diseases +MONDO:0024282 rare diseases +MONDO:0024283 gard_rare diseases +MONDO:0024283 rare diseases +MONDO:0024284 gard_rare diseases +MONDO:0024284 rare diseases +MONDO:0024285 gard_rare diseases +MONDO:0024285 rare diseases +MONDO:0024286 otar diseases +MONDO:0024287 otar diseases +MONDO:0024290 otar diseases +MONDO:0024291 otar diseases +MONDO:0024292 otar diseases +MONDO:0024294 otar diseases +MONDO:0024295 otar diseases +MONDO:0024296 otar diseases +MONDO:0024298 otar diseases +MONDO:0024299 gard_rare diseases +MONDO:0024299 otar diseases +MONDO:0024299 rare diseases +MONDO:0024300 gard_rare diseases +MONDO:0024300 otar diseases +MONDO:0024300 rare diseases +MONDO:0024304 gard_rare diseases +MONDO:0024304 rare diseases +MONDO:0024305 otar diseases +MONDO:0024307 gard_rare diseases +MONDO:0024307 nord_rare diseases +MONDO:0024307 otar diseases +MONDO:0024307 rare diseases +MONDO:0024308 otar diseases +MONDO:0024309 clingen diseases +MONDO:0024309 gard_rare diseases +MONDO:0024309 nord_rare diseases +MONDO:0024309 rare diseases +MONDO:0024311 gard_rare diseases +MONDO:0024311 rare diseases +MONDO:0024312 gard_rare diseases +MONDO:0024312 rare diseases +MONDO:0024313 otar diseases +MONDO:0024314 gard_rare diseases +MONDO:0024314 rare diseases +MONDO:0024315 gard_rare diseases +MONDO:0024315 rare diseases +MONDO:0024318 gard_rare diseases +MONDO:0024318 otar diseases +MONDO:0024318 rare diseases +MONDO:0024322 otar diseases +MONDO:0024323 gard_rare diseases +MONDO:0024323 rare diseases +MONDO:0024325 gard_rare diseases +MONDO:0024325 rare diseases +MONDO:0024331 otar diseases +MONDO:0024332 otar diseases +MONDO:0024333 gard_rare diseases +MONDO:0024333 rare diseases +MONDO:0024334 gard_rare diseases +MONDO:0024334 otar diseases +MONDO:0024334 rare diseases +MONDO:0024336 gard_rare diseases +MONDO:0024336 nord_rare diseases +MONDO:0024336 ordo_subtype_of_a_disorder diseases +MONDO:0024336 rare diseases +MONDO:0024337 otar diseases +MONDO:0024338 otar diseases +MONDO:0024339 gard_rare diseases +MONDO:0024339 nord_rare diseases +MONDO:0024339 otar diseases +MONDO:0024339 rare diseases +MONDO:0024340 gard_rare diseases +MONDO:0024340 nord_rare diseases +MONDO:0024340 rare diseases +MONDO:0024352 otar diseases +MONDO:0024355 otar diseases +MONDO:0024358 otar diseases +MONDO:0024361 obsoletion_candidate diseases +MONDO:0024361 otar diseases +MONDO:0024387 otar diseases +MONDO:0024388 otar diseases +MONDO:0024389 otar diseases +MONDO:0024416 gard_rare diseases +MONDO:0024416 rare diseases +MONDO:0024417 otar diseases +MONDO:0024418 gard_rare diseases +MONDO:0024418 nord_rare diseases +MONDO:0024418 rare diseases +MONDO:0024419 otar diseases +MONDO:0024431 otar diseases +MONDO:0024432 gard_rare diseases +MONDO:0024432 otar diseases +MONDO:0024432 rare diseases +MONDO:0024454 gard_rare diseases +MONDO:0024454 rare diseases +MONDO:0024455 gard_rare diseases +MONDO:0024455 nord_rare diseases +MONDO:0024455 rare diseases +MONDO:0024456 clingen diseases +MONDO:0024456 gard_rare diseases +MONDO:0024456 nord_rare diseases +MONDO:0024456 rare diseases +MONDO:0024457 gard_rare diseases +MONDO:0024457 nord_rare diseases +MONDO:0024457 ordo_disorder diseases +MONDO:0024457 orphanet_rare diseases +MONDO:0024457 otar diseases +MONDO:0024457 rare diseases +MONDO:0024458 otar diseases +MONDO:0024458 rare_grouping diseases +MONDO:0024462 inferred_rare diseases +MONDO:0024462 rare diseases +MONDO:0024463 gard_rare diseases +MONDO:0024463 nord_rare diseases +MONDO:0024463 rare diseases +MONDO:0024464 gard_rare diseases +MONDO:0024464 nord_rare diseases +MONDO:0024464 otar diseases +MONDO:0024464 rare diseases +MONDO:0024465 gard_rare diseases +MONDO:0024465 nord_rare diseases +MONDO:0024465 rare diseases +MONDO:0024466 gard_rare diseases +MONDO:0024466 nord_rare diseases +MONDO:0024466 rare diseases +MONDO:0024468 otar diseases +MONDO:0024469 otar diseases +MONDO:0024470 otar diseases +MONDO:0024472 gard_rare diseases +MONDO:0024472 nord_rare diseases +MONDO:0024472 ordo_disorder diseases +MONDO:0024472 ordo_etiological_subtype diseases +MONDO:0024472 orphanet_rare diseases +MONDO:0024472 rare diseases +MONDO:0024473 gard_rare diseases +MONDO:0024473 nord_rare diseases +MONDO:0024473 rare diseases +MONDO:0024474 otar diseases +MONDO:0024475 otar diseases +MONDO:0024476 otar diseases +MONDO:0024477 otar diseases +MONDO:0024478 otar diseases +MONDO:0024479 otar diseases +MONDO:0024481 otar diseases +MONDO:0024483 otar diseases +MONDO:0024498 gard_rare diseases +MONDO:0024498 predisposition diseases +MONDO:0024498 rare diseases +MONDO:0024499 gard_rare diseases +MONDO:0024499 nord_rare diseases +MONDO:0024499 rare diseases +MONDO:0024500 gard_rare diseases +MONDO:0024500 otar diseases +MONDO:0024500 rare diseases +MONDO:0024501 gard_rare diseases +MONDO:0024501 otar diseases +MONDO:0024501 rare diseases +MONDO:0024502 gard_rare diseases +MONDO:0024502 rare diseases +MONDO:0024503 disease_grouping diseases +MONDO:0024503 gard_rare diseases +MONDO:0024503 nord_rare diseases +MONDO:0024503 ordo_group_of_disorders diseases +MONDO:0024503 otar diseases +MONDO:0024503 rare diseases +MONDO:0024504 gard_rare diseases +MONDO:0024504 nord_rare diseases +MONDO:0024504 ordo_disorder diseases +MONDO:0024504 orphanet_rare diseases +MONDO:0024504 rare diseases +MONDO:0024506 gard_rare diseases +MONDO:0024506 nord_rare diseases +MONDO:0024506 rare diseases +MONDO:0024507 gard_rare diseases +MONDO:0024507 nord_rare diseases +MONDO:0024507 rare diseases +MONDO:0024508 gard_rare diseases +MONDO:0024508 rare diseases +MONDO:0024516 otar diseases +MONDO:0024517 gard_rare diseases +MONDO:0024517 nord_rare diseases +MONDO:0024517 rare diseases +MONDO:0024518 gard_rare diseases +MONDO:0024518 rare diseases +MONDO:0024519 gard_rare diseases +MONDO:0024519 nord_rare diseases +MONDO:0024519 otar diseases +MONDO:0024519 rare diseases +MONDO:0024520 gard_rare diseases +MONDO:0024520 nord_rare diseases +MONDO:0024520 rare diseases +MONDO:0024521 gard_rare diseases +MONDO:0024521 nord_rare diseases +MONDO:0024521 rare diseases +MONDO:0024522 gard_rare diseases +MONDO:0024522 rare diseases +MONDO:0024523 gard_rare diseases +MONDO:0024523 nord_rare diseases +MONDO:0024523 rare diseases +MONDO:0024524 gard_rare diseases +MONDO:0024524 rare diseases +MONDO:0024525 gard_rare diseases +MONDO:0024525 nord_rare diseases +MONDO:0024525 otar diseases +MONDO:0024525 rare diseases +MONDO:0024526 gard_rare diseases +MONDO:0024526 nord_rare diseases +MONDO:0024526 rare diseases +MONDO:0024527 gard_rare diseases +MONDO:0024527 nord_rare diseases +MONDO:0024527 rare diseases +MONDO:0024528 gard_rare diseases +MONDO:0024528 otar diseases +MONDO:0024528 rare diseases +MONDO:0024529 gard_rare diseases +MONDO:0024529 nord_rare diseases +MONDO:0024529 rare diseases +MONDO:0024530 gard_rare diseases +MONDO:0024530 rare diseases +MONDO:0024531 gard_rare diseases +MONDO:0024531 rare diseases +MONDO:0024532 gard_rare diseases +MONDO:0024532 nord_rare diseases +MONDO:0024532 rare diseases +MONDO:0024533 gard_rare diseases +MONDO:0024533 nord_rare diseases +MONDO:0024533 rare diseases +MONDO:0024534 gard_rare diseases +MONDO:0024534 nord_rare diseases +MONDO:0024534 rare diseases +MONDO:0024535 gard_rare diseases +MONDO:0024535 nord_rare diseases +MONDO:0024535 rare diseases +MONDO:0024536 gard_rare diseases +MONDO:0024536 nord_rare diseases +MONDO:0024536 rare diseases +MONDO:0024537 clingen diseases +MONDO:0024537 gard_rare diseases +MONDO:0024537 nord_rare diseases +MONDO:0024537 ordo_subtype_of_a_disorder diseases +MONDO:0024537 rare diseases +MONDO:0024538 gard_rare diseases +MONDO:0024538 rare diseases +MONDO:0024539 gard_rare diseases +MONDO:0024539 nord_rare diseases +MONDO:0024539 rare diseases +MONDO:0024540 gard_rare diseases +MONDO:0024540 rare diseases +MONDO:0024541 gard_rare diseases +MONDO:0024541 nord_rare diseases +MONDO:0024541 rare diseases +MONDO:0024542 clingen diseases +MONDO:0024542 gard_rare diseases +MONDO:0024542 nord_rare diseases +MONDO:0024542 rare diseases +MONDO:0024543 gard_rare diseases +MONDO:0024543 nord_rare diseases +MONDO:0024543 rare diseases +MONDO:0024545 gard_rare diseases +MONDO:0024545 rare diseases +MONDO:0024546 gard_rare diseases +MONDO:0024546 nord_rare diseases +MONDO:0024546 otar diseases +MONDO:0024546 rare diseases +MONDO:0024547 clingen diseases +MONDO:0024547 gard_rare diseases +MONDO:0024547 nord_rare diseases +MONDO:0024547 rare diseases +MONDO:0024548 gard_rare diseases +MONDO:0024548 nord_rare diseases +MONDO:0024548 ordo_subtype_of_a_disorder diseases +MONDO:0024548 otar diseases +MONDO:0024548 rare diseases +MONDO:0024549 gard_rare diseases +MONDO:0024549 nord_rare diseases +MONDO:0024549 rare diseases +MONDO:0024550 gard_rare diseases +MONDO:0024550 nord_rare diseases +MONDO:0024550 rare diseases +MONDO:0024551 gard_rare diseases +MONDO:0024551 nord_rare diseases +MONDO:0024551 ordo_disorder diseases +MONDO:0024551 orphanet_rare diseases +MONDO:0024551 rare diseases +MONDO:0024552 gard_rare diseases +MONDO:0024552 nord_rare diseases +MONDO:0024552 rare diseases +MONDO:0024553 gard_rare diseases +MONDO:0024553 nord_rare diseases +MONDO:0024553 rare diseases +MONDO:0024554 gard_rare diseases +MONDO:0024554 rare diseases +MONDO:0024555 gard_rare diseases +MONDO:0024555 nord_rare diseases +MONDO:0024555 rare diseases +MONDO:0024556 gard_rare diseases +MONDO:0024556 nord_rare diseases +MONDO:0024556 rare diseases +MONDO:0024557 gard_rare diseases +MONDO:0024557 nord_rare diseases +MONDO:0024557 ordo_disorder diseases +MONDO:0024557 orphanet_rare diseases +MONDO:0024557 rare diseases +MONDO:0024558 clingen diseases +MONDO:0024558 gard_rare diseases +MONDO:0024558 nord_rare diseases +MONDO:0024558 rare diseases +MONDO:0024559 gard_rare diseases +MONDO:0024559 nord_rare diseases +MONDO:0024559 ordo_disorder diseases +MONDO:0024559 orphanet_rare diseases +MONDO:0024559 rare diseases +MONDO:0024560 gard_rare diseases +MONDO:0024560 nord_rare diseases +MONDO:0024560 rare diseases +MONDO:0024561 gard_rare diseases +MONDO:0024561 nord_rare diseases +MONDO:0024561 rare diseases +MONDO:0024562 gard_rare diseases +MONDO:0024562 rare diseases +MONDO:0024564 gard_rare diseases +MONDO:0024564 nord_rare diseases +MONDO:0024564 rare diseases +MONDO:0024565 gard_rare diseases +MONDO:0024565 nord_rare diseases +MONDO:0024565 rare diseases +MONDO:0024566 gard_rare diseases +MONDO:0024566 nord_rare diseases +MONDO:0024566 rare diseases +MONDO:0024567 gard_rare diseases +MONDO:0024567 nord_rare diseases +MONDO:0024567 rare diseases +MONDO:0024568 gard_rare diseases +MONDO:0024568 nord_rare diseases +MONDO:0024568 ordo_disorder diseases +MONDO:0024568 orphanet_rare diseases +MONDO:0024568 otar diseases +MONDO:0024568 rare diseases +MONDO:0024569 gard_rare diseases +MONDO:0024569 nord_rare diseases +MONDO:0024569 rare diseases +MONDO:0024570 gard_rare diseases +MONDO:0024570 nord_rare diseases +MONDO:0024570 rare diseases +MONDO:0024571 otar diseases +MONDO:0024572 otar diseases +MONDO:0024573 inferred_rare diseases +MONDO:0024573 otar diseases +MONDO:0024573 rare diseases +MONDO:0024574 gard_rare diseases +MONDO:0024574 otar diseases +MONDO:0024574 rare diseases +MONDO:0024575 otar diseases +MONDO:0024582 otar diseases +MONDO:0024607 gard_rare diseases +MONDO:0024607 rare diseases +MONDO:0024609 gard_rare diseases +MONDO:0024609 nord_rare diseases +MONDO:0024609 ordo_subtype_of_a_disorder diseases +MONDO:0024609 otar diseases +MONDO:0024609 rare diseases +MONDO:0024611 gard_rare diseases +MONDO:0024611 otar diseases +MONDO:0024611 rare diseases +MONDO:0024615 gard_rare diseases +MONDO:0024615 otar diseases +MONDO:0024615 rare diseases +MONDO:0024617 gard_rare diseases +MONDO:0024617 rare diseases +MONDO:0024618 otar diseases +MONDO:0024619 gard_rare diseases +MONDO:0024619 otar diseases +MONDO:0024619 rare diseases +MONDO:0024620 gard_rare diseases +MONDO:0024620 rare diseases +MONDO:0024621 otar diseases +MONDO:0024622 gard_rare diseases +MONDO:0024622 otar diseases +MONDO:0024622 rare diseases +MONDO:0024623 rare_grouping diseases +MONDO:0024625 otar diseases +MONDO:0024633 otar diseases +MONDO:0024634 otar diseases +MONDO:0024635 otar diseases +MONDO:0024636 otar diseases +MONDO:0024637 otar diseases +MONDO:0024638 gard_rare diseases +MONDO:0024638 rare diseases +MONDO:0024639 gard_rare diseases +MONDO:0024639 rare diseases +MONDO:0024642 gard_rare diseases +MONDO:0024642 rare diseases +MONDO:0024643 otar diseases +MONDO:0024644 otar diseases +MONDO:0024645 otar diseases +MONDO:0024647 otar diseases +MONDO:0024648 gard_rare diseases +MONDO:0024648 rare diseases +MONDO:0024649 gard_rare diseases +MONDO:0024649 otar diseases +MONDO:0024649 rare diseases +MONDO:0024650 gard_rare diseases +MONDO:0024650 nord_rare diseases +MONDO:0024650 rare diseases +MONDO:0024651 gard_rare diseases +MONDO:0024651 rare diseases +MONDO:0024653 gard_rare diseases +MONDO:0024653 otar diseases +MONDO:0024653 rare diseases +MONDO:0024656 gard_rare diseases +MONDO:0024656 otar diseases +MONDO:0024656 rare diseases +MONDO:0024658 gard_rare diseases +MONDO:0024658 rare diseases +MONDO:0024659 gard_rare diseases +MONDO:0024659 rare diseases +MONDO:0024660 otar diseases +MONDO:0024661 otar diseases +MONDO:0024662 otar diseases +MONDO:0024663 gard_rare diseases +MONDO:0024663 rare diseases +MONDO:0024664 otar diseases +MONDO:0024665 gard_rare diseases +MONDO:0024665 rare diseases +MONDO:0024666 otar diseases +MONDO:0024673 gard_rare diseases +MONDO:0024673 rare diseases +MONDO:0024674 gard_rare diseases +MONDO:0024674 nord_rare diseases +MONDO:0024674 rare diseases +MONDO:0024675 gard_rare diseases +MONDO:0024675 rare diseases +MONDO:0024676 gard_rare diseases +MONDO:0024676 rare diseases +MONDO:0024677 gard_rare diseases +MONDO:0024677 otar diseases +MONDO:0024677 rare diseases +MONDO:0024685 gard_rare diseases +MONDO:0024685 rare diseases +MONDO:0024686 gard_rare diseases +MONDO:0024686 nord_rare diseases +MONDO:0024686 ordo_disorder diseases +MONDO:0024686 orphanet_rare diseases +MONDO:0024686 rare diseases +MONDO:0024744 gard_rare diseases +MONDO:0024744 rare diseases +MONDO:0024746 gard_rare diseases +MONDO:0024746 rare diseases +MONDO:0024757 otar diseases +MONDO:0024770 gard_rare diseases +MONDO:0024770 nord_rare diseases +MONDO:0024770 rare diseases +MONDO:0024771 gard_rare diseases +MONDO:0024771 rare diseases +MONDO:0024772 gard_rare diseases +MONDO:0024772 nord_rare diseases +MONDO:0024772 rare diseases +MONDO:0024781 gard_rare diseases +MONDO:0024781 ordo_disorder diseases +MONDO:0024781 orphanet_rare diseases +MONDO:0024781 rare diseases +MONDO:0024857 gard_rare diseases +MONDO:0024857 rare diseases +MONDO:0024861 gard_rare diseases +MONDO:0024861 rare diseases +MONDO:0024863 gard_rare diseases +MONDO:0024863 rare diseases +MONDO:0024864 gard_rare diseases +MONDO:0024864 rare diseases +MONDO:0024868 gard_rare diseases +MONDO:0024868 rare diseases +MONDO:0024873 gard_rare diseases +MONDO:0024873 rare diseases +MONDO:0024878 otar diseases +MONDO:0024879 otar diseases +MONDO:0024880 otar diseases +MONDO:0024881 otar diseases +MONDO:0024882 otar diseases +MONDO:0024883 otar diseases +MONDO:0024884 gard_rare diseases +MONDO:0024884 rare diseases +MONDO:0024885 gard_rare diseases +MONDO:0024885 otar diseases +MONDO:0024885 rare diseases +MONDO:0024890 otar diseases +MONDO:0024892 gard_rare diseases +MONDO:0024892 otar diseases +MONDO:0024892 rare diseases +MONDO:0024893 gard_rare diseases +MONDO:0024893 rare diseases +MONDO:0024905 otar diseases +MONDO:0024913 otar diseases +MONDO:0024934 otar diseases +MONDO:0024950 otar diseases +MONDO:0024954 gard_rare diseases +MONDO:0024954 rare diseases +MONDO:0024990 otar diseases +MONDO:0025003 otar diseases +MONDO:0025193 gard_rare diseases +MONDO:0025193 nord_rare diseases +MONDO:0025193 ordo_disorder diseases +MONDO:0025193 ordo_inheritance_inconsistent diseases +MONDO:0025193 orphanet_rare diseases +MONDO:0025193 otar diseases +MONDO:0025193 rare diseases +MONDO:0025294 otar diseases +MONDO:0025303 gard_rare diseases +MONDO:0025303 nord_rare diseases +MONDO:0025303 otar diseases +MONDO:0025303 rare diseases +MONDO:0025353 gard_rare diseases +MONDO:0025353 nord_rare diseases +MONDO:0025353 rare diseases +MONDO:0025354 clingen diseases +MONDO:0025354 otar diseases +MONDO:0025371 otar diseases +MONDO:0025445 gard_rare diseases +MONDO:0025445 otar diseases +MONDO:0025445 rare diseases +MONDO:0025514 gard_rare diseases +MONDO:0025514 nord_rare diseases +MONDO:0025514 ordo_disorder diseases +MONDO:0025514 orphanet_rare diseases +MONDO:0025514 rare diseases +MONDO:0025622 gard_rare diseases +MONDO:0025622 nord_rare diseases +MONDO:0025622 rare diseases +MONDO:0025667 gard_rare diseases +MONDO:0025667 nord_rare diseases +MONDO:0025667 ordo_disorder diseases +MONDO:0025667 orphanet_rare diseases +MONDO:0025667 rare diseases +MONDO:0025690 gard_rare diseases +MONDO:0025690 rare diseases +MONDO:0025691 gard_rare diseases +MONDO:0025691 nord_rare diseases +MONDO:0025691 rare diseases +MONDO:0025699 gard_rare diseases +MONDO:0025699 nord_rare diseases +MONDO:0025699 rare diseases +MONDO:0025701 gard_rare diseases +MONDO:0025701 nord_rare diseases +MONDO:0025701 rare diseases +MONDO:0025708 gard_rare diseases +MONDO:0025708 otar diseases +MONDO:0025708 rare diseases +MONDO:0025712 gard_rare diseases +MONDO:0025712 rare diseases +MONDO:0025713 gard_rare diseases +MONDO:0025713 rare diseases +MONDO:0025986 otar diseases +MONDO:0026045 otar diseases +MONDO:0026720 gard_rare diseases +MONDO:0026720 rare diseases +MONDO:0026721 gard_rare diseases +MONDO:0026721 rare diseases +MONDO:0026722 otar diseases +MONDO:0026723 gard_rare diseases +MONDO:0026723 nord_rare diseases +MONDO:0026723 rare diseases +MONDO:0026726 gard_rare diseases +MONDO:0026726 rare diseases +MONDO:0026727 gard_rare diseases +MONDO:0026727 rare diseases +MONDO:0026729 gard_rare diseases +MONDO:0026729 rare diseases +MONDO:0026730 clingen diseases +MONDO:0026730 gard_rare diseases +MONDO:0026730 nord_rare diseases +MONDO:0026730 otar diseases +MONDO:0026730 rare diseases +MONDO:0026731 gard_rare diseases +MONDO:0026731 nord_rare diseases +MONDO:0026731 rare diseases +MONDO:0026732 gard_rare diseases +MONDO:0026732 nord_rare diseases +MONDO:0026732 rare diseases +MONDO:0026733 gard_rare diseases +MONDO:0026733 nord_rare diseases +MONDO:0026733 otar diseases +MONDO:0026733 rare diseases +MONDO:0026762 gard_rare diseases +MONDO:0026762 nord_rare diseases +MONDO:0026762 rare diseases +MONDO:0026763 gard_rare diseases +MONDO:0026763 nord_rare diseases +MONDO:0026763 rare diseases +MONDO:0026765 gard_rare diseases +MONDO:0026765 rare diseases +MONDO:0026767 otar diseases +MONDO:0026771 gard_rare diseases +MONDO:0026771 nord_rare diseases +MONDO:0026771 rare diseases +MONDO:0026777 gard_rare diseases +MONDO:0026777 nord_rare diseases +MONDO:0026777 ordo_disorder diseases +MONDO:0026777 orphanet_rare diseases +MONDO:0026777 rare diseases +MONDO:0027026 gard_rare diseases +MONDO:0027026 nord_rare diseases +MONDO:0027026 rare diseases +MONDO:0027029 gard_rare diseases +MONDO:0027029 rare diseases +MONDO:0027048 gard_rare diseases +MONDO:0027048 nord_rare diseases +MONDO:0027048 rare diseases +MONDO:0027068 gard_rare diseases +MONDO:0027068 rare diseases +MONDO:0027069 gard_rare diseases +MONDO:0027069 rare diseases +MONDO:0027353 gard_rare diseases +MONDO:0027353 rare diseases +MONDO:0027407 gard_rare diseases +MONDO:0027407 nord_rare diseases +MONDO:0027407 otar diseases +MONDO:0027407 rare diseases +MONDO:0027451 gard_rare diseases +MONDO:0027451 nord_rare diseases +MONDO:0027451 rare diseases +MONDO:0027462 gard_rare diseases +MONDO:0027462 nord_rare diseases +MONDO:0027462 rare diseases +MONDO:0027676 gard_rare diseases +MONDO:0027676 nord_rare diseases +MONDO:0027676 rare diseases +MONDO:0027694 clingen diseases +MONDO:0027694 gard_rare diseases +MONDO:0027694 nord_rare diseases +MONDO:0027694 rare diseases +MONDO:0027749 disease_grouping diseases +MONDO:0027749 gard_rare diseases +MONDO:0027749 ordo_group_of_disorders diseases +MONDO:0027749 otar diseases +MONDO:0027749 rare diseases +MONDO:0027766 otar diseases +MONDO:0027767 otar diseases +MONDO:0027772 gard_rare diseases +MONDO:0027772 otar diseases +MONDO:0027772 rare diseases +MONDO:0028226 disease_grouping diseases +MONDO:0028226 gard_rare diseases +MONDO:0028226 ordo_group_of_disorders diseases +MONDO:0028226 otar diseases +MONDO:0028226 rare diseases +MONDO:0029000 harrisons_view diseases +MONDO:0029000 otar diseases +MONDO:0029000 rare_grouping diseases +MONDO:0029130 gard_rare diseases +MONDO:0029130 nord_rare diseases +MONDO:0029130 otar diseases +MONDO:0029130 rare diseases +MONDO:0029131 clingen diseases +MONDO:0029131 otar diseases +MONDO:0029132 gard_rare diseases +MONDO:0029132 rare diseases +MONDO:0029133 gard_rare diseases +MONDO:0029133 otar diseases +MONDO:0029133 rare diseases +MONDO:0029134 gard_rare diseases +MONDO:0029134 nord_rare diseases +MONDO:0029134 ordo_disorder diseases +MONDO:0029134 orphanet_rare diseases +MONDO:0029134 otar diseases +MONDO:0029134 rare diseases +MONDO:0029135 gard_rare diseases +MONDO:0029135 otar diseases +MONDO:0029135 rare diseases +MONDO:0029136 gard_rare diseases +MONDO:0029136 nord_rare diseases +MONDO:0029136 ordo_disorder diseases +MONDO:0029136 orphanet_rare diseases +MONDO:0029136 otar diseases +MONDO:0029136 rare diseases +MONDO:0029137 gard_rare diseases +MONDO:0029137 nord_rare diseases +MONDO:0029137 otar diseases +MONDO:0029137 rare diseases +MONDO:0029138 gard_rare diseases +MONDO:0029138 nord_rare diseases +MONDO:0029138 rare diseases +MONDO:0029140 gard_rare diseases +MONDO:0029140 otar diseases +MONDO:0029140 rare diseases +MONDO:0029141 gard_rare diseases +MONDO:0029141 nord_rare diseases +MONDO:0029141 rare diseases +MONDO:0029142 gard_rare diseases +MONDO:0029142 nord_rare diseases +MONDO:0029142 rare diseases +MONDO:0029143 otar diseases +MONDO:0029144 clingen diseases +MONDO:0029144 otar diseases +MONDO:0029145 gard_rare diseases +MONDO:0029145 rare diseases +MONDO:0029147 gard_rare diseases +MONDO:0029147 rare diseases +MONDO:0029148 gard_rare diseases +MONDO:0029148 rare diseases +MONDO:0030006 gard_rare diseases +MONDO:0030006 nord_rare diseases +MONDO:0030006 ordo_disorder diseases +MONDO:0030006 orphanet_rare diseases +MONDO:0030006 otar diseases +MONDO:0030006 rare diseases +MONDO:0030007 gard_rare diseases +MONDO:0030007 otar diseases +MONDO:0030007 rare diseases +MONDO:0030008 gard_rare diseases +MONDO:0030008 otar diseases +MONDO:0030008 rare diseases +MONDO:0030009 gard_rare diseases +MONDO:0030009 nord_rare diseases +MONDO:0030009 rare diseases +MONDO:0030010 gard_rare diseases +MONDO:0030010 rare diseases +MONDO:0030013 otar diseases +MONDO:0030014 gard_rare diseases +MONDO:0030014 rare diseases +MONDO:0030015 gard_rare diseases +MONDO:0030015 nord_rare diseases +MONDO:0030015 otar diseases +MONDO:0030015 rare diseases +MONDO:0030017 gard_rare diseases +MONDO:0030017 otar diseases +MONDO:0030017 rare diseases +MONDO:0030019 gard_rare diseases +MONDO:0030019 nord_rare diseases +MONDO:0030019 otar diseases +MONDO:0030019 rare diseases +MONDO:0030020 gard_rare diseases +MONDO:0030020 otar diseases +MONDO:0030020 rare diseases +MONDO:0030024 otar diseases +MONDO:0030025 otar diseases +MONDO:0030027 otar diseases +MONDO:0030028 otar diseases +MONDO:0030029 otar diseases +MONDO:0030030 otar diseases +MONDO:0030031 gard_rare diseases +MONDO:0030031 nord_rare diseases +MONDO:0030031 otar diseases +MONDO:0030031 rare diseases +MONDO:0030033 otar diseases +MONDO:0030034 gard_rare diseases +MONDO:0030034 nord_rare diseases +MONDO:0030034 otar diseases +MONDO:0030034 rare diseases +MONDO:0030035 otar diseases +MONDO:0030036 otar diseases +MONDO:0030037 gard_rare diseases +MONDO:0030037 otar diseases +MONDO:0030037 rare diseases +MONDO:0030038 otar diseases +MONDO:0030042 otar diseases +MONDO:0030043 gard_rare diseases +MONDO:0030043 otar diseases +MONDO:0030043 rare diseases +MONDO:0030044 gard_rare diseases +MONDO:0030044 otar diseases +MONDO:0030044 rare diseases +MONDO:0030045 gard_rare diseases +MONDO:0030045 nord_rare diseases +MONDO:0030045 ordo_disorder diseases +MONDO:0030045 orphanet_rare diseases +MONDO:0030045 otar diseases +MONDO:0030045 rare diseases +MONDO:0030046 otar diseases +MONDO:0030047 otar diseases +MONDO:0030048 gard_rare diseases +MONDO:0030048 nord_rare diseases +MONDO:0030048 otar diseases +MONDO:0030048 rare diseases +MONDO:0030049 otar diseases +MONDO:0030051 clingen diseases +MONDO:0030051 gard_rare diseases +MONDO:0030051 otar diseases +MONDO:0030051 rare diseases +MONDO:0030054 gard_rare diseases +MONDO:0030054 nord_rare diseases +MONDO:0030054 otar diseases +MONDO:0030054 rare diseases +MONDO:0030055 gard_rare diseases +MONDO:0030055 otar diseases +MONDO:0030055 rare diseases +MONDO:0030056 gard_rare diseases +MONDO:0030056 nord_rare diseases +MONDO:0030056 rare diseases +MONDO:0030057 gard_rare diseases +MONDO:0030057 otar diseases +MONDO:0030057 rare diseases +MONDO:0030058 gard_rare diseases +MONDO:0030058 nord_rare diseases +MONDO:0030058 otar diseases +MONDO:0030058 rare diseases +MONDO:0030059 gard_rare diseases +MONDO:0030059 nord_rare diseases +MONDO:0030059 otar diseases +MONDO:0030059 rare diseases +MONDO:0030060 clingen diseases +MONDO:0030060 otar diseases +MONDO:0030061 gard_rare diseases +MONDO:0030061 nord_rare diseases +MONDO:0030061 otar diseases +MONDO:0030061 rare diseases +MONDO:0030062 gard_rare diseases +MONDO:0030062 nord_rare diseases +MONDO:0030062 otar diseases +MONDO:0030062 rare diseases +MONDO:0030063 gard_rare diseases +MONDO:0030063 otar diseases +MONDO:0030063 rare diseases +MONDO:0030064 gard_rare diseases +MONDO:0030064 nord_rare diseases +MONDO:0030064 otar diseases +MONDO:0030064 rare diseases +MONDO:0030065 otar diseases +MONDO:0030066 gard_rare diseases +MONDO:0030066 nord_rare diseases +MONDO:0030066 otar diseases +MONDO:0030066 rare diseases +MONDO:0030067 gard_rare diseases +MONDO:0030067 nord_rare diseases +MONDO:0030067 otar diseases +MONDO:0030067 rare diseases +MONDO:0030069 gard_rare diseases +MONDO:0030069 nord_rare diseases +MONDO:0030069 otar diseases +MONDO:0030069 rare diseases +MONDO:0030070 gard_rare diseases +MONDO:0030070 nord_rare diseases +MONDO:0030070 otar diseases +MONDO:0030070 rare diseases +MONDO:0030071 otar diseases +MONDO:0030072 gard_rare diseases +MONDO:0030072 nord_rare diseases +MONDO:0030072 otar diseases +MONDO:0030072 rare diseases +MONDO:0030073 clingen diseases +MONDO:0030073 gard_rare diseases +MONDO:0030073 ordo_disorder diseases +MONDO:0030073 orphanet_rare diseases +MONDO:0030073 otar diseases +MONDO:0030073 rare diseases +MONDO:0030074 gard_rare diseases +MONDO:0030074 ordo_disorder diseases +MONDO:0030074 orphanet_rare diseases +MONDO:0030074 otar diseases +MONDO:0030074 rare diseases +MONDO:0030077 gard_rare diseases +MONDO:0030077 rare diseases +MONDO:0030087 gard_rare diseases +MONDO:0030087 nord_rare diseases +MONDO:0030087 otar diseases +MONDO:0030087 rare diseases +MONDO:0030088 gard_rare diseases +MONDO:0030088 nord_rare diseases +MONDO:0030088 otar diseases +MONDO:0030088 rare diseases +MONDO:0030089 gard_rare diseases +MONDO:0030089 nord_rare diseases +MONDO:0030089 otar diseases +MONDO:0030089 rare diseases +MONDO:0030105 gard_rare diseases +MONDO:0030105 nord_rare diseases +MONDO:0030105 ordo_disorder diseases +MONDO:0030105 orphanet_rare diseases +MONDO:0030105 otar diseases +MONDO:0030105 rare diseases +MONDO:0030116 gard_rare diseases +MONDO:0030116 nord_rare diseases +MONDO:0030116 rare diseases +MONDO:0030118 gard_rare diseases +MONDO:0030118 nord_rare diseases +MONDO:0030118 otar diseases +MONDO:0030118 rare diseases +MONDO:0030134 gard_rare diseases +MONDO:0030134 nord_rare diseases +MONDO:0030134 otar diseases +MONDO:0030134 rare diseases +MONDO:0030258 gard_rare diseases +MONDO:0030258 nord_rare diseases +MONDO:0030258 ordo_disorder diseases +MONDO:0030258 orphanet_rare diseases +MONDO:0030258 rare diseases +MONDO:0030259 gard_rare diseases +MONDO:0030259 nord_rare diseases +MONDO:0030259 rare diseases +MONDO:0030260 gard_rare diseases +MONDO:0030260 nord_rare diseases +MONDO:0030260 otar diseases +MONDO:0030260 rare diseases +MONDO:0030261 gard_rare diseases +MONDO:0030261 nord_rare diseases +MONDO:0030261 rare diseases +MONDO:0030263 gard_rare diseases +MONDO:0030263 nord_rare diseases +MONDO:0030263 rare diseases +MONDO:0030268 gard_rare diseases +MONDO:0030268 nord_rare diseases +MONDO:0030268 rare diseases +MONDO:0030270 gard_rare diseases +MONDO:0030270 nord_rare diseases +MONDO:0030270 rare diseases +MONDO:0030281 gard_rare diseases +MONDO:0030281 nord_rare diseases +MONDO:0030281 rare diseases +MONDO:0030293 gard_rare diseases +MONDO:0030293 rare diseases +MONDO:0030298 gard_rare diseases +MONDO:0030298 rare diseases +MONDO:0030300 gard_rare diseases +MONDO:0030300 nord_rare diseases +MONDO:0030300 rare diseases +MONDO:0030309 gard_rare diseases +MONDO:0030309 rare diseases +MONDO:0030311 gard_rare diseases +MONDO:0030311 rare diseases +MONDO:0030312 gard_rare diseases +MONDO:0030312 nord_rare diseases +MONDO:0030312 rare diseases +MONDO:0030316 gard_rare diseases +MONDO:0030316 nord_rare diseases +MONDO:0030316 rare diseases +MONDO:0030317 gard_rare diseases +MONDO:0030317 nord_rare diseases +MONDO:0030317 rare diseases +MONDO:0030318 gard_rare diseases +MONDO:0030318 nord_rare diseases +MONDO:0030318 rare diseases +MONDO:0030323 clingen diseases +MONDO:0030323 gard_rare diseases +MONDO:0030323 nord_rare diseases +MONDO:0030323 rare diseases +MONDO:0030326 gard_rare diseases +MONDO:0030326 rare diseases +MONDO:0030330 gard_rare diseases +MONDO:0030330 nord_rare diseases +MONDO:0030330 rare diseases +MONDO:0030331 gard_rare diseases +MONDO:0030331 nord_rare diseases +MONDO:0030331 rare diseases +MONDO:0030332 gard_rare diseases +MONDO:0030332 nord_rare diseases +MONDO:0030332 rare diseases +MONDO:0030333 clingen diseases +MONDO:0030337 gard_rare diseases +MONDO:0030337 nord_rare diseases +MONDO:0030337 rare diseases +MONDO:0030339 gard_rare diseases +MONDO:0030339 nord_rare diseases +MONDO:0030339 rare diseases +MONDO:0030341 gard_rare diseases +MONDO:0030341 nord_rare diseases +MONDO:0030341 rare diseases +MONDO:0030346 gard_rare diseases +MONDO:0030346 nord_rare diseases +MONDO:0030346 rare diseases +MONDO:0030353 gard_rare diseases +MONDO:0030353 nord_rare diseases +MONDO:0030353 otar diseases +MONDO:0030353 rare diseases +MONDO:0030354 gard_rare diseases +MONDO:0030354 nord_rare diseases +MONDO:0030354 rare diseases +MONDO:0030355 gard_rare diseases +MONDO:0030355 nord_rare diseases +MONDO:0030355 rare diseases +MONDO:0030356 gard_rare diseases +MONDO:0030356 nord_rare diseases +MONDO:0030356 otar diseases +MONDO:0030356 rare diseases +MONDO:0030360 gard_rare diseases +MONDO:0030360 nord_rare diseases +MONDO:0030360 rare diseases +MONDO:0030361 gard_rare diseases +MONDO:0030361 nord_rare diseases +MONDO:0030361 rare diseases +MONDO:0030362 gard_rare diseases +MONDO:0030362 nord_rare diseases +MONDO:0030362 otar diseases +MONDO:0030362 rare diseases +MONDO:0030366 gard_rare diseases +MONDO:0030366 nord_rare diseases +MONDO:0030366 rare diseases +MONDO:0030376 gard_rare diseases +MONDO:0030376 rare diseases +MONDO:0030378 gard_rare diseases +MONDO:0030378 rare diseases +MONDO:0030423 gard_rare diseases +MONDO:0030423 otar diseases +MONDO:0030423 rare diseases +MONDO:0030433 gard_rare diseases +MONDO:0030433 nord_rare diseases +MONDO:0030433 rare diseases +MONDO:0030436 gard_rare diseases +MONDO:0030436 nord_rare diseases +MONDO:0030436 rare diseases +MONDO:0030437 gard_rare diseases +MONDO:0030437 rare diseases +MONDO:0030438 gard_rare diseases +MONDO:0030438 nord_rare diseases +MONDO:0030438 rare diseases +MONDO:0030440 gard_rare diseases +MONDO:0030440 nord_rare diseases +MONDO:0030440 rare diseases +MONDO:0030449 gard_rare diseases +MONDO:0030449 nord_rare diseases +MONDO:0030449 rare diseases +MONDO:0030453 gard_rare diseases +MONDO:0030453 nord_rare diseases +MONDO:0030453 rare diseases +MONDO:0030454 gard_rare diseases +MONDO:0030454 nord_rare diseases +MONDO:0030454 rare diseases +MONDO:0030455 gard_rare diseases +MONDO:0030455 nord_rare diseases +MONDO:0030455 rare diseases +MONDO:0030456 gard_rare diseases +MONDO:0030456 rare diseases +MONDO:0030458 gard_rare diseases +MONDO:0030458 nord_rare diseases +MONDO:0030458 otar diseases +MONDO:0030458 rare diseases +MONDO:0030462 gard_rare diseases +MONDO:0030462 nord_rare diseases +MONDO:0030462 rare diseases +MONDO:0030471 gard_rare diseases +MONDO:0030471 nord_rare diseases +MONDO:0030471 rare diseases +MONDO:0030472 gard_rare diseases +MONDO:0030472 nord_rare diseases +MONDO:0030472 otar diseases +MONDO:0030472 rare diseases +MONDO:0030473 gard_rare diseases +MONDO:0030473 nord_rare diseases +MONDO:0030473 otar diseases +MONDO:0030473 rare diseases +MONDO:0030474 gard_rare diseases +MONDO:0030474 nord_rare diseases +MONDO:0030474 rare diseases +MONDO:0030475 gard_rare diseases +MONDO:0030475 nord_rare diseases +MONDO:0030475 rare diseases +MONDO:0030476 gard_rare diseases +MONDO:0030476 nord_rare diseases +MONDO:0030476 rare diseases +MONDO:0030480 gard_rare diseases +MONDO:0030480 nord_rare diseases +MONDO:0030480 rare diseases +MONDO:0030482 gard_rare diseases +MONDO:0030482 ordo_disorder diseases +MONDO:0030482 orphanet_rare diseases +MONDO:0030482 rare diseases +MONDO:0030486 gard_rare diseases +MONDO:0030486 nord_rare diseases +MONDO:0030486 rare diseases +MONDO:0030487 gard_rare diseases +MONDO:0030487 nord_rare diseases +MONDO:0030487 rare diseases +MONDO:0030489 gard_rare diseases +MONDO:0030489 nord_rare diseases +MONDO:0030489 rare diseases +MONDO:0030498 clingen diseases +MONDO:0030500 gard_rare diseases +MONDO:0030500 nord_rare diseases +MONDO:0030500 rare diseases +MONDO:0030502 gard_rare diseases +MONDO:0030502 otar diseases +MONDO:0030502 rare diseases +MONDO:0030503 gard_rare diseases +MONDO:0030503 nord_rare diseases +MONDO:0030503 rare diseases +MONDO:0030505 gard_rare diseases +MONDO:0030505 nord_rare diseases +MONDO:0030505 rare diseases +MONDO:0030506 gard_rare diseases +MONDO:0030506 nord_rare diseases +MONDO:0030506 rare diseases +MONDO:0030512 gard_rare diseases +MONDO:0030512 ordo_disorder diseases +MONDO:0030512 orphanet_rare diseases +MONDO:0030512 rare diseases +MONDO:0030513 gard_rare diseases +MONDO:0030513 nord_rare diseases +MONDO:0030513 rare diseases +MONDO:0030514 gard_rare diseases +MONDO:0030514 nord_rare diseases +MONDO:0030514 rare diseases +MONDO:0030517 gard_rare diseases +MONDO:0030517 nord_rare diseases +MONDO:0030517 rare diseases +MONDO:0030518 gard_rare diseases +MONDO:0030518 nord_rare diseases +MONDO:0030518 rare diseases +MONDO:0030519 gard_rare diseases +MONDO:0030519 nord_rare diseases +MONDO:0030519 rare diseases +MONDO:0030524 gard_rare diseases +MONDO:0030524 rare diseases +MONDO:0030525 gard_rare diseases +MONDO:0030525 nord_rare diseases +MONDO:0030525 rare diseases +MONDO:0030527 gard_rare diseases +MONDO:0030527 nord_rare diseases +MONDO:0030527 rare diseases +MONDO:0030529 clingen diseases +MONDO:0030529 gard_rare diseases +MONDO:0030529 nord_rare diseases +MONDO:0030529 rare diseases +MONDO:0030533 gard_rare diseases +MONDO:0030533 nord_rare diseases +MONDO:0030533 rare diseases +MONDO:0030534 gard_rare diseases +MONDO:0030534 rare diseases +MONDO:0030535 gard_rare diseases +MONDO:0030535 nord_rare diseases +MONDO:0030535 rare diseases +MONDO:0030538 gard_rare diseases +MONDO:0030538 nord_rare diseases +MONDO:0030538 rare diseases +MONDO:0030543 gard_rare diseases +MONDO:0030543 rare diseases +MONDO:0030549 gard_rare diseases +MONDO:0030549 nord_rare diseases +MONDO:0030549 rare diseases +MONDO:0030553 gard_rare diseases +MONDO:0030553 nord_rare diseases +MONDO:0030553 rare diseases +MONDO:0030604 gard_rare diseases +MONDO:0030604 rare diseases +MONDO:0030619 gard_rare diseases +MONDO:0030619 nord_rare diseases +MONDO:0030619 rare diseases +MONDO:0030673 gard_rare diseases +MONDO:0030673 ordo_disorder diseases +MONDO:0030673 orphanet_rare diseases +MONDO:0030673 rare diseases +MONDO:0030676 gard_rare diseases +MONDO:0030676 nord_rare diseases +MONDO:0030676 rare diseases +MONDO:0030677 gard_rare diseases +MONDO:0030677 nord_rare diseases +MONDO:0030677 rare diseases +MONDO:0030679 gard_rare diseases +MONDO:0030679 nord_rare diseases +MONDO:0030679 rare diseases +MONDO:0030680 gard_rare diseases +MONDO:0030680 nord_rare diseases +MONDO:0030680 rare diseases +MONDO:0030681 gard_rare diseases +MONDO:0030681 nord_rare diseases +MONDO:0030681 rare diseases +MONDO:0030684 gard_rare diseases +MONDO:0030684 rare diseases +MONDO:0030689 gard_rare diseases +MONDO:0030689 nord_rare diseases +MONDO:0030689 rare diseases +MONDO:0030690 gard_rare diseases +MONDO:0030690 nord_rare diseases +MONDO:0030690 rare diseases +MONDO:0030693 otar diseases +MONDO:0030695 gard_rare diseases +MONDO:0030695 nord_rare diseases +MONDO:0030695 rare diseases +MONDO:0030696 gard_rare diseases +MONDO:0030696 rare diseases +MONDO:0030700 gard_rare diseases +MONDO:0030700 rare diseases +MONDO:0030701 gard_rare diseases +MONDO:0030701 rare diseases +MONDO:0030703 gard_rare diseases +MONDO:0030703 rare diseases +MONDO:0030711 gard_rare diseases +MONDO:0030711 nord_rare diseases +MONDO:0030711 rare diseases +MONDO:0030712 gard_rare diseases +MONDO:0030712 nord_rare diseases +MONDO:0030712 rare diseases +MONDO:0030714 gard_rare diseases +MONDO:0030714 rare diseases +MONDO:0030717 clingen diseases +MONDO:0030719 gard_rare diseases +MONDO:0030719 nord_rare diseases +MONDO:0030719 rare diseases +MONDO:0030723 gard_rare diseases +MONDO:0030723 nord_rare diseases +MONDO:0030723 rare diseases +MONDO:0030724 gard_rare diseases +MONDO:0030724 nord_rare diseases +MONDO:0030724 rare diseases +MONDO:0030726 gard_rare diseases +MONDO:0030726 nord_rare diseases +MONDO:0030726 rare diseases +MONDO:0030727 gard_rare diseases +MONDO:0030727 nord_rare diseases +MONDO:0030727 rare diseases +MONDO:0030731 gard_rare diseases +MONDO:0030731 nord_rare diseases +MONDO:0030731 rare diseases +MONDO:0030736 gard_rare diseases +MONDO:0030736 nord_rare diseases +MONDO:0030736 rare diseases +MONDO:0030746 gard_rare diseases +MONDO:0030746 nord_rare diseases +MONDO:0030746 rare diseases +MONDO:0030747 gard_rare diseases +MONDO:0030747 nord_rare diseases +MONDO:0030747 rare diseases +MONDO:0030748 gard_rare diseases +MONDO:0030748 nord_rare diseases +MONDO:0030748 rare diseases +MONDO:0030749 gard_rare diseases +MONDO:0030749 nord_rare diseases +MONDO:0030749 rare diseases +MONDO:0030750 gard_rare diseases +MONDO:0030750 nord_rare diseases +MONDO:0030750 rare diseases +MONDO:0030756 otar diseases +MONDO:0030768 gard_rare diseases +MONDO:0030768 nord_rare diseases +MONDO:0030768 otar diseases +MONDO:0030768 rare diseases +MONDO:0030770 gard_rare diseases +MONDO:0030770 rare diseases +MONDO:0030781 gard_rare diseases +MONDO:0030781 otar diseases +MONDO:0030781 rare diseases +MONDO:0030785 gard_rare diseases +MONDO:0030785 nord_rare diseases +MONDO:0030785 rare diseases +MONDO:0030797 gard_rare diseases +MONDO:0030797 nord_rare diseases +MONDO:0030797 rare diseases +MONDO:0030800 gard_rare diseases +MONDO:0030800 nord_rare diseases +MONDO:0030800 rare diseases +MONDO:0030801 gard_rare diseases +MONDO:0030801 nord_rare diseases +MONDO:0030801 rare diseases +MONDO:0030805 gard_rare diseases +MONDO:0030805 nord_rare diseases +MONDO:0030805 ordo_disorder diseases +MONDO:0030805 orphanet_rare diseases +MONDO:0030805 rare diseases +MONDO:0030809 otar diseases +MONDO:0030810 gard_rare diseases +MONDO:0030810 nord_rare diseases +MONDO:0030810 rare diseases +MONDO:0030815 gard_rare diseases +MONDO:0030815 nord_rare diseases +MONDO:0030815 rare diseases +MONDO:0030819 gard_rare diseases +MONDO:0030819 rare diseases +MONDO:0030822 gard_rare diseases +MONDO:0030822 nord_rare diseases +MONDO:0030822 rare diseases +MONDO:0030827 gard_rare diseases +MONDO:0030827 nord_rare diseases +MONDO:0030827 rare diseases +MONDO:0030837 gard_rare diseases +MONDO:0030837 rare diseases +MONDO:0030840 gard_rare diseases +MONDO:0030840 rare diseases +MONDO:0030841 gard_rare diseases +MONDO:0030841 rare diseases +MONDO:0030843 gard_rare diseases +MONDO:0030843 rare diseases +MONDO:0030844 otar diseases +MONDO:0030846 gard_rare diseases +MONDO:0030846 otar diseases +MONDO:0030846 rare diseases +MONDO:0030847 gard_rare diseases +MONDO:0030847 nord_rare diseases +MONDO:0030847 otar diseases +MONDO:0030847 rare diseases +MONDO:0030849 gard_rare diseases +MONDO:0030849 rare diseases +MONDO:0030854 clingen diseases +MONDO:0030854 gard_rare diseases +MONDO:0030854 rare diseases +MONDO:0030855 clingen diseases +MONDO:0030855 gard_rare diseases +MONDO:0030855 rare diseases +MONDO:0030856 gard_rare diseases +MONDO:0030856 nord_rare diseases +MONDO:0030856 rare diseases +MONDO:0030858 gard_rare diseases +MONDO:0030858 rare diseases +MONDO:0030859 gard_rare diseases +MONDO:0030859 nord_rare diseases +MONDO:0030859 rare diseases +MONDO:0030860 gard_rare diseases +MONDO:0030860 rare diseases +MONDO:0030861 gard_rare diseases +MONDO:0030861 otar diseases +MONDO:0030861 rare diseases +MONDO:0030862 gard_rare diseases +MONDO:0030862 nord_rare diseases +MONDO:0030862 rare diseases +MONDO:0030864 gard_rare diseases +MONDO:0030864 nord_rare diseases +MONDO:0030864 rare diseases +MONDO:0030866 clingen diseases +MONDO:0030866 otar diseases +MONDO:0030867 clingen diseases +MONDO:0030867 gard_rare diseases +MONDO:0030867 nord_rare diseases +MONDO:0030867 otar diseases +MONDO:0030867 rare diseases +MONDO:0030868 otar diseases +MONDO:0030869 otar diseases +MONDO:0030870 gard_rare diseases +MONDO:0030870 nord_rare diseases +MONDO:0030870 rare diseases +MONDO:0030872 clingen diseases +MONDO:0030872 gard_rare diseases +MONDO:0030872 nord_rare diseases +MONDO:0030872 rare diseases +MONDO:0030875 clingen diseases +MONDO:0030875 gard_rare diseases +MONDO:0030875 nord_rare diseases +MONDO:0030875 rare diseases +MONDO:0030878 gard_rare diseases +MONDO:0030878 rare diseases +MONDO:0030880 gard_rare diseases +MONDO:0030880 ordo_disorder diseases +MONDO:0030880 orphanet_rare diseases +MONDO:0030880 rare diseases +MONDO:0030881 gard_rare diseases +MONDO:0030881 nord_rare diseases +MONDO:0030881 rare diseases +MONDO:0030883 gard_rare diseases +MONDO:0030883 nord_rare diseases +MONDO:0030883 rare diseases +MONDO:0030885 clingen diseases +MONDO:0030885 gard_rare diseases +MONDO:0030885 nord_rare diseases +MONDO:0030885 rare diseases +MONDO:0030886 gard_rare diseases +MONDO:0030886 nord_rare diseases +MONDO:0030886 rare diseases +MONDO:0030887 gard_rare diseases +MONDO:0030887 nord_rare diseases +MONDO:0030887 rare diseases +MONDO:0030890 gard_rare diseases +MONDO:0030890 nord_rare diseases +MONDO:0030890 rare diseases +MONDO:0030893 otar diseases +MONDO:0030894 gard_rare diseases +MONDO:0030894 nord_rare diseases +MONDO:0030894 ordo_disorder diseases +MONDO:0030894 orphanet_rare diseases +MONDO:0030894 rare diseases +MONDO:0030895 gard_rare diseases +MONDO:0030895 rare diseases +MONDO:0030896 gard_rare diseases +MONDO:0030896 nord_rare diseases +MONDO:0030896 rare diseases +MONDO:0030897 gard_rare diseases +MONDO:0030897 rare diseases +MONDO:0030898 clingen diseases +MONDO:0030898 gard_rare diseases +MONDO:0030898 ordo_disorder diseases +MONDO:0030898 orphanet_rare diseases +MONDO:0030898 otar diseases +MONDO:0030898 rare diseases +MONDO:0030899 gard_rare diseases +MONDO:0030899 nord_rare diseases +MONDO:0030899 ordo_disorder diseases +MONDO:0030899 orphanet_rare diseases +MONDO:0030899 rare diseases +MONDO:0030900 otar diseases +MONDO:0030902 gard_rare diseases +MONDO:0030902 rare diseases +MONDO:0030903 gard_rare diseases +MONDO:0030903 nord_rare diseases +MONDO:0030903 rare diseases +MONDO:0030905 gard_rare diseases +MONDO:0030905 nord_rare diseases +MONDO:0030905 rare diseases +MONDO:0030907 clingen diseases +MONDO:0030907 gard_rare diseases +MONDO:0030907 nord_rare diseases +MONDO:0030907 otar diseases +MONDO:0030907 rare diseases +MONDO:0030908 gard_rare diseases +MONDO:0030908 nord_rare diseases +MONDO:0030908 otar diseases +MONDO:0030908 rare diseases +MONDO:0030909 gard_rare diseases +MONDO:0030909 nord_rare diseases +MONDO:0030909 rare diseases +MONDO:0030910 gard_rare diseases +MONDO:0030910 nord_rare diseases +MONDO:0030910 otar diseases +MONDO:0030910 rare diseases +MONDO:0030911 gard_rare diseases +MONDO:0030911 nord_rare diseases +MONDO:0030911 rare diseases +MONDO:0030912 gard_rare diseases +MONDO:0030912 nord_rare diseases +MONDO:0030912 ordo_disorder diseases +MONDO:0030912 ordo_malformation_syndrome diseases +MONDO:0030912 orphanet_rare diseases +MONDO:0030912 otar diseases +MONDO:0030912 rare diseases +MONDO:0030913 gard_rare diseases +MONDO:0030913 nord_rare diseases +MONDO:0030913 ordo_disorder diseases +MONDO:0030913 ordo_malformation_syndrome diseases +MONDO:0030913 orphanet_rare diseases +MONDO:0030913 rare diseases +MONDO:0030914 gard_rare diseases +MONDO:0030914 nord_rare diseases +MONDO:0030914 ordo_disorder diseases +MONDO:0030914 orphanet_rare diseases +MONDO:0030914 otar diseases +MONDO:0030914 rare diseases +MONDO:0030915 gard_rare diseases +MONDO:0030915 nord_rare diseases +MONDO:0030915 rare diseases +MONDO:0030916 gard_rare diseases +MONDO:0030916 nord_rare diseases +MONDO:0030916 otar diseases +MONDO:0030916 rare diseases +MONDO:0030917 gard_rare diseases +MONDO:0030917 nord_rare diseases +MONDO:0030917 otar diseases +MONDO:0030917 rare diseases +MONDO:0030918 gard_rare diseases +MONDO:0030918 nord_rare diseases +MONDO:0030918 otar diseases +MONDO:0030918 rare diseases +MONDO:0030919 gard_rare diseases +MONDO:0030919 nord_rare diseases +MONDO:0030919 otar diseases +MONDO:0030919 rare diseases +MONDO:0030920 gard_rare diseases +MONDO:0030920 nord_rare diseases +MONDO:0030920 rare diseases +MONDO:0030921 gard_rare diseases +MONDO:0030921 nord_rare diseases +MONDO:0030921 rare diseases +MONDO:0030922 gard_rare diseases +MONDO:0030922 nord_rare diseases +MONDO:0030922 otar diseases +MONDO:0030922 rare diseases +MONDO:0030923 clingen diseases +MONDO:0030923 gard_rare diseases +MONDO:0030923 otar diseases +MONDO:0030923 rare diseases +MONDO:0030924 gard_rare diseases +MONDO:0030924 nord_rare diseases +MONDO:0030924 rare diseases +MONDO:0030925 gard_rare diseases +MONDO:0030925 rare diseases +MONDO:0030926 otar diseases +MONDO:0030927 gard_rare diseases +MONDO:0030927 rare diseases +MONDO:0030928 gard_rare diseases +MONDO:0030928 nord_rare diseases +MONDO:0030928 rare diseases +MONDO:0030929 gard_rare diseases +MONDO:0030929 nord_rare diseases +MONDO:0030929 rare diseases +MONDO:0030930 gard_rare diseases +MONDO:0030930 rare diseases +MONDO:0030931 gard_rare diseases +MONDO:0030931 nord_rare diseases +MONDO:0030931 rare diseases +MONDO:0030933 gard_rare diseases +MONDO:0030933 nord_rare diseases +MONDO:0030933 rare diseases +MONDO:0030934 gard_rare diseases +MONDO:0030934 rare diseases +MONDO:0030935 gard_rare diseases +MONDO:0030935 rare diseases +MONDO:0030936 gard_rare diseases +MONDO:0030936 nord_rare diseases +MONDO:0030936 rare diseases +MONDO:0030937 gard_rare diseases +MONDO:0030937 otar diseases +MONDO:0030937 rare diseases +MONDO:0030938 gard_rare diseases +MONDO:0030938 otar diseases +MONDO:0030938 rare diseases +MONDO:0030939 gard_rare diseases +MONDO:0030939 nord_rare diseases +MONDO:0030939 rare diseases +MONDO:0030941 gard_rare diseases +MONDO:0030941 nord_rare diseases +MONDO:0030941 rare diseases +MONDO:0030947 gard_rare diseases +MONDO:0030947 nord_rare diseases +MONDO:0030947 ordo_disorder diseases +MONDO:0030947 orphanet_rare diseases +MONDO:0030947 rare diseases +MONDO:0030957 gard_rare diseases +MONDO:0030957 nord_rare diseases +MONDO:0030957 rare diseases +MONDO:0030958 gard_rare diseases +MONDO:0030958 nord_rare diseases +MONDO:0030958 rare diseases +MONDO:0030961 gard_rare diseases +MONDO:0030961 nord_rare diseases +MONDO:0030961 rare diseases +MONDO:0030962 gard_rare diseases +MONDO:0030962 rare diseases +MONDO:0030963 otar diseases +MONDO:0030968 gard_rare diseases +MONDO:0030968 nord_rare diseases +MONDO:0030968 rare diseases +MONDO:0030974 gard_rare diseases +MONDO:0030974 rare diseases +MONDO:0030975 gard_rare diseases +MONDO:0030975 nord_rare diseases +MONDO:0030975 rare diseases +MONDO:0030977 gard_rare diseases +MONDO:0030977 rare diseases +MONDO:0030978 gard_rare diseases +MONDO:0030978 rare diseases +MONDO:0030979 gard_rare diseases +MONDO:0030979 rare diseases +MONDO:0030981 gard_rare diseases +MONDO:0030981 nord_rare diseases +MONDO:0030981 otar diseases +MONDO:0030981 rare diseases +MONDO:0030982 gard_rare diseases +MONDO:0030982 rare diseases +MONDO:0030983 gard_rare diseases +MONDO:0030983 rare diseases +MONDO:0030985 gard_rare diseases +MONDO:0030985 nord_rare diseases +MONDO:0030985 rare diseases +MONDO:0030991 otar diseases +MONDO:0030994 gard_rare diseases +MONDO:0030994 otar diseases +MONDO:0030994 rare diseases +MONDO:0030995 gard_rare diseases +MONDO:0030995 otar diseases +MONDO:0030995 rare diseases +MONDO:0030996 gard_rare diseases +MONDO:0030996 nord_rare diseases +MONDO:0030996 otar diseases +MONDO:0030996 rare diseases +MONDO:0030997 gard_rare diseases +MONDO:0030997 rare diseases +MONDO:0030998 gard_rare diseases +MONDO:0030998 nord_rare diseases +MONDO:0030998 rare diseases +MONDO:0030999 gard_rare diseases +MONDO:0030999 rare diseases +MONDO:0031001 otar diseases +MONDO:0031003 gard_rare diseases +MONDO:0031003 rare diseases +MONDO:0031007 gard_rare diseases +MONDO:0031007 nord_rare diseases +MONDO:0031007 ordo_disorder diseases +MONDO:0031007 orphanet_rare diseases +MONDO:0031007 rare diseases +MONDO:0031008 gard_rare diseases +MONDO:0031008 nord_rare diseases +MONDO:0031008 ordo_disorder diseases +MONDO:0031008 orphanet_rare diseases +MONDO:0031008 rare diseases +MONDO:0031009 gard_rare diseases +MONDO:0031009 nord_rare diseases +MONDO:0031009 rare diseases +MONDO:0031010 gard_rare diseases +MONDO:0031010 nord_rare diseases +MONDO:0031010 rare diseases +MONDO:0031011 gard_rare diseases +MONDO:0031011 rare diseases +MONDO:0031012 gard_rare diseases +MONDO:0031012 rare diseases +MONDO:0031019 gard_rare diseases +MONDO:0031019 ordo_disorder diseases +MONDO:0031019 orphanet_rare diseases +MONDO:0031019 rare diseases +MONDO:0031021 gard_rare diseases +MONDO:0031021 nord_rare diseases +MONDO:0031021 rare diseases +MONDO:0031028 gard_rare diseases +MONDO:0031028 nord_rare diseases +MONDO:0031028 rare diseases +MONDO:0031031 gard_rare diseases +MONDO:0031031 nord_rare diseases +MONDO:0031031 rare diseases +MONDO:0031037 gard_rare diseases +MONDO:0031037 nord_rare diseases +MONDO:0031037 ordo_disorder diseases +MONDO:0031037 ordo_malformation_syndrome diseases +MONDO:0031037 orphanet_rare diseases +MONDO:0031037 otar diseases +MONDO:0031037 rare diseases +MONDO:0031040 gard_rare diseases +MONDO:0031040 nord_rare diseases +MONDO:0031040 rare diseases +MONDO:0031043 gard_rare diseases +MONDO:0031043 nord_rare diseases +MONDO:0031043 rare diseases +MONDO:0031044 gard_rare diseases +MONDO:0031044 nord_rare diseases +MONDO:0031044 rare diseases +MONDO:0031045 gard_rare diseases +MONDO:0031045 nord_rare diseases +MONDO:0031045 rare diseases +MONDO:0031047 gard_rare diseases +MONDO:0031047 nord_rare diseases +MONDO:0031047 rare diseases +MONDO:0031052 gard_rare diseases +MONDO:0031052 nord_rare diseases +MONDO:0031052 rare diseases +MONDO:0031054 gard_rare diseases +MONDO:0031054 nord_rare diseases +MONDO:0031054 rare diseases +MONDO:0031055 gard_rare diseases +MONDO:0031055 nord_rare diseases +MONDO:0031055 rare diseases +MONDO:0031057 gard_rare diseases +MONDO:0031057 nord_rare diseases +MONDO:0031057 rare diseases +MONDO:0031060 gard_rare diseases +MONDO:0031060 nord_rare diseases +MONDO:0031060 rare diseases +MONDO:0031061 otar diseases +MONDO:0031062 gard_rare diseases +MONDO:0031062 nord_rare diseases +MONDO:0031062 rare diseases +MONDO:0031068 gard_rare diseases +MONDO:0031068 nord_rare diseases +MONDO:0031068 rare diseases +MONDO:0031071 gard_rare diseases +MONDO:0031071 nord_rare diseases +MONDO:0031071 rare diseases +MONDO:0031084 gard_rare diseases +MONDO:0031084 rare diseases +MONDO:0031166 gard_rare diseases +MONDO:0031166 otar diseases +MONDO:0031166 rare diseases +MONDO:0031169 gard_rare diseases +MONDO:0031169 nord_rare diseases +MONDO:0031169 otar diseases +MONDO:0031169 rare diseases +MONDO:0031213 gard_rare diseases +MONDO:0031213 ordo_disorder diseases +MONDO:0031213 orphanet_rare diseases +MONDO:0031213 otar diseases +MONDO:0031213 rare diseases +MONDO:0031219 gard_rare diseases +MONDO:0031219 ordo_disorder diseases +MONDO:0031219 orphanet_rare diseases +MONDO:0031219 otar diseases +MONDO:0031219 rare diseases +MONDO:0031230 gard_rare diseases +MONDO:0031230 rare diseases +MONDO:0031257 gard_rare diseases +MONDO:0031257 ordo_disorder diseases +MONDO:0031257 orphanet_rare diseases +MONDO:0031257 rare diseases +MONDO:0031280 otar diseases +MONDO:0031322 gard_rare diseases +MONDO:0031322 n_of_one diseases +MONDO:0031322 nord_rare diseases +MONDO:0031322 ordo_disorder diseases +MONDO:0031322 orphanet_rare diseases +MONDO:0031322 rare diseases +MONDO:0031323 otar diseases +MONDO:0031332 gard_rare diseases +MONDO:0031332 nord_rare diseases +MONDO:0031332 otar diseases +MONDO:0031332 rare diseases +MONDO:0031376 gard_rare diseases +MONDO:0031376 rare diseases +MONDO:0031384 gard_rare diseases +MONDO:0031384 nord_rare diseases +MONDO:0031384 rare diseases +MONDO:0031415 gard_rare diseases +MONDO:0031415 ordo_disorder diseases +MONDO:0031415 orphanet_rare diseases +MONDO:0031415 rare diseases +MONDO:0031421 gard_rare diseases +MONDO:0031421 nord_rare diseases +MONDO:0031421 ordo_disorder diseases +MONDO:0031421 orphanet_rare diseases +MONDO:0031421 otar diseases +MONDO:0031421 rare diseases +MONDO:0031422 gard_rare diseases +MONDO:0031422 rare diseases +MONDO:0031439 otar diseases +MONDO:0031446 gard_rare diseases +MONDO:0031446 nord_rare diseases +MONDO:0031446 ordo_disorder diseases +MONDO:0031446 orphanet_rare diseases +MONDO:0031446 otar diseases +MONDO:0031446 rare diseases +MONDO:0031447 clingen diseases +MONDO:0031447 gard_rare diseases +MONDO:0031447 rare diseases +MONDO:0031481 gard_rare diseases +MONDO:0031481 nord_rare diseases +MONDO:0031481 ordo_disorder diseases +MONDO:0031481 orphanet_rare diseases +MONDO:0031481 otar diseases +MONDO:0031481 rare diseases +MONDO:0031520 gard_rare diseases +MONDO:0031520 nord_rare diseases +MONDO:0031520 obsoletion_candidate diseases +MONDO:0031520 rare diseases +MONDO:0031615 gard_rare diseases +MONDO:0031615 nord_rare diseases +MONDO:0031615 rare diseases +MONDO:0032485 gard_rare diseases +MONDO:0032485 nord_rare diseases +MONDO:0032485 otar diseases +MONDO:0032485 rare diseases +MONDO:0032526 gard_rare diseases +MONDO:0032526 nord_rare diseases +MONDO:0032526 ordo_disorder diseases +MONDO:0032526 orphanet_rare diseases +MONDO:0032526 rare diseases +MONDO:0032564 gard_rare diseases +MONDO:0032564 nord_rare diseases +MONDO:0032564 rare diseases +MONDO:0032567 gard_rare diseases +MONDO:0032567 nord_rare diseases +MONDO:0032567 rare diseases +MONDO:0032569 gard_rare diseases +MONDO:0032569 nord_rare diseases +MONDO:0032569 rare diseases +MONDO:0032570 gard_rare diseases +MONDO:0032570 nord_rare diseases +MONDO:0032570 rare diseases +MONDO:0032571 gard_rare diseases +MONDO:0032571 nord_rare diseases +MONDO:0032571 rare diseases +MONDO:0032573 gard_rare diseases +MONDO:0032573 nord_rare diseases +MONDO:0032573 rare diseases +MONDO:0032577 gard_rare diseases +MONDO:0032577 nord_rare diseases +MONDO:0032577 rare diseases +MONDO:0032579 clingen diseases +MONDO:0032580 gard_rare diseases +MONDO:0032580 rare diseases +MONDO:0032581 gard_rare diseases +MONDO:0032581 rare diseases +MONDO:0032582 gard_rare diseases +MONDO:0032582 rare diseases +MONDO:0032583 gard_rare diseases +MONDO:0032583 nord_rare diseases +MONDO:0032583 rare diseases +MONDO:0032584 gard_rare diseases +MONDO:0032584 nord_rare diseases +MONDO:0032584 rare diseases +MONDO:0032588 gard_rare diseases +MONDO:0032588 nord_rare diseases +MONDO:0032588 rare diseases +MONDO:0032590 gard_rare diseases +MONDO:0032590 nord_rare diseases +MONDO:0032590 rare diseases +MONDO:0032591 gard_rare diseases +MONDO:0032591 nord_rare diseases +MONDO:0032591 otar diseases +MONDO:0032591 rare diseases +MONDO:0032592 gard_rare diseases +MONDO:0032592 nord_rare diseases +MONDO:0032592 rare diseases +MONDO:0032594 gard_rare diseases +MONDO:0032594 otar diseases +MONDO:0032594 rare diseases +MONDO:0032596 gard_rare diseases +MONDO:0032596 nord_rare diseases +MONDO:0032596 rare diseases +MONDO:0032597 gard_rare diseases +MONDO:0032597 nord_rare diseases +MONDO:0032597 rare diseases +MONDO:0032598 gard_rare diseases +MONDO:0032598 nord_rare diseases +MONDO:0032598 rare diseases +MONDO:0032599 gard_rare diseases +MONDO:0032599 rare diseases +MONDO:0032600 clingen diseases +MONDO:0032600 gard_rare diseases +MONDO:0032600 nord_rare diseases +MONDO:0032600 ordo_disorder diseases +MONDO:0032600 orphanet_rare diseases +MONDO:0032600 rare diseases +MONDO:0032601 gard_rare diseases +MONDO:0032601 nord_rare diseases +MONDO:0032601 ordo_disorder diseases +MONDO:0032601 orphanet_rare diseases +MONDO:0032601 rare diseases +MONDO:0032603 gard_rare diseases +MONDO:0032603 nord_rare diseases +MONDO:0032603 rare diseases +MONDO:0032604 gard_rare diseases +MONDO:0032604 nord_rare diseases +MONDO:0032604 rare diseases +MONDO:0032605 gard_rare diseases +MONDO:0032605 nord_rare diseases +MONDO:0032605 rare diseases +MONDO:0032606 gard_rare diseases +MONDO:0032606 rare diseases +MONDO:0032608 gard_rare diseases +MONDO:0032608 rare diseases +MONDO:0032609 gard_rare diseases +MONDO:0032609 rare diseases +MONDO:0032610 gard_rare diseases +MONDO:0032610 otar diseases +MONDO:0032610 rare diseases +MONDO:0032611 gard_rare diseases +MONDO:0032611 rare diseases +MONDO:0032612 gard_rare diseases +MONDO:0032612 rare diseases +MONDO:0032613 gard_rare diseases +MONDO:0032613 rare diseases +MONDO:0032615 gard_rare diseases +MONDO:0032615 rare diseases +MONDO:0032616 gard_rare diseases +MONDO:0032616 rare diseases +MONDO:0032617 gard_rare diseases +MONDO:0032617 rare diseases +MONDO:0032618 gard_rare diseases +MONDO:0032618 rare diseases +MONDO:0032619 gard_rare diseases +MONDO:0032619 rare diseases +MONDO:0032620 gard_rare diseases +MONDO:0032620 rare diseases +MONDO:0032621 gard_rare diseases +MONDO:0032621 rare diseases +MONDO:0032622 gard_rare diseases +MONDO:0032622 rare diseases +MONDO:0032623 gard_rare diseases +MONDO:0032623 rare diseases +MONDO:0032624 gard_rare diseases +MONDO:0032624 rare diseases +MONDO:0032625 gard_rare diseases +MONDO:0032625 rare diseases +MONDO:0032626 gard_rare diseases +MONDO:0032626 rare diseases +MONDO:0032627 gard_rare diseases +MONDO:0032627 rare diseases +MONDO:0032628 gard_rare diseases +MONDO:0032628 rare diseases +MONDO:0032629 gard_rare diseases +MONDO:0032629 rare diseases +MONDO:0032630 gard_rare diseases +MONDO:0032630 rare diseases +MONDO:0032631 gard_rare diseases +MONDO:0032631 rare diseases +MONDO:0032632 gard_rare diseases +MONDO:0032632 rare diseases +MONDO:0032633 gard_rare diseases +MONDO:0032633 rare diseases +MONDO:0032634 gard_rare diseases +MONDO:0032634 rare diseases +MONDO:0032635 gard_rare diseases +MONDO:0032635 rare diseases +MONDO:0032636 gard_rare diseases +MONDO:0032636 rare diseases +MONDO:0032637 gard_rare diseases +MONDO:0032637 nord_rare diseases +MONDO:0032637 otar diseases +MONDO:0032637 rare diseases +MONDO:0032639 gard_rare diseases +MONDO:0032639 nord_rare diseases +MONDO:0032639 rare diseases +MONDO:0032641 gard_rare diseases +MONDO:0032641 nord_rare diseases +MONDO:0032641 otar diseases +MONDO:0032641 rare diseases +MONDO:0032642 gard_rare diseases +MONDO:0032642 nord_rare diseases +MONDO:0032642 ordo_disorder diseases +MONDO:0032642 orphanet_rare diseases +MONDO:0032642 rare diseases +MONDO:0032643 gard_rare diseases +MONDO:0032643 nord_rare diseases +MONDO:0032643 ordo_disorder diseases +MONDO:0032643 orphanet_rare diseases +MONDO:0032643 rare diseases +MONDO:0032646 gard_rare diseases +MONDO:0032646 nord_rare diseases +MONDO:0032646 rare diseases +MONDO:0032649 gard_rare diseases +MONDO:0032649 rare diseases +MONDO:0032653 gard_rare diseases +MONDO:0032653 ordo_disorder diseases +MONDO:0032653 orphanet_rare diseases +MONDO:0032653 rare diseases +MONDO:0032654 gard_rare diseases +MONDO:0032654 nord_rare diseases +MONDO:0032654 rare diseases +MONDO:0032657 gard_rare diseases +MONDO:0032657 nord_rare diseases +MONDO:0032657 rare diseases +MONDO:0032660 gard_rare diseases +MONDO:0032660 nord_rare diseases +MONDO:0032660 rare diseases +MONDO:0032661 gard_rare diseases +MONDO:0032661 rare diseases +MONDO:0032662 gard_rare diseases +MONDO:0032662 nord_rare diseases +MONDO:0032662 rare diseases +MONDO:0032663 gard_rare diseases +MONDO:0032663 nord_rare diseases +MONDO:0032663 rare diseases +MONDO:0032664 gard_rare diseases +MONDO:0032664 nord_rare diseases +MONDO:0032664 otar diseases +MONDO:0032664 rare diseases +MONDO:0032665 gard_rare diseases +MONDO:0032665 nord_rare diseases +MONDO:0032665 rare diseases +MONDO:0032668 gard_rare diseases +MONDO:0032668 nord_rare diseases +MONDO:0032668 rare diseases +MONDO:0032669 gard_rare diseases +MONDO:0032669 nord_rare diseases +MONDO:0032669 rare diseases +MONDO:0032670 gard_rare diseases +MONDO:0032670 nord_rare diseases +MONDO:0032670 rare diseases +MONDO:0032672 gard_rare diseases +MONDO:0032672 nord_rare diseases +MONDO:0032672 ordo_disorder diseases +MONDO:0032672 orphanet_rare diseases +MONDO:0032672 rare diseases +MONDO:0032673 gard_rare diseases +MONDO:0032673 rare diseases +MONDO:0032675 gard_rare diseases +MONDO:0032675 nord_rare diseases +MONDO:0032675 rare diseases +MONDO:0032677 gard_rare diseases +MONDO:0032677 nord_rare diseases +MONDO:0032677 ordo_disorder diseases +MONDO:0032677 orphanet_rare diseases +MONDO:0032677 otar diseases +MONDO:0032677 rare diseases +MONDO:0032678 gard_rare diseases +MONDO:0032678 mondo_rare diseases +MONDO:0032678 nord_rare diseases +MONDO:0032678 ordo_disorder diseases +MONDO:0032678 orphanet_rare diseases +MONDO:0032678 rare diseases +MONDO:0032679 gard_rare diseases +MONDO:0032679 rare diseases +MONDO:0032680 gard_rare diseases +MONDO:0032680 rare diseases +MONDO:0032681 otar diseases +MONDO:0032684 gard_rare diseases +MONDO:0032684 nord_rare diseases +MONDO:0032684 otar diseases +MONDO:0032684 rare diseases +MONDO:0032685 clingen diseases +MONDO:0032687 gard_rare diseases +MONDO:0032687 otar diseases +MONDO:0032687 rare diseases +MONDO:0032688 gard_rare diseases +MONDO:0032688 ordo_disorder diseases +MONDO:0032688 orphanet_rare diseases +MONDO:0032688 otar diseases +MONDO:0032688 rare diseases +MONDO:0032689 gard_rare diseases +MONDO:0032689 nord_rare diseases +MONDO:0032689 rare diseases +MONDO:0032691 gard_rare diseases +MONDO:0032691 nord_rare diseases +MONDO:0032691 rare diseases +MONDO:0032692 gard_rare diseases +MONDO:0032692 nord_rare diseases +MONDO:0032692 rare diseases +MONDO:0032693 gard_rare diseases +MONDO:0032693 nord_rare diseases +MONDO:0032693 rare diseases +MONDO:0032694 gard_rare diseases +MONDO:0032694 nord_rare diseases +MONDO:0032694 rare diseases +MONDO:0032697 otar diseases +MONDO:0032698 otar diseases +MONDO:0032702 gard_rare diseases +MONDO:0032702 nord_rare diseases +MONDO:0032702 rare diseases +MONDO:0032703 gard_rare diseases +MONDO:0032703 nord_rare diseases +MONDO:0032703 rare diseases +MONDO:0032705 gard_rare diseases +MONDO:0032705 nord_rare diseases +MONDO:0032705 ordo_disorder diseases +MONDO:0032705 orphanet_rare diseases +MONDO:0032705 rare diseases +MONDO:0032706 gard_rare diseases +MONDO:0032706 nord_rare diseases +MONDO:0032706 rare diseases +MONDO:0032707 clingen diseases +MONDO:0032710 gard_rare diseases +MONDO:0032710 nord_rare diseases +MONDO:0032710 rare diseases +MONDO:0032712 gard_rare diseases +MONDO:0032712 rare diseases +MONDO:0032714 gard_rare diseases +MONDO:0032714 nord_rare diseases +MONDO:0032714 ordo_disorder diseases +MONDO:0032714 orphanet_rare diseases +MONDO:0032714 rare diseases +MONDO:0032715 gard_rare diseases +MONDO:0032715 nord_rare diseases +MONDO:0032715 rare diseases +MONDO:0032716 gard_rare diseases +MONDO:0032716 nord_rare diseases +MONDO:0032716 ordo_disorder diseases +MONDO:0032716 orphanet_rare diseases +MONDO:0032716 rare diseases +MONDO:0032717 gard_rare diseases +MONDO:0032717 rare diseases +MONDO:0032721 gard_rare diseases +MONDO:0032721 nord_rare diseases +MONDO:0032721 rare diseases +MONDO:0032723 clingen diseases +MONDO:0032724 gard_rare diseases +MONDO:0032724 nord_rare diseases +MONDO:0032724 ordo_disorder diseases +MONDO:0032724 orphanet_rare diseases +MONDO:0032724 rare diseases +MONDO:0032725 gard_rare diseases +MONDO:0032725 nord_rare diseases +MONDO:0032725 rare diseases +MONDO:0032726 gard_rare diseases +MONDO:0032726 nord_rare diseases +MONDO:0032726 ordo_disorder diseases +MONDO:0032726 orphanet_rare diseases +MONDO:0032726 rare diseases +MONDO:0032728 gard_rare diseases +MONDO:0032728 nord_rare diseases +MONDO:0032728 otar diseases +MONDO:0032728 rare diseases +MONDO:0032729 gard_rare diseases +MONDO:0032729 nord_rare diseases +MONDO:0032729 rare diseases +MONDO:0032730 gard_rare diseases +MONDO:0032730 nord_rare diseases +MONDO:0032730 rare diseases +MONDO:0032732 gard_rare diseases +MONDO:0032732 nord_rare diseases +MONDO:0032732 rare diseases +MONDO:0032735 gard_rare diseases +MONDO:0032735 rare diseases +MONDO:0032737 gard_rare diseases +MONDO:0032737 ordo_disorder diseases +MONDO:0032737 orphanet_rare diseases +MONDO:0032737 otar diseases +MONDO:0032737 rare diseases +MONDO:0032740 gard_rare diseases +MONDO:0032740 nord_rare diseases +MONDO:0032740 rare diseases +MONDO:0032744 gard_rare diseases +MONDO:0032744 rare diseases +MONDO:0032745 clingen diseases +MONDO:0032745 gard_rare diseases +MONDO:0032745 otar diseases +MONDO:0032745 rare diseases +MONDO:0032746 gard_rare diseases +MONDO:0032746 rare diseases +MONDO:0032747 gard_rare diseases +MONDO:0032747 rare diseases +MONDO:0032748 clingen diseases +MONDO:0032748 gard_rare diseases +MONDO:0032748 rare diseases +MONDO:0032749 gard_rare diseases +MONDO:0032749 nord_rare diseases +MONDO:0032749 rare diseases +MONDO:0032750 gard_rare diseases +MONDO:0032750 nord_rare diseases +MONDO:0032750 rare diseases +MONDO:0032751 gard_rare diseases +MONDO:0032751 nord_rare diseases +MONDO:0032751 otar diseases +MONDO:0032751 rare diseases +MONDO:0032752 gard_rare diseases +MONDO:0032752 nord_rare diseases +MONDO:0032752 rare diseases +MONDO:0032753 gard_rare diseases +MONDO:0032753 nord_rare diseases +MONDO:0032753 rare diseases +MONDO:0032755 clingen diseases +MONDO:0032755 otar diseases +MONDO:0032756 gard_rare diseases +MONDO:0032756 rare diseases +MONDO:0032757 clingen diseases +MONDO:0032757 gard_rare diseases +MONDO:0032757 nord_rare diseases +MONDO:0032757 rare diseases +MONDO:0032760 otar diseases +MONDO:0032761 gard_rare diseases +MONDO:0032761 nord_rare diseases +MONDO:0032761 rare diseases +MONDO:0032762 gard_rare diseases +MONDO:0032762 nord_rare diseases +MONDO:0032762 rare diseases +MONDO:0032763 clingen diseases +MONDO:0032763 otar diseases +MONDO:0032764 clingen diseases +MONDO:0032765 gard_rare diseases +MONDO:0032765 nord_rare diseases +MONDO:0032765 rare diseases +MONDO:0032766 gard_rare diseases +MONDO:0032766 nord_rare diseases +MONDO:0032766 rare diseases +MONDO:0032767 gard_rare diseases +MONDO:0032767 nord_rare diseases +MONDO:0032767 rare diseases +MONDO:0032768 gard_rare diseases +MONDO:0032768 nord_rare diseases +MONDO:0032768 rare diseases +MONDO:0032770 gard_rare diseases +MONDO:0032770 rare diseases +MONDO:0032771 gard_rare diseases +MONDO:0032771 nord_rare diseases +MONDO:0032771 rare diseases +MONDO:0032773 gard_rare diseases +MONDO:0032773 rare diseases +MONDO:0032776 gard_rare diseases +MONDO:0032776 nord_rare diseases +MONDO:0032776 rare diseases +MONDO:0032777 gard_rare diseases +MONDO:0032777 rare diseases +MONDO:0032778 gard_rare diseases +MONDO:0032778 nord_rare diseases +MONDO:0032778 rare diseases +MONDO:0032780 gard_rare diseases +MONDO:0032780 ordo_disorder diseases +MONDO:0032780 orphanet_rare diseases +MONDO:0032780 rare diseases +MONDO:0032781 otar diseases +MONDO:0032783 gard_rare diseases +MONDO:0032783 nord_rare diseases +MONDO:0032783 rare diseases +MONDO:0032785 gard_rare diseases +MONDO:0032785 nord_rare diseases +MONDO:0032785 rare diseases +MONDO:0032786 gard_rare diseases +MONDO:0032786 nord_rare diseases +MONDO:0032786 rare diseases +MONDO:0032787 clingen diseases +MONDO:0032787 gard_rare diseases +MONDO:0032787 nord_rare diseases +MONDO:0032787 otar diseases +MONDO:0032787 rare diseases +MONDO:0032789 gard_rare diseases +MONDO:0032789 nord_rare diseases +MONDO:0032789 rare diseases +MONDO:0032790 otar diseases +MONDO:0032791 gard_rare diseases +MONDO:0032791 nord_rare diseases +MONDO:0032791 rare diseases +MONDO:0032792 gard_rare diseases +MONDO:0032792 nord_rare diseases +MONDO:0032792 rare diseases +MONDO:0032794 gard_rare diseases +MONDO:0032794 nord_rare diseases +MONDO:0032794 rare diseases +MONDO:0032795 clingen diseases +MONDO:0032795 gard_rare diseases +MONDO:0032795 nord_rare diseases +MONDO:0032795 otar diseases +MONDO:0032795 rare diseases +MONDO:0032796 gard_rare diseases +MONDO:0032796 nord_rare diseases +MONDO:0032796 rare diseases +MONDO:0032797 gard_rare diseases +MONDO:0032797 rare diseases +MONDO:0032799 gard_rare diseases +MONDO:0032799 otar diseases +MONDO:0032799 rare diseases +MONDO:0032800 gard_rare diseases +MONDO:0032800 nord_rare diseases +MONDO:0032800 rare diseases +MONDO:0032801 gard_rare diseases +MONDO:0032801 nord_rare diseases +MONDO:0032801 rare diseases +MONDO:0032802 gard_rare diseases +MONDO:0032802 nord_rare diseases +MONDO:0032802 rare diseases +MONDO:0032803 gard_rare diseases +MONDO:0032803 rare diseases +MONDO:0032804 gard_rare diseases +MONDO:0032804 nord_rare diseases +MONDO:0032804 rare diseases +MONDO:0032805 otar diseases +MONDO:0032806 gard_rare diseases +MONDO:0032806 nord_rare diseases +MONDO:0032806 rare diseases +MONDO:0032808 gard_rare diseases +MONDO:0032808 nord_rare diseases +MONDO:0032808 rare diseases +MONDO:0032811 gard_rare diseases +MONDO:0032811 nord_rare diseases +MONDO:0032811 rare diseases +MONDO:0032812 gard_rare diseases +MONDO:0032812 nord_rare diseases +MONDO:0032812 rare diseases +MONDO:0032813 gard_rare diseases +MONDO:0032813 nord_rare diseases +MONDO:0032813 rare diseases +MONDO:0032814 gard_rare diseases +MONDO:0032814 ordo_disorder diseases +MONDO:0032814 orphanet_rare diseases +MONDO:0032814 rare diseases +MONDO:0032815 gard_rare diseases +MONDO:0032815 rare diseases +MONDO:0032816 gard_rare diseases +MONDO:0032816 rare diseases +MONDO:0032819 gard_rare diseases +MONDO:0032819 nord_rare diseases +MONDO:0032819 ordo_disorder diseases +MONDO:0032819 orphanet_rare diseases +MONDO:0032819 rare diseases +MONDO:0032821 gard_rare diseases +MONDO:0032821 rare diseases +MONDO:0032822 gard_rare diseases +MONDO:0032822 nord_rare diseases +MONDO:0032822 rare diseases +MONDO:0032823 gard_rare diseases +MONDO:0032823 nord_rare diseases +MONDO:0032823 rare diseases +MONDO:0032824 clingen diseases +MONDO:0032829 clingen diseases +MONDO:0032830 gard_rare diseases +MONDO:0032830 ordo_disorder diseases +MONDO:0032830 orphanet_rare diseases +MONDO:0032830 rare diseases +MONDO:0032831 gard_rare diseases +MONDO:0032831 nord_rare diseases +MONDO:0032831 ordo_disorder diseases +MONDO:0032831 orphanet_rare diseases +MONDO:0032831 rare diseases +MONDO:0032834 gard_rare diseases +MONDO:0032834 nord_rare diseases +MONDO:0032834 rare diseases +MONDO:0032835 gard_rare diseases +MONDO:0032835 nord_rare diseases +MONDO:0032835 rare diseases +MONDO:0032836 clingen diseases +MONDO:0032836 obsoletion_candidate diseases +MONDO:0032837 gard_rare diseases +MONDO:0032837 rare diseases +MONDO:0032839 gard_rare diseases +MONDO:0032839 nord_rare diseases +MONDO:0032839 rare diseases +MONDO:0032841 gard_rare diseases +MONDO:0032841 rare diseases +MONDO:0032842 clingen diseases +MONDO:0032843 otar diseases +MONDO:0032844 gard_rare diseases +MONDO:0032844 nord_rare diseases +MONDO:0032844 rare diseases +MONDO:0032845 clingen diseases +MONDO:0032845 gard_rare diseases +MONDO:0032845 rare diseases +MONDO:0032846 gard_rare diseases +MONDO:0032846 rare diseases +MONDO:0032851 gard_rare diseases +MONDO:0032851 rare diseases +MONDO:0032852 gard_rare diseases +MONDO:0032852 rare diseases +MONDO:0032854 gard_rare diseases +MONDO:0032854 nord_rare diseases +MONDO:0032854 rare diseases +MONDO:0032855 gard_rare diseases +MONDO:0032855 rare diseases +MONDO:0032858 gard_rare diseases +MONDO:0032858 nord_rare diseases +MONDO:0032858 rare diseases +MONDO:0032859 gard_rare diseases +MONDO:0032859 rare diseases +MONDO:0032860 gard_rare diseases +MONDO:0032860 nord_rare diseases +MONDO:0032860 rare diseases +MONDO:0032862 gard_rare diseases +MONDO:0032862 rare diseases +MONDO:0032863 gard_rare diseases +MONDO:0032863 rare diseases +MONDO:0032865 gard_rare diseases +MONDO:0032865 nord_rare diseases +MONDO:0032865 rare diseases +MONDO:0032867 gard_rare diseases +MONDO:0032867 rare diseases +MONDO:0032869 gard_rare diseases +MONDO:0032869 rare diseases +MONDO:0032870 gard_rare diseases +MONDO:0032870 rare diseases +MONDO:0032871 gard_rare diseases +MONDO:0032871 nord_rare diseases +MONDO:0032871 rare diseases +MONDO:0032872 clingen diseases +MONDO:0032872 gard_rare diseases +MONDO:0032872 nord_rare diseases +MONDO:0032872 rare diseases +MONDO:0032873 gard_rare diseases +MONDO:0032873 nord_rare diseases +MONDO:0032873 rare diseases +MONDO:0032874 clingen diseases +MONDO:0032874 gard_rare diseases +MONDO:0032874 nord_rare diseases +MONDO:0032874 otar diseases +MONDO:0032874 rare diseases +MONDO:0032880 gard_rare diseases +MONDO:0032880 nord_rare diseases +MONDO:0032880 rare diseases +MONDO:0032881 gard_rare diseases +MONDO:0032881 nord_rare diseases +MONDO:0032881 rare diseases +MONDO:0032882 clingen diseases +MONDO:0032882 gard_rare diseases +MONDO:0032882 ordo_disorder diseases +MONDO:0032882 orphanet_rare diseases +MONDO:0032882 otar diseases +MONDO:0032882 rare diseases +MONDO:0032884 otar diseases +MONDO:0032885 otar diseases +MONDO:0032886 otar diseases +MONDO:0032887 otar diseases +MONDO:0032888 otar diseases +MONDO:0032889 clingen diseases +MONDO:0032889 otar diseases +MONDO:0032890 otar diseases +MONDO:0032891 gard_rare diseases +MONDO:0032891 nord_rare diseases +MONDO:0032891 otar diseases +MONDO:0032891 rare diseases +MONDO:0032892 otar diseases +MONDO:0032893 otar diseases +MONDO:0032894 otar diseases +MONDO:0032895 gard_rare diseases +MONDO:0032895 nord_rare diseases +MONDO:0032895 otar diseases +MONDO:0032895 rare diseases +MONDO:0032896 gard_rare diseases +MONDO:0032896 otar diseases +MONDO:0032896 rare diseases +MONDO:0032897 otar diseases +MONDO:0032898 gard_rare diseases +MONDO:0032898 otar diseases +MONDO:0032898 rare diseases +MONDO:0032899 gard_rare diseases +MONDO:0032899 nord_rare diseases +MONDO:0032899 otar diseases +MONDO:0032899 rare diseases +MONDO:0032900 otar diseases +MONDO:0032901 otar diseases +MONDO:0032902 gard_rare diseases +MONDO:0032902 nord_rare diseases +MONDO:0032902 otar diseases +MONDO:0032902 rare diseases +MONDO:0032903 gard_rare diseases +MONDO:0032903 nord_rare diseases +MONDO:0032903 otar diseases +MONDO:0032903 rare diseases +MONDO:0032904 gard_rare diseases +MONDO:0032904 nord_rare diseases +MONDO:0032904 otar diseases +MONDO:0032904 rare diseases +MONDO:0032905 gard_rare diseases +MONDO:0032905 otar diseases +MONDO:0032905 rare diseases +MONDO:0032906 gard_rare diseases +MONDO:0032906 ordo_disorder diseases +MONDO:0032906 orphanet_rare diseases +MONDO:0032906 otar diseases +MONDO:0032906 rare diseases +MONDO:0032907 gard_rare diseases +MONDO:0032907 nord_rare diseases +MONDO:0032907 otar diseases +MONDO:0032907 rare diseases +MONDO:0032908 otar diseases +MONDO:0032909 gard_rare diseases +MONDO:0032909 otar diseases +MONDO:0032909 rare diseases +MONDO:0032910 gard_rare diseases +MONDO:0032910 otar diseases +MONDO:0032910 rare diseases +MONDO:0032911 gard_rare diseases +MONDO:0032911 nord_rare diseases +MONDO:0032911 otar diseases +MONDO:0032911 rare diseases +MONDO:0032912 gard_rare diseases +MONDO:0032912 nord_rare diseases +MONDO:0032912 otar diseases +MONDO:0032912 rare diseases +MONDO:0032913 clingen diseases +MONDO:0032913 otar diseases +MONDO:0032914 gard_rare diseases +MONDO:0032914 nord_rare diseases +MONDO:0032914 otar diseases +MONDO:0032914 rare diseases +MONDO:0032915 gard_rare diseases +MONDO:0032915 otar diseases +MONDO:0032915 rare diseases +MONDO:0032916 gard_rare diseases +MONDO:0032916 otar diseases +MONDO:0032916 rare diseases +MONDO:0032917 gard_rare diseases +MONDO:0032917 nord_rare diseases +MONDO:0032917 otar diseases +MONDO:0032917 rare diseases +MONDO:0032918 gard_rare diseases +MONDO:0032918 nord_rare diseases +MONDO:0032918 otar diseases +MONDO:0032918 rare diseases +MONDO:0032919 gard_rare diseases +MONDO:0032919 nord_rare diseases +MONDO:0032919 otar diseases +MONDO:0032919 rare diseases +MONDO:0032920 gard_rare diseases +MONDO:0032920 otar diseases +MONDO:0032920 rare diseases +MONDO:0032921 otar diseases +MONDO:0032922 otar diseases +MONDO:0032923 gard_rare diseases +MONDO:0032923 nord_rare diseases +MONDO:0032923 otar diseases +MONDO:0032923 rare diseases +MONDO:0032924 gard_rare diseases +MONDO:0032924 nord_rare diseases +MONDO:0032924 otar diseases +MONDO:0032924 rare diseases +MONDO:0032925 otar diseases +MONDO:0032926 otar diseases +MONDO:0032927 otar diseases +MONDO:0032928 otar diseases +MONDO:0032930 otar diseases +MONDO:0032931 gard_rare diseases +MONDO:0032931 nord_rare diseases +MONDO:0032931 ordo_disorder diseases +MONDO:0032931 orphanet_rare diseases +MONDO:0032931 otar diseases +MONDO:0032931 rare diseases +MONDO:0032932 gard_rare diseases +MONDO:0032932 otar diseases +MONDO:0032932 rare diseases +MONDO:0032933 gard_rare diseases +MONDO:0032933 nord_rare diseases +MONDO:0032933 ordo_disorder diseases +MONDO:0032933 orphanet_rare diseases +MONDO:0032933 rare diseases +MONDO:0032934 clingen diseases +MONDO:0032934 otar diseases +MONDO:0032935 otar diseases +MONDO:0032936 gard_rare diseases +MONDO:0032936 otar diseases +MONDO:0032936 rare diseases +MONDO:0032937 gard_rare diseases +MONDO:0032937 otar diseases +MONDO:0032937 rare diseases +MONDO:0032938 gard_rare diseases +MONDO:0032938 otar diseases +MONDO:0032938 rare diseases +MONDO:0032939 gard_rare diseases +MONDO:0032939 nord_rare diseases +MONDO:0032939 otar diseases +MONDO:0032939 rare diseases +MONDO:0032940 gard_rare diseases +MONDO:0032940 nord_rare diseases +MONDO:0032940 otar diseases +MONDO:0032940 rare diseases +MONDO:0032941 otar diseases +MONDO:0032942 otar diseases +MONDO:0032943 otar diseases +MONDO:0033004 gard_rare diseases +MONDO:0033004 nord_rare diseases +MONDO:0033004 rare diseases +MONDO:0033005 gard_rare diseases +MONDO:0033005 nord_rare diseases +MONDO:0033005 rare diseases +MONDO:0033006 gard_rare diseases +MONDO:0033006 nord_rare diseases +MONDO:0033006 otar diseases +MONDO:0033006 rare diseases +MONDO:0033007 gard_rare diseases +MONDO:0033007 nord_rare diseases +MONDO:0033007 rare diseases +MONDO:0033008 gard_rare diseases +MONDO:0033008 nord_rare diseases +MONDO:0033008 rare diseases +MONDO:0033009 gard_rare diseases +MONDO:0033009 nord_rare diseases +MONDO:0033009 rare diseases +MONDO:0033010 gard_rare diseases +MONDO:0033010 nord_rare diseases +MONDO:0033010 rare diseases +MONDO:0033012 gard_rare diseases +MONDO:0033012 nord_rare diseases +MONDO:0033012 rare diseases +MONDO:0033013 gard_rare diseases +MONDO:0033013 nord_rare diseases +MONDO:0033013 rare diseases +MONDO:0033014 clingen diseases +MONDO:0033014 gard_rare diseases +MONDO:0033014 nord_rare diseases +MONDO:0033014 otar diseases +MONDO:0033014 rare diseases +MONDO:0033015 gard_rare diseases +MONDO:0033015 nord_rare diseases +MONDO:0033015 rare diseases +MONDO:0033043 gard_rare diseases +MONDO:0033043 nord_rare diseases +MONDO:0033043 ordo_disorder diseases +MONDO:0033043 orphanet_rare diseases +MONDO:0033043 otar diseases +MONDO:0033043 rare diseases +MONDO:0033044 gard_rare diseases +MONDO:0033044 rare diseases +MONDO:0033045 gard_rare diseases +MONDO:0033045 nord_rare diseases +MONDO:0033045 rare diseases +MONDO:0033046 gard_rare diseases +MONDO:0033046 nord_rare diseases +MONDO:0033046 rare diseases +MONDO:0033047 gard_rare diseases +MONDO:0033047 nord_rare diseases +MONDO:0033047 rare diseases +MONDO:0033091 gard_rare diseases +MONDO:0033091 nord_rare diseases +MONDO:0033091 rare diseases +MONDO:0033092 gard_rare diseases +MONDO:0033092 nord_rare diseases +MONDO:0033092 rare diseases +MONDO:0033115 clingen diseases +MONDO:0033115 gard_rare diseases +MONDO:0033115 nord_rare diseases +MONDO:0033115 rare diseases +MONDO:0033116 gard_rare diseases +MONDO:0033116 nord_rare diseases +MONDO:0033116 rare diseases +MONDO:0033123 gard_rare diseases +MONDO:0033123 nord_rare diseases +MONDO:0033123 rare diseases +MONDO:0033135 gard_rare diseases +MONDO:0033135 nord_rare diseases +MONDO:0033135 ordo_disorder diseases +MONDO:0033135 orphanet_rare diseases +MONDO:0033135 rare diseases +MONDO:0033198 gard_rare diseases +MONDO:0033198 nord_rare diseases +MONDO:0033198 rare diseases +MONDO:0033199 gard_rare diseases +MONDO:0033199 nord_rare diseases +MONDO:0033199 rare diseases +MONDO:0033200 gard_rare diseases +MONDO:0033200 nord_rare diseases +MONDO:0033200 rare diseases +MONDO:0033201 gard_rare diseases +MONDO:0033201 nord_rare diseases +MONDO:0033201 otar diseases +MONDO:0033201 rare diseases +MONDO:0033202 gard_rare diseases +MONDO:0033202 nord_rare diseases +MONDO:0033202 rare diseases +MONDO:0033203 gard_rare diseases +MONDO:0033203 nord_rare diseases +MONDO:0033203 ordo_disorder diseases +MONDO:0033203 orphanet_rare diseases +MONDO:0033203 rare diseases +MONDO:0033204 clingen diseases +MONDO:0033204 gard_rare diseases +MONDO:0033204 nord_rare diseases +MONDO:0033204 otar diseases +MONDO:0033204 rare diseases +MONDO:0033258 gard_rare diseases +MONDO:0033258 nord_rare diseases +MONDO:0033258 rare diseases +MONDO:0033259 gard_rare diseases +MONDO:0033259 nord_rare diseases +MONDO:0033259 rare diseases +MONDO:0033260 gard_rare diseases +MONDO:0033260 nord_rare diseases +MONDO:0033260 rare diseases +MONDO:0033261 gard_rare diseases +MONDO:0033261 nord_rare diseases +MONDO:0033261 rare diseases +MONDO:0033281 gard_rare diseases +MONDO:0033281 nord_rare diseases +MONDO:0033281 rare diseases +MONDO:0033282 gard_rare diseases +MONDO:0033282 nord_rare diseases +MONDO:0033282 ordo_disorder diseases +MONDO:0033282 orphanet_rare diseases +MONDO:0033282 rare diseases +MONDO:0033304 gard_rare diseases +MONDO:0033304 rare diseases +MONDO:0033308 clingen diseases +MONDO:0033308 gard_rare diseases +MONDO:0033308 nord_rare diseases +MONDO:0033308 rare diseases +MONDO:0033309 gard_rare diseases +MONDO:0033309 nord_rare diseases +MONDO:0033309 rare diseases +MONDO:0033310 gard_rare diseases +MONDO:0033310 nord_rare diseases +MONDO:0033310 rare diseases +MONDO:0033311 gard_rare diseases +MONDO:0033311 nord_rare diseases +MONDO:0033311 rare diseases +MONDO:0033352 gard_rare diseases +MONDO:0033352 otar diseases +MONDO:0033352 rare diseases +MONDO:0033361 gard_rare diseases +MONDO:0033361 nord_rare diseases +MONDO:0033361 otar diseases +MONDO:0033361 rare diseases +MONDO:0033362 gard_rare diseases +MONDO:0033362 nord_rare diseases +MONDO:0033362 rare diseases +MONDO:0033363 gard_rare diseases +MONDO:0033363 nord_rare diseases +MONDO:0033363 otar diseases +MONDO:0033363 rare diseases +MONDO:0033364 gard_rare diseases +MONDO:0033364 nord_rare diseases +MONDO:0033364 rare diseases +MONDO:0033365 gard_rare diseases +MONDO:0033365 nord_rare diseases +MONDO:0033365 rare diseases +MONDO:0033366 gard_rare diseases +MONDO:0033366 nord_rare diseases +MONDO:0033366 rare diseases +MONDO:0033367 gard_rare diseases +MONDO:0033367 nord_rare diseases +MONDO:0033367 rare diseases +MONDO:0033368 gard_rare diseases +MONDO:0033368 nord_rare diseases +MONDO:0033368 rare diseases +MONDO:0033369 gard_rare diseases +MONDO:0033369 nord_rare diseases +MONDO:0033369 rare diseases +MONDO:0033370 gard_rare diseases +MONDO:0033370 nord_rare diseases +MONDO:0033370 rare diseases +MONDO:0033371 gard_rare diseases +MONDO:0033371 nord_rare diseases +MONDO:0033371 rare diseases +MONDO:0033372 gard_rare diseases +MONDO:0033372 nord_rare diseases +MONDO:0033372 rare diseases +MONDO:0033373 gard_rare diseases +MONDO:0033373 nord_rare diseases +MONDO:0033373 rare diseases +MONDO:0033374 gard_rare diseases +MONDO:0033374 nord_rare diseases +MONDO:0033374 otar diseases +MONDO:0033374 rare diseases +MONDO:0033375 gard_rare diseases +MONDO:0033375 nord_rare diseases +MONDO:0033375 rare diseases +MONDO:0033479 gard_rare diseases +MONDO:0033479 nord_rare diseases +MONDO:0033479 ordo_disorder diseases +MONDO:0033479 orphanet_rare diseases +MONDO:0033479 rare diseases +MONDO:0033480 gard_rare diseases +MONDO:0033480 nord_rare diseases +MONDO:0033480 ordo_disorder diseases +MONDO:0033480 orphanet_rare diseases +MONDO:0033480 rare diseases +MONDO:0033481 gard_rare diseases +MONDO:0033481 nord_rare diseases +MONDO:0033481 ordo_disorder diseases +MONDO:0033481 orphanet_rare diseases +MONDO:0033481 rare diseases +MONDO:0033482 gard_rare diseases +MONDO:0033482 nord_rare diseases +MONDO:0033482 ordo_disorder diseases +MONDO:0033482 orphanet_rare diseases +MONDO:0033482 otar diseases +MONDO:0033482 rare diseases +MONDO:0033483 gard_rare diseases +MONDO:0033483 nord_rare diseases +MONDO:0033483 rare diseases +MONDO:0033485 gard_rare diseases +MONDO:0033485 nord_rare diseases +MONDO:0033485 rare diseases +MONDO:0033486 gard_rare diseases +MONDO:0033486 nord_rare diseases +MONDO:0033486 rare diseases +MONDO:0033492 gard_rare diseases +MONDO:0033492 nord_rare diseases +MONDO:0033492 rare diseases +MONDO:0033493 gard_rare diseases +MONDO:0033493 nord_rare diseases +MONDO:0033493 rare diseases +MONDO:0033532 otar diseases +MONDO:0033533 gard_rare diseases +MONDO:0033533 otar diseases +MONDO:0033533 rare diseases +MONDO:0033534 gard_rare diseases +MONDO:0033534 otar diseases +MONDO:0033534 rare diseases +MONDO:0033537 gard_rare diseases +MONDO:0033537 otar diseases +MONDO:0033537 rare diseases +MONDO:0033541 otar diseases +MONDO:0033542 otar diseases +MONDO:0033543 otar diseases +MONDO:0033544 gard_rare diseases +MONDO:0033544 otar diseases +MONDO:0033544 rare diseases +MONDO:0033545 gard_rare diseases +MONDO:0033545 otar diseases +MONDO:0033545 rare diseases +MONDO:0033546 otar diseases +MONDO:0033547 gard_rare diseases +MONDO:0033547 otar diseases +MONDO:0033547 rare diseases +MONDO:0033548 gard_rare diseases +MONDO:0033548 otar diseases +MONDO:0033548 rare diseases +MONDO:0033549 gard_rare diseases +MONDO:0033549 otar diseases +MONDO:0033549 rare diseases +MONDO:0033551 otar diseases +MONDO:0033554 clingen diseases +MONDO:0033554 gard_rare diseases +MONDO:0033554 nord_rare diseases +MONDO:0033554 otar diseases +MONDO:0033554 rare diseases +MONDO:0033555 clingen diseases +MONDO:0033555 gard_rare diseases +MONDO:0033555 nord_rare diseases +MONDO:0033555 otar diseases +MONDO:0033555 rare diseases +MONDO:0033556 gard_rare diseases +MONDO:0033556 otar diseases +MONDO:0033556 rare diseases +MONDO:0033557 gard_rare diseases +MONDO:0033557 nord_rare diseases +MONDO:0033557 otar diseases +MONDO:0033557 rare diseases +MONDO:0033558 otar diseases +MONDO:0033559 gard_rare diseases +MONDO:0033559 otar diseases +MONDO:0033559 rare diseases +MONDO:0033560 gard_rare diseases +MONDO:0033560 otar diseases +MONDO:0033560 rare diseases +MONDO:0033561 otar diseases +MONDO:0033562 gard_rare diseases +MONDO:0033562 otar diseases +MONDO:0033562 rare diseases +MONDO:0033563 gard_rare diseases +MONDO:0033563 nord_rare diseases +MONDO:0033563 otar diseases +MONDO:0033563 rare diseases +MONDO:0033564 gard_rare diseases +MONDO:0033564 otar diseases +MONDO:0033564 rare diseases +MONDO:0033565 gard_rare diseases +MONDO:0033565 otar diseases +MONDO:0033565 rare diseases +MONDO:0033566 gard_rare diseases +MONDO:0033566 otar diseases +MONDO:0033566 rare diseases +MONDO:0033569 otar diseases +MONDO:0033570 otar diseases +MONDO:0033572 gard_rare diseases +MONDO:0033572 otar diseases +MONDO:0033572 rare diseases +MONDO:0033613 gard_rare diseases +MONDO:0033613 ordo_disorder diseases +MONDO:0033613 orphanet_rare diseases +MONDO:0033613 otar diseases +MONDO:0033613 rare diseases +MONDO:0033614 gard_rare diseases +MONDO:0033614 ordo_disorder diseases +MONDO:0033614 orphanet_rare diseases +MONDO:0033614 otar diseases +MONDO:0033614 rare diseases +MONDO:0033615 gard_rare diseases +MONDO:0033615 nord_rare diseases +MONDO:0033615 otar diseases +MONDO:0033615 rare diseases +MONDO:0033618 otar diseases +MONDO:0033619 gard_rare diseases +MONDO:0033619 otar diseases +MONDO:0033619 rare diseases +MONDO:0033620 gard_rare diseases +MONDO:0033620 otar diseases +MONDO:0033620 rare diseases +MONDO:0033621 otar diseases +MONDO:0033622 otar diseases +MONDO:0033630 gard_rare diseases +MONDO:0033630 otar diseases +MONDO:0033630 rare diseases +MONDO:0033631 gard_rare diseases +MONDO:0033631 rare diseases +MONDO:0033635 gard_rare diseases +MONDO:0033635 otar diseases +MONDO:0033635 rare diseases +MONDO:0033636 gard_rare diseases +MONDO:0033636 otar diseases +MONDO:0033636 rare diseases +MONDO:0033637 gard_rare diseases +MONDO:0033637 otar diseases +MONDO:0033637 rare diseases +MONDO:0033638 gard_rare diseases +MONDO:0033638 otar diseases +MONDO:0033638 rare diseases +MONDO:0033639 gard_rare diseases +MONDO:0033639 otar diseases +MONDO:0033639 rare diseases +MONDO:0033640 gard_rare diseases +MONDO:0033640 rare diseases +MONDO:0033642 gard_rare diseases +MONDO:0033642 nord_rare diseases +MONDO:0033642 ordo_disorder diseases +MONDO:0033642 orphanet_rare diseases +MONDO:0033642 rare diseases +MONDO:0033643 otar diseases +MONDO:0033644 gard_rare diseases +MONDO:0033644 rare diseases +MONDO:0033645 gard_rare diseases +MONDO:0033645 otar diseases +MONDO:0033645 rare diseases +MONDO:0033646 gard_rare diseases +MONDO:0033646 otar diseases +MONDO:0033646 rare diseases +MONDO:0033649 gard_rare diseases +MONDO:0033649 otar diseases +MONDO:0033649 rare diseases +MONDO:0033650 gard_rare diseases +MONDO:0033650 otar diseases +MONDO:0033650 rare diseases +MONDO:0033651 gard_rare diseases +MONDO:0033651 otar diseases +MONDO:0033651 rare diseases +MONDO:0033652 gard_rare diseases +MONDO:0033652 otar diseases +MONDO:0033652 rare diseases +MONDO:0033653 gard_rare diseases +MONDO:0033653 otar diseases +MONDO:0033653 rare diseases +MONDO:0033654 gard_rare diseases +MONDO:0033654 otar diseases +MONDO:0033654 rare diseases +MONDO:0033655 gard_rare diseases +MONDO:0033655 otar diseases +MONDO:0033655 rare diseases +MONDO:0033656 gard_rare diseases +MONDO:0033656 otar diseases +MONDO:0033656 rare diseases +MONDO:0033657 gard_rare diseases +MONDO:0033657 nord_rare diseases +MONDO:0033657 rare diseases +MONDO:0033658 gard_rare diseases +MONDO:0033658 rare diseases +MONDO:0033662 gard_rare diseases +MONDO:0033662 rare diseases +MONDO:0033664 otar diseases +MONDO:0033665 gard_rare diseases +MONDO:0033665 nord_rare diseases +MONDO:0033665 otar diseases +MONDO:0033665 rare diseases +MONDO:0033667 gard_rare diseases +MONDO:0033667 otar diseases +MONDO:0033667 rare diseases +MONDO:0033668 gard_rare diseases +MONDO:0033668 nord_rare diseases +MONDO:0033668 rare diseases +MONDO:0033669 gard_rare diseases +MONDO:0033669 nord_rare diseases +MONDO:0033669 rare diseases +MONDO:0033670 gard_rare diseases +MONDO:0033670 nord_rare diseases +MONDO:0033670 rare diseases +MONDO:0033671 otar diseases +MONDO:0033672 gard_rare diseases +MONDO:0033672 ordo_disorder diseases +MONDO:0033672 orphanet_rare diseases +MONDO:0033672 rare diseases +MONDO:0033673 clingen diseases +MONDO:0033673 otar diseases +MONDO:0033682 gard_rare diseases +MONDO:0033682 nord_rare diseases +MONDO:0033682 ordo_disorder diseases +MONDO:0033682 orphanet_rare diseases +MONDO:0033682 rare diseases +MONDO:0033683 gard_rare diseases +MONDO:0033683 nord_rare diseases +MONDO:0033683 ordo_disorder diseases +MONDO:0033683 orphanet_rare diseases +MONDO:0033683 otar diseases +MONDO:0033683 rare diseases +MONDO:0033717 gard_rare diseases +MONDO:0033717 nord_rare diseases +MONDO:0033717 ordo_disorder diseases +MONDO:0033717 orphanet_rare diseases +MONDO:0033717 rare diseases +MONDO:0033809 gard_rare diseases +MONDO:0033809 nord_rare diseases +MONDO:0033809 ordo_disorder diseases +MONDO:0033809 orphanet_rare diseases +MONDO:0033809 rare diseases +MONDO:0033810 gard_rare diseases +MONDO:0033810 nord_rare diseases +MONDO:0033810 ordo_disorder diseases +MONDO:0033810 orphanet_rare diseases +MONDO:0033810 rare diseases +MONDO:0033816 gard_rare diseases +MONDO:0033816 nord_rare diseases +MONDO:0033816 ordo_disorder diseases +MONDO:0033816 orphanet_rare diseases +MONDO:0033816 rare diseases +MONDO:0033818 gard_rare diseases +MONDO:0033818 nord_rare diseases +MONDO:0033818 ordo_disorder diseases +MONDO:0033818 orphanet_rare diseases +MONDO:0033818 rare diseases +MONDO:0033821 gard_rare diseases +MONDO:0033821 nord_rare diseases +MONDO:0033821 ordo_disorder diseases +MONDO:0033821 orphanet_rare diseases +MONDO:0033821 rare diseases +MONDO:0033838 gard_rare diseases +MONDO:0033838 nord_rare diseases +MONDO:0033838 ordo_disorder diseases +MONDO:0033838 orphanet_rare diseases +MONDO:0033838 rare diseases +MONDO:0033839 gard_rare diseases +MONDO:0033839 nord_rare diseases +MONDO:0033839 ordo_disorder diseases +MONDO:0033839 orphanet_rare diseases +MONDO:0033839 rare diseases +MONDO:0033850 gard_rare diseases +MONDO:0033850 nord_rare diseases +MONDO:0033850 ordo_disorder diseases +MONDO:0033850 orphanet_rare diseases +MONDO:0033850 rare diseases +MONDO:0033853 gard_rare diseases +MONDO:0033853 nord_rare diseases +MONDO:0033853 ordo_disorder diseases +MONDO:0033853 orphanet_rare diseases +MONDO:0033853 rare diseases +MONDO:0033856 gard_rare diseases +MONDO:0033856 n_of_one diseases +MONDO:0033856 nord_rare diseases +MONDO:0033856 ordo_disorder diseases +MONDO:0033856 orphanet_rare diseases +MONDO:0033856 rare diseases +MONDO:0033862 gard_rare diseases +MONDO:0033862 nord_rare diseases +MONDO:0033862 ordo_disorder diseases +MONDO:0033862 orphanet_rare diseases +MONDO:0033862 rare diseases +MONDO:0033864 gard_rare diseases +MONDO:0033864 nord_rare diseases +MONDO:0033864 ordo_disorder diseases +MONDO:0033864 orphanet_rare diseases +MONDO:0033864 otar diseases +MONDO:0033864 rare diseases +MONDO:0033885 gard_rare diseases +MONDO:0033885 rare diseases +MONDO:0033925 gard_rare diseases +MONDO:0033925 nord_rare diseases +MONDO:0033925 ordo_disorder diseases +MONDO:0033925 orphanet_rare diseases +MONDO:0033925 rare diseases +MONDO:0033926 gard_rare diseases +MONDO:0033926 nord_rare diseases +MONDO:0033926 ordo_disorder diseases +MONDO:0033926 orphanet_rare diseases +MONDO:0033926 rare diseases +MONDO:0033938 gard_rare diseases +MONDO:0033938 nord_rare diseases +MONDO:0033938 ordo_disorder diseases +MONDO:0033938 orphanet_rare diseases +MONDO:0033938 rare diseases +MONDO:0033946 clingen diseases +MONDO:0033946 gard_rare diseases +MONDO:0033946 nord_rare diseases +MONDO:0033946 ordo_disorder diseases +MONDO:0033946 orphanet_rare diseases +MONDO:0033946 otar diseases +MONDO:0033946 rare diseases +MONDO:0033948 gard_rare diseases +MONDO:0033948 nord_rare diseases +MONDO:0033948 ordo_disorder diseases +MONDO:0033948 orphanet_rare diseases +MONDO:0033948 rare diseases +MONDO:0033954 gard_rare diseases +MONDO:0033954 nord_rare diseases +MONDO:0033954 ordo_disorder diseases +MONDO:0033954 orphanet_rare diseases +MONDO:0033954 rare diseases +MONDO:0033968 gard_rare diseases +MONDO:0033968 nord_rare diseases +MONDO:0033968 ordo_disorder diseases +MONDO:0033968 orphanet_rare diseases +MONDO:0033968 rare diseases +MONDO:0033969 gard_rare diseases +MONDO:0033969 nord_rare diseases +MONDO:0033969 ordo_disorder diseases +MONDO:0033969 orphanet_rare diseases +MONDO:0033969 rare diseases +MONDO:0033980 gard_rare diseases +MONDO:0033980 nord_rare diseases +MONDO:0033980 ordo_disorder diseases +MONDO:0033980 orphanet_rare diseases +MONDO:0033980 rare diseases +MONDO:0034021 gard_rare diseases +MONDO:0034021 ordo_disorder diseases +MONDO:0034021 orphanet_rare diseases +MONDO:0034021 rare diseases +MONDO:0034022 gard_rare diseases +MONDO:0034022 nord_rare diseases +MONDO:0034022 ordo_disorder diseases +MONDO:0034022 orphanet_rare diseases +MONDO:0034022 otar diseases +MONDO:0034022 rare diseases +MONDO:0034041 gard_rare diseases +MONDO:0034041 nord_rare diseases +MONDO:0034041 ordo_disorder diseases +MONDO:0034041 orphanet_rare diseases +MONDO:0034041 rare diseases +MONDO:0034054 gard_rare diseases +MONDO:0034054 nord_rare diseases +MONDO:0034054 ordo_disorder diseases +MONDO:0034054 orphanet_rare diseases +MONDO:0034054 rare diseases +MONDO:0034092 gard_rare diseases +MONDO:0034092 nord_rare diseases +MONDO:0034092 ordo_disorder diseases +MONDO:0034092 orphanet_rare diseases +MONDO:0034092 rare diseases +MONDO:0034099 gard_rare diseases +MONDO:0034099 nord_rare diseases +MONDO:0034099 ordo_disorder diseases +MONDO:0034099 orphanet_rare diseases +MONDO:0034099 rare diseases +MONDO:0034103 gard_rare diseases +MONDO:0034103 nord_rare diseases +MONDO:0034103 ordo_disorder diseases +MONDO:0034103 orphanet_rare diseases +MONDO:0034103 otar diseases +MONDO:0034103 rare diseases +MONDO:0034106 gard_rare diseases +MONDO:0034106 nord_rare diseases +MONDO:0034106 ordo_disorder diseases +MONDO:0034106 orphanet_rare diseases +MONDO:0034106 rare diseases +MONDO:0034109 gard_rare diseases +MONDO:0034109 nord_rare diseases +MONDO:0034109 ordo_disorder diseases +MONDO:0034109 orphanet_rare diseases +MONDO:0034109 rare diseases +MONDO:0034110 gard_rare diseases +MONDO:0034110 nord_rare diseases +MONDO:0034110 ordo_disorder diseases +MONDO:0034110 orphanet_rare diseases +MONDO:0034110 rare diseases +MONDO:0034121 gard_rare diseases +MONDO:0034121 nord_rare diseases +MONDO:0034121 ordo_disorder diseases +MONDO:0034121 orphanet_rare diseases +MONDO:0034121 rare diseases +MONDO:0034127 gard_rare diseases +MONDO:0034127 nord_rare diseases +MONDO:0034127 ordo_disorder diseases +MONDO:0034127 orphanet_rare diseases +MONDO:0034127 rare diseases +MONDO:0034142 gard_rare diseases +MONDO:0034142 nord_rare diseases +MONDO:0034142 ordo_disorder diseases +MONDO:0034142 orphanet_rare diseases +MONDO:0034142 rare diseases +MONDO:0034143 gard_rare diseases +MONDO:0034143 nord_rare diseases +MONDO:0034143 ordo_disorder diseases +MONDO:0034143 orphanet_rare diseases +MONDO:0034143 rare diseases +MONDO:0034145 gard_rare diseases +MONDO:0034145 nord_rare diseases +MONDO:0034145 ordo_disorder diseases +MONDO:0034145 orphanet_rare diseases +MONDO:0034145 otar diseases +MONDO:0034145 rare diseases +MONDO:0034146 gard_rare diseases +MONDO:0034146 nord_rare diseases +MONDO:0034146 ordo_disorder diseases +MONDO:0034146 orphanet_rare diseases +MONDO:0034146 rare diseases +MONDO:0034150 gard_rare diseases +MONDO:0034150 nord_rare diseases +MONDO:0034150 ordo_disorder diseases +MONDO:0034150 orphanet_rare diseases +MONDO:0034150 rare diseases +MONDO:0034186 gard_rare diseases +MONDO:0034186 nord_rare diseases +MONDO:0034186 ordo_disorder diseases +MONDO:0034186 orphanet_rare diseases +MONDO:0034186 rare diseases +MONDO:0034189 gard_rare diseases +MONDO:0034189 nord_rare diseases +MONDO:0034189 ordo_disorder diseases +MONDO:0034189 orphanet_rare diseases +MONDO:0034189 rare diseases +MONDO:0034204 gard_rare diseases +MONDO:0034204 nord_rare diseases +MONDO:0034204 ordo_disorder diseases +MONDO:0034204 orphanet_rare diseases +MONDO:0034204 otar diseases +MONDO:0034204 rare diseases +MONDO:0034212 nord_rare diseases +MONDO:0034212 ordo_disorder diseases +MONDO:0034212 orphanet_rare diseases +MONDO:0034212 rare diseases +MONDO:0034216 gard_rare diseases +MONDO:0034216 nord_rare diseases +MONDO:0034216 ordo_disorder diseases +MONDO:0034216 orphanet_rare diseases +MONDO:0034216 rare diseases +MONDO:0034556 gard_rare diseases +MONDO:0034556 rare diseases +MONDO:0034676 gard_rare diseases +MONDO:0034676 nord_rare diseases +MONDO:0034676 ordo_disorder diseases +MONDO:0034676 orphanet_rare diseases +MONDO:0034676 rare diseases +MONDO:0034820 gard_rare diseases +MONDO:0034820 nord_rare diseases +MONDO:0034820 ordo_disorder diseases +MONDO:0034820 orphanet_rare diseases +MONDO:0034820 rare diseases +MONDO:0034823 gard_rare diseases +MONDO:0034823 nord_rare diseases +MONDO:0034823 obsoletion_candidate diseases +MONDO:0034823 ordo_disorder diseases +MONDO:0034823 orphanet_rare diseases +MONDO:0034823 rare diseases +MONDO:0034846 gard_rare diseases +MONDO:0034846 nord_rare diseases +MONDO:0034846 ordo_disorder diseases +MONDO:0034846 orphanet_rare diseases +MONDO:0034846 rare diseases +MONDO:0034895 gard_rare diseases +MONDO:0034895 nord_rare diseases +MONDO:0034895 ordo_disorder diseases +MONDO:0034895 orphanet_rare diseases +MONDO:0034895 rare diseases +MONDO:0034971 gard_rare diseases +MONDO:0034971 nord_rare diseases +MONDO:0034971 ordo_disorder diseases +MONDO:0034971 orphanet_rare diseases +MONDO:0034971 rare diseases +MONDO:0034976 gard_rare diseases +MONDO:0034976 nord_rare diseases +MONDO:0034976 ordo_disorder diseases +MONDO:0034976 orphanet_rare diseases +MONDO:0034976 otar diseases +MONDO:0034976 rare diseases +MONDO:0034978 gard_rare diseases +MONDO:0034978 nord_rare diseases +MONDO:0034978 ordo_disorder diseases +MONDO:0034978 orphanet_rare diseases +MONDO:0034978 rare diseases +MONDO:0034987 gard_rare diseases +MONDO:0034987 nord_rare diseases +MONDO:0034987 ordo_disorder diseases +MONDO:0034987 orphanet_rare diseases +MONDO:0034987 rare diseases +MONDO:0034989 gard_rare diseases +MONDO:0034989 nord_rare diseases +MONDO:0034989 ordo_disorder diseases +MONDO:0034989 orphanet_rare diseases +MONDO:0034989 rare diseases +MONDO:0034991 gard_rare diseases +MONDO:0034991 ordo_disorder diseases +MONDO:0034991 orphanet_rare diseases +MONDO:0034991 rare diseases +MONDO:0035004 gard_rare diseases +MONDO:0035004 nord_rare diseases +MONDO:0035004 ordo_disorder diseases +MONDO:0035004 orphanet_rare diseases +MONDO:0035004 rare diseases +MONDO:0035008 gard_rare diseases +MONDO:0035008 nord_rare diseases +MONDO:0035008 ordo_disorder diseases +MONDO:0035008 orphanet_rare diseases +MONDO:0035008 rare diseases +MONDO:0035009 gard_rare diseases +MONDO:0035009 nord_rare diseases +MONDO:0035009 ordo_disorder diseases +MONDO:0035009 orphanet_rare diseases +MONDO:0035009 rare diseases +MONDO:0035018 gard_rare diseases +MONDO:0035018 nord_rare diseases +MONDO:0035018 ordo_disorder diseases +MONDO:0035018 orphanet_rare diseases +MONDO:0035018 rare diseases +MONDO:0035027 gard_rare diseases +MONDO:0035027 nord_rare diseases +MONDO:0035027 ordo_disorder diseases +MONDO:0035027 orphanet_rare diseases +MONDO:0035027 rare diseases +MONDO:0035105 gard_rare diseases +MONDO:0035105 nord_rare diseases +MONDO:0035105 ordo_disorder diseases +MONDO:0035105 orphanet_rare diseases +MONDO:0035105 rare diseases +MONDO:0035112 gard_rare diseases +MONDO:0035112 nord_rare diseases +MONDO:0035112 ordo_disorder diseases +MONDO:0035112 orphanet_rare diseases +MONDO:0035112 rare diseases +MONDO:0035117 gard_rare diseases +MONDO:0035117 nord_rare diseases +MONDO:0035117 ordo_disorder diseases +MONDO:0035117 orphanet_rare diseases +MONDO:0035117 rare diseases +MONDO:0035121 gard_rare diseases +MONDO:0035121 nord_rare diseases +MONDO:0035121 ordo_disorder diseases +MONDO:0035121 orphanet_rare diseases +MONDO:0035121 rare diseases +MONDO:0035122 gard_rare diseases +MONDO:0035122 nord_rare diseases +MONDO:0035122 ordo_disorder diseases +MONDO:0035122 orphanet_rare diseases +MONDO:0035122 rare diseases +MONDO:0035124 gard_rare diseases +MONDO:0035124 nord_rare diseases +MONDO:0035124 ordo_disorder diseases +MONDO:0035124 orphanet_rare diseases +MONDO:0035124 rare diseases +MONDO:0035133 clingen diseases +MONDO:0035133 gard_rare diseases +MONDO:0035133 nord_rare diseases +MONDO:0035133 ordo_disorder diseases +MONDO:0035133 orphanet_rare diseases +MONDO:0035133 otar diseases +MONDO:0035133 rare diseases +MONDO:0035136 gard_rare diseases +MONDO:0035136 nord_rare diseases +MONDO:0035136 ordo_disorder diseases +MONDO:0035136 orphanet_rare diseases +MONDO:0035136 rare diseases +MONDO:0035149 gard_rare diseases +MONDO:0035149 nord_rare diseases +MONDO:0035149 ordo_disorder diseases +MONDO:0035149 orphanet_rare diseases +MONDO:0035149 rare diseases +MONDO:0035151 gard_rare diseases +MONDO:0035151 nord_rare diseases +MONDO:0035151 ordo_disorder diseases +MONDO:0035151 orphanet_rare diseases +MONDO:0035151 rare diseases +MONDO:0035153 gard_rare diseases +MONDO:0035153 nord_rare diseases +MONDO:0035153 ordo_subtype_of_a_disorder diseases +MONDO:0035153 rare diseases +MONDO:0035159 gard_rare diseases +MONDO:0035159 nord_rare diseases +MONDO:0035159 ordo_disorder diseases +MONDO:0035159 orphanet_rare diseases +MONDO:0035159 rare diseases +MONDO:0035161 gard_rare diseases +MONDO:0035161 ordo_subtype_of_a_disorder diseases +MONDO:0035161 rare diseases +MONDO:0035173 gard_rare diseases +MONDO:0035173 nord_rare diseases +MONDO:0035173 ordo_disorder diseases +MONDO:0035173 orphanet_rare diseases +MONDO:0035173 rare diseases +MONDO:0035220 gard_rare diseases +MONDO:0035220 nord_rare diseases +MONDO:0035220 ordo_subtype_of_a_disorder diseases +MONDO:0035220 rare diseases +MONDO:0035235 gard_rare diseases +MONDO:0035235 nord_rare diseases +MONDO:0035235 ordo_subtype_of_a_disorder diseases +MONDO:0035235 rare diseases +MONDO:0035236 gard_rare diseases +MONDO:0035236 nord_rare diseases +MONDO:0035236 ordo_subtype_of_a_disorder diseases +MONDO:0035236 rare diseases +MONDO:0035237 gard_rare diseases +MONDO:0035237 nord_rare diseases +MONDO:0035237 ordo_subtype_of_a_disorder diseases +MONDO:0035237 rare diseases +MONDO:0035238 gard_rare diseases +MONDO:0035238 nord_rare diseases +MONDO:0035238 ordo_subtype_of_a_disorder diseases +MONDO:0035238 rare diseases +MONDO:0035290 gard_rare diseases +MONDO:0035290 nord_rare diseases +MONDO:0035290 ordo_subtype_of_a_disorder diseases +MONDO:0035290 otar diseases +MONDO:0035290 rare diseases +MONDO:0035293 gard_rare diseases +MONDO:0035293 nord_rare diseases +MONDO:0035293 ordo_subtype_of_a_disorder diseases +MONDO:0035293 rare diseases +MONDO:0035295 gard_rare diseases +MONDO:0035295 nord_rare diseases +MONDO:0035295 ordo_subtype_of_a_disorder diseases +MONDO:0035295 rare diseases +MONDO:0035312 gard_rare diseases +MONDO:0035312 nord_rare diseases +MONDO:0035312 ordo_subtype_of_a_disorder diseases +MONDO:0035312 rare diseases +MONDO:0035313 gard_rare diseases +MONDO:0035313 nord_rare diseases +MONDO:0035313 ordo_subtype_of_a_disorder diseases +MONDO:0035313 rare diseases +MONDO:0035320 gard_rare diseases +MONDO:0035320 nord_rare diseases +MONDO:0035320 ordo_subtype_of_a_disorder diseases +MONDO:0035320 rare diseases +MONDO:0035321 gard_rare diseases +MONDO:0035321 nord_rare diseases +MONDO:0035321 ordo_subtype_of_a_disorder diseases +MONDO:0035321 rare diseases +MONDO:0035337 gard_rare diseases +MONDO:0035337 nord_rare diseases +MONDO:0035337 ordo_disorder diseases +MONDO:0035337 orphanet_rare diseases +MONDO:0035337 rare diseases +MONDO:0035344 gard_rare diseases +MONDO:0035344 nord_rare diseases +MONDO:0035344 ordo_disorder diseases +MONDO:0035344 orphanet_rare diseases +MONDO:0035344 rare diseases +MONDO:0035345 gard_rare diseases +MONDO:0035345 nord_rare diseases +MONDO:0035345 ordo_disorder diseases +MONDO:0035345 orphanet_rare diseases +MONDO:0035345 rare diseases +MONDO:0035349 gard_rare diseases +MONDO:0035349 nord_rare diseases +MONDO:0035349 ordo_disorder diseases +MONDO:0035349 orphanet_rare diseases +MONDO:0035349 rare diseases +MONDO:0035350 nord_rare diseases +MONDO:0035350 ordo_disorder diseases +MONDO:0035350 orphanet_rare diseases +MONDO:0035350 rare diseases +MONDO:0035357 gard_rare diseases +MONDO:0035357 nord_rare diseases +MONDO:0035357 ordo_disorder diseases +MONDO:0035357 orphanet_rare diseases +MONDO:0035357 rare diseases +MONDO:0035362 gard_rare diseases +MONDO:0035362 nord_rare diseases +MONDO:0035362 ordo_disorder diseases +MONDO:0035362 orphanet_rare diseases +MONDO:0035362 rare diseases +MONDO:0035370 gard_rare diseases +MONDO:0035370 nord_rare diseases +MONDO:0035370 ordo_disorder diseases +MONDO:0035370 orphanet_rare diseases +MONDO:0035370 rare diseases +MONDO:0035375 gard_rare diseases +MONDO:0035375 nord_rare diseases +MONDO:0035375 ordo_disorder diseases +MONDO:0035375 orphanet_rare diseases +MONDO:0035375 rare diseases +MONDO:0035383 gard_rare diseases +MONDO:0035383 ordo_disorder diseases +MONDO:0035383 orphanet_rare diseases +MONDO:0035383 rare diseases +MONDO:0035400 gard_rare diseases +MONDO:0035400 nord_rare diseases +MONDO:0035400 ordo_subtype_of_a_disorder diseases +MONDO:0035400 rare diseases +MONDO:0035401 gard_rare diseases +MONDO:0035401 ordo_subtype_of_a_disorder diseases +MONDO:0035401 rare diseases +MONDO:0035402 gard_rare diseases +MONDO:0035402 ordo_subtype_of_a_disorder diseases +MONDO:0035402 rare diseases +MONDO:0035403 gard_rare diseases +MONDO:0035403 nord_rare diseases +MONDO:0035403 ordo_subtype_of_a_disorder diseases +MONDO:0035403 rare diseases +MONDO:0035404 gard_rare diseases +MONDO:0035404 nord_rare diseases +MONDO:0035404 ordo_subtype_of_a_disorder diseases +MONDO:0035404 rare diseases +MONDO:0035405 gard_rare diseases +MONDO:0035405 nord_rare diseases +MONDO:0035405 ordo_subtype_of_a_disorder diseases +MONDO:0035405 rare diseases +MONDO:0035406 gard_rare diseases +MONDO:0035406 nord_rare diseases +MONDO:0035406 ordo_subtype_of_a_disorder diseases +MONDO:0035406 rare diseases +MONDO:0035407 gard_rare diseases +MONDO:0035407 nord_rare diseases +MONDO:0035407 ordo_subtype_of_a_disorder diseases +MONDO:0035407 rare diseases +MONDO:0035408 gard_rare diseases +MONDO:0035408 nord_rare diseases +MONDO:0035408 ordo_subtype_of_a_disorder diseases +MONDO:0035408 rare diseases +MONDO:0035410 gard_rare diseases +MONDO:0035410 nord_rare diseases +MONDO:0035410 ordo_subtype_of_a_disorder diseases +MONDO:0035410 rare diseases +MONDO:0035411 gard_rare diseases +MONDO:0035411 ordo_subtype_of_a_disorder diseases +MONDO:0035411 rare diseases +MONDO:0035423 gard_rare diseases +MONDO:0035423 nord_rare diseases +MONDO:0035423 ordo_disorder diseases +MONDO:0035423 orphanet_rare diseases +MONDO:0035423 rare diseases +MONDO:0035432 gard_rare diseases +MONDO:0035432 nord_rare diseases +MONDO:0035432 ordo_disorder diseases +MONDO:0035432 orphanet_rare diseases +MONDO:0035432 rare diseases +MONDO:0035433 gard_rare diseases +MONDO:0035433 nord_rare diseases +MONDO:0035433 ordo_disorder diseases +MONDO:0035433 orphanet_rare diseases +MONDO:0035433 rare diseases +MONDO:0035437 gard_rare diseases +MONDO:0035437 nord_rare diseases +MONDO:0035437 ordo_disorder diseases +MONDO:0035437 orphanet_rare diseases +MONDO:0035437 rare diseases +MONDO:0035441 gard_rare diseases +MONDO:0035441 nord_rare diseases +MONDO:0035441 ordo_disorder diseases +MONDO:0035441 orphanet_rare diseases +MONDO:0035441 rare diseases +MONDO:0035444 gard_rare diseases +MONDO:0035444 nord_rare diseases +MONDO:0035444 ordo_subtype_of_a_disorder diseases +MONDO:0035444 rare diseases +MONDO:0035445 gard_rare diseases +MONDO:0035445 nord_rare diseases +MONDO:0035445 ordo_subtype_of_a_disorder diseases +MONDO:0035445 rare diseases +MONDO:0035447 gard_rare diseases +MONDO:0035447 nord_rare diseases +MONDO:0035447 ordo_disorder diseases +MONDO:0035447 orphanet_rare diseases +MONDO:0035447 rare diseases +MONDO:0035449 gard_rare diseases +MONDO:0035449 nord_rare diseases +MONDO:0035449 ordo_subtype_of_a_disorder diseases +MONDO:0035449 rare diseases +MONDO:0035450 gard_rare diseases +MONDO:0035450 nord_rare diseases +MONDO:0035450 ordo_subtype_of_a_disorder diseases +MONDO:0035450 rare diseases +MONDO:0035452 gard_rare diseases +MONDO:0035452 nord_rare diseases +MONDO:0035452 ordo_disorder diseases +MONDO:0035452 orphanet_rare diseases +MONDO:0035452 rare diseases +MONDO:0035454 gard_rare diseases +MONDO:0035454 nord_rare diseases +MONDO:0035454 ordo_disorder diseases +MONDO:0035454 orphanet_rare diseases +MONDO:0035454 rare diseases +MONDO:0035459 gard_rare diseases +MONDO:0035459 nord_rare diseases +MONDO:0035459 ordo_subtype_of_a_disorder diseases +MONDO:0035459 rare diseases +MONDO:0035460 gard_rare diseases +MONDO:0035460 nord_rare diseases +MONDO:0035460 ordo_subtype_of_a_disorder diseases +MONDO:0035460 rare diseases +MONDO:0035472 gard_rare diseases +MONDO:0035472 ordo_disorder diseases +MONDO:0035472 orphanet_rare diseases +MONDO:0035472 rare diseases +MONDO:0035473 gard_rare diseases +MONDO:0035473 nord_rare diseases +MONDO:0035473 ordo_disorder diseases +MONDO:0035473 orphanet_rare diseases +MONDO:0035473 rare diseases +MONDO:0035474 clingen diseases +MONDO:0035474 gard_rare diseases +MONDO:0035474 nord_rare diseases +MONDO:0035474 ordo_disorder diseases +MONDO:0035474 orphanet_rare diseases +MONDO:0035474 rare diseases +MONDO:0035475 gard_rare diseases +MONDO:0035475 nord_rare diseases +MONDO:0035475 ordo_disorder diseases +MONDO:0035475 orphanet_rare diseases +MONDO:0035475 rare diseases +MONDO:0035499 gard_rare diseases +MONDO:0035499 ordo_disorder diseases +MONDO:0035499 orphanet_rare diseases +MONDO:0035499 rare diseases +MONDO:0035500 gard_rare diseases +MONDO:0035500 nord_rare diseases +MONDO:0035500 ordo_disorder diseases +MONDO:0035500 orphanet_rare diseases +MONDO:0035500 rare diseases +MONDO:0035511 gard_rare diseases +MONDO:0035511 nord_rare diseases +MONDO:0035511 ordo_disorder diseases +MONDO:0035511 orphanet_rare diseases +MONDO:0035511 rare diseases +MONDO:0035521 gard_rare diseases +MONDO:0035521 nord_rare diseases +MONDO:0035521 ordo_disorder diseases +MONDO:0035521 orphanet_rare diseases +MONDO:0035521 rare diseases +MONDO:0035524 gard_rare diseases +MONDO:0035524 nord_rare diseases +MONDO:0035524 ordo_subtype_of_a_disorder diseases +MONDO:0035524 rare diseases +MONDO:0035525 gard_rare diseases +MONDO:0035525 nord_rare diseases +MONDO:0035525 ordo_subtype_of_a_disorder diseases +MONDO:0035525 otar diseases +MONDO:0035525 rare diseases +MONDO:0035529 gard_rare diseases +MONDO:0035529 nord_rare diseases +MONDO:0035529 ordo_disorder diseases +MONDO:0035529 orphanet_rare diseases +MONDO:0035529 rare diseases +MONDO:0035534 gard_rare diseases +MONDO:0035534 nord_rare diseases +MONDO:0035534 ordo_disorder diseases +MONDO:0035534 orphanet_rare diseases +MONDO:0035534 rare diseases +MONDO:0035540 gard_rare diseases +MONDO:0035540 ordo_group_of_disorders diseases +MONDO:0035540 rare diseases +MONDO:0035551 gard_rare diseases +MONDO:0035551 nord_rare diseases +MONDO:0035551 ordo_disorder diseases +MONDO:0035551 orphanet_rare diseases +MONDO:0035551 rare diseases +MONDO:0035562 gard_rare diseases +MONDO:0035562 nord_rare diseases +MONDO:0035562 ordo_group_of_disorders diseases +MONDO:0035562 rare diseases +MONDO:0035584 gard_rare diseases +MONDO:0035584 nord_rare diseases +MONDO:0035584 ordo_disorder diseases +MONDO:0035584 orphanet_rare diseases +MONDO:0035584 rare diseases +MONDO:0035586 gard_rare diseases +MONDO:0035586 nord_rare diseases +MONDO:0035586 ordo_disorder diseases +MONDO:0035586 orphanet_rare diseases +MONDO:0035586 rare diseases +MONDO:0035592 gard_rare diseases +MONDO:0035592 nord_rare diseases +MONDO:0035592 ordo_disorder diseases +MONDO:0035592 orphanet_rare diseases +MONDO:0035592 rare diseases +MONDO:0035605 gard_rare diseases +MONDO:0035605 nord_rare diseases +MONDO:0035605 ordo_subtype_of_a_disorder diseases +MONDO:0035605 rare diseases +MONDO:0035614 gard_rare diseases +MONDO:0035614 nord_rare diseases +MONDO:0035614 ordo_disorder diseases +MONDO:0035614 orphanet_rare diseases +MONDO:0035614 rare diseases +MONDO:0035639 gard_rare diseases +MONDO:0035639 nord_rare diseases +MONDO:0035639 ordo_subtype_of_a_disorder diseases +MONDO:0035639 rare diseases +MONDO:0035642 gard_rare diseases +MONDO:0035642 nord_rare diseases +MONDO:0035642 ordo_subtype_of_a_disorder diseases +MONDO:0035642 rare diseases +MONDO:0035646 gard_rare diseases +MONDO:0035646 nord_rare diseases +MONDO:0035646 ordo_subtype_of_a_disorder diseases +MONDO:0035646 rare diseases +MONDO:0035647 gard_rare diseases +MONDO:0035647 nord_rare diseases +MONDO:0035647 ordo_subtype_of_a_disorder diseases +MONDO:0035647 rare diseases +MONDO:0035648 gard_rare diseases +MONDO:0035648 nord_rare diseases +MONDO:0035648 ordo_subtype_of_a_disorder diseases +MONDO:0035648 rare diseases +MONDO:0035649 gard_rare diseases +MONDO:0035649 nord_rare diseases +MONDO:0035649 ordo_subtype_of_a_disorder diseases +MONDO:0035649 rare diseases +MONDO:0035650 gard_rare diseases +MONDO:0035650 nord_rare diseases +MONDO:0035650 ordo_subtype_of_a_disorder diseases +MONDO:0035650 rare diseases +MONDO:0035651 gard_rare diseases +MONDO:0035651 nord_rare diseases +MONDO:0035651 ordo_disorder diseases +MONDO:0035651 orphanet_rare diseases +MONDO:0035651 rare diseases +MONDO:0035660 gard_rare diseases +MONDO:0035660 nord_rare diseases +MONDO:0035660 ordo_disorder diseases +MONDO:0035660 orphanet_rare diseases +MONDO:0035660 rare diseases +MONDO:0035661 gard_rare diseases +MONDO:0035661 nord_rare diseases +MONDO:0035661 ordo_disorder diseases +MONDO:0035661 orphanet_rare diseases +MONDO:0035661 rare diseases +MONDO:0035663 gard_rare diseases +MONDO:0035663 nord_rare diseases +MONDO:0035663 ordo_subtype_of_a_disorder diseases +MONDO:0035663 rare diseases +MONDO:0035664 gard_rare diseases +MONDO:0035664 nord_rare diseases +MONDO:0035664 ordo_subtype_of_a_disorder diseases +MONDO:0035664 rare diseases +MONDO:0035665 gard_rare diseases +MONDO:0035665 nord_rare diseases +MONDO:0035665 ordo_subtype_of_a_disorder diseases +MONDO:0035665 rare diseases +MONDO:0035666 gard_rare diseases +MONDO:0035666 nord_rare diseases +MONDO:0035666 ordo_subtype_of_a_disorder diseases +MONDO:0035666 rare diseases +MONDO:0035667 gard_rare diseases +MONDO:0035667 nord_rare diseases +MONDO:0035667 ordo_subtype_of_a_disorder diseases +MONDO:0035667 rare diseases +MONDO:0035668 gard_rare diseases +MONDO:0035668 nord_rare diseases +MONDO:0035668 ordo_subtype_of_a_disorder diseases +MONDO:0035668 rare diseases +MONDO:0035669 gard_rare diseases +MONDO:0035669 nord_rare diseases +MONDO:0035669 ordo_subtype_of_a_disorder diseases +MONDO:0035669 rare diseases +MONDO:0035670 gard_rare diseases +MONDO:0035670 nord_rare diseases +MONDO:0035670 ordo_subtype_of_a_disorder diseases +MONDO:0035670 rare diseases +MONDO:0035678 gard_rare diseases +MONDO:0035678 nord_rare diseases +MONDO:0035678 ordo_subtype_of_a_disorder diseases +MONDO:0035678 rare diseases +MONDO:0035679 gard_rare diseases +MONDO:0035679 nord_rare diseases +MONDO:0035679 ordo_subtype_of_a_disorder diseases +MONDO:0035679 rare diseases +MONDO:0035694 clingen diseases +MONDO:0035694 gard_rare diseases +MONDO:0035694 nord_rare diseases +MONDO:0035694 ordo_disorder diseases +MONDO:0035694 orphanet_rare diseases +MONDO:0035694 rare diseases +MONDO:0035696 gard_rare diseases +MONDO:0035696 nord_rare diseases +MONDO:0035696 ordo_subtype_of_a_disorder diseases +MONDO:0035696 rare diseases +MONDO:0035706 gard_rare diseases +MONDO:0035706 nord_rare diseases +MONDO:0035706 ordo_disorder diseases +MONDO:0035706 orphanet_rare diseases +MONDO:0035706 rare diseases +MONDO:0035707 gard_rare diseases +MONDO:0035707 nord_rare diseases +MONDO:0035707 ordo_disorder diseases +MONDO:0035707 orphanet_rare diseases +MONDO:0035707 rare diseases +MONDO:0035713 gard_rare diseases +MONDO:0035713 nord_rare diseases +MONDO:0035713 ordo_subtype_of_a_disorder diseases +MONDO:0035713 rare diseases +MONDO:0035734 gard_rare diseases +MONDO:0035734 nord_rare diseases +MONDO:0035734 ordo_subtype_of_a_disorder diseases +MONDO:0035734 rare diseases +MONDO:0035735 gard_rare diseases +MONDO:0035735 nord_rare diseases +MONDO:0035735 ordo_disorder diseases +MONDO:0035735 orphanet_rare diseases +MONDO:0035735 rare diseases +MONDO:0035736 gard_rare diseases +MONDO:0035736 nord_rare diseases +MONDO:0035736 ordo_disorder diseases +MONDO:0035736 orphanet_rare diseases +MONDO:0035736 rare diseases +MONDO:0035737 gard_rare diseases +MONDO:0035737 nord_rare diseases +MONDO:0035737 ordo_disorder diseases +MONDO:0035737 orphanet_rare diseases +MONDO:0035737 rare diseases +MONDO:0035738 gard_rare diseases +MONDO:0035738 nord_rare diseases +MONDO:0035738 ordo_disorder diseases +MONDO:0035738 orphanet_rare diseases +MONDO:0035738 rare diseases +MONDO:0035740 gard_rare diseases +MONDO:0035740 nord_rare diseases +MONDO:0035740 ordo_disorder diseases +MONDO:0035740 orphanet_rare diseases +MONDO:0035740 rare diseases +MONDO:0035742 gard_rare diseases +MONDO:0035742 nord_rare diseases +MONDO:0035742 ordo_disorder diseases +MONDO:0035742 orphanet_rare diseases +MONDO:0035742 rare diseases +MONDO:0035743 gard_rare diseases +MONDO:0035743 nord_rare diseases +MONDO:0035743 ordo_subtype_of_a_disorder diseases +MONDO:0035743 rare diseases +MONDO:0035759 gard_rare diseases +MONDO:0035759 nord_rare diseases +MONDO:0035759 ordo_subtype_of_a_disorder diseases +MONDO:0035759 rare diseases +MONDO:0035763 gard_rare diseases +MONDO:0035763 nord_rare diseases +MONDO:0035763 ordo_disorder diseases +MONDO:0035763 orphanet_rare diseases +MONDO:0035763 rare diseases +MONDO:0035764 gard_rare diseases +MONDO:0035764 nord_rare diseases +MONDO:0035764 ordo_disorder diseases +MONDO:0035764 orphanet_rare diseases +MONDO:0035764 rare diseases +MONDO:0035774 gard_rare diseases +MONDO:0035774 ordo_disorder diseases +MONDO:0035774 orphanet_rare diseases +MONDO:0035774 rare diseases +MONDO:0035775 gard_rare diseases +MONDO:0035775 nord_rare diseases +MONDO:0035775 ordo_disorder diseases +MONDO:0035775 orphanet_rare diseases +MONDO:0035775 rare diseases +MONDO:0035776 gard_rare diseases +MONDO:0035776 nord_rare diseases +MONDO:0035776 ordo_disorder diseases +MONDO:0035776 orphanet_rare diseases +MONDO:0035776 rare diseases +MONDO:0035777 gard_rare diseases +MONDO:0035777 nord_rare diseases +MONDO:0035777 ordo_disorder diseases +MONDO:0035777 orphanet_rare diseases +MONDO:0035777 rare diseases +MONDO:0035782 gard_rare diseases +MONDO:0035782 nord_rare diseases +MONDO:0035782 ordo_subtype_of_a_disorder diseases +MONDO:0035782 rare diseases +MONDO:0035783 gard_rare diseases +MONDO:0035783 nord_rare diseases +MONDO:0035783 ordo_subtype_of_a_disorder diseases +MONDO:0035783 rare diseases +MONDO:0035819 gard_rare diseases +MONDO:0035819 nord_rare diseases +MONDO:0035819 ordo_disorder diseases +MONDO:0035819 orphanet_rare diseases +MONDO:0035819 rare diseases +MONDO:0035821 gard_rare diseases +MONDO:0035821 nord_rare diseases +MONDO:0035821 ordo_disorder diseases +MONDO:0035821 orphanet_rare diseases +MONDO:0035821 rare diseases +MONDO:0035823 gard_rare diseases +MONDO:0035823 nord_rare diseases +MONDO:0035823 ordo_disorder diseases +MONDO:0035823 orphanet_rare diseases +MONDO:0035823 rare diseases +MONDO:0035824 gard_rare diseases +MONDO:0035824 nord_rare diseases +MONDO:0035824 ordo_disorder diseases +MONDO:0035824 orphanet_rare diseases +MONDO:0035824 rare diseases +MONDO:0035826 gard_rare diseases +MONDO:0035826 nord_rare diseases +MONDO:0035826 ordo_disorder diseases +MONDO:0035826 orphanet_rare diseases +MONDO:0035826 rare diseases +MONDO:0035838 gard_rare diseases +MONDO:0035838 nord_rare diseases +MONDO:0035838 ordo_subtype_of_a_disorder diseases +MONDO:0035838 rare diseases +MONDO:0035879 gard_rare diseases +MONDO:0035879 nord_rare diseases +MONDO:0035879 ordo_disorder diseases +MONDO:0035879 orphanet_rare diseases +MONDO:0035879 rare diseases +MONDO:0035882 gard_rare diseases +MONDO:0035882 nord_rare diseases +MONDO:0035882 ordo_disorder diseases +MONDO:0035882 orphanet_rare diseases +MONDO:0035882 rare diseases +MONDO:0035892 gard_rare diseases +MONDO:0035892 nord_rare diseases +MONDO:0035892 ordo_disorder diseases +MONDO:0035892 orphanet_rare diseases +MONDO:0035892 rare diseases +MONDO:0035930 gard_rare diseases +MONDO:0035930 nord_rare diseases +MONDO:0035930 ordo_subtype_of_a_disorder diseases +MONDO:0035930 rare diseases +MONDO:0035940 gard_rare diseases +MONDO:0035940 nord_rare diseases +MONDO:0035940 ordo_subtype_of_a_disorder diseases +MONDO:0035940 rare diseases +MONDO:0035941 gard_rare diseases +MONDO:0035941 nord_rare diseases +MONDO:0035941 ordo_subtype_of_a_disorder diseases +MONDO:0035941 rare diseases +MONDO:0035942 gard_rare diseases +MONDO:0035942 nord_rare diseases +MONDO:0035942 ordo_subtype_of_a_disorder diseases +MONDO:0035942 rare diseases +MONDO:0035943 gard_rare diseases +MONDO:0035943 nord_rare diseases +MONDO:0035943 ordo_subtype_of_a_disorder diseases +MONDO:0035943 rare diseases +MONDO:0035944 gard_rare diseases +MONDO:0035944 nord_rare diseases +MONDO:0035944 ordo_subtype_of_a_disorder diseases +MONDO:0035944 rare diseases +MONDO:0035945 gard_rare diseases +MONDO:0035945 nord_rare diseases +MONDO:0035945 ordo_subtype_of_a_disorder diseases +MONDO:0035945 rare diseases +MONDO:0036042 clingen diseases +MONDO:0036042 gard_rare diseases +MONDO:0036042 nord_rare diseases +MONDO:0036042 ordo_group_of_disorders diseases +MONDO:0036042 rare diseases +MONDO:0036045 gard_rare diseases +MONDO:0036045 nord_rare diseases +MONDO:0036045 ordo_disorder diseases +MONDO:0036045 orphanet_rare diseases +MONDO:0036045 rare diseases +MONDO:0036189 gard_rare diseases +MONDO:0036189 nord_rare diseases +MONDO:0036189 ordo_disorder diseases +MONDO:0036189 orphanet_rare diseases +MONDO:0036189 rare diseases +MONDO:0036193 gard_rare diseases +MONDO:0036193 nord_rare diseases +MONDO:0036193 ordo_disorder diseases +MONDO:0036193 orphanet_rare diseases +MONDO:0036193 rare diseases +MONDO:0036212 gard_rare diseases +MONDO:0036212 nord_rare diseases +MONDO:0036212 ordo_disorder diseases +MONDO:0036212 orphanet_rare diseases +MONDO:0036212 rare diseases +MONDO:0036217 gard_rare diseases +MONDO:0036217 nord_rare diseases +MONDO:0036217 ordo_subtype_of_a_disorder diseases +MONDO:0036217 rare diseases +MONDO:0036218 gard_rare diseases +MONDO:0036218 nord_rare diseases +MONDO:0036218 ordo_subtype_of_a_disorder diseases +MONDO:0036218 rare diseases +MONDO:0036482 gard_rare diseases +MONDO:0036482 nord_rare diseases +MONDO:0036482 rare diseases +MONDO:0036483 gard_rare diseases +MONDO:0036483 nord_rare diseases +MONDO:0036483 rare diseases +MONDO:0036484 gard_rare diseases +MONDO:0036484 nord_rare diseases +MONDO:0036484 otar diseases +MONDO:0036484 rare diseases +MONDO:0036511 otar diseases +MONDO:0036591 gard_rare diseases +MONDO:0036591 otar diseases +MONDO:0036591 rare diseases +MONDO:0036688 otar diseases +MONDO:0036696 gard_rare diseases +MONDO:0036696 otar diseases +MONDO:0036696 rare diseases +MONDO:0036870 otar diseases +MONDO:0036918 gard_rare diseases +MONDO:0036918 nord_rare diseases +MONDO:0036918 ordo_disorder diseases +MONDO:0036918 orphanet_rare diseases +MONDO:0036918 rare diseases +MONDO:0036976 otar diseases +MONDO:0037003 otar diseases +MONDO:0037105 gard_rare diseases +MONDO:0037105 rare diseases +MONDO:0037149 gard_rare diseases +MONDO:0037149 nord_rare diseases +MONDO:0037149 ordo_subtype_of_a_disorder diseases +MONDO:0037149 rare diseases +MONDO:0037251 gard_rare diseases +MONDO:0037251 rare diseases +MONDO:0037254 otar diseases +MONDO:0037255 otar diseases +MONDO:0037256 otar diseases +MONDO:0037398 gard_rare diseases +MONDO:0037398 nord_rare diseases +MONDO:0037398 ordo_disorder diseases +MONDO:0037398 orphanet_rare diseases +MONDO:0037398 rare diseases +MONDO:0037736 otar diseases +MONDO:0037737 gard_rare diseases +MONDO:0037737 otar diseases +MONDO:0037737 rare diseases +MONDO:0037744 gard_rare diseases +MONDO:0037744 rare diseases +MONDO:0037745 otar diseases +MONDO:0037748 otar diseases +MONDO:0037792 otar diseases +MONDO:0037821 otar diseases +MONDO:0037829 otar diseases +MONDO:0037847 otar diseases +MONDO:0037858 clingen diseases +MONDO:0037858 gard_rare diseases +MONDO:0037858 otar diseases +MONDO:0037858 rare diseases +MONDO:0037871 otar diseases +MONDO:0037872 otar diseases +MONDO:0037938 gard_rare diseases +MONDO:0037938 rare diseases +MONDO:0037939 otar diseases +MONDO:0040500 gard_rare diseases +MONDO:0040500 nord_rare diseases +MONDO:0040500 otar diseases +MONDO:0040500 rare diseases +MONDO:0040501 gard_rare diseases +MONDO:0040501 rare diseases +MONDO:0040502 gard_rare diseases +MONDO:0040502 nord_rare diseases +MONDO:0040502 rare diseases +MONDO:0040503 gard_rare diseases +MONDO:0040503 nord_rare diseases +MONDO:0040503 rare diseases +MONDO:0040566 gard_rare diseases +MONDO:0040566 otar diseases +MONDO:0040566 rare diseases +MONDO:0040653 gard_rare diseases +MONDO:0040653 otar diseases +MONDO:0040653 rare diseases +MONDO:0040654 gard_rare diseases +MONDO:0040654 rare diseases +MONDO:0040671 inferred_rare diseases +MONDO:0040671 rare diseases +MONDO:0040673 gard_rare diseases +MONDO:0040673 rare diseases +MONDO:0040675 otar diseases +MONDO:0040677 otar diseases +MONDO:0040678 otar diseases +MONDO:0040679 gard_rare diseases +MONDO:0040679 otar diseases +MONDO:0040679 rare diseases +MONDO:0040700 gard_rare diseases +MONDO:0040700 rare diseases +MONDO:0040753 gard_rare diseases +MONDO:0040753 rare diseases +MONDO:0040925 gard_rare diseases +MONDO:0040925 nord_rare diseases +MONDO:0040925 rare diseases +MONDO:0040998 otar diseases +MONDO:0041052 inferred_rare diseases +MONDO:0041052 otar diseases +MONDO:0041052 rare diseases +MONDO:0041086 otar diseases +MONDO:0041093 gard_rare diseases +MONDO:0041093 rare diseases +MONDO:0041167 gard_rare diseases +MONDO:0041167 rare diseases +MONDO:0041182 gard_rare diseases +MONDO:0041182 otar diseases +MONDO:0041182 rare diseases +MONDO:0041186 gard_rare diseases +MONDO:0041186 ordo_disorder diseases +MONDO:0041186 orphanet_rare diseases +MONDO:0041186 rare diseases +MONDO:0041259 gard_rare diseases +MONDO:0041259 rare diseases +MONDO:0041261 otar diseases +MONDO:0041447 otar diseases +MONDO:0041751 gard_rare diseases +MONDO:0041751 rare diseases +MONDO:0041752 gard_rare diseases +MONDO:0041752 rare diseases +MONDO:0041755 gard_rare diseases +MONDO:0041755 nord_rare diseases +MONDO:0041755 rare diseases +MONDO:0041806 gard_rare diseases +MONDO:0041806 rare diseases +MONDO:0041825 gard_rare diseases +MONDO:0041825 otar diseases +MONDO:0041825 rare diseases +MONDO:0041996 gard_rare diseases +MONDO:0041996 rare diseases +MONDO:0042233 otar diseases +MONDO:0042370 otar diseases +MONDO:0042433 gard_rare diseases +MONDO:0042433 rare diseases +MONDO:0042452 gard_rare diseases +MONDO:0042452 rare diseases +MONDO:0042458 gard_rare diseases +MONDO:0042458 rare diseases +MONDO:0042484 gard_rare diseases +MONDO:0042484 nord_rare diseases +MONDO:0042484 rare diseases +MONDO:0042485 otar diseases +MONDO:0042486 gard_rare diseases +MONDO:0042486 nord_rare diseases +MONDO:0042486 predisposition diseases +MONDO:0042486 rare diseases +MONDO:0042487 otar diseases +MONDO:0042488 otar diseases +MONDO:0042490 gard_rare diseases +MONDO:0042490 nord_rare diseases +MONDO:0042490 otar diseases +MONDO:0042490 rare diseases +MONDO:0042491 gard_rare diseases +MONDO:0042491 rare diseases +MONDO:0042493 gard_rare diseases +MONDO:0042493 otar diseases +MONDO:0042493 rare diseases +MONDO:0042494 gard_rare diseases +MONDO:0042494 nord_rare diseases +MONDO:0042494 rare diseases +MONDO:0042499 gard_rare diseases +MONDO:0042499 nord_rare diseases +MONDO:0042499 rare diseases +MONDO:0042724 obsoletion_candidate diseases +MONDO:0042727 gard_rare diseases +MONDO:0042727 nord_rare diseases +MONDO:0042727 ordo_subtype_of_a_disorder diseases +MONDO:0042727 rare diseases +MONDO:0042961 gard_rare diseases +MONDO:0042961 rare diseases +MONDO:0042962 gard_rare diseases +MONDO:0042962 nord_rare diseases +MONDO:0042962 rare diseases +MONDO:0042963 gard_rare diseases +MONDO:0042963 nord_rare diseases +MONDO:0042963 rare diseases +MONDO:0042964 gard_rare diseases +MONDO:0042964 rare diseases +MONDO:0042965 gard_rare diseases +MONDO:0042965 obsoletion_candidate diseases +MONDO:0042965 rare diseases +MONDO:0042968 gard_rare diseases +MONDO:0042968 rare diseases +MONDO:0042969 gard_rare diseases +MONDO:0042969 rare diseases +MONDO:0042971 gard_rare diseases +MONDO:0042971 rare diseases +MONDO:0042974 gard_rare diseases +MONDO:0042974 nord_rare diseases +MONDO:0042974 rare diseases +MONDO:0042975 gard_rare diseases +MONDO:0042975 rare diseases +MONDO:0042976 otar diseases +MONDO:0042977 gard_rare diseases +MONDO:0042977 nord_rare diseases +MONDO:0042977 rare diseases +MONDO:0042979 gard_rare diseases +MONDO:0042979 otar diseases +MONDO:0042979 rare diseases +MONDO:0042980 gard_rare diseases +MONDO:0042980 rare diseases +MONDO:0042981 gard_rare diseases +MONDO:0042981 nord_rare diseases +MONDO:0042981 otar diseases +MONDO:0042981 rare diseases +MONDO:0042982 clingen diseases +MONDO:0042982 otar diseases +MONDO:0042982 predisposition diseases +MONDO:0042983 otar diseases +MONDO:0043003 otar diseases +MONDO:0043004 gard_rare diseases +MONDO:0043004 rare diseases +MONDO:0043009 disease_grouping diseases +MONDO:0043009 gard_rare diseases +MONDO:0043009 ordo_group_of_disorders diseases +MONDO:0043009 rare diseases +MONDO:0043069 gard_rare diseases +MONDO:0043069 rare diseases +MONDO:0043075 gard_rare diseases +MONDO:0043075 rare diseases +MONDO:0043077 gard_rare diseases +MONDO:0043077 rare diseases +MONDO:0043083 gard_rare diseases +MONDO:0043083 rare diseases +MONDO:0043085 gard_rare diseases +MONDO:0043085 rare diseases +MONDO:0043089 gard_rare diseases +MONDO:0043089 nord_rare diseases +MONDO:0043089 rare diseases +MONDO:0043094 gard_rare diseases +MONDO:0043094 rare diseases +MONDO:0043096 gard_rare diseases +MONDO:0043096 rare diseases +MONDO:0043099 gard_rare diseases +MONDO:0043099 nord_rare diseases +MONDO:0043099 rare diseases +MONDO:0043103 gard_rare diseases +MONDO:0043103 nord_rare diseases +MONDO:0043103 rare diseases +MONDO:0043106 gard_rare diseases +MONDO:0043106 nord_rare diseases +MONDO:0043106 rare diseases +MONDO:0043108 gard_rare diseases +MONDO:0043108 nord_rare diseases +MONDO:0043108 rare diseases +MONDO:0043110 gard_rare diseases +MONDO:0043110 nord_rare diseases +MONDO:0043110 rare diseases +MONDO:0043116 gard_rare diseases +MONDO:0043116 rare diseases +MONDO:0043120 gard_rare diseases +MONDO:0043120 rare diseases +MONDO:0043123 gard_rare diseases +MONDO:0043123 rare diseases +MONDO:0043127 gard_rare diseases +MONDO:0043127 nord_rare diseases +MONDO:0043127 rare diseases +MONDO:0043131 gard_rare diseases +MONDO:0043131 rare diseases +MONDO:0043133 gard_rare diseases +MONDO:0043133 rare diseases +MONDO:0043137 gard_rare diseases +MONDO:0043137 nord_rare diseases +MONDO:0043137 rare diseases +MONDO:0043139 gard_rare diseases +MONDO:0043139 rare diseases +MONDO:0043141 gard_rare diseases +MONDO:0043141 nord_rare diseases +MONDO:0043141 rare diseases +MONDO:0043143 gard_rare diseases +MONDO:0043143 ordo_disorder diseases +MONDO:0043143 ordo_malformation_syndrome diseases +MONDO:0043143 orphanet_rare diseases +MONDO:0043143 rare diseases +MONDO:0043162 gard_rare diseases +MONDO:0043162 rare diseases +MONDO:0043164 gard_rare diseases +MONDO:0043164 ordo_disorder diseases +MONDO:0043164 orphanet_rare diseases +MONDO:0043164 rare diseases +MONDO:0043168 gard_rare diseases +MONDO:0043168 nord_rare diseases +MONDO:0043168 rare diseases +MONDO:0043176 gard_rare diseases +MONDO:0043176 rare diseases +MONDO:0043191 gard_rare diseases +MONDO:0043191 rare diseases +MONDO:0043207 gard_rare diseases +MONDO:0043207 nord_rare diseases +MONDO:0043207 rare diseases +MONDO:0043209 gard_rare diseases +MONDO:0043209 otar diseases +MONDO:0043209 rare diseases +MONDO:0043218 otar diseases +MONDO:0043219 gard_rare diseases +MONDO:0043219 nord_rare diseases +MONDO:0043219 rare diseases +MONDO:0043224 otar diseases +MONDO:0043226 gard_rare diseases +MONDO:0043226 rare diseases +MONDO:0043230 otar diseases +MONDO:0043233 otar diseases +MONDO:0043237 otar diseases +MONDO:0043243 otar diseases +MONDO:0043257 gard_rare diseases +MONDO:0043257 ordo_disorder diseases +MONDO:0043257 orphanet_rare diseases +MONDO:0043257 rare diseases +MONDO:0043267 gard_rare diseases +MONDO:0043267 nord_rare diseases +MONDO:0043267 rare diseases +MONDO:0043277 gard_rare diseases +MONDO:0043277 nord_rare diseases +MONDO:0043277 rare diseases +MONDO:0043283 gard_rare diseases +MONDO:0043283 rare diseases +MONDO:0043294 gard_rare diseases +MONDO:0043294 rare diseases +MONDO:0043317 gard_rare diseases +MONDO:0043317 ordo_subtype_of_a_disorder diseases +MONDO:0043317 rare diseases +MONDO:0043320 gard_rare diseases +MONDO:0043320 rare diseases +MONDO:0043330 gard_rare diseases +MONDO:0043330 nord_rare diseases +MONDO:0043330 ordo_clinical_syndrome diseases +MONDO:0043330 ordo_disorder diseases +MONDO:0043330 orphanet_rare diseases +MONDO:0043330 rare diseases +MONDO:0043346 gard_rare diseases +MONDO:0043346 rare diseases +MONDO:0043358 gard_rare diseases +MONDO:0043358 rare diseases +MONDO:0043364 gard_rare diseases +MONDO:0043364 nord_rare diseases +MONDO:0043364 otar diseases +MONDO:0043364 rare diseases +MONDO:0043373 gard_rare diseases +MONDO:0043373 nord_rare diseases +MONDO:0043373 ordo_disorder diseases +MONDO:0043373 orphanet_rare diseases +MONDO:0043373 rare diseases +MONDO:0043424 otar diseases +MONDO:0043452 gard_rare diseases +MONDO:0043452 otar diseases +MONDO:0043452 rare diseases +MONDO:0043455 gard_rare diseases +MONDO:0043455 rare diseases +MONDO:0043459 disease_grouping diseases +MONDO:0043459 gard_rare diseases +MONDO:0043459 ordo_group_of_disorders diseases +MONDO:0043459 otar diseases +MONDO:0043459 rare diseases +MONDO:0043472 gard_rare diseases +MONDO:0043472 nord_rare diseases +MONDO:0043472 rare diseases +MONDO:0043494 gard_rare diseases +MONDO:0043494 otar diseases +MONDO:0043494 rare diseases +MONDO:0043510 otar diseases +MONDO:0043537 inferred_rare diseases +MONDO:0043537 rare diseases +MONDO:0043541 otar diseases +MONDO:0043543 harrisons_view diseases +MONDO:0043544 otar diseases +MONDO:0043576 gard_rare diseases +MONDO:0043576 rare diseases +MONDO:0043579 otar diseases +MONDO:0043678 gard_rare diseases +MONDO:0043678 rare diseases +MONDO:0043693 otar diseases +MONDO:0043735 gard_rare diseases +MONDO:0043735 rare diseases +MONDO:0043765 otar diseases +MONDO:0043768 gard_rare diseases +MONDO:0043768 otar diseases +MONDO:0043768 rare diseases +MONDO:0043771 gard_rare diseases +MONDO:0043771 otar diseases +MONDO:0043771 rare diseases +MONDO:0043775 gard_rare diseases +MONDO:0043775 rare diseases +MONDO:0043797 gard_rare diseases +MONDO:0043797 ordo_disorder diseases +MONDO:0043797 orphanet_rare diseases +MONDO:0043797 rare diseases +MONDO:0043836 gard_rare diseases +MONDO:0043836 rare diseases +MONDO:0043839 otar diseases +MONDO:0043862 otar diseases +MONDO:0043875 gard_rare diseases +MONDO:0043875 nord_rare diseases +MONDO:0043875 rare diseases +MONDO:0043878 gard_rare diseases +MONDO:0043878 otar diseases +MONDO:0043878 rare diseases +MONDO:0043904 gard_rare diseases +MONDO:0043904 rare diseases +MONDO:0043905 otar diseases +MONDO:0043919 gard_rare diseases +MONDO:0043919 rare diseases +MONDO:0043959 otar diseases +MONDO:0043982 gard_rare diseases +MONDO:0043982 rare diseases +MONDO:0043985 gard_rare diseases +MONDO:0043985 rare diseases +MONDO:0044001 otar diseases +MONDO:0044013 otar diseases +MONDO:0044014 otar diseases +MONDO:0044037 gard_rare diseases +MONDO:0044037 rare diseases +MONDO:0044067 gard_rare diseases +MONDO:0044067 ordo_disorder diseases +MONDO:0044067 orphanet_rare diseases +MONDO:0044067 rare diseases +MONDO:0044070 gard_rare diseases +MONDO:0044070 rare diseases +MONDO:0044113 gard_rare diseases +MONDO:0044113 rare diseases +MONDO:0044137 otar diseases +MONDO:0044138 gard_rare diseases +MONDO:0044138 rare diseases +MONDO:0044200 disease_grouping diseases +MONDO:0044200 gard_rare diseases +MONDO:0044200 ordo_group_of_disorders diseases +MONDO:0044200 otar diseases +MONDO:0044200 rare diseases +MONDO:0044201 disease_grouping diseases +MONDO:0044201 gard_rare diseases +MONDO:0044201 obsoletion_candidate diseases +MONDO:0044201 ordo_group_of_disorders diseases +MONDO:0044201 otar diseases +MONDO:0044201 rare diseases +MONDO:0044202 gard_rare diseases +MONDO:0044202 nord_rare diseases +MONDO:0044202 ordo_disorder diseases +MONDO:0044202 orphanet_rare diseases +MONDO:0044202 otar diseases +MONDO:0044202 rare diseases +MONDO:0044203 otar diseases +MONDO:0044204 gard_rare diseases +MONDO:0044204 nord_rare diseases +MONDO:0044204 rare diseases +MONDO:0044205 gard_rare diseases +MONDO:0044205 nord_rare diseases +MONDO:0044205 rare diseases +MONDO:0044206 gard_rare diseases +MONDO:0044206 nord_rare diseases +MONDO:0044206 otar diseases +MONDO:0044206 rare diseases +MONDO:0044207 gard_rare diseases +MONDO:0044207 nord_rare diseases +MONDO:0044207 rare diseases +MONDO:0044208 gard_rare diseases +MONDO:0044208 nord_rare diseases +MONDO:0044208 rare diseases +MONDO:0044209 gard_rare diseases +MONDO:0044209 nord_rare diseases +MONDO:0044209 rare diseases +MONDO:0044210 gard_rare diseases +MONDO:0044210 rare diseases +MONDO:0044211 otar diseases +MONDO:0044299 gard_rare diseases +MONDO:0044299 nord_rare diseases +MONDO:0044299 rare diseases +MONDO:0044300 gard_rare diseases +MONDO:0044300 ordo_subtype_of_a_disorder diseases +MONDO:0044300 rare diseases +MONDO:0044302 gard_rare diseases +MONDO:0044302 ordo_disorder diseases +MONDO:0044302 orphanet_rare diseases +MONDO:0044302 otar diseases +MONDO:0044302 rare diseases +MONDO:0044303 otar diseases +MONDO:0044304 clingen diseases +MONDO:0044304 gard_rare diseases +MONDO:0044304 nord_rare diseases +MONDO:0044304 ordo_disorder diseases +MONDO:0044304 orphanet_rare diseases +MONDO:0044304 otar diseases +MONDO:0044304 rare diseases +MONDO:0044305 gard_rare diseases +MONDO:0044305 nord_rare diseases +MONDO:0044305 rare diseases +MONDO:0044306 gard_rare diseases +MONDO:0044306 nord_rare diseases +MONDO:0044306 ordo_disorder diseases +MONDO:0044306 orphanet_rare diseases +MONDO:0044306 otar diseases +MONDO:0044306 rare diseases +MONDO:0044308 gard_rare diseases +MONDO:0044308 nord_rare diseases +MONDO:0044308 rare diseases +MONDO:0044309 gard_rare diseases +MONDO:0044309 nord_rare diseases +MONDO:0044309 rare diseases +MONDO:0044310 gard_rare diseases +MONDO:0044310 nord_rare diseases +MONDO:0044310 rare diseases +MONDO:0044312 gard_rare diseases +MONDO:0044312 nord_rare diseases +MONDO:0044312 otar diseases +MONDO:0044312 rare diseases +MONDO:0044313 gard_rare diseases +MONDO:0044313 nord_rare diseases +MONDO:0044313 rare diseases +MONDO:0044314 gard_rare diseases +MONDO:0044314 nord_rare diseases +MONDO:0044314 rare diseases +MONDO:0044316 clingen diseases +MONDO:0044316 otar diseases +MONDO:0044317 gard_rare diseases +MONDO:0044317 nord_rare diseases +MONDO:0044317 rare diseases +MONDO:0044318 gard_rare diseases +MONDO:0044318 nord_rare diseases +MONDO:0044318 ordo_disorder diseases +MONDO:0044318 orphanet_rare diseases +MONDO:0044318 otar diseases +MONDO:0044318 rare diseases +MONDO:0044319 gard_rare diseases +MONDO:0044319 nord_rare diseases +MONDO:0044319 ordo_disorder diseases +MONDO:0044319 ordo_malformation_syndrome diseases +MONDO:0044319 orphanet_rare diseases +MONDO:0044319 otar diseases +MONDO:0044319 rare diseases +MONDO:0044320 gard_rare diseases +MONDO:0044320 nord_rare diseases +MONDO:0044320 rare diseases +MONDO:0044321 gard_rare diseases +MONDO:0044321 rare diseases +MONDO:0044322 otar diseases +MONDO:0044323 gard_rare diseases +MONDO:0044323 nord_rare diseases +MONDO:0044323 ordo_disorder diseases +MONDO:0044323 orphanet_rare diseases +MONDO:0044323 rare diseases +MONDO:0044324 gard_rare diseases +MONDO:0044324 nord_rare diseases +MONDO:0044324 otar diseases +MONDO:0044324 rare diseases +MONDO:0044325 gard_rare diseases +MONDO:0044325 nord_rare diseases +MONDO:0044325 otar diseases +MONDO:0044325 rare diseases +MONDO:0044326 gard_rare diseases +MONDO:0044326 nord_rare diseases +MONDO:0044326 otar diseases +MONDO:0044326 rare diseases +MONDO:0044327 gard_rare diseases +MONDO:0044327 otar diseases +MONDO:0044327 rare diseases +MONDO:0044328 gard_rare diseases +MONDO:0044328 nord_rare diseases +MONDO:0044328 rare diseases +MONDO:0044329 gard_rare diseases +MONDO:0044329 nord_rare diseases +MONDO:0044329 rare diseases +MONDO:0044330 gard_rare diseases +MONDO:0044330 nord_rare diseases +MONDO:0044330 rare diseases +MONDO:0044332 gard_rare diseases +MONDO:0044332 nord_rare diseases +MONDO:0044332 ordo_disorder diseases +MONDO:0044332 orphanet_rare diseases +MONDO:0044332 rare diseases +MONDO:0044334 otar diseases +MONDO:0044335 otar diseases +MONDO:0044337 gard_rare diseases +MONDO:0044337 rare diseases +MONDO:0044343 otar diseases +MONDO:0044344 gard_rare diseases +MONDO:0044344 rare diseases +MONDO:0044345 gard_rare diseases +MONDO:0044345 nord_rare diseases +MONDO:0044345 rare diseases +MONDO:0044347 gard_rare diseases +MONDO:0044347 otar diseases +MONDO:0044347 rare diseases +MONDO:0044348 gard_rare diseases +MONDO:0044348 otar diseases +MONDO:0044348 rare diseases +MONDO:0044349 gard_rare diseases +MONDO:0044349 rare diseases +MONDO:0044350 gard_rare diseases +MONDO:0044350 nord_rare diseases +MONDO:0044350 rare diseases +MONDO:0044351 gard_rare diseases +MONDO:0044351 rare diseases +MONDO:0044355 gard_rare diseases +MONDO:0044355 nord_rare diseases +MONDO:0044355 ordo_disorder diseases +MONDO:0044355 orphanet_rare diseases +MONDO:0044355 rare diseases +MONDO:0044406 gard_rare diseases +MONDO:0044406 nord_rare diseases +MONDO:0044406 ordo_disorder diseases +MONDO:0044406 ordo_malformation_syndrome diseases +MONDO:0044406 orphanet_rare diseases +MONDO:0044406 rare diseases +MONDO:0044617 gard_rare diseases +MONDO:0044617 nord_rare diseases +MONDO:0044617 ordo_disorder diseases +MONDO:0044617 ordo_malformation_syndrome diseases +MONDO:0044617 orphanet_rare diseases +MONDO:0044617 rare diseases +MONDO:0044619 nord_rare diseases +MONDO:0044619 ordo_disorder diseases +MONDO:0044619 ordo_malformation_syndrome diseases +MONDO:0044619 orphanet_rare diseases +MONDO:0044619 rare diseases +MONDO:0044621 gard_rare diseases +MONDO:0044621 nord_rare diseases +MONDO:0044621 ordo_disorder diseases +MONDO:0044621 ordo_malformation_syndrome diseases +MONDO:0044621 orphanet_rare diseases +MONDO:0044621 rare diseases +MONDO:0044622 gard_rare diseases +MONDO:0044622 nord_rare diseases +MONDO:0044622 ordo_disorder diseases +MONDO:0044622 orphanet_rare diseases +MONDO:0044622 rare diseases +MONDO:0044624 gard_rare diseases +MONDO:0044624 nord_rare diseases +MONDO:0044624 ordo_disorder diseases +MONDO:0044624 orphanet_rare diseases +MONDO:0044624 rare diseases +MONDO:0044625 gard_rare diseases +MONDO:0044625 nord_rare diseases +MONDO:0044625 ordo_disorder diseases +MONDO:0044625 orphanet_rare diseases +MONDO:0044625 rare diseases +MONDO:0044626 gard_rare diseases +MONDO:0044626 nord_rare diseases +MONDO:0044626 ordo_disorder diseases +MONDO:0044626 orphanet_rare diseases +MONDO:0044626 otar diseases +MONDO:0044626 rare diseases +MONDO:0044627 gard_rare diseases +MONDO:0044627 nord_rare diseases +MONDO:0044627 ordo_disorder diseases +MONDO:0044627 orphanet_rare diseases +MONDO:0044627 rare diseases +MONDO:0044628 gard_rare diseases +MONDO:0044628 nord_rare diseases +MONDO:0044628 ordo_disorder diseases +MONDO:0044628 ordo_malformation_syndrome diseases +MONDO:0044628 orphanet_rare diseases +MONDO:0044628 rare diseases +MONDO:0044629 gard_rare diseases +MONDO:0044629 nord_rare diseases +MONDO:0044629 ordo_disorder diseases +MONDO:0044629 ordo_malformation_syndrome diseases +MONDO:0044629 orphanet_rare diseases +MONDO:0044629 rare diseases +MONDO:0044632 gard_rare diseases +MONDO:0044632 nord_rare diseases +MONDO:0044632 ordo_disorder diseases +MONDO:0044632 ordo_morphological_anomaly diseases +MONDO:0044632 orphanet_rare diseases +MONDO:0044632 rare diseases +MONDO:0044633 gard_rare diseases +MONDO:0044633 nord_rare diseases +MONDO:0044633 ordo_disorder diseases +MONDO:0044633 orphanet_rare diseases +MONDO:0044633 rare diseases +MONDO:0044634 gard_rare diseases +MONDO:0044634 nord_rare diseases +MONDO:0044634 ordo_disorder diseases +MONDO:0044634 ordo_malformation_syndrome diseases +MONDO:0044634 orphanet_rare diseases +MONDO:0044634 rare diseases +MONDO:0044635 clingen diseases +MONDO:0044635 gard_rare diseases +MONDO:0044635 nord_rare diseases +MONDO:0044635 ordo_disorder diseases +MONDO:0044635 orphanet_rare diseases +MONDO:0044635 otar diseases +MONDO:0044635 rare diseases +MONDO:0044637 gard_rare diseases +MONDO:0044637 nord_rare diseases +MONDO:0044637 ordo_disorder diseases +MONDO:0044637 orphanet_rare diseases +MONDO:0044637 rare diseases +MONDO:0044638 gard_rare diseases +MONDO:0044638 nord_rare diseases +MONDO:0044638 ordo_disorder diseases +MONDO:0044638 orphanet_rare diseases +MONDO:0044638 otar diseases +MONDO:0044638 rare diseases +MONDO:0044640 gard_rare diseases +MONDO:0044640 nord_rare diseases +MONDO:0044640 ordo_disorder diseases +MONDO:0044640 orphanet_rare diseases +MONDO:0044640 rare diseases +MONDO:0044641 gard_rare diseases +MONDO:0044641 nord_rare diseases +MONDO:0044641 ordo_disorder diseases +MONDO:0044641 ordo_malformation_syndrome diseases +MONDO:0044641 orphanet_rare diseases +MONDO:0044641 rare diseases +MONDO:0044642 gard_rare diseases +MONDO:0044642 nord_rare diseases +MONDO:0044642 ordo_disorder diseases +MONDO:0044642 orphanet_rare diseases +MONDO:0044642 rare diseases +MONDO:0044643 gard_rare diseases +MONDO:0044643 nord_rare diseases +MONDO:0044643 ordo_disorder diseases +MONDO:0044643 ordo_malformation_syndrome diseases +MONDO:0044643 orphanet_rare diseases +MONDO:0044643 rare diseases +MONDO:0044644 gard_rare diseases +MONDO:0044644 nord_rare diseases +MONDO:0044644 ordo_disorder diseases +MONDO:0044644 ordo_morphological_anomaly diseases +MONDO:0044644 orphanet_rare diseases +MONDO:0044644 rare diseases +MONDO:0044645 gard_rare diseases +MONDO:0044645 nord_rare diseases +MONDO:0044645 ordo_disorder diseases +MONDO:0044645 orphanet_rare diseases +MONDO:0044645 rare diseases +MONDO:0044646 gard_rare diseases +MONDO:0044646 nord_rare diseases +MONDO:0044646 ordo_disorder diseases +MONDO:0044646 ordo_malformation_syndrome diseases +MONDO:0044646 orphanet_rare diseases +MONDO:0044646 otar diseases +MONDO:0044646 rare diseases +MONDO:0044647 gard_rare diseases +MONDO:0044647 nord_rare diseases +MONDO:0044647 ordo_disorder diseases +MONDO:0044647 orphanet_rare diseases +MONDO:0044647 rare diseases +MONDO:0044648 gard_rare diseases +MONDO:0044648 nord_rare diseases +MONDO:0044648 ordo_disorder diseases +MONDO:0044648 orphanet_rare diseases +MONDO:0044648 rare diseases +MONDO:0044649 gard_rare diseases +MONDO:0044649 nord_rare diseases +MONDO:0044649 ordo_disorder diseases +MONDO:0044649 ordo_malformation_syndrome diseases +MONDO:0044649 orphanet_rare diseases +MONDO:0044649 rare diseases +MONDO:0044651 gard_rare diseases +MONDO:0044651 nord_rare diseases +MONDO:0044651 ordo_disorder diseases +MONDO:0044651 orphanet_rare diseases +MONDO:0044651 rare diseases +MONDO:0044656 gard_rare diseases +MONDO:0044656 nord_rare diseases +MONDO:0044656 ordo_disorder diseases +MONDO:0044656 orphanet_rare diseases +MONDO:0044656 rare diseases +MONDO:0044657 gard_rare diseases +MONDO:0044657 nord_rare diseases +MONDO:0044657 ordo_disorder diseases +MONDO:0044657 orphanet_rare diseases +MONDO:0044657 rare diseases +MONDO:0044660 gard_rare diseases +MONDO:0044660 nord_rare diseases +MONDO:0044660 ordo_disorder diseases +MONDO:0044660 orphanet_rare diseases +MONDO:0044660 otar diseases +MONDO:0044660 rare diseases +MONDO:0044663 gard_rare diseases +MONDO:0044663 nord_rare diseases +MONDO:0044663 ordo_disorder diseases +MONDO:0044663 orphanet_rare diseases +MONDO:0044663 rare diseases +MONDO:0044675 gard_rare diseases +MONDO:0044675 nord_rare diseases +MONDO:0044675 ordo_disorder diseases +MONDO:0044675 ordo_malformation_syndrome diseases +MONDO:0044675 orphanet_rare diseases +MONDO:0044675 rare diseases +MONDO:0044682 gard_rare diseases +MONDO:0044682 nord_rare diseases +MONDO:0044682 ordo_disorder diseases +MONDO:0044682 orphanet_rare diseases +MONDO:0044682 rare diseases +MONDO:0044685 disease_grouping diseases +MONDO:0044685 gard_rare diseases +MONDO:0044685 ordo_group_of_disorders diseases +MONDO:0044685 rare diseases +MONDO:0044687 gard_rare diseases +MONDO:0044687 nord_rare diseases +MONDO:0044687 ordo_disorder diseases +MONDO:0044687 orphanet_rare diseases +MONDO:0044687 rare diseases +MONDO:0044688 gard_rare diseases +MONDO:0044688 nord_rare diseases +MONDO:0044688 ordo_disorder diseases +MONDO:0044688 orphanet_rare diseases +MONDO:0044688 rare diseases +MONDO:0044689 gard_rare diseases +MONDO:0044689 ordo_disorder diseases +MONDO:0044689 orphanet_rare diseases +MONDO:0044689 rare diseases +MONDO:0044690 gard_rare diseases +MONDO:0044690 ordo_disorder diseases +MONDO:0044690 orphanet_rare diseases +MONDO:0044690 rare diseases +MONDO:0044696 gard_rare diseases +MONDO:0044696 nord_rare diseases +MONDO:0044696 ordo_disorder diseases +MONDO:0044696 ordo_malformation_syndrome diseases +MONDO:0044696 orphanet_rare diseases +MONDO:0044696 otar diseases +MONDO:0044696 rare diseases +MONDO:0044699 clingen diseases +MONDO:0044699 gard_rare diseases +MONDO:0044699 nord_rare diseases +MONDO:0044699 ordo_disorder diseases +MONDO:0044699 ordo_malformation_syndrome diseases +MONDO:0044699 orphanet_rare diseases +MONDO:0044699 rare diseases +MONDO:0044700 gard_rare diseases +MONDO:0044700 nord_rare diseases +MONDO:0044700 ordo_etiological_subtype diseases +MONDO:0044700 ordo_subtype_of_a_disorder diseases +MONDO:0044700 rare diseases +MONDO:0044701 gard_rare diseases +MONDO:0044701 nord_rare diseases +MONDO:0044701 ordo_disorder diseases +MONDO:0044701 orphanet_rare diseases +MONDO:0044701 rare diseases +MONDO:0044702 gard_rare diseases +MONDO:0044702 nord_rare diseases +MONDO:0044702 ordo_disorder diseases +MONDO:0044702 ordo_malformation_syndrome diseases +MONDO:0044702 orphanet_rare diseases +MONDO:0044702 rare diseases +MONDO:0044704 gard_rare diseases +MONDO:0044704 nord_rare diseases +MONDO:0044704 ordo_disorder diseases +MONDO:0044704 orphanet_rare diseases +MONDO:0044704 otar diseases +MONDO:0044704 rare diseases +MONDO:0044705 gard_rare diseases +MONDO:0044705 nord_rare diseases +MONDO:0044705 ordo_disorder diseases +MONDO:0044705 orphanet_rare diseases +MONDO:0044705 otar diseases +MONDO:0044705 rare diseases +MONDO:0044709 gard_rare diseases +MONDO:0044709 ordo_disorder diseases +MONDO:0044709 ordo_morphological_anomaly diseases +MONDO:0044709 orphanet_rare diseases +MONDO:0044709 rare diseases +MONDO:0044710 disease_grouping diseases +MONDO:0044710 gard_rare diseases +MONDO:0044710 ordo_group_of_disorders diseases +MONDO:0044710 otar diseases +MONDO:0044710 rare diseases +MONDO:0044714 gard_rare diseases +MONDO:0044714 nord_rare diseases +MONDO:0044714 ordo_disorder diseases +MONDO:0044714 orphanet_rare diseases +MONDO:0044714 otar diseases +MONDO:0044714 rare diseases +MONDO:0044715 gard_rare diseases +MONDO:0044715 nord_rare diseases +MONDO:0044715 ordo_disorder diseases +MONDO:0044715 ordo_malformation_syndrome diseases +MONDO:0044715 orphanet_rare diseases +MONDO:0044715 rare diseases +MONDO:0044717 gard_rare diseases +MONDO:0044717 nord_rare diseases +MONDO:0044717 ordo_disorder diseases +MONDO:0044717 ordo_malformation_syndrome diseases +MONDO:0044717 orphanet_rare diseases +MONDO:0044717 rare diseases +MONDO:0044718 gard_rare diseases +MONDO:0044718 nord_rare diseases +MONDO:0044718 ordo_disorder diseases +MONDO:0044718 orphanet_rare diseases +MONDO:0044718 otar diseases +MONDO:0044718 rare diseases +MONDO:0044719 gard_rare diseases +MONDO:0044719 nord_rare diseases +MONDO:0044719 ordo_disorder diseases +MONDO:0044719 orphanet_rare diseases +MONDO:0044719 rare diseases +MONDO:0044720 gard_rare diseases +MONDO:0044720 nord_rare diseases +MONDO:0044720 ordo_disorder diseases +MONDO:0044720 orphanet_rare diseases +MONDO:0044720 otar diseases +MONDO:0044720 rare diseases +MONDO:0044721 clingen diseases +MONDO:0044721 gard_rare diseases +MONDO:0044721 nord_rare diseases +MONDO:0044721 ordo_disorder diseases +MONDO:0044721 orphanet_rare diseases +MONDO:0044721 rare diseases +MONDO:0044723 clingen diseases +MONDO:0044723 gard_rare diseases +MONDO:0044723 ordo_disorder diseases +MONDO:0044723 orphanet_rare diseases +MONDO:0044723 rare diseases +MONDO:0044724 clingen diseases +MONDO:0044724 gard_rare diseases +MONDO:0044724 nord_rare diseases +MONDO:0044724 ordo_disorder diseases +MONDO:0044724 orphanet_rare diseases +MONDO:0044724 otar diseases +MONDO:0044724 rare diseases +MONDO:0044725 gard_rare diseases +MONDO:0044725 nord_rare diseases +MONDO:0044725 ordo_disorder diseases +MONDO:0044725 orphanet_rare diseases +MONDO:0044725 otar diseases +MONDO:0044725 rare diseases +MONDO:0044726 gard_rare diseases +MONDO:0044726 nord_rare diseases +MONDO:0044726 ordo_disorder diseases +MONDO:0044726 orphanet_rare diseases +MONDO:0044726 otar diseases +MONDO:0044726 rare diseases +MONDO:0044727 gard_rare diseases +MONDO:0044727 nord_rare diseases +MONDO:0044727 ordo_disorder diseases +MONDO:0044727 orphanet_rare diseases +MONDO:0044727 rare diseases +MONDO:0044737 gard_rare diseases +MONDO:0044737 nord_rare diseases +MONDO:0044737 ordo_disorder diseases +MONDO:0044737 orphanet_rare diseases +MONDO:0044737 rare diseases +MONDO:0044738 gard_rare diseases +MONDO:0044738 nord_rare diseases +MONDO:0044738 ordo_disorder diseases +MONDO:0044738 ordo_malformation_syndrome diseases +MONDO:0044738 orphanet_rare diseases +MONDO:0044738 otar diseases +MONDO:0044738 rare diseases +MONDO:0044739 gard_rare diseases +MONDO:0044739 nord_rare diseases +MONDO:0044739 ordo_subtype_of_a_disorder diseases +MONDO:0044739 rare diseases +MONDO:0044740 gard_rare diseases +MONDO:0044740 nord_rare diseases +MONDO:0044740 ordo_histopathological_subtype diseases +MONDO:0044740 ordo_subtype_of_a_disorder diseases +MONDO:0044740 otar diseases +MONDO:0044740 rare diseases +MONDO:0044742 gard_rare diseases +MONDO:0044742 nord_rare diseases +MONDO:0044742 ordo_disorder diseases +MONDO:0044742 orphanet_rare diseases +MONDO:0044742 rare diseases +MONDO:0044743 otar diseases +MONDO:0044744 gard_rare diseases +MONDO:0044744 otar diseases +MONDO:0044744 rare diseases +MONDO:0044745 otar diseases +MONDO:0044749 gard_rare diseases +MONDO:0044749 nord_rare diseases +MONDO:0044749 rare diseases +MONDO:0044750 otar diseases +MONDO:0044751 otar diseases +MONDO:0044764 inferred_rare diseases +MONDO:0044764 rare diseases +MONDO:0044765 otar diseases +MONDO:0044767 gard_rare diseases +MONDO:0044767 rare diseases +MONDO:0044768 gard_rare diseases +MONDO:0044768 rare diseases +MONDO:0044776 gard_rare diseases +MONDO:0044776 nord_rare diseases +MONDO:0044776 rare diseases +MONDO:0044777 gard_rare diseases +MONDO:0044777 nord_rare diseases +MONDO:0044777 rare diseases +MONDO:0044778 gard_rare diseases +MONDO:0044778 nord_rare diseases +MONDO:0044778 ordo_disorder diseases +MONDO:0044778 orphanet_rare diseases +MONDO:0044778 rare diseases +MONDO:0044782 otar diseases +MONDO:0044784 otar diseases +MONDO:0044785 otar diseases +MONDO:0044787 gard_rare diseases +MONDO:0044787 nord_rare diseases +MONDO:0044787 otar diseases +MONDO:0044787 rare diseases +MONDO:0044788 gard_rare diseases +MONDO:0044788 rare diseases +MONDO:0044791 gard_rare diseases +MONDO:0044791 ordo_disorder diseases +MONDO:0044791 orphanet_rare diseases +MONDO:0044791 otar diseases +MONDO:0044791 rare diseases +MONDO:0044792 gard_rare diseases +MONDO:0044792 nord_rare diseases +MONDO:0044792 ordo_disorder diseases +MONDO:0044792 orphanet_rare diseases +MONDO:0044792 otar diseases +MONDO:0044792 rare diseases +MONDO:0044793 otar diseases +MONDO:0044794 otar diseases +MONDO:0044807 disease_grouping diseases +MONDO:0044807 gard_rare diseases +MONDO:0044807 ordo_group_of_disorders diseases +MONDO:0044807 otar diseases +MONDO:0044807 rare diseases +MONDO:0044816 gard_rare diseases +MONDO:0044816 rare diseases +MONDO:0044871 gard_rare diseases +MONDO:0044871 nord_rare diseases +MONDO:0044871 rare diseases +MONDO:0044873 gard_rare diseases +MONDO:0044873 rare diseases +MONDO:0044874 gard_rare diseases +MONDO:0044874 nord_rare diseases +MONDO:0044874 rare diseases +MONDO:0044877 gard_rare diseases +MONDO:0044877 ordo_disorder diseases +MONDO:0044877 orphanet_rare diseases +MONDO:0044877 otar diseases +MONDO:0044877 rare diseases +MONDO:0044878 gard_rare diseases +MONDO:0044878 rare diseases +MONDO:0044881 gard_rare diseases +MONDO:0044881 otar diseases +MONDO:0044881 rare diseases +MONDO:0044884 gard_rare diseases +MONDO:0044884 nord_rare diseases +MONDO:0044884 rare diseases +MONDO:0044887 gard_rare diseases +MONDO:0044887 otar diseases +MONDO:0044887 rare diseases +MONDO:0044889 gard_rare diseases +MONDO:0044889 nord_rare diseases +MONDO:0044889 otar diseases +MONDO:0044889 rare diseases +MONDO:0044903 gard_rare diseases +MONDO:0044903 nord_rare diseases +MONDO:0044903 otar diseases +MONDO:0044903 rare diseases +MONDO:0044915 otar diseases +MONDO:0044916 gard_rare diseases +MONDO:0044916 otar diseases +MONDO:0044916 rare diseases +MONDO:0044917 gard_rare diseases +MONDO:0044917 nord_rare diseases +MONDO:0044917 otar diseases +MONDO:0044917 rare diseases +MONDO:0044919 otar diseases +MONDO:0044921 gard_rare diseases +MONDO:0044921 rare diseases +MONDO:0044923 gard_rare diseases +MONDO:0044923 nord_rare diseases +MONDO:0044923 rare diseases +MONDO:0044925 otar diseases +MONDO:0044926 otar diseases +MONDO:0044937 otar diseases +MONDO:0044956 gard_rare diseases +MONDO:0044956 rare diseases +MONDO:0044964 gard_rare diseases +MONDO:0044964 otar diseases +MONDO:0044964 rare diseases +MONDO:0044970 clingen diseases +MONDO:0044970 otar diseases +MONDO:0044970 rare_grouping diseases +MONDO:0044972 gard_rare diseases +MONDO:0044972 otar diseases +MONDO:0044972 rare diseases +MONDO:0044983 otar diseases +MONDO:0044991 otar diseases +MONDO:0044992 otar diseases +MONDO:0044993 otar diseases +MONDO:0045002 otar diseases +MONDO:0045008 gard_rare diseases +MONDO:0045008 otar diseases +MONDO:0045008 rare diseases +MONDO:0045010 gard_rare diseases +MONDO:0045010 rare diseases +MONDO:0045011 otar diseases +MONDO:0045012 otar diseases +MONDO:0045014 gard_rare diseases +MONDO:0045014 otar diseases +MONDO:0045014 rare diseases +MONDO:0045016 gard_rare diseases +MONDO:0045016 rare diseases +MONDO:0045017 gard_rare diseases +MONDO:0045017 otar diseases +MONDO:0045017 rare diseases +MONDO:0045018 otar diseases +MONDO:0045020 otar diseases +MONDO:0045022 otar diseases +MONDO:0045023 gard_rare diseases +MONDO:0045023 rare diseases +MONDO:0045024 harrisons_view diseases +MONDO:0045024 otar diseases +MONDO:0045024 rare_grouping diseases +MONDO:0045038 gard_rare diseases +MONDO:0045038 rare diseases +MONDO:0045039 gard_rare diseases +MONDO:0045039 rare diseases +MONDO:0045044 rare_grouping diseases +MONDO:0045045 gard_rare diseases +MONDO:0045045 rare diseases +MONDO:0045046 gard_rare diseases +MONDO:0045046 rare diseases +MONDO:0045047 gard_rare diseases +MONDO:0045047 nord_rare diseases +MONDO:0045047 rare diseases +MONDO:0045048 otar diseases +MONDO:0045050 otar diseases +MONDO:0045054 otar diseases +MONDO:0045056 gard_rare diseases +MONDO:0045056 otar diseases +MONDO:0045056 rare diseases +MONDO:0045057 otar diseases +MONDO:0045058 gard_rare diseases +MONDO:0045058 rare diseases +MONDO:0045063 gard_rare diseases +MONDO:0045063 otar diseases +MONDO:0045063 rare diseases +MONDO:0045068 gard_rare diseases +MONDO:0045068 otar diseases +MONDO:0045068 rare diseases +MONDO:0045069 otar diseases +MONDO:0045070 otar diseases +MONDO:0045071 gard_rare diseases +MONDO:0045071 rare diseases +MONDO:0049221 otar diseases +MONDO:0049222 gard_rare diseases +MONDO:0049222 nord_rare diseases +MONDO:0049222 rare diseases +MONDO:0049223 gard_rare diseases +MONDO:0049223 nord_rare diseases +MONDO:0049223 rare diseases +MONDO:0054549 gard_rare diseases +MONDO:0054549 nord_rare diseases +MONDO:0054549 rare diseases +MONDO:0054550 gard_rare diseases +MONDO:0054550 nord_rare diseases +MONDO:0054550 rare diseases +MONDO:0054551 gard_rare diseases +MONDO:0054551 nord_rare diseases +MONDO:0054551 rare diseases +MONDO:0054559 gard_rare diseases +MONDO:0054559 nord_rare diseases +MONDO:0054559 ordo_disorder diseases +MONDO:0054559 orphanet_rare diseases +MONDO:0054559 otar diseases +MONDO:0054559 rare diseases +MONDO:0054560 gard_rare diseases +MONDO:0054560 nord_rare diseases +MONDO:0054560 rare diseases +MONDO:0054561 gard_rare diseases +MONDO:0054561 nord_rare diseases +MONDO:0054561 rare diseases +MONDO:0054565 gard_rare diseases +MONDO:0054565 nord_rare diseases +MONDO:0054565 otar diseases +MONDO:0054565 rare diseases +MONDO:0054573 otar diseases +MONDO:0054577 clingen diseases +MONDO:0054577 gard_rare diseases +MONDO:0054577 nord_rare diseases +MONDO:0054577 rare diseases +MONDO:0054581 gard_rare diseases +MONDO:0054581 nord_rare diseases +MONDO:0054581 rare diseases +MONDO:0054582 gard_rare diseases +MONDO:0054582 nord_rare diseases +MONDO:0054582 rare diseases +MONDO:0054588 gard_rare diseases +MONDO:0054588 nord_rare diseases +MONDO:0054588 rare diseases +MONDO:0054591 otar diseases +MONDO:0054593 gard_rare diseases +MONDO:0054593 nord_rare diseases +MONDO:0054593 rare diseases +MONDO:0054601 gard_rare diseases +MONDO:0054601 nord_rare diseases +MONDO:0054601 rare diseases +MONDO:0054602 gard_rare diseases +MONDO:0054602 nord_rare diseases +MONDO:0054602 rare diseases +MONDO:0054615 clingen diseases +MONDO:0054615 gard_rare diseases +MONDO:0054615 rare diseases +MONDO:0054636 gard_rare diseases +MONDO:0054636 nord_rare diseases +MONDO:0054636 ordo_disorder diseases +MONDO:0054636 orphanet_rare diseases +MONDO:0054636 otar diseases +MONDO:0054636 rare diseases +MONDO:0054637 gard_rare diseases +MONDO:0054637 nord_rare diseases +MONDO:0054637 rare diseases +MONDO:0054654 gard_rare diseases +MONDO:0054654 rare diseases +MONDO:0054665 gard_rare diseases +MONDO:0054665 nord_rare diseases +MONDO:0054665 rare diseases +MONDO:0054666 gard_rare diseases +MONDO:0054666 nord_rare diseases +MONDO:0054666 rare diseases +MONDO:0054669 gard_rare diseases +MONDO:0054669 nord_rare diseases +MONDO:0054669 ordo_disorder diseases +MONDO:0054669 orphanet_rare diseases +MONDO:0054669 rare diseases +MONDO:0054677 gard_rare diseases +MONDO:0054677 rare diseases +MONDO:0054680 gard_rare diseases +MONDO:0054680 nord_rare diseases +MONDO:0054680 ordo_disorder diseases +MONDO:0054680 orphanet_rare diseases +MONDO:0054680 rare diseases +MONDO:0054691 clingen diseases +MONDO:0054691 gard_rare diseases +MONDO:0054691 nord_rare diseases +MONDO:0054691 otar diseases +MONDO:0054691 rare diseases +MONDO:0054695 clingen diseases +MONDO:0054695 gard_rare diseases +MONDO:0054695 otar diseases +MONDO:0054695 rare diseases +MONDO:0054696 clingen diseases +MONDO:0054697 clingen diseases +MONDO:0054698 gard_rare diseases +MONDO:0054698 nord_rare diseases +MONDO:0054698 rare diseases +MONDO:0054699 gard_rare diseases +MONDO:0054699 nord_rare diseases +MONDO:0054699 otar diseases +MONDO:0054699 rare diseases +MONDO:0054700 gard_rare diseases +MONDO:0054700 nord_rare diseases +MONDO:0054700 otar diseases +MONDO:0054700 rare diseases +MONDO:0054701 gard_rare diseases +MONDO:0054701 nord_rare diseases +MONDO:0054701 otar diseases +MONDO:0054701 rare diseases +MONDO:0054708 gard_rare diseases +MONDO:0054708 nord_rare diseases +MONDO:0054708 rare diseases +MONDO:0054716 gard_rare diseases +MONDO:0054716 nord_rare diseases +MONDO:0054716 rare diseases +MONDO:0054722 gard_rare diseases +MONDO:0054722 nord_rare diseases +MONDO:0054722 rare diseases +MONDO:0054723 clingen diseases +MONDO:0054723 gard_rare diseases +MONDO:0054723 rare diseases +MONDO:0054724 gard_rare diseases +MONDO:0054724 rare diseases +MONDO:0054726 gard_rare diseases +MONDO:0054726 otar diseases +MONDO:0054726 rare diseases +MONDO:0054727 gard_rare diseases +MONDO:0054727 otar diseases +MONDO:0054727 rare diseases +MONDO:0054728 otar diseases +MONDO:0054729 gard_rare diseases +MONDO:0054729 otar diseases +MONDO:0054729 rare diseases +MONDO:0054730 otar diseases +MONDO:0054731 clingen diseases +MONDO:0054731 gard_rare diseases +MONDO:0054731 rare diseases +MONDO:0054732 gard_rare diseases +MONDO:0054732 otar diseases +MONDO:0054732 rare diseases +MONDO:0054733 otar diseases +MONDO:0054736 gard_rare diseases +MONDO:0054736 nord_rare diseases +MONDO:0054736 rare diseases +MONDO:0054737 gard_rare diseases +MONDO:0054737 nord_rare diseases +MONDO:0054737 rare diseases +MONDO:0054738 gard_rare diseases +MONDO:0054738 nord_rare diseases +MONDO:0054738 rare diseases +MONDO:0054739 clingen diseases +MONDO:0054739 gard_rare diseases +MONDO:0054739 nord_rare diseases +MONDO:0054739 rare diseases +MONDO:0054740 gard_rare diseases +MONDO:0054740 nord_rare diseases +MONDO:0054740 rare diseases +MONDO:0054741 gard_rare diseases +MONDO:0054741 ordo_disorder diseases +MONDO:0054741 orphanet_rare diseases +MONDO:0054741 otar diseases +MONDO:0054741 rare diseases +MONDO:0054742 gard_rare diseases +MONDO:0054742 otar diseases +MONDO:0054742 rare diseases +MONDO:0054743 clingen diseases +MONDO:0054743 gard_rare diseases +MONDO:0054743 otar diseases +MONDO:0054743 rare diseases +MONDO:0054748 clingen diseases +MONDO:0054748 gard_rare diseases +MONDO:0054748 nord_rare diseases +MONDO:0054748 otar diseases +MONDO:0054748 rare diseases +MONDO:0054752 gard_rare diseases +MONDO:0054752 nord_rare diseases +MONDO:0054752 rare diseases +MONDO:0054761 gard_rare diseases +MONDO:0054761 nord_rare diseases +MONDO:0054761 rare diseases +MONDO:0054763 gard_rare diseases +MONDO:0054763 nord_rare diseases +MONDO:0054763 rare diseases +MONDO:0054764 gard_rare diseases +MONDO:0054764 nord_rare diseases +MONDO:0054764 otar diseases +MONDO:0054764 rare diseases +MONDO:0054765 gard_rare diseases +MONDO:0054765 rare diseases +MONDO:0054770 gard_rare diseases +MONDO:0054770 nord_rare diseases +MONDO:0054770 rare diseases +MONDO:0054771 gard_rare diseases +MONDO:0054771 nord_rare diseases +MONDO:0054771 rare diseases +MONDO:0054776 gard_rare diseases +MONDO:0054776 nord_rare diseases +MONDO:0054776 rare diseases +MONDO:0054780 gard_rare diseases +MONDO:0054780 nord_rare diseases +MONDO:0054780 rare diseases +MONDO:0054781 gard_rare diseases +MONDO:0054781 otar diseases +MONDO:0054781 rare diseases +MONDO:0054782 gard_rare diseases +MONDO:0054782 nord_rare diseases +MONDO:0054782 otar diseases +MONDO:0054782 rare diseases +MONDO:0054785 gard_rare diseases +MONDO:0054785 nord_rare diseases +MONDO:0054785 ordo_disorder diseases +MONDO:0054785 orphanet_rare diseases +MONDO:0054785 otar diseases +MONDO:0054785 rare diseases +MONDO:0054791 gard_rare diseases +MONDO:0054791 nord_rare diseases +MONDO:0054791 rare diseases +MONDO:0054794 gard_rare diseases +MONDO:0054794 nord_rare diseases +MONDO:0054794 otar diseases +MONDO:0054794 rare diseases +MONDO:0054801 gard_rare diseases +MONDO:0054801 nord_rare diseases +MONDO:0054801 otar diseases +MONDO:0054801 rare diseases +MONDO:0054802 gard_rare diseases +MONDO:0054802 nord_rare diseases +MONDO:0054802 rare diseases +MONDO:0054804 gard_rare diseases +MONDO:0054804 nord_rare diseases +MONDO:0054804 rare diseases +MONDO:0054805 gard_rare diseases +MONDO:0054805 nord_rare diseases +MONDO:0054805 rare diseases +MONDO:0054806 gard_rare diseases +MONDO:0054806 nord_rare diseases +MONDO:0054806 rare diseases +MONDO:0054813 gard_rare diseases +MONDO:0054813 nord_rare diseases +MONDO:0054813 ordo_disorder diseases +MONDO:0054813 orphanet_rare diseases +MONDO:0054813 otar diseases +MONDO:0054813 rare diseases +MONDO:0054817 gard_rare diseases +MONDO:0054817 nord_rare diseases +MONDO:0054817 otar diseases +MONDO:0054817 rare diseases +MONDO:0054831 gard_rare diseases +MONDO:0054831 nord_rare diseases +MONDO:0054831 rare diseases +MONDO:0054832 gard_rare diseases +MONDO:0054832 nord_rare diseases +MONDO:0054832 rare diseases +MONDO:0054833 clingen diseases +MONDO:0054833 gard_rare diseases +MONDO:0054833 nord_rare diseases +MONDO:0054833 ordo_disorder diseases +MONDO:0054833 orphanet_rare diseases +MONDO:0054833 otar diseases +MONDO:0054833 rare diseases +MONDO:0054835 gard_rare diseases +MONDO:0054835 nord_rare diseases +MONDO:0054835 otar diseases +MONDO:0054835 rare diseases +MONDO:0054837 gard_rare diseases +MONDO:0054837 nord_rare diseases +MONDO:0054837 otar diseases +MONDO:0054837 rare diseases +MONDO:0054838 gard_rare diseases +MONDO:0054838 nord_rare diseases +MONDO:0054838 rare diseases +MONDO:0054842 clingen diseases +MONDO:0054842 gard_rare diseases +MONDO:0054842 nord_rare diseases +MONDO:0054842 otar diseases +MONDO:0054842 rare diseases +MONDO:0054843 clingen diseases +MONDO:0054843 gard_rare diseases +MONDO:0054843 nord_rare diseases +MONDO:0054843 otar diseases +MONDO:0054843 rare diseases +MONDO:0054844 gard_rare diseases +MONDO:0054844 nord_rare diseases +MONDO:0054844 rare diseases +MONDO:0054845 gard_rare diseases +MONDO:0054845 nord_rare diseases +MONDO:0054845 otar diseases +MONDO:0054845 rare diseases +MONDO:0054846 gard_rare diseases +MONDO:0054846 nord_rare diseases +MONDO:0054846 rare diseases +MONDO:0054847 gard_rare diseases +MONDO:0054847 nord_rare diseases +MONDO:0054847 rare diseases +MONDO:0054850 gard_rare diseases +MONDO:0054850 nord_rare diseases +MONDO:0054850 rare diseases +MONDO:0054852 gard_rare diseases +MONDO:0054852 nord_rare diseases +MONDO:0054852 otar diseases +MONDO:0054852 rare diseases +MONDO:0054860 gard_rare diseases +MONDO:0054860 nord_rare diseases +MONDO:0054860 otar diseases +MONDO:0054860 rare diseases +MONDO:0054861 gard_rare diseases +MONDO:0054861 nord_rare diseases +MONDO:0054861 rare diseases +MONDO:0054862 gard_rare diseases +MONDO:0054862 nord_rare diseases +MONDO:0054862 rare diseases +MONDO:0054865 clingen diseases +MONDO:0054865 gard_rare diseases +MONDO:0054865 ordo_disorder diseases +MONDO:0054865 orphanet_rare diseases +MONDO:0054865 otar diseases +MONDO:0054865 rare diseases +MONDO:0054867 gard_rare diseases +MONDO:0054867 rare diseases +MONDO:0054869 gard_rare diseases +MONDO:0054869 rare diseases +MONDO:0056795 gard_rare diseases +MONDO:0056795 rare diseases +MONDO:0056797 otar diseases +MONDO:0056798 otar diseases +MONDO:0056799 otar diseases +MONDO:0056802 otar diseases +MONDO:0056805 inferred_rare diseases +MONDO:0056805 rare diseases +MONDO:0056806 otar diseases +MONDO:0056815 gard_rare diseases +MONDO:0056815 otar diseases +MONDO:0056815 rare diseases +MONDO:0056816 gard_rare diseases +MONDO:0056816 rare diseases +MONDO:0056817 gard_rare diseases +MONDO:0056817 rare diseases +MONDO:0056819 otar diseases +MONDO:0056820 otar diseases +MONDO:0060455 gard_rare diseases +MONDO:0060455 nord_rare diseases +MONDO:0060455 rare diseases +MONDO:0060457 otar diseases +MONDO:0060486 gard_rare diseases +MONDO:0060486 nord_rare diseases +MONDO:0060486 rare diseases +MONDO:0060489 gard_rare diseases +MONDO:0060489 nord_rare diseases +MONDO:0060489 rare diseases +MONDO:0060490 gard_rare diseases +MONDO:0060490 ordo_disorder diseases +MONDO:0060490 orphanet_rare diseases +MONDO:0060490 otar diseases +MONDO:0060490 rare diseases +MONDO:0060491 gard_rare diseases +MONDO:0060491 otar diseases +MONDO:0060491 rare diseases +MONDO:0060496 clingen diseases +MONDO:0060502 gard_rare diseases +MONDO:0060502 nord_rare diseases +MONDO:0060502 ordo_disorder diseases +MONDO:0060502 ordo_malformation_syndrome diseases +MONDO:0060502 orphanet_rare diseases +MONDO:0060502 otar diseases +MONDO:0060502 rare diseases +MONDO:0060507 gard_rare diseases +MONDO:0060507 ordo_disorder diseases +MONDO:0060507 orphanet_rare diseases +MONDO:0060507 otar diseases +MONDO:0060507 rare diseases +MONDO:0060510 clingen diseases +MONDO:0060510 gard_rare diseases +MONDO:0060510 otar diseases +MONDO:0060510 rare diseases +MONDO:0060527 clingen diseases +MONDO:0060527 otar diseases +MONDO:0060532 gard_rare diseases +MONDO:0060532 ordo_disorder diseases +MONDO:0060532 orphanet_rare diseases +MONDO:0060532 otar diseases +MONDO:0060532 rare diseases +MONDO:0060533 gard_rare diseases +MONDO:0060533 nord_rare diseases +MONDO:0060533 ordo_subtype_of_a_disorder diseases +MONDO:0060533 otar diseases +MONDO:0060533 rare diseases +MONDO:0060549 clingen diseases +MONDO:0060549 gard_rare diseases +MONDO:0060549 ordo_disorder diseases +MONDO:0060549 orphanet_rare diseases +MONDO:0060549 otar diseases +MONDO:0060549 rare diseases +MONDO:0060550 gard_rare diseases +MONDO:0060550 nord_rare diseases +MONDO:0060550 rare diseases +MONDO:0060551 otar diseases +MONDO:0060554 clingen diseases +MONDO:0060554 gard_rare diseases +MONDO:0060554 nord_rare diseases +MONDO:0060554 otar diseases +MONDO:0060554 rare diseases +MONDO:0060555 clingen diseases +MONDO:0060555 gard_rare diseases +MONDO:0060555 nord_rare diseases +MONDO:0060555 otar diseases +MONDO:0060555 rare diseases +MONDO:0060556 gard_rare diseases +MONDO:0060556 nord_rare diseases +MONDO:0060556 ordo_disorder diseases +MONDO:0060556 ordo_malformation_syndrome diseases +MONDO:0060556 orphanet_rare diseases +MONDO:0060556 otar diseases +MONDO:0060556 rare diseases +MONDO:0060564 gard_rare diseases +MONDO:0060564 nord_rare diseases +MONDO:0060564 ordo_disorder diseases +MONDO:0060564 orphanet_rare diseases +MONDO:0060564 rare diseases +MONDO:0060568 gard_rare diseases +MONDO:0060568 nord_rare diseases +MONDO:0060568 ordo_disorder diseases +MONDO:0060568 ordo_malformation_syndrome diseases +MONDO:0060568 orphanet_rare diseases +MONDO:0060568 rare diseases +MONDO:0060577 clingen diseases +MONDO:0060577 gard_rare diseases +MONDO:0060577 otar diseases +MONDO:0060577 rare diseases +MONDO:0060578 gard_rare diseases +MONDO:0060578 nord_rare diseases +MONDO:0060578 ordo_disorder diseases +MONDO:0060578 orphanet_rare diseases +MONDO:0060578 otar diseases +MONDO:0060578 rare diseases +MONDO:0060582 gard_rare diseases +MONDO:0060582 ordo_disorder diseases +MONDO:0060582 orphanet_rare diseases +MONDO:0060582 otar diseases +MONDO:0060582 rare diseases +MONDO:0060583 clingen diseases +MONDO:0060583 otar diseases +MONDO:0060585 gard_rare diseases +MONDO:0060585 nord_rare diseases +MONDO:0060585 rare diseases +MONDO:0060589 otar diseases +MONDO:0060591 otar diseases +MONDO:0060592 clingen diseases +MONDO:0060596 gard_rare diseases +MONDO:0060596 nord_rare diseases +MONDO:0060596 otar diseases +MONDO:0060596 rare diseases +MONDO:0060611 gard_rare diseases +MONDO:0060611 ordo_disorder diseases +MONDO:0060611 orphanet_rare diseases +MONDO:0060611 otar diseases +MONDO:0060611 rare diseases +MONDO:0060621 otar diseases +MONDO:0060622 gard_rare diseases +MONDO:0060622 ordo_disorder diseases +MONDO:0060622 orphanet_rare diseases +MONDO:0060622 otar diseases +MONDO:0060622 rare diseases +MONDO:0060624 otar diseases +MONDO:0060627 clingen diseases +MONDO:0060627 gard_rare diseases +MONDO:0060627 nord_rare diseases +MONDO:0060627 ordo_disorder diseases +MONDO:0060627 ordo_malformation_syndrome diseases +MONDO:0060627 orphanet_rare diseases +MONDO:0060627 otar diseases +MONDO:0060627 rare diseases +MONDO:0060629 otar diseases +MONDO:0060631 gard_rare diseases +MONDO:0060631 nord_rare diseases +MONDO:0060631 ordo_disorder diseases +MONDO:0060631 orphanet_rare diseases +MONDO:0060631 otar diseases +MONDO:0060631 rare diseases +MONDO:0060640 otar diseases +MONDO:0060641 otar diseases +MONDO:0060642 otar diseases +MONDO:0060650 clingen diseases +MONDO:0060650 gard_rare diseases +MONDO:0060650 nord_rare diseases +MONDO:0060650 otar diseases +MONDO:0060650 rare diseases +MONDO:0060663 otar diseases +MONDO:0060664 otar diseases +MONDO:0060666 otar diseases +MONDO:0060677 gard_rare diseases +MONDO:0060677 nord_rare diseases +MONDO:0060677 rare diseases +MONDO:0060702 gard_rare diseases +MONDO:0060702 nord_rare diseases +MONDO:0060702 otar diseases +MONDO:0060702 rare diseases +MONDO:0060704 otar diseases +MONDO:0060707 gard_rare diseases +MONDO:0060707 nord_rare diseases +MONDO:0060707 ordo_disorder diseases +MONDO:0060707 orphanet_rare diseases +MONDO:0060707 otar diseases +MONDO:0060707 rare diseases +MONDO:0060711 otar diseases +MONDO:0060713 otar diseases +MONDO:0060714 gard_rare diseases +MONDO:0060714 nord_rare diseases +MONDO:0060714 otar diseases +MONDO:0060714 rare diseases +MONDO:0060715 gard_rare diseases +MONDO:0060715 nord_rare diseases +MONDO:0060715 otar diseases +MONDO:0060715 rare diseases +MONDO:0060720 gard_rare diseases +MONDO:0060720 otar diseases +MONDO:0060720 rare diseases +MONDO:0060724 gard_rare diseases +MONDO:0060724 otar diseases +MONDO:0060724 rare diseases +MONDO:0060729 gard_rare diseases +MONDO:0060729 nord_rare diseases +MONDO:0060729 otar diseases +MONDO:0060729 rare diseases +MONDO:0060732 gard_rare diseases +MONDO:0060732 nord_rare diseases +MONDO:0060732 rare diseases +MONDO:0060733 otar diseases +MONDO:0060745 otar diseases +MONDO:0060752 otar diseases +MONDO:0060758 gard_rare diseases +MONDO:0060758 nord_rare diseases +MONDO:0060758 otar diseases +MONDO:0060758 rare diseases +MONDO:0060759 gard_rare diseases +MONDO:0060759 nord_rare diseases +MONDO:0060759 ordo_disorder diseases +MONDO:0060759 orphanet_rare diseases +MONDO:0060759 otar diseases +MONDO:0060759 rare diseases +MONDO:0060760 otar diseases +MONDO:0060761 otar diseases +MONDO:0060763 otar diseases +MONDO:0060764 gard_rare diseases +MONDO:0060764 nord_rare diseases +MONDO:0060764 rare diseases +MONDO:0060765 otar diseases +MONDO:0060778 gard_rare diseases +MONDO:0060778 rare diseases +MONDO:0060779 gard_rare diseases +MONDO:0060779 otar diseases +MONDO:0060779 rare diseases +MONDO:0060781 gard_rare diseases +MONDO:0060781 rare diseases +MONDO:0060782 gard_rare diseases +MONDO:0060782 rare diseases +MONDO:0060783 gard_rare diseases +MONDO:0060783 rare diseases +MONDO:0100000 clingen diseases +MONDO:0100000 gard_rare diseases +MONDO:0100000 nord_rare diseases +MONDO:0100000 otar diseases +MONDO:0100000 rare diseases +MONDO:0100004 gard_rare diseases +MONDO:0100004 rare diseases +MONDO:0100006 gard_rare diseases +MONDO:0100006 nord_rare diseases +MONDO:0100006 rare diseases +MONDO:0100009 clingen diseases +MONDO:0100009 otar diseases +MONDO:0100010 otar diseases +MONDO:0100012 gard_rare diseases +MONDO:0100012 rare diseases +MONDO:0100013 gard_rare diseases +MONDO:0100013 rare diseases +MONDO:0100015 gard_rare diseases +MONDO:0100015 rare diseases +MONDO:0100016 gard_rare diseases +MONDO:0100016 rare diseases +MONDO:0100017 gard_rare diseases +MONDO:0100017 nord_rare diseases +MONDO:0100017 otar diseases +MONDO:0100017 rare diseases +MONDO:0100018 gard_rare diseases +MONDO:0100018 rare diseases +MONDO:0100019 gard_rare diseases +MONDO:0100019 nord_rare diseases +MONDO:0100019 rare diseases +MONDO:0100020 gard_rare diseases +MONDO:0100020 rare diseases +MONDO:0100021 gard_rare diseases +MONDO:0100021 nord_rare diseases +MONDO:0100021 rare diseases +MONDO:0100022 gard_rare diseases +MONDO:0100022 rare diseases +MONDO:0100025 gard_rare diseases +MONDO:0100025 nord_rare diseases +MONDO:0100025 rare diseases +MONDO:0100026 gard_rare diseases +MONDO:0100026 rare diseases +MONDO:0100030 gard_rare diseases +MONDO:0100030 rare diseases +MONDO:0100031 gard_rare diseases +MONDO:0100031 rare diseases +MONDO:0100032 gard_rare diseases +MONDO:0100032 nord_rare diseases +MONDO:0100032 obsoletion_candidate diseases +MONDO:0100032 rare diseases +MONDO:0100033 otar diseases +MONDO:0100034 gard_rare diseases +MONDO:0100034 rare diseases +MONDO:0100035 otar diseases +MONDO:0100037 gard_rare diseases +MONDO:0100037 rare diseases +MONDO:0100038 clingen diseases +MONDO:0100038 gard_rare diseases +MONDO:0100038 ordo_disorder diseases +MONDO:0100038 orphanet_rare diseases +MONDO:0100038 otar diseases +MONDO:0100038 rare diseases +MONDO:0100039 clingen diseases +MONDO:0100039 gard_rare diseases +MONDO:0100039 nord_rare diseases +MONDO:0100039 otar diseases +MONDO:0100039 rare diseases +MONDO:0100040 clingen diseases +MONDO:0100040 gard_rare diseases +MONDO:0100040 nord_rare diseases +MONDO:0100040 otar diseases +MONDO:0100040 rare diseases +MONDO:0100041 gard_rare diseases +MONDO:0100041 rare diseases +MONDO:0100044 gard_rare diseases +MONDO:0100044 nord_rare diseases +MONDO:0100044 rare diseases +MONDO:0100050 gard_rare diseases +MONDO:0100050 nord_rare diseases +MONDO:0100050 rare diseases +MONDO:0100051 gard_rare diseases +MONDO:0100051 rare diseases +MONDO:0100052 gard_rare diseases +MONDO:0100052 rare diseases +MONDO:0100053 otar diseases +MONDO:0100054 otar diseases +MONDO:0100055 gard_rare diseases +MONDO:0100055 rare diseases +MONDO:0100058 clingen diseases +MONDO:0100058 gard_rare diseases +MONDO:0100058 otar diseases +MONDO:0100058 rare diseases +MONDO:0100059 gard_rare diseases +MONDO:0100059 rare diseases +MONDO:0100060 gard_rare diseases +MONDO:0100060 rare diseases +MONDO:0100061 clingen diseases +MONDO:0100061 gard_rare diseases +MONDO:0100061 otar diseases +MONDO:0100061 rare diseases +MONDO:0100062 clingen diseases +MONDO:0100062 gard_rare diseases +MONDO:0100062 nord_rare diseases +MONDO:0100062 ordo_clinical_syndrome diseases +MONDO:0100062 ordo_disorder diseases +MONDO:0100062 orphanet_rare diseases +MONDO:0100062 otar diseases +MONDO:0100062 rare diseases +MONDO:0100064 clingen diseases +MONDO:0100064 gard_rare diseases +MONDO:0100064 otar diseases +MONDO:0100064 rare diseases +MONDO:0100065 gard_rare diseases +MONDO:0100065 rare diseases +MONDO:0100066 gard_rare diseases +MONDO:0100066 rare diseases +MONDO:0100067 gard_rare diseases +MONDO:0100067 rare diseases +MONDO:0100068 gard_rare diseases +MONDO:0100068 nord_rare diseases +MONDO:0100068 rare diseases +MONDO:0100069 clingen diseases +MONDO:0100069 otar diseases +MONDO:0100070 otar diseases +MONDO:0100073 otar diseases +MONDO:0100077 gard_rare diseases +MONDO:0100077 nord_rare diseases +MONDO:0100077 rare diseases +MONDO:0100079 gard_rare diseases +MONDO:0100079 nord_rare diseases +MONDO:0100079 rare diseases +MONDO:0100081 otar diseases +MONDO:0100082 gard_rare diseases +MONDO:0100082 nord_rare diseases +MONDO:0100082 rare diseases +MONDO:0100083 gard_rare diseases +MONDO:0100083 nord_rare diseases +MONDO:0100083 otar diseases +MONDO:0100083 rare diseases +MONDO:0100084 clingen diseases +MONDO:0100084 gard_rare diseases +MONDO:0100084 otar diseases +MONDO:0100084 rare diseases +MONDO:0100085 gard_rare diseases +MONDO:0100085 rare diseases +MONDO:0100086 harrisons_view diseases +MONDO:0100086 otar diseases +MONDO:0100087 otar diseases +MONDO:0100089 clingen diseases +MONDO:0100089 gard_rare diseases +MONDO:0100089 nord_rare diseases +MONDO:0100089 otar diseases +MONDO:0100089 rare diseases +MONDO:0100090 gard_rare diseases +MONDO:0100090 nord_rare diseases +MONDO:0100090 rare diseases +MONDO:0100091 gard_rare diseases +MONDO:0100091 nord_rare diseases +MONDO:0100091 otar diseases +MONDO:0100091 rare diseases +MONDO:0100092 gard_rare diseases +MONDO:0100092 nord_rare diseases +MONDO:0100092 rare diseases +MONDO:0100093 gard_rare diseases +MONDO:0100093 nord_rare diseases +MONDO:0100093 rare diseases +MONDO:0100095 gard_rare diseases +MONDO:0100095 otar diseases +MONDO:0100095 rare diseases +MONDO:0100096 otar diseases +MONDO:0100097 gard_rare diseases +MONDO:0100097 nord_rare diseases +MONDO:0100097 rare diseases +MONDO:0100098 gard_rare diseases +MONDO:0100098 nord_rare diseases +MONDO:0100098 rare diseases +MONDO:0100100 clingen diseases +MONDO:0100100 gard_rare diseases +MONDO:0100100 otar diseases +MONDO:0100100 rare diseases +MONDO:0100101 gard_rare diseases +MONDO:0100101 nord_rare diseases +MONDO:0100101 ordo_disorder diseases +MONDO:0100101 orphanet_rare diseases +MONDO:0100101 otar diseases +MONDO:0100101 rare diseases +MONDO:0100102 gard_rare diseases +MONDO:0100102 nord_rare diseases +MONDO:0100102 rare diseases +MONDO:0100103 gard_rare diseases +MONDO:0100103 nord_rare diseases +MONDO:0100103 rare diseases +MONDO:0100104 gard_rare diseases +MONDO:0100104 nord_rare diseases +MONDO:0100104 rare diseases +MONDO:0100105 gard_rare diseases +MONDO:0100105 nord_rare diseases +MONDO:0100105 rare diseases +MONDO:0100107 gard_rare diseases +MONDO:0100107 rare diseases +MONDO:0100108 clingen diseases +MONDO:0100108 gard_rare diseases +MONDO:0100108 otar diseases +MONDO:0100108 rare diseases +MONDO:0100111 clingen diseases +MONDO:0100112 clingen diseases +MONDO:0100112 gard_rare diseases +MONDO:0100112 otar diseases +MONDO:0100112 rare diseases +MONDO:0100113 gard_rare diseases +MONDO:0100113 rare diseases +MONDO:0100114 gard_rare diseases +MONDO:0100114 otar diseases +MONDO:0100114 rare diseases +MONDO:0100115 gard_rare diseases +MONDO:0100115 ordo_disorder diseases +MONDO:0100115 orphanet_rare diseases +MONDO:0100115 rare diseases +MONDO:0100116 gard_rare diseases +MONDO:0100116 nord_rare diseases +MONDO:0100116 ordo_disorder diseases +MONDO:0100116 orphanet_rare diseases +MONDO:0100116 otar diseases +MONDO:0100116 rare diseases +MONDO:0100118 otar diseases +MONDO:0100119 gard_rare diseases +MONDO:0100119 nord_rare diseases +MONDO:0100119 rare diseases +MONDO:0100120 otar diseases +MONDO:0100121 clingen diseases +MONDO:0100121 gard_rare diseases +MONDO:0100121 otar diseases +MONDO:0100121 rare diseases +MONDO:0100122 clingen diseases +MONDO:0100122 gard_rare diseases +MONDO:0100122 otar diseases +MONDO:0100122 rare diseases +MONDO:0100124 clingen diseases +MONDO:0100124 disease_grouping diseases +MONDO:0100124 gard_rare diseases +MONDO:0100124 nord_rare diseases +MONDO:0100124 otar diseases +MONDO:0100124 rare diseases +MONDO:0100126 clingen diseases +MONDO:0100126 gard_rare diseases +MONDO:0100126 otar diseases +MONDO:0100126 rare diseases +MONDO:0100129 gard_rare diseases +MONDO:0100129 rare diseases +MONDO:0100130 gard_rare diseases +MONDO:0100130 nord_rare diseases +MONDO:0100130 ordo_disorder diseases +MONDO:0100130 orphanet_rare diseases +MONDO:0100130 otar diseases +MONDO:0100130 rare diseases +MONDO:0100131 otar diseases +MONDO:0100132 gard_rare diseases +MONDO:0100132 rare diseases +MONDO:0100133 gard_rare diseases +MONDO:0100133 nord_rare diseases +MONDO:0100133 ordo_disorder diseases +MONDO:0100133 orphanet_rare diseases +MONDO:0100133 otar diseases +MONDO:0100133 rare diseases +MONDO:0100134 gard_rare diseases +MONDO:0100134 rare diseases +MONDO:0100135 clingen diseases +MONDO:0100135 gard_rare diseases +MONDO:0100135 nord_rare diseases +MONDO:0100135 rare diseases +MONDO:0100137 gard_rare diseases +MONDO:0100137 otar diseases +MONDO:0100137 rare diseases +MONDO:0100138 gard_rare diseases +MONDO:0100138 rare diseases +MONDO:0100146 clingen diseases +MONDO:0100146 gard_rare diseases +MONDO:0100146 nord_rare diseases +MONDO:0100146 otar diseases +MONDO:0100146 rare diseases +MONDO:0100147 clingen diseases +MONDO:0100147 gard_rare diseases +MONDO:0100147 nord_rare diseases +MONDO:0100147 ordo_disorder diseases +MONDO:0100147 orphanet_rare diseases +MONDO:0100147 otar diseases +MONDO:0100147 rare diseases +MONDO:0100148 clingen diseases +MONDO:0100148 inferred_rare diseases +MONDO:0100148 otar diseases +MONDO:0100148 rare diseases +MONDO:0100149 clingen diseases +MONDO:0100149 gard_rare diseases +MONDO:0100149 rare diseases +MONDO:0100150 clingen diseases +MONDO:0100150 gard_rare diseases +MONDO:0100150 otar diseases +MONDO:0100150 rare diseases +MONDO:0100151 gard_rare diseases +MONDO:0100151 rare diseases +MONDO:0100152 clingen diseases +MONDO:0100152 gard_rare diseases +MONDO:0100152 otar diseases +MONDO:0100152 rare diseases +MONDO:0100153 clingen diseases +MONDO:0100155 clingen diseases +MONDO:0100156 gard_rare diseases +MONDO:0100156 nord_rare diseases +MONDO:0100156 rare diseases +MONDO:0100157 gard_rare diseases +MONDO:0100157 nord_rare diseases +MONDO:0100157 otar diseases +MONDO:0100157 rare diseases +MONDO:0100158 clingen diseases +MONDO:0100158 gard_rare diseases +MONDO:0100158 rare diseases +MONDO:0100161 inferred_rare diseases +MONDO:0100161 rare diseases +MONDO:0100162 clingen diseases +MONDO:0100162 otar diseases +MONDO:0100163 gard_rare diseases +MONDO:0100163 rare diseases +MONDO:0100164 gard_rare diseases +MONDO:0100164 nord_rare diseases +MONDO:0100164 ordo_disorder diseases +MONDO:0100164 orphanet_rare diseases +MONDO:0100164 otar diseases +MONDO:0100164 rare diseases +MONDO:0100165 gard_rare diseases +MONDO:0100165 nord_rare diseases +MONDO:0100165 rare diseases +MONDO:0100168 gard_rare diseases +MONDO:0100168 rare diseases +MONDO:0100169 gard_rare diseases +MONDO:0100169 rare diseases +MONDO:0100172 otar diseases +MONDO:0100173 gard_rare diseases +MONDO:0100173 rare diseases +MONDO:0100175 clingen diseases +MONDO:0100175 gard_rare diseases +MONDO:0100175 otar diseases +MONDO:0100175 rare diseases +MONDO:0100176 clingen diseases +MONDO:0100176 otar diseases +MONDO:0100184 clingen diseases +MONDO:0100184 gard_rare diseases +MONDO:0100184 otar diseases +MONDO:0100184 rare diseases +MONDO:0100186 gard_rare diseases +MONDO:0100186 nord_rare diseases +MONDO:0100186 ordo_subtype_of_a_disorder diseases +MONDO:0100186 otar diseases +MONDO:0100186 rare diseases +MONDO:0100188 gard_rare diseases +MONDO:0100188 nord_rare diseases +MONDO:0100188 rare diseases +MONDO:0100191 otar diseases +MONDO:0100194 gard_rare diseases +MONDO:0100194 nord_rare diseases +MONDO:0100194 rare diseases +MONDO:0100195 gard_rare diseases +MONDO:0100195 nord_rare diseases +MONDO:0100195 rare diseases +MONDO:0100196 clingen diseases +MONDO:0100196 gard_rare diseases +MONDO:0100196 otar diseases +MONDO:0100196 rare diseases +MONDO:0100199 gard_rare diseases +MONDO:0100199 rare diseases +MONDO:0100200 clingen diseases +MONDO:0100200 gard_rare diseases +MONDO:0100200 otar diseases +MONDO:0100200 rare diseases +MONDO:0100207 clingen diseases +MONDO:0100207 otar diseases +MONDO:0100208 gard_rare diseases +MONDO:0100208 rare diseases +MONDO:0100210 gard_rare diseases +MONDO:0100210 rare diseases +MONDO:0100211 gard_rare diseases +MONDO:0100211 nord_rare diseases +MONDO:0100211 ordo_disorder diseases +MONDO:0100211 orphanet_rare diseases +MONDO:0100211 otar diseases +MONDO:0100211 rare diseases +MONDO:0100212 gard_rare diseases +MONDO:0100212 nord_rare diseases +MONDO:0100212 ordo_disorder diseases +MONDO:0100212 orphanet_rare diseases +MONDO:0100212 otar diseases +MONDO:0100212 rare diseases +MONDO:0100213 clingen diseases +MONDO:0100213 gard_rare diseases +MONDO:0100213 nord_rare diseases +MONDO:0100213 otar diseases +MONDO:0100213 rare diseases +MONDO:0100214 gard_rare diseases +MONDO:0100214 otar diseases +MONDO:0100214 rare diseases +MONDO:0100215 gard_rare diseases +MONDO:0100215 nord_rare diseases +MONDO:0100215 ordo_disorder diseases +MONDO:0100215 orphanet_rare diseases +MONDO:0100215 otar diseases +MONDO:0100215 rare diseases +MONDO:0100216 clingen diseases +MONDO:0100216 gard_rare diseases +MONDO:0100216 ordo_disorder diseases +MONDO:0100216 orphanet_rare diseases +MONDO:0100216 rare diseases +MONDO:0100218 gard_rare diseases +MONDO:0100218 nord_rare diseases +MONDO:0100218 otar diseases +MONDO:0100218 rare diseases +MONDO:0100219 gard_rare diseases +MONDO:0100219 nord_rare diseases +MONDO:0100219 otar diseases +MONDO:0100219 rare diseases +MONDO:0100220 gard_rare diseases +MONDO:0100220 otar diseases +MONDO:0100220 rare diseases +MONDO:0100221 gard_rare diseases +MONDO:0100221 nord_rare diseases +MONDO:0100221 otar diseases +MONDO:0100221 rare diseases +MONDO:0100222 gard_rare diseases +MONDO:0100222 rare diseases +MONDO:0100223 gard_rare diseases +MONDO:0100223 rare diseases +MONDO:0100224 gard_rare diseases +MONDO:0100224 rare diseases +MONDO:0100225 clingen diseases +MONDO:0100225 gard_rare diseases +MONDO:0100225 otar diseases +MONDO:0100225 rare diseases +MONDO:0100227 clingen diseases +MONDO:0100227 gard_rare diseases +MONDO:0100227 otar diseases +MONDO:0100227 rare diseases +MONDO:0100228 clingen diseases +MONDO:0100228 gard_rare diseases +MONDO:0100228 otar diseases +MONDO:0100228 rare diseases +MONDO:0100230 clingen diseases +MONDO:0100230 gard_rare diseases +MONDO:0100230 rare diseases +MONDO:0100234 gard_rare diseases +MONDO:0100234 nord_rare diseases +MONDO:0100234 ordo_disorder diseases +MONDO:0100234 orphanet_rare diseases +MONDO:0100234 otar diseases +MONDO:0100234 rare diseases +MONDO:0100235 gard_rare diseases +MONDO:0100235 rare diseases +MONDO:0100237 gard_rare diseases +MONDO:0100237 otar diseases +MONDO:0100237 rare diseases +MONDO:0100238 gard_rare diseases +MONDO:0100238 rare diseases +MONDO:0100240 gard_rare diseases +MONDO:0100240 otar diseases +MONDO:0100240 rare diseases +MONDO:0100241 gard_rare diseases +MONDO:0100241 otar diseases +MONDO:0100241 rare diseases +MONDO:0100242 gard_rare diseases +MONDO:0100242 rare diseases +MONDO:0100244 gard_rare diseases +MONDO:0100244 nord_rare diseases +MONDO:0100244 ordo_disorder diseases +MONDO:0100244 orphanet_rare diseases +MONDO:0100244 otar diseases +MONDO:0100244 rare diseases +MONDO:0100247 gard_rare diseases +MONDO:0100247 nord_rare diseases +MONDO:0100247 otar diseases +MONDO:0100247 rare diseases +MONDO:0100248 gard_rare diseases +MONDO:0100248 rare diseases +MONDO:0100249 gard_rare diseases +MONDO:0100249 nord_rare diseases +MONDO:0100249 ordo_disorder diseases +MONDO:0100249 ordo_malformation_syndrome diseases +MONDO:0100249 orphanet_rare diseases +MONDO:0100249 otar diseases +MONDO:0100249 rare diseases +MONDO:0100250 gard_rare diseases +MONDO:0100250 nord_rare diseases +MONDO:0100250 rare diseases +MONDO:0100251 gard_rare diseases +MONDO:0100251 nord_rare diseases +MONDO:0100251 ordo_subtype_of_a_disorder diseases +MONDO:0100251 rare diseases +MONDO:0100252 gard_rare diseases +MONDO:0100252 nord_rare diseases +MONDO:0100252 rare diseases +MONDO:0100253 clingen diseases +MONDO:0100253 gard_rare diseases +MONDO:0100253 nord_rare diseases +MONDO:0100253 ordo_disorder diseases +MONDO:0100253 ordo_malformation_syndrome diseases +MONDO:0100253 orphanet_rare diseases +MONDO:0100253 otar diseases +MONDO:0100253 rare diseases +MONDO:0100254 inferred_rare diseases +MONDO:0100254 rare diseases +MONDO:0100255 clingen diseases +MONDO:0100255 gard_rare diseases +MONDO:0100255 nord_rare diseases +MONDO:0100255 ordo_disorder diseases +MONDO:0100255 orphanet_rare diseases +MONDO:0100255 otar diseases +MONDO:0100255 rare diseases +MONDO:0100256 clingen diseases +MONDO:0100256 gard_rare diseases +MONDO:0100256 rare diseases +MONDO:0100257 gard_rare diseases +MONDO:0100257 rare diseases +MONDO:0100258 clingen diseases +MONDO:0100258 gard_rare diseases +MONDO:0100258 otar diseases +MONDO:0100258 rare diseases +MONDO:0100259 disease_grouping diseases +MONDO:0100259 gard_rare diseases +MONDO:0100259 otar diseases +MONDO:0100259 rare diseases +MONDO:0100260 disease_grouping diseases +MONDO:0100260 gard_rare diseases +MONDO:0100260 nord_rare diseases +MONDO:0100260 rare diseases +MONDO:0100261 disease_grouping diseases +MONDO:0100261 gard_rare diseases +MONDO:0100261 rare diseases +MONDO:0100262 disease_grouping diseases +MONDO:0100262 gard_rare diseases +MONDO:0100262 otar diseases +MONDO:0100262 rare diseases +MONDO:0100263 disease_grouping diseases +MONDO:0100263 gard_rare diseases +MONDO:0100263 rare diseases +MONDO:0100264 disease_grouping diseases +MONDO:0100264 gard_rare diseases +MONDO:0100264 rare diseases +MONDO:0100265 gard_rare diseases +MONDO:0100265 rare diseases +MONDO:0100266 disease_grouping diseases +MONDO:0100266 gard_rare diseases +MONDO:0100266 nord_rare diseases +MONDO:0100266 rare diseases +MONDO:0100267 disease_grouping diseases +MONDO:0100267 gard_rare diseases +MONDO:0100267 rare diseases +MONDO:0100268 disease_grouping diseases +MONDO:0100268 gard_rare diseases +MONDO:0100268 rare diseases +MONDO:0100269 disease_grouping diseases +MONDO:0100269 gard_rare diseases +MONDO:0100269 otar diseases +MONDO:0100269 rare diseases +MONDO:0100270 disease_grouping diseases +MONDO:0100270 gard_rare diseases +MONDO:0100270 rare diseases +MONDO:0100271 disease_grouping diseases +MONDO:0100271 gard_rare diseases +MONDO:0100271 rare diseases +MONDO:0100272 gard_rare diseases +MONDO:0100272 rare diseases +MONDO:0100273 clingen diseases +MONDO:0100273 gard_rare diseases +MONDO:0100273 otar diseases +MONDO:0100273 rare diseases +MONDO:0100274 clingen diseases +MONDO:0100274 gard_rare diseases +MONDO:0100274 otar diseases +MONDO:0100274 rare diseases +MONDO:0100275 gard_rare diseases +MONDO:0100275 rare diseases +MONDO:0100276 gard_rare diseases +MONDO:0100276 rare diseases +MONDO:0100277 disease_grouping diseases +MONDO:0100277 gard_rare diseases +MONDO:0100277 rare diseases +MONDO:0100278 clingen diseases +MONDO:0100278 gard_rare diseases +MONDO:0100278 otar diseases +MONDO:0100278 rare diseases +MONDO:0100279 disease_grouping diseases +MONDO:0100279 gard_rare diseases +MONDO:0100279 rare diseases +MONDO:0100280 gard_rare diseases +MONDO:0100280 nord_rare diseases +MONDO:0100280 ordo_disorder diseases +MONDO:0100280 orphanet_rare diseases +MONDO:0100280 otar diseases +MONDO:0100280 rare diseases +MONDO:0100281 gard_rare diseases +MONDO:0100281 predisposition diseases +MONDO:0100281 rare diseases +MONDO:0100283 clingen diseases +MONDO:0100283 gard_rare diseases +MONDO:0100283 otar diseases +MONDO:0100283 rare diseases +MONDO:0100284 clingen diseases +MONDO:0100284 otar diseases +MONDO:0100285 gard_rare diseases +MONDO:0100285 nord_rare diseases +MONDO:0100285 rare diseases +MONDO:0100287 clingen diseases +MONDO:0100287 gard_rare diseases +MONDO:0100287 rare diseases +MONDO:0100288 gard_rare diseases +MONDO:0100288 nord_rare diseases +MONDO:0100288 rare diseases +MONDO:0100289 gard_rare diseases +MONDO:0100289 nord_rare diseases +MONDO:0100289 ordo_disorder diseases +MONDO:0100289 orphanet_rare diseases +MONDO:0100289 otar diseases +MONDO:0100289 rare diseases +MONDO:0100290 gard_rare diseases +MONDO:0100290 rare diseases +MONDO:0100291 gard_rare diseases +MONDO:0100291 nord_rare diseases +MONDO:0100291 rare diseases +MONDO:0100292 gard_rare diseases +MONDO:0100292 rare diseases +MONDO:0100293 gard_rare diseases +MONDO:0100293 rare diseases +MONDO:0100294 gard_rare diseases +MONDO:0100294 nord_rare diseases +MONDO:0100294 ordo_disorder diseases +MONDO:0100294 orphanet_rare diseases +MONDO:0100294 otar diseases +MONDO:0100294 rare diseases +MONDO:0100296 gard_rare diseases +MONDO:0100296 nord_rare diseases +MONDO:0100296 otar diseases +MONDO:0100296 rare diseases +MONDO:0100298 gard_rare diseases +MONDO:0100298 rare diseases +MONDO:0100299 clingen diseases +MONDO:0100299 gard_rare diseases +MONDO:0100299 rare diseases +MONDO:0100301 gard_rare diseases +MONDO:0100301 rare diseases +MONDO:0100302 gard_rare diseases +MONDO:0100302 rare diseases +MONDO:0100303 gard_rare diseases +MONDO:0100303 rare diseases +MONDO:0100304 gard_rare diseases +MONDO:0100304 rare diseases +MONDO:0100305 clingen diseases +MONDO:0100305 gard_rare diseases +MONDO:0100305 rare diseases +MONDO:0100306 gard_rare diseases +MONDO:0100306 rare diseases +MONDO:0100307 gard_rare diseases +MONDO:0100307 rare diseases +MONDO:0100308 otar diseases +MONDO:0100309 disease_grouping diseases +MONDO:0100309 gard_rare diseases +MONDO:0100309 mondo_rare diseases +MONDO:0100309 nord_rare diseases +MONDO:0100309 ordo_group_of_disorders diseases +MONDO:0100309 otar diseases +MONDO:0100309 rare diseases +MONDO:0100310 gard_rare diseases +MONDO:0100310 otar diseases +MONDO:0100310 rare diseases +MONDO:0100313 gard_rare diseases +MONDO:0100313 otar diseases +MONDO:0100313 rare diseases +MONDO:0100314 gard_rare diseases +MONDO:0100314 rare diseases +MONDO:0100315 gard_rare diseases +MONDO:0100315 rare diseases +MONDO:0100316 gard_rare diseases +MONDO:0100316 prototype_pattern diseases +MONDO:0100316 rare diseases +MONDO:0100317 clingen diseases +MONDO:0100317 gard_rare diseases +MONDO:0100317 otar diseases +MONDO:0100317 rare diseases +MONDO:0100319 gard_rare diseases +MONDO:0100319 rare diseases +MONDO:0100322 disease_grouping diseases +MONDO:0100322 gard_rare diseases +MONDO:0100322 rare diseases +MONDO:0100323 gard_rare diseases +MONDO:0100323 rare diseases +MONDO:0100324 gard_rare diseases +MONDO:0100324 rare diseases +MONDO:0100325 gard_rare diseases +MONDO:0100325 nord_rare diseases +MONDO:0100325 ordo_disorder diseases +MONDO:0100325 ordo_malformation_syndrome diseases +MONDO:0100325 orphanet_rare diseases +MONDO:0100325 otar diseases +MONDO:0100325 rare diseases +MONDO:0100326 clingen diseases +MONDO:0100326 gard_rare diseases +MONDO:0100326 nord_rare diseases +MONDO:0100326 ordo_disorder diseases +MONDO:0100326 orphanet_rare diseases +MONDO:0100326 otar diseases +MONDO:0100326 rare diseases +MONDO:0100327 gard_rare diseases +MONDO:0100327 otar diseases +MONDO:0100327 rare diseases +MONDO:0100328 otar diseases +MONDO:0100330 otar diseases +MONDO:0100337 clingen diseases +MONDO:0100337 otar diseases +MONDO:0100338 otar diseases +MONDO:0100339 clingen diseases +MONDO:0100339 gard_rare diseases +MONDO:0100339 nord_rare diseases +MONDO:0100339 ordo_disorder diseases +MONDO:0100339 orphanet_rare diseases +MONDO:0100339 otar diseases +MONDO:0100339 rare diseases +MONDO:0100340 gard_rare diseases +MONDO:0100340 nord_rare diseases +MONDO:0100340 rare diseases +MONDO:0100342 disease_grouping diseases +MONDO:0100342 gard_rare diseases +MONDO:0100342 otar diseases +MONDO:0100342 rare diseases +MONDO:0100344 gard_rare diseases +MONDO:0100344 nord_rare diseases +MONDO:0100344 ordo_subtype_of_a_disorder diseases +MONDO:0100344 rare diseases +MONDO:0100345 gard_rare diseases +MONDO:0100345 otar diseases +MONDO:0100345 rare diseases +MONDO:0100346 clingen diseases +MONDO:0100346 gard_rare diseases +MONDO:0100346 rare diseases +MONDO:0100347 gard_rare diseases +MONDO:0100347 nord_rare diseases +MONDO:0100347 ordo_clinical_syndrome diseases +MONDO:0100347 ordo_disorder diseases +MONDO:0100347 orphanet_rare diseases +MONDO:0100347 otar diseases +MONDO:0100347 rare diseases +MONDO:0100348 gard_rare diseases +MONDO:0100348 otar diseases +MONDO:0100348 rare diseases +MONDO:0100349 gard_rare diseases +MONDO:0100349 nord_rare diseases +MONDO:0100349 ordo_disorder diseases +MONDO:0100349 orphanet_rare diseases +MONDO:0100349 rare diseases +MONDO:0100350 gard_rare diseases +MONDO:0100350 nord_rare diseases +MONDO:0100350 ordo_disorder diseases +MONDO:0100350 orphanet_rare diseases +MONDO:0100350 otar diseases +MONDO:0100350 rare diseases +MONDO:0100351 clingen diseases +MONDO:0100351 gard_rare diseases +MONDO:0100351 rare diseases +MONDO:0100352 gard_rare diseases +MONDO:0100352 nord_rare diseases +MONDO:0100352 otar diseases +MONDO:0100352 rare diseases +MONDO:0100354 gard_rare diseases +MONDO:0100354 nord_rare diseases +MONDO:0100354 ordo_disorder diseases +MONDO:0100354 ordo_malformation_syndrome diseases +MONDO:0100354 orphanet_rare diseases +MONDO:0100354 otar diseases +MONDO:0100354 rare diseases +MONDO:0100358 clingen diseases +MONDO:0100358 disease_grouping diseases +MONDO:0100358 gard_rare diseases +MONDO:0100358 otar diseases +MONDO:0100358 rare diseases +MONDO:0100365 gard_rare diseases +MONDO:0100365 rare diseases +MONDO:0100367 gard_rare diseases +MONDO:0100367 ordo_disorder diseases +MONDO:0100367 orphanet_rare diseases +MONDO:0100367 rare diseases +MONDO:0100368 clingen diseases +MONDO:0100368 gard_rare diseases +MONDO:0100368 nord_rare diseases +MONDO:0100368 rare diseases +MONDO:0100372 gard_rare diseases +MONDO:0100372 rare diseases +MONDO:0100373 gard_rare diseases +MONDO:0100373 rare diseases +MONDO:0100374 gard_rare diseases +MONDO:0100374 rare diseases +MONDO:0100375 gard_rare diseases +MONDO:0100375 rare diseases +MONDO:0100376 gard_rare diseases +MONDO:0100376 rare diseases +MONDO:0100377 gard_rare diseases +MONDO:0100377 rare diseases +MONDO:0100378 gard_rare diseases +MONDO:0100378 nord_rare diseases +MONDO:0100378 rare diseases +MONDO:0100379 gard_rare diseases +MONDO:0100379 nord_rare diseases +MONDO:0100379 rare diseases +MONDO:0100380 gard_rare diseases +MONDO:0100380 rare diseases +MONDO:0100381 gard_rare diseases +MONDO:0100381 rare diseases +MONDO:0100382 gard_rare diseases +MONDO:0100382 rare diseases +MONDO:0100383 gard_rare diseases +MONDO:0100383 rare diseases +MONDO:0100384 gard_rare diseases +MONDO:0100384 rare diseases +MONDO:0100385 gard_rare diseases +MONDO:0100385 rare diseases +MONDO:0100386 gard_rare diseases +MONDO:0100386 nord_rare diseases +MONDO:0100386 rare diseases +MONDO:0100387 gard_rare diseases +MONDO:0100387 rare diseases +MONDO:0100388 gard_rare diseases +MONDO:0100388 rare diseases +MONDO:0100389 gard_rare diseases +MONDO:0100389 rare diseases +MONDO:0100390 gard_rare diseases +MONDO:0100390 rare diseases +MONDO:0100391 gard_rare diseases +MONDO:0100391 rare diseases +MONDO:0100392 gard_rare diseases +MONDO:0100392 rare diseases +MONDO:0100393 gard_rare diseases +MONDO:0100393 rare diseases +MONDO:0100394 gard_rare diseases +MONDO:0100394 rare diseases +MONDO:0100395 gard_rare diseases +MONDO:0100395 nord_rare diseases +MONDO:0100395 rare diseases +MONDO:0100396 gard_rare diseases +MONDO:0100396 rare diseases +MONDO:0100397 gard_rare diseases +MONDO:0100397 rare diseases +MONDO:0100398 gard_rare diseases +MONDO:0100398 rare diseases +MONDO:0100399 gard_rare diseases +MONDO:0100399 rare diseases +MONDO:0100400 gard_rare diseases +MONDO:0100400 rare diseases +MONDO:0100401 gard_rare diseases +MONDO:0100401 rare diseases +MONDO:0100402 gard_rare diseases +MONDO:0100402 rare diseases +MONDO:0100403 gard_rare diseases +MONDO:0100403 nord_rare diseases +MONDO:0100403 rare diseases +MONDO:0100404 gard_rare diseases +MONDO:0100404 rare diseases +MONDO:0100405 gard_rare diseases +MONDO:0100405 rare diseases +MONDO:0100406 gard_rare diseases +MONDO:0100406 rare diseases +MONDO:0100407 gard_rare diseases +MONDO:0100407 rare diseases +MONDO:0100408 gard_rare diseases +MONDO:0100408 rare diseases +MONDO:0100409 gard_rare diseases +MONDO:0100409 otar diseases +MONDO:0100409 rare diseases +MONDO:0100410 gard_rare diseases +MONDO:0100410 rare diseases +MONDO:0100412 gard_rare diseases +MONDO:0100412 nord_rare diseases +MONDO:0100412 rare diseases +MONDO:0100413 gard_rare diseases +MONDO:0100413 rare diseases +MONDO:0100414 gard_rare diseases +MONDO:0100414 nord_rare diseases +MONDO:0100414 rare diseases +MONDO:0100415 gard_rare diseases +MONDO:0100415 rare diseases +MONDO:0100416 gard_rare diseases +MONDO:0100416 rare diseases +MONDO:0100417 gard_rare diseases +MONDO:0100417 rare diseases +MONDO:0100418 gard_rare diseases +MONDO:0100418 rare diseases +MONDO:0100419 gard_rare diseases +MONDO:0100419 rare diseases +MONDO:0100420 gard_rare diseases +MONDO:0100420 rare diseases +MONDO:0100421 gard_rare diseases +MONDO:0100421 rare diseases +MONDO:0100422 gard_rare diseases +MONDO:0100422 rare diseases +MONDO:0100423 gard_rare diseases +MONDO:0100423 rare diseases +MONDO:0100424 gard_rare diseases +MONDO:0100424 rare diseases +MONDO:0100425 gard_rare diseases +MONDO:0100425 rare diseases +MONDO:0100428 gard_rare diseases +MONDO:0100428 rare diseases +MONDO:0100429 gard_rare diseases +MONDO:0100429 nord_rare diseases +MONDO:0100429 ordo_disorder diseases +MONDO:0100429 orphanet_rare diseases +MONDO:0100429 rare diseases +MONDO:0100431 gard_rare diseases +MONDO:0100431 otar diseases +MONDO:0100431 rare diseases +MONDO:0100432 clingen diseases +MONDO:0100433 clingen diseases +MONDO:0100433 gard_rare diseases +MONDO:0100433 nord_rare diseases +MONDO:0100433 rare diseases +MONDO:0100435 clingen diseases +MONDO:0100435 gard_rare diseases +MONDO:0100435 nord_rare diseases +MONDO:0100435 rare diseases +MONDO:0100437 clingen diseases +MONDO:0100437 gard_rare diseases +MONDO:0100437 rare diseases +MONDO:0100438 clingen diseases +MONDO:0100438 gard_rare diseases +MONDO:0100438 rare diseases +MONDO:0100439 gard_rare diseases +MONDO:0100439 rare diseases +MONDO:0100441 clingen diseases +MONDO:0100441 gard_rare diseases +MONDO:0100441 rare diseases +MONDO:0100442 clingen diseases +MONDO:0100442 gard_rare diseases +MONDO:0100442 nord_rare diseases +MONDO:0100442 rare diseases +MONDO:0100443 clingen diseases +MONDO:0100443 gard_rare diseases +MONDO:0100443 nord_rare diseases +MONDO:0100443 otar diseases +MONDO:0100443 rare diseases +MONDO:0100444 clingen diseases +MONDO:0100444 gard_rare diseases +MONDO:0100444 otar diseases +MONDO:0100444 rare diseases +MONDO:0100445 clingen diseases +MONDO:0100445 gard_rare diseases +MONDO:0100445 rare diseases +MONDO:0100446 clingen diseases +MONDO:0100446 gard_rare diseases +MONDO:0100446 rare diseases +MONDO:0100447 clingen diseases +MONDO:0100447 gard_rare diseases +MONDO:0100447 rare diseases +MONDO:0100448 clingen diseases +MONDO:0100448 gard_rare diseases +MONDO:0100448 nord_rare diseases +MONDO:0100448 rare diseases +MONDO:0100449 clingen diseases +MONDO:0100449 gard_rare diseases +MONDO:0100449 nord_rare diseases +MONDO:0100449 otar diseases +MONDO:0100449 rare diseases +MONDO:0100450 clingen diseases +MONDO:0100450 gard_rare diseases +MONDO:0100450 nord_rare diseases +MONDO:0100450 ordo_disorder diseases +MONDO:0100450 orphanet_rare diseases +MONDO:0100450 rare diseases +MONDO:0100451 clingen diseases +MONDO:0100451 gard_rare diseases +MONDO:0100451 rare diseases +MONDO:0100452 clingen diseases +MONDO:0100452 gard_rare diseases +MONDO:0100452 nord_rare diseases +MONDO:0100452 rare diseases +MONDO:0100453 clingen diseases +MONDO:0100453 gard_rare diseases +MONDO:0100453 rare diseases +MONDO:0100454 gard_rare diseases +MONDO:0100454 nord_rare diseases +MONDO:0100454 rare diseases +MONDO:0100455 clingen diseases +MONDO:0100455 gard_rare diseases +MONDO:0100455 otar diseases +MONDO:0100455 rare diseases +MONDO:0100456 clingen diseases +MONDO:0100456 inferred_rare diseases +MONDO:0100456 rare diseases +MONDO:0100457 gard_rare diseases +MONDO:0100457 rare diseases +MONDO:0100458 clingen diseases +MONDO:0100462 gard_rare diseases +MONDO:0100462 nord_rare diseases +MONDO:0100462 ordo_disorder diseases +MONDO:0100462 orphanet_rare diseases +MONDO:0100462 rare diseases +MONDO:0100463 gard_rare diseases +MONDO:0100463 rare diseases +MONDO:0100464 clingen diseases +MONDO:0100464 gard_rare diseases +MONDO:0100464 otar diseases +MONDO:0100464 rare diseases +MONDO:0100465 clingen diseases +MONDO:0100465 inferred_rare diseases +MONDO:0100465 rare diseases +MONDO:0100466 gard_rare diseases +MONDO:0100466 nord_rare diseases +MONDO:0100466 ordo_disorder diseases +MONDO:0100466 orphanet_rare diseases +MONDO:0100466 rare diseases +MONDO:0100467 gard_rare diseases +MONDO:0100467 nord_rare diseases +MONDO:0100467 rare diseases +MONDO:0100468 gard_rare diseases +MONDO:0100468 rare diseases +MONDO:0100472 clingen diseases +MONDO:0100472 gard_rare diseases +MONDO:0100472 otar diseases +MONDO:0100472 rare diseases +MONDO:0100473 gard_rare diseases +MONDO:0100473 rare diseases +MONDO:0100474 gard_rare diseases +MONDO:0100474 rare diseases +MONDO:0100475 gard_rare diseases +MONDO:0100475 rare diseases +MONDO:0100477 gard_rare diseases +MONDO:0100477 rare diseases +MONDO:0100478 clingen diseases +MONDO:0100479 gard_rare diseases +MONDO:0100479 rare diseases +MONDO:0100480 gard_rare diseases +MONDO:0100480 nord_rare diseases +MONDO:0100480 ordo_disorder diseases +MONDO:0100480 orphanet_rare diseases +MONDO:0100480 rare diseases +MONDO:0100481 gard_rare diseases +MONDO:0100481 rare diseases +MONDO:0100482 gard_rare diseases +MONDO:0100482 rare diseases +MONDO:0100483 gard_rare diseases +MONDO:0100483 rare diseases +MONDO:0100484 clingen diseases +MONDO:0100484 gard_rare diseases +MONDO:0100484 rare diseases +MONDO:0100485 clingen diseases +MONDO:0100487 clingen diseases +MONDO:0100487 gard_rare diseases +MONDO:0100487 nord_rare diseases +MONDO:0100487 rare diseases +MONDO:0100488 gard_rare diseases +MONDO:0100488 rare diseases +MONDO:0100490 gard_rare diseases +MONDO:0100490 nord_rare diseases +MONDO:0100490 rare diseases +MONDO:0100491 gard_rare diseases +MONDO:0100491 nord_rare diseases +MONDO:0100491 ordo_disorder diseases +MONDO:0100491 orphanet_rare diseases +MONDO:0100491 rare diseases +MONDO:0100493 gard_rare diseases +MONDO:0100493 otar diseases +MONDO:0100493 rare diseases +MONDO:0100494 gard_rare diseases +MONDO:0100494 rare diseases +MONDO:0100495 gard_rare diseases +MONDO:0100495 rare diseases +MONDO:0100496 gard_rare diseases +MONDO:0100496 rare diseases +MONDO:0100497 gard_rare diseases +MONDO:0100497 rare diseases +MONDO:0100498 clingen diseases +MONDO:0100498 gard_rare diseases +MONDO:0100498 otar diseases +MONDO:0100498 rare diseases +MONDO:0100499 gard_rare diseases +MONDO:0100499 rare diseases +MONDO:0100501 gard_rare diseases +MONDO:0100501 rare diseases +MONDO:0100502 clingen diseases +MONDO:0100502 gard_rare diseases +MONDO:0100502 rare diseases +MONDO:0100506 clingen diseases +MONDO:0100506 gard_rare diseases +MONDO:0100506 rare diseases +MONDO:0100507 gard_rare diseases +MONDO:0100507 rare diseases +MONDO:0100508 gard_rare diseases +MONDO:0100508 ordo_disorder diseases +MONDO:0100508 orphanet_rare diseases +MONDO:0100508 rare diseases +MONDO:0100509 clingen diseases +MONDO:0100509 gard_rare diseases +MONDO:0100509 otar diseases +MONDO:0100509 rare diseases +MONDO:0100510 gard_rare diseases +MONDO:0100510 nord_rare diseases +MONDO:0100510 otar diseases +MONDO:0100510 rare diseases +MONDO:0100512 disease_grouping diseases +MONDO:0100512 gard_rare diseases +MONDO:0100512 ordo_group_of_disorders diseases +MONDO:0100512 rare diseases +MONDO:0100513 clingen diseases +MONDO:0100514 gard_rare diseases +MONDO:0100514 otar diseases +MONDO:0100514 rare diseases +MONDO:0100515 clingen diseases +MONDO:0100515 gard_rare diseases +MONDO:0100515 otar diseases +MONDO:0100515 rare diseases +MONDO:0100516 clingen diseases +MONDO:0100516 inferred_rare diseases +MONDO:0100516 otar diseases +MONDO:0100516 rare diseases +MONDO:0100517 gard_rare diseases +MONDO:0100517 rare diseases +MONDO:0100520 clingen diseases +MONDO:0100522 gard_rare diseases +MONDO:0100522 rare diseases +MONDO:0100524 gard_rare diseases +MONDO:0100524 rare diseases +MONDO:0100527 gard_rare diseases +MONDO:0100527 ordo_subtype_of_a_disorder diseases +MONDO:0100527 rare diseases +MONDO:0100528 gard_rare diseases +MONDO:0100528 ordo_subtype_of_a_disorder diseases +MONDO:0100528 rare diseases +MONDO:0100529 gard_rare diseases +MONDO:0100529 rare diseases +MONDO:0100530 gard_rare diseases +MONDO:0100530 rare diseases +MONDO:0100531 gard_rare diseases +MONDO:0100531 rare diseases +MONDO:0100534 gard_rare diseases +MONDO:0100534 rare diseases +MONDO:0100535 gard_rare diseases +MONDO:0100535 rare diseases +MONDO:0100536 gard_rare diseases +MONDO:0100536 rare diseases +MONDO:0100537 gard_rare diseases +MONDO:0100537 rare diseases +MONDO:0100538 gard_rare diseases +MONDO:0100538 rare diseases +MONDO:0100539 gard_rare diseases +MONDO:0100539 rare diseases +MONDO:0100542 gard_rare diseases +MONDO:0100542 rare diseases +MONDO:0100543 gard_rare diseases +MONDO:0100543 rare diseases +MONDO:0100544 gard_rare diseases +MONDO:0100544 rare diseases +MONDO:0100546 gard_rare diseases +MONDO:0100546 rare diseases +MONDO:0100550 gard_rare diseases +MONDO:0100550 rare diseases +MONDO:0100551 inferred_rare diseases +MONDO:0100551 rare diseases +MONDO:0100552 gard_rare diseases +MONDO:0100552 ordo_disorder diseases +MONDO:0100552 orphanet_rare diseases +MONDO:0100552 rare diseases +MONDO:0100553 gard_rare diseases +MONDO:0100553 rare diseases +MONDO:0100554 gard_rare diseases +MONDO:0100554 rare diseases +MONDO:0100559 gard_rare diseases +MONDO:0100559 rare diseases +MONDO:0100561 gard_rare diseases +MONDO:0100561 rare diseases +MONDO:0100562 gard_rare diseases +MONDO:0100562 rare diseases +MONDO:0100563 gard_rare diseases +MONDO:0100563 rare diseases +MONDO:0100564 gard_rare diseases +MONDO:0100564 rare diseases +MONDO:0100565 gard_rare diseases +MONDO:0100565 rare diseases +MONDO:0100566 gard_rare diseases +MONDO:0100566 ordo_disorder diseases +MONDO:0100566 orphanet_rare diseases +MONDO:0100566 rare diseases +MONDO:0100567 gard_rare diseases +MONDO:0100567 ordo_disorder diseases +MONDO:0100567 orphanet_rare diseases +MONDO:0100567 rare diseases +MONDO:0100569 gard_rare diseases +MONDO:0100569 rare diseases +MONDO:0100570 gard_rare diseases +MONDO:0100570 rare diseases +MONDO:0200000 gard_rare diseases +MONDO:0200000 rare diseases +MONDO:0300000 gard_rare diseases +MONDO:0300000 rare diseases +MONDO:0400004 gard_rare diseases +MONDO:0400004 nord_rare diseases +MONDO:0400004 rare diseases +MONDO:0500000 gard_rare diseases +MONDO:0500000 nord_rare diseases +MONDO:0500000 rare diseases +MONDO:0550003 clingen diseases +MONDO:0550003 gard_rare diseases +MONDO:0550003 rare diseases +MONDO:0600001 clingen diseases +MONDO:0600001 gard_rare diseases +MONDO:0600001 mondo_rare diseases +MONDO:0600001 otar diseases +MONDO:0600001 rare diseases +MONDO:0600002 otar diseases +MONDO:0600003 gard_rare diseases +MONDO:0600003 mondo_rare diseases +MONDO:0600003 rare diseases +MONDO:0600009 gard_rare diseases +MONDO:0600009 rare diseases +MONDO:0600010 gard_rare diseases +MONDO:0600010 rare diseases +MONDO:0600011 gard_rare diseases +MONDO:0600011 rare diseases +MONDO:0600014 gard_rare diseases +MONDO:0600014 rare diseases +MONDO:0600016 gard_rare diseases +MONDO:0600016 nord_rare diseases +MONDO:0600016 rare diseases +MONDO:0600017 gard_rare diseases +MONDO:0600017 rare diseases +MONDO:0600018 gard_rare diseases +MONDO:0600018 rare diseases +MONDO:0600019 gard_rare diseases +MONDO:0600019 rare diseases +MONDO:0600023 gard_rare diseases +MONDO:0600023 otar diseases +MONDO:0600023 rare diseases +MONDO:0600024 gard_rare diseases +MONDO:0600024 rare diseases +MONDO:0600027 gard_rare diseases +MONDO:0600027 rare diseases +MONDO:0600030 gard_rare diseases +MONDO:0600030 nord_rare diseases +MONDO:0600030 ordo_subtype_of_a_disorder diseases +MONDO:0600030 otar diseases +MONDO:0600030 rare diseases +MONDO:0700000 clingen diseases +MONDO:0700000 gard_rare diseases +MONDO:0700000 nord_rare diseases +MONDO:0700000 otar diseases +MONDO:0700000 rare diseases +MONDO:0700002 clingen diseases +MONDO:0700002 otar diseases +MONDO:0700003 harrisons_view diseases +MONDO:0700003 otar diseases +MONDO:0700003 rare_grouping diseases +MONDO:0700008 gard_rare diseases +MONDO:0700008 rare diseases +MONDO:0700009 gard_rare diseases +MONDO:0700009 rare diseases +MONDO:0700010 gard_rare diseases +MONDO:0700010 rare diseases +MONDO:0700011 gard_rare diseases +MONDO:0700011 rare diseases +MONDO:0700012 gard_rare diseases +MONDO:0700012 rare diseases +MONDO:0700013 gard_rare diseases +MONDO:0700013 rare diseases +MONDO:0700014 gard_rare diseases +MONDO:0700014 rare diseases +MONDO:0700015 gard_rare diseases +MONDO:0700015 rare diseases +MONDO:0700016 gard_rare diseases +MONDO:0700016 rare diseases +MONDO:0700017 gard_rare diseases +MONDO:0700017 rare diseases +MONDO:0700018 gard_rare diseases +MONDO:0700018 rare diseases +MONDO:0700019 gard_rare diseases +MONDO:0700019 rare diseases +MONDO:0700020 gard_rare diseases +MONDO:0700020 rare diseases +MONDO:0700021 gard_rare diseases +MONDO:0700021 rare diseases +MONDO:0700022 gard_rare diseases +MONDO:0700022 rare diseases +MONDO:0700023 gard_rare diseases +MONDO:0700023 rare diseases +MONDO:0700024 gard_rare diseases +MONDO:0700024 rare diseases +MONDO:0700025 gard_rare diseases +MONDO:0700025 rare diseases +MONDO:0700026 gard_rare diseases +MONDO:0700026 rare diseases +MONDO:0700027 gard_rare diseases +MONDO:0700027 otar diseases +MONDO:0700027 rare diseases +MONDO:0700028 gard_rare diseases +MONDO:0700028 rare diseases +MONDO:0700029 gard_rare diseases +MONDO:0700029 rare diseases +MONDO:0700030 gard_rare diseases +MONDO:0700030 nord_rare diseases +MONDO:0700030 rare diseases +MONDO:0700031 gard_rare diseases +MONDO:0700031 rare diseases +MONDO:0700032 gard_rare diseases +MONDO:0700032 rare diseases +MONDO:0700033 gard_rare diseases +MONDO:0700033 rare diseases +MONDO:0700034 gard_rare diseases +MONDO:0700034 rare diseases +MONDO:0700035 gard_rare diseases +MONDO:0700035 rare diseases +MONDO:0700037 gard_rare diseases +MONDO:0700037 mondo_rare diseases +MONDO:0700037 rare diseases +MONDO:0700039 gard_rare diseases +MONDO:0700039 nord_rare diseases +MONDO:0700039 rare diseases +MONDO:0700041 inferred_rare diseases +MONDO:0700041 rare diseases +MONDO:0700043 gard_rare diseases +MONDO:0700043 rare diseases +MONDO:0700044 inferred_rare diseases +MONDO:0700044 rare diseases +MONDO:0700047 gard_rare diseases +MONDO:0700047 rare diseases +MONDO:0700054 clingen diseases +MONDO:0700054 gard_rare diseases +MONDO:0700054 rare diseases +MONDO:0700055 otar diseases +MONDO:0700060 gard_rare diseases +MONDO:0700060 rare diseases +MONDO:0700064 gard_rare diseases +MONDO:0700064 otar diseases +MONDO:0700064 rare diseases +MONDO:0700065 gard_rare diseases +MONDO:0700065 otar diseases +MONDO:0700065 rare diseases +MONDO:0700066 clingen diseases +MONDO:0700066 gard_rare diseases +MONDO:0700066 otar diseases +MONDO:0700066 rare diseases +MONDO:0700067 clingen diseases +MONDO:0700067 gard_rare diseases +MONDO:0700067 otar diseases +MONDO:0700067 rare diseases +MONDO:0700068 clingen diseases +MONDO:0700068 gard_rare diseases +MONDO:0700068 otar diseases +MONDO:0700068 rare diseases +MONDO:0700069 clingen diseases +MONDO:0700069 gard_rare diseases +MONDO:0700069 otar diseases +MONDO:0700069 rare diseases +MONDO:0700070 clingen diseases +MONDO:0700070 gard_rare diseases +MONDO:0700070 otar diseases +MONDO:0700070 rare diseases +MONDO:0700071 clingen diseases +MONDO:0700071 gard_rare diseases +MONDO:0700071 otar diseases +MONDO:0700071 rare diseases +MONDO:0700073 gard_rare diseases +MONDO:0700073 nord_rare diseases +MONDO:0700073 rare diseases +MONDO:0700074 gard_rare diseases +MONDO:0700074 rare diseases +MONDO:0700075 gard_rare diseases +MONDO:0700075 rare diseases +MONDO:0700076 gard_rare diseases +MONDO:0700076 rare diseases +MONDO:0700080 clingen diseases +MONDO:0700080 otar diseases +MONDO:0700081 gard_rare diseases +MONDO:0700081 otar diseases +MONDO:0700081 rare diseases +MONDO:0700082 gard_rare diseases +MONDO:0700082 rare diseases +MONDO:0700083 gard_rare diseases +MONDO:0700083 rare diseases +MONDO:0700084 clingen diseases +MONDO:0700084 gard_rare diseases +MONDO:0700084 otar diseases +MONDO:0700084 rare diseases +MONDO:0700085 gard_rare diseases +MONDO:0700085 rare diseases +MONDO:0700086 gard_rare diseases +MONDO:0700086 otar diseases +MONDO:0700086 rare diseases +MONDO:0700087 gard_rare diseases +MONDO:0700087 nord_rare diseases +MONDO:0700087 otar diseases +MONDO:0700087 rare diseases +MONDO:0700088 gard_rare diseases +MONDO:0700088 nord_rare diseases +MONDO:0700088 ordo_disorder diseases +MONDO:0700088 orphanet_rare diseases +MONDO:0700088 otar diseases +MONDO:0700088 rare diseases +MONDO:0700089 gard_rare diseases +MONDO:0700089 nord_rare diseases +MONDO:0700089 otar diseases +MONDO:0700089 rare diseases +MONDO:0700090 gard_rare diseases +MONDO:0700090 nord_rare diseases +MONDO:0700090 rare diseases +MONDO:0700091 gard_rare diseases +MONDO:0700091 rare diseases +MONDO:0700092 otar diseases +MONDO:0700093 gard_rare diseases +MONDO:0700093 rare diseases +MONDO:0700094 gard_rare diseases +MONDO:0700094 rare diseases +MONDO:0700096 rare_grouping diseases +MONDO:0700107 gard_rare diseases +MONDO:0700107 nord_rare diseases +MONDO:0700107 rare diseases +MONDO:0700112 gard_rare diseases +MONDO:0700112 nord_rare diseases +MONDO:0700112 otar diseases +MONDO:0700112 rare diseases +MONDO:0700116 gard_rare diseases +MONDO:0700116 rare diseases +MONDO:0700117 clingen diseases +MONDO:0700117 gard_rare diseases +MONDO:0700117 nord_rare diseases +MONDO:0700117 otar diseases +MONDO:0700117 rare diseases +MONDO:0700118 gard_rare diseases +MONDO:0700118 rare diseases +MONDO:0700119 gard_rare diseases +MONDO:0700119 rare diseases +MONDO:0700120 otar diseases +MONDO:0700123 clingen diseases +MONDO:0700124 gard_rare diseases +MONDO:0700124 rare diseases +MONDO:0700125 gard_rare diseases +MONDO:0700125 nord_rare diseases +MONDO:0700125 rare diseases +MONDO:0700126 gard_rare diseases +MONDO:0700126 rare diseases +MONDO:0700127 gard_rare diseases +MONDO:0700127 rare diseases +MONDO:0700128 gard_rare diseases +MONDO:0700128 rare diseases +MONDO:0700129 gard_rare diseases +MONDO:0700129 rare diseases +MONDO:0700130 gard_rare diseases +MONDO:0700130 rare diseases +MONDO:0700200 gard_rare diseases +MONDO:0700200 rare diseases +MONDO:0700220 gard_rare diseases +MONDO:0700220 ordo_disorder diseases +MONDO:0700220 orphanet_rare diseases +MONDO:0700220 otar diseases +MONDO:0700220 rare diseases +MONDO:0700221 gard_rare diseases +MONDO:0700221 rare diseases +MONDO:0700222 gard_rare diseases +MONDO:0700222 rare diseases +MONDO:0700223 gard_rare diseases +MONDO:0700223 otar diseases +MONDO:0700223 rare diseases +MONDO:0700224 gard_rare diseases +MONDO:0700224 rare diseases +MONDO:0700226 otar diseases +MONDO:0700227 gard_rare diseases +MONDO:0700227 rare diseases +MONDO:0700228 gard_rare diseases +MONDO:0700228 rare diseases +MONDO:0700229 gard_rare diseases +MONDO:0700229 rare diseases +MONDO:0700231 gard_rare diseases +MONDO:0700231 rare diseases +MONDO:0700232 gard_rare diseases +MONDO:0700232 rare diseases +MONDO:0700233 gard_rare diseases +MONDO:0700233 rare diseases +MONDO:0700234 gard_rare diseases +MONDO:0700234 rare diseases +MONDO:0700235 gard_rare diseases +MONDO:0700235 rare diseases +MONDO:0700236 gard_rare diseases +MONDO:0700236 rare diseases +MONDO:0700237 gard_rare diseases +MONDO:0700237 rare diseases +MONDO:0700238 gard_rare diseases +MONDO:0700238 rare diseases +MONDO:0700239 gard_rare diseases +MONDO:0700239 rare diseases +MONDO:0700240 gard_rare diseases +MONDO:0700240 rare diseases +MONDO:0700241 gard_rare diseases +MONDO:0700241 rare diseases +MONDO:0700242 gard_rare diseases +MONDO:0700242 rare diseases +MONDO:0700243 gard_rare diseases +MONDO:0700243 rare diseases +MONDO:0700244 gard_rare diseases +MONDO:0700244 rare diseases +MONDO:0700245 gard_rare diseases +MONDO:0700245 rare diseases +MONDO:0700247 gard_rare diseases +MONDO:0700247 rare diseases +MONDO:0700248 gard_rare diseases +MONDO:0700248 rare diseases +MONDO:0700249 gard_rare diseases +MONDO:0700249 rare diseases +MONDO:0700250 gard_rare diseases +MONDO:0700250 rare diseases +MONDO:0700253 gard_rare diseases +MONDO:0700253 rare diseases +MONDO:0700256 gard_rare diseases +MONDO:0700256 rare diseases +MONDO:0700257 gard_rare diseases +MONDO:0700257 rare diseases +MONDO:0700258 gard_rare diseases +MONDO:0700258 rare diseases +MONDO:0700259 gard_rare diseases +MONDO:0700259 rare diseases +MONDO:0700260 gard_rare diseases +MONDO:0700260 rare diseases +MONDO:0700261 gard_rare diseases +MONDO:0700261 rare diseases +MONDO:0700262 gard_rare diseases +MONDO:0700262 rare diseases +MONDO:0700263 gard_rare diseases +MONDO:0700263 rare diseases +MONDO:0700264 gard_rare diseases +MONDO:0700264 ordo_group_of_disorders diseases +MONDO:0700264 rare diseases +MONDO:0700267 gard_rare diseases +MONDO:0700267 rare diseases +MONDO:0700268 gard_rare diseases +MONDO:0700268 rare diseases +MONDO:0700269 gard_rare diseases +MONDO:0700269 rare diseases +MONDO:0700270 gard_rare diseases +MONDO:0700270 rare diseases +MONDO:0700271 gard_rare diseases +MONDO:0700271 rare diseases +MONDO:0700272 gard_rare diseases +MONDO:0700272 rare diseases +MONDO:0700273 gard_rare diseases +MONDO:0700273 rare diseases +MONDO:0700274 gard_rare diseases +MONDO:0700274 rare diseases +MONDO:0800025 gard_rare diseases +MONDO:0800025 ordo_disorder diseases +MONDO:0800025 ordo_malformation_syndrome diseases +MONDO:0800025 orphanet_rare diseases +MONDO:0800025 rare diseases +MONDO:0800026 clingen diseases +MONDO:0800026 gard_rare diseases +MONDO:0800026 nord_rare diseases +MONDO:0800026 ordo_disorder diseases +MONDO:0800026 orphanet_rare diseases +MONDO:0800026 rare diseases +MONDO:0800027 gard_rare diseases +MONDO:0800027 nord_rare diseases +MONDO:0800027 ordo_disorder diseases +MONDO:0800027 orphanet_rare diseases +MONDO:0800027 rare diseases +MONDO:0800028 gard_rare diseases +MONDO:0800028 nord_rare diseases +MONDO:0800028 ordo_disorder diseases +MONDO:0800028 orphanet_rare diseases +MONDO:0800028 rare diseases +MONDO:0800029 clingen diseases +MONDO:0800029 gard_rare diseases +MONDO:0800029 nord_rare diseases +MONDO:0800029 ordo_disorder diseases +MONDO:0800029 orphanet_rare diseases +MONDO:0800029 rare diseases +MONDO:0800030 gard_rare diseases +MONDO:0800030 nord_rare diseases +MONDO:0800030 ordo_disorder diseases +MONDO:0800030 orphanet_rare diseases +MONDO:0800030 rare diseases +MONDO:0800032 gard_rare diseases +MONDO:0800032 rare diseases +MONDO:0800033 gard_rare diseases +MONDO:0800033 rare diseases +MONDO:0800034 gard_rare diseases +MONDO:0800034 rare diseases +MONDO:0800035 gard_rare diseases +MONDO:0800035 rare diseases +MONDO:0800036 gard_rare diseases +MONDO:0800036 rare diseases +MONDO:0800037 gard_rare diseases +MONDO:0800037 rare diseases +MONDO:0800038 gard_rare diseases +MONDO:0800038 rare diseases +MONDO:0800039 gard_rare diseases +MONDO:0800039 rare diseases +MONDO:0800040 gard_rare diseases +MONDO:0800040 rare diseases +MONDO:0800041 gard_rare diseases +MONDO:0800041 rare diseases +MONDO:0800042 gard_rare diseases +MONDO:0800042 rare diseases +MONDO:0800043 gard_rare diseases +MONDO:0800043 nord_rare diseases +MONDO:0800043 ordo_disorder diseases +MONDO:0800043 ordo_malformation_syndrome diseases +MONDO:0800043 orphanet_rare diseases +MONDO:0800043 rare diseases +MONDO:0800044 clingen diseases +MONDO:0800044 gard_rare diseases +MONDO:0800044 nord_rare diseases +MONDO:0800044 ordo_disorder diseases +MONDO:0800044 orphanet_rare diseases +MONDO:0800044 rare diseases +MONDO:0800045 gard_rare diseases +MONDO:0800045 nord_rare diseases +MONDO:0800045 ordo_disorder diseases +MONDO:0800045 orphanet_rare diseases +MONDO:0800045 rare diseases +MONDO:0800046 gard_rare diseases +MONDO:0800046 nord_rare diseases +MONDO:0800046 ordo_disorder diseases +MONDO:0800046 orphanet_rare diseases +MONDO:0800046 rare diseases +MONDO:0800047 clingen diseases +MONDO:0800047 gard_rare diseases +MONDO:0800047 nord_rare diseases +MONDO:0800047 rare diseases +MONDO:0800063 gard_rare diseases +MONDO:0800063 rare diseases +MONDO:0800064 gard_rare diseases +MONDO:0800064 rare diseases +MONDO:0800066 gard_rare diseases +MONDO:0800066 rare diseases +MONDO:0800080 gard_rare diseases +MONDO:0800080 rare diseases +MONDO:0800088 gard_rare diseases +MONDO:0800088 ordo_group_of_disorders diseases +MONDO:0800088 otar diseases +MONDO:0800088 rare diseases +MONDO:0800096 gard_rare diseases +MONDO:0800096 otar diseases +MONDO:0800096 rare diseases +MONDO:0800098 clingen diseases +MONDO:0800098 gard_rare diseases +MONDO:0800098 rare diseases +MONDO:0800099 clingen diseases +MONDO:0800099 gard_rare diseases +MONDO:0800099 rare diseases +MONDO:0800100 gard_rare diseases +MONDO:0800100 rare diseases +MONDO:0800101 clingen diseases +MONDO:0800101 gard_rare diseases +MONDO:0800101 rare diseases +MONDO:0800102 clingen diseases +MONDO:0800102 gard_rare diseases +MONDO:0800102 rare diseases +MONDO:0800103 gard_rare diseases +MONDO:0800103 nord_rare diseases +MONDO:0800103 rare diseases +MONDO:0800104 gard_rare diseases +MONDO:0800104 nord_rare diseases +MONDO:0800104 rare diseases +MONDO:0800109 gard_rare diseases +MONDO:0800109 rare diseases +MONDO:0800110 gard_rare diseases +MONDO:0800110 rare diseases +MONDO:0800111 gard_rare diseases +MONDO:0800111 rare diseases +MONDO:0800112 obsoletion_candidate diseases +MONDO:0800113 gard_rare diseases +MONDO:0800113 otar diseases +MONDO:0800113 rare diseases +MONDO:0800114 gard_rare diseases +MONDO:0800114 rare diseases +MONDO:0800121 gard_rare diseases +MONDO:0800121 rare diseases +MONDO:0800123 gard_rare diseases +MONDO:0800123 rare diseases +MONDO:0800124 gard_rare diseases +MONDO:0800124 rare diseases +MONDO:0800125 gard_rare diseases +MONDO:0800125 rare diseases +MONDO:0800127 gard_rare diseases +MONDO:0800127 rare diseases +MONDO:0800128 gard_rare diseases +MONDO:0800128 nord_rare diseases +MONDO:0800128 rare diseases +MONDO:0800129 gard_rare diseases +MONDO:0800129 nord_rare diseases +MONDO:0800129 rare diseases +MONDO:0800130 gard_rare diseases +MONDO:0800130 nord_rare diseases +MONDO:0800130 rare diseases +MONDO:0800131 gard_rare diseases +MONDO:0800131 nord_rare diseases +MONDO:0800131 rare diseases +MONDO:0800133 gard_rare diseases +MONDO:0800133 nord_rare diseases +MONDO:0800133 rare diseases +MONDO:0800135 gard_rare diseases +MONDO:0800135 rare diseases +MONDO:0800136 gard_rare diseases +MONDO:0800136 nord_rare diseases +MONDO:0800136 rare diseases +MONDO:0800137 gard_rare diseases +MONDO:0800137 nord_rare diseases +MONDO:0800137 rare diseases +MONDO:0800139 clingen diseases +MONDO:0800139 gard_rare diseases +MONDO:0800139 nord_rare diseases +MONDO:0800139 rare diseases +MONDO:0800140 gard_rare diseases +MONDO:0800140 nord_rare diseases +MONDO:0800140 rare diseases +MONDO:0800141 gard_rare diseases +MONDO:0800141 nord_rare diseases +MONDO:0800141 rare diseases +MONDO:0800145 clingen diseases +MONDO:0800145 gard_rare diseases +MONDO:0800145 rare diseases +MONDO:0800146 gard_rare diseases +MONDO:0800146 nord_rare diseases +MONDO:0800146 rare diseases +MONDO:0800147 gard_rare diseases +MONDO:0800147 nord_rare diseases +MONDO:0800147 rare diseases +MONDO:0800148 gard_rare diseases +MONDO:0800148 nord_rare diseases +MONDO:0800148 rare diseases +MONDO:0800149 gard_rare diseases +MONDO:0800149 rare diseases +MONDO:0800152 gard_rare diseases +MONDO:0800152 rare diseases +MONDO:0800153 gard_rare diseases +MONDO:0800153 rare diseases +MONDO:0800154 gard_rare diseases +MONDO:0800154 rare diseases +MONDO:0800155 gard_rare diseases +MONDO:0800155 rare diseases +MONDO:0800156 gard_rare diseases +MONDO:0800156 rare diseases +MONDO:0800157 gard_rare diseases +MONDO:0800157 rare diseases +MONDO:0800158 gard_rare diseases +MONDO:0800158 rare diseases +MONDO:0800159 gard_rare diseases +MONDO:0800159 otar diseases +MONDO:0800159 rare diseases +MONDO:0800166 gard_rare diseases +MONDO:0800166 nord_rare diseases +MONDO:0800166 otar diseases +MONDO:0800166 rare diseases +MONDO:0800167 clingen diseases +MONDO:0800167 gard_rare diseases +MONDO:0800167 nord_rare diseases +MONDO:0800167 ordo_disorder diseases +MONDO:0800167 ordo_malformation_syndrome diseases +MONDO:0800167 orphanet_rare diseases +MONDO:0800167 otar diseases +MONDO:0800167 rare diseases +MONDO:0800175 gard_rare diseases +MONDO:0800175 nord_rare diseases +MONDO:0800175 ordo_disorder diseases +MONDO:0800175 orphanet_rare diseases +MONDO:0800175 rare diseases +MONDO:0800180 clingen diseases +MONDO:0800180 gard_rare diseases +MONDO:0800180 otar diseases +MONDO:0800180 rare diseases +MONDO:0800181 clingen diseases +MONDO:0800181 gard_rare diseases +MONDO:0800181 otar diseases +MONDO:0800181 rare diseases +MONDO:0800182 clingen diseases +MONDO:0800182 gard_rare diseases +MONDO:0800182 rare diseases +MONDO:0800183 clingen diseases +MONDO:0800183 gard_rare diseases +MONDO:0800183 otar diseases +MONDO:0800183 rare diseases +MONDO:0800196 gard_rare diseases +MONDO:0800196 nord_rare diseases +MONDO:0800196 rare diseases +MONDO:0800197 gard_rare diseases +MONDO:0800197 rare diseases +MONDO:0800198 gard_rare diseases +MONDO:0800198 nord_rare diseases +MONDO:0800198 rare diseases +MONDO:0800200 gard_rare diseases +MONDO:0800200 rare diseases +MONDO:0800201 gard_rare diseases +MONDO:0800201 nord_rare diseases +MONDO:0800201 rare diseases +MONDO:0800204 gard_rare diseases +MONDO:0800204 nord_rare diseases +MONDO:0800204 rare diseases +MONDO:0800206 gard_rare diseases +MONDO:0800206 rare diseases +MONDO:0800207 gard_rare diseases +MONDO:0800207 otar diseases +MONDO:0800207 rare diseases +MONDO:0800209 gard_rare diseases +MONDO:0800209 rare diseases +MONDO:0800210 gard_rare diseases +MONDO:0800210 rare diseases +MONDO:0800290 gard_rare diseases +MONDO:0800290 rare diseases +MONDO:0800291 gard_rare diseases +MONDO:0800291 nord_rare diseases +MONDO:0800291 rare diseases +MONDO:0800298 gard_rare diseases +MONDO:0800298 rare diseases +MONDO:0800301 gard_rare diseases +MONDO:0800301 rare diseases +MONDO:0800302 gard_rare diseases +MONDO:0800302 nord_rare diseases +MONDO:0800302 rare diseases +MONDO:0800304 gard_rare diseases +MONDO:0800304 rare diseases +MONDO:0800305 gard_rare diseases +MONDO:0800305 rare diseases +MONDO:0800306 gard_rare diseases +MONDO:0800306 rare diseases +MONDO:0800307 gard_rare diseases +MONDO:0800307 rare diseases +MONDO:0800308 gard_rare diseases +MONDO:0800308 rare diseases +MONDO:0800311 gard_rare diseases +MONDO:0800311 rare diseases +MONDO:0800312 gard_rare diseases +MONDO:0800312 rare diseases +MONDO:0800313 gard_rare diseases +MONDO:0800313 rare diseases +MONDO:0800314 gard_rare diseases +MONDO:0800314 nord_rare diseases +MONDO:0800314 rare diseases +MONDO:0800317 gard_rare diseases +MONDO:0800317 rare diseases +MONDO:0800318 gard_rare diseases +MONDO:0800318 rare diseases +MONDO:0800321 gard_rare diseases +MONDO:0800321 rare diseases +MONDO:0800323 gard_rare diseases +MONDO:0800323 rare diseases +MONDO:0800324 gard_rare diseases +MONDO:0800324 rare diseases +MONDO:0800326 gard_rare diseases +MONDO:0800326 rare diseases +MONDO:0800328 gard_rare diseases +MONDO:0800328 rare diseases +MONDO:0800330 gard_rare diseases +MONDO:0800330 rare diseases +MONDO:0800331 gard_rare diseases +MONDO:0800331 rare diseases +MONDO:0800335 gard_rare diseases +MONDO:0800335 rare diseases +MONDO:0800339 gard_rare diseases +MONDO:0800339 rare diseases +MONDO:0800341 gard_rare diseases +MONDO:0800341 rare diseases +MONDO:0800345 gard_rare diseases +MONDO:0800345 rare diseases +MONDO:0800346 gard_rare diseases +MONDO:0800346 rare diseases +MONDO:0800347 gard_rare diseases +MONDO:0800347 rare diseases +MONDO:0800348 gard_rare diseases +MONDO:0800348 rare diseases +MONDO:0800349 gard_rare diseases +MONDO:0800349 rare diseases +MONDO:0800350 gard_rare diseases +MONDO:0800350 rare diseases +MONDO:0800351 gard_rare diseases +MONDO:0800351 rare diseases +MONDO:0800352 gard_rare diseases +MONDO:0800352 nord_rare diseases +MONDO:0800352 rare diseases +MONDO:0800353 gard_rare diseases +MONDO:0800353 rare diseases +MONDO:0800356 gard_rare diseases +MONDO:0800356 nord_rare diseases +MONDO:0800356 rare diseases +MONDO:0800357 gard_rare diseases +MONDO:0800357 rare diseases +MONDO:0800359 gard_rare diseases +MONDO:0800359 nord_rare diseases +MONDO:0800359 rare diseases +MONDO:0800363 gard_rare diseases +MONDO:0800363 rare diseases +MONDO:0800364 gard_rare diseases +MONDO:0800364 rare diseases +MONDO:0800365 gard_rare diseases +MONDO:0800365 nord_rare diseases +MONDO:0800365 otar diseases +MONDO:0800365 rare diseases +MONDO:0800366 gard_rare diseases +MONDO:0800366 rare diseases +MONDO:0800367 gard_rare diseases +MONDO:0800367 nord_rare diseases +MONDO:0800367 rare diseases +MONDO:0800368 gard_rare diseases +MONDO:0800368 nord_rare diseases +MONDO:0800368 rare diseases +MONDO:0800369 gard_rare diseases +MONDO:0800369 rare diseases +MONDO:0800370 gard_rare diseases +MONDO:0800370 nord_rare diseases +MONDO:0800370 rare diseases +MONDO:0800371 gard_rare diseases +MONDO:0800371 rare diseases +MONDO:0800372 gard_rare diseases +MONDO:0800372 nord_rare diseases +MONDO:0800372 rare diseases +MONDO:0800373 otar diseases +MONDO:0800374 gard_rare diseases +MONDO:0800374 rare diseases +MONDO:0800375 gard_rare diseases +MONDO:0800375 nord_rare diseases +MONDO:0800375 rare diseases +MONDO:0800376 gard_rare diseases +MONDO:0800376 nord_rare diseases +MONDO:0800376 rare diseases +MONDO:0800377 gard_rare diseases +MONDO:0800377 rare diseases +MONDO:0800381 gard_rare diseases +MONDO:0800381 rare diseases +MONDO:0800382 gard_rare diseases +MONDO:0800382 rare diseases +MONDO:0800383 gard_rare diseases +MONDO:0800383 nord_rare diseases +MONDO:0800383 rare diseases +MONDO:0800384 gard_rare diseases +MONDO:0800384 rare diseases +MONDO:0800385 gard_rare diseases +MONDO:0800385 rare diseases +MONDO:0800391 clingen diseases +MONDO:0800391 gard_rare diseases +MONDO:0800391 rare diseases +MONDO:0800392 clingen diseases +MONDO:0800392 gard_rare diseases +MONDO:0800392 rare diseases +MONDO:0800393 clingen diseases +MONDO:0800393 gard_rare diseases +MONDO:0800393 rare diseases +MONDO:0800394 clingen diseases +MONDO:0800394 gard_rare diseases +MONDO:0800394 rare diseases +MONDO:0800395 clingen diseases +MONDO:0800395 gard_rare diseases +MONDO:0800395 rare diseases +MONDO:0800396 clingen diseases +MONDO:0800396 gard_rare diseases +MONDO:0800396 rare diseases +MONDO:0800397 clingen diseases +MONDO:0800397 gard_rare diseases +MONDO:0800397 rare diseases +MONDO:0800398 clingen diseases +MONDO:0800398 gard_rare diseases +MONDO:0800398 rare diseases +MONDO:0800399 clingen diseases +MONDO:0800399 gard_rare diseases +MONDO:0800399 rare diseases +MONDO:0800400 clingen diseases +MONDO:0800400 gard_rare diseases +MONDO:0800400 rare diseases +MONDO:0800401 clingen diseases +MONDO:0800401 gard_rare diseases +MONDO:0800401 rare diseases +MONDO:0800402 clingen diseases +MONDO:0800402 gard_rare diseases +MONDO:0800402 rare diseases +MONDO:0800403 clingen diseases +MONDO:0800403 gard_rare diseases +MONDO:0800403 rare diseases +MONDO:0800404 clingen diseases +MONDO:0800404 gard_rare diseases +MONDO:0800404 rare diseases +MONDO:0800405 clingen diseases +MONDO:0800405 gard_rare diseases +MONDO:0800405 rare diseases +MONDO:0800406 clingen diseases +MONDO:0800406 gard_rare diseases +MONDO:0800406 otar diseases +MONDO:0800406 rare diseases +MONDO:0800407 clingen diseases +MONDO:0800407 gard_rare diseases +MONDO:0800407 rare diseases +MONDO:0800418 gard_rare diseases +MONDO:0800418 rare diseases +MONDO:0800419 gard_rare diseases +MONDO:0800419 rare diseases +MONDO:0800420 gard_rare diseases +MONDO:0800420 rare diseases +MONDO:0800423 gard_rare diseases +MONDO:0800423 rare diseases +MONDO:0800424 gard_rare diseases +MONDO:0800424 rare diseases +MONDO:0800433 gard_rare diseases +MONDO:0800433 rare diseases +MONDO:0800434 gard_rare diseases +MONDO:0800434 rare diseases +MONDO:0800435 gard_rare diseases +MONDO:0800435 rare diseases +MONDO:0800436 gard_rare diseases +MONDO:0800436 ordo_disorder diseases +MONDO:0800436 ordo_malformation_syndrome diseases +MONDO:0800436 orphanet_rare diseases +MONDO:0800436 rare diseases +MONDO:0800437 gard_rare diseases +MONDO:0800437 ordo_malformation_syndrome diseases +MONDO:0800437 rare diseases +MONDO:0800438 gard_rare diseases +MONDO:0800438 ordo_disorder diseases +MONDO:0800438 ordo_malformation_syndrome diseases +MONDO:0800438 orphanet_rare diseases +MONDO:0800438 rare diseases +MONDO:0800439 clingen diseases +MONDO:0800439 inferred_rare diseases +MONDO:0800439 rare diseases +MONDO:0800441 clingen diseases +MONDO:0800441 gard_rare diseases +MONDO:0800441 rare diseases +MONDO:0800443 inferred_rare diseases +MONDO:0800443 rare diseases +MONDO:0800445 gard_rare diseases +MONDO:0800445 ordo_disorder diseases +MONDO:0800445 ordo_malformation_syndrome diseases +MONDO:0800445 orphanet_rare diseases +MONDO:0800445 rare diseases +MONDO:0800446 gard_rare diseases +MONDO:0800446 ordo_disorder diseases +MONDO:0800446 orphanet_rare diseases +MONDO:0800446 rare diseases +MONDO:0800448 gard_rare diseases +MONDO:0800448 ordo_disorder diseases +MONDO:0800448 orphanet_rare diseases +MONDO:0800448 otar diseases +MONDO:0800448 rare diseases +MONDO:0800449 gard_rare diseases +MONDO:0800449 ordo_disorder diseases +MONDO:0800449 orphanet_rare diseases +MONDO:0800449 rare diseases +MONDO:0800451 gard_rare diseases +MONDO:0800451 rare diseases +MONDO:0800452 gard_rare diseases +MONDO:0800452 ordo_disorder diseases +MONDO:0800452 orphanet_rare diseases +MONDO:0800452 rare diseases +MONDO:0800453 gard_rare diseases +MONDO:0800453 ordo_disorder diseases +MONDO:0800453 orphanet_rare diseases +MONDO:0800453 rare diseases +MONDO:0800458 gard_rare diseases +MONDO:0800458 rare diseases +MONDO:0800460 gard_rare diseases +MONDO:0800460 rare diseases +MONDO:0800462 gard_rare diseases +MONDO:0800462 rare diseases +MONDO:0800463 gard_rare diseases +MONDO:0800463 rare diseases +MONDO:0800464 gard_rare diseases +MONDO:0800464 rare diseases +MONDO:0800465 gard_rare diseases +MONDO:0800465 rare diseases +MONDO:0800467 gard_rare diseases +MONDO:0800467 rare diseases +MONDO:0800468 gard_rare diseases +MONDO:0800468 rare diseases +MONDO:0800469 gard_rare diseases +MONDO:0800469 rare diseases +MONDO:0800470 gard_rare diseases +MONDO:0800470 rare diseases +MONDO:0800472 gard_rare diseases +MONDO:0800472 rare diseases +MONDO:0800475 inferred_rare diseases +MONDO:0800475 rare diseases +MONDO:0800479 gard_rare diseases +MONDO:0800479 rare diseases +MONDO:0800480 gard_rare diseases +MONDO:0800480 rare diseases +MONDO:0800483 gard_rare diseases +MONDO:0800483 rare diseases +MONDO:0800484 gard_rare diseases +MONDO:0800484 rare diseases +MONDO:0800485 gard_rare diseases +MONDO:0800485 rare diseases +MONDO:0850001 gard_rare diseases +MONDO:0850001 ordo_disorder diseases +MONDO:0850001 orphanet_rare diseases +MONDO:0850001 rare diseases +MONDO:0850007 gard_rare diseases +MONDO:0850007 ordo_group_of_disorders diseases +MONDO:0850007 rare diseases +MONDO:0850008 gard_rare diseases +MONDO:0850008 ordo_group_of_disorders diseases +MONDO:0850008 rare diseases +MONDO:0850009 gard_rare diseases +MONDO:0850009 ordo_group_of_disorders diseases +MONDO:0850009 rare diseases +MONDO:0850010 gard_rare diseases +MONDO:0850010 ordo_group_of_disorders diseases +MONDO:0850010 rare diseases +MONDO:0850013 gard_rare diseases +MONDO:0850013 nord_rare diseases +MONDO:0850013 ordo_disorder diseases +MONDO:0850013 orphanet_rare diseases +MONDO:0850013 rare diseases +MONDO:0850014 gard_rare diseases +MONDO:0850014 nord_rare diseases +MONDO:0850014 ordo_disorder diseases +MONDO:0850014 orphanet_rare diseases +MONDO:0850014 rare diseases +MONDO:0850015 gard_rare diseases +MONDO:0850015 nord_rare diseases +MONDO:0850015 ordo_disorder diseases +MONDO:0850015 orphanet_rare diseases +MONDO:0850015 rare diseases +MONDO:0850030 gard_rare diseases +MONDO:0850030 ordo_group_of_disorders diseases +MONDO:0850030 rare diseases +MONDO:0850046 gard_rare diseases +MONDO:0850046 nord_rare diseases +MONDO:0850046 ordo_disorder diseases +MONDO:0850046 orphanet_rare diseases +MONDO:0850046 rare diseases +MONDO:0850048 gard_rare diseases +MONDO:0850048 nord_rare diseases +MONDO:0850048 ordo_disorder diseases +MONDO:0850048 orphanet_rare diseases +MONDO:0850048 rare diseases +MONDO:0850049 gard_rare diseases +MONDO:0850049 nord_rare diseases +MONDO:0850049 ordo_disorder diseases +MONDO:0850049 orphanet_rare diseases +MONDO:0850049 rare diseases +MONDO:0850050 gard_rare diseases +MONDO:0850050 nord_rare diseases +MONDO:0850050 ordo_disorder diseases +MONDO:0850050 orphanet_rare diseases +MONDO:0850050 rare diseases +MONDO:0850053 gard_rare diseases +MONDO:0850053 ordo_disorder diseases +MONDO:0850053 orphanet_rare diseases +MONDO:0850053 rare diseases +MONDO:0850054 gard_rare diseases +MONDO:0850054 ordo_subtype_of_a_disorder diseases +MONDO:0850054 rare diseases +MONDO:0850058 gard_rare diseases +MONDO:0850058 nord_rare diseases +MONDO:0850058 ordo_disorder diseases +MONDO:0850058 orphanet_rare diseases +MONDO:0850058 rare diseases +MONDO:0850059 gard_rare diseases +MONDO:0850059 nord_rare diseases +MONDO:0850059 ordo_disorder diseases +MONDO:0850059 orphanet_rare diseases +MONDO:0850059 rare diseases +MONDO:0850064 gard_rare diseases +MONDO:0850064 ordo_group_of_disorders diseases +MONDO:0850064 rare diseases +MONDO:0850065 gard_rare diseases +MONDO:0850065 ordo_disorder diseases +MONDO:0850065 orphanet_rare diseases +MONDO:0850065 rare diseases +MONDO:0850066 gard_rare diseases +MONDO:0850066 ordo_disorder diseases +MONDO:0850066 orphanet_rare diseases +MONDO:0850066 rare diseases +MONDO:0850067 gard_rare diseases +MONDO:0850067 nord_rare diseases +MONDO:0850067 ordo_disorder diseases +MONDO:0850067 orphanet_rare diseases +MONDO:0850067 rare diseases +MONDO:0850068 gard_rare diseases +MONDO:0850068 nord_rare diseases +MONDO:0850068 ordo_disorder diseases +MONDO:0850068 orphanet_rare diseases +MONDO:0850068 rare diseases +MONDO:0850069 gard_rare diseases +MONDO:0850069 ordo_disorder diseases +MONDO:0850069 orphanet_rare diseases +MONDO:0850069 rare diseases +MONDO:0850070 gard_rare diseases +MONDO:0850070 nord_rare diseases +MONDO:0850070 ordo_disorder diseases +MONDO:0850070 orphanet_rare diseases +MONDO:0850070 rare diseases +MONDO:0850071 gard_rare diseases +MONDO:0850071 nord_rare diseases +MONDO:0850071 ordo_disorder diseases +MONDO:0850071 orphanet_rare diseases +MONDO:0850071 rare diseases +MONDO:0850072 gard_rare diseases +MONDO:0850072 ordo_group_of_disorders diseases +MONDO:0850072 rare diseases +MONDO:0850073 gard_rare diseases +MONDO:0850073 ordo_disorder diseases +MONDO:0850073 orphanet_rare diseases +MONDO:0850073 rare diseases +MONDO:0850074 gard_rare diseases +MONDO:0850074 ordo_disorder diseases +MONDO:0850074 orphanet_rare diseases +MONDO:0850074 rare diseases +MONDO:0850075 gard_rare diseases +MONDO:0850075 ordo_disorder diseases +MONDO:0850075 orphanet_rare diseases +MONDO:0850075 rare diseases +MONDO:0850076 gard_rare diseases +MONDO:0850076 ordo_disorder diseases +MONDO:0850076 orphanet_rare diseases +MONDO:0850076 rare diseases +MONDO:0850077 gard_rare diseases +MONDO:0850077 ordo_group_of_disorders diseases +MONDO:0850077 rare diseases +MONDO:0850078 gard_rare diseases +MONDO:0850078 ordo_disorder diseases +MONDO:0850078 orphanet_rare diseases +MONDO:0850078 rare diseases +MONDO:0850079 gard_rare diseases +MONDO:0850079 ordo_disorder diseases +MONDO:0850079 orphanet_rare diseases +MONDO:0850079 rare diseases +MONDO:0850080 gard_rare diseases +MONDO:0850080 ordo_disorder diseases +MONDO:0850080 orphanet_rare diseases +MONDO:0850080 rare diseases +MONDO:0850081 gard_rare diseases +MONDO:0850081 ordo_disorder diseases +MONDO:0850081 orphanet_rare diseases +MONDO:0850081 rare diseases +MONDO:0850082 gard_rare diseases +MONDO:0850082 ordo_disorder diseases +MONDO:0850082 orphanet_rare diseases +MONDO:0850082 rare diseases +MONDO:0850083 gard_rare diseases +MONDO:0850083 ordo_disorder diseases +MONDO:0850083 orphanet_rare diseases +MONDO:0850083 rare diseases +MONDO:0850084 gard_rare diseases +MONDO:0850084 ordo_disorder diseases +MONDO:0850084 orphanet_rare diseases +MONDO:0850084 rare diseases +MONDO:0850087 gard_rare diseases +MONDO:0850087 nord_rare diseases +MONDO:0850087 ordo_disorder diseases +MONDO:0850087 orphanet_rare diseases +MONDO:0850087 rare diseases +MONDO:0850088 gard_rare diseases +MONDO:0850088 ordo_disorder diseases +MONDO:0850088 orphanet_rare diseases +MONDO:0850088 rare diseases +MONDO:0850089 gard_rare diseases +MONDO:0850089 nord_rare diseases +MONDO:0850089 ordo_disorder diseases +MONDO:0850089 orphanet_rare diseases +MONDO:0850089 rare diseases +MONDO:0850090 gard_rare diseases +MONDO:0850090 nord_rare diseases +MONDO:0850090 ordo_disorder diseases +MONDO:0850090 orphanet_rare diseases +MONDO:0850090 rare diseases +MONDO:0850093 otar diseases +MONDO:0850095 gard_rare diseases +MONDO:0850095 nord_rare diseases +MONDO:0850095 ordo_disorder diseases +MONDO:0850095 orphanet_rare diseases +MONDO:0850095 rare diseases +MONDO:0850096 gard_rare diseases +MONDO:0850096 ordo_disorder diseases +MONDO:0850096 orphanet_rare diseases +MONDO:0850096 rare diseases +MONDO:0850097 gard_rare diseases +MONDO:0850097 nord_rare diseases +MONDO:0850097 ordo_disorder diseases +MONDO:0850097 orphanet_rare diseases +MONDO:0850097 rare diseases +MONDO:0850099 gard_rare diseases +MONDO:0850099 ordo_disorder diseases +MONDO:0850099 orphanet_rare diseases +MONDO:0850099 rare diseases +MONDO:0850100 gard_rare diseases +MONDO:0850100 nord_rare diseases +MONDO:0850100 ordo_disorder diseases +MONDO:0850100 orphanet_rare diseases +MONDO:0850100 rare diseases +MONDO:0850102 gard_rare diseases +MONDO:0850102 nord_rare diseases +MONDO:0850102 ordo_disorder diseases +MONDO:0850102 orphanet_rare diseases +MONDO:0850102 rare diseases +MONDO:0850103 gard_rare diseases +MONDO:0850103 nord_rare diseases +MONDO:0850103 ordo_disorder diseases +MONDO:0850103 orphanet_rare diseases +MONDO:0850103 rare diseases +MONDO:0850104 gard_rare diseases +MONDO:0850104 nord_rare diseases +MONDO:0850104 ordo_disorder diseases +MONDO:0850104 orphanet_rare diseases +MONDO:0850104 rare diseases +MONDO:0850105 gard_rare diseases +MONDO:0850105 nord_rare diseases +MONDO:0850105 ordo_disorder diseases +MONDO:0850105 orphanet_rare diseases +MONDO:0850105 rare diseases +MONDO:0850106 gard_rare diseases +MONDO:0850106 nord_rare diseases +MONDO:0850106 ordo_disorder diseases +MONDO:0850106 orphanet_rare diseases +MONDO:0850106 rare diseases +MONDO:0850107 gard_rare diseases +MONDO:0850107 ordo_disorder diseases +MONDO:0850107 orphanet_rare diseases +MONDO:0850107 rare diseases +MONDO:0850108 gard_rare diseases +MONDO:0850108 nord_rare diseases +MONDO:0850108 ordo_disorder diseases +MONDO:0850108 orphanet_rare diseases +MONDO:0850108 rare diseases +MONDO:0850109 gard_rare diseases +MONDO:0850109 nord_rare diseases +MONDO:0850109 ordo_disorder diseases +MONDO:0850109 orphanet_rare diseases +MONDO:0850109 rare diseases +MONDO:0850112 gard_rare diseases +MONDO:0850112 rare diseases +MONDO:0850115 gard_rare diseases +MONDO:0850115 nord_rare diseases +MONDO:0850115 ordo_disorder diseases +MONDO:0850115 orphanet_rare diseases +MONDO:0850115 rare diseases +MONDO:0850122 gard_rare diseases +MONDO:0850122 rare diseases +MONDO:0850126 inferred_rare diseases +MONDO:0850126 rare diseases +MONDO:0850127 gard_rare diseases +MONDO:0850127 rare diseases +MONDO:0850144 inferred_rare diseases +MONDO:0850144 rare diseases +MONDO:0850151 gard_rare diseases +MONDO:0850151 rare diseases +MONDO:0850156 gard_rare diseases +MONDO:0850156 rare diseases +MONDO:0850157 gard_rare diseases +MONDO:0850157 rare diseases +MONDO:0850160 gard_rare diseases +MONDO:0850160 rare diseases +MONDO:0850161 gard_rare diseases +MONDO:0850161 rare diseases +MONDO:0850162 gard_rare diseases +MONDO:0850162 rare diseases +MONDO:0850170 gard_rare diseases +MONDO:0850170 rare diseases +MONDO:0850196 gard_rare diseases +MONDO:0850196 rare diseases +MONDO:0850197 gard_rare diseases +MONDO:0850197 rare diseases +MONDO:0850198 gard_rare diseases +MONDO:0850198 rare diseases +MONDO:0850199 gard_rare diseases +MONDO:0850199 rare diseases +MONDO:0850200 gard_rare diseases +MONDO:0850200 rare diseases +MONDO:0850225 gard_rare diseases +MONDO:0850225 rare diseases +MONDO:0850267 gard_rare diseases +MONDO:0850267 rare diseases +MONDO:0850269 gard_rare diseases +MONDO:0850269 rare diseases +MONDO:0850271 gard_rare diseases +MONDO:0850271 rare diseases +MONDO:0850301 gard_rare diseases +MONDO:0850301 rare diseases +MONDO:0850302 gard_rare diseases +MONDO:0850302 rare diseases +MONDO:0850303 gard_rare diseases +MONDO:0850303 rare diseases +MONDO:0850312 gard_rare diseases +MONDO:0850312 rare diseases +MONDO:0850332 gard_rare diseases +MONDO:0850332 rare diseases +MONDO:0850333 gard_rare diseases +MONDO:0850333 rare diseases +MONDO:0850335 gard_rare diseases +MONDO:0850335 rare diseases +MONDO:0850338 gard_rare diseases +MONDO:0850338 rare diseases +MONDO:0850339 gard_rare diseases +MONDO:0850339 rare diseases +MONDO:0850340 gard_rare diseases +MONDO:0850340 rare diseases +MONDO:0850346 gard_rare diseases +MONDO:0850346 rare diseases +MONDO:0850347 gard_rare diseases +MONDO:0850347 rare diseases +MONDO:0850349 gard_rare diseases +MONDO:0850349 rare diseases +MONDO:0850368 gard_rare diseases +MONDO:0850368 rare diseases +MONDO:0850388 gard_rare diseases +MONDO:0850388 rare diseases +MONDO:0850415 gard_rare diseases +MONDO:0850415 rare diseases +MONDO:0850417 gard_rare diseases +MONDO:0850417 rare diseases +MONDO:0850418 gard_rare diseases +MONDO:0850418 rare diseases +MONDO:0850419 gard_rare diseases +MONDO:0850419 rare diseases +MONDO:0850426 gard_rare diseases +MONDO:0850426 rare diseases +MONDO:0850449 gard_rare diseases +MONDO:0850449 rare diseases +MONDO:0850450 gard_rare diseases +MONDO:0850450 rare diseases +MONDO:0850451 gard_rare diseases +MONDO:0850451 rare diseases +MONDO:0850452 gard_rare diseases +MONDO:0850452 rare diseases +MONDO:0850459 gard_rare diseases +MONDO:0850459 rare diseases +MONDO:0850461 gard_rare diseases +MONDO:0850461 rare diseases +MONDO:0850468 gard_rare diseases +MONDO:0850468 rare diseases +MONDO:0850469 gard_rare diseases +MONDO:0850469 rare diseases +MONDO:0850470 gard_rare diseases +MONDO:0850470 rare diseases +MONDO:0850471 gard_rare diseases +MONDO:0850471 rare diseases +MONDO:0850472 gard_rare diseases +MONDO:0850472 rare diseases +MONDO:0850473 gard_rare diseases +MONDO:0850473 rare diseases +MONDO:0850492 gard_rare diseases +MONDO:0850492 rare diseases +MONDO:0850495 gard_rare diseases +MONDO:0850495 rare diseases +MONDO:0850514 gard_rare diseases +MONDO:0850514 rare diseases +MONDO:0850519 gard_rare diseases +MONDO:0850519 rare diseases +MONDO:0850812 gard_rare diseases +MONDO:0850812 rare diseases +MONDO:0858916 gard_rare diseases +MONDO:0858916 rare diseases +MONDO:0858939 gard_rare diseases +MONDO:0858939 rare diseases +MONDO:0858940 gard_rare diseases +MONDO:0858940 otar diseases +MONDO:0858940 rare diseases +MONDO:0858956 otar diseases +MONDO:0858958 gard_rare diseases +MONDO:0858958 rare diseases +MONDO:0858960 gard_rare diseases +MONDO:0858960 rare diseases +MONDO:0858967 gard_rare diseases +MONDO:0858967 rare diseases +MONDO:0858997 gard_rare diseases +MONDO:0858997 ordo_disorder diseases +MONDO:0858997 orphanet_rare diseases +MONDO:0858997 rare diseases +MONDO:0858998 gard_rare diseases +MONDO:0858998 ordo_disorder diseases +MONDO:0858998 orphanet_rare diseases +MONDO:0858998 rare diseases +MONDO:0858999 gard_rare diseases +MONDO:0858999 ordo_disorder diseases +MONDO:0858999 orphanet_rare diseases +MONDO:0858999 rare diseases +MONDO:0859000 gard_rare diseases +MONDO:0859000 ordo_disorder diseases +MONDO:0859000 orphanet_rare diseases +MONDO:0859000 rare diseases +MONDO:0859001 gard_rare diseases +MONDO:0859001 ordo_disorder diseases +MONDO:0859001 orphanet_rare diseases +MONDO:0859001 rare diseases +MONDO:0859002 gard_rare diseases +MONDO:0859002 ordo_disorder diseases +MONDO:0859002 orphanet_rare diseases +MONDO:0859002 rare diseases +MONDO:0859003 gard_rare diseases +MONDO:0859003 ordo_disorder diseases +MONDO:0859003 orphanet_rare diseases +MONDO:0859003 rare diseases +MONDO:0859004 gard_rare diseases +MONDO:0859004 ordo_disorder diseases +MONDO:0859004 orphanet_rare diseases +MONDO:0859004 rare diseases +MONDO:0859005 gard_rare diseases +MONDO:0859005 ordo_disorder diseases +MONDO:0859005 orphanet_rare diseases +MONDO:0859005 rare diseases +MONDO:0859006 gard_rare diseases +MONDO:0859006 ordo_disorder diseases +MONDO:0859006 orphanet_rare diseases +MONDO:0859006 rare diseases +MONDO:0859007 gard_rare diseases +MONDO:0859007 ordo_disorder diseases +MONDO:0859007 orphanet_rare diseases +MONDO:0859007 rare diseases +MONDO:0859008 gard_rare diseases +MONDO:0859008 ordo_group_of_disorders diseases +MONDO:0859008 rare diseases +MONDO:0859046 gard_rare diseases +MONDO:0859046 rare diseases +MONDO:0859081 gard_rare diseases +MONDO:0859081 rare diseases +MONDO:0859082 gard_rare diseases +MONDO:0859082 rare diseases +MONDO:0859083 gard_rare diseases +MONDO:0859083 rare diseases +MONDO:0859086 gard_rare diseases +MONDO:0859086 rare diseases +MONDO:0859136 clingen diseases +MONDO:0859136 gard_rare diseases +MONDO:0859136 rare diseases +MONDO:0859139 gard_rare diseases +MONDO:0859139 ordo_disorder diseases +MONDO:0859139 orphanet_rare diseases +MONDO:0859139 rare diseases +MONDO:0859141 gard_rare diseases +MONDO:0859141 rare diseases +MONDO:0859144 gard_rare diseases +MONDO:0859144 rare diseases +MONDO:0859147 gard_rare diseases +MONDO:0859147 rare diseases +MONDO:0859154 gard_rare diseases +MONDO:0859154 nord_rare diseases +MONDO:0859154 rare diseases +MONDO:0859155 gard_rare diseases +MONDO:0859155 rare diseases +MONDO:0859156 gard_rare diseases +MONDO:0859156 rare diseases +MONDO:0859157 gard_rare diseases +MONDO:0859157 rare diseases +MONDO:0859160 gard_rare diseases +MONDO:0859160 rare diseases +MONDO:0859168 gard_rare diseases +MONDO:0859168 rare diseases +MONDO:0859172 gard_rare diseases +MONDO:0859172 rare diseases +MONDO:0859173 gard_rare diseases +MONDO:0859173 rare diseases +MONDO:0859175 gard_rare diseases +MONDO:0859175 rare diseases +MONDO:0859192 gard_rare diseases +MONDO:0859192 rare diseases +MONDO:0859200 gard_rare diseases +MONDO:0859200 ordo_disorder diseases +MONDO:0859200 orphanet_rare diseases +MONDO:0859200 rare diseases +MONDO:0859203 gard_rare diseases +MONDO:0859203 rare diseases +MONDO:0859210 gard_rare diseases +MONDO:0859210 rare diseases +MONDO:0859222 gard_rare diseases +MONDO:0859222 rare diseases +MONDO:0859223 gard_rare diseases +MONDO:0859223 rare diseases +MONDO:0859226 gard_rare diseases +MONDO:0859226 rare diseases +MONDO:0859228 gard_rare diseases +MONDO:0859228 rare diseases +MONDO:0859233 gard_rare diseases +MONDO:0859233 rare diseases +MONDO:0859234 gard_rare diseases +MONDO:0859234 rare diseases +MONDO:0859235 gard_rare diseases +MONDO:0859235 rare diseases +MONDO:0859237 gard_rare diseases +MONDO:0859237 rare diseases +MONDO:0859238 gard_rare diseases +MONDO:0859238 rare diseases +MONDO:0859242 gard_rare diseases +MONDO:0859242 rare diseases +MONDO:0859245 gard_rare diseases +MONDO:0859245 rare diseases +MONDO:0859246 gard_rare diseases +MONDO:0859246 rare diseases +MONDO:0859248 gard_rare diseases +MONDO:0859248 rare diseases +MONDO:0859255 gard_rare diseases +MONDO:0859255 rare diseases +MONDO:0859264 gard_rare diseases +MONDO:0859264 rare diseases +MONDO:0859267 gard_rare diseases +MONDO:0859267 rare diseases +MONDO:0859279 gard_rare diseases +MONDO:0859279 rare diseases +MONDO:0859290 gard_rare diseases +MONDO:0859290 rare diseases +MONDO:0859300 gard_rare diseases +MONDO:0859300 rare diseases +MONDO:0859308 gard_rare diseases +MONDO:0859308 rare diseases +MONDO:0859309 gard_rare diseases +MONDO:0859309 rare diseases +MONDO:0859310 gard_rare diseases +MONDO:0859310 rare diseases +MONDO:0859311 gard_rare diseases +MONDO:0859311 rare diseases +MONDO:0859314 gard_rare diseases +MONDO:0859314 rare diseases +MONDO:0859317 gard_rare diseases +MONDO:0859317 rare diseases +MONDO:0859318 gard_rare diseases +MONDO:0859318 rare diseases +MONDO:0859319 gard_rare diseases +MONDO:0859319 rare diseases +MONDO:0859320 gard_rare diseases +MONDO:0859320 rare diseases +MONDO:0859321 gard_rare diseases +MONDO:0859321 rare diseases +MONDO:0859323 gard_rare diseases +MONDO:0859323 rare diseases +MONDO:0859325 gard_rare diseases +MONDO:0859325 rare diseases +MONDO:0859327 gard_rare diseases +MONDO:0859327 rare diseases +MONDO:0859328 gard_rare diseases +MONDO:0859328 rare diseases +MONDO:0859329 gard_rare diseases +MONDO:0859329 rare diseases +MONDO:0859334 gard_rare diseases +MONDO:0859334 rare diseases +MONDO:0859335 gard_rare diseases +MONDO:0859335 rare diseases +MONDO:0859337 gard_rare diseases +MONDO:0859337 rare diseases +MONDO:0859339 gard_rare diseases +MONDO:0859339 rare diseases +MONDO:0859340 gard_rare diseases +MONDO:0859340 rare diseases +MONDO:0859342 gard_rare diseases +MONDO:0859342 rare diseases +MONDO:0859345 obsoletion_candidate diseases +MONDO:0859346 gard_rare diseases +MONDO:0859346 rare diseases +MONDO:0859353 gard_rare diseases +MONDO:0859353 rare diseases +MONDO:0859355 gard_rare diseases +MONDO:0859355 rare diseases +MONDO:0859356 gard_rare diseases +MONDO:0859356 rare diseases +MONDO:0859357 gard_rare diseases +MONDO:0859357 rare diseases +MONDO:0859358 gard_rare diseases +MONDO:0859358 rare diseases +MONDO:0859360 gard_rare diseases +MONDO:0859360 rare diseases +MONDO:0859362 gard_rare diseases +MONDO:0859362 rare diseases +MONDO:0859363 gard_rare diseases +MONDO:0859363 rare diseases +MONDO:0859366 gard_rare diseases +MONDO:0859366 rare diseases +MONDO:0859367 gard_rare diseases +MONDO:0859367 rare diseases +MONDO:0859368 gard_rare diseases +MONDO:0859368 rare diseases +MONDO:0859372 gard_rare diseases +MONDO:0859372 rare diseases +MONDO:0859373 gard_rare diseases +MONDO:0859373 rare diseases +MONDO:0859374 gard_rare diseases +MONDO:0859374 rare diseases +MONDO:0859378 gard_rare diseases +MONDO:0859378 rare diseases +MONDO:0859379 gard_rare diseases +MONDO:0859379 rare diseases +MONDO:0859380 gard_rare diseases +MONDO:0859380 rare diseases +MONDO:0859381 gard_rare diseases +MONDO:0859381 rare diseases +MONDO:0859383 gard_rare diseases +MONDO:0859383 otar diseases +MONDO:0859383 rare diseases +MONDO:0859390 gard_rare diseases +MONDO:0859390 rare diseases +MONDO:0859514 gard_rare diseases +MONDO:0859514 rare diseases +MONDO:0859515 gard_rare diseases +MONDO:0859515 rare diseases +MONDO:0859517 gard_rare diseases +MONDO:0859517 rare diseases +MONDO:0859518 gard_rare diseases +MONDO:0859518 rare diseases +MONDO:0859520 gard_rare diseases +MONDO:0859520 rare diseases +MONDO:0859523 gard_rare diseases +MONDO:0859523 rare diseases +MONDO:0859524 gard_rare diseases +MONDO:0859524 rare diseases +MONDO:0859525 gard_rare diseases +MONDO:0859525 rare diseases +MONDO:0859527 gard_rare diseases +MONDO:0859527 rare diseases +MONDO:0859528 gard_rare diseases +MONDO:0859528 rare diseases +MONDO:0859529 gard_rare diseases +MONDO:0859529 rare diseases +MONDO:0859530 gard_rare diseases +MONDO:0859530 rare diseases +MONDO:0859564 gard_rare diseases +MONDO:0859564 rare diseases +MONDO:0859565 gard_rare diseases +MONDO:0859565 rare diseases +MONDO:0859568 gard_rare diseases +MONDO:0859568 rare diseases +MONDO:0859571 gard_rare diseases +MONDO:0859571 rare diseases +MONDO:0859573 gard_rare diseases +MONDO:0859573 rare diseases +MONDO:0859574 gard_rare diseases +MONDO:0859574 rare diseases +MONDO:0859575 gard_rare diseases +MONDO:0859575 rare diseases +MONDO:0859576 gard_rare diseases +MONDO:0859576 rare diseases +MONDO:0859577 gard_rare diseases +MONDO:0859577 rare diseases +MONDO:0859578 gard_rare diseases +MONDO:0859578 rare diseases +MONDO:0859588 gard_rare diseases +MONDO:0859588 rare diseases +MONDO:0859591 gard_rare diseases +MONDO:0859591 rare diseases +MONDO:0859592 gard_rare diseases +MONDO:0859592 rare diseases +MONDO:0859597 gard_rare diseases +MONDO:0859597 rare diseases +MONDO:0859598 gard_rare diseases +MONDO:0859598 rare diseases +MONDO:0859614 gard_rare diseases +MONDO:0859614 rare diseases +MONDO:0859615 gard_rare diseases +MONDO:0859615 rare diseases +MONDO:0859692 gard_rare diseases +MONDO:0859692 ordo_group_of_disorders diseases +MONDO:0859692 rare diseases +MONDO:0859747 gard_rare diseases +MONDO:0859747 rare diseases +MONDO:0859748 gard_rare diseases +MONDO:0859748 rare diseases +MONDO:0859749 gard_rare diseases +MONDO:0859749 rare diseases +MONDO:0859761 gard_rare diseases +MONDO:0859761 ordo_subtype_of_a_disorder diseases +MONDO:0859761 rare diseases +MONDO:0859762 gard_rare diseases +MONDO:0859762 ordo_subtype_of_a_disorder diseases +MONDO:0859762 rare diseases +MONDO:0859763 gard_rare diseases +MONDO:0859763 ordo_disorder diseases +MONDO:0859763 orphanet_rare diseases +MONDO:0859763 rare diseases +MONDO:0859764 gard_rare diseases +MONDO:0859764 ordo_disorder diseases +MONDO:0859764 orphanet_rare diseases +MONDO:0859764 rare diseases +MONDO:0859765 gard_rare diseases +MONDO:0859765 ordo_disorder diseases +MONDO:0859765 orphanet_rare diseases +MONDO:0859765 rare diseases +MONDO:0956962 gard_rare diseases +MONDO:0956962 rare diseases +MONDO:0956964 gard_rare diseases +MONDO:0956964 rare diseases +MONDO:0956965 gard_rare diseases +MONDO:0956965 rare diseases +MONDO:0956966 gard_rare diseases +MONDO:0956966 rare diseases +MONDO:0956967 gard_rare diseases +MONDO:0956967 rare diseases +MONDO:0956981 gard_rare diseases +MONDO:0956981 rare diseases +MONDO:0956983 gard_rare diseases +MONDO:0956983 rare diseases +MONDO:0956984 gard_rare diseases +MONDO:0956984 rare diseases +MONDO:0956987 gard_rare diseases +MONDO:0956987 rare diseases +MONDO:0956988 gard_rare diseases +MONDO:0956988 rare diseases +MONDO:0956990 gard_rare diseases +MONDO:0956990 rare diseases +MONDO:0956991 gard_rare diseases +MONDO:0956991 rare diseases +MONDO:0956992 gard_rare diseases +MONDO:0956992 rare diseases +MONDO:0956993 gard_rare diseases +MONDO:0956993 rare diseases +MONDO:0956994 gard_rare diseases +MONDO:0956994 rare diseases +MONDO:0956995 gard_rare diseases +MONDO:0956995 rare diseases +MONDO:0956996 gard_rare diseases +MONDO:0956996 rare diseases +MONDO:0956997 gard_rare diseases +MONDO:0956997 rare diseases +MONDO:0957003 gard_rare diseases +MONDO:0957003 ordo_group_of_disorders diseases +MONDO:0957003 rare diseases +MONDO:0957008 gard_rare diseases +MONDO:0957008 ordo_group_of_disorders diseases +MONDO:0957008 rare diseases +MONDO:0957018 gard_rare diseases +MONDO:0957018 ordo_group_of_disorders diseases +MONDO:0957018 rare diseases +MONDO:0957048 gard_rare diseases +MONDO:0957048 ordo_group_of_disorders diseases +MONDO:0957048 rare diseases +MONDO:0957097 gard_rare diseases +MONDO:0957097 ordo_group_of_disorders diseases +MONDO:0957097 rare diseases +MONDO:0957111 gard_rare diseases +MONDO:0957111 ordo_group_of_disorders diseases +MONDO:0957111 rare diseases +MONDO:0957112 gard_rare diseases +MONDO:0957112 ordo_group_of_disorders diseases +MONDO:0957112 rare diseases +MONDO:0957113 gard_rare diseases +MONDO:0957113 ordo_group_of_disorders diseases +MONDO:0957113 rare diseases +MONDO:0957114 gard_rare diseases +MONDO:0957114 ordo_group_of_disorders diseases +MONDO:0957114 rare diseases +MONDO:0957115 gard_rare diseases +MONDO:0957115 ordo_group_of_disorders diseases +MONDO:0957115 rare diseases +MONDO:0957196 gard_rare diseases +MONDO:0957196 rare diseases +MONDO:0957197 gard_rare diseases +MONDO:0957197 rare diseases +MONDO:0957203 gard_rare diseases +MONDO:0957203 rare diseases +MONDO:0957208 gard_rare diseases +MONDO:0957208 rare diseases +MONDO:0957215 gard_rare diseases +MONDO:0957215 rare diseases +MONDO:0957216 gard_rare diseases +MONDO:0957216 rare diseases +MONDO:0957221 gard_rare diseases +MONDO:0957221 rare diseases +MONDO:0957224 gard_rare diseases +MONDO:0957224 rare diseases +MONDO:0957225 gard_rare diseases +MONDO:0957225 rare diseases +MONDO:0957240 gard_rare diseases +MONDO:0957240 rare diseases +MONDO:0957247 gard_rare diseases +MONDO:0957247 rare diseases +MONDO:0957248 gard_rare diseases +MONDO:0957248 rare diseases +MONDO:0957252 gard_rare diseases +MONDO:0957252 rare diseases +MONDO:0957254 gard_rare diseases +MONDO:0957254 rare diseases +MONDO:0957255 gard_rare diseases +MONDO:0957255 rare diseases +MONDO:0957261 gard_rare diseases +MONDO:0957261 rare diseases +MONDO:0957262 gard_rare diseases +MONDO:0957262 rare diseases +MONDO:0957263 gard_rare diseases +MONDO:0957263 rare diseases +MONDO:0957264 gard_rare diseases +MONDO:0957264 rare diseases +MONDO:0957265 gard_rare diseases +MONDO:0957265 rare diseases +MONDO:0957270 gard_rare diseases +MONDO:0957270 ordo_disorder diseases +MONDO:0957270 orphanet_rare diseases +MONDO:0957270 rare diseases +MONDO:0957271 gard_rare diseases +MONDO:0957271 rare diseases +MONDO:0957273 gard_rare diseases +MONDO:0957273 rare diseases +MONDO:0957274 gard_rare diseases +MONDO:0957274 rare diseases +MONDO:0957279 gard_rare diseases +MONDO:0957279 rare diseases +MONDO:0957281 gard_rare diseases +MONDO:0957281 rare diseases +MONDO:0957284 gard_rare diseases +MONDO:0957284 rare diseases +MONDO:0957288 gard_rare diseases +MONDO:0957288 rare diseases +MONDO:0957294 gard_rare diseases +MONDO:0957294 rare diseases +MONDO:0957303 gard_rare diseases +MONDO:0957303 rare diseases +MONDO:0957308 gard_rare diseases +MONDO:0957308 rare diseases +MONDO:0957309 gard_rare diseases +MONDO:0957309 rare diseases +MONDO:0957314 gard_rare diseases +MONDO:0957314 rare diseases +MONDO:0957319 gard_rare diseases +MONDO:0957319 obsoletion_candidate diseases +MONDO:0957319 rare diseases +MONDO:0957337 gard_rare diseases +MONDO:0957337 ordo_group_of_disorders diseases +MONDO:0957337 rare diseases +MONDO:0957341 gard_rare diseases +MONDO:0957341 ordo_group_of_disorders diseases +MONDO:0957341 rare diseases +MONDO:0957382 gard_rare diseases +MONDO:0957382 rare diseases +MONDO:0957385 gard_rare diseases +MONDO:0957385 rare diseases +MONDO:0957396 gard_rare diseases +MONDO:0957396 rare diseases +MONDO:0957397 gard_rare diseases +MONDO:0957397 ordo_disorder diseases +MONDO:0957397 orphanet_rare diseases +MONDO:0957397 rare diseases +MONDO:0957403 gard_rare diseases +MONDO:0957403 ordo_group_of_disorders diseases +MONDO:0957403 rare diseases +MONDO:0957405 gard_rare diseases +MONDO:0957405 ordo_group_of_disorders diseases +MONDO:0957405 rare diseases +MONDO:0957408 gard_rare diseases +MONDO:0957408 ordo_group_of_disorders diseases +MONDO:0957408 rare diseases +MONDO:0957421 gard_rare diseases +MONDO:0957421 ordo_disorder diseases +MONDO:0957421 orphanet_rare diseases +MONDO:0957421 rare diseases +MONDO:0957423 gard_rare diseases +MONDO:0957423 ordo_disorder diseases +MONDO:0957423 orphanet_rare diseases +MONDO:0957423 rare diseases +MONDO:0957426 gard_rare diseases +MONDO:0957426 ordo_disorder diseases +MONDO:0957426 orphanet_rare diseases +MONDO:0957426 rare diseases +MONDO:0957427 gard_rare diseases +MONDO:0957427 ordo_subtype_of_a_disorder diseases +MONDO:0957427 rare diseases +MONDO:0957428 gard_rare diseases +MONDO:0957428 ordo_subtype_of_a_disorder diseases +MONDO:0957428 rare diseases +MONDO:0957430 gard_rare diseases +MONDO:0957430 ordo_disorder diseases +MONDO:0957430 orphanet_rare diseases +MONDO:0957430 rare diseases +MONDO:0957431 gard_rare diseases +MONDO:0957431 ordo_group_of_disorders diseases +MONDO:0957431 rare diseases +MONDO:0957432 gard_rare diseases +MONDO:0957432 ordo_disorder diseases +MONDO:0957432 orphanet_rare diseases +MONDO:0957432 rare diseases +MONDO:0957433 gard_rare diseases +MONDO:0957433 ordo_disorder diseases +MONDO:0957433 orphanet_rare diseases +MONDO:0957433 rare diseases +MONDO:0957442 gard_rare diseases +MONDO:0957442 ordo_disorder diseases +MONDO:0957442 orphanet_rare diseases +MONDO:0957442 rare diseases +MONDO:0957443 gard_rare diseases +MONDO:0957443 ordo_disorder diseases +MONDO:0957443 orphanet_rare diseases +MONDO:0957443 rare diseases +MONDO:0957451 gard_rare diseases +MONDO:0957451 ordo_disorder diseases +MONDO:0957451 orphanet_rare diseases +MONDO:0957451 rare diseases +MONDO:0957452 gard_rare diseases +MONDO:0957452 ordo_disorder diseases +MONDO:0957452 orphanet_rare diseases +MONDO:0957452 rare diseases +MONDO:0957453 gard_rare diseases +MONDO:0957453 ordo_subtype_of_a_disorder diseases +MONDO:0957453 rare diseases +MONDO:0957454 gard_rare diseases +MONDO:0957454 ordo_subtype_of_a_disorder diseases +MONDO:0957454 rare diseases +MONDO:0957456 gard_rare diseases +MONDO:0957456 ordo_subtype_of_a_disorder diseases +MONDO:0957456 rare diseases +MONDO:0957458 gard_rare diseases +MONDO:0957458 ordo_subtype_of_a_disorder diseases +MONDO:0957458 rare diseases +MONDO:0957459 gard_rare diseases +MONDO:0957459 ordo_disorder diseases +MONDO:0957459 orphanet_rare diseases +MONDO:0957459 rare diseases +MONDO:0957460 gard_rare diseases +MONDO:0957460 ordo_disorder diseases +MONDO:0957460 orphanet_rare diseases +MONDO:0957460 rare diseases +MONDO:0957461 gard_rare diseases +MONDO:0957461 ordo_disorder diseases +MONDO:0957461 orphanet_rare diseases +MONDO:0957461 rare diseases +MONDO:0957462 gard_rare diseases +MONDO:0957462 ordo_disorder diseases +MONDO:0957462 orphanet_rare diseases +MONDO:0957462 rare diseases +MONDO:0957463 gard_rare diseases +MONDO:0957463 ordo_disorder diseases +MONDO:0957463 orphanet_rare diseases +MONDO:0957463 rare diseases +MONDO:0957464 gard_rare diseases +MONDO:0957464 ordo_disorder diseases +MONDO:0957464 orphanet_rare diseases +MONDO:0957464 rare diseases +MONDO:0957465 gard_rare diseases +MONDO:0957465 ordo_disorder diseases +MONDO:0957465 orphanet_rare diseases +MONDO:0957465 rare diseases +MONDO:0957466 gard_rare diseases +MONDO:0957466 ordo_disorder diseases +MONDO:0957466 orphanet_rare diseases +MONDO:0957466 rare diseases +MONDO:0957467 gard_rare diseases +MONDO:0957467 ordo_disorder diseases +MONDO:0957467 orphanet_rare diseases +MONDO:0957467 rare diseases +MONDO:0957473 gard_rare diseases +MONDO:0957473 ordo_disorder diseases +MONDO:0957473 orphanet_rare diseases +MONDO:0957473 rare diseases +MONDO:0957476 gard_rare diseases +MONDO:0957476 ordo_disorder diseases +MONDO:0957476 orphanet_rare diseases +MONDO:0957476 rare diseases +MONDO:0957477 gard_rare diseases +MONDO:0957477 ordo_disorder diseases +MONDO:0957477 orphanet_rare diseases +MONDO:0957477 rare diseases +MONDO:0957481 gard_rare diseases +MONDO:0957481 ordo_disorder diseases +MONDO:0957481 orphanet_rare diseases +MONDO:0957481 rare diseases +MONDO:0957487 gard_rare diseases +MONDO:0957487 ordo_disorder diseases +MONDO:0957487 orphanet_rare diseases +MONDO:0957487 rare diseases +MONDO:0957494 gard_rare diseases +MONDO:0957494 rare diseases +MONDO:0957495 gard_rare diseases +MONDO:0957495 rare diseases +MONDO:0957496 gard_rare diseases +MONDO:0957496 rare diseases +MONDO:0957524 gard_rare diseases +MONDO:0957524 rare diseases +MONDO:0957536 gard_rare diseases +MONDO:0957536 rare diseases +MONDO:0957537 gard_rare diseases +MONDO:0957537 rare diseases +MONDO:0957538 gard_rare diseases +MONDO:0957538 rare diseases +MONDO:0957539 gard_rare diseases +MONDO:0957539 rare diseases +MONDO:0957540 gard_rare diseases +MONDO:0957540 rare diseases +MONDO:0957542 gard_rare diseases +MONDO:0957542 rare diseases +MONDO:0957543 gard_rare diseases +MONDO:0957543 rare diseases +MONDO:0957544 gard_rare diseases +MONDO:0957544 rare diseases +MONDO:0957545 gard_rare diseases +MONDO:0957545 rare diseases +MONDO:0957556 gard_rare diseases +MONDO:0957556 ordo_disorder diseases +MONDO:0957556 orphanet_rare diseases +MONDO:0957556 rare diseases +MONDO:0957572 gard_rare diseases +MONDO:0957572 rare diseases +MONDO:0957577 gard_rare diseases +MONDO:0957577 rare diseases +MONDO:0957578 gard_rare diseases +MONDO:0957578 rare diseases +MONDO:0957580 gard_rare diseases +MONDO:0957580 rare diseases +MONDO:0957595 gard_rare diseases +MONDO:0957595 rare diseases +MONDO:0957780 gard_rare diseases +MONDO:0957780 rare diseases +MONDO:0957783 gard_rare diseases +MONDO:0957783 rare diseases +MONDO:0957788 gard_rare diseases +MONDO:0957788 rare diseases +MONDO:0957807 gard_rare diseases +MONDO:0957807 rare diseases +MONDO:0957809 gard_rare diseases +MONDO:0957809 rare diseases +MONDO:0957811 gard_rare diseases +MONDO:0957811 rare diseases +MONDO:0957812 gard_rare diseases +MONDO:0957812 rare diseases +MONDO:0957813 gard_rare diseases +MONDO:0957813 rare diseases +MONDO:0957819 gard_rare diseases +MONDO:0957819 rare diseases +MONDO:0957820 gard_rare diseases +MONDO:0957820 rare diseases +MONDO:0957822 gard_rare diseases +MONDO:0957822 rare diseases +MONDO:0957824 gard_rare diseases +MONDO:0957824 rare diseases +MONDO:0957825 gard_rare diseases +MONDO:0957825 rare diseases +MONDO:0957870 gard_rare diseases +MONDO:0957870 rare diseases +MONDO:0957871 gard_rare diseases +MONDO:0957871 rare diseases +MONDO:0957872 gard_rare diseases +MONDO:0957872 rare diseases +MONDO:0957873 gard_rare diseases +MONDO:0957873 rare diseases +MONDO:0957874 gard_rare diseases +MONDO:0957874 rare diseases +MONDO:0957875 gard_rare diseases +MONDO:0957875 rare diseases +MONDO:0957876 gard_rare diseases +MONDO:0957876 rare diseases +MONDO:0957912 gard_rare diseases +MONDO:0957912 rare diseases +MONDO:0957921 gard_rare diseases +MONDO:0957921 rare diseases +MONDO:0957922 gard_rare diseases +MONDO:0957922 rare diseases +MONDO:0957928 gard_rare diseases +MONDO:0957928 rare diseases +MONDO:0957935 gard_rare diseases +MONDO:0957935 rare diseases +MONDO:0957953 gard_rare diseases +MONDO:0957953 rare diseases +MONDO:0957954 gard_rare diseases +MONDO:0957954 rare diseases +MONDO:0957958 gard_rare diseases +MONDO:0957958 rare diseases +MONDO:0957978 gard_rare diseases +MONDO:0957978 rare diseases +MONDO:0957984 gard_rare diseases +MONDO:0957984 rare diseases +MONDO:0957988 gard_rare diseases +MONDO:0957988 rare diseases +MONDO:0957991 gard_rare diseases +MONDO:0957991 rare diseases +MONDO:0957992 gard_rare diseases +MONDO:0957992 rare diseases +MONDO:0957993 gard_rare diseases +MONDO:0957993 rare diseases +MONDO:0957999 gard_rare diseases +MONDO:0957999 rare diseases +MONDO:0958000 gard_rare diseases +MONDO:0958000 rare diseases +MONDO:0958006 gard_rare diseases +MONDO:0958006 rare diseases +MONDO:0958009 gard_rare diseases +MONDO:0958009 rare diseases +MONDO:0958012 gard_rare diseases +MONDO:0958012 rare diseases +MONDO:0958013 gard_rare diseases +MONDO:0958013 rare diseases +MONDO:0958017 gard_rare diseases +MONDO:0958017 rare diseases +MONDO:0958018 gard_rare diseases +MONDO:0958018 rare diseases +MONDO:0958022 gard_rare diseases +MONDO:0958022 rare diseases +MONDO:0958023 gard_rare diseases +MONDO:0958023 rare diseases +MONDO:0958034 gard_rare diseases +MONDO:0958034 rare diseases +MONDO:0958035 gard_rare diseases +MONDO:0958035 rare diseases +MONDO:0958071 gard_rare diseases +MONDO:0958071 ordo_subtype_of_a_disorder diseases +MONDO:0958071 rare diseases +MONDO:0958075 gard_rare diseases +MONDO:0958075 ordo_disorder diseases +MONDO:0958075 orphanet_rare diseases +MONDO:0958075 rare diseases +MONDO:0958076 gard_rare diseases +MONDO:0958076 ordo_disorder diseases +MONDO:0958076 orphanet_rare diseases +MONDO:0958076 rare diseases +MONDO:0958077 gard_rare diseases +MONDO:0958077 ordo_group_of_disorders diseases +MONDO:0958077 rare diseases +MONDO:0958083 gard_rare diseases +MONDO:0958083 ordo_disorder diseases +MONDO:0958083 orphanet_rare diseases +MONDO:0958083 rare diseases +MONDO:0958085 gard_rare diseases +MONDO:0958085 ordo_disorder diseases +MONDO:0958085 orphanet_rare diseases +MONDO:0958085 rare diseases +MONDO:0958091 gard_rare diseases +MONDO:0958091 ordo_disorder diseases +MONDO:0958091 orphanet_rare diseases +MONDO:0958091 rare diseases +MONDO:0958093 gard_rare diseases +MONDO:0958093 ordo_disorder diseases +MONDO:0958093 orphanet_rare diseases +MONDO:0958093 rare diseases +MONDO:0958094 gard_rare diseases +MONDO:0958094 ordo_disorder diseases +MONDO:0958094 orphanet_rare diseases +MONDO:0958094 rare diseases +MONDO:0958095 gard_rare diseases +MONDO:0958095 ordo_disorder diseases +MONDO:0958095 orphanet_rare diseases +MONDO:0958095 rare diseases +MONDO:0958096 gard_rare diseases +MONDO:0958096 ordo_disorder diseases +MONDO:0958096 orphanet_rare diseases +MONDO:0958096 rare diseases +MONDO:0958097 gard_rare diseases +MONDO:0958097 ordo_disorder diseases +MONDO:0958097 orphanet_rare diseases +MONDO:0958097 rare diseases +MONDO:0958098 gard_rare diseases +MONDO:0958098 ordo_disorder diseases +MONDO:0958098 orphanet_rare diseases +MONDO:0958098 rare diseases +MONDO:0958099 gard_rare diseases +MONDO:0958099 ordo_disorder diseases +MONDO:0958099 orphanet_rare diseases +MONDO:0958099 rare diseases +MONDO:0958101 gard_rare diseases +MONDO:0958101 ordo_disorder diseases +MONDO:0958101 orphanet_rare diseases +MONDO:0958101 rare diseases +MONDO:0958104 gard_rare diseases +MONDO:0958104 ordo_subtype_of_a_disorder diseases +MONDO:0958104 rare diseases +MONDO:0958106 gard_rare diseases +MONDO:0958106 ordo_disorder diseases +MONDO:0958106 orphanet_rare diseases +MONDO:0958106 rare diseases +MONDO:0958110 gard_rare diseases +MONDO:0958110 ordo_disorder diseases +MONDO:0958110 orphanet_rare diseases +MONDO:0958110 rare diseases +MONDO:0958115 gard_rare diseases +MONDO:0958115 ordo_disorder diseases +MONDO:0958115 orphanet_rare diseases +MONDO:0958115 rare diseases +MONDO:0958116 gard_rare diseases +MONDO:0958116 ordo_disorder diseases +MONDO:0958116 orphanet_rare diseases +MONDO:0958116 rare diseases +MONDO:0958117 gard_rare diseases +MONDO:0958117 ordo_disorder diseases +MONDO:0958117 orphanet_rare diseases +MONDO:0958117 rare diseases +MONDO:0958118 gard_rare diseases +MONDO:0958118 ordo_disorder diseases +MONDO:0958118 orphanet_rare diseases +MONDO:0958118 rare diseases +MONDO:0958119 gard_rare diseases +MONDO:0958119 ordo_disorder diseases +MONDO:0958119 orphanet_rare diseases +MONDO:0958119 rare diseases +MONDO:0958120 gard_rare diseases +MONDO:0958120 ordo_disorder diseases +MONDO:0958120 orphanet_rare diseases +MONDO:0958120 rare diseases +MONDO:0958122 gard_rare diseases +MONDO:0958122 ordo_disorder diseases +MONDO:0958122 orphanet_rare diseases +MONDO:0958122 rare diseases +MONDO:0958123 gard_rare diseases +MONDO:0958123 ordo_disorder diseases +MONDO:0958123 orphanet_rare diseases +MONDO:0958123 rare diseases +MONDO:0958127 gard_rare diseases +MONDO:0958127 ordo_disorder diseases +MONDO:0958127 orphanet_rare diseases +MONDO:0958127 rare diseases +MONDO:0958128 gard_rare diseases +MONDO:0958128 ordo_disorder diseases +MONDO:0958128 orphanet_rare diseases +MONDO:0958128 rare diseases +MONDO:0958129 gard_rare diseases +MONDO:0958129 ordo_disorder diseases +MONDO:0958129 orphanet_rare diseases +MONDO:0958129 rare diseases +MONDO:0958130 gard_rare diseases +MONDO:0958130 ordo_disorder diseases +MONDO:0958130 orphanet_rare diseases +MONDO:0958130 rare diseases +MONDO:0958137 gard_rare diseases +MONDO:0958137 ordo_disorder diseases +MONDO:0958137 orphanet_rare diseases +MONDO:0958137 rare diseases +MONDO:0958138 gard_rare diseases +MONDO:0958138 ordo_disorder diseases +MONDO:0958138 orphanet_rare diseases +MONDO:0958138 rare diseases +MONDO:0958161 gard_rare diseases +MONDO:0958161 rare diseases +MONDO:0958162 gard_rare diseases +MONDO:0958162 rare diseases +MONDO:0958164 gard_rare diseases +MONDO:0958164 rare diseases +MONDO:0958165 gard_rare diseases +MONDO:0958165 rare diseases +MONDO:0958174 gard_rare diseases +MONDO:0958174 rare diseases +MONDO:0958175 gard_rare diseases +MONDO:0958175 rare diseases +MONDO:0958176 gard_rare diseases +MONDO:0958176 rare diseases +MONDO:0958177 gard_rare diseases +MONDO:0958177 rare diseases +MONDO:0958179 gard_rare diseases +MONDO:0958179 rare diseases +MONDO:0958180 gard_rare diseases +MONDO:0958180 rare diseases +MONDO:0958181 gard_rare diseases +MONDO:0958181 rare diseases +MONDO:0958182 gard_rare diseases +MONDO:0958182 rare diseases +MONDO:0958183 gard_rare diseases +MONDO:0958183 rare diseases +MONDO:0958184 gard_rare diseases +MONDO:0958184 rare diseases +MONDO:0958185 gard_rare diseases +MONDO:0958185 rare diseases +MONDO:0958187 gard_rare diseases +MONDO:0958187 rare diseases +MONDO:0958188 gard_rare diseases +MONDO:0958188 rare diseases +MONDO:0958189 gard_rare diseases +MONDO:0958189 rare diseases +MONDO:0958190 gard_rare diseases +MONDO:0958190 rare diseases +MONDO:0958192 gard_rare diseases +MONDO:0958192 rare diseases +MONDO:0958194 gard_rare diseases +MONDO:0958194 rare diseases +MONDO:0958195 gard_rare diseases +MONDO:0958195 rare diseases +MONDO:0958197 gard_rare diseases +MONDO:0958197 rare diseases +MONDO:0958199 gard_rare diseases +MONDO:0958199 rare diseases +MONDO:0958200 gard_rare diseases +MONDO:0958200 rare diseases +MONDO:0958202 gard_rare diseases +MONDO:0958202 rare diseases +MONDO:0958204 gard_rare diseases +MONDO:0958204 rare diseases +MONDO:0958226 gard_rare diseases +MONDO:0958226 rare diseases +MONDO:0958228 gard_rare diseases +MONDO:0958228 rare diseases +MONDO:0958230 gard_rare diseases +MONDO:0958230 rare diseases +MONDO:0958232 gard_rare diseases +MONDO:0958232 rare diseases +MONDO:0958233 gard_rare diseases +MONDO:0958233 rare diseases +MONDO:0958234 gard_rare diseases +MONDO:0958234 rare diseases +MONDO:0958235 gard_rare diseases +MONDO:0958235 rare diseases +MONDO:0958236 gard_rare diseases +MONDO:0958236 rare diseases +MONDO:0958239 gard_rare diseases +MONDO:0958239 rare diseases +MONDO:0958241 gard_rare diseases +MONDO:0958241 rare diseases +MONDO:0958256 gard_rare diseases +MONDO:0958256 ordo_disorder diseases +MONDO:0958256 orphanet_rare diseases +MONDO:0958256 rare diseases +MONDO:0958257 gard_rare diseases +MONDO:0958257 ordo_disorder diseases +MONDO:0958257 orphanet_rare diseases +MONDO:0958257 rare diseases +MONDO:0958258 gard_rare diseases +MONDO:0958258 ordo_disorder diseases +MONDO:0958258 orphanet_rare diseases +MONDO:0958258 rare diseases +MONDO:0958259 gard_rare diseases +MONDO:0958259 ordo_group_of_disorders diseases +MONDO:0958259 rare diseases +MONDO:0958260 gard_rare diseases +MONDO:0958260 ordo_group_of_disorders diseases +MONDO:0958260 rare diseases +MONDO:0958262 gard_rare diseases +MONDO:0958262 ordo_disorder diseases +MONDO:0958262 orphanet_rare diseases +MONDO:0958262 rare diseases +MONDO:0958263 gard_rare diseases +MONDO:0958263 ordo_disorder diseases +MONDO:0958263 orphanet_rare diseases +MONDO:0958263 rare diseases +MONDO:0958264 gard_rare diseases +MONDO:0958264 ordo_disorder diseases +MONDO:0958264 orphanet_rare diseases +MONDO:0958264 rare diseases +MONDO:0958265 gard_rare diseases +MONDO:0958265 ordo_disorder diseases +MONDO:0958265 orphanet_rare diseases +MONDO:0958265 rare diseases +MONDO:0958266 gard_rare diseases +MONDO:0958266 ordo_disorder diseases +MONDO:0958266 orphanet_rare diseases +MONDO:0958266 rare diseases +MONDO:0958267 gard_rare diseases +MONDO:0958267 ordo_disorder diseases +MONDO:0958267 orphanet_rare diseases +MONDO:0958267 rare diseases +MONDO:0958268 gard_rare diseases +MONDO:0958268 ordo_disorder diseases +MONDO:0958268 orphanet_rare diseases +MONDO:0958268 rare diseases +MONDO:0958269 gard_rare diseases +MONDO:0958269 ordo_disorder diseases +MONDO:0958269 orphanet_rare diseases +MONDO:0958269 rare diseases +MONDO:0958270 gard_rare diseases +MONDO:0958270 ordo_group_of_disorders diseases +MONDO:0958270 rare diseases +MONDO:0958273 gard_rare diseases +MONDO:0958273 ordo_subtype_of_a_disorder diseases +MONDO:0958273 rare diseases +MONDO:0958274 gard_rare diseases +MONDO:0958274 ordo_subtype_of_a_disorder diseases +MONDO:0958274 rare diseases +MONDO:0958275 gard_rare diseases +MONDO:0958275 ordo_disorder diseases +MONDO:0958275 orphanet_rare diseases +MONDO:0958275 rare diseases +MONDO:0958277 gard_rare diseases +MONDO:0958277 rare diseases +MONDO:0958302 gard_rare diseases +MONDO:0958302 rare diseases +MONDO:0958303 gard_rare diseases +MONDO:0958303 rare diseases +MONDO:0958324 gard_rare diseases +MONDO:0958324 rare diseases +MONDO:0958325 gard_rare diseases +MONDO:0958325 rare diseases +MONDO:0958326 gard_rare diseases +MONDO:0958326 rare diseases +MONDO:0958328 gard_rare diseases +MONDO:0958328 rare diseases +MONDO:0958330 gard_rare diseases +MONDO:0958330 rare diseases +MONDO:0958331 gard_rare diseases +MONDO:0958331 rare diseases +MONDO:0958332 gard_rare diseases +MONDO:0958332 rare diseases +MONDO:0958333 gard_rare diseases +MONDO:0958333 rare diseases +MONDO:0958334 gard_rare diseases +MONDO:0958334 rare diseases +MONDO:0958335 gard_rare diseases +MONDO:0958335 rare diseases +MONDO:0958342 gard_rare diseases +MONDO:0958342 ordo_disorder diseases +MONDO:0958342 orphanet_rare diseases +MONDO:0958342 rare diseases +MONDO:0958343 gard_rare diseases +MONDO:0958343 ordo_disorder diseases +MONDO:0958343 orphanet_rare diseases +MONDO:0958343 rare diseases +MONDO:0958344 gard_rare diseases +MONDO:0958344 ordo_disorder diseases +MONDO:0958344 orphanet_rare diseases +MONDO:0958344 rare diseases +MONDO:0958345 gard_rare diseases +MONDO:0958345 ordo_group_of_disorders diseases +MONDO:0958345 rare diseases +MONDO:0958346 gard_rare diseases +MONDO:0958346 ordo_disorder diseases +MONDO:0958346 orphanet_rare diseases +MONDO:0958346 rare diseases +MONDO:0958347 gard_rare diseases +MONDO:0958347 ordo_disorder diseases +MONDO:0958347 orphanet_rare diseases +MONDO:0958347 rare diseases +MONDO:0958348 gard_rare diseases +MONDO:0958348 ordo_disorder diseases +MONDO:0958348 orphanet_rare diseases +MONDO:0958348 rare diseases +MONDO:0958349 gard_rare diseases +MONDO:0958349 ordo_disorder diseases +MONDO:0958349 orphanet_rare diseases +MONDO:0958349 rare diseases +MONDO:0958350 gard_rare diseases +MONDO:0958350 ordo_group_of_disorders diseases +MONDO:0958350 rare diseases +MONDO:0958351 gard_rare diseases +MONDO:0958351 ordo_subtype_of_a_disorder diseases +MONDO:0958351 rare diseases +MONDO:0958352 gard_rare diseases +MONDO:0958352 ordo_subtype_of_a_disorder diseases +MONDO:0958352 rare diseases +MONDO:0958353 gard_rare diseases +MONDO:0958353 ordo_disorder diseases +MONDO:0958353 orphanet_rare diseases +MONDO:0958353 rare diseases +MONDO:0958354 gard_rare diseases +MONDO:0958354 ordo_disorder diseases +MONDO:0958354 orphanet_rare diseases +MONDO:0958354 rare diseases +MONDO:0958355 gard_rare diseases +MONDO:0958355 ordo_disorder diseases +MONDO:0958355 orphanet_rare diseases +MONDO:0958355 rare diseases +MONDO:0958356 gard_rare diseases +MONDO:0958356 ordo_disorder diseases +MONDO:0958356 orphanet_rare diseases +MONDO:0958356 rare diseases +MONDO:0958357 gard_rare diseases +MONDO:0958357 ordo_disorder diseases +MONDO:0958357 orphanet_rare diseases +MONDO:0958357 rare diseases +MONDO:0968944 gard_rare diseases +MONDO:0968944 rare diseases +MONDO:0968946 gard_rare diseases +MONDO:0968946 rare diseases +MONDO:0968949 gard_rare diseases +MONDO:0968949 rare diseases +MONDO:0968951 gard_rare diseases +MONDO:0968951 rare diseases +MONDO:0968955 gard_rare diseases +MONDO:0968955 ordo_subtype_of_a_disorder diseases +MONDO:0968955 rare diseases +MONDO:0968959 gard_rare diseases +MONDO:0968959 ordo_disorder diseases +MONDO:0968959 orphanet_rare diseases +MONDO:0968959 rare diseases +MONDO:0968974 gard_rare diseases +MONDO:0968974 rare diseases +MONDO:0968977 inferred_rare diseases +MONDO:0968977 rare diseases +MONDO:0968980 inferred_rare diseases +MONDO:0968980 rare diseases +MONDO:0968981 inferred_rare diseases +MONDO:0968981 rare diseases +MONDO:0968983 inferred_rare diseases +MONDO:0968983 rare diseases +MONDO:0968986 ordo_disorder diseases +MONDO:0968986 orphanet_rare diseases +MONDO:0968986 rare diseases +MONDO:0968987 ordo_disorder diseases +MONDO:0968987 orphanet_rare diseases +MONDO:0968987 rare diseases +MONDO:0968988 inferred_rare diseases +MONDO:0968988 ordo_group_of_disorders diseases +MONDO:0968988 rare diseases +MONDO:0968989 ordo_disorder diseases +MONDO:0968989 orphanet_rare diseases +MONDO:0968989 rare diseases +MONDO:1010000 gard_rare diseases +MONDO:1010000 mondo_rare diseases +MONDO:1010000 rare diseases +MONDO:1030000 inferred_rare diseases +MONDO:1030000 rare diseases +MONDO:8000000 otar diseases +MONDO:8000004 gard_rare diseases +MONDO:8000004 rare diseases +MONDO:8000006 gard_rare diseases +MONDO:8000006 nord_rare diseases +MONDO:8000006 ordo_disorder diseases +MONDO:8000006 orphanet_rare diseases +MONDO:8000006 rare diseases +MONDO:8000008 gard_rare diseases +MONDO:8000008 nord_rare diseases +MONDO:8000008 ordo_disorder diseases +MONDO:8000008 orphanet_rare diseases +MONDO:8000008 rare diseases +MONDO:8000010 gard_rare diseases +MONDO:8000010 ordo_disorder diseases +MONDO:8000010 orphanet_rare diseases +MONDO:8000010 otar diseases +MONDO:8000010 rare diseases +MONDO:8000011 gard_rare diseases +MONDO:8000011 nord_rare diseases +MONDO:8000011 ordo_subtype_of_a_disorder diseases +MONDO:8000011 rare diseases +MONDO:8000012 gard_rare diseases +MONDO:8000012 nord_rare diseases +MONDO:8000012 ordo_disorder diseases +MONDO:8000012 orphanet_rare diseases +MONDO:8000012 rare diseases +MONDO:8000014 gard_rare diseases +MONDO:8000014 rare diseases +MONDO:8000015 gard_rare diseases +MONDO:8000015 nord_rare diseases +MONDO:8000015 ordo_disorder diseases +MONDO:8000015 ordo_morphological_anomaly diseases +MONDO:8000015 orphanet_rare diseases +MONDO:8000015 rare diseases +MONDO:8000018 nord_rare diseases +MONDO:8000018 rare diseases +MONDO:8000019 gard_rare diseases +MONDO:8000019 rare diseases +MONDO:8000023 gard_rare diseases +MONDO:8000023 rare diseases +MONDO:8000024 gard_rare diseases +MONDO:8000024 nord_rare diseases +MONDO:8000024 rare diseases +MONDO:0021135 obsoletion_candidate characteristics +MONDO:0021136 obsoletion_candidate characteristics +MONDO:0021137 obsoletion_candidate characteristics +MONDO:0000065 predisposition susceptibilities +MONDO:0000070 predisposition susceptibilities +MONDO:0000093 obsoletion_candidate susceptibilities +MONDO:0000093 predisposition susceptibilities +MONDO:0000108 predisposition susceptibilities +MONDO:0000141 gard_rare susceptibilities +MONDO:0000141 nord_rare susceptibilities +MONDO:0000141 ordo_disorder susceptibilities +MONDO:0000141 ordo_malformation_syndrome susceptibilities +MONDO:0000141 orphanet_rare susceptibilities +MONDO:0000141 otar susceptibilities +MONDO:0000141 rare susceptibilities +MONDO:0000144 predisposition susceptibilities +MONDO:0000162 predisposition susceptibilities +MONDO:0001734 clingen susceptibilities +MONDO:0001734 gard_rare susceptibilities +MONDO:0001734 nord_rare susceptibilities +MONDO:0001734 ordo_disorder susceptibilities +MONDO:0001734 orphanet_rare susceptibilities +MONDO:0001734 otar susceptibilities +MONDO:0001734 rare susceptibilities +MONDO:0003582 gard_rare susceptibilities +MONDO:0003582 nord_rare susceptibilities +MONDO:0003582 ordo_disorder susceptibilities +MONDO:0003582 orphanet_rare susceptibilities +MONDO:0003582 otar susceptibilities +MONDO:0003582 predisposition susceptibilities +MONDO:0003582 rare susceptibilities +MONDO:0004951 predisposition susceptibilities +MONDO:0005508 gard_rare susceptibilities +MONDO:0005508 nord_rare susceptibilities +MONDO:0005508 ordo_disorder susceptibilities +MONDO:0005508 orphanet_rare susceptibilities +MONDO:0005508 otar susceptibilities +MONDO:0005508 rare susceptibilities +MONDO:0005835 clingen susceptibilities +MONDO:0005835 gard_rare susceptibilities +MONDO:0005835 nord_rare susceptibilities +MONDO:0005835 ordo_disorder susceptibilities +MONDO:0005835 orphanet_rare susceptibilities +MONDO:0005835 otar susceptibilities +MONDO:0005835 rare susceptibilities +MONDO:0007039 clingen susceptibilities +MONDO:0007039 gard_rare susceptibilities +MONDO:0007039 nord_rare susceptibilities +MONDO:0007039 ordo_disorder susceptibilities +MONDO:0007039 orphanet_rare susceptibilities +MONDO:0007039 otar susceptibilities +MONDO:0007039 rare susceptibilities +MONDO:0007053 predisposition susceptibilities +MONDO:0007126 predisposition susceptibilities +MONDO:0007187 clingen susceptibilities +MONDO:0007187 gard_rare susceptibilities +MONDO:0007187 nord_rare susceptibilities +MONDO:0007187 ordo_disorder susceptibilities +MONDO:0007187 ordo_malformation_syndrome susceptibilities +MONDO:0007187 orphanet_rare susceptibilities +MONDO:0007187 otar susceptibilities +MONDO:0007187 rare susceptibilities +MONDO:0007190 inferred_rare susceptibilities +MONDO:0007190 predisposition susceptibilities +MONDO:0007190 rare susceptibilities +MONDO:0007203 gard_rare susceptibilities +MONDO:0007203 nord_rare susceptibilities +MONDO:0007203 ordo_disorder susceptibilities +MONDO:0007203 ordo_malformation_syndrome susceptibilities +MONDO:0007203 orphanet_rare susceptibilities +MONDO:0007203 otar susceptibilities +MONDO:0007203 rare susceptibilities +MONDO:0007315 gard_rare susceptibilities +MONDO:0007315 nord_rare susceptibilities +MONDO:0007315 ordo_disorder susceptibilities +MONDO:0007315 ordo_malformation_syndrome susceptibilities +MONDO:0007315 orphanet_rare susceptibilities +MONDO:0007315 otar susceptibilities +MONDO:0007315 rare susceptibilities +MONDO:0007356 gard_rare susceptibilities +MONDO:0007356 nord_rare susceptibilities +MONDO:0007356 rare susceptibilities +MONDO:0007462 predisposition susceptibilities +MONDO:0007462 prototype_pattern susceptibilities +MONDO:0007485 gard_rare susceptibilities +MONDO:0007485 nord_rare susceptibilities +MONDO:0007485 prototype_pattern susceptibilities +MONDO:0007485 rare susceptibilities +MONDO:0007487 predisposition susceptibilities +MONDO:0007534 gard_rare susceptibilities +MONDO:0007534 nord_rare susceptibilities +MONDO:0007534 ordo_disorder susceptibilities +MONDO:0007534 ordo_malformation_syndrome susceptibilities +MONDO:0007534 orphanet_rare susceptibilities +MONDO:0007534 otar susceptibilities +MONDO:0007534 rare susceptibilities +MONDO:0007540 clingen susceptibilities +MONDO:0007540 gard_rare susceptibilities +MONDO:0007540 nord_rare susceptibilities +MONDO:0007540 ordo_disorder susceptibilities +MONDO:0007540 orphanet_rare susceptibilities +MONDO:0007540 otar susceptibilities +MONDO:0007540 rare susceptibilities +MONDO:0007541 predisposition susceptibilities +MONDO:0007565 gard_rare susceptibilities +MONDO:0007565 nord_rare susceptibilities +MONDO:0007565 ordo_subtype_of_a_disorder susceptibilities +MONDO:0007565 otar susceptibilities +MONDO:0007565 rare susceptibilities +MONDO:0007566 clingen susceptibilities +MONDO:0007566 gard_rare susceptibilities +MONDO:0007566 nord_rare susceptibilities +MONDO:0007566 ordo_disorder susceptibilities +MONDO:0007566 orphanet_rare susceptibilities +MONDO:0007566 otar susceptibilities +MONDO:0007566 rare susceptibilities +MONDO:0007573 inferred_rare susceptibilities +MONDO:0007573 rare susceptibilities +MONDO:0007585 clingen susceptibilities +MONDO:0007585 gard_rare susceptibilities +MONDO:0007585 nord_rare susceptibilities +MONDO:0007585 otar susceptibilities +MONDO:0007585 rare susceptibilities +MONDO:0007586 clingen susceptibilities +MONDO:0007586 gard_rare susceptibilities +MONDO:0007586 nord_rare susceptibilities +MONDO:0007586 otar susceptibilities +MONDO:0007586 rare susceptibilities +MONDO:0007681 gard_rare susceptibilities +MONDO:0007681 nord_rare susceptibilities +MONDO:0007681 ordo_disorder susceptibilities +MONDO:0007681 orphanet_rare susceptibilities +MONDO:0007681 otar susceptibilities +MONDO:0007681 rare susceptibilities +MONDO:0007704 predisposition susceptibilities +MONDO:0007723 predisposition susceptibilities +MONDO:0007767 gard_rare susceptibilities +MONDO:0007767 nord_rare susceptibilities +MONDO:0007767 rare susceptibilities +MONDO:0007768 clingen susceptibilities +MONDO:0007768 gard_rare susceptibilities +MONDO:0007768 nord_rare susceptibilities +MONDO:0007768 ordo_disorder susceptibilities +MONDO:0007768 orphanet_rare susceptibilities +MONDO:0007768 otar susceptibilities +MONDO:0007768 rare susceptibilities +MONDO:0007781 otar susceptibilities +MONDO:0007783 clingen susceptibilities +MONDO:0007783 predisposition susceptibilities +MONDO:0007814 gard_rare susceptibilities +MONDO:0007814 nord_rare susceptibilities +MONDO:0007814 rare susceptibilities +MONDO:0007845 inferred_rare susceptibilities +MONDO:0007845 predisposition susceptibilities +MONDO:0007845 rare susceptibilities +MONDO:0007888 clingen susceptibilities +MONDO:0007888 gard_rare susceptibilities +MONDO:0007888 nord_rare susceptibilities +MONDO:0007888 ordo_disorder susceptibilities +MONDO:0007888 orphanet_rare susceptibilities +MONDO:0007888 otar susceptibilities +MONDO:0007888 rare susceptibilities +MONDO:0007924 gard_rare susceptibilities +MONDO:0007924 nord_rare susceptibilities +MONDO:0007924 ordo_disorder susceptibilities +MONDO:0007924 ordo_malformation_syndrome susceptibilities +MONDO:0007924 orphanet_rare susceptibilities +MONDO:0007924 otar susceptibilities +MONDO:0007924 rare susceptibilities +MONDO:0007939 predisposition susceptibilities +MONDO:0007940 predisposition susceptibilities +MONDO:0007958 gard_rare susceptibilities +MONDO:0007958 nord_rare susceptibilities +MONDO:0007958 ordo_disorder susceptibilities +MONDO:0007958 orphanet_rare susceptibilities +MONDO:0007958 otar susceptibilities +MONDO:0007958 rare susceptibilities +MONDO:0007963 inferred_rare susceptibilities +MONDO:0007963 predisposition susceptibilities +MONDO:0007963 rare susceptibilities +MONDO:0007964 nord_rare susceptibilities +MONDO:0007964 predisposition susceptibilities +MONDO:0007964 rare susceptibilities +MONDO:0007966 gard_rare susceptibilities +MONDO:0007966 predisposition susceptibilities +MONDO:0007966 rare susceptibilities +MONDO:0007967 gard_rare susceptibilities +MONDO:0007967 nord_rare susceptibilities +MONDO:0007967 ordo_disorder susceptibilities +MONDO:0007967 orphanet_rare susceptibilities +MONDO:0007967 rare susceptibilities +MONDO:0008000 predisposition susceptibilities +MONDO:0008018 gard_rare susceptibilities +MONDO:0008018 nord_rare susceptibilities +MONDO:0008018 otar susceptibilities +MONDO:0008018 rare susceptibilities +MONDO:0008067 inferred_rare susceptibilities +MONDO:0008067 predisposition susceptibilities +MONDO:0008067 rare susceptibilities +MONDO:0008072 predisposition susceptibilities +MONDO:0008075 gard_rare susceptibilities +MONDO:0008075 nord_rare susceptibilities +MONDO:0008075 ordo_disorder susceptibilities +MONDO:0008075 orphanet_rare susceptibilities +MONDO:0008075 otar susceptibilities +MONDO:0008075 rare susceptibilities +MONDO:0008078 gard_rare susceptibilities +MONDO:0008078 nord_rare susceptibilities +MONDO:0008078 rare susceptibilities +MONDO:0008080 gard_rare susceptibilities +MONDO:0008080 nord_rare susceptibilities +MONDO:0008080 rare susceptibilities +MONDO:0008081 gard_rare susceptibilities +MONDO:0008081 nord_rare susceptibilities +MONDO:0008081 rare susceptibilities +MONDO:0008082 clingen susceptibilities +MONDO:0008082 gard_rare susceptibilities +MONDO:0008082 nord_rare susceptibilities +MONDO:0008082 ordo_subtype_of_a_disorder susceptibilities +MONDO:0008082 otar susceptibilities +MONDO:0008082 rare susceptibilities +MONDO:0008143 predisposition susceptibilities +MONDO:0008162 predisposition susceptibilities +MONDO:0008234 clingen susceptibilities +MONDO:0008234 gard_rare susceptibilities +MONDO:0008234 nord_rare susceptibilities +MONDO:0008234 ordo_subtype_of_a_disorder susceptibilities +MONDO:0008234 otar susceptibilities +MONDO:0008234 rare susceptibilities +MONDO:0008276 gard_rare susceptibilities +MONDO:0008276 nord_rare susceptibilities +MONDO:0008276 ordo_subtype_of_a_disorder susceptibilities +MONDO:0008276 otar susceptibilities +MONDO:0008276 rare susceptibilities +MONDO:0008278 clingen susceptibilities +MONDO:0008278 gard_rare susceptibilities +MONDO:0008278 nord_rare susceptibilities +MONDO:0008278 otar susceptibilities +MONDO:0008278 rare susceptibilities +MONDO:0008280 clingen susceptibilities +MONDO:0008280 gard_rare susceptibilities +MONDO:0008280 nord_rare susceptibilities +MONDO:0008280 ordo_disorder susceptibilities +MONDO:0008280 orphanet_rare susceptibilities +MONDO:0008280 otar susceptibilities +MONDO:0008280 rare susceptibilities +MONDO:0008283 gard_rare susceptibilities +MONDO:0008283 nord_rare susceptibilities +MONDO:0008283 ordo_disorder susceptibilities +MONDO:0008283 orphanet_rare susceptibilities +MONDO:0008283 otar susceptibilities +MONDO:0008283 rare susceptibilities +MONDO:0008313 predisposition susceptibilities +MONDO:0008334 predisposition susceptibilities +MONDO:0008344 predisposition susceptibilities +MONDO:0008399 predisposition susceptibilities +MONDO:0008419 predisposition susceptibilities +MONDO:0008468 predisposition susceptibilities +MONDO:0008498 predisposition susceptibilities +MONDO:0008570 predisposition susceptibilities +MONDO:0008612 gard_rare susceptibilities +MONDO:0008612 nord_rare susceptibilities +MONDO:0008612 rare susceptibilities +MONDO:0008672 gard_rare susceptibilities +MONDO:0008672 otar susceptibilities +MONDO:0008672 rare susceptibilities +MONDO:0008681 gard_rare susceptibilities +MONDO:0008681 nord_rare susceptibilities +MONDO:0008681 ordo_disorder susceptibilities +MONDO:0008681 ordo_malformation_syndrome susceptibilities +MONDO:0008681 orphanet_rare susceptibilities +MONDO:0008681 otar susceptibilities +MONDO:0008681 rare susceptibilities +MONDO:0008905 nord_rare susceptibilities +MONDO:0008905 ordo_disorder susceptibilities +MONDO:0008905 orphanet_rare susceptibilities +MONDO:0008905 rare susceptibilities +MONDO:0008930 predisposition susceptibilities +MONDO:0009136 gard_rare susceptibilities +MONDO:0009136 nord_rare susceptibilities +MONDO:0009136 prototype_pattern susceptibilities +MONDO:0009136 rare susceptibilities +MONDO:0009335 predisposition susceptibilities +MONDO:0009409 predisposition susceptibilities +MONDO:0009413 clingen susceptibilities +MONDO:0009413 gard_rare susceptibilities +MONDO:0009413 nord_rare susceptibilities +MONDO:0009413 otar susceptibilities +MONDO:0009413 rare susceptibilities +MONDO:0009500 predisposition susceptibilities +MONDO:0009518 predisposition susceptibilities +MONDO:0009741 inferred_rare susceptibilities +MONDO:0009741 predisposition susceptibilities +MONDO:0009741 rare susceptibilities +MONDO:0009759 clingen susceptibilities +MONDO:0009759 gard_rare susceptibilities +MONDO:0009759 nord_rare susceptibilities +MONDO:0009759 rare susceptibilities +MONDO:0009789 predisposition susceptibilities +MONDO:0009990 gard_rare susceptibilities +MONDO:0009990 nord_rare susceptibilities +MONDO:0009990 ordo_disorder susceptibilities +MONDO:0009990 ordo_malformation_syndrome susceptibilities +MONDO:0009990 orphanet_rare susceptibilities +MONDO:0009990 otar susceptibilities +MONDO:0009990 rare susceptibilities +MONDO:0010002 clingen susceptibilities +MONDO:0010002 gard_rare susceptibilities +MONDO:0010002 nord_rare susceptibilities +MONDO:0010002 ordo_disorder susceptibilities +MONDO:0010002 orphanet_rare susceptibilities +MONDO:0010002 otar susceptibilities +MONDO:0010002 rare susceptibilities +MONDO:0010159 clingen susceptibilities +MONDO:0010159 gard_rare susceptibilities +MONDO:0010159 nord_rare susceptibilities +MONDO:0010159 otar susceptibilities +MONDO:0010159 rare susceptibilities +MONDO:0010253 predisposition susceptibilities +MONDO:0010255 predisposition susceptibilities +MONDO:0010282 predisposition susceptibilities +MONDO:0010304 predisposition susceptibilities +MONDO:0010321 predisposition susceptibilities +MONDO:0010331 predisposition susceptibilities +MONDO:0010340 predisposition susceptibilities +MONDO:0010341 predisposition susceptibilities +MONDO:0010342 predisposition susceptibilities +MONDO:0010343 predisposition susceptibilities +MONDO:0010348 predisposition susceptibilities +MONDO:0010389 nord_rare susceptibilities +MONDO:0010389 ordo_etiological_subtype susceptibilities +MONDO:0010389 ordo_subtype_of_a_disorder susceptibilities +MONDO:0010389 predisposition susceptibilities +MONDO:0010389 rare susceptibilities +MONDO:0010433 predisposition susceptibilities +MONDO:0010440 predisposition susceptibilities +MONDO:0010449 predisposition susceptibilities +MONDO:0010469 predisposition susceptibilities +MONDO:0010518 clingen susceptibilities +MONDO:0010518 gard_rare susceptibilities +MONDO:0010518 nord_rare susceptibilities +MONDO:0010518 ordo_disorder susceptibilities +MONDO:0010518 orphanet_rare susceptibilities +MONDO:0010518 otar susceptibilities +MONDO:0010518 rare susceptibilities +MONDO:0010584 clingen susceptibilities +MONDO:0010584 gard_rare susceptibilities +MONDO:0010584 nord_rare susceptibilities +MONDO:0010584 otar susceptibilities +MONDO:0010584 rare susceptibilities +MONDO:0010640 predisposition susceptibilities +MONDO:0010686 gard_rare susceptibilities +MONDO:0010686 nord_rare susceptibilities +MONDO:0010686 ordo_disorder susceptibilities +MONDO:0010686 ordo_malformation_syndrome susceptibilities +MONDO:0010686 orphanet_rare susceptibilities +MONDO:0010686 otar susceptibilities +MONDO:0010686 rare susceptibilities +MONDO:0010833 predisposition susceptibilities +MONDO:0010834 predisposition susceptibilities +MONDO:0010843 predisposition susceptibilities +MONDO:0010846 gard_rare susceptibilities +MONDO:0010846 nord_rare susceptibilities +MONDO:0010846 rare susceptibilities +MONDO:0010853 predisposition susceptibilities +MONDO:0010893 predisposition susceptibilities +MONDO:0010918 predisposition susceptibilities +MONDO:0010940 predisposition susceptibilities +MONDO:0011023 clingen susceptibilities +MONDO:0011023 gard_rare susceptibilities +MONDO:0011023 nord_rare susceptibilities +MONDO:0011023 ordo_disorder susceptibilities +MONDO:0011023 orphanet_rare susceptibilities +MONDO:0011023 otar susceptibilities +MONDO:0011023 rare susceptibilities +MONDO:0011035 gard_rare susceptibilities +MONDO:0011035 nord_rare susceptibilities +MONDO:0011035 ordo_disorder susceptibilities +MONDO:0011035 ordo_malformation_syndrome susceptibilities +MONDO:0011035 orphanet_rare susceptibilities +MONDO:0011035 otar susceptibilities +MONDO:0011035 rare susceptibilities +MONDO:0011037 predisposition susceptibilities +MONDO:0011071 clingen susceptibilities +MONDO:0011071 gard_rare susceptibilities +MONDO:0011071 nord_rare susceptibilities +MONDO:0011071 ordo_disorder susceptibilities +MONDO:0011071 orphanet_rare susceptibilities +MONDO:0011071 otar susceptibilities +MONDO:0011071 rare susceptibilities +MONDO:0011114 gard_rare susceptibilities +MONDO:0011114 nord_rare susceptibilities +MONDO:0011114 ordo_subtype_of_a_disorder susceptibilities +MONDO:0011114 otar susceptibilities +MONDO:0011114 rare susceptibilities +MONDO:0011138 predisposition susceptibilities +MONDO:0011163 predisposition susceptibilities +MONDO:0011164 predisposition susceptibilities +MONDO:0011167 predisposition susceptibilities +MONDO:0011179 predisposition susceptibilities +MONDO:0011207 predisposition susceptibilities +MONDO:0011314 predisposition susceptibilities +MONDO:0011361 inferred_rare susceptibilities +MONDO:0011361 predisposition susceptibilities +MONDO:0011361 rare susceptibilities +MONDO:0011373 predisposition susceptibilities +MONDO:0011384 predisposition susceptibilities +MONDO:0011386 predisposition susceptibilities +MONDO:0011409 predisposition susceptibilities +MONDO:0011418 predisposition susceptibilities +MONDO:0011427 predisposition susceptibilities +MONDO:0011440 predisposition susceptibilities +MONDO:0011450 clingen susceptibilities +MONDO:0011450 gard_rare susceptibilities +MONDO:0011450 nord_rare susceptibilities +MONDO:0011450 predisposition susceptibilities +MONDO:0011450 rare susceptibilities +MONDO:0011491 predisposition susceptibilities +MONDO:0011512 clingen susceptibilities +MONDO:0011512 gard_rare susceptibilities +MONDO:0011512 nord_rare susceptibilities +MONDO:0011512 ordo_disorder susceptibilities +MONDO:0011512 orphanet_rare susceptibilities +MONDO:0011512 otar susceptibilities +MONDO:0011512 rare susceptibilities +MONDO:0011520 predisposition susceptibilities +MONDO:0011556 predisposition susceptibilities +MONDO:0011560 predisposition susceptibilities +MONDO:0011607 predisposition susceptibilities +MONDO:0011622 predisposition susceptibilities +MONDO:0011627 predisposition susceptibilities +MONDO:0011650 predisposition susceptibilities +MONDO:0011684 predisposition susceptibilities +MONDO:0011685 predisposition susceptibilities +MONDO:0011689 predisposition susceptibilities +MONDO:0011693 clingen susceptibilities +MONDO:0011693 predisposition susceptibilities +MONDO:0011695 inferred_rare susceptibilities +MONDO:0011695 predisposition susceptibilities +MONDO:0011695 rare susceptibilities +MONDO:0011696 inferred_rare susceptibilities +MONDO:0011696 predisposition susceptibilities +MONDO:0011696 rare susceptibilities +MONDO:0011713 clingen susceptibilities +MONDO:0011713 gard_rare susceptibilities +MONDO:0011713 nord_rare susceptibilities +MONDO:0011713 rare susceptibilities +MONDO:0011727 predisposition susceptibilities +MONDO:0011729 predisposition susceptibilities +MONDO:0011739 inferred_rare susceptibilities +MONDO:0011739 predisposition susceptibilities +MONDO:0011739 rare susceptibilities +MONDO:0011740 gard_rare susceptibilities +MONDO:0011740 nord_rare susceptibilities +MONDO:0011740 ordo_disorder susceptibilities +MONDO:0011740 orphanet_rare susceptibilities +MONDO:0011740 otar susceptibilities +MONDO:0011740 rare susceptibilities +MONDO:0011741 predisposition susceptibilities +MONDO:0011742 predisposition susceptibilities +MONDO:0011747 predisposition susceptibilities +MONDO:0011753 predisposition susceptibilities +MONDO:0011775 gard_rare susceptibilities +MONDO:0011775 predisposition susceptibilities +MONDO:0011775 rare susceptibilities +MONDO:0011789 clingen susceptibilities +MONDO:0011789 gard_rare susceptibilities +MONDO:0011789 nord_rare susceptibilities +MONDO:0011789 otar susceptibilities +MONDO:0011789 rare susceptibilities +MONDO:0011793 predisposition susceptibilities +MONDO:0011800 gard_rare susceptibilities +MONDO:0011800 rare susceptibilities +MONDO:0011805 predisposition susceptibilities +MONDO:0011807 predisposition susceptibilities +MONDO:0011815 predisposition susceptibilities +MONDO:0011817 predisposition susceptibilities +MONDO:0011820 predisposition susceptibilities +MONDO:0011824 predisposition susceptibilities +MONDO:0011845 predisposition susceptibilities +MONDO:0011846 predisposition susceptibilities +MONDO:0011847 predisposition susceptibilities +MONDO:0011850 predisposition susceptibilities +MONDO:0011851 predisposition susceptibilities +MONDO:0011860 predisposition susceptibilities +MONDO:0011864 clingen susceptibilities +MONDO:0011864 gard_rare susceptibilities +MONDO:0011864 nord_rare susceptibilities +MONDO:0011864 rare susceptibilities +MONDO:0011875 predisposition susceptibilities +MONDO:0011892 predisposition susceptibilities +MONDO:0011896 predisposition susceptibilities +MONDO:0011917 predisposition susceptibilities +MONDO:0011919 predisposition susceptibilities +MONDO:0011923 predisposition susceptibilities +MONDO:0011931 gard_rare susceptibilities +MONDO:0011931 predisposition susceptibilities +MONDO:0011931 rare susceptibilities +MONDO:0011941 predisposition susceptibilities +MONDO:0011942 predisposition susceptibilities +MONDO:0011943 predisposition susceptibilities +MONDO:0011944 predisposition susceptibilities +MONDO:0011954 inferred_rare susceptibilities +MONDO:0011954 predisposition susceptibilities +MONDO:0011954 rare susceptibilities +MONDO:0011956 predisposition susceptibilities +MONDO:0011980 predisposition susceptibilities +MONDO:0011981 predisposition susceptibilities +MONDO:0011982 predisposition susceptibilities +MONDO:0011983 predisposition susceptibilities +MONDO:0012009 predisposition susceptibilities +MONDO:0012010 predisposition susceptibilities +MONDO:0012027 predisposition susceptibilities +MONDO:0012028 predisposition susceptibilities +MONDO:0012036 predisposition susceptibilities +MONDO:0012039 predisposition susceptibilities +MONDO:0012041 clingen susceptibilities +MONDO:0012041 gard_rare susceptibilities +MONDO:0012041 nord_rare susceptibilities +MONDO:0012041 ordo_subtype_of_a_disorder susceptibilities +MONDO:0012041 otar susceptibilities +MONDO:0012041 rare susceptibilities +MONDO:0012042 predisposition susceptibilities +MONDO:0012057 predisposition susceptibilities +MONDO:0012058 predisposition susceptibilities +MONDO:0012067 predisposition susceptibilities +MONDO:0012079 predisposition susceptibilities +MONDO:0012082 predisposition susceptibilities +MONDO:0012109 predisposition susceptibilities +MONDO:0012113 predisposition susceptibilities +MONDO:0012115 predisposition susceptibilities +MONDO:0012119 predisposition susceptibilities +MONDO:0012132 clingen susceptibilities +MONDO:0012132 gard_rare susceptibilities +MONDO:0012132 predisposition susceptibilities +MONDO:0012132 rare susceptibilities +MONDO:0012134 predisposition susceptibilities +MONDO:0012135 predisposition susceptibilities +MONDO:0012141 predisposition susceptibilities +MONDO:0012147 predisposition susceptibilities +MONDO:0012149 predisposition susceptibilities +MONDO:0012150 predisposition susceptibilities +MONDO:0012151 predisposition susceptibilities +MONDO:0012152 predisposition susceptibilities +MONDO:0012159 gard_rare susceptibilities +MONDO:0012159 rare susceptibilities +MONDO:0012161 clingen susceptibilities +MONDO:0012161 nord_rare susceptibilities +MONDO:0012161 ordo_disorder susceptibilities +MONDO:0012161 orphanet_rare susceptibilities +MONDO:0012161 predisposition susceptibilities +MONDO:0012161 rare susceptibilities +MONDO:0012168 predisposition susceptibilities +MONDO:0012183 clingen susceptibilities +MONDO:0012183 inferred_rare susceptibilities +MONDO:0012183 predisposition susceptibilities +MONDO:0012183 rare susceptibilities +MONDO:0012202 predisposition susceptibilities +MONDO:0012210 predisposition susceptibilities +MONDO:0012249 gard_rare susceptibilities +MONDO:0012249 nord_rare susceptibilities +MONDO:0012249 rare susceptibilities +MONDO:0012252 clingen susceptibilities +MONDO:0012252 gard_rare susceptibilities +MONDO:0012252 nord_rare susceptibilities +MONDO:0012252 rare susceptibilities +MONDO:0012261 predisposition susceptibilities +MONDO:0012263 predisposition susceptibilities +MONDO:0012292 predisposition susceptibilities +MONDO:0012303 predisposition susceptibilities +MONDO:0012318 inferred_rare susceptibilities +MONDO:0012318 predisposition susceptibilities +MONDO:0012318 rare susceptibilities +MONDO:0012331 predisposition susceptibilities +MONDO:0012338 predisposition susceptibilities +MONDO:0012339 predisposition susceptibilities +MONDO:0012340 predisposition susceptibilities +MONDO:0012341 predisposition susceptibilities +MONDO:0012358 predisposition susceptibilities +MONDO:0012361 predisposition susceptibilities +MONDO:0012369 predisposition susceptibilities +MONDO:0012377 predisposition susceptibilities +MONDO:0012379 predisposition susceptibilities +MONDO:0012402 predisposition susceptibilities +MONDO:0012403 predisposition susceptibilities +MONDO:0012404 predisposition susceptibilities +MONDO:0012405 gard_rare susceptibilities +MONDO:0012405 nord_rare susceptibilities +MONDO:0012405 rare susceptibilities +MONDO:0012406 gard_rare susceptibilities +MONDO:0012406 nord_rare susceptibilities +MONDO:0012406 rare susceptibilities +MONDO:0012440 predisposition susceptibilities +MONDO:0012441 predisposition susceptibilities +MONDO:0012458 predisposition susceptibilities +MONDO:0012459 predisposition susceptibilities +MONDO:0012466 predisposition susceptibilities +MONDO:0012482 predisposition susceptibilities +MONDO:0012488 predisposition susceptibilities +MONDO:0012492 predisposition susceptibilities +MONDO:0012493 predisposition susceptibilities +MONDO:0012499 predisposition susceptibilities +MONDO:0012533 predisposition susceptibilities +MONDO:0012548 gard_rare susceptibilities +MONDO:0012548 nord_rare susceptibilities +MONDO:0012548 ordo_disorder susceptibilities +MONDO:0012548 orphanet_rare susceptibilities +MONDO:0012548 otar susceptibilities +MONDO:0012548 rare susceptibilities +MONDO:0012552 clingen susceptibilities +MONDO:0012552 gard_rare susceptibilities +MONDO:0012552 nord_rare susceptibilities +MONDO:0012552 ordo_disorder susceptibilities +MONDO:0012552 orphanet_rare susceptibilities +MONDO:0012552 otar susceptibilities +MONDO:0012552 rare susceptibilities +MONDO:0012566 predisposition susceptibilities +MONDO:0012567 predisposition susceptibilities +MONDO:0012577 predisposition susceptibilities +MONDO:0012578 predisposition susceptibilities +MONDO:0012584 predisposition susceptibilities +MONDO:0012585 predisposition susceptibilities +MONDO:0012587 predisposition susceptibilities +MONDO:0012595 predisposition susceptibilities +MONDO:0012599 predisposition susceptibilities +MONDO:0012600 predisposition susceptibilities +MONDO:0012601 predisposition susceptibilities +MONDO:0012606 predisposition susceptibilities +MONDO:0012607 predisposition susceptibilities +MONDO:0012627 predisposition susceptibilities +MONDO:0012628 predisposition susceptibilities +MONDO:0012636 predisposition susceptibilities +MONDO:0012641 predisposition susceptibilities +MONDO:0012655 predisposition susceptibilities +MONDO:0012660 predisposition susceptibilities +MONDO:0012661 predisposition susceptibilities +MONDO:0012666 predisposition susceptibilities +MONDO:0012673 gard_rare susceptibilities +MONDO:0012673 predisposition susceptibilities +MONDO:0012673 rare susceptibilities +MONDO:0012702 predisposition susceptibilities +MONDO:0012710 predisposition susceptibilities +MONDO:0012715 predisposition susceptibilities +MONDO:0012760 predisposition susceptibilities +MONDO:0012763 predisposition susceptibilities +MONDO:0012771 predisposition susceptibilities +MONDO:0012776 predisposition susceptibilities +MONDO:0012777 predisposition susceptibilities +MONDO:0012778 predisposition susceptibilities +MONDO:0012779 predisposition susceptibilities +MONDO:0012780 predisposition susceptibilities +MONDO:0012781 predisposition susceptibilities +MONDO:0012782 predisposition susceptibilities +MONDO:0012788 predisposition susceptibilities +MONDO:0012800 gard_rare susceptibilities +MONDO:0012800 nord_rare susceptibilities +MONDO:0012800 rare susceptibilities +MONDO:0012801 predisposition susceptibilities +MONDO:0012820 gard_rare susceptibilities +MONDO:0012820 predisposition susceptibilities +MONDO:0012820 rare susceptibilities +MONDO:0012821 gard_rare susceptibilities +MONDO:0012821 predisposition susceptibilities +MONDO:0012821 rare susceptibilities +MONDO:0012822 gard_rare susceptibilities +MONDO:0012822 predisposition susceptibilities +MONDO:0012822 rare susceptibilities +MONDO:0012823 gard_rare susceptibilities +MONDO:0012823 predisposition susceptibilities +MONDO:0012823 rare susceptibilities +MONDO:0012826 predisposition susceptibilities +MONDO:0012827 predisposition susceptibilities +MONDO:0012834 predisposition susceptibilities +MONDO:0012835 predisposition susceptibilities +MONDO:0012836 predisposition susceptibilities +MONDO:0012842 gard_rare susceptibilities +MONDO:0012842 predisposition susceptibilities +MONDO:0012842 rare susceptibilities +MONDO:0012843 predisposition susceptibilities +MONDO:0012862 predisposition susceptibilities +MONDO:0012863 predisposition susceptibilities +MONDO:0012884 predisposition susceptibilities +MONDO:0012888 predisposition susceptibilities +MONDO:0012889 predisposition susceptibilities +MONDO:0012893 predisposition susceptibilities +MONDO:0012898 predisposition susceptibilities +MONDO:0012913 gard_rare susceptibilities +MONDO:0012913 nord_rare susceptibilities +MONDO:0012913 rare susceptibilities +MONDO:0012931 clingen susceptibilities +MONDO:0012931 predisposition susceptibilities +MONDO:0012933 clingen susceptibilities +MONDO:0012933 predisposition susceptibilities +MONDO:0012934 inferred_rare susceptibilities +MONDO:0012934 predisposition susceptibilities +MONDO:0012934 rare susceptibilities +MONDO:0012935 inferred_rare susceptibilities +MONDO:0012935 predisposition susceptibilities +MONDO:0012935 rare susceptibilities +MONDO:0012936 inferred_rare susceptibilities +MONDO:0012936 predisposition susceptibilities +MONDO:0012936 rare susceptibilities +MONDO:0012942 gard_rare susceptibilities +MONDO:0012942 rare susceptibilities +MONDO:0012951 gard_rare susceptibilities +MONDO:0012951 predisposition susceptibilities +MONDO:0012951 rare susceptibilities +MONDO:0012952 gard_rare susceptibilities +MONDO:0012952 predisposition susceptibilities +MONDO:0012952 rare susceptibilities +MONDO:0012953 inferred_rare susceptibilities +MONDO:0012953 predisposition susceptibilities +MONDO:0012953 rare susceptibilities +MONDO:0012954 gard_rare susceptibilities +MONDO:0012954 predisposition susceptibilities +MONDO:0012954 rare susceptibilities +MONDO:0012955 gard_rare susceptibilities +MONDO:0012955 predisposition susceptibilities +MONDO:0012955 rare susceptibilities +MONDO:0012956 predisposition susceptibilities +MONDO:0012957 predisposition susceptibilities +MONDO:0012958 predisposition susceptibilities +MONDO:0012962 predisposition susceptibilities +MONDO:0012963 predisposition susceptibilities +MONDO:0012966 predisposition susceptibilities +MONDO:0012969 predisposition susceptibilities +MONDO:0012970 predisposition susceptibilities +MONDO:0012971 predisposition susceptibilities +MONDO:0013020 predisposition susceptibilities +MONDO:0013022 predisposition susceptibilities +MONDO:0013032 predisposition susceptibilities +MONDO:0013045 predisposition susceptibilities +MONDO:0013075 predisposition susceptibilities +MONDO:0013076 predisposition susceptibilities +MONDO:0013083 clingen susceptibilities +MONDO:0013083 inferred_rare susceptibilities +MONDO:0013083 predisposition susceptibilities +MONDO:0013083 rare susceptibilities +MONDO:0013084 inferred_rare susceptibilities +MONDO:0013084 predisposition susceptibilities +MONDO:0013084 rare susceptibilities +MONDO:0013085 inferred_rare susceptibilities +MONDO:0013085 predisposition susceptibilities +MONDO:0013085 rare susceptibilities +MONDO:0013086 inferred_rare susceptibilities +MONDO:0013086 predisposition susceptibilities +MONDO:0013086 rare susceptibilities +MONDO:0013088 inferred_rare susceptibilities +MONDO:0013088 predisposition susceptibilities +MONDO:0013088 rare susceptibilities +MONDO:0013092 gard_rare susceptibilities +MONDO:0013092 predisposition susceptibilities +MONDO:0013092 rare susceptibilities +MONDO:0013093 gard_rare susceptibilities +MONDO:0013093 predisposition susceptibilities +MONDO:0013093 rare susceptibilities +MONDO:0013094 gard_rare susceptibilities +MONDO:0013094 rare susceptibilities +MONDO:0013095 gard_rare susceptibilities +MONDO:0013095 rare susceptibilities +MONDO:0013096 gard_rare susceptibilities +MONDO:0013096 rare susceptibilities +MONDO:0013097 gard_rare susceptibilities +MONDO:0013097 rare susceptibilities +MONDO:0013101 predisposition susceptibilities +MONDO:0013102 predisposition susceptibilities +MONDO:0013103 predisposition susceptibilities +MONDO:0013104 predisposition susceptibilities +MONDO:0013105 predisposition susceptibilities +MONDO:0013106 predisposition susceptibilities +MONDO:0013108 gard_rare susceptibilities +MONDO:0013108 predisposition susceptibilities +MONDO:0013108 rare susceptibilities +MONDO:0013109 gard_rare susceptibilities +MONDO:0013109 predisposition susceptibilities +MONDO:0013109 rare susceptibilities +MONDO:0013124 predisposition susceptibilities +MONDO:0013133 inferred_rare susceptibilities +MONDO:0013133 predisposition susceptibilities +MONDO:0013133 rare susceptibilities +MONDO:0013152 predisposition susceptibilities +MONDO:0013180 predisposition susceptibilities +MONDO:0013185 predisposition susceptibilities +MONDO:0013192 predisposition susceptibilities +MONDO:0013193 predisposition susceptibilities +MONDO:0013196 gard_rare susceptibilities +MONDO:0013196 nord_rare susceptibilities +MONDO:0013196 otar susceptibilities +MONDO:0013196 rare susceptibilities +MONDO:0013199 gard_rare susceptibilities +MONDO:0013199 nord_rare susceptibilities +MONDO:0013199 rare susceptibilities +MONDO:0013224 clingen susceptibilities +MONDO:0013224 gard_rare susceptibilities +MONDO:0013224 nord_rare susceptibilities +MONDO:0013224 rare susceptibilities +MONDO:0013235 inferred_rare susceptibilities +MONDO:0013235 predisposition susceptibilities +MONDO:0013235 rare susceptibilities +MONDO:0013236 inferred_rare susceptibilities +MONDO:0013236 predisposition susceptibilities +MONDO:0013236 rare susceptibilities +MONDO:0013246 predisposition susceptibilities +MONDO:0013253 predisposition susceptibilities +MONDO:0013257 predisposition susceptibilities +MONDO:0013258 predisposition susceptibilities +MONDO:0013265 predisposition susceptibilities +MONDO:0013283 clingen susceptibilities +MONDO:0013283 gard_rare susceptibilities +MONDO:0013283 nord_rare susceptibilities +MONDO:0013283 rare susceptibilities +MONDO:0013284 clingen susceptibilities +MONDO:0013284 gard_rare susceptibilities +MONDO:0013284 nord_rare susceptibilities +MONDO:0013284 otar susceptibilities +MONDO:0013284 rare susceptibilities +MONDO:0013285 clingen susceptibilities +MONDO:0013285 gard_rare susceptibilities +MONDO:0013285 nord_rare susceptibilities +MONDO:0013285 rare susceptibilities +MONDO:0013286 clingen susceptibilities +MONDO:0013286 gard_rare susceptibilities +MONDO:0013286 nord_rare susceptibilities +MONDO:0013286 otar susceptibilities +MONDO:0013286 rare susceptibilities +MONDO:0013303 predisposition susceptibilities +MONDO:0013340 predisposition susceptibilities +MONDO:0013344 predisposition susceptibilities +MONDO:0013357 gard_rare susceptibilities +MONDO:0013357 nord_rare susceptibilities +MONDO:0013357 ordo_disorder susceptibilities +MONDO:0013357 ordo_malformation_syndrome susceptibilities +MONDO:0013357 ordo_subtype_of_a_disorder susceptibilities +MONDO:0013357 orphanet_rare susceptibilities +MONDO:0013357 otar susceptibilities +MONDO:0013357 rare susceptibilities +MONDO:0013383 predisposition susceptibilities +MONDO:0013384 predisposition susceptibilities +MONDO:0013496 predisposition susceptibilities +MONDO:0013510 inferred_rare susceptibilities +MONDO:0013510 predisposition susceptibilities +MONDO:0013510 rare susceptibilities +MONDO:0013519 gard_rare susceptibilities +MONDO:0013519 nord_rare susceptibilities +MONDO:0013519 rare susceptibilities +MONDO:0013520 gard_rare susceptibilities +MONDO:0013520 nord_rare susceptibilities +MONDO:0013520 rare susceptibilities +MONDO:0013521 clingen susceptibilities +MONDO:0013521 gard_rare susceptibilities +MONDO:0013521 nord_rare susceptibilities +MONDO:0013521 otar susceptibilities +MONDO:0013521 rare susceptibilities +MONDO:0013522 gard_rare susceptibilities +MONDO:0013522 nord_rare susceptibilities +MONDO:0013522 otar susceptibilities +MONDO:0013522 rare susceptibilities +MONDO:0013554 predisposition susceptibilities +MONDO:0013562 predisposition susceptibilities +MONDO:0013568 predisposition susceptibilities +MONDO:0013582 clingen susceptibilities +MONDO:0013582 gard_rare susceptibilities +MONDO:0013582 nord_rare susceptibilities +MONDO:0013582 rare susceptibilities +MONDO:0013631 gard_rare susceptibilities +MONDO:0013631 rare susceptibilities +MONDO:0013633 predisposition susceptibilities +MONDO:0013639 predisposition susceptibilities +MONDO:0013653 predisposition susceptibilities +MONDO:0013665 predisposition susceptibilities +MONDO:0013669 predisposition susceptibilities +MONDO:0013685 inferred_rare susceptibilities +MONDO:0013685 predisposition susceptibilities +MONDO:0013685 rare susceptibilities +MONDO:0013692 clingen susceptibilities +MONDO:0013692 gard_rare susceptibilities +MONDO:0013692 nord_rare susceptibilities +MONDO:0013692 ordo_disorder susceptibilities +MONDO:0013692 orphanet_rare susceptibilities +MONDO:0013692 otar susceptibilities +MONDO:0013692 rare susceptibilities +MONDO:0013695 gard_rare susceptibilities +MONDO:0013695 nord_rare susceptibilities +MONDO:0013695 rare susceptibilities +MONDO:0013699 gard_rare susceptibilities +MONDO:0013699 nord_rare susceptibilities +MONDO:0013699 rare susceptibilities +MONDO:0013710 gard_rare susceptibilities +MONDO:0013710 nord_rare susceptibilities +MONDO:0013710 rare susceptibilities +MONDO:0013713 predisposition susceptibilities +MONDO:0013723 predisposition susceptibilities +MONDO:0013724 predisposition susceptibilities +MONDO:0013725 clingen susceptibilities +MONDO:0013725 gard_rare susceptibilities +MONDO:0013725 nord_rare susceptibilities +MONDO:0013725 rare susceptibilities +MONDO:0013727 predisposition susceptibilities +MONDO:0013728 predisposition susceptibilities +MONDO:0013729 predisposition susceptibilities +MONDO:0013759 ordo_disorder susceptibilities +MONDO:0013759 orphanet_rare susceptibilities +MONDO:0013759 predisposition susceptibilities +MONDO:0013759 rare susceptibilities +MONDO:0013765 predisposition susceptibilities +MONDO:0013806 gard_rare susceptibilities +MONDO:0013806 nord_rare susceptibilities +MONDO:0013806 ordo_disorder susceptibilities +MONDO:0013806 orphanet_rare susceptibilities +MONDO:0013806 otar susceptibilities +MONDO:0013806 rare susceptibilities +MONDO:0013808 gard_rare susceptibilities +MONDO:0013808 nord_rare susceptibilities +MONDO:0013808 ordo_disorder susceptibilities +MONDO:0013808 orphanet_rare susceptibilities +MONDO:0013808 otar susceptibilities +MONDO:0013808 rare susceptibilities +MONDO:0013846 predisposition susceptibilities +MONDO:0013855 predisposition susceptibilities +MONDO:0013862 clingen susceptibilities +MONDO:0013862 gard_rare susceptibilities +MONDO:0013862 nord_rare susceptibilities +MONDO:0013862 otar susceptibilities +MONDO:0013862 rare susceptibilities +MONDO:0013863 clingen susceptibilities +MONDO:0013863 gard_rare susceptibilities +MONDO:0013863 nord_rare susceptibilities +MONDO:0013863 ordo_disorder susceptibilities +MONDO:0013863 orphanet_rare susceptibilities +MONDO:0013863 otar susceptibilities +MONDO:0013863 rare susceptibilities +MONDO:0013876 gard_rare susceptibilities +MONDO:0013876 predisposition susceptibilities +MONDO:0013876 rare susceptibilities +MONDO:0013893 predisposition susceptibilities +MONDO:0013908 predisposition susceptibilities +MONDO:0013919 predisposition susceptibilities +MONDO:0013920 predisposition susceptibilities +MONDO:0013921 predisposition susceptibilities +MONDO:0013954 nord_rare susceptibilities +MONDO:0013954 ordo_disorder susceptibilities +MONDO:0013954 orphanet_rare susceptibilities +MONDO:0013954 predisposition susceptibilities +MONDO:0013954 rare susceptibilities +MONDO:0013955 nord_rare susceptibilities +MONDO:0013955 ordo_disorder susceptibilities +MONDO:0013955 orphanet_rare susceptibilities +MONDO:0013955 predisposition susceptibilities +MONDO:0013955 rare susceptibilities +MONDO:0013956 nord_rare susceptibilities +MONDO:0013956 ordo_disorder susceptibilities +MONDO:0013956 orphanet_rare susceptibilities +MONDO:0013956 predisposition susceptibilities +MONDO:0013956 rare susceptibilities +MONDO:0013957 nord_rare susceptibilities +MONDO:0013957 ordo_disorder susceptibilities +MONDO:0013957 orphanet_rare susceptibilities +MONDO:0013957 predisposition susceptibilities +MONDO:0013957 rare susceptibilities +MONDO:0014017 ordo_disorder susceptibilities +MONDO:0014017 orphanet_rare susceptibilities +MONDO:0014017 predisposition susceptibilities +MONDO:0014017 rare susceptibilities +MONDO:0014038 inferred_rare susceptibilities +MONDO:0014038 predisposition susceptibilities +MONDO:0014038 rare susceptibilities +MONDO:0014041 predisposition susceptibilities +MONDO:0014056 inferred_rare susceptibilities +MONDO:0014056 predisposition susceptibilities +MONDO:0014056 rare susceptibilities +MONDO:0014076 gard_rare susceptibilities +MONDO:0014076 nord_rare susceptibilities +MONDO:0014076 otar susceptibilities +MONDO:0014076 rare susceptibilities +MONDO:0014079 predisposition susceptibilities +MONDO:0014151 predisposition susceptibilities +MONDO:0014232 predisposition susceptibilities +MONDO:0014241 gard_rare susceptibilities +MONDO:0014241 predisposition susceptibilities +MONDO:0014241 rare susceptibilities +MONDO:0014251 predisposition susceptibilities +MONDO:0014260 clingen susceptibilities +MONDO:0014260 gard_rare susceptibilities +MONDO:0014260 nord_rare susceptibilities +MONDO:0014260 otar susceptibilities +MONDO:0014260 rare susceptibilities +MONDO:0014281 inferred_rare susceptibilities +MONDO:0014281 predisposition susceptibilities +MONDO:0014281 rare susceptibilities +MONDO:0014299 gard_rare susceptibilities +MONDO:0014299 nord_rare susceptibilities +MONDO:0014299 rare susceptibilities +MONDO:0014338 gard_rare susceptibilities +MONDO:0014338 nord_rare susceptibilities +MONDO:0014338 ordo_disorder susceptibilities +MONDO:0014338 orphanet_rare susceptibilities +MONDO:0014338 rare susceptibilities +MONDO:0014368 gard_rare susceptibilities +MONDO:0014368 predisposition susceptibilities +MONDO:0014368 rare susceptibilities +MONDO:0014429 nord_rare susceptibilities +MONDO:0014429 ordo_disorder susceptibilities +MONDO:0014429 orphanet_rare susceptibilities +MONDO:0014429 predisposition susceptibilities +MONDO:0014429 rare susceptibilities +MONDO:0014494 predisposition susceptibilities +MONDO:0014502 nord_rare susceptibilities +MONDO:0014502 ordo_disorder susceptibilities +MONDO:0014502 orphanet_rare susceptibilities +MONDO:0014502 predisposition susceptibilities +MONDO:0014502 rare susceptibilities +MONDO:0014519 predisposition susceptibilities +MONDO:0014527 gard_rare susceptibilities +MONDO:0014527 nord_rare susceptibilities +MONDO:0014527 ordo_disorder susceptibilities +MONDO:0014527 orphanet_rare susceptibilities +MONDO:0014527 otar susceptibilities +MONDO:0014527 rare susceptibilities +MONDO:0014536 clingen susceptibilities +MONDO:0014536 gard_rare susceptibilities +MONDO:0014536 nord_rare susceptibilities +MONDO:0014536 otar susceptibilities +MONDO:0014536 rare susceptibilities +MONDO:0014600 gard_rare susceptibilities +MONDO:0014600 nord_rare susceptibilities +MONDO:0014600 rare susceptibilities +MONDO:0014613 gard_rare susceptibilities +MONDO:0014613 nord_rare susceptibilities +MONDO:0014613 rare susceptibilities +MONDO:0014630 gard_rare susceptibilities +MONDO:0014630 nord_rare susceptibilities +MONDO:0014630 ordo_subtype_of_a_disorder susceptibilities +MONDO:0014630 rare susceptibilities +MONDO:0014680 predisposition susceptibilities +MONDO:0014690 gard_rare susceptibilities +MONDO:0014690 nord_rare susceptibilities +MONDO:0014690 rare susceptibilities +MONDO:0014697 clingen susceptibilities +MONDO:0014697 gard_rare susceptibilities +MONDO:0014697 nord_rare susceptibilities +MONDO:0014697 rare susceptibilities +MONDO:0014710 nord_rare susceptibilities +MONDO:0014710 ordo_disorder susceptibilities +MONDO:0014710 orphanet_rare susceptibilities +MONDO:0014710 predisposition susceptibilities +MONDO:0014710 rare susceptibilities +MONDO:0014734 predisposition susceptibilities +MONDO:0014774 inferred_rare susceptibilities +MONDO:0014774 predisposition susceptibilities +MONDO:0014774 rare susceptibilities +MONDO:0014786 predisposition susceptibilities +MONDO:0014809 clingen susceptibilities +MONDO:0014809 gard_rare susceptibilities +MONDO:0014809 nord_rare susceptibilities +MONDO:0014809 ordo_disorder susceptibilities +MONDO:0014809 orphanet_rare susceptibilities +MONDO:0014809 otar susceptibilities +MONDO:0014809 rare susceptibilities +MONDO:0014810 clingen susceptibilities +MONDO:0014810 gard_rare susceptibilities +MONDO:0014810 nord_rare susceptibilities +MONDO:0014810 ordo_disorder susceptibilities +MONDO:0014810 orphanet_rare susceptibilities +MONDO:0014810 otar susceptibilities +MONDO:0014810 rare susceptibilities +MONDO:0014902 inferred_rare susceptibilities +MONDO:0014902 predisposition susceptibilities +MONDO:0014902 rare susceptibilities +MONDO:0014919 clingen susceptibilities +MONDO:0014919 gard_rare susceptibilities +MONDO:0014919 nord_rare susceptibilities +MONDO:0014919 otar susceptibilities +MONDO:0014919 rare susceptibilities +MONDO:0015027 gard_rare susceptibilities +MONDO:0015027 nord_rare susceptibilities +MONDO:0015027 ordo_disorder susceptibilities +MONDO:0015027 orphanet_rare susceptibilities +MONDO:0015027 otar susceptibilities +MONDO:0015027 rare susceptibilities +MONDO:0015185 disease_grouping susceptibilities +MONDO:0015185 gard_rare susceptibilities +MONDO:0015185 ordo_group_of_disorders susceptibilities +MONDO:0015185 otar susceptibilities +MONDO:0015185 rare susceptibilities +MONDO:0015356 disease_grouping susceptibilities +MONDO:0015356 gard_rare susceptibilities +MONDO:0015356 ordo_group_of_disorders susceptibilities +MONDO:0015356 otar susceptibilities +MONDO:0015356 predisposition susceptibilities +MONDO:0015356 rare susceptibilities +MONDO:0015517 clingen susceptibilities +MONDO:0015517 gard_rare susceptibilities +MONDO:0015517 nord_rare susceptibilities +MONDO:0015517 ordo_disorder susceptibilities +MONDO:0015517 orphanet_rare susceptibilities +MONDO:0015517 otar susceptibilities +MONDO:0015517 rare susceptibilities +MONDO:0015524 gard_rare susceptibilities +MONDO:0015524 ordo_disorder susceptibilities +MONDO:0015524 orphanet_rare susceptibilities +MONDO:0015524 otar susceptibilities +MONDO:0015524 rare susceptibilities +MONDO:0015780 clingen susceptibilities +MONDO:0015780 gard_rare susceptibilities +MONDO:0015780 nord_rare susceptibilities +MONDO:0015780 ordo_disorder susceptibilities +MONDO:0015780 orphanet_rare susceptibilities +MONDO:0015780 otar susceptibilities +MONDO:0015780 rare susceptibilities +MONDO:0016362 gard_rare susceptibilities +MONDO:0016362 nord_rare susceptibilities +MONDO:0016362 ordo_disorder susceptibilities +MONDO:0016362 orphanet_rare susceptibilities +MONDO:0016362 otar susceptibilities +MONDO:0016362 rare susceptibilities +MONDO:0016368 gard_rare susceptibilities +MONDO:0016368 nord_rare susceptibilities +MONDO:0016368 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016368 otar susceptibilities +MONDO:0016368 rare susceptibilities +MONDO:0016369 gard_rare susceptibilities +MONDO:0016369 nord_rare susceptibilities +MONDO:0016369 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016369 otar susceptibilities +MONDO:0016369 rare susceptibilities +MONDO:0016473 gard_rare susceptibilities +MONDO:0016473 nord_rare susceptibilities +MONDO:0016473 ordo_disorder susceptibilities +MONDO:0016473 orphanet_rare susceptibilities +MONDO:0016473 otar susceptibilities +MONDO:0016473 rare susceptibilities +MONDO:0016475 gard_rare susceptibilities +MONDO:0016475 nord_rare susceptibilities +MONDO:0016475 ordo_etiological_subtype susceptibilities +MONDO:0016475 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016475 otar susceptibilities +MONDO:0016475 rare susceptibilities +MONDO:0016476 gard_rare susceptibilities +MONDO:0016476 nord_rare susceptibilities +MONDO:0016476 ordo_etiological_subtype susceptibilities +MONDO:0016476 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016476 otar susceptibilities +MONDO:0016476 rare susceptibilities +MONDO:0016477 gard_rare susceptibilities +MONDO:0016477 nord_rare susceptibilities +MONDO:0016477 ordo_etiological_subtype susceptibilities +MONDO:0016477 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016477 rare susceptibilities +MONDO:0016478 gard_rare susceptibilities +MONDO:0016478 nord_rare susceptibilities +MONDO:0016478 ordo_etiological_subtype susceptibilities +MONDO:0016478 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016478 rare susceptibilities +MONDO:0016547 gard_rare susceptibilities +MONDO:0016547 nord_rare susceptibilities +MONDO:0016547 ordo_etiological_subtype susceptibilities +MONDO:0016547 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016547 otar susceptibilities +MONDO:0016547 rare susceptibilities +MONDO:0016613 gard_rare susceptibilities +MONDO:0016613 nord_rare susceptibilities +MONDO:0016613 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016613 otar susceptibilities +MONDO:0016613 rare susceptibilities +MONDO:0016860 gard_rare susceptibilities +MONDO:0016860 nord_rare susceptibilities +MONDO:0016860 ordo_etiological_subtype susceptibilities +MONDO:0016860 ordo_subtype_of_a_disorder susceptibilities +MONDO:0016860 otar susceptibilities +MONDO:0016860 rare susceptibilities +MONDO:0017169 disease_grouping susceptibilities +MONDO:0017169 gard_rare susceptibilities +MONDO:0017169 nord_rare susceptibilities +MONDO:0017169 ordo_group_of_disorders susceptibilities +MONDO:0017169 otar susceptibilities +MONDO:0017169 rare susceptibilities +MONDO:0017380 clingen susceptibilities +MONDO:0017380 gard_rare susceptibilities +MONDO:0017380 nord_rare susceptibilities +MONDO:0017380 ordo_disorder susceptibilities +MONDO:0017380 orphanet_rare susceptibilities +MONDO:0017380 otar susceptibilities +MONDO:0017380 rare susceptibilities +MONDO:0017407 gard_rare susceptibilities +MONDO:0017407 nord_rare susceptibilities +MONDO:0017407 ordo_disorder susceptibilities +MONDO:0017407 orphanet_rare susceptibilities +MONDO:0017407 otar susceptibilities +MONDO:0017407 rare susceptibilities +MONDO:0017571 gard_rare susceptibilities +MONDO:0017571 nord_rare susceptibilities +MONDO:0017571 ordo_disorder susceptibilities +MONDO:0017571 orphanet_rare susceptibilities +MONDO:0017571 otar susceptibilities +MONDO:0017571 rare susceptibilities +MONDO:0017900 nord_rare susceptibilities +MONDO:0017900 ordo_disorder susceptibilities +MONDO:0017900 orphanet_rare susceptibilities +MONDO:0017900 predisposition susceptibilities +MONDO:0017900 rare susceptibilities +MONDO:0017901 nord_rare susceptibilities +MONDO:0017901 ordo_disorder susceptibilities +MONDO:0017901 orphanet_rare susceptibilities +MONDO:0017901 predisposition susceptibilities +MONDO:0017901 rare susceptibilities +MONDO:0017902 ordo_disorder susceptibilities +MONDO:0017902 orphanet_rare susceptibilities +MONDO:0017902 predisposition susceptibilities +MONDO:0017902 rare susceptibilities +MONDO:0017903 nord_rare susceptibilities +MONDO:0017903 ordo_disorder susceptibilities +MONDO:0017903 orphanet_rare susceptibilities +MONDO:0017903 predisposition susceptibilities +MONDO:0017903 rare susceptibilities +MONDO:0017905 nord_rare susceptibilities +MONDO:0017905 ordo_disorder susceptibilities +MONDO:0017905 orphanet_rare susceptibilities +MONDO:0017905 predisposition susceptibilities +MONDO:0017905 rare susceptibilities +MONDO:0018045 gard_rare susceptibilities +MONDO:0018045 nord_rare susceptibilities +MONDO:0018045 ordo_disorder susceptibilities +MONDO:0018045 orphanet_rare susceptibilities +MONDO:0018045 otar susceptibilities +MONDO:0018045 rare susceptibilities +MONDO:0018070 gard_rare susceptibilities +MONDO:0018070 nord_rare susceptibilities +MONDO:0018070 rare susceptibilities +MONDO:0018160 gard_rare susceptibilities +MONDO:0018160 nord_rare susceptibilities +MONDO:0018160 ordo_subtype_of_a_disorder susceptibilities +MONDO:0018160 otar susceptibilities +MONDO:0018160 rare susceptibilities +MONDO:0018208 gard_rare susceptibilities +MONDO:0018208 nord_rare susceptibilities +MONDO:0018208 ordo_etiological_subtype susceptibilities +MONDO:0018208 ordo_subtype_of_a_disorder susceptibilities +MONDO:0018208 otar susceptibilities +MONDO:0018208 rare susceptibilities +MONDO:0018426 gard_rare susceptibilities +MONDO:0018426 nord_rare susceptibilities +MONDO:0018426 ordo_subtype_of_a_disorder susceptibilities +MONDO:0018426 otar susceptibilities +MONDO:0018426 rare susceptibilities +MONDO:0018453 gard_rare susceptibilities +MONDO:0018453 nord_rare susceptibilities +MONDO:0018453 ordo_disorder susceptibilities +MONDO:0018453 orphanet_rare susceptibilities +MONDO:0018453 otar susceptibilities +MONDO:0018453 rare susceptibilities +MONDO:0018604 gard_rare susceptibilities +MONDO:0018604 nord_rare susceptibilities +MONDO:0018604 ordo_disorder susceptibilities +MONDO:0018604 orphanet_rare susceptibilities +MONDO:0018604 rare susceptibilities +MONDO:0018630 clingen susceptibilities +MONDO:0018630 disease_grouping susceptibilities +MONDO:0018630 gard_rare susceptibilities +MONDO:0018630 nord_rare susceptibilities +MONDO:0018630 ordo_group_of_disorders susceptibilities +MONDO:0018630 otar susceptibilities +MONDO:0018630 rare susceptibilities +MONDO:0018643 ordo_disorder susceptibilities +MONDO:0018643 orphanet_rare susceptibilities +MONDO:0018643 predisposition susceptibilities +MONDO:0018643 rare susceptibilities +MONDO:0018653 gard_rare susceptibilities +MONDO:0018653 nord_rare susceptibilities +MONDO:0018653 ordo_subtype_of_a_disorder susceptibilities +MONDO:0018653 otar susceptibilities +MONDO:0018653 rare susceptibilities +MONDO:0018875 gard_rare susceptibilities +MONDO:0018875 nord_rare susceptibilities +MONDO:0018875 ordo_disorder susceptibilities +MONDO:0018875 orphanet_rare susceptibilities +MONDO:0018875 otar susceptibilities +MONDO:0018875 rare susceptibilities +MONDO:0018893 gard_rare susceptibilities +MONDO:0018893 nord_rare susceptibilities +MONDO:0018893 ordo_disorder susceptibilities +MONDO:0018893 ordo_malformation_syndrome susceptibilities +MONDO:0018893 orphanet_rare susceptibilities +MONDO:0018893 rare susceptibilities +MONDO:0018975 clingen susceptibilities +MONDO:0018975 gard_rare susceptibilities +MONDO:0018975 nord_rare susceptibilities +MONDO:0018975 ordo_disorder susceptibilities +MONDO:0018975 orphanet_rare susceptibilities +MONDO:0018975 otar susceptibilities +MONDO:0018975 rare susceptibilities +MONDO:0019003 gard_rare susceptibilities +MONDO:0019003 nord_rare susceptibilities +MONDO:0019003 ordo_disorder susceptibilities +MONDO:0019003 orphanet_rare susceptibilities +MONDO:0019003 otar susceptibilities +MONDO:0019003 rare susceptibilities +MONDO:0019146 disease_grouping susceptibilities +MONDO:0019146 ordo_group_of_disorders susceptibilities +MONDO:0019146 predisposition susceptibilities +MONDO:0019190 gard_rare susceptibilities +MONDO:0019190 nord_rare susceptibilities +MONDO:0019190 ordo_subtype_of_a_disorder susceptibilities +MONDO:0019190 otar susceptibilities +MONDO:0019190 rare susceptibilities +MONDO:0019336 gard_rare susceptibilities +MONDO:0019336 nord_rare susceptibilities +MONDO:0019336 ordo_subtype_of_a_disorder susceptibilities +MONDO:0019336 otar susceptibilities +MONDO:0019336 rare susceptibilities +MONDO:0019738 gard_rare susceptibilities +MONDO:0019738 ordo_etiological_subtype susceptibilities +MONDO:0019738 otar susceptibilities +MONDO:0019738 rare susceptibilities +MONDO:0019739 gard_rare susceptibilities +MONDO:0019739 nord_rare susceptibilities +MONDO:0019739 ordo_etiological_subtype susceptibilities +MONDO:0019739 ordo_subtype_of_a_disorder susceptibilities +MONDO:0019739 otar susceptibilities +MONDO:0019739 rare susceptibilities +MONDO:0019875 gard_rare susceptibilities +MONDO:0019875 nord_rare susceptibilities +MONDO:0019875 ordo_etiological_subtype susceptibilities +MONDO:0019875 ordo_subtype_of_a_disorder susceptibilities +MONDO:0019875 rare susceptibilities +MONDO:0019923 gard_rare susceptibilities +MONDO:0019923 nord_rare susceptibilities +MONDO:0019923 ordo_etiological_subtype susceptibilities +MONDO:0019923 ordo_subtype_of_a_disorder susceptibilities +MONDO:0019923 rare susceptibilities +MONDO:0020497 gard_rare susceptibilities +MONDO:0020497 nord_rare susceptibilities +MONDO:0020497 ordo_subtype_of_a_disorder susceptibilities +MONDO:0020497 otar susceptibilities +MONDO:0020497 rare susceptibilities +MONDO:0020530 nord_rare susceptibilities +MONDO:0020530 ordo_disorder susceptibilities +MONDO:0020530 orphanet_rare susceptibilities +MONDO:0020530 predisposition susceptibilities +MONDO:0020530 rare susceptibilities +MONDO:0020573 predisposition susceptibilities +MONDO:0020636 predisposition susceptibilities +MONDO:0020637 predisposition susceptibilities +MONDO:0020705 predisposition susceptibilities +MONDO:0020752 predisposition susceptibilities +MONDO:0020836 predisposition susceptibilities +MONDO:0021012 predisposition susceptibilities +MONDO:0021024 predisposition susceptibilities +MONDO:0021055 gard_rare susceptibilities +MONDO:0021055 nord_rare susceptibilities +MONDO:0021055 ordo_disorder susceptibilities +MONDO:0021055 orphanet_rare susceptibilities +MONDO:0021055 otar susceptibilities +MONDO:0021055 rare susceptibilities +MONDO:0021056 gard_rare susceptibilities +MONDO:0021056 nord_rare susceptibilities +MONDO:0021056 otar susceptibilities +MONDO:0021056 rare susceptibilities +MONDO:0021057 clingen susceptibilities +MONDO:0021057 gard_rare susceptibilities +MONDO:0021057 otar susceptibilities +MONDO:0021057 rare susceptibilities +MONDO:0021061 gard_rare susceptibilities +MONDO:0021061 nord_rare susceptibilities +MONDO:0021061 otar susceptibilities +MONDO:0021061 rare susceptibilities +MONDO:0021571 predisposition susceptibilities +MONDO:0021838 gard_rare susceptibilities +MONDO:0021838 n_of_one susceptibilities +MONDO:0021838 rare susceptibilities +MONDO:0023182 gard_rare susceptibilities +MONDO:0023182 rare susceptibilities +MONDO:0024462 inferred_rare susceptibilities +MONDO:0024462 rare susceptibilities +MONDO:0024498 gard_rare susceptibilities +MONDO:0024498 predisposition susceptibilities +MONDO:0024498 rare susceptibilities +MONDO:0024512 predisposition susceptibilities +MONDO:0024517 gard_rare susceptibilities +MONDO:0024517 nord_rare susceptibilities +MONDO:0024517 rare susceptibilities +MONDO:0024563 predisposition susceptibilities +MONDO:0024570 gard_rare susceptibilities +MONDO:0024570 nord_rare susceptibilities +MONDO:0024570 rare susceptibilities +MONDO:0027353 gard_rare susceptibilities +MONDO:0027353 rare susceptibilities +MONDO:0031057 gard_rare susceptibilities +MONDO:0031057 nord_rare susceptibilities +MONDO:0031057 rare susceptibilities +MONDO:0032666 clingen susceptibilities +MONDO:0032867 gard_rare susceptibilities +MONDO:0032867 rare susceptibilities +MONDO:0035547 nord_rare susceptibilities +MONDO:0035547 obsoletion_candidate susceptibilities +MONDO:0035547 ordo_disorder susceptibilities +MONDO:0035547 orphanet_rare susceptibilities +MONDO:0035547 rare susceptibilities +MONDO:0035548 nord_rare susceptibilities +MONDO:0035548 ordo_disorder susceptibilities +MONDO:0035548 orphanet_rare susceptibilities +MONDO:0035548 rare susceptibilities +MONDO:0042486 gard_rare susceptibilities +MONDO:0042486 nord_rare susceptibilities +MONDO:0042486 predisposition susceptibilities +MONDO:0042486 rare susceptibilities +MONDO:0042489 predisposition susceptibilities +MONDO:0042977 gard_rare susceptibilities +MONDO:0042977 nord_rare susceptibilities +MONDO:0042977 rare susceptibilities +MONDO:0044300 gard_rare susceptibilities +MONDO:0044300 ordo_subtype_of_a_disorder susceptibilities +MONDO:0044300 rare susceptibilities +MONDO:0044301 predisposition susceptibilities +MONDO:0054691 clingen susceptibilities +MONDO:0054691 gard_rare susceptibilities +MONDO:0054691 nord_rare susceptibilities +MONDO:0054691 otar susceptibilities +MONDO:0054691 rare susceptibilities +MONDO:0054736 gard_rare susceptibilities +MONDO:0054736 nord_rare susceptibilities +MONDO:0054736 rare susceptibilities +MONDO:0054750 clingen susceptibilities +MONDO:0054750 predisposition susceptibilities +MONDO:0054754 predisposition susceptibilities +MONDO:0060670 clingen susceptibilities +MONDO:0060670 predisposition susceptibilities +MONDO:0060671 predisposition susceptibilities +MONDO:0100083 gard_rare susceptibilities +MONDO:0100083 nord_rare susceptibilities +MONDO:0100083 otar susceptibilities +MONDO:0100083 rare susceptibilities +MONDO:0100152 clingen susceptibilities +MONDO:0100152 gard_rare susceptibilities +MONDO:0100152 otar susceptibilities +MONDO:0100152 rare susceptibilities +MONDO:0100173 gard_rare susceptibilities +MONDO:0100173 rare susceptibilities +MONDO:0100199 gard_rare susceptibilities +MONDO:0100199 rare susceptibilities +MONDO:0100242 gard_rare susceptibilities +MONDO:0100242 rare susceptibilities +MONDO:0100287 clingen susceptibilities +MONDO:0100287 gard_rare susceptibilities +MONDO:0100287 rare susceptibilities +MONDO:0100290 gard_rare susceptibilities +MONDO:0100290 rare susceptibilities +MONDO:0100301 gard_rare susceptibilities +MONDO:0100301 rare susceptibilities +MONDO:0100351 clingen susceptibilities +MONDO:0100351 gard_rare susceptibilities +MONDO:0100351 rare susceptibilities +MONDO:0100488 gard_rare susceptibilities +MONDO:0100488 rare susceptibilities +MONDO:0100502 clingen susceptibilities +MONDO:0100502 gard_rare susceptibilities +MONDO:0100502 rare susceptibilities +MONDO:0700041 inferred_rare susceptibilities +MONDO:0700041 rare susceptibilities +MONDO:0700267 gard_rare susceptibilities +MONDO:0700267 rare susceptibilities +MONDO:0700268 gard_rare susceptibilities +MONDO:0700268 rare susceptibilities +MONDO:0700269 gard_rare susceptibilities +MONDO:0700269 rare susceptibilities +MONDO:0700270 gard_rare susceptibilities +MONDO:0700270 rare susceptibilities +MONDO:0700271 gard_rare susceptibilities +MONDO:0700271 rare susceptibilities +MONDO:0700272 gard_rare susceptibilities +MONDO:0700272 rare susceptibilities +MONDO:0700273 gard_rare susceptibilities +MONDO:0700273 rare susceptibilities +MONDO:0700274 gard_rare susceptibilities +MONDO:0700274 rare susceptibilities +MONDO:0800149 gard_rare susceptibilities +MONDO:0800149 rare susceptibilities +MONDO:0800268 predisposition susceptibilities +MONDO:0800290 gard_rare susceptibilities +MONDO:0800290 rare susceptibilities +MONDO:0800366 gard_rare susceptibilities +MONDO:0800366 rare susceptibilities +MONDO:0800370 gard_rare susceptibilities +MONDO:0800370 nord_rare susceptibilities +MONDO:0800370 rare susceptibilities +MONDO:0800416 predisposition susceptibilities +MONDO:0800418 gard_rare susceptibilities +MONDO:0800418 rare susceptibilities +MONDO:0800419 gard_rare susceptibilities +MONDO:0800419 rare susceptibilities +MONDO:0800420 gard_rare susceptibilities +MONDO:0800420 rare susceptibilities +MONDO:0800423 gard_rare susceptibilities +MONDO:0800423 rare susceptibilities +MONDO:0800424 gard_rare susceptibilities +MONDO:0800424 rare susceptibilities +MONDO:0800433 gard_rare susceptibilities +MONDO:0800433 rare susceptibilities +MONDO:0800434 gard_rare susceptibilities +MONDO:0800434 rare susceptibilities +MONDO:0800435 gard_rare susceptibilities +MONDO:0800435 rare susceptibilities +MONDO:0800447 predisposition susceptibilities +MONDO:0800467 gard_rare susceptibilities +MONDO:0800467 rare susceptibilities +MONDO:0850064 gard_rare susceptibilities +MONDO:0850064 ordo_group_of_disorders susceptibilities +MONDO:0850064 rare susceptibilities +MONDO:0859008 gard_rare susceptibilities +MONDO:0859008 ordo_group_of_disorders susceptibilities +MONDO:0859008 rare susceptibilities +MONDO:0859267 gard_rare susceptibilities +MONDO:0859267 rare susceptibilities +MONDO:0859319 gard_rare susceptibilities +MONDO:0859319 rare susceptibilities +MONDO:0859329 gard_rare susceptibilities +MONDO:0859329 rare susceptibilities +MONDO:0859346 gard_rare susceptibilities +MONDO:0859346 rare susceptibilities +MONDO:0859575 gard_rare susceptibilities +MONDO:0859575 rare susceptibilities +MONDO:0859576 gard_rare susceptibilities +MONDO:0859576 rare susceptibilities +MONDO:0859763 gard_rare susceptibilities +MONDO:0859763 ordo_disorder susceptibilities +MONDO:0859763 orphanet_rare susceptibilities +MONDO:0859763 rare susceptibilities +MONDO:0859764 gard_rare susceptibilities +MONDO:0859764 ordo_disorder susceptibilities +MONDO:0859764 orphanet_rare susceptibilities +MONDO:0859764 rare susceptibilities +MONDO:0859765 gard_rare susceptibilities +MONDO:0859765 ordo_disorder susceptibilities +MONDO:0859765 orphanet_rare susceptibilities +MONDO:0859765 rare susceptibilities +MONDO:0958013 gard_rare susceptibilities +MONDO:0958013 rare susceptibilities +MONDO:0958174 gard_rare susceptibilities +MONDO:0958174 rare susceptibilities +MONDO:0958189 gard_rare susceptibilities +MONDO:0958189 rare susceptibilities +MONDO:0005203 otar injuries +MONDO:0005309 otar injuries +MONDO:0005315 otar injuries +MONDO:0005315 other_hierarchy injuries +MONDO:0005319 otar injuries +MONDO:0005319 other_hierarchy injuries +MONDO:0005320 otar injuries +MONDO:0005320 other_hierarchy injuries +MONDO:0005322 otar injuries +MONDO:0005325 otar injuries +MONDO:0005327 otar injuries +MONDO:0005621 otar injuries +MONDO:0015796 gard_rare injuries +MONDO:0015796 ordo_clinical_situation injuries +MONDO:0015796 ordo_disorder injuries +MONDO:0015796 orphanet_rare injuries +MONDO:0015796 otar injuries +MONDO:0015796 rare injuries +MONDO:0021178 harrisons_view injuries +MONDO:0021178 otar injuries +MONDO:0021178 other_hierarchy injuries +MONDO:0037747 otar injuries +MONDO:0043510 otar injuries +MONDO:0043797 gard_rare injuries +MONDO:0043797 ordo_disorder injuries +MONDO:0043797 orphanet_rare injuries +MONDO:0043797 rare injuries +MONDO:0044745 otar injuries +MONDO:0100075 otar injuries diff --git a/src/scripts/notebooks/mondo_synonyms.csv b/src/scripts/notebooks/mondo_synonyms.csv new file mode 100644 index 0000000000..7785a8a8ef --- /dev/null +++ b/src/scripts/notebooks/mondo_synonyms.csv @@ -0,0 +1,11 @@ +id synonym synonym_type xrefs predicate group +MONDO:0000001 condition NCIT:C2991 hasExactSynonym disease +MONDO:0000001 disease NCIT:C2991 hasExactSynonym disease +MONDO:0000001 disease or disorder NCIT:C2991 hasExactSynonym disease +MONDO:0000001 disease or disorder, non-neoplastic NCIT:C2991 hasExactSynonym disease +MONDO:0000001 diseases NCIT:C2991 hasExactSynonym disease +MONDO:0000001 diseases and disorders NCIT:C2991 hasExactSynonym disease +MONDO:0000001 disorder NCIT:C2991 hasExactSynonym disease +MONDO:0000001 disorders NCIT:C2991 hasExactSynonym disease +MONDO:0000001 medical condition hasExactSynonym disease +MONDO:0000001 other disease NCIT:C2991 hasExactSynonym disease diff --git a/src/scripts/notebooks/poetry.lock b/src/scripts/notebooks/poetry.lock new file mode 100644 index 0000000000..327ea0f3fe --- /dev/null +++ b/src/scripts/notebooks/poetry.lock @@ -0,0 +1,2768 @@ +# This file is automatically @generated by Poetry 1.7.1 and should not be changed by hand. + +[[package]] +name = "airium" +version = "0.2.6" +description = "Easy and quick html builder with natural syntax correspondence (python->html). No templates needed. Serves pure pythonic library with no dependencies." +optional = false +python-versions = "*" +files = [ + {file = "airium-0.2.6-py3-none-any.whl", hash = "sha256:50af5cf491e084f27909e29a93550b4170e587cde01334d58c6249644ee8c6c2"}, + {file = "airium-0.2.6.tar.gz", hash = "sha256:ccab36b798b6cce3d0c5074e52ce8059f6e82991caae4985f42cadfad80b1de4"}, +] + +[package.extras] +dev = ["pytest (>=6.2,<7.0)", "pytest-cov (>=3.0,<4.0)", "pytest-mock (>=3.6,<4.0)"] +parse = ["beautifulsoup4 (>=4.10.0,<5.0)", "requests (>=2.12.0,<3)"] + +[[package]] +name = "annotated-types" +version = "0.7.0" +description = "Reusable constraint types to use with typing.Annotated" +optional = false +python-versions = ">=3.8" +files = [ + {file = "annotated_types-0.7.0-py3-none-any.whl", hash = "sha256:1f02e8b43a8fbbc3f3e0d4f0f4bfc8131bcb4eebe8849b8e5c773f3a1c582a53"}, + {file = "annotated_types-0.7.0.tar.gz", hash = "sha256:aff07c09a53a08bc8cfccb9c85b05f1aa9a2a6f23728d790723543408344ce89"}, +] + +[[package]] +name = "antlr4-python3-runtime" +version = "4.9.3" +description = "ANTLR 4.9.3 runtime for Python 3.7" +optional = false +python-versions = "*" +files = [ + {file = "antlr4-python3-runtime-4.9.3.tar.gz", hash = "sha256:f224469b4168294902bb1efa80a8bf7855f24c99aef99cbefc1bcd3cce77881b"}, +] + +[[package]] +name = "anyio" +version = "4.4.0" +description = "High level compatibility layer for multiple asynchronous event loop implementations" +optional = false +python-versions = ">=3.8" +files = [ + {file = "anyio-4.4.0-py3-none-any.whl", hash = "sha256:c1b2d8f46a8a812513012e1107cb0e68c17159a7a594208005a57dc776e1bdc7"}, + {file = "anyio-4.4.0.tar.gz", hash = "sha256:5aadc6a1bbb7cdb0bede386cac5e2940f5e2ff3aa20277e991cf028e0585ce94"}, +] + +[package.dependencies] +idna = ">=2.8" +sniffio = ">=1.1" + +[package.extras] +doc = ["Sphinx (>=7)", "packaging", "sphinx-autodoc-typehints (>=1.2.0)", "sphinx-rtd-theme"] +test = ["anyio[trio]", "coverage[toml] (>=7)", "exceptiongroup (>=1.2.0)", "hypothesis (>=4.0)", "psutil (>=5.9)", "pytest (>=7.0)", "pytest-mock (>=3.6.1)", "trustme", "uvloop (>=0.17)"] +trio = ["trio (>=0.23)"] + +[[package]] +name = "appdirs" +version = "1.4.4" +description = "A small Python module for determining appropriate platform-specific dirs, e.g. a \"user data dir\"." +optional = false +python-versions = "*" +files = [ + {file = "appdirs-1.4.4-py2.py3-none-any.whl", hash = "sha256:a841dacd6b99318a741b166adb07e19ee71a274450e68237b4650ca1055ab128"}, + {file = "appdirs-1.4.4.tar.gz", hash = "sha256:7d5d0167b2b1ba821647616af46a749d1c653740dd0d2415100fe26e27afdf41"}, +] + +[[package]] +name = "attrs" +version = "23.2.0" +description = "Classes Without Boilerplate" +optional = false +python-versions = ">=3.7" +files = [ + {file = "attrs-23.2.0-py3-none-any.whl", hash = "sha256:99b87a485a5820b23b879f04c2305b44b951b502fd64be915879d77a7e8fc6f1"}, + {file = "attrs-23.2.0.tar.gz", hash = "sha256:935dc3b529c262f6cf76e50877d35a4bd3c1de194fd41f47a2b7ae8f19971f30"}, +] + +[package.extras] +cov = ["attrs[tests]", "coverage[toml] (>=5.3)"] +dev = ["attrs[tests]", "pre-commit"] +docs = ["furo", "myst-parser", "sphinx", "sphinx-notfound-page", "sphinxcontrib-towncrier", "towncrier", "zope-interface"] +tests = ["attrs[tests-no-zope]", "zope-interface"] +tests-mypy = ["mypy (>=1.6)", "pytest-mypy-plugins"] +tests-no-zope = ["attrs[tests-mypy]", "cloudpickle", "hypothesis", "pympler", "pytest (>=4.3.0)", "pytest-xdist[psutil]"] + +[[package]] +name = "bcp47" +version = "0.1.0" +description = "Language tags made easy" +optional = false +python-versions = "*" +files = [ + {file = "bcp47-0.1.0-py3-none-any.whl", hash = "sha256:a567b7fe881c900916a9db62ac8f792370c7ddf2664e601b74eeed35d8758aa5"}, + {file = "bcp47-0.1.0.tar.gz", hash = "sha256:37cc7a03fd696149ebfe7de785c5bad473f911eddac8415cf479584049cf03d5"}, +] + +[[package]] +name = "cattrs" +version = "23.2.3" +description = "Composable complex class support for attrs and dataclasses." +optional = false +python-versions = ">=3.8" +files = [ + {file = "cattrs-23.2.3-py3-none-any.whl", hash = "sha256:0341994d94971052e9ee70662542699a3162ea1e0c62f7ce1b4a57f563685108"}, + {file = "cattrs-23.2.3.tar.gz", hash = "sha256:a934090d95abaa9e911dac357e3a8699e0b4b14f8529bcc7d2b1ad9d51672b9f"}, +] + +[package.dependencies] +attrs = ">=23.1.0" + +[package.extras] +bson = ["pymongo (>=4.4.0)"] +cbor2 = ["cbor2 (>=5.4.6)"] +msgpack = ["msgpack (>=1.0.5)"] +orjson = ["orjson (>=3.9.2)"] +pyyaml = ["pyyaml (>=6.0)"] +tomlkit = ["tomlkit (>=0.11.8)"] +ujson = ["ujson (>=5.7.0)"] + +[[package]] +name = "certifi" +version = "2024.6.2" +description = "Python package for providing Mozilla's CA Bundle." +optional = false +python-versions = ">=3.6" +files = [ + {file = "certifi-2024.6.2-py3-none-any.whl", hash = "sha256:ddc6c8ce995e6987e7faf5e3f1b02b302836a0e5d98ece18392cb1a36c72ad56"}, + {file = "certifi-2024.6.2.tar.gz", hash = "sha256:3cd43f1c6fa7dedc5899d69d3ad0398fd018ad1a17fba83ddaf78aa46c747516"}, +] + +[[package]] +name = "chardet" +version = "5.2.0" +description = "Universal encoding detector for Python 3" +optional = false +python-versions = ">=3.7" +files = [ + {file = "chardet-5.2.0-py3-none-any.whl", hash = "sha256:e1cf59446890a00105fe7b7912492ea04b6e6f06d4b742b2c788469e34c82970"}, + {file = "chardet-5.2.0.tar.gz", hash = "sha256:1b3b6ff479a8c414bc3fa2c0852995695c4a026dcd6d0633b2dd092ca39c1cf7"}, +] + +[[package]] +name = "charset-normalizer" +version = "3.3.2" +description = "The Real First Universal Charset Detector. Open, modern and actively maintained alternative to Chardet." +optional = false +python-versions = ">=3.7.0" +files = [ + {file = "charset-normalizer-3.3.2.tar.gz", hash = "sha256:f30c3cb33b24454a82faecaf01b19c18562b1e89558fb6c56de4d9118a032fd5"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-macosx_10_9_universal2.whl", hash = "sha256:25baf083bf6f6b341f4121c2f3c548875ee6f5339300e08be3f2b2ba1721cdd3"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:06435b539f889b1f6f4ac1758871aae42dc3a8c0e24ac9e60c2384973ad73027"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:9063e24fdb1e498ab71cb7419e24622516c4a04476b17a2dab57e8baa30d6e03"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:6897af51655e3691ff853668779c7bad41579facacf5fd7253b0133308cf000d"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:1d3193f4a680c64b4b6a9115943538edb896edc190f0b222e73761716519268e"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:cd70574b12bb8a4d2aaa0094515df2463cb429d8536cfb6c7ce983246983e5a6"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:8465322196c8b4d7ab6d1e049e4c5cb460d0394da4a27d23cc242fbf0034b6b5"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:a9a8e9031d613fd2009c182b69c7b2c1ef8239a0efb1df3f7c8da66d5dd3d537"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:beb58fe5cdb101e3a055192ac291b7a21e3b7ef4f67fa1d74e331a7f2124341c"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-musllinux_1_1_i686.whl", hash = "sha256:e06ed3eb3218bc64786f7db41917d4e686cc4856944f53d5bdf83a6884432e12"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-musllinux_1_1_ppc64le.whl", hash = "sha256:2e81c7b9c8979ce92ed306c249d46894776a909505d8f5a4ba55b14206e3222f"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-musllinux_1_1_s390x.whl", hash = "sha256:572c3763a264ba47b3cf708a44ce965d98555f618ca42c926a9c1616d8f34269"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:fd1abc0d89e30cc4e02e4064dc67fcc51bd941eb395c502aac3ec19fab46b519"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-win32.whl", hash = "sha256:3d47fa203a7bd9c5b6cee4736ee84ca03b8ef23193c0d1ca99b5089f72645c73"}, + {file = "charset_normalizer-3.3.2-cp310-cp310-win_amd64.whl", hash = "sha256:10955842570876604d404661fbccbc9c7e684caf432c09c715ec38fbae45ae09"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-macosx_10_9_universal2.whl", hash = "sha256:802fe99cca7457642125a8a88a084cef28ff0cf9407060f7b93dca5aa25480db"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:573f6eac48f4769d667c4442081b1794f52919e7edada77495aaed9236d13a96"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:549a3a73da901d5bc3ce8d24e0600d1fa85524c10287f6004fbab87672bf3e1e"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:f27273b60488abe721a075bcca6d7f3964f9f6f067c8c4c605743023d7d3944f"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:1ceae2f17a9c33cb48e3263960dc5fc8005351ee19db217e9b1bb15d28c02574"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:65f6f63034100ead094b8744b3b97965785388f308a64cf8d7c34f2f2e5be0c4"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:753f10e867343b4511128c6ed8c82f7bec3bd026875576dfd88483c5c73b2fd8"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:4a78b2b446bd7c934f5dcedc588903fb2f5eec172f3d29e52a9096a43722adfc"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:e537484df0d8f426ce2afb2d0f8e1c3d0b114b83f8850e5f2fbea0e797bd82ae"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-musllinux_1_1_i686.whl", hash = "sha256:eb6904c354526e758fda7167b33005998fb68c46fbc10e013ca97f21ca5c8887"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-musllinux_1_1_ppc64le.whl", hash = "sha256:deb6be0ac38ece9ba87dea880e438f25ca3eddfac8b002a2ec3d9183a454e8ae"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-musllinux_1_1_s390x.whl", hash = "sha256:4ab2fe47fae9e0f9dee8c04187ce5d09f48eabe611be8259444906793ab7cbce"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:80402cd6ee291dcb72644d6eac93785fe2c8b9cb30893c1af5b8fdd753b9d40f"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-win32.whl", hash = "sha256:7cd13a2e3ddeed6913a65e66e94b51d80a041145a026c27e6bb76c31a853c6ab"}, + {file = "charset_normalizer-3.3.2-cp311-cp311-win_amd64.whl", hash = "sha256:663946639d296df6a2bb2aa51b60a2454ca1cb29835324c640dafb5ff2131a77"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-macosx_10_9_universal2.whl", hash = "sha256:0b2b64d2bb6d3fb9112bafa732def486049e63de9618b5843bcdd081d8144cd8"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:ddbb2551d7e0102e7252db79ba445cdab71b26640817ab1e3e3648dad515003b"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:55086ee1064215781fff39a1af09518bc9255b50d6333f2e4c74ca09fac6a8f6"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:8f4a014bc36d3c57402e2977dada34f9c12300af536839dc38c0beab8878f38a"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:a10af20b82360ab00827f916a6058451b723b4e65030c5a18577c8b2de5b3389"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:8d756e44e94489e49571086ef83b2bb8ce311e730092d2c34ca8f7d925cb20aa"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:90d558489962fd4918143277a773316e56c72da56ec7aa3dc3dbbe20fdfed15b"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:6ac7ffc7ad6d040517be39eb591cac5ff87416c2537df6ba3cba3bae290c0fed"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:7ed9e526742851e8d5cc9e6cf41427dfc6068d4f5a3bb03659444b4cabf6bc26"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-musllinux_1_1_i686.whl", hash = "sha256:8bdb58ff7ba23002a4c5808d608e4e6c687175724f54a5dade5fa8c67b604e4d"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-musllinux_1_1_ppc64le.whl", hash = "sha256:6b3251890fff30ee142c44144871185dbe13b11bab478a88887a639655be1068"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-musllinux_1_1_s390x.whl", hash = "sha256:b4a23f61ce87adf89be746c8a8974fe1c823c891d8f86eb218bb957c924bb143"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:efcb3f6676480691518c177e3b465bcddf57cea040302f9f4e6e191af91174d4"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-win32.whl", hash = "sha256:d965bba47ddeec8cd560687584e88cf699fd28f192ceb452d1d7ee807c5597b7"}, + {file = "charset_normalizer-3.3.2-cp312-cp312-win_amd64.whl", hash = "sha256:96b02a3dc4381e5494fad39be677abcb5e6634bf7b4fa83a6dd3112607547001"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:95f2a5796329323b8f0512e09dbb7a1860c46a39da62ecb2324f116fa8fdc85c"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:c002b4ffc0be611f0d9da932eb0f704fe2602a9a949d1f738e4c34c75b0863d5"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:a981a536974bbc7a512cf44ed14938cf01030a99e9b3a06dd59578882f06f985"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:3287761bc4ee9e33561a7e058c72ac0938c4f57fe49a09eae428fd88aafe7bb6"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:42cb296636fcc8b0644486d15c12376cb9fa75443e00fb25de0b8602e64c1714"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:0a55554a2fa0d408816b3b5cedf0045f4b8e1a6065aec45849de2d6f3f8e9786"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-musllinux_1_1_aarch64.whl", hash = "sha256:c083af607d2515612056a31f0a8d9e0fcb5876b7bfc0abad3ecd275bc4ebc2d5"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-musllinux_1_1_i686.whl", hash = "sha256:87d1351268731db79e0f8e745d92493ee2841c974128ef629dc518b937d9194c"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-musllinux_1_1_ppc64le.whl", hash = "sha256:bd8f7df7d12c2db9fab40bdd87a7c09b1530128315d047a086fa3ae3435cb3a8"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-musllinux_1_1_s390x.whl", hash = "sha256:c180f51afb394e165eafe4ac2936a14bee3eb10debc9d9e4db8958fe36afe711"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-musllinux_1_1_x86_64.whl", hash = "sha256:8c622a5fe39a48f78944a87d4fb8a53ee07344641b0562c540d840748571b811"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-win32.whl", hash = "sha256:db364eca23f876da6f9e16c9da0df51aa4f104a972735574842618b8c6d999d4"}, + {file = "charset_normalizer-3.3.2-cp37-cp37m-win_amd64.whl", hash = "sha256:86216b5cee4b06df986d214f664305142d9c76df9b6512be2738aa72a2048f99"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-macosx_10_9_universal2.whl", hash = "sha256:6463effa3186ea09411d50efc7d85360b38d5f09b870c48e4600f63af490e56a"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:6c4caeef8fa63d06bd437cd4bdcf3ffefe6738fb1b25951440d80dc7df8c03ac"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:37e55c8e51c236f95b033f6fb391d7d7970ba5fe7ff453dad675e88cf303377a"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:fb69256e180cb6c8a894fee62b3afebae785babc1ee98b81cdf68bbca1987f33"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:ae5f4161f18c61806f411a13b0310bea87f987c7d2ecdbdaad0e94eb2e404238"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:b2b0a0c0517616b6869869f8c581d4eb2dd83a4d79e0ebcb7d373ef9956aeb0a"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:45485e01ff4d3630ec0d9617310448a8702f70e9c01906b0d0118bdf9d124cf2"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:eb00ed941194665c332bf8e078baf037d6c35d7c4f3102ea2d4f16ca94a26dc8"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:2127566c664442652f024c837091890cb1942c30937add288223dc895793f898"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-musllinux_1_1_i686.whl", hash = "sha256:a50aebfa173e157099939b17f18600f72f84eed3049e743b68ad15bd69b6bf99"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-musllinux_1_1_ppc64le.whl", hash = "sha256:4d0d1650369165a14e14e1e47b372cfcb31d6ab44e6e33cb2d4e57265290044d"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-musllinux_1_1_s390x.whl", hash = "sha256:923c0c831b7cfcb071580d3f46c4baf50f174be571576556269530f4bbd79d04"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:06a81e93cd441c56a9b65d8e1d043daeb97a3d0856d177d5c90ba85acb3db087"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-win32.whl", hash = "sha256:6ef1d82a3af9d3eecdba2321dc1b3c238245d890843e040e41e470ffa64c3e25"}, + {file = "charset_normalizer-3.3.2-cp38-cp38-win_amd64.whl", hash = "sha256:eb8821e09e916165e160797a6c17edda0679379a4be5c716c260e836e122f54b"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-macosx_10_9_universal2.whl", hash = "sha256:c235ebd9baae02f1b77bcea61bce332cb4331dc3617d254df3323aa01ab47bd4"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:5b4c145409bef602a690e7cfad0a15a55c13320ff7a3ad7ca59c13bb8ba4d45d"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:68d1f8a9e9e37c1223b656399be5d6b448dea850bed7d0f87a8311f1ff3dabb0"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:22afcb9f253dac0696b5a4be4a1c0f8762f8239e21b99680099abd9b2b1b2269"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:e27ad930a842b4c5eb8ac0016b0a54f5aebbe679340c26101df33424142c143c"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:1f79682fbe303db92bc2b1136016a38a42e835d932bab5b3b1bfcfbf0640e519"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:b261ccdec7821281dade748d088bb6e9b69e6d15b30652b74cbbac25e280b796"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:122c7fa62b130ed55f8f285bfd56d5f4b4a5b503609d181f9ad85e55c89f4185"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:d0eccceffcb53201b5bfebb52600a5fb483a20b61da9dbc885f8b103cbe7598c"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-musllinux_1_1_i686.whl", hash = "sha256:9f96df6923e21816da7e0ad3fd47dd8f94b2a5ce594e00677c0013018b813458"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-musllinux_1_1_ppc64le.whl", hash = "sha256:7f04c839ed0b6b98b1a7501a002144b76c18fb1c1850c8b98d458ac269e26ed2"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-musllinux_1_1_s390x.whl", hash = "sha256:34d1c8da1e78d2e001f363791c98a272bb734000fcef47a491c1e3b0505657a8"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:ff8fa367d09b717b2a17a052544193ad76cd49979c805768879cb63d9ca50561"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-win32.whl", hash = "sha256:aed38f6e4fb3f5d6bf81bfa990a07806be9d83cf7bacef998ab1a9bd660a581f"}, + {file = "charset_normalizer-3.3.2-cp39-cp39-win_amd64.whl", hash = "sha256:b01b88d45a6fcb69667cd6d2f7a9aeb4bf53760d7fc536bf679ec94fe9f3ff3d"}, + {file = "charset_normalizer-3.3.2-py3-none-any.whl", hash = "sha256:3e4d1f6587322d2788836a99c69062fbb091331ec940e02d12d179c1d53e25fc"}, +] + +[[package]] +name = "class-resolver" +version = "0.4.3" +description = "Lookup and instantiate classes with style." +optional = false +python-versions = ">=3.7" +files = [ + {file = "class_resolver-0.4.3-py3-none-any.whl", hash = "sha256:9a0e3420edc262f1eb357580ff607ddc5806b9c0d19354a6f3dede15a69fbea0"}, + {file = "class_resolver-0.4.3.tar.gz", hash = "sha256:18bb9983cb377f669e5900979de4aa65449d95ead61838fa12862958998c71a2"}, +] + +[package.extras] +click = ["click"] +docdata = ["docdata"] +docs = ["sphinx", "sphinx-autodoc-typehints", "sphinx-automodapi", "sphinx-rtd-theme"] +numpy = ["numpy"] +optuna = ["optuna"] +ray = ["ray[tune] (<2.0.0)"] +sklearn = ["scikit-learn"] +tests = ["coverage", "docdata", "pytest"] +torch = ["torch"] +torch-geometric = ["torch", "torch-geometric", "torch-sparse"] + +[[package]] +name = "click" +version = "8.1.7" +description = "Composable command line interface toolkit" +optional = false +python-versions = ">=3.7" +files = [ + {file = "click-8.1.7-py3-none-any.whl", hash = "sha256:ae74fb96c20a0277a1d615f1e4d73c8414f5a98db8b799a7931d1582f3390c28"}, + {file = "click-8.1.7.tar.gz", hash = "sha256:ca9853ad459e787e2192211578cc907e7594e294c7ccc834310722b41b9ca6de"}, +] + +[package.dependencies] +colorama = {version = "*", markers = "platform_system == \"Windows\""} + +[[package]] +name = "colorama" +version = "0.4.6" +description = "Cross-platform colored terminal text." +optional = false +python-versions = "!=3.0.*,!=3.1.*,!=3.2.*,!=3.3.*,!=3.4.*,!=3.5.*,!=3.6.*,>=2.7" +files = [ + {file = "colorama-0.4.6-py2.py3-none-any.whl", hash = "sha256:4f1d9991f5acc0ca119f9d443620b77f9d6b33703e51011c16baf57afb285fc6"}, + {file = "colorama-0.4.6.tar.gz", hash = "sha256:08695f5cb7ed6e0531a20572697297273c47b8cae5a63ffc6d6ed5c201be6e44"}, +] + +[[package]] +name = "curies" +version = "0.7.9" +description = "Idiomatic conversion between URIs and compact URIs (CURIEs)." +optional = false +python-versions = ">=3.8" +files = [ + {file = "curies-0.7.9-py3-none-any.whl", hash = "sha256:e4c5beb91642376953c94db0ee2fb5d2b011c3b16749516436114ba61442f260"}, + {file = "curies-0.7.9.tar.gz", hash = "sha256:3b63c5fea7b0e967629a3a384b1a8c59b56c503487c1dcbacddeab59e25db4d8"}, +] + +[package.dependencies] +pydantic = "*" +pytrie = "*" +requests = "*" + +[package.extras] +docs = ["sphinx", "sphinx-automodapi", "sphinx-rtd-theme"] +fastapi = ["defusedxml", "fastapi", "httpx", "python-multipart", "uvicorn"] +flask = ["defusedxml", "flask"] +pandas = ["pandas"] +rdflib = ["rdflib"] +tests = ["coverage", "pytest"] + +[[package]] +name = "defusedxml" +version = "0.7.1" +description = "XML bomb protection for Python stdlib modules" +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*, !=3.3.*, !=3.4.*" +files = [ + {file = "defusedxml-0.7.1-py2.py3-none-any.whl", hash = "sha256:a352e7e428770286cc899e2542b6cdaedb2b4953ff269a210103ec58f6198a61"}, + {file = "defusedxml-0.7.1.tar.gz", hash = "sha256:1bb3032db185915b62d7c6209c5a8792be6a32ab2fedacc84e01b52c51aa3e69"}, +] + +[[package]] +name = "deprecated" +version = "1.2.14" +description = "Python @deprecated decorator to deprecate old python classes, functions or methods." +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*, !=3.3.*" +files = [ + {file = "Deprecated-1.2.14-py2.py3-none-any.whl", hash = "sha256:6fac8b097794a90302bdbb17b9b815e732d3c4720583ff1b198499d78470466c"}, + {file = "Deprecated-1.2.14.tar.gz", hash = "sha256:e5323eb936458dccc2582dc6f9c322c852a775a27065ff2b0c4970b9d53d01b3"}, +] + +[package.dependencies] +wrapt = ">=1.10,<2" + +[package.extras] +dev = ["PyTest", "PyTest-Cov", "bump2version (<1)", "sphinx (<2)", "tox"] + +[[package]] +name = "deprecation" +version = "2.1.0" +description = "A library to handle automated deprecations" +optional = false +python-versions = "*" +files = [ + {file = "deprecation-2.1.0-py2.py3-none-any.whl", hash = "sha256:a10811591210e1fb0e768a8c25517cabeabcba6f0bf96564f8ff45189f90b14a"}, + {file = "deprecation-2.1.0.tar.gz", hash = "sha256:72b3bde64e5d778694b0cf68178aed03d15e15477116add3fb773e581f9518ff"}, +] + +[package.dependencies] +packaging = "*" + +[[package]] +name = "distro" +version = "1.9.0" +description = "Distro - an OS platform information API" +optional = false +python-versions = ">=3.6" +files = [ + {file = "distro-1.9.0-py3-none-any.whl", hash = "sha256:7bffd925d65168f85027d8da9af6bddab658135b840670a223589bc0c8ef02b2"}, + {file = "distro-1.9.0.tar.gz", hash = "sha256:2fa77c6fd8940f116ee1d6b94a2f90b13b5ea8d019b98bc8bafdcabcdd9bdbed"}, +] + +[[package]] +name = "eutils" +version = "0.6.0" +description = "\"Python interface to NCBI's eutilities API\"" +optional = false +python-versions = ">=3.6" +files = [ + {file = "eutils-0.6.0-py2.py3-none-any.whl", hash = "sha256:4938c4baff6ca52141204ff3eff3a91ec1e83e52a6c5d92e7163585117b96566"}, + {file = "eutils-0.6.0.tar.gz", hash = "sha256:3515178c0aadb836206a3eee2bc9f340f3213c13b53632e058eb58a9219d03cf"}, +] + +[package.dependencies] +lxml = "*" +pytz = "*" +requests = "*" + +[package.extras] +dev = ["flake8", "ipython", "mock", "pytest", "pytest-cov", "restview", "setuptools", "sphinx", "sphinx-rtd-theme", "tox", "vcrpy", "yapf"] + +[[package]] +name = "fastobo" +version = "0.12.3" +description = "Faultless AST for Open Biomedical Ontologies in Python." +optional = false +python-versions = ">=3.7" +files = [ + {file = "fastobo-0.12.3-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:79fe4f5ba1ec1a2bc1ca0d65834cfc622db639128ba89019328937e623c54094"}, + {file = "fastobo-0.12.3-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:21c347ec270d0ef6e120ba701370a8ef20953654b397d2814f62595d4d7c0062"}, + {file = "fastobo-0.12.3-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:42b5cc3676bfbe902632075455eb8faef2e3c2812423bb172e0c9bb905e93e04"}, + {file = "fastobo-0.12.3-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:922e61874e3c436c1990fb741f69b15c8395d1c760c569f2b4f024c7d315a0f4"}, + {file = "fastobo-0.12.3-cp310-cp310-win_amd64.whl", hash = "sha256:c8f73c80ae92fd7ba8e0532880b53308200563a7ce2137ed751dd3bfb5dcde88"}, + {file = "fastobo-0.12.3-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:7862627caf2deda767a8b5278f7da3bf6cb8173130505f7aed03c41d5b512de9"}, + {file = "fastobo-0.12.3-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:b496e003db5ae1d27de3c5078a3a00d1bcb84b436eb68461a55efd3af979bbc6"}, + {file = "fastobo-0.12.3-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:2fed9875760ea2f0d7d9a3697f83a3168c3cd46005b41096dafbae97220a9637"}, + {file = "fastobo-0.12.3-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:debab1d3144506a9b4c0d98261ecf7bdcadb5f420843358188b11bc9312aec90"}, + {file = "fastobo-0.12.3-cp311-cp311-win_amd64.whl", hash = "sha256:5566f9f54f836e29edbdae15d22b11982db73fedfaefcbe5cc9f10f2568179a4"}, + {file = "fastobo-0.12.3-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:a9d6502e397bcb644ada900e33ea70683006c23598758f829be7210e375f7952"}, + {file = "fastobo-0.12.3-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:673aa41d260869ba6ae07aaa716c78cb26203662e61b3e401b006d85d748cf76"}, + {file = "fastobo-0.12.3-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:68841568868408ac1b020d436ce29de50c7457031051d8d7389dc8d838cb244f"}, + {file = "fastobo-0.12.3-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:09714ec07d4b0211a3ada40b7b1bfcca64aa01ba24c50d39c4d367bea058f996"}, + {file = "fastobo-0.12.3-cp312-cp312-win_amd64.whl", hash = "sha256:fa6aaa4380825692c863f2cf9a0ad667973af8dd9162fd8282331464489b3f6c"}, + {file = "fastobo-0.12.3-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:fa546543209f3ce95b23c767dd4c2ae4181a81526e8ab2df4a0c079b4073ef72"}, + {file = "fastobo-0.12.3-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:9739bb54c025679108a1ba8638f327ddddb68d7cdd666fd9009a72597a590560"}, + {file = "fastobo-0.12.3-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d7cce0096b09a73fef542c17899f84db1234aff7d6bc12c1b8b86e109613bfa0"}, + {file = "fastobo-0.12.3-cp37-cp37m-win_amd64.whl", hash = "sha256:64e028355b7ca9fb4d2b8f688759e04a7c48c08db55aaafdc599dca9bc4d70fe"}, + {file = "fastobo-0.12.3-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:525cf2eebb584e5e2a2fe7c9aca4172109a8bdc008cf5699d14ffbd15a136cae"}, + {file = "fastobo-0.12.3-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:727743ff6353eb5d2982568e585b7b69fed9f6e63a141ebbbbd3f5d79a4ea8bd"}, + {file = "fastobo-0.12.3-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:5a73ba3d593d420675691e53698cdc21b4500b17036ee80bd26b5acea03192e8"}, + {file = "fastobo-0.12.3-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:377ecc157842a10ecc8a00c8d9ea9f380010cbb1ee123db42b7aca78d6c12cd9"}, + {file = "fastobo-0.12.3-cp38-cp38-win_amd64.whl", hash = "sha256:bd6d4c7be54900022f85403b5c65f80b2b27997e185920a5e50471bf66e7ff08"}, + {file = "fastobo-0.12.3-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:eea6e991a4e9c0f9e4c752125f72c22ed27fb8ea3c08e4610b1264c3a3100979"}, + {file = "fastobo-0.12.3-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:e1ea49a9f0b8c8a51d920cb2782c88ddb66f44e81db55ee876ccbc6a2c3a12d2"}, + {file = "fastobo-0.12.3-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:5cdbd0c52a5d0d43035b21294579b73439889e4af08eb5739dc94a59caaa861f"}, + {file = "fastobo-0.12.3-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:c6acd98a335375c384e236b1e37867150b3b067f3a161c0cfe6a3dcf74aa9bd0"}, + {file = "fastobo-0.12.3-cp39-cp39-win_amd64.whl", hash = "sha256:32ce37ba36f3b5e7b6642b6c0e5b9a0a6d95f78e5e98901f45cbbc958665fe46"}, + {file = "fastobo-0.12.3-pp310-pypy310_pp73-macosx_10_9_x86_64.whl", hash = "sha256:c8fba47c98201d0c3b0c515e1ded7608a1f3015a5a0a34df8d6cbf201d58a00e"}, + {file = "fastobo-0.12.3-pp310-pypy310_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4071609ee8c8e87b03b2e786c6bd6d6845eb3580410bf95ee29c445699a99530"}, + {file = "fastobo-0.12.3-pp310-pypy310_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:34781dd51ad9589e6b73bf6c3854edd22a6aba4d78d9ef17fcba3448b8501abe"}, + {file = "fastobo-0.12.3-pp310-pypy310_pp73-win_amd64.whl", hash = "sha256:958da0f135270da6fcfb8181114e5f631e77bc11ad897112039764af19085183"}, + {file = "fastobo-0.12.3-pp37-pypy37_pp73-macosx_10_9_x86_64.whl", hash = "sha256:75977f4cbdfd7b371b9c4107de953c3bd1a57201cec7c877a9a64eff7817b8ce"}, + {file = "fastobo-0.12.3-pp37-pypy37_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4589124050eab5517416a357b8e0c50ecbd36a7caaf3428b3b403f8147858986"}, + {file = "fastobo-0.12.3-pp37-pypy37_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:4c3bdbc447398a21b5ea35195bf1541f8634d86680ed763b71aa99928859bc2e"}, + {file = "fastobo-0.12.3-pp37-pypy37_pp73-win_amd64.whl", hash = "sha256:29f5180c37428af74ff80f08a4889d13fb716a6ee858debd00ac805f7c4f792b"}, + {file = "fastobo-0.12.3-pp38-pypy38_pp73-macosx_10_9_x86_64.whl", hash = "sha256:9e6d701d9f69a94222c621c86ef47fa7d2cebed0a0f455a2c9144a0a8227d4ea"}, + {file = "fastobo-0.12.3-pp38-pypy38_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d21581d8a22b0acf2db2b987e76c19be3b9e5a714e290690e2858b533bd882a5"}, + {file = "fastobo-0.12.3-pp38-pypy38_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:3b676acbf95579a72b1fae985442a583a15f2cc358efd061ab304a1f6e14269a"}, + {file = "fastobo-0.12.3-pp38-pypy38_pp73-win_amd64.whl", hash = "sha256:3f245df99769d08c007aa2630b9ca0c2aca628371512f48aaf61953f67625b05"}, + {file = "fastobo-0.12.3-pp39-pypy39_pp73-macosx_10_9_x86_64.whl", hash = "sha256:dc566c24d891ab21eb985fbc73d1b5ef3bfa3f096473060cfddbab8b00669756"}, + {file = "fastobo-0.12.3-pp39-pypy39_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:75205475ce0d6cedd5074107c3719b2c8df4e14cc5d481b1a28a5639418705cd"}, + {file = "fastobo-0.12.3-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e180e7dcf53e6fc774230d8a53212c7f710b2265ef2b3b07fe4fc75226bae17c"}, + {file = "fastobo-0.12.3-pp39-pypy39_pp73-win_amd64.whl", hash = "sha256:5e6f20a884c9409e9968e77ee74d407564814f2360dfc35440de268d753ad85e"}, + {file = "fastobo-0.12.3.tar.gz", hash = "sha256:f375932a24b078706797eb9296740f2d2e6987a34309bda7c9f235aba1d74217"}, +] + +[[package]] +name = "funowl" +version = "0.2.3" +description = "Python rendering of the OWL Functional syntax" +optional = false +python-versions = ">=3.7" +files = [ + {file = "funowl-0.2.3-py3-none-any.whl", hash = "sha256:4c4328d03c7815cd61d6691f0fafc78dc9a78ec3dcab4c83afb64d125ad3660e"}, + {file = "funowl-0.2.3.tar.gz", hash = "sha256:eecc2f58d792c714f6671a826cb2744e80cd3019fa56b3c8539ce69c8d874126"}, +] + +[package.dependencies] +bcp47 = "*" +jsonasobj = "*" +pyjsg = ">=0.11.6" +rdflib = ">=6.2.0,<8" +rdflib-shim = "*" +rfc3987 = "*" + +[[package]] +name = "greenlet" +version = "3.0.3" +description = "Lightweight in-process concurrent programming" +optional = false +python-versions = ">=3.7" +files = [ + {file = "greenlet-3.0.3-cp310-cp310-macosx_11_0_universal2.whl", hash = "sha256:9da2bd29ed9e4f15955dd1595ad7bc9320308a3b766ef7f837e23ad4b4aac31a"}, + {file = "greenlet-3.0.3-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d353cadd6083fdb056bb46ed07e4340b0869c305c8ca54ef9da3421acbdf6881"}, + {file = "greenlet-3.0.3-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:dca1e2f3ca00b84a396bc1bce13dd21f680f035314d2379c4160c98153b2059b"}, + {file = "greenlet-3.0.3-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:3ed7fb269f15dc662787f4119ec300ad0702fa1b19d2135a37c2c4de6fadfd4a"}, + {file = "greenlet-3.0.3-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:dd4f49ae60e10adbc94b45c0b5e6a179acc1736cf7a90160b404076ee283cf83"}, + {file = "greenlet-3.0.3-cp310-cp310-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:73a411ef564e0e097dbe7e866bb2dda0f027e072b04da387282b02c308807405"}, + {file = "greenlet-3.0.3-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:7f362975f2d179f9e26928c5b517524e89dd48530a0202570d55ad6ca5d8a56f"}, + {file = "greenlet-3.0.3-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:649dde7de1a5eceb258f9cb00bdf50e978c9db1b996964cd80703614c86495eb"}, + {file = "greenlet-3.0.3-cp310-cp310-win_amd64.whl", hash = "sha256:68834da854554926fbedd38c76e60c4a2e3198c6fbed520b106a8986445caaf9"}, + {file = "greenlet-3.0.3-cp311-cp311-macosx_11_0_universal2.whl", hash = "sha256:b1b5667cced97081bf57b8fa1d6bfca67814b0afd38208d52538316e9422fc61"}, + {file = "greenlet-3.0.3-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:52f59dd9c96ad2fc0d5724107444f76eb20aaccb675bf825df6435acb7703559"}, + {file = "greenlet-3.0.3-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:afaff6cf5200befd5cec055b07d1c0a5a06c040fe5ad148abcd11ba6ab9b114e"}, + {file = "greenlet-3.0.3-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:fe754d231288e1e64323cfad462fcee8f0288654c10bdf4f603a39ed923bef33"}, + {file = "greenlet-3.0.3-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:2797aa5aedac23af156bbb5a6aa2cd3427ada2972c828244eb7d1b9255846379"}, + {file = "greenlet-3.0.3-cp311-cp311-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:b7f009caad047246ed379e1c4dbcb8b020f0a390667ea74d2387be2998f58a22"}, + {file = "greenlet-3.0.3-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:c5e1536de2aad7bf62e27baf79225d0d64360d4168cf2e6becb91baf1ed074f3"}, + {file = "greenlet-3.0.3-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:894393ce10ceac937e56ec00bb71c4c2f8209ad516e96033e4b3b1de270e200d"}, + {file = "greenlet-3.0.3-cp311-cp311-win_amd64.whl", hash = "sha256:1ea188d4f49089fc6fb283845ab18a2518d279c7cd9da1065d7a84e991748728"}, + {file = "greenlet-3.0.3-cp312-cp312-macosx_11_0_universal2.whl", hash = "sha256:70fb482fdf2c707765ab5f0b6655e9cfcf3780d8d87355a063547b41177599be"}, + {file = "greenlet-3.0.3-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d4d1ac74f5c0c0524e4a24335350edad7e5f03b9532da7ea4d3c54d527784f2e"}, + {file = "greenlet-3.0.3-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:149e94a2dd82d19838fe4b2259f1b6b9957d5ba1b25640d2380bea9c5df37676"}, + {file = "greenlet-3.0.3-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:15d79dd26056573940fcb8c7413d84118086f2ec1a8acdfa854631084393efcc"}, + {file = "greenlet-3.0.3-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:881b7db1ebff4ba09aaaeae6aa491daeb226c8150fc20e836ad00041bcb11230"}, + {file = "greenlet-3.0.3-cp312-cp312-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:fcd2469d6a2cf298f198f0487e0a5b1a47a42ca0fa4dfd1b6862c999f018ebbf"}, + {file = "greenlet-3.0.3-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:1f672519db1796ca0d8753f9e78ec02355e862d0998193038c7073045899f305"}, + {file = "greenlet-3.0.3-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:2516a9957eed41dd8f1ec0c604f1cdc86758b587d964668b5b196a9db5bfcde6"}, + {file = "greenlet-3.0.3-cp312-cp312-win_amd64.whl", hash = "sha256:bba5387a6975598857d86de9eac14210a49d554a77eb8261cc68b7d082f78ce2"}, + {file = "greenlet-3.0.3-cp37-cp37m-macosx_11_0_universal2.whl", hash = "sha256:5b51e85cb5ceda94e79d019ed36b35386e8c37d22f07d6a751cb659b180d5274"}, + {file = "greenlet-3.0.3-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:daf3cb43b7cf2ba96d614252ce1684c1bccee6b2183a01328c98d36fcd7d5cb0"}, + {file = "greenlet-3.0.3-cp37-cp37m-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:99bf650dc5d69546e076f413a87481ee1d2d09aaaaaca058c9251b6d8c14783f"}, + {file = "greenlet-3.0.3-cp37-cp37m-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:2dd6e660effd852586b6a8478a1d244b8dc90ab5b1321751d2ea15deb49ed414"}, + {file = "greenlet-3.0.3-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e3391d1e16e2a5a1507d83e4a8b100f4ee626e8eca43cf2cadb543de69827c4c"}, + {file = "greenlet-3.0.3-cp37-cp37m-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:e1f145462f1fa6e4a4ae3c0f782e580ce44d57c8f2c7aae1b6fa88c0b2efdb41"}, + {file = "greenlet-3.0.3-cp37-cp37m-musllinux_1_1_aarch64.whl", hash = "sha256:1a7191e42732df52cb5f39d3527217e7ab73cae2cb3694d241e18f53d84ea9a7"}, + {file = "greenlet-3.0.3-cp37-cp37m-musllinux_1_1_x86_64.whl", hash = "sha256:0448abc479fab28b00cb472d278828b3ccca164531daab4e970a0458786055d6"}, + {file = "greenlet-3.0.3-cp37-cp37m-win32.whl", hash = "sha256:b542be2440edc2d48547b5923c408cbe0fc94afb9f18741faa6ae970dbcb9b6d"}, + {file = "greenlet-3.0.3-cp37-cp37m-win_amd64.whl", hash = "sha256:01bc7ea167cf943b4c802068e178bbf70ae2e8c080467070d01bfa02f337ee67"}, + {file = "greenlet-3.0.3-cp38-cp38-macosx_11_0_universal2.whl", hash = "sha256:1996cb9306c8595335bb157d133daf5cf9f693ef413e7673cb07e3e5871379ca"}, + {file = "greenlet-3.0.3-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:3ddc0f794e6ad661e321caa8d2f0a55ce01213c74722587256fb6566049a8b04"}, + {file = "greenlet-3.0.3-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:c9db1c18f0eaad2f804728c67d6c610778456e3e1cc4ab4bbd5eeb8e6053c6fc"}, + {file = "greenlet-3.0.3-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:7170375bcc99f1a2fbd9c306f5be8764eaf3ac6b5cb968862cad4c7057756506"}, + {file = "greenlet-3.0.3-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:6b66c9c1e7ccabad3a7d037b2bcb740122a7b17a53734b7d72a344ce39882a1b"}, + {file = "greenlet-3.0.3-cp38-cp38-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:098d86f528c855ead3479afe84b49242e174ed262456c342d70fc7f972bc13c4"}, + {file = "greenlet-3.0.3-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:81bb9c6d52e8321f09c3d165b2a78c680506d9af285bfccbad9fb7ad5a5da3e5"}, + {file = "greenlet-3.0.3-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:fd096eb7ffef17c456cfa587523c5f92321ae02427ff955bebe9e3c63bc9f0da"}, + {file = "greenlet-3.0.3-cp38-cp38-win32.whl", hash = "sha256:d46677c85c5ba00a9cb6f7a00b2bfa6f812192d2c9f7d9c4f6a55b60216712f3"}, + {file = "greenlet-3.0.3-cp38-cp38-win_amd64.whl", hash = "sha256:419b386f84949bf0e7c73e6032e3457b82a787c1ab4a0e43732898a761cc9dbf"}, + {file = "greenlet-3.0.3-cp39-cp39-macosx_11_0_universal2.whl", hash = "sha256:da70d4d51c8b306bb7a031d5cff6cc25ad253affe89b70352af5f1cb68e74b53"}, + {file = "greenlet-3.0.3-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:086152f8fbc5955df88382e8a75984e2bb1c892ad2e3c80a2508954e52295257"}, + {file = "greenlet-3.0.3-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:d73a9fe764d77f87f8ec26a0c85144d6a951a6c438dfe50487df5595c6373eac"}, + {file = "greenlet-3.0.3-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:b7dcbe92cc99f08c8dd11f930de4d99ef756c3591a5377d1d9cd7dd5e896da71"}, + {file = "greenlet-3.0.3-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:1551a8195c0d4a68fac7a4325efac0d541b48def35feb49d803674ac32582f61"}, + {file = "greenlet-3.0.3-cp39-cp39-manylinux_2_24_x86_64.manylinux_2_28_x86_64.whl", hash = "sha256:64d7675ad83578e3fc149b617a444fab8efdafc9385471f868eb5ff83e446b8b"}, + {file = "greenlet-3.0.3-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:b37eef18ea55f2ffd8f00ff8fe7c8d3818abd3e25fb73fae2ca3b672e333a7a6"}, + {file = "greenlet-3.0.3-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:77457465d89b8263bca14759d7c1684df840b6811b2499838cc5b040a8b5b113"}, + {file = "greenlet-3.0.3-cp39-cp39-win32.whl", hash = "sha256:57e8974f23e47dac22b83436bdcf23080ade568ce77df33159e019d161ce1d1e"}, + {file = "greenlet-3.0.3-cp39-cp39-win_amd64.whl", hash = "sha256:c5ee858cfe08f34712f548c3c363e807e7186f03ad7a5039ebadb29e8c6be067"}, + {file = "greenlet-3.0.3.tar.gz", hash = "sha256:43374442353259554ce33599da8b692d5aa96f8976d567d4badf263371fbe491"}, +] + +[package.extras] +docs = ["Sphinx", "furo"] +test = ["objgraph", "psutil"] + +[[package]] +name = "h11" +version = "0.14.0" +description = "A pure-Python, bring-your-own-I/O implementation of HTTP/1.1" +optional = false +python-versions = ">=3.7" +files = [ + {file = "h11-0.14.0-py3-none-any.whl", hash = "sha256:e3fe4ac4b851c468cc8363d500db52c2ead036020723024a109d37346efaa761"}, + {file = "h11-0.14.0.tar.gz", hash = "sha256:8f19fbbe99e72420ff35c00b27a34cb9937e902a8b810e2c88300c6f0a3b699d"}, +] + +[[package]] +name = "hbreader" +version = "0.9.1" +description = "Honey Badger reader - a generic file/url/string open and read tool" +optional = false +python-versions = ">=3.7" +files = [ + {file = "hbreader-0.9.1-py3-none-any.whl", hash = "sha256:9a6e76c9d1afc1b977374a5dc430a1ebb0ea0488205546d4678d6e31cc5f6801"}, + {file = "hbreader-0.9.1.tar.gz", hash = "sha256:d2c132f8ba6276d794c66224c3297cec25c8079d0a4cf019c061611e0a3b94fa"}, +] + +[[package]] +name = "httpcore" +version = "1.0.5" +description = "A minimal low-level HTTP client." +optional = false +python-versions = ">=3.8" +files = [ + {file = "httpcore-1.0.5-py3-none-any.whl", hash = "sha256:421f18bac248b25d310f3cacd198d55b8e6125c107797b609ff9b7a6ba7991b5"}, + {file = "httpcore-1.0.5.tar.gz", hash = "sha256:34a38e2f9291467ee3b44e89dd52615370e152954ba21721378a87b2960f7a61"}, +] + +[package.dependencies] +certifi = "*" +h11 = ">=0.13,<0.15" + +[package.extras] +asyncio = ["anyio (>=4.0,<5.0)"] +http2 = ["h2 (>=3,<5)"] +socks = ["socksio (==1.*)"] +trio = ["trio (>=0.22.0,<0.26.0)"] + +[[package]] +name = "httpx" +version = "0.27.0" +description = "The next generation HTTP client." +optional = false +python-versions = ">=3.8" +files = [ + {file = "httpx-0.27.0-py3-none-any.whl", hash = "sha256:71d5465162c13681bff01ad59b2cc68dd838ea1f10e51574bac27103f00c91a5"}, + {file = "httpx-0.27.0.tar.gz", hash = "sha256:a0cb88a46f32dc874e04ee956e4c2764aba2aa228f650b06788ba6bda2962ab5"}, +] + +[package.dependencies] +anyio = "*" +certifi = "*" +httpcore = "==1.*" +idna = "*" +sniffio = "*" + +[package.extras] +brotli = ["brotli", "brotlicffi"] +cli = ["click (==8.*)", "pygments (==2.*)", "rich (>=10,<14)"] +http2 = ["h2 (>=3,<5)"] +socks = ["socksio (==1.*)"] + +[[package]] +name = "idna" +version = "3.7" +description = "Internationalized Domain Names in Applications (IDNA)" +optional = false +python-versions = ">=3.5" +files = [ + {file = "idna-3.7-py3-none-any.whl", hash = "sha256:82fee1fc78add43492d3a1898bfa6d8a904cc97d8427f683ed8e798d07761aa0"}, + {file = "idna-3.7.tar.gz", hash = "sha256:028ff3aadf0609c1fd278d8ea3089299412a7a8b9bd005dd08b9f8285bcb5cfc"}, +] + +[[package]] +name = "ijson" +version = "3.3.0" +description = "Iterative JSON parser with standard Python iterator interfaces" +optional = false +python-versions = "*" +files = [ + {file = "ijson-3.3.0-cp310-cp310-macosx_10_9_universal2.whl", hash = "sha256:7f7a5250599c366369fbf3bc4e176f5daa28eb6bc7d6130d02462ed335361675"}, + {file = "ijson-3.3.0-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:f87a7e52f79059f9c58f6886c262061065eb6f7554a587be7ed3aa63e6b71b34"}, + {file = "ijson-3.3.0-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:b73b493af9e947caed75d329676b1b801d673b17481962823a3e55fe529c8b8b"}, + {file = "ijson-3.3.0-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d5576415f3d76290b160aa093ff968f8bf6de7d681e16e463a0134106b506f49"}, + {file = "ijson-3.3.0-cp310-cp310-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:4e9ffe358d5fdd6b878a8a364e96e15ca7ca57b92a48f588378cef315a8b019e"}, + {file = "ijson-3.3.0-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:8643c255a25824ddd0895c59f2319c019e13e949dc37162f876c41a283361527"}, + {file = "ijson-3.3.0-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:df3ab5e078cab19f7eaeef1d5f063103e1ebf8c26d059767b26a6a0ad8b250a3"}, + {file = "ijson-3.3.0-cp310-cp310-musllinux_1_2_i686.whl", hash = "sha256:3dc1fb02c6ed0bae1b4bf96971258bf88aea72051b6e4cebae97cff7090c0607"}, + {file = "ijson-3.3.0-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:e9afd97339fc5a20f0542c971f90f3ca97e73d3050cdc488d540b63fae45329a"}, + {file = "ijson-3.3.0-cp310-cp310-win32.whl", hash = "sha256:844c0d1c04c40fd1b60f148dc829d3f69b2de789d0ba239c35136efe9a386529"}, + {file = "ijson-3.3.0-cp310-cp310-win_amd64.whl", hash = "sha256:d654d045adafdcc6c100e8e911508a2eedbd2a1b5f93f930ba13ea67d7704ee9"}, + {file = "ijson-3.3.0-cp311-cp311-macosx_10_9_universal2.whl", hash = "sha256:501dce8eaa537e728aa35810656aa00460a2547dcb60937c8139f36ec344d7fc"}, + {file = "ijson-3.3.0-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:658ba9cad0374d37b38c9893f4864f284cdcc7d32041f9808fba8c7bcaadf134"}, + {file = "ijson-3.3.0-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:2636cb8c0f1023ef16173f4b9a233bcdb1df11c400c603d5f299fac143ca8d70"}, + {file = "ijson-3.3.0-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:cd174b90db68c3bcca273e9391934a25d76929d727dc75224bf244446b28b03b"}, + {file = "ijson-3.3.0-cp311-cp311-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:97a9aea46e2a8371c4cf5386d881de833ed782901ac9f67ebcb63bb3b7d115af"}, + {file = "ijson-3.3.0-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:c594c0abe69d9d6099f4ece17763d53072f65ba60b372d8ba6de8695ce6ee39e"}, + {file = "ijson-3.3.0-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:8e0ff16c224d9bfe4e9e6bd0395826096cda4a3ef51e6c301e1b61007ee2bd24"}, + {file = "ijson-3.3.0-cp311-cp311-musllinux_1_2_i686.whl", hash = "sha256:0015354011303175eae7e2ef5136414e91de2298e5a2e9580ed100b728c07e51"}, + {file = "ijson-3.3.0-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:034642558afa57351a0ffe6de89e63907c4cf6849070cc10a3b2542dccda1afe"}, + {file = "ijson-3.3.0-cp311-cp311-win32.whl", hash = "sha256:192e4b65495978b0bce0c78e859d14772e841724d3269fc1667dc6d2f53cc0ea"}, + {file = "ijson-3.3.0-cp311-cp311-win_amd64.whl", hash = "sha256:72e3488453754bdb45c878e31ce557ea87e1eb0f8b4fc610373da35e8074ce42"}, + {file = "ijson-3.3.0-cp312-cp312-macosx_10_9_universal2.whl", hash = "sha256:988e959f2f3d59ebd9c2962ae71b97c0df58323910d0b368cc190ad07429d1bb"}, + {file = "ijson-3.3.0-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:b2f73f0d0fce5300f23a1383d19b44d103bb113b57a69c36fd95b7c03099b181"}, + {file = "ijson-3.3.0-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:0ee57a28c6bf523d7cb0513096e4eb4dac16cd935695049de7608ec110c2b751"}, + {file = "ijson-3.3.0-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:e0155a8f079c688c2ccaea05de1ad69877995c547ba3d3612c1c336edc12a3a5"}, + {file = "ijson-3.3.0-cp312-cp312-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:7ab00721304af1ae1afa4313ecfa1bf16b07f55ef91e4a5b93aeaa3e2bd7917c"}, + {file = "ijson-3.3.0-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:40ee3821ee90be0f0e95dcf9862d786a7439bd1113e370736bfdf197e9765bfb"}, + {file = "ijson-3.3.0-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:da3b6987a0bc3e6d0f721b42c7a0198ef897ae50579547b0345f7f02486898f5"}, + {file = "ijson-3.3.0-cp312-cp312-musllinux_1_2_i686.whl", hash = "sha256:63afea5f2d50d931feb20dcc50954e23cef4127606cc0ecf7a27128ed9f9a9e6"}, + {file = "ijson-3.3.0-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:b5c3e285e0735fd8c5a26d177eca8b52512cdd8687ca86ec77a0c66e9c510182"}, + {file = "ijson-3.3.0-cp312-cp312-win32.whl", hash = "sha256:907f3a8674e489abdcb0206723e5560a5cb1fa42470dcc637942d7b10f28b695"}, + {file = "ijson-3.3.0-cp312-cp312-win_amd64.whl", hash = "sha256:8f890d04ad33262d0c77ead53c85f13abfb82f2c8f078dfbf24b78f59534dfdd"}, + {file = "ijson-3.3.0-cp36-cp36m-macosx_10_9_x86_64.whl", hash = "sha256:b9d85a02e77ee8ea6d9e3fd5d515bcc3d798d9c1ea54817e5feb97a9bc5d52fe"}, + {file = "ijson-3.3.0-cp36-cp36m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:e6576cdc36d5a09b0c1a3d81e13a45d41a6763188f9eaae2da2839e8a4240bce"}, + {file = "ijson-3.3.0-cp36-cp36m-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:e5589225c2da4bb732c9c370c5961c39a6db72cf69fb2a28868a5413ed7f39e6"}, + {file = "ijson-3.3.0-cp36-cp36m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:ad04cf38164d983e85f9cba2804566c0160b47086dcca4cf059f7e26c5ace8ca"}, + {file = "ijson-3.3.0-cp36-cp36m-musllinux_1_2_aarch64.whl", hash = "sha256:a3b730ef664b2ef0e99dec01b6573b9b085c766400af363833e08ebc1e38eb2f"}, + {file = "ijson-3.3.0-cp36-cp36m-musllinux_1_2_i686.whl", hash = "sha256:4690e3af7b134298055993fcbea161598d23b6d3ede11b12dca6815d82d101d5"}, + {file = "ijson-3.3.0-cp36-cp36m-musllinux_1_2_x86_64.whl", hash = "sha256:aaa6bfc2180c31a45fac35d40e3312a3d09954638ce0b2e9424a88e24d262a13"}, + {file = "ijson-3.3.0-cp36-cp36m-win32.whl", hash = "sha256:44367090a5a876809eb24943f31e470ba372aaa0d7396b92b953dda953a95d14"}, + {file = "ijson-3.3.0-cp36-cp36m-win_amd64.whl", hash = "sha256:7e2b3e9ca957153557d06c50a26abaf0d0d6c0ddf462271854c968277a6b5372"}, + {file = "ijson-3.3.0-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:47c144117e5c0e2babb559bc8f3f76153863b8dd90b2d550c51dab5f4b84a87f"}, + {file = "ijson-3.3.0-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:29ce02af5fbf9ba6abb70765e66930aedf73311c7d840478f1ccecac53fefbf3"}, + {file = "ijson-3.3.0-cp37-cp37m-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:4ac6c3eeed25e3e2cb9b379b48196413e40ac4e2239d910bb33e4e7f6c137745"}, + {file = "ijson-3.3.0-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d92e339c69b585e7b1d857308ad3ca1636b899e4557897ccd91bb9e4a56c965b"}, + {file = "ijson-3.3.0-cp37-cp37m-musllinux_1_2_aarch64.whl", hash = "sha256:8c85447569041939111b8c7dbf6f8fa7a0eb5b2c4aebb3c3bec0fb50d7025121"}, + {file = "ijson-3.3.0-cp37-cp37m-musllinux_1_2_i686.whl", hash = "sha256:542c1e8fddf082159a5d759ee1412c73e944a9a2412077ed00b303ff796907dc"}, + {file = "ijson-3.3.0-cp37-cp37m-musllinux_1_2_x86_64.whl", hash = "sha256:30cfea40936afb33b57d24ceaf60d0a2e3d5c1f2335ba2623f21d560737cc730"}, + {file = "ijson-3.3.0-cp37-cp37m-win32.whl", hash = "sha256:6b661a959226ad0d255e49b77dba1d13782f028589a42dc3172398dd3814c797"}, + {file = "ijson-3.3.0-cp37-cp37m-win_amd64.whl", hash = "sha256:0b003501ee0301dbf07d1597482009295e16d647bb177ce52076c2d5e64113e0"}, + {file = "ijson-3.3.0-cp38-cp38-macosx_10_9_universal2.whl", hash = "sha256:3e8d8de44effe2dbd0d8f3eb9840344b2d5b4cc284a14eb8678aec31d1b6bea8"}, + {file = "ijson-3.3.0-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:9cd5c03c63ae06d4f876b9844c5898d0044c7940ff7460db9f4cd984ac7862b5"}, + {file = "ijson-3.3.0-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:04366e7e4a4078d410845e58a2987fd9c45e63df70773d7b6e87ceef771b51ee"}, + {file = "ijson-3.3.0-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:de7c1ddb80fa7a3ab045266dca169004b93f284756ad198306533b792774f10a"}, + {file = "ijson-3.3.0-cp38-cp38-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:8851584fb931cffc0caa395f6980525fd5116eab8f73ece9d95e6f9c2c326c4c"}, + {file = "ijson-3.3.0-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:bdcfc88347fd981e53c33d832ce4d3e981a0d696b712fbcb45dcc1a43fe65c65"}, + {file = "ijson-3.3.0-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:3917b2b3d0dbbe3296505da52b3cb0befbaf76119b2edaff30bd448af20b5400"}, + {file = "ijson-3.3.0-cp38-cp38-musllinux_1_2_i686.whl", hash = "sha256:e10c14535abc7ddf3fd024aa36563cd8ab5d2bb6234a5d22c77c30e30fa4fb2b"}, + {file = "ijson-3.3.0-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:3aba5c4f97f4e2ce854b5591a8b0711ca3b0c64d1b253b04ea7b004b0a197ef6"}, + {file = "ijson-3.3.0-cp38-cp38-win32.whl", hash = "sha256:b325f42e26659df1a0de66fdb5cde8dd48613da9c99c07d04e9fb9e254b7ee1c"}, + {file = "ijson-3.3.0-cp38-cp38-win_amd64.whl", hash = "sha256:ff835906f84451e143f31c4ce8ad73d83ef4476b944c2a2da91aec8b649570e1"}, + {file = "ijson-3.3.0-cp39-cp39-macosx_10_9_universal2.whl", hash = "sha256:3c556f5553368dff690c11d0a1fb435d4ff1f84382d904ccc2dc53beb27ba62e"}, + {file = "ijson-3.3.0-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:e4396b55a364a03ff7e71a34828c3ed0c506814dd1f50e16ebed3fc447d5188e"}, + {file = "ijson-3.3.0-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:e6850ae33529d1e43791b30575070670070d5fe007c37f5d06aebc1dd152ab3f"}, + {file = "ijson-3.3.0-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:36aa56d68ea8def26778eb21576ae13f27b4a47263a7a2581ab2ef58b8de4451"}, + {file = "ijson-3.3.0-cp39-cp39-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:a7ec759c4a0fc820ad5dc6a58e9c391e7b16edcb618056baedbedbb9ea3b1524"}, + {file = "ijson-3.3.0-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:b51bab2c4e545dde93cb6d6bb34bf63300b7cd06716f195dd92d9255df728331"}, + {file = "ijson-3.3.0-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:92355f95a0e4da96d4c404aa3cff2ff033f9180a9515f813255e1526551298c1"}, + {file = "ijson-3.3.0-cp39-cp39-musllinux_1_2_i686.whl", hash = "sha256:8795e88adff5aa3c248c1edce932db003d37a623b5787669ccf205c422b91e4a"}, + {file = "ijson-3.3.0-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:8f83f553f4cde6d3d4eaf58ec11c939c94a0ec545c5b287461cafb184f4b3a14"}, + {file = "ijson-3.3.0-cp39-cp39-win32.whl", hash = "sha256:ead50635fb56577c07eff3e557dac39533e0fe603000684eea2af3ed1ad8f941"}, + {file = "ijson-3.3.0-cp39-cp39-win_amd64.whl", hash = "sha256:c8a9befb0c0369f0cf5c1b94178d0d78f66d9cebb9265b36be6e4f66236076b8"}, + {file = "ijson-3.3.0-pp310-pypy310_pp73-macosx_10_9_x86_64.whl", hash = "sha256:2af323a8aec8a50fa9effa6d640691a30a9f8c4925bd5364a1ca97f1ac6b9b5c"}, + {file = "ijson-3.3.0-pp310-pypy310_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:f64f01795119880023ba3ce43072283a393f0b90f52b66cc0ea1a89aa64a9ccb"}, + {file = "ijson-3.3.0-pp310-pypy310_pp73-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:a716e05547a39b788deaf22725490855337fc36613288aa8ae1601dc8c525553"}, + {file = "ijson-3.3.0-pp310-pypy310_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:473f5d921fadc135d1ad698e2697025045cd8ed7e5e842258295012d8a3bc702"}, + {file = "ijson-3.3.0-pp310-pypy310_pp73-win_amd64.whl", hash = "sha256:dd26b396bc3a1e85f4acebeadbf627fa6117b97f4c10b177d5779577c6607744"}, + {file = "ijson-3.3.0-pp37-pypy37_pp73-macosx_10_9_x86_64.whl", hash = "sha256:25fd49031cdf5fd5f1fd21cb45259a64dad30b67e64f745cc8926af1c8c243d3"}, + {file = "ijson-3.3.0-pp37-pypy37_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4b72178b1e565d06ab19319965022b36ef41bcea7ea153b32ec31194bec032a2"}, + {file = "ijson-3.3.0-pp37-pypy37_pp73-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:7d0b6b637d05dbdb29d0bfac2ed8425bb369e7af5271b0cc7cf8b801cb7360c2"}, + {file = "ijson-3.3.0-pp37-pypy37_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:5378d0baa59ae422905c5f182ea0fd74fe7e52a23e3821067a7d58c8306b2191"}, + {file = "ijson-3.3.0-pp37-pypy37_pp73-win_amd64.whl", hash = "sha256:99f5c8ab048ee4233cc4f2b461b205cbe01194f6201018174ac269bf09995749"}, + {file = "ijson-3.3.0-pp38-pypy38_pp73-macosx_10_9_x86_64.whl", hash = "sha256:45ff05de889f3dc3d37a59d02096948ce470699f2368b32113954818b21aa74a"}, + {file = "ijson-3.3.0-pp38-pypy38_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:1efb521090dd6cefa7aafd120581947b29af1713c902ff54336b7c7130f04c47"}, + {file = "ijson-3.3.0-pp38-pypy38_pp73-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:87c727691858fd3a1c085d9980d12395517fcbbf02c69fbb22dede8ee03422da"}, + {file = "ijson-3.3.0-pp38-pypy38_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:0420c24e50389bc251b43c8ed379ab3e3ba065ac8262d98beb6735ab14844460"}, + {file = "ijson-3.3.0-pp38-pypy38_pp73-win_amd64.whl", hash = "sha256:8fdf3721a2aa7d96577970f5604bd81f426969c1822d467f07b3d844fa2fecc7"}, + {file = "ijson-3.3.0-pp39-pypy39_pp73-macosx_10_9_x86_64.whl", hash = "sha256:891f95c036df1bc95309951940f8eea8537f102fa65715cdc5aae20b8523813b"}, + {file = "ijson-3.3.0-pp39-pypy39_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:ed1336a2a6e5c427f419da0154e775834abcbc8ddd703004108121c6dd9eba9d"}, + {file = "ijson-3.3.0-pp39-pypy39_pp73-manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:f0c819f83e4f7b7f7463b2dc10d626a8be0c85fbc7b3db0edc098c2b16ac968e"}, + {file = "ijson-3.3.0-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:33afc25057377a6a43c892de34d229a86f89ea6c4ca3dd3db0dcd17becae0dbb"}, + {file = "ijson-3.3.0-pp39-pypy39_pp73-win_amd64.whl", hash = "sha256:7914d0cf083471856e9bc2001102a20f08e82311dfc8cf1a91aa422f9414a0d6"}, + {file = "ijson-3.3.0.tar.gz", hash = "sha256:7f172e6ba1bee0d4c8f8ebd639577bfe429dee0f3f96775a067b8bae4492d8a0"}, +] + +[[package]] +name = "importlib-resources" +version = "6.4.0" +description = "Read resources from Python packages" +optional = false +python-versions = ">=3.8" +files = [ + {file = "importlib_resources-6.4.0-py3-none-any.whl", hash = "sha256:50d10f043df931902d4194ea07ec57960f66a80449ff867bfe782b4c486ba78c"}, + {file = "importlib_resources-6.4.0.tar.gz", hash = "sha256:cdb2b453b8046ca4e3798eb1d84f3cce1446a0e8e7b5ef4efb600f19fc398145"}, +] + +[package.extras] +docs = ["furo", "jaraco.packaging (>=9.3)", "jaraco.tidelift (>=1.4)", "rst.linker (>=1.9)", "sphinx (<7.2.5)", "sphinx (>=3.5)", "sphinx-lint"] +testing = ["jaraco.test (>=5.4)", "pytest (>=6)", "pytest-checkdocs (>=2.4)", "pytest-cov", "pytest-enabler (>=2.2)", "pytest-mypy", "pytest-ruff (>=0.2.1)", "zipp (>=3.17)"] + +[[package]] +name = "iniconfig" +version = "2.0.0" +description = "brain-dead simple config-ini parsing" +optional = false +python-versions = ">=3.7" +files = [ + {file = "iniconfig-2.0.0-py3-none-any.whl", hash = "sha256:b6a85871a79d2e3b22d2d1b94ac2824226a63c6b741c88f7ae975f18b6778374"}, + {file = "iniconfig-2.0.0.tar.gz", hash = "sha256:2d91e135bf72d31a410b17c16da610a82cb55f6b0477d1a902134b24a455b8b3"}, +] + +[[package]] +name = "isodate" +version = "0.6.1" +description = "An ISO 8601 date/time/duration parser and formatter" +optional = false +python-versions = "*" +files = [ + {file = "isodate-0.6.1-py2.py3-none-any.whl", hash = "sha256:0751eece944162659049d35f4f549ed815792b38793f07cf73381c1c87cbed96"}, + {file = "isodate-0.6.1.tar.gz", hash = "sha256:48c5881de7e8b0a0d648cb024c8062dc84e7b840ed81e864c7614fd3c127bde9"}, +] + +[package.dependencies] +six = "*" + +[[package]] +name = "json-flattener" +version = "0.1.9" +description = "Python library for denormalizing nested dicts or json objects to tables and back" +optional = false +python-versions = ">=3.7.0" +files = [ + {file = "json_flattener-0.1.9-py3-none-any.whl", hash = "sha256:6b027746f08bf37a75270f30c6690c7149d5f704d8af1740c346a3a1236bc941"}, + {file = "json_flattener-0.1.9.tar.gz", hash = "sha256:84cf8523045ffb124301a602602201665fcb003a171ece87e6f46ed02f7f0c15"}, +] + +[package.dependencies] +click = "*" +pyyaml = "*" + +[[package]] +name = "jsonasobj" +version = "1.3.1" +description = "JSON as python objects" +optional = false +python-versions = "*" +files = [ + {file = "jsonasobj-1.3.1-py3-none-any.whl", hash = "sha256:b9e329dc1ceaae7cf5d5b214684a0b100e0dad0be6d5bbabac281ec35ddeca65"}, + {file = "jsonasobj-1.3.1.tar.gz", hash = "sha256:d52e0544a54a08f6ea3f77fa3387271e3648655e0eace2f21e825c26370e44a2"}, +] + +[[package]] +name = "jsonasobj2" +version = "1.0.4" +description = "JSON as python objects - version 2" +optional = false +python-versions = ">=3.6" +files = [ + {file = "jsonasobj2-1.0.4-py3-none-any.whl", hash = "sha256:12e86f86324d54fcf60632db94ea74488d5314e3da554c994fe1e2c6f29acb79"}, + {file = "jsonasobj2-1.0.4.tar.gz", hash = "sha256:f50b1668ef478004aa487b2d2d094c304e5cb6b79337809f4a1f2975cc7fbb4e"}, +] + +[package.dependencies] +hbreader = "*" + +[[package]] +name = "jsonlines" +version = "4.0.0" +description = "Library with helpers for the jsonlines file format" +optional = false +python-versions = ">=3.8" +files = [ + {file = "jsonlines-4.0.0-py3-none-any.whl", hash = "sha256:185b334ff2ca5a91362993f42e83588a360cf95ce4b71a73548502bda52a7c55"}, + {file = "jsonlines-4.0.0.tar.gz", hash = "sha256:0c6d2c09117550c089995247f605ae4cf77dd1533041d366351f6f298822ea74"}, +] + +[package.dependencies] +attrs = ">=19.2.0" + +[[package]] +name = "jsonpatch" +version = "1.33" +description = "Apply JSON-Patches (RFC 6902)" +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*, !=3.3.*, !=3.4.*, !=3.5.*, !=3.6.*" +files = [ + {file = "jsonpatch-1.33-py2.py3-none-any.whl", hash = "sha256:0ae28c0cd062bbd8b8ecc26d7d164fbbea9652a1a3693f3b956c1eae5145dade"}, + {file = "jsonpatch-1.33.tar.gz", hash = "sha256:9fcd4009c41e6d12348b4a0ff2563ba56a2923a7dfee731d004e212e1ee5030c"}, +] + +[package.dependencies] +jsonpointer = ">=1.9" + +[[package]] +name = "jsonpointer" +version = "3.0.0" +description = "Identify specific nodes in a JSON document (RFC 6901)" +optional = false +python-versions = ">=3.7" +files = [ + {file = "jsonpointer-3.0.0-py2.py3-none-any.whl", hash = "sha256:13e088adc14fca8b6aa8177c044e12701e6ad4b28ff10e65f2267a90109c9942"}, + {file = "jsonpointer-3.0.0.tar.gz", hash = "sha256:2b2d729f2091522d61c3b31f82e11870f60b68f43fbc705cb76bf4b832af59ef"}, +] + +[[package]] +name = "jsonschema" +version = "4.22.0" +description = "An implementation of JSON Schema validation for Python" +optional = false +python-versions = ">=3.8" +files = [ + {file = "jsonschema-4.22.0-py3-none-any.whl", hash = "sha256:ff4cfd6b1367a40e7bc6411caec72effadd3db0bbe5017de188f2d6108335802"}, + {file = "jsonschema-4.22.0.tar.gz", hash = "sha256:5b22d434a45935119af990552c862e5d6d564e8f6601206b305a61fdf661a2b7"}, +] + +[package.dependencies] +attrs = ">=22.2.0" +jsonschema-specifications = ">=2023.03.6" +referencing = ">=0.28.4" +rpds-py = ">=0.7.1" + +[package.extras] +format = ["fqdn", "idna", "isoduration", "jsonpointer (>1.13)", "rfc3339-validator", "rfc3987", "uri-template", "webcolors (>=1.11)"] +format-nongpl = ["fqdn", "idna", "isoduration", "jsonpointer (>1.13)", "rfc3339-validator", "rfc3986-validator (>0.1.0)", "uri-template", "webcolors (>=1.11)"] + +[[package]] +name = "jsonschema-specifications" +version = "2023.12.1" +description = "The JSON Schema meta-schemas and vocabularies, exposed as a Registry" +optional = false +python-versions = ">=3.8" +files = [ + {file = "jsonschema_specifications-2023.12.1-py3-none-any.whl", hash = "sha256:87e4fdf3a94858b8a2ba2778d9ba57d8a9cafca7c7489c46ba0d30a8bc6a9c3c"}, + {file = "jsonschema_specifications-2023.12.1.tar.gz", hash = "sha256:48a76787b3e70f5ed53f1160d2b81f586e4ca6d1548c5de7085d1682674764cc"}, +] + +[package.dependencies] +referencing = ">=0.31.0" + +[[package]] +name = "kgcl-rdflib" +version = "0.5.0" +description = "Schema for the KGCL project." +optional = false +python-versions = ">=3.8,<4.0" +files = [ + {file = "kgcl_rdflib-0.5.0-py3-none-any.whl", hash = "sha256:214c011eac692384dd18397e455af2a7375f6a2f71fa318df245e8826678f454"}, + {file = "kgcl_rdflib-0.5.0.tar.gz", hash = "sha256:19e34690316714b9c500e1749a35d1a0d17282f2a38cd2b1fd3d7d8cf5e6013d"}, +] + +[package.dependencies] +kgcl-schema = ">=0.5.0" +linkml-runtime = ">=1.1.24" + +[[package]] +name = "kgcl-schema" +version = "0.6.8" +description = "Schema for the KGCL project." +optional = false +python-versions = "<4.0,>=3.9" +files = [ + {file = "kgcl_schema-0.6.8-py3-none-any.whl", hash = "sha256:84deb921203c5b94c9fa6386e7fec24593162abbccdadeb78a5f7231c0c75803"}, + {file = "kgcl_schema-0.6.8.tar.gz", hash = "sha256:7520e8fc7cd1546e3212ae868fae410720c4f2cea0e0a5e85ac277f63941d8bd"}, +] + +[package.dependencies] +curies = ">=0.6.0" +lark = ">=1.1.2" +linkml-runtime = ">=1.1.24" +prefixmaps = ">=0.2.0,<0.3.0" + +[[package]] +name = "langchain-core" +version = "0.2.7" +description = "Building applications with LLMs through composability" +optional = false +python-versions = "<4.0,>=3.8.1" +files = [ + {file = "langchain_core-0.2.7-py3-none-any.whl", hash = "sha256:fd02e153c898486dd728d634684ffc64bc257ff2ba443dc7e53d017ac0bf4658"}, + {file = "langchain_core-0.2.7.tar.gz", hash = "sha256:b0b1b6dfbdedb39426fcb8bd3f07e40eec7964856e3fc384c420ca6dba61b34e"}, +] + +[package.dependencies] +jsonpatch = ">=1.33,<2.0" +langsmith = ">=0.1.75,<0.2.0" +packaging = ">=23.2,<25" +pydantic = ">=1,<3" +PyYAML = ">=5.3" +tenacity = ">=8.1.0,<9.0.0" + +[[package]] +name = "langchain-openai" +version = "0.1.8" +description = "An integration package connecting OpenAI and LangChain" +optional = false +python-versions = "<4.0,>=3.8.1" +files = [ + {file = "langchain_openai-0.1.8-py3-none-any.whl", hash = "sha256:8125c84223e9f43b05defbca64eedbcf362fd78a680de6c25e64f973b34a8063"}, + {file = "langchain_openai-0.1.8.tar.gz", hash = "sha256:a11fcce15def7917c44232abda6baaa63dfc79fe44be1531eea650d39a44cd95"}, +] + +[package.dependencies] +langchain-core = ">=0.2.2,<0.3" +openai = ">=1.26.0,<2.0.0" +tiktoken = ">=0.7,<1" + +[[package]] +name = "langsmith" +version = "0.1.77" +description = "Client library to connect to the LangSmith LLM Tracing and Evaluation Platform." +optional = false +python-versions = "<4.0,>=3.8.1" +files = [ + {file = "langsmith-0.1.77-py3-none-any.whl", hash = "sha256:2202cc21b1ed7e7b9e5d2af2694be28898afa048c09fdf09f620cbd9301755ae"}, + {file = "langsmith-0.1.77.tar.gz", hash = "sha256:4ace09077a9a4e412afeb4b517ca68e7de7b07f36e4792dc8236ac5207c0c0c7"}, +] + +[package.dependencies] +orjson = ">=3.9.14,<4.0.0" +pydantic = ">=1,<3" +requests = ">=2,<3" + +[[package]] +name = "lark" +version = "1.1.9" +description = "a modern parsing library" +optional = false +python-versions = ">=3.6" +files = [ + {file = "lark-1.1.9-py3-none-any.whl", hash = "sha256:a0dd3a87289f8ccbb325901e4222e723e7d745dbfc1803eaf5f3d2ace19cf2db"}, + {file = "lark-1.1.9.tar.gz", hash = "sha256:15fa5236490824c2c4aba0e22d2d6d823575dcaf4cdd1848e34b6ad836240fba"}, +] + +[package.extras] +atomic-cache = ["atomicwrites"] +interegular = ["interegular (>=0.3.1,<0.4.0)"] +nearley = ["js2py"] +regex = ["regex"] + +[[package]] +name = "linkml-renderer" +version = "0.3.0" +description = "linkml-renderer" +optional = false +python-versions = ">=3.8,<4.0" +files = [ + {file = "linkml_renderer-0.3.0-py3-none-any.whl", hash = "sha256:9b2c0207751c8b5abb814b67fa1ae0f2a4dce80637d56ed770f74a40d4fee614"}, + {file = "linkml_renderer-0.3.0.tar.gz", hash = "sha256:59441022182d1386ef761ad4d055a23cef5707e0070400e2f6860893751c05f8"}, +] + +[package.dependencies] +airium = ">=0.2.5,<0.3.0" +click = ">=8.1.3,<9.0.0" +linkml-runtime = ">=1.4.1" +pydantic = "*" + +[[package]] +name = "linkml-runtime" +version = "1.7.7" +description = "Runtime environment for LinkML, the Linked open data modeling language" +optional = false +python-versions = "<4.0,>=3.8" +files = [ + {file = "linkml_runtime-1.7.7-py3-none-any.whl", hash = "sha256:1556db30cda1191de2f70c3b949eb45c31b2ed66ca525bf38ee99f992f2451d7"}, + {file = "linkml_runtime-1.7.7.tar.gz", hash = "sha256:f471b765056b38ff3eb1372d167b86a67e188ef472c16abf4f6cd91097a82a11"}, +] + +[package.dependencies] +click = "*" +curies = ">=0.5.4" +deprecated = "*" +hbreader = "*" +json-flattener = ">=0.1.9" +jsonasobj2 = ">=1.0.4,<2.dev0" +jsonschema = ">=3.2.0" +prefixcommons = ">=0.1.12" +prefixmaps = ">=0.1.4" +pydantic = ">=1.10.2,<3.0.0" +pyyaml = "*" +rdflib = ">=6.0.0" +requests = "*" + +[[package]] +name = "lxml" +version = "5.2.2" +description = "Powerful and Pythonic XML processing library combining libxml2/libxslt with the ElementTree API." +optional = false +python-versions = ">=3.6" +files = [ + {file = "lxml-5.2.2-cp310-cp310-macosx_10_9_universal2.whl", hash = "sha256:364d03207f3e603922d0d3932ef363d55bbf48e3647395765f9bfcbdf6d23632"}, + {file = "lxml-5.2.2-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:50127c186f191b8917ea2fb8b206fbebe87fd414a6084d15568c27d0a21d60db"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:74e4f025ef3db1c6da4460dd27c118d8cd136d0391da4e387a15e48e5c975147"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:981a06a3076997adf7c743dcd0d7a0415582661e2517c7d961493572e909aa1d"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:aef5474d913d3b05e613906ba4090433c515e13ea49c837aca18bde190853dff"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:1e275ea572389e41e8b039ac076a46cb87ee6b8542df3fff26f5baab43713bca"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f5b65529bb2f21ac7861a0e94fdbf5dc0daab41497d18223b46ee8515e5ad297"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_28_aarch64.whl", hash = "sha256:bcc98f911f10278d1daf14b87d65325851a1d29153caaf146877ec37031d5f36"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_28_ppc64le.whl", hash = "sha256:b47633251727c8fe279f34025844b3b3a3e40cd1b198356d003aa146258d13a2"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_28_s390x.whl", hash = "sha256:fbc9d316552f9ef7bba39f4edfad4a734d3d6f93341232a9dddadec4f15d425f"}, + {file = "lxml-5.2.2-cp310-cp310-manylinux_2_28_x86_64.whl", hash = "sha256:13e69be35391ce72712184f69000cda04fc89689429179bc4c0ae5f0b7a8c21b"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:3b6a30a9ab040b3f545b697cb3adbf3696c05a3a68aad172e3fd7ca73ab3c835"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_1_ppc64le.whl", hash = "sha256:a233bb68625a85126ac9f1fc66d24337d6e8a0f9207b688eec2e7c880f012ec0"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_1_s390x.whl", hash = "sha256:dfa7c241073d8f2b8e8dbc7803c434f57dbb83ae2a3d7892dd068d99e96efe2c"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:1a7aca7964ac4bb07680d5c9d63b9d7028cace3e2d43175cb50bba8c5ad33316"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:ae4073a60ab98529ab8a72ebf429f2a8cc612619a8c04e08bed27450d52103c0"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_2_ppc64le.whl", hash = "sha256:ffb2be176fed4457e445fe540617f0252a72a8bc56208fd65a690fdb1f57660b"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_2_s390x.whl", hash = "sha256:e290d79a4107d7d794634ce3e985b9ae4f920380a813717adf61804904dc4393"}, + {file = "lxml-5.2.2-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:96e85aa09274955bb6bd483eaf5b12abadade01010478154b0ec70284c1b1526"}, + {file = "lxml-5.2.2-cp310-cp310-win32.whl", hash = "sha256:f956196ef61369f1685d14dad80611488d8dc1ef00be57c0c5a03064005b0f30"}, + {file = "lxml-5.2.2-cp310-cp310-win_amd64.whl", hash = "sha256:875a3f90d7eb5c5d77e529080d95140eacb3c6d13ad5b616ee8095447b1d22e7"}, + {file = "lxml-5.2.2-cp311-cp311-macosx_10_9_universal2.whl", hash = "sha256:45f9494613160d0405682f9eee781c7e6d1bf45f819654eb249f8f46a2c22545"}, + {file = "lxml-5.2.2-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:b0b3f2df149efb242cee2ffdeb6674b7f30d23c9a7af26595099afaf46ef4e88"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:d28cb356f119a437cc58a13f8135ab8a4c8ece18159eb9194b0d269ec4e28083"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:657a972f46bbefdbba2d4f14413c0d079f9ae243bd68193cb5061b9732fa54c1"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:b74b9ea10063efb77a965a8d5f4182806fbf59ed068b3c3fd6f30d2ac7bee734"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:07542787f86112d46d07d4f3c4e7c760282011b354d012dc4141cc12a68cef5f"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:303f540ad2dddd35b92415b74b900c749ec2010e703ab3bfd6660979d01fd4ed"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_28_aarch64.whl", hash = "sha256:2eb2227ce1ff998faf0cd7fe85bbf086aa41dfc5af3b1d80867ecfe75fb68df3"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_28_ppc64le.whl", hash = "sha256:1d8a701774dfc42a2f0b8ccdfe7dbc140500d1049e0632a611985d943fcf12df"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_28_s390x.whl", hash = "sha256:56793b7a1a091a7c286b5f4aa1fe4ae5d1446fe742d00cdf2ffb1077865db10d"}, + {file = "lxml-5.2.2-cp311-cp311-manylinux_2_28_x86_64.whl", hash = "sha256:eb00b549b13bd6d884c863554566095bf6fa9c3cecb2e7b399c4bc7904cb33b5"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:1a2569a1f15ae6c8c64108a2cd2b4a858fc1e13d25846be0666fc144715e32ab"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_1_ppc64le.whl", hash = "sha256:8cf85a6e40ff1f37fe0f25719aadf443686b1ac7652593dc53c7ef9b8492b115"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_1_s390x.whl", hash = "sha256:d237ba6664b8e60fd90b8549a149a74fcc675272e0e95539a00522e4ca688b04"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:0b3f5016e00ae7630a4b83d0868fca1e3d494c78a75b1c7252606a3a1c5fc2ad"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:23441e2b5339bc54dc949e9e675fa35efe858108404ef9aa92f0456929ef6fe8"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_2_ppc64le.whl", hash = "sha256:2fb0ba3e8566548d6c8e7dd82a8229ff47bd8fb8c2da237607ac8e5a1b8312e5"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_2_s390x.whl", hash = "sha256:79d1fb9252e7e2cfe4de6e9a6610c7cbb99b9708e2c3e29057f487de5a9eaefa"}, + {file = "lxml-5.2.2-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:6dcc3d17eac1df7859ae01202e9bb11ffa8c98949dcbeb1069c8b9a75917e01b"}, + {file = "lxml-5.2.2-cp311-cp311-win32.whl", hash = "sha256:4c30a2f83677876465f44c018830f608fa3c6a8a466eb223535035fbc16f3438"}, + {file = "lxml-5.2.2-cp311-cp311-win_amd64.whl", hash = "sha256:49095a38eb333aaf44c06052fd2ec3b8f23e19747ca7ec6f6c954ffea6dbf7be"}, + {file = "lxml-5.2.2-cp312-cp312-macosx_10_9_universal2.whl", hash = "sha256:7429e7faa1a60cad26ae4227f4dd0459efde239e494c7312624ce228e04f6391"}, + {file = "lxml-5.2.2-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:50ccb5d355961c0f12f6cf24b7187dbabd5433f29e15147a67995474f27d1776"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:dc911208b18842a3a57266d8e51fc3cfaccee90a5351b92079beed912a7914c2"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:33ce9e786753743159799fdf8e92a5da351158c4bfb6f2db0bf31e7892a1feb5"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:ec87c44f619380878bd49ca109669c9f221d9ae6883a5bcb3616785fa8f94c97"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:08ea0f606808354eb8f2dfaac095963cb25d9d28e27edcc375d7b30ab01abbf6"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:75a9632f1d4f698b2e6e2e1ada40e71f369b15d69baddb8968dcc8e683839b18"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_28_aarch64.whl", hash = "sha256:74da9f97daec6928567b48c90ea2c82a106b2d500f397eeb8941e47d30b1ca85"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_28_ppc64le.whl", hash = "sha256:0969e92af09c5687d769731e3f39ed62427cc72176cebb54b7a9d52cc4fa3b73"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_28_s390x.whl", hash = "sha256:9164361769b6ca7769079f4d426a41df6164879f7f3568be9086e15baca61466"}, + {file = "lxml-5.2.2-cp312-cp312-manylinux_2_28_x86_64.whl", hash = "sha256:d26a618ae1766279f2660aca0081b2220aca6bd1aa06b2cf73f07383faf48927"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:ab67ed772c584b7ef2379797bf14b82df9aa5f7438c5b9a09624dd834c1c1aaf"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_1_ppc64le.whl", hash = "sha256:3d1e35572a56941b32c239774d7e9ad724074d37f90c7a7d499ab98761bd80cf"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_1_s390x.whl", hash = "sha256:8268cbcd48c5375f46e000adb1390572c98879eb4f77910c6053d25cc3ac2c67"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:e282aedd63c639c07c3857097fc0e236f984ceb4089a8b284da1c526491e3f3d"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:6dfdc2bfe69e9adf0df4915949c22a25b39d175d599bf98e7ddf620a13678585"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_2_ppc64le.whl", hash = "sha256:4aefd911793b5d2d7a921233a54c90329bf3d4a6817dc465f12ffdfe4fc7b8fe"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_2_s390x.whl", hash = "sha256:8b8df03a9e995b6211dafa63b32f9d405881518ff1ddd775db4e7b98fb545e1c"}, + {file = "lxml-5.2.2-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:f11ae142f3a322d44513de1018b50f474f8f736bc3cd91d969f464b5bfef8836"}, + {file = "lxml-5.2.2-cp312-cp312-win32.whl", hash = "sha256:16a8326e51fcdffc886294c1e70b11ddccec836516a343f9ed0f82aac043c24a"}, + {file = "lxml-5.2.2-cp312-cp312-win_amd64.whl", hash = "sha256:bbc4b80af581e18568ff07f6395c02114d05f4865c2812a1f02f2eaecf0bfd48"}, + {file = "lxml-5.2.2-cp36-cp36m-macosx_10_9_x86_64.whl", hash = "sha256:e3d9d13603410b72787579769469af730c38f2f25505573a5888a94b62b920f8"}, + {file = "lxml-5.2.2-cp36-cp36m-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:38b67afb0a06b8575948641c1d6d68e41b83a3abeae2ca9eed2ac59892b36706"}, + {file = "lxml-5.2.2-cp36-cp36m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:c689d0d5381f56de7bd6966a4541bff6e08bf8d3871bbd89a0c6ab18aa699573"}, + {file = "lxml-5.2.2-cp36-cp36m-manylinux_2_28_x86_64.whl", hash = "sha256:cf2a978c795b54c539f47964ec05e35c05bd045db5ca1e8366988c7f2fe6b3ce"}, + {file = "lxml-5.2.2-cp36-cp36m-manylinux_2_5_x86_64.manylinux1_x86_64.whl", hash = "sha256:739e36ef7412b2bd940f75b278749106e6d025e40027c0b94a17ef7968d55d56"}, + {file = "lxml-5.2.2-cp36-cp36m-musllinux_1_1_x86_64.whl", hash = "sha256:d8bbcd21769594dbba9c37d3c819e2d5847656ca99c747ddb31ac1701d0c0ed9"}, + {file = "lxml-5.2.2-cp36-cp36m-musllinux_1_2_x86_64.whl", hash = "sha256:2304d3c93f2258ccf2cf7a6ba8c761d76ef84948d87bf9664e14d203da2cd264"}, + {file = "lxml-5.2.2-cp36-cp36m-win32.whl", hash = "sha256:02437fb7308386867c8b7b0e5bc4cd4b04548b1c5d089ffb8e7b31009b961dc3"}, + {file = "lxml-5.2.2-cp36-cp36m-win_amd64.whl", hash = "sha256:edcfa83e03370032a489430215c1e7783128808fd3e2e0a3225deee278585196"}, + {file = "lxml-5.2.2-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:28bf95177400066596cdbcfc933312493799382879da504633d16cf60bba735b"}, + {file = "lxml-5.2.2-cp37-cp37m-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:3a745cc98d504d5bd2c19b10c79c61c7c3df9222629f1b6210c0368177589fb8"}, + {file = "lxml-5.2.2-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:b336b0416828022bfd5a2e3083e7f5ba54b96242159f83c7e3eebaec752f1716"}, + {file = "lxml-5.2.2-cp37-cp37m-manylinux_2_28_x86_64.whl", hash = "sha256:4bc6cb140a7a0ad1f7bc37e018d0ed690b7b6520ade518285dc3171f7a117905"}, + {file = "lxml-5.2.2-cp37-cp37m-musllinux_1_1_x86_64.whl", hash = "sha256:57f0a0bbc9868e10ebe874e9f129d2917750adf008fe7b9c1598c0fbbfdde6a6"}, + {file = "lxml-5.2.2-cp37-cp37m-musllinux_1_2_x86_64.whl", hash = "sha256:60499fe961b21264e17a471ec296dcbf4365fbea611bf9e303ab69db7159ce61"}, + {file = "lxml-5.2.2-cp37-cp37m-win32.whl", hash = "sha256:d9b342c76003c6b9336a80efcc766748a333573abf9350f4094ee46b006ec18f"}, + {file = "lxml-5.2.2-cp37-cp37m-win_amd64.whl", hash = "sha256:b16db2770517b8799c79aa80f4053cd6f8b716f21f8aca962725a9565ce3ee40"}, + {file = "lxml-5.2.2-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:7ed07b3062b055d7a7f9d6557a251cc655eed0b3152b76de619516621c56f5d3"}, + {file = "lxml-5.2.2-cp38-cp38-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:f60fdd125d85bf9c279ffb8e94c78c51b3b6a37711464e1f5f31078b45002421"}, + {file = "lxml-5.2.2-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:8a7e24cb69ee5f32e003f50e016d5fde438010c1022c96738b04fc2423e61706"}, + {file = "lxml-5.2.2-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:23cfafd56887eaed93d07bc4547abd5e09d837a002b791e9767765492a75883f"}, + {file = "lxml-5.2.2-cp38-cp38-manylinux_2_28_aarch64.whl", hash = "sha256:19b4e485cd07b7d83e3fe3b72132e7df70bfac22b14fe4bf7a23822c3a35bff5"}, + {file = "lxml-5.2.2-cp38-cp38-manylinux_2_28_x86_64.whl", hash = "sha256:7ce7ad8abebe737ad6143d9d3bf94b88b93365ea30a5b81f6877ec9c0dee0a48"}, + {file = "lxml-5.2.2-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:e49b052b768bb74f58c7dda4e0bdf7b79d43a9204ca584ffe1fb48a6f3c84c66"}, + {file = "lxml-5.2.2-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:d14a0d029a4e176795cef99c056d58067c06195e0c7e2dbb293bf95c08f772a3"}, + {file = "lxml-5.2.2-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:be49ad33819d7dcc28a309b86d4ed98e1a65f3075c6acd3cd4fe32103235222b"}, + {file = "lxml-5.2.2-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:a6d17e0370d2516d5bb9062c7b4cb731cff921fc875644c3d751ad857ba9c5b1"}, + {file = "lxml-5.2.2-cp38-cp38-win32.whl", hash = "sha256:5b8c041b6265e08eac8a724b74b655404070b636a8dd6d7a13c3adc07882ef30"}, + {file = "lxml-5.2.2-cp38-cp38-win_amd64.whl", hash = "sha256:f61efaf4bed1cc0860e567d2ecb2363974d414f7f1f124b1df368bbf183453a6"}, + {file = "lxml-5.2.2-cp39-cp39-macosx_10_9_universal2.whl", hash = "sha256:fb91819461b1b56d06fa4bcf86617fac795f6a99d12239fb0c68dbeba41a0a30"}, + {file = "lxml-5.2.2-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:d4ed0c7cbecde7194cd3228c044e86bf73e30a23505af852857c09c24e77ec5d"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_12_i686.manylinux2010_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:54401c77a63cc7d6dc4b4e173bb484f28a5607f3df71484709fe037c92d4f0ed"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:625e3ef310e7fa3a761d48ca7ea1f9d8718a32b1542e727d584d82f4453d5eeb"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:519895c99c815a1a24a926d5b60627ce5ea48e9f639a5cd328bda0515ea0f10c"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:c7079d5eb1c1315a858bbf180000757db8ad904a89476653232db835c3114001"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:343ab62e9ca78094f2306aefed67dcfad61c4683f87eee48ff2fd74902447726"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_28_aarch64.whl", hash = "sha256:cd9e78285da6c9ba2d5c769628f43ef66d96ac3085e59b10ad4f3707980710d3"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_28_ppc64le.whl", hash = "sha256:546cf886f6242dff9ec206331209db9c8e1643ae642dea5fdbecae2453cb50fd"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_28_s390x.whl", hash = "sha256:02f6a8eb6512fdc2fd4ca10a49c341c4e109aa6e9448cc4859af5b949622715a"}, + {file = "lxml-5.2.2-cp39-cp39-manylinux_2_28_x86_64.whl", hash = "sha256:339ee4a4704bc724757cd5dd9dc8cf4d00980f5d3e6e06d5847c1b594ace68ab"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:0a028b61a2e357ace98b1615fc03f76eb517cc028993964fe08ad514b1e8892d"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_1_ppc64le.whl", hash = "sha256:f90e552ecbad426eab352e7b2933091f2be77115bb16f09f78404861c8322981"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_1_s390x.whl", hash = "sha256:d83e2d94b69bf31ead2fa45f0acdef0757fa0458a129734f59f67f3d2eb7ef32"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:a02d3c48f9bb1e10c7788d92c0c7db6f2002d024ab6e74d6f45ae33e3d0288a3"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:6d68ce8e7b2075390e8ac1e1d3a99e8b6372c694bbe612632606d1d546794207"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_2_ppc64le.whl", hash = "sha256:453d037e09a5176d92ec0fd282e934ed26d806331a8b70ab431a81e2fbabf56d"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_2_s390x.whl", hash = "sha256:3b019d4ee84b683342af793b56bb35034bd749e4cbdd3d33f7d1107790f8c472"}, + {file = "lxml-5.2.2-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:cb3942960f0beb9f46e2a71a3aca220d1ca32feb5a398656be934320804c0df9"}, + {file = "lxml-5.2.2-cp39-cp39-win32.whl", hash = "sha256:ac6540c9fff6e3813d29d0403ee7a81897f1d8ecc09a8ff84d2eea70ede1cdbf"}, + {file = "lxml-5.2.2-cp39-cp39-win_amd64.whl", hash = "sha256:610b5c77428a50269f38a534057444c249976433f40f53e3b47e68349cca1425"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-macosx_10_9_x86_64.whl", hash = "sha256:b537bd04d7ccd7c6350cdaaaad911f6312cbd61e6e6045542f781c7f8b2e99d2"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4820c02195d6dfb7b8508ff276752f6b2ff8b64ae5d13ebe02e7667e035000b9"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f2a09f6184f17a80897172863a655467da2b11151ec98ba8d7af89f17bf63dae"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-manylinux_2_28_aarch64.whl", hash = "sha256:76acba4c66c47d27c8365e7c10b3d8016a7da83d3191d053a58382311a8bf4e1"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-manylinux_2_28_x86_64.whl", hash = "sha256:b128092c927eaf485928cec0c28f6b8bead277e28acf56800e972aa2c2abd7a2"}, + {file = "lxml-5.2.2-pp310-pypy310_pp73-win_amd64.whl", hash = "sha256:ae791f6bd43305aade8c0e22f816b34f3b72b6c820477aab4d18473a37e8090b"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-macosx_10_9_x86_64.whl", hash = "sha256:a2f6a1bc2460e643785a2cde17293bd7a8f990884b822f7bca47bee0a82fc66b"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:8e8d351ff44c1638cb6e980623d517abd9f580d2e53bfcd18d8941c052a5a009"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:bec4bd9133420c5c52d562469c754f27c5c9e36ee06abc169612c959bd7dbb07"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-manylinux_2_28_aarch64.whl", hash = "sha256:55ce6b6d803890bd3cc89975fca9de1dff39729b43b73cb15ddd933b8bc20484"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-manylinux_2_28_x86_64.whl", hash = "sha256:8ab6a358d1286498d80fe67bd3d69fcbc7d1359b45b41e74c4a26964ca99c3f8"}, + {file = "lxml-5.2.2-pp37-pypy37_pp73-win_amd64.whl", hash = "sha256:06668e39e1f3c065349c51ac27ae430719d7806c026fec462e5693b08b95696b"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-macosx_10_9_x86_64.whl", hash = "sha256:9cd5323344d8ebb9fb5e96da5de5ad4ebab993bbf51674259dbe9d7a18049525"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:89feb82ca055af0fe797a2323ec9043b26bc371365847dbe83c7fd2e2f181c34"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e481bba1e11ba585fb06db666bfc23dbe181dbafc7b25776156120bf12e0d5a6"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-manylinux_2_28_aarch64.whl", hash = "sha256:9d6c6ea6a11ca0ff9cd0390b885984ed31157c168565702959c25e2191674a14"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-manylinux_2_28_x86_64.whl", hash = "sha256:3d98de734abee23e61f6b8c2e08a88453ada7d6486dc7cdc82922a03968928db"}, + {file = "lxml-5.2.2-pp38-pypy38_pp73-win_amd64.whl", hash = "sha256:69ab77a1373f1e7563e0fb5a29a8440367dec051da6c7405333699d07444f511"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-macosx_10_9_x86_64.whl", hash = "sha256:34e17913c431f5ae01d8658dbf792fdc457073dcdfbb31dc0cc6ab256e664a8d"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:05f8757b03208c3f50097761be2dea0aba02e94f0dc7023ed73a7bb14ff11eb0"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:6a520b4f9974b0a0a6ed73c2154de57cdfd0c8800f4f15ab2b73238ffed0b36e"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-manylinux_2_28_aarch64.whl", hash = "sha256:5e097646944b66207023bc3c634827de858aebc226d5d4d6d16f0b77566ea182"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-manylinux_2_28_x86_64.whl", hash = "sha256:b5e4ef22ff25bfd4ede5f8fb30f7b24446345f3e79d9b7455aef2836437bc38a"}, + {file = "lxml-5.2.2-pp39-pypy39_pp73-win_amd64.whl", hash = "sha256:ff69a9a0b4b17d78170c73abe2ab12084bdf1691550c5629ad1fe7849433f324"}, + {file = "lxml-5.2.2.tar.gz", hash = "sha256:bb2dc4898180bea79863d5487e5f9c7c34297414bad54bcd0f0852aee9cfdb87"}, +] + +[package.extras] +cssselect = ["cssselect (>=0.7)"] +html-clean = ["lxml-html-clean"] +html5 = ["html5lib"] +htmlsoup = ["BeautifulSoup4"] +source = ["Cython (>=3.0.10)"] + +[[package]] +name = "more-click" +version = "0.1.2" +description = "More click." +optional = false +python-versions = ">=3.7" +files = [ + {file = "more_click-0.1.2-py3-none-any.whl", hash = "sha256:f6387af37ef7e7423bd94b72a81a53c79c5086a3bfe5cc035da534ff0c2a0a9e"}, + {file = "more_click-0.1.2.tar.gz", hash = "sha256:085da66d5a9b823c5d912a888dca1fa0c8b3a14ed1b21ea9c8a1b814857a3981"}, +] + +[package.dependencies] +click = "*" + +[package.extras] +tests = ["coverage", "pytest"] + +[[package]] +name = "ndex2" +version = "3.8.0" +description = "Nice CX Python includes a client and a data model." +optional = false +python-versions = "*" +files = [ + {file = "ndex2-3.8.0-py2.py3-none-any.whl", hash = "sha256:c00e4748489f3f523df2524917b7be921c590fffd8a860a5077e1504f47afcc2"}, + {file = "ndex2-3.8.0.tar.gz", hash = "sha256:9f4d7f4b9594664191fba5c6512e315ed47b13bc416df5769802f87a7c22d1c8"}, +] + +[package.dependencies] +ijson = "*" +networkx = "*" +numpy = "*" +pandas = "*" +requests = "*" +requests-toolbelt = "*" +six = "*" +urllib3 = ">=1.16" + +[[package]] +name = "networkx" +version = "3.3" +description = "Python package for creating and manipulating graphs and networks" +optional = false +python-versions = ">=3.10" +files = [ + {file = "networkx-3.3-py3-none-any.whl", hash = "sha256:28575580c6ebdaf4505b22c6256a2b9de86b316dc63ba9e93abde3d78dfdbcf2"}, + {file = "networkx-3.3.tar.gz", hash = "sha256:0c127d8b2f4865f59ae9cb8aafcd60b5c70f3241ebd66f7defad7c4ab90126c9"}, +] + +[package.extras] +default = ["matplotlib (>=3.6)", "numpy (>=1.23)", "pandas (>=1.4)", "scipy (>=1.9,!=1.11.0,!=1.11.1)"] +developer = ["changelist (==0.5)", "mypy (>=1.1)", "pre-commit (>=3.2)", "rtoml"] +doc = ["myst-nb (>=1.0)", "numpydoc (>=1.7)", "pillow (>=9.4)", "pydata-sphinx-theme (>=0.14)", "sphinx (>=7)", "sphinx-gallery (>=0.14)", "texext (>=0.6.7)"] +extra = ["lxml (>=4.6)", "pydot (>=2.0)", "pygraphviz (>=1.12)", "sympy (>=1.10)"] +test = ["pytest (>=7.2)", "pytest-cov (>=4.0)"] + +[[package]] +name = "numpy" +version = "1.26.4" +description = "Fundamental package for array computing in Python" +optional = false +python-versions = ">=3.9" +files = [ + {file = "numpy-1.26.4-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:9ff0f4f29c51e2803569d7a51c2304de5554655a60c5d776e35b4a41413830d0"}, + {file = "numpy-1.26.4-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:2e4ee3380d6de9c9ec04745830fd9e2eccb3e6cf790d39d7b98ffd19b0dd754a"}, + {file = "numpy-1.26.4-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d209d8969599b27ad20994c8e41936ee0964e6da07478d6c35016bc386b66ad4"}, + {file = "numpy-1.26.4-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:ffa75af20b44f8dba823498024771d5ac50620e6915abac414251bd971b4529f"}, + {file = "numpy-1.26.4-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:62b8e4b1e28009ef2846b4c7852046736bab361f7aeadeb6a5b89ebec3c7055a"}, + {file = "numpy-1.26.4-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:a4abb4f9001ad2858e7ac189089c42178fcce737e4169dc61321660f1a96c7d2"}, + {file = "numpy-1.26.4-cp310-cp310-win32.whl", hash = "sha256:bfe25acf8b437eb2a8b2d49d443800a5f18508cd811fea3181723922a8a82b07"}, + {file = "numpy-1.26.4-cp310-cp310-win_amd64.whl", hash = "sha256:b97fe8060236edf3662adfc2c633f56a08ae30560c56310562cb4f95500022d5"}, + {file = "numpy-1.26.4-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:4c66707fabe114439db9068ee468c26bbdf909cac0fb58686a42a24de1760c71"}, + {file = "numpy-1.26.4-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:edd8b5fe47dab091176d21bb6de568acdd906d1887a4584a15a9a96a1dca06ef"}, + {file = "numpy-1.26.4-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:7ab55401287bfec946ced39700c053796e7cc0e3acbef09993a9ad2adba6ca6e"}, + {file = "numpy-1.26.4-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:666dbfb6ec68962c033a450943ded891bed2d54e6755e35e5835d63f4f6931d5"}, + {file = "numpy-1.26.4-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:96ff0b2ad353d8f990b63294c8986f1ec3cb19d749234014f4e7eb0112ceba5a"}, + {file = "numpy-1.26.4-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:60dedbb91afcbfdc9bc0b1f3f402804070deed7392c23eb7a7f07fa857868e8a"}, + {file = "numpy-1.26.4-cp311-cp311-win32.whl", hash = "sha256:1af303d6b2210eb850fcf03064d364652b7120803a0b872f5211f5234b399f20"}, + {file = "numpy-1.26.4-cp311-cp311-win_amd64.whl", hash = "sha256:cd25bcecc4974d09257ffcd1f098ee778f7834c3ad767fe5db785be9a4aa9cb2"}, + {file = "numpy-1.26.4-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:b3ce300f3644fb06443ee2222c2201dd3a89ea6040541412b8fa189341847218"}, + {file = "numpy-1.26.4-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:03a8c78d01d9781b28a6989f6fa1bb2c4f2d51201cf99d3dd875df6fbd96b23b"}, + {file = "numpy-1.26.4-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:9fad7dcb1aac3c7f0584a5a8133e3a43eeb2fe127f47e3632d43d677c66c102b"}, + {file = "numpy-1.26.4-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:675d61ffbfa78604709862923189bad94014bef562cc35cf61d3a07bba02a7ed"}, + {file = "numpy-1.26.4-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:ab47dbe5cc8210f55aa58e4805fe224dac469cde56b9f731a4c098b91917159a"}, + {file = "numpy-1.26.4-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:1dda2e7b4ec9dd512f84935c5f126c8bd8b9f2fc001e9f54af255e8c5f16b0e0"}, + {file = "numpy-1.26.4-cp312-cp312-win32.whl", hash = "sha256:50193e430acfc1346175fcbdaa28ffec49947a06918b7b92130744e81e640110"}, + {file = "numpy-1.26.4-cp312-cp312-win_amd64.whl", hash = "sha256:08beddf13648eb95f8d867350f6a018a4be2e5ad54c8d8caed89ebca558b2818"}, + {file = "numpy-1.26.4-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:7349ab0fa0c429c82442a27a9673fc802ffdb7c7775fad780226cb234965e53c"}, + {file = "numpy-1.26.4-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:52b8b60467cd7dd1e9ed082188b4e6bb35aa5cdd01777621a1658910745b90be"}, + {file = "numpy-1.26.4-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d5241e0a80d808d70546c697135da2c613f30e28251ff8307eb72ba696945764"}, + {file = "numpy-1.26.4-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f870204a840a60da0b12273ef34f7051e98c3b5961b61b0c2c1be6dfd64fbcd3"}, + {file = "numpy-1.26.4-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:679b0076f67ecc0138fd2ede3a8fd196dddc2ad3254069bcb9faf9a79b1cebcd"}, + {file = "numpy-1.26.4-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:47711010ad8555514b434df65f7d7b076bb8261df1ca9bb78f53d3b2db02e95c"}, + {file = "numpy-1.26.4-cp39-cp39-win32.whl", hash = "sha256:a354325ee03388678242a4d7ebcd08b5c727033fcff3b2f536aea978e15ee9e6"}, + {file = "numpy-1.26.4-cp39-cp39-win_amd64.whl", hash = "sha256:3373d5d70a5fe74a2c1bb6d2cfd9609ecf686d47a2d7b1d37a8f3b6bf6003aea"}, + {file = "numpy-1.26.4-pp39-pypy39_pp73-macosx_10_9_x86_64.whl", hash = "sha256:afedb719a9dcfc7eaf2287b839d8198e06dcd4cb5d276a3df279231138e83d30"}, + {file = "numpy-1.26.4-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:95a7476c59002f2f6c590b9b7b998306fba6a5aa646b1e22ddfeaf8f78c3a29c"}, + {file = "numpy-1.26.4-pp39-pypy39_pp73-win_amd64.whl", hash = "sha256:7e50d0a0cc3189f9cb0aeb3a6a6af18c16f59f004b866cd2be1c14b36134a4a0"}, + {file = "numpy-1.26.4.tar.gz", hash = "sha256:2a02aba9ed12e4ac4eb3ea9421c420301a0c6460d9830d74a9df87efa4912010"}, +] + +[[package]] +name = "oaklib" +version = "0.6.9" +description = "Ontology Access Kit: Python library for common ontology operations over a variety of backends" +optional = false +python-versions = "<4.0.0,>=3.9" +files = [ + {file = "oaklib-0.6.9-py3-none-any.whl", hash = "sha256:88fa11859fe0ba314c22db69a6a9d2da8d51afcf21430d07e4e203a92eb9147a"}, + {file = "oaklib-0.6.9.tar.gz", hash = "sha256:9c9ca505a6cf84059fe906a6749cffb6a129875003c3c5501f042900b43f2dc9"}, +] + +[package.dependencies] +airium = ">=0.2.5" +appdirs = ">=1.4.4" +class-resolver = ">=0.4.2" +click = "*" +curies = ">=0.6.6" +defusedxml = ">=0.7.1,<0.8.0" +eutils = ">=0.6.0" +funowl = ">=0.2.0" +jsonlines = ">=4.0.0,<5.0.0" +kgcl-rdflib = "0.5.0" +kgcl-schema = ">=0.6.8,<0.7.0" +linkml-renderer = ">=0.3.0" +linkml-runtime = ">=1.5.3" +ndex2 = ">=3.5.0,<4.0.0" +networkx = ">=2.7.1" +ols-client = ">=0.1.1" +ontoportal-client = ">=0.0.3" +prefixmaps = ">=0.1.2" +pronto = ">=2.5.0" +pydantic = "*" +pysolr = ">=3.9.0,<4.0.0" +pystow = ">=0.5.0" +ratelimit = ">=2.2.1" +requests-cache = ">=1.0.1,<2.0.0" +semsql = ">=0.3.1" +SPARQLWrapper = "*" +SQLAlchemy = ">=1.4.32" +sssom = ">=0.4.4,<0.5.0" +tenacity = ">=8.2.3,<9.0.0" + +[package.extras] +gilda = ["gilda (>=1.0.0)", "urllib3 (<2)"] +llm = ["aiohttp", "html2text", "llm"] +semsimian = ["semsimian (>=0.2.16)"] + +[[package]] +name = "ols-client" +version = "0.1.4" +description = "A client to the EBI Ontology Lookup Service" +optional = false +python-versions = ">=3.7" +files = [ + {file = "ols_client-0.1.4-py3-none-any.whl", hash = "sha256:7bdca0590042e07cc7ee3ef3fba99c3b6862cde6c8835afb129de31284b3e010"}, + {file = "ols_client-0.1.4.tar.gz", hash = "sha256:cd2a0f39107f39eaf0f40b9098f12d442cf3d43e28228e63feb407d0aeb44470"}, +] + +[package.dependencies] +class-resolver = "*" +click = "*" +more-click = "*" +pystow = "*" +requests = "*" + +[package.extras] +docs = ["sphinx", "sphinx-autodoc-typehints", "sphinx-automodapi", "sphinx-click", "sphinx-rtd-theme"] +tests = ["coverage", "pytest"] + +[[package]] +name = "ontoportal-client" +version = "0.0.4" +description = "A client to BioPortal and other OntoPortal instances." +optional = false +python-versions = ">=3.7" +files = [ + {file = "ontoportal_client-0.0.4-py3-none-any.whl", hash = "sha256:0dedd4ce003e0b6c1128fa05101e57bcc128ad79a6c9fcae66037d2447706c4c"}, + {file = "ontoportal_client-0.0.4.tar.gz", hash = "sha256:1bf7edcb94db3ed68ea9a64c620056f0517f7e209826b05dbfda8fe27384fa48"}, +] + +[package.dependencies] +pystow = "*" +typing-extensions = "*" + +[package.extras] +docs = ["sphinx", "sphinx-autodoc-typehints", "sphinx-automodapi", "sphinx-rtd-theme"] +tests = ["coverage", "pytest", "unittest-templates"] + +[[package]] +name = "openai" +version = "1.34.0" +description = "The official Python library for the openai API" +optional = false +python-versions = ">=3.7.1" +files = [ + {file = "openai-1.34.0-py3-none-any.whl", hash = "sha256:018623c2f795424044675c6230fa3bfbf98d9e0aab45d8fd116f2efb2cfb6b7e"}, + {file = "openai-1.34.0.tar.gz", hash = "sha256:95c8e2da4acd6958e626186957d656597613587195abd0fb2527566a93e76770"}, +] + +[package.dependencies] +anyio = ">=3.5.0,<5" +distro = ">=1.7.0,<2" +httpx = ">=0.23.0,<1" +pydantic = ">=1.9.0,<3" +sniffio = "*" +tqdm = ">4" +typing-extensions = ">=4.7,<5" + +[package.extras] +datalib = ["numpy (>=1)", "pandas (>=1.2.3)", "pandas-stubs (>=1.1.0.11)"] + +[[package]] +name = "orjson" +version = "3.10.5" +description = "Fast, correct Python JSON library supporting dataclasses, datetimes, and numpy" +optional = false +python-versions = ">=3.8" +files = [ + {file = "orjson-3.10.5-cp310-cp310-macosx_10_15_x86_64.macosx_11_0_arm64.macosx_10_15_universal2.whl", hash = "sha256:545d493c1f560d5ccfc134803ceb8955a14c3fcb47bbb4b2fee0232646d0b932"}, + {file = "orjson-3.10.5-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:f4324929c2dd917598212bfd554757feca3e5e0fa60da08be11b4aa8b90013c1"}, + {file = "orjson-3.10.5-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:8c13ca5e2ddded0ce6a927ea5a9f27cae77eee4c75547b4297252cb20c4d30e6"}, + {file = "orjson-3.10.5-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:b6c8e30adfa52c025f042a87f450a6b9ea29649d828e0fec4858ed5e6caecf63"}, + {file = "orjson-3.10.5-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:338fd4f071b242f26e9ca802f443edc588fa4ab60bfa81f38beaedf42eda226c"}, + {file = "orjson-3.10.5-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:6970ed7a3126cfed873c5d21ece1cd5d6f83ca6c9afb71bbae21a0b034588d96"}, + {file = "orjson-3.10.5-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:235dadefb793ad12f7fa11e98a480db1f7c6469ff9e3da5e73c7809c700d746b"}, + {file = "orjson-3.10.5-cp310-none-win32.whl", hash = "sha256:be79e2393679eda6a590638abda16d167754393f5d0850dcbca2d0c3735cebe2"}, + {file = "orjson-3.10.5-cp310-none-win_amd64.whl", hash = "sha256:c4a65310ccb5c9910c47b078ba78e2787cb3878cdded1702ac3d0da71ddc5228"}, + {file = "orjson-3.10.5-cp311-cp311-macosx_10_15_x86_64.macosx_11_0_arm64.macosx_10_15_universal2.whl", hash = "sha256:cdf7365063e80899ae3a697def1277c17a7df7ccfc979990a403dfe77bb54d40"}, + {file = "orjson-3.10.5-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:6b68742c469745d0e6ca5724506858f75e2f1e5b59a4315861f9e2b1df77775a"}, + {file = "orjson-3.10.5-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:7d10cc1b594951522e35a3463da19e899abe6ca95f3c84c69e9e901e0bd93d38"}, + {file = "orjson-3.10.5-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:dcbe82b35d1ac43b0d84072408330fd3295c2896973112d495e7234f7e3da2e1"}, + {file = "orjson-3.10.5-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:10c0eb7e0c75e1e486c7563fe231b40fdd658a035ae125c6ba651ca3b07936f5"}, + {file = "orjson-3.10.5-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:53ed1c879b10de56f35daf06dbc4a0d9a5db98f6ee853c2dbd3ee9d13e6f302f"}, + {file = "orjson-3.10.5-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:099e81a5975237fda3100f918839af95f42f981447ba8f47adb7b6a3cdb078fa"}, + {file = "orjson-3.10.5-cp311-none-win32.whl", hash = "sha256:1146bf85ea37ac421594107195db8bc77104f74bc83e8ee21a2e58596bfb2f04"}, + {file = "orjson-3.10.5-cp311-none-win_amd64.whl", hash = "sha256:36a10f43c5f3a55c2f680efe07aa93ef4a342d2960dd2b1b7ea2dd764fe4a37c"}, + {file = "orjson-3.10.5-cp312-cp312-macosx_10_15_x86_64.macosx_11_0_arm64.macosx_10_15_universal2.whl", hash = "sha256:68f85ecae7af14a585a563ac741b0547a3f291de81cd1e20903e79f25170458f"}, + {file = "orjson-3.10.5-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:28afa96f496474ce60d3340fe8d9a263aa93ea01201cd2bad844c45cd21f5268"}, + {file = "orjson-3.10.5-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:9cd684927af3e11b6e754df80b9ffafd9fb6adcaa9d3e8fdd5891be5a5cad51e"}, + {file = "orjson-3.10.5-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:3d21b9983da032505f7050795e98b5d9eee0df903258951566ecc358f6696969"}, + {file = "orjson-3.10.5-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:1ad1de7fef79736dde8c3554e75361ec351158a906d747bd901a52a5c9c8d24b"}, + {file = "orjson-3.10.5-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:2d97531cdfe9bdd76d492e69800afd97e5930cb0da6a825646667b2c6c6c0211"}, + {file = "orjson-3.10.5-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:d69858c32f09c3e1ce44b617b3ebba1aba030e777000ebdf72b0d8e365d0b2b3"}, + {file = "orjson-3.10.5-cp312-none-win32.whl", hash = "sha256:64c9cc089f127e5875901ac05e5c25aa13cfa5dbbbd9602bda51e5c611d6e3e2"}, + {file = "orjson-3.10.5-cp312-none-win_amd64.whl", hash = "sha256:b2efbd67feff8c1f7728937c0d7f6ca8c25ec81373dc8db4ef394c1d93d13dc5"}, + {file = "orjson-3.10.5-cp38-cp38-macosx_10_15_x86_64.macosx_11_0_arm64.macosx_10_15_universal2.whl", hash = "sha256:03b565c3b93f5d6e001db48b747d31ea3819b89abf041ee10ac6988886d18e01"}, + {file = "orjson-3.10.5-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:584c902ec19ab7928fd5add1783c909094cc53f31ac7acfada817b0847975f26"}, + {file = "orjson-3.10.5-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:5a35455cc0b0b3a1eaf67224035f5388591ec72b9b6136d66b49a553ce9eb1e6"}, + {file = "orjson-3.10.5-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:1670fe88b116c2745a3a30b0f099b699a02bb3482c2591514baf5433819e4f4d"}, + {file = "orjson-3.10.5-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:185c394ef45b18b9a7d8e8f333606e2e8194a50c6e3c664215aae8cf42c5385e"}, + {file = "orjson-3.10.5-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:ca0b3a94ac8d3886c9581b9f9de3ce858263865fdaa383fbc31c310b9eac07c9"}, + {file = "orjson-3.10.5-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:dfc91d4720d48e2a709e9c368d5125b4b5899dced34b5400c3837dadc7d6271b"}, + {file = "orjson-3.10.5-cp38-none-win32.whl", hash = "sha256:c05f16701ab2a4ca146d0bca950af254cb7c02f3c01fca8efbbad82d23b3d9d4"}, + {file = "orjson-3.10.5-cp38-none-win_amd64.whl", hash = "sha256:8a11d459338f96a9aa7f232ba95679fc0c7cedbd1b990d736467894210205c09"}, + {file = "orjson-3.10.5-cp39-cp39-macosx_10_15_x86_64.macosx_11_0_arm64.macosx_10_15_universal2.whl", hash = "sha256:85c89131d7b3218db1b24c4abecea92fd6c7f9fab87441cfc342d3acc725d807"}, + {file = "orjson-3.10.5-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:fb66215277a230c456f9038d5e2d84778141643207f85336ef8d2a9da26bd7ca"}, + {file = "orjson-3.10.5-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:51bbcdea96cdefa4a9b4461e690c75ad4e33796530d182bdd5c38980202c134a"}, + {file = "orjson-3.10.5-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:dbead71dbe65f959b7bd8cf91e0e11d5338033eba34c114f69078d59827ee139"}, + {file = "orjson-3.10.5-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:5df58d206e78c40da118a8c14fc189207fffdcb1f21b3b4c9c0c18e839b5a214"}, + {file = "orjson-3.10.5-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:c4057c3b511bb8aef605616bd3f1f002a697c7e4da6adf095ca5b84c0fd43595"}, + {file = "orjson-3.10.5-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:b39e006b00c57125ab974362e740c14a0c6a66ff695bff44615dcf4a70ce2b86"}, + {file = "orjson-3.10.5-cp39-none-win32.whl", hash = "sha256:eded5138cc565a9d618e111c6d5c2547bbdd951114eb822f7f6309e04db0fb47"}, + {file = "orjson-3.10.5-cp39-none-win_amd64.whl", hash = "sha256:cc28e90a7cae7fcba2493953cff61da5a52950e78dc2dacfe931a317ee3d8de7"}, + {file = "orjson-3.10.5.tar.gz", hash = "sha256:7a5baef8a4284405d96c90c7c62b755e9ef1ada84c2406c24a9ebec86b89f46d"}, +] + +[[package]] +name = "packaging" +version = "24.1" +description = "Core utilities for Python packages" +optional = false +python-versions = ">=3.8" +files = [ + {file = "packaging-24.1-py3-none-any.whl", hash = "sha256:5b8f2217dbdbd2f7f384c41c628544e6d52f2d0f53c6d0c3ea61aa5d1d7ff124"}, + {file = "packaging-24.1.tar.gz", hash = "sha256:026ed72c8ed3fcce5bf8950572258698927fd1dbda10a5e981cdf0ac37f4f002"}, +] + +[[package]] +name = "pandas" +version = "2.2.2" +description = "Powerful data structures for data analysis, time series, and statistics" +optional = false +python-versions = ">=3.9" +files = [ + {file = "pandas-2.2.2-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:90c6fca2acf139569e74e8781709dccb6fe25940488755716d1d354d6bc58bce"}, + {file = "pandas-2.2.2-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:c7adfc142dac335d8c1e0dcbd37eb8617eac386596eb9e1a1b77791cf2498238"}, + {file = "pandas-2.2.2-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4abfe0be0d7221be4f12552995e58723c7422c80a659da13ca382697de830c08"}, + {file = "pandas-2.2.2-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:8635c16bf3d99040fdf3ca3db669a7250ddf49c55dc4aa8fe0ae0fa8d6dcc1f0"}, + {file = "pandas-2.2.2-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:40ae1dffb3967a52203105a077415a86044a2bea011b5f321c6aa64b379a3f51"}, + {file = "pandas-2.2.2-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:8e5a0b00e1e56a842f922e7fae8ae4077aee4af0acb5ae3622bd4b4c30aedf99"}, + {file = "pandas-2.2.2-cp310-cp310-win_amd64.whl", hash = "sha256:ddf818e4e6c7c6f4f7c8a12709696d193976b591cc7dc50588d3d1a6b5dc8772"}, + {file = "pandas-2.2.2-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:696039430f7a562b74fa45f540aca068ea85fa34c244d0deee539cb6d70aa288"}, + {file = "pandas-2.2.2-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:8e90497254aacacbc4ea6ae5e7a8cd75629d6ad2b30025a4a8b09aa4faf55151"}, + {file = "pandas-2.2.2-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:58b84b91b0b9f4bafac2a0ac55002280c094dfc6402402332c0913a59654ab2b"}, + {file = "pandas-2.2.2-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:6d2123dc9ad6a814bcdea0f099885276b31b24f7edf40f6cdbc0912672e22eee"}, + {file = "pandas-2.2.2-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:2925720037f06e89af896c70bca73459d7e6a4be96f9de79e2d440bd499fe0db"}, + {file = "pandas-2.2.2-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:0cace394b6ea70c01ca1595f839cf193df35d1575986e484ad35c4aeae7266c1"}, + {file = "pandas-2.2.2-cp311-cp311-win_amd64.whl", hash = "sha256:873d13d177501a28b2756375d59816c365e42ed8417b41665f346289adc68d24"}, + {file = "pandas-2.2.2-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:9dfde2a0ddef507a631dc9dc4af6a9489d5e2e740e226ad426a05cabfbd7c8ef"}, + {file = "pandas-2.2.2-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:e9b79011ff7a0f4b1d6da6a61aa1aa604fb312d6647de5bad20013682d1429ce"}, + {file = "pandas-2.2.2-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:1cb51fe389360f3b5a4d57dbd2848a5f033350336ca3b340d1c53a1fad33bcad"}, + {file = "pandas-2.2.2-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:eee3a87076c0756de40b05c5e9a6069c035ba43e8dd71c379e68cab2c20f16ad"}, + {file = "pandas-2.2.2-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:3e374f59e440d4ab45ca2fffde54b81ac3834cf5ae2cdfa69c90bc03bde04d76"}, + {file = "pandas-2.2.2-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:43498c0bdb43d55cb162cdc8c06fac328ccb5d2eabe3cadeb3529ae6f0517c32"}, + {file = "pandas-2.2.2-cp312-cp312-win_amd64.whl", hash = "sha256:d187d355ecec3629624fccb01d104da7d7f391db0311145817525281e2804d23"}, + {file = "pandas-2.2.2-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:0ca6377b8fca51815f382bd0b697a0814c8bda55115678cbc94c30aacbb6eff2"}, + {file = "pandas-2.2.2-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:9057e6aa78a584bc93a13f0a9bf7e753a5e9770a30b4d758b8d5f2a62a9433cd"}, + {file = "pandas-2.2.2-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:001910ad31abc7bf06f49dcc903755d2f7f3a9186c0c040b827e522e9cef0863"}, + {file = "pandas-2.2.2-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:66b479b0bd07204e37583c191535505410daa8df638fd8e75ae1b383851fe921"}, + {file = "pandas-2.2.2-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:a77e9d1c386196879aa5eb712e77461aaee433e54c68cf253053a73b7e49c33a"}, + {file = "pandas-2.2.2-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:92fd6b027924a7e178ac202cfbe25e53368db90d56872d20ffae94b96c7acc57"}, + {file = "pandas-2.2.2-cp39-cp39-win_amd64.whl", hash = "sha256:640cef9aa381b60e296db324337a554aeeb883ead99dc8f6c18e81a93942f5f4"}, + {file = "pandas-2.2.2.tar.gz", hash = "sha256:9e79019aba43cb4fda9e4d983f8e88ca0373adbb697ae9c6c43093218de28b54"}, +] + +[package.dependencies] +numpy = [ + {version = ">=1.23.2", markers = "python_version == \"3.11\""}, + {version = ">=1.26.0", markers = "python_version >= \"3.12\""}, +] +python-dateutil = ">=2.8.2" +pytz = ">=2020.1" +tzdata = ">=2022.7" + +[package.extras] +all = ["PyQt5 (>=5.15.9)", "SQLAlchemy (>=2.0.0)", "adbc-driver-postgresql (>=0.8.0)", "adbc-driver-sqlite (>=0.8.0)", "beautifulsoup4 (>=4.11.2)", "bottleneck (>=1.3.6)", "dataframe-api-compat (>=0.1.7)", "fastparquet (>=2022.12.0)", "fsspec (>=2022.11.0)", "gcsfs (>=2022.11.0)", "html5lib (>=1.1)", "hypothesis (>=6.46.1)", "jinja2 (>=3.1.2)", "lxml (>=4.9.2)", "matplotlib (>=3.6.3)", "numba (>=0.56.4)", "numexpr (>=2.8.4)", "odfpy (>=1.4.1)", "openpyxl (>=3.1.0)", "pandas-gbq (>=0.19.0)", "psycopg2 (>=2.9.6)", "pyarrow (>=10.0.1)", "pymysql (>=1.0.2)", "pyreadstat (>=1.2.0)", "pytest (>=7.3.2)", "pytest-xdist (>=2.2.0)", "python-calamine (>=0.1.7)", "pyxlsb (>=1.0.10)", "qtpy (>=2.3.0)", "s3fs (>=2022.11.0)", "scipy (>=1.10.0)", "tables (>=3.8.0)", "tabulate (>=0.9.0)", "xarray (>=2022.12.0)", "xlrd (>=2.0.1)", "xlsxwriter (>=3.0.5)", "zstandard (>=0.19.0)"] +aws = ["s3fs (>=2022.11.0)"] +clipboard = ["PyQt5 (>=5.15.9)", "qtpy (>=2.3.0)"] +compression = ["zstandard (>=0.19.0)"] +computation = ["scipy (>=1.10.0)", "xarray (>=2022.12.0)"] +consortium-standard = ["dataframe-api-compat (>=0.1.7)"] +excel = ["odfpy (>=1.4.1)", "openpyxl (>=3.1.0)", "python-calamine (>=0.1.7)", "pyxlsb (>=1.0.10)", "xlrd (>=2.0.1)", "xlsxwriter (>=3.0.5)"] +feather = ["pyarrow (>=10.0.1)"] +fss = ["fsspec (>=2022.11.0)"] +gcp = ["gcsfs (>=2022.11.0)", "pandas-gbq (>=0.19.0)"] +hdf5 = ["tables (>=3.8.0)"] +html = ["beautifulsoup4 (>=4.11.2)", "html5lib (>=1.1)", "lxml (>=4.9.2)"] +mysql = ["SQLAlchemy (>=2.0.0)", "pymysql (>=1.0.2)"] +output-formatting = ["jinja2 (>=3.1.2)", "tabulate (>=0.9.0)"] +parquet = ["pyarrow (>=10.0.1)"] +performance = ["bottleneck (>=1.3.6)", "numba (>=0.56.4)", "numexpr (>=2.8.4)"] +plot = ["matplotlib (>=3.6.3)"] +postgresql = ["SQLAlchemy (>=2.0.0)", "adbc-driver-postgresql (>=0.8.0)", "psycopg2 (>=2.9.6)"] +pyarrow = ["pyarrow (>=10.0.1)"] +spss = ["pyreadstat (>=1.2.0)"] +sql-other = ["SQLAlchemy (>=2.0.0)", "adbc-driver-postgresql (>=0.8.0)", "adbc-driver-sqlite (>=0.8.0)"] +test = ["hypothesis (>=6.46.1)", "pytest (>=7.3.2)", "pytest-xdist (>=2.2.0)"] +xml = ["lxml (>=4.9.2)"] + +[[package]] +name = "pansql" +version = "0.0.1" +description = "sqldf for pandas" +optional = false +python-versions = "*" +files = [ + {file = "pansql-0.0.1-py3-none-any.whl", hash = "sha256:0c49d8c23e418ac065af767ed350c544c0d6d96dc04e2faa1f8b37851d404988"}, + {file = "pansql-0.0.1.tar.gz", hash = "sha256:61091112442c5d663ea5c042b6327a9b6b94c6687831677dddda46f292532e29"}, +] + +[package.dependencies] +numpy = "*" +pandas = "*" +sqlalchemy = "*" + +[[package]] +name = "platformdirs" +version = "4.2.2" +description = "A small Python package for determining appropriate platform-specific dirs, e.g. a `user data dir`." +optional = false +python-versions = ">=3.8" +files = [ + {file = "platformdirs-4.2.2-py3-none-any.whl", hash = "sha256:2d7a1657e36a80ea911db832a8a6ece5ee53d8de21edd5cc5879af6530b1bfee"}, + {file = "platformdirs-4.2.2.tar.gz", hash = "sha256:38b7b51f512eed9e84a22788b4bce1de17c0adb134d6becb09836e37d8654cd3"}, +] + +[package.extras] +docs = ["furo (>=2023.9.10)", "proselint (>=0.13)", "sphinx (>=7.2.6)", "sphinx-autodoc-typehints (>=1.25.2)"] +test = ["appdirs (==1.4.4)", "covdefaults (>=2.3)", "pytest (>=7.4.3)", "pytest-cov (>=4.1)", "pytest-mock (>=3.12)"] +type = ["mypy (>=1.8)"] + +[[package]] +name = "pluggy" +version = "1.5.0" +description = "plugin and hook calling mechanisms for python" +optional = false +python-versions = ">=3.8" +files = [ + {file = "pluggy-1.5.0-py3-none-any.whl", hash = "sha256:44e1ad92c8ca002de6377e165f3e0f1be63266ab4d554740532335b9d75ea669"}, + {file = "pluggy-1.5.0.tar.gz", hash = "sha256:2cffa88e94fdc978c4c574f15f9e59b7f4201d439195c3715ca9e2486f1d0cf1"}, +] + +[package.extras] +dev = ["pre-commit", "tox"] +testing = ["pytest", "pytest-benchmark"] + +[[package]] +name = "prefixcommons" +version = "0.1.12" +description = "A python API for working with ID prefixes" +optional = false +python-versions = ">=3.7,<4.0" +files = [ + {file = "prefixcommons-0.1.12-py3-none-any.whl", hash = "sha256:16dbc0a1f775e003c724f19a694fcfa3174608f5c8b0e893d494cf8098ac7f8b"}, + {file = "prefixcommons-0.1.12.tar.gz", hash = "sha256:22c4e2d37b63487b3ab48f0495b70f14564cb346a15220f23919eb0c1851f69f"}, +] + +[package.dependencies] +click = ">=8.1.3,<9.0.0" +pytest-logging = ">=2015.11.4,<2016.0.0" +PyYAML = ">=6.0,<7.0" +requests = ">=2.28.1,<3.0.0" + +[[package]] +name = "prefixmaps" +version = "0.2.4" +description = "A python library for retrieving semantic prefix maps" +optional = false +python-versions = "<4.0,>=3.8" +files = [ + {file = "prefixmaps-0.2.4-py3-none-any.whl", hash = "sha256:89bf0e6fb08c276f754f9624c42adf2e87c64ee92a3dde1f7eff01f22d85b512"}, + {file = "prefixmaps-0.2.4.tar.gz", hash = "sha256:ae86a1b31189d0516d199756d5808f75f44b39e86546c356cc78c0fe8d2078af"}, +] + +[package.dependencies] +curies = ">=0.5.3" +pyyaml = ">=5.3.1" + +[[package]] +name = "pronto" +version = "2.5.7" +description = "Python frontend to ontologies." +optional = false +python-versions = ">=3.7" +files = [ + {file = "pronto-2.5.7-py2.py3-none-any.whl", hash = "sha256:d7a053cb1735353ef1c708226e77d051a1a32906b5c77f89f9d99c6ca5b5c985"}, + {file = "pronto-2.5.7.tar.gz", hash = "sha256:014a5b02064781d6edd7ca5b4f63b13342dd9b5322248f5a4740f48a98464629"}, +] + +[package.dependencies] +chardet = ">=5.0,<6.0" +fastobo = ">=0.12.2,<0.13.0" +networkx = ">=2.3,<4.0" +python-dateutil = ">=2.8,<3.0" + +[[package]] +name = "pydantic" +version = "2.7.4" +description = "Data validation using Python type hints" +optional = false +python-versions = ">=3.8" +files = [ + {file = "pydantic-2.7.4-py3-none-any.whl", hash = "sha256:ee8538d41ccb9c0a9ad3e0e5f07bf15ed8015b481ced539a1759d8cc89ae90d0"}, + {file = "pydantic-2.7.4.tar.gz", hash = "sha256:0c84efd9548d545f63ac0060c1e4d39bb9b14db8b3c0652338aecc07b5adec52"}, +] + +[package.dependencies] +annotated-types = ">=0.4.0" +pydantic-core = "2.18.4" +typing-extensions = ">=4.6.1" + +[package.extras] +email = ["email-validator (>=2.0.0)"] + +[[package]] +name = "pydantic-core" +version = "2.18.4" +description = "Core functionality for Pydantic validation and serialization" +optional = false +python-versions = ">=3.8" +files = [ + {file = "pydantic_core-2.18.4-cp310-cp310-macosx_10_12_x86_64.whl", hash = "sha256:f76d0ad001edd426b92233d45c746fd08f467d56100fd8f30e9ace4b005266e4"}, + {file = "pydantic_core-2.18.4-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:59ff3e89f4eaf14050c8022011862df275b552caef8082e37b542b066ce1ff26"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a55b5b16c839df1070bc113c1f7f94a0af4433fcfa1b41799ce7606e5c79ce0a"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:4d0dcc59664fcb8974b356fe0a18a672d6d7cf9f54746c05f43275fc48636851"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:8951eee36c57cd128f779e641e21eb40bc5073eb28b2d23f33eb0ef14ffb3f5d"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:4701b19f7e3a06ea655513f7938de6f108123bf7c86bbebb1196eb9bd35cf724"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e00a3f196329e08e43d99b79b286d60ce46bed10f2280d25a1718399457e06be"}, + {file = "pydantic_core-2.18.4-cp310-cp310-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:97736815b9cc893b2b7f663628e63f436018b75f44854c8027040e05230eeddb"}, + {file = "pydantic_core-2.18.4-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:6891a2ae0e8692679c07728819b6e2b822fb30ca7445f67bbf6509b25a96332c"}, + {file = "pydantic_core-2.18.4-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:bc4ff9805858bd54d1a20efff925ccd89c9d2e7cf4986144b30802bf78091c3e"}, + {file = "pydantic_core-2.18.4-cp310-none-win32.whl", hash = "sha256:1b4de2e51bbcb61fdebd0ab86ef28062704f62c82bbf4addc4e37fa4b00b7cbc"}, + {file = "pydantic_core-2.18.4-cp310-none-win_amd64.whl", hash = "sha256:6a750aec7bf431517a9fd78cb93c97b9b0c496090fee84a47a0d23668976b4b0"}, + {file = "pydantic_core-2.18.4-cp311-cp311-macosx_10_12_x86_64.whl", hash = "sha256:942ba11e7dfb66dc70f9ae66b33452f51ac7bb90676da39a7345e99ffb55402d"}, + {file = "pydantic_core-2.18.4-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:b2ebef0e0b4454320274f5e83a41844c63438fdc874ea40a8b5b4ecb7693f1c4"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a642295cd0c8df1b86fc3dced1d067874c353a188dc8e0f744626d49e9aa51c4"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:5f09baa656c904807e832cf9cce799c6460c450c4ad80803517032da0cd062e2"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:98906207f29bc2c459ff64fa007afd10a8c8ac080f7e4d5beff4c97086a3dabd"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:19894b95aacfa98e7cb093cd7881a0c76f55731efad31073db4521e2b6ff5b7d"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:0fbbdc827fe5e42e4d196c746b890b3d72876bdbf160b0eafe9f0334525119c8"}, + {file = "pydantic_core-2.18.4-cp311-cp311-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:f85d05aa0918283cf29a30b547b4df2fbb56b45b135f9e35b6807cb28bc47951"}, + {file = "pydantic_core-2.18.4-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:e85637bc8fe81ddb73fda9e56bab24560bdddfa98aa64f87aaa4e4b6730c23d2"}, + {file = "pydantic_core-2.18.4-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:2f5966897e5461f818e136b8451d0551a2e77259eb0f73a837027b47dc95dab9"}, + {file = "pydantic_core-2.18.4-cp311-none-win32.whl", hash = "sha256:44c7486a4228413c317952e9d89598bcdfb06399735e49e0f8df643e1ccd0558"}, + {file = "pydantic_core-2.18.4-cp311-none-win_amd64.whl", hash = "sha256:8a7164fe2005d03c64fd3b85649891cd4953a8de53107940bf272500ba8a788b"}, + {file = "pydantic_core-2.18.4-cp311-none-win_arm64.whl", hash = "sha256:4e99bc050fe65c450344421017f98298a97cefc18c53bb2f7b3531eb39bc7805"}, + {file = "pydantic_core-2.18.4-cp312-cp312-macosx_10_12_x86_64.whl", hash = "sha256:6f5c4d41b2771c730ea1c34e458e781b18cc668d194958e0112455fff4e402b2"}, + {file = "pydantic_core-2.18.4-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:2fdf2156aa3d017fddf8aea5adfba9f777db1d6022d392b682d2a8329e087cef"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4748321b5078216070b151d5271ef3e7cc905ab170bbfd27d5c83ee3ec436695"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:847a35c4d58721c5dc3dba599878ebbdfd96784f3fb8bb2c356e123bdcd73f34"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:3c40d4eaad41f78e3bbda31b89edc46a3f3dc6e171bf0ecf097ff7a0ffff7cb1"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:21a5e440dbe315ab9825fcd459b8814bb92b27c974cbc23c3e8baa2b76890077"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:01dd777215e2aa86dfd664daed5957704b769e726626393438f9c87690ce78c3"}, + {file = "pydantic_core-2.18.4-cp312-cp312-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:4b06beb3b3f1479d32befd1f3079cc47b34fa2da62457cdf6c963393340b56e9"}, + {file = "pydantic_core-2.18.4-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:564d7922e4b13a16b98772441879fcdcbe82ff50daa622d681dd682175ea918c"}, + {file = "pydantic_core-2.18.4-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:0eb2a4f660fcd8e2b1c90ad566db2b98d7f3f4717c64fe0a83e0adb39766d5b8"}, + {file = "pydantic_core-2.18.4-cp312-none-win32.whl", hash = "sha256:8b8bab4c97248095ae0c4455b5a1cd1cdd96e4e4769306ab19dda135ea4cdb07"}, + {file = "pydantic_core-2.18.4-cp312-none-win_amd64.whl", hash = "sha256:14601cdb733d741b8958224030e2bfe21a4a881fb3dd6fbb21f071cabd48fa0a"}, + {file = "pydantic_core-2.18.4-cp312-none-win_arm64.whl", hash = "sha256:c1322d7dd74713dcc157a2b7898a564ab091ca6c58302d5c7b4c07296e3fd00f"}, + {file = "pydantic_core-2.18.4-cp38-cp38-macosx_10_12_x86_64.whl", hash = "sha256:823be1deb01793da05ecb0484d6c9e20baebb39bd42b5d72636ae9cf8350dbd2"}, + {file = "pydantic_core-2.18.4-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:ebef0dd9bf9b812bf75bda96743f2a6c5734a02092ae7f721c048d156d5fabae"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:ae1d6df168efb88d7d522664693607b80b4080be6750c913eefb77e34c12c71a"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:f9899c94762343f2cc2fc64c13e7cae4c3cc65cdfc87dd810a31654c9b7358cc"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:99457f184ad90235cfe8461c4d70ab7dd2680e28821c29eca00252ba90308c78"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:18f469a3d2a2fdafe99296a87e8a4c37748b5080a26b806a707f25a902c040a8"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:b7cdf28938ac6b8b49ae5e92f2735056a7ba99c9b110a474473fd71185c1af5d"}, + {file = "pydantic_core-2.18.4-cp38-cp38-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:938cb21650855054dc54dfd9120a851c974f95450f00683399006aa6e8abb057"}, + {file = "pydantic_core-2.18.4-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:44cd83ab6a51da80fb5adbd9560e26018e2ac7826f9626bc06ca3dc074cd198b"}, + {file = "pydantic_core-2.18.4-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:972658f4a72d02b8abfa2581d92d59f59897d2e9f7e708fdabe922f9087773af"}, + {file = "pydantic_core-2.18.4-cp38-none-win32.whl", hash = "sha256:1d886dc848e60cb7666f771e406acae54ab279b9f1e4143babc9c2258213daa2"}, + {file = "pydantic_core-2.18.4-cp38-none-win_amd64.whl", hash = "sha256:bb4462bd43c2460774914b8525f79b00f8f407c945d50881568f294c1d9b4443"}, + {file = "pydantic_core-2.18.4-cp39-cp39-macosx_10_12_x86_64.whl", hash = "sha256:44a688331d4a4e2129140a8118479443bd6f1905231138971372fcde37e43528"}, + {file = "pydantic_core-2.18.4-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:a2fdd81edd64342c85ac7cf2753ccae0b79bf2dfa063785503cb85a7d3593223"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:86110d7e1907ab36691f80b33eb2da87d780f4739ae773e5fc83fb272f88825f"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:46387e38bd641b3ee5ce247563b60c5ca098da9c56c75c157a05eaa0933ed154"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:123c3cec203e3f5ac7b000bd82235f1a3eced8665b63d18be751f115588fea30"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:dc1803ac5c32ec324c5261c7209e8f8ce88e83254c4e1aebdc8b0a39f9ddb443"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:53db086f9f6ab2b4061958d9c276d1dbe3690e8dd727d6abf2321d6cce37fa94"}, + {file = "pydantic_core-2.18.4-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:abc267fa9837245cc28ea6929f19fa335f3dc330a35d2e45509b6566dc18be23"}, + {file = "pydantic_core-2.18.4-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:a0d829524aaefdebccb869eed855e2d04c21d2d7479b6cada7ace5448416597b"}, + {file = "pydantic_core-2.18.4-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:509daade3b8649f80d4e5ff21aa5673e4ebe58590b25fe42fac5f0f52c6f034a"}, + {file = "pydantic_core-2.18.4-cp39-none-win32.whl", hash = "sha256:ca26a1e73c48cfc54c4a76ff78df3727b9d9f4ccc8dbee4ae3f73306a591676d"}, + {file = "pydantic_core-2.18.4-cp39-none-win_amd64.whl", hash = "sha256:c67598100338d5d985db1b3d21f3619ef392e185e71b8d52bceacc4a7771ea7e"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-macosx_10_12_x86_64.whl", hash = "sha256:574d92eac874f7f4db0ca653514d823a0d22e2354359d0759e3f6a406db5d55d"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-macosx_11_0_arm64.whl", hash = "sha256:1f4d26ceb5eb9eed4af91bebeae4b06c3fb28966ca3a8fb765208cf6b51102ab"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:77450e6d20016ec41f43ca4a6c63e9fdde03f0ae3fe90e7c27bdbeaece8b1ed4"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d323a01da91851a4f17bf592faf46149c9169d68430b3146dcba2bb5e5719abc"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:43d447dd2ae072a0065389092a231283f62d960030ecd27565672bd40746c507"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-musllinux_1_1_aarch64.whl", hash = "sha256:578e24f761f3b425834f297b9935e1ce2e30f51400964ce4801002435a1b41ef"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-musllinux_1_1_x86_64.whl", hash = "sha256:81b5efb2f126454586d0f40c4d834010979cb80785173d1586df845a632e4e6d"}, + {file = "pydantic_core-2.18.4-pp310-pypy310_pp73-win_amd64.whl", hash = "sha256:ab86ce7c8f9bea87b9d12c7f0af71102acbf5ecbc66c17796cff45dae54ef9a5"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-macosx_10_12_x86_64.whl", hash = "sha256:90afc12421df2b1b4dcc975f814e21bc1754640d502a2fbcc6d41e77af5ec312"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-macosx_11_0_arm64.whl", hash = "sha256:51991a89639a912c17bef4b45c87bd83593aee0437d8102556af4885811d59f5"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:293afe532740370aba8c060882f7d26cfd00c94cae32fd2e212a3a6e3b7bc15e"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:b48ece5bde2e768197a2d0f6e925f9d7e3e826f0ad2271120f8144a9db18d5c8"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:eae237477a873ab46e8dd748e515c72c0c804fb380fbe6c85533c7de51f23a8f"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-musllinux_1_1_aarch64.whl", hash = "sha256:834b5230b5dfc0c1ec37b2fda433b271cbbc0e507560b5d1588e2cc1148cf1ce"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-musllinux_1_1_x86_64.whl", hash = "sha256:e858ac0a25074ba4bce653f9b5d0a85b7456eaddadc0ce82d3878c22489fa4ee"}, + {file = "pydantic_core-2.18.4-pp39-pypy39_pp73-win_amd64.whl", hash = "sha256:2fd41f6eff4c20778d717af1cc50eca52f5afe7805ee530a4fbd0bae284f16e9"}, + {file = "pydantic_core-2.18.4.tar.gz", hash = "sha256:ec3beeada09ff865c344ff3bc2f427f5e6c26401cc6113d77e372c3fdac73864"}, +] + +[package.dependencies] +typing-extensions = ">=4.6.0,<4.7.0 || >4.7.0" + +[[package]] +name = "pyjsg" +version = "0.11.10" +description = "Python JSON Schema Grammar interpreter" +optional = false +python-versions = "*" +files = [ + {file = "PyJSG-0.11.10-py3-none-any.whl", hash = "sha256:10af60ff42219be7e85bf7f11c19b648715b0b29eb2ddbd269e87069a7c3f26d"}, + {file = "PyJSG-0.11.10.tar.gz", hash = "sha256:4bd6e3ff2833fa2b395bbe803a2d72a5f0bab5b7285bccd0da1a1bc0aee88bfa"}, +] + +[package.dependencies] +antlr4-python3-runtime = ">=4.9.3,<4.10.0" +jsonasobj = ">=1.2.1" + +[[package]] +name = "pyparsing" +version = "3.1.2" +description = "pyparsing module - Classes and methods to define and execute parsing grammars" +optional = false +python-versions = ">=3.6.8" +files = [ + {file = "pyparsing-3.1.2-py3-none-any.whl", hash = "sha256:f9db75911801ed778fe61bb643079ff86601aca99fcae6345aa67292038fb742"}, + {file = "pyparsing-3.1.2.tar.gz", hash = "sha256:a1bac0ce561155ecc3ed78ca94d3c9378656ad4c94c1270de543f621420f94ad"}, +] + +[package.extras] +diagrams = ["jinja2", "railroad-diagrams"] + +[[package]] +name = "pysolr" +version = "3.9.0" +description = "Lightweight Python client for Apache Solr" +optional = false +python-versions = "*" +files = [ + {file = "pysolr-3.9.0.tar.gz", hash = "sha256:6ef05feb87c614894243eddc62e9b0a6134a889c159ae868655cf6cd749545e6"}, +] + +[package.dependencies] +requests = ">=2.9.1" + +[package.extras] +solrcloud = ["kazoo (>=2.5.0)"] + +[[package]] +name = "pystow" +version = "0.5.4" +description = "Easily pick a place to store data for your python package." +optional = false +python-versions = ">=3.7" +files = [ + {file = "pystow-0.5.4-py3-none-any.whl", hash = "sha256:c377cc9fff11127007e60eb5c4dc18f2ffd986c0d0cec27134cdcd4c805bc7d8"}, + {file = "pystow-0.5.4.tar.gz", hash = "sha256:2692180cb405bd77259bee6c7f4db545d10e81939980064730609f21750567ff"}, +] + +[package.dependencies] +click = "*" +requests = "*" +tqdm = "*" + +[package.extras] +aws = ["boto3"] +docs = ["sphinx", "sphinx-autodoc-typehints", "sphinx-automodapi", "sphinx-click", "sphinx-rtd-theme"] +pandas = ["pandas"] +rdf = ["rdflib"] +tests = ["coverage", "pytest", "requests-file"] +xml = ["lxml"] + +[[package]] +name = "pytest" +version = "8.2.2" +description = "pytest: simple powerful testing with Python" +optional = false +python-versions = ">=3.8" +files = [ + {file = "pytest-8.2.2-py3-none-any.whl", hash = "sha256:c434598117762e2bd304e526244f67bf66bbd7b5d6cf22138be51ff661980343"}, + {file = "pytest-8.2.2.tar.gz", hash = "sha256:de4bb8104e201939ccdc688b27a89a7be2079b22e2bd2b07f806b6ba71117977"}, +] + +[package.dependencies] +colorama = {version = "*", markers = "sys_platform == \"win32\""} +iniconfig = "*" +packaging = "*" +pluggy = ">=1.5,<2.0" + +[package.extras] +dev = ["argcomplete", "attrs (>=19.2)", "hypothesis (>=3.56)", "mock", "pygments (>=2.7.2)", "requests", "setuptools", "xmlschema"] + +[[package]] +name = "pytest-logging" +version = "2015.11.4" +description = "Configures logging and allows tweaking the log level with a py.test flag" +optional = false +python-versions = "*" +files = [ + {file = "pytest-logging-2015.11.4.tar.gz", hash = "sha256:cec5c85ecf18aab7b2ead5498a31b9f758680ef5a902b9054ab3f2bdbb77c896"}, +] + +[package.dependencies] +pytest = ">=2.8.1" + +[[package]] +name = "python-dateutil" +version = "2.9.0.post0" +description = "Extensions to the standard Python datetime module" +optional = false +python-versions = "!=3.0.*,!=3.1.*,!=3.2.*,>=2.7" +files = [ + {file = "python-dateutil-2.9.0.post0.tar.gz", hash = "sha256:37dd54208da7e1cd875388217d5e00ebd4179249f90fb72437e91a35459a0ad3"}, + {file = "python_dateutil-2.9.0.post0-py2.py3-none-any.whl", hash = "sha256:a8b2bc7bffae282281c8140a97d3aa9c14da0b136dfe83f850eea9a5f7470427"}, +] + +[package.dependencies] +six = ">=1.5" + +[[package]] +name = "pytrie" +version = "0.4.0" +description = "A pure Python implementation of the trie data structure." +optional = false +python-versions = "*" +files = [ + {file = "PyTrie-0.4.0.tar.gz", hash = "sha256:8f4488f402d3465993fb6b6efa09866849ed8cda7903b50647b7d0342b805379"}, +] + +[package.dependencies] +sortedcontainers = "*" + +[[package]] +name = "pytz" +version = "2024.1" +description = "World timezone definitions, modern and historical" +optional = false +python-versions = "*" +files = [ + {file = "pytz-2024.1-py2.py3-none-any.whl", hash = "sha256:328171f4e3623139da4983451950b28e95ac706e13f3f2630a879749e7a8b319"}, + {file = "pytz-2024.1.tar.gz", hash = "sha256:2a29735ea9c18baf14b448846bde5a48030ed267578472d8955cd0e7443a9812"}, +] + +[[package]] +name = "pyyaml" +version = "6.0.1" +description = "YAML parser and emitter for Python" +optional = false +python-versions = ">=3.6" +files = [ + {file = "PyYAML-6.0.1-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:d858aa552c999bc8a8d57426ed01e40bef403cd8ccdd0fc5f6f04a00414cac2a"}, + {file = "PyYAML-6.0.1-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:fd66fc5d0da6d9815ba2cebeb4205f95818ff4b79c3ebe268e75d961704af52f"}, + {file = "PyYAML-6.0.1-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:69b023b2b4daa7548bcfbd4aa3da05b3a74b772db9e23b982788168117739938"}, + {file = "PyYAML-6.0.1-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:81e0b275a9ecc9c0c0c07b4b90ba548307583c125f54d5b6946cfee6360c733d"}, + {file = "PyYAML-6.0.1-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:ba336e390cd8e4d1739f42dfe9bb83a3cc2e80f567d8805e11b46f4a943f5515"}, + {file = "PyYAML-6.0.1-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:326c013efe8048858a6d312ddd31d56e468118ad4cdeda36c719bf5bb6192290"}, + {file = "PyYAML-6.0.1-cp310-cp310-win32.whl", hash = "sha256:bd4af7373a854424dabd882decdc5579653d7868b8fb26dc7d0e99f823aa5924"}, + {file = "PyYAML-6.0.1-cp310-cp310-win_amd64.whl", hash = "sha256:fd1592b3fdf65fff2ad0004b5e363300ef59ced41c2e6b3a99d4089fa8c5435d"}, + {file = "PyYAML-6.0.1-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:6965a7bc3cf88e5a1c3bd2e0b5c22f8d677dc88a455344035f03399034eb3007"}, + {file = "PyYAML-6.0.1-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:f003ed9ad21d6a4713f0a9b5a7a0a79e08dd0f221aff4525a2be4c346ee60aab"}, + {file = "PyYAML-6.0.1-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:42f8152b8dbc4fe7d96729ec2b99c7097d656dc1213a3229ca5383f973a5ed6d"}, + {file = "PyYAML-6.0.1-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:062582fca9fabdd2c8b54a3ef1c978d786e0f6b3a1510e0ac93ef59e0ddae2bc"}, + {file = "PyYAML-6.0.1-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d2b04aac4d386b172d5b9692e2d2da8de7bfb6c387fa4f801fbf6fb2e6ba4673"}, + {file = "PyYAML-6.0.1-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:e7d73685e87afe9f3b36c799222440d6cf362062f78be1013661b00c5c6f678b"}, + {file = "PyYAML-6.0.1-cp311-cp311-win32.whl", hash = "sha256:1635fd110e8d85d55237ab316b5b011de701ea0f29d07611174a1b42f1444741"}, + {file = "PyYAML-6.0.1-cp311-cp311-win_amd64.whl", hash = "sha256:bf07ee2fef7014951eeb99f56f39c9bb4af143d8aa3c21b1677805985307da34"}, + {file = "PyYAML-6.0.1-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:855fb52b0dc35af121542a76b9a84f8d1cd886ea97c84703eaa6d88e37a2ad28"}, + {file = "PyYAML-6.0.1-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:40df9b996c2b73138957fe23a16a4f0ba614f4c0efce1e9406a184b6d07fa3a9"}, + {file = "PyYAML-6.0.1-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a08c6f0fe150303c1c6b71ebcd7213c2858041a7e01975da3a99aed1e7a378ef"}, + {file = "PyYAML-6.0.1-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:6c22bec3fbe2524cde73d7ada88f6566758a8f7227bfbf93a408a9d86bcc12a0"}, + {file = "PyYAML-6.0.1-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:8d4e9c88387b0f5c7d5f281e55304de64cf7f9c0021a3525bd3b1c542da3b0e4"}, + {file = "PyYAML-6.0.1-cp312-cp312-win32.whl", hash = "sha256:d483d2cdf104e7c9fa60c544d92981f12ad66a457afae824d146093b8c294c54"}, + {file = "PyYAML-6.0.1-cp312-cp312-win_amd64.whl", hash = "sha256:0d3304d8c0adc42be59c5f8a4d9e3d7379e6955ad754aa9d6ab7a398b59dd1df"}, + {file = "PyYAML-6.0.1-cp36-cp36m-macosx_10_9_x86_64.whl", hash = "sha256:50550eb667afee136e9a77d6dc71ae76a44df8b3e51e41b77f6de2932bfe0f47"}, + {file = "PyYAML-6.0.1-cp36-cp36m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:1fe35611261b29bd1de0070f0b2f47cb6ff71fa6595c077e42bd0c419fa27b98"}, + {file = "PyYAML-6.0.1-cp36-cp36m-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:704219a11b772aea0d8ecd7058d0082713c3562b4e271b849ad7dc4a5c90c13c"}, + {file = "PyYAML-6.0.1-cp36-cp36m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:afd7e57eddb1a54f0f1a974bc4391af8bcce0b444685d936840f125cf046d5bd"}, + {file = "PyYAML-6.0.1-cp36-cp36m-win32.whl", hash = "sha256:fca0e3a251908a499833aa292323f32437106001d436eca0e6e7833256674585"}, + {file = "PyYAML-6.0.1-cp36-cp36m-win_amd64.whl", hash = "sha256:f22ac1c3cac4dbc50079e965eba2c1058622631e526bd9afd45fedd49ba781fa"}, + {file = "PyYAML-6.0.1-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:b1275ad35a5d18c62a7220633c913e1b42d44b46ee12554e5fd39c70a243d6a3"}, + {file = "PyYAML-6.0.1-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:18aeb1bf9a78867dc38b259769503436b7c72f7a1f1f4c93ff9a17de54319b27"}, + {file = "PyYAML-6.0.1-cp37-cp37m-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:596106435fa6ad000c2991a98fa58eeb8656ef2325d7e158344fb33864ed87e3"}, + {file = "PyYAML-6.0.1-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:baa90d3f661d43131ca170712d903e6295d1f7a0f595074f151c0aed377c9b9c"}, + {file = "PyYAML-6.0.1-cp37-cp37m-win32.whl", hash = "sha256:9046c58c4395dff28dd494285c82ba00b546adfc7ef001486fbf0324bc174fba"}, + {file = "PyYAML-6.0.1-cp37-cp37m-win_amd64.whl", hash = "sha256:4fb147e7a67ef577a588a0e2c17b6db51dda102c71de36f8549b6816a96e1867"}, + {file = "PyYAML-6.0.1-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:1d4c7e777c441b20e32f52bd377e0c409713e8bb1386e1099c2415f26e479595"}, + {file = "PyYAML-6.0.1-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a0cd17c15d3bb3fa06978b4e8958dcdc6e0174ccea823003a106c7d4d7899ac5"}, + {file = "PyYAML-6.0.1-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:28c119d996beec18c05208a8bd78cbe4007878c6dd15091efb73a30e90539696"}, + {file = "PyYAML-6.0.1-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:7e07cbde391ba96ab58e532ff4803f79c4129397514e1413a7dc761ccd755735"}, + {file = "PyYAML-6.0.1-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:49a183be227561de579b4a36efbb21b3eab9651dd81b1858589f796549873dd6"}, + {file = "PyYAML-6.0.1-cp38-cp38-win32.whl", hash = "sha256:184c5108a2aca3c5b3d3bf9395d50893a7ab82a38004c8f61c258d4428e80206"}, + {file = "PyYAML-6.0.1-cp38-cp38-win_amd64.whl", hash = "sha256:1e2722cc9fbb45d9b87631ac70924c11d3a401b2d7f410cc0e3bbf249f2dca62"}, + {file = "PyYAML-6.0.1-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:9eb6caa9a297fc2c2fb8862bc5370d0303ddba53ba97e71f08023b6cd73d16a8"}, + {file = "PyYAML-6.0.1-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:c8098ddcc2a85b61647b2590f825f3db38891662cfc2fc776415143f599bb859"}, + {file = "PyYAML-6.0.1-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:5773183b6446b2c99bb77e77595dd486303b4faab2b086e7b17bc6bef28865f6"}, + {file = "PyYAML-6.0.1-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:b786eecbdf8499b9ca1d697215862083bd6d2a99965554781d0d8d1ad31e13a0"}, + {file = "PyYAML-6.0.1-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:bc1bf2925a1ecd43da378f4db9e4f799775d6367bdb94671027b73b393a7c42c"}, + {file = "PyYAML-6.0.1-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:04ac92ad1925b2cff1db0cfebffb6ffc43457495c9b3c39d3fcae417d7125dc5"}, + {file = "PyYAML-6.0.1-cp39-cp39-win32.whl", hash = "sha256:faca3bdcf85b2fc05d06ff3fbc1f83e1391b3e724afa3feba7d13eeab355484c"}, + {file = "PyYAML-6.0.1-cp39-cp39-win_amd64.whl", hash = "sha256:510c9deebc5c0225e8c96813043e62b680ba2f9c50a08d3724c7f28a747d1486"}, + {file = "PyYAML-6.0.1.tar.gz", hash = "sha256:bfdf460b1736c775f2ba9f6a92bca30bc2095067b8a9d77876d1fad6cc3b4a43"}, +] + +[[package]] +name = "ratelimit" +version = "2.2.1" +description = "API rate limit decorator" +optional = false +python-versions = "*" +files = [ + {file = "ratelimit-2.2.1.tar.gz", hash = "sha256:af8a9b64b821529aca09ebaf6d8d279100d766f19e90b5059ac6a718ca6dee42"}, +] + +[[package]] +name = "rdflib" +version = "7.0.0" +description = "RDFLib is a Python library for working with RDF, a simple yet powerful language for representing information." +optional = false +python-versions = ">=3.8.1,<4.0.0" +files = [ + {file = "rdflib-7.0.0-py3-none-any.whl", hash = "sha256:0438920912a642c866a513de6fe8a0001bd86ef975057d6962c79ce4771687cd"}, + {file = "rdflib-7.0.0.tar.gz", hash = "sha256:9995eb8569428059b8c1affd26b25eac510d64f5043d9ce8c84e0d0036e995ae"}, +] + +[package.dependencies] +isodate = ">=0.6.0,<0.7.0" +pyparsing = ">=2.1.0,<4" + +[package.extras] +berkeleydb = ["berkeleydb (>=18.1.0,<19.0.0)"] +html = ["html5lib (>=1.0,<2.0)"] +lxml = ["lxml (>=4.3.0,<5.0.0)"] +networkx = ["networkx (>=2.0.0,<3.0.0)"] + +[[package]] +name = "rdflib-jsonld" +version = "0.6.1" +description = "rdflib extension adding JSON-LD parser and serializer" +optional = false +python-versions = "*" +files = [ + {file = "rdflib-jsonld-0.6.1.tar.gz", hash = "sha256:eda5a42a2e09f80d4da78e32b5c684bccdf275368f1541e6b7bcddfb1382a0e0"}, + {file = "rdflib_jsonld-0.6.1-py2.py3-none-any.whl", hash = "sha256:bcf84317e947a661bae0a3f2aee1eced697075fc4ac4db6065a3340ea0f10fc2"}, +] + +[package.dependencies] +rdflib = ">=5.0.0" + +[[package]] +name = "rdflib-shim" +version = "1.0.3" +description = "Shim for rdflib 5 and 6 incompatibilities" +optional = false +python-versions = ">=3.7" +files = [ + {file = "rdflib_shim-1.0.3-py3-none-any.whl", hash = "sha256:7a853e7750ef1e9bf4e35dea27d54e02d4ed087de5a9e0c329c4a6d82d647081"}, + {file = "rdflib_shim-1.0.3.tar.gz", hash = "sha256:d955d11e2986aab42b6830ca56ac6bc9c893abd1d049a161c6de2f1b99d4fc0d"}, +] + +[package.dependencies] +rdflib = ">=5.0.0" +rdflib-jsonld = "0.6.1" + +[[package]] +name = "referencing" +version = "0.35.1" +description = "JSON Referencing + Python" +optional = false +python-versions = ">=3.8" +files = [ + {file = "referencing-0.35.1-py3-none-any.whl", hash = "sha256:eda6d3234d62814d1c64e305c1331c9a3a6132da475ab6382eaa997b21ee75de"}, + {file = "referencing-0.35.1.tar.gz", hash = "sha256:25b42124a6c8b632a425174f24087783efb348a6f1e0008e63cd4466fedf703c"}, +] + +[package.dependencies] +attrs = ">=22.2.0" +rpds-py = ">=0.7.0" + +[[package]] +name = "regex" +version = "2024.5.15" +description = "Alternative regular expression module, to replace re." +optional = false +python-versions = ">=3.8" +files = [ + {file = "regex-2024.5.15-cp310-cp310-macosx_10_9_universal2.whl", hash = "sha256:a81e3cfbae20378d75185171587cbf756015ccb14840702944f014e0d93ea09f"}, + {file = "regex-2024.5.15-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:7b59138b219ffa8979013be7bc85bb60c6f7b7575df3d56dc1e403a438c7a3f6"}, + {file = "regex-2024.5.15-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:a0bd000c6e266927cb7a1bc39d55be95c4b4f65c5be53e659537537e019232b1"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:5eaa7ddaf517aa095fa8da0b5015c44d03da83f5bd49c87961e3c997daed0de7"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:ba68168daedb2c0bab7fd7e00ced5ba90aebf91024dea3c88ad5063c2a562cca"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:6e8d717bca3a6e2064fc3a08df5cbe366369f4b052dcd21b7416e6d71620dca1"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:1337b7dbef9b2f71121cdbf1e97e40de33ff114801263b275aafd75303bd62b5"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:f9ebd0a36102fcad2f03696e8af4ae682793a5d30b46c647eaf280d6cfb32796"}, + {file = "regex-2024.5.15-cp310-cp310-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_12_x86_64.manylinux2010_x86_64.whl", hash = "sha256:9efa1a32ad3a3ea112224897cdaeb6aa00381627f567179c0314f7b65d354c62"}, + {file = "regex-2024.5.15-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:1595f2d10dff3d805e054ebdc41c124753631b6a471b976963c7b28543cf13b0"}, + {file = "regex-2024.5.15-cp310-cp310-musllinux_1_2_i686.whl", hash = "sha256:b802512f3e1f480f41ab5f2cfc0e2f761f08a1f41092d6718868082fc0d27143"}, + {file = "regex-2024.5.15-cp310-cp310-musllinux_1_2_ppc64le.whl", hash = "sha256:a0981022dccabca811e8171f913de05720590c915b033b7e601f35ce4ea7019f"}, + {file = "regex-2024.5.15-cp310-cp310-musllinux_1_2_s390x.whl", hash = "sha256:19068a6a79cf99a19ccefa44610491e9ca02c2be3305c7760d3831d38a467a6f"}, + {file = "regex-2024.5.15-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:1b5269484f6126eee5e687785e83c6b60aad7663dafe842b34691157e5083e53"}, + {file = "regex-2024.5.15-cp310-cp310-win32.whl", hash = "sha256:ada150c5adfa8fbcbf321c30c751dc67d2f12f15bd183ffe4ec7cde351d945b3"}, + {file = "regex-2024.5.15-cp310-cp310-win_amd64.whl", hash = "sha256:ac394ff680fc46b97487941f5e6ae49a9f30ea41c6c6804832063f14b2a5a145"}, + {file = "regex-2024.5.15-cp311-cp311-macosx_10_9_universal2.whl", hash = "sha256:f5b1dff3ad008dccf18e652283f5e5339d70bf8ba7c98bf848ac33db10f7bc7a"}, + {file = "regex-2024.5.15-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:c6a2b494a76983df8e3d3feea9b9ffdd558b247e60b92f877f93a1ff43d26656"}, + {file = "regex-2024.5.15-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:a32b96f15c8ab2e7d27655969a23895eb799de3665fa94349f3b2fbfd547236f"}, + {file = "regex-2024.5.15-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:10002e86e6068d9e1c91eae8295ef690f02f913c57db120b58fdd35a6bb1af35"}, + {file = "regex-2024.5.15-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:ec54d5afa89c19c6dd8541a133be51ee1017a38b412b1321ccb8d6ddbeb4cf7d"}, + {file = "regex-2024.5.15-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:10e4ce0dca9ae7a66e6089bb29355d4432caed736acae36fef0fdd7879f0b0cb"}, + {file = "regex-2024.5.15-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:3e507ff1e74373c4d3038195fdd2af30d297b4f0950eeda6f515ae3d84a1770f"}, + {file = "regex-2024.5.15-cp311-cp311-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:d1f059a4d795e646e1c37665b9d06062c62d0e8cc3c511fe01315973a6542e40"}, + {file = "regex-2024.5.15-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:0721931ad5fe0dda45d07f9820b90b2148ccdd8e45bb9e9b42a146cb4f695649"}, + {file = "regex-2024.5.15-cp311-cp311-musllinux_1_2_i686.whl", hash = "sha256:833616ddc75ad595dee848ad984d067f2f31be645d603e4d158bba656bbf516c"}, + {file = "regex-2024.5.15-cp311-cp311-musllinux_1_2_ppc64le.whl", hash = "sha256:287eb7f54fc81546346207c533ad3c2c51a8d61075127d7f6d79aaf96cdee890"}, + {file = "regex-2024.5.15-cp311-cp311-musllinux_1_2_s390x.whl", hash = "sha256:19dfb1c504781a136a80ecd1fff9f16dddf5bb43cec6871778c8a907a085bb3d"}, + {file = "regex-2024.5.15-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:119af6e56dce35e8dfb5222573b50c89e5508d94d55713c75126b753f834de68"}, + {file = "regex-2024.5.15-cp311-cp311-win32.whl", hash = "sha256:1c1c174d6ec38d6c8a7504087358ce9213d4332f6293a94fbf5249992ba54efa"}, + {file = "regex-2024.5.15-cp311-cp311-win_amd64.whl", hash = "sha256:9e717956dcfd656f5055cc70996ee2cc82ac5149517fc8e1b60261b907740201"}, + {file = "regex-2024.5.15-cp312-cp312-macosx_10_9_universal2.whl", hash = "sha256:632b01153e5248c134007209b5c6348a544ce96c46005d8456de1d552455b014"}, + {file = "regex-2024.5.15-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:e64198f6b856d48192bf921421fdd8ad8eb35e179086e99e99f711957ffedd6e"}, + {file = "regex-2024.5.15-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:68811ab14087b2f6e0fc0c2bae9ad689ea3584cad6917fc57be6a48bbd012c49"}, + {file = "regex-2024.5.15-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:f8ec0c2fea1e886a19c3bee0cd19d862b3aa75dcdfb42ebe8ed30708df64687a"}, + {file = "regex-2024.5.15-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:d0c0c0003c10f54a591d220997dd27d953cd9ccc1a7294b40a4be5312be8797b"}, + {file = "regex-2024.5.15-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:2431b9e263af1953c55abbd3e2efca67ca80a3de8a0437cb58e2421f8184717a"}, + {file = "regex-2024.5.15-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:4a605586358893b483976cffc1723fb0f83e526e8f14c6e6614e75919d9862cf"}, + {file = "regex-2024.5.15-cp312-cp312-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:391d7f7f1e409d192dba8bcd42d3e4cf9e598f3979cdaed6ab11288da88cb9f2"}, + {file = "regex-2024.5.15-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:9ff11639a8d98969c863d4617595eb5425fd12f7c5ef6621a4b74b71ed8726d5"}, + {file = "regex-2024.5.15-cp312-cp312-musllinux_1_2_i686.whl", hash = "sha256:4eee78a04e6c67e8391edd4dad3279828dd66ac4b79570ec998e2155d2e59fd5"}, + {file = "regex-2024.5.15-cp312-cp312-musllinux_1_2_ppc64le.whl", hash = "sha256:8fe45aa3f4aa57faabbc9cb46a93363edd6197cbc43523daea044e9ff2fea83e"}, + {file = "regex-2024.5.15-cp312-cp312-musllinux_1_2_s390x.whl", hash = "sha256:d0a3d8d6acf0c78a1fff0e210d224b821081330b8524e3e2bc5a68ef6ab5803d"}, + {file = "regex-2024.5.15-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:c486b4106066d502495b3025a0a7251bf37ea9540433940a23419461ab9f2a80"}, + {file = "regex-2024.5.15-cp312-cp312-win32.whl", hash = "sha256:c49e15eac7c149f3670b3e27f1f28a2c1ddeccd3a2812cba953e01be2ab9b5fe"}, + {file = "regex-2024.5.15-cp312-cp312-win_amd64.whl", hash = "sha256:673b5a6da4557b975c6c90198588181029c60793835ce02f497ea817ff647cb2"}, + {file = "regex-2024.5.15-cp38-cp38-macosx_10_9_universal2.whl", hash = "sha256:87e2a9c29e672fc65523fb47a90d429b70ef72b901b4e4b1bd42387caf0d6835"}, + {file = "regex-2024.5.15-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:c3bea0ba8b73b71b37ac833a7f3fd53825924165da6a924aec78c13032f20850"}, + {file = "regex-2024.5.15-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:bfc4f82cabe54f1e7f206fd3d30fda143f84a63fe7d64a81558d6e5f2e5aaba9"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:e5bb9425fe881d578aeca0b2b4b3d314ec88738706f66f219c194d67179337cb"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:64c65783e96e563103d641760664125e91bd85d8e49566ee560ded4da0d3e704"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:cf2430df4148b08fb4324b848672514b1385ae3807651f3567871f130a728cc3"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:5397de3219a8b08ae9540c48f602996aa6b0b65d5a61683e233af8605c42b0f2"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:455705d34b4154a80ead722f4f185b04c4237e8e8e33f265cd0798d0e44825fa"}, + {file = "regex-2024.5.15-cp38-cp38-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_12_x86_64.manylinux2010_x86_64.whl", hash = "sha256:b2b6f1b3bb6f640c1a92be3bbfbcb18657b125b99ecf141fb3310b5282c7d4ed"}, + {file = "regex-2024.5.15-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:3ad070b823ca5890cab606c940522d05d3d22395d432f4aaaf9d5b1653e47ced"}, + {file = "regex-2024.5.15-cp38-cp38-musllinux_1_2_i686.whl", hash = "sha256:5b5467acbfc153847d5adb21e21e29847bcb5870e65c94c9206d20eb4e99a384"}, + {file = "regex-2024.5.15-cp38-cp38-musllinux_1_2_ppc64le.whl", hash = "sha256:e6662686aeb633ad65be2a42b4cb00178b3fbf7b91878f9446075c404ada552f"}, + {file = "regex-2024.5.15-cp38-cp38-musllinux_1_2_s390x.whl", hash = "sha256:2b4c884767504c0e2401babe8b5b7aea9148680d2e157fa28f01529d1f7fcf67"}, + {file = "regex-2024.5.15-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:3cd7874d57f13bf70078f1ff02b8b0aa48d5b9ed25fc48547516c6aba36f5741"}, + {file = "regex-2024.5.15-cp38-cp38-win32.whl", hash = "sha256:e4682f5ba31f475d58884045c1a97a860a007d44938c4c0895f41d64481edbc9"}, + {file = "regex-2024.5.15-cp38-cp38-win_amd64.whl", hash = "sha256:d99ceffa25ac45d150e30bd9ed14ec6039f2aad0ffa6bb87a5936f5782fc1569"}, + {file = "regex-2024.5.15-cp39-cp39-macosx_10_9_universal2.whl", hash = "sha256:13cdaf31bed30a1e1c2453ef6015aa0983e1366fad2667657dbcac7b02f67133"}, + {file = "regex-2024.5.15-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:cac27dcaa821ca271855a32188aa61d12decb6fe45ffe3e722401fe61e323cd1"}, + {file = "regex-2024.5.15-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:7dbe2467273b875ea2de38ded4eba86cbcbc9a1a6d0aa11dcf7bd2e67859c435"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:64f18a9a3513a99c4bef0e3efd4c4a5b11228b48aa80743be822b71e132ae4f5"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:d347a741ea871c2e278fde6c48f85136c96b8659b632fb57a7d1ce1872547600"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:1878b8301ed011704aea4c806a3cadbd76f84dece1ec09cc9e4dc934cfa5d4da"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:4babf07ad476aaf7830d77000874d7611704a7fcf68c9c2ad151f5d94ae4bfc4"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:35cb514e137cb3488bce23352af3e12fb0dbedd1ee6e60da053c69fb1b29cc6c"}, + {file = "regex-2024.5.15-cp39-cp39-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_12_x86_64.manylinux2010_x86_64.whl", hash = "sha256:cdd09d47c0b2efee9378679f8510ee6955d329424c659ab3c5e3a6edea696294"}, + {file = "regex-2024.5.15-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:72d7a99cd6b8f958e85fc6ca5b37c4303294954eac1376535b03c2a43eb72629"}, + {file = "regex-2024.5.15-cp39-cp39-musllinux_1_2_i686.whl", hash = "sha256:a094801d379ab20c2135529948cb84d417a2169b9bdceda2a36f5f10977ebc16"}, + {file = "regex-2024.5.15-cp39-cp39-musllinux_1_2_ppc64le.whl", hash = "sha256:c0c18345010870e58238790a6779a1219b4d97bd2e77e1140e8ee5d14df071aa"}, + {file = "regex-2024.5.15-cp39-cp39-musllinux_1_2_s390x.whl", hash = "sha256:16093f563098448ff6b1fa68170e4acbef94e6b6a4e25e10eae8598bb1694b5d"}, + {file = "regex-2024.5.15-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:e38a7d4e8f633a33b4c7350fbd8bad3b70bf81439ac67ac38916c4a86b465456"}, + {file = "regex-2024.5.15-cp39-cp39-win32.whl", hash = "sha256:71a455a3c584a88f654b64feccc1e25876066c4f5ef26cd6dd711308aa538694"}, + {file = "regex-2024.5.15-cp39-cp39-win_amd64.whl", hash = "sha256:cab12877a9bdafde5500206d1020a584355a97884dfd388af3699e9137bf7388"}, + {file = "regex-2024.5.15.tar.gz", hash = "sha256:d3ee02d9e5f482cc8309134a91eeaacbdd2261ba111b0fef3748eeb4913e6a2c"}, +] + +[[package]] +name = "requests" +version = "2.32.3" +description = "Python HTTP for Humans." +optional = false +python-versions = ">=3.8" +files = [ + {file = "requests-2.32.3-py3-none-any.whl", hash = "sha256:70761cfe03c773ceb22aa2f671b4757976145175cdfca038c02654d061d6dcc6"}, + {file = "requests-2.32.3.tar.gz", hash = "sha256:55365417734eb18255590a9ff9eb97e9e1da868d4ccd6402399eaf68af20a760"}, +] + +[package.dependencies] +certifi = ">=2017.4.17" +charset-normalizer = ">=2,<4" +idna = ">=2.5,<4" +urllib3 = ">=1.21.1,<3" + +[package.extras] +socks = ["PySocks (>=1.5.6,!=1.5.7)"] +use-chardet-on-py3 = ["chardet (>=3.0.2,<6)"] + +[[package]] +name = "requests-cache" +version = "1.2.0" +description = "A persistent cache for python requests" +optional = false +python-versions = ">=3.8" +files = [ + {file = "requests_cache-1.2.0-py3-none-any.whl", hash = "sha256:490324301bf0cb924ff4e6324bd2613453e7e1f847353928b08adb0fdfb7f722"}, + {file = "requests_cache-1.2.0.tar.gz", hash = "sha256:db1c709ca343cc1cd5b6c8b1a5387298eceed02306a6040760db538c885e3838"}, +] + +[package.dependencies] +attrs = ">=21.2" +cattrs = ">=22.2" +platformdirs = ">=2.5" +requests = ">=2.22" +url-normalize = ">=1.4" +urllib3 = ">=1.25.5" + +[package.extras] +all = ["boto3 (>=1.15)", "botocore (>=1.18)", "itsdangerous (>=2.0)", "pymongo (>=3)", "pyyaml (>=6.0.1)", "redis (>=3)", "ujson (>=5.4)"] +bson = ["bson (>=0.5)"] +docs = ["furo (>=2023.3,<2024.0)", "linkify-it-py (>=2.0,<3.0)", "myst-parser (>=1.0,<2.0)", "sphinx (>=5.0.2,<6.0.0)", "sphinx-autodoc-typehints (>=1.19)", "sphinx-automodapi (>=0.14)", "sphinx-copybutton (>=0.5)", "sphinx-design (>=0.2)", "sphinx-notfound-page (>=0.8)", "sphinxcontrib-apidoc (>=0.3)", "sphinxext-opengraph (>=0.9)"] +dynamodb = ["boto3 (>=1.15)", "botocore (>=1.18)"] +json = ["ujson (>=5.4)"] +mongodb = ["pymongo (>=3)"] +redis = ["redis (>=3)"] +security = ["itsdangerous (>=2.0)"] +yaml = ["pyyaml (>=6.0.1)"] + +[[package]] +name = "requests-toolbelt" +version = "1.0.0" +description = "A utility belt for advanced users of python-requests" +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*, !=3.3.*" +files = [ + {file = "requests-toolbelt-1.0.0.tar.gz", hash = "sha256:7681a0a3d047012b5bdc0ee37d7f8f07ebe76ab08caeccfc3921ce23c88d5bc6"}, + {file = "requests_toolbelt-1.0.0-py2.py3-none-any.whl", hash = "sha256:cccfdd665f0a24fcf4726e690f65639d272bb0637b9b92dfd91a5568ccf6bd06"}, +] + +[package.dependencies] +requests = ">=2.0.1,<3.0.0" + +[[package]] +name = "rfc3987" +version = "1.3.8" +description = "Parsing and validation of URIs (RFC 3986) and IRIs (RFC 3987)" +optional = false +python-versions = "*" +files = [ + {file = "rfc3987-1.3.8-py2.py3-none-any.whl", hash = "sha256:10702b1e51e5658843460b189b185c0366d2cf4cff716f13111b0ea9fd2dce53"}, + {file = "rfc3987-1.3.8.tar.gz", hash = "sha256:d3c4d257a560d544e9826b38bc81db676890c79ab9d7ac92b39c7a253d5ca733"}, +] + +[[package]] +name = "rpds-py" +version = "0.18.1" +description = "Python bindings to Rust's persistent data structures (rpds)" +optional = false +python-versions = ">=3.8" +files = [ + {file = "rpds_py-0.18.1-cp310-cp310-macosx_10_12_x86_64.whl", hash = "sha256:d31dea506d718693b6b2cffc0648a8929bdc51c70a311b2770f09611caa10d53"}, + {file = "rpds_py-0.18.1-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:732672fbc449bab754e0b15356c077cc31566df874964d4801ab14f71951ea80"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:4a98a1f0552b5f227a3d6422dbd61bc6f30db170939bd87ed14f3c339aa6c7c9"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:7f1944ce16401aad1e3f7d312247b3d5de7981f634dc9dfe90da72b87d37887d"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:38e14fb4e370885c4ecd734f093a2225ee52dc384b86fa55fe3f74638b2cfb09"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:08d74b184f9ab6289b87b19fe6a6d1a97fbfea84b8a3e745e87a5de3029bf944"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d70129cef4a8d979caa37e7fe957202e7eee8ea02c5e16455bc9808a59c6b2f0"}, + {file = "rpds_py-0.18.1-cp310-cp310-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:ce0bb20e3a11bd04461324a6a798af34d503f8d6f1aa3d2aa8901ceaf039176d"}, + {file = "rpds_py-0.18.1-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:81c5196a790032e0fc2464c0b4ab95f8610f96f1f2fa3d4deacce6a79852da60"}, + {file = "rpds_py-0.18.1-cp310-cp310-musllinux_1_2_i686.whl", hash = "sha256:f3027be483868c99b4985fda802a57a67fdf30c5d9a50338d9db646d590198da"}, + {file = "rpds_py-0.18.1-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:d44607f98caa2961bab4fa3c4309724b185b464cdc3ba6f3d7340bac3ec97cc1"}, + {file = "rpds_py-0.18.1-cp310-none-win32.whl", hash = "sha256:c273e795e7a0f1fddd46e1e3cb8be15634c29ae8ff31c196debb620e1edb9333"}, + {file = "rpds_py-0.18.1-cp310-none-win_amd64.whl", hash = "sha256:8352f48d511de5f973e4f2f9412736d7dea76c69faa6d36bcf885b50c758ab9a"}, + {file = "rpds_py-0.18.1-cp311-cp311-macosx_10_12_x86_64.whl", hash = "sha256:6b5ff7e1d63a8281654b5e2896d7f08799378e594f09cf3674e832ecaf396ce8"}, + {file = "rpds_py-0.18.1-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:8927638a4d4137a289e41d0fd631551e89fa346d6dbcfc31ad627557d03ceb6d"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:154bf5c93d79558b44e5b50cc354aa0459e518e83677791e6adb0b039b7aa6a7"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:07f2139741e5deb2c5154a7b9629bc5aa48c766b643c1a6750d16f865a82c5fc"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:8c7672e9fba7425f79019db9945b16e308ed8bc89348c23d955c8c0540da0a07"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:489bdfe1abd0406eba6b3bb4fdc87c7fa40f1031de073d0cfb744634cc8fa261"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:3c20f05e8e3d4fc76875fc9cb8cf24b90a63f5a1b4c5b9273f0e8225e169b100"}, + {file = "rpds_py-0.18.1-cp311-cp311-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:967342e045564cef76dfcf1edb700b1e20838d83b1aa02ab313e6a497cf923b8"}, + {file = "rpds_py-0.18.1-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:2cc7c1a47f3a63282ab0f422d90ddac4aa3034e39fc66a559ab93041e6505da7"}, + {file = "rpds_py-0.18.1-cp311-cp311-musllinux_1_2_i686.whl", hash = "sha256:f7afbfee1157e0f9376c00bb232e80a60e59ed716e3211a80cb8506550671e6e"}, + {file = "rpds_py-0.18.1-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:9e6934d70dc50f9f8ea47081ceafdec09245fd9f6032669c3b45705dea096b88"}, + {file = "rpds_py-0.18.1-cp311-none-win32.whl", hash = "sha256:c69882964516dc143083d3795cb508e806b09fc3800fd0d4cddc1df6c36e76bb"}, + {file = "rpds_py-0.18.1-cp311-none-win_amd64.whl", hash = "sha256:70a838f7754483bcdc830444952fd89645569e7452e3226de4a613a4c1793fb2"}, + {file = "rpds_py-0.18.1-cp312-cp312-macosx_10_12_x86_64.whl", hash = "sha256:3dd3cd86e1db5aadd334e011eba4e29d37a104b403e8ca24dcd6703c68ca55b3"}, + {file = "rpds_py-0.18.1-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:05f3d615099bd9b13ecf2fc9cf2d839ad3f20239c678f461c753e93755d629ee"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:35b2b771b13eee8729a5049c976197ff58a27a3829c018a04341bcf1ae409b2b"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:ee17cd26b97d537af8f33635ef38be873073d516fd425e80559f4585a7b90c43"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:b646bf655b135ccf4522ed43d6902af37d3f5dbcf0da66c769a2b3938b9d8184"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:19ba472b9606c36716062c023afa2484d1e4220548751bda14f725a7de17b4f6"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:6e30ac5e329098903262dc5bdd7e2086e0256aa762cc8b744f9e7bf2a427d3f8"}, + {file = "rpds_py-0.18.1-cp312-cp312-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:d58ad6317d188c43750cb76e9deacf6051d0f884d87dc6518e0280438648a9ac"}, + {file = "rpds_py-0.18.1-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:e1735502458621921cee039c47318cb90b51d532c2766593be6207eec53e5c4c"}, + {file = "rpds_py-0.18.1-cp312-cp312-musllinux_1_2_i686.whl", hash = "sha256:f5bab211605d91db0e2995a17b5c6ee5edec1270e46223e513eaa20da20076ac"}, + {file = "rpds_py-0.18.1-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:2fc24a329a717f9e2448f8cd1f960f9dac4e45b6224d60734edeb67499bab03a"}, + {file = "rpds_py-0.18.1-cp312-none-win32.whl", hash = "sha256:1805d5901779662d599d0e2e4159d8a82c0b05faa86ef9222bf974572286b2b6"}, + {file = "rpds_py-0.18.1-cp312-none-win_amd64.whl", hash = "sha256:720edcb916df872d80f80a1cc5ea9058300b97721efda8651efcd938a9c70a72"}, + {file = "rpds_py-0.18.1-cp38-cp38-macosx_10_12_x86_64.whl", hash = "sha256:c827576e2fa017a081346dce87d532a5310241648eb3700af9a571a6e9fc7e74"}, + {file = "rpds_py-0.18.1-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:aa3679e751408d75a0b4d8d26d6647b6d9326f5e35c00a7ccd82b78ef64f65f8"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:0abeee75434e2ee2d142d650d1e54ac1f8b01e6e6abdde8ffd6eeac6e9c38e20"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:ed402d6153c5d519a0faf1bb69898e97fb31613b49da27a84a13935ea9164dfc"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:338dee44b0cef8b70fd2ef54b4e09bb1b97fc6c3a58fea5db6cc083fd9fc2724"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:7750569d9526199c5b97e5a9f8d96a13300950d910cf04a861d96f4273d5b104"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:607345bd5912aacc0c5a63d45a1f73fef29e697884f7e861094e443187c02be5"}, + {file = "rpds_py-0.18.1-cp38-cp38-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:207c82978115baa1fd8d706d720b4a4d2b0913df1c78c85ba73fe6c5804505f0"}, + {file = "rpds_py-0.18.1-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:6d1e42d2735d437e7e80bab4d78eb2e459af48c0a46e686ea35f690b93db792d"}, + {file = "rpds_py-0.18.1-cp38-cp38-musllinux_1_2_i686.whl", hash = "sha256:5463c47c08630007dc0fe99fb480ea4f34a89712410592380425a9b4e1611d8e"}, + {file = "rpds_py-0.18.1-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:06d218939e1bf2ca50e6b0ec700ffe755e5216a8230ab3e87c059ebb4ea06afc"}, + {file = "rpds_py-0.18.1-cp38-none-win32.whl", hash = "sha256:312fe69b4fe1ffbe76520a7676b1e5ac06ddf7826d764cc10265c3b53f96dbe9"}, + {file = "rpds_py-0.18.1-cp38-none-win_amd64.whl", hash = "sha256:9437ca26784120a279f3137ee080b0e717012c42921eb07861b412340f85bae2"}, + {file = "rpds_py-0.18.1-cp39-cp39-macosx_10_12_x86_64.whl", hash = "sha256:19e515b78c3fc1039dd7da0a33c28c3154458f947f4dc198d3c72db2b6b5dc93"}, + {file = "rpds_py-0.18.1-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:a7b28c5b066bca9a4eb4e2f2663012debe680f097979d880657f00e1c30875a0"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:673fdbbf668dd958eff750e500495ef3f611e2ecc209464f661bc82e9838991e"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:d960de62227635d2e61068f42a6cb6aae91a7fe00fca0e3aeed17667c8a34611"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:352a88dc7892f1da66b6027af06a2e7e5d53fe05924cc2cfc56495b586a10b72"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:4e0ee01ad8260184db21468a6e1c37afa0529acc12c3a697ee498d3c2c4dcaf3"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e4c39ad2f512b4041343ea3c7894339e4ca7839ac38ca83d68a832fc8b3748ab"}, + {file = "rpds_py-0.18.1-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:aaa71ee43a703c321906813bb252f69524f02aa05bf4eec85f0c41d5d62d0f4c"}, + {file = "rpds_py-0.18.1-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:6cd8098517c64a85e790657e7b1e509b9fe07487fd358e19431cb120f7d96338"}, + {file = "rpds_py-0.18.1-cp39-cp39-musllinux_1_2_i686.whl", hash = "sha256:4adec039b8e2928983f885c53b7cc4cda8965b62b6596501a0308d2703f8af1b"}, + {file = "rpds_py-0.18.1-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:32b7daaa3e9389db3695964ce8e566e3413b0c43e3394c05e4b243a4cd7bef26"}, + {file = "rpds_py-0.18.1-cp39-none-win32.whl", hash = "sha256:2625f03b105328729f9450c8badda34d5243231eef6535f80064d57035738360"}, + {file = "rpds_py-0.18.1-cp39-none-win_amd64.whl", hash = "sha256:bf18932d0003c8c4d51a39f244231986ab23ee057d235a12b2684ea26a353590"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-macosx_10_12_x86_64.whl", hash = "sha256:cbfbea39ba64f5e53ae2915de36f130588bba71245b418060ec3330ebf85678e"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-macosx_11_0_arm64.whl", hash = "sha256:a3d456ff2a6a4d2adcdf3c1c960a36f4fd2fec6e3b4902a42a384d17cf4e7a65"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:7700936ef9d006b7ef605dc53aa364da2de5a3aa65516a1f3ce73bf82ecfc7ae"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:51584acc5916212e1bf45edd17f3a6b05fe0cbb40482d25e619f824dccb679de"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:942695a206a58d2575033ff1e42b12b2aece98d6003c6bc739fbf33d1773b12f"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:b906b5f58892813e5ba5c6056d6a5ad08f358ba49f046d910ad992196ea61397"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f6f8e3fecca256fefc91bb6765a693d96692459d7d4c644660a9fff32e517843"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:7732770412bab81c5a9f6d20aeb60ae943a9b36dcd990d876a773526468e7163"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-musllinux_1_2_aarch64.whl", hash = "sha256:bd1105b50ede37461c1d51b9698c4f4be6e13e69a908ab7751e3807985fc0346"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-musllinux_1_2_i686.whl", hash = "sha256:618916f5535784960f3ecf8111581f4ad31d347c3de66d02e728de460a46303c"}, + {file = "rpds_py-0.18.1-pp310-pypy310_pp73-musllinux_1_2_x86_64.whl", hash = "sha256:17c6d2155e2423f7e79e3bb18151c686d40db42d8645e7977442170c360194d4"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-macosx_10_12_x86_64.whl", hash = "sha256:6c4c4c3f878df21faf5fac86eda32671c27889e13570645a9eea0a1abdd50922"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-macosx_11_0_arm64.whl", hash = "sha256:fab6ce90574645a0d6c58890e9bcaac8d94dff54fb51c69e5522a7358b80ab64"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:531796fb842b53f2695e94dc338929e9f9dbf473b64710c28af5a160b2a8927d"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:740884bc62a5e2bbb31e584f5d23b32320fd75d79f916f15a788d527a5e83644"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:998125738de0158f088aef3cb264a34251908dd2e5d9966774fdab7402edfab7"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:e2be6e9dd4111d5b31ba3b74d17da54a8319d8168890fbaea4b9e5c3de630ae5"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d0cee71bc618cd93716f3c1bf56653740d2d13ddbd47673efa8bf41435a60daa"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:2c3caec4ec5cd1d18e5dd6ae5194d24ed12785212a90b37f5f7f06b8bedd7139"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-musllinux_1_2_aarch64.whl", hash = "sha256:27bba383e8c5231cd559affe169ca0b96ec78d39909ffd817f28b166d7ddd4d8"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-musllinux_1_2_i686.whl", hash = "sha256:a888e8bdb45916234b99da2d859566f1e8a1d2275a801bb8e4a9644e3c7e7909"}, + {file = "rpds_py-0.18.1-pp38-pypy38_pp73-musllinux_1_2_x86_64.whl", hash = "sha256:6031b25fb1b06327b43d841f33842b383beba399884f8228a6bb3df3088485ff"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-macosx_10_12_x86_64.whl", hash = "sha256:48c2faaa8adfacefcbfdb5f2e2e7bdad081e5ace8d182e5f4ade971f128e6bb3"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-macosx_11_0_arm64.whl", hash = "sha256:d85164315bd68c0806768dc6bb0429c6f95c354f87485ee3593c4f6b14def2bd"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:6afd80f6c79893cfc0574956f78a0add8c76e3696f2d6a15bca2c66c415cf2d4"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_17_armv7l.manylinux2014_armv7l.whl", hash = "sha256:fa242ac1ff583e4ec7771141606aafc92b361cd90a05c30d93e343a0c2d82a89"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_17_ppc64le.manylinux2014_ppc64le.whl", hash = "sha256:d21be4770ff4e08698e1e8e0bce06edb6ea0626e7c8f560bc08222880aca6a6f"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:5c45a639e93a0c5d4b788b2613bd637468edd62f8f95ebc6fcc303d58ab3f0a8"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:910e71711d1055b2768181efa0a17537b2622afeb0424116619817007f8a2b10"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-manylinux_2_5_i686.manylinux1_i686.whl", hash = "sha256:b9bb1f182a97880f6078283b3505a707057c42bf55d8fca604f70dedfdc0772a"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-musllinux_1_2_aarch64.whl", hash = "sha256:1d54f74f40b1f7aaa595a02ff42ef38ca654b1469bef7d52867da474243cc633"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-musllinux_1_2_i686.whl", hash = "sha256:8d2e182c9ee01135e11e9676e9a62dfad791a7a467738f06726872374a83db49"}, + {file = "rpds_py-0.18.1-pp39-pypy39_pp73-musllinux_1_2_x86_64.whl", hash = "sha256:636a15acc588f70fda1661234761f9ed9ad79ebed3f2125d44be0862708b666e"}, + {file = "rpds_py-0.18.1.tar.gz", hash = "sha256:dc48b479d540770c811fbd1eb9ba2bb66951863e448efec2e2c102625328e92f"}, +] + +[[package]] +name = "scipy" +version = "1.13.1" +description = "Fundamental algorithms for scientific computing in Python" +optional = false +python-versions = ">=3.9" +files = [ + {file = "scipy-1.13.1-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:20335853b85e9a49ff7572ab453794298bcf0354d8068c5f6775a0eabf350aca"}, + {file = "scipy-1.13.1-cp310-cp310-macosx_12_0_arm64.whl", hash = "sha256:d605e9c23906d1994f55ace80e0125c587f96c020037ea6aa98d01b4bd2e222f"}, + {file = "scipy-1.13.1-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:cfa31f1def5c819b19ecc3a8b52d28ffdcc7ed52bb20c9a7589669dd3c250989"}, + {file = "scipy-1.13.1-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f26264b282b9da0952a024ae34710c2aff7d27480ee91a2e82b7b7073c24722f"}, + {file = "scipy-1.13.1-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:eccfa1906eacc02de42d70ef4aecea45415f5be17e72b61bafcfd329bdc52e94"}, + {file = "scipy-1.13.1-cp310-cp310-win_amd64.whl", hash = "sha256:2831f0dc9c5ea9edd6e51e6e769b655f08ec6db6e2e10f86ef39bd32eb11da54"}, + {file = "scipy-1.13.1-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:27e52b09c0d3a1d5b63e1105f24177e544a222b43611aaf5bc44d4a0979e32f9"}, + {file = "scipy-1.13.1-cp311-cp311-macosx_12_0_arm64.whl", hash = "sha256:54f430b00f0133e2224c3ba42b805bfd0086fe488835effa33fa291561932326"}, + {file = "scipy-1.13.1-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:e89369d27f9e7b0884ae559a3a956e77c02114cc60a6058b4e5011572eea9299"}, + {file = "scipy-1.13.1-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:a78b4b3345f1b6f68a763c6e25c0c9a23a9fd0f39f5f3d200efe8feda560a5fa"}, + {file = "scipy-1.13.1-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:45484bee6d65633752c490404513b9ef02475b4284c4cfab0ef946def50b3f59"}, + {file = "scipy-1.13.1-cp311-cp311-win_amd64.whl", hash = "sha256:5713f62f781eebd8d597eb3f88b8bf9274e79eeabf63afb4a737abc6c84ad37b"}, + {file = "scipy-1.13.1-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:5d72782f39716b2b3509cd7c33cdc08c96f2f4d2b06d51e52fb45a19ca0c86a1"}, + {file = "scipy-1.13.1-cp312-cp312-macosx_12_0_arm64.whl", hash = "sha256:017367484ce5498445aade74b1d5ab377acdc65e27095155e448c88497755a5d"}, + {file = "scipy-1.13.1-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:949ae67db5fa78a86e8fa644b9a6b07252f449dcf74247108c50e1d20d2b4627"}, + {file = "scipy-1.13.1-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:de3ade0e53bc1f21358aa74ff4830235d716211d7d077e340c7349bc3542e884"}, + {file = "scipy-1.13.1-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:2ac65fb503dad64218c228e2dc2d0a0193f7904747db43014645ae139c8fad16"}, + {file = "scipy-1.13.1-cp312-cp312-win_amd64.whl", hash = "sha256:cdd7dacfb95fea358916410ec61bbc20440f7860333aee6d882bb8046264e949"}, + {file = "scipy-1.13.1-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:436bbb42a94a8aeef855d755ce5a465479c721e9d684de76bf61a62e7c2b81d5"}, + {file = "scipy-1.13.1-cp39-cp39-macosx_12_0_arm64.whl", hash = "sha256:8335549ebbca860c52bf3d02f80784e91a004b71b059e3eea9678ba994796a24"}, + {file = "scipy-1.13.1-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:d533654b7d221a6a97304ab63c41c96473ff04459e404b83275b60aa8f4b7004"}, + {file = "scipy-1.13.1-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:637e98dcf185ba7f8e663e122ebf908c4702420477ae52a04f9908707456ba4d"}, + {file = "scipy-1.13.1-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:a014c2b3697bde71724244f63de2476925596c24285c7a637364761f8710891c"}, + {file = "scipy-1.13.1-cp39-cp39-win_amd64.whl", hash = "sha256:392e4ec766654852c25ebad4f64e4e584cf19820b980bc04960bca0b0cd6eaa2"}, + {file = "scipy-1.13.1.tar.gz", hash = "sha256:095a87a0312b08dfd6a6155cbbd310a8c51800fc931b8c0b84003014b874ed3c"}, +] + +[package.dependencies] +numpy = ">=1.22.4,<2.3" + +[package.extras] +dev = ["cython-lint (>=0.12.2)", "doit (>=0.36.0)", "mypy", "pycodestyle", "pydevtool", "rich-click", "ruff", "types-psutil", "typing_extensions"] +doc = ["jupyterlite-pyodide-kernel", "jupyterlite-sphinx (>=0.12.0)", "jupytext", "matplotlib (>=3.5)", "myst-nb", "numpydoc", "pooch", "pydata-sphinx-theme (>=0.15.2)", "sphinx (>=5.0.0)", "sphinx-design (>=0.4.0)"] +test = ["array-api-strict", "asv", "gmpy2", "hypothesis (>=6.30)", "mpmath", "pooch", "pytest", "pytest-cov", "pytest-timeout", "pytest-xdist", "scikit-umfpack", "threadpoolctl"] + +[[package]] +name = "semsql" +version = "0.3.3" +description = "" +optional = false +python-versions = ">=3.8,<4.0" +files = [ + {file = "semsql-0.3.3-py3-none-any.whl", hash = "sha256:7249cf1faf61dabf2605a06dd0955775e1adad2e462e3f95ebbb1b7caed0e54c"}, + {file = "semsql-0.3.3.tar.gz", hash = "sha256:af75543bbe7469b856f58653d490095527f3653c6b499e27a714c6da78f1d185"}, +] + +[package.dependencies] +click = ">=8.1.3,<9.0.0" +linkml-runtime = ">=1.2.15,<2.0.0" +SQLAlchemy-Utils = ">=0.38.2,<0.39.0" + +[[package]] +name = "six" +version = "1.16.0" +description = "Python 2 and 3 compatibility utilities" +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*" +files = [ + {file = "six-1.16.0-py2.py3-none-any.whl", hash = "sha256:8abb2f1d86890a2dfb989f9a77cfcfd3e47c2a354b01111771326f8aa26e0254"}, + {file = "six-1.16.0.tar.gz", hash = "sha256:1e61c37477a1626458e36f7b1d82aa5c9b094fa4802892072e49de9c60c4c926"}, +] + +[[package]] +name = "sniffio" +version = "1.3.1" +description = "Sniff out which async library your code is running under" +optional = false +python-versions = ">=3.7" +files = [ + {file = "sniffio-1.3.1-py3-none-any.whl", hash = "sha256:2f6da418d1f1e0fddd844478f41680e794e6051915791a034ff65e5f100525a2"}, + {file = "sniffio-1.3.1.tar.gz", hash = "sha256:f4324edc670a0f49750a81b895f35c3adb843cca46f0530f79fc1babb23789dc"}, +] + +[[package]] +name = "sortedcontainers" +version = "2.4.0" +description = "Sorted Containers -- Sorted List, Sorted Dict, Sorted Set" +optional = false +python-versions = "*" +files = [ + {file = "sortedcontainers-2.4.0-py2.py3-none-any.whl", hash = "sha256:a163dcaede0f1c021485e957a39245190e74249897e2ae4b2aa38595db237ee0"}, + {file = "sortedcontainers-2.4.0.tar.gz", hash = "sha256:25caa5a06cc30b6b83d11423433f65d1f9d76c4c6a0c90e3379eaa43b9bfdb88"}, +] + +[[package]] +name = "sparqlwrapper" +version = "2.0.0" +description = "SPARQL Endpoint interface to Python" +optional = false +python-versions = ">=3.7" +files = [ + {file = "SPARQLWrapper-2.0.0-py3-none-any.whl", hash = "sha256:c99a7204fff676ee28e6acef327dc1ff8451c6f7217dcd8d49e8872f324a8a20"}, + {file = "SPARQLWrapper-2.0.0.tar.gz", hash = "sha256:3fed3ebcc77617a4a74d2644b86fd88e0f32e7f7003ac7b2b334c026201731f1"}, +] + +[package.dependencies] +rdflib = ">=6.1.1" + +[package.extras] +dev = ["mypy (>=0.931)", "pandas (>=1.3.5)", "pandas-stubs (>=1.2.0.48)", "setuptools (>=3.7.1)"] +docs = ["sphinx (<5)", "sphinx-rtd-theme"] +keepalive = ["keepalive (>=0.5)"] +pandas = ["pandas (>=1.3.5)"] + +[[package]] +name = "sqlalchemy" +version = "2.0.30" +description = "Database Abstraction Library" +optional = false +python-versions = ">=3.7" +files = [ + {file = "SQLAlchemy-2.0.30-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:3b48154678e76445c7ded1896715ce05319f74b1e73cf82d4f8b59b46e9c0ddc"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:2753743c2afd061bb95a61a51bbb6a1a11ac1c44292fad898f10c9839a7f75b2"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a7bfc726d167f425d4c16269a9a10fe8630ff6d14b683d588044dcef2d0f6be7"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:c4f61ada6979223013d9ab83a3ed003ded6959eae37d0d685db2c147e9143797"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:3a365eda439b7a00732638f11072907c1bc8e351c7665e7e5da91b169af794af"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:bba002a9447b291548e8d66fd8c96a6a7ed4f2def0bb155f4f0a1309fd2735d5"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-win32.whl", hash = "sha256:0138c5c16be3600923fa2169532205d18891b28afa817cb49b50e08f62198bb8"}, + {file = "SQLAlchemy-2.0.30-cp310-cp310-win_amd64.whl", hash = "sha256:99650e9f4cf3ad0d409fed3eec4f071fadd032e9a5edc7270cd646a26446feeb"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:955991a09f0992c68a499791a753523f50f71a6885531568404fa0f231832aa0"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:f69e4c756ee2686767eb80f94c0125c8b0a0b87ede03eacc5c8ae3b54b99dc46"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:69c9db1ce00e59e8dd09d7bae852a9add716efdc070a3e2068377e6ff0d6fdaa"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:a1429a4b0f709f19ff3b0cf13675b2b9bfa8a7e79990003207a011c0db880a13"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:efedba7e13aa9a6c8407c48facfdfa108a5a4128e35f4c68f20c3407e4376aa9"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:16863e2b132b761891d6c49f0a0f70030e0bcac4fd208117f6b7e053e68668d0"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-win32.whl", hash = "sha256:2ecabd9ccaa6e914e3dbb2aa46b76dede7eadc8cbf1b8083c94d936bcd5ffb49"}, + {file = "SQLAlchemy-2.0.30-cp311-cp311-win_amd64.whl", hash = "sha256:0b3f4c438e37d22b83e640f825ef0f37b95db9aa2d68203f2c9549375d0b2260"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:5a79d65395ac5e6b0c2890935bad892eabb911c4aa8e8015067ddb37eea3d56c"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:9a5baf9267b752390252889f0c802ea13b52dfee5e369527da229189b8bd592e"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:3cb5a646930c5123f8461f6468901573f334c2c63c795b9af350063a736d0134"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:296230899df0b77dec4eb799bcea6fbe39a43707ce7bb166519c97b583cfcab3"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:c62d401223f468eb4da32627bffc0c78ed516b03bb8a34a58be54d618b74d472"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:3b69e934f0f2b677ec111b4d83f92dc1a3210a779f69bf905273192cf4ed433e"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-win32.whl", hash = "sha256:77d2edb1f54aff37e3318f611637171e8ec71472f1fdc7348b41dcb226f93d90"}, + {file = "SQLAlchemy-2.0.30-cp312-cp312-win_amd64.whl", hash = "sha256:b6c7ec2b1f4969fc19b65b7059ed00497e25f54069407a8701091beb69e591a5"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:5a8e3b0a7e09e94be7510d1661339d6b52daf202ed2f5b1f9f48ea34ee6f2d57"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:b60203c63e8f984df92035610c5fb76d941254cf5d19751faab7d33b21e5ddc0"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f1dc3eabd8c0232ee8387fbe03e0a62220a6f089e278b1f0aaf5e2d6210741ad"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-musllinux_1_1_aarch64.whl", hash = "sha256:40ad017c672c00b9b663fcfcd5f0864a0a97828e2ee7ab0c140dc84058d194cf"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-musllinux_1_1_x86_64.whl", hash = "sha256:e42203d8d20dc704604862977b1470a122e4892791fe3ed165f041e4bf447a1b"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-win32.whl", hash = "sha256:2a4f4da89c74435f2bc61878cd08f3646b699e7d2eba97144030d1be44e27584"}, + {file = "SQLAlchemy-2.0.30-cp37-cp37m-win_amd64.whl", hash = "sha256:b6bf767d14b77f6a18b6982cbbf29d71bede087edae495d11ab358280f304d8e"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:bc0c53579650a891f9b83fa3cecd4e00218e071d0ba00c4890f5be0c34887ed3"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:311710f9a2ee235f1403537b10c7687214bb1f2b9ebb52702c5aa4a77f0b3af7"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:408f8b0e2c04677e9c93f40eef3ab22f550fecb3011b187f66a096395ff3d9fd"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:37a4b4fb0dd4d2669070fb05b8b8824afd0af57587393015baee1cf9890242d9"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:a943d297126c9230719c27fcbbeab57ecd5d15b0bd6bfd26e91bfcfe64220621"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:0a089e218654e740a41388893e090d2e2c22c29028c9d1353feb38638820bbeb"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-win32.whl", hash = "sha256:fa561138a64f949f3e889eb9ab8c58e1504ab351d6cf55259dc4c248eaa19da6"}, + {file = "SQLAlchemy-2.0.30-cp38-cp38-win_amd64.whl", hash = "sha256:7d74336c65705b986d12a7e337ba27ab2b9d819993851b140efdf029248e818e"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:ae8c62fe2480dd61c532ccafdbce9b29dacc126fe8be0d9a927ca3e699b9491a"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:2383146973a15435e4717f94c7509982770e3e54974c71f76500a0136f22810b"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:8409de825f2c3b62ab15788635ccaec0c881c3f12a8af2b12ae4910a0a9aeef6"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:0094c5dc698a5f78d3d1539853e8ecec02516b62b8223c970c86d44e7a80f6c7"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:edc16a50f5e1b7a06a2dcc1f2205b0b961074c123ed17ebda726f376a5ab0953"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:f7703c2010355dd28f53deb644a05fc30f796bd8598b43f0ba678878780b6e4c"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-win32.whl", hash = "sha256:1f9a727312ff6ad5248a4367358e2cf7e625e98b1028b1d7ab7b806b7d757513"}, + {file = "SQLAlchemy-2.0.30-cp39-cp39-win_amd64.whl", hash = "sha256:a0ef36b28534f2a5771191be6edb44cc2673c7b2edf6deac6562400288664221"}, + {file = "SQLAlchemy-2.0.30-py3-none-any.whl", hash = "sha256:7108d569d3990c71e26a42f60474b4c02c8586c4681af5fd67e51a044fdea86a"}, + {file = "SQLAlchemy-2.0.30.tar.gz", hash = "sha256:2b1708916730f4830bc69d6f49d37f7698b5bd7530aca7f04f785f8849e95255"}, +] + +[package.dependencies] +greenlet = {version = "!=0.4.17", markers = "platform_machine == \"aarch64\" or platform_machine == \"ppc64le\" or platform_machine == \"x86_64\" or platform_machine == \"amd64\" or platform_machine == \"AMD64\" or platform_machine == \"win32\" or platform_machine == \"WIN32\""} +typing-extensions = ">=4.6.0" + +[package.extras] +aiomysql = ["aiomysql (>=0.2.0)", "greenlet (!=0.4.17)"] +aioodbc = ["aioodbc", "greenlet (!=0.4.17)"] +aiosqlite = ["aiosqlite", "greenlet (!=0.4.17)", "typing_extensions (!=3.10.0.1)"] +asyncio = ["greenlet (!=0.4.17)"] +asyncmy = ["asyncmy (>=0.2.3,!=0.2.4,!=0.2.6)", "greenlet (!=0.4.17)"] +mariadb-connector = ["mariadb (>=1.0.1,!=1.1.2,!=1.1.5)"] +mssql = ["pyodbc"] +mssql-pymssql = ["pymssql"] +mssql-pyodbc = ["pyodbc"] +mypy = ["mypy (>=0.910)"] +mysql = ["mysqlclient (>=1.4.0)"] +mysql-connector = ["mysql-connector-python"] +oracle = ["cx_oracle (>=8)"] +oracle-oracledb = ["oracledb (>=1.0.1)"] +postgresql = ["psycopg2 (>=2.7)"] +postgresql-asyncpg = ["asyncpg", "greenlet (!=0.4.17)"] +postgresql-pg8000 = ["pg8000 (>=1.29.1)"] +postgresql-psycopg = ["psycopg (>=3.0.7)"] +postgresql-psycopg2binary = ["psycopg2-binary"] +postgresql-psycopg2cffi = ["psycopg2cffi"] +postgresql-psycopgbinary = ["psycopg[binary] (>=3.0.7)"] +pymysql = ["pymysql"] +sqlcipher = ["sqlcipher3_binary"] + +[[package]] +name = "sqlalchemy-utils" +version = "0.38.3" +description = "Various utility functions for SQLAlchemy." +optional = false +python-versions = "~=3.6" +files = [ + {file = "SQLAlchemy-Utils-0.38.3.tar.gz", hash = "sha256:9f9afba607a40455cf703adfa9846584bf26168a0c5a60a70063b70d65051f4d"}, + {file = "SQLAlchemy_Utils-0.38.3-py3-none-any.whl", hash = "sha256:5c13b5d08adfaa85f3d4e8ec09a75136216fad41346980d02974a70a77988bf9"}, +] + +[package.dependencies] +SQLAlchemy = ">=1.3" + +[package.extras] +arrow = ["arrow (>=0.3.4)"] +babel = ["Babel (>=1.3)"] +color = ["colour (>=0.0.4)"] +encrypted = ["cryptography (>=0.6)"] +intervals = ["intervals (>=0.7.1)"] +password = ["passlib (>=1.6,<2.0)"] +pendulum = ["pendulum (>=2.0.5)"] +phone = ["phonenumbers (>=5.9.2)"] +test = ["Jinja2 (>=2.3)", "Pygments (>=1.2)", "backports.zoneinfo", "docutils (>=0.10)", "flake8 (>=2.4.0)", "flexmock (>=0.9.7)", "isort (>=4.2.2)", "pg8000 (>=1.12.4)", "psycopg2 (>=2.5.1)", "psycopg2cffi (>=2.8.1)", "pymysql", "pyodbc", "pytest (>=2.7.1)", "python-dateutil (>=2.6)", "pytz (>=2014.2)"] +test-all = ["Babel (>=1.3)", "Jinja2 (>=2.3)", "Pygments (>=1.2)", "arrow (>=0.3.4)", "backports.zoneinfo", "colour (>=0.0.4)", "cryptography (>=0.6)", "docutils (>=0.10)", "flake8 (>=2.4.0)", "flexmock (>=0.9.7)", "furl (>=0.4.1)", "intervals (>=0.7.1)", "isort (>=4.2.2)", "passlib (>=1.6,<2.0)", "pendulum (>=2.0.5)", "pg8000 (>=1.12.4)", "phonenumbers (>=5.9.2)", "psycopg2 (>=2.5.1)", "psycopg2cffi (>=2.8.1)", "pymysql", "pyodbc", "pytest (>=2.7.1)", "python-dateutil", "python-dateutil (>=2.6)", "pytz (>=2014.2)"] +timezone = ["python-dateutil"] +url = ["furl (>=0.4.1)"] + +[[package]] +name = "sssom" +version = "0.4.9" +description = "Operations on SSSOM mapping tables" +optional = false +python-versions = "<4.0,>=3.8" +files = [ + {file = "sssom-0.4.9-py3-none-any.whl", hash = "sha256:54af580957947175dfcc96e7ce2323ea3b476eb58b6e7a2e95d8c3e10c6393f4"}, + {file = "sssom-0.4.9.tar.gz", hash = "sha256:16674d58aa37ab82c1f6f69d317c0bdc6eedd59e8d809fcbc87f5f1e1eefdbf1"}, +] + +[package.dependencies] +click = ">=8.1.6" +curies = ">=0.7.3" +deprecation = ">=2.1.0,<3.0.0" +importlib-resources = ">=6.1.1,<7.0.0" +linkml-runtime = ">=1.7.5,<2.0.0" +networkx = {version = ">=3.1", extras = ["networkx"]} +pandas = ">1.0.3" +pansql = {version = ">=0.0.1", extras = ["pansql"]} +pyyaml = ">=6.0.1,<7.0.0" +rdflib = ">=6.0.0" +scipy = {version = "*", extras = ["scipy"]} +sparqlwrapper = ">=2.0.0" +sssom-schema = ">=0.15.2,<0.16.0" +validators = ">=0.20.0" + +[[package]] +name = "sssom-schema" +version = "0.15.2" +description = "SSSOM is a Simple Standard for Sharing Ontology Mappings." +optional = false +python-versions = "<4.0,>=3.8" +files = [ + {file = "sssom_schema-0.15.2-py3-none-any.whl", hash = "sha256:41112586160d5e57a7cfedab22dfd0c21d1e3e1a86805f7fe31918a9b664ca15"}, + {file = "sssom_schema-0.15.2.tar.gz", hash = "sha256:c759ee8f9e4a7e5e8249b58198189b2e48e297ff31a918d4af64a89ed30938da"}, +] + +[package.dependencies] +linkml-runtime = "*" + +[[package]] +name = "tenacity" +version = "8.3.0" +description = "Retry code until it succeeds" +optional = false +python-versions = ">=3.8" +files = [ + {file = "tenacity-8.3.0-py3-none-any.whl", hash = "sha256:3649f6443dbc0d9b01b9d8020a9c4ec7a1ff5f6f3c6c8a036ef371f573fe9185"}, + {file = "tenacity-8.3.0.tar.gz", hash = "sha256:953d4e6ad24357bceffbc9707bc74349aca9d245f68eb65419cf0c249a1949a2"}, +] + +[package.extras] +doc = ["reno", "sphinx"] +test = ["pytest", "tornado (>=4.5)", "typeguard"] + +[[package]] +name = "tiktoken" +version = "0.7.0" +description = "tiktoken is a fast BPE tokeniser for use with OpenAI's models" +optional = false +python-versions = ">=3.8" +files = [ + {file = "tiktoken-0.7.0-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:485f3cc6aba7c6b6ce388ba634fbba656d9ee27f766216f45146beb4ac18b25f"}, + {file = "tiktoken-0.7.0-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:e54be9a2cd2f6d6ffa3517b064983fb695c9a9d8aa7d574d1ef3c3f931a99225"}, + {file = "tiktoken-0.7.0-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:79383a6e2c654c6040e5f8506f3750db9ddd71b550c724e673203b4f6b4b4590"}, + {file = "tiktoken-0.7.0-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:5d4511c52caacf3c4981d1ae2df85908bd31853f33d30b345c8b6830763f769c"}, + {file = "tiktoken-0.7.0-cp310-cp310-musllinux_1_2_aarch64.whl", hash = "sha256:13c94efacdd3de9aff824a788353aa5749c0faee1fbe3816df365ea450b82311"}, + {file = "tiktoken-0.7.0-cp310-cp310-musllinux_1_2_x86_64.whl", hash = "sha256:8e58c7eb29d2ab35a7a8929cbeea60216a4ccdf42efa8974d8e176d50c9a3df5"}, + {file = "tiktoken-0.7.0-cp310-cp310-win_amd64.whl", hash = "sha256:21a20c3bd1dd3e55b91c1331bf25f4af522c525e771691adbc9a69336fa7f702"}, + {file = "tiktoken-0.7.0-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:10c7674f81e6e350fcbed7c09a65bca9356eaab27fb2dac65a1e440f2bcfe30f"}, + {file = "tiktoken-0.7.0-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:084cec29713bc9d4189a937f8a35dbdfa785bd1235a34c1124fe2323821ee93f"}, + {file = "tiktoken-0.7.0-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:811229fde1652fedcca7c6dfe76724d0908775b353556d8a71ed74d866f73f7b"}, + {file = "tiktoken-0.7.0-cp311-cp311-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:86b6e7dc2e7ad1b3757e8a24597415bafcfb454cebf9a33a01f2e6ba2e663992"}, + {file = "tiktoken-0.7.0-cp311-cp311-musllinux_1_2_aarch64.whl", hash = "sha256:1063c5748be36344c7e18c7913c53e2cca116764c2080177e57d62c7ad4576d1"}, + {file = "tiktoken-0.7.0-cp311-cp311-musllinux_1_2_x86_64.whl", hash = "sha256:20295d21419bfcca092644f7e2f2138ff947a6eb8cfc732c09cc7d76988d4a89"}, + {file = "tiktoken-0.7.0-cp311-cp311-win_amd64.whl", hash = "sha256:959d993749b083acc57a317cbc643fb85c014d055b2119b739487288f4e5d1cb"}, + {file = "tiktoken-0.7.0-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:71c55d066388c55a9c00f61d2c456a6086673ab7dec22dd739c23f77195b1908"}, + {file = "tiktoken-0.7.0-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:09ed925bccaa8043e34c519fbb2f99110bd07c6fd67714793c21ac298e449410"}, + {file = "tiktoken-0.7.0-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:03c6c40ff1db0f48a7b4d2dafeae73a5607aacb472fa11f125e7baf9dce73704"}, + {file = "tiktoken-0.7.0-cp312-cp312-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:d20b5c6af30e621b4aca094ee61777a44118f52d886dbe4f02b70dfe05c15350"}, + {file = "tiktoken-0.7.0-cp312-cp312-musllinux_1_2_aarch64.whl", hash = "sha256:d427614c3e074004efa2f2411e16c826f9df427d3c70a54725cae860f09e4bf4"}, + {file = "tiktoken-0.7.0-cp312-cp312-musllinux_1_2_x86_64.whl", hash = "sha256:8c46d7af7b8c6987fac9b9f61041b452afe92eb087d29c9ce54951280f899a97"}, + {file = "tiktoken-0.7.0-cp312-cp312-win_amd64.whl", hash = "sha256:0bc603c30b9e371e7c4c7935aba02af5994a909fc3c0fe66e7004070858d3f8f"}, + {file = "tiktoken-0.7.0-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:2398fecd38c921bcd68418675a6d155fad5f5e14c2e92fcf5fe566fa5485a858"}, + {file = "tiktoken-0.7.0-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:8f5f6afb52fb8a7ea1c811e435e4188f2bef81b5e0f7a8635cc79b0eef0193d6"}, + {file = "tiktoken-0.7.0-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:861f9ee616766d736be4147abac500732b505bf7013cfaf019b85892637f235e"}, + {file = "tiktoken-0.7.0-cp38-cp38-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:54031f95c6939f6b78122c0aa03a93273a96365103793a22e1793ee86da31685"}, + {file = "tiktoken-0.7.0-cp38-cp38-musllinux_1_2_aarch64.whl", hash = "sha256:fffdcb319b614cf14f04d02a52e26b1d1ae14a570f90e9b55461a72672f7b13d"}, + {file = "tiktoken-0.7.0-cp38-cp38-musllinux_1_2_x86_64.whl", hash = "sha256:c72baaeaefa03ff9ba9688624143c858d1f6b755bb85d456d59e529e17234769"}, + {file = "tiktoken-0.7.0-cp38-cp38-win_amd64.whl", hash = "sha256:131b8aeb043a8f112aad9f46011dced25d62629091e51d9dc1adbf4a1cc6aa98"}, + {file = "tiktoken-0.7.0-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:cabc6dc77460df44ec5b879e68692c63551ae4fae7460dd4ff17181df75f1db7"}, + {file = "tiktoken-0.7.0-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:8d57f29171255f74c0aeacd0651e29aa47dff6f070cb9f35ebc14c82278f3b25"}, + {file = "tiktoken-0.7.0-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:2ee92776fdbb3efa02a83f968c19d4997a55c8e9ce7be821ceee04a1d1ee149c"}, + {file = "tiktoken-0.7.0-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:e215292e99cb41fbc96988ef62ea63bb0ce1e15f2c147a61acc319f8b4cbe5bf"}, + {file = "tiktoken-0.7.0-cp39-cp39-musllinux_1_2_aarch64.whl", hash = "sha256:8a81bac94769cab437dd3ab0b8a4bc4e0f9cf6835bcaa88de71f39af1791727a"}, + {file = "tiktoken-0.7.0-cp39-cp39-musllinux_1_2_x86_64.whl", hash = "sha256:d6d73ea93e91d5ca771256dfc9d1d29f5a554b83821a1dc0891987636e0ae226"}, + {file = "tiktoken-0.7.0-cp39-cp39-win_amd64.whl", hash = "sha256:2bcb28ddf79ffa424f171dfeef9a4daff61a94c631ca6813f43967cb263b83b9"}, + {file = "tiktoken-0.7.0.tar.gz", hash = "sha256:1077266e949c24e0291f6c350433c6f0971365ece2b173a23bc3b9f9defef6b6"}, +] + +[package.dependencies] +regex = ">=2022.1.18" +requests = ">=2.26.0" + +[package.extras] +blobfile = ["blobfile (>=2)"] + +[[package]] +name = "tqdm" +version = "4.66.4" +description = "Fast, Extensible Progress Meter" +optional = false +python-versions = ">=3.7" +files = [ + {file = "tqdm-4.66.4-py3-none-any.whl", hash = "sha256:b75ca56b413b030bc3f00af51fd2c1a1a5eac6a0c1cca83cbb37a5c52abce644"}, + {file = "tqdm-4.66.4.tar.gz", hash = "sha256:e4d936c9de8727928f3be6079590e97d9abfe8d39a590be678eb5919ffc186bb"}, +] + +[package.dependencies] +colorama = {version = "*", markers = "platform_system == \"Windows\""} + +[package.extras] +dev = ["pytest (>=6)", "pytest-cov", "pytest-timeout", "pytest-xdist"] +notebook = ["ipywidgets (>=6)"] +slack = ["slack-sdk"] +telegram = ["requests"] + +[[package]] +name = "typing-extensions" +version = "4.12.2" +description = "Backported and Experimental Type Hints for Python 3.8+" +optional = false +python-versions = ">=3.8" +files = [ + {file = "typing_extensions-4.12.2-py3-none-any.whl", hash = "sha256:04e5ca0351e0f3f85c6853954072df659d0d13fac324d0072316b67d7794700d"}, + {file = "typing_extensions-4.12.2.tar.gz", hash = "sha256:1a7ead55c7e559dd4dee8856e3a88b41225abfe1ce8df57b7c13915fe121ffb8"}, +] + +[[package]] +name = "tzdata" +version = "2024.1" +description = "Provider of IANA time zone data" +optional = false +python-versions = ">=2" +files = [ + {file = "tzdata-2024.1-py2.py3-none-any.whl", hash = "sha256:9068bc196136463f5245e51efda838afa15aaeca9903f49050dfa2679db4d252"}, + {file = "tzdata-2024.1.tar.gz", hash = "sha256:2674120f8d891909751c38abcdfd386ac0a5a1127954fbc332af6b5ceae07efd"}, +] + +[[package]] +name = "url-normalize" +version = "1.4.3" +description = "URL normalization for Python" +optional = false +python-versions = ">=2.7, !=3.0.*, !=3.1.*, !=3.2.*, !=3.3.*, !=3.4.*, !=3.5.*" +files = [ + {file = "url-normalize-1.4.3.tar.gz", hash = "sha256:d23d3a070ac52a67b83a1c59a0e68f8608d1cd538783b401bc9de2c0fac999b2"}, + {file = "url_normalize-1.4.3-py2.py3-none-any.whl", hash = "sha256:ec3c301f04e5bb676d333a7fa162fa977ad2ca04b7e652bfc9fac4e405728eed"}, +] + +[package.dependencies] +six = "*" + +[[package]] +name = "urllib3" +version = "2.2.1" +description = "HTTP library with thread-safe connection pooling, file post, and more." +optional = false +python-versions = ">=3.8" +files = [ + {file = "urllib3-2.2.1-py3-none-any.whl", hash = "sha256:450b20ec296a467077128bff42b73080516e71b56ff59a60a02bef2232c4fa9d"}, + {file = "urllib3-2.2.1.tar.gz", hash = "sha256:d0570876c61ab9e520d776c38acbbb5b05a776d3f9ff98a5c8fd5162a444cf19"}, +] + +[package.extras] +brotli = ["brotli (>=1.0.9)", "brotlicffi (>=0.8.0)"] +h2 = ["h2 (>=4,<5)"] +socks = ["pysocks (>=1.5.6,!=1.5.7,<2.0)"] +zstd = ["zstandard (>=0.18.0)"] + +[[package]] +name = "validators" +version = "0.28.3" +description = "Python Data Validation for Humans™" +optional = false +python-versions = ">=3.8" +files = [ + {file = "validators-0.28.3-py3-none-any.whl", hash = "sha256:53cafa854f13850156259d9cc479b864ee901f6a96e6b109e6fc33f98f37d99f"}, + {file = "validators-0.28.3.tar.gz", hash = "sha256:c6c79840bcde9ba77b19f6218f7738188115e27830cbaff43264bc4ed24c429d"}, +] + +[[package]] +name = "wrapt" +version = "1.16.0" +description = "Module for decorators, wrappers and monkey patching." +optional = false +python-versions = ">=3.6" +files = [ + {file = "wrapt-1.16.0-cp310-cp310-macosx_10_9_x86_64.whl", hash = "sha256:ffa565331890b90056c01db69c0fe634a776f8019c143a5ae265f9c6bc4bd6d4"}, + {file = "wrapt-1.16.0-cp310-cp310-macosx_11_0_arm64.whl", hash = "sha256:e4fdb9275308292e880dcbeb12546df7f3e0f96c6b41197e0cf37d2826359020"}, + {file = "wrapt-1.16.0-cp310-cp310-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:bb2dee3874a500de01c93d5c71415fcaef1d858370d405824783e7a8ef5db440"}, + {file = "wrapt-1.16.0-cp310-cp310-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:2a88e6010048489cda82b1326889ec075a8c856c2e6a256072b28eaee3ccf487"}, + {file = "wrapt-1.16.0-cp310-cp310-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:ac83a914ebaf589b69f7d0a1277602ff494e21f4c2f743313414378f8f50a4cf"}, + {file = "wrapt-1.16.0-cp310-cp310-musllinux_1_1_aarch64.whl", hash = "sha256:73aa7d98215d39b8455f103de64391cb79dfcad601701a3aa0dddacf74911d72"}, + {file = "wrapt-1.16.0-cp310-cp310-musllinux_1_1_i686.whl", hash = "sha256:807cc8543a477ab7422f1120a217054f958a66ef7314f76dd9e77d3f02cdccd0"}, + {file = "wrapt-1.16.0-cp310-cp310-musllinux_1_1_x86_64.whl", hash = "sha256:bf5703fdeb350e36885f2875d853ce13172ae281c56e509f4e6eca049bdfb136"}, + {file = "wrapt-1.16.0-cp310-cp310-win32.whl", hash = "sha256:f6b2d0c6703c988d334f297aa5df18c45e97b0af3679bb75059e0e0bd8b1069d"}, + {file = "wrapt-1.16.0-cp310-cp310-win_amd64.whl", hash = "sha256:decbfa2f618fa8ed81c95ee18a387ff973143c656ef800c9f24fb7e9c16054e2"}, + {file = "wrapt-1.16.0-cp311-cp311-macosx_10_9_x86_64.whl", hash = "sha256:1a5db485fe2de4403f13fafdc231b0dbae5eca4359232d2efc79025527375b09"}, + {file = "wrapt-1.16.0-cp311-cp311-macosx_11_0_arm64.whl", hash = "sha256:75ea7d0ee2a15733684badb16de6794894ed9c55aa5e9903260922f0482e687d"}, + {file = "wrapt-1.16.0-cp311-cp311-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a452f9ca3e3267cd4d0fcf2edd0d035b1934ac2bd7e0e57ac91ad6b95c0c6389"}, + {file = "wrapt-1.16.0-cp311-cp311-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:43aa59eadec7890d9958748db829df269f0368521ba6dc68cc172d5d03ed8060"}, + {file = "wrapt-1.16.0-cp311-cp311-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:72554a23c78a8e7aa02abbd699d129eead8b147a23c56e08d08dfc29cfdddca1"}, + {file = "wrapt-1.16.0-cp311-cp311-musllinux_1_1_aarch64.whl", hash = "sha256:d2efee35b4b0a347e0d99d28e884dfd82797852d62fcd7ebdeee26f3ceb72cf3"}, + {file = "wrapt-1.16.0-cp311-cp311-musllinux_1_1_i686.whl", hash = "sha256:6dcfcffe73710be01d90cae08c3e548d90932d37b39ef83969ae135d36ef3956"}, + {file = "wrapt-1.16.0-cp311-cp311-musllinux_1_1_x86_64.whl", hash = "sha256:eb6e651000a19c96f452c85132811d25e9264d836951022d6e81df2fff38337d"}, + {file = "wrapt-1.16.0-cp311-cp311-win32.whl", hash = "sha256:66027d667efe95cc4fa945af59f92c5a02c6f5bb6012bff9e60542c74c75c362"}, + {file = "wrapt-1.16.0-cp311-cp311-win_amd64.whl", hash = "sha256:aefbc4cb0a54f91af643660a0a150ce2c090d3652cf4052a5397fb2de549cd89"}, + {file = "wrapt-1.16.0-cp312-cp312-macosx_10_9_x86_64.whl", hash = "sha256:5eb404d89131ec9b4f748fa5cfb5346802e5ee8836f57d516576e61f304f3b7b"}, + {file = "wrapt-1.16.0-cp312-cp312-macosx_11_0_arm64.whl", hash = "sha256:9090c9e676d5236a6948330e83cb89969f433b1943a558968f659ead07cb3b36"}, + {file = "wrapt-1.16.0-cp312-cp312-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:94265b00870aa407bd0cbcfd536f17ecde43b94fb8d228560a1e9d3041462d73"}, + {file = "wrapt-1.16.0-cp312-cp312-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:f2058f813d4f2b5e3a9eb2eb3faf8f1d99b81c3e51aeda4b168406443e8ba809"}, + {file = "wrapt-1.16.0-cp312-cp312-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:98b5e1f498a8ca1858a1cdbffb023bfd954da4e3fa2c0cb5853d40014557248b"}, + {file = "wrapt-1.16.0-cp312-cp312-musllinux_1_1_aarch64.whl", hash = "sha256:14d7dc606219cdd7405133c713f2c218d4252f2a469003f8c46bb92d5d095d81"}, + {file = "wrapt-1.16.0-cp312-cp312-musllinux_1_1_i686.whl", hash = "sha256:49aac49dc4782cb04f58986e81ea0b4768e4ff197b57324dcbd7699c5dfb40b9"}, + {file = "wrapt-1.16.0-cp312-cp312-musllinux_1_1_x86_64.whl", hash = "sha256:418abb18146475c310d7a6dc71143d6f7adec5b004ac9ce08dc7a34e2babdc5c"}, + {file = "wrapt-1.16.0-cp312-cp312-win32.whl", hash = "sha256:685f568fa5e627e93f3b52fda002c7ed2fa1800b50ce51f6ed1d572d8ab3e7fc"}, + {file = "wrapt-1.16.0-cp312-cp312-win_amd64.whl", hash = "sha256:dcdba5c86e368442528f7060039eda390cc4091bfd1dca41e8046af7c910dda8"}, + {file = "wrapt-1.16.0-cp36-cp36m-macosx_10_9_x86_64.whl", hash = "sha256:d462f28826f4657968ae51d2181a074dfe03c200d6131690b7d65d55b0f360f8"}, + {file = "wrapt-1.16.0-cp36-cp36m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:a33a747400b94b6d6b8a165e4480264a64a78c8a4c734b62136062e9a248dd39"}, + {file = "wrapt-1.16.0-cp36-cp36m-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:b3646eefa23daeba62643a58aac816945cadc0afaf21800a1421eeba5f6cfb9c"}, + {file = "wrapt-1.16.0-cp36-cp36m-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:3ebf019be5c09d400cf7b024aa52b1f3aeebeff51550d007e92c3c1c4afc2a40"}, + {file = "wrapt-1.16.0-cp36-cp36m-musllinux_1_1_aarch64.whl", hash = "sha256:0d2691979e93d06a95a26257adb7bfd0c93818e89b1406f5a28f36e0d8c1e1fc"}, + {file = "wrapt-1.16.0-cp36-cp36m-musllinux_1_1_i686.whl", hash = "sha256:1acd723ee2a8826f3d53910255643e33673e1d11db84ce5880675954183ec47e"}, + {file = "wrapt-1.16.0-cp36-cp36m-musllinux_1_1_x86_64.whl", hash = "sha256:bc57efac2da352a51cc4658878a68d2b1b67dbe9d33c36cb826ca449d80a8465"}, + {file = "wrapt-1.16.0-cp36-cp36m-win32.whl", hash = "sha256:da4813f751142436b075ed7aa012a8778aa43a99f7b36afe9b742d3ed8bdc95e"}, + {file = "wrapt-1.16.0-cp36-cp36m-win_amd64.whl", hash = "sha256:6f6eac2360f2d543cc875a0e5efd413b6cbd483cb3ad7ebf888884a6e0d2e966"}, + {file = "wrapt-1.16.0-cp37-cp37m-macosx_10_9_x86_64.whl", hash = "sha256:a0ea261ce52b5952bf669684a251a66df239ec6d441ccb59ec7afa882265d593"}, + {file = "wrapt-1.16.0-cp37-cp37m-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:7bd2d7ff69a2cac767fbf7a2b206add2e9a210e57947dd7ce03e25d03d2de292"}, + {file = "wrapt-1.16.0-cp37-cp37m-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:9159485323798c8dc530a224bd3ffcf76659319ccc7bbd52e01e73bd0241a0c5"}, + {file = "wrapt-1.16.0-cp37-cp37m-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:a86373cf37cd7764f2201b76496aba58a52e76dedfaa698ef9e9688bfd9e41cf"}, + {file = "wrapt-1.16.0-cp37-cp37m-musllinux_1_1_aarch64.whl", hash = "sha256:73870c364c11f03ed072dda68ff7aea6d2a3a5c3fe250d917a429c7432e15228"}, + {file = "wrapt-1.16.0-cp37-cp37m-musllinux_1_1_i686.whl", hash = "sha256:b935ae30c6e7400022b50f8d359c03ed233d45b725cfdd299462f41ee5ffba6f"}, + {file = "wrapt-1.16.0-cp37-cp37m-musllinux_1_1_x86_64.whl", hash = "sha256:db98ad84a55eb09b3c32a96c576476777e87c520a34e2519d3e59c44710c002c"}, + {file = "wrapt-1.16.0-cp37-cp37m-win32.whl", hash = "sha256:9153ed35fc5e4fa3b2fe97bddaa7cbec0ed22412b85bcdaf54aeba92ea37428c"}, + {file = "wrapt-1.16.0-cp37-cp37m-win_amd64.whl", hash = "sha256:66dfbaa7cfa3eb707bbfcd46dab2bc6207b005cbc9caa2199bcbc81d95071a00"}, + {file = "wrapt-1.16.0-cp38-cp38-macosx_10_9_x86_64.whl", hash = "sha256:1dd50a2696ff89f57bd8847647a1c363b687d3d796dc30d4dd4a9d1689a706f0"}, + {file = "wrapt-1.16.0-cp38-cp38-macosx_11_0_arm64.whl", hash = "sha256:44a2754372e32ab315734c6c73b24351d06e77ffff6ae27d2ecf14cf3d229202"}, + {file = "wrapt-1.16.0-cp38-cp38-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:8e9723528b9f787dc59168369e42ae1c3b0d3fadb2f1a71de14531d321ee05b0"}, + {file = "wrapt-1.16.0-cp38-cp38-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:dbed418ba5c3dce92619656802cc5355cb679e58d0d89b50f116e4a9d5a9603e"}, + {file = "wrapt-1.16.0-cp38-cp38-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:941988b89b4fd6b41c3f0bfb20e92bd23746579736b7343283297c4c8cbae68f"}, + {file = "wrapt-1.16.0-cp38-cp38-musllinux_1_1_aarch64.whl", hash = "sha256:6a42cd0cfa8ffc1915aef79cb4284f6383d8a3e9dcca70c445dcfdd639d51267"}, + {file = "wrapt-1.16.0-cp38-cp38-musllinux_1_1_i686.whl", hash = "sha256:1ca9b6085e4f866bd584fb135a041bfc32cab916e69f714a7d1d397f8c4891ca"}, + {file = "wrapt-1.16.0-cp38-cp38-musllinux_1_1_x86_64.whl", hash = "sha256:d5e49454f19ef621089e204f862388d29e6e8d8b162efce05208913dde5b9ad6"}, + {file = "wrapt-1.16.0-cp38-cp38-win32.whl", hash = "sha256:c31f72b1b6624c9d863fc095da460802f43a7c6868c5dda140f51da24fd47d7b"}, + {file = "wrapt-1.16.0-cp38-cp38-win_amd64.whl", hash = "sha256:490b0ee15c1a55be9c1bd8609b8cecd60e325f0575fc98f50058eae366e01f41"}, + {file = "wrapt-1.16.0-cp39-cp39-macosx_10_9_x86_64.whl", hash = "sha256:9b201ae332c3637a42f02d1045e1d0cccfdc41f1f2f801dafbaa7e9b4797bfc2"}, + {file = "wrapt-1.16.0-cp39-cp39-macosx_11_0_arm64.whl", hash = "sha256:2076fad65c6736184e77d7d4729b63a6d1ae0b70da4868adeec40989858eb3fb"}, + {file = "wrapt-1.16.0-cp39-cp39-manylinux_2_17_aarch64.manylinux2014_aarch64.whl", hash = "sha256:c5cd603b575ebceca7da5a3a251e69561bec509e0b46e4993e1cac402b7247b8"}, + {file = "wrapt-1.16.0-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:b47cfad9e9bbbed2339081f4e346c93ecd7ab504299403320bf85f7f85c7d46c"}, + {file = "wrapt-1.16.0-cp39-cp39-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:f8212564d49c50eb4565e502814f694e240c55551a5f1bc841d4fcaabb0a9b8a"}, + {file = "wrapt-1.16.0-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:5f15814a33e42b04e3de432e573aa557f9f0f56458745c2074952f564c50e664"}, + {file = "wrapt-1.16.0-cp39-cp39-musllinux_1_1_i686.whl", hash = "sha256:db2e408d983b0e61e238cf579c09ef7020560441906ca990fe8412153e3b291f"}, + {file = "wrapt-1.16.0-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:edfad1d29c73f9b863ebe7082ae9321374ccb10879eeabc84ba3b69f2579d537"}, + {file = "wrapt-1.16.0-cp39-cp39-win32.whl", hash = "sha256:ed867c42c268f876097248e05b6117a65bcd1e63b779e916fe2e33cd6fd0d3c3"}, + {file = "wrapt-1.16.0-cp39-cp39-win_amd64.whl", hash = "sha256:eb1b046be06b0fce7249f1d025cd359b4b80fc1c3e24ad9eca33e0dcdb2e4a35"}, + {file = "wrapt-1.16.0-py3-none-any.whl", hash = "sha256:6906c4100a8fcbf2fa735f6059214bb13b97f75b1a61777fcf6432121ef12ef1"}, + {file = "wrapt-1.16.0.tar.gz", hash = "sha256:5f370f952971e7d17c7d1ead40e49f32345a7f7a5373571ef44d800d06b1899d"}, +] + +[metadata] +lock-version = "2.0" +python-versions = "^3.11" +content-hash = "39cb350b0bc05b5cb3e8231f423b228c39ae5f8ab4966c43c48ee084f6f76ad7" diff --git a/src/scripts/notebooks/pyproject.toml b/src/scripts/notebooks/pyproject.toml new file mode 100644 index 0000000000..e52879e7d4 --- /dev/null +++ b/src/scripts/notebooks/pyproject.toml @@ -0,0 +1,17 @@ +[tool.poetry] +name = "mondo-ai" +version = "0.1.0" +description = "" +authors = ["Nico Matentzoglu "] +readme = "README.md" + +[tool.poetry.dependencies] +python = "^3.11" +oaklib = "^0.6.9" +langchain-core = "^0.2.7" +langchain-openai = "^0.1.8" + + +[build-system] +requires = ["poetry-core"] +build-backend = "poetry.core.masonry.api" diff --git a/src/scripts/notebooks/reviewed_mappings.tsv b/src/scripts/notebooks/reviewed_mappings.tsv new file mode 100644 index 0000000000..99796e7ea6 --- /dev/null +++ b/src/scripts/notebooks/reviewed_mappings.tsv @@ -0,0 +1,50 @@ +subject_id subject_label predicate_id predicate_modifier object_id object_label mapping_justification mapping_tool confidence subject_match_field object_match_field match_string comment +MONDO:0016733 ganglioglioma skos:closeMatch not NCIT:C27362 Childhood Ganglioglioma semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label childhood ganglioglioma The term 'ganglioglioma' is a broader category that includes both childhood and adult cases, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is not appropriate to consider them as close matches. +MONDO:0016733 ganglioglioma skos:exactMatch not NCIT:C27362 Childhood Ganglioglioma semapv:MappingChaining 0.475 The term 'ganglioglioma' encompasses both childhood and adult forms of the disease, whereas 'Childhood Ganglioglioma' is specific to pediatric cases. Therefore, it is incorrect to consider them as exact matches. +MONDO:0022096 pyogenic granuloma skos:closeMatch not NCIT:C3480 Lobular Capillary Hemangioma semapv:LexicalMatching oaklib 0.5 ['oio:hasRelatedSynonym'] ['rdfs:label'] lobular capillary hemangioma Pyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true. +MONDO:0022096 pyogenic granuloma skos:closeMatch not NCIT:C3480 Lobular Capillary Hemangioma semapv:LexicalMatching oaklib 0.5 ['oio:hasRelatedSynonym'] ['rdfs:label'] lobular capillary hemangioma Pyogenic granuloma, although sometimes used synonymously with lobular capillary hemangioma, can present in various forms not strictly classified as lobular capillary hemangiomas. Therefore, this mapping may not always hold true. +MONDO:0006292 malignant mesothelioma skos:closeMatch NCIT:C8420 Diffuse Malignant Mesothelioma semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label diffuse malignant mesothelioma +MONDO:0006292 malignant mesothelioma skos:exactMatch not NCIT:C8420 Diffuse Malignant Mesothelioma semapv:MappingChaining 0.475 The term 'malignant mesothelioma' is broader and not an exact match for 'Diffuse Malignant Mesothelioma'. +MONDO:0007959 medulloblastoma skos:closeMatch not NCIT:C27294 Localized Primitive Neuroectodermal Tumor semapv:LexicalMatching oaklib 0.5 ['oio:hasRelatedSynonym'] ['rdfs:label'] localized primitive neuroectodermal tumor Medulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor. +MONDO:0007959 medulloblastoma skos:exactMatch not NCIT:C27294 Localized Primitive Neuroectodermal Tumor semapv:MappingChaining 0.475 Medulloblastoma and Localized Primitive Neuroectodermal Tumor are distinct entities; medulloblastoma is a specific type of primitive neuroectodermal tumor but not synonymous with localized primitive neuroectodermal tumor. +MONDO:0006292 malignant mesothelioma skos:closeMatch not NCIT:C27926 Asbestos-Related Malignant Mesothelioma semapv:LexicalMatching oaklib 0.5 ['oio:hasNarrowSynonym'] ['rdfs:label'] ['asbestos-related malignant mesothelioma'] Malignant mesothelioma is a broader category that includes asbestos-related malignant mesothelioma as a subset. Therefore, this should not be a 'closeMatch'. +MONDO:0006292 malignant mesothelioma skos:exactMatch not NCIT:C27926 Asbestos-Related Malignant Mesothelioma semapv:MappingChaining 0.475 Malignant mesothelioma is a more general term than asbestos-related malignant mesothelioma. Therefore, they are not exact matches. +MONDO:0006312 myofibroma skos:closeMatch not NCIT:C27498 Infantile Hemangiopericytoma semapv:LexicalMatching oaklib 0.5 ['oio:hasRelatedSynonym'] ['rdfs:label'] ['infantile hemangiopericytoma'] Myofibroma and Infantile Hemangiopericytoma are distinct entities. Myofibroma is a benign neoplasm of myofibroblasts, whereas Infantile Hemangiopericytoma is a vascular tumor. The lexical match is misleading. +MONDO:0016824 infantile myofibromatosis skos:exactMatch NCIT:C27498 Infantile Hemangiopericytoma semapv:LexicalMatching oaklib 0.8 ['oio:hasExactSynonym'] ['rdfs:label'] ['infantile hemangiopericytoma'] Infantile myofibromatosis and Infantile Hemangiopericytoma are different conditions. Infantile myofibromatosis is characterized by the presence of multiple myofibromas, while Infantile Hemangiopericytoma is a rare vascular tumor. The lexical match does not imply they are the same disease. +MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch NCIT:C192096 Intratubular Embryonal Carcinoma semapv:LexicalMatching oaklib 0.8 ['oio:hasExactSynonym'] ['rdfs:label'] ['intratubular embryonal carcinoma'] +MONDO:0004520 intratubular embryonal carcinoma skos:exactMatch NCIT:C192096 Intratubular Embryonal Carcinoma semapv:LexicalMatching oaklib 0.849779 ['rdfs:label'] ['rdfs:label'] ['intratubular embryonal carcinoma'] +MONDO:0018177 glioblastoma skos:exactMatch not NCIT:C39750 Glioblastoma, IDH-Wildtype semapv:MappingChaining 0.475 The subject label 'glioblastoma' is too general to be an exact match for 'Glioblastoma, IDH-Wildtype', as the latter specifies a particular genetic subtype. +MONDO:0850335 IDH-wildtype glioblastoma skos:exactMatch NCIT:C39750 Glioblastoma, IDH-Wildtype semapv:MappingChaining 0.475 This mapping is correct as 'IDH-wildtype glioblastoma' accurately matches 'Glioblastoma, IDH-Wildtype'. +MONDO:0003766 thalamic cancer skos:closeMatch not NCIT:C6221 Thalamic Neoplasm semapv:LexicalMatching oaklib 0.5 ['oio:hasRelatedSynonym'] ['rdfs:label'] thalamic neoplasm Thalamic cancer and thalamic neoplasm are not exact matches; cancer is a type of neoplasm, but a neoplasm does not necessarily imply malignancy. +MONDO:0003766 thalamic cancer skos:exactMatch not NCIT:C6221 Thalamic Neoplasm semapv:MappingChaining 0.475 Thalamic cancer is a specific type of thalamic neoplasm. An exact match is not appropriate due to the broader scope of 'neoplasm' compared to 'cancer'. +MONDO:0016733 ganglioglioma skos:closeMatch not NCIT:C27363 Adult Ganglioglioma semapv:LexicalMatching oaklib 0.5 oio:hasNarrowSynonym rdfs:label adult ganglioglioma Ganglioglioma is a broad category, whereas Adult Ganglioglioma specifically refers to a subset of gangliogliomas occurring in adults. A close match is not appropriate; it should be a narrower match. +MONDO:0016733 ganglioglioma skos:exactMatch not NCIT:C27363 Adult Ganglioglioma semapv:MappingChaining 0.475 Ganglioglioma is a general term that includes various subtypes, including those in adults and children. An exact match is not appropriate because Adult Ganglioglioma is a more specific condition. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['oio:hasDbXref-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semapv:LexicalMatching oaklib 0.5 ['rdf:ID'] ['skos:relatedMatch-INVERSE'] ['mondo:0000503'] Duplicate row: Lung adenocarcinoma in situ is a different type of carcinoma and not equivalent to Stage 0 Lung Adenosquamous Carcinoma. +MONDO:0000503 lung adenocarcinoma in situ skos:closeMatch not NCIT:C8748 Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7 semap +MONDO:0015686 primary peritoneal carcinoma skos:exactMatch not NCIT:C4182 Serous Surface Papillary Carcinoma semapv:LexicalMatching oaklib 0.8 oio:hasExactSynonym rdfs:label serous surface papillary carcinoma The term 'primary peritoneal carcinoma' is broader than 'Serous Surface Papillary Carcinoma' and not specific enough to consider an exact match. +MONDO:0002368 papillary serous cystadenocarcinoma skos:exactMatch NCIT:C4182 Serous Surface Papillary Carcinoma semapv:MappingChaining 0.475 Generated by matching the object of a Mondo mapping to the object of a source mapping. +MONDO:0006055 sex cord-stromal tumor skos:closeMatch not NCIT:C39948 Malignant Testicular Sex Cord-Stromal Tumor semapv:LexicalMatching oaklib 0.5 ['oio:hasNarrowSynonym'] ['rdfs:label'] malignant testicular sex cord-stromal tumor The subject 'sex cord-stromal tumor' is a broader term and does not specifically refer to 'malignant testicular sex cord-stromal tumor'. +MONDO:0003125 testicular sex cord-stromal neoplasm skos:exactMatch NCIT:C39948 Malignant Testicular Sex Cord-Stromal Tumor semapv:MappingChaining 0.475 Generated by matching the object of a Mondo mapping to the object of a source mapping. +MONDO:0016642 meningioma skos:closeMatch not NCIT:C7048 Supratentorial Meningioma semapv:LexicalMatching oaklib 0.5 oio:hasRelatedSynonym rdfs:label supratentorial meningioma The subject label 'meningioma' is too broad compared to the specific term 'Supratentorial Meningioma'. Hence, this is not a close match. +MONDO:0850303 supratentorial meningioma skos:exactMatch NCIT:C7048 Supratentorial Meningioma semapv:LexicalMatching oaklib 0.849779 rdfs:label rdfs:label supratentorial meningioma +MONDO:0011655 alveolar soft part sarcoma skos:closeMatch NCIT:C8092 Childhood Alveolar Soft Part Sarcoma semapv:LexicalMatching oaklib 0.5 ['oio:hasNarrowSynonym'] ['rdfs:label'] ['childhood alveolar soft part sarcoma'] +MONDO:0011655 alveolar soft part sarcoma skos:exactMatch not NCIT:C8092 Childhood Alveolar Soft Part Sarcoma semapv:MappingChaining 0.475 Generated by matching the object of a Mondo mapping to the object of a source mapping. Alveolar soft part sarcoma is a broader term and not an exact match for Childhood Alveolar Soft Part Sarcoma. diff --git a/src/scripts/notebooks/sssom_pydantic.py b/src/scripts/notebooks/sssom_pydantic.py new file mode 100644 index 0000000000..3021c51299 --- /dev/null +++ b/src/scripts/notebooks/sssom_pydantic.py @@ -0,0 +1,249 @@ +from __future__ import annotations +from datetime import datetime, date +from enum import Enum +from typing import List, Dict, Optional, Any, Union +from pydantic import BaseModel as BaseModel, ConfigDict, Field +import sys +if sys.version_info >= (3, 8): + from typing import Literal +else: + from typing_extensions import Literal + + +metamodel_version = "None" +version = "None" + +class WeakRefShimBaseModel(BaseModel): + __slots__ = '__weakref__' + +class ConfiguredBaseModel(WeakRefShimBaseModel, + validate_assignment = True, + validate_all = True, + underscore_attrs_are_private = True, + extra = 'forbid', + arbitrary_types_allowed = True, + use_enum_values = True): + pass + + +class EntityTypeEnum(str, Enum): + + + owl_class = "owl class" + + owl_object_property = "owl object property" + + owl_data_property = "owl data property" + + owl_annotation_property = "owl annotation property" + + owl_named_individual = "owl named individual" + + skos_concept = "skos concept" + + rdfs_resource = "rdfs resource" + + rdfs_class = "rdfs class" + + rdfs_literal = "rdfs literal" + + rdfs_datatype = "rdfs datatype" + + rdf_property = "rdf property" + + + +class PredicateModifierEnum(str, Enum): + + # Negating the mapping predicate. The meaning of the triple becomes subject_id is not a predicate_id match to object_id. + Not = "Not" + + + +class MappingCardinalityEnum(str, Enum): + + # One-to-one mapping + number_1COLON1 = "1:1" + # One-to-many mapping + number_1COLONn = "1:n" + # Many-to-one mapping + nCOLON1 = "n:1" + # One-to-none mapping + number_1COLON0 = "1:0" + # None-to-one mapping + number_0COLON1 = "0:1" + # Many-to-many mapping + nCOLONn = "n:n" + + + +class MappingSet(ConfiguredBaseModel): + """ + Represents a set of mappings + """ + curie_map: Optional[Dict[str, Prefix]] = Field(default_factory=dict, description="""A dictionary that contains prefixes as keys and their URI expansions as values.""") + mappings: Optional[List[Mapping]] = Field(default_factory=list, description="""Contains a list of mapping objects""") + mapping_set_id: str = Field(..., description="""A globally unique identifier for the mapping set (not each individual mapping). Should be IRI, ideally resolvable.""") + mapping_set_version: Optional[str] = Field(None, description="""A version string for the mapping.""") + mapping_set_source: Optional[List[str]] = Field(default_factory=list, description="""A mapping set or set of mapping set that was used to derive the mapping set.""") + mapping_set_title: Optional[str] = Field(None, description="""The display name of a mapping set.""") + mapping_set_description: Optional[str] = Field(None, description="""A description of the mapping set.""") + creator_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups responsible for the creation of the mapping. The creator is the agent that put the mapping in its published form, which may be different from the author, which is a person that was actively involved in the assertion of the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + creator_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the creator of this mapping. In the spirit of provenance, consider using creator_id instead.""") + license: str = Field(..., description="""A url to the license of the mapping. In absence of a license we assume no license.""") + subject_type: Optional[EntityTypeEnum] = Field(None, description="""The type of entity that is being mapped.""") + subject_source: Optional[str] = Field(None, description="""URI of vocabulary or identifier source for the subject.""") + subject_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the subject term.""") + object_type: Optional[EntityTypeEnum] = Field(None, description="""The type of entity that is being mapped.""") + object_source: Optional[str] = Field(None, description="""URI of vocabulary or identifier source for the object.""") + object_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the object term.""") + mapping_provider: Optional[str] = Field(None, description="""URL pointing to the source that provided the mapping, for example an ontology that already contains the mappings, or a database from which it was derived.""") + mapping_tool: Optional[str] = Field(None, description="""A reference to the tool or algorithm that was used to generate the mapping. Should be a URL pointing to more info about it, but can be free text.""") + mapping_tool_version: Optional[str] = Field(None, description="""Version string that denotes the version of the mapping tool used.""") + mapping_date: Optional[date] = Field(None, description="""The date the mapping was asserted. This is different from the date the mapping was published or compiled in a SSSOM file.""") + publication_date: Optional[date] = Field(None, description="""The date the mapping was published. This is different from the date the mapping was asserted.""") + subject_match_field: Optional[List[str]] = Field(default_factory=list, description="""A list of properties (term annotations on the subject) that was used for the match.""") + object_match_field: Optional[List[str]] = Field(default_factory=list, description="""A list of properties (term annotations on the object) that was used for the match.""") + subject_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the fields of the subject. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.""") + object_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the fields of the object. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.""") + see_also: Optional[List[str]] = Field(default_factory=list, description="""A URL specific for the mapping instance. E.g. for kboom we have a per-mapping image that shows surrounding axioms that drive probability. Could also be a github issue URL that discussed a complicated alignment""") + issue_tracker: Optional[str] = Field(None, description="""A URL location of the issue tracker for this entity.""") + other: Optional[str] = Field(None, description="""Pipe separated list of key value pairs for properties not part of the SSSOM spec. Can be used to encode additional provenance data.""") + comment: Optional[str] = Field(None, description="""Free text field containing either curator notes or text generated by tool providing additional informative information.""") + + +class Mapping(ConfiguredBaseModel): + """ + Represents an individual mapping between a pair of entities + """ + subject_id: str = Field(..., description="""The ID of the subject of the mapping.""") + subject_label: Optional[str] = Field(None, description="""The label of subject of the mapping""") + subject_category: Optional[str] = Field(None, description="""The conceptual category to which the subject belongs to. This can be a string denoting the category or a term from a controlled vocabulary. This slot is deliberately underspecified. Conceptual categories can range from those that are found in general upper ontologies such as BFO (e.g. process, temporal region, etc) to those that serve as upper ontologies in specific domains, such as COB or BioLink (e.g. gene, disease, chemical entity). The purpose of this optional field is documentation for human reviewers - when a category is known and documented clearly, the cost of interpreting and evaluating the mapping decreases.""") + predicate_id: str = Field(..., description="""The ID of the predicate or relation that relates the subject and object of this match.""") + predicate_label: Optional[str] = Field(None, description="""The label of the predicate/relation of the mapping""") + predicate_modifier: Optional[PredicateModifierEnum] = Field(None, description="""A modifier for negating the prediate. See https://github.com/mapping-commons/sssom/issues/40 for discussion""") + object_id: str = Field(..., description="""The ID of the object of the mapping.""") + object_label: Optional[str] = Field(None, description="""The label of object of the mapping""") + object_category: Optional[str] = Field(None, description="""The conceptual category to which the subject belongs to. This can be a string denoting the category or a term from a controlled vocabulary. This slot is deliberately underspecified. Conceptual categories can range from those that are found in general upper ontologies such as BFO (e.g. process, temporal region, etc) to those that serve as upper ontologies in specific domains, such as COB or BioLink (e.g. gene, disease, chemical entity). The purpose of this optional field is documentation for human reviewers - when a category is known and documented clearly, the cost of interpreting and evaluating the mapping decreases.""") + mapping_justification: str = Field(..., description="""A mapping justification is an action (or the written representation of that action) of showing a mapping to be right or reasonable.""") + author_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups responsible for asserting the mappings. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + author_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the author of this mapping. In the spirit of provenance, consider using author_id instead.""") + reviewer_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups that reviewed and confirmed the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + reviewer_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the reviewer of this mapping. In the spirit of provenance, consider using reviewer_id instead.""") + creator_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups responsible for the creation of the mapping. The creator is the agent that put the mapping in its published form, which may be different from the author, which is a person that was actively involved in the assertion of the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + creator_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the creator of this mapping. In the spirit of provenance, consider using creator_id instead.""") + license: Optional[str] = Field(None, description="""A url to the license of the mapping. In absence of a license we assume no license.""") + subject_type: Optional[EntityTypeEnum] = Field(None, description="""The type of entity that is being mapped.""") + subject_source: Optional[str] = Field(None, description="""URI of vocabulary or identifier source for the subject.""") + subject_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the subject term.""") + object_type: Optional[EntityTypeEnum] = Field(None, description="""The type of entity that is being mapped.""") + object_source: Optional[str] = Field(None, description="""URI of vocabulary or identifier source for the object.""") + object_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the object term.""") + mapping_provider: Optional[str] = Field(None, description="""URL pointing to the source that provided the mapping, for example an ontology that already contains the mappings, or a database from which it was derived.""") + mapping_source: Optional[str] = Field(None, description="""The mapping set this mapping was originally defined in. mapping_source is used for example when merging multiple mapping sets or deriving one mapping set from another.""") + mapping_cardinality: Optional[MappingCardinalityEnum] = Field(None, description="""A string indicating whether this mapping is from a 1:1 (the subject_id maps to a single object_id), 1:n (the subject maps to more than one object_id), n:1, 1:0, 0:1 or n:n group. Note that this is a convenience field that should be derivable from the mapping set.""") + mapping_tool: Optional[str] = Field(None, description="""A reference to the tool or algorithm that was used to generate the mapping. Should be a URL pointing to more info about it, but can be free text.""") + mapping_tool_version: Optional[str] = Field(None, description="""Version string that denotes the version of the mapping tool used.""") + mapping_date: Optional[date] = Field(None, description="""The date the mapping was asserted. This is different from the date the mapping was published or compiled in a SSSOM file.""") + publication_date: Optional[date] = Field(None, description="""The date the mapping was published. This is different from the date the mapping was asserted.""") + confidence: Optional[float] = Field(None, description="""A score between 0 and 1 to denote the confidence or probability that the match is correct, where 1 denotes total confidence.""") + curation_rule: Optional[List[str]] = Field(default_factory=list, description="""A curation rule is a (potentially) complex condition executed by an agent that led to the establishment of a mapping. Curation rules often involve complex domain-specific considerations, which are hard to capture in an automated fashion. The curation rule is captured as a resource rather than a string, which enables higher levels of transparency and sharing across mapping sets. The URI representation of the curation rule is expected to be a resolvable identifier which provides details about the nature of the curation rule.""") + curation_rule_text: Optional[List[str]] = Field(default_factory=list, description="""A curation rule is a (potentially) complex condition executed by an agent that led to the establishment of a mapping. Curation rules often involve complex domain-specific considerations, which are hard to capture in an automated fashion. The curation rule should be captured as a resource (entity reference) rather than a string (see curation_rule element), which enables higher levels of transparency and sharing across mapping sets. The textual representation of curation rule is intended to be used in cases where (1) the creation of a resource is not practical from the perspective of the mapping_provider and (2) as an additional piece of metadata to augment the curation_rule element with a human readable text.""") + subject_match_field: Optional[List[str]] = Field(default_factory=list, description="""A list of properties (term annotations on the subject) that was used for the match.""") + object_match_field: Optional[List[str]] = Field(default_factory=list, description="""A list of properties (term annotations on the object) that was used for the match.""") + match_string: Optional[List[str]] = Field(default_factory=list, description="""String that is shared by subj/obj. It is recommended to indicate the fields for the match using the object and subject_match_field slots.""") + subject_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the fields of the subject. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.""") + object_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the fields of the object. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.""") + semantic_similarity_score: Optional[float] = Field(None, description="""A score between 0 and 1 to denote the semantic similarity, where 1 denotes equivalence.""") + semantic_similarity_measure: Optional[str] = Field(None, description="""The measure used for computing the the semantic similarity score. To make processing this field as unambiguous as possible, we recommend using wikidata identifiers, but wikipedia pages could also be acceptable.""") + see_also: Optional[List[str]] = Field(default_factory=list, description="""A URL specific for the mapping instance. E.g. for kboom we have a per-mapping image that shows surrounding axioms that drive probability. Could also be a github issue URL that discussed a complicated alignment""") + issue_tracker_item: Optional[str] = Field(None, description="""The issue tracker item discussing this mapping.""") + other: Optional[str] = Field(None, description="""Pipe separated list of key value pairs for properties not part of the SSSOM spec. Can be used to encode additional provenance data.""") + comment: Optional[str] = Field(None, description="""Free text field containing either curator notes or text generated by tool providing additional informative information.""") + + +class LiteralMapping(ConfiguredBaseModel): + """ + Represents an individual mapping between a literal and an entity. Note that this schema has been created on 01.08.2023 and is subject to change. + """ + literal: str = Field(..., description="""The literal being mapped""") + literal_datatype: Optional[str] = Field(None, description="""The datatype of the literal being mapped""") + predicate_id: str = Field(..., description="""The ID of the predicate or relation that relates the subject and object of this match.""") + predicate_label: Optional[str] = Field(None, description="""The label of the predicate/relation of the mapping""") + predicate_modifier: Optional[PredicateModifierEnum] = Field(None, description="""A modifier for negating the prediate. See https://github.com/mapping-commons/sssom/issues/40 for discussion""") + object_id: str = Field(..., description="""The ID of the object of the mapping.""") + object_label: Optional[str] = Field(None, description="""The label of object of the mapping""") + object_category: Optional[str] = Field(None, description="""The conceptual category to which the subject belongs to. This can be a string denoting the category or a term from a controlled vocabulary. This slot is deliberately underspecified. Conceptual categories can range from those that are found in general upper ontologies such as BFO (e.g. process, temporal region, etc) to those that serve as upper ontologies in specific domains, such as COB or BioLink (e.g. gene, disease, chemical entity). The purpose of this optional field is documentation for human reviewers - when a category is known and documented clearly, the cost of interpreting and evaluating the mapping decreases.""") + mapping_justification: str = Field(..., description="""A mapping justification is an action (or the written representation of that action) of showing a mapping to be right or reasonable.""") + author_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups responsible for asserting the mappings. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + author_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the author of this mapping. In the spirit of provenance, consider using author_id instead.""") + reviewer_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups that reviewed and confirmed the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + reviewer_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the reviewer of this mapping. In the spirit of provenance, consider using reviewer_id instead.""") + creator_id: Optional[List[str]] = Field(default_factory=list, description="""Identifies the persons or groups responsible for the creation of the mapping. The creator is the agent that put the mapping in its published form, which may be different from the author, which is a person that was actively involved in the assertion of the mapping. Recommended to be a list of ORCIDs or otherwise identifying URIs.""") + creator_label: Optional[List[str]] = Field(default_factory=list, description="""A string identifying the creator of this mapping. In the spirit of provenance, consider using creator_id instead.""") + license: Optional[str] = Field(None, description="""A url to the license of the mapping. In absence of a license we assume no license.""") + literal_source: Optional[str] = Field(None, description="""URI of ontology source for the literal.""") + literal_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the literal.""") + object_type: Optional[EntityTypeEnum] = Field(None, description="""The type of entity that is being mapped.""") + object_source: Optional[str] = Field(None, description="""URI of vocabulary or identifier source for the object.""") + object_source_version: Optional[str] = Field(None, description="""Version IRI or version string of the source of the object term.""") + mapping_provider: Optional[str] = Field(None, description="""URL pointing to the source that provided the mapping, for example an ontology that already contains the mappings, or a database from which it was derived.""") + mapping_source: Optional[str] = Field(None, description="""The mapping set this mapping was originally defined in. mapping_source is used for example when merging multiple mapping sets or deriving one mapping set from another.""") + mapping_cardinality: Optional[MappingCardinalityEnum] = Field(None, description="""A string indicating whether this mapping is from a 1:1 (the subject_id maps to a single object_id), 1:n (the subject maps to more than one object_id), n:1, 1:0, 0:1 or n:n group. Note that this is a convenience field that should be derivable from the mapping set.""") + mapping_tool: Optional[str] = Field(None, description="""A reference to the tool or algorithm that was used to generate the mapping. Should be a URL pointing to more info about it, but can be free text.""") + mapping_tool_version: Optional[str] = Field(None, description="""Version string that denotes the version of the mapping tool used.""") + mapping_date: Optional[date] = Field(None, description="""The date the mapping was asserted. This is different from the date the mapping was published or compiled in a SSSOM file.""") + confidence: Optional[float] = Field(None, description="""A score between 0 and 1 to denote the confidence or probability that the match is correct, where 1 denotes total confidence.""") + object_match_field: Optional[List[str]] = Field(default_factory=list, description="""A list of properties (term annotations on the object) that was used for the match.""") + match_string: Optional[List[str]] = Field(default_factory=list, description="""String that is shared by subj/obj. It is recommended to indicate the fields for the match using the object and subject_match_field slots.""") + literal_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the literal.""") + object_preprocessing: Optional[List[str]] = Field(default_factory=list, description="""Method of preprocessing applied to the fields of the object. If different preprocessing steps were performed on different fields, it is recommended to store the match in separate rows.""") + similarity_score: Optional[float] = Field(None, description="""A score between 0 and 1 to denote the similarity, where 1 denotes equivalence.""") + similarity_measure: Optional[str] = Field(None, description="""The measure used for computing the the similarity score. To make processing this field as unambiguous as possible, we recommend using wikidata identifiers, but wikipedia pages could also be acceptable.""") + see_also: Optional[List[str]] = Field(default_factory=list, description="""A URL specific for the mapping instance. E.g. for kboom we have a per-mapping image that shows surrounding axioms that drive probability. Could also be a github issue URL that discussed a complicated alignment""") + other: Optional[str] = Field(None, description="""Pipe separated list of key value pairs for properties not part of the SSSOM spec. Can be used to encode additional provenance data.""") + comment: Optional[str] = Field(None, description="""Free text field containing either curator notes or text generated by tool providing additional informative information.""") + + +class MappingRegistry(ConfiguredBaseModel): + """ + A registry for managing mapping sets. It holds a set of mapping set references, and can import other registries. + """ + mapping_registry_id: str = Field(..., description="""The unique identifier of a mapping registry.""") + mapping_registry_title: Optional[str] = Field(None, description="""The title of a mapping registry.""") + mapping_registry_description: Optional[str] = Field(None, description="""The description of a mapping registry.""") + imports: Optional[List[str]] = Field(default_factory=list, description="""A list of registries that should be imported into this one.""") + mapping_set_references: Optional[List[MappingSetReference]] = Field(default_factory=list, description="""A list of mapping set references.""") + documentation: Optional[str] = Field(None, description="""A URL to the documentation of this mapping commons.""") + homepage: Optional[str] = Field(None, description="""A URL to a homepage of this mapping commons.""") + issue_tracker: Optional[str] = Field(None, description="""A URL location of the issue tracker for this entity.""") + + +class MappingSetReference(ConfiguredBaseModel): + """ + A reference to a mapping set. It allows to augment mapping set metadata from the perspective of the registry, for example, providing confidence, or a local filename or a grouping. + """ + mapping_set_id: str = Field(..., description="""A globally unique identifier for the mapping set (not each individual mapping). Should be IRI, ideally resolvable.""") + mirror_from: Optional[str] = Field(None, description="""A URL location from which to obtain a resource, such as a mapping set.""") + registry_confidence: Optional[float] = Field(None, description="""This value is set by the registry that indexes the mapping set. It reflects the confidence the registry has in the correctness of the mappings in the mapping set.""") + mapping_set_group: Optional[str] = Field(None, description="""Set by the owners of the mapping registry. A way to group .""") + last_updated: Optional[date] = Field(None, description="""The date this reference was last updated.""") + local_name: Optional[str] = Field(None, description="""The local name assigned to file that corresponds to the downloaded mapping set.""") + + +class Prefix(ConfiguredBaseModel): + + prefix_name: str = Field(...) + prefix_url: Optional[str] = Field(None) + + + +# Update forward refs +# see https://pydantic-docs.helpmanual.io/usage/postponed_annotations/ +MappingSet.update_forward_refs() +Mapping.update_forward_refs() +LiteralMapping.update_forward_refs() +MappingRegistry.update_forward_refs() +MappingSetReference.update_forward_refs() +Prefix.update_forward_refs() + diff --git a/src/sparql/reports/all_synonym_data.sparql b/src/sparql/reports/all_synonym_data.sparql new file mode 100644 index 0000000000..7541d8f7c5 --- /dev/null +++ b/src/sparql/reports/all_synonym_data.sparql @@ -0,0 +1,37 @@ +PREFIX skos: +PREFIX rdf: +PREFIX rdfs: +PREFIX IAO: +PREFIX OMO: +PREFIX MONDO: +PREFIX owl: +prefix oboInOwl: + +# description: Checks if a proper obsolesence reason was documented for this class + +SELECT ?entity ?synonym ?synonym_property ?xref ?st1 ?st2 WHERE { + VALUES ?synonym_property { + oboInOwl:hasExactSynonym + oboInOwl:hasRelatedSynonym + oboInOwl:hasBroadSynonym + oboInOwl:hasNarrowSynonym + rdfs:label + } + ?entity ?synonym_property ?synonym . + FILTER (isIRI(?entity) && STRSTARTS(str(?entity), "http://purl.obolibrary.org/obo/MONDO_")) + + OPTIONAL { + ?ax owl:annotatedSource ?entity ; + owl:annotatedProperty ?synonym_property ; + owl:annotatedTarget ?synonym ; + oboInOwl:hasDbXref ?xref . + OPTIONAL { + ?ax oboInOwl:hasSynonymType ?st1 . + } + OPTIONAL { + ?ax oboInOwl:hasSynonymType ?st2 . + FILTER(?st1!=?st2) + } + } + +} \ No newline at end of file diff --git a/src/sparql/reports/clingen-non-exact.sparql b/src/sparql/reports/clingen-non-exact.sparql new file mode 100644 index 0000000000..330c1372c6 --- /dev/null +++ b/src/sparql/reports/clingen-non-exact.sparql @@ -0,0 +1,20 @@ +PREFIX rdf: +PREFIX rdfs: +PREFIX IAO: +PREFIX OMO: +PREFIX MONDO: +PREFIX owl: +prefix oboInOwl: + +# description: Checks if a proper obsolesence reason was documented for this class + +SELECT ?entity ?label ?value ?synonym_property WHERE { + ?entity rdfs:label ?label . + VALUES ?synonym_property { oboInOwl:hasRelatedSynonym oboInOwl:hasNarrowSynonym oboInOwl:hasBroadSynonym oboInOwl:hasCloseSynonym } + [] owl:annotatedSource ?entity ; + owl:annotatedProperty ?synonym_property ; + owl:annotatedTarget ?value ; + oboInOwl:hasSynonymType . + + FILTER (isIRI(?entity) && STRSTARTS(str(?entity), "http://purl.obolibrary.org/obo/MONDO_")) +} \ No newline at end of file diff --git a/src/sparql/reports/efo-preferred-external.sparql b/src/sparql/reports/efo-preferred-external.sparql new file mode 100644 index 0000000000..f0b0d896d7 --- /dev/null +++ b/src/sparql/reports/efo-preferred-external.sparql @@ -0,0 +1,19 @@ +PREFIX skos: +PREFIX rdf: +PREFIX rdfs: +PREFIX IAO: +PREFIX OMO: +PREFIX MONDO: +PREFIX owl: +prefix oboInOwl: + +# description: Checks if a proper obsolesence reason was documented for this class + +SELECT ?entity ?xref WHERE { + [] owl:annotatedSource ?entity ; + owl:annotatedProperty oboInOwl:hasDbXref ; + owl:annotatedTarget ?xref ; + oboInOwl:source "MONDO:preferredExternal" . + FILTER (isIRI(?entity) && STRSTARTS(str(?entity), "http://purl.obolibrary.org/obo/MONDO_")) + FILTER(STRSTARTS(?xref,"EFO:")) +} \ No newline at end of file diff --git a/src/sparql/reports/ordo_obsolete_disorder.sparql b/src/sparql/reports/ordo_obsolete_disorder.sparql new file mode 100644 index 0000000000..baf508abe9 --- /dev/null +++ b/src/sparql/reports/ordo_obsolete_disorder.sparql @@ -0,0 +1,32 @@ +PREFIX owl: +PREFIX skos: +PREFIX rdf: +PREFIX rdfs: +prefix oio: +PREFIX MONDO: +SELECT + +?mondo_curie ?label +(GROUP_CONCAT(DISTINCT STR(?xref); separator="|") as ?xrefs) +(GROUP_CONCAT(DISTINCT STR(?subset); separator=", ") as ?subsets) +(GROUP_CONCAT(DISTINCT STR(?exact_match); separator=", ") as ?exact_matches) + +WHERE { + ?mondo_id owl:deprecated true . + ?mondo_id oio:inSubset . + + OPTIONAL { + ?mondo_id rdfs:label ?label . + } + OPTIONAL { + ?mondo_id oio:inSubset ?subset . + } + OPTIONAL { + ?mondo_id oio:hasDbXref ?xref . + } + OPTIONAL { + ?mondo_id skos:exactMatch ?exact_match . + } + BIND(REPLACE(REPLACE(STR(?mondo_id),"http://purl.obolibrary.org/obo/",""),"_",":") as ?mondo_curie) + +} GROUP BY ?mondo_curie ?label \ No newline at end of file diff --git a/src/sparql/reports/rare-inferred-report.sparql b/src/sparql/reports/rare-inferred-report.sparql new file mode 100644 index 0000000000..e4558bc406 --- /dev/null +++ b/src/sparql/reports/rare-inferred-report.sparql @@ -0,0 +1,24 @@ +prefix IAO: +prefix rdfs: +prefix oio: +prefix def: +prefix owl: +PREFIX xsd: + +SELECT ?cls ?label (GROUP_CONCAT(DISTINCT STR(?parent); separator="|") as ?parent_ids) (GROUP_CONCAT(DISTINCT STR(?parent_label); separator="|") as ?parent_labels) + +WHERE +{ + + ?cls . + ?cls rdfs:label ?label . + ?cls rdfs:subClassOf ?parent . + ?parent rdfs:label ?parent_label . + ?parent . + + FILTER NOT EXISTS { + ?parent . + } + + FILTER( !isBlank(?cls) && STRSTARTS(str(?cls), "http://purl.obolibrary.org/obo/MONDO_")) +} GROUP BY ?cls ?label \ No newline at end of file diff --git a/src/sparql/reports/rare_subset_analysis.sparql b/src/sparql/reports/rare_subset_analysis.sparql new file mode 100644 index 0000000000..79ef204a6e --- /dev/null +++ b/src/sparql/reports/rare_subset_analysis.sparql @@ -0,0 +1,711 @@ +PREFIX owl: +PREFIX xsd: +PREFIX rdf: +PREFIX rdfs: +PREFIX oio: +PREFIX MONDO: + +SELECT ?mondo_curie ?label ?deprecated + (IF(BOUND(?subset_rare), "yes", "no") AS ?rare) + (IF(BOUND(?subset_gard_rare), "yes", "no") AS ?gard) + (IF(BOUND(?subset_orphanet_rare), "yes", "no") AS ?orphanet) + (IF(BOUND(?subset_nord_rare), "yes", "no") AS ?nord) + (IF(BOUND(?subset_mondo_rare), "yes", "no") AS ?mondo_rare) + (IF(BOUND(?subset_clingen), "yes", "no") AS ?clingen) + (IF(BOUND(?subset_disease_grouping), "yes", "no") AS ?general_grouping) + (IF(BOUND(?subset_rare_grouping), "yes", "no") AS ?rare_grouping) + (IF(BOUND(?subset_inferred_rare), "yes", "no") AS ?inferred_rare) + (IF(BOUND(?subset_obsoletion_candidate), "yes", "no") AS ?obsoletion_candidate) + (IF(BOUND(?subset_ordo_clinical_subtype), "yes", "no") AS ?ordo_disorder_subtype) + (IF(BOUND(?subset_ordo_group_of_disorders), "yes", "no") AS ?ordo_group_of_disorders) + (IF(BOUND(?subset_ordo_disorder), "yes", "no") AS ?ordo_disorder) + (GROUP_CONCAT(DISTINCT STR(?xref); separator="|") as ?xrefs) + (GROUP_CONCAT(DISTINCT STR(?ancestor_label); separator=", ") as ?ancestors) + +WHERE { + + # These are 636 or so Mondo + # VALUES ?mondo_id { + # MONDO:0100569 + # MONDO:0100161 + # MONDO:0958303 + # MONDO:0020813 + # MONDO:0011163 + # MONDO:0005361 + # MONDO:0016312 + # MONDO:0017975 + # MONDO:0005550 + # MONDO:0958328 + # MONDO:0013920 + # MONDO:0957991 + # MONDO:0700242 + # MONDO:0021500 + # MONDO:0013253 + # MONDO:0019722 + # MONDO:0011450 + # MONDO:0000927 + # MONDO:0018738 + # MONDO:0700234 + # MONDO:0013092 + # MONDO:0019288 + # MONDO:0957993 + # MONDO:0014680 + # MONDO:0958197 + # MONDO:0957912 + # MONDO:0023179 + # MONDO:0006215 + # MONDO:0012933 + # MONDO:0800480 + # MONDO:0958356 + # MONDO:0012763 + # MONDO:0700261 + # MONDO:0958017 + # MONDO:0957922 + # MONDO:0800464 + # MONDO:0021154 + # MONDO:0100564 + # MONDO:0011739 + # MONDO:0007810 + # MONDO:0018230 + # MONDO:0012042 + # MONDO:0040671 + # MONDO:0012134 + # MONDO:0020725 + # MONDO:0968944 + # MONDO:0005071 + # MONDO:0018102 + # MONDO:0011917 + # MONDO:0800419 + # MONDO:0023910 + # MONDO:0004397 + # MONDO:0012952 + # MONDO:0957953 + # MONDO:0013108 + # MONDO:0012823 + # MONDO:0005267 + # MONDO:0011941 + # MONDO:0700228 + # MONDO:0018548 + # MONDO:0009741 + # MONDO:0024573 + # MONDO:0958179 + # MONDO:0800183 + # MONDO:0020010 + # MONDO:0957807 + # MONDO:0011741 + # MONDO:0968959 + # MONDO:0007190 + # MONDO:0013568 + # MONDO:0015714 + # MONDO:0800468 + # MONDO:0016017 + # MONDO:0014429 + # MONDO:0007488 + # MONDO:0800463 + # MONDO:0002409 + # MONDO:0957809 + # MONDO:0012935 + # MONDO:0002281 + # MONDO:0010640 + # MONDO:0017902 + # MONDO:0012936 + # MONDO:0019146 + # MONDO:0016005 + # MONDO:0012843 + # MONDO:0012842 + # MONDO:0700244 + # MONDO:0800187 + # MONDO:0007028 + # MONDO:0004995 + # MONDO:0958332 + # MONDO:0014710 + # MONDO:0700041 + # MONDO:0957319 + # MONDO:0013084 + # MONDO:0020120 + # MONDO:0019755 + # MONDO:0013427 + # MONDO:0003250 + # MONDO:0957572 + # MONDO:0956993 + # MONDO:0014774 + # MONDO:0043537 + # MONDO:0013340 + # MONDO:0700236 + # MONDO:0958174 + # MONDO:0008067 + # MONDO:0957780 + # MONDO:0000088 + # MONDO:0859050 + # MONDO:0008856 + # MONDO:0012953 + # MONDO:0016330 + # MONDO:0013639 + # MONDO:0013957 + # MONDO:0700237 + # MONDO:0958233 + # MONDO:0045044 + # MONDO:0012655 + # MONDO:0958235 + # MONDO:0957872 + # MONDO:0100559 + # MONDO:0003939 + # MONDO:0956987 + # MONDO:0013096 + # MONDO:0007275 + # MONDO:0017901 + # MONDO:0017863 + # MONDO:0958176 + # MONDO:0800483 + # MONDO:0006065 + # MONDO:0006217 + # MONDO:0021522 + # MONDO:0003749 + # MONDO:0005385 + # MONDO:0005093 + # MONDO:0002356 + # MONDO:0957921 + # MONDO:0005137 + # MONDO:0010564 + # MONDO:0011164 + # MONDO:0023865 + # MONDO:0016677 + # MONDO:0012606 + # MONDO:0005150 + # MONDO:0016064 + # MONDO:0017772 + # MONDO:0008226 + # MONDO:0958183 + # MONDO:0000645 + # MONDO:0013086 + # MONDO:0004067 + # MONDO:0019040 + # MONDO:0016231 + # MONDO:0004298 + # MONDO:0957577 + # MONDO:0001479 + # MONDO:0013094 + # MONDO:0957822 + # MONDO:0957870 + # MONDO:0023243 + # MONDO:0013193 + # MONDO:0005172 + # MONDO:0100536 + # MONDO:0013633 + # MONDO:0003832 + # MONDO:0958162 + # MONDO:0100553 + # MONDO:0013045 + # MONDO:0021515 + # MONDO:0018173 + # MONDO:0957874 + # MONDO:0800479 + # MONDO:0007783 + # MONDO:0958354 + # MONDO:0957984 + # MONDO:0022454 + # MONDO:0958236 + # MONDO:0012934 + # MONDO:0957813 + # MONDO:0700003 + # MONDO:0041052 + # MONDO:0006476 + # MONDO:0017903 + # MONDO:0100301 + # MONDO:0957871 + # MONDO:0956984 + # MONDO:0700238 + # MONDO:0013088 + # MONDO:0060671 + # MONDO:0956995 + # MONDO:0007573 + # MONDO:0012595 + # MONDO:0035547 + # MONDO:0014241 + # MONDO:0006107 + # MONDO:0013510 + # MONDO:0012161 + # MONDO:0850126 + # MONDO:0013908 + # MONDO:0100570 + # MONDO:0100537 + # MONDO:0005066 + # MONDO:0012942 + # MONDO:0005411 + # MONDO:0956990 + # MONDO:0010833 + # MONDO:0700259 + # MONDO:0021001 + # MONDO:0013921 + # MONDO:0007966 + # MONDO:0958018 + # MONDO:0012141 + # MONDO:0002081 + # MONDO:0000816 + # MONDO:0019278 + # MONDO:0100173 + # MONDO:0021512 + # MONDO:0011361 + # MONDO:0021484 + # MONDO:0958330 + # MONDO:0021468 + # MONDO:0700273 + # MONDO:0957954 + # MONDO:0958241 + # MONDO:0007476 + # MONDO:0012144 + # MONDO:0958199 + # MONDO:0006104 + # MONDO:0958189 + # MONDO:0005039 + # MONDO:0054754 + # MONDO:0958161 + # MONDO:0016103 + # MONDO:0019632 + # MONDO:0013235 + # MONDO:0020581 + # MONDO:0001761 + # MONDO:0021511 + # MONDO:0700233 + # MONDO:0006823 + # MONDO:0013956 + # MONDO:0016037 + # MONDO:0958226 + # MONDO:0016105 + # MONDO:0000631 + # MONDO:0100561 + # MONDO:0015967 + # MONDO:0015925 + # MONDO:0958234 + # MONDO:0958023 + # MONDO:0700257 + # MONDO:0011607 + # MONDO:0002602 + # MONDO:0012951 + # MONDO:0011696 + # MONDO:0100544 + # MONDO:0700232 + # MONDO:0958326 + # MONDO:0958035 + # MONDO:0024623 + # MONDO:0000259 + # MONDO:0800470 + # MONDO:0029000 + # MONDO:0957935 + # MONDO:0700260 + # MONDO:0700253 + # MONDO:0011742 + # MONDO:0958012 + # MONDO:0958185 + # MONDO:0100542 + # MONDO:0958188 + # MONDO:0021759 + # MONDO:0013383 + # MONDO:0700231 + # MONDO:0958184 + # MONDO:0024458 + # MONDO:0958333 + # MONDO:0013954 + # MONDO:0012466 + # MONDO:0013876 + # MONDO:0002451 + # MONDO:0005061 + # MONDO:0020058 + # MONDO:0020636 + # MONDO:0004335 + # MONDO:0015713 + # MONDO:0958009 + # MONDO:0003220 + # MONDO:0957524 + # MONDO:0012159 + # MONDO:0013257 + # MONDO:0100199 + # MONDO:0957875 + # MONDO:0700262 + # MONDO:0700248 + # MONDO:0021166 + # MONDO:0045024 + # MONDO:0004994 + # MONDO:0013562 + # MONDO:0958180 + # MONDO:0010565 + # MONDO:0956967 + # MONDO:8000018 + # MONDO:0014502 + # MONDO:0012954 + # MONDO:0017256 + # MONDO:0000373 + # MONDO:0012318 + # MONDO:0958331 + # MONDO:0008608 + # MONDO:0800460 + # MONDO:0958182 + # MONDO:0958202 + # MONDO:0015914 + # MONDO:0700272 + # MONDO:0017204 + # MONDO:0957820 + # MONDO:0008399 + # MONDO:0958165 + # MONDO:0003620 + # MONDO:0958302 + # MONDO:0008685 + # MONDO:0004907 + # MONDO:0800424 + # MONDO:0013083 + # MONDO:0014902 + # MONDO:0021527 + # MONDO:0013669 + # MONDO:0044619 + # MONDO:0958352 + # MONDO:0957811 + # MONDO:0013185 + # MONDO:0958190 + # MONDO:0005570 + # MONDO:0100562 + # MONDO:0056805 + # MONDO:0957197 + # MONDO:0017014 + # MONDO:0007939 + # MONDO:0700224 + # MONDO:0700249 + # MONDO:0034212 + # MONDO:0012889 + # MONDO:0016226 + # MONDO:0043455 + # MONDO:0011775 + # MONDO:0700270 + # MONDO:0017900 + # MONDO:0000387 + # MONDO:0019290 + # MONDO:0021477 + # MONDO:0020530 + # MONDO:0958343 + # MONDO:0016242 + # MONDO:0019283 + # MONDO:0958351 + # MONDO:0012955 + # MONDO:0032667 + # MONDO:0100563 + # MONDO:0021443 + # MONDO:0958175 + # MONDO:0005775 + # MONDO:0100538 + # MONDO:0016225 + # MONDO:0009500 + # MONDO:0002118 + # MONDO:0023180 + # MONDO:0014017 + # MONDO:0001245 + # MONDO:0019544 + # MONDO:0956981 + # MONDO:0021048 + # MONDO:0007628 + # MONDO:0013109 + # MONDO:0012482 + # MONDO:0968951 + # MONDO:0004139 + # MONDO:0002145 + # MONDO:0957876 + # MONDO:0013095 + # MONDO:0016625 + # MONDO:0850144 + # MONDO:0032644 + # MONDO:0011954 + # MONDO:0957788 + # MONDO:0700258 + # MONDO:0005046 + # MONDO:0800434 + # MONDO:0958334 + # MONDO:0003333 + # MONDO:0700235 + # MONDO:0957999 + # MONDO:0700247 + # MONDO:0014281 + # MONDO:0700243 + # MONDO:0019056 + # MONDO:0968974 + # MONDO:0700227 + # MONDO:0004148 + # MONDO:0100539 + # MONDO:0958022 + # MONDO:0019296 + # MONDO:0011800 + # MONDO:0011348 + # MONDO:0006103 + # MONDO:0001357 + # MONDO:0100550 + # MONDO:0005349 + # MONDO:0035548 + # MONDO:0100543 + # MONDO:0017019 + # MONDO:0011931 + # MONDO:0956966 + # MONDO:0012132 + # MONDO:0957196 + # MONDO:0012822 + # MONDO:0018643 + # MONDO:0956992 + # MONDO:0956994 + # MONDO:0956964 + # MONDO:0007940 + # MONDO:0006858 + # MONDO:0958353 + # MONDO:0957825 + # MONDO:0019956 + # MONDO:0958006 + # MONDO:0957988 + # MONDO:0013384 + # MONDO:0005062 + # MONDO:0957783 + # MONDO:0002025 + # MONDO:0013097 + # MONDO:0700263 + # MONDO:0003900 + # MONDO:0044764 + # MONDO:0019293 + # MONDO:0100502 + # MONDO:0800433 + # MONDO:0007964 + # MONDO:0100567 + # MONDO:0019512 + # MONDO:0100546 + # MONDO:0956996 + # MONDO:0008410 + # MONDO:0958187 + # MONDO:0019054 + # MONDO:0956991 + # MONDO:0024498 + # MONDO:0016752 + # MONDO:0011207 + # MONDO:0015871 + # MONDO:0957978 + # MONDO:0800469 + # MONDO:0013653 + # MONDO:0009518 + # MONDO:0013665 + # MONDO:0007972 + # MONDO:0958000 + # MONDO:0958230 + # MONDO:0100534 + # MONDO:0010834 + # MONDO:0019530 + # MONDO:0700256 + # MONDO:0003924 + # MONDO:0020212 + # MONDO:0700239 + # MONDO:0005087 + # MONDO:0958013 + # MONDO:0011627 + # MONDO:0002051 + # MONDO:0019545 + # MONDO:0007723 + # MONDO:0957873 + # MONDO:0800435 + # MONDO:0700229 + # MONDO:0968955 + # MONDO:0100565 + # MONDO:0007845 + # MONDO:0019289 + # MONDO:0968946 + # MONDO:0005045 + # MONDO:0005020 + # MONDO:0011695 + # MONDO:0956965 + # MONDO:0968949 + # MONDO:0032867 + # MONDO:0014056 + # MONDO:0957958 + # MONDO:0014232 + # MONDO:0800462 + # MONDO:0021483 + # MONDO:0014251 + # MONDO:0001356 + # MONDO:0859310 + # MONDO:0014038 + # MONDO:0958335 + # MONDO:0008327 + # MONDO:0003847 + # MONDO:0957580 + # MONDO:0957819 + # MONDO:0020759 + # MONDO:0800484 + # MONDO:0017026 + # MONDO:0013236 + # MONDO:0012820 + # MONDO:0013955 + # MONDO:0017394 + # MONDO:0958201 + # MONDO:0016511 + # MONDO:0030781 + # MONDO:0012627 + # MONDO:0018908 + # MONDO:0003054 + # MONDO:0013685 + # MONDO:0044970 + # MONDO:0021439 + # MONDO:0700274 + # MONDO:0958324 + # MONDO:0011182 + # MONDO:0013085 + # MONDO:0958164 + # MONDO:0958277 + # MONDO:0044070 + # MONDO:0002280 + # MONDO:0956962 + # MONDO:0018741 + # MONDO:0018754 + # MONDO:0022714 + # MONDO:0100535 + # MONDO:0010389 + # MONDO:0700271 + # MONDO:0011896 + # MONDO:0958181 + # MONDO:0011860 + # MONDO:0957578 + # MONDO:0700250 + # MONDO:0017859 + # MONDO:0013759 + # MONDO:0018547 + # MONDO:0800418 + # MONDO:0012821 + # MONDO:0956988 + # MONDO:0000827 + # MONDO:0007745 + # MONDO:0020439 + # MONDO:0012931 + # MONDO:0002254 + # MONDO:0700245 + # MONDO:0008905 + # MONDO:0958034 + # MONDO:0700240 + # MONDO:0015337 + # MONDO:0013631 + # MONDO:0008570 + # MONDO:0016010 + # MONDO:0700096 + # MONDO:0100566 + # MONDO:0016004 + # MONDO:0002667 + # MONDO:0800472 + # MONDO:0700241 + # MONDO:0001703 + # MONDO:0000499 + # MONDO:0017168 + # MONDO:0013577 + # MONDO:0957928 + # MONDO:0800420 + # MONDO:0958192 + # MONDO:0958195 + # MONDO:0012710 + # MONDO:0958177 + # MONDO:0700268 + # MONDO:0019294 + # MONDO:0007963 + # MONDO:0800467 + # MONDO:0035350 + # MONDO:0012898 + # MONDO:0957992 + # MONDO:0100488 + # MONDO:0957595 + # MONDO:0019268 + # MONDO:0958204 + # MONDO:0004149 + # MONDO:0012888 + # MONDO:0700269 + # MONDO:0100317 + # MONDO:0957812 + # MONDO:0010282 + # MONDO:0100003 + # MONDO:0958228 + # MONDO:0009335 + # MONDO:0000638 + # MONDO:0017905 + # MONDO:0958194 + # MONDO:0958232 + # MONDO:0013093 + # MONDO:0956997 + # MONDO:0000070 + # MONDO:0958239 + # MONDO:0008231 + # MONDO:0012673 + # MONDO:0800485 + # MONDO:0957303 + # MONDO:0014494 + # MONDO:0958200 + # MONDO:0054750 + # MONDO:0800423 + # MONDO:0012183 + # MONDO:0700267 + # MONDO:0005151 + # MONDO:0010893 + # MONDO:0100242 + # MONDO:0012839 + # MONDO:0957824 + # MONDO:0023178 + # MONDO:0958357 + # MONDO:0800458 + # MONDO:0020637 + # MONDO:0024462 + # MONDO:0958355 + # MONDO:0800465 + # MONDO:0958325 + # MONDO:0001341 + # MONDO:0013133 + # MONDO:0033619 + # MONDO:0006220 + # MONDO:0956983 + # MONDO:0013020 + # MONDO:0030376 + # MONDO:0021147 + # MONDO:0012682 + # } + + OPTIONAL { ?mondo_id rdfs:label ?label . } + OPTIONAL { + VALUES ?rare_ancestor_subset { + + + + + } + ?mondo_id rdfs:subClassOf* ?ancestor . ?ancestor rdfs:label ?ancestor_label . ?ancestor oio:inSubset ?rare_ancestor_subset . + FILTER(STRSTARTS(str(?ancestor), "http://purl.obolibrary.org/obo/MONDO_")) } + OPTIONAL { ?mondo_id oio:hasDbXref ?xref . } + OPTIONAL { ?mondo_id oio:inSubset ?subset_rare . FILTER(STR(?subset_rare) = "http://purl.obolibrary.org/obo/mondo#rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_gard_rare . FILTER(STR(?subset_gard_rare) = "http://purl.obolibrary.org/obo/mondo#gard_rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_orphanet_rare . FILTER(STR(?subset_orphanet_rare) = "http://purl.obolibrary.org/obo/mondo#orphanet_rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_mondo_rare . FILTER(STR(?subset_mondo_rare) = "http://purl.obolibrary.org/obo/mondo#mondo_rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_nord_rare . FILTER(STR(?subset_nord_rare) = "http://purl.obolibrary.org/obo/mondo#nord_rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_disease_grouping . FILTER(STR(?subset_disease_grouping) = "http://purl.obolibrary.org/obo/mondo#disease_grouping") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_inferred_rare . FILTER(STR(?subset_inferred_rare) = "http://purl.obolibrary.org/obo/mondo#inferred_rare") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_obsoletion_candidate . FILTER(STR(?subset_obsoletion_candidate) = "http://purl.obolibrary.org/obo/mondo#obsoletion_candidate") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_rare_grouping . FILTER(STR(?subset_rare_grouping) = "http://purl.obolibrary.org/obo/mondo#rare_grouping") } + OPTIONAL { ?mondo_id owl:deprecated ?deprecated . } + OPTIONAL { ?mondo_id oio:inSubset ?subset_ordo_clinical_subtype . FILTER(STR(?subset_ordo_clinical_subtype) = "http://purl.obolibrary.org/obo/mondo#ordo_clinical_subtype") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_ordo_group_of_disorders . FILTER(STR(?subset_ordo_group_of_disorders) = "http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_clingen . FILTER(STR(?subset_clingen) = "http://purl.obolibrary.org/obo/mondo#clingen") } + OPTIONAL { ?mondo_id oio:inSubset ?subset_ordo_disorder . FILTER(STR(?subset_ordo_disorder) = "http://purl.obolibrary.org/obo/mondo#ordo_disorder") } + BIND(REPLACE(REPLACE(STR(?mondo_id),"http://purl.obolibrary.org/obo/",""),"_",":") as ?mondo_curie) + FILTER (isIRI(?mondo_id) && STRSTARTS(str(?mondo_id), "http://purl.obolibrary.org/obo/MONDO_")) +} GROUP BY ?mondo_curie ?label ?deprecated +?rare +?gard +?orphanet +?nord +?mondo_rare +?clingen +?general_grouping ?rare_grouping ?inferred_rare ?obsoletion_candidate ?ordo_disorder_subtype ?ordo_group_of_disorders ?ordo_disorder +?subset_rare +?subset_gard_rare +?subset_orphanet_rare +?subset_nord_rare +?subset_clingen +?subset_disease_grouping +?subset_rare_grouping +?subset_inferred_rare +?subset_obsoletion_candidate +?subset_ordo_clinical_subtype +?subset_ordo_group_of_disorders +?subset_ordo_disorder +?subset_mondo_rare \ No newline at end of file diff --git a/src/sparql/signature/clingen-subset.sparql b/src/sparql/signature/clingen-subset.sparql new file mode 100644 index 0000000000..980af6f123 --- /dev/null +++ b/src/sparql/signature/clingen-subset.sparql @@ -0,0 +1,25 @@ +prefix IAO: +prefix rdfs: +prefix oio: +prefix def: +prefix owl: +PREFIX xsd: + +# The Clingen subset is defined as all IDS used by clingen +# and all their parent classes. + +SELECT DISTINCT ?cls WHERE +{ + { + ?cls . + } + UNION { + ?child . + ?child rdfs:subClassOf* ?cls . + } + FILTER NOT EXISTS { + ?cls owl:deprecated "true"^^xsd:boolean + } + FILTER( !isBlank(?cls) && STRSTARTS(str(?cls), "http://purl.obolibrary.org/obo/MONDO_")) +} + \ No newline at end of file diff --git a/src/sparql/signature/rare-subset-related-entity.sparql b/src/sparql/signature/rare-subset-related-entity.sparql index d01efb578c..1048032850 100644 --- a/src/sparql/signature/rare-subset-related-entity.sparql +++ b/src/sparql/signature/rare-subset-related-entity.sparql @@ -5,7 +5,7 @@ prefix def: prefix owl: PREFIX xsd: -# Get all classes related to diseases that +# Get all classes related to diseases that related via RO:0004003 or SELECT DISTINCT ?entity WHERE { VALUES ?property { RO:0004003 } diff --git a/src/sparql/update/clingen-labels.ru b/src/sparql/update/clingen-labels.ru new file mode 100644 index 0000000000..157d659298 --- /dev/null +++ b/src/sparql/update/clingen-labels.ru @@ -0,0 +1,36 @@ +PREFIX rdf: +PREFIX rdfs: +PREFIX IAO: +PREFIX OMO: +PREFIX MONDO: +PREFIX owl: +prefix oboInOwl: + +# description: Replaces the standard label with the clingen preferred label + +DELETE { + ?entity rdfs:label ?label . +} + +INSERT { +?entity rdfs:label ?clingen_label . +[] rdf:type owl:Axiom ; + owl:annotatedSource ?entity ; + owl:annotatedProperty oboInOwl:hasExactSynonym ; + owl:annotatedTarget ?label ; + oboInOwl:hasSynonymType . +} + +WHERE { + ?entity rdfs:label ?label . + VALUES ?synonym_property { oboInOwl:hasExactSynonym } + ?entity ?synonym_property ?clingen_label . + [] owl:annotatedSource ?entity ; + owl:annotatedProperty ?synonym_property ; + owl:annotatedTarget ?clingen_label ; + oboInOwl:hasSynonymType . + + FILTER(STR(?label)!=STR(?clingen_label)) + + FILTER (isIRI(?entity) && STRSTARTS(str(?entity), "http://purl.obolibrary.org/obo/MONDO_")) +} \ No newline at end of file