{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0013477/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"characteristic",
"familial cardiomyopathy",
"disease",
"muscle tissue disorder",
"cardiovascular disorder",
"musculoskeletal system disorder",
"familial hypertrophic cardiomyopathy",
"experimental factor",
"cardiomyopathy",
"entity",
"realizable",
"human disease",
"disposition",
"hypertrophic cardiomyopathy",
"intrinsic cardiomyopathy",
"cardiogenetic disease",
"hereditary disease",
"hypertrophic cardiomyopathy 20",
"heart disease",
"musculoskeletal system disease",
"heart disorder",
"continuant",
"genetic disorder",
"cardiovascular disease"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:59:39.651302+00:00",
"name": "MONDO_0013477",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:13:20.577208+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "hypertrophic cardiomyopathy 20",
"synonyms": [
"cardiomyopathy, hypertrophic, 20",
"cardiomyopathy, familial hypertrophic, type 20",
"NEXN hypertrophic cardiomyopathy",
"hypertrophic cardiomyopathy caused by mutation in NEXN",
"cardiomyopathy familial hypertrophic 20",
"hypertrophic cardiomyopathy type 20",
"CMH20"
],
"term_id": "MONDO:0013477",
"term_name": "hypertrophic cardiomyopathy 20",
"uuid": "fe83a6af-bf8b-40be-b622-c84a08e37f22"
}