{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0014073/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"heart disorder",
"dilated cardiomyopathy",
"familial cardiomyopathy",
"intrinsic cardiomyopathy",
"cardiovascular disease",
"musculoskeletal system disorder",
"entity",
"hereditary disease",
"experimental factor",
"familial dilated cardiomyopathy",
"realizable",
"human disease",
"cardiogenetic disease",
"genetic disorder",
"continuant",
"musculoskeletal system disease",
"cardiovascular disorder",
"dilated cardiomyopathy 1II",
"characteristic",
"heart disease",
"muscle tissue disorder",
"cardiomyopathy",
"disposition",
"disease"
],
"audit": {},
"creation_timestamp": "2023-11-03T21:55:20.219635+00:00",
"name": "MONDO_0014073",
"ontology": "MONDO",
"release_timestamp": "2023-11-06T21:04:39.343829+00:00",
"schema_version": "4",
"status": "released",
"submitted_by": {
"@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
"title": "Ingrid Youngworth"
},
"summary": "dilated cardiomyopathy 1II",
"synonyms": [
"CMD1II",
"cardiomyopathy, dilated, type 1II",
"dilated cardiomyopathy type 1II",
"familial isolated dilated cardiomyopathy caused by mutation in CRYAB",
"CRYAB familial isolated dilated cardiomyopathy"
],
"term_id": "MONDO:0014073",
"term_name": "dilated cardiomyopathy 1II",
"uuid": "eb9f835d-1149-435f-b1b4-0f453f097dda"
}