{
"@context": "/terms/",
"@id": "/phenotype-terms/MONDO_0014073/",
"@type": [
"PhenotypeTerm",
"OntologyTerm",
"Item"
],
"ancestors": [
"heart disease",
"musculoskeletal system disease",
"dilated cardiomyopathy",
"experimental factor",
"hereditary disease",
"cardiomyopathy",
"entity",
"continuant",
"muscle tissue disorder",
"realizable",
"human disease",
"familial cardiomyopathy",
"heart disorder",
"dilated cardiomyopathy 1II",
"intrinsic cardiomyopathy",
"familial isolated dilated cardiomyopathy",
"cardiovascular disease",
"musculoskeletal system disorder",
"disease",
"genetic disorder",
"cardiogenetic disease",
"familial dilated cardiomyopathy",
"cardiovascular disorder",
"disposition",
"characteristic"
],
"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": [
"cardiomyopathy, dilated, type 1II",
"CRYAB familial isolated dilated cardiomyopathy",
"dilated cardiomyopathy type 1II",
"CMD1II",
"familial isolated dilated cardiomyopathy caused by mutation in CRYAB"
],
"term_id": "MONDO:0014073",
"term_name": "dilated cardiomyopathy 1II",
"uuid": "eb9f835d-1149-435f-b1b4-0f453f097dda"
}