MONDO:0013477

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0013477/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "cardiovascular disorder",
11        "entity",
12        "muscle tissue disorder",
13        "musculoskeletal system disease",
14        "heart disorder",
15        "genetic disorder",
16        "musculoskeletal system disorder",
17        "cardiogenetic disease",
18        "intrinsic cardiomyopathy",
19        "hereditary disease",
20        "hypertrophic cardiomyopathy 20",
21        "disease",
22        "continuant",
23        "familial hypertrophic cardiomyopathy",
24        "familial cardiomyopathy",
25        "human disease",
26        "cardiovascular disease",
27        "characteristic",
28        "experimental factor",
29        "cardiomyopathy",
30        "heart disease",
31        "realizable",
32        "hypertrophic cardiomyopathy",
33        "disposition"
34    ],
35    "audit": {},
36    "creation_timestamp": "2023-11-03T21:59:39.651302+00:00",
37    "name": "MONDO_0013477",
38    "ontology": "MONDO",
39    "release_timestamp": "2023-11-06T21:13:20.577208+00:00",
40    "schema_version": "4",
41    "status": "released",
42    "submitted_by": {
43        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
44        "title": "Ingrid Youngworth"
45    },
46    "summary": "hypertrophic cardiomyopathy 20",
47    "synonyms": [
48        "hypertrophic cardiomyopathy type 20",
49        "CMH20",
50        "cardiomyopathy, hypertrophic, 20",
51        "NEXN hypertrophic cardiomyopathy",
52        "cardiomyopathy, familial hypertrophic, type 20",
53        "cardiomyopathy familial hypertrophic 20",
54        "hypertrophic cardiomyopathy caused by mutation in NEXN"
55    ],
56    "term_id": "MONDO:0013477",
57    "term_name": "hypertrophic cardiomyopathy 20",
58    "uuid": "fe83a6af-bf8b-40be-b622-c84a08e37f22"
59}