MONDO:0018958

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0018958/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "musculoskeletal system disease",
11        "muscular disease",
12        "entity",
13        "experimental factor",
14        "disease",
15        "human disease",
16        "characteristic",
17        "hereditary disease",
18        "realizable",
19        "myopathy",
20        "hereditary skeletal muscle disorder",
21        "congenital myopathy",
22        "nemaline myopathy",
23        "congenital structural myopathy",
24        "genetic disorder",
25        "continuant",
26        "musculoskeletal system disorder",
27        "skeletal muscle disorder",
28        "disposition",
29        "muscle tissue disorder"
30    ],
31    "audit": {},
32    "creation_timestamp": "2023-11-03T21:57:52.995254+00:00",
33    "name": "MONDO_0018958",
34    "ontology": "MONDO",
35    "release_timestamp": "2023-11-06T21:09:54.954869+00:00",
36    "schema_version": "4",
37    "status": "released",
38    "submitted_by": {
39        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
40        "title": "Ingrid Youngworth"
41    },
42    "summary": "nemaline myopathy",
43    "synonyms": [
44        "nemaline body disease",
45        "nemaline rod myopathy",
46        "nemaline myopathy",
47        "NEM",
48        "rod myopathy",
49        "NM"
50    ],
51    "term_id": "MONDO:0018958",
52    "term_name": "nemaline myopathy",
53    "uuid": "eff96d19-0968-4417-b425-e03814ebe884"
54}