MONDO:0008476

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0008476/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "collagenopathy",
11        "skeletal system disease",
12        "skeletal system disorder",
13        "entity",
14        "disorder of development or morphogenesis",
15        "type 2 collagenopathy",
16        "musculoskeletal system disease",
17        "skeletal dysplasia",
18        "genetic disorder",
19        "musculoskeletal system disorder",
20        "hereditary disorder of connective tissue",
21        "spondyloepimetaphyseal dysplasia",
22        "hereditary disease",
23        "disease",
24        "continuant",
25        "connective tissue disease",
26        "spondylometaphyseal dysplasia",
27        "connective tissue disorder",
28        "bone disease",
29        "spondyloepimetaphyseal dysplasia, Strudwick type",
30        "osteochondrodysplasia",
31        "human disease",
32        "bone development disease",
33        "characteristic",
34        "bone disorder",
35        "experimental factor",
36        "syndromic disease",
37        "realizable",
38        "disposition"
39    ],
40    "audit": {},
41    "creation_timestamp": "2023-11-03T21:55:01.071663+00:00",
42    "name": "MONDO_0008476",
43    "ontology": "MONDO",
44    "release_timestamp": "2023-11-06T21:04:03.171507+00:00",
45    "schema_version": "4",
46    "status": "released",
47    "submitted_by": {
48        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
49        "title": "Ingrid Youngworth"
50    },
51    "summary": "spondyloepimetaphyseal dysplasia, Strudwick type",
52    "synonyms": [
53        "spondyloepimetaphyseal dysplasia, Strudwick type"
54    ],
55    "term_id": "MONDO:0008476",
56    "term_name": "spondyloepimetaphyseal dysplasia, Strudwick type",
57    "uuid": "f06d9da9-70f3-4070-8f6d-5af498c7dbc9"
58}