MONDO:0008009

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0008009/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "hereditary skin disorder",
11        "monilethrix",
12        "autosomal genetic disease",
13        "autosomal dominant disease",
14        "disease",
15        "skin disease",
16        "characteristic",
17        "realizable",
18        "experimental factor",
19        "continuant",
20        "integumentary system disease",
21        "human disease",
22        "entity",
23        "disposition",
24        "genetic disorder",
25        "skin disorder",
26        "integumentary system disorder",
27        "hereditary disease"
28    ],
29    "audit": {},
30    "creation_timestamp": "2023-11-03T21:56:22.827535+00:00",
31    "name": "MONDO_0008009",
32    "ontology": "MONDO",
33    "release_timestamp": "2023-11-06T21:06:53.190941+00:00",
34    "schema_version": "4",
35    "status": "released",
36    "submitted_by": {
37        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
38        "title": "Ingrid Youngworth"
39    },
40    "summary": "monilethrix",
41    "synonyms": [
42        "moniliform hair syndrome",
43        "monilethrix"
44    ],
45    "term_id": "MONDO:0008009",
46    "term_name": "monilethrix",
47    "uuid": "f6423123-7d82-4d20-a857-aacb2d4aff4c"
48}