MONDO:0010713

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0010713/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "realizable",
11        "inborn error of immunity",
12        "disposition",
13        "disease",
14        "immune deficiency disease",
15        "entity",
16        "human disease",
17        "immune system disorder",
18        "hereditary disease",
19        "immune system disease",
20        "properdin deficiency, X-linked",
21        "characteristic",
22        "genetic disorder",
23        "continuant",
24        "experimental factor"
25    ],
26    "audit": {},
27    "creation_timestamp": "2023-11-03T21:56:46.488193+00:00",
28    "name": "MONDO_0010713",
29    "ontology": "MONDO",
30    "release_timestamp": "2023-11-06T21:07:38.529687+00:00",
31    "schema_version": "4",
32    "status": "released",
33    "submitted_by": {
34        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
35        "title": "Ingrid Youngworth"
36    },
37    "summary": "properdin deficiency, X-linked",
38    "synonyms": [
39        "properdin deficiency, X-linked",
40        "properdin deficiency, X-linked, X-linked recessive"
41    ],
42    "term_id": "MONDO:0010713",
43    "term_name": "properdin deficiency, X-linked",
44    "uuid": "f2b02b30-5f2d-41e6-84cb-c5a2df2b2440"
45}