MONDO:0011458

released
1{
2    "@context": "/terms/",
3    "@id": "/phenotype-terms/MONDO_0011458/",
4    "@type": [
5        "PhenotypeTerm",
6        "OntologyTerm",
7        "Item"
8    ],
9    "ancestors": [
10        "Leber congenital amaurosis 4",
11        "disorder of visual system",
12        "entity",
13        "inherited retinal dystrophy",
14        "cone-rod dystrophy",
15        "genetic disorder",
16        "hereditary disease",
17        "disease of orbital region",
18        "disease",
19        "continuant",
20        "disorder of orbital region",
21        "psychiatric disorder",
22        "retinopathy",
23        "Leber congenital amaurosis",
24        "eye disease",
25        "human disease",
26        "characteristic",
27        "hereditary neurological disease",
28        "AIPL1-related retinopathy",
29        "experimental factor",
30        "retinal degeneration",
31        "eye disorder",
32        "retinal disorder",
33        "nervous system disorder",
34        "perceptual disorders",
35        "nervous system disease",
36        "head and neck disorder",
37        "realizable",
38        "congenital nervous system disorder",
39        "disposition"
40    ],
41    "audit": {},
42    "creation_timestamp": "2023-11-03T21:58:47.115941+00:00",
43    "name": "MONDO_0011458",
44    "ontology": "MONDO",
45    "release_timestamp": "2023-11-06T21:11:39.686973+00:00",
46    "schema_version": "4",
47    "status": "released",
48    "submitted_by": {
49        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
50        "title": "Ingrid Youngworth"
51    },
52    "summary": "Leber congenital amaurosis 4",
53    "synonyms": [
54        "Leber congenital amaurosis type 4",
55        "Leber congenital amaurosis 4",
56        "Leber congenital amaurosis caused by mutation in AIPL1",
57        "AIPL1 Leber congenital amaurosis",
58        "LCA4"
59    ],
60    "term_id": "MONDO:0011458",
61    "term_name": "Leber congenital amaurosis 4",
62    "uuid": "f3581aa9-3839-4d26-a784-69dea5976ba8"
63}