MONDO:0011458

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0011458/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "human disease",
        "disorder of visual system",
        "realizable",
        "AIPL1-related retinopathy",
        "retinopathy",
        "experimental factor",
        "eye disorder",
        "continuant",
        "inherited retinal dystrophy",
        "Leber congenital amaurosis",
        "disease of orbital region",
        "cone-rod dystrophy",
        "entity",
        "disorder of orbital region",
        "psychiatric disorder",
        "Leber congenital amaurosis 4",
        "retinal degeneration",
        "congenital nervous system disorder",
        "eye disease",
        "hereditary neurological disease",
        "hereditary disease",
        "nervous system disorder",
        "perceptual disorders",
        "genetic disorder",
        "characteristic",
        "head and neck disorder",
        "disposition",
        "disease",
        "nervous system disease",
        "retinal disorder"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:58:47.115941+00:00",
    "name": "MONDO_0011458",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:11:39.686973+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "Leber congenital amaurosis 4",
    "synonyms": [
        "Leber congenital amaurosis 4",
        "LCA4",
        "Leber congenital amaurosis caused by mutation in AIPL1",
        "AIPL1 Leber congenital amaurosis",
        "Leber congenital amaurosis type 4"
    ],
    "term_id": "MONDO:0011458",
    "term_name": "Leber congenital amaurosis 4",
    "uuid": "f3581aa9-3839-4d26-a784-69dea5976ba8"
}