MONDO:0013866

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0013866/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "inborn errors of metabolism",
        "brain disorder",
        "hereditary dementia",
        "central nervous system disorder",
        "disease",
        "lysosomal lipid storage disorder",
        "human disease",
        "experimental factor",
        "dementia",
        "entity",
        "mental or behavioural disorder",
        "brain disease",
        "central nervous system disease",
        "neuronal ceroid lipofuscinosis",
        "genetic disorder",
        "cerebral lipidosis with dementia",
        "nervous system disorder",
        "hereditary disease",
        "nervous system disease",
        "cognitive disorder",
        "neurodegenerative disease",
        "inherited neurodegenerative disorder",
        "lysosomal storage disease",
        "psychiatric disorder",
        "continuant",
        "realizable",
        "disposition",
        "characteristic",
        "inherited lipid metabolism disorder",
        "hereditary neurological disease",
        "neuronal ceroid lipofuscinosis 11",
        "metabolic disease",
        "adult neuronal ceroid lipofuscinosis"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:50:12.033392+00:00",
    "name": "MONDO_0013866",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:33:09.661706+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "neuronal ceroid lipofuscinosis 11",
    "synonyms": [
        "neuronal ceroid lipofuscinosis caused by mutation in GRN",
        "CLN11",
        "Grn neuronal ceroid lipofuscinosis",
        "neuronal ceroid lipofuscinosis type 11",
        "ceroid lipofuscinosis, neuronal, type 11",
        "neuronal ceroid lipofuscinosis caused by mutation in Grn",
        "GRN neuronal ceroid lipofuscinosis"
    ],
    "term_id": "MONDO:0013866",
    "term_name": "neuronal ceroid lipofuscinosis 11",
    "uuid": "fc2760c5-1fc9-457c-9d5c-1f47699435d6"
}