MONDO:0013761

{
    "@context": "/terms/",
    "@id": "/phenotype-terms/MONDO_0013761/",
    "@type": [
        "PhenotypeTerm",
        "OntologyTerm",
        "Item"
    ],
    "ancestors": [
        "human disease",
        "entity",
        "hereditary disease",
        "childhood encephalopathy due to thiamine pyrophosphokinase deficiency",
        "metabolic disease",
        "characteristic",
        "disorder of vitamin and non-protein cofactor absorption and transport",
        "continuant",
        "inborn errors of metabolism",
        "experimental factor",
        "disease",
        "disorder of metabolite absorption and transport",
        "realizable",
        "thiamine-responsive dysfunction syndrome",
        "disposition",
        "genetic disorder",
        "disorder of thiamine metabolism and transport"
    ],
    "audit": {},
    "creation_timestamp": "2023-11-03T21:53:12.706229+00:00",
    "name": "MONDO_0013761",
    "ontology": "MONDO",
    "release_timestamp": "2023-11-06T21:39:18.165013+00:00",
    "schema_version": "4",
    "status": "released",
    "submitted_by": {
        "@id": "/users/85c75ed3-269b-4273-b4ba-e269ee350dd6/",
        "title": "Ingrid Youngworth"
    },
    "summary": "childhood encephalopathy due to thiamine pyrophosphokinase deficiency",
    "synonyms": [
        "childhood encephalopathy due to thiamine pyrophosphokinase deficiency"
    ],
    "term_id": "MONDO:0013761",
    "term_name": "childhood encephalopathy due to thiamine pyrophosphokinase deficiency",
    "uuid": "fdf4cc58-f3a2-46dc-ba23-666deb5d31c7"
}