{
    "disease_id": "DOID:0111837",
    "recommended_name": {
        "id": "DOID:0111837",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111837",
        "name": "congenital nongoitrous hypothyroidism 8",
        "description": "A congenital hypothyroidism characterized by relatively mild central hypothyroidism that has_material_basis_in heterozygous or hemizygous mutation in the TBL1X gene on chromosome Xp22.3-p22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111837",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111837",
            "name": "CHNG8",
            "description": ""
        },
        {
            "id": "MONDO:0026731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026731",
            "name": "hypothyroidism, congenital, nongoitrous, 8",
            "description": ""
        },
        {
            "id": "MONDO:0026731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026731",
            "name": "CHNG8",
            "description": ""
        },
        {
            "id": "MONDO:0026731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026731",
            "name": "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 8",
            "description": ""
        },
        {
            "id": "MIM:301033",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301033",
            "name": "Hypothyroidism, congenital, non-goitrous, 8",
            "description": "Hypothyroidism, congenital, non-goitrous, 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111837"
    ],
    "unlinked_id_list": []
}