{
    "disease_id": "DOID:0070128",
    "recommended_name": {
        "id": "DOID:0070128",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070128",
        "name": "congenital nongoitrous hypothyroidism 6",
        "description": "A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070128",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070128",
            "name": "CHNG6",
            "description": ""
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "congenital nongoitrous hypothyroidism 6",
            "description": "Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the THRA gene."
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "CHNG6",
            "description": ""
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "THRA hypothyroidism, congenital, nongoitrous",
            "description": ""
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "hypothyroidism, congenital, nongoitrous caused by mutation in THRA",
            "description": ""
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "hypothyroidism, congenital, nongoitrous, 6",
            "description": ""
        },
        {
            "id": "MONDO:0013757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013757",
            "name": "hypothyroidism, congenital, nongoitrous, type 6",
            "description": ""
        },
        {
            "id": "MIM:614450",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614450",
            "name": "Hypothyroidism, congenital, non-goitrous, 6",
            "description": "Hypothyroidism, congenital, non-goitrous, 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070128"
    ],
    "unlinked_id_list": []
}