{
    "disease_id": "DOID:0070125",
    "recommended_name": {
        "id": "DOID:0070125",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070125",
        "name": "congenital nongoitrous hypothyroidism 5",
        "description": "A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "DOID:0070125",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070125",
            "name": "CHNG5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "hypothyroidism, congenital, nongoitrous, 5",
            "description": "Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene."
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "CHNG5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "NKX2-5 hypothyroidism, congenital, nongoitrous",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "hypothyroidism, congenital nongoitrous, 5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "hypothyroidism, congenital, nongoitrous, 5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "hypothyroidism, congenital, nongoitrous, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0009154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009154",
            "name": "congenital nongoitrous hypothyroidism 5",
            "description": ""
        },
        {
            "id": "MIM:225250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/225250",
            "name": "Hypothyroidism, congenital, non-goitrous, 5",
            "description": "Hypothyroidism, congenital, non-goitrous, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070125"
    ],
    "unlinked_id_list": []
}