{
    "disease_id": "DOID:0112189",
    "recommended_name": {
        "id": "DOID:0112189",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112189",
        "name": "thyroid dyshormonogenesis 6",
        "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in DUOX2 on chromosome 15q21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112189",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112189",
            "name": "TDH6",
            "description": ""
        },
        {
            "id": "DOID:0112189",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112189",
            "name": "genetic defect in thyroid hormonogenesis 6",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "thyroid dyshormonogenesis 6",
            "description": "Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOX2 gene."
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "DUOX2 familial thyroid dyshormonogenesis",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "familial thyroid dyshormonogenesis caused by mutation in DUOX2",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "thyroid dyshormonogenesis 6",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "thyroid dyshormonogenesis type 6",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "TDH6",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "hypothyroidism, congenital, due to dyshormonogenesis, 6",
            "description": ""
        },
        {
            "id": "MONDO:0011792",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011792",
            "name": "thyroid hormonogenesis, genetic defect in, 6",
            "description": ""
        },
        {
            "id": "MIM:607200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607200",
            "name": "Thyroid dyshormonogenesis 6",
            "description": "Thyroid dyshormonogenesis 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112189"
    ],
    "unlinked_id_list": []
}