{
    "disease_id": "DOID:0112188",
    "recommended_name": {
        "id": "DOID:0112188",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112188",
        "name": "thyroid dyshormonogenesis 4",
        "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in IYD on chromosome 6q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112188",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112188",
            "name": "TDH4",
            "description": ""
        },
        {
            "id": "DOID:0112188",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112188",
            "name": "deiodinase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112188",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112188",
            "name": "genetic defect in thyroid hormonogenesis 4",
            "description": ""
        },
        {
            "id": "DOID:0112188",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112188",
            "name": "iodotyrosine dehalogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "thyroid dyshormonogenesis 4",
            "description": "Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the IYD gene."
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "IYD familial thyroid dyshormonogenesis",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "TDH4",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "familial thyroid dyshormonogenesis caused by mutation in IYD",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "hypothyroidism, congenital, due to dyshormonogenesis, 4",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "thyroid dyshormonogenesis 4",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "thyroid dyshormonogenesis type 4",
            "description": ""
        },
        {
            "id": "MONDO:0010136",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010136",
            "name": "thyroid hormonogenesis, genetic defect in, 4",
            "description": ""
        },
        {
            "id": "MIM:274800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/274800",
            "name": "Thyroid dyshormonogenesis 4",
            "description": "Thyroid dyshormonogenesis 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112188"
    ],
    "unlinked_id_list": []
}