{
    "disease_id": "DOID:0112185",
    "recommended_name": {
        "id": "DOID:0112185",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112185",
        "name": "thyroid dyshormonogenesis 1",
        "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in SLC5A5 on chromosome 19p13.11."
    },
    "synonyms": [
        {
            "id": "DOID:0112185",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112185",
            "name": "TDH1",
            "description": ""
        },
        {
            "id": "DOID:0112185",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112185",
            "name": "genetic defect in thyroid hormonogenesis 1",
            "description": ""
        },
        {
            "id": "DOID:0112185",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112185",
            "name": "iodide accumulation, transport, or trapping defect",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "thyroid dyshormonogenesis 1",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "TDH1",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "familial thyroid dyshormonogenesis 1",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "hypothyroidism, congenital, due to dyshormonogenesis, 1",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "iodine accumulation, transport, or trapping defect",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "thyroid dyshormonogenesis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0020716",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020716",
            "name": "thyroid hormonogenesis, genetic defect in, 1",
            "description": ""
        },
        {
            "id": "MIM:274400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/274400",
            "name": "Thyroid dyshormonogenesis 1",
            "description": "Thyroid dyshormonogenesis 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112185"
    ],
    "unlinked_id_list": []
}