{
    "disease_id": "DOID:0080219",
    "recommended_name": {
        "id": "DOID:0080219",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080219",
        "name": "dystransthyretinemic hyperthyroxinemia",
        "description": "A hyperthyroxinemia that is characterized by an increased affinity for thyroxine (T4) by transthyretin in clinically euthyroid individuals and that has_material_basis_in heterozygous mutation in the TTR gene on chromosome 18q12."
    },
    "synonyms": [
        {
            "id": "MONDO:0007785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007785",
            "name": "hyperthyroxinemia, dystransthyretinemic",
            "description": ""
        },
        {
            "id": "MONDO:0007785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007785",
            "name": "hyperthyroxinemia, dystransthyretinemic",
            "description": ""
        },
        {
            "id": "MONDO:0007785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007785",
            "name": "DTTRH",
            "description": ""
        },
        {
            "id": "MIM:145680",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/145680",
            "name": "Hyperthyroxinemia, dystransthyretinemic",
            "description": "Hyperthyroxinemia, dystransthyretinemic"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080219"
    ],
    "unlinked_id_list": []
}