{
    "disease_id": "DOID:0080219", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "hyperthyroxinemia, dystransthyretinemic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "hyperthyroxinemia, dystransthyretinemic; DTTRH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "dystransthyretinemic Euthyroidal hyperthyroxinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "Euthryroidal hyperthyroxinemia 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "hyperthyroxinemia, Dysprealbuminemic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007785", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007785", 
            "name": "DTTRH"
        }, 
        {
            "url": "https://www.omim.org/entry/145680", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:145680", 
            "name": "Hyperthyroxinemia, dystransthyretinemic"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080219", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080219", 
        "name": "dystransthyretinemic hyperthyroxinemia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/145680", 
            "id": "145680", 
            "database": "MIM"
        }
    ]
}