{
    "disease_id": "DOID:0080267",
    "recommended_name": {
        "id": "DOID:0080267",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080267",
        "name": "autosomal dominant nonsyndromic deafness 71",
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the DMXL2 gene on chromosome 15q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0033258",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033258",
            "name": "deafness, autosomal dominant 71",
            "description": ""
        },
        {
            "id": "MONDO:0033258",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033258",
            "name": "deafness, autosomal dominant 71; DFNA71",
            "description": ""
        },
        {
            "id": "MONDO:0033258",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033258",
            "name": "DFNA71",
            "description": ""
        },
        {
            "id": "MONDO:0033258",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033258",
            "name": "autosomal dominant nonsyndromic deafness 71",
            "description": ""
        },
        {
            "id": "MIM:617605",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617605",
            "name": "Deafness, autosomal dominant, 71",
            "description": "Deafness, autosomal dominant, 71"
        }
    ]
}