{
    "disease_id": "DOID:0110586", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "deafness, autosomal dominant 65"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "deafness, autosomal dominant 65; DFNA65"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "deafness, autosomal dominant type 65"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "DFNA65"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "TBC1D24 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014470", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014470", 
            "name": "autosomal dominant deafness 65"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110586", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110586", 
            "name": "DFNA65"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110586", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110586", 
            "name": "autosomal dominant deafness 65"
        }, 
        {
            "url": "https://www.omim.org/entry/616044", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616044", 
            "name": "Deafness, autosomal dominant, 65"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110586", 
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110586", 
        "name": "autosomal dominant nonsyndromic deafness 65"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616044", 
            "id": "616044", 
            "database": "MIM"
        }
    ]
}