{
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    "synonyms": [
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            "description": "", 
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            "description": "", 
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            "description": "", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011102", 
            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011102", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011102", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in TECTA"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011102", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110544", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110544", 
            "name": "DFNA12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110544", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110544", 
            "name": "DFNA8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110544", 
            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110544", 
            "name": "autosomal dominant deafness 8"
        }, 
        {
            "url": "https://www.omim.org/entry/601543", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601543", 
            "name": "Deafness, autosomal dominant, 12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110544", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.", 
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        "name": "autosomal dominant nonsyndromic deafness 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601543", 
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            "database": "MIM"
        }
    ]
}