{
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            "description": "", 
            "resource": "MONDO", 
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            "name": "DFNA68"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014740", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014740", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014740", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014740", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014740", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014740", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110589", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110589", 
            "name": "DFNA68"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110589", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616707", 
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        }
    ], 
    "recommended_name": {
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        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the HOMER2 gene on chromosome 15q25.", 
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    }, 
    "evidence": [
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            "id": "616707", 
            "database": "MIM"
        }
    ]
}
