{
    "disease_id": "DOID:0110587", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "CD164 autosomal dominant nonsyndromic deafness"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014854", 
            "name": "deafness, autosomal dominant type 66"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014854", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in CD164"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014854", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014854", 
            "name": "autosomal dominant nonsyndromic deafness type 66"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110587", 
            "name": "DFNA66"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110587", 
            "name": "autosomal dominant deafness 66"
        }, 
        {
            "url": "https://www.omim.org/entry/616969", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616969", 
            "name": "Deafness, autosomal dominant, 66"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110587", 
        "description": "An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CD164 gene on chromosome 6q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110587", 
        "name": "autosomal dominant nonsyndromic deafness 66"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616969", 
            "id": "616969", 
            "database": "MIM"
        }
    ]
}