{
    "disease_id": "DOID:0110584", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "deafness, autosomal dominant 6; DFNA6"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "DFNA6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "deafness, autosomal dominant 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "autosomal dominant deafness 38"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "autosomal dominant nonsyndromic deafness type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "DFNA38"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "autosomal dominant deafness 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "WFS1 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010963", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010963", 
            "name": "DFNA14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "DFNA14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "DFNA38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "DFNA6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "autosomal dominant deafness 14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "autosomal dominant deafness 38"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110584", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110584", 
            "name": "autosomal dominant deafness 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110584", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110584", 
        "name": "autosomal dominant nonsyndromic deafness 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110584#disease-associations", 
            "id": "0110584", 
            "database": "Alliance of Genome Resources"
        }
    ]
}