{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "autosomal dominant deafness 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "DFNA2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in GJB3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "deafness, autosomal dominant 2B; DFNA2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "deafness, autosomal dominant 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "deafness, autosomal dominant type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "autosomal dominant nonsyndromic deafness type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012976", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012976", 
            "name": "GJB3 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110559", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110559", 
            "name": "DFNA2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110559", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110559", 
            "name": "autosomal dominant deafness 2B"
        }, 
        {
            "url": "https://www.omim.org/entry/612644", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612644", 
            "name": "Deafness, autosomal dominant, 2B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110559", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110559", 
        "name": "autosomal dominant nonsyndromic deafness 2B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612644", 
            "id": "612644", 
            "database": "MIM"
        }
    ]
}