{
    "disease_id": "DOID:0110577", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "chromosome 9Q21.11 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "deafness, autosomal dominant 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "deafness, autosomal dominant type 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "deafness, autosomal dominant 51; DFNA51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "autosomal dominant deafness 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "autosomal dominant nonsyndromic deafness type 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013305", 
            "name": "DFNA51"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110577", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110577", 
            "name": "DFNA51"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110577", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110577", 
            "name": "autosomal dominant deafness 51"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110577", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110577", 
            "name": "chromosome 9q21.11 duplication syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110577", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has_material_basis_in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110577", 
        "name": "autosomal dominant nonsyndromic deafness 51"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110577#disease-associations", 
            "id": "0110577", 
            "database": "Alliance of Genome Resources"
        }
    ]
}