{
    "disease_id": "DOID:0110593", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "autosomal dominant nonsyndromic deafness type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "deafness, autosomal dominant type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "deafness, autosomal dominant 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "DFNA9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "COCH autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in COCH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "autosomal dominant deafness 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011058", 
            "name": "deafness, autosomal dominant 9; DFNA9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110593", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110593", 
            "name": "DFNA9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110593", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110593", 
            "name": "autosomal dominant deafness 9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110593", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110593", 
        "name": "autosomal dominant nonsyndromic deafness 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110593#disease-associations", 
            "id": "0110593", 
            "database": "Alliance of Genome Resources"
        }
    ]
}