{
    "disease_id": "DOID:0110571", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "autosomal dominant nonsyndromic deafness type 48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "deafness, autosomal dominant type 48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "autosomal dominant deafness 48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "deafness, autosomal dominant 48; DFNA48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in MYO1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "MYO1A autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "DFNA48"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011920", 
            "name": "deafness, autosomal dominant 48"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110571", 
            "name": "DFNA48"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110571", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110571", 
            "name": "autosomal dominant deafness 48"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110571", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110571", 
        "name": "autosomal dominant nonsyndromic deafness 48"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110571#disease-associations", 
            "id": "0110571", 
            "database": "Alliance of Genome Resources"
        }
    ]
}