{
    "disease_id": "DOID:0110546", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in POU4F3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "deafness, autosomal dominant 15; DFNA15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "POU4F3 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "deafness, autosomal dominant 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "deafness, autosomal dominant type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "autosomal dominant nonsyndromic deafness type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "autosomal dominant deafness 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011226", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011226", 
            "name": "DFNA15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110546", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110546", 
            "name": "DFNA15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110546", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110546", 
            "name": "autosomal dominant deafness 15"
        }, 
        {
            "url": "https://www.omim.org/entry/602459", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:602459", 
            "name": "Deafness, autosomal dominant, 15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110546", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110546", 
        "name": "autosomal dominant nonsyndromic deafness 15"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602459", 
            "id": "602459", 
            "database": "MIM"
        }
    ]
}