{
    "disease_id": "DOID:0110552", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "deafness, autosomal dominant type 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "DFNA 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in MYO6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "autosomal dominant deafness 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "MYO6 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "deafness, autosomal dominant nonsyndromic sensorineural 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "deafness, autosomal dominant 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "autosomal dominant nonsyndromic deafness type 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "deafness, autosomal dominant 22, with hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "deafness, autosomal dominant 22; DFNA22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011660", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011660", 
            "name": "DFNA22"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110552", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110552", 
            "name": "DFNA22"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110552", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110552", 
            "name": "autosomal dominant deafness 22"
        }, 
        {
            "url": "https://www.omim.org/entry/606346", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:606346", 
            "name": "Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110552", 
        "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 MYO6 gene on chromosome 6q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110552", 
        "name": "autosomal dominant nonsyndromic deafness 22"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/606346", 
            "id": "606346", 
            "database": "MIM"
        }
    ]
}