{
    "disease_id": "DOID:0110591", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011074", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011074", 
            "name": "DFNA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011074", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011074", 
            "name": "deafness, autosomal dominant 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011074", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011074", 
            "name": "autosomal dominant nonsyndromic deafness type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011074", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011074", 
            "name": "autosomal dominant deafness 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011074", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011074", 
            "name": "deafness, autosomal dominant 7; DFNA7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110591", 
            "name": "DFNA7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110591", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110591", 
            "name": "autosomal dominant deafness 7"
        }, 
        {
            "url": "https://www.omim.org/entry/601412", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:601412", 
            "name": "Deafness, autosomal dominant, 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110591", 
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by progressive high-tone hearing loss and has_material_basis_in variation in the chromosome region 1q21-q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110591", 
        "name": "autosomal dominant nonsyndromic deafness 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/601412", 
            "id": "601412", 
            "database": "MIM"
        }
    ]
}