{
    "disease_id": "DOID:0110548", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "autosomal dominant nonsyndromic deafness type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "nonsyndromic hereditary deafness DFNA17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "MYH9 autosomal dominant nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "DFNA17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "deafness, autosomal dominant 17; DFNA17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "autosomal dominant deafness 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in MYH9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "Cochleosaccular Degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "deafness, autosomal dominant 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011350", 
            "name": "deafness, autosomal dominant nonsyndromic sensorineural 17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110548", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110548", 
            "name": "DFNA17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110548", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110548", 
            "name": "autosomal dominant deafness 17"
        }, 
        {
            "url": "https://www.omim.org/entry/603622", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:603622", 
            "name": "Deafness, autosomal dominant, 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110548", 
        "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 MYH9 gene on chromosome 22q12.", 
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        "id": "DOID:0110548", 
        "name": "autosomal dominant nonsyndromic deafness 17"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/603622", 
            "id": "603622", 
            "database": "MIM"
        }
    ]
}