{
    "disease_id": "DOID:0060690", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "autosomal dominant auditory neuropathy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "auditory neuropathy, autosomal dominant, 1; AUNA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "auditory neuropathy caused by mutation in DIAPH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "DIAPH3 auditory neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "auditory neuropathy, nonsyndromic dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "auditory neuropathy, autosomal dominant, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "AUNA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "nonsyndromic dominant auditory neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "NSDAN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012196", 
            "name": "auditory neuropathy, autosomal dominant, 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060690", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060690", 
            "name": "AUNA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060690", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060690", 
            "name": "NSDAN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060690", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060690", 
            "name": "nonsyndromic dominant auditory neuropathy"
        }, 
        {
            "url": "https://www.omim.org/entry/609129", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:609129", 
            "name": "Auditory neuropathy, autosomal dominant, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060690", 
        "description": "An autosomal dominant nonsyndromic deafness characterized by  preservation of outer hair cell function and abnormal or absent auditory brainstem responses that has_material_basis_in heterozygous mutation in the DIAPH3 gene on chromosome 13q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060690", 
        "name": "autosomal dominant auditory neuropathy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609129", 
            "id": "609129", 
            "database": "MIM"
        }
    ]
}