{
    "disease_id": "DOID:0111751", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "mitochondrial non-syndromic sensorineural deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "mitochondrial non-syndromic neurosensory deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "deafness, nonsyndromic sensorineural, mitochondrial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "isolated mitochondrial neurosensory deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "deafness, isolated, due to mitochondrial transmission"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010779", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010779", 
            "name": "isolated mitochondrial sensorineural deafness"
        }, 
        {
            "url": "https://www.omim.org/entry/500008", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:500008", 
            "name": "Deafness, sensorineural, mitochondrial"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111751", 
        "description": "A sensorineural hearing loss that has_material_basis_in mutation in one of several different mitochondrial genes including; MTRNR1, MTTS1, MTCO1, MTTH, MTND1, and MTTI.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111751", 
        "name": "mitochondrial nonsyndromic sensorineural deafness"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500008", 
            "id": "500008", 
            "database": "MIM"
        }
    ]
}