{
    "disease_id": "DOID:0111752",
    "recommended_name": {
        "id": "DOID:0111752",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111752",
        "name": "autosomal-mitochondrial sensorineural deafness",
        "description": "A sensorineural hearing loss characterized by progressive, severe to profound deafness that has_material_basis_in digenic inheritance of mutations in the mitochondrial gene MTRNR1 and an unidentified nuclear gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0009090",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009090",
            "name": "deafness, sensorineural, autosomal-mitochondrial type",
            "description": ""
        },
        {
            "id": "MONDO:0009090",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009090",
            "name": "deafness, sensorineural, autosomal-mitochondrial type",
            "description": ""
        }
    ]
}