{
    "disease_id": "DOID:0110829", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110829", 
        "description": "An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has_material_basis_in mutation in the MTTS2 gene in the mitochondrial genome.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110829", 
        "name": "retinitis pigmentosa-deafness syndrome"
    }
}
