{
    "disease_id": "DOID:0112143", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112143", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112143", 
            "name": "RP86"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112143", 
        "description": "A retinitis pigmentosa characterized by night blindness followed by progressive narrowing of visual fields and decline in visual acuity that has_material_basis_in mutation in KIAA1549 on chromosome 7q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112143", 
        "name": "retinitis pigmentosa 86"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618613", 
            "id": "618613", 
            "database": "MIM"
        }
    ]
}