{
    "disease_id": "DOID:0112145", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112145", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112145", 
            "name": "RP88"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112145", 
        "description": "A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that has_material_basis_in homozygous or compound heterozygous mutation in RP1L1 on chromosome 8p23.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112145", 
        "name": "retinitis pigmentosa 88"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618826", 
            "id": "618826", 
            "database": "MIM"
        }
    ]
}