{
    "disease_id": "DOID:0112145",
    "recommended_name": {
        "id": "DOID:0112145",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112145",
        "name": "retinitis pigmentosa 88",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0112145",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112145",
            "name": "RP88",
            "description": ""
        },
        {
            "id": "MIM:618826",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618826",
            "name": "Retinitis pigmentosa 88",
            "description": "Retinitis pigmentosa 88"
        }
    ]
}