{
    "disease_id": "DOID:0112144",
    "recommended_name": {
        "id": "DOID:0112144",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112144",
        "name": "retinitis pigmentosa 87",
        "description": "A retinitis pigmentosa characterized by slowly progressive visual disturbance and extensive choroid/retinal atrophy that has_material_basis_in heterozygous mutation in the RPE65 gene on chromosome 1p31.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112144",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112144",
            "name": "RP87",
            "description": ""
        },
        {
            "id": "DOID:0112144",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112144",
            "name": "retinitis pigmentosa 87 with choroidal involvement",
            "description": ""
        },
        {
            "id": "MONDO:0032873",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032873",
            "name": "retinitis pigmentosa 87 with choroidal involvement",
            "description": ""
        },
        {
            "id": "MONDO:0032873",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032873",
            "name": "RP87",
            "description": ""
        },
        {
            "id": "MIM:618697",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618697",
            "name": "Retinitis pigmentosa 87 with choroidal involvement",
            "description": "Retinitis pigmentosa 87 with choroidal involvement"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112144"
    ],
    "unlinked_id_list": []
}