{
    "disease_id": "DOID:0061112",
    "recommended_name": {
        "id": "DOID:0061112",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061112",
        "name": "retinitis pigmentosa 95",
        "description": "A retinitis pigmentosa characterized by pale optic discs, attenuation of retinal vessels, and atrophy of the retinal pigment epithelium with bone-spicule pigmentation that has_material_basis_in homozygous or compound heterozygous mutation in the RAX2 gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0061112",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061112",
            "name": "RP95",
            "description": ""
        },
        {
            "id": "MONDO:0859308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859308",
            "name": "retinitis pigmentosa 95",
            "description": ""
        },
        {
            "id": "MIM:620102",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620102",
            "name": "Retinitis pigmentosa 95",
            "description": "Retinitis pigmentosa 95"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061112"
    ],
    "unlinked_id_list": []
}