{
    "disease_id": "DOID:0061298",
    "recommended_name": {
        "id": "DOID:0061298",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061298",
        "name": "retinitis pigmentosa 100",
        "description": "A retinitis pigmentosa characterized by the onset of night blindness in childhood or young adulthood, followed by progressive visual field constriction and that has_material_basis_in compound heterozygous mutation in the TBC1D32 gene on chromosome 6q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0979574",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0979574",
            "name": "retinitis pigmentosa 100",
            "description": ""
        },
        {
            "id": "MIM:621280",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/621280",
            "name": "Retinitis pigmentosa 100",
            "description": "Retinitis pigmentosa 100"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061298"
    ],
    "unlinked_id_list": []
}