{
    "disease_id": "DOID:0080292",
    "recommended_name": {
        "id": "DOID:0080292",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080292",
        "name": "retinitis pigmentosa 81",
        "description": "A retinitis pigmentosa that has_material_basis_in homozygous mutation in the IFT43 gene on chromosome 14q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0036482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0036482",
            "name": "retinitis pigmentosa 81",
            "description": ""
        },
        {
            "id": "MONDO:0036482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0036482",
            "name": "retinitis pigmentosa 81",
            "description": ""
        },
        {
            "id": "MONDO:0036482",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0036482",
            "name": "RP81",
            "description": ""
        },
        {
            "id": "MIM:617871",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617871",
            "name": "Retinitis pigmentosa 81",
            "description": "Retinitis pigmentosa 81"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080292"
    ],
    "unlinked_id_list": []
}