{
    "disease_id": "DOID:0110408",
    "recommended_name": {
        "id": "DOID:0110408",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110408",
        "name": "retinitis pigmentosa 11",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110408",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110408",
            "name": "RP11",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "retinitis pigmentosa 11",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF31 gene."
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "PRPF31 retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "RP11",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "retinitis pigmentosa 11",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "retinitis pigmentosa caused by mutation in PRPF31",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "retinitis pigmentosa type 11",
            "description": ""
        },
        {
            "id": "MONDO:0010828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010828",
            "name": "RP 11",
            "description": ""
        },
        {
            "id": "MIM:600138",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600138",
            "name": "Retinitis pigmentosa 11",
            "description": "Retinitis pigmentosa 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110408"
    ],
    "unlinked_id_list": []
}