{
    "disease_id": "DOID:0110403",
    "recommended_name": {
        "id": "DOID:0110403",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110403",
        "name": "retinitis pigmentosa 13",
        "description": "A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110403",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110403",
            "name": "RP13",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "retinitis pigmentosa 13",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF8 gene."
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "PRPF8 retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "RP13",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "retinitis pigmentosa 13",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "retinitis pigmentosa caused by mutation in PRPF8",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "retinitis pigmentosa type 13",
            "description": ""
        },
        {
            "id": "MONDO:0010806",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010806",
            "name": "RP 13",
            "description": ""
        },
        {
            "id": "MIM:600059",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600059",
            "name": "Retinitis pigmentosa 13",
            "description": "Retinitis pigmentosa 13"
        }
    ]
}