{
    "disease_id": "DOID:0110352",
    "recommended_name": {
        "id": "DOID:0110352",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110352",
        "name": "retinitis pigmentosa 59",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11."
    },
    "synonyms": [
        {
            "id": "DOID:0110352",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110352",
            "name": "RP59",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "retinitis pigmentosa 59",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the DHDDS gene."
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "retinitis pigmentosa type 59",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "DHDDS retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "retinitis pigmentosa 59; RP59",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "retinitis pigmentosa caused by mutation in DHDDS",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "RP59",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "congenital disorder of glycosylation, type Ibb",
            "description": ""
        },
        {
            "id": "MONDO:0013468",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013468",
            "name": "retinitis pigmentosa 59",
            "description": ""
        },
        {
            "id": "MIM:613861",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613861",
            "name": "Retinitis pigmentosa 59",
            "description": "Retinitis pigmentosa 59"
        }
    ]
}