{
    "disease_id": "DOID:0110409",
    "recommended_name": {
        "id": "DOID:0110409",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110409",
        "name": "retinitis pigmentosa 46",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the IDH3B on chromosome 20p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110409",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110409",
            "name": "RP46",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa 46",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene."
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa type 46",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa 46",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "IDH3B retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "RP46",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa 46; RP46",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa, autosomal recessive, Idh3B-related",
            "description": ""
        },
        {
            "id": "MONDO:0012943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012943",
            "name": "retinitis pigmentosa caused by mutation in IDH3B",
            "description": ""
        },
        {
            "id": "MIM:612572",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612572",
            "name": "Retinitis pigmentosa 46",
            "description": "Retinitis pigmentosa 46"
        }
    ]
}