{
    "disease_id": "DOID:0112147",
    "recommended_name": {
        "id": "DOID:0112147",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112147",
        "name": "retinitis pigmentosa 90",
        "description": "A retinitis pigmentosa characterized by onset in the first decade of life of night blindness that has_material_basis_in homozygous or compound heterozygous mutation in IDH3A on chromosome 15q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112147",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112147",
            "name": "RP90",
            "description": ""
        },
        {
            "id": "MONDO:0033563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033563",
            "name": "retinitis pigmentosa 90",
            "description": ""
        },
        {
            "id": "MONDO:0033563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033563",
            "name": "RETINITIS PIGMENTOSA 90",
            "description": ""
        },
        {
            "id": "MONDO:0033563",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033563",
            "name": "RP90",
            "description": ""
        },
        {
            "id": "MIM:619007",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619007",
            "name": "Retinitis pigmentosa 90",
            "description": "Retinitis pigmentosa 90"
        }
    ]
}