{
    "disease_id": "DOID:0110355",
    "recommended_name": {
        "id": "DOID:0110355",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110355",
        "name": "retinitis pigmentosa 32",
        "description": "A retinitis pigmentosa that has_material_basis_in variation in the chromosome region 1p21.3-p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110355",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110355",
            "name": "RP32",
            "description": ""
        },
        {
            "id": "MONDO:0012363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012363",
            "name": "retinitis pigmentosa 32",
            "description": "A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3."
        },
        {
            "id": "MONDO:0012363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012363",
            "name": "RP32",
            "description": ""
        },
        {
            "id": "MONDO:0012363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012363",
            "name": "retinitis pigmentosa 32",
            "description": ""
        },
        {
            "id": "MONDO:0012363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012363",
            "name": "retinitis pigmentosa type 32",
            "description": ""
        },
        {
            "id": "MIM:609913",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609913",
            "name": "Retinitis pigmentosa 32",
            "description": "Retinitis pigmentosa 32"
        }
    ]
}