{
    "disease_id": "DOID:0112146",
    "recommended_name": {
        "id": "DOID:0112146",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112146",
        "name": "retinitis pigmentosa 89",
        "description": "A retinitis pigmentosa characterized by onset of retinitis pigmentosa in the first decade of life and additional features of ciliopathy that has_material_basis_in heterozygous mutation in the KIF3B gene on chromosome 20q11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0112146",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112146",
            "name": "RP89",
            "description": ""
        },
        {
            "id": "MONDO:0030071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030071",
            "name": "retinitis pigmentosa 89",
            "description": ""
        },
        {
            "id": "MONDO:0030071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030071",
            "name": "RETINITIS PIGMENTOSA 89",
            "description": ""
        },
        {
            "id": "MONDO:0030071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030071",
            "name": "RP89",
            "description": ""
        },
        {
            "id": "MONDO:0030071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030071",
            "name": "retinitis pigmentosa 89",
            "description": ""
        },
        {
            "id": "MIM:618955",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618955",
            "name": "Retinitis pigmentosa 89",
            "description": "Retinitis pigmentosa 89"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112146"
    ],
    "unlinked_id_list": []
}