{
    "disease_id": "DOID:0081449",
    "recommended_name": {
        "id": "DOID:0081449",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081449",
        "name": "cone-rod dystrophy 24",
        "description": "A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11."
    },
    "synonyms": [
        {
            "id": "MONDO:0957240",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957240",
            "name": "cone-rod dystrophy 24",
            "description": ""
        },
        {
            "id": "MIM:620342",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620342",
            "name": "Cone-rod dystrophy 24",
            "description": "Cone-rod dystrophy 24"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081449"
    ],
    "unlinked_id_list": []
}