{
    "disease_id": "DOID:0110713",
    "recommended_name": {
        "id": "DOID:0110713",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110713",
        "name": "Oguchi disease-2",
        "description": "A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous mutation in the GRK1 gene on chromosome 13q34."
    },
    "synonyms": [
        {
            "id": "DOID:0110713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110713",
            "name": "CSNBO2",
            "description": ""
        },
        {
            "id": "DOID:0110713",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110713",
            "name": "congenital stationary night blindness Oguchi type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013259",
            "name": "Oguchi disease-2",
            "description": "Any Oguchi disease in which the cause of the disease is a mutation in the GRK1 gene."
        },
        {
            "id": "MONDO:0013259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013259",
            "name": "CSNBO2",
            "description": ""
        },
        {
            "id": "MONDO:0013259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013259",
            "name": "GRK1 Oguchi disease",
            "description": ""
        },
        {
            "id": "MONDO:0013259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013259",
            "name": "Oguchi disease caused by mutation in GRK1",
            "description": ""
        },
        {
            "id": "MONDO:0013259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013259",
            "name": "Oguchi disease type 2",
            "description": ""
        },
        {
            "id": "MIM:613411",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613411",
            "name": "Night blindness, congenital stationary, Oguchi type 2",
            "description": "Night blindness, congenital stationary, Oguchi type 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110713"
    ],
    "unlinked_id_list": []
}