{
    "disease_id": "DOID:0110713", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "GRK1 Oguchi disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "Oguchi disease 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "Oguchi disease type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "congenital stationary night blindness Oguchi type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "Oguchi disease caused by mutation in GRK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "CSNBO2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013259", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013259", 
            "name": "night blindness, congenital stationary, Oguchi type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110713", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110713", 
            "name": "CSNBO2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110713", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110713", 
            "name": "congenital stationary night blindness Oguchi type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110713", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110713", 
        "name": "Oguchi disease-2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110713#disease-associations", 
            "id": "0110713", 
            "database": "Alliance of Genome Resources"
        }
    ]
}