{
    "disease_id": "DOID:0110871", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "congenital stationary night blindness caused by mutation in CACNA1F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "congenital stationary night blindness 2A X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "night blindness, congenital stationary, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "congenital stationary night blindness type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "night blindness, congenital stationary, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "night blindness, congenital stationary, type 2A; CSNB2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "CACNA1F congenital stationary night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "CSNB2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010241", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010241", 
            "name": "CSNB, incomplete, X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110871", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110871", 
            "name": "congenital stationary night blindness 2A X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110871", 
        "description": "A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110871", 
        "name": "congenital stationary night blindness 2A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110871#disease-associations", 
            "id": "0110871", 
            "database": "Alliance of Genome Resources"
        }
    ]
}