{
    "disease_id": "DOID:0110714", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014614", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014614", 
            "name": "CSNB1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014614", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014614", 
            "name": "night blindness, congenital stationary, type 1G; CSNB1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014614", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014614", 
            "name": "night blindness, congenital stationary, type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014614", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014614", 
            "name": "congenital stationary night blindness type 1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110714", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110714", 
            "name": "CSNB1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110714", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110714", 
            "name": "congenital stationary night blindness type 1G"
        }, 
        {
            "url": "https://www.omim.org/entry/616389", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616389", 
            "name": "Night blindness, congenital stationary, 1G"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110714", 
        "description": "A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the GNAT1 gene on chromosome 3p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110714", 
        "name": "congenital stationary night blindness 1G"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616389", 
            "id": "616389", 
            "database": "MIM"
        }
    ]
}