{
    "disease_id": "DOID:0110715", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "CSNBAD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "congenital stationary night blindness autosomal dominant type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "Nougaret type congenital stationary night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "night blindness, congenital stationary, autosomal dominant 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "night blindness, congenital stationary, Nougaret type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "night blindness, congenital stationary, autosomal dominant type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012497", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012497", 
            "name": "night blindness, congenital stationary, autosomal dominant 3; CSNBAD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110715", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110715", 
            "name": "CSNBAD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110715", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110715", 
            "name": "Nougaret type congenital stationary night blindness"
        }, 
        {
            "url": "https://www.omim.org/entry/610444", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610444", 
            "name": "Night blindness, congenital stationary, autosomal dominant 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110715", 
        "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110715", 
        "name": "congenital stationary night blindness autosomal dominant 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610444", 
            "id": "610444", 
            "database": "MIM"
        }
    ]
}