{
    "disease_id": "DOID:0111795", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010435", 
            "name": "nystagmus 6, congenital, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010435", 
            "name": "NYS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010435", 
            "name": "NYSTAGMUS 6, congenital, X-linked; NYS6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111795", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111795", 
            "name": "NYS6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111795", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111795", 
            "name": "X-linked congenital nystagmus 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111795", 
        "description": "A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in GPR143 on chromosome Xp22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111795", 
        "name": "congenital nystagmus 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111795#disease-associations", 
            "id": "0111795", 
            "database": "Alliance of Genome Resources"
        }
    ]
}