{
    "disease_id": "DOID:0111790", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "nystagmus 1, congenital, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus, infantile idiopathic, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "NYS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "NYSTAGMUS 1, congenital, X-linked; NYS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus, infantile idiopathic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus 1, infantile, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus 1, congenital, X- linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Xlpan"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "congenital nystagmus caused by mutation in FRMD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus, congenital motor, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "Nystagmus, infantile periodic alternating, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010693", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010693", 
            "name": "FRMD7 congenital nystagmus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111790", 
            "name": "NYS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111790", 
            "name": "X-linked infantile nystagmus 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111790", 
            "name": "congenital motor nystagmus 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111790", 
        "description": "A congenital nystagmus that has_material_basis_in mutation in FRMD7 on chromosome Xq26.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111790", 
        "name": "congenital nystagmus 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111790#disease-associations", 
            "id": "0111790", 
            "database": "Alliance of Genome Resources"
        }
    ]
}