{
    "disease_id": "DOID:0111796",
    "recommended_name": {
        "id": "DOID:0111796",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111796",
        "name": "congenital nystagmus 5",
        "description": "A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4."
    },
    "synonyms": [
        {
            "id": "DOID:0111796",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111796",
            "name": "NYS5",
            "description": ""
        },
        {
            "id": "DOID:0111796",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111796",
            "name": "X-linked congenital nystagmus 5",
            "description": ""
        },
        {
            "id": "MONDO:0010369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010369",
            "name": "NYS5",
            "description": ""
        },
        {
            "id": "MONDO:0010369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010369",
            "name": "NYS5",
            "description": ""
        },
        {
            "id": "MONDO:0010369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010369",
            "name": "NYSTAGMUS 5, congenital, X-linked; NYS5",
            "description": ""
        },
        {
            "id": "MONDO:0010369",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010369",
            "name": "NYSTAGMUS 5, congenital, X-linked",
            "description": ""
        }
    ]
}