{
    "disease_id": "DOID:0111790",
    "recommended_name": {
        "id": "DOID:0111790",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111790",
        "name": "congenital nystagmus 1",
        "description": "A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene (FERM domain-containing-7) on chromosome Xq26."
    },
    "synonyms": [
        {
            "id": "DOID:0111790",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111790",
            "name": "NYS1",
            "description": ""
        },
        {
            "id": "DOID:0111790",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111790",
            "name": "X-linked infantile nystagmus 1",
            "description": ""
        },
        {
            "id": "DOID:0111790",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111790",
            "name": "congenital motor nystagmus 1",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "nystagmus 1, congenital, X-linked",
            "description": "Any congenital nystagmus in which the cause of the disease is a mutation in the FRMD7 gene."
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "FRMD7 congenital nystagmus",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "congenital nystagmus caused by mutation in FRMD7",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "nystagmus 1, congenital, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "NYS1",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "Nystagmus 1, congenital, X- linked",
            "description": ""
        },
        {
            "id": "MONDO:0010693",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010693",
            "name": "Nystagmus, infantile idiopathic",
            "description": ""
        },
        {
            "id": "MIM:310700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/310700",
            "name": "Nystagmus 1, congenital, X-linked",
            "description": "Nystagmus 1, congenital, X-linked"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111790"
    ],
    "unlinked_id_list": []
}