{
    "disease_id": "DOID:0061178",
    "recommended_name": {
        "id": "DOID:0061178",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061178",
        "name": "autosomal recessive congenital nystagmus 8",
        "description": "A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2."
    },
    "synonyms": [
        {
            "id": "MONDO:0009762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009762",
            "name": "nystagmus, congenital, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009762",
            "name": "nystagmus, congenital, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009762",
            "name": "Nystagmus, congenital motor, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:257400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/257400",
            "name": "Nystagmus 8, congenital, autosomal recessive",
            "description": "Nystagmus 8, congenital, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061178"
    ],
    "unlinked_id_list": []
}