{
    "disease_id": "DOID:0081424",
    "recommended_name": {
        "id": "DOID:0081424",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081424",
        "name": "familial focal epilepsy with variable foci 4",
        "description": "A familial focal epilepsy with variable foci that is characterized by onset of focal seizures in the first years of life and that has_material_basis_in heterozygous mutation in the SCN3A gene on chromosome 2q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0054776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054776",
            "name": "epilepsy, familial focal, with variable foci 4",
            "description": ""
        },
        {
            "id": "MONDO:0054776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054776",
            "name": "FFEVF4",
            "description": ""
        },
        {
            "id": "MIM:617935",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617935",
            "name": "Epilepsy, familial focal, with variable foci 4",
            "description": "Epilepsy, familial focal, with variable foci 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081424"
    ],
    "unlinked_id_list": []
}