{
    "disease_id": "DOID:0081421",
    "recommended_name": {
        "id": "DOID:0081421",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081421",
        "name": "familial focal epilepsy with variable foci 1",
        "description": "A familial focal epilepsy with variable foci that is characterized by focal seizures arising from different cortical regions in different family members and that has_material_basis_in heterozygous mutation in the DEPDC5 gene on chromosome 22q12."
    },
    "synonyms": [
        {
            "id": "MONDO:0024556",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024556",
            "name": "epilepsy, familial focal, with variable foci 1",
            "description": "Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the DEPDC5 gene."
        },
        {
            "id": "MONDO:0024556",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024556",
            "name": "DEPDC5 epilepsy, familial focal, with variable foci",
            "description": ""
        },
        {
            "id": "MONDO:0024556",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024556",
            "name": "epilepsy, familial focal, with variable foci 1",
            "description": ""
        },
        {
            "id": "MONDO:0024556",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024556",
            "name": "epilepsy, familial focal, with variable foci caused by mutation in DEPDC5",
            "description": ""
        },
        {
            "id": "MONDO:0024556",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024556",
            "name": "FFEVF1",
            "description": ""
        },
        {
            "id": "MIM:604364",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604364",
            "name": "Epilepsy, familial focal, with variable foci 1",
            "description": "Epilepsy, familial focal, with variable foci 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081421"
    ],
    "unlinked_id_list": []
}