{
    "disease_id": "DOID:0081420",
    "recommended_name": {
        "id": "DOID:0081420",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081420",
        "name": "familial focal epilepsy with variable foci",
        "description": "A focal epilepsy that is characterized by focal seizures, with seizure onset in a discrete area of the brain including the temporal, frontal, parietal, and occipital lobes, with focal seizures arising from different cortical regions in different family members."
    },
    "synonyms": [
        {
            "id": "DOID:0081420",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081420",
            "name": "DEPDC5-related epilepsy",
            "description": ""
        },
        {
            "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": "DOID:0081421",
            "label": "familial focal epilepsy with variable foci 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0081422",
            "label": "familial focal epilepsy with variable foci 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0081423",
            "label": "familial focal epilepsy with variable foci 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0081424",
            "label": "familial focal epilepsy with variable foci 4",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0081424",
        "DOID:0081421",
        "DOID:0081422",
        "DOID:0081423",
        "DOID:0081420"
    ],
    "unlinked_id_list": []
}