{
    "disease_id": "DOID:0081423",
    "recommended_name": {
        "id": "DOID:0081423",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081423",
        "name": "familial focal epilepsy with variable foci 3",
        "description": "A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL3 gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "epilepsy, familial focal, with variable foci 3",
            "description": "Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL3 gene."
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "FFEVF3",
            "description": ""
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "NPRL3 epilepsy, familial focal, with variable foci",
            "description": ""
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "epilepsy, familial focal, with variable foci 3",
            "description": ""
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "epilepsy, familial focal, with variable foci 3; FFEVF3",
            "description": ""
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "epilepsy, familial focal, with variable foci caused by mutation in NPRL3",
            "description": ""
        },
        {
            "id": "MONDO:0014925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014925",
            "name": "epilepsy, familial focal, with variable foci type 3",
            "description": ""
        },
        {
            "id": "MIM:617118",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617118",
            "name": "Epilepsy, familial focal, with variable foci 3",
            "description": "Epilepsy, familial focal, with variable foci 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081423"
    ],
    "unlinked_id_list": []
}