{
    "disease_id": "DOID:0081422",
    "recommended_name": {
        "id": "DOID:0081422",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081422",
        "name": "familial focal epilepsy with variable foci 2",
        "description": "A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL2 gene on chromosome 3p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "epilepsy, familial focal, with variable foci 2",
            "description": "Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL2 gene."
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "FFEVF2",
            "description": ""
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "NPRL2 epilepsy, familial focal, with variable foci",
            "description": ""
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "epilepsy, familial focal, with variable foci 2",
            "description": ""
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "epilepsy, familial focal, with variable foci 2; FFEVF2",
            "description": ""
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "epilepsy, familial focal, with variable foci caused by mutation in NPRL2",
            "description": ""
        },
        {
            "id": "MONDO:0014924",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014924",
            "name": "epilepsy, familial focal, with variable foci type 2",
            "description": ""
        },
        {
            "id": "MIM:617116",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617116",
            "name": "Epilepsy, familial focal, with variable foci 2",
            "description": "Epilepsy, familial focal, with variable foci 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081422"
    ],
    "unlinked_id_list": []
}