{
    "disease_id": "DOID:0081116",
    "recommended_name": {
        "id": "DOID:0081116",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081116",
        "name": "benign familial infantile seizures 3",
        "description": "A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutations in the SCN2A gene on chromosome 2q24."
    },
    "synonyms": [
        {
            "id": "DOID:0081116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081116",
            "name": "Benign Familial Infantile Seizures, 3",
            "description": ""
        },
        {
            "id": "DOID:0081116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081116",
            "name": "benign familial neonatal-infantile seizures",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "seizures, benign familial infantile, 3",
            "description": "Any benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN2A gene."
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "BFNIS",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "SCN2A benign familial infantile epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "benign familial infantile epilepsy caused by mutation in SCN2A",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "benign familial neonatal-infantile seizures",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "benign neonatal-infantile epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "seizures, benign familial infantile, 3",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "seizures, benign familial infantile, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "BFIS3",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "benign familial infantile convulsions",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "convulsions benign familial neonatal",
            "description": ""
        },
        {
            "id": "MONDO:0011904",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011904",
            "name": "epilepsy, benign neonatal-infantile",
            "description": ""
        },
        {
            "id": "MIM:607745",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607745",
            "name": "Seizures, benign familial infantile, 3",
            "description": "Seizures, benign familial infantile, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081116"
    ],
    "unlinked_id_list": []
}