{
    "disease_id": "DOID:0111312",
    "recommended_name": {
        "id": "DOID:0111312",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111312",
        "name": "obsolete idiopathic generalized epilepsy 11",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1."
    },
    "synonyms": [
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 11",
            "description": "An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene."
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "CLCN2 generalised epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "CLCN2 generalized epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "EIG11",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 11",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "generalised epilepsy caused by mutation in CLCN2",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "generalized epilepsy caused by mutation in CLCN2",
            "description": ""
        },
        {
            "id": "MONDO:0011875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011875",
            "name": "susceptibility to idiopathic generalised epilepsy 11",
            "description": ""
        },
        {
            "id": "MIM:607628",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607628",
            "name": "Juvenile absence epilepsy 2",
            "description": "Juvenile absence epilepsy 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111312"
    ],
    "unlinked_id_list": []
}