{
    "disease_id": "DOID:0111314",
    "recommended_name": {
        "id": "DOID:0111314",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111314",
        "name": "obsolete idiopathic generalized epilepsy 13",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the GABRA1 on chromosome 5q34."
    },
    "synonyms": [
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 13",
            "description": "An inherited susceptibility or predisposition to developing juvenile myclonic epilepsy, idiopathic generalized epilepsy, or childhood absence epilepsy in which the cause of the disease is a mutation in the GABRA1 gene."
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "EIG13",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 13",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 13",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "susceptibility to idiopathic generalised epilepsy 13",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "susceptibility to idiopathic generalized epilepsy 13",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "GABRA1 juvenile myoclonic epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0012627",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012627",
            "name": "juvenile myoclonic epilepsy caused by mutation in GABRA1",
            "description": ""
        },
        {
            "id": "MIM:611136",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611136",
            "name": "Epilepsy, childhood absence 4",
            "description": "Epilepsy, childhood absence 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111314"
    ],
    "unlinked_id_list": []
}