{
    "disease_id": "DOID:0111292",
    "recommended_name": {
        "id": "DOID:0111292",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111292",
        "name": "obsolete idiopathic generalized epilepsy 10",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in variation in the GABRD on chromosome 1p36.33."
    },
    "synonyms": [
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 10",
            "description": "An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the GABRD gene."
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "EIG10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "epilepsy, idiopathic generalized, 10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "epilepsy, juvenile myoclonic, susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "susceptibility to idiopathic generalised epilepsy 10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "susceptibility to idiopathic generalized epilepsy 10",
            "description": ""
        },
        {
            "id": "MONDO:0013103",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013103",
            "name": "generalised epilepsy with febrile seizures plus, type 5, susceptibility to",
            "description": ""
        },
        {
            "id": "MIM:613060",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613060",
            "name": "Epilepsy, idiopathic generalized 10",
            "description": "Epilepsy, idiopathic generalized 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111292"
    ],
    "unlinked_id_list": []
}