{
    "disease_id": "DOID:0111322",
    "recommended_name": {
        "id": "DOID:0111322",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111322",
        "name": "obsolete idiopathic generalized epilepsy 8",
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CASR on chromosome 3q13.3-q21.1."
    },
    "synonyms": [
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 8",
            "description": "Any generalized epilepsy in which the cause of the disease is a mutation in the CASR gene."
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "CASR generalised epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "CASR generalized epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "epilepsy idiopathic generalized, susceptibility to, 8",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "epilepsy, idiopathic generalized, susceptibility to, 8",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "generalised epilepsy caused by mutation in CASR",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "generalized epilepsy caused by mutation in CASR",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "EIG8",
            "description": ""
        },
        {
            "id": "MONDO:0013032",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013032",
            "name": "susceptibility to idiopathic generalised epilepsy 8",
            "description": ""
        },
        {
            "id": "MIM:612899",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612899",
            "name": "Epilepsy, idiopathic generalized 8",
            "description": "Epilepsy, idiopathic generalized 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111322"
    ],
    "unlinked_id_list": []
}