{
    "disease_id": "DOID:0111312", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "epilepsy, juvenile absence, susceptibility to, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "EIG11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "epilepsy, juvenile myoclonic, susceptibility to, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "generalised epilepsy caused by mutation in CLCN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "epilepsy, idiopathic generalized, susceptibility to, 11; EIG11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "susceptibility to idiopathic generalized epilepsy 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011875", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011875", 
            "name": "CLCN2 generalised epilepsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111312", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111312", 
            "name": "EIG11"
        }, 
        {
            "url": "https://www.omim.org/entry/607628", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607628", 
            "name": "Juvenile absence epilepsy 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111312", 
        "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111312", 
        "name": "idiopathic generalized epilepsy 11"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607628", 
            "id": "607628", 
            "database": "MIM"
        }
    ]
}