epilepsy, idiopathic generalized, susceptibility to, 11
MONDO:0011875
Also Known As
CLCN2 generalised epilepsyCLCN2 generalized epilepsyEIG11epilepsy, idiopathic generalized, susceptibility to, 11epilepsy, idiopathic generalized, susceptibility to, type 11generalised epilepsy caused by mutation in CLCN2generalized epilepsy caused by mutation in CLCN2epilepsy, juvenile absence, susceptibility to, 2epilepsy, juvenile myoclonic, susceptibility to, 8susceptibility to idiopathic generalised epilepsy 11susceptibility to idiopathic generalized epilepsy 11
Definition
An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene.