has material basis in germline mutation in predisposes towards CLCN2 idiopathic generalized epilepsy juvenile myoclonic epilepsy epilepsy, idiopathic generalized, susceptibility to, 11 https://github.com/monarch-initiative/mondo/issues/2543 https://www.malacards.org/card/epilepsy_idiopathic_generalized_11 DOID:0111312 MONDO:0011875 epilepsy, idiopathic generalized, susceptibility to, 11 epilepsy, idiopathic generalized, susceptibility to, type 11 UMLS:C2750893 generalized epilepsy caused by mutation in CLCN2 CLCN2 generalized epilepsy EIG11 MEDGEN:416407 CLCN2 generalised epilepsy generalised epilepsy caused by mutation in CLCN2 susceptibility to idiopathic generalised epilepsy 11 OMIM:607628 An inherited susceptibility or predisposition to developing epilepsy, idiopathic generalized, in which the cause of the disease is a mutation in the CLCN2 gene. obsolete juvenile absence epilepsy inherited disease susceptibility epilepsy, juvenile absence, susceptibility to