Epilepsy, childhood absence, susceptibility to, 6

An inherited susceptibility or predisposition to developing child absence epilepsy or idiopathic generalized epilepsy, in which the cause of the disease is a mutation in the CACNA1H gene.

Also known as: ECA6, epilepsy, childhood absence, susceptibility to, 6, epilepsy, childhood absence, susceptibility to, type 6, susceptibility to childhood absence epilepsy 6, CACNA1H childhood absence epilepsy, childhood absence epilepsy caused by mutation in CACNA1H, epilepsy, idiopathic generalized, susceptibility to, 6

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, childhood absence, susceptibility to, 6 itself.