Epilepsy, idiopathic generalized, susceptibility to, 8

MONDO:0013032

Any generalized epilepsy in which the cause of the disease is a mutation in the CASR gene.

Also known as: CASR generalised epilepsy, CASR generalized epilepsy, epilepsy idiopathic generalized, susceptibility to, 8, epilepsy, idiopathic generalized, susceptibility to, 8, epilepsy, idiopathic generalized, susceptibility to, type 8, generalised epilepsy caused by mutation in CASR, generalized epilepsy caused by mutation in CASR, EIG8

0 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, idiopathic generalized, susceptibility to, 8 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Inherited disease susceptibility (1316)

Including sub-types (0) Tagged with Epilepsy, idiopathic generalized, susceptibility to, 8 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.