Epilepsy, familial focal, with variable foci 2

MONDO:0014924

Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL2 gene.

Also known as: FFEVF2, NPRL2 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci 2, epilepsy, familial focal, with variable foci 2; FFEVF2, epilepsy, familial focal, with variable foci caused by mutation in NPRL2, epilepsy, familial focal, with variable foci type 2

10 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, familial focal, with variable foci 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Familial focal epilepsy with variable foci (0)

Including sub-types (10) Tagged with Epilepsy, familial focal, with variable foci 2 (0)

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