Epilepsy, familial focal, with variable foci 2

Definition

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

Also known as 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, FFEVF2, NPRL2 epilepsy, familial focal, with variable foci — per MONDO

Also identified as

• DOID 0081422 per MONDO
• OMIM 617116 per MONDO
• UMLS C4310709 per MONDO