familial focal epilepsy with variable foci epilepsy, familial focal, with variable foci 1 OMIM:604364 MONDO:0024556 NCIT:C161005 Any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the DEPDC5 gene. FFEVF1 epilepsy, familial focal, with variable foci caused by mutation in DEPDC5 DEPDC5 epilepsy, familial focal, with variable foci DOID:0081421 GARD:0018202 UMLS:C4551983 epilepsy, familial focal, with variable foci 1 MEDGEN:1641798