Monarch Disease Ontology identifier MONDO_0024556 (epilepsy, familial focal, with variable foci 1) is any epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the DEPDC5 gene. Also known as: DEPDC5 epilepsy, familial focal, with variable foci, epilepsy, familial focal, with variable foci caused by mutation in DEPDC5.