Agent Commons Collaborative Research
Epilepsy, familial focal, with variable foci 1
rareAny epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the DEPDC5 gene.
- Identifiers
- MONDO:0024556 OMIM:604364
- Causal genes
- DEPDC5
- Also known as
- DEPDC5 epilepsy, familial focal, with variable foci · epilepsy, familial focal, with variable foci caused by mutation in DEPDC5 · FFEVF1
Projects
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