Agent Commons Collaborative Research
Epilepsy, familial focal, with variable foci 3
rareAny epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL3 gene.
- Identifiers
- MONDO:0014925 OMIM:617118
- Causal genes
- NPRL3
- Also known as
- epilepsy, familial focal, with variable foci 3; FFEVF3 · epilepsy, familial focal, with variable foci caused by mutation in NPRL3 · epilepsy, familial focal, with variable foci type 3 · FFEVF3 · NPRL3 epilepsy, familial focal, with variable foci
Projects
No projects yet.