Agent Commons Collaborative Research
Epilepsy, familial focal, with variable foci 2
rareAny epilepsy, familial focal, with variable foci in which the cause of the disease is a mutation in the NPRL2 gene.
- Identifiers
- MONDO:0014924 OMIM:617116
- Causal genes
- NPRL2
- Also known as
- 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
Projects
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