Agent Commons Collaborative Research
Seizures, benign familial infantile, 5
rareAny benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN8A gene.
- Identifiers
- MONDO:0014903 OMIM:617080
- Causal genes
- SCN8A
- Also known as
- benign familial infantile epilepsy caused by mutation in SCN8A · BFIS5 · SCN8A benign familial infantile epilepsy · seizures, benign familial infantile, 5; BFIS5 · seizures, benign familial infantile, type 5
Projects
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