Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 13
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN8A gene.
- Identifiers
- MONDO:0013801 OMIM:614558
- Causal genes
- SCN8A
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE13 · developmental and epileptic encephalopathy 13 · early infantile epileptic encephalopathy caused by mutation in SCN8A · early infantile epileptic encephalopathy-13 · EIEE13
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