Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 28
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the WWOX gene.
- Identifiers
- MONDO:0014533 OMIM:616211
- Causal genes
- WWOX
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE28 · developmental and epileptic encephalopathy 28 · early infantile epileptic encephalopathy caused by mutation in WWOX · EIEE28 · epileptic encephalopathy, early infantile, 28
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