Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 41
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC1A2 gene.
- Identifiers
- MONDO:0014916 OMIM:617105
- Causal genes
- SLC1A2
- Part of
- Early-infantile DEENeonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE41 · developmental and epileptic encephalopathy 41 · early infantile epileptic encephalopathy caused by mutation in SLC1A2 · EIEE41 · epileptic encephalopathy, early infantile, 41
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