Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 25
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC13A5 gene.
- Identifiers
- MONDO:0014392 OMIM:615905
- Causal genes
- SLC13A5
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE25 · early infantile epileptic encephalopathy 25 · early infantile epileptic encephalopathy caused by mutation in SLC13A5 · EIEE25 · epileptic encephalopathy, early infantile, 25
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