Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 5
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SPTAN1 gene.
- Identifiers
- MONDO:0013277 OMIM:613477
- Causal genes
- SPTAN1
- Also known as
- DEE5 · developmental and epileptic encephalopathy 5 · early infantile epileptic encephalopathy caused by mutation in SPTAN1 · EIEE5 · epileptic encephalopathy, early infantile, 5
Projects
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