Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 37
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the FRRS1L gene.
- Identifiers
- MONDO:0014859 OMIM:616981
- Causal genes
- FRRS1L
- Also known as
- DEE37 · developmental and epileptic encephalopathy 37 · early infantile epileptic encephalopathy caused by mutation in FRRS1L · EIEE37 · epileptic encephalopathy, early infantile, 37
Projects
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