Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 47
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the FGF12 gene.
- Identifiers
- MONDO:0014949 OMIM:617166
- Causal genes
- FGF12
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE47 · developmental and epileptic encephalopathy 47 · early infantile epileptic encephalopathy caused by mutation in FGF12 · EIEE47 · epileptic encephalopathy, early infantile, 47
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