Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 33
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the EEF1A2 gene.
- Identifiers
- MONDO:0014625 OMIM:616409
- Causal genes
- EEF1A2
- Part of
- Neonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- DEE33 · developmental and epileptic encephalopathy 33 · early infantile epileptic encephalopathy caused by mutation in EEF1A2 · EEF1A2 early infantile epileptic encephalopathy · EEF1A2-Related Neurodevelopmental Disorder
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