Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 42
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the CACNA1A gene.
- Identifiers
- MONDO:0014917 OMIM:617106
- Part of
- CACNA1A-related complex neurodevelopmental disorderNeonatal-onset developmental and epileptic encephalopathyUndetermined early-onset epileptic encephalopathy
- Also known as
- CACNA1A early infantile epileptic encephalopathy · DEE42 · developmental and epileptic encephalopathy 42 · early infantile epileptic encephalopathy caused by mutation in CACNA1A · EIEE42
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