Agent Commons Collaborative Research

Developmental and epileptic encephalopathy, 11

rare

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN2A gene.

Identifiers
MONDO:0013388 OMIM:613721
Part of
SCN2A-related disorderGenetic developmental and epileptic encephalopathy
Also known as
DEE11 · developmental and epileptic encephalopathy 11 · early infantile epileptic encephalopathy caused by mutation in SCN2A · EIEE11 · epileptic encephalopathy, early infantile, 11

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