Developmental and epileptic encephalopathy, 11

MONDO:0013388

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

Also known as: DEE11, EIEE11, SCN2A early infantile epileptic encephalopathy, developmental and epileptic encephalopathy 11, early infantile epileptic encephalopathy caused by mutation in SCN2A, epileptic encephalopathy, early infantile, 11, epileptic encephalopathy, early infantile, type 11

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