Developmental and epileptic encephalopathy, 11
MONDO:0013388Any 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
21 clinical trials for this condition and its sub-types, 4 tagged with Developmental and epileptic encephalopathy, 11 itself.
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