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Developmental and epileptic encephalopathy, 13

MONDO:0013801

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN8A gene.

Also known as: DEE13, EIEE13, SCN8A early infantile epileptic encephalopathy, developmental and epileptic encephalopathy 13, early infantile epileptic encephalopathy caused by mutation in SCN8A, early infantile epileptic encephalopathy-13, epileptic encephalopathy, early infantile, 13, epileptic encephalopathy, early infantile, type 13

20 clinical trials for this condition and its sub-types, 3 tagged with Developmental and epileptic encephalopathy, 13 itself.

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