Developmental and epileptic encephalopathy, 31A

Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.

Also known as: DEE31, DNM1-encephalopathy and neurodevelopmental disorder, DNM1-related epilepsy and neurodevelopmental disorder, EIEE31, developmental and epileptic encephalopathy 31, early infantile epileptic encephalopathy caused by mutation in DNM1, epileptic encephalopathy, early infantile, 31, epileptic encephalopathy, early infantile, type 31

18 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 31A itself.