DNM1-encephalopathy and neurodevelopmental disorder

MONDO:0700339

A developmental and epileptic encephalopathy in which the cause of the disease is a variation in the DNM1 gene.

Also known as: DNM1-related DEE, DNM1-related developmental and epileptic encephalopathy

17 clinical trials for this condition and its sub-types, 0 tagged with DNM1-encephalopathy and neurodevelopmental disorder itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of DNM1-encephalopathy and neurodevelopmental disorder

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.