Myoclonic dystonia 15

MONDO:0011844

A myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11.

Also known as: dystonia-15, myoclonic, myoclonic dystonia type 15, DYT15, dystonia 15, myoclonic

14 clinical trials for this condition and its sub-types, 0 tagged with Myoclonic dystonia 15 itself.

Where it sits in the disease tree

Part of

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