Myoclonic dystonia 26

MONDO:0014620

Any myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene.

Also known as: KCTD17 myoclonus-dystonia syndrome, myoclonic dystonia type 26, myoclonus-dystonia syndrome caused by mutation in KCTD17, DYT26, dystonia 26, myoclonic

14 clinical trials for this condition and its sub-types, 0 tagged with Myoclonic dystonia 26 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Myoclonus-dystonia syndrome (3)

Including sub-types (14) Tagged with Myoclonic dystonia 26 (0)

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