myoclonic dystonia 26

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

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


Synonyms

  • DYT26
  • KCTD17 myoclonus-dystonia syndrome
  • dystonia 26, myoclonic
  • myoclonic dystonia type 26
  • myoclonus-dystonia syndrome caused by mutation in KCTD17DYT26
  • KCTD17 myoclonus-dystonia syndrome
  • dystonia 26, myoclonic
  • myoclonic dystonia type 26
  • myoclonus-dystonia syndrome caused by mutation in KCTD17