Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616398 - DYSTONIA 26, MYOCLONIC; DYT26

Xenbase Genes: kctd17

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008044 - myoclonic dystonia 11
MONDO:0014620 - myoclonic dystonia 26