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:614408 - MOVED TO 160150

Xenbase Genes: myf6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008048 - autosomal dominant centronuclear myopathy
MONDO:0013736 - myopathy, centronuclear, 3