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:160150 - MYOPATHY, CENTRONUCLEAR, 1; CNM1

Xenbase Genes: myf6, mtmr14, dnm2

Human Disease Resource: MIM

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

Disease Ontology (DO):
DOID:14717 - centronuclear myopathy