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)
OMIM:160150 - MYOPATHY, CENTRONUCLEAR, 1; CNM1

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

In Mondo Disease Ontology:
MONDO:0008048 - autosomal dominant centronuclear myopathy

Human Disease Resources: OMIM

Xenbase Genes: myf6, mtmr14, dnm2