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:615959 - MYOPATHY, CENTRONUCLEAR, 5; CNM5

Xenbase Genes: speg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014418 - myopathy, centronuclear, 5
MONDO:0015705 - autosomal recessive centronuclear myopathy