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:255160 - CONGENITAL MYOPATHY 7B, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; CMYO7B

Xenbase Genes: myh7l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009708 - dorsal pancreas
MONDO:0018889 - hyaline body myopathy

Disease Ontology (DO):
DOID:0111268 - autosomal recessive hyaline body myopathy