inclusion body myopathy-3 Gene Set

Dataset	OMIM Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms. (Human Disease Ontology, DOID_3429)
External Link	http://www.omim.org/entry/605637
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Genes

1 genes associated with the inclusion body myopathy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol	Name
MYH2	myosin, heavy chain 2, skeletal muscle, adult