Inclusion Body Myopathy 3, Autosomal Dominant Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C565311
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Genes

1 genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MYH2 myosin, heavy chain 2, skeletal muscle, adult 2.88009