inclusion body myopathy, autosomal recessive Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/600737
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Genes

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

Symbol Name
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase