Inclusion body myopathy 2 Gene Set

Dataset ClinVar Gene-Phenotype 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/600737
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Genes

1 genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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