|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|GNE||glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase|