|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterized by exercise intolerance. (Orphanet Rare Disease Ontology, Orphanet_715)|
|Downloads & Tools|
1 genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset.
|PHKA1||phosphorylase kinase, alpha 1 (muscle)||2.88009|