|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A glycogen metabolism disorder that has_material_basis_in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. (Human Disease Ontology, DOID_2747)|
|Downloads & Tools|
2 genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset.