|Dataset||GAD 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|
4 genes associated with the disease glycogen storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.