|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome. (Human Disease Ontology, DOID_2752)|
|Downloads & Tools|
2 genes associated with the disease glycogen storage disease type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.