Glycogen Storage Disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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2 genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PHKA2 phosphorylase kinase, alpha 2 (liver) 2.88009
GYG1 glycogenin 1 2.88009