Glycogen Storage Disease Type II Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006009
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Genes

1 genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GAA glucosidase, alpha; acid 2.88009