glycogen storage disease ii Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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)
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Genes

1 genes involed in the disease glycogen storage disease ii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
GAA glucosidase, alpha; acid