Term Name:	glycogen storage disease II
Synonyms:	acid maltase deficiency, deficiency of glucoamylase, deficiency of maltase, Generalized glycogenosis, Glycogen storage disease 2, glycogen storage disease type II, Glycogen storage disease, type II, Glycogenosis, type 2, Lysosomal alpha-1,4-glucosidase deficiency, Pompe's disease
Definition:	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.
Ontology:	Human Disease [DOID:2752]   ( DOID:2752 )