Glycogen storage disease type II

glycogen storage disease II

Acid Maltase Deficiency, Generalized gangliosidosis, Glucosidase acid-1,4-alpha deficiency, Glycogen storage disease type ii, Glycogen storage disease type IIb, Glycogen storage disease type iib, Glycogenosis type II, GSD II, GSD type II, infantile-onset Pompe disease, Infantile acid maltase deficiency, IOPD, Pompe's diseas, Pompe's disease, Pompe disease, Pompeii disease, Type II glycogen storage disease

acid maltase deficiency, Alpha-1,4-glucosidase acid deficiency, Alpha-1,4-Glucosidase Deficiency, Cardiomegalia Glycogenica Diffusa, deficiency of glucoamylase, deficiency of maltase, Gaa Deficiency, Generalized glycogenosis, Glycogen storage disease, type II, Glycogen storage disease due to acid maltase deficiency, GLYCOGEN STORAGE DISEASE II, GLYCOGEN STORAGE DISEASE II; GSD2, Glycogen storage disease type 2, glycogen storage disease type II, Glycogenosis, Generalized, Cardiac Form, Glycogenosis, type 2, Glycogenosis due to acid maltase deficiency, Glycogenosis type 2, Glycogenosis type II, GSD2, Gsd 2, GSD due to acid maltase deficiency, GSD type 2, GSD type II, Lysosomal alpha-1,4-glucosidase deficiency, Pompe's disease, Pompe disease