glycogen storage disease II glycogen storage disease due to acid maltase deficiency, infantile onset icd11.foundation:1496243702 Pompe disease, infantile onset NANDO:1200139 Orphanet:308552 glycogenosis type 2, infantile onset SCTID:722302009 GSD due to acid maltase deficiency, infantile onset alpha-1,4-glucosidase acid deficiency, infantile onset GARD:0021310 GSD type 2, infantile onset glycogen storage disease type II, infantile onset Glycogen storage disease due to acid maltase deficiency, infantile onset is the most severe form of glycogen storage disease due to acid maltase deficiency, characterized by cardiomegaly with respiratory distress, muscle weakness and feeding difficulties. It is often fatal. NANDO:2201229 MEDGEN:923868 UMLS:C3888924 glycogen storage disease type 2, infantile onset MONDO:0017694 glycogenosis due to acid maltase deficiency, infantile onset OMIM:232300 glycogenosis type II, infantile onset GSD type II, infantile onset