| Disease Aliases (36) | Acid alpha-glucosidase deficiency, infantile-onset Acid maltase deficiency Acid maltase deficiency disease Acid maltase deficiency, infantile-onset Aglucosidase alfa Alpha-1,4-glucosidase acid deficiency Cardiomegalia glycogenica diffusa Deficiency of alpha-glucosidase Deficiency of glucoamylase Deficiency of lysosomal alpha-glucosidase Deficiency of maltase Gaa deficiency, infantile-onset Gaa glycogen storage disease Generalised glycogenosis Generalized glycogenosis Glucosidase acid-1,4-alpha deficiency Glycogen heart disease Glycogen storage disease caused by mutation in gaa Glycogen storage disease due to acid maltase deficiency Glycogen storage disease ii Glycogen storage disease ii, infantile-onset Glycogen storage disease type 2 Glycogen storage disease type ii (pompe disease) Glycogenosis due to acid maltase deficiency Glycogenosis type 2 Glycogenosis type ii Glycogenosis, generalized, cardiac form Glycogenosis, type 2 Gsd due to acid maltase deficiency Gsd ii Gsd type 2 Gsd type ii Iopd Lysosomal alpha-1,4-glucosidase deficiency Pompe disease Pompe disease, infantile-onset |
Associated Genes (0) | |||||||
| Cross-references of Glycogen storage disease, type II | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |