E74.0 Glycogen storage diseaseNon-billable header with 7 child codes.
E74.00 Glycogen storage disease, unspecifiedE74.01 von Gierke diseaseE74.02 Pompe diseaseE74.03 Cori diseaseE74.04 McArdle diseaseE74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiencyE74.09 Other glycogen storage diseaseG73.7 Myopathy in diseases classified elsewhere ("glycogen storage disease (E74.0-)")I43 Cardiomyopathy in diseases classified elsewhere ("glycogen storage disease (E74.0-)")N16 Renal tubulo-interstitial disorders in diseases classified elsewhere ("glycogen storage disease (E74.0-)")G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of carbohydrate metabolism (E73-E74)")