E72.5 Disorders of glycine metabolismNon-billable header with 6 child codes.
E72.50 Disorder of glycine metabolism, unspecifiedE72.51 Non-ketotic hyperglycinemiaE72.52 TrimethylaminuriaE72.53 Primary hyperoxaluriaE72.54 Secondary hyperoxaluriaE72.59 Other disorders of glycine metabolismG11 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 amino-acid metabolism (E70-E72)")R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")E72.22 Arginosuccinic aciduriaE72.23 CitrullinemiaE72.29 Other disorders of urea cycle metabolismE72.3 Disorders of lysine and hydroxylysine metabolismE72.4 Disorders of ornithine metabolismE72.5 Disorders of glycine metabolism (this code)E72.50 Disorder of glycine metabolism, unspecifiedE72.51 Non-ketotic hyperglycinemiaE72.52 TrimethylaminuriaE72.53 Primary hyperoxaluriaE72.530 Primary hyperoxaluria, type 1