E72.51 Non-ketotic hyperglycinemiaBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Defines the logic of DRG(s) 642 in MDC 10.
270.7 Other disturbances of straight-chain amino-acid metabolism (approximate)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 amino-acid metabolism (E70-E72)")R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")E72.29 Other disorders of urea cycle metabolismE72.3 Disorders of lysine and hydroxylysine metabolismE72.4 Disorders of ornithine metabolismE72.5 Disorders of glycine metabolismE72.50 Disorder of glycine metabolism, unspecifiedE72.51 Non-ketotic hyperglycinemia (this code)E72.52 TrimethylaminuriaE72.53 Primary hyperoxaluriaE72.530 Primary hyperoxaluria, type 1E72.538 Other specified primary hyperoxaluriaE72.539 Primary hyperoxaluria, unspecified