E72.548 Other secondary hyperoxaluriaBillable ICD-10-CM code, FY2026.
Defines the logic of DRG(s) 695-696 in MDC 11.
E72.53 Primary hyperoxaluria ("secondary hyperoxaluria (E72.54-)")R82.992 Hyperoxaluria ("secondary hyperoxaluria (E72.54-)")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)")E72.538 Other specified primary hyperoxaluriaE72.539 Primary hyperoxaluria, unspecifiedE72.54 Secondary hyperoxaluriaE72.540 Dietary hyperoxaluriaE72.541 Enteric hyperoxaluriaE72.548 Other secondary hyperoxaluria (this code)E72.549 Secondary hyperoxaluria, unspecifiedE72.59 Other disorders of glycine metabolismE72.8 Other specified disorders of amino-acid metabolismE72.81 Disorders of gamma aminobutyric acid metabolismE72.89 Other specified disorders of amino-acid metabolism