E72.549 Secondary hyperoxaluria, unspecifiedBillable 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)")E72.539 Primary hyperoxaluria, unspecifiedE72.54 Secondary hyperoxaluriaE72.540 Dietary hyperoxaluriaE72.541 Enteric hyperoxaluriaE72.548 Other secondary hyperoxaluriaE72.549 Secondary hyperoxaluria, unspecified (this code)E72.59 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 metabolismE72.9 Disorder of amino-acid metabolism, unspecified