E83.119 Hemochromatosis, unspecifiedBillable ICD-10-CM code, FY2026.
Defines the logic of DRG(s) 642 in MDC 10.
275.03 Other hemochromatosis (approximate)M14.8 Arthropathies in other specified diseases classified elsewhere ("hemochromatosis (E83.11-)")P78.84 Gestational alloimmune liver disease ("hemochromatosis (E83.11-)")J84.03 Idiopathic pulmonary hemosiderosis ("disorders of iron metabolism (E83.1-)")E61 Deficiency of other nutrient elements ("disorders of mineral metabolism (E83.-)")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)")R79.0 Abnormal level of blood mineral ("disorders of mineral metabolism (E83.-)")E83.10 Disorder of iron metabolism, unspecifiedE83.11 HemochromatosisE83.110 Hereditary hemochromatosisE83.111 Hemochromatosis due to repeated red blood cell transfusionsE83.118 Other hemochromatosisE83.119 Hemochromatosis, unspecified (this code)E83.19 Other disorders of iron metabolismE83.2 Disorders of zinc metabolismE83.3 Disorders of phosphorus metabolism and phosphatasesE83.30 Disorder of phosphorus metabolism, unspecifiedE83.31 Familial hypophosphatemia