D59.32 Hereditary hemolytic-uremic syndromeBillable ICD-10-CM code, FY2026. Acts as a Major Complication or Comorbidity (MCC) as a secondary diagnosis.
Defines the logic of DRG(s) 791 in MDC 15.
D69.1 Qualitative platelet defects ("hemolytic-uremic syndrome (D59.3-)")M31.11 Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA] ("hemolytic uremic syndrome (D59.3-)")N08 Glomerular disorders in diseases classified elsewhere ("hemolytic-uremic syndrome (D59.3-)")M90.5 Osteonecrosis in diseases classified elsewhere ("hemoglobinopathy (D50-D64)")R71 Abnormality of red blood cells ("anemias (D50-D64)")D59.19 Other autoimmune hemolytic anemiaD59.2 Drug-induced nonautoimmune hemolytic anemiaD59.3 Hemolytic-uremic syndromeD59.30 Hemolytic-uremic syndrome, unspecifiedD59.31 Infection-associated hemolytic-uremic syndromeD59.32 Hereditary hemolytic-uremic syndrome (this code)D59.39 Other hemolytic-uremic syndromeD59.4 Other nonautoimmune hemolytic anemiasD59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]D59.6 Hemoglobinuria due to hemolysis from other external causesD59.8 Other acquired hemolytic anemias