M31.19 Other thrombotic microangiopathyBillable ICD-10-CM code, FY2026. Acts as a Major Complication or Comorbidity (MCC) as a secondary diagnosis.
Defines the logic of DRG(s) 545-547 in MDC 08.
D68.5 Primary thrombophilia ("thrombotic thrombocytopenic purpura (M31.19)")D69 Purpura and other hemorrhagic conditions ("thrombotic thrombocytopenic purpura (M31.19)")I77 Other disorders of arteries and arterioles ("collagen (vascular) diseases (M30-M36)")J82 Pulmonary eosinophilia, not elsewhere classified ("pulmonary eosinophilia due to systemic connective tissue disorders (M30-M36)")J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere ("systemic connective tissue disorders (M30-M36)")L94 Other localized connective tissue disorders ("systemic connective tissue disorders (M30-M36)")M31 Other necrotizing vasculopathiesM31.0 Hypersensitivity angiitisM31.1 Thrombotic microangiopathyM31.10 Thrombotic microangiopathy, unspecifiedM31.11 Hematopoietic stem cell transplantation-associated thrombotic microangiopathy [HSCT-TMA]M31.19 Other thrombotic microangiopathy (this code)M31.2 Lethal midline granulomaM31.3 Wegener's granulomatosisM31.30 Wegener's granulomatosis without renal involvementM31.31 Wegener's granulomatosis with renal involvementM31.4 Aortic arch syndrome [Takayasu]