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3B65 Thrombotic microangiopathy, not elsewhere classified

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Thrombotic microangiopathies are microvascular occlusive disorders characterised by systemic or intrarenal aggregation of platelets, thrombocytopenia, and mechanical injury to erythrocytes. Thrombotic thrombocytopenic purpura (TTP) and haemolytic–uremic syndrome (HUS) represent a spectrum of thrombotic microangiopathies. In TTP, systemic microvascular aggregation of platelets causes ischemia in the brain and other organs. In HUS, platelet–fibrin thrombi predominantly occlude the renal circulation.

code elsewhere

• Thrombotic thrombocytopenic purpura  (3B64.14)
• Haemolytic uraemic syndrome  (3A21.2)
• Methylcobalamin deficiency type cbl G  (5C50.B)
• Hereditary haemolytic uraemic syndrome  (3A10.Y)

postcoordination

synonyms

• Thrombotic microangiopathy, not elsewhere classified
• Acute intravascular thrombotic microangiopathy
• Acute intravascular thrombi microangiopathy
• Chronic intravascular thrombotic microangiopathy
• Chronic intravascular thrombi microangiopathy

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