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
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Course - only one may be selected
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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