Fibrinolytic defects

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

A disease caused by determinants arising during the antenatal period, after birth or genetically inherited factors, affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.

sections/codes in this section (3B50-3B51)

• Inherited fibrinolytic defects  (3B50)
• Acquired fibrinolytic defects  (3B51)

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