3B50 Inherited fibrinolytic defects

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

A disease caused by genetically inherited mutations 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.

code elsewhere

• Hypoplasminogenaemia  (DA0D.3)

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

• Congenital alpha-2 antiplasmin deficiency  (3B50.0)
• Congenital plasminogen activator inhibitor type 1 deficiency  (3B50.1)
• Other specified inherited fibrinolytic defects  (3B50.Y)
• Inherited fibrinolytic defects, unspecified  (3B50.Z)

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