ICD-11 code : L2-3B5;
Preferred Label : Fibrinolytic defects;
ICD-11 definition : 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.;
Origin ID : 1881300992;
Automatic exact mappings (from CISMeF team)
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.
