ICD·index Chapters ENESDE
3B50-3B51 block

Fibrinolytic defects

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.

2 subordinate codes

Nearby in Coagulation defects, purpura or other haemorrhagic or related conditions