ICD-11 classes
03 Diseases of the blood or blood-forming organs
Coagulation defects, purpura or other haemorrhagic or...
Fibrinolytic defects
ICD-11 Fibrinolytic defects
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.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis contains 2 clarifying diagnoses:
- 3B50 — Inherited fibrinolytic defects
It contains 5 clarifying diagnoses. - 3B51 — Acquired fibrinolytic defects