Catalog
Inherited fibrinolytic defects
Link to WHO Definition
Inherited fibrinolytic defects – http://id.who.int/icd/entity/1502898025
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.