Inherited fibrinolytic defects (Q39608): Difference between revisions
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Revision as of 05:05, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B50 |
||
| English | Inherited fibrinolytic defects |
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. |
