Fibrinolytic defects (Q52735): Difference between revisions
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Revision as of 00:03, 14 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1881300992 |
||
| English | 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. |
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CID11:ID_1881300992
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dki-india-ID_1881300992
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