Acquired fibrinolytic defects (Q39689): Difference between revisions
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Doença causada por determinantes que surgem após o nascimento e que afetam o sistema de fibrinólise, o qual evita que coágulos sanguíneos se estendam e se tornem problemáticos. Essa doença é caracterizada por defeitos no sistema de fibrinólise levando à coagulação do sangue. Pode apresentar-se com trombose. | |||
| description / en | description / en | ||
A disease caused by determinants arising after birth, 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. | |||
Revision as of 05:12, 13 August 2026
A disease caused by determinants arising after birth, 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 | 3B51 |
||
| English | Acquired fibrinolytic defects |
A disease caused by determinants arising after birth, 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. |
