Inherited fibrinolytic defects (Q39608): Difference between revisions
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Doença causada por mutações geneticamente herdadas que afetam o sistema de fibrinólise que 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 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. | |||
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. |
