Inherited fibrinolytic defects (Q39608)
From determinar.ia.br - Determine suas informações
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. |
Statements
CID11:3B50
0 references
dki-india-3B50
0 references
Concluído
0 references
