3B51
获得性纤维蛋白溶解缺陷
Acquired fibrinolytic defects
- 上级条目
- 纤维蛋白溶解缺陷
- 层级
- 4 级
定义
一种由出生后产生的影响因素引起的疾病，影响到防止血凝块生长和形成问题的纤维蛋白溶解系统。这种疾病特点是纤维蛋白溶解系统的缺陷导致血液凝固。本病可表现为血栓形成。
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.
索引词 可用于检索该条目的同义词与别名
- 获得性纤维蛋白溶解缺陷
- 药物性纤溶异常
- 药剂性纤溶异常
- 使用组织型纤溶酶原激活剂引起的纤溶异常
- 使用tPA[组织型纤溶酶原激活剂]引起的纤溶异常 [possible translation]
- 使用tPA[组织型纤溶酶原激活剂]引起的纤溶异常
- 使用尿激酶引起的纤溶异常
- 使用其他药物引起的纤溶异常
英文词条（7）
- Acquired fibrinolytic defects
- Drug-induced fibrinolytic disorder
- medicament-induced fibrinolytic disorder
- Fibrinolytic disorder due to administration of tissue-type plasminogen activator
- Fibrinolytic disorder due to administration of tPA - [ tissue-type plasminogen activator]
- Fibrinolytic disorder due to administration of urokinase
- Fibrinolytic disorder due to administration of other drugs
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。