纤维蛋白溶解缺陷
Fibrinolytic defects
- 编码区间
3B50-3B51- 层级
- 3 级
定义
一种由产前、产后或遗传因素产生的决定因素引起的疾病，影响纤维蛋白溶解系统，防止血凝块生长和形成问题。这种疾病特点是纤溶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 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.
子条目 共 2 条
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。