3A80.0
原发性遗传性红细胞增多症
Primary inherited erythrocytosis
- 上级条目
- 3A80 先天性红细胞增多症
- 层级
- 5 级
定义
由遗传因素引起的导致红细胞浓度变化的疾病。这种疾病特点是体内红细胞浓度高，导致血液流动缓慢。通过基因检测识别突变。
A disease caused by genetically inherited factors leading to changes in the concentration of red blood cells. This disease is characterised by having a high concentration of red blood cells in the body leading to slow flow of blood. Confirmation is by identification of mutations by genetic testing.
索引词 可用于检索该条目的同义词与别名
- 原发性遗传性红细胞增多症
- 原发性遗传性红细胞增多症
- 原发性家族性红细胞增多症
- HIF2A突变引起的红细胞增多症
- PHD2突变引起的红细胞增多症
- VHL突变引起的红细胞增多症
- Chuvash红细胞增多症
- Chuvash红细胞增多症
- Von Hippel-Lindau依赖性红细胞增多症
- EPOR突变引起的原发性家族性红细胞增多症
- 其他突变引起的原发性家族性红细胞增多症
英文词条（11）
- Primary inherited erythrocytosis
- Primary familial polycythaemia
- Primary inherited polycythaemia
- Polycythaemia due to HIF2A mutation
- Polycythaemia due to PHD2 mutation
- Polycythaemia due to VHL mutation
- Chuvash erythrocytosis
- Chuvash polycythaemia
- Von Hippel-Lindau-dependent polycythaemia
- Primary familial polycythaemia due to EPOR mutation
- Primary familial polycythaemia due to other mutations
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。