3A51.9
血红蛋白O病
Haemoglobin O disease
- 层级
- 4 级
定义
一种由编码血红蛋白O的基因的双亲遗传引起的疾病。这种疾病特征是血红蛋白分子的一条球蛋白链结构异常。本病可表现为轻度溶血性贫血，胆结石风险增加，脾脏肿大，关节疼痛发作，感染风险增加。这种疾病是通过基因检测鉴定血红蛋白O基因来确诊。
A disease caused by the bi-parental inheritance of the gene that encodes for haemoglobin O. This disease is characterised by abnormal structure of one of the globin chains of the haemoglobin molecule. This disease may present with mild haemolytic anaemia, increased risk for gallstones, enlarged spleen, episodes of joint pain, and increased risk of infection. This disease is confirmed by identification of the haemoglobin O gene by genetic testing.
索引词 可用于检索该条目的同义词与别名
- 血红蛋白O病
- 阿拉伯病
英文词条（2）
- Haemoglobin O disease
- Arab disease
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。