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常染色体隐性遗传病 meaning in Chinese

autosomal recessive inherited disease
autosome recessive disease

Examples

  1. Complex vertebral malformation ( cvm ) , a lethal autosomal recessive inherited defect in holstein breed , was newly reported in demark
    摘要荷斯坦奶牛脊柱畸形综合征是近年新发现的一种常染色体隐性遗传病,该病对纯合子胎儿是致死性的。
  2. Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption , liver disease , or numerous transfusions )
    血色素沉着症或可以是原发的(病因大概为常染色体隐性遗传病) ,也可以是继发的(过多的铁摄取或吸收、肝脏疾病、大量输血) 。
  3. Wilson " s disease is the consequence of toxic accumulation of copper initially in the liver and later in extrahepatic sites , this disorder is inherited in autosomal recessive manner and is present in 1 in 30000 individuals in all populations
    其中研究最多的是铜代谢异常所引起的wilson ' s病,这种病是常染色体隐性遗传病,如果肝脏中铜浓度达到毒性水平,将引发急性肝炎,其发生率为三万分之一。

Related Words

  1. 隐性遗传氨基酸尿代谢异常
  2. 染色体分离
  3. 染色体损害
  4. 破裂染色体
  5. 染色体斑
  6. 畸变染色体
  7. 亲本染色体
  8. 染色体带
  9. 染色体裂
  10. x染色体
  11. 常染色体隐性遗传
  12. 常染色体隐性遗传氨酰脯基氨酸酶缺乏
  13. 常染色体隐性遗传特性
  14. 常染色体隐性遗传性聋
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