ICD-11 编码查询_国际疾病分类第 11 版中文版_在线疾病编码检索工具
LD45.1

父源单亲二倍体

Uniparental disomies of paternal origin

上级条目
LD45 单亲二倍体
层级
4 级

定义

任何由父亲遗传两个同源染色体副本而未从母亲遗传引起的任何疾病。通过观察相同的染色体对,并通过基因检测与父系染色体匹配确诊。

Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.

索引词 可用于检索该条目的同义词与别名

  • 父源单亲二倍体
  • 父源性1号染色体单亲二倍体
  • 父源性4号染色体单亲二倍体
  • 父源性5号染色体单亲二倍体
  • 父源性6号染色体单亲二倍体
  • 父源性7号染色体单亲二倍体
  • 父源性11号染色体单亲二倍体
  • 父源性13号染色体单亲二倍体
  • 父源性14号染色体单亲二倍体
  • 父源性15号染色体单亲二倍体
  • 父源性20号染色体单亲二倍体
  • 父源性21号染色体单亲二倍体
  • 父源性X染色体单亲二倍体
英文词条(13)
  • Uniparental disomies of paternal origin
  • Paternal uniparental disomy of chromosome 1
  • Paternal uniparental disomy of chromosome 4
  • Paternal uniparental disomy of chromosome 5
  • Paternal uniparental disomy of chromosome 6
  • Paternal uniparental disomy of chromosome 7
  • Paternal uniparental disomy of chromosome 11
  • Paternal uniparental disomy of chromosome 13
  • Paternal uniparental disomy of chromosome 14
  • Paternal uniparental disomy of chromosome 15
  • Paternal uniparental disomy of chromosome 20
  • Paternal uniparental disomy of chromosome 21
  • Paternal uniparental disomy of chromosome X

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。