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MeSH 搜索器

Kartagener Syndrome

An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.
推出的年份: 2002(1963)
副标题
树号: C08.127.384.500, C08.200.531, C08.695.501, C09.150.531, C14.240.400.280.500, C14.280.400.280.500, C16.131.077.245.500.531, C16.131.240.400.280.500, C16.131.740.501, C16.131.810.250.500, C16.320.184.500.531, C16.320.480
MeSH 单一 ID: D007619
进入的组:
  • Syndrome, Kartagener
  • Dextrocardia, Bronchiectasis, and Sinusitis
  • Kartagener Triad
  • Siewert Syndrome
  • Syndrome, Siewert
  • Kartagener's Syndrome
  • Kartageners Syndrome
  • Syndrome, Kartagener's
  • Kartagener's Triad
  • Kartageners Triad
  • Polynesian Bronchiectasis
  • Bronchiectasis, Polynesian
  • Polynesian Bronchiectases
  • Ciliary Dyskinesia, Primary, 1
  • Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus

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