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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.

Year introduced: 2002 (1963)

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Tree Number(s): C08.127.384.500, C08.200.531, C08.695.501, C09.150.531, C14.240.400.280.500, C14.280.400.280.500, C16., C16.131.240.400.280.500, C16.131.740.501, C16.131.810.250.500, C16.320.184.500.531, C16.320.480

MeSH Unique ID: D007619

Entry Terms:

  • 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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