MeSH Browser

MeSH Heading: Kartagener Syndrome
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; C16.131.077.245.500.531; C16.131.240.400.280.500; C16.131.740.501; C16.131.810.250.500; C16.320.184.500.531; C16.320.480
Unique ID: D007619
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D007619
Scope Note: 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.
Entry Term(s): Ciliary Dyskinesia, Primary, 1; Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus; Dextrocardia, Bronchiectasis, and Sinusitis; Kartagener Triad; Kartagener's Syndrome; Kartagener's Triad; Polynesian Bronchiectasis; Siewert Syndrome
Public MeSH Note: 2002; see KARTAGENER'S SYNDROME 1990-2001; see KARTAGENER TRIAD 1963-1989; for CILIARY DYSKINESIA, PRIMARY see CILIARY MOTILITY DISORDERS 1992-2001
History Note: 2002 (1963); for CILIARY DYSKINESIA, PRIMARY use CILIARY MOTILITY DISORDERS 1992-2001
Date Established: 2002/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/03/01

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0011929
Scope Note: 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.
Terms: Kartagener Syndrome Preferred Term
Term UI T443993
Date04/24/2001
LexicalTag EPO
ThesaurusID; Kartagener's Syndrome
Term UI T022899
Date01/01/1999
LexicalTag EPO
ThesaurusID NLM (1966); Kartagener's Triad
Term UI T022900
Date01/23/1989
LexicalTag EPO
ThesaurusID NLM (1990); Kartagener Triad
Term UI T443994
Date04/24/2001
LexicalTag EPO
ThesaurusID NLM (2002); Siewert Syndrome
Term UI T680922
Date09/06/2006
LexicalTag EPO
ThesaurusID; Dextrocardia, Bronchiectasis, and Sinusitis
Term UI T781716
Date12/06/2010
LexicalTag NON
ThesaurusID

Kartagener Syndrome MeSH Descriptor Data 2025