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Descriptor English: Kartagener Syndrome
Descriptor Spanish: Síndrome de Kartagener
Descriptor Portuguese: Síndrome de Kartagener
Descriptor French: Syndrome de Kartagener
Entry term(s): Bronchiectasis, Polynesian
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
Kartageners Syndrome
Kartageners Triad
Polynesian Bronchiectases
Polynesian Bronchiectasis
Siewert Syndrome
Syndrome, Kartagener
Syndrome, Kartagener's
Syndrome, Siewert
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
RDF Unique Identifier: https://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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
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
DeCS ID: 28293
Unique ID: D007619
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2002/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/03/01
Kartagener Syndrome - Preferred
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.
Preferred term Kartagener Syndrome
Entry term(s) Dextrocardia, Bronchiectasis, and Sinusitis
Kartagener Triad
Kartagener's Syndrome
Kartagener's Triad
Kartageners Syndrome
Kartageners Triad
Siewert Syndrome
Syndrome, Kartagener
Syndrome, Kartagener's
Syndrome, Siewert
Polynesian Bronchiectasis - Narrower
Concept UI M000629770
Preferred term Polynesian Bronchiectasis
Entry term(s) Bronchiectasis, Polynesian
Polynesian Bronchiectases
Ciliary Dyskinesia, Primary, 1 - Narrower
Concept UI M000629767
Preferred term Ciliary Dyskinesia, Primary, 1
Entry term(s) Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus



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