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Descriptor English: Gardner Syndrome
Descriptor Spanish: Síndrome de Gardner
Descriptor síndrome de Gardner
Scope note: Variante de POLIPOSIS COLI ADENOMATOSA causada por la mutación del gen APC (GENES APC), en el CROMOSOMA 5. Se caracteriza, aunque no exclusivamente, por la presencia de múltiples pólipos en el colon, pero también por PÓLIPOS ADENOMATOSOS fuera del colon, en el TRACTO GASTROINTESTINAL SUPERIOR, el OJO, la PIEL, el CRÁNEO, los HUESOS FACIALES, y como neoplasia maligna en otros órganos aparte del tracto gastrointestinal.
Descriptor Portuguese: Síndrome de Gardner
Descriptor French: Syndrome de Gardner
Entry term(s): Gardner Syndromes
Gardner's Syndrome
Gardner's Syndromes
Gardners Syndrome
Syndrome, Gardner
Syndrome, Gardner's
Syndromes, Gardner
Syndromes, Gardner's
Tree number(s): C04.557.470.035.215.100.500
C04.588.274.476.411.307.089.393
C04.700.100.392
C06.301.371.411.307.090.500
C06.405.249.411.307.090.500
C06.405.469.158.356.090.500
C06.405.469.491.307.090.500
C06.405.469.578.249.393
C16.131.077.393
C16.320.700.100.393
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D005736
Scope note: A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract.
Allowable Qualifiers: BL blood
BS blood supply
CF cerebrospinal fluid
CH chemistry
CI chemically induced
CL classification
CN congenital
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
SC secondary
SU surgery
TH therapy
UL ultrastructure
UR urine
VE veterinary
VI virology
Previous Indexing: Colonic Neoplasms (1966-1980)
Intestinal Polyps/FG (1968-1980)
Neoplasms, Multiple Primary (1966-1980)
Public MeSH Note: 1981
History Note: 1981
Related: Adenomatous Polyposis Coli MeSH
Adenomatous Polyposis Coli Protein MeSH
Genes, APC MeSH
DeCS ID: 22472
Unique ID: D005736
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1981/01/01
Date of Entry: 1980/04/04
Revision Date: 2015/06/01
Gardner Syndrome - Preferred
Concept UI M0008991
Scope note A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract.
Preferred term Gardner Syndrome
Entry term(s) Gardner Syndromes
Gardner's Syndrome
Gardner's Syndromes
Gardners Syndrome
Syndrome, Gardner
Syndrome, Gardner's
Syndromes, Gardner
Syndromes, Gardner's



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