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Descritor em português: Síndrome de Gardner
Descritor em inglês: Gardner Syndrome
Descritor em espanhol: Síndrome de Gardner
Descritor síndrome de Gardner
Nota de escopo: 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.
Descritor em francês: Syndrome de Gardner
Termo(s) alternativo(s): Gardner Syndromes
Gardner's Syndrome
Gardner's Syndromes
Gardners Syndrome
Syndrome, Gardner
Syndrome, Gardner's
Syndromes, Gardner
Syndromes, Gardner's
Código(s) hierárquico(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
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D005736
Nota de escopo: 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.
Qualificadores permitidos: 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
Indexação Anterior: Colonic Neoplasms (1966-1980)
Intestinal Polyps/FG (1968-1980)
Neoplasms, Multiple Primary (1966-1980)
Nota MeSH pública: 1981
Nota histórica: 1981
Veja também os descritores: Adenomatous Polyposis Coli MeSH
Adenomatous Polyposis Coli Protein MeSH
Genes, APC MeSH
Identificador DeCS: 22472
ID do descritor: D005736
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1981
Data de entrada: 04/04/1980
Data de revisão: 01/06/2015
Gardner Syndrome - Conceito preferido
Identificador do conceito M0008991
Nota de escopo 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.
Termo preferido Gardner Syndrome
Termo(s) alternativo(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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