Gardner Syndrome [Gardnerův syndrom]

topical
21
Terms

Gardner's Syndrome

Persistent link   https://www.medvik.cz/link/D005736
Definition

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.

DUI
D005736 MeSH Browser
CUI
M0008991
Previous indexing
Colonic Neoplasms (1966-1980); Intestinal Polyps/FG (1968-1980); Neoplasms, Multiple Primary (1966-1980)
History note
1981
Public note
1981

Allowable subheadings

BL
blood
BS
blood supply
CF
cerebrospinal fluid
CI
chemically induced
CH
chemistry
CL
classification 1
CO
complications 3
CN
congenital
DI
diagnosis 7
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics 10
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 3
PP
physiopathology 1
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SC
secondary
SU
surgery 3
TH
therapy 1
UL
ultrastructure
UR
urine
VE
veterinary
VI
virology

C Diseases
C04 Neoplasms 12 832
C04.557 Neoplasms by Histologic Type 270
C04.557.470 Neoplasms, Glandular and Epithelial 75
C04.557.470.035 Adenoma 728
C04.557.470.035.215 Adenomatous Polyps 67
C04.557.470.035.215.100 Adenomatous Polyposis Coli 93
C04.557.470.035.215.100.500 Gardner Syndrome 21
C04.588 Neoplasms by Site 77
C04.588.274 Digestive System Neoplasms 219
C04.588.274.476 Gastrointestinal Neoplasms 679
C04.588.274.476.411 Intestinal Neoplasms 426
C04.588.274.476.411.307 Colorectal Neoplasms 3 658
C04.588.274.476.411.307.089 Adenomatous Polyposis Coli 93
C04.588.274.476.411.307.089.393 Gardner Syndrome 21
C04.700 Neoplastic Syndromes, Hereditary 144
C04.700.100 Adenomatous Polyposis Coli 93
C04.700.100.392 Gardner Syndrome 21
C06 Digestive System Diseases 674
C06.301 Digestive System Neoplasms 219
C06.301.371 Gastrointestinal Neoplasms 679
C06.301.371.411 Intestinal Neoplasms 426
C06.301.371.411.307 Colorectal Neoplasms 3 658
C06.301.371.411.307.090 Adenomatous Polyposis Coli 93
C06.301.371.411.307.090.500 Gardner Syndrome 21
C06.405 Gastrointestinal Diseases 1 751
C06.405.249 Gastrointestinal Neoplasms 679
C06.405.249.411 Intestinal Neoplasms 426
C06.405.249.411.307 Colorectal Neoplasms 3 658
C06.405.249.411.307.090 Adenomatous Polyposis Coli 93
C06.405.249.411.307.090.500 Gardner Syndrome 21
C06.405.469 Intestinal Diseases 757
C06.405.469.158 Colonic Diseases 217
C06.405.469.158.356 Colorectal Neoplasms 3 658
C06.405.469.158.356.090 Adenomatous Polyposis Coli 93
C06.405.469.158.356.090.500 Gardner Syndrome 21
C06.405.469.491 Intestinal Neoplasms 426
C06.405.469.491.307 Colorectal Neoplasms 3 658
C06.405.469.491.307.090 Adenomatous Polyposis Coli 93
C06.405.469.491.307.090.500 Gardner Syndrome 21
C06.405.469.578 Intestinal Polyposis 28
C06.405.469.578.249 Adenomatous Polyposis Coli 93
C06.405.469.578.249.393 Gardner Syndrome 21
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.077 Abnormalities, Multiple 330
C16.131.077.019 22q11 Deletion Syndrome 2
C16.131.077.065 Alagille Syndrome 19
C16.131.077.095 Angelman Syndrome 35
C16.131.077.121 Barth Syndrome 6
C16.131.077.130 Basal Cell Nevus Syndrome 33
C16.131.077.133 Beckwith-Wiedemann Syndrome 17
C16.131.077.137 Bloom Syndrome 11
C16.131.077.208 Branchio-Oto-Renal Syndrome 5
C16.131.077.229 Carney Complex 8
C16.131.077.245 Ciliopathies 9
C16.131.077.250 Cockayne Syndrome 4
C16.131.077.256 Costello Syndrome 3
C16.131.077.262 Cri-du-Chat Syndrome 11
C16.131.077.272 De Lange Syndrome 4
C16.131.077.299 Deaf-Blind Disorders 65
C16.131.077.313 Donohue Syndrome 1
C16.131.077.327 Down Syndrome 510
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.371 Fraser Syndrome 2
C16.131.077.393 Gardner Syndrome 21
C16.131.077.401 Heterotaxy Syndrome 7
C16.131.077.410 Holoprosencephaly 9
C16.131.077.445 Incontinentia Pigmenti 19
C16.131.077.477 Isolated Noncompaction of the Ventricular Myocardium 11
C16.131.077.509 Laurence-Moon Syndrome 6
C16.131.077.525 LEOPARD Syndrome 11
C16.131.077.537 Loeys-Dietz Syndrome 7
C16.131.077.550 Marfan Syndrome 105
C16.131.077.578 Mobius Syndrome 10
C16.131.077.592 Monilethrix 1
C16.131.077.606 Nail-Patella Syndrome 8
C16.131.077.619 Netherton Syndrome 2
C16.131.077.633 Nevus, Sebaceous of Jadassohn 7
C16.131.077.662 Oculocerebrorenal Syndrome 9
C16.131.077.676 Orofaciodigital Syndromes 7
C16.131.077.690 Pallister-Hall Syndrome
C16.131.077.696 Pentalogy of Cantrell 1
C16.131.077.703 POEMS Syndrome 35
C16.131.077.717 Polycystic Kidney Diseases 83
C16.131.077.730 Prader-Willi Syndrome 92
C16.131.077.735 Prolidase Deficiency
C16.131.077.740 Proteus Syndrome 8
C16.131.077.745 Prune Belly Syndrome 3
C16.131.077.790 Rubella Syndrome, Congenital 20
C16.131.077.804 Rubinstein-Taybi Syndrome 12
C16.131.077.850 Short Rib-Polydactyly Syndrome 3
C16.131.077.855 Silver-Russell Syndrome 3
C16.131.077.860 Smith-Lemli-Opitz Syndrome 30
C16.131.077.879 Smith-Magenis Syndrome 2
C16.131.077.889 Sotos Syndrome 4
C16.131.077.899 Trichothiodystrophy Syndromes 1
C16.131.077.919 Trisomy 13 Syndrome 6
C16.131.077.929 Trisomy 18 Syndrome 5
C16.131.077.938 Waardenburg Syndrome 10
C16.131.077.941 Weill-Marchesani Syndrome 1
C16.131.077.944 Wolf-Hirschhorn Syndrome
C16.131.077.970 Zellweger Syndrome 10
C16.320 Genetic Diseases, Inborn 1 215
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.700.100 Adenomatous Polyposis Coli 93
C16.320.700.100.393 Gardner Syndrome 21

Adenomatous Polyposis Coli, Attenuated Disease MeSH Browser

Intestinal polyposis, osteomas, sebaceous cysts Disease MeSH Browser

Samson Gardner syndrome Disease MeSH Browser

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