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Descriptor English: Colorectal Neoplasms, Hereditary Nonpolyposis
Descriptor Spanish: Neoplasias Colorrectales Hereditarias sin Poliposis
Descriptor neoplasias colorrectales hereditarias sin poliposis
Entry term(s) cancer colorrectal hereditario sin poliposis
cáncer colorrectal hereditario no asociado a poliposis
cáncer colorrectal hereditario no polipósico
cáncer colorrectal hereditario no polipósico de tipo 1
cáncer colorrectal hereditario sin poliposis de tipo 1
cáncer de colon familiar no polipósico
cáncer de colon familiar no polipósico de tipo 1
cáncer de colon familiar sin poliposis de tipo 1
cáncer de colon hereditario no polipósico
cáncer de colon hereditario sin poliposis
neoplasias colorrectales no polipósicas hereditarias
neoplasias colorrectales sin poliposis hereditarias
neoplasias colorrectales sin poliposis hereditarias familiares
síndrome de Lynch
síndrome de Lynch de tipo I
Scope note: Grupo de enfermedades hereditarias de carácter autosómico dominante en las que el CÁNCER DE COLON se desarrolla a partir de adenomas aislados. A diferencia de la POLIPOSIS COLÓNICA FAMILIAR, en la que existen cientos de pólipos, las neoplasias colorrectales hereditarias no polipósicas aparecen mucho más tarde, en la cuarta o quinta década de la vida. Las NCNPH se han asociado con mutaciones germinales en los genes reparadores de errores de emparejamiento (GREE). Se subdividen en síndrome de Lynch I o cáncer de colon específico, y SÍNDROME DE LYNCH II, que incluye el cáncer extracólico.
Descriptor Portuguese: Neoplasias Colorretais Hereditárias sem Polipose
Descriptor French: Tumeurs colorectales héréditaires sans polypose
Entry term(s): Colon Cancer, Familial Nonpolyposis
Colon Cancer, Familial Nonpolyposis, Type 1
Colorectal Cancer Hereditary Nonpolyposis
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
Familial Nonpolyposis Colon Cancer
Familial Nonpolyposis Colon Cancer Type 1
Hereditary Nonpolyposis Colon Cancer
Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer Type 1
Hereditary Nonpolyposis Colorectal Neoplasms
Lynch Cancer Family Syndrome I
Lynch Syndrome
Lynch Syndrome I
Syndrome, Lynch
Tree number(s): C04.588.274.476.411.307.190
C04.700.250
C06.301.371.411.307.190
C06.405.249.411.307.190
C06.405.469.158.356.190
C06.405.469.491.307.190
C16.320.700.250
C18.452.284.255
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D003123
Scope note: A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer.
Allowable Qualifiers: BL blood
BS blood supply
CF cerebrospinal fluid
CH chemistry
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
SC secondary
SU surgery
TH therapy
UL ultrastructure
UR urine
VE veterinary
VI virology
Public MeSH Note: 87
History Note: 87
Entry Version: COLORECTAL NEOPL HEREDITARY NONPOLYPOSIS
DeCS ID: 24009
Unique ID: D003123
NLM Classification: WI 529
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1987/01/01
Date of Entry: 1986/06/24
Revision Date: 2020/02/06
Colorectal Neoplasms, Hereditary Nonpolyposis - Preferred
Concept UI M0004834
Scope note A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer.
Preferred term Colorectal Neoplasms, Hereditary Nonpolyposis
Entry term(s) Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Cancer - Narrower
Concept UI M0444331
Scope note HNPCC with no history of associated cancers.
Preferred term Hereditary Nonpolyposis Colorectal Cancer
Entry term(s) Colon Cancer, Familial Nonpolyposis
Colorectal Cancer Hereditary Nonpolyposis
Familial Nonpolyposis Colon Cancer
Hereditary Nonpolyposis Colon Cancer
Lynch Syndrome - Narrower
Concept UI M000655656
Preferred term Lynch Syndrome
Entry term(s) Syndrome, Lynch
Lynch Syndrome I - Narrower
Concept UI M000738553
Preferred term Lynch Syndrome I
Entry term(s) Colon Cancer, Familial Nonpolyposis, Type 1
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
Familial Nonpolyposis Colon Cancer Type 1
Hereditary Nonpolyposis Colorectal Cancer Type 1
Lynch Cancer Family Syndrome I



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