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Concept information

Preferred term

Colorectal Neoplasms, Hereditary Nonpolyposis  

Type

  • Topical Descriptor

Narrower concepts

Entry terms

  • Familial Nonpolyposis Colon Cancer
  • Hereditary Nonpolyposis Colorectal Neoplasms

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.

History note

  • 87

In other languages

  • Finnish

  • hereditaarinen ei-polypoottinen paksusuolisyöpä
  • hereditary non-polypotic colorectal cancer
  • hereditäärinen ei-polypoottinen paksusuolisyöpä
  • HNPCC
  • Lynch
  • Lynchin oireyhtymä
  • Lynchin syndrooma
  • perinnöllinen ei-polypoottinen koolonkarsinooma
  • perinnöllinen ei-polypoottinen paksusuolen syöpä
  • perinnöllinen ei-polypoottinen paksusuolisyöpä
  • periytyvä ei-polypoottinen paksusuolen syöpä
  • Swedish

  • Lynchs syndrom
  • Ärftlig icke-polypos kolorektalcancer

URI

http://www.yso.fi/onto/mesh/D003123

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