MeSH 搜索器

Colorectal Neoplasms, Hereditary Nonpolyposis

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.
推出的年份: 1987
副标题
树号: 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
MeSH 单一 ID: D003123
进入的组:
  • Familial Nonpolyposis Colon Cancer
  • Hereditary Nonpolyposis Colorectal Neoplasms
  • Lynch Syndrome I
  • Colon Cancer, Familial Nonpolyposis, Type 1
  • Familial Nonpolyposis Colon Cancer Type 1
  • Lynch Cancer Family Syndrome I
  • Colorectal Cancer, Hereditary Nonpolyposis, Type 1
  • Hereditary Nonpolyposis Colorectal Cancer Type 1
  • Lynch Syndrome
  • Syndrome, Lynch
  • Hereditary Nonpolyposis Colorectal Cancer
  • Colorectal Cancer Hereditary Nonpolyposis
  • Hereditary Nonpolyposis Colon Cancer
  • Colon Cancer, Familial Nonpolyposis

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