Hereditary nonpolyposis colorectal cancer (Q97091): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 13:07, 16 August 2026
Lynch syndrome (HNPCC or Hereditary nonpolyposis colorectal cancer) is an autosomal dominant genetic condition which has a high risk of colon cancer as well as other cancers including stomach, small intestine, liver, gallbladder ducts, upper urinary tract, brain, skin, and prostate. Women with this disorder also have a high risk of cancer of the endometrium (lining of the uterus) and ovaries.The increased risk for these cancers is due to inherited mutations that impair DNA mismatch repair.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_8113015 |
||
| English | Hereditary nonpolyposis colorectal cancer |
Lynch syndrome (HNPCC or Hereditary nonpolyposis colorectal cancer) is an autosomal dominant genetic condition which has a high risk of colon cancer as well as other cancers including stomach, small intestine, liver, gallbladder ducts, upper urinary tract, brain, skin, and prostate. Women with this disorder also have a high risk of cancer of the endometrium (lining of the uterus) and ovaries.The increased risk for these cancers is due to inherited mutations that impair DNA mismatch repair. |
Statements
CID11:ID_8113015
0 references
dki-india-ID_8113015
0 references
Concluído
0 references
