Hereditary nonpolyposis colorectal cancer

Preferred Label : Hereditary nonpolyposis colorectal cancer;

ICD-11 definition : 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.;

Details

Origin ID

8113015;

Currated CISMeF NLP mapping
- Colorectal cancer, hereditary nonpolyposis [OMIM phenotypic series]
- Hereditary Nonpolyposis Colorectal Cancer Syndrome [NCIt concept]
- Hereditary non-polyposis colorectal cancer syndrome [MedDRA Preferred Term]
- Hereditary nonpolyposis colon cancer [ORDO Disease]
- Hereditary nonpolyposis colon cancer (disorder) [SNOMED CT concept]
- Hereditary nonpolyposis colorectal cancer [PASCAL descriptor]
- Lynch syndrome [ORDO Disease]
- Lynch syndrome [DO Concept]
- Lynch syndrome [MedDRA LLT]
- hereditary nonpolyposis colorectal cancer [MeSH concept]
- hereditary nonpolyposis colorectal cancer [Disease (Nov.)]
See also inter- (CISMeF)
- Lynch syndrome (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- Lynch Syndrome [NCIt concept]
- colorectal neoplasms, hereditary nonpolyposis [MeSH Descriptor]
- colorectal neoplasms, hereditary nonpolyposis [MeSH concept]
- lynch syndrome I (site-specific colonic cancer) [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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