lynch syndrome I (site-specific colonic cancer) - CISMeF

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CISMeF

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Lynch syndrome I (site-specific colonic cancer)MeSH Supplementary Concept

Preferred Label : lynch syndrome I (site-specific colonic cancer);

Details

Origin ID

C537261;

UMLS CUI

C2931459;

Currated CISMeF NLP mapping
- Hereditary non-polyposis colorectal cancer syndrome [MedDRA Preferred Term]
- Hereditary nonpolyposis colon cancer (disorder) [SNOMED CT concept]
- Hereditary nonpolyposis colorectal cancer [PASCAL descriptor]
- Lynch Syndrome [NCIt concept]
- Lynch syndrome [ORDO Disease]
- Lynch syndrome (disorder) [SNOMED CT concept]
- colorectal neoplasms, hereditary nonpolyposis [MeSH Descriptor]
- hereditary nonpolyposis colorectal cancer [Disease (Nov.)]
- hereditary nonpolyposis colorectal neoplasm [Disease (Nov.)]
MeSH term(s) associated for indexing
- colorectal neoplasms, hereditary nonpolyposis [MeSH Descriptor]
Record concept(s)
- Lynch syndrome I (site-specific colonic cancer) [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Familial nonpolyposis colorectal cancer [ICD-11 More detail]
- Hereditary nonpolyposis colon cancer [ORDO Disease]
- Hereditary nonpolyposis colorectal cancer [ICD-11 More detail]
- Lynch syndrome [MedDRA LLT]
Validated automatic mappings to NTBT
- hereditary nonpolyposis colorectal neoplasm [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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03/05/2025

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