Colorectal cancer, hereditary nonpolyposis, type 6

Preferred Label : Colorectal cancer, hereditary nonpolyposis, type 6;

Symbol : HNPCC6;

CISMeF acronym : HNPCC6;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Colon cancer, hereditary nonpolyposis, type 6;

Prefixed ID : #614331;

Details

Origin ID

614331;

UMLS CUI

C1860896;

Currated CISMeF NLP mapping
- colorectal cancer, hereditary nonpolyposis, type 6 [MeSH concept]
- colorectal cancer, hereditary nonpolyposis, type 6 [MeSH Supplementary Concept]
- hereditary nonpolyposis colorectal cancer type 6 [DO Concept]
DO Cross reference
- hereditary nonpolyposis colorectal cancer type 6 [DO Concept]
Genes related to phenotype
- Transforming growth factor-beta receptor, type II [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hereditary nonpolyposis colorectal carcinoma [HPO term]
ORDO concept(s)
- Lynch syndrome [ORDO Disease]
See also inter- (CISMeF)
- TGFBR2 wt Allele [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- colorectal cancer, hereditary nonpolyposis, type 6 [MeSH Supplementary Concept]
- colorectal cancer, hereditary nonpolyposis, type 6 [MeSH concept]

Keyword's position in hierarchy(ies) :

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