Lynch syndrome 8

Preferred Label : Lynch syndrome 8;

Symbol : LYNCH8;

CISMeF acronym : HNPCC8;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Colorectal cancer, hereditary nonpolyposis, type 8; HNPCC8;

Prefixed ID : #613244;

Details

Origin ID

613244;

UMLS CUI

C2750471;

Currated CISMeF NLP mapping
- colorectal cancer, hereditary nonpolyposis, type 8 [MeSH concept]
- colorectal cancer, hereditary nonpolyposis, type 8 [MeSH Supplementary Concept]
- hereditary nonpolyposis colorectal cancer type 8 [DO Concept]
DO Cross reference
- hereditary nonpolyposis colorectal cancer type 8 [DO Concept]
Genes related to phenotype
- Epithelial cellular adhesion molecule [OMIM gene]
HPO term(s)
- Hereditary nonpolyposis colorectal carcinoma [HPO term]
ORDO concept(s)
- Lynch syndrome [ORDO Disease]
See also inter- (CISMeF)
- EPCAM wt Allele [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- colorectal cancer, hereditary nonpolyposis, type 8 [MeSH Supplementary Concept]
- colorectal cancer, hereditary nonpolyposis, type 8 [MeSH concept]

Keyword's position in hierarchy(ies) :

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