Lynch syndrome 4

Preferred Label : Lynch syndrome 4;

Symbol : LYNCH4;

CISMeF acronym : HNPCC4;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : HNPCC4; Colorectal cancer, hereditary nonpolyposis, type 4;

Prefixed ID : #614337;

Details

Origin ID

614337;

UMLS CUI

C1838333;

Currated CISMeF NLP mapping
- colorectal cancer, hereditary nonpolyposis, type 4 [MeSH concept]
- colorectal cancer, hereditary nonpolyposis, type 4 [MeSH Supplementary Concept]
- hereditary nonpolyposis colorectal cancer type 4 [DO Concept]
DO Cross reference
- hereditary nonpolyposis colorectal cancer type 4 [DO Concept]
Genes related to phenotype
- Pms1 homolog 2, mismatch repair system component [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Endometrial carcinoma [HPO term]
- Hereditary nonpolyposis colorectal carcinoma [HPO term]
- Ovarian neoplasm [HPO term]
ORDO concept(s)
- Lynch syndrome [ORDO Disease]
See also inter- (CISMeF)
- PMS1 homolog 2, mismatch repair system component [ORDO Gene]
- PMS1 homolog 2, mismatch repair system component [HGNC gene]
- PMS2 wt Allele [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- colorectal cancer, hereditary nonpolyposis, type 4 [MeSH Supplementary Concept]
- colorectal cancer, hereditary nonpolyposis, type 4 [MeSH concept]

Keyword's position in hierarchy(ies) :

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