Sessile serrated polyposis cancer syndrome

Preferred Label : Sessile serrated polyposis cancer syndrome;

Symbol : SSPCS;

CISMeF acronym : SSPCS;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the ring finger protein-43 gene (RNF43, 612482.0001);

Neoplasia : Extracolonic cancers, susceptibility to (in some patients); Colorectal carcinoma, susceptibility to (in some patients);

Prefixed ID : #617108;

Details

Origin ID

617108;

UMLS CUI

C4310714;

Automatic exact mappings (from CISMeF team)
- RNF43 wt Allele [NCIt concept]
Genes related to phenotype
- Ring finger protein 43 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Serrated intestinal polyps [HPO term]
ORDO concept(s)
- Serrated polyposis syndrome [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients