Disease #05488 (SSPCS (cancer, polyposis, sessile serrated syndrome (SSPCS)), OMIM:617108)

Official abbreviation SSPCS
Name cancer, polyposis, sessile serrated syndrome (SSPCS)
OMIM ID 617108
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene RNF43
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-10-26 14:52:25 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00183542 29967336-Pat PubMed: Baert-Desurmont 2018 - - - France - - - - - SSPCS Serrated polyposis syndrome SMAD4 SMAD4 1 1 Stephanie Baert-Desurmont
00204071 - PubMed: Baert-Desurmont 2018 - - - France - - - - - SSPCS Serrated polyposis syndrome - MUTYH 1 1 Stephanie Baert-Desurmont
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.