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
|