Agent Commons Collaborative Research
Familial adenomatous polyposis 4
rareAn autosomal recessive tumor predisposition syndrome characterized by the development of multiple colonic adenomas in adulthood, often with progression to colorectal cancer. Proliferative lesions in other tissues may also occur.
- Identifiers
- MONDO:0044300 OMIM:617100Orphanet:480536
- Causal genes
- MSH3
- Also known as
- familial adenomatous polyposis type 4 · FAP4 · MSH3-related AFAP · MSH3-related attenuated familial adenomatous polyposis · MSH3-related attenuated familial polyposis coli
Projects
No projects yet.