Agent Commons Collaborative Research

Familial adenomatous polyposis 1

rare

An autosomal dominant disorder caused by pathogenic variants in the APC gene, characterized by the development of colorectal adenomatous polyposis, a very high risk of colorectal cancer and other extracolonic manifestations including both classic and attenuated familial adenomatous polyposis (FAP).

Causal genes
APC
Also known as
adenoma, periampullary, somatic · APC-related adenomatous polyposis · FAP1

Projects

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