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Familial adenomatous polyposis 2

MONDO:0012041

An autosomal recessive hereditary cancer predisposition disorder caused by pathogenic variants in the MUTYH gene. It is characterized by an increased risk of colorectal adenomatous polyposis and carcinomas.

Also known as: FAP2, MAP, MUTYH-associated polyposis, MUTYH-related AFAP, MUTYH-related adenomatous polyposis, adenomas, multiple colorectal, autosomal recessive, colorectal adenomatous polyposis, autosomal recessive, familial adenomatous polyposis 2

34 clinical trials for this condition and its sub-types, 1 tagged with Familial adenomatous polyposis 2 itself.

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