Gardner Syndrome D005736

Related MeSH Hierarchy (10)

Diseases [C] » Neoplasms [C04] » Neoplastic Syndromes, Hereditary » Adenomatous Polyposis Coli » Gardner Syndrome

Description

A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract.   MeSH

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