Other Names for this Disease
- MAP syndrome
- Autosomal recessive familial adenomatous polyposis
- Autosomal recessive multiple colorectal adenomas
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 This condition, a milder form of familial adenomatous polyposis (FAP), is sometimes called autosomal recessive familial adenomatous polyposis because it is inherited in an autosomal recessive manner. People with this condition have fewer polyps than those with the classic type of FAP; fewer than 100 polyps typically develop, rather than hundreds or thousands. They may also be at increased risk for upper gastrointestinal polyps. MYH-associated polyposis is caused by mutations in the MYH gene.MYH-associated polyposis is an inherited condition characterized by the development of multiple adenomatous colon polyps and an increased risk of colorectal cancer.
Last updated: 6/28/2011
- MYH-Associated Polyposis. Cancer.Net. September 2010; http://www.cancer.net/patient/Cancer+Types/MYH-Associated+Polyposis. Accessed 6/28/2011.
- Familial adenomatous polyposis. Genetics Home Reference (GHR). April 2008; http://ghr.nlm.nih.gov/condition/familial-adenomatous-polyposis. Accessed 6/28/2011.
- Genetics Home Reference (GHR) contains information on MYH-associated polyposis. This website is maintained by the National Library of Medicine.
- The Johns Hopkins Cancer Risk Assessment Program provides information about polyposis and MYH gene. Click on the link to go access this information.
- The National Cancer Institute provides the most current information on cancer for patients, health professionals, and the general public.
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- PubMed is a searchable database of medical literature and lists journal articles that discuss MYH-associated polyposis. Click on the link to view a sample search on this topic.