Structured Summary
Abstract
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.
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Broader headings
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Synonyms
8 entry terms
- Gardner's Syndrome
- Gardner Syndromes
- Gardner's Syndromes
- Gardners Syndrome
- Syndrome, Gardner
- Syndrome, Gardner's
- Syndromes, Gardner
- Syndromes, Gardner's
MeSH Record
Aspects Covered
39 allowable subheadings
Indexed with the subheadings blood, blood supply, cerebrospinal fluid, chemically induced, chemistry, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, secondary, surgery, therapy, ultrastructure, urine, veterinary, virology.
MeSH Record
History Note
1981
MeSH Record
Previous Indexing
- Colonic Neoplasms (1966-1980)
- Intestinal Polyps/FG (1968-1980)
- Neoplasms, Multiple Primary (1966-1980)
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AMA Style
References
- National Library of Medicine. Gardner Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D005736. http://id.nlm.nih.gov/mesh/2026/D005736
- Gardner Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Gardner%27s_syndrome
- Gardner Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1702335