| FAP | familial adenomatous polyposis; familial amyloid polyneuropathy; fatty acid polyunsaturated; fatty a... |
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| AP | accessory pathway; accounts payable; acid phosphatase; acinar parenchyma; action potential; active p... |
| APC | acetylsalicylic acid, phenacetin, and caffeine; activated protein C; adenoidal-pharyngeal-conjunctiv... |
| CFPR | Canadian Familial Polyposis Registry |
| FPC | familial polyposis coli; family planning clinic; fish protein concentrate |
| FAP | Familial Adenomatous Polyposis |
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| FAP | Familial adenomatous polyposis coli |
| APC | Adenomatous Polyposis Coli |
| APC | Adenomatous polyposis coli protein |
| APC | adenomatous polyposis coli gene |
| familial adenomatous polyposis | <gastroenterology> Genetic disease with numerous precancerous polyps in the colon and rectum. Also called familial polyposis. (12 Dec 1998) |
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| adenomatous polyposis coli | An autosomal dominant polyposis syndrome in which the colon contains few to thousands of adenomatous polyps, often occurring by age 15 to 25. (12 Dec 1998) |
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| familial intestinal polyposis | Begins usually in late childhood; polyps increase in numbers, causing symptoms of chronic colitis, and carcinoma of the colon almost invariably develops in untreated cases; autosomal dominant inheritance. In the Gardner syndrome there are extracolonic changes (desmoid tumours, etc.). Synonym: polyposis coli. Hamartomatous polyposis of the small or large intestine, Peutz-Jeghers syndrome with melanin spots on the lips, less common, miscellaneous, rare, and doubtful occurrences. Synonym: familial intestinal polyposis. (05 Mar 2000) |
| familial polyposis | An inherited condition in which several hundred polyps develop in the colon and rectum. (12 Dec 1998) |
| familial polyposis coli | <gastroenterology, oncology> A inherited, disorder where there are multiple adenomatous polyps (up to several thousand) in the colon. Malignant degeneration of the polyps (to colon carcinoma) occurs in virtually 100% by age 40. Inheritance: autosomal dominant. (27 Sep 1997) |
| adenomatous | Relating to an adenoma, and to some types of glandular hyperplasia. (05 Mar 2000) |
| adenomatous colon polyps | <radiology> Probability of malignancy by size and type Size (cm) less than 1 1-2 greater than 2 --------------------------- tubular 1% 10% 34% mixed (TV) 4% 9% 45% villous 10% 10% 54%, most colon polyps (90%) are hyperplastic (size less than 5 mm) (12 Dec 1998) |
| adenomatous goiter | An enlargement of the thyroid gland due to the growth of one or more encapsulated adenomas or multiple nonencapsulated colloid nodules within its substance. (05 Mar 2000) |
| adenomatous polyp | A polyp that consists of benign neoplastic tissue derived from glandular epithelium. Synonym: cellular polyp, polypoid adenoma. (05 Mar 2000) |
| adenomatous polyps | Benign neoplasms derived from glandular epithelium. (12 Dec 1998) |
| multiple intestinal polyposis | Begins usually in late childhood; polyps increase in numbers, causing symptoms of chronic colitis, and carcinoma of the colon almost invariably develops in untreated cases; autosomal dominant inheritance. In the Gardner syndrome there are extracolonic changes (desmoid tumours, etc.). Synonym: polyposis coli. Hamartomatous polyposis of the small or large intestine, Peutz-Jeghers syndrome with melanin spots on the lips, less common, miscellaneous, rare, and doubtful occurrences. Synonym: familial intestinal polyposis. (05 Mar 2000) |
| polyposis | Presence of several polyps. Origin: polyp + G. -osis, condition (05 Mar 2000) |
| polyposis coli | Hereditary disorder (Mendelian dominant) characterised by the development of hundreds of adenomatous polyps in the large intestine, which show a tendency to progress to malignancy. The APC gene has also been implicated in a chromosome 5 gastric and pancreatic cancer. (18 Nov 1997) |
| polyposis syndromes | <radiology> Inher. Malig. Type familial polyposis coli dom and adenoma Gardner syndrome dom and Turcot syndrome rec CNS Peutz-Jeghers syndrome dom (+) hamartoma Cowden syndrome dom ? juvenile polyposis coli (?) - juvenile Cronkhite-Canada syndrome (12 Dec 1998) |
| juvenile polyposis coli | <radiology> Benign polyposis, inheritance uncertain, inflammatory or retention polyps: round, smooth, soft, mucin-filled, non-neoplastic, onset less than 10 yrs, polyps can prolapse through anus, associated with diarrhoea, protein loss see: polyposis syndromes, Cronkhite-Canada syndrome (12 Dec 1998) |
| filiform polyposis | <radiology> Benign, non-specific sequela of diffuse, severe mucosal inflammation, UC, Crohn's, XR: thin, straight filling defects, resembles stalks of polyps without heads (12 Dec 1998) |
| familial adenomatous polyposis |
FAP. An inherited condition in which numerous polyps (growths that protrude from mucous membranes) form on the inside walls of the colon and rectum. It increases the risk for colorectal cancer. Also called familial polyposis.
출처: www.stjude.org/glossary
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| familial adenomatous polyposis |
A rare genetic disorder of the intestines characterized by "carpet-like" growths of polyps that develop along the inner walls of the colon. These areas of abnormal growth typically develop at a relatively young age.
출처: www.ehealthmd.com/library/colon-cancer/Colon-Cance...
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| familial adenomatous polyposis |
a hereditary syndrome characterized by the formation of many polyps in the colon and rectum, some of which ultimately develop into colorectal cancer.
출처: www.nutrabio.com/Definitions/definitions_f.htm
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| familial adenomatous polyposis |
An inherited condition in which hundreds of potentially cancerous polyps develop in the colon and rectum.
출처: aspin.asu.edu/geneinfo/glos-f.htm
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| familial adenomatous polyposis |
Also known as Gardner
출처: www.vh.org/adult/patient/cancercenter/prevention/p...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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