| ¿µ¹® | iron deficiency anemia | ÇÑ±Û | ö°áÇ̺óÇ÷ |
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| ¿µ¹® | alimentary canal | ÇÑ±Û | ¼ÒȰü |
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| ¿µ¹® | alimentary tract | ÇÑ±Û | ¼ÒȰü, ¿µ¾ç°ü |
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| ¼³¸í | ÀÔ¿¡¼ ½ÃÀÛÇÏ¿© Ç×¹®À¸·Î ³¡³ª´Â ¼Òȸ¦ ´ã´çÇÏ´Â À̸£´Â ¸». À§Ã¢ÀÚ°üÀ̶ó°íµµ ºÒ¸°´Ù. |
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| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
|---|---|
| ATA | alimentary toxic aleukia; American Thyroid Association; aminotriazole; antithymic activity; antithyr... |
| BAPV | bovine alimentary papilloma virus |
| IGD | idiopathic growth hormone deficiency; interglobal distance; isolated gonadotropin deficiency |
| MCD | magnetic circular dichroism; mast-cell degranulation; mean cell diameter; mean of consecutive differ... |
| CARDIAC | Cardiovascular Disease and Alimentary Comparison |
|---|---|
| ATD | 1-antitrypsin deficiency |
| AMD | Acid maltase deficiency |
| AIDS | Acquire Immune Deficiency Syndrome |
| AIDS | Acquired Immune Deficiency Disease Syndrome |
| alimentary | <gastroenterology> Pertaining to food or nutritive material or to the organs of digestion. (18 Nov 1997) |
|---|---|
| alimentary apparatus | The organs that are responsible for getting food into and out of the body and for making use of food to keep the body healthy. These include the mouth, oesophagus, stomach, liver, gallbladder, pancreas, small intestine, colon, and rectum. (12 Dec 1998) |
| alimentary canal | <anatomy> The digestive tract. (27 Sep 1997) |
| alimentary diabetes | Glycosuria developing after the ingestion of a moderate amount of sugar or starch, which normally is disposed of without appearing in the urine, because rate of intestinal absorption exceeds capacity of the liver and the other tissues to remove the glucose, thus allowing blood glucose levels to become high enough for renal excretion to occur. Synonym: alimentary diabetes, digestive glycosuria. (05 Mar 2000) |
| alimentary glycosuria | Glycosuria developing after the ingestion of a moderate amount of sugar or starch, which normally is disposed of without appearing in the urine, because rate of intestinal absorption exceeds capacity of the liver and the other tissues to remove the glucose, thus allowing blood glucose levels to become high enough for renal excretion to occur. Synonym: alimentary diabetes, digestive glycosuria. (05 Mar 2000) |
| alimentary lipaemia | Relatively transient lipaemia occurring after the ingestion of foods with a large content of fat. Synonym: postprandial lipaemia. (05 Mar 2000) |
| alimentary osteopathy | Bone disease due to dietary deficiency. (05 Mar 2000) |
| alimentary system | The organs that are responsible for getting food into and out of the body and for making use of food to keep the body healthy. These include the mouth, oesophagus, stomach, liver, gallbladder, pancreas, small intestine, colon, and rectum. (12 Dec 1998) |
| alimentary tract | The passage leading from the mouth to the anus through the pharynx, oesophagus, stomach, and intestine. Synonym: alimentary canal, alimentary tract, digestive tube, tubus digestorius. (05 Mar 2000) |
| alimentary tract smear | A group of cytologic specimens containing material from the mouth (oral smear), oesophagus and stomach (gastric smear), duodenum (paraduodenal smear), and colon, obtained by specialised lavage techniques; used principally for the diagnosis of cancer of those areas. (05 Mar 2000) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| alpha-1 antitrypsin deficiency | <chest medicine> Deficiency of the protease inhibitor alpha-1 antitrypsin, leads primarily to degradation of elastin of the alveolar walls, as well as other structural proteins of a variety of tissues. The lack of this protein leads to damage of various organs, but mainly to the lung and liver. symptoms may become apparent at a very early age or in adulthood, manifesting either as shortness of breath or liver related symptoms (jaundice, fatigue, fluid in the abdomen, mental changes, or gastrointestinal bleeding). There are several options for treatment of the lung disease, including replacement of the missing protein. Treatment of the liver disease is a well-timed liver transplant (12 Dec 1998) |
| alpha-1-proteinase deficiency | Absence of a serum proteinase inhibitor that may cause nodular non-suppurative panniculitis. (05 Mar 2000) |
| alpha-antitrypsin deficiency | <enzyme> A specific enzyme (alpha 1 antitrypsinase) that when absent genetically can result in panacinar emphysema (lung disease) and liver disease. There is no specific treatment for this condition other than supportive care for the liver and lung complications. Medications such as alpha-1proteinase inhibitor is given regularly to these patients. Incidence: approximately 1 in 10,000. (02 Jan 1998) |
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