| ¿µ¹® | periodontal disease | ÇÑ±Û | Ä¡ÁÖº´ |
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| ¼³¸í | ÀÕ¸ö°ú Ä¡¾Æ, ±×¸®°í ±× ÁÖÀ§ »ÀÀÇ ¿°Áõ°ú ÅðÇ༺ º¯È¸¦ ¸»ÇÔ. Ä¡·á¿¡ ÀÖ¾î¼ ÀÕ¸öÀÇ Á¦°Å°¡ ÇʼöÀûÀÌ´Ù. ÀÕ¸öÀÇ Á¦°Å´Â »õ·Î¿î ÀÕ¸öÀÇ »ý¼ºÀ» Á¶ÀåÇÑ´Ù. |
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| ¿µ¹® | Crohn's disease | ÇÑ±Û | Å©·Ðº´ |
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| ¼³¸í | ¸¸¼ºÀûÀ̰í Àç¹ßÀ» ÀßÇϴ âÀÚÀÇ ¿°ÁõÀ» Ư¡À¸·Î ÇÏ´Â º´. ÀåÀÇ º®Àº ¾ÈÂÊ¿¡¼ºÎÅÍ Á¡¸·, Á¡¸·ÇÏÁ¶Á÷, ±ÙÀ°Ãþ, À帷ÀÇ 4°³ÀÇ ÃþÀ¸·Î ÀÌ·ç¾îÁ® Àִµ¥, Å©·Ðº´Àº ÀÌ ¸ðµç ÃþÀÇ ¿°ÁõÀ» µ¿¹ÝÇÑ´Ù. ÀåÀÇ ¸ðµç ºÎºÐ¿¡¼ »ý±æ ¼ö°¡ ÀÖÁö¸¸ ÁÖ·Î ¸·Ã¢ÀÚ¿Í ¿¬°áµÇ´Â ūâÀÚÀÇ ¸»´ÜºÎ¿¡ °¡Àå ¸¹ÀÌ »ý±ä´Ù. âÀÚÀÇ ÀüÃþÀÇ ¿°ÁõÀ¸·Î ÀÎÇØ¼ ÀåÀÇ Æó¼â³ª ±«¾çÀ» ¸¸µé¸ç Á¾Á¾ õ°øµÈ´Ù. |
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| ¿µ¹® | Paget's disease | ÇÑ±Û | ÆÄÁ¦Æ®º´ |
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| ¼³¸í | 1. »ÀÆÄÁ¦Æ®º´. º¯Çü¼º »À¿°. »ÀÈí¼ö ÈÄ »ÀÇü¼ºÀÌ ¹Ýº¹ÀûÀ¸·Î °úµµÇÏ°Ô ÀϾ´Â °ÍÀ¸·Î, »õ·Ó°Ô Çü¼ºµÈ »À´Â ¹«Áú¼ÇÏ°í ±¸Á¶ÀûÀ¸·Î °ß°íÇÏÁö ¸øÇÏ´Ù. »ÀÈí¼öÀÇ Áõ°¡°¡ ¹Ýº¹µÇ°í ÀÌ¾î¼ °úÀ׺¸¼ö¸¦ ²ÒÇÏ¿© ¾àÇÏ°í º¯ÇüµÈ »ÀÀÇ ºÎÇǰ¡ Áõ°¡µÇ´Â °ÍÀ» Ư¡À¸·Î ÇÏ´Â »Àº´ÀÌ´Ù. ±ÃµÕ»ÀÀÇ ¸¸°î, ÆíÆò»ÀÀÇ º¯ÇüÀ» ÀÏÀ¸Å°°í, µ¿Åë ¹× º´Àû °ñÀýÀ» ¼ö¹ÝÇÑ´Ù. 2. À¯¹æÆÄÁ¦Æ®º´. Á¥²ÉÆÇ ¹× Á¥²ÀÁöÀÇ ¿°Áõ¼º ¾Ï¼º Áúº´À¸·Î¼ º¸ÅëÀº Á¥»ù ¹× À¯¹æ ±íÀº °÷ÀÇ ¾ÏÀ» µ¿¹ÝÇÑ´Ù. º¸Åë Áß³âºÎÀο¡°Ô ¹ß»ýÇÑ´Ù. |
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| ¿µ¹® | Parkinson disease | ÇÑ±Û | ÆÄŲ½¼º´ |
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| ¼³¸í | ³ªÀÌµç »ç¶÷¿¡°Ô ¹ß»ýÇÏ´Â ½Å°æ°èÀÇ ÅðÇິÀÌ´Ù. ÁÖ·Î ¿îµ¿À» ´ã´çÇÏ´Â Áß°£³úºÎÀ§°¡ ħ¹üµÈ´Ù. ¿øÀÎÀº ¹ÙÀÌ·¯½º, ¾à¹°, ȤÀº µ¿¸Æ°æÈÁõ µîÀ¸·Î ¾Ë·ÁÁø °æ¿ìµµ ÀÖÀ¸³ª, ¿øÀÎÀ» ¾Ë ¼ö ¾ø´Â °æ¿ì°¡ ¸¹´Ù. Áõ»óÀº °¡¸é¾ó±¼, ¾²·¯Áú °Í °°Àº °ÉÀ½°ÉÀÌ, ¼Õ¶³¸², ±ÙÀ°ÀÇ °Á÷, ¾ÕÀ¸·Î ±â¿ï¾îÁø ÀÚ¼¼ µîÀÓ. Ä¡·á´Â Ưº°ÇÑ °ÍÀÌ ¾øÀ¸¸ç, ´ë°³ º¸Á¸Àû Ä¡·á(¿ÏÄ¡¸¦ ¸ñÀûÀ¸·Î ÇÏÁö ¾Ê°í ´ÜÁö ȯÀÚÀÇ »ýȰÀ» º¸Á¶ÇØÁÖ´Â Á¤µµÀÇ Ä¡·á)¸¦ ½ÃÇàÇÑ´Ù. ÃÖ±Ù, Á×Àº žÆÀÇ ³ú¸¦ À̽ÄÇÏ´Â ³ú À̽ļú¿¡ ÀÇÇÑ Ä¡·áÈ¿°ú°¡ ³ô´Ù´Â º¸°í°¡ ÀÖ´Ù. |
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| ¿µ¹® | endemic disease | ÇÑ±Û | dzÅ亴 |
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| ¼³¸í | Àΰ£»çȸ¿¡ Ç×»ó Á¸ÀçÇÏÁö¸¸ Ư¼öÇÑ ±âÈijª ÅäÁú·Î ÀÎÇÏ¿© ƯÁ¤Áö¿ª¿¡¸¸ Á¸ÀçÇÏ´Â »ç¸Á·üÀÌ ³·°í, ÀÓ»óÀûÀ¸·Îµµ µå¹°°Ô º¼ ¼ö ÀÖ´Â º´. ƯÈ÷ ±× ÅäÁöÀÇ Ç³Åä-±âÈÄ-»ý¹°-Åä¾ç µîÀÇ ÀÚ¿¬È¯°æ°ú ±× Áö¹æ ÁÖ¹ÎÀÇ Ç³¼Ó-½À°ü-ÀνÀ µîÀÌ º¹ÀâÇÏ°Ô ¾ôÇô¼ »ý±ä Ư¼öÇÑ º´À» °¡¸®Å²´Ù. ÀϹÝÀûÀ¸·Î ±× Áö¹æ ÁÖ¹ÎÀÇ »ç¸Á·üÀº ±×´ÙÁö ³ôÁö ¾ÊÁö¸¸ ±ÙÀýµÇ±â ¾î·Á¿î °ÍÀÌ Æ¯Â¡ÀÌ´Ù. Áö¹æº´À̶ó´Â ¸»Àº ¾î´À Áö¹æ¿¡ ÇÑÁ¤ÇÏ¿© º¼ ¼ö ÀÖ´Â º´À̶ó´Â Á¡¿¡¼´Â °°Áö¸¸, dzÅäȯ°æ°ú ¹ÐÁ¢ÇÑ °ü°è°¡ ÀÖ´Ù´Â µ¥¼ º¸¸é dzÅ亴À̶ó´Â ¿ë¾î°¡ ÀûÀýÇÏ´Ù. ±¹³»ÀûÀ¸·Î´Â ÂêÂê°¡¹«½Ãº´, ¾ß»ýÅä³¢º´, ·¾Å佺ÇǶóÁõ µîÀÌ ¾Ë·ÁÁ® ÀÖ°í, ¼¼°èÀûÀ¸·Î´Â ¸»¶ó¸®¾Æ, Ȳ¿, ÆäÆ®½º, ÀϺ»ÁÖÇ÷ÈíÃæÁõ µîÀÌ ¾Ë·ÁÁ® ÀÖ´Ù. |
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| CAD | cadaver, cadaveric; cold agglutinin disease; compressed air disease; computer-assisted design; compu... |
|---|---|
| CSD | carotid sinus denervation; cat scratch disease; combined system disease; conditionally streptomycin ... |
| CVD | cardiovascular disease; cerebrovascular disease; collagen vascular disease; color-vision-deviant |
| GBD | gallbladder disease; gender behavior disorder; glass blower's disease; granulomatous bowel disease |
| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
| beta-cystathionase | <enzyme> An enzyme catalyzing the hydrolysis of l-cystathionine to pyruvate, l-homocysteine, and NH3. See: cystathionine gamma-lyase. Synonym: beta-cystathionase, cystine lyase. (05 Mar 2000) |
|---|---|
| beta-D-fucosidase | <enzyme> Catalyses hydrolysis of terminal non-reducing beta-d-fucose residues in beta-d-fucosides; also hydrolyzes beta-d-galactosides Registry number: EC 3.2.1.38 Synonym: beta-d-fucoside fucohydrolase (26 Jun 1999) |
| beta-d-galactosidase | A sugar-splitting enzyme that catalyses the hydrolysis of lactose into d-glucose and d-galactose, and that of other beta-d-galactosides; it also catalyses galactotransferase reactions; a deficiency of beta-d -galactosidase leads to problems in the intestinal digestion of lactose; used in the production of milk products for adults who do not have the intestinal enzyme; a defect of one isozyme of beta-d-galactosidase is associated with Morquio's syndrome type B. Compare: lactase persistence, lactase restriction. Synonym: lactase. (05 Mar 2000) |
| beta-D-galactoside alpha 2-6-sialyltransferase | <enzyme> Catalyses the reaction of cmp-n-acetylneuraminate and galactosylglycoprotein to yield cmp and n-acetylneuraminylgalactosylglycoprotein; cd75 and cd75w antigen were removed as sys - it is not equivalent to the enzyme. Registry number: EC 2.4.99.1 Synonym: cmp-n-acetylneuraminate-d-galactosyl-glycoprotein n-acetylneurainyltransferase, cmp-n-acetylneuraminate-beta-galactoside alpha-2,6-sialyltransferase, beta-galactosyl(1-4)n-acetylglucosaminide alpha(2-6)-sialyltransferase, gal-glcnac(2-6)-sialyltransferase, cmp-n-acetylneuraminic acid-lactose sialytransferase, cmp-acetylneuraminate galactoside (alpha 2-6)-sialyltransferase, cmp-n-acetylneuraminate-galactosylglycoprotein sialyltransferase, alpha 2-6-sialyltransferase, cmp-sialic acid-n-acetyllactosaminide alpha (2-6)-sialyltransferase, cmp-neuac-galactoside (alpha 2-6)-sialyltransferase, gal-1-4-glcnac alpha(2-6)-sialyltransferase, siat-1, beta-galctoside alpha2,6-sialyltransferase (26 Jun 1999) |
| beta-d-glucosidase | A glucohydrolase similar to alpha-d-glucosidase, but attacking beta-glucosides and releasing beta-d-glucose. Synonym: amygdalase, cellobiase, gentiobiase. (05 Mar 2000) |
| beta-d-glucuronidase | <enzyme> An enzyme catalyzing the hydrolysis of various beta-d-glucuronides, liberating free d-glucuronic acid and an alcohol; a deficiency of this enzyme is associated with Sly syndrome. Synonym: glusulase, glycuronidase. (05 Mar 2000) |
| beta-d-glucuronidase deficiency | A rare deficiency of beta-d-glucuronidase; an autosomal recessive disorder with several allelic forms, characterised by abnormal mucopolysaccharide metabolism leading to progressive mental deterioration, splenic and hepatic enlargement, and dysostosis multiplex. Synonym: mucopolysaccharidase. (05 Mar 2000) |
| beta-D-mannosidase | <enzyme> Catalyses hydrolysis of terminal, non-reducing beta-d-mannose residues in beta-d-mannosides Registry number: EC 3.2.1.25 Synonym: mannanase, beta-mannosidase, mana gene product (26 Jun 1999) |
| beta-DNA | <molecular biology> The normal form of DNA found in organisms, which exists as a right-handed helix. (09 Oct 1997) |
| beta-d thalassaemia | Thalassaemia due to a gene that depresses synthesis of both beta-and d-globin chains by the chromosome bearing the abnormal gene. Heterozygous state: thalassaemia minor with Hb F comprising 5 to 30% of total haemoglobin but distributed unevenly among cells, Hb A2 reduced or normal. Homozygous state: moderate anaemia with only Hb F present, no Hb A or Hb A2. Synonym: F thalassaemia. (05 Mar 2000) |
| beta emission | <radiobiology> Form of nuclear decay where a neutron splits into a proton plus electron plus neutrino set. The proton stays in the nucleus but the electron (beta ray) is ejected. (09 Oct 1997) |
| beta-endorphin | <chemical> A peptide consisting of amino acid sequence 61-91 of the endogenous pituitary hormone beta-lipotropin. The first four amino acids show a common tetrapeptide sequence with methionine- and leucine enkephalin. The compound shows opiate-like activity. Injection of beta-endorphin induces a profound analgesia of the whole body for several hours. This action is reversed after administration of naloxone. Chemical name: beta-Endorphin (12 Dec 1998) |
| beta error | The statistical error (said to be of the second kind or type II) made in testing when it is concluded that something is negative when it really is positive. Beta error is often referred to as a false negative. (12 Dec 1998) |
| beta-farnesene | 7,11-Dimethyl-3-methylene-1,6,10-dodecatriene;one of the two isomers (trans) that occurs in the alarm pheromone of some aphids and also in various essential oils. (05 Mar 2000) |
| beta-farnesene synthase | <enzyme> Catalyses conversion of farnesyl diphosphate to beta-farnesene; genbank af024615 Registry number: EC 3.6.1.- (26 Jun 1999) |
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