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"alpha chain disease"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • hemoglobin M disease
    Çì¸ð±Û·ÎºóMº´
  • hemoglobin S-C disease
    Çì¸ð±Û·ÎºóS-Cº´
  • hemolytic disease
    ¿ëÇ÷º´
  • hemorrhagic disease
    ÃâÇ÷º´
  • hepatolenticular disease
    °£·»ÁîÇÙº´
  • hereditary disease
    À¯Àüº´
  • heredodegenerative disease
    À¯Àüº¯¼ºº´
  • herpetic disease
    Ç츣Æä½ºº´
  • hidebound disease
    Çǰñ»óÁ¢º´
  • hip-joint disease
    ¾ûµ¢°üÀýº´, °í°üÀýº´
  • Hirschsprung¡¯s disease
    È÷¸£½´½´ÇÁ·îº´
  • hand-foot-mouth disease
    ¼Õ¹ßÀÔº´
  • Hand-Schuller-Christian disease
    ÇÚµå-½¯·¯-Å©¸®½ºÃµº´
  • Hodgkin¡¯s disease
    È£ÁöŲº´
  • holoendemic disease
    ¼Ò¾ÆÇ³Å亴
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  • ¿µ¹®
    ÇѱÛ
  • hookworm disease
    ±¸Ã溴
  • hunger disease
    ±â¾Æº´
  • hyaline membrane disease
    À¯¸®Áú¸·º´
  • hydatid disease
    Æ÷Ãæº´
  • hyperbaric disease
    °í¾Ðº´
  • hyperendemic disease
    °ú´ÙºóµµÇ³Å亴
  • hypertensive disease
    °íÇ÷¾ÐÁúȯ
  • hypertensive heart disease
    °íÇ÷¾Ð½ÉÀ庴, °íÇ÷¾Ð½ÉÀåÁúȯ
  • hypertensive vascular disease
    °íÇ÷¾ÐÇ÷°üº´
  • iatrogenic disease
    ¿øÀÎºÒ¸íº´
  • idiopathic disease
    Ư¹ßº´, Àڹߺ´
  • immune deposit disease
    ¸é¿ªÄ§Âøº´
  • immune-complex disease
    ¸é¿ªº¹ÇÕüº´
  • immunodeficiency disease
    ¸é¿ª°áÇ̺´
  • immunological disease
    ¸é¿ªÁúȯ
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  • ¿µ¹®
    ÇѱÛ
  • Hodgkin s disease =malignant lymphoma
    È£ÁîŲº´.
  • Hodgkin s disease =malignant lymphoma
    È£ÁîŲº´.
  • Huntingtons disease
    ÇãÆÃÅæ¹«µµº´
  • Huntingtons disease
    ÇåÆÃÅæ º´
  • Hyaline membrane disease
    À¯¸®Áú¸·º´(ë¤×ãòõدܻ)
  • Internation Classification of Disease(ICD)
    ±¹Á¦Áúº´ºÐ·ù.
  • Jacob-Creutzfeldt disease
    ¾ßÄß-Å©·çÃ÷ÆçÆ®º´
  • Johnes disease
    ÁÔÁúȯ
  • Kahler s disease
    Ä®·¯º´.
  • Kawasaki disease
    °¡¿Í»ç³¢º´, Á¡¸·ÇǺθ²ÇÁÀý ÁõÈıº (±Þ¼º¿­¼º)
  • Kawasaki disease => mucocutaneous lymph node syndrome
    °¡¿Í»çŰ º´
  • Kimura disease
    ±â¹«¶ó º´
  • Krabbe s disease
    Å©¶óº£º´.
  • Krabbes disease
    Å©·¹º£º´
  • Kyrles disease = hyperkeratosis folliculitis
    ۸¦·¹ º´
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  • ¿µ¹®
    ÇѱÛ
  • alzheimers disease
    ¾ËÂêÇÏÀ̸Ӻ´(¡­Ü»)
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼º Èæ³»Àå ¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼ºÈæ¾Ï½Ã¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amyloid disease
    ¾Æ¹Ð·ÎÀ̵庴(¡­Ü»).
  • andersen disease
    ¾Ø´õ½¼º´<--Áúȯ>
  • angiospasmodic disease
    Ç÷°ü¿¬Ã༺ Áúȯ.
  • aortic valvular disease
    ´ëµ¿¸ÆÆÇÁúȯ(¡­òðü´).
  • aphthous fever =foot and mouth disease
    ¾ÆÇÁŸ¼º¿­(¡­æð).
  • apocrine miliaria => Fox Fordyce disease
    ¾ÆÆ÷Å©¸° ÇÑÁø
  • arbovirus disease
    ¾Æ¸£º¸¹ÙÀÌ·¯½ºº´(¡­Ü»)
  • arteriosclerotic cardiovascular disease
    µ¿¸Æ°æÈ­¼º ½ÉÇ÷°üº´(¡­ãýúìηܻ).
  • arteriosclerotic heart disease
    µ¿¸Æ°æÈ­¼º ½ÉÁúȯ(ãýòðü´).
  • arthropod-borne viral disease
    ÀýÁöµ¿¹° ¸Å°³ ¹ÙÀÌ·¯½ºº´
  • arthropod-borne viral disease
    ÀýÁöµ¿¹°¸Å°³¹ÙÀÌ·¯½º,¾Æº¸¹ÙÀÌ·¯½º
  • association disease
    ¿¬»óº´
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BCKA branched-chain keto acid
BCT brachiocephalic trunk; branched-chain amino acid transferase
CH constant domain of H chain
CL constant domain of L chain; lung compliance
CSCI corticosterone side-chain isomerase
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 13
alpha-BuTx Alpha-Bungarotoxin
alpha-GAL Alpha-Galactosidase
alpha-LA Alpha-Lactalbumin
alpha-MSH Alpha-Melanocyte stimulating hormone
alpha-MPT alpha-methyl-L-p-tyrosine
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Langdon-Down's disease
    ·©µ·-´Ù¿î º´
  • Larsen-Johansson disease
    ¶ó¸£¼¾-¿äÇѽ¼ º´
  • law of prophylaxis for infectious disease
    Àü¿°º´ ¿¹¹æ¹ý
  • legal communicable disease
    ¹ýÁ¤ Àü¿°º´
    Àü¿°º´ ¿¹¹æ¹ý Á¦2Á¶ 1Ç׿¡¼­ ¿­°Å ±ÔÁ¤Çϰí ÀÖ´Â Àü¿°º´. Á¦1Á¾, Á¦2Á¾ ¹× Á¦3Á¾À¸·Î ³ª´©¾îÁø´Ù. 93³â 12¿ù ¼öÁ¤, °áÁ¤µÈ ¹ýÁ¤ Àü¿°º´Àº ¸ðµÎ 28Á¾ÀÌ´Ù. Áï, Á¦1Á¾Àº ÄÝ·¹¶ó, Æä½ºÆ®, ¹ßÁøÆ¼Çª½º, ÀåÆ¼Çª½º, ÆÄ¶óƼǪ½º, µðÇÁÅ׸®¾Æ, ¼¼±Õ¼º ÀÌÁú, Ȳ¿­, Á¦2Á¾Àº Æú¸®¿À, ¹éÀÏÇØ, È«¿ª, À¯Ç༺ ÀÌÇϼ±¿°, ÀϺ» ³ú¿°, °ø¼öº´, ¸»¶ó¸®¾Æ, ¹ßÁø¿­, ¼ºÈ«¿­, Àç±Í¿­, ¾Æ¸Þ¹Ù¼º ÀÌÁú, ¼ö¸· ±¸±Õ¼º ¼ö¸·¿°, À¯Ç༺ ÃâÇ÷¿­, ÆÄ»ódz, ÈÄõ¼º ¸é¿ª °áÇÌÁõ, ·¾Å佺ÇǶóÁõ, ¾²¾²°¡¹«½Ã º´, Á¦3Á¾Àº °áÇÙ, ¼ºº´, ³ªº´À¸·Î µÇ¾î ÀÖ´Ù. Àü¿°º´ ¿¹¹æ¹ýÀº ¹ýÁ¤ Àü¿°º´¿¡ ´ëÇÑ ÀÇ»ç, È£ÁÖ, ¼¼´ëÁÖ, ±âŸ °¢ ±â°üÀÇ ±â°üÀåÀ̳ª °æ¿µÀÚ, ±º ºÎ´ëÀå µîÀÇ ½Å°í ¹× º¸°í Àǹ«¿Í °Ç°­ Áø´Ü, ¿¹¹æ Á¢Á¾, °Ý¸®, ÀÔ¿ø Á¶Ä¡, °¢Á¾ ¿¹¹æ Á¶Ä¡ µîÀ» ±ÔÁ¤Çϰí ÀÖ´Ù.
  • Legg-Calve-Perthes disease
    ·¹±×-Ä®º£-ÆÆä¸£Å×½
  • Legionnaires'disease
    ÀçÇⱺÀÎ º´
    Legionella °¨¿°Àº »çȸ ȹµæ Æó·ÅÀÇ 3-4¹øÂ°·Î ÈçÇÑ ¿øÀÎÀÌ´Ù. ¿øÀÎÀ» Àß ¸ð¸£´Â Æó·ÅÀÇ °æ¿ì´Â ¾ðÁ¦µçÁö °í·ÁÇØ¾ß ÇÑ´Ù. ÀçÇⱺÀÎ º´Àº ¸é¿ª ÀúÇÏÀÚ¿Í Èí¿¬ÀÚ, ¸¸¼º Æó ÁúȯÀÚ¿¡¼­ Á»´õ ÈçÇÏ´Ù. ·¹Áö¿À³Ú¶óÁõÀÇ Áý´Ü ¹ß»ýÀº »þ¿ö±â³ª ¼öµµ²ÀÁö¿Í ¿¡¾îÄÁÀÇ ³Ã°¢ ž°ú °°Àº ¿À¿°µÈ ¼ö¿ø°ú ¿¬°üµÇ¾î ÀÖ´Ù. ÀÌ º´Àº °´´ãÀÇ ±×¶÷ ¿°»ö¿¡¼­ ±ÕÀÌ º¸ÀÌÁö ¾Ê±â ¶§¹®¿¡ ÈçÈ÷ ºñÁ¤Çü Æó·ÅÀ̶ó°í ÇÑ´Ù. ±×·¯³ª ÀÌ º´ÀÇ ÀÓ»ó Áõ»óÀº °í¿­°ú Áßµ¶¼º ¿Ü°ß, ´Á¸·¿°, È­³ó¼º °´´ã
  • Letter Siwe disease
    ·¹ÅÍ·¯ ½Ã¿þ º´
    ¾Ç¼º Á¶Á÷±¸ÁõÀ̳ª ¾Ç¼º ÀÓÆÄÁ¾°ú °°Àº ¾çÅÂÀÌ´Ù. 2¼¼ ÀÌÇÏÀÇ À¯¾Æ¿¡ ¹ßº´ÇÏ°í ´ë°³ Ä¡¸íÀûÀÌ´Ù. ±âº»ÀûÀÎ º´¸® ¼Ò°ßÀº ÀÓÆÄÀý, ÇǺÎ, Æó, °ñ¼öÀÇ º´¹ßÀ̳ª °£ ºñ´ë¸¦ ÃÊ·¡ÇÏ´Â ¼¼¸Á³»Çǰè ÁúȯÀ¸·Î º´º¯ÀÇ ÁøÇà ¼Óµµ°¡ ºü¸£±â ¶§¹®¿¡ ¹æ»ç¼±ÇÐÀû °Ë»ç°¡ ºÒ°¡´ÉÇÏ´Ù.
  • linear IgA disease
    ¼±»ó ¸é¿ª ±Û·ÎºÒ¸° A Áúȯ
  • liver disease
    °£ Áúȯ
  • lung disease
    Æó Áúȯ
  • lymphoproliferative disease
    ÀÓÆÄ ¼¼Æ÷ Áõ½Ä¼º Áúȯ
  • Majocci's disease
    ¸¶¿äŰ º´
    Àڹݺ´.
  • Malassez's disease
    ¸»¶ó¼¼ º´
    °íȯÀÇ ³¶Æ÷.
  • manager disease
    ¸Å´ÏÀú º´
    ¿©·¯ °¡Áö º¹ÀâÇÑ ¾÷¹«¿¡ ¹Ù»Ú°Ô ½Ã´Þ¸®´Â °ü¸® Á÷±ÞÀÇ »ç¶÷¿¡°Ô¼­ ÈçÈ÷ º¼ ¼ö ÀÖ´Â º´. Çù½ÉÁõ, ƯÈ÷ °ü»ó µ¿¸Æ Ç÷ÀüÁõ µîÀÇ ½ÉÀå Ç÷°ü°è Áõ¼¼µé¸¸À» °¡¸®Å°´Â °ÍÀ̾ú´Âµ¥ Á¡Â÷·Î È®´ëµÇ¾î ¼ÒÈ­¼º ±Ë¾ç, ´ç´¢º´, ³ëÀÌ·ÎÁ¦, Ç÷¾Ð Àå¾Ö µîµµ Æ÷ÇԵȴÙ.
  • maple syrum urine disease
    ´Üdz ³ª¹« ½Ã·´ º´
    Ãø¼â, ¾Æ¹Ì³ë»ê ´ë»çÀÇ È¿¼Ò °á¼Õ¿¡ ÀÇÇÑ À¯Àüº´À¸·Î, Ç÷Àå ¹× ¿äÁß¿¡¼­ ŰÅä»ê
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alpha-ketoglutaramic acid H2N-COCH2CH2COCOOH;a metabolite of glutamine formed by the action of glutamine aminotransferase; elevated in certain cases of hepatocoma.
Synonym: 2-oxoglutaric acid.
(05 Mar 2000)
alpha-ketoglutarate A salt or ester of alpha-ketoglutaric acid.
Alpha-ketoglutarate dehydrogenase, an enzyme that catalyses the oxidative decarboxylation of 2-ketoglutaric acid to succinyldihydrolipoate; the succinyl group is later transferred to CoA and the reduced lipoate is oxidised by NAD+; a complex that is a part of the tricarboxylic acid cycle.
Synonym: 2-oxoglutarate dehydrogenase, alpha-ketoglutarate dehydrogenase complex.
(05 Mar 2000)
alpha-ketoglutarate dehydrogenase complex alpha-ketoglutarate dehydrogenase
alpha-ketoglutarate permease <chemical> From E coli; 432-amino acid protein; amino acid sequence given in first source
Synonym: kGTP gene product, wita protein, alpha-ketoglutarate transporter
(26 Jun 1999)
alpha-ketoisocaproate oxygenase <enzyme> From rat liver cytosol; oxidatively decarboxylates and hydroxylates alpha-ketoisocaporate to form beta-hydroxyisovalerate; requires fe(2+) and thiol; activated by ascorbate
Registry number: EC 1.13.11.-
Synonym: 2-ketoisocaproate oxygenase, alpha-ketoisocaproate dioxygenase
(26 Jun 1999)
alpha-ketosuccinamic acid NH2-CO-CH2-CO-COOH;the transamination product of asparagine; acted upon by &omega;-amidase.
(05 Mar 2000)
alpha-lactyl-thiamin pyrophosphate An intermediate formed in the oxidative decarboxylation of pyruvate.
Compare: pyruvate dehydrogenase (lipoamide).
Synonym: alpha-lactyl-thiamin pyrophosphate.
(05 Mar 2000)
alpha-l-iduronidase <enzyme> An enzyme that hydrolyzes terminal desulfated alpha-l-iduronic acid residues of dermatan sulfate and of heparan sulfate; a deficiency of this enzyme is associated with Hurler syndrome and Scheie syndrome.
(05 Mar 2000)
alpha-linolenic acid <chemical> (z,z,z)-9,12,15-octadecatrienoic acid. A fatty acid that is found in plants and involved in the formation of prostaglandins.
Chemical name: 9,12,15-Octadecatrienoic acid, (Z,Z,Z)-
(12 Dec 1998)
alpha-macroglobulins Glycoproteins with a molecular weight of approximately 620,000 to 680,000. Precipitation by electrophoresis is in the alpha region. They include alpha 1-macroglobulins and alpha 2-macroglobulins. These proteins exhibit trypsin-, chymotrypsin-, thrombin-, and plasmin-binding activity and function as hormonal transporters.
(12 Dec 1998)
alpha-mannosidase <enzyme> Catalyses hydrolysis of terminal, non-reducing alpha-d-mannose residues in alpha-d-mannosides
Registry number: EC 3.2.1.24
Synonym: alpha-d-mannoside mannohydrolase, alpha-d-mannosidase, neutral alpha-mannosidase, alpha mannosidase a, alpha mannosidase b, lysosomal alpha-mannosidase, laman
(26 Jun 1999)
alpha-methylacyl-CoA racemase <enzyme> Involved in catabolism of branched-chain fatty acids derived from isoprenoids; acts on pristanoyl-CoA and trihydroxycoprostanoyl-CoA, but not on 3-methyl branched-chain or linear-chain acyl coas; amino acid sequence has been determined; genbank u89905 (rat) and u89906 (mouse); also isolated from human liver
Registry number: EC 5.1.99.-
Synonym: meac CoA racemase
(26 Jun 1999)
alpha methyl dopa <drug> An antihypertensive drug, preferred in pregnant patients.
(18 Nov 1997)
alpha-methyltyrosine <chemical> An inhibitor of the enzyme tyrosine 3-monooxygenase, and consequently of the synthesis of catecholamines. It is used to control the symptoms of excessive sympathetic stimulation in patients with pheochromocytoma and decreases the frequency and severity of hypertensive attacks and related symptoms in most patients. (martindale, the extra pharmacopoeia, 30th ed)
Pharmacological action: enzyme inhibitors.
(12 Dec 1998)
alpha-msh <chemical> A 13-amino acid peptide derived from the anterior pituitary gland in man and from the pars intermedia in lower vertebrates. Its amino acid sequence is identical to the first 13 amino acids of acth. It influences the formation of deposition of melanin in the body and produces colour changes in the skin of amphibians, fishes and reptiles. It is secreted in humans only during foetal life and occasionally during pregnancy.
Chemical name: alpha-Melanotropin (pig)
(12 Dec 1998)
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