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"cold agglutinin 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.
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  • ¿µ¹®
    ÇѱÛ
  • disease entity
    Áúº´´ÜÀ§, Áúº´¸í
  • disease free survival
    ¹«º´»ýÁ¸
  • disease odds ratio
    Áúº´±³Â÷ºñ, Áúº´½Â»êºñ
  • disease potential
    Áúº´ÀáÀç·Â
  • disease registry
    Áúº´µî·Ïü°è
  • disease susceptibility
    Áúº´°¨¼ö¼º
  • disease taxonomy
    Áúº´ºÐ·ùÇÐ
  • extramammary Paget disease
    À¯¹æ¿ÜÆÄÁ¦Æ®º´
  • extrapyramidal disease
    ÇǶó¹Ìµå¹Ù±ù±æº´, Ãßü¿Ü·Îº´
  • endemic disease
    dzÅ亴, Áö¹æÀ¯Çິ
  • enzootic disease
    µ¿¹°Áö¹æº´, µ¿¹°ÅäÂøº´
  • epidemic disease
    À¯Çິ
  • Fabry disease
    ÆÄºê¸®º´
  • fat deficiency disease
    Áö¹æ°áÇ̺´
  • febrile disease
    ¿­º´
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  • ¿µ¹®
    ÇѱÛ
  • disease susceptibility
    Áúº´°¨¼ö¼º
  • disease taxonomy
    Áúº´ºÐ·ùÇÐ
  • disease vector
    Áúº´¸Å°³Ã¼
  • disease free survival
    ¹«º´»ýÁ¸
  • disease frequency survey
    Áúº´ºóµµÁ¶»ç
  • disease odds ratio
    Áúº´±³Â÷ºñ
  • dust disease
    ¸ÕÁöº´
  • endemic disease
    dzÅ亴
  • enzootic disease
    µ¿¹°ÅäÂøº´
  • epidemic disease
    À¯Çິ
  • epidermal-epithelial viral disease
    Ç¥ÇÇ»óÇǹÙÀÌ·¯½ºº´
  • exotic disease
    ¿Ü·¡º´
  • extraarticular rheumatic disease
    °üÀý¿Ü·ù¸¶Æ¼½ºº´
  • extrapyramidal disease
    Ãßü¿Ü·Îº´
  • fat deficiency disease
    Áö¹æ°áÇÌÁõ
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  • ¿µ¹®
    ÇѱÛ
  • 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´
  • Lebers disease
    ·¹º£¸£º´
  • Legionnaires disease
    ·¹±â¿À³Ú¶óÁõ, ÀçÇⱺÀÎȸº´
  • Leiners disease
    ¶óÀÌ³Ê º´
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  • ¿µ¹®
    ÇѱÛ
  • allergic disease
    ¾Ë·¹¸£±â(¼º) Áúȯ
  • allergic respiratory disease
    ¾Ë·¹¸£±â¼º È£Èí±âº´
  • allergic skin disease
    ¾Ë·¹¸£±â(¼º)ÇǺΠÁúȯ
  • allergic skin disease
    ¾Ë·¹¸£±â[¼º] ÇǺκ´
  • alpha (¥á) chain disease
    ¾ËÆÄ»ç½½º´, ¾ËÆÄ¼âº´
  • alpha chain disease
    ¾ËÆÄ¼âº´(¡­áðÜ»).
  • alpha chain disease
    ¾ËÆÄ¼âÁúȯ
  • alpha-chain disease
    ¾ËÆÄ¼â Áúȯ(¡­áð òðü´)
  • alports syndrome(disease)
    ¾ËÆ÷Æ® ÁõÈıº(º´)(¡­ñøý¦ÏØ)
  • aluminium dust disease
    ¾Ë·ç¹Ì´½°¡·çº´(ÊÙËÓ).
  • 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>
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CSTT cold-stimulation time test
CWS cell wall skeleton; chest wall stimulation; child welfare service; cold water-soluble; cotton wool s...
CWT cold water treatment
H&C hot and cold
IHCA individual health care account; isocapnic hyperventilation with cold air
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PNA Peanut agglutinin
PSA Pisum sativum agglutinin
RCA Ricinis communis agglutinin
RCAI Ricinus Communis Agglutinin
RCA-120 Ricinus Communis Agglutinin-120
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Ebstein anomaly disease
    ¿¦½ºÅ¸ÀÎ º´
    ¿ì½É½Ç°ú ¿ì½É¹æ »çÀÌ¿¡ ÀÖ´Â »ï÷ÆÇ
  • epizootic hemorrhagic disease
    °¡Ãà À¯Ç༺ ÃâÇ÷¼º Áúȯ
  • F1 hybrid disease
    F1 ÇÏÀ̺긮µå Áúȯ
    ÇÑÂÊ ¾î¹öÀÌÀÇ ¸é¿ª ´ã´ç ¼¼Æ÷¸¦ F
  • Fabry Anderson disease
    ÆÐºê¸® ¾Ø´õ½¼ Áúȯ
  • febrile disease
    ¿­¼º Áúȯ
  • fifth disease
    Á¦ 5º´
  • flat Bowen's disease
    ÆíÆò Bowen Áúȯ
  • focal disease
    ÃÊÁ¡¼º Áúȯ
  • following chronic infectious disease
    ¸¸¼º °¨¿° ÁúȯÀÇ ÃßÀû
  • Fordyce's disease
    Æ÷¿À´ÙÀ̽º º´
  • Hailey-Hailey disease
    ÇìÀϸ® ÇìÀϸ® º´
    °¡Á·¼º ¾ç¼º ¸¸¼º õÆ÷â. °æºÎ, ¾×¿Í, ¼­ÇýºÎ¿¡ ÀÛÀº ¼öÆ÷ ¹× Å« ¼öÆ÷°¡ ¹Ýº¹ÇÏ¿© ¹ß»ýÇÏ´Â Èñ±ÍÇÑ À¯Àü¼º Áúȯ. »ó¿°»öü ¿ì¼º À¯ÀüÀ» ÇÏ¸ç ºÒ¿ÏÀüÇÑ Ç¥ÇöÀ²À» °¡Áø´Ù. ¸ð³¶ °¢È­Áõ°ú À¯»çÇÏ°Ô »ý°¢ÇÏ¸ç ºÎÂø ¹Ý³» ¼¼Æ÷°£ Á¢ÃËÃþÀÇ ¼Ò½Ç ¶Ç´Â ´ç±è¼¼»çÀÇ °áÇÔÀ» µé°í ÀÖ´Ù.
  • hand and foot disease
    ¼Õ¹ß º´, ¼öÁ· º´
  • hand foot and mouth disease
    ¼öÁ·±¸ º´, ¼Õ¹ßÀÔ º´, ¼Õ¹ß ¹× ±¸°­ Áúȯ, ¼Õ-¹ß-±¸°­ Áúȯ
    1. ÄÛ»çŰ ¹ÙÀÌ·¯½º¿¡ ÀÇÇØ »ý±ä µå¹® Àå ¹ÙÀÌ·¯½º¼º °¨¿° Áúȯ. 2. °æÁõÀ̳ª ´ë´ÜÈ÷ °¨¿°·ÂÀÌ ÀÖ´Â ¼Ò¾ÆÀÇ ¹ÙÀÌ·¯½º º´À¸·Î¼­, ÀÔ, ¼öÁ·¿¡ ¼öÆ÷¼º º´º¯À» º¼ ¼ö ÀÖ´Â °ÍÀÌ ±× Ư¡ÀÌ´Ù. 3. ÄÛ»çŰ ¹ÙÀÌ·¯½º A16ÀÇ °¨¿°À¸·Î ¼Õ, ¹ß, ÇÏÁö, ÀÔ¼Ó¿¡ ÀÛÀº ¼öÆ÷°¡ »ý±â´Â Áúº´. ÁÖ·Î Á¥¸ÔÀÌ¿¡°Ô Àß ³ªÅ¸³ª´Â °¨¿°ÁõÀε¥, 6°³¿ù ¹Ì¸¸ÀÇ Á¥¸ÔÀÌ¿Í 4¼¼ ÀÌ»óÀÇ ¾î¸°ÀÌ¿¡°Ô´Â µå¹°°Ô °¨¿°µÈ´Ù. ³²ÀÚ ¾î¸°ÀÌ¿¡°Ô ¸¹°í ¼ºÀο¡°Ôµµ ³ªÅ¸³­´Ù. ¿©¸§Ã¶¿¡ ÁÖ·Î ¹ßº´Çϰí 4~6Àϰ£ÀÇ Àẹ±â¸¦ °ÅÄ£´Ù. Áõ¼¼´Â ´ëü·Î °¡º±´Ù. 1957³â ij³ª´Ù Åä·ÐÅä¿¡¼­ À¯ÇàÇßÀ» ¶§ ·Îºó½¼ µîÀÌ ÀÌ Áõ¼¼¿¡ ´ëÇØ ±â·ÏÇß°í, ´º¿åÁÖ ÄÛ»çŰ¿¡¼­ óÀ½À¸·Î ÀÌ ¹ÙÀÌ·¯½º¸¦ ºÐ¸®½ÃŲ µ¥¼­ ±× Áö¹æ¸íÀ» µû¼­ ¸í¸íÇÏ¿´´Ù. ±× ´ç½Ã º´¿øÃ¼´Â ÄÛ»çŰ A16 ¹ÙÀÌ·¯½º¿´À¸³ª, ÈÄ¿¡ ÄÛ»çŰ A5, A10°ú ¿£Å×·Î ¹ÙÀÌ·¯½º 71Çü¿¡ ÀÇÇØ¼­µµ °°Àº Áõ¼¼ÀÇ º´ÀÌ ³ªÅ¸³­´Ù´Â °ÍÀÌ ¹àÇôÁ³´Ù. ÁÖ·Î ºñ¸» °¨¿°, °æ±¸ °¨¿°À¸·Î Àü¿°µÈ´Ù.
  • Hand Schuller Christian disease
    ÇÑÆ® ½¶·¯ Å©¸®½ºÂù º´, ÇÚµå ½¶·¯ Å©¸®½ºÂù º´, Hand-Schuller-Christian º´
    1. ´Ù¼Ò¼º È£»ê¼º À°¾ÆÁ¾ÀÌ 5¼¼ ÀÌÀü¿¡ ¹ßº´ÇÏ´Â °æ¿ì¿¡ »ç¿ëÇÏ´Â ¿ë¾î. ¹ß¿­, Àü½Å¼º Àμ³, µÎÇÇ¿Í À̰ü ÇǺÎÀÇ Áö·ç¼º ¹ßÁø, ÁßÀÌ¿°, À¯¾çµ¹±â¿° ¹× Ä¡Àº¿°°ú »ó±âµµ ¿°ÁõÀ» ÈçÈ÷ µ¿¹ÝÇÑ´Ù. 2. °æµµÀÇ ¸²ÇÁÀý Á¾´ë, °£ºñ Á¾´ë°¡ ÃÊ·¡µÉ ¼ö ÀÖ°í ÆóÀå³»¿¡ À°¾ÆÁ¾ Çü¼º ¶Ç´Â °£ÇæÀûÀÎ ¹Ì»ý¹° °¨¿°¿¡ ÀÇÇÑ °ÍÀ¸·Î º¸ÀÌ´Â ¹Ì¸¸¼º Æó¿° ¼Ò°ßÀ» º¼ ¼ö ÀÖ´Ù. 3. ¾î¸°ÀÌ ¹× 10´ë Ãʹݿ¡ ¹ßº´Çϸç 3´ë Áõ»óÀ¸·Î´Â ¾È±¸ µ¹ÃâÁõ, °ñ º´¼Ò, ´¢ºØÁõ
  • Hand-Schuller-Christian disease
    ÇÚµå-½¯·¯-Å©¸®½ºÂù º´
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
Azorean disease A rare form of hereditary ataxia, characterised by onset in early adult life of progressive, spinocerebellar and extrapyramidal disease with external ophthalmoplegia, rigidity dystonia symptoms, and, often, peripheral amyotrophy; found predominantly in people of Azorean ancestry; autosomal dominant inheritance.
Synonym: Azorean disease, Portuguese-Azorean disease.
Origin: Surnames of two families studied in major descriptions of the disease.
(05 Mar 2000)
bacterial wilt disease <botany> A plant disease common in cucumber and muskmelon caused by the bacteria Erwinia tracheiphila which causes wilting and shriveling of the stems and leaves.
(09 Oct 1997)
Baelz' disease An acquired disorder, of unknown aetiology, of the lower lip characterised by swelling, ulceration, crusting, mucous gland hyperplasia, abscesses, and sinus tracts.
Synonym: Baelz' disease, myxadenitis labialis, Volkmann's cheilitis.
(05 Mar 2000)
Balo's disease Encephalitis that is clinically similar to adrenoleukodystrophy, but pathologically characterised by concentric globes or circles of demyelination of cerebral white matter separated by normal tissue.
Synonym: Balo's disease.
(05 Mar 2000)
Baltic myoclonus disease One of the familial light sensitive myoclonic epilepsies. Unlike Lafora body polymyoclonus, where inclusion bodies are seen in the brain cells, the prognosis is often favourable. Probably an autosomal recessive disorder.
(05 Mar 2000)
Bamberger-Marie disease hypertrophic pulmonary osteoarthropathy
Bamberger's disease A spasmodic affection of the muscles of the lower extremities.
Synonym: Bamberger's disease, dancing spasm, Gowers disease.
(05 Mar 2000)
Bang's disease A disease in cattle caused by Brucella abortus; in pregnant cows, characterised by abortion late in pregnancy, followed by retained placenta and metritis; in bulls, orchitis and epididymitis may occur; the organism may localise in the udder and thus appear in milk from infected cows.
Synonym: Bang's disease.
(05 Mar 2000)
Bannister's disease A vascular reaction involving the deep dermis or subcutaneous or submucal tissues, representing localised oedema caused by dilatation and increased permeability of the capillaries and characterised by development of giant wheals.
(18 Nov 1997)
Banti's disease <syndrome> Chronic congestive splenomegaly that occurs primarily in children as a sequel to hypertension in the portal or splenic veins, usually as a result of thrombosis of the veins; anaemia, splenomegaly, and irregular episodes of gastrointestinal bleeding are usually observed, with ascites, jaundice, leukopenia, and thrombocytopenia developing in various conbinations.
Synonym: Banti's disease, splenic anaemia.
(05 Mar 2000)
Barclay-Baron disease Dysphagia caused by food becoming lodged above the epiglottis.
Synonym: Barclay-Baron disease.
(05 Mar 2000)
Barlow's disease infantile scurvy
Barraquer's disease A condition characterised by a complete loss of the subcutaneous fat of the upper part of the torso, the arms, neck, and face, sometimes with an increase of fat in the tissues about and below the pelvis.
Synonym: Barraquer's disease, lipodystrophia progessiva superior, partial lipoatrophy, Simons' disease.
(05 Mar 2000)
bartter's disease Hypertrophy and hyperplasia of the juxtaglomerular cells, producing hypokalaemic alkalosis and hyperaldosteronism, characterised by absence of hypertension in the presence of markedly increased plasma renin concentrations, and by insensitivity to the pressor effects of angiotensin. It usually affects children, is perhaps hereditary, and may be associated with other anomalies, such as mental retardation and short stature. It is also called juxtaglomerular cell aplasia.
(12 Dec 1998)
Basedow's disease <endocrinology> A common cause of hyperthyroidism thought to be caused by an underlying autoimmune mechanism.
(27 Sep 1997)
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