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  • ¿µ¹®
    ÇѱÛ
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀûº´, ´ç¿øÃàÀûº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • granulomatous disease
    À°¾ÆÁ¾º´
  • Greenfield¡¯s disease
    ±×¸°Çʵ庴
  • Hartnup¡¯s disease
    ÇÏÆ®³Òº´
  • Hashimoto¡¯s disease
    ÇϽøðÅ亴
  • hyperendemic disease
    °ú´ÙºóµµÇ³Å亴, °ú´ÙÁö¹æÀ¯Çິ
  • hypertensive disease
    °íÇ÷¾Ðº´
  • hypertensive heart disease
    °íÇ÷¾Ð½ÉÀ庴, °íÇ÷¾Ð½ÉÀåÁúȯ
  • hypertensive vascular disease
    °íÇ÷¾ÐÇ÷°üº´
  • heart disease
    ½ÉÀ庴
  • heart muscle disease
    ½ÉÀå±ÙÀ°º´, ½É±ÙÁúȯ
  • heavy-chain disease
    ¹«°Å¿î»ç½½º´, Á߼⺴
  • hemoglobin C disease
    Çì¸ð±Û·ÎºóCº´
  • hemoglobin disease
    Çì¸ð±Û·Îºóº´, Ç÷»ö¼Òº´
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  • ¿µ¹®
    ÇѱÛ
  • helminthic disease
    ¿¬Ã溴
  • hemisoimmune disease
    ÀûÇ÷±¸µ¿Á¾¸é¿ªº´
  • hemoglobin disease
    Çì¸ð±Û·Îºóº´, Ç÷»ö¼Òº´
  • hemolytic disease
    ¿ëÇ÷º´, ¿ëÇ÷Áúȯ
  • hemorrhagic disease
    ÃâÇ÷º´
  • hemp disease
    ¸¶¼¶À¯º´
  • hepatolenticular disease
    °£·»ÁîÇÙº´
  • hepatolienal disease
    °£Áö¶óº´, °£ºñÀ庴
  • hereditary disease
    À¯Àüº´
  • heredoconstitutional disease
    À¯ÀüüÁúº´
  • heredodegenerative disease
    À¯Àüº¯¼ºÁõ
  • herpetic disease
    Ç츣Æä½ºº´
  • hidebound disease
    (¢¡scleroderma) ÇǺΰæÈ­Áõ, ÇǺα»À½Áõ
  • hip-joint disease
    ¾ûµ¢°üÀýº´, °í°üÀýº´
  • holoendemic disease
    ¼Ò¾ÆÇ³Å亴
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  • ¿µ¹®
    ÇѱÛ
  • Pompe disease
    ÆûÆäº´
  • Pompes disease
    ÆûÆä¾¾ º´
  • Pott s disease
    Æ÷Æ®º´ ôÃßÄ«¸®¿¡½º .
  • Potts disease
    Æ÷Æ®º´, ôÃßÄ«¸®¿¡½º .
  • Pseudo Hurler disease
    °¡¼ºÇæ·¯º´
  • Raynaud s disease
    ·¹À̳뺴.
  • Refsum s disease
    ·¹ÇÁ¼ûº´.
  • Refsums disease
    ·¹ÇÁ¼û º´
  • Ritter disease
    ¸®ÅÍ º´
  • Rombergs disease = Romberg syndrome
    ·Òº£¸£Å©º´
  • Schilder s disease
    ½Ç´õº´.
  • Sheehans disease
    ½ÃÇѺ´
  • Sj?rens disease
    ¼î±×·»º´, ¼î±×·»ÁõÈıº
  • Stargardts disease=>fundus flavimaculatus
    ½ºÅ¸°¡¸£Æ®º´
  • Stills disease
    ½ºÆ¿ º´
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  • ¿µ¹®
    ÇѱÛ
  • acquired heart disease =AHD
    ÈÄõ¼º ½ÉÁúȯ(¡­ãýòðü´).
  • acute demyelinating disease
    ±Þ¼º Å»¼öÃʼº Áúȯ(¡­÷­âÐõ¦àõòðü´).
  • acute febrile neutrophilic dermatosis ; Sweet disease
    ±Þ¼º À¯¿­ È£Áß±¸¼º ÇǺÎÁõ.
  • acute febrile neutrophilic dermatosis = Sweet disease
    ±Þ¼º À¯¿­ È£Áß±¸¼º ÇǺÎÁõ
  • acute infectious disease
    ±Þ¼º °¨¿°Áúȯ
  • acute infectious disease =AID
    ±Þ¼º Àü¿°º´(¡­îîæøÜ»).
  • acute respiratory disease =ARD
    ±Þ¼º È£Èí±âº´(¡­û¼ýåÐïÜ»).
  • acute respiratory disease =ARD
    ±Þ¼º È£Èí±âº´(¡­û¼ýåÐïÜ»).
  • addisons disease
    ¾Öµð½¼º´(¡­Ü»)
  • addisons disease
    ¾Öµð½¼º´<<ºÎ½Å±â´ÉºÎÀü>>
  • adipose tissue disease
    Áö¹æÁ¶Á÷Áúȯ.
  • adjuvant disease
    ¾ÖÁÖ¹øÆ®º´.
  • adrenal cortex disease
    ºÎ½ÅÇÇÁúÁúȯ(Üùãìù«òõòðü´).
  • adult disease
    ¼ºÀκ´(à÷ìÑÜ»).
  • african sleeping disease
    ¾ÆÇÁ¸®Ä« ¼ö¸éº´(¡­â²ØùÜ»)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 13
UPJ Uretero-Pelvic Junction
FPD feto-pelvic disproportion; flame photometric detector
IPTX intermittent pelvic traction
LBPF long bone or pelvic fracture
NPE neurogenic pulmonary edema; neuropsychologic examination; no palpable enlargement; normal pelvic exa...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 13
AOSD Adult Onset Still's Disease
ASD Adult Still's disease
APKD Adult polycystic kidney disease
ABD Adynamic Bone Disease
ATSDR Agency for Toxic Substances and Disease Registry
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Lane's disease
    ·¹ÀÎ º´
    ¸¸¼º Àå Æó»öÁõ.
  • 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.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 13
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)
basilar interstitial lung disease <radiology> B bronchiectasis, A asbestosis, D drugs / DIP, L lymphangitic metastasis / LAM, A aspiration, S sarcoidosis, S scleroderma
(12 Dec 1998)
batten disease <disease> This congenital disorder strikes between the ages of 5 and 10, causing the afflicted child to suddenly go blind. The child begins to suffer fromseizures and mental deterioration, afflicted individuals typically diebefore the age of 20. The disease is caused by the accumulation of toxicproteins in nerve cells, the root of the disorder is a mutation of a geneon chromosome 16.
(09 Oct 1997)
Batten-Mayou disease Cerebral sphingolipidosis, late infantile and juvenile types.
(05 Mar 2000)
Bayle's disease <neurology> Slight or incomplete paralysis.
Origin: Gr. = relaxation
(18 Nov 1997)
Bazin's disease A type of panniculitis characterised histologically by the presence of granulomas, vasculitis, and necrosis. It is traditionally considered to be the tuberculous counterpart of nodular vasculitis, but is now known to occur without tuberculous precedent. It is seen most commonly in adolescent and menopausal women, is initiated or exacerbated by cold weather, and typically presents as one or more recurrent erythrocyanotic nodules or plaques on the calves. The nodules may progress to form indurations, ulcerations, and scars.
(12 Dec 1998)
Bechterew's disease Arthritis and osteitis deformans involving the spinal column; marked by nodular deposits at the edges of the intervertebral disks with ossification of the ligaments and bony ankylosis of the intervertebral articulations, it results in a rounded kyphosis with rigidity.
Synonym: Bechterew's disease, poker back, Strumpell's disease.
(05 Mar 2000)
Becker's disease An obscure South African cardiomyopathy leading to rapidly fatal congestive heart failure and idiopathic mural endomyocardial disease.
(05 Mar 2000)
Begbie's disease Localised chorea.
(05 Mar 2000)
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