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¿µ¹® Parkinson disease ÇÑ±Û ÆÄŲ½¼º´
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¿µ¹® endemic disease ÇÑ±Û Ç³Å亴
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¿µ¹® Hodgkin's disease ÇÑ±Û È£ÁöŲº´
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  • ¿µ¹®
    ÇѱÛ
  • deficiency disease
    °áÇ̺´
  • degenerative disease
    ÅðÇິ, º¯¼ºº´
  • degenerative joint disease
    ÅðÇà°üÀýº´
  • demyelinating disease
    ¸»ÀÌÁýÅ»¶ôº´, Å»¼öÃʺ´
  • dense deposit disease
    °í¹ÐµµÄ§Âøº´
  • depression spectrum disease
    ¿ì¿ï½ºÆåÆ®·³º´
  • de Quervain¡¯s disease
    µåÄù¸£¹ðº´
  • diarrheal disease
    ¼³»çº´
  • diffuse Lewy body disease
    ±¤¹üÀ§·¹ºñ¼Òüº´
  • digestive tract disease
    ¼ÒÈ­°üº´
  • disease
    º´, Áúº´, Áúȯ
  • disease control
    Áúº´°ü¸®
  • disease entity
    Áúº´´ÜÀ§, Áúº´¸í
  • disease free survival
    ¹«º´»ýÁ¸
  • disease odds ratio
    Áúº´±³Â÷ºñ, Áúº´½Â»êºñ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • diarrheal disease
    ¼³»çº´
  • diffuse collagen disease
    ±¤¹üÀ§¾Æ±³Áúº´, ¹Ì¸¸¾Æ±³Áúº´
  • diffuse interstitial pulmonary disease
    ±¤¹üÀ§»çÀÌÁúÆóº´, ¹Ì¸¸°£ÁúÆóº´
  • digestive tract disease
    ¼ÒÈ­°üº´
  • disease detection
    Áúº´¹ß°ß
  • disease entity
    Áúº´´ÜÀ§, Áúº´¸í
  • disease potential
    Áúº´ÀáÀç·Â
  • disease registry
    Áúº´µî·Ïü°è
  • 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´
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • Fox Fordyce disease
    Æø½º-Æ÷´ÙÀ̽ºº´
  • Gauchers disease
    °í¼Îº´
  • Gerstmann-Strauissler-Scheinker disease(GSS)
    °Ô¸£½ºÆ®¸¸ ½´Åõ·ÎÀ̽½·¯ »þÀ×Ä¿ º´
  • Gilchrist disease
    ±æÅ©¸®½ºÆ®º´
  • Gilchrists disease => North American blastomycosis
    ºÏ¾Æ¸Þ¸®Ä« ºÐ¾Æ Áø±ÕÁõ
  • Graves disease
    ±×·¹À̺꽺 º´
  • Graves disease
    ±×·¹À̺꾾º´(Ü»)
  • Graves disease
    ±×¶óºê½ºº´
  • Graves disease
    ±×·¹À̺꽺º´
  • Grovers disease => transient acantholytic dermatosis
    Àϰú¼º ±Ø¼¼Æ÷ÇØ¸® ÇǺÎÁõ
  • Gunthers disease => congenital erythropoietic porphyria
    ¼±Ãµ¼º ÀûÇ÷±¸ Á¶Ç÷¼º Æ÷¸£ÇǸ° Áõ
  • H chain disease
    H-¼âº´, Á߼⺴.
  • H chain disease
    Á߼⺴
  • Hailey-Hailey disease = familial benign chronic pemphigus
    ÇìÀϸ®-ÇìÀϸ®º´
  • Hand Schueller Christian disease
    ÇÚµå-½¯·¯-Å©¸®½ºÂùº´.
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • bacterial disease
    ¼¼±ÕÁúȯ
  • bacterial disease
    ¼¼±Õ¼º Áúȯ(¡­òðü´)
  • bacterial disease
    ¼¼±Õ¼º Áúȯ(¡­òðü´).
  • bauxite fume disease
    º¸¿ÀÅ©»çÀÌÆ® Áõ±âº´.
  • bergers disease
    ¹ö°Åº´(¡­Ü»)
  • beriberi heart disease
    °¢±â½ÉÁúȯ(ÊÅѨãýòðü´)
  • beriberi heart disease
    °¢±â½ÉÁúȯ.
  • biliary tract disease
    ´ãµµÁúȯ
  • bird fanciers disease
    Á¶·ù»çÀ°ÀÚº´.
  • bird fanoiers disease
    Á¶·ù»çÀ°ÀÚº´(ðè×¾ÞøëÀí­Ü»)
  • black disease
    ±«»ç¼º °£¿°(ÎÕÞÝàõÊÜæú) ¡ì¾çÀÇ¡í.
  • black disease
    ±«»ç¼º °£¿°(ÎÕÞÝàõÊÜæú) ¡ì¾çÀÇ¡í.
  • black jaundice =Winckels disease
    ÈæÈ²´Þ(ÈæÈ²´Þ).
  • black jaundice =Winckels disease
    ÈæÈ²´Þ(ýÙüÜÓ¸).
  • bleeders disease
    Ç÷¿ìº´(úìéÒ Ü»).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
GD gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ...
ICD I-cell disease; immune complex disease; implantable cardioverter defibrillator; impulse-control diso...
ID identification; iditol dehydrogenase; immunodeficiency; immunodiffusion; immunoglobulin deficiency; ...
ILD interstitial lung disease; intraoperative localization device; ischemic leg disease; ischemic limb d...
LD labor and delivery; laboratory data; labyrinthine defect; lactate dehydrogenase; laser Doppler; lear...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
ADV Aujeszky Disease Virus
AITD Autoimmune Thyroid Disease
ATD Autoimmune thyroid disease
ADPKD Autosomal Dominant Polycystic Kidney Disease
ARPKD Autosomal recessive polycystic kidney disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • cyanotic heart disease
    û»ö¼º ½ÉÀå Áúȯ
  • cytomegalic inclusion disease
    ¼¼Æ÷ °Å´ë¼º ºÀÀÔü º´, °Å´ë ¼¼Æ÷ ºÀÀÔü Áúȯ
  • cytomegaloviral disease
    °Å´ë ¼¼Æ÷ ¹ÙÀÌ·¯½º Áúȯ
  • Darier's disease
    ´ë¸®¾î º´
    µ¿ÀǾî=
  • degenerative brain disease
    ÅðÇ༺ ³ú Áúȯ
  • degenerative disease
    ÅðÇ༺ Áúȯ
  • degenerative joint disease
    ÅðÇ༺ °üÀý Áúȯ
    °üÀý ±¸Á¶¹°¿¡ ÀûÀÀ ÇѰ踦 ³Ñ¾î¼­´Â ÈûÀÌ °è¼Ó °¡ÇØÁö¸é °üÀý¸é, Ȱ¸·, °üÀý³¶¿¡ ¿°Áõ¼º º´º¯ÀÌ »ý±â´Â °æ¿ì.
  • demyelination disease
    Å»¼öÃÊ Áúȯ
    ½Å°æ¿¡ ¼öÃʰ¡ ¾ø¾î¼­ µµ¾à Àüµµ°¡ ÀϾÁö ¾Ê¾Æ ¾ß±âµÇ´Â Áúȯµé.
  • dercums disease
    ´õÄÄ º´
  • devics disease
    µ¥ºò º´
    µ¿ÀǾî=o
  • digestive tract disease
    ¼ÒÈ­±â °èÅë Áúȯ
  • disease
    º´, Áúº´, Áúȯ
    ÀÎÁö °¡´ÉÇÑ ÀÏ·ÃÀÇ Â¡ÈÄ¿Í Áõ»ó, ½Åü ¼Ò°ßÀÌ Æ¯Â¡ÀÎ Áúº´
  • disease entity
    Áúº´ ´ÜÀ§
  • disease of the esophagus
    ½Äµµ Áúȯ
  • disease of the lymphreticular system
    ¸²ÇÁ ¼¼¸Á³»ÇǰèÀÇ Áúȯ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
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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