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"localised small bowel 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
  • neuromuscular disease
    ½Å°æ±Ù(À°)º´
  • neuropathic joint disease
    ½Å°æº´¼º°üÀýº´
  • notifiable disease
    ½Å°í´ë»óº´, ¹ß»ýº¸°íº´
  • nutritional deficiency disease
    ¿µ¾ç°áÇ̺´
  • nutritional disease
    ¿µ¾çº´, ¿µ¾ç¼ºÁúȯ
  • occlusive cerebrovascular disease
    Æó¼â³úÇ÷°üº´, Æó¼â³úÇ÷°üÁúȯ
  • occupational dental disease
    Á÷¾÷Ä¡°úº´
  • occupational disease
    Á÷¾÷º´
  • organic disease
    ±âÁúº´
  • Osgood-Schlatter disease
    ¿À½º±Â-½¶¶óÅͺ´
  • obstructive pulmonary disease
    Æó¼âÆóº´
  • Owren¡¯s disease
    ¿Àºê·»º´
  • phytanic acid storage disease
    ÇÇź»êÃàÀûº´
  • Pick disease
    ÇȺ´
  • pigeon breeder¡¯s disease
    ºñµÑ±â»çÀ°ÀÚº´
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  • ¿µ¹®
    ÇѱÛ
  • posttransplant lymphoproliferative disease
    À̽ÄÈĸ鿪Áõ½Äº´
  • prenatal disease
    Ãâ»ýÀüº´
  • primary pigmented nodular adrenocortical disease
    ÀÏÂ÷»ö¼ÒÄ§Âø°áÁ¤ºÎ½Å°ÑÁúº´
  • professional disease
    Á÷¾÷º´
  • protozoan disease
    ¿øÃ溴
  • psychosomatic disease
    Á¤½Å½Åüº´
  • pulmonary disease
    Æóº´
  • pulseless disease
    ¹«¸Æ¹Úº´, ¹«¸Æº´
  • pyramidal disease
    ÇǶó¹Ô½Å°æ·Îº´, Ãßü½Å°æ·Îº´
  • quarantinable disease
    °Ë¿ªÁúȯ
  • rat-bite disease
    Áã¹°±âº´
  • Raynaud¡¯s disease
    ·¹À̳뺴
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
  • renal disease
    ÄáÆÏº´, ½ÅÀ庴
  • reported communicable disease
    ½Å°íµÈÀü¿°º´
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • granulomatous disease
    À°¾ÆÁ¾¼º Áúȯ
  • granulomatous disease of childhood
    ¼Ò¾ÆÀ°¾ÆÁ¾¼º Áúȯ.
  • granulomatous disease of childhood
    ¼Ò¾Æ À°¾ÆÁ¾¼º Áúȯ
  • graves disease
    ±×·¹À̺꽺 º´, Grave º´
  • grinder s disease ; silicosis
    ±ÔÆóÁõ, ºÐ¼â±â°øº´.
  • grinder s disease ; silicosis
    ±ÔÆóÁõ.
  • hallervoden-spatz disease
    ÇÒ·¯º¸µç-½´ÆÄÂê º´, Hallervoden-Spatz º´
  • hand and foot disease
    ¼ö Á· Áúȯ£¨â¢ðëòðü´£©£¬¼Õ ¹ß º´, ¼ö Á· º´ (â¢ðëÜ»).
  • hand foot and mouth disease
    ¼Õ¹ßÀÔº´ (¡­Ü»), ¼öÁ·±¸º´(â¢ðëϢܻ).
  • hand foot and mouth disease
    ¼Õ¹ßÀÔº´ (¡­Ü»), ¼öÁ·±¸º´(â¢ðëϢܻ)
  • hand-foot-mouth disease
    ¼öÁ·±¸º´
  • hand-schueller-christian disease
    ÇÚµå-½¯·¯-Å©¸®½ºÂùº´
  • hanseniasis = Hansens disease
    ÇѼ¾º´
  • hansens disease
    ÇѼ¾ º´, Hansen º´
  • hard pad disease
    °æÃ´Áõ(Ìãô²ñø).
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
  • consumption disease
    ¼Ò¸ð¼º Áúȯ.
  • contagious disease
    Àü¿°º´
  • contagious disease
    (Á¢ÃË)Àü¿°º´(ïÈõºîîæøÜ»), (Á¢ÃË)°¨¿°Áõ(¡­Êïæøñø).
  • copper storage disease
    µ¿ÀúÀåÁúȯ(ÔÞîÍíúòðü´).
  • coris disease
    ÄÚ¸®º´(¡­Ü»)
  • coronary artery disease
    °ü(»ó)µ¿¸ÆÁúȯ(¡­òðü´).
  • coronary artery disease
    ½ÉÀ嵿¸ÆÁúȯ(ãýíôÔÑØæòðü´)
  • coronary disease
    °ü(»ó)Áúȯ(ήßÒòðü´).
  • coronary heart disease
    °ü(»ó)µ¿¸Æ½ÉÁúȯ(ήßÒÔÑØæãýòðü´).
  • coronary heart disease
    ½ÉÀ嵿¸Æ¼º ½ÉÁúȯ(ãýíôÔÑØæàõ ãýòðü´)
  • counterfeit disease
    ²Òº´, °¡º´.
  • creeping disease
    Æ÷ÇàÁø(ú¼òÖ) ÇÇºÎÆÄÇàÁõ(ù«Ý±÷òú¼ñø)[Á¤½Å]Æ÷ÇàÁõ
  • creeping eruption =c. disease
    Æ÷ÇàÁø( ú¼òÖ), ÇÇºÎÆÄÇàÁõ(ù« ݱ÷òú¼ñø).
  • creutzfeldt-jakob disease
    Å©·ÎÀÌÃ÷ÆçÆ®¾ßÄߺ´(¡­Ü»)
  • crohns disease
    Å©·Ð º´(¡­Ü»)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
BSAP brief short-action potential; brief, small, abundant potentials
cal small calorie
CDPS calcium-dependent protease small subunit
CSC blow on blow (administration of small amounts of drugs at short intervals) [Fr. coup sur coup]; coll...
LAST left anterior small thoracotomy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
STR small tandem repeat
SYF small yellow follicles
18S small-subunit
AIDS Acquired Immune Deficiency Disease Syndrome
AIDS Acquired Immunodeficiency Disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • restrictive pulmonary disease
    ±¸¼Ó¼º Æó Áúȯ
  • retimal degenerative disease
    ¸Á¸· ÅðÇ༺ Áúȯ
    ±¹¼Ò ¸ð¼¼ Ç÷°ü °æÈ­¿Í ±¸¸Û Çü¼º°ú ÇÔ²² ¸Á¸· ÃÊÀÚü Á¢Ã˸éÀ» ħ¹üÇϰųª ¶Ç´Â ¸Á¸· ÃÊÀÚü À¯Âø°ú ÃÊÀÚü ¾×È­°¡ ¸Á¸· °ßÀÎ, ¸Á¸·ÀÇ ¸»±Á ¸ð¾ç ÆÄ¿­, ±×¸®°í ¹Ú¸®¸¦ ÀÏÀ¸Å°´Â ºÐ¸®µÈ ºÎÀ§·Î¼­ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
  • rheumatic disease
    ·ù¸¶Æ¼¼º Áúȯ, ·ù¸¶Æ¼½º¼º Áúȯ
  • rheumatic valvular disease
    ·ù¸¶Æ¼½º¼º ÆÇ¸· Áúȯ
  • rheumatoid disease
    ·ù¸¶Æ¼½º¾ç Áúȯ
    Ư¡À¸·Î¼­ Ȱ¸·¿°. °üÀý ÆÄ±«, °üÀý º¯Çü µîÀÇ °üÀýħ½ÀÀ» ÁÖ·Î ÇÏ´Â Àü½Å¼º Áúȯ.
  • Riga-Fede disease
    ¸®°¡-Æäµ¥º´
    ¼Ò¾ÆÀÇ ¼³¼Ò´ëÀÇ À°¾ÆÁ¾À¸·Î ÇÏ¾Ç ÁßÀýÄ¡¿¡ ÀÇÇÑ ¸¶Âû ÈÄ¿¡ »ý±ä´Ù.
  • saccharine disease
    »çÄ«¸° º´
    ½ÄÀ̼º ¼¶À¯¿Í ´Ü¹éÁúÀ» Á¦°ÅÇϰí Á¤Á¦ÇÑ ÇÔ¼öź¼Ò ½Ä»ç¸¦ °úµµÇÏ°Ô ¼·ÃëÇÏ¿© »ý±â´Â Áúº´¿¡ ´ëÇÏ¿© Á¦Ã¢µÈ ¿ë¾îÀÌ´Ù. À̰Ϳ¡´Â ´ç´¢º´, ½ÉÇ÷°ü Áúȯ, º¯ºñ, ºñ¸¸Áõ ¹× ¼ÒÈ­¼º ±Ë¾ç µîÀÌ Æ÷ÇԵȴÙ.
  • salivary gland disease
    Ÿ¾×¼± Áúȯ
  • Saunders' disease
    »ç¿î´õÁî º´
    Á¥¸ÔÀÌ¿¡°Ô °ú·®ÀÇ Åº¼öÈ­¹° À½½ÄÀ» ÁÖ¾úÀ» ¶§ ÀϾ´Â ¼ÒÈ­ Àå¾Ö¿¡¼­ º¼ ¼ö ÀÖ´Â À§ÇèÇÑ Áõ»ó. ±¸Åä, ³ú Áõ»ó, ¼øÈ¯ Àå¾Ö°¡ Ư¡ÀÌ´Ù.
  • Schamberg's disease ¸¸¼º, ¹«Áõ»ó¼º ÇǺΠÁúȯÀ¸·Î »çÃá±â¿Í Àå³â±âÀÇ ³²ÀÚ¿¡°Ô ¹ß»ýÇÑ´Ù. ¾Õ Á¤°­ÀÌ, ¹ß¸ñ, ¹ß, ¹ß°¡¶ô µî¿¡ ±¹ÇÑÇÏ¿© ³ªÅ¸³ª´Â µî»ö ¶Ç´Â ´ãȲ °¥»öÀÇ °¡ÀåÀÚ¸®¿¡ Àû»öÁ¡À» °¡Áø ¹Ý»ó ¹ßÁøÀ» Ư¡À¸·Î ÇÑ´Ù.

    Schanz's syndrome

    ¼¢Áî ÁõÈıº
    ÇǷΰ¨, ôÃß µ¹±âÀÇ ¾ÐÅë, º¹¿ÍÀ§¿¡¼­ÀÇ µ¿Åë, ôÃß ¸¸°î µî, ôÃßÀÇ ¼è¾àÀ» ³ªÅ¸³»´Â ÀÏ·ÃÀÇ ÁõÈÄ.
  • Schilder's disease
    ½¯´õº´
    1. 1912³â¿¡ ±âÀçÇÑ ¼Ò¾Æ ¹× ÀþÀºÀÌ¿¡°Ô ÀϾ´Â ¿øÀÎ ºÒ¸íÀÇ µå¹® ÁúȯÀ¸·Î¼­, ÁÖ·Î ´ë³ú ¹Ý±¸¸¦ ħ¹üÇϸç, Á¶±â¿¡ Àå´Ô, ±Í¸Ó°Å¸®, °¨°¢Àå¿¡ µîÀÇ Áõ»óÀÌ ³ªÅ¸³­´Ù. 2. ¹éÁú³úÁõÀÇ ¾Æ±Þ¼º ¶Ç´Â ¸¸¼ºÇüÀ¸·Î ¼Ò¾Æ ¹× û³â¿¡°Ô¼­ º¼ ¼ö ÀÖ´Ù. ÀÓ»óÁõ»óÀ¸·Î´Â ½Ç¸í, ³­Ã», ¾çÃø¼º °æ·Ã, ÁøÇ༺ Á¤½ÅȲÆó µîÀÌ ³ªÅ¸³­´Ù. ´ë³ú ¹éÁúÀÇ ±¤¹üÇÑ ÆÄ±«°¡ ÀÖ°í, °øµ¿ÀÌ Çü¼ºµÈ´Ù. º¸Åë »ê¹ßÀûÀ¸·Î ¹ß»ýÇϳª °¡Á·¼ºÀÇ º´ÇüÀ¸·Îµµ º¸°íµÇ¾î ÀÖ´Ù.
  • Schmorl's disease
    ½¬¸ð¸¦ º´
    1. ÀÎÁ¢ÇÑ º¹Ã¼ºÎ¿¡ÀÇ ¼öÇÙ Å»Ãâ.
  • Scholz's disease
    ¼ñÃ÷ º´
    ¹éÁú ³úÁõÀÇ °¡Á· ¼ºÇüÀ¸·Î ¹Ý¼º ¿­¼º À¯Àü. 8¼¼ °æ¿¡ ½ÃÀÛÇÏ¿© ³ú¹éÁúÀÇ Å»¼öÈ­, °¨°¢¼º ½Ç¾îÁõ, ÇÇÁú¼º ½Ç¸í, ³­Ã», Çã¾à, »çÁöÀÇ °æ·Ã, ¿ÏÀü ¸¶ºñ, Ä¡¸Å°¡ Ư¡ÀÌ´Ù.
  • seasonal disease
    °èÀýº´
    °èÀý¿¡ µû¶ó ¹ß»ýÇÏ´Â º´ÀÇ ÃÑĪ. °èÀýÀÇ º¯È­°¡ º´À» ÀÏÀ¸Å²´Ù´Â °ÍÀ» óÀ½ ±â·ÏÇÑ »ç¶÷Àº È÷Æ÷Å©¶óÅ×½º¿´´Âµ¥, À̸¦ ±Ù´ë ÀÇÇÐÀûÀÎ ¹æ¹ýÀ¸·Î ¿¬±¸ÇÑ »ç¶÷Àº µ¶ÀÏÀÇ µ¥ ·ç´õ¿´´Ù. ±×´Â ±â´Ü ±³Ã¼ ¶§ÀÇ Àü¼± Åë°ú¿Í °¢Á¾ Áúº´°úÀÇ °ü·ÃÀ» Åë°èÇÐÀûÀ¸·Î Á¶»çÇÏ¿´À¸¸ç, ƯÈ÷ ºÏ¹Ý±¸ÀÇ °èÀý°ú °ü°è°¡ ±íÀº Áúº´ÀÇ ¿¬°£ºÐÆ÷Ç¥´Â °èÀýº´ ͏°´õÀÇ ½ÃÃʷμ­ À¯¸íÇÏ´Ù. ¾î¶² º´À» °èÀýº´À¸·Î Ãë±ÞÇϱâ À§Çؼ­´Â, ±× º´ÀÇ À¯¹ßÀÎÀÚ ¶Ç´Â ±× º´À» Àü¿°½ÃŰ´Â À§»ý °ïÃæ µîÀÌ °èÀýÀûÀ¸·Î º¯µ¿Çϰí ÀÖ´Ù´Â Á¡, ¶Ç´Â Àΰ£ ÀÚü°¡ ±× º´¿¡ °É¸®±â ½¬¿î »óŰ¡ °èÀý¿¡ ÀÇÇØ¼­ Á¿ìµÈ´Ù´Â Á¡ µîÀÌ ¾î¶»°Ô ¼­·Î ¾ôÇô ÀÖ´ÂÁö Á¶»çÇÒ Çʿ䰡 ÀÖ´Ù. Çѱ¹ÀÇ °æ¿ì, ¾î¸°ÀÌÀÇ ¼ÒÈ­±â º´À̳ª ´Üµ¶ µîÀÇ ÇǺΠÁúȯÀº ¿©¸§¿¡ ¸¹°í, °Ü¿ï¿¡¼­ º½¿¡ À̸£·¯ Â÷°í ¸Þ¸¶¸¥ ±âÈÄÀÏ ¶§¿¡´Â °¨±â, Æó·Å, ±Þ¼º ±â°üÁö¿° µîÀÌ ¸¹´Ù.
  • self limited disease
    ÀÚ±â ÇÑÁ¤¼º Áúȯ
    Áúȯ ÀÚüÀÇ ¼ºÁú ¶§¹®¿¡ ÀÏÁ¤Çϰí ÇÑÁ¤µÈ °æ°í¸¦ ÃëÇÏ´Â Áúȯ.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
camurati-engelmann disease <radiology> Sclerosing diaphyseal dysplasia, does not involve metaphysis, epiphysis, or bone marrow cavity Cf: Albers-Schoenberg disease
(12 Dec 1998)
canavan disease Spongy degeneration of cerebral white matter, a rare autosomal recessive form of leukodystrophy. It is characterised by early onset, widespread demyelination and vacuolation of the white matter that gives rise to a spongy appearance, severe mental retardation, megalocephaly, atony of the neck muscles, spasticity of the extremities, and blindness. Death occurs at about 18 months of age.
(12 Dec 1998)
Canavan's disease Autosomal recessive degenerative disease of infancy; mostly in Jewish infants; onset typically within first 3-4 months of birth, consisting of blindness, psychomotor regression, enlarged head, optic atrophy, hypotonia, spasticity, increased N-acetylaspartic acid urinary excretion. MRI shows enlarged brain, decreased attenuation of cerebral and cerebellar white matter, and normal ventricles. Pathologically, there is increased brain volume and weight, and spongy degeneration in the subcortical white matter.
See: leukodystrophy.
Synonym: Canavan's sclerosis, Canavan-van Bogaert-Bertrand disease, spongy degeneration of infancy.
(05 Mar 2000)
Canavan-van Bogaert-Bertrand disease Autosomal recessive degenerative disease of infancy; mostly in Jewish infants; onset typically within first 3-4 months of birth, consisting of blindness, psychomotor regression, enlarged head, optic atrophy, hypotonia, spasticity, increased N-acetylaspartic acid urinary excretion. MRI shows enlarged brain, decreased attenuation of cerebral and cerebellar white matter, and normal ventricles. Pathologically, there is increased brain volume and weight, and spongy degeneration in the subcortical white matter.
See: leukodystrophy.
Synonym: Canavan's sclerosis, Canavan-van Bogaert-Bertrand disease, spongy degeneration of infancy.
(05 Mar 2000)
cancer, hodgkin's disease A type of lymphoma (cancer of the lymphatic system). The most common symptom of Hodgkin's disease is a painless swelling in the lymph nodes in the neck, underarm, or groin. Hodgkin's disease is diagnosed when abnormal tissue is detected by a pathologist after a biopsy of an enlarged lymph node. Treatment usually includes radiation therapy or chemotherapy. Regular follow-up examinations are important after treatment for Hodgkin's disease. Patients treated for Hodgkin's disease have an increased risk of developing other types of cancer later in life, especially leukaemia.
(12 Dec 1998)
canine parvovirus disease An acute disease of dogs with a variable mortality rate caused by the canine parvovirus; seen in three distinct clinical forms; a generalised neonatal disease, a severe nonsuppurative myocarditis, and a frequently fatal enteritis.
(05 Mar 2000)
carcinoid heart disease Cardiac manifestation of malignant carcinoid syndrome. It is a unique form of fibrosis involving the endocardium, primarily of the right heart. The fibrous deposits tend to cause constriction of the tricuspid and pulmonary valves.
(12 Dec 1998)
caroli disease <radiology> Communicating, cavernous ectasia of the intrahepatic bile ducts, rare, autosomal recessive, usually detected in young adults, no cirrhosis or portal hypertension, predisposed to calculus formation, benign course, but.. Recurrent cholangitis most likely to be liver abscesses most likely to be death, associated with medullary sponge kidney (renal tubular ectasia) in 80%
(12 Dec 1998)
caroli's disease Congenital cystic dilatation of the intrahepatic bile ducts. It consists of 2 types: simple, with bile duct dilatation or ectasia alone, and complex, with associated extensive hepatic fibrosis and portal hypertension. Benign renal tubular ectasia is associated with both types.
(12 Dec 1998)
rabbit haemorrhagic disease A highly infectious disease of rabbits, caused by a calicivirus and characterised by haemorrhagic lesions, particularly affecting the lungs and liver; since it was first identified in China in 1984, it has been reported from Korea, it has spread through Europe, and it has reached North Africa and Mexico.
(05 Mar 2000)
machado-joseph disease A progressive degenerative disease of the central nervous system occurring in portuguese-azorean families, having a variety of forms and inherited as an autosomal dominant trait. There are four major types: type I: with pyramidal and extrapyramidal deficits; type II: with cerebellar, pyramidal and extrapyramidal deficits; type III: with cerebellar deficits and distal sensorimotor neuropathy; type IV: with parkinsonism and distal sensory neuropathy. It was originally reported in two portuguese-azorean families in massachusettes (machado), then in another portuguese family (thomas), and later in a third family in california (joseph, who settled there in 1845). It has been reported also in japanese families.
(12 Dec 1998)
Paas' disease A familial skeletal deformation marked by coxa valga, double patella, shortening of the middle and terminal phalanges of fingers and toes, deformities of the elbows, scoliosis, and spondylitis deformans of the lumbar vertebrae; all of these manifestations may be unilateral or bilateral.
(05 Mar 2000)
Gairdner's disease <disease> Attacks of cardiac distress accompanied by apprehension.
Synonym: angina pectoris sine dolore, angor pectoris.
(05 Mar 2000)
Pacheco's disease A highly contagious, acute disease of psittacine birds caused by a herpesvirus and characterised by bright yellow urates with scant faeces, icterus, and terminal anorexia.
(05 Mar 2000)
Pacheco's parrot disease virus Probably a virus of the family Herpesviridae, possibly related to the virus of infectious laryngotracheitis.
Synonym: parrot virus.
(05 Mar 2000)
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