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"Genetic Predisposition to 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
  • lower motor neuron disease
    ¾Æ·¡¿îµ¿½Å°æ¼¼Æ÷º´, ÇÏÀ§¿îµ¿½Å°æ¿øº´
  • lysosomal storage disease
    ¿ëÇØ¼ÒüÃàÀûº´, ¸®¼ÒÁ»ÃàÀûº´
  • Mikulicz¡¯s disease
    ¹ÌÄð¸®Ä¡º´
  • Minamata disease
    ¹Ì³ª¸¶Å¸º´
  • miner¡¯s disease
    ±¤ºÎº´
  • minimal change disease
    ¹Ì¼¼º¯È­º´
  • malabsorption disease
    Èí¼öÀå¾Öº´
  • mixed connective tissue disease
    È¥ÇÕ°áÇÕÁ¶Á÷º´
  • molecular disease
    ºÐÀÚº´
  • Monge disease
    ¸ùÇ캴
  • motor neuron disease
    ¿îµ¿½Å°æ¼¼Æ÷º´, ¿îµ¿½Å°æ¿øº´
  • mountain disease
    °í»êº´
  • moyamoya disease
    ¸ð¾ß¸ð¾ßº´
  • muscle disease
    ±ÙÀ°º´
  • mycobacterial disease
    Ç×»ê±Õº´, ¹ÌÄÚ¹ÚÅ׸®¾Æº´
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  • ¿µ¹®
    ÇѱÛ
  • neuromuscular disease
    ½Å°æ±ÙÀ°º´
  • neuronal storage disease
    ½Å°æ¼¼Æ÷ÀúÀ庴
  • neuropathic joint disease
    ½Å°æº´Áõ°üÀýº´
  • notifiable disease
    ½Å°í´ë»óÁúº´
  • nutritional disease
    ¿µ¾çº´
  • nutritional deficiency disease
    ¿µ¾ç°áÇ̺´
  • obliterative arterial disease
    Æó»öµ¿¸Æº´
  • obstructive pulmonary disease
    Æó¼âÆóº´
  • occlusive cerebrovascular disease
    Æó¼â³úÇ÷°üÁúȯ
  • occupational disease
    Á÷¾÷º´
  • occupational dental disease
    Á÷¾÷Ä¡°úº´
  • oculoglandular disease
    ´«»ùº´
  • oral disease
    ÀÔº´, ±¸°­Áúȯ
  • organic disease
    ±âÁúº´
  • pandemic disease
    ¹üÀ¯Çິ
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  • ¿µ¹®
    ÇѱÛ
  • 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´
  • Takahara disease
    ´ÙÄ«Ç϶óº´
  • Takayasu disease
    Ÿī¾ß¼öº´
  • Theilers disease
    ŸÀÏ·¯¸¶¿ì½º Ư¹ß¼º ³úô¼ö¿°
  • Thornwaldts disease
    Àεγ¶¿°
  • Tietzes disease
    ƼÂź´.
  • VDRL test= venereal disease research laboratory test
    ¼ºº´¿¬±¸¼Ò½ÄÅ×½ºÆ®.
  • VDRL test= venereal disease research laboratory test
    ¼ºº´¿¬±¸¼Ò½ÄÅ×½ºÆ®.
  • Von Recklinghausens disease(neurofibromatosis)
    Æù·¹Å¬¸µÇÏ¿ìÁ¨º´<½Å°æ¼¶À¯Á¾Áõ>.
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  • ¿µ¹®
    ÇѱÛ
  • cine magulomatous disease
  • climatic disease
    ±âÈĺ´(˻̷ËÓ).
  • cold agglutinin disease
    ÇÑ·©ÀÀÁýÁúȯ(¡­ëêó¢òðü´).
  • cold hemagglutinin disease
    ÇÑ·©(Àû)Ç÷±¸ÀÀÁý¼Ò Áúȯ
  • cold hemagglutinin disease=CHD
    ÇÑ·©Ç÷±¸ÀÀÁý¼Òº´
  • collagen disease
    ±³¿ø(Áú)º´(Îïê«òõÜ»).
  • collagen disease
    ±³¿ø(Áú)º´(Îïê«òõÜ»). ÄݶóÁ¨º´(¡­Ü»)
  • collagen-vascular disease
    ±³¿ø-Ç÷°ü Áúȯ
  • comb disease
    °è°üº´.
  • combined immunodeficiency disease
    º¹ÇÕÇü¸é¿ª°áÇÌÁúȯ
  • combined immunodeficiency disease
    º¹ÇÕÇü ¸é¿ª°áÇÌÁúȯ
  • combined system disease
    º¹ÇÕ°èÅëÁúȯ.
  • combined valvular disease
    º¹ÇÕÆÇ¸·Áúȯ.
  • communicable disease
    Àü¿°º´
  • communicable disease control
    Àü¿°º´°ü¸®(ÊÙË´Ëö), Àü¿°º´¿¹¹æ.
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
OHD hydroxyvitamin D; Office of Human Development; Ondine-Hirschsprung disease; organic heart disease
PAIN pyoderma gangrenosum, aphthous stomatitis, inflammatory eye disease, erythema nodosum [disorders ass...
PAOD peripheral arterial occlusive disease; peripheral arteriosclerotic occlusive disease
PKD polycystic kidney disease; proliferative kidney disease
PMD Pelizaeus-Merzbacher disease; posterior mandibular depth; primary myocardial disease; private medici...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
CBD Chronic beryllium disease
CBDC Chronic bullous disease of childhood
cGVHD Chronic graft versus host disease
cGVHD Chronic graft-vs.-host disease
CIBD Chronic inflammatory bowel disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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.
  • sexually transmitted disease
    ¼º Àü¿°¼º Áúȯ
    Åë»óÀûÀÎ ¼º±³¿¡ ÀÇÇÑ ¼ºº´À» Æ÷ÇÔÇÏ¿©, ¼º±³´Â ¾Æ´ÏÁö¸¸ À¯»çÇÑ ¼º ÇàÀ§·Î °¨¿°µÇ´Â ¸ðµç Áúȯ. ¼º¿¡ ´ëÇÑ »çȸ °ü½ÀÀº Áö³­ ¼ö ½Ê ³â¿¡ °ÉÃÄ ¸¹ÀÌ º¯È­ÇÏ¿´À¸¸ç, 1970³â´ë¿¡ À̸£·¯ ¼º ÇàÀ§ÀÇ ´Ù¾ç¼ºÀÌ µÎµå·¯Áö°Ô ³ªÅ¸³µ´Ù. Áï, À̼º°£ÀÇ ¼º±³»Ó¸¸ ¾Æ´Ï¶ó µ¿¼º°£¿¡ ÇàÇÏ¿©Áö´Â ¿©·¯ ÇüÅÂÀÇ ¼º ÇàÀ§, ¿©·¯ »ó´ëÀÚ¿ÍÀÇ ¼º °ü°è, ´Ù¾çÇÑ ¼º ±â±³ ¹× ±¸°­ ¼º±â ¼º ÇàÀ§ µî ´Ù¾çÇØÁ³À¸¸ç, ÀÌ¿¡ µû¶ó °¨¿°ÀÇ Á¾·ùµµ Áõ°¡ÇÏ¿´´Ù. ¶ÇÇÑ °¨¿° °æ·Îµµ Åë»óÀû ¼º±³ ¿Ü¿¡ ±¸°­ ¹× ¼º±â¿¡ÀÇ ÀÔ¸ÂÃã¿¡ ÀÇÇÑ °æ±¸ °¨¿°, µ¿¼º¾Ö ³²¼º°£¿¡ ÇàÇÏ¿©Áö´Â Ç×¹® ¼º±³ ¹× ¿©·¯ »ç¶÷ÀÌ ¾î¿ï·Á ºÒ°áÇÏ°Ô À̺ÎÀÚ¸®¸¦ °°ÀÌ »ç¿ëÇÏ´Â µ¥¼­ ¿À´Â ±â»ýÃæ °¨¿° µî ¿©·¯ °¡Áö°¡ ÀÖ´Ù. ¼º Àü¿°¼º ÁúȯÀ» ÀÏÀ¸Å°´Â º´¿øÃ¼µµ ´Ù¾çÇÏ¿©, ´ëº°ÇØ º¸¸é, ¼¼±Õ, ¹ÙÀÌ·¯½º, Ŭ¶ó¹Ìµð¾Æ Æ®¶óÄÚ¸¶Æ¼½º
  • silo-filler's disease
    »çÀÏ·Î Ãæ¸¸ °¡½ºº´
    ¶§¶§·Î ±Þ¼º Æó ºÎÁ¾À» ¼ö¹ÝÇÏ´Â ÆóÀÇ ¿°ÁõÀ¸·Î, »çÀϷο¡ ¸ðÀÎ Àڱؼº °¡½ºÀÇ ÈíÀÔÀÌ ¿øÀÎÀÌ´Ù.
  • Simmonds' disease
    ½Ã¸óµå º´, ½Ã¸óÁ
    1. ÇϼöüÀÇ À§ÃàÀ¸·Î ÀÎÇØ ±ØµµÀÇ ¼è¾à, ¼Ò¸ð, ¹× Á¤½Å Àå¾Ö¸¦ À¯¹ßÇϰí, Á¶·Î, Å»¸ð, ¼º¿å °¨Åð, ±âÃÊ ´ë»ç ÀúÇÏ µîÀ» Ư¡À¸·Î Çϴµ¥ ÁÖ·Î ¿©ÀÚ¿¡¼­ º¼ ¼ö ÀÖ´Ù. 2. somatotro
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
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)
vagabond's disease Excoriations and melanoderma caused by scratching the bites of the body louse, Pediculus corporis.
Synonym: Greenhow's disease, vagabond's disease, vagrant's disease.
Racial melanoderma, the normally dark skin of blacks and certain other races.
Senile melanoderma, cutaneous pigmentation occurring in the aged.
Synonym: melasma universale.
(05 Mar 2000)
gallbladder disease <gastroenterology, surgery> An inflammatory condition of the gallbladder that usually results from the presence of gallstones and repeated bouts of cholecystitis.
(27 Sep 1997)
paget disease <radiology> Disease of unknown aetiology involving destruction and reparation, age greater than 40y; M:F 2:1, skull, osteoporosis circumscripta (outer table destroyed only), cotton wool appearance, increased hat size!, spine, monostotic vertebral involvment usually, pelvis, affected in 2/3 cases, consists of cortical thickening, enlargement of pubis/ischium, coarse trabecular pattern, extremities, blade of grass appearance, elevation of alk phos (up to 20X), normal calcium, normal phosphorus, complications: path fractures in 8% cases (usually femur = shepard's crook), malignant degeneration (usually osteosarcoma-50%, fibrosarcoma-25%)
(12 Dec 1998)
paget disease of breast <radiology> Form of ductal carcinoma, associated with eczematous changes of the nipple
(12 Dec 1998)
Paget's disease <disease, rheumatology> This is a disease of bone that initially results in the excessive resorption of bone (by osteoclasts) followed by the replacement of normal bone marrow with vascular and fibrous tissue.
Many patients are asymptomatic and diagnosed by routine X-rays.
(13 Nov 1997)
paget's disease, extramammary A rare cutaneous neoplasm that occurs in the elderly. It develops more frequently in women and predominantly involves apocrine gland-bearing areas, especially the vulva, scrotum, and perianal areas. The lesions develop as erythematous scaly patches that progress to crusted, pruritic, erythematous plaques. The clinical differential diagnosis includes squamous cell carcinoma in situ and superficial fungal infection. It is generally thought to be an adenocarcinoma of the epidermis, from which it extends into the contiguous epithelium of hair follicles and eccrine sweat ducts. (devita jr et al., cancer: principles & practice of oncology, 3d ed, p1478)
(12 Dec 1998)
paget's disease, mammary An intraductal carcinoma of the breast extending to involve the nipple and areola, characterised clinically by eczema-like inflammatory skin changes and histologically by infiltration of the dermis by malignant cells (paget's cells).
(12 Dec 1998)
Paget's disease of the nipple <oncology, tumour> A cancer of the nipple.
(16 Dec 1997)
vagrant's disease Excoriations and melanoderma caused by scratching the bites of the body louse, Pediculus corporis.
Synonym: Greenhow's disease, vagabond's disease, vagrant's disease.
Racial melanoderma, the normally dark skin of blacks and certain other races.
Senile melanoderma, cutaneous pigmentation occurring in the aged.
Synonym: melasma universale.
(05 Mar 2000)
mad cow disease A new disease of cattle, first reported in 1986 in Great Britain, characterised clinically by apprehensive behaviour, hyperesthesia, and ataxia and histopathologically by spongiform changes in the gray-matter neuropil of the brain stem; it is thought to be caused by an agent, possibly a prion, similar to that observed as the cause of scrapie.
Synonym: mad cow disease.
(05 Mar 2000)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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