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"generalized obstructive lung 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
  • Menetrier disease
    ¸Þ³×Æ®¸®¿¡º´
  • metabolic disease
    ´ë»çº´, ´ë»çÁúȯ
  • metazoan disease
    ÈÄ»ýµ¿¹°º´
  • microdrepanocytic disease
    ÀÛÀº³´ÀûÇ÷±¸º´
  • neoplastic disease
    ½Å»ý¹°º´, Á¾¾çº´
  • nervous disease
    ½Å°æ°èÁúȯ, ½Å°æº´
  • neurohypophysial disease
    ½Å°æ³úÇϼöüº´
  • 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´
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  • ¿µ¹®
    ÇѱÛ
  • periapical disease
    Ä¡±Ù´ÜÁÖÀ§º´, Ä¡¾Æ³¡ÁÖÀ§º´
  • pericardial disease
    ½ÉÀ帷º´
  • periodontal disease
    Ä¡ÁÖº´, Ä¡±Ù¸·º´
  • peripheral vascular disease
    ¸»ÃÊÇ÷°üº´
  • pigeon breeder¡¯s disease
    ºñµÑ±â»çÀ°»çº´
  • pneumatic hammer disease
    ¾ÐÂø°ø±âÇØ¸ÓÁõ
  • polycystic kidney disease
    ¹µÁÖ¸Ó´ÏÄáÆÏº´, ´Ù³¶ÄáÆÏº´
  • 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´
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  • ¿µ¹®
    ÇѱÛ
  • 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·¼ºÈæ¾Ï½Ã¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼º Èæ³»Àå ¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amyloid disease
    ¾Æ¹Ð·ÎÀ̵庴(¡­Ü»).
  • andersen disease
    ¾Ø´õ½¼º´<--Áúȯ>
  • angiospasmodic disease
    Ç÷°ü¿¬Ã༺ Áúȯ.
  • aortic valvular disease
    ´ëµ¿¸ÆÆÇÁúȯ(¡­òðü´).
  • aphthous fever =foot and mouth disease
    ¾ÆÇÁŸ¼º¿­(¡­æð).
  • apocrine miliaria => Fox Fordyce disease
    ¾ÆÆ÷Å©¸° ÇÑÁø
  • arbovirus disease
    ¾Æ¸£º¸¹ÙÀÌ·¯½ºº´(¡­Ü»)
  • arthropod-borne viral disease
    ÀýÁöµ¿¹° ¸Å°³ ¹ÙÀÌ·¯½ºº´
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  • ¿µ¹®
    ÇѱÛ
  • 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>
  • angiospasmodic disease
    Ç÷°ü¿¬Ã༺ Áúȯ.
  • aortic valvular disease
    ´ëµ¿¸ÆÆÇÁúȯ(¡­òðü´).
  • aphthous fever =foot and mouth disease
    ¾ÆÇÁŸ¼º¿­(¡­æð).
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LL large lymphocyte; lateral leminiscus; left lateral; left leg; left lower; left lung; lepromatous [in...
OILD occupational immunologic lung disease
SCLD sickle-cell chronic lung disease
AFP Alpha(¥á) Feto-Protein [HP 1826, 1858, 1859, 2265]
  ; Oncofetal Antigens
 &nbs...
BZ Disease Brill Zinsser Disease
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LLL lower lung lobe
LALN lung associated lymph node
LT lung transplant
L-Tx lung transplantation
NSCCL non-small cell carcinoma of the lung
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • sporadic disease
    »ê¹ß Áúȯ, »ê¹ß¼º Áúȯ
  • sterility disease
    ºÒÀÓ¼º Áúȯ
  • Still's disease
    ½ºÆ¿ Áúȯ, ½ºÆ¿ º´
    µ¿ÀǾî=juvenile rheumatoid arthritis. 1. Ç÷û¿¡ ÀÌ»óÀÌ ³ªÅ¸³ªÁö ¾Ê´Â °üÀý¿°À¸·Î¼­ Á¾Á¾ ¹ß¿­°ú ¸²ÇÁÀýº´ÁõÀÌ µ¿¹ÝµÇ¸ç 16¼¼ ÀÌÀü¿¡ ½ÃÀÛÇÏ´Â °üÀý¿°ÀÇ 70%¸¦ Â÷ÁöÇÑ´Ù. 2. ¼Ò¾Æ¼º ¸²ÇÁÁ¾ ºñÁ¾¼º À§Ãà ´Ù¹ß¼º °üÀý¿°. ¼Ò¾Æ¿¡ »ý±â´Â ¸¸¼º ´Ù¹ß¼º °üÀý¿°ÀÇ ÀÏÁ¾. ¸²ÇÁÀý Á¾Ã¢, ºñÁ¾, ºÒ±ÔÄ¢¼º ¹ß¿­ÀÌ Æ¯Â¡ÀÌ´Ù.
  • storage pool disease
    ÀúÀåÁ¶º´
    ÀÀÁýÁ¦, ¿¡Çdz×ÇÁ¸°, ¿ÜÀμº ADP, Æ®·Òºó µî¿¡ ¹ÝÀÀÇÏ¿© ADP¸¦ ¹æÃâÇÏ´Â Ç÷¼ÒÆÇ ±â´É ºÎÀü¿¡ ÀÇÇÑ Ç÷¾× ÀÀ°í Àå¾Ö, °¡º­¿î ÃâÇ÷ Áõ»ó, ÃâÇ÷ ½Ã°£ Áö¿¬, ±³¿øÁúÀ̳ª Æ®·Òºó¿¡ ´ëÇÑ ÀÀÁý ¹ÝÀÀÀÇ °¨Å𸦠Ư¡À¸·Î ÇÑ´Ù.
  • stripe disease
    ¼±Á¶º´
  • strumpell's disease Ãø»è °æÈ­ÁõÀÇ À¯ÀüÇüÀ¸·Î ÀÌ Áúº´¿¡¼­ÀÇ °æ·ÃÀº ÁÖ·Î ¹ß¿¡ ÇÑÁ¤µÇ¾î ÀϾ´Ù.

    strychnine

    ½ºÆ®¸®Å©´Ñ
    ±Øµµ·Î µ¶¼ºÀÌ °­ÇÑ ¾ËÄ®·ÎÀ̵å. ÁÖ·Î Strychnos nuxvomica ¹× StrychnosÀÇ ´Ù¸¥ Á¾¿¡¼­ ¾ò¾îÁö¸ç, ½Å°æ Ãæµ¿ÀÇ Á¢ÇպΠÈĺÎÀÇ ¾ïÁ¦¸¦ Â÷´ÜÇÔÀ¸·Î½á ÁßÃß ½Å°æ°èÀÇ ¸ðµç ºÎºÐÀ» ÈïºÐ½ÃŲ´Ù. ÁßÃß ½Å°æ°èÀÇ ÈïºÐÁ¦·Î »ç¿ëµÇ°í ÀÖÀ¸¸ç, ÀÌÀü¿¡´Â °í¹Ì °­ÀåÁ¦, ¼øÈ¯ ÀÚ±ØÁ¦·Î ¶Ç´Â ¼³»çÁ¦¿Í ¾Æ¿ï·¯ »ç¿ëµÇ¾ú´Ù.
  • subacute disease
    ¾Æ±Þ¼º Áúȯ
  • systemic degenerative joint disease
    Àü½Å¼º ÅðÇ༺ °üÀý Áúȯ
  • tay-sachs disease Èæ³»À强 °¡Á·¼º ¹éÄ¡ÀÇ ¿µ¾ÆÇü.

    tazettine

    ŸÁ¦Æ¾
  • temporomandibular joint disease
    ÃøµÎÇϾǰüÀý Áúȯ
  • Thomsen's disease : ¼±Ãµ¼º ±Ù±äÀåÁõ.

    thoracalgia

    È亮Åë
  • thromboembolic disease
    Ç÷Àü »öÀü¼º Áúȯ
  • thyrotoxic heart disease
    °©»ó¼± Áßµ¶¼º ½ÉÀ庴
    °©»ó¼± ±â´É Ç×Áø°ú °ü·ÃÇÑ ½ÉÀå ÁúȯÀ¸·Î ½É¹æ ¼¼µ¿. ½ÉÀå È®´ë, ¿ïÇ÷¼º ½ÉºÎÀü µîÀÌ ³ªÅ¸³­´Ù.
  • tropical disease
    ¿­´ëº´
    °í¿Â ´Ù½ÀÇÏ°í ¹Ì°³¹ß Áö¿ªÀÌ ¸¹Àº ¿­´ë Áö¹æ¿¡¼­ ¸¹ÀÌ ¹ß»ýÇÏ´Â º´. ´ëÇ¥ÀûÀÎ °ÍÀ¸·Î´Â ¾Æ¸Þ¹Ù Àû¸®, Ä®¶ó¾ÆÀÚ¸£
  • tubulo-interstitial disease
    ¼¼´¢°ü-°£Áú¼º Áúȯ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 20
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)
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