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  • ¿µ¹®
    ÇѱÛ
  • lipid storage disease
    ÁöÁúÃàÀûº´
  • liver disease
    °£Áúȯ, °£º´
  • 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´
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  • ¿µ¹®
    ÇѱÛ
  • microdrepanocytic disease
    ÀÛÀº³´ÀûÇ÷±¸º´
  • miner¡¯s disease
    ±¤ºÎº´
  • minimal change disease
    ÃÖ¼Òº¯È­ÄáÆÏº´Áõ
  • mixed connective tissue disease
    È¥ÇÕ°áÇÕÁ¶Á÷º´, ½Â¸ðÆÇ¸·º´
  • molecular disease
    ºÐÀÚº´
  • motor neuron disease
    ¿îµ¿½Å°æ¼¼Æ÷º´
  • mountain disease
    °í»êº´
  • moyamoya disease
    ¸ð¾ß¸ð¾ßº´
  • muscle disease
    ±ÙÀ°º´
  • mycobacterial disease
    Ç×»ê±Õº´
  • mycoplasma disease
    ¹ÌÄÚÇö󽺸¶º´
  • neoplastic disease
    Á¾¾çº´, ½Å»ý¹°º´
  • nervous disease
    ½Å°æº´
  • neurohypophysial disease
    ½Å°æ³úÇϼöüº´
  • neuromuscular disease
    ½Å°æ±ÙÀ°º´
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  • ¿µ¹®
    ÇѱÛ
  • gestational trophoblastic disease
    Àӽżº¿µ¾ç¸ð¼¼Æ÷Áúȯ(¡­ç½å×Ù½á¬øàòðü´)
  • glomerular disease
    »ç±¸Ã¼Áúº´
  • glomerular disease
    »ç±¸Ã¼Áúȯ(ÞêϹô÷òðü´)
  • glucose storage disease
    ´çÃàÀûÁúȯ.
  • glucuronidase deficiency disease
    ±Û·çÅ¥·Î´Ïµ¥À̽º °áÇÌÁõ
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀû Áúȯ.
  • glycogen storage disease
    ´ç¿ø ÃàÀûÁúȯ(ÓØê«õëîÝòðü´)
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀûÁúȯ
  • graft versus host disease
    ´ë¼÷ÁÖÀÌ½ÄÆíÁúȯ
  • graft versus host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´.
  • graft versus host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë ¼÷ÁÖº´
  • granulomatous disease
    À°¾ÆÁ¾¼º Áúȯ.
  • granulomatous disease
    À°¾ÆÁ¾¼º Áúȯ
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  • ¿µ¹®
    ÇѱÛ
  • bone disease
    °ñÁúȯ
  • bone disease =osteopathy
    °ñ Áúȯ(Íéòðü´).
  • bone disease, marble
    ´ë¸®¼® °ñÁúȯ
  • bournevilles disease
    ºÎ¸£´Àºä º´(¡­Ü»)
  • bowens disease
    º¸À¢ º´(¡­Ü»)
  • breast,cystic disease
    ³¶(Á¾)¼º Áúȯ (Ò¥ðþàõòðü´)
  • breast,fibrocystic disease
    ¼¶À¯ ³¶¼º Áúȯ(àéë«Ò¥àõòðü´)
  • bridegrooms disease
    ½Å¶ûº´(ãæÕÍÜ»)
  • brill-zinsser disease
    ºê¸±ÂðÀúº´ (¡­Ü»)
  • brittle bone disease
    ÆÄ¼â°ñ (÷òáïÍé)
  • broad beta disease
    ±¤º£Å¸º´
  • buergers disease
    ¹ö°Å º´ (¡­Ü»)
  • buffalo disease
    ¹°¼Ò³ú¿°(¡­Òàæú).
  • bullous disease
    ¼öÆ÷¼º Áúȯ(â©øÞàõ òðü´)
  • bullous disease
    ¼öÆ÷¼º Áúȯ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
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...
PRAGMATIC pregnancy, rheumatoid arthritis, acromegaly, glucose metabolism disorders, mechanical injury, amyloi...
PVD patient very disturbed; peripheral vascular disease; portal vein dilation; posterior vitreous detach...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
ACKD Acquired cystic kidney disease
ARCD Acquired renal cystic disease
AGVHD Acute graft-versus-host disease
aGVHD Acute graft-vs.-host disease
AOSD Adult Onset Still's Disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • previous dental disease
    ÀÌÀüÀÇ Ä¡°ú Áúȯ
  • professional disease
    Àü¹®Á÷º´, Á÷¾÷º´
  • progress of disease
    º´ÀÇ °æ°ú, º´ÀÇ ÁøÇà
    Áúº´ÀÌ ¾ÕÀ¸·Î ÁøÇàÇÏ¿© ¿øÇÏÁö ¾Ê´Â °á°ú¸¦ ÃëÇÏ´Â °Í
  • psychological disease
    ½É¸® Áúȯ
  • quarantinable disease
    °Ë¿ª Áúȯ
  • Raynaud's disease
    ·¹ÀÌ³ë º´
    ¿ø¹ß¼º ¶Ç´Â Ư¹ß¼º Ç÷°ü Àå¾Ö·Î ¾çÃøÀÇ ·¹À̳ë Çö»óÀÇ ¹ßÀÛÀÌ Æ¯Â¡. ³²¼ºº¸´Ù´Â ¿©¼ºÀÌ ¹ßº´Çϱ⠽±´Ù.
  • reactive disease
    ¹ÝÀÀ¼º Áúȯ
  • Recklinghausen's disease
    Recklinghausen º´
    ´Ù¹ß, ´ÙÇü¼º ½Å°æ ¼¶À¯Á¾À̸ç, ±× ¹Û¿¡µµ »À, ÁßÃß ½Å°æ, ÀÚÀ² ½Å°æ µî¿¡µµ Á¾·ù¸¦ Çü¼ºÇÏ´Â ÇϳªÀÇ µ¶¸³ ÁúȯÀÌ´Ù. º´¸íÀº µ¶ÀÏÀÇ º´¸®ÇÐÀÚ F.D.von ·¹Å¬¸µÇÏ¿ìÁ¨
  • Refsum's disease
    ·¹ÇÁ¼¶ º´
    ÆÄÀÌź»ê
  • renal atheroembolic disease
    ½ÅÁ×»ó Àü»öº´, ½ÅÁ×Á¾ »öÀüº´
  • renal disease
    ½Å Áúȯ
  • Rendu Osler Weber disease
    ·»µÎ ¿À½½·¯ ¿þ¹ö º´
  • restrictive heart disease
    ±¸¼Ó¼º ½É Áúȯ
  • 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.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
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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