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  • ¿µ¹®
    ÇѱÛ
  • nutritional deficiency syndrome
    ¿µ¾ç°áÇÌÁõÈıº
  • Ogilvie syndrome
    ¿À±æºñÁõÈıº
  • oral-facial-digital syndrome
    ÀÔ¾ó±¼¼Õ°¡¶ôÁõÈıº, ±¸°­¾È¸é¼öÁ·ÁöÁõÈıº
  • orbital apex syndrome
    ´«È®²ÀÁöÁõÈıº, ¾È¿Í÷´ÜÁõÈıº
  • organic mental syndrome
    ±âÁú¼ºÁ¤½ÅÁõÈıº
  • Osler-Weber-Rendu syndrome
    ¿À½½·¯-¿þ¹ö-¶ûµÚÁõÈıº
  • obstructive sleep apnea syndrome
    Æó¼â¼ö¸é¹«È£ÈíÁõÈıº
  • overlap syndrome
    °ãħÁõÈıº, Áߺ¹ÁõÈıº
  • overuse syndrome
    °ú»ç¿ëÁõÈıº, °ú¿ëÁõÈıº
  • overwear syndrome
    °úµµÂø¿ëÁõÈıº
  • Pancoast syndrome
    ÆÒÄÚ½ºÆ®ÁõÈıº
  • Pickwickian syndrome
    ÇÈÀ¨ÁõÈıº
  • Pierre Robin syndrome
    ÇÇ¿¡¸£·Î¹ðÁõÈıº
  • placental transfusion syndrome
    ŹݼöÇ÷ÁõÈıº
  • polycystic ovarian syndrome
    ´Ù³¶³­¼ÒÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
  • ¿µ¹®
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  • sleep apnea syndrome
    ¼ö¸é¹«È£ÈíÁõÈıº
  • sleep choking syndrome
    ¼ö¸éÁú½ÄÁõÈıº
  • somatizing syndrome
    ½ÅüȭÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº
  • stiff-man syndrome
    ±ÙÀ°°­Á÷ÁõÈıº
  • stroke syndrome
    ÁßdzÁõÈıº
  • sudden infant death syndrome
    ¿µ¾Æ±Þ»çÁõÈıº
  • sudden manhood death syndrome
    ûÀå³â±Þ»çÁõÈıº
  • superior orbital fissure syndrome
    À§´«È®Æ´»õÁõÈıº
  • supine hypotensive syndrome
    ´©¿îÀÚ¼¼ÀúÇ÷¾ÐÁõÈıº
  • tabetic syndrome
    ¼Ò¸ðÁõÁõÈıº, Ÿº£½ºÁõÈıº
  • tarsal tunnel syndrome
    ¹ß¸ñ±¼ÁõÈıº, Á·±Ù°üÁõÈıº
  • testicular feminization syndrome
    °íȯ¿©¼ºÈ­ÁõÈıº
  • thalamic syndrome
    ½Ã»óÁõÈıÙ
  • time zone change syndrome
    (¢¡jet lag syndrome) ºñÇà½ÃÂ÷ÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
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  • acute tubular necrosis
    ±Þ¼º ¼¼´¢°ü±«»ç (¡­á¬èñηÎÕÞÝ).
  • acute tubular necrosis
    ±Þ¼º¼¼´¢°ü±«»ç(¡­á¬Òãη)
  • acute tubular necrosis, ATN
    ±Þ¼º ¼¼´¢°ü ±«»ç
  • acute ulcerative colitis
    ±Þ¼º ±Ë¾ç¼º ´ëÀå¿°(¡­Ï÷åËàõÓÞ æú).
  • acute ulcerative gingivitis
    ±Þ¼º ±Ë¾ç¼º Ä¡Àº¿°(¡­Ï÷åËàõöÍó»æú).
  • acute undifferentiated
    ±Þ¼º ¹ÌºÐÈ­.[Á¤½Å]±Þ¼º ¹ÌºÐÇü(¡­Ú±ÝÂû¡).
  • acute undifferentiated leukemia
    ±Þ¼º ¹ÌºÐÈ­¼º ¹éÇ÷º´
  • acute urethritis
    ±Þ¼º ¿äµµ¿°
  • acute urinary retention
    ±Þ¼º ¿äÆó
  • acute urticaria
    ±Þ¼º(Ðáàõ) µÎµå·¯±â
  • acute variceal hemorrhage
    ±Þ¼º Á¤¸Æ·ùÃâÇ÷(¡­ð¡Øæ×»õóúì).
  • acute viral hepatitis
    ±Þ¼º ¹ÙÀÌ·¯½º°£¿°(¡­ÊÜæú).
  • acute viral hepatitis
    ±Þ¼º¹ÙÀÌ·¯½º¼º °£¿° (~ÊÜæú)
  • acute yellow atrophy
    ±Þ¼º Ȳ»öÀ§Ãà(Áõ)(ÐáàõüÜßäê×õêñø) °£(ÊÜ)ÀÇ .
  • acute yellow atrophy
    ±Þ¼º Ȳ»öÀ§Ãà(Áõ)(ÐáàõüÜßäê×õêñø) °£(ÊÜ)
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  • acute myelogenous leukemia
    ±Þ¼º °ñ¼ö¼º ¹éÇ÷º´(¡­ÍéâÐàõÛÜúìÜ»).
  • acute myelomonocytic leukemia
    ±Þ¼º °ñ¼ö´Ü±¸ ¹éÇ÷º´
  • acute myocarditis
    ±Þ¼º ½É±Ù¿°(¡­ãýÐÉæú).
  • acute myopathy
    ±Þ¼º ±Ùº´Áõ(¡­ÐÉÜ»ñø).
  • acute myopathy
    ±Þ¼º ±Ùº´Áõ(¡­ÐÉÜ»ñø).
  • acute necrotic otitis media
    ±Þ¼º ±«»ç(¼º) ÁßÀÌ¿°
  • acute necrotizing enterocolitis
    ±Þ¼º±«»ç¼ºÀ§Àå¿°(¡­ÎÕÞÝàõêÖíóæú).
  • acute necrotizing enterocolitis
    ±Þ¼º ±«»ç¼º ÀüÀå¿°(¡­ÎÕÞÝàõîï æú).
  • acute necrotizing hemorrhagic encephalomyelitis
    ±Þ¼º ±«»çÃâÇ÷¼º ³úô¼ö¿°(¡­ÎÕÞÝõóúìàõÒàô±âÐæú).
  • acute necrotizing retinitis
    ±Þ¼º±«»ç¸Á¸·¿°
  • acute necrotizing ulcerative gingivitis
    ±Þ¼º ±«»ç±Ë¾ç¼º Ä¡Àº¿°
  • acute necrotizing ulcerative gingivitis
    ±Þ¼º±«»ç±Ë¾ç¼º Ä¡Àº¿°
  • acute nephritis
    ±Þ¼º ½Å¿°(Ðáàõãìæú).
  • acute obliterating bronchiolitis
    ±Þ¼º Æó¼â¼º ¼¼±â°üÁö¿°(¡­øÍáðàõá¬Ñ¨Î·ò¨æú).
  • acute orchitis
    ±Þ¼º °íȯ¿°
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
BH base hospital; benzalkonium and heparin; bill of health; birth history; Bishop-Harman [instruments];...
BHI biosynthetic human insulin; brain-heart infusion [broth]; British Humanities Index; Bureau of Health...
BHIA brain-heart infusion agar
BHI-ac brain-heart infusion broth with acetone
BHIB brain-heart infusion broth
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 17
AFP Acute Flaccid Paralysis
aGVHD Acute GVHD
AHC Acute Hemorrhagic Conjunctivitis
AIP Acute Intermittent Porphyria
AL Acute Leukemia
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
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    ¼³¸í
  • cerebrohepatorenal syndrome
    ³ú°£ ½Å ÁõÈıº
  • cervical fusion syndrome
    °æºÎ À¯ÇÕ ÁõÈıº
  • cervicobrachial syndrome
    °æ »ó¿Ï ÁõÈıº
  • Cestans syndrome
    ¼¼½ºÅº ÁõÈıº
  • Charcot-Wilbrand syndrome
    »þ¸£ÄÚ-ºôºê¶õµå ÁõÈıº
  • chiasmal syndrome
    ½Ã ½Å°æ ±³Â÷ºÎ ÁõÈıº
  • Chilaiditis syndrome
    ų¶óÀÌµðÆ¼ ÁõÈıº
    °áÀå ¶Ç´Â ¼ÒÀåÀÇ ÀϺΰ¡ °£°ú Ⱦ°æ¸· »çÀÌ¿¡ °¨µ·ÇÏ¿© ÀϾ´Â ÁõÈıº.
  • cholecysto-hepatic flexure adhesion syndrome
    ´ã³¶ °áÀå °£°îºÎ À¯Âø ÁõÈıº
  • Chotzen's syndrome
    ÄÚþ ÁõÈıº
    ÷µÎÇÕÁöÁõÀ» ³ªÅ¸³»´Â »ó¿°»öü¼º ¿ì¼ºÀ¸·Î À¯ÀüµÇ´Â À¯Àü¼º Áúȯ.
  • chromaosomal breakage syndrome

    chromate

    Á¦ 2Å©·Ò»ê¿°
    1. Á¦2 Å©·Ò»êÀÇ ¸ðµç ¿°. 2. Á¦2Å©·Ò»ê¿° ¼ö¿ë¼ºÀÇ. Á¦2Å©·Î»ê¿°ÀÇ ÀÛ¿ëÀ» ½±°Ô ¹Þ¾ÆµéÀÌ´Â. 3. Å©·Ò»ê¿°.
  • chromosomal syndrome
    ¿°»öü ÁõÈıº
  • chromosome longarm deletion syndrome
    ¿°»öü ÀåÁö °á¼Õ ÁõÈıº
  • chromosome-breakage syndrome
    ¿°»öü-ºÐÇØ ÁõÈıº
  • chronic fatigue syndrome
    ¸¸¼º ÇÇ·Î ÁõÈıº
    ½±°Ô ÇǰïÇϰí ÁöÄ¡¸ç ¸öÀÌ ³ª¸¥ÇØÁö´Â µîÀÇ ÇÇ·Î Áõ¼¼°¡ 6°³¿ù ÀÌ»ó ¸¸¼ºÀûÀ¸·Î Áö¼ÓÇÏ´Â Áõ»ó. È®½ÇÇÑ ¿øÀÎÀº ¹àÇôÁ® ÀÖÁö ¾Ê°í, ¹ÙÀÌ·¯½º °¨¿°ÀÌ ±× ¿øÀÎÀÇ Çϳª·Î ÃßÁ¤µÈ´Ù. Æò¼Ò °Ç°­ÇÑ »ç¶÷¿¡°Ô¼­ °¨±â³ª ¸ö»ì ±â¿îÀÌ ÀÖ´Ù°¡ ÀÌ·± ÇǷΰ¡ ³ªÅ¸³­´Ù. ´ëü·Î Ưº°ÇÑ Ä¡·á°¡ ÇÊ¿ä¾øÀÌ ÀúÀý·Î Ä¡À¯µÇ³ª ÇǷθ¦ ´À³¢°Ô ÇÏ´Â ´Ù¸¥ Áúº´ÀÇ À¯¹«¸¦ È®ÀÎÇÏ´Â °ÍÀÌ Áß¿äÇÏ´Ù. ƯÈ÷ ½ºÆ®·¹½º, ¿ì¿ïÁõ, ºÒ¾ÈÀå¾Ö µî°ú °°Àº Á¤½ÅÀû ¹®Á¦°¡ ¾à 50 %¸¦ Â÷ÁöÇϸç, ½ÅüÀû ÁúȯÀ¸·Î´Â ´ç´¢º´, °©»ó¼± Áúȯ, ¸¸¼º È£Èí±â Áúȯ, ºóÇ÷, °áÇÙ, °£¿°, ½ÅÀå ÁúȯÀ̳ª ¾Ï µî¿¡ ÀÇÇØ¼­µµ ¸¸¼ºÀû ÇǷΰ¨À» ´À³¥ ¼ö ÀÖ´Ù. ÀÌ¿Í °°Àº ÁúȯÀÌ ¾ø´Â °ÍÀÌ ÆÇ¸íµÇ¸é ¸¸¼º ÇÇ·Î ÁõÈıºÀ¸·Î Áø´ÜÇÒ ¼ö ÀÖ´Ù.
  • chronic infantile neurological cutaneous articular syndrome
    ¸¸¼º À¯¾Æ ½Å°æ ÇǺαº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 17
Ahumada-Del Castillo syndrome <syndrome> Unphysiological lactation and amenorrhoea not following pregnancy characterised by hyperprolactinaemia and a pituitary adenoma.
Synonym: Argonz-Del Castillo syndrome.
(05 Mar 2000)
Aicardi's syndrome <syndrome> Agenesis of the corpus collosum with infantile spasms in female babies.
(05 Mar 2000)
alagille syndrome <syndrome> Hypoplasia of the hepatic ducts, congenital pulmonary artery stenosis, facial abnormalities, and other congenital malformations, particularly skeletal. It is often presented as jaundice during the neonatal period. It is an autosomal recessive disease generally manifesting during childhood. "arteriohepatic" refers to the pulmonary artery and the intrahepatic bile ducts, not to the hepatic artery.
(12 Dec 1998)
Albright's syndrome <syndrome> A condition of cystic bone growth that results from abnormal bone development. May occur with bone lesions, skin pigmentation and endocrine abnormalities.
See: McCune-Albright syndrome.
(27 Sep 1997)
alcohol amnestic syndrome <syndrome> An amnestic syndrome resulting from alcoholism; alcoholic "blackouts." Cf.: Korsakoff's syndrome.
(05 Mar 2000)
Aldrich syndrome <syndrome> An sex-linked (X chromosome) genetic disorder occurring in male children that is characterised by thrombocytopenia, eczema, melena and susceptibility to bacterial infections. Death often occurs from severe haemorrhage or overwhelming sepsis.
Inheritance: sex-linked (X chromosome).
(27 Sep 1997)
Alezzandrini's syndrome <syndrome> A rare syndrome appearing in adolescents and young adults, characterised by unilateral degenerative retinitis, followed by ipsilateral poliosis and facial vitiligo, and occasionally bilateral perceptive deafness.
(05 Mar 2000)
Alice in Wonderland syndrome <syndrome> The illusion of dreams, feelings of levitation, and alteration in the sense of the passage of time, sometimes associated with migraine, epilepsy, and various diseases of the parietal lobe of the brain.
(05 Mar 2000)
Allen-Masters syndrome <syndrome> Pelvic pain resulting from an old laceration of the broad ligament received during delivery.
(05 Mar 2000)
Alpert syndrome <syndrome> A usually inherited disorder characterised by premature closing of the cranial suture lines resulting in a peaked shaped head and abnormal facial appearance. Since it is usually autosomal dominant one or both parents also have the disorder.
Surgery is used to correct skull and facial abnormalities.
Inheritance: autosomal dominant.
(27 Sep 1997)
Alport's syndrome <syndrome> Progressive microscopic haematuria leading to chronic renal failure earlier in males, accompanied by defects such as sensorineural hearing loss, lenticonus, and maculopathy; autosomal dominant, autosomal recessive, and X-linked forms known.
(05 Mar 2000)
Alport syndrome <syndrome> An uncommon inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected.
Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision.
Incidence: 1 in 50,000.
Inheritance: sex-linked autosomal dominant.
(15 Nov 1997)
Alstrom's syndrome <syndrome> Retinal degeneration with nystagmus and loss of central vision, associated with obesity in childhood; sensorineural hearing loss and diabetes mellitus usually occur after age 10; autosomal recessive inheritance.
(05 Mar 2000)
amenorrhoea-galactorrhoea syndrome <syndrome> Unphysiologic lactation from endocrinological causes or from a pituitary tumour.
(05 Mar 2000)
amnestic syndrome <syndrome> May occur as a sequel to chronic alcohol abuse. Features include personality changes, confabulation, psychosis, disorientation, polyneuritis, insomnia and hallucinations.
(27 Sep 1997)
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