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  • ¿µ¹®
    ÇѱÛ
  • hematologic disorder
    Ç÷¾×Àå¾Ö
  • hemostatic disorder
    ÁöÇ÷Àå¾Ö, Ç÷¾×ÀÀ°íÀå¾Ö
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hormonal disorder
    È£¸£¸óÀå¾Ö, ³»ºÐºñÀå¾Ö
  • ion channel disorder
    ÀÌ¿ÂÅë·ÎÁúȯ
  • immune disorder
    ¸é¿ªÁúȯ, ¸é¿ªÀå¾Ö
  • immunoproliferative disorder
    ¸é¿ªÁõ½ÄÀå¾Ö
  • impulse control disorder
    Ãæµ¿Á¶ÀýÀå¾Ö
  • identity disorder
    Á¤Ã¼¼ºÀå¾Ö
  • intermittent explosive disorder
    °£ÇæÆø¹ßÀå¾Ö
  • intestinal motility disorder
    âÀڿÀå¾Ö, Àå¿îµ¿Àå¾Ö
  • language disorder
    ¾ð¾îÀå¾Ö
  • learning disorder
    ÇнÀÀå¾Ö
  • lymphoproliferative disorder
    ¸²ÇÁ¼¼Æ÷Áõ½ÄÁúȯ
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  • ¿µ¹®
    ÇѱÛ
  • extrapyramidal disorder
    Ãßü¿Ü·ÎÀå¾Ö
  • factitious disorder
    ÀÎÀ§ÀûÀå¾Ö
  • fanatic personality disorder
    ±¤½ÅÀΰÝÀå¾Ö
  • female sexual arousal disorder
    ¿©¼º¼ºÀûÈïºÐÀå¾Ö
  • functional disorder
    ±â´ÉÀå¾Ö
  • generalized anxiety disorder
    ¹üºÒ¾ÈÀå¾Ö
  • hearing disorder
    û·ÂÀå¾Ö
  • hematologic disorder
    Ç÷¾×Àå¾Ö
  • hemostatic disorder
    Ç÷¾×ÀÀ°íÀÌ»ó
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hormonal disorder
    ³»ºÐºñÀå¾Ö, È£¸£¸óÀå¾Ö
  • hyperkinetic disorder
    ¿îµ¿°ú´ÙÀå¾Ö, ¿îµ¿°ú´ÙÁúȯ
  • hyperkinetic impulse disorder
    ¿îµ¿°ú´ÙÃæµ¿Àå¾Ö
  • hypersensitivity disorder
    °ú¹ÎÁúȯ
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    ÇѱÛ
  • personality disorder, asocial
    ºñ»çȸ¼º ÀΰÝÀå¾Ö
  • personality disorder, asthenic
    ¹«·ÂÁõÀû(ÙíÕôñøîÜ) ÀΰÝÀå¾Ö
  • personality disorder, avoidant
    ȸÇǼº(üÞù­àõ) ÀΰÝÀå¾Ö
  • personality disorder, borderline
    °æ°è¼º(ÌÑÍ£àõ) ÀΰÝÀå¾Ö
  • personality disorder, compulsive
    °­¹Ú¼º ÀΰÝÀå¾Ö
  • personality disorder, dependent
    ÀÇÁ¸¼º(ëîðíàõ) ÀΰÝÀå¾Ö
  • personality disorder, dissocial
    »ç±³°ï¶õ¼º ÀΰÝÀå¾Ö
  • personality disorder, emotionally unstable
    Á¤¼­ºÒ¾ÈÁ¤¼º ÀΰÝÀå¾Ö
  • personality disorder, explosive
    Æø¹ß¼º ÀΰÝÀå¾Ö
  • personality disorder, fanatic
    ±¤½ÅÀû ÀΰÝÀå¾Ö
  • personality disorder, histrionic
    È÷½ºÅ׸®¾ç ÀΰÝÀå¾Ö
  • personality disorder, hysterical
    È÷½ºÅ׸®¼º ÀΰÝÀå¾Ö
  • personality disorder, immature
    ¹Ì¼÷(Ú±âÙ)¼º ÀΰÝÀå¾Ö
  • personality disorder, inadequate
    ºÎÀû°Ý¼º ÀΰÝÀå¾Ö
  • personality disorder, multiple
    ´ÙÁß(Òýñì) ÀΰÝÀå¾Ö
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  • jealous type
    ÁúÅõÇü(òì÷àúþ)
  • langhans-type giant cell
    ¶û±×Çѽº°Å´ë¼¼Æ÷, Langerhans °Å´ë¼¼Æ÷(¡­ËÝÓÞá¬øà)
  • lepromatous type
    ³ªÁ¾Çü(ÑÛðþúþ)
  • lepromatous type
    ³ªÁ¾Çü(ÑÛðþúþ).
  • leptosomatic type
    ¸¶¸¥Çü(¡­úþ).
  • limb girdle type
    Áö´ëÇü.
  • linear array type
    ¼±Çü ¹è¿­½Ä (àÊû¡ ÛÕÖªãÒ)
  • linear type constitution
    ¼±Ã¼Çü.
  • lymphatic type
    ¸²ÇÁÇü(¡­úþ).
  • mating type
    ±³¹èÇü
  • men type
    MEN Çü(¡­ û¡)
  • meningeal type
    ¼ö¸·Çü(âÐØ¯úþ).
  • metaphyseal dysostosis dominant type
    °ñ °£´Ü¼º À̰ñÁõ ¿ì¼ºÇü(ÍéÊÏÓ®àõì¶ÍéñøéÐàõúþ).
  • metaplastic bone (type)
    È­»ý°ñ(Çü)(ûùßæÍéû¡).
  • mixed type of artery
    È¥ÇÕÇüµ¿¸Æ
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CPD calcium pyrophosphate deposition; cephalopelvic disproportion; cerebelloparenchymal disorder; childh...
CTD carpal tunnel decompression; chest tube drainage; congenital thymic dysplasia; connective tissue dis...
E-ADD epileptic attentional deficit disorder
ED early-decision [applicant]; early differentiation; ectodermal dysplasia; ectopic depolarization; eff...
EDI eating disorder inventory; electronic data interchange
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
LLPDD Late Luteal Phase Dysphoric Disorder
LPD Lymphoproliferative disorder
M.P.D. Multiple Personality Disorder
MPD Myeloproliferative disorder
NPD Narcissistic personality disorder
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
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  • dissociative identity disorder
    ÇØ¸®¼º ÁÖü¼º Àå¾Ö, ÇØ¸®¼º ÁÖü¼º º´
  • dominated inherited disorder
    ¿ì¼º À¯Àü Áúȯ
  • drug induced disorder
    ¾à¹° À¯¹ß¼º Áúȯ
  • dysthmic disorder
    ±âºÐ º¯Á¶Áõ
  • dysthymic disorder
    ±âºÐ º¯Á¶¼º Àå¾Ö
  • endocrine disorder
    ³»ºÐºñ Àå¾Ö
  • enzyme disorder
    È¿¼Ò Àå¾Ö
  • functional mandibular disorder
    ±â´ÉÀû ÇÏ¾Ç Àå¾Ö
    ºñÁ¤»óÀûÀÎ ÇÏ¾Ç ¿îµ¿À̳ª ÀÛ¿ë°ú °ü·ÃµÈ Àå¾Ö.
  • habit and impulse disorder
    ½À°ü ¹× Ãæµ¿ Àå¾Ö, ½À°ü ¹× Ãæµ¿º´
  • headache disorder
    µÎÅë Àå¾Ö
  • hemologic disorder
    Ç÷¾× Àå¾Ö
  • hemolytic disorder
    ¿ëÇ÷¼º Áúȯ
  • hemorrhagic disorder
    ÃâÇ÷ Àå¾Ö
    ÁöÇ÷À» ¹æÇØÇÏ´Â ¿ä¼Ò¸¦ °¡Áø º´.
  • iatrogenic disorder
    ÀǼº Àå¾Ö, ÀÇ¿ø¼º Àå¾Ö
  • identity disorder
    ÁÖü¼º Àå¾Ö
    Á÷¾÷ ¼±Á¤, ¼ºÀû Áö³²·Â, Çൿ, µµ´öÀû °¡Ä¡°ü µî¿¡ ´ëÇÑ ºÒÈ®½Å°ú ÇÔ²², ÀÚ±âÀÚ½ÅÀÇ ±¹¸éÀ» ºñ±³Àû ÀϰüµÈ Àüü¿¡ ÀÏÄ¡½ÃŰÁö ¸øÇϰí ÀÚ½ÅÀÇ ÀνÄÀ» ¼ö¿ëÇÏÁö ¸øÇÏ´Â °Í¿¡ ´ëÇÑ ½ÉÇÑ ÁÖ°üÀû °í³ú·Î, 3°³¿ù ȤÀº ±× ÀÌ»ó Áö¼ÓµÇ¸ç, »çÃá±â Èıâ û¼Ò³â¿¡ °¡Àå ÈçÈ÷ ³ªÅ¸³­´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
botulinum toxin type a <chemical> A neurotoxin produced by clostridium botulinum. When consumed in contaminated food it can cause paralysis and death. In its purified form, it has been used in the treatment of blepharospasm and strabismus.
Pharmacological action: neuromuscular agents.
(12 Dec 1998)
bovine adenovirus type 3 proteinase <enzyme> Amino acid sequence given in first source
Registry number: EC 3.4.-
Synonym: bav-3 proteinase
(26 Jun 1999)
bovine adenovirus type 7 proteinase <enzyme> Amino acid sequence given in first source
Registry number: EC 3.4.-
Synonym: bav-7 proteinase
(26 Jun 1999)
buffalo type Term used to describe the distribution of a fat deposit seen posteriorly over the upper thoracic vertebrae; seen in hyperadrenocorticalism (Cushing's syndrome).
Synonym: buffalo hump.
(05 Mar 2000)
vaccination, haemophilus influenzae type b See vaccination, hib.
(12 Dec 1998)
gastroenteritis virus type A A RNA virus, about 27 nm in diameter, which has not been cultured in vitro; it is the cause of epidemic nonbacterial gastroenteritis; at least five antigenically distinct serotypes have been recognised, including the Norwalk agent. These viruses are probably classified with the Caliciviruses in the family Caliciviridae.
Synonym: gastroenteritis virus type A.
(05 Mar 2000)
gastroenteritis virus type B <virology> Genus of the Reoviridae having a double layered capsid and 11 double stranded RNA molecules in the genome. They have a wheel like appearance in the electron microscope and cause acute diarrhoeal disease in their mammalian and avian hosts.
Probably the most important cause of severe dehydrating diarrhoea in children under three years of age worldwide.
Symptoms include nausea, vomiting, low-grade fever and diarrhoea. Aggressive fluid replacement is generally required.
(27 Sep 1997)
gaucher's disease, type 1 A progressive genetic disease caused by a defect in an enzyme. The enzyme, called glucocerebrosidase, is needed to break down the chemical glucocerebroside. The enzyme defect in persons with Gaucher's disease (GD) leads to the accumulation of glucocerebroside in the spleen, liver, and lymph nodes. The most common early sign is enlargement of the spleen (located in the upper left abdomen). Other signs include low red blood cell counts (anaemia), a decrease in blood clotting cells (platelets), increased pigmentation of the skin, and a yellow fatty spot on the white of the eye (a pinguecula). Severe bone involvement can lead to pain and collapse of the bone of the hips, shoulders, and spine. The GD gene is on chromosome 1. The disease is a recessive trait. Both parents carry a GD gene and transmit it for their child with the disease. The parents' risk of a child with the disease is 1 in 4 with each pregnancy. This type of Gaucher's disease (noncerebral juvenile Gaucher's disease) is most common in Ashkenazi Jews (of European origin) and is the most common genetic disease among Jews in the United States.
(12 Dec 1998)
Recklinghausen's disease type I type 2 neurofibromatosis
mating type gene Genes that, in Saccharomyces cerevisiae specify into which of the two mating types (a and _) a particular cell falls. Only unlike mating type haploids will fuse. The interest derives from the way in which mating type is switched, the existing gene is removed and a new gene, derived from a (silent) master copy elsewhere in the genome is spliced in. Later this gene will in its turn be replaced by a new copy of the old gene, also derived from a silent master. The a and _ genes code for pheromones that affect cells of the opposite mating type. Similar mating type genes are known from other yeasts and the switching mechanism (cassette mechanism) may be used more generally.
(18 Nov 1997)
viral hepatitis type A A virus disease with a short incubation period (usually 15 to 50 days), caused by hepatitis A virus, a member of the family Picornaviridae, often transmitted by faecal-oral route; may be inapparent, mild, severe, or occasionally fatal and occurs sporadically or in epidemics, commonly in school-age children and young adults; necrosis of periportal liver cells with lymphocytic and plasma cell infiltration is characteristic and jaundice is a common symptom.
Synonym: epidemic hepatitis, hepatitis A, infectious hepatitis, MS-1 hepatitis, short incubation hepatitis, virus A hepatitis.
(05 Mar 2000)
viral hepatitis type B A virus disease with a long incubation period (usually 50 to 160 days), caused by hepatitis B virus, a DNA virus and member of the family Hepadnoviridae, usually transmitted by injection of infected blood or blood derivatives or by use of contaminated needles, lancets, or other instruments; clinically and pathologically similar to viral hepatitis type A, but there is no cross-protective immunity; HBsAg is found in the serum and the hepatitis delta virus occurs in some patients.
Synonym: hepatitis B, serum hepatitis, transfusion hepatitis, virus B hepatitis.
(05 Mar 2000)
viral hepatitis type C Principal cause of non-A, non-B posttransfusion hepatitis caused by an RNA virus that may be related to Flaviviridae family.
Synonym: hepatitis C, virus C hepatitis.
(05 Mar 2000)
viral hepatitis type D Acute or chronic hepatitis caused by the hepatitis delta virus, a defective RNA virus requiring HBV for replication. The acute type occurs in two forms: 1) coinfection, the simultaneous occurrence of hepatitis B virus and hepatitis delta virus infections, which usually is self-limiting; 2) superinfection, the appearance of hepatitis delta virus infection in a hepatitis B virus carrier, which often leads to chronic hepatitis The chronic type appears to be more severe than other types of viral hepatitis.
Synonym: delta hepatitis, hepatitis D.
(05 Mar 2000)
viral hepatitis type E Hepatitis caused by a nonenveloped, single-stranded, positive-sense RNA virus 27-34 nm in diameter, unrelated to other hepatitis; it is the principal cause of enterically transmitted, waterborne, epidemic NANB hepatitis occurring primarily in Asia and Africa.
Synonym: hepatitis E.
(05 Mar 2000)
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