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  • ¿µ¹®
    ÇѱÛ
  • cardiovascular disease
    ½É(Àå)Ç÷°üÁúȯ
  • Caroli disease
    Ä«·Ñ¸®º´
  • cat-scratch disease
    °í¾çÀÌÇÒÅ¡º´
  • celiac disease
    º¹°­º´, º¹°­Áúȯ
  • Center for Disease Control and Prevention
    Áúº´°ü¸®¿¹¹æ¼¾ÅÍ
  • central core disease
    Áß½ÉÇÙº´, Áß½ÉÄھ
  • caloric disease
    °í¿Âº´
  • cerebrovascular disease
    ³úÇ÷°üÁúȯ, ³úÇ÷°üº´
  • Charcot-Marie-Tooth disease
    »þ¸£ÄÚ-¸¶¸®-Åõ½ºº´
  • Canavan disease
    ij³Ê¹øº´
  • cholesteryl ester storage disease
    ÄÝ·¹½ºÅ×·Ñ¿¡½ºÅ׸£ÃàÀûº´
  • chronic granulomatous disease
    ¸¸¼ºÀ°¾ÆÁ¾º´
  • chronic obstructive pulmonary disease
    ¸¸¼ºÆó¼âÆóÁúȯ
  • deficiency disease
    °áÇ̺´
  • degenerative disease
    ÅðÇິ, º¯¼ºº´
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  • ¿µ¹®
    ÇѱÛ
  • compressed-air disease
    °¡¾Ðº´
  • congenital heart disease
    ¼±Ãµ½ÉÀ庴
  • connate disease
    ¼±Ãµº´
  • connective tissue disease
    °áÇÕÁ¶Á÷º´
  • constitutional disease
    üÁúº´
  • constrictive heart disease
    ±³Âø½ÉÀ庴
  • consumption disease
    ¼Ò¸ðº´
  • contagious disease
    Á¢ÃËÀü¿°º´
  • copper storage disease
    ±¸¸®ÀúÀ庴
  • coronary artery disease
    ½ÉÀ嵿¸Æº´, °ü»óµ¿¸Æº´
  • corticospinal tract disease
    °ÑÁúô¼ö·Îº´
  • counterfeit disease
    ²Òº´
  • creeping disease
    ±â´Âº´
  • cystic kidney disease
    ÁÖ¸Ó´ÏÄáÆÏº´, ³¶¼º½ÅÀ庴
  • cystine disease
    ½Ã½ºÆ¾º´
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  • ¿µ¹®
    ÇѱÛ
  • Dorfman-Chanarin syndrome = neutral lipid storage disease
    Áß¼ºÁö¹æÃàÀûÁõ
  • Dowling-Degos disease = reticular pigmented anomaly of the flexures
    ±¼ÃøºÎ ¸Á»ó»ö¼ÒÀÌ»ó(Áõ)
  • Duhrings disease => dermatitis herpetiformis
    Æ÷Áø»ó ÇǺο°
  • Duncans disease .
    ´øÄ­¾¾º´
  • Eagles disease
    À̱۽ºº´
  • Eales disease
    ÀϽºº´
  • Ebola disease
    ¿¡º¼¶óº´
  • Ebola disease
    ¿¡º¼¶ó º´
  • Fabrys disease
    ÆÄºê¸®º´
  • Fabrys disease
    ÆÄºê¸®º´.
  • Fabrys disease
    ÆÄºê¸®º´
  • Farber s disease
    ÆÄ¾Æ¹öº´.
  • Fordyce s disease
    Æ÷¿À´ÙÀ̽ºº´.
  • Fordyces disease
    Æ÷´ÙÀ̽ºº´
  • Fordyces disease
    Æ÷¿À´ÙÀ̽ºº´
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  • ¿µ¹®
    ÇѱÛ
  • tumor,mixed
    È¥ÇÕ
  • aberrant type
    ÀÌÇü(ì¶úþ)
  • abortive type
    ºÎÀüÇü(ÝÕîïúþ).
  • acute fulminating type
    ±Þ¼º Àü°ÝÇü.
  • agammaglobulinemia,x-linked, bruton type
    ¼º¿°»öü ¿¬°ü¼º, ºê·çÅæÇü(àõæøßäô÷ æáμàõ, ¡­úþ)
  • anovulatory type
    ¹«¹è¶õÇü
  • association type
    ¿¬»óÀ¯Çü
  • asthenia type
    ¹«·ÂüÇü.
  • atypical type
    ºñÁ¤Çü ÇüÅÂ
  • bell type
    Á¾¸ð¾ç, Á¾Çü.
  • blood group =b. type
    Ç÷¾×Çü(Ì´ËâÌ´).
  • blood group =b. type
    Ç÷¾×Çü(úìäûû¡).
  • blood type
    Ç÷¾×Çü(Ì´ËâÌ´).
  • blood type
    Ç÷¾×Çü(úìäûúþ)
  • body type
    üÇü
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CVD cardiovascular disease; cerebrovascular disease; collagen vascular disease; color-vision-deviant
GBD gallbladder disease; gender behavior disorder; glass blower's disease; granulomatous bowel disease
GD gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ...
ICD I-cell disease; immune complex disease; implantable cardioverter defibrillator; impulse-control diso...
ID identification; iditol dehydrogenase; immunodeficiency; immunodiffusion; immunoglobulin deficiency; ...
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MMT Mixed mesodermal tumor
MM Mixed micelles
NONMEM NON-linear Mixed Effects Modelling
Nonmem Non-Linear Mixed Effects Model
SMLR Syngeneic mixed lymphocyte reaction
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Banti's disease
    ¹ÝƼ º´
    Ãʱ⿡´Â ºñÁ¾ ¹× ¹üÇ÷±¸ °¨¼ÒÁõÀ» µ¿¹ÝÇÏ´Â ºñÀåÀÇ ¿ø¹ß¼º ÁúȯÀ¸·Î ±â·ÏµÇ¾úÀ¸³ª, ÈÄ¿¡ ¹®¸Æ¾Ð Ç×Áø¿¡ ÀÇÇÑ ÀÌÂ÷ÀûÀÎ °ÍÀ¸·Î ÀÎÁ¤µÇ¾ú´Ù.
  • Barcoo disease
    ¹Ù¸£Äíº´
    µ¿ÀǾî=desert sore.
  • Barthelemy's disease
    ¹Ù¸£ÅÚ·¹¹Ì º´
    ¾ó±¼ÀÇ °áÇÙ¼º µÎâ ºñ½ÁÇÑ ÁÂâ.
  • Basedow's disease
    ¹Ù¼¼µµ¿ì º´
    µ¿ÀǾî=Graves' disease. °©»ó¼± ±â´ÉÇ×ÁøÁõ.
  • Bazin's disease
    ¹ÙÁø º´
    µ¿ÀǾî=erythema induratum.
  • Beard's disease
    º£¾îµå º´
    µ¿ÀǾî=neurasthenia.
  • Beau's disease
    º¸¿ì º´
    µ¿ÀǾî=cardiac insufficiendy.
  • Bernard-Soulier disease
    º£¸£³ª¸£-¼ú¸®¿¡ º´, Bernard-Soulier º´
    Å©±â¿Í ÇüŰ¡ ´Ù¾çÇÑ Ç÷¼ÒÆÇÀ» Ư¡À¸·Î ÇÏ´Â »ó¿°»öü ¿­¼º À¯Àü¼º ÁúȯÀ¸·Î, Ç÷¼ÒÆÇ ¸·Àº Ç÷Àå vWF
  • Bernhardt's disease
    º£¸¥Çϸ£Æ® º´
    µ¿ÀǾî=meralgia
  • Best's disease
    º£½ºÆ® º´
    µ¿ÀǾî=congenital macular degeneration.
  • black disease
    Èæ»ö º´
    ¾çÀÇ Àü¿°¼º ±«»ç¼º °£¿°. ¹Ì±¹, ¿À½ºÆ®·¹Àϸ®¾Æ¿¡¼­ÀÇ ¾çÀÇ Ä¡»çº´ÀÌ¸ç ¶§¶§·Î »ç¶÷¿¡°Ôµµ »ý±ä´Ù. °£ÀåÀÇ ±«»ç°¡ ±× Ư¡ÀÌ¸ç ³ëºñ±Õ¿¡ ÀÇÇÏ¿© ÀϾ´Ù.
  • bleeder's disease
    Ç÷¿ìº´
    ÃâÇ÷À» Àß ÀÏÀ¸Å°°Å³ª ÃâÇ÷ ¼ÒÁúÀÌ ÀÖ´Â Áúº´.
  • Blocq's disease
    ºí·Ï º´
    µ¿ÀǾî=astasia, abasia.
  • blood disease
    Ç÷¾× ÀÌ»ó
    µ¿ÀǾî=hemic disease.
  • bone disease
    °ñ Áúȯ
    µ¿ÀǾî=osteo
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 10
Haemophilus influenzae type B vaccine A conjugate of oligosaccharides of the capsular antigen of H. Influenzae type B and diphtheria CRM protein.
(05 Mar 2000)
pre-excitation, mahaim-type A form of pre-excitation characterised by a normal pr interval and a long qrs interval with a delta wave.
(12 Dec 1998)
Hermansky-Pudlak syndrome type VI An autosomal recessive deficiency of pigment in skin, hair, and eyes; in the tyrosinase negative type, there is an absence of tyrosinase; in the tyrosinase positive type, there is normal tyrosinase which cannot enter pigment cells; it is transmitted by an autosomal recessive inheritance. The compound heterozygote is normal so the two forms are not allelic.
There are several types: type IA is characterised by absence of tyrosinase with life-long complete absence of melanin, marked photophobia, and nystagmus. Type IB, yellow albinism with low or absent tyrosinase; improves with age.
Type II, with normal tyrosinase activity is the most common; hair darkens and nevi and freckles develop.
Type III is characterised by absent tyrosinase but pigmentation of the iris in the first decade.
Type IV in Africans with normal tyrosinase.
Type V with red hair.
Type VI, Hermansky-Padlak syndrome, with haemorrhage due to platelet deficiency and low to absent tyrosinase.
Synonym: Hermansky-Pudlak syndrome type VI.
(05 Mar 2000)
herpes simplex type 1 A virus that causes cold sores and fever blisters.
(12 Dec 1998)
herpes simplex type 2 Different from herpes simplex type 1, herpes simplex 2 causes genital herpes.
(12 Dec 1998)
herpes simplex virus type 1 UL13 protein kinase <enzyme> Phosphorylates icp22 and involved in the accumulation of alpha and gamma mrnas and proteins in the infected cells; aa sequence has been determined
Registry number: EC 2.7.1.-
Synonym: ul13 protein kinase, hsv-1, hsv-1 ul13 protein, hsv-1 ul13 pk, u(l)13 protein kinase, protein kinase ul13
(26 Jun 1999)
Schilling type of monocytic leukaemia See: monocytic leukaemia.
(05 Mar 2000)
protoporphyrinogen type III The immediate precursor of protoporphyrin III in haem biosynthesis; elevated in cases of variegate porphyria.
(05 Mar 2000)
protoporphyrinogen type III oxidase A mitochondrial enzyme that uses O2 to convert protoporphyrinogen type III to protoporphyrin type III in haem biosynthesis; a deficiency of this enzyme is associated with variegate porphyria.
(05 Mar 2000)
protoporphyrin type III 2,7,12,18-Tetramethyl-3,8-divinylporphin-13,17dipropionic acid;the principal protoporphyrin found in nature (one of 15 possible isomers), characterised by the presence of 4 methyl groups, 2 vinyl groups, and 2 propionic acid side chains; a porphyrin derivative that, with iron, forms the haem of haemoglobin and the prosthetic groups of myoglobin, catalase, cytochromes, etc.
(05 Mar 2000)
P-type ATPase <enzyme> One of three major classes of ion transport ATPases, characterised by vanadate sensitivity and a phosphorylated intermediate. The archetype is the sodium pump.
See: F-type ATPase, V-type ATPase.
(18 Nov 1997)
H-type fistula <gastroenterology, surgery> A rare form of congenital tracheoesophageal fistula in which there is no oesophageal atresia, manifest as aspiration pneumonias.
Synonym: H-type tracheoesophageal fistula.
(05 Mar 2000)
H-type tracheoesophageal fistula <gastroenterology, surgery> A rare form of congenital tracheoesophageal fistula in which there is no oesophageal atresia, manifest as aspiration pneumonias.
Synonym: H-type tracheoesophageal fistula.
(05 Mar 2000)
serine-type D-Ala-D-Ala carboxypeptidase <enzyme> Cleaves between d-ala residues of bacterial cell wall peptidoglycan; also catalyses transpeptidation of peptidyl-alanyl moieties that are n-acyl substituents of d-alanine
Registry number: EC 3.4.16.4
Synonym: ala-ala carboxypeptidase, serine-type, dd-peptidase, d-alanyl-d-alanine-carboxypeptidase
(26 Jun 1999)
hyperlipoproteinaemia type III A rather uncommon form of familial hyperlipaemia characterised by the presence of lipoproteins of abnormal composition. The main abnormal lipoproteins are called beta-vldl and have a different apoprotein content and a higher proportion of cholesterol relative to triglyceride than normal vldl.
(12 Dec 1998)
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