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"Niemann-Pick disease type C"¿¡ ´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
  • 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´
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
  • ¿µ¹®
    ÇѱÛ
  • 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´
  • cystine storage disease
    ½Ã½ºÆ¾ÃàÀûº´
  • cytomegalic inclusion disease
    ¼¼Æ÷°Å´ëÆ÷ÇÔº´
  • disease control
    Áúº´°ü¸®
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
  • ¿µ¹®
    ÇѱÛ
  • Christmas disease=hemophilia B
    Å©¸®½º¸¶½ºº´=Ç÷¿ìº´ B
  • Clostridial disease
    Ŭ·Î½ºÆ®¸®µð¿òº´
  • Coats disease
    ÄÚ¿ìÃ÷º´
  • Coats disease
    ÄÚ¿ìÃ÷º´
  • Corvisart s disease
    ÄÚ¸£ºñÀÚ¸£º´.
  • Coutons disease
    ÄíÅ뺴.
  • Creutzfeld-Jakob disease
    Å©·ÎÀÌÃ÷ÆçÆ®-¾ßÄߺ´.
  • Creutzfeld-Jakob disease
    Å©·ÎÀÌÃ÷ÆçÆ®-¾ßÄߺ´.
  • Creutzfeldt-Jakob disease
    Å©·ÎÀÌÃ÷ÆçÆ®-¾ßÄß º´
  • Creutzfeldt-Jakob disease(CJD)
    Å©·ÎÀÌÃ÷ÆçÆ®¾ßÄߺ´
  • Crohns disease
    Å©·Ðº´
  • Crohns disease
    Å©·Ðº´.
  • Crouzons disease =craniofacial dysostosis
    µÎ°³¾È¸éȸ°ñºÎÀüÁõ, Å©·ç Á¾º´ µÎ°³¾È¸éÀ̰ñÁõ .
  • Cushings disease
    Äí½Ìº´.
  • Dariers disease => keratosis follicularis
    ´Ù¸®¿¡ º´
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
  • ¿µ¹®
    ÇѱÛ
  • muscular type of artery
    ±ÙÀ°Çüµ¿¸Æ
  • muscular type of lymphatic vessel
    ±ÙÀ°Çü¸²ÇÁ°ü
  • muscular type of vein
    ±ÙÀ°ÇüÁ¤¸Æ
  • mutation, plaque-type
    ÇöóÅ©Çü µ¹¿¬º¯ÀÌ
  • on off type
    Á¡¸êÇü(ïÇØþúþ).
  • on type
    Áß½ÉÇü.
  • onion skin type
    ¾çÆÄ²®Áú¸ð¾ç
  • organic reaction type
    ±âÁú¼º ¹ÝÀÀÇü(¡­Úãëëúþ).
  • ovulatory type
    ¹è¶õÇü
  • particle, C-type
    CÇü ÀÔÀÚ (·¹Æ®·Î¹ÙÀÌ·¯½ºÀÇ)
  • personality disorder, mixed type
    È¥ÀçÇü(ûèî¤úþ) ÀΰÝÀå¾Ö
  • personality, type A
    AÇü ÀΰÝ
  • personality, type B
    BÇü ÀΰÝ
  • phage type
    ÆÄÁöÇü
  • phage type
    ÆÄÁöÇü(¡­úþ).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
LD labor and delivery; laboratory data; labyrinthine defect; lactate dehydrogenase; laser Doppler; lear...
NSD Nairobi sheep disease; neonatal staphylococcal disease; neurosecretory dysfunction; night sleep depr...
NVD nausea, vomiting, and diarrhea; neck vein distention; neovascularization of the disk; neurovesicle d...
SD Sandhoff disease; senile dementia; septal defect; serologically defined; serologically detectable; s...
SVD single vessel disease; singular value decomposition; small vessel disease; spontaneous vaginal deliv...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 8
AT1 Angiotensin II type 1
AT1-R Angiotensin II type 1 receptor
AT1 Angiotensin II receptor type 1
AT1 Angiotensin type 1 receptor
AT2 Angiotensin II type 2
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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
  • Bowen's disease
    º¸À¢ º´, º¸À¢ Áúȯ
    1. À¯¿øÇüÀÇ °æ°è. ¼±¸íÇÑ Èë°¥»ö ³»Áö °¥»öÀÇ ±¹¼ÒÀû º´º¯À» Çü¼ºÇÑ´Ù. ±¸°­ Á¡¸·ÀÇ Àû»ö, ¹é»ö ¹ÝÁ¡À¸·Î ¶Ñ·ÇÇÑ ºÒ±ÔÄ¢ÇÑ ¼ºÀåÀ» ÇÑ´Ù. °¡Çǰ¡ µ¤È÷¸é¼­ ¿ø½É»óÀ¸·Î È®´ëÇϴµ¥ Ç¥ÇÇ ³»¾ÏÀÇ »óŸ¦ À¯ÁöÇÏ¸ç ±âÀúÃþ¿¡ ÆÄ±«, Áõ½Ä, ÀüÀ̸¦ ³ªÅ¸³»´Â °ÍÀº »ó´çÈ÷ ÁøÇàÇÑ °æ¿ìÀÌ´Ù. Ä¡·á¹ýÀ¸·Î¼­´Â ÀýÁ¦, Ç×¾ÏÁ¦ ¿¬°í°¡ »ç¿ëµÈ´Ù. 2. ³»Àå ¾Ï°ú °ü·Ã ÀÖ´Â ºñħÀ±¼º ¾ÏÁ¾À¸·Î µå¹°°Ô ¹ß»ýÇÏ¸ç ³²¼º, ¿©¼º ¸ðµÎ ¼º±â¿¡ ¹ß»ýÇÑ´Ù. 3. »óÇdz»ÀÇ ¾Ç¼º Á¾¾çÀÌ´Ù. ¾Ç¼º ¼ºÀåÀº °Ç°­ÇÑ ±âÀú¸·°ú ÇÔ²² »óÇÇ¿¡ Á¦ÇѵȴÙ. ÇǺδ ¸î °³ÀÇ À¶±âµÈ Á¡À» µ¿¹ÝÇÑ Ã¤ ºÓ°Ô ³ªÅ¸³ª¸ç ºÎºÐÀûÀ¸·Î Àμ³ÀÌ Çü¼ºµÇ¾î ÀÖ°í ºÎºÐÀûÀ¸·Î Á¥¾î ÀÖ´Ù. Áß¾Ó¿¡ À§ÃàÀ̳ª ±Ë¾çÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù. 4. ºñ±³Àû µå¹® ÁúȯÀ¸·Î ³ëÃâ ¶Ç´Â ºñ³ëÃâ ºÎÀ§¿¡ »ý±æ ¼ö ÀÖ´Ù. º´º¯Àº ÀÛ°í
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 8
Swiss type agammaglobulinaemia Group of rare congenital disorders characterised by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an x-linked or autosomal recessive defect. About half of the patients with autosomal recessive scid are deficient in the enzyme adenosine deaminase.
(12 Dec 1998)
deoxyribonucleases, type III site-specific <enzyme> Enzyme systems composed of two subunits and requiring ATP and magnesium for endonucleolytic activity; they do not function as atpases. They exist as complexes with modification methylases of similar specificity.
The systems recognise specific short DNA sequences and cleave a short distance, about 24 to 27 bases, away from the recognition sequence to give specific double-stranded fragments with terminal 5'-phosphates. Enzymes from different microorganisms with the same specificity are called isoschizomers.
Registry number: EC 3.1.21.5
(12 Dec 1998)
deoxyribonucleases, type II site-specific <enzyme> Enzyme systems containing a single subunit and requiring only magnesium for endonucleolytic activity. The corresponding modification methylases are separate enzymes. The systems recognise specific short DNA sequences and cleave either within, or at a short specific distance from, the recognition sequence to give specific double-stranded fragments with terminal 5'-phosphates. Enzymes from different microorganisms with the same specificity are called isoschizomers.
Registry number: EC 3.1.21.4
(12 Dec 1998)
deoxyribonucleases, type I site-specific <enzyme> Enzyme systems containing three different subunits and requiring ATP, s-adenosylmethionine, and magnesium for endonucleolytic activity to give random double-stranded fragments with terminal 5'-phosphates. They function also as DNA-dependent atpases and modification methylases, catalyzing the reactions of EC 2.1.1.72 and EC 2.1.1.73 with similar site-specificity. The systems recognise specific short DNA sequences and cleave at sites remote from the recognition sequence. Enzymes from different microorganisms with the same specificity are called isoschizomers.
Registry number: EC 3.1.21.3
(12 Dec 1998)
diabetes, type 1 Insulin dependent diabetes or juvenile diabetes.
(12 Dec 1998)
diabetes, type 2 Non-insulin dependent diabetes, adult-onset diabetes or insulin-resistant diabetes.
(12 Dec 1998)
immunization, haemophilus influenzae type b See immunization, hib.
(12 Dec 1998)
influenza type a A common acute viral infection of the nasopharynx and respiratory tract which occurs in epidemic forms. A common cause is the Influenza a virus. Annual vaccination is recommended for those in high risk groups (health care workers, elderly and immunocompromised) for influenza infection.
Common symptoms include runny nose, fever, weakness, headache, body aches, muscle aches, nausea and back pain. Treatment of symptoms has been successful with amantadine or rimantadine.
(27 Sep 1997)
interferon type I <chemical> Interferon secreted by leukocytes, fibroblasts, or lymphoblasts in response to viruses or interferon inducers other than mitogens, antigens, or allo-antigens. They include alpha- and beta-interferons (interferon-alpha and interferon-beta).
Pharmacological action: antineoplastic agent, antiviral agents.
(12 Dec 1998)
interferon type II <chemical> The major interferon produced by mitogenically or antigenically stimulated lymphocytes. It is structurally different from type I interferon (interferon type I) and its major activity is immunoregulation. It has been implicated in the expression of class II histocompatibility antigens in cells that do not normally produce them, leading to autoimmune disease.
Pharmacological action: antineoplastic agent, antiviral agents.
Chemical name: Interferon-gamma (human lymphocyte protein moiety reduced)
(12 Dec 1998)
ocean-type fish An anadromous fish that shows no indication on its scales or other hard parts of an extended freshwater residence early in its life.
(09 Oct 1997)
Ellis type 1 glomerulonephritis An obsolete designation for glomerulonephritis presenting as acute glomerulonephritis, followed by complete recovery in most cases, or the development of rapidly progressive glomerulonephritis, or incomplete remission with persistent proteinuria and subsequent development of chronic glomerulonephritis.
Synonym: Ellis type 1 nephritis.
(05 Mar 2000)
Ellis type 1 nephritis An obsolete designation for glomerulonephritis presenting as acute glomerulonephritis, followed by complete recovery in most cases, or the development of rapidly progressive glomerulonephritis, or incomplete remission with persistent proteinuria and subsequent development of chronic glomerulonephritis.
Synonym: Ellis type 1 nephritis.
(05 Mar 2000)
Ellis type 2 glomerulonephritis An obsolete designation for glomerulonephritis which is usually not related to preceding bacterial infection; characterised by an insidious onset of the nephrotic syndrome, failure of complete remission, and eventual development of chronic renal failure. The kidneys usually show membranous glomerulonephritis.
Synonym: Ellis type 2 nephritis.
(05 Mar 2000)
Ellis type 2 nephritis An obsolete designation for glomerulonephritis which is usually not related to preceding bacterial infection; characterised by an insidious onset of the nephrotic syndrome, failure of complete remission, and eventual development of chronic renal failure. The kidneys usually show membranous glomerulonephritis.
Synonym: Ellis type 2 nephritis.
(05 Mar 2000)
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