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"Stickler syndrome, type II"¿¡ ´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
  • Dandy-Walker syndrome
    ´íµð-¿öÄ¿ÁõÈıº
  • dead-in-bed syndrome
    ħ´ë»ç¸ÁÁõÈıº
  • dialysis disequilibrium syndrome
    Åõ¼®ºÒ±ÕÇüÁõÈıº
  • Diamond-Blackfan syndrome
    ´ÙÀ̾Ƹóµå-ºí·¢ÆÇÁõÈıº
  • Down syndrome
    ´Ù¿îÁõÈıº
  • exfoliation syndrome
    ¹ÚÅ»ÁõÈıº
  • ectrodactyly-ectodermal dysplasia clefting syndrome
    °áÁö¿Ü¹è¿±Çü¼ºÀ̻󰥸²ÁõÈıº
  • extrapyramidal syndrome
    ÇǶó¹Ìµå¹Ù±ù±æÁõÈıº, Ãßü¿Ü·ÎÁõÈıº
  • empty nest syndrome
    ºóµÕÁöÁõÈıº
  • empty sella syndrome
    ºó¾ÈÀåÁõÈıº
  • entrapment syndrome
    Æ÷ÂøÁõÈıº
  • eosinophilia-myalgia syndrome
    È£»ê±¸Áõ°¡±Ù(À°)ÅëÁõÁõÈıº
  • epidermal nevus syndrome
    Ç¥ÇǸð¹ÝÁõÈıº
  • ectopic ACTH syndrome
    µý°÷ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸óÁõÈıº, À̼ҼººÎ½ÅÇÇÁúÀÚ±ØÈ£¸£¸óÁõÈıº
  • facet syndrome
    ÈİüÀýÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
  • concentration camp syndrome
    ¼ö¿ë¼ÒÁõÈıº
  • congenital constriction ring syndrome
    ¼±ÃµÇùÂø°í¸®ÁõÈıº
  • cor pulmonale syndrome
    Æó½ÉÀåÁõÈıº, ÇãÆÄ½ÉÀåÁõÈıº
  • cord compression syndrome
    ô¼ö¾Ð¹ÚÁõÈıº
  • cranial nerve syndrome
    ³ú½Å°æÁõÈıº
  • craniofacial syndrome
    ¸Ó¸®¾ó±¼ÁõÈıº
  • cri du chat syndrome
    (¢¡cat¡¯s cry) °í¾çÀÌ¿ïÀ½ÁõÈıº
  • cubital tunnel syndrome
    ÆÈ²ß±¼ÁõÈıº
  • culture-bound syndrome
    ¹®È­±ÇÁõÈıº
  • defibrination syndrome
    Å»¼¶À¯¼ÒÁõÈıº
  • deficit syndrome
    °áÇÌÁõÈıº
  • delayed sleep phase syndrome
    ¼ö¸éÀ§»óÁö¿¬ÁõÈıº
  • depersonalization-derealization syndrome
    ÀÌÀκñÇö½Ç°¨ÁõÈıº
  • discontinuation syndrome
    ºÒ¿¬¼ÓÁõÈıº
  • dissociation syndrome
    ÇØ¸®ÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Conradi-Hunermann syndrome => chondrodysplasia punctata, autosomal dom
    »ó¿°»öü ¿ì¼ºÇü Á¡»ó¿¬°ñ ÀÌÇü¼º
  • Costens syndrome
    ÄÚ½ºÅÙ ÁõÈıº
  • Cotards syndrome
    ÄÚŸ¸£ÁõÈıº.
  • Cri du chat syndrome ºÒ
    ¹¦¼ºÁõÈıº.
  • Cronkhite Canada syndrome
    Å©·ÐÄ«ÀÌÆ® Ä«³ª´Ù ÁõÈıº
  • Crouzon syndrome
    Å©·ÎÁ¸ ÁõÈıº
  • Crouzons syndrome = craniofacial dysostosis
    µÎ°³¾ó±¼ À̰ñÁõ
  • Crouzons syndrome=>craniofacial dysostosis
    Å©·çÁ¸ÁõÈıº
  • Cushing syndrome
    Äí½ÌÁõÈıº
  • Cushing syndrome
    Äí½Ì ÁõÈıº
  • Cushingoid syndrome
    Äí½Ì¾çÁõÈıº.
  • Cushings syndrome
    Äí½ÌÁõÈıº.
  • Cushings syndrome
    Äí½ÌÁõÈıº
  • DaCostas syndrome
    ´ÙÄÚ½ºÅ¸ ÁõÈıº(~ñøý¦ÏØ)
  • De Sanctis-Caccione syndrome = xerodermic idiocy
    °ÇÇǼº ¹éÄ¡
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
  • ¿µ¹®
    ÇѱÛ
  • phased linear array type
    À§»óÂ÷ ¼±Çü ¹è¿­½Ä
  • phthisic type
    ³ëÁõº¸Çü( ñøÜÁúþ).
  • phthisic type
    ³ëÁõº¸Çü(Ò¾ñøÜÁúþ)
  • pilus, type 1
    Á¦1Çü ¼¶¸ð
  • plaque-type mutation
    ÇöóÅ©Çü µ¹¿¬º¯ÀÌ
  • platelet-type
    Ç÷¼ÒÆÇÇü(û¡)
  • pneumocyte type i
    È£ÈíÇãÆÄ²Ê¸®¼¼Æ÷
  • pneumocyte type ii
    °ú¸³ÇãÆÄ²Ê¸®¼¼Æ÷
  • precision type attachment
    Á¤¹ÐÇü¾îÅÂÄ¡ ¸ÕÆ®.
  • propagative type
    Áõ½ÄÇü(Ì¡ËàÌ´).
  • protease inhibitor type
  • pseudorabies virus (Suid herpesvirus type 1)
    ½´µµ·¹À̺ñ½º¹ÙÀÌ·¯½º (Á¦1Çü µÅÁö Ç츣Æä½º¹ÙÀÌ·¯½º, ¿¾ Herpesvirus suis)
  • pyknic body type
    ºñ¸¸Çü ½ÅüÀ¯Çü
  • regular type
    ±ÔÄ¢Çü
  • repository type of penicillin
    ÀúÀåÇü(îÍíúû¡) Æä´Ï½Ç¸°.
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
SFB Sanfilippo syndrome type B; saphenofemoral bypass; surgical foreign body
TC target cell; taurocholate; temperature compensation; teratocarcinoma; tertiary cleavage; tetracyclin...
WSI Waardenburg syndrome type I
ADS acute death syndrome; acute diarrheal syndrome; Alcohol Dependence Scale; alternative delivery syste...
AIS Abbreviated Injury Scale; amniotic infection syndrome; androgen insensitivity syndrome; anterior int...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 9
AT(1)R Angiotensin type 1 receptor
AT(2) Angiotensin type 2
Anti-HIV-1 Anti-human immunodeficiency virus type 1
HIV-1 Anti-human immunodeficiency virus type 1
B-CLL B cell Type
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • Ashermans syndrome
    ¾Æ¼Å¸¸ ÁõÈıº
    Àڱó» ¿ìÂø¿¡ ÀÇÇÏ¿© Áö¼Ó¼º ¹«¿ù°æ°ú ÀÌÂ÷¼º ºÒÀÓÀÌ ³ªÅ¸³ª´Â °Í. º¸Åë Àڱó» ¼ÒÆÄÀÇ °á°ú·Î ÀϾ´Ù.
  • atypical or mixed organic brain syndrome
    ºñÁ¤Çü ³»Áö È¥ÇÕÇü ±âÁú¼º ³ú ÁõÈıº
  • atypical schizophrenic syndrome
    ºñÁ¤Çü Á¤½ÅºÐ¿­¼º ÁõÈıº
  • autoerythrocyte sensitization syndrome
    ÀÚ°¡ ÀûÇ÷±¸ °¨ÀÛ ÁõÈıº
    ÁÖ·Î ÀþÀº ¿©ÀÚ¿¡°Ô º¼ ¼ö ÀÖ´Â ÀÚ¹Ý ¹ÝÀÀÀÇ ÀÏÁ¾À¸·Î ¿Ü»ó ¾øÀÌ ¶Ç´Â ºÒ¿ÏÀü ¿Ü»ó ÈÄ ½Åü¿¡ ÀÚ¿¬ÀûÀ¸·Î µ¿ÅëÀ» µ¿¹ÝÇÏ°í ¹Ýº¹ÇÏ¿© ´Üµ¶ ¶Ç´Â ´Ù¹ß¼º ¹Ý»ó ÃâÇ÷ÀÌ ³ªÅ¸³­´Ù. ¸¹Àº Áõ·Ê¿¡¼­ ÀûÇ÷±¸ ±¸¼º ¼ººÐ¿¡ ´ëÇÑ °ú¹Î¼ºÀÌ ¿øÀÎÀ¸·Î »ý°¢µÇ³ª, ¹éÇ÷±¸°¡ ¿øÀÎÀ¸·Î »ý°¢µÇ´Â ¿¹µµ ÀÖ´Ù. Á¤¼­Àû Àå¾Ö°¡ ¹ßº´ °á½Ç ÀÎÀÚ·Î º¸ÀδÙ.
  • Axenfeld syndrome
    ¾Ç¼¾ÆçÆ® ÁõÈıº
  • B-K mole syndrome
    B-K ¸ð¹Ý ÁõÈıº
  • Barters syndrome
    ¹ÙÅÍ ÁõÈıº
  • basal ganglion calcification syndrome
    ±âÀú ½Å°æÀý ¼®È¸È­ ÁõÈıº
  • battered child syndrome
    ÇÇÇÐ´ë¾Æ ÁõÈıº, ¾Æµ¿ Çдë ÁõÈıº, ¼Ò¾Æ Çдë ÁõÈıº
    ¾Æµ¿ÀÇ »À ¹× ¿¬ºÎ Á¶Á÷¿¡ ´Ù¼öÀÇ ¿Ü»ó¼º º´º¯À» ³ªÅ¸³»´Â °ÍÀ¸·Î¼­ Á¾Á¾ °æ¸·ÇÏ Ç÷Á¾À» ¼ö¹ÝÇÑ´Ù. ÀÌ·± º´º¯Àº º¸Åë ¼ºÀÎÀÇ °íÀÇÀûÀÎ °¡ÇØ¿¡ ÀÇÇØ »ý±ä´Ù. ºÎ¸ðµéÀÌ 3¼¼ ÀÌÇÏ Æ¯È÷ 1¼¼ ÀÌÇÏÀÇ À¯¾Æ¸¦ ¹«ºÐº°ÇÏ°Ô ¶§¸®°Å³ª ±âŸ ¹æ¹ýÀ¸·Î ÇдëÇÔÀ¸·Î½á ÀϾ´Â ½Åü Áõ»ó. ¹Ì±¹ÀÇ ¼Ò¾Æ°ú ÀÇ»ç H. ÄÍÇÁ µîÀÌ ¹Ì±¹ Àü¿ª¿¡ °ÉÃÄ Á¶»çÇÏ¿´À¸¸ç, 1962³âÀÌ·¡ ¼±Áø Á¦±¹¿¡ ³Î¸® ¾Ë·ÁÁø Çö»óÀÌ´Ù. ÁÖ·Î, ¨ç ÇÇÇÏ ÃâÇ÷, Àý»ó, È­»ó µîÀÇ ÇǺΠÁõ¼¼, ¨è Àü½ÅÀÇ °ñÀý, Å»±¸, ¨é µÎ°³³» ÃâÇ÷À̳ª °æ¸·ÇÏÇ÷Á¾, ¨ê Àå±â ÆÄ¿­ ¹× ³»ÃâÇ÷ µî º¹ºÎÀÇ ¼Õ»ó, ¨ë ¼ºÀå ¹ß´Þ ÀåÇØ µîÀ» º¼ ¼ö ÀÖ´Ù. À̰ÍÀº ¿À´Ã³¯ÀÇ ¼±Áø Á¦±¹ÀÇ ±Þ¼ÓÇÑ °¡Á¤ ºØ±« Çö»ó°ú °ü·ÃÇÏ¿© ÀϾ´Â Áõ¼¼ÀÌ´Ù. ºÎºÎ°£ÀÇ °¥µîÀÌ ±Ø½ÉÇØÁö¸é À̵éÀº ¼­·Î °£ÆíÇÏ°Ô Çì¾îÁ®¾ß ÇÑ´Ù°í »ý°¢Çϰí À̶§ ¾î¸°¾ÆÀ̵éÀÌ Àå¾Ö¹°À̶ó ¹Ï°Ô µÇ¾î ¾Æ¹« ÁË ¾ø´Â ¾ÆÀ̵éÀ» ¸¶±¸ ÆøÇàÇÏ´Â µîÀÇ ÇдëÇàÀ§°¡ ³ªÅ¸³­´Ù. Çд븦 °¡ÇÏ´Â ºÎ¸ðµéÀº Á¤¼­ÀûÀ¸·Î ¹Ì¼÷ÇÑ È÷½ºÅ׸® ¼º°ÝÀÚ, ¼ºÀû ºÒ°¨Áõ, °ø°Ý¼º ¼º°ÝÀÚ, ¾ËÄÚ¿Ã Áßµ¶ÀÚ, ¸Á»óÇüÀÇ Á¤½ÅºÐ¿­Áõ ȯÀÚ µî¿¡¼­ º¼ ¼ö ÀÖ´Ù. À̶§ Çд븦 ¹ÞÀº ¾ÆÀ̵éÀº Á¤½Å ¹ß´Þ Àå¾ÖÁõ, ¹ÝÇ×Àû ¼º°Ý, °íÁýÀÌ ¼¾ Ç×¹®±âÀû °íÂøÁõ µîÀÇ Æ¯Â¡À» ³ªÅ¸³½´Ù. ÀÌ·¯ÇÑ Çö»óÀº Çѱ¹ÀÇ »çȸ ¹®È­¿¡¼­´Â ¾ÆÁ÷ Èñ±ÍÇÏÁö¸¸ ±Ù´ëÈ­, ÇÙ°¡Á·È­, ¿©±ÇÀÇ ½ÅÀå, ¾ËÄÚ¿Ã Àα¸ÀÇ Áõ°¡, »çȸÀû ½ºÆ®·¹½º ¿äÀÎÀÇ Áõ´ë·Î Á¡Á¡ Áõ°¡µÈ´Ù.
  • Bechet syndrome
    º£Ã¼Æ® ÁõÈıº
    º£Ã¼Æ® ÁõÈıºÀº ¹Ýº¹µÇ´Â ±¸°­ ¹× ¼º±âÀÇ ±Ë¾ç°ú ´« ¹× ÇǺΠµîÀ» ħ¹üÇÏ´Â ¿©·¯ ±â°ü¿¡ ¿À´Â ÁúȯÀÌ´Ù. ¾ÆÁ÷±îÁö È®½ÇÇÑ ¿øÀÎÀº ¸ð¸£Áö¸¸ Ç÷°ü¿°ÀÌ ÁÖµÈ º´¸® ¼Ò°ßÀ̰í ÀÚ°¡ Ç×ü°¡ 50%¿¡¼­ ÃâÇöÇÏ´Â °ÍÀ¸·Î º¸¾Æ¼­ ÀÚ°¡¸é¿ª ÁúȯÀÇ Çϳª¶ó°í »ý°¢Çϰí ÀÖ´Ù. Áõ»óÀÇ Á¤µµ´Â ½Ã°£ÀÌ °¡¸é ´úÇØÁö°í ½ÉÇÑ ÇÕº´ÁõÀÌ ¾ø´Â ÇÑ ¼ö¸í°ú´Â °ü°è°¡ ¾ø´Ù. ±×·¯³ª Ä¡·á´Â Ưº°ÇÑ °ÍÀÌ ¾ø°í ´ëÁõÀûÀÌ°í °æÇèÀûÀÎ Ä¡·á¸¦ ÇϰԵǾî Áõ»ó¿¡ µû¶ó¼­
  • Behcet's syndrome
    º£Ã¼Æ® ÁõÈıº, Behcet ÁõÈıº
    ±¸°­, ´«, ¼º±âÀÇ º´¼Ò°¡ Ư¡ÀΠƯ¹ß¼º Áúȯ. ´«¿¡¼­ º¼ ¼ö ÀÖ´Â ¼Ò°ßÀº Æ÷µµ¸·¿°, ¸Á¸·¿° ¹× °á¸·¿°À̰í, ¼º±â¿¡ ³ªÅ¸³ª´Â ¼Ò°ßÀº ´ë°³°¡ ÇÇºÎ¿Í Á¡¸·ÀÇ ±Ë¾çÀ̸ç, ±¸°­¿¡ ³ªÅ¸³ª´Â ¼Ò°ßÀº À¯»ç ¾ÆÇÁŸ¼º ±Ë¾çÀÌ´Ù. Áø´ÜÀº ÀÓ»ó ¼Ò°ß¿¡ ±Ù°ÅÇÑ´Ù. Ä¡·á¿¡´Â Àü½Å¼º ÄÚ¸£Æ¼ÄÚ½ºÅ×·ÎÀ̵å Åõ¿©¸¦ ÀÌ¿ë. À¯ÀüÀû ¿ä¼Ò°¡ ÀÖ´Ù°í º¸°íµÇ°í ÀÖ´Ù.
  • big heart syndrome
    °Å½É ÁõÈıº
  • black cardiac syndrome
    Èæ½ÉÀå ÁõÈıº
  • Boerhaave syndrome
    ºÆ¸£ÇϺ£ ÁõÈıº
    ±¸Åä·Î ÀÎÇØ ½ÄµµÀÇ ÀÚ¿¬ÀûÀÎ ÆÄ¿­À» ¸»Çϴµ¥ µ¿Åë°ú ¹ß¿­À» ¼ö¹ÝÇÑ °ß°©°ñ¾È ȤÀº Èä°ñÇÏ µ¿ÅëÀ» È£¼ÒÇÏ°í ¼îÅ© »óŰ¡ ¹ß»ýÇϱ⵵ ÇÑ´Ù. ±¤¹üÀ§ÇÑ ±«»ç¼º Á¾°Ýµ¿¿°Àº ÆíÃø ȤÀº ¾çÃø¼º ³óÈäÀ» ÃÊ·¡½Ã۱⵵ ÇÏ¿© 24~48½Ã°£³» »ç¸Á½Ã۱⵵ ÇÑ´Ù. ÀÓ»ó Áõ»óÀº ÈäºÎ X-¼± »çÁø»ó °æºÎ Á¶Á÷¸é°ú Á¾°Ýµ¿³» °ø±â°¡ ³ªÅ¸³ª°í Á¾°Ýµ¿ »óÀÌ È®´ëµÇ°í Á¾°Ýµ¿¿¡ ¾×¸é»ó°ú µå¹°°Ô ½É³¶°ú ÅëÇØ ½É³¶³» ¾×¸é»óÀÌ º¸À̱⵵ ÇÑ´Ù. ½Äµµ Á¶¿µ¼úµµ Áø´ÜÀÌ °¡´ÉÇÏ¸é °¡´ÉÇÑ ÇÑ ºü¸¥ Áø´Ü°ú Ä¡·á¸¸ÀÌ È¯ÀÚÀÇ »ýÁ¸À²À» ³ôÀÏ ¼ö ÀÖ´Ù.
  • bottle mouse syndrome
    ¿ìÀ¯º´ ¿ì½Ä
    Àå½Ã°£ ¿ìÀ¯¸¦ ¹°°í ÀÖ´Â À¯¾Æ¿¡ È£¹ß, ÇÏ¾Ç ÀýÄ¡¿¡´Â ¿ì½ÄÁõÀÌ ¾ø´Ù.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 9
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)
Ellis type II <nephrology> A type of nephritis that is characterised by low serum albumin, large amount of protein in the urine and swelling (oedema). Swelling, weight gain, high blood pressure and anorexia are key features. Nephrotic syndrome can be seen with a number of illness that cause damage to the kidney glomerulus.
Examples include diabetes, hereditary disorders, lupus, multiple myeloma, amyloidosis, glomerulonephritis, minimal change disease and membranous glomerulonephritis.
(27 Sep 1997)
erotomanic type of paranoid disorder The false belief that one is loved by another such as a movie star or a casual acquaintance.
(05 Mar 2000)
tuberculin-type hypersensitivity A local or generalised response that begins 24 to 48 hours after exposure to an antigen.
See: cell-mediated reaction.
Synonym: contact hypersensitivity, delayed hypersensitivity, late reaction, tuberculin-type hypersensitivity.
(05 Mar 2000)
jealous type of paranoid disorder The false belief that one's spouse or lover is unfaithful and leading to repeated confrontation, or the taking of extraordinary steps to intervene in the imagined infidelity.
(05 Mar 2000)
type 1. The mark or impression of something; stamp; impressed sign; emblem.
2. Form or character impressed; style; semblance.
3. A figure or representation of something to come; a token; a sign; a symbol; correlative to antitype.
4. That which possesses or exemplifies characteristic qualities; the representative.
<biology> Specifically: A general form or structure common to a number of individuals; hence, the ideal representation of a species, genus, or other group, combining the essential characteristics; an animal or plant possessing or exemplifying the essential characteristics of a species, genus, or other group. Also, a group or division of animals having a certain typical or characteristic structure of body maintained within the group.
<chemistry> A simple compound, used as a mode or pattern to which other compounds are conveniently regarded as being related, and from which they may be actually or theoretically derived.
The fundamental types used to express the simplest and most essential chemical relations are hydrochloric acid, HCl; water, H2O; ammonia, NH3; and methane, CH4.
5. A raised letter, figure, accent, or other character, cast in metal or cut in wood, used in printing. Such letters or characters, in general, or the whole quantity of them used in printing, spoken of collectively; any number or mass of such letters or characters, however disposed.
Origin: F. Type; cf. It. Tipo, from L. Typus a figure, image, a form, type, character, Gr. The mark of a blow, impression, form of character, model, from the root of to beat, strike; cf. Skr. Tup to hurt.
Source: Websters Dictionary
(01 Mar 1998)
type 1 dextrocardia Displacement of the heart to the right side of the chest with mirror transposition of the cardiac chambers together with transposition of the abdominal viscera.
Synonym: type 1 dextrocardia.
(05 Mar 2000)
type 1 diabetes <endocrinology> Also referred to as juvenile onset diabetes. Underlying cause is likely genetic. Usually treated with daily insulin dosing. Insulin is necessary for the body to properly utilise glucose. Without insulin, glucose accumulates in the bloodstream.
(27 Sep 1997)
type 1 glycogenosis Glycogenosis due to glucose-6-phosphatase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure, particularly in liver and kidney.
Synonym: Gierke's disease, glucose-6-phosphatase hepatorenal glycogenosis, von Gierke's disease.
(05 Mar 2000)
Type 1 GM1 gangliosidosis One of the hereditary metabolic diseases of infancy; resembles Tay-Sachs disease, except other organ systems (bone, liver, kidney) are affected.
Synonym: familial neuroviscerolipidosis, pseudo-Hurler disease, Type 1 GM1 gangliosidosis.
(05 Mar 2000)
type 2 astrocyte <pathology> A glial cell found in vertebrate brain, named for its characteristic star like shape.
Astrocytes lend both mechanical and metabolic support for neurons, regulating the environment in which they function.
See: oligodendrocytes.
(18 Nov 1997)
type 2 dextrocardia Dextrocardia with mirror transposition of the cardiac chambers but without displacement of the abdominal viscera.
Synonym: type 2 dextrocardia.
(05 Mar 2000)
type 2 diabetes <endocrinology> Also referred to as adult-onset diabetes. More common in the middle-age, overweight individual. Usually treated by diet control, weight reduction or oral hypoglycemic agents.
(27 Sep 1997)
type 2 glycogenosis Glycogenosis due to lysosomal alpha-1,4-glucosidase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure in heart, muscle, liver, and nervous system.
Synonym: generalised glycogenosis, Pompe's disease.
(05 Mar 2000)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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  • Á¦Ç°¸í
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    ±¸ºÐ/º¸Çè±Þ¿©
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  • Á¦Ç°¸í
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