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  • deficiency (nanismus)
    °áÇÌ(³­ÀåÀÌÁõ)
  • diabetes mellitus,insulin deficiency
    Àν¶¸° °áÇÌÁõ(¡­ÌÀù¹ñø)
  • dietary deficiency
    ½ÄÀ̼º ¿µ¾ç°áÇÌ(½ÄÀ̼º¿µ¾ç°áÇÌ).
  • dietary deficiency
    ½ÄÀ̼º ¿µ¾ç°áÇÌ(ãÝìÈàõç½å×ÌÀù¹).
  • diphosphatase deficiency
    µðÆ÷½ºÆÄŸÁ¦°áÇÌ(Áõ)
  • disaccaridase deficiency
    ÀÌ´çºÐÇØÈ¿¼Ò°áÇÌ(ì£ÓØÝÂú°ý£áÈÌÀù¹)
  • disaccharidase deficiency
    ÀÌ´ç·ùºÐÇØÈ¿¼Ò°áÇÌÁõ
  • disaccharide deficiency
    ÀÌź´ç°áÇÌ
  • dissacharidase deficiency syndrome
    ÀÌ´ç·ùºÐÇØÈ¿¼Ò °áÇÌÁõÈıº(¡­ÌÀù¹ñøý¦ÏØ ).
  • electrolyte deficiency syndrome
    ÀüÇØÁú °áÇÌÁõÈıº(ï³ú°òõÌÀù¹ñøý¦ÏØ).
  • enzyme deficiency
    È¿¼Ò°áÇÌ(Áõ)
  • erythrocyte enzyme deficiency
    ÀûÇ÷±¸È¿¼Ò°áÇÌÁõ
  • erythropoietin deficiency anemia
    ¿¡¸®Æ®·ÎÆ÷¿¡Æ¾ °áÇ̼º ºóÇ÷, ÀûÇ÷
  • factor deficiency
    Á¦ÀÎÀÚ°áÇÌÁõ(ð¯ì×í­ÌÀù¹ñø).
  • factor ix deficiency
    Á¦9ÀÎÀÚ °áÇÌ(Áõ)
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SSPG steady state plasma glucose
SSPI steady state plasma insulin
SS-PSE Schizophrenic Subscale of the Present State Examination
STAI State Trait Anxiety Inventory
STIC Science and Technology Information Center; serum trypsin inhibition capacity; solid-state transducer...
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LPD Luteal phase deficiency
MPHD Multiple Pituitary Hormone Deficiency
MSD Multiple Sulfatase Deficiency
MAIDS Murine acquired immune deficiency syndrome
NOD/SCID Nonobese diabetic/severe combined immune deficiency
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leukocyte adhesion deficiency An inherited disorder (autosomal recessive) in which there is a defective CD18 adherence complex that disturbs leukocyte chemotaxis. It is characterised by recurrent bacterial infections and impaired wound healing.
(05 Mar 2000)
leukocyte-adhesion deficiency syndrome <syndrome> Rare, autosomal recessive disorder caused by deficiency of the beta 2 integrin receptors (receptors, leukocyte-adhesion) comprising the CD11/CD18 family of glycoproteins. The syndrome is characterised by abnormal adhesion-dependent functions, especially defective tissue emigration of neutrophils, leading to recurrent infection.
(12 Dec 1998)
lipoprotein lipase deficiency, familial A rare familial condition characterised by massive chylomicronaemia and decreased levels of other lipoproteins. It is due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyses an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood.
(12 Dec 1998)
luteal phase deficiency Inadequate function of the corpus luteum that may prevent a fertilized egg from implanting in the uterus or may lead to early pregnancy loss.
(09 Oct 1997)
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