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  • ¿µ¹®
    ÇѱÛ
  • defect rate
    °áÇÔ·ü
  • differentiation defect
    ºÐÈ­°áÇÔ
  • endocardial cushion defect
    ½É(Àå)³»¸·À¶±â°á¼Õ
  • field defect
    ½Ã¾ß°á¼Õ
  • filling defect
    Ãæ¸¸°á¼Õ
  • fusion defect
    À¶ÇÕ°áÇÔ
  • gene defect
    À¯ÀüÀÚ°á¼Õ
  • genetic defect
    À¯Àü°á¼Õ
  • growth defect
    ¼ºÀå°áÇÔ
  • hearing defect
    û°¢Àå¾Ö
  • heritable defect
    À¯Àü°áÇÔ
  • incongruous field defect
    ºÒÀÏÄ¡½Ã¾ß°á¼Õ
  • interatrial septal defect
    ½É¹æ»çÀ̸·°á¼Õ, ½É¹æÁ߰ݰá¼Õ
  • interventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • luteal phase defect
    Ȳ(»ö)ü±â°á¼Õ
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  • ¿µ¹®
    ÇѱÛ
  • conduction defect
    ÀüµµÀå¾Ö
  • congenital defect
    ¼±Ãµ°áÇÔ, ¼±Ãµ°á¼Õ(Áõ)
  • congruous field defect
    ÀÏÄ¡½Ã¾ß°áÇÔ
  • conjunction defect
    °áÇÕ°áÇÔ
  • cortical sensory defect
    °ÑÁú°¨°¢°á¼Õ
  • defect
    °áÇÔ, °á¼Õ(Áõ)
  • defect rate
    °áÇÔ·ü
  • differentiation defect
    ºÐÈ­°áÇÔ
  • endocardial cushion defect
    ½ÉÀå³»¸·À¶±â°á¼Õ
  • field defect
    ½Ã¾ß°á¼Õ
  • fusion defect
    À¶ÇÕ°áÇÔ
  • gene defect
    À¯ÀüÀÚ°á¼Õ
  • genetic defect
    À¯Àü°áÇÔ
  • growth defect
    ¼ºÀå°áÇÔ
  • hearing defect
    û°¢Àå¾Ö
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  • ¿µ¹®
    ÇѱÛ
  • gene defect
    À¯ÀüÀÚ°á¼Õ<--°á¿©>
  • genetic defect
    À¯ÀüÀû °áÇÔ(¡­ÌÀùè).
  • genetic defect
    À¯ÀüÀÚ°áÇÔ
  • genetic defect
    À¯ÀüÀû °áÇÔ.
  • growth defect
    ¼ºÀå°áÇÔ
  • hearing defect
    û·ÂÀå¾Ö
  • heart defect
    ½ÉÀå°áÇÔ
  • heart septal defect
    ½ÉÁ߰ݰá¼Õ(Áõ)(ãýñḛ́ÌÀáßñø).
  • heritable defect
    À¯Àü°áÇÔ
  • high ventricular septal defect
    °íÀ§½É½ÇÁ߰ݰá¼Õ.
  • placental defect
    ŹݰáÇÔ
  • plication defect
    ÁÖ¸§Çü¼º°áÇÔ
  • plication defect (schistomyelia)
    ÁÖ¸§Çü¼º°áÇÔ (ô¼ö°¥¸²Áõ)
  • postnatal defect
    Ãâ»ýÀÌÈİáÇÔ
  • prenatal defect
    Ãâ»ýÀÌÀü°áÇÔ
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  • ¿µ¹®
    ÇѱÛ
  • platelet sequestration
    Ç÷¼ÒÆÇ°Ý¸®(̰×î)
  • platelet survival measurement
    Ç÷¼ÒÆÇ»ýÁ¸´ÉÃøÁ¤
  • platelet transfusion
    Ç÷¼ÒÆÇ¼öÇ÷
  • platelet transfusion
    Ç÷¼ÒÆÇ¼öÇ÷(¡­âÃúì).
  • platelet,adhesion
    À¯Âø(ë¨ó·),ºÎÂø(ݾó·),Á¢Âø(ïÈó·)
  • platelet,aggregation
    ÀÀÁý(ëêó¢), ÀÀ±«(ëêÎÔ)
  • platelet-activating factor (PAF)
    Ç÷¼ÒÆÇ Ȱ¼ºÈ­ÀÎÀÚ
  • platelet-activating factor (paf)
    Ç÷¼ÒÆÇȰ¼ºÈ­ÀÎÀÚ(úìá³÷ùüÀàõûùì×í­)
  • platelet-derived growth factor
    Ç÷¼ÒÆÇÀ¯·¡ Áõ½ÄÀÎÀÚ
  • platelet-derived growth factor(PDGF)
    Ç÷¼ÒÆÇ À¯·¡ ¼ºÀå ÀÎÀÚ
  • platelet-derived growth factor(pdgf)
    ÆÇ-À¯µµ¼ºÀåÀÎÀÚ(úìá³÷ù-ë¯Óôà÷íþì×í­)
  • platelet-specific antigens
    Ç÷¼ÒÆÇƯÀÌÇ׿ø
  • platelet-type
    Ç÷¼ÒÆÇÇü(û¡)
  • therapeutic platelet-leukapheresis
    Ä¡·áÀû Ç÷¼ÒÆÇ¹éÇ÷±¸¼ººÐäÁý¼ú
  • thrombocyte [blood platelet]
    Ç÷¼ÒÆÇ
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    ÇѱÛ
  • Synthesis defect (Tyrosinosis)
    ÇÕ¼º°áÇÔ (ŸÀ̷νÅÁõ)
    [¿¾ ¿ë¾î] ÇÕ¼º°áÇÔ
  • Morphologic defect
    ÇüŰáÇÔ
    [¿¾ ¿ë¾î] ÇüÅÂÇÐÀû°áÇÔ
  • Contents defect
    ³»¿ë°áÇÔ
    [¿¾ ¿ë¾î] ³»¿ë°áÇÔ
  • Growth defect
    ¼ºÀå°áÇÔ
    [¿¾ ¿ë¾î] ¼ºÀå°áÇÔ
  • Defect of nose
    ÄÚ°áÇÔ
    [¿¾ ¿ë¾î] ºñ°áÇÔ
  • Defect of blood vessel
    Ç÷°ü°áÇÔ
    [¿¾ ¿ë¾î] Ç÷°ü°áÇÔ
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APSD aorticopulmonary septal defect
AREDYLD acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes [syndrome]
AVSD atrioventricular septal defect
COVESDEM costovertebral segmentation defect with mesomelia [syndrome]
CSD carotid sinus denervation; cat scratch disease; combined system disease; conditionally streptomycin ...
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HIV/AIDS Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome
MAIDS Murine acquired immune deficiency syndrome
AIDS Non-acquired immunodeficiency syndrome
NHAP Nursing Home-Acquired Pneumonia
PAM Primary acquired melanosis
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    ÇѱÛ
    ¼³¸í
  • congenital defect
    ¼±Ãµ¼º °á¼Õ, ¼±Ãµ¼º °á¼ÕÁõ, ¼±ÃµÀû °á¼Õ
  • congenital heart defect
    ¼±Ãµ¼º ½É³» °á¼ÕÁõ
  • defect
    °á¼Õ, °á¿©, ±âÇü, °áÇÔ, ºÎÀü, ºÎÀç, ¼Õ»ó
  • ectodermal defect
    ¿Ü¹è¿± °á¼Õ, ¿Ü¹è¿± °á¼ÕÁõ
  • enzymatic defect
    È¿¼Ò °á¼ÕÁõ, È¿¼Ò °á¼Õ
  • filling defect
    Ãæ¸¸ °á¼Õ
  • hearing defect
    û·Â Àå¾Ö
    ºÎºÐÀûÀ¸·Î ȤÀº ¿ÏÀüÈ÷ µé¸®Áö ¾Ê´Â °Í.
  • heart septal defect
    ½É Áß°Ý °á¼Õ, ½É Áß°Ý °á¼ÕÁõ
  • interventricular septal defect
    ½É½Ç Áß°Ý °á¼ÕÁõ
  • metabolic defect of amino acid
    ¾Æ¹Ì³ë»ê ´ë»ç °áÇÔ
    ¾Ëİſ ´¢Áõ.
  • metabolic defect of pigment
    »ö¼Ò ´ë»ç °áÇÔ
  • morphologic defect
    ÇüÅ °áÇÔ
  • ostium primum atrial septal defect
    ÀÏÂ÷ °øÇü ½É¹æ Áß°Ý °á¼Õ
  • paraplacental chorionic defect
    ÅÂ¹Ý °ç À¶¸ð¸· °áÇÔ
  • perceptual defect
    Áö°¢ °á¼Õ
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relative afferent pupillary defect An asymmetry of the pupillomotor input between the two eyes; tested by alternating the light from one eye to the other and comparing the direct light reactions.
(05 Mar 2000)
metaphysial fibrous cortical defect A small (less than 2 to 3 cm in diameter) fibrous cortical d.
(05 Mar 2000)
complete endocardial cushion defect <radiology> Arteriovenous canal components: low atrial septal defect (ostium primum), high VSD, cleft anterior leaflet of mitral valve, cleft septal leaflet of tricuspid valve, one AV valve common to RV and LV with 5-6 leaflets findings: 4-chamber enlargement (R greater than L), mitral insufficiency, associated with congestive heart failure and Eisenmenger syndrome, gooseneck deformity on angiogram (elongation and narrowing of the LV outflow tract during diastole) see also: endocardial cushion defect, partial endocardial cushion defect
(12 Dec 1998)
congenital defect A birth defect.
(12 Dec 1998)
congenital ectodermal defect Incomplete development of the epidermis and skin appendages; the skin is smooth and hairless, the facies abnormal, and the teeth and nails may be affected; sweating may be deficient.
Synonym: congenital ectodermal dysplasia.
(05 Mar 2000)
coupling defect See: familial goiter.
(05 Mar 2000)
postinfarction ventricular septal defect A defect developed in the ventricular septum resulting from rupture of an acute myocardial infarction.
(05 Mar 2000)
salt-losing defect Renal tubular abnormality causing loss of sodium in the urine.
(05 Mar 2000)
septal defect, atrial A hole in the septum, the wall, between the atria, the upper chambers of the heart. Commonly called an asd. Asds are a major class of heart deformity that is present at birth (congenital cardiac malformation).
(12 Dec 1998)
septal defect, ventricular A hole in the interventricular septum, the wall between the ventricles, the lower chambers of the heart. Commonly called a vsd. Vsds are a common class of heart deformity that is present at birth (congenital cardiac malformation).
(12 Dec 1998)
neural tube defect <neurology, paediatrics> Abnormal development during embryonic life of the neural tube producing congenital malformations of the nervous system due to closure failure of the neural tube.
The structure gives rise to the central nervous system (the brain and spinal cord), and failure to close results in anencephaly (absence of the cranial vault and absence of most or all of the cerebral hemispheres of the brain) and spina bifida or meningomyelocele (open spina with exposure and protusion of the spinal cord).
The risk of neuroal tube defects can be decreased by the mother taking folic acid during pregnancy.
(04 Jul 1999)
defect 1. Want or absence of something necessary for completeness or perfection; deficiency; opposed to superfluity. "Errors have been corrected, and defects supplied." (Davies)
2. Failing; fault; imperfection, whether physical or moral; blemish; as, a defect in the ear or eye; a defect in timber or iron; a defect of memory or judgment. "Trust not yourself; but, your defects to know, Make use of every friend any every foe." (Pope) "Among boys little tenderness is shown to personal defects." (Macaulay)
Synonym: Deficiency, imperfection, blemish. See Fault.
Origin: L. Defectus, fr. Deficere, defectum, to desert, fail, be wanting; de- + facere = to make, do. See Fact, Feat, and cf. Deficit.
Source: Websters Dictionary
(01 Mar 1998)
defect, atrial septal A hole in the septum, the wall, between the atria, the upper chambers of the heart. Commonly called an ASD. ASDs are a major class of congenital cardiac malformation.
(12 Dec 1998)
defect, enzyme An abnormality in the protein (enzyme) important in catalyzing a normal biochemical reaction in the body. Disorders result from a deficiency (or functional abnormality) of an enzyme. Archibald Garrod in 1902 was the first to attribute a disease to an enzyme defect: an inborn error of metabolism. Today, newborns are routinely screened for certain enzyme defects such as phenylketonuria (PKU) and galactosaemia, an error in the handling (metabolism) of the sugar galactose.
(12 Dec 1998)
defect, ventricular septal Hole in the interventricular septum, the wall between the ventricles (lower chambers of the heart). Commonly called a VSD. VSDs are a common class of heart deformity present at birth (congenital cardiac malformation).
(17 Dec 1998)
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