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  • ¿µ¹®
    ÇѱÛ
  • conjunction defect
    °áÇÕ°áÇÔ
  • cortical sensory defect
    °ÑÁú°¨°¢°á¼Õ, ÇÇÁú°¨°¢°á¼Õ
  • canalization defect
    °üÇü¼º°áÇÔ
  • defect
    1. °áÇÔ, °á¼Õ(Áõ) 2. Àå¾Ö
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • 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
  • heritable defect
    À¯Àü°áÇÔ
  • hour-glass filling defect
    ¸ð·¡½Ã°èÃæ¸¸°á¼Õ
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  • ¿µ¹®
    ÇѱÛ
  • postnatal defect
    Ãâ»ýÀÌÈİáÇÔ
  • prenatal defect
    Ãâ»ýÀÌÀü°áÇÔ
  • primum atrial septal defect
    ÀÏÂ÷°ø½É¹æÁ߰ݰá¼Õ(Áõ).
  • primum atrial septal defect
    ÀÏÂ÷°ø½É¹æÁ߰ݰá¼Õ(Áõ)(ìéó­°ø½É¹æÁß°ÝÌÀáß(ñø))
  • promeiotic defect
    °¨¼öºÐ¿­ÀÌÀü°áÇÔ
  • quantum defect
    ¾çÀÚ°á¼Õ.
  • relative afferent pupillary defect
    »ó´ëÀû±¸½É¼ºµ¿°ø¿îµ¿Àå¾Ö
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè).
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè)
  • Intermediate part(commissura) of bulb
    Áú¾î±Í¸Á¿ïÁß°£ºÎºÐ
  • Iridial part of retina
    ¸Á¸·È«Ã¼ºÎºÐ
  • Iridic part of retina
    ¸Á¸·È«Ã¤[Á¶¸®°³]ºÎºÐ
  • Laibal part
    ÀÔ¼úºÎºÐ
  • Lateral(part of) globus pallidus
    °¡ÂÊâ¹éÇÙ
  • abdominal part
    ¹èºÎºÐ
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    ÇѱÛ
  • muscular atrophy
    ±ÙÀ§Ãà(¡­ê×õê)
  • muscular atrophy
    ±ÙÀ§Ãà(ÐÉê×õê).
  • muscular branch
    ±ÙÀ°°¡Áö, ±ÙÁö(ÐÉò«).
  • muscular branch
    ±ÙÀ° °¡Áö, ±ÙÁö(ÐÉò«).
  • muscular branch to thyrohyoideus
    ¹æÆÐ¸ñ»Ô±Ù°¡Áö
  • muscular branches
    ±ÙÀ°°¡Áö
  • muscular cirrus organ
    ±ÙÀ°¼º À½°æºÎÀ§, ±ÙÀ°¼º À½°æºÎ(ÐÉë¿àõëä Ý»).
  • muscular coat
    ±ÙÀ°Ãþ, ±ÙÃþ(ÐÉöµ).
  • muscular coat
    ±ÙÀ°Ãþ
  • muscular coat myometrium
    ±ÙÀ°Ãþ ÀڱñÙÀ°Ãþ
  • muscular coat of pharynx
    ÀεαÙÀ°Ãþ
  • muscular contraction
    ±Ù ¼öÃà(ÐÉâ¥õê), ±ÙÀ° ¼öÃà.
  • muscular contraction
    ±Ù¼öÃà(ÐÉâ¥õê), ±ÙÀ°¼öÃà.
  • muscular contracture
    ±Ù ±¸Ãà(ÐÉϬõê).
  • muscular contracture
    ±Ù±¸Ãà(ÐÉϬõê).
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    ÇѱÛ
  • Defect of urogenital organ
    ºñ´¢»ý½Ä±â°ü°áÇÔ
    [¿¾ ¿ë¾î] ºñ´¢»ý½Ä±â°ü°áÇÔ
  • Defect of Skeleton
    »À´ë°áÇÔ
    [¿¾ ¿ë¾î] °ñ°Ý°áÇÔ
  • Septation defect
    »çÀ̸·Çü¼º°áÇÔ
    [¿¾ ¿ë¾î] Áß°ÝÇü¼º°áÇÔ
  • Metabolic defect of pigment (Methemoglobinemia)
    »ö¼Ò´ë»ç°áÇÔ(¸ÞÆ®Çì¸ð±×·ÎºóÇ÷Áõ)
    [¿¾ ¿ë¾î] »ö¼Ò´ë»ç°áÇÔ(¸ÞÆ®Çì¸ð±×·ÎºóÇ÷Áõ)
  • Gametic defect
    »ý½ÄÀÚ°áÇÔ
    [¿¾ ¿ë¾î] »ý½ÄÀÚ°áÇÔ
  • Defect of gametogenesis
    »ý½ÄÀڹ߻ý°áÇÔ
    [¿¾ ¿ë¾î] »ý½ÄÀÚÇü¼º°áÇÔ
  • Congenital defect
    ¼±Ãµ°áÇÔ
    [¿¾ ¿ë¾î] ¼±Ãµ¼º°áÇÔ
  • Congenital metabolic defect
    ¼±Ãµ´ë»ç°áÇÔ
    [¿¾ ¿ë¾î] ¼±Ãµ¼º´ë»ç¼º°áÇÔ
  • Defect of alimentary tract
    ¼ÒÈ­°ü°áÇÔ
    [¿¾ ¿ë¾î] ¼ÒÈ­°ü°áÇÔ
  • Defect of fertilization
    ¼öÁ¤°áÇÔ
    [¿¾ ¿ë¾î] ¼öÁ¤°áÇÔ
  • Metabolic defect of steroid (Adrenogenital syndrome)
    ½ºÅ×·ÎÀ̵å´ë»ç°áÇÔ(ºÎ½Å»ý½Ä±âÁõÈıº)
    [¿¾ ¿ë¾î] ½ºÅ×·ÎÀ̵å´ë»ç°áÇÔ(ºÎ½Å»ý½Ä±âÁõÈıº)
  • Neural defect (Imbecility)
    ½Å°æ°áÇÌ(Ä¡¿ì)
    [¿¾ ¿ë¾î] ½Å°æ°áÇÔ
  • Ventricular septal defect
    ½É½Ç»çÀ̸·°áÇÔ
    [¿¾ ¿ë¾î] ½É½ÇÁ߰ݰáÇÔ
  • Defect of heart
    ½ÉÀå°áÇÔ
    [¿¾ ¿ë¾î] ½ÉÀå°áÇÔ
  • Heart defect
    ½ÉÀå°áÇÔ
    [¿¾ ¿ë¾î] ½ÉÀå°áÇÔ
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BDM Becker's muscular dystrophy
BMD Becker's muscular dystrophy; Boehringer Mannheim Diagnostics; bone marrow depression; bone mineral d...
CASMD congenital atonic sclerotic muscular dystrophy
CMS children's medical services; Christian Medical Society; chronic myelodysplastic syndrome; chromosome...
COD-MD cerebro-ocular dysplasia-muscular dystrophy [syndrome]
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 4
VFD visual field defect
BMD Becker Muscular Dystrophy
CMD Congenital muscular dystrophies
CMD Congenital muscular dystrophy
CMT Congenital muscular torticollis
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    ÇѱÛ
    ¼³¸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
  • peroxidase defect
    °ú»êÈ­È¿¼Ò °á¼Õ
  • punch out defect
    ±¸¸Û °á¼Õ
  • qualitative platelet defect
    Á¤»ó Ç÷¼ÒÆÇ °áÇÌÁõ, ÁúÀû Ç÷¼ÒÆÇ °áÇÔ
  • quantum defect
    ¾çÀÚ °á¼Õ
  • skeletal defect
    °ñ°Ý °á¼Õ
  • small atrial septal defect
    ¹Ì¼¼ ½É¹æ Áß°Ý °á¼Õ
  • substance defect
    ¹°Áú °áÇÌ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 4
childhood muscular dystrophy The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females).
Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy.
(05 Mar 2000)
peroneal muscular atrophy A group of three familial peripheral neuromuscular disorders, sharing the common feature of marked wasting of the more distal extremities, particularly the peroneal muscle groups, resulting in "stork legs." Two of the three subtypes are hereditary sensorimotor polyneuropathies, one demyelinating in type and the other axon loss in type, while the third subgroup is an anterior horn cell disorder. It usually involves the legs before the arms; pes cavus is often the first sign; autosomal dominant, autosomal recessive, and X-linked recessive types, with severity related to genetic type.
Synonym: Charcot-Marie-Tooth disease.
(05 Mar 2000)
circular layer of muscular coat The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ).
Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae.
(05 Mar 2000)
circular layers of muscular tunics The inner, circular layer of the smooth muscle of the muscular coat. Nomina Anatomica lists circular layers of muscular coats (stratum circulare tunicae muscularis...) of the following: 1) colon (... Coli ); 2) rectum (... Recti ); 3) small intestine (... Intestini tenuis ); 4) stomach (... Gastrici ).
Synonym: stratum circulare tunicae muscularis gastricae, stratum circulare tunicae.
(05 Mar 2000)
Werdnig-Hoffmann muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
muscular <anatomy> Pertaining to or composing muscle.
Origin: L. Muscularis
(18 Nov 1997)
muscular artery <anatomy, artery> An artery with a tunica media composed principally of circularly arranged smooth muscle.
Synonym: distributing artery, medium artery.
(05 Mar 2000)
muscular asthenopia Asthenopia due to imbalance of the extrinsic ocular muscles.
(05 Mar 2000)
muscular atrophy Derangement in size and number of muscle fibres occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.
(12 Dec 1998)
muscular atrophy, spinal Progressive degenerative disorder of motor neurons in the spinal cord, brainstem, and motor cortex, manifested clinically by muscular weakness, atrophy, and corticospinal tract signs in varying combinations.
(12 Dec 1998)
muscular branches Usually unnamed branches of nerves or vessels that supply the muscles.
Synonym: rami musculares.
(05 Mar 2000)
muscular coat The muscular, usually middle, layer of a tubular structure; for most of the gastrointestinal tract, it consists of an outer longitudinal layer of muscle and an inner circular layer.
Synonym: tunica muscularis.
(05 Mar 2000)
muscular coat of bronchi Muscular layer of the bronchial wall.
Synonym: tunica muscularis bronchiorum.
(05 Mar 2000)
muscular coat of colon Muscular layer of the wall of the colon.
Synonym: tunica muscularis coli.
(05 Mar 2000)
muscular coat of ductus deferens Muscular layer of the wall of the ductus deferens.
Synonym: tunica muscularis ductus deferentis.
(05 Mar 2000)
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