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"malignant carcinoid syndrome"¿¡ ´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
  • rotator cuff syndrome
    ȸÀü±Ù°³ÁõÈıº, µ¹¸²±Ù¶ìÁõÈıº
  • runting syndrome
    ¼Ò¸ðÁõÈıº, ¿Ö¼ÒÁõÈıº
  • Raynaud¡¯s syndrome
    ·¹À̳ëÁõÈıº
  • radial tunnel syndrome
    ³ëÂʱ¼ÁõÈıº, ¿äÃø±¼ÁõÈıº
  • refeeding syndrome
    ¿µ¾çÀç°³ÁõÈıº, ±Þ½ÄÀç°³ÁõÈıº
  • Reiter¡¯s syndrome
    ¶óÀÌÅÍÁõÈıº
  • respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº
  • radicular syndrome
    ½Å°æ»Ñ¸®ÁõÈıº, ½Å°æ±ÙÁõÈıº
  • retraction syndrome
    ¾È±¸ÈÄÅðÁõÈıº
  • scalded skin syndrome
    È­»óÇǺÎÁõÈıº
  • staphylococcal scalded skin syndrome
    Æ÷µµ¾Ë±Õ¼º¿­»óÇǺÎÁõÈıº, Æ÷µµ±¸±Õ¼º¿­»óÇǺÎÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº, ÀåÁ¤Ã¼ÁõÈıº
  • Steele-Richardson-Olszewski syndrome
    ½ºÆ¿-¸®Ã³µå½¼-¿Ã½ºÁ¦ºê½ºÅ°ÁõÈıº
  • Scheie syndrome
    »þÀÌ¿¡ÁõÈıº
  • Stevens-Johnson syndrome
    ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
  • stiff-man syndrome
    ±ÙÀ°°­Á÷ÁõÈıº
  • stroke syndrome
    ÁßdzÁõÈıº
  • sudden infant death syndrome
    ¿µ¾Æ±Þ»çÁõÈıº
  • sudden manhood death syndrome
    ûÀå³â±Þ»çÁõÈıº
  • superior orbital fissure syndrome
    À§´«È®Æ´»õÁõÈıº
  • supine hypotensive syndrome
    ´©¿îÀÚ¼¼ÀúÇ÷¾ÐÁõÈıº
  • tabetic syndrome
    ¼Ò¸ðÁõÁõÈıº, Ÿº£½ºÁõÈıº
  • tarsal tunnel syndrome
    ¹ß¸ñ±¼ÁõÈıº, Á·±Ù°üÁõÈıº
  • testicular feminization syndrome
    °íȯ¿©¼ºÈ­ÁõÈıº
  • thalamic syndrome
    ½Ã»óÁõÈıÙ
  • time zone change syndrome
    (¢¡jet lag syndrome) ºñÇà½ÃÂ÷ÁõÈıº
  • toxic shock syndrome
    µ¶¼ÒÃæ°ÝÁõÈıº
  • transurethral resection syndrome
    °æ¿äµµÀýÁ¦ÈÄÁõÈıº
  • trisomy 18 syndrome
    18¼¼¿°»öüÁõÈıº
  • ulnar tunnel syndrome
    ÀÚ»À±¼ÁõÈıº, ô°ñ°üÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
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  • WPW syndrome
    WPWÁõÈıº, ºÎÀüµµ·ÎÁõÈıº .
  • Waardenburgs syndrome
    ¹Ù¸£µ§ºÎ¸£Å© ÁõÈıº
  • Wallenbergs syndrome
    ¹ß·»º£¸£Å©ÁõÈıº.
  • Waterhouse Friderichsen syndrome
    ¿ö¾îÅÍÇϿ콺-ÇÁ¸®µ¥¸®Å©¼¾ÁõÈıº.
  • Waterhouse-Friderichsen syndrome
    ¿öÅÍÇϿ콺-ÇÁ¸®µ¥¸¯¼¾ ÁõÈıº
  • Weber syndrome
    ¿þ¹öÁõÈıº
  • Weber-Cocayne syndrome
    ¿þ¹ö ÄÚÄÉÀÎ ÁõÈıº
  • Webers syndrome
    ¿þ¹öÁõÈıº.
  • Werners syndrome
    º£¸£³ÊÁõÈıº.
  • Wernicke Korsakoff syndrome
    º£¸£´ÏÄÉ-ÄÚ¸£»çÄÚÇÁÁõÈıº.
  • Wiskott-Aldrich syndrome
    ºñ½ºÄÚÆ®-¿Ãµå¸®Ä¡ ÁõÈıº
  • Wiskott-Aldrich syndrome
    À§½ºÄÚÆ® ¿Ãµå¸®È÷ ÁõÈıº
  • Wolff-Parkinson-White syndrome
    ¿ùÇÁÆÄŲ½¼È­ÀÌÆ® ÁõÈıº
  • Wyburn-Mason syndrome
    À§¹ø¸Å½¼ ÁõÈıº
  • X-linked lymphoproliferative syndrome
    ¼º¿°»öü ¿¬°ü ¸²ÇÁÁõ½Ä ÁõÈıº
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  • brittle hair syndrome
    Ãë¾à¸ð¹ßÁõÈıº
  • broad thumb-hallux syndrome
    ±¤¾öÁö¼Õ,¹ß°¡¶ôÁõÈıº
  • bronze baby syndrome
    ûµ¿»ö¾Æ±âÁõÈıº
  • bruising syndrome
    Ÿ¹Ú»óÁõÈıº.
  • budd-chiari syndrome
    ¹Ùµå-Ű¾Æ¸® ÁõÈıº (¡­ñøý¦ÏØ)
  • bulbar syndrome
    ¿¬¼öÁõÈıº(æÅâÐñøý¦ÏØ)
  • burning feet syndrome
    ÀÛ¿­°¢ÁõÈıº(¡­ñøý¦ÏØ), ¼ÒÀÛÁ·ÁõÈıº(áÀíÇðëñøý¦ÏØ).
  • camptomelic syndrome
    ±¼Áö ÁõÈıº.[¼Ò¾Æ]Áöü ±¼°î ÁõÈıº(ò¶ô÷ÏÝÍØñøý¦ÏØ) .
  • camptomelic syndrome
    ±¼ÁöÁõÈıº.¼Ò¾ÆÁöü±¼°îÁõÈıº(ò¶ô÷ÏÝÍØñøý¦ÏØ) .
  • capillary leak syndrome
    ¸ð¼¼Ç÷°ü´©ÃâÁõÈıº
  • caplans syndrome
    ijÀÌÇöõ ÁõÈıº (¡­ñøý¦ÏØ)
  • carbohydrate malabsorption syndrome
    ´çÁúÈí¼öºÒ·®ÁõÈıº(ÓØòõýåâ¥ÝÕÕÞñøý¦ÏØ)
  • cardiofacial syndrome
    ½É¾È¸é ÁõÈıº(ãýäÔØüñøý¦ÏØ)
  • cardiofaciocutaneous syndrome
    ½ÉÀå¾ó±¼ÇǺÎÁõÈıº
  • carotid sinus syndrome
    °æµ¿¸Æµ¿ÁõÈıº(¡­ñøý¦ÏØ).
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AIS Abbreviated Injury Scale; amniotic infection syndrome; androgen insensitivity syndrome; anterior int...
AS acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis...
BLS bare lymphocyte syndrome; basic life support; blind loop syndrome; blood and lymphatic system; blood...
BS Bachelor of Science; Bachelor of Surgery; Bacillus subtilis; Bartter syndrome; base strap; bedside; ...
CAS calcarine sulcus; calcific aortic stenosis; Cancer Attitude Survey; carbohydrate-active steroid; car...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
CFS Cancer Family Syndrome
CDGS Carbohydrate Deficient Glycoprotein Syndrome
CSS Carotid Sinus Syndrome
C.T.S. Carpal Tunnel Syndrome
CES Cat Eye Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
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    ¼³¸í
  • hypotonic syndrome
    ÀúÀå ÁõÈıº
  • hypoventilation syndrome
    È£Èí ÀúÇÏ ÁõÈıº
  • ICE syndrome
    ȫä °¢¸· ³»ÇÇ ÁõÈıº
    iridocorneal endothelial syndromeÀÇ ¾àÀÚ.
  • ileal diverticulum meckel syndrome
    µ¹ âÀÚ °ç ÁÖ¸Ó´Ï ¸ßÄÌ ÁõÈıº
  • immersion foot syndrome
    ħ¼öÁ· ÁõÈıº
  • immune amnesia syndrome
    ¸é¿ª ±â¾ï »ó½Ç ÁõÈıº
  • immunoproliferative syndrome
    ¸é¿ª Áõ½Ä¼º ÁõÈıº
  • imposter syndrome
    ÇùÀâ²Û ÁõÈıº
  • inappropriate ADH syndrome
    ADH ºÎÀûÇÕ ºÐºñ ÁõÈıº
  • infantile stiff skin syndrome
    ¿µ¾Æ ÇǺΠ°æÁ÷ ÁõÈıº
  • inspissated bile syndrome
    ³óÃà ´ãÁó ÁõÈıº
  • intermediate syndrome
    Áß°£Çü ÁõÈıº
  • iridocorneal-endothelial syndrome
    ȫä °¢¸· ³»ÇÇ ÁõÈıº
  • iris-nevus syndrome
    ȫä ¸ð¹Ý ÁõÈıº
  • irritation syndrome
    ÀÚ±Ø ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
caplan syndrome <radiology> Combination of: necrobiotic rheumatoid lung nodules, coal worker's pneumoconiosis Findings: round, peripheral nodules (0.5 - 5.0 cm), with or without cavitation, nodules associated with subcutaneous rheumatoid nodules
(12 Dec 1998)
carbohydrate-deficient glycoprotein syndrome <syndrome> An inborn error of carbohydrate metabolism manifesting as a genetic multisystem disorder of autosomal recessive inheritance. A predominant feature is severe central and peripheral nervous system involvement resulting in psychomotor retardation, seizures, cerebellar ataxia, and other symptoms which include growth retardation, retinitis pigmentosa, hypothyroidism, and fatty liver. The notable biochemical feature is the deficiency of a large number of blood glycoproteins and decreased activities of various blood coagulation factors.
(12 Dec 1998)
carbonic anhydrase II deficiency syndrome <syndrome> An inherited deficiency of carbonic anhydrase II that results in osteopetrosis and metabolic acidosis.
Synonym: osteopetrosis with renal tubular acidosis.
(05 Mar 2000)
cardiofacial syndrome <syndrome> Transient or persistent unilateral partial lower facial paresis accompanying some congenital heart disease.
A group of syndromes characterised by congenital cardiovascular, bone, soft tissue, and facial abnormalities. Examples include Rubinstein-Taybi syndrome, Noonan's syndrome and Williams' syndrome.
Synonym: Williams' syndrome.
(05 Mar 2000)
carney syndrome <radiology> Association of: pheochromocytoma, paraganglioma (functioning), chondroma (mult. Chondromatous hamartomas?)
(12 Dec 1998)
Caroli's syndrome <syndrome> Congenital malformation of the bile ducts leading to formation of multifocal dilatations and cysts.
(05 Mar 2000)
Gaisbock's syndrome Polycythemia associated with hypertension, but without splenomegaly.
Synonym: Gaisbock's syndrome.
(05 Mar 2000)
VACTERL syndrome <syndrome> Abnormalities of vertebrae, anus, cardiovascular tree, trachea, oesophagus, renal system, and limb buds associated with administration of sex steroids during early pregnancy.
(05 Mar 2000)
pacemaker syndrome <syndrome> The occurrence of symptoms relating to the loss of atrial-ventricular synchrony in ventricularly paced patients, or symptoms caused by inadequate timing of atrial and ventricular contractions in paced patients.
(05 Mar 2000)
Macleod's syndrome A state in which the roentgenographic density of one lung (or one lobe) is markedly less than the density of the other(s) because of the presence of air trapped during expiration.
Synonym: Macleod's syndrome, Swyer-James syndrome.
(05 Mar 2000)
pachydermoperiostosis syndrome <radiology> Idiopathic, familial hypertrophic osteoarthropathy, boys at puberty, blacks more than whites, familial, periosteal reaction, thick skin: extremities and forehead, hyperhidrosis, relatively pain free
(12 Dec 1998)
radial aplasia-thrombocytopenia syndrome <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome.
(12 Dec 1998)
Paget-von Schrotter syndrome <syndrome> Stress thrombosis or spontaneous thrombosis of the subclavian or axillary vein; a thoracic-outlet syndrome.
Synonym: effort-induced thrombosis.
(05 Mar 2000)
radicular syndrome A group of symptoms resulting from any interference with the intradural portion of one or more spinal nerve roots; the chief symptoms are pain, paresthesia, hypesthesia, or hyperesthesia, motor, trophic, and reflex disturbances.
(05 Mar 2000)
painful-bruising syndrome <syndrome> An intense inflammatory reaction to slight extravasation of blood, due to an allergic sensitivity to red blood cells; more commonly seen in adult women.
(05 Mar 2000)
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