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  • ¿µ¹®
    ÇѱÛ
  • oral-facial-digital syndrome
    ÀÔ¾ó±¼¼Õ°¡¶ôÁõÈıº, ±¸°­¾È¸é¼öÁ·ÁöÁõÈıº
  • orbital apex syndrome
    ´«È®²ÀÁöÁõÈıº, ¾È¿Í÷´ÜÁõÈıº
  • organic brain syndrome
    ±âÁú¼º³úÁõÈıº
  • organic mental syndrome
    ±âÁú¼ºÁ¤½ÅÁõÈıº
  • Osler-Weber-Rendu syndrome
    ¿À½½·¯-¿þ¹ö-¶ûµÚÁõÈıº
  • obstructive sleep apnea syndrome
    Æó¼â¼ö¸é¹«È£ÈíÁõÈıº
  • overlap syndrome
    °ãħÁõÈıº, Áߺ¹ÁõÈıº
  • overuse syndrome
    °ú»ç¿ëÁõÈıº, °ú¿ëÁõÈıº
  • overwear syndrome
    °úµµÂø¿ëÁõÈıº
  • Pancoast syndrome
    ÆÒÄÚ½ºÆ®ÁõÈıº
  • Pickwickian syndrome
    ÇÈÀ¨ÁõÈıº
  • Pierre Robin syndrome
    ÇÇ¿¡¸£·Î¹ðÁõÈıº
  • placental transfusion syndrome
    ŹݼöÇ÷ÁõÈıº
  • polycystic ovarian syndrome
    ´Ù³¶³­¼ÒÁõÈıº
  • postmenopausal syndrome
    Æó°æÈÄÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • post-infarction syndrome
    °æ»öÈÄÁõÈıº
  • postelectric shock syndrome
    Àü±âÃæ°ÝÈÄÁõÈıº
  • postencephalitic behavioral syndrome
    ³ú¿°ÈÄÇൿÁõÈıº
  • postmenopausal syndrome
    Æó°æÈÄÁõÈıº
  • postpartum mood syndrome
    »êÈıâºÐÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
  • presbyophrenia syndrome
    ³ëÀÎÄ¡¸Å
  • prodromal radiation syndrome
    Á¶Áü¹æ»ç¼±ÁõÈıº
  • prune-belly syndrome
    ¸»¸°´ëÃßÁõÈıº
  • psychomotor syndrome
    Á¤½Å¿îµ¿ÁõÈıº
  • punch-drunken syndrome
    (¢¡boxer¡¯s dementia) ±ÇÅõ¼±¼öÄ¡¸Å
  • quadrilateral space syndrome
    ³×¸ð°ø°£ÁõÈıº
  • radicular syndrome
    ½Å°æ»Ñ¸®ÁõÈıº
  • respiratory distress syndrome
    È£Èí°ï¶õÁõÈıº
  • retraction syndrome
    ¾È±¸ÈÄÅðÁõÈıº
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  • ¿µ¹®
    ÇѱÛ
  • Ushers syndrome
    ¾Æ¼ÅÁõÈıº
  • V-syndrome
    VÁõÈıº
  • V-syndrome
    V ÁõÈıº
  • Vogt-Koyanagi syndrome
    Æ÷±×Æ® °í¾ß³ª±â ÁõÈıº
  • Vogt-Koyanagi-Harada syndrome
    º¸Å©Æ®-°í¾ß³ª±â-Ç϶ó´Ù ÁõÈıº
  • 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.
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  • ¿µ¹®
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  • apathetic-akinetic syndrome
    ¹«°¨µ¿-¹«µ¿ÀÛ ÁõÈıº
  • aphasic and apraxic syndrome
    ½Ç¾î½ÇÇàÁõÈıº(ã÷åÞãùú¼ñøý¦ÏØ).
  • aqueous mis-direction syndrome
    ¹æ¼öÈ帧ÀÌ»óÁõÈıº
  • ards(adult respiratory disress syndrome)
    ARDS(¼ºÀÎÈ£Èí°ï¶õÁõÈıº)(à÷ìÑû¼ýåÍÝÑññøý¦ÏØ)
  • arthritis-dermatitis syndrome
    °üÀý¿°-ÇǺο° ÁõÈıº
  • ashermans syndrome
    ¾Æ¼Å¸¸ ÁõÈıº
  • asphyctic syndrome
    Áú½ÄÁõÈıº.
  • atomic bomb syndrome
    ¿ø(ÀÚ)Æø(ź)ÁõÈıº.
  • atypical or mixed organic brain syndrome
    ºñÁ¤Çü ³»Áö È¥ÇÕÇü ±âÁú¼º ³úÁõÈıº
  • atypical schizophrenic syndrome
    ºñÁ¤Çü Á¤½ÅºÐ¿­¼º ÁõÈıº
  • auriculotemporal nerve syndrome
    À̰³ÃøµÎ½Å°æÁõÈıº.
  • auriculotemporal syndrome
    À̰³ÃøµÎÁõÈıº(¡­ñøý¦ÏØ).
  • auriculotemporal syndrome
    À̰³ÃøµÎ ÁõÈıº(ì¼Ë¿ö°Ôé ñøý¦ÏØ)
  • bantis syndrome
    ¹ÝƼÁõÈıº(¡­ñøý¦ÏØ)
  • bartters syndrome
    ¹ÙÅÍ ÁõÈıº(¡­ñøý¦ÏØ)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
LGS Langer-Giedion syndrome; Lennox-Gastaut syndrome; limb girdle syndrome
MPS meconium plug syndrome; medial premotor system; Member of the Pharmaceutical Society; microbial prof...
NBS N-bromosuccinimide; National Bureau of Standards; neuroblastoma supressor; nevoid basal cell carcino...
PES Patient Escort Service; photoelectron spectroscopy; physicians' equity services; polyethylene sulfon...
PSS painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
RR MS relapsing remitting multiple sclerosis
MDS 7--myelodysplastic syndrome
ACS Abdominal compartment syndrome
AIDS Acquire Immune Deficiency Syndrome
AIDS Acquired Immune Deficiency Disease Syndrome
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    ¼³¸í
  • Hamman-Rich syndrome
    ÇÔ¸¸- ¸®Ä¡ ÁõÈıº, ÇØ¸Õ-¸®Ä¡ ÁõÈıº, ÇÜ¸Õ ¸®Ä¡ ÁõÈıº
    Ư¹ß¼º ¹Ì¸¸¼º °£Áú¼º Æó¿°.
  • hand shoulder syndrome
    ¼Õ-¾î±ú ÁõÈıº
  • HELLP syndrome
    HELLP ÁõÈıº
  • hematopoietic syndrome
    Á¶Ç÷ ÁõÈıº
  • hemolytic-uremic syndrome
    ¿ëÇ÷¼º ¿äµ¶ ÁõÈıº
  • Henoch Schoenlein syndrome
    Çì³ëÈ£-½¨¶óÀÎ ÁõÈıº
  • hepatocerebral syndrome
    °£ ³ú ÁõÈıº
  • hepatoovarian syndrome
    °£ ³­¼Ò ÁõÈıº
  • hepatorenal syndrome
    °£ ½Å ÁõÈıº
    °£ Áõ»ó°ú ÇÔ²² ¿äÁß¿¡ ´Ü¹é, ¿øÁÖ°¡ ³ªÅ¸³ª°í, ¿äÀÇ ºÐ·®ÀÌ °¨¼ÒÇÏ´Â »óÅÂ. °£°ú ½ÅÀåÀÌ µ¿½Ã¿¡ Àå¾Ö¸¦ ÀÏÀ¸Å°´Â ÀÏÀº ÀÓ»ó¿¡¼­ ¿¾³¯ºÎÅÍ ÀÎÁ¤µÇ¾î ¿Ô´Ù. ±× ÀÌÀ¯´Â, ù° ¼¼±ÕÀÇ °¨¿°À¸·Î ÀÎÇÑ °£ ½Å¿°, µÑ° °£ Áßµ¶, ¼Â° °£ °æº¯, ³Ý° ¹ÙÀÌ·¯½º¼ºÀ¸·Î ÀÎÇÑ °Í µîÀÌ ÀÖ´Ù.
  • heritable melanoma syndrome
    À¯Àü¼º Èæ»öÁ¾ ÁõÈıº
  • histiocytosis syndrome
    Á¶Á÷±¸Áõ ÁõÈıº
  • Holt Oram syndrome
    ȦƮ-¿À¶÷ ÁõÈıº
  • Horner's syndrome
    È£³Ê ÁõÈıº, Horner ÁõÈıº
    ÆíÃø¼º Ãൿ ¼öÁõ, ±×¸®°í ¾È¸é Å»¼öÁõÀÌ Æ¯Â¡ÀÎ ½Å°æ¼º »óÅ·μ­ º¸Åë °æºÎ ±³°¨¼º ¸¶ºñ·ÎºÎÅÍ ¹ß»ýµÈ´Ù.
  • Horton's syndrome
    Horton ÁõÈıº
    cluster headache¸¦ º¸½Ã¿À.
  • Hurler-Scheie syndrome
    Çæ·¯-»þÀÌ¿¡ ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
Budd's syndrome <syndrome> Thrombosis of the hepatic vein with great enlargement of the liver and extensive development of collateral vessels, intractable ascites, and severe portal hypertension.
Synonym: Budd's syndrome, Budd-Chiari syndrome, Chiari's disease, Chiari-Budd syndrome, Rokitansky's disease.
(05 Mar 2000)
Burger-Grutz syndrome Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance.
See: familial lipoprotein lipase inhibitor.
Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia.
(05 Mar 2000)
burner syndrome <syndrome> Multiple episodes of upper extremity burning pain, sometimes accompanied by shoulder girdle weakness, experienced during contact sports, especially football, with each forceful blow to the head or shoulder; attributed to an upper trunk brachial plexopathy.
(05 Mar 2000)
Burnett's syndrome <syndrome> A form of metabolic acidosis that can result from the excessive consumption of milk (calcium) and antacids (sodium bicarbonate) over a prolonged period of time. This can result in calcium deposits in the kidneys and body tissues.
Symptoms include nausea, vomiting and weakness. May be seen as a complication of peptic ulcer therapy.
(27 Sep 1997)
burning foot syndrome <syndrome> A disorder observed in prisoners-of-war in World War II, now believed to be due to a pantothenate deficiency.
(05 Mar 2000)
burning mouth syndrome <syndrome> A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders.
(12 Dec 1998)
burning vulva syndrome <syndrome> Persistent vulvodynia in which a physical cause has not been identified.
(05 Mar 2000)
Buschke-Ollendorf syndrome Osteopoikilosis with skin lesions, most commonly small elastic fibrous nodules on the posterior aspects of the thighs and buttocks; irregular autosomal dominant inheritance.
Synonym: Buschke-Ollendorf syndrome.
Origin: osteo-+ G. Derma, skin, + poikilos, dappled, + -osis, condition
(05 Mar 2000)
Caffey-Kempe syndrome <radiology> Multiple assymetrical fractures, separation of distal epiphyses, irregularity and fragmentation of metaphyses, bucket-handle fracture, corner fracture of elbow, knee, ankle (sudden twisting motion), isolated spiral fracture, extensive periosteal reaction (subperiosteal haemorrhage), exuberant callus formation, cortical hyperostosis extending to epiphyseal plate, avulsion fracture at ligamentous insertion, subdural haematoma (most common), brain atrophy (up to 100%), infarction (50%), subdural hygroma, encephalomalacia, porencephaly
(12 Dec 1998)
Caffey-Silverman syndrome Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood.
Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome.
(05 Mar 2000)
Caffey's syndrome Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood.
Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome.
(05 Mar 2000)
camptomelic syndrome <syndrome> Also associated with flat facies, short vertebrae, hypoplastic scapula, and bowed tibia.
Synonym: osteochondrodysplasia.
(05 Mar 2000)
cantrell syndrome <radiology> Herniation of gut into pericardial sac, common anterior communication in diaphragm and pericardium, associated with congenital defects of sternum, heart, mesentery, anterior abdominal wall, must be excluded in presence of omphalocele, ** diaphragmatic hernia
(12 Dec 1998)
capgras syndrome <syndrome> A psychotic disorder characterised by the patient's conviction that certain important or familiar persons in his environment are not real but are "doubles" of themselves or imposters.
(12 Dec 1998)
Capgras' syndrome <syndrome> The delusional belief that a person (or persons) close to the schizophrenic patient has been substituted for by one or more impostors; may have an organic aetiology.
Synonym: Capgras' phenomenon, illusion of doubles.
(05 Mar 2000)
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