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  • ¿µ¹®
    ÇѱÛ
  • Prader-Willi syndrome
    ÇÁ·¡´õ-Àª¸®ÁõÈıº
  • premenstrual syndrome
    ¿ù°æÀüÁõÈıº
  • prune-belly syndrome
    ¸»¸°´ëÃß¹èÁõÈıº
  • pulmonary overinflation syndrome
    Æó°úµµÆØÃ¢ÁõÈıº
  • paraneoplastic syndrome
    ½Å»ý¹°µþ¸²ÁõÈıº
  • Parinaud syndrome
    ÆÄ¸®³ëÁõÈıº
  • parkinsonian syndrome
    ÆÄŲ½¼ÁõÈıº
  • Peutz-Jeghers syndrome
    Æ÷ÀÌÃ÷-Á¦°Å½ºÁõÈıº
  • quadrilateral space syndrome
    ³×¸ð°ø°£ÁõÈıº
  • 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
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  • ¿µ¹®
    ÇѱÛ
  • shock syndrome
    Ãæ°ÝÁõÈıº
  • short bowel syndrome
    ÀÛÀºÃ¢ÀÚÁõÈıº
  • shoulder-hand syndrome
    ¾î±ú¼ÕÁõÈıº
  • sleep apnea syndrome
    ¼ö¸é¹«È£ÈíÁõÈıº
  • sleep choking syndrome
    ¼ö¸éÁú½ÄÁõÈıº
  • somatizing syndrome
    ½ÅüȭÁõÈıº
  • stasis syndrome
    âÀÚÁ¤Ã¼ÁõÈıº
  • 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
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
    ÇѱÛ
  • Turners syndrome
    ÅÍ³Ê ÁõÈıº
  • 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.
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  • ¿µ¹®
    ÇѱÛ
  • blind spot syndrome
    ¸ÍÁ¡ÁõÈıº(ØîïÇñøý¦ÏØ).
  • blooms syndrome
    ºí·ç¿ò ÁõÈıº (¡­ñøý¦ÏØ)
  • blue rubber-bleb nevus syndrome
    û»ö°í¹«¼öÆ÷¸ð¹ÝÁõÈıº
  • blue rubber-bleb nevus syndrome
    û»ö°í¹«¼öÆ÷¸ð¹ÝÁõÈıº(ôìßä¡­â©øÜÙ½Úèñøý¦ÏØ)
  • borderline syndrome
    °æ°è¼º ÁõÈıº
  • bradycardia tachycardia syndrome
    ¼­ºó¸Æ ÁõÈıº(ßïÞµØæ ñøý¥ÏØ).
  • bradycardia tachycardia syndrome
    ¼øÈ¯¼­¸Æºó¸ÆÁõÈıº.
  • bradytachycardia syndrome
    ¼­ºó¸ÆÁõÈıº(ßïÞºØæñøý¦ÏØ).
  • brain death syndrome
    ³ú»çÁõÈıº(ÒàÞÝñøý¦ÏØ).
  • brain stem syndrome
    ³ú°£ÁõÈıº(¡­ñøý¦ÏØ).
  • brain syndrome
    ³úÁõÈıº
  • brain syndrome, acute, chronic
    ±Þ¼º, ¸¸¼º ³úÁõÈıº.
  • breast/ovarian familial cancer syndrome
    À¯¹æ/³­¼Ò °¡Á·¼º ¾ÏÁõÈıº
  • brittle hair syndrome
    Ãë¾à¸ð¹ßÁõÈıº
  • broad thumb-hallux syndrome
    ±¤¾öÁö¼Õ,¹ß°¡¶ôÁõÈıº
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
CV cardiac volume; cardiovascular; carotenoid vesicle; cell volume; central venous; cephalic vein; cere...
ELECTZ electrosurgical loop excision of the cervical transformation zone
HCTU home cervical traction unit
HeLa Helen Lake [human cervical carcinoma cells]
HEp-1 human cervical carcinoma cells
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 16
CHS Che'diak-Higashi syndrome
CCS Chronic Compartment Syndrome
CFS Chronic Fatigue Syndrome
CPPS Chronic Pelvic Pain Syndrome
CSS Churg Strauss Syndrome
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
  • ¿µ¹®
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  • 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
  • Hutchinson's syndrome
    ÇãÄ£½¼ ÁõÈıº
    °£Áú °¢¸·¿°, ¹Ì·Î Áúȯ, ÇãÄ£½¼ Ä¡¾ÆÀÇ º¹ÇÕÀ¸·Î ¼±Ãµ ¸Åµ¶¿¡¼­ º¼ ¼ö ÀÖ´Ù. ¼±Ãµ¼º ¸Åµ¶ÀÇ Áõ»óÀ¸·Î ÇãÄ£½¼ 3ÁÖÁõÀ¸·Î Áø´ÜÇÒ ¼ö ÀÖ´Ù. ¸Åµ¶Àº 1Â÷, 2Â÷, 3Â÷ÀÇ ´Ü°è¸¦ º¸À̸ç À¯Àü¼ºÀ» ¶ì°í ÀÖ´Ù.
  • hyperimmunoglobulin E syndrome
    °ú¸é¿ª ±Û·ÎºÒ¸° E ÁõÈıº
  • hyperkinetic heart syndrome
    °ú¿îµ¿¼º ½ÉÁõÈÄ, °ú¿îµ¿¼º ½ÉÁõÈıº
  • hypermobility syndrome
    °ú¿îµ¿ ÁõÈıº
  • hyperstimulation syndrome
    °úÀÚ±Ø ÁõÈıº
  • hyperviscosity syndrome
    °íÁ¡µµ ÁõÈıº
    °ñ¼öÁ¾ ´Ü¹éÀÌ °ú´ÙÇÏ°Ô »ý¼ºµÈ °ÍÀÌ ÀÀÁýµÇ¾î ³ªÅ¸³­´Ù. ´Ù¹ß¼º °ñ¼öÁ¾ ȯÀÚÀÇ ¾à 7%¿¡¼­ º¼ ¼ö ÀÖ´Ù.
  • hypogenetic lung syndrome
    Àú¹ß»ý Æó ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 16
Bauer's syndrome <syndrome> Aortitis and aortic endocarditis as a little recognised manifestation of rheumatoid arthritis.
(05 Mar 2000)
Bazex's syndrome <syndrome> Erythematous to plum-coloured scaly acral skin lesions, paronychia, and nail dysplasia; associated with cancer of the upper respiratory or upper alimentary tract.
Synonym: paraneoplastic acrokeratosis.
(05 Mar 2000)
Beckwith syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
Beckwith-Wiedemann syndrome <syndrome> This syndrome, of unknown cause, is characterised by a group of the following findings: large tongue, organ enlargement (visceromegaly), large body size, umbilical hernia and neonatal hypoglycaemia. Evidence suggests a genetic lesion. Birth weight is often more than 8 pounds. Complications include Wilm's tumour, seizures, aspiration and hypoglycaemia.
(27 Sep 1997)
Behcet's syndrome <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil).
(27 Sep 1997)
Behr's syndrome <syndrome> Adult or presenile form of heredomacular degeneration.
Synonym: Behr's disease.
(05 Mar 2000)
Benedikt's syndrome <syndrome> Hemiplegia with clonic spasm or tremor and oculomotor paralysis on the opposite side.
(05 Mar 2000)
Beradinelli's syndrome <syndrome> The clinical findings of accelerated growth, lipodystrophy with muscular hypertrophy, hepatomegaly and lipaemia.
(27 Sep 1997)
Bernard-Horner syndrome <syndrome> A nerve condition which involves a dropping eyelid (ptosis), constricted pupil, enophthalmos and lack of sweating on one side of the face. Often seen in association with injury (for example neck fracture, penetrating injury) to the cervical sympathetic nerve trunk in the neck or a Pancoast tumour involving both the upper and lower brachial plexus.
(29 Sep 1997)
Bernard-Sergent syndrome Severe adrenocortical insufficiency when an intercurrent illness or trauma causes an increased demand for adrenocortical hormones in a patient with adrenal insufficiency due to disease or use of relatively large amounts of similar hormones as therapy; characterised by nausea, vomiting, hypotension, and frequently hyperthemia, hyponatraemia, hyperkalaemia, and hypoglycaemia; can be fatal if untreated.
Synonym: addisonian crisis, adrenal crisis, Bernard-Sergent syndrome.
(05 Mar 2000)
Bernard Soulier syndrome <haematology, syndrome> A congenital disorder where the platelets lack receptors which allow them to adhere to the walls of blood vessels. The genetic deficiency in platelet membrane glycoprotein Ib allows platelets to aggregate normally (c.f. Glanzmann's thrombasthenia) but they do not stick to collagen of sub endothelial basement membrane. The net result is a platelet function disorder that causes a prolonged bleeding time.
Symptoms include nosebleeds, easy bruising, heavy menstrual periods, bleeding gums and increased post-operative bleeding. Avoidance of aspirin, anti-inflammatories or any other agents which can cause bleeding is critical.
(06 Oct 1997)
bernard syndrome <syndrome> A complex of abnormal findings, namely sinking in of one eyeball, ipsilateral ptosis (drooping of the upper eyelid on the same side) and miosis (constriction of the pupil of that eye) together with anhidosis (lack of sweating) and flushing of the affected side of the face.
Due to paralysis of certain nerves (specifically, the cervical sympathetic nerves). Also called Horner-Bernard syndrome, Bernard-Horner syndrome and Horner's ptosis, but best known today as Horner syndrome.
(12 Dec 1998)
Bernhardt-Roth syndrome <symptom> A tingling, formication, itching, and other forms of paresthesia in the outer side of the lower part of the thigh in the area of distribution of the lateral femoral cutaneous nerve; there may be pain, but the skin is usually hypesthetic to the touch.
Synonym: Bernhardt's disease, Bernhardt-Roth syndrome, Roth's disease, Roth-Bernhardt disease.
(21 Sep 2000)
Bernheim's syndrome <syndrome> Systemic congestion resembling the consequences of right heart failure (enlarged liver, distended neck veins, and oedema) without pulmonary congestion in subjects with left ventricular enlargement from any cause.
A reduction in the size of the right ventricular cavity is found by contrast imaging or echocardiography or at postmortem due to encroachment by the hypertrophied or aneurysmal ventricular septum.
(14 Aug 2000)
Besnier-Boeck-Schaumann syndrome <disease> Disease of unknown aetiology in which there are chronic inflammatory granulomatous lesions in lymph nodes and other organs.
(18 Nov 1997)
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