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"egg drop 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®
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  • combined immunodeficiency syndrome
    º¹Çո鿪°áÇÌÁõÈıº
  • compartment syndrome
    ±¸È¹ÁõÈıº
  • complex regional pain syndrome
    º¹ÇÕºÎÀ§ÅëÁõÁõÈıº
  • compression syndrome
    ¾Ð¹ÚÁõÈıº
  • congenital rubella syndrome
    ¼±ÃµÇ³ÁøÁõÈıº
  • Conn¡¯s syndrome
    ÄÜÁõÈıº
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵åÁõÈıº
  • CREST syndrome
    Å©·¹½ºÆ®ÁõÈıº
  • cri du chat syndrome
    °í¾çÀÌ¿ïÀ½ÁõÈıº
  • Crigler-Najjar syndrome
    Å©¸®±Û·¯-³ªÀÚ¸£ÁõÈıº
  • Cronkhite-Canada syndrome
    Å©·ÐÅ©ÇÏÀÌÆ®-ij³ª´ÙÁõÈıº
  • Crouzon¡¯s syndrome
    Å©·çÁ¾ÁõÈıº
  • crush syndrome
    À¸±þÁõÈıº, ¾Ð±ËÁõÈıº
  • cubital tunnel syndrome
    ÆÈ²ß±¼ÁõÈıº, ÁÖ°üÀýÅͳÎÁõÈıº
  • culture-bound syndrome
    ¹®È­±ÇÁõÈıº
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
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    ÇѱÛ
  • blast syndrome
    Æø¹ßÁõÈıº
  • blind loop syndrome
    (¢¡stasis syndrome) âÀÚÁ¤Ã¼ÁõÈıº
  • blind spot syndrome
    ¸ÍÁ¡ÁõÈıº
  • brain death syndrome
    ³ú»çÁõÈıº
  • branchial arch syndrome
    ¾Æ°¡¹Ì±ÁÀÌÁõÈıº
  • branchio-otorenal syndrome
    ¾Æ°¡¹Ì±ÍÄáÆÏÁõÈıº
  • brittle hair syndrome
    Ãë¾à¸ð¹ßÁõÈıº
  • bronze baby syndrome
    ûµ¿»ö¾Æ±âÁõÈıº
  • Brown-Sequard syndrome
    ºê¶ó¿î¼¼±î¸£ÁõÈıº
  • bruising syndrome
    (¢¡simple purpura) ´Ü¼øÀÚ»ö¹Ý
  • camptomelic syndrome
    ±¼ÁöÁõÈıº, Áöü±¼°îÁõÈıº
  • capsular block syndrome
    ÇǸ·Æó¼âÁõÈıº
  • capsule contracture syndrome
    ¼öÁ¤Ã¼³¶¼öÃàÁõÈıº
  • carbohydrate malabsorption syndrome
    ´çÁúÈí¼öºÒ·®ÁõÈıº
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵åÁõÈıº
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • Crouzons syndrome=>craniofacial dysostosis
    Å©·çÁ¸ÁõÈıº
  • Cushing syndrome
    Äí½ÌÁõÈıº
  • Cushing syndrome
    Äí½Ì ÁõÈıº
  • Cushingoid syndrome
    Äí½Ì¾çÁõÈıº.
  • Cushings syndrome
    Äí½ÌÁõÈıº.
  • Cushings syndrome
    Äí½ÌÁõÈıº
  • DaCostas syndrome
    ´ÙÄÚ½ºÅ¸ ÁõÈıº(~ñøý¦ÏØ)
  • De Sanctis-Caccione syndrome = xerodermic idiocy
    °ÇÇǼº ¹éÄ¡
  • Defibrillation syndrome
    Å»¼¶À¯¼ÒÁõÈıº
  • Devies syndrome
    µ¥ºòÁõÈıº
  • Di Guglielmo syndrome
    µð±¸±Û¸®¿¤¸ðÁõÈıº, ÀûÇ÷º´¼º °ñ¼öÁõ
  • DiGeorges syndrome => thymic-parathyroid aplasia
    µðÁÒÁö ÁõÈıº
  • Dorfman-Chanarin syndrome = neutral lipid storage disease
    Áß¼ºÁö¹æÃàÀûÁõ
  • Down syndrome
    ´Ù¿îÁõÈıº
  • Downs syndrome
    ´Ù¿îÁõÈıº
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
    ÇѱÛ
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acquired immune deficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌÁõÈıº(ý­ô¸àõ Øóæ¹ÌÀù¹ñøý¦ÏØ)
  • acquired immunodeficiency syndrome
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acquired immunodeficiency syndrome
    ÈÄõ¼º¸é¿ª°áÇÌÁõ
  • acquired immunodeficiency syndrome (AIDS)
    ÈÄõ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • acquired immunodeficiency syndrome(AIDS)
    ÈÄõ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • acute brain syndrome
    ±Þ¼º ³úÁõÈıº(¡­Òàñøý¦ÏØ).
  • acute fulminating meningococcemia ; Waterhouse Friderichsen syndrome
    ±Þ¼º Àü°Ý¼º ¼ö¸·±¸±Õ±ÕÇ÷Áõ.
  • acute radiation syndrome
    ±Þ¼º¹æ»ç¼±ÁõÈıº
  • acute radiation syndrome
    ±Þ¼º¹æ»ç¼±ÁõÈıº(¡­Û¯ÞÒàÊñøý¦ÏØ)
  • adherence syndrome, Johnson
    ÁÔ½¼À¯ÂøÁõÈıº
  • adhesive syndrome
    À¯ÂøÁõÈıº
  • adrenal cortex,cushings syndrome
    Äí½ÌÁõÈıº(¡­ñøý¦ÏØ)
  • adrenal virilizing syndrome
    ºÎ½Å¼º ³²¼ºÈ­ ÁõÈıº(¡­ñøý¦ÏØ).
  • adrenogenital syndrome
    ºÎ½Å¼º±â ÁõÈıº
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
EYA egg yolk agar
HEL hen egg white lysozyme; human embryonic lung; human erythroleukemia
HEP hemolysis end point; hepatoerythropoietic porphyria; high egg passage [virus]; high-energy phosphate...
LD-EYA Lombard-Dowell egg yolk agar
LD-NEYA Lombard-Dowell neomycin egg yolk agar
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 6
EYL egg yolk lecithin
EPC egg yolk phosphatidycholine
EYPC egg yolk phosphatidyl choline
EggPC egg yolk phosphatidylcholine
EYP egg yolk phospholipid
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
  • ¿µ¹®
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  • Boerhaave syndrome
    ºÆ¸£ÇϺ£ ÁõÈıº
    ±¸Åä·Î ÀÎÇØ ½ÄµµÀÇ ÀÚ¿¬ÀûÀÎ ÆÄ¿­À» ¸»Çϴµ¥ µ¿Åë°ú ¹ß¿­À» ¼ö¹ÝÇÑ °ß°©°ñ¾È ȤÀº Èä°ñÇÏ µ¿ÅëÀ» È£¼ÒÇÏ°í ¼îÅ© »óŰ¡ ¹ß»ýÇϱ⵵ ÇÑ´Ù. ±¤¹üÀ§ÇÑ ±«»ç¼º Á¾°Ýµ¿¿°Àº ÆíÃø ȤÀº ¾çÃø¼º ³óÈäÀ» ÃÊ·¡½Ã۱⵵ ÇÏ¿© 24~48½Ã°£³» »ç¸Á½Ã۱⵵ ÇÑ´Ù. ÀÓ»ó Áõ»óÀº ÈäºÎ X-¼± »çÁø»ó °æºÎ Á¶Á÷¸é°ú Á¾°Ýµ¿³» °ø±â°¡ ³ªÅ¸³ª°í Á¾°Ýµ¿ »óÀÌ È®´ëµÇ°í Á¾°Ýµ¿¿¡ ¾×¸é»ó°ú µå¹°°Ô ½É³¶°ú ÅëÇØ ½É³¶³» ¾×¸é»óÀÌ º¸À̱⵵ ÇÑ´Ù. ½Äµµ Á¶¿µ¼úµµ Áø´ÜÀÌ °¡´ÉÇÏ¸é °¡´ÉÇÑ ÇÑ ºü¸¥ Áø´Ü°ú Ä¡·á¸¸ÀÌ È¯ÀÚÀÇ »ýÁ¸À²À» ³ôÀÏ ¼ö ÀÖ´Ù.
  • bottle mouse syndrome
    ¿ìÀ¯º´ ¿ì½Ä
    Àå½Ã°£ ¿ìÀ¯¸¦ ¹°°í ÀÖ´Â À¯¾Æ¿¡ È£¹ß, ÇÏ¾Ç ÀýÄ¡¿¡´Â ¿ì½ÄÁõÀÌ ¾ø´Ù.
  • brain death syndrome
    ³ú»ç ÁõÈıº
  • brain stem syndrome
    ³ú°£ ÁõÈıº
  • Briquets syndrome
    ºê¸®ÄÉ ÁõÈıº
    µ¿ÀǾî=ataxia syndrome. ºê¸®ÄÉ ¿îµ¿ ½ÇÁ¶ ÁõÈıº.
  • brittle hair syndrome
    Ãë¾à ¸ð¹ß ÁõÈıº
  • bronze baby syndrome
    ûµ¿»ö ¾Æ±â ÁõÈıº
  • bruising syndrome
    Ÿ¹Ú»ó ÁõÈıº
  • burning feel syndrome
    ÀÛ¿­°¨ ÁõÈıº, ¼ÒÀÛÁ· ÁõÈıº
  • Bäfverstedt's syndrome
    º£Æä¸£½ºÅׯ® ÁõÈıº
  • capillary leak syndrome
    ¸ð¼¼Ç÷°ü ´©Ãâ ÁõÈıº
  • caplans syndrome
    ijÀÌÇöõ ÁõÈıº
  • carcinoid syndrome
    Ä«¸£½Ã³ëÀ̵å ÁõÈıº
  • cardiofaciocutaneous syndrome
    ½ÉÀå-¾ó±¼-ÇǺΠÁõÈıº
  • carotid artery syndrome
    °æµ¿¸Æ ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
aglossia-adactylia syndrome <syndrome> Congenital absence or hypoplasia of the tongue, associated with absence of the digits.
(05 Mar 2000)
Ahumada-Del Castillo syndrome <syndrome> Unphysiological lactation and amenorrhoea not following pregnancy characterised by hyperprolactinaemia and a pituitary adenoma.
Synonym: Argonz-Del Castillo syndrome.
(05 Mar 2000)
Aicardi's syndrome <syndrome> Agenesis of the corpus collosum with infantile spasms in female babies.
(05 Mar 2000)
alagille syndrome <syndrome> Hypoplasia of the hepatic ducts, congenital pulmonary artery stenosis, facial abnormalities, and other congenital malformations, particularly skeletal. It is often presented as jaundice during the neonatal period. It is an autosomal recessive disease generally manifesting during childhood. "arteriohepatic" refers to the pulmonary artery and the intrahepatic bile ducts, not to the hepatic artery.
(12 Dec 1998)
Albright's syndrome <syndrome> A condition of cystic bone growth that results from abnormal bone development. May occur with bone lesions, skin pigmentation and endocrine abnormalities.
See: McCune-Albright syndrome.
(27 Sep 1997)
alcohol amnestic syndrome <syndrome> An amnestic syndrome resulting from alcoholism; alcoholic "blackouts." Cf.: Korsakoff's syndrome.
(05 Mar 2000)
Aldrich syndrome <syndrome> An sex-linked (X chromosome) genetic disorder occurring in male children that is characterised by thrombocytopenia, eczema, melena and susceptibility to bacterial infections. Death often occurs from severe haemorrhage or overwhelming sepsis.
Inheritance: sex-linked (X chromosome).
(27 Sep 1997)
Alezzandrini's syndrome <syndrome> A rare syndrome appearing in adolescents and young adults, characterised by unilateral degenerative retinitis, followed by ipsilateral poliosis and facial vitiligo, and occasionally bilateral perceptive deafness.
(05 Mar 2000)
Alice in Wonderland syndrome <syndrome> The illusion of dreams, feelings of levitation, and alteration in the sense of the passage of time, sometimes associated with migraine, epilepsy, and various diseases of the parietal lobe of the brain.
(05 Mar 2000)
Allen-Masters syndrome <syndrome> Pelvic pain resulting from an old laceration of the broad ligament received during delivery.
(05 Mar 2000)
Alpert syndrome <syndrome> A usually inherited disorder characterised by premature closing of the cranial suture lines resulting in a peaked shaped head and abnormal facial appearance. Since it is usually autosomal dominant one or both parents also have the disorder.
Surgery is used to correct skull and facial abnormalities.
Inheritance: autosomal dominant.
(27 Sep 1997)
Alport's syndrome <syndrome> Progressive microscopic haematuria leading to chronic renal failure earlier in males, accompanied by defects such as sensorineural hearing loss, lenticonus, and maculopathy; autosomal dominant, autosomal recessive, and X-linked forms known.
(05 Mar 2000)
Alport syndrome <syndrome> An uncommon inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected.
Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision.
Incidence: 1 in 50,000.
Inheritance: sex-linked autosomal dominant.
(15 Nov 1997)
Alstrom's syndrome <syndrome> Retinal degeneration with nystagmus and loss of central vision, associated with obesity in childhood; sensorineural hearing loss and diabetes mellitus usually occur after age 10; autosomal recessive inheritance.
(05 Mar 2000)
amenorrhoea-galactorrhoea syndrome <syndrome> Unphysiologic lactation from endocrinological causes or from a pituitary tumour.
(05 Mar 2000)
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