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    ÇѱÛ
  • congenital laryngeal stridor
    ¼±ÃµÈĵα׷·°Å¸²
  • congenital megacolon
    ¼±Ãµ°Å´ëÀß·ÏâÀÚ, ¼±Ãµ°Å´ë°áÀå
  • congenital nonbullous icthyosiform erythroderma
    ¼±Ãµºñ¹°Áýºñ´ÃÁõ¸ð¾çÈ«»öÇǺÎ(Áõ), ¼±Ãµºñ¼öÆ÷ºñ´ÃÁõ¸ð¾çÈ«»öÇǺÎ(Áõ)
  • congenital oculomotor apraxia
    ¼±ÃµÈ´º¸±â¸øÇÔ(Áõ), ¼±ÃµÈ´º¸±â½ÇÇàÁõ
  • congenital preauricular fistula
    ¼±Ãµ±Ó¹ÙÄû¾Õ»û±æ, ¼±ÃµÀÌÀüºÎ´©°ø
  • congenital rubella syndrome
    ¼±ÃµÇ³ÁøÁõÈıº
  • congenital syphilis
    ¼±Ãµ¸Åµ¶
  • congenital torticollis
    ¼±Ãµ±â¿î¸ñ, ¼±Ãµ»ç°æ
  • congenital toxoplasmosis
    ¼±ÃµÅå¼ÒÆ÷ÀÚÃæÁõ
  • congenital word deafness
    ¼±Ãµ¸»±Í¸ÔÀ½, ¼±Ãµ¾î³ó
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 8 ÆäÀÌÁö: 3
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  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • congenital laryngeal stridor
    ¼±ÃµÈĵα׷·°Å¸²
  • congenital nonbullous icthyosiform erythroderma
    ¼±Ãµºñ¹°Áýºñ´ÃÇǺÎÁõ¸ð¾çÈ«»öÇǺÎÁõ
  • congenital preauricular fistula
    ¼±Ãµ±Ó¹ÙÄû¾Õ»û±æ, ¼±ÃµÀÌÀüºÎ´©°ø
  • congenital telangiectatic erythema
    ¼±Ãµ¸ð¼¼Ç÷°üÈ®ÀåÈ«¹Ý
  • congenital word deafness
    ¼±Ãµ¸»±Í¸ÔÀ½
  • discrete subvalvular congenital aortic stenosis
    ºÐ¸®¼±ÃµÆÇ¸·¹Ø´ëµ¿¸ÆÇùÂøÁõ
  • giant congenital pigmented nevus
    ¼±Ãµ°Å´ë»ö¼ÒÄ§Âø¸ð¹Ý
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  • iris pattern
    ȫ乫´Ì(ÆÐÅÏ)
  • iris pigment
    ȫä»ö¼Ò(¡­ßäáÈ).
  • iris plane lens
    ȫä¸é·»Áî
  • iris process
    ȫäµ¹±â
  • iris prolapse
    ȫäŻÃâ
  • iris retractors
    ȫäÈÅ
  • iris root
    ȫä±ÙºÎ
  • iris scissors
    ȫä°¡À§
  • iris spatula
    ȫäÁÖ°Æ.
  • iris sphincter
    µ¿°ø°ý¾à±Ù
  • iris stroma
    ȫä°£Áú
  • iris-nevus syndrome
    ȫä¸ð¹ÝÁõÈıº
  • iris-supported intraocular lens
    ȫäÁöÁö·»Áî
  • lesser arterial circle of iris
    ÀÛÀºÈ«Ã¤µ¿¸Æ°í¸®
  • lesser circle of iris
    ȫä¼Òµ¿¸Æ·û(ûöóôá³ÔÑØæëÌ).
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CHA Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi...
CHD Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis...
CEA Carcino-Embryonic Antigen [HP 1825-6]
  ; Oncofetal Antigens
  ; Glycopro...
HIVD Herniation(Herniated) of Inter-Vertebral Disc
  - Cervical HIVD
   &...
PEEP Positive End-Expiratory Pressure
  ? Ix
    1. PaO2 < 60 mmHg, ...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
ARM Ano-Rectal Malformations
AVM Arterio-Venous malformations
CVM Cardiovascular malformations
CM Cavernous Malformations
DAVM dural arterio-venous malformations
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  • congenital epulis
    ¼±Ãµ¼º ¿¡Çª¸®½º, ¼±Ãµ¼º Ä¡ÀºÁ¾
    Ãâ»ý ½Ã Á¸ÀçÇÏ´Â »ó¾Ç Ä¡ÀºÀÇ µ¹ÃâµÈ Á¾¹°·Î ºñƯÀÌÀûÀÌ´Ù. ½Å»ý¾Æ¿¡°Ô¸¸ ³ªÅ¸³ª´Â À¯°æ¼º Á¾¹°·Î °ú¸³ ¼¼Æ÷¼º ±Ù¸ð¼¼Æ÷Áõ°ú Á¶Á÷»óÀÌ À¯»çÇÏ¿© µÎ º´¼ÒÀÇ ±â¿øÀÌ °°´Ù´Â ÇÐÀÚµµ ÀÖ°í, ¹ß»ý ºÎÀ§°¡ ÀüÀÚ´Â »ó¾Ç ÀüÄ¡ºÎÀ̰í Ãâ»ý ½ÃºÎÅÍ Á¸ÀçÇϰí ÈÄÀÚ´Â Çô¿¡ ¹ß»ýµÇ¸ç ¾î´À ¿¬·ÉÃþ¿¡¼­³ª ¹ß»ýÇϹǷΠµÎ º´¼Ò´Â º°°³ÀÌ´Ù. ÀüÀÚ´Â Á¾¾ç Á¶Á÷¿¡¼­ °¡²û Ä¡¼º »óÇÇ Àܻ簡 ¹ß°ßµÇ¾î Ä¡¹èÀÇ ¹ßÀ° ÀÌ»óÀ¸·Î ¾ß±âµÈ´Ù°í º»´Ù. È£¹ß ºÎÀ§´Â »ó¾Ç ÀüÄ¡ºÎ·Î ±¸Çü ¶Ç´Â ³­¿øÇüÀ̸ç Á÷°æÀÌ 0.5-2.5cm Á¤µµÀÇ ¾ç¼º Áõ½Ä¹°·Î ³²¾Æº¸´Ù ¿©¾Æ¿¡¼­ 10¹èÁ¤µµ ºó¹ßÇÏ´Ù. Á¾¾çÀ» ÀÌ·ç´Â ¼¼Æ÷µéÀº Å©°í ´Ù°¢ÇüÀ̸ç, ¼¼Æ÷ÁúÀº ¿¡¿À½Å¿¡ ¿°»öµÇ¸ç °ú¸³ »óÀ̸ç ÇÙÀº ÀÛ°í ÆíÀçµÇ¾î ÀÖ´Ù.
  • congenital erythropoietic porphyria
    ¼±ÃµÀû ÀûÇ÷±¸ »ý¼º Æ÷¸£ÇǸ°Áõ
  • congenital fibrosis syndrome
    ¼±Ãµ ¼¶À¯Áõ ÁõÈıº
  • congenital fracture
    ¼±Ãµ¼º °ñÀý
  • congenital glaucoma
    ¼±Ãµ¼º ³ì³»Àå
    ³ì³»ÀåÀ̶õ ¾È¾Ð »ó½ÂÀ¸·Î ÀÎÇÏ¿© ´Ù¾çÇÑ Àå¾Ö±ºÀ» ÀÌ·ç¸ç ½Ã½Å°æ À§Ãà°ú ½Ã¾ß °á¼ÕÀ» ÃÊ·¡ÇÏ´Â ÁúȯÀÌ´Ù. ÀÌ Áß ¼±Ãµ¼º ³ì³»ÀåÀº Ãâ»ý ÈÄ 3³â À̳»¿¡ ¹ß»ýÇÏ´Â ¿µ¾Æ ³ì³»Àå°ú ±× ÀÌÈÄ¿¡ ¹ß»ýÇÏ´Â ¿¬¼Ò ³ì³»ÀåÀ¸·Î ³ª´©¾îÁø´Ù.
  • congenital granular cell epulis
    ¼±ÃµÀû °ú¸³¼¼Æ÷¼º Ä¡ÀºÁ¾
  • congenital heart defect
    ¼±Ãµ¼º ½É³» °á¼ÕÁõ
  • congenital hemolytic anemia
    ¼±Ãµ¼º ¿ëÇ÷¼º ºóÇ÷
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  • congenital hypothyroidism
    ¼±Ãµ¼º °©»ó¼± ±â´ÉÀúÇÏÁõ
  • congenital immunity
    ¼±Ãµ¼º ¸é¿ª
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ
  • congenital intracranial tumor
    ¼±Ãµ¼º µÎ°³³» Á¾¾ç
  • congenital leukokeratosis
    ¼±Ãµ¼º ¹é»ö °¢È­Áõ
  • congenital macroginbivae
    ¼±Ãµ¼º Ä¡Àº ºñ´ëÁõ
  • congenital megaureter
    ¼±Ãµ¼º °Å´ë¿ä°ü
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
iris neoplasms Tumours of the iris characterised by increased pigmentation of melanocytes. Iris nevi are composed of proliferated melanocytes and are associated with neurofibromatosis and malignant melanoma of the choroid and ciliary body. Malignant melanoma of the iris often originates from preexisting nevi.
(12 Dec 1998)
iris-nevus syndrome <syndrome> Syndrome of glaucoma, iris atrophy, decreased corneal endothelium, anterior peripheral synechia, and multiple iris nodules.
Synonym: Cogan-Reese syndrome, iris-nevus syndrome.
(05 Mar 2000)
iris pits Colobomas affecting the stroma of the iris with pigment epithelium intact.
(05 Mar 2000)
tremulous iris Agitated motion of the iris.
Synonym: tremulous iris.
Origin: irido-+ G. Doneo, to shake to and fro
(05 Mar 2000)
erythema iris Concentric rings of erythema varying in intensity, characteristic of erythema multiforme.
Synonym: herpes iris.
(05 Mar 2000)
essential progressive atrophy of iris Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years.
(05 Mar 2000)
folds of iris Numerous very fine, almost microscopic, radial folds on the posterior surface of the iris that extend around the pupillary margin.
Synonym: plicae iridis.
(05 Mar 2000)
lesser arterial circle of iris An arterial circle near the pupillary margin of the iris.
Synonym: circulus arteriosus iridis minor.
(05 Mar 2000)
lesser ring of iris The narrow inner zone of the iris.
Synonym: annulus iridis minor.
(05 Mar 2000)
lichen iris Ringworm with concentric rings of erythematous papules.
(05 Mar 2000)
adrenal hyperplasia, congenital A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form.
(12 Dec 1998)
anaemia, dyserythropoietic, congenital A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test.
(12 Dec 1998)
anaemia, haemolytic, congenital Haemolytic anaemia due to various intrinsic defects of the erythrocyte.
(12 Dec 1998)
anaemia, haemolytic, congenital nonspherocytic Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated.
(12 Dec 1998)
bovine congenital ataxia An autosomal recessive ataxia seen in several European breeds of cattle.
(05 Mar 2000)
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