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"congenital"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
  • congenital cloaca
    ¼±Ãµ¼º ÃѹèÃâ°­(¡­õÅÛÉõóË·).
  • congenital clumsiness
    ¼±Ãµ¼º(à»ô¸àõ)¼­Åõ¸§.
  • congenital color vision defect
    ¼±Ãµ»ö°¢ÀÌ»ó
  • congenital contractural arachnodactyly
    ¼±Ãµ¼º ¼öÃ༺ °Å¹Ì¼Õ¹ß°¡¶ô
  • congenital coronary arteriovenous fistula
    ¼±Ãµ¼º °ü»óµ¿Á¤¸Æ·ç.
  • congenital cystic eye
    ¼±Ãµ³¶Æ÷¾È
  • congenital deafness
    ¼±Ãµ(¼º) ³­Ã», ¼±Ãµ(¼º) ±Í¸Ó°Å
  • congenital debility<³ª> debilitas vitae con gen ita
    ¼±Ãµ(¼º) ¾àÁú(¡­å°òõ ).
  • congenital defect
    ¼±Ãµ¼º °á¼Õ(Áõ)(¡­ÌÀáßñø).
  • congenital defect
    ¼±Ãµ°áÇÔ
  • congenital deficiency of glucuronyl transfe ra se
    ¼±Ãµ¼º ±Û·çÄí·Ð»ê Àü À§È¿¼Ò°áÇÌÁõ(¡­ï®êÈý£áÈÌÀù¹ñø).
  • congenital deformation
    ¼±Ãµ¼º ±âÇü(¡­Ñ±û¡)
  • congenital diaphragmatic hernia
    ¼±Ãµ¼º Ⱦ°Ý¸·Ç츣´Ï¾Æ<Å»Àå>.
  • congenital dilatation of colon
    ¼±Ãµ¼º °áÀåÈ®Àå(Áõ)(¡­°áÀåÈ®ÀåÁõ).
  • congenital diplegia
    ¼±Ãµ¼º ¾çÃø¸¶ºñ(¡­å»ö° Ýö).
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    ÇѱÛ
  • nipple,congenital conversion
    ¼±Ãµ¼º Àüȯ(à»ô¸àõ ï®üµ)
  • polar congenital cataract
    ±Ø¼º¼±Ãµ¹é³»Àå
  • pulverulent congenital cataract
    °¡·ç¸ð¾ç¼±Ãµ¹é³»Àå, ºÐ¸»»ó¼±Ãµ¹é³»Àå
  • reduplicated congenital cataract
    Áߺ¹¼±Ãµ¹é³»Àå
  • syphilis congenita =congenital s. ³ª
    ¼±Ãµ¸Åµ¶(à»ô¸ØÞÔ¸).
  • syphilis congenita =congenital s. ³ª
    ¼±Ãµ¸Åµ¶(à»ô¸ØÞÔ¸)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
CAD cadaver, cadaveric; cold agglutinin disease; compressed air disease; computer-assisted design; compu...
CAH chronic active hepatitis; chronic aggressive hepatitis; combined atrial hypertrophy; congenital adre...
CALP congenital absence of left pericardium
CAS calcarine sulcus; calcific aortic stenosis; Cancer Attitude Survey; carbohydrate-active steroid; car...
CASMD congenital atonic sclerotic muscular dystrophy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
CMS Congenital Myasthenic Syndromes
CNS Congenital Nephrotic Syndrome
CN Congenital Nystagmus
CRS Congenital Rubella Syndrome
CAVD Congenital absence of the vas deferens
Çѱ¹Ç¥ÁØÁúº´»çÀκзù ¾àÀÚ ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • Q73.0
    Congenital absence of unspecified limb(s)
    »ó¼¼ºÒ¸í »çÁöÀÇ ¼±Ãµ °á¿©
  • Q71.1
    Congenital absence of upper arm and forearm with hand present
    ¼ÕÀÌ ÀÖ´Â À§ÆÈ ¹× ¾Æ·¡ÆÈÀÇ ¼±Ãµ °á¿©
  • Q52.0
    Congenital absence of vagina
    ÁúÀÇ ¼±Ãµ °á¿©
  • Q16.0
    Congenital absence of(ear) auricle
    ±Ó¹ÙÄûÀÇ ¼±Ãµ °á¿©
  • Q42.2
    Congenital absence, atresia and stenosis of anus with fistula
    »û±æ(´©°ø)À» µ¿¹ÝÇÑ Ç×¹®ÀÇ ¼±Ãµ °á¿©, Æó¼â ¹× ÇùÂø
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • 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
  • congenital missing tooh
    ¼±Ãµ¼º °á¼ÕÄ¡
  • congenital muscle disorder
    ¼±Ãµ¼º ±Ù Àå¾Ö
  • congenital myotonia
    ¼±Ãµ¼º ±Ù°æÁ÷Áõ
  • congenital nonocclusion
    ¼±Ãµ¼º °³±³
  • congenital nystagmus
    ¼±Ãµ¼º ¾ÈÁø
    ÁÖ½ÃÀÇ ¸ðµç À§Ä¡°¡ ¼öÆòÀÎ ÁøÀÚ¼º ¶Ç´Â À²µ¿¼º ¾ÈÁøÀ̸ç, ÆøÁÖ¿¡ ÀÇÇØ ¾àÈ­µÇ¸ç, ȯÀÚ´Â ¸Õ °Å¸®º¸´Ù °¡±î¿î °Å¸®¿¡¼­ ´õ Àß º»´Ù.
  • congenital pachyonychia
    ¼±ÃµÀû ¼Õ, ¹ßÅé °æ°íÁõ
  • congenital pigmented nevus
    ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý
    Åë»óÀûÀÎ »ö¼Ò¼º ¸ð¹ÝÀº Ãâ»ý ÈÄ¿¡ ¹ß»ýÇϳª ¾à 1%ÀÇ ½Å»ý¾Æ´Â Ãâ»ý ½ÃºÎÅÍ ¸ð¹ÝÀ» °¡Áö°í ÀÖÀ¸¸ç, À̰ÍÀ» ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹ÝÀ̶ó°í ÇÑ´Ù. ´ëºÎºÐÀÇ °æ¿ì ÈÄõ¼º ¸ð¹Ýº¸´Ù Ä¿¼­ 1.5cm ÀÌ»óÀÌ°í ¶§·Î´Â 20cm¸¦ ÃʰúÇÏ´Â °æ¿ì°¡ Àִµ¥ À̸¦ '°Å´ë ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý'À̶ó°í ºÎ¸¥´Ù. ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý¿¡¼­ Áß¿äÇÑ °ÍÀº ¾Ç¼º ÀüȯÀÇ ºóµµ°¡ ÀϹÝÀο¡ ºñÇØ ³ô´Ù´Â °ÍÀÌ´Ù. °Å´ë ¸ð¹Ý¿¡¼­´Â ¾à 6.3³»Áö 12%°¡ ¾Ç¼º Èæ»öÁ¾À¸·Î ÀÌÇàÇÏ¸ç ºñ°Å´ë ¸ð¹Ýµµ Àû¾îµµ 1%
  • congenital porphyria
    ¼±Ãµ¼º Æ÷¸£ÇǸ®¾Æ ´ë»ç Àå¾Ö, ¼±Ãµ¼º Æ÷¸£ÇǸ°Áõ
    ¼±Ãµ¼º Æ÷¸£ÇǸ°
  • congenital Q-T syndrome
    ¼±Ãµ¼º QT ÁõÈıº
  • congenital rubella syndrome
    ¼±Ãµ¼º dzÁø ÁõÈıº
    žư¡ ¸ðü ³»¿¡¼­ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î »ý±â´Â ÀÌ»ó Áõ¼¼. ÀӽŠÃʱâÀÇ ÀÓ»êºÎ°¡ dzÁø¿¡ °É¸®¸é žư¡ ¹ßÀ° Ãʱ⿡ dzÁø ¹ÙÀÌ·¯½º¿¡ Ä§ÇØµÇ¾î Ãâ»ý ÈÄ¿¡ ´«ÀÇ ÀÌ»ó
  • congenital spastic paraplegia
    ¼±Ãµ¼º ¿¬Ãà´ë¸¶ºñ
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    ÇѱÛ
    ¼³¸í
  • 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
  • congenital missing tooh
    ¼±Ãµ¼º °á¼ÕÄ¡
  • congenital muscle disorder
    ¼±Ãµ¼º ±Ù Àå¾Ö
  • congenital myotonia
    ¼±Ãµ¼º ±Ù°æÁ÷Áõ
  • congenital nonocclusion
    ¼±Ãµ¼º °³±³
  • congenital nystagmus
    ¼±Ãµ¼º ¾ÈÁø
    ÁÖ½ÃÀÇ ¸ðµç À§Ä¡°¡ ¼öÆòÀÎ ÁøÀÚ¼º ¶Ç´Â À²µ¿¼º ¾ÈÁøÀ̸ç, ÆøÁÖ¿¡ ÀÇÇØ ¾àÈ­µÇ¸ç, ȯÀÚ´Â ¸Õ °Å¸®º¸´Ù °¡±î¿î °Å¸®¿¡¼­ ´õ Àß º»´Ù.
  • congenital pachyonychia
    ¼±ÃµÀû ¼Õ, ¹ßÅé °æ°íÁõ
  • congenital pigmented nevus
    ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý
    Åë»óÀûÀÎ »ö¼Ò¼º ¸ð¹ÝÀº Ãâ»ý ÈÄ¿¡ ¹ß»ýÇϳª ¾à 1%ÀÇ ½Å»ý¾Æ´Â Ãâ»ý ½ÃºÎÅÍ ¸ð¹ÝÀ» °¡Áö°í ÀÖÀ¸¸ç, À̰ÍÀ» ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹ÝÀ̶ó°í ÇÑ´Ù. ´ëºÎºÐÀÇ °æ¿ì ÈÄõ¼º ¸ð¹Ýº¸´Ù Ä¿¼­ 1.5cm ÀÌ»óÀÌ°í ¶§·Î´Â 20cm¸¦ ÃʰúÇÏ´Â °æ¿ì°¡ Àִµ¥ À̸¦ '°Å´ë ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý'À̶ó°í ºÎ¸¥´Ù. ¼±Ãµ¼º »ö¼Ò¼º ¸ð¹Ý¿¡¼­ Áß¿äÇÑ °ÍÀº ¾Ç¼º ÀüȯÀÇ ºóµµ°¡ ÀϹÝÀο¡ ºñÇØ ³ô´Ù´Â °ÍÀÌ´Ù. °Å´ë ¸ð¹Ý¿¡¼­´Â ¾à 6.3³»Áö 12%°¡ ¾Ç¼º Èæ»öÁ¾À¸·Î ÀÌÇàÇÏ¸ç ºñ°Å´ë ¸ð¹Ýµµ Àû¾îµµ 1%
  • congenital porphyria
    ¼±Ãµ¼º Æ÷¸£ÇǸ®¾Æ ´ë»ç Àå¾Ö, ¼±Ãµ¼º Æ÷¸£ÇǸ°Áõ
    ¼±Ãµ¼º Æ÷¸£ÇǸ°
  • congenital Q-T syndrome
    ¼±Ãµ¼º QT ÁõÈıº
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
congenital epulis of newborn A congenital benign nodular tumour of the alveolar ridge, of unknown histogenesis; histologically, it is composed of large cells with a granular cytoplasm similar to that of a granular cell tumour (myoblastoma).
(05 Mar 2000)
congenital erythropoietic porphyria A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. Acute intermittent porphyria is a rare inherited (autosomal dominant) form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differntiated measuring various blood prophyrins.
Inheritance: autosomal dominant.
(27 Sep 1997)
congenital facial diplegia <syndrome> A developmental bilateral facial paralysis usually associated with oculomotor or other neurological disorders.
Synonym: congenital facial diplegia.
(05 Mar 2000)
congenital fibrosis of the extraocular muscles An autosomal dominant disorder associated with blepharoptosis and absence of eye movements.
(05 Mar 2000)
congenital generalised fibromatosis Multiple subcutaneous and visceral fibrous tumours present at birth; a rare disorder often fatal in the first week of life, although sometimes undergoing spontaneous remission; probable autosomal recessive inheritance.
(05 Mar 2000)
congenital giant pigmented nevus These large pigmented (often hairy) congenital nevi are important because of their increased risk (10 to 15%) of conversion into malignant melanoma. A biopsy can confirm if cells have turned malignant. Any change in a pre-existing nevus should prompt a physician evaluation.
(27 Sep 1997)
congenital glaucoma An affection of infancy, marked by an increase of intraocular pressure with enlargement of the eyeball.
Synonym: congenital glaucoma, hydrophthalmia, hydrophthalmos, hydrophthalmus.
Origin: G. Bous, ox, + ophthalmos, eye
(05 Mar 2000)
congenital haemolytic anaemia Accelerated destruction of red blood cells due to an inherited defect, such as in the membrane in hereditary spherocytosis.
(05 Mar 2000)
congenital haemolytic icterus <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane.
This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged.
Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal.
(27 Sep 1997)
congenital haemolytic jaundice <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane.
This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged.
Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal.
(27 Sep 1997)
congenital heart block Atrioventricular block present in utero or at birth and usually of advanced or complete degree.
(05 Mar 2000)
congenital heart disease Heart disease that is present from birth.
Examples include atrial septal defect, ventricular septal defect, aortic stenosis and tetralogy of Fallot.
(27 Sep 1997)
congenital hernia of the diaphragm A condition present at birth where there is abnormal protrusion of abdominal contents upward through a defect in the diaphragm. This condition is treated as a surgical emergency due to interference with the infant's breathing. Smaller, less serious diaphragmatic hernias may also be seen in adults.
(27 Sep 1997)
congenital hip dislocation A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints.
(27 Sep 1997)
congenital hip dysplasia A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints.
Origin: Gr. Plassein = to form
(27 Sep 1997)
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congenital palatopharyngeal incompetence CPI; a congenital variety of velopharyngeal insufficiency.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
congenital afibrinogenemia a rare autosomal recessive hemorrhagic coagulation disorder, characterized by complete incoagulability of the blood; hemorrhagic manifestations vary from mild to serious.
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
congenital alopecia alopecia congenita
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
congenital A condition that is present at birth resulting from either heredity or environmental influences or both.
Ãâó: www.geocities.com/coloboma_group/words.html
congenital A characteristic of an animal that is present at birth. It may be inherited or induced by events that occur during pregnancy.
Ãâó: www.peteducation.com/dict_alpha_listing.cfm
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