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  • congenital word deafness
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  • discrete subvalvular congenital aortic stenosis
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  • giant congenital pigmented nevus
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  • congenital anodontia
    ¼±Ãµ¼º ¹«Ä¡(Áõ)(¡­ÙíöÍñø).
  • congenital anomaly
    ¼±Ãµ(¼º) ÀÌ»ó(ì¶ßÈ).
  • congenital aortic stenosis
    ¼±Ãµ¼º ´ëµ¿¸ÆÆÇ ÇùÂø(Áõ)(¡­ÓÞÔÑØæ÷ûúõó¸ñø).
  • congenital aural atresia
    ¼±Ãµ(¼º) ÀÌÆó¼âÁõ
  • congenital aural fistula =fistulus auris congenit
    ¼±Ãµ(¼º) ÀÌ·ç(°ø)
  • congenital auricular fistula
    ¼±Ãµ¼º ±Ó¹ÙÄû ´©Ãâ°ü
  • congenital bile duct atresia
    ÀÏ¹Ý ¼±Ãµ¼º ´ã°üÆó¼â(Áõ)(¡­ÓÅηøÍáðñø).
  • congenital bullous ichthyosiform erythroderma
    ¼±Ãµ¼º ¼öÆ÷¼º¾î¸°¼±¾ç È«ÇÇÁõ
  • congenital cataract
    ¼±Ãµ¹é³»Àå(à»ô¸ÛÜÒ®î¡).
  • congenital cataract
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  • congenital cause
    ¼±ÃµÀû ¿øÀÎ(¡­ê«ì×).
  • congenital central hypoventilation syndrome
    ¼±Ãµ¼º ÁßÃß¼º °ú¼Òȯ±â ÁõÈıº(à»ô¸àõñéõÒàõΦá´üµÑ¨ñøý¦ÏØ)
  • congenital cerebellar ataxia
    ¼±Ãµ¼º ¼Ò³ú¼º (¿îµ¿)½ÇÁ¶(¡­á³Òààõê¡ÔÑã÷ðà).
  • congenital cervical fistula<³ª> f. colli congenita
    ¼±Ãµ¼º °æ·ç(°ø)(¡­°æ·ç°ø).
  • congenital cholesteatoma
    ¼±Ãµ(¼º) ÁøÁÖÁ¾
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CAH   1) Chronic Active Hepatitis
  2) Congenital Adrenal Hyperplasia
CEP Congenital Erythropoetic Porphyria(= Gnther Disease; ¼±Ãµ¼º Á¶Ç÷±â¼º Porphyria
CHD   1) Congenital Heart Disease
  2) Common Hepatic Duct
ACED anhydrotic congenital ectodermal dysplasia
CAD cadaver, cadaveric; cold agglutinin disease; compressed air disease; computer-assisted design; compu...
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CRS Congenital Rubella Syndrome
CAVD Congenital absence of the vas deferens
CBAVD Congenital bilateal absence of the vas deferens
CCHS Congenital central hypoventilation syndrome
CCD Congenital chloride diarrhea
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  • congenital heart defect
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  • congenital hemolytic anemia
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    ÈÄõ¼º ¿ëÇ÷¼º ºóÇ÷¿¡ ´ëÀÀÇÏ¿©, ÀûÇ÷±¸ÀÇ ¼±ÃµÀûÀÎ ´ë»ç ÀÌ»ó¿¡ ÀÇÇØ ÀϾ´Â ¿ëÇ÷¼º ºóÇ÷ÀÇ ÃÑĪÀÌ´Ù. ±× ¿øÀÎÀº ¨ç ÀûÇ÷±¸ ¸· ÀÌ»ó¿¡ ÀÇÇÑ °Í
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  • congenital immunity
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  • congenital macroginbivae
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  • congenital missing tooh
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  • congenital muscle disorder
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  • congenital myotonia
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  • congenital pachyonychia
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congenital anaemia <haematology> A condition which develops in the foetus due to an incompatibility between the mother's blood type (RH factor) and the baby's. Maternal antibodies, which enter the foetal circulation during delivery attack the baby's red blood cells leading to haemolysis (rupture of the cells).
Symptoms include an infant with an enlarged liver and spleen, swelling, jaundice and anaemia.
(27 Sep 1997)
congenital ankyloblepharon Congenital adhesion of the upper and lower eyelid by bands of tissue.
Synonym: filiform adnatum.
Origin: ankylo-+ G. Blepharon, eyelid
(05 Mar 2000)
congenital antithrombin III deficiency Antithrombin III is a protein which stimulates the removal of blood clots in the bloodstream. Small blood clots form normally within the bloodstream, but are normally dissolved via the bodys antithrombin III. The deficiency of antithrombin III will result in an increased risk for blood clot formation causing organ damage. This is an inherited as a autosomal dominant trait.
Inheritance: autosomal dominant.
(27 Sep 1997)
congenital aplasia of thymus diGeorge syndrome
congenital aplastic anaemia <haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant.
Origin: Gr. Haima = blood
(13 Nov 1997)
congenital atonic pseudoparalysis Atonic pseudoparalysis of congenital origin (neither familial nor hereditary), observed especially in infants and characterised by absences of muscular tone only in muscles innervated by the spinal nerves.
Synonym: congenital atonic pseudoparalysis, myatonia congenita, Oppenheim's disease, Oppenheim's syndrome.
An indefinite term for a number of congenital neuromuscular disorders that cause generalised myotonia in young children, and that have a benign course (static or regressive).
(05 Mar 2000)
congenital baldness Absence of all hair at birth, associated with psychomotor epilepsy; autosomal dominant inheritance.
Synonym: congenital baldness, hypotrichiasis.
(05 Mar 2000)
congenital bronchiectasis Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Although rarely congenital, it is most often an acquired condition in childhood.
(27 Sep 1997)
congenital cardiomyopathy <radiology> Endocardial fibroelastosis, myocarditis, glycogen storage disease (Pompe's), anomalous origin of left coronary artery from pulmonary artery
(12 Dec 1998)
congenital cataract A cataract or clouding or the lens of the eye, that occurs in the foetus at some time during pregnancy. Children with Down's syndrome and galactosaemia have an increased incidence of congenital cataracts.
Treatment includes cataract removal and the insertion of an artificial lens.
(27 Sep 1997)
congenital cerebellar atrophy Familial disorder that causes degeneration of various cells in the cerebellum. Two types are recognised, one in which the granular layer cells degenerate, the other in which the Purkinje cells degenerate.
(05 Mar 2000)
congenital cerebral aneurysm Localised dilation of a cerebral vessel; usually a berry aneurysm.
(05 Mar 2000)
congenital choreoathetosis A type of cerebral palsy manifested predominantly as bilateral involuntary movements, beginning at about the age of 3 years, and preceded by generalised hypotonia and delayed motor development. Due to various causes, including kernicterus and birth hypoxia.
Synonym: congenital choreoathetosis, double congenital athetosis, Vogt syndrome.
(05 Mar 2000)
congenital clasped thumb with mental retardation See: Clasped thumbs and mental retardation.
(12 Dec 1998)
congenital conus A congenital inferior crescent on the choroid at the edge of the optic disk; not associated with myopia.
Synonym: congenital conus.
(05 Mar 2000)
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