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  • congenital hypoplastic anemia
    ¼±Ãµ¼º Çü¼ººÎÀü¼º ºóÇ÷
  • congenital ichthyosiform erythroderma
    ¼±Ãµ¾î¸°¼±Çü È«ÇÇÁõ
  • congenital ichthyosis
    ¼±Ãµ(¼º) ¾î¸°¼±(¡­åàìçàÈ).
  • congenital ichthyosis
    ¼±Ãµ¼º(à»ô¸àõ)¾î¸°¼±(åà×÷àÈ)
  • congenital idiopathic methemoglobinuria
    ¼±Ãµ(¼º) Ư¹ß¼º ¸ÞÆ®Çì¸ð±Û·Îºó¿ä Áõ(à»ô¸àõ÷åÛ¡àõ¡­èññø).
  • congenital immunity
    ¼±Ãµ¼º ¸é¿ª(¡­Øóæ¹).
  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º ¸é¿ª°áÇÌ ÁõÈıº
  • congenital immunodeficiency syndrome
    ¼±Ãµ¼º¸é¿ª°áÇÌÁõ(Èıº)
  • congenital immunologic thrombocytopenia
    ¼±Ãµ¼º ¸é¿ª¼º Ç÷¼ÒÆÇ°¨¼ÒÁõ(¡­Øóæ¹ àõúìá³÷ùÊõá´ñø).
  • congenital incontinence
    ¼±Ãµ¼º ½Ç±Ý(¡­ã÷Ð×).
  • congenital infantile hemiplegia
    ¼±Ãµ¼º ¿µ¾Æ¼º Æí¸¶ºñ.
  • congenital infection
    ¼±Ãµ°¨¿°
  • congenital intracranial tumor
    ¼±Ãµ¼º µÎ°³(°­)³»Á¾¾ç(¡­ÔéËÏË·Ò®ðþ åË).
  • congenital intussusception
    ¼±ÃµÃ¢ÀÚ°ãħÁõ
  • congenital laryngeal spasm
    ¼±Ãµ(¼º) Èĵο¬Ãà
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CIA chemiluminescent immunoassay; chymotrypsin inhibitor activity; colony-inhibiting activity; congenita...
CIBHA congenital inclusion-body hemolytic anemia
CLAH congenital lipoid adrenal hyperplasia
CLAS congenital localized absence of skin
CLD chloride diarrhea; chronic liver disease; chronic lung disease; congenital limb deficiency; crystal ...
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CMT Congenital muscular torticollis
CMD Congenital myotonic dystrophy
CSNB Congenital stationary night blindness
CS Congenital syphilis
FCMD Fukuyama congenital muscular dystrophy
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syphilis, congenital Syphilis acquired in utero and manifested by any of several characteristic tooth (hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur.
(12 Dec 1998)
disease, congenital heart A birth defect of the heart or great blood vessels (like the aorta).
(12 Dec 1998)
double congenital athetosis 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)
ichthyosiform erythroderma, congenital Designation for several severe forms of ichthyosis, present at birth, that are characterised by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalised scaling. The forms include bullous (hyperkeratosis, epidermolytic), non-bullous (ichthyosis, lamellar), wet type, and dry type.
(12 Dec 1998)
toxoplasmosis, congenital Congenital infection with toxoplasma gondii characterised by lesions of the central nervous system.
(12 Dec 1998)
foot deformities, congenital Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth.
(12 Dec 1998)
limb deformities, congenital Congenital structural deformities of the upper and lower extremities collectively or unspecified.
(12 Dec 1998)
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