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  • congenital choreoathetosis
    ¼±Ãµ¼º ¹«µµº´(¡­ÙñÔ°Ü»)¾ÆÅ×Åä½Ã½º.
  • congenital circumscribed alopecia
    ¼±Ãµ¼º ±¹ÇѼº Å»¸ð(Áõ)
  • 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>.
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CLD chloride diarrhea; chronic liver disease; chronic lung disease; congenital limb deficiency; crystal ...
CM California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ...
CMD campomelic dysplasia; camptomelic dwarfism; cartilage matrix deficiency; chief medical director; chi...
CMG canine or congenital myasthenia gravis; chopped meat glucose [medium]; cystometrography, cystometrog...
CMH cardiomyopathy, hypertrophic; community mental health [services or program]; congenital malformation...
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SCN Severe congenital neutropenia
CCHD cyanotic congenital heart disease
MCA/MR multiple congenital anomalies mental retardation
MCA multiple congenital anomaly
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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)
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
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