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  • congenital rubella syndrome
    ¼±Ãµ¼ºÇ³ÁøÁõ(Èıº)
  • congenital spastic paraplegia
    ¼±Ãµ¼º ¿¬Ãà´ë¸¶ºñ(¡­ÕýõêÓß Ýö).
  • congenital spherocytic anemia
    ¼±Ãµ¼º ±¸»óÀûÇ÷±¸ºóÇ÷(¡­Ï¹ßÒîåúìϹ޸úì).
  • congenital strabismus
    ¼±Ãµ»ç½Ã
  • congenital stridor
    ¼±Ãµ¼º õ¸í(¡­ô·Ù°).
  • congenital syphilis
    ¼±Ãµ¼º¸Åµ¶
  • congenital syphilis
    ¹Ì»ý¹° ¼±Ãµ¼º ¸Åµ¶(¡­ØÞÔ¸).
  • congenital syphilis
    ¼±Ãµ¼º ¸Åµ¶
  • congenital sypohilis
  • congenital telangiectatic erythema
    ¼±Ãµ¼º(à»ô¸àõ) ¸ð¼¼Ç÷°üÈ®À强 È«¹Ý(Ù½á¬úìηüªíåàõ ûõÚè)
  • congenital torticollis
  • congenital toxoplasmosis
    ¼±Ãµ¼º Åå¼ÒÇö󽺸¶Áõ(¡­ñø).
  • congenital tuberculosis
  • congenital urethral valve
    ¼±Ãµ¼º ¿äµµÆÇ¸·(¡­èñÔ³÷ûد).
  • congenital varicella
    ¼±Ãµ¼º ¼öµÎ
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CMSD congenital myocardial sympathetic dysinnervation
CN caudate nucleus; cellulose nitrate; charge nurse; child nutrition; chloroacetophenone; clinical nurs...
CNF chronic nodular fibrositis; congenital nephrotic syndrome of the Finnish [type]
CNHD congenital nonspherocytic hemolytic disease
CNS central nervous system; clinical nurse specialist; coagulase-negative staphylococci; congenital neph...
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CCHD cyanotic congenital heart disease
MCA/MR multiple congenital anomalies mental retardation
MCA multiple congenital anomaly
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  • Q34.1
    Congenital cyst of mediastinum
    Á¾°Ýµ¿ÀÇ ¼±Ãµ ³¶Á¾
  • Q33.0
    Congenital cystic lung
    ¼±Ãµ ³¶¼º Æó
  • P35.1
    Congenital cytomegalovirus infection
    ¼±Ãµ °Å´ë¼¼Æ÷¹ÙÀÌ·¯½º °¨¿°
  • Q66
    Congenital deformities of feet
    ¹ßÀÇ ¼±Ãµ º¯Çü
  • Q65
    Congenital deformities of hip
    ¾ûµ¢°üÀýÀÇ ¼±Ãµ º¯Çü
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congenital a. of newborn erythroblastosis fetalis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital abducens-facial p. Möbius syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital adrenal h. a group of inherited disorders in which deficiencies of enzymes that catalyze the biosynthesis of cortisol result in compensatory hypersecretion of corticotropin and subsequent adrenal hyperplasia as well as excessive androgen production. There are several different forms, numbered in order of increasing severity, of which the most common type is type III, or 21-hydroxylase deficiency (see accompanying table). They range from “classic” forms present at birth with severe salt wasting or hypertension and pseudohermaphroditism to less severe “nonclassic” forms of later onset. See also deficiency conditions at names of specific enzymes.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital aregenerative a. congenital hypoplastic a. (def. 1).
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital articular r. rigid or deformed joints in newborn calves or lambs; a hereditary variety is seen among Charolais cattle, and a type acquired in utero is part of the Akabane virus disease. Called also congenital arthrogryposis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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