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MACDP Metropolitan Atlanta Congenital Defects Program
MCA major coronary artery; Maternity Center Association; medical care administration; methylcholanthrene...
MCA/MR multiple congenital anomaly/mental retardation [syndrome]
PAMC pterygoarthromyodysplasia congenital
SCA self-care agency; severe congenital anomaly; sickle-cell anemia; single-camera autostereoscopic [ima...
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  • E03.1
    Congenital hypothyroidism without goitre
    °©»ó»ùÁ¾À» µ¿¹ÝÇÏÁö ¾ÊÀº ¼±Ãµ °©»ó»ù ±â´ÉÀúÇÏÁõ
  • P94.2
    Congenital hypotonia
    ¼±Ãµ ±äÀå°ú¼Ò
  • Q80
    Congenital ichthyosis
    ¼±Ãµ ºñ´ÃÁõ
  • Q80.9
    Congenital ichthyosis, unspecified
    »ó¼¼ºÒ¸íÀÇ ¼±Ãµ ºñ´ÃÁõ
  • P37.9
    Congenital infectious or parasitic disease, unspecified
    »ó¼¼ºÒ¸íÀÇ ¼±Ãµ °¨¿°¼º ¶Ç´Â ±â»ýÃæ¼º Áúȯ
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congenital multiple f. see infantile myofibromatosis, under myofibromatosis.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital n. nephritis existing at birth, such as in congenital syphilitic nephritis or Alport's syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital nonspherocytic hemolytic a. any of a heterogeneous group of inherited anemias characterized by shortened red blood cell survival, lack of spherocytosis, and normal osmotic fragility associated with erythrocyte membrane defects, multiple intracellular enzyme deficiencies or other defects, or unstable hemoglobins. The most common enzyme defects are in glucose-6-phosphate dehydrogenase or pyruvate kinase.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital p. Fanconi syndrome (def. 1).
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
congenital palatopharyngeal i. a congenital variety of velopharyngeal insufficiency.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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