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fibróza cystická

  1. Subject h.fibróza cystická
    Subject h.Cystic Fibrosis
    Entry termsmukoviscidóza
    English X referencesMucoviscidosis
    Scope note in EnglishAn autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
    See also reference (FX) in Slovak regulátor vodivosti pri cystickej fibróze, transmembránový
    myši inbredné CFTR
    See also reference (FX) in English Cystic Fibrosis Transmembrane Conductance Regulator
    Mice, Inbred CFTR
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Number of the records: 1  

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