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fibróza cystická
Record number d003550 Date 06.06.2025 Type M - MESH Topical term fibróza cystická Other term English (Pseudonym) Mucoviscidosis
Slovak (Pseudonym) mukoviscidóza
See also (Skutočné meno) myši inbredné CFTR
(Skutočné meno) regulátor vodivosti pri cystickej fibróze, transmembránový
(Later heading) potenie
UDC C06.689.202C08.381.187C16.320.190C16.614.213 Note An 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. 
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Number of the records: 1