encyclopedia of medical concepts
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Cystic Fibrosis

More information in Books or onNLM PubMed
Definition: 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.  a specific disease entity: do not use for fibrocystic states of various organs   
See Also Cystic Fibrosis Transmembrane Conductance Regulato; Mice, Inbred CFTR
Other names Mucoviscidosis; Pancreas Fibrocystic Diseases; Pancreas Fibrocystic Disease; Fibrosis, Cystic; Cystic Fibrosis, Pulmonary; Cystic Fibrosis, Pancreatic; Pulmonary Cystic Fibrosis; Pancreatic Cystic Fibrosis; Fibrocystic Disease of Pancreas
 
SubstanceCAS Registry & nameCategoriesSource
Follicular hamartoma alopecia cystic fibrosis  0   *Alopecia *Cystic Fibrosis *Hamartoma.
Lubani Al Saleh Teebi syndrome  0   *Anemia, Megaloblastic *Cystic Fibrosis *Intellectual Disability *Helicobacter Infections Face/abnormalities.
CLCA4 protein, human  0   *Chloride Channels Cystic Fibrosis. Hum Genet. 2004 Nov;115(6):483-91
MucA protein, Pseudomonas  0   *Bacterial Proteins Cystic Fibrosis Pseudomonas aeruginosa. Infect Immun 1997 Sep;65(9):3838-46
DNASE1 protein, human  EC 3.1.21.1   *Deoxyribonuclease I Cystic Fibrosis. JAMA 1994 Feb 16;271(7):494PULMOZYME

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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