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CFPR Canadian Familial Polyposis Registry
CFR case-fatality ratio; citrovorum-factor rescue; Code of Federal Regulations; complement-fixation reaction; correct fast reaction; cycloc flow reduction
CFS Chronic Fatigue Syndrome
CFS cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; crush fracture syndrome; culture fluid supernatant; Cystic Fibrosis Society
CFSE crystal field stabilization energy
CFSTI Clearinghouse for Federal Scientific and Technical Information
CFT cardiolipin flocculation test; clinical full time; complement-fixation test
CFTR cystic fibrosis transmembrane conductance regulator
CFU Colony Forming Unit
CFU colony-forming unit
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CF competence factor
CF constant frequency
CF conventional fractionation
CF cord factor
CF cytotoxic factor
CF1 Chloroplast F1-ATPase
CF1 Coupling Factor 1
CFA Cellular fatty acid
CFA Chicken fetal antigen
CFA Colonization factor antigen
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Cf Cystic Fibrosis - A genetic condition usually fatal in early adulthood, in which the secretion of thick mucus in respiratory and digestive systems (due to an error in chloride metabolism) inhibits oxygen and nutrient absorption.
Ãâó: www.findhealer.com/glossary/acronym.php3
CFS A group of symptoms, of unknown cause, characterized by unexplained fatigue, weakness, muscle pain, feeling poorly, trouble thinking, and sometimes, fever and/or lymph node swelling.
Ãâó: www.gulflink.osd.mil/medsearch/glossary/glossary_c...
CFIDS A synonym for chronic fatigue syndrome used by some patients and physicians. It should be stressed, however, that no immune dysfunction or aberration has been persuasively linked to chronic fatigue syndrome.
Ãâó: counsellingresource.com/distress/chronic/cfs/gloss...
Cf A recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties.
Ãâó: www.ornl.gov/sci/techresources/Human_Genome/public...
Cf A genetic disease involving a sticky buildup of mucus in the lungs (which makes breathing difficult and leads to infections), as well as pancreatic insufficiency (which leads to digestive problems). It is a recessive disease, occurring only when a child inherits two mutated copies of the CF gene--one from each parent.
Ãâó: www.med.nyu.edu/rcr/rcr/glossary.html
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