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Preferred Term:

cystic fibrosis

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.
Concept Schemes:
https://lod.nal.usda.gov/nalt-core
NALT Full
URI:
https://lod.nal.usda.gov/nalt/31334
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RDF/XMLCreated 2006-01-19, last modified 2018-05-15