cystic fibrosis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. (Human Disease Ontology, DOID_1485)
External Link http://www.omim.org/entry/219700
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Genes

1 genes associated with the cystic fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)