chronic bronchitis Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A bronchial disease that is an inflammation of the bronchial tubes. It is caused by bacteria and viruses. The disease has_symptom cough with mucus, has_symptom shortness of breath, has_symptom low fever and has_symptom chest tightness. (Human Disease Ontology, DOID_6132)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0004469
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Genes

12 genes associated with the chronic bronchitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ARMC4	armadillo repeat containing 4
C21ORF59	chromosome 21 open reading frame 59
CCDC65	coiled-coil domain containing 65
DNAAF5	dynein, axonemal, assembly factor 5
DNMT3B	DNA (cytosine-5-)-methyltransferase 3 beta
LRRC6	leucine rich repeat containing 6
SCNN1A	sodium channel, non voltage gated 1 alpha subunit
SCNN1B	sodium channel, non voltage gated 1 beta subunit
SCNN1G	sodium channel, non voltage gated 1 gamma subunit
SPAG1	sperm associated antigen 1
ZBTB24	zinc finger and BTB domain containing 24
ZMYND10	zinc finger, MYND-type containing 10