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)
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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