Bronchiolitis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A lung disease that is an inflammation of the bronchioles, the smallest air passages of the lungs. It is caused by viruses and bacteria. The disease has_symptom cough, has_symptom wheezing, has_symptom shortness of breath, has_symptom fever, has_symptom nasal flaring in infants and has_symptom bluish skin due to lack of oxygen. (Human Disease Ontology, DOID_2942)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001988
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Genes

5 genes/proteins associated with the disease Bronchiolitis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RMDN2 regulator of microtubule dynamics 2 1.08442
IL6 interleukin 6 1.07163
SPP1 secreted phosphoprotein 1 1.06333
CCL2 chemokine (C-C motif) ligand 2 1.02746
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2 1.01137