pneumonia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing. (Human Disease Ontology, DOID_552)
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Genes

9 genes associated with the disease pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
GSTM1 glutathione S-transferase mu 1
IL10 interleukin 10
IL1RN interleukin 1 receptor antagonist
LTA lymphotoxin alpha
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TNF tumor necrosis factor
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B