Idiopathic Pulmonary Fibrosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An idiopathic interstitial pneumonia which is a distinctive type of chronic fibrosing interstitial pneumonia with thick scarring in the lung creating a honeycomb appearance. The main symptoms start insidiously as shortness of breath on exertion, cough, and diminished stamina. Other common complaints include weight loss and fatigue. The level of oxygen in the blood decreases, and the skin may take on a bluish tinge (called cyanosis) and the ends of the fingers may become thick or club-shape. In most people, symptoms worsen over a period ranging from about 6 months to several years. (Human Disease Ontology, DOID_0050156)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D054990
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Genes

13 genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DSP desmoplakin 2.88009
SFTPA2 surfactant protein A2 2.88009
FAM13A family with sequence similarity 13, member A 2.88009
DPP9 dipeptidyl-peptidase 9 2.88009
ATP11A ATPase, class VI, type 11A 2.88009
TERT telomerase reverse transcriptase 2.88009
TERC telomerase RNA component 2.88009
MUC5B mucin 5B, oligomeric mucus/gel-forming 2.88009
SFTPC surfactant protein C 2.88009
ELMOD2 ELMO/CED-12 domain containing 2 2.88009
OBFC1 oligonucleotide/oligosaccharide-binding fold containing 1 2.88009
PLAU plasminogen activator, urokinase 2.88009
SFTPA1 surfactant protein A1 2.88009