idiopathic pulmonary fibrosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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)
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Genes

6 genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ELMOD2 ELMO/CED-12 domain containing 2
MICA MHC class I polypeptide-related sequence A
SFTPA1 surfactant protein A1
SFTPA2 surfactant protein A2
SFTPC surfactant protein C
TERT telomerase reverse transcriptase