Idiopathic pulmonary fibrosis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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 https://www.ebi.ac.uk/gwas/search?query=Idiopathic pulmonary fibrosis
Similar Terms
Downloads & Tools

Genes

4 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
TOLLIP toll interacting protein 0.626595
MAPT-AS1 MAPT antisense RNA 1 0.455873
TERT telomerase reverse transcriptase 0.389385
MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 2 0.104568