idiopathic pulmonary fibrosis Gene Set

Dataset PhosphoSitePlus Phosphosite-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)
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Genes

1 proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Symbol Name
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa