Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0050156 - idiopathic pulmonary fibrosis


Disease Ontology Definition:A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.

Synonyms: cryptogenic fibrosing alveolitis, FIBROCYSTIC PULMONARY DYSPLASIA, idiopathic pulmonary fibrosis, IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL

Xenbase Genes : sftpc, elmod2, muc5b, tert, sftpa1, sftpa2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008345 - obsolete idiopathic pulmonary fibrosis


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), idiopathic interstitial pneumonia (is_a), interstitial lung disease (is_a), pulmonary fibrosis (is_a)