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Summary Literature (1)
DOID:0050156 - interstitial lung disease 2

Disease Ontology Definition:An interstitial lung disease pulmonary fibrosis that is characterized by scarring of the lung and that has_material_basis_in heterozygous mutation in the SFTPA2 gene on chromosome 10q22.

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

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

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


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

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