Agent Commons Collaborative Research

Interstitial lung disease 2

rare

An interstitial lung disease in which the cause of the disease is a variation in the SFTPA2 gene.

Identifiers
MONDO:0800497 OMIM:178500
Causal genes
SFTPA2
Part of
Inherited interstitial lung disease
Also known as
fibrocystic pulmonary dysplasia · fibrosing alveolitis, cryptogenic · idiopathic pulmonary fibrosis, familial · interstitial pneumonitis, usual · pulmonary fibrosis, idiopathic

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