Interstitial lung disease 2

MONDO:0800497

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

Also known as: fibrocystic pulmonary dysplasia, fibrosing alveolitis, cryptogenic, idiopathic pulmonary fibrosis, familial, interstitial pneumonitis, usual, pulmonary fibrosis, idiopathic

61 clinical trials for this condition and its sub-types, 2 tagged with Interstitial lung disease 2 itself.

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Where it sits in the disease tree

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↑ Inherited interstitial lung disease (11)

Including sub-types (61) Tagged with Interstitial lung disease 2 (2)

Trials to join now! 1 Not yet recruiting 1

Can a breath test predict lung scarring? new study seeks answers

Knowledge-focused Recruiting now

This observational study aims to find early biomarkers that can predict if a person's lung scarring (pulmonary fibrosis) will get worse quickly. Researchers will follow 450 adults with various types of interstitial lung disease, including IPF and other fibrotic conditions. Partic…

Sponsor: Amsterdam UMC, location VUmc • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:31 UTC

Interstitial lung disease 2

Where it sits in the disease tree

Can a breath test predict lung scarring? new study seeks answers