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Fig. 1 | BMC Pulmonary Medicine

Fig. 1

From: Clustering of lung diseases in the family of interstitial lung disease patients

Fig. 1

Percentage of patients who reported relatives with ILD (a) and non-ILD lung disease (b) per diagnosis group. ILD patient diagnosis groups: HP = hypersensitivity pneumonitis; IPF = idiopathic pulmonary fibrosis; uPF = unclassifiable pulmonary fibrosis; non-IPF IIP = idiopathic interstitial pneumonia other than IPF; aidILD = autoimmune disease interstitial lung disease; oILD = other interstitial lung disease

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