Interstitial lung disease endpoints

Description

interstitial lung disease: A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.

Data source
FinnGen phenocode ILD_ENDPOINTS
Include ILD, IPF, ILD_SYST_AUTO
First defined in version DF2
Ontology
DOID 3082
GWAS catalog 0004244
MESH D017563
SNOMED CT 233703007

Key figures

Sex All Female Male
Number of individuals 16604 10056 6548
Unadjusted prevalence (%) 9.52 10.14 8.71
Mean age at first event (years) 47.38 46.29 49.06
Case fatality at 5-years (%) 3.0 2.09 4.4

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 4 4 4
Recurrence at 6 months (%) 61.77 61.82 61.68

Associations

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