Other insterstitial pulmonary diseases

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 J10_OTHERINSTPULM
Hospital Discharge registry ICD-10: J84, ICD-9: 516/515, ICD-8: 48499|51701
Cause of Death registry ICD-10: J84, ICD-9: 515/516, ICD-8: 48499|51701
Level in the ICD-hierarchy 3
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 994 449 545
Unadjusted prevalence (%) 0.75 0.6 0.95
Mean age at first event (years) 64.24 62.84 65.4
Median number of events / individual 3 3 3

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 59.96 61.92 58.35
Case fatality at 5-years (%) 19.22 14.03 23.49

Associations