Patients with interstitial lung disease (ILD) for whom we propose genetic testing
| Idiopathic or non-idiopathic ILD with at least one of the following: |
| Familial ILD |
| Cryptogenic pulmonary fibrosis <50 years old |
| Rare syndrome (table 1) or telomeropathy assessed as personal, or familial history of: |
| Bone-marrow failure, thrombocytopenia or myelodysplasia |
| Dyskeratosis congenita |
| Cryptogenic cirrhosis |