An instance of interstitial lung disease that is caused by an inherited modification of the individual's genome.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Pulmonary fibrosis and/or bone marrow failure, telomere-related | MONDO:0000148 | 9 | |
| Familial hypocalciuric hypercalcemia | MONDO:0018458 | 3 | |
| Hermansky-Pudlak syndrome with pulmonary fibrosis | MONDO:0016501 | 2 | |
| Rajab interstitial lung disease with brain calcifications | MONDO:0100214 | 2 | |
| Lane Hamilton syndrome | MONDO:0800124 | ||
| Niemann-Pick disease type B | MONDO:0011871 | SMPD1 | |
| SFTPC-related interstitial lung disease | MONDO:0018603 | SFTPC | |
| Alveolar capillary dysplasia with misalignment of pulmonary veins | MONDO:0009934 | FOXF1 | |
| Hypersensitivity pneumonitis, familial | MONDO:0007776 | ||
| Interstitial lung disease 1 | MONDO:0030608 | SFTPA1 | |
| Interstitial lung disease 2 | MONDO:0800497 | SFTPA2 | |
| Interstitial lung disease due to ABCA3 deficiency | MONDO:0012582 | ABCA3 | |
| Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome | MONDO:0012757 |
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