An interstitial lung disease in which the cause of the disease is a variation in the SFTPA2 gene.
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pulmonary fibrosis and/or bone marrow failure, telomere-related
MONDO:0000148
hypersensitivity pneumonitis, familial
MONDO:0007776
alveolar capillary dysplasia with misalignment of pulmonary veins
MONDO:0009934
Niemann-Pick disease type B
MONDO:0011871
interstitial lung disease due to ABCA3 deficiency
MONDO:0012582
lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
MONDO:0012757