Term Name: | interstitial lung disease 2 |
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Synonyms: | cryptogenic fibrosing alveolitis, FIBROCYSTIC PULMONARY DYSPLASIA, idiopathic pulmonary fibrosis, IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL |
Definition: | An interstitial lung disease pulmonary fibrosis that is characterized by scarring of the lung and that has_material_basis_in heterozygous mutation in the SFTPA2 gene on chromosome 10q22. |
Ontology: | Human Disease [DOID:0050156] ( DOID:0050156 ) |