interstitial lung disease 2 (DOID:0050156)
Alliance: disease page
Synonyms: cryptogenic fibrosing alveolitis; FIBROCYSTIC PULMONARY DYSPLASIA; idiopathic pulmonary fibrosis; IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
Alt IDs: OMIM:178500, EFO:0000768, ICD10CM:J84.112, ICD9CM:516.31, MESH:D054990, NCI:C35716, UMLS_CUI:C1800706
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.