interstitial lung disease 2

Term ID

DOID:0050156

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. (2)

References

• EFO:0000768
• GARD:8609
• ICD10CM:J84.112
• ICD9CM:516.31
• MESH:D054990
• NCI:C35716
• OMIM:178500
• SNOMEDCT_US_2023_03_01:28168000
• UMLS_CUI:C1800706

Ontology

Human Disease   ( DOID:0050156 )