OBO ID: DOID:0050156
Term Name: idiopathic pulmonary fibrosis Search Ontology:
Synonyms:
  • cryptogenic fibrosing alveolitis
  • FIBROCYSTIC PULMONARY DYSPLASIA
  • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
Definition: A pulmonary fibrosis that is characterized by scarring of the lung. https://www.pulmonaryfibrosis.org/life-with-pf/about-ipf
References:
  • EFO:0000768
  • GARD:8609
  • ICD10CM:J84.112
  • ICD9CM:516.31
  • MESH:D054990
  • NCI:C35716
  • OMIM:178500
  • SNOMEDCT_US_2022_03_01:28168000
  • UMLS_CUI:C1800706
Ontology: Human Disease   (DOID:0050156)
OTHER idiopathic pulmonary fibrosis PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MUC5B {Pulmonary fibrosis, idiopathic, susceptibility to} 178500
SFTPA2 Interstitial lung disease 2 178500
ZEBRAFISH MODELS
Fish Conditions Citations
WT xenotransplantation Xia et al., 2014
PHENOTYPE No data available

CITATIONS (1)