Terminology Service for NFDI4Health

idiopathic pulmonary fibrosis

Go to external page http://www.ebi.ac.uk/efo/EFO_0000768


Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause. [ ]

Term info

Label

idiopathic pulmonary fibrosis

Synonyms
  • CFA
  • UIP
  • cryptogenic fibrosing alveolitis
  • fibrocystic pulmonary dysplasia
  • idiopathic pulmonary fibrosis
  • idiopathic pulmonary fibrosis, familial
  • usual interstitial pneumonia
database cross reference
Subsets

gard_rare, ordo_disease

closeMatch

http://purl.obolibrary.org/obo/NCIT_C35715, http://identifiers.org/snomedct/426437004, http://identifiers.org/snomedct/700250006, http://identifiers.org/snomedct/28168000, http://linkedlifedata.com/resource/umls/id/C1800706, http://identifiers.org/snomedct/233721005, http://identifiers.org/snomedct/237121003

exactMatch

http://purl.obolibrary.org/obo/NCIT_C35716, http://identifiers.org/omim/178500, http://identifiers.org/meddra/10021240, http://identifiers.org/mesh/D054990, http://purl.obolibrary.org/obo/DOID_0050156, http://identifiers.org/snomedct/196125002

gwas trait

true

has related synonym

pulmonary fibrosis, idiopathic, familial idiopathic pulmonary fibrosis, Hamman-rich disease, interstitial pneumonitis, usual, fibrosing alveolitis, cryptogenic, IPF, fibrosing alveolitis

see also

https://rarediseases.info.nih.gov/diseases/8609/idiopathic-pulmonary-fibrosis

Term relations