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. [ Orphanet:2032 ]

Synonyms: idiopathic pulmonary fibrosis, familial usual interstitial pneumonia fibrocystic pulmonary dysplasia idiopathic pulmonary fibrosis UIP cryptogenic fibrosing alveolitis CFA

This is just here as a test because I lose it

Term information

database cross reference
  • MONDO:0008345
  • MESH:D054990 (Orphanet:2032)
  • COHD:45763750 (MONDO:equivalentTo)
  • ICD10:J84.112 (MONDO:equivalentTo)
  • EFO:0000768 (MONDO:equivalentTo)
  • MedDRA:10021240 (Orphanet:2032)
  • SCTID:196125002 (MONDO:equivalentTo)
  • NCIT:C35716 (MONDO:equivalentTo)
  • GARD:0008609 (MONDO:equivalentTo)
  • ICD10:J84.1 (Orphanet:2032)
  • ICD9:516.31 (EFO:0000768)
  • Orphanet:2032 (OMIM:178500)
  • DOID:0050156 (MONDO:equivalentTo)
  • OMIM:178500 (Orphanet:2032)
Subsets

gard_rare, ordo_disease

closeMatch

http://purl.obolibrary.org/obo/NCIT_C35715

http://identifiers.org/snomedct/426437004

http://identifiers.org/snomedct/700250006

http://linkedlifedata.com/resource/umls/id/C1800706

http://identifiers.org/snomedct/28168000

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

http://purl.obolibrary.org/obo/Orphanet_2032

gwas trait

true

has related synonym

pulmonary fibrosis, idiopathic

familial idiopathic pulmonary fibrosis

Hamman-rich disease

interstitial pneumonitis, usual

fibrosing alveolitis, cryptogenic

fibrosing alveolitis

IPF

id

EFO:0000768

see also

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