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idiopathic pulmonary fibrosis

^ 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. [ Orphanet:2032 ]

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

Term info

database cross reference
  • MedDRA:10021240 (Orphanet:2032)
  • ICD9:516.31 (EFO:0000768)
  • OMIM:178500 (Orphanet:2032)
  • COHD:45763750 (MONDO:equivalentTo)
  • NCIt:C35716
  • MONDO:0008345
  • ICD10:J84.112 (MONDO:equivalentTo)
  • OMIM:616373 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
  • MESH:D054990 (Orphanet:2032)
  • SCTID:196125002 (MONDO:kboom-pr-0.73/0.45/0.11)
  • Orphanet:2032 (OMIM:178500)
  • OMIM:614742 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
  • MSH:D054990
  • OMIM:616371 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
  • ICD10:J84.1 (Orphanet:2032)
  • GARD:0008609 (MONDO:equivalentTo)
  • DOID:0050156 (MONDO:equivalentTo)
  • NCIT:C35716 (MONDO:equivalentTo)
  • SNOMEDCT:700250006
Subsets

gard_rare, ordo_disease

closeMatch

http://identifiers.org/snomedct/426437004, http://purl.obolibrary.org/obo/NCIT_C35715, 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://identifiers.org/omim/178500, http://purl.obolibrary.org/obo/NCIT_C35716, 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, pulmonary fibrosis, idiopathic; IPF, 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

term editor

Tomasz Adamusiak, James Malone