Chronic progressive interstitial lung disorder characterized by the replacement of the lung tissue by connective tissue, leading to progressive dyspnea, respiratory failure, or right heart failure. Causes include chronic inflammatory processes, exposure to environmental irritants, radiation therapy, autoimmune disorders, certain drugs, or it may be idiopathic (no identifiable cause). [ NCIT:P378 ]

Synonyms: fibrosis of lung pulmonary interstitial fibrosis

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C26869 (MONDO:equivalentTo)
  • SCTID:51615001 (MONDO:equivalentTo)
  • MEDGEN:11028 (MONDO:equivalentTo)
  • MESH:D011658 (MONDO:equivalentTo)
  • UMLS:C0034069 (MONDO:equivalentTo)
  • DOID:3770 (MONDO:equivalentTo)
  • EFO:0009448 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare

exactMatch

http://identifiers.org/snomedct/51615001

http://purl.obolibrary.org/obo/NCIT_C26869

http://purl.obolibrary.org/obo/DOID_3770

http://linkedlifedata.com/resource/umls/id/C0034069

http://identifiers.org/medgen/11028

http://identifiers.org/mesh/D011658

id

MONDO:0002771

Term relations