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interstitial lung disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0015925

A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. [ MESH:D017563 ]

Synonyms: ILD interstitial lung disease

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:J80-J84 (https://orcid.org/0000-0002-4142-7153)
  • SCTID:233703007 (MONDO:equivalentTo)
  • Orphanet:182095 (MONDO:equivalentTo)
  • UMLS:C5441745 (MONDO:equivalentTo)
  • MEDGEN:1788738 (MONDO:equivalentTo)
  • NCIT:C164315 (MONDO:equivalentTo)
  • MedDRA:10022611 (Orphanet:182095/e)
  • MESH:D017563 (Orphanet:182095/e)
  • DOID:3082 (MONDO:equivalentTo)
  • EFO:0004244 (MONDO:equivalentTo)
Subsets

otar, disease_grouping, ordo_group_of_disorders

abbreviation
ILD [ Orphanet:182095 DOID:3082 ]

closeMatch

http://identifiers.org/meddra/10022611

exactMatch

http://purl.obolibrary.org/obo/NCIT_C164315

http://www.orpha.net/ORDO/Orphanet_182095

http://identifiers.org/medgen/1788738

http://linkedlifedata.com/resource/umls/id/C5441745

http://identifiers.org/mesh/D017563

http://purl.obolibrary.org/obo/DOID_3082

http://identifiers.org/snomedct/233703007

http://purl.bioontology.org/ontology/ICD10CM/J80-J84

id

MONDO:0015925

Term relations