interstitial lung disease
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 ]
Term info
- ICD10CM:J80-J84 (https://orcid.org/0000-0002-4142-7153)
- DOID:3082 (MONDO:equivalentTo)
- MESH:D017563 (Orphanet:182095/e)
- UMLS:C0206062 (Orphanet:182095/e)
- GARD:0013336 (MONDO:equivalentTo)
- NCIT:C164315 (MONDO:equivalentTo)
- SCTID:233703007 (MONDO:equivalentTo)
- MedDRA:10022611 (Orphanet:182095/e)
- Orphanet:182095 (MONDO:equivalentTo)
- EFO:0004244 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10022611
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.
http://purl.obolibrary.org/obo/NCIT_C164315, http://identifiers.org/mesh/D017563, http://purl.obolibrary.org/obo/Orphanet_182095, http://purl.obolibrary.org/obo/DOID_3082, http://purl.bioontology.org/ontology/ICD10CM/J80-J84, http://linkedlifedata.com/resource/umls/id/C0206062, http://identifiers.org/snomedct/233703007
ILD, interstitial lung disease
MONDO:0015925