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
Term information
- DOID:3082 (MONDO:equivalentTo)
- SCTID:233703007 (MONDO:equivalentTo)
- UMLS:C5441745 (MONDO:equivalentTo)
- MedDRA:10022611 (Orphanet:182095/e)
- NCIT:C164315 (MONDO:equivalentTo)
- EFO:0004244 (MONDO:equivalentTo)
- MESH:D017563 (Orphanet:182095/e)
- Orphanet:182095 (MONDO:equivalentTo)
- ICD10CM:J80-J84 (https://orcid.org/0000-0002-4142-7153)
- MEDGEN:1788738 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, harrisons_view_respiratory_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, ordo_group_of_disorders, mondo_top_grouping_respiratory_system_disorder
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://purl.bioontology.org/ontology/ICD10CM/J80-J84
http://identifiers.org/snomedct/233703007
http://www.ebi.ac.uk/efo/EFO_0004244