DOID:0050156

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • musculoskeletal system disease
              • connective tissue disease
                • interstitial lung disease
                  • pulmonary fibrosis
                    • idiopathic pulmonary fibrosis
            • respiratory system disease
              • lower respiratory tract disease
                • lung disease
                  • interstitial lung disease
                    • pulmonary fibrosis
                      • idiopathic pulmonary fibrosis
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • idiopathic pulmonary fibrosis ^xsd:string
• comment
  • OMIM mapping confirmed by DO. [SN]. ^xsd:string
• definition
  • A pulmonary fibrosis that is characterized by scarring of the lung. ^xsd:string
    • oio:hasDbXref
      • url:https://www.pulmonaryfibrosis.org/life-with-pf/about-ipf ^xsd:string
• has exact synonym
  • FIBROCYSTIC PULMONARY DYSPLASIA ^@en
  • IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL ^@en
  • cryptogenic fibrosing alveolitis ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:0050156 ^xsd:string
• in_subset
  • obo:doid#NCIthesaurus
  • obo:doid#DO_rare_slim
• oio:hasDbXref
  • ICD9CM:516.31 ^xsd:string
  • UMLS_CUI:C1800706 ^xsd:string
  • SNOMEDCT_US_2023_03_01:28168000 ^xsd:string
  • OMIM:178500 ^xsd:string
  • EFO:0000768 ^xsd:string
  • NCI:C35716 ^xsd:string
  • ICD10CM:J84.112 ^xsd:string
  • GARD:8609 ^xsd:string
  • MESH:D054990 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • pulmonary fibrosis