DOID:1485

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • genetic disease
            • monogenic disease
              • autosomal genetic disease
                • autosomal recessive disease
                  • cystic fibrosis
          • syndrome
            • cystic fibrosis
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • cystic fibrosis ^xsd:string
• comment
  • OMIM mapping confirmed by DO. [SN]. ^xsd:string
• definition
  • A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs. ^xsd:string
    • dce:type
      • obo:ECO_0007637
      • obo:ECO_0007638
    • oio:hasDbXref
      • url:http://en.wikipedia.org/wiki/Cystic_fibrosis ^xsd:string
      • url:http://ghr.nlm.nih.gov/condition/cystic-fibrosis ^xsd:string
      • url:http://www.nhlbi.nih.gov/health/health-topics/topics/cf/ ^xsd:string
      • url:https://www.genome.gov/Genetic-Disorders/Cystic-Fibrosis ^xsd:string
• has exact match
  • MESH:D003550 ^xsd:string
• has exact synonym
  • mucoviscidosis ^@en
  • CF ^@en
• has_alternative_id
  • DOID:12447 ^xsd:string
  • DOID:14395 ^xsd:string
  • DOID:1484 ^xsd:string
  • DOID:13383 ^xsd:string
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:1485 ^xsd:string
• in_subset
  • obo:doid#DO_rare_slim
  • obo:doid#NCIthesaurus
• oio:hasDbXref
  • MESH:D003550 ^xsd:string
  • NCI:C2975 ^xsd:string
  • ORDO:586 ^xsd:string
  • OMIM:219700 ^xsd:string
  • GARD:6233 ^xsd:string
  • ICD10CM:E84 ^xsd:string
  • SNOMEDCT_US_2023_03_01:85809002 ^xsd:string
  • ICD9CM:277.0 ^xsd:string
  • UMLS_CUI:C0010674 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • syndrome
  • autosomal recessive disease