DOID:418

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • musculoskeletal system disease
              • connective tissue disease
                • rheumatic disease
                  • scleroderma
                    • systemic scleroderma
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • systemic scleroderma ^xsd:string
• definition
  • A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. ^xsd:string
    • dce:type
      • obo:ECO_0007637
    • oio:hasDbXref
      • url:https://ghr.nlm.nih.gov/condition/systemic-scleroderma ^xsd:string
    • rdfs:comment
      • sn:IEDB ^xsd:string
• has exact synonym
  • systemic sclerosis ^@en
  • Scleroderma ^@en
  • Scleroderma syndrome ^@en
  • progressive systemic sclerosis ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:418 ^xsd:string
• in_subset
  • obo:doid#DO_rare_slim
  • obo:doid#NCIthesaurus
• oio:hasDbXref
  • ICD9CM:710.1 ^xsd:string
  • EFO:0000717 ^xsd:string
  • MESH:D012595 ^xsd:string
  • SNOMEDCT_US_2023_03_01:89155008 ^xsd:string
  • NCI:C72070 ^xsd:string
  • OMIM:181750 ^xsd:string
  • UMLS_CUI:C0036421 ^xsd:string
  • GARD:9748 ^xsd:string
  • ICD10CM:M34.0 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • scleroderma