DOID:12531

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • hematopoietic system disease
              • blood coagulation disease
                • von Willebrand's disease
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • von Willebrand's disease ^xsd:string
• comment
  • OMIM mapping confirmed by DO. [SN]. ^xsd:string
• definition
  • A blood coagulation disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. ^xsd:string
    • dce:type
      • obo:ECO_0007637
      • obo:ECO_0007638
    • oio:hasDbXref
      • url:http://en.wikipedia.org/wiki/Von_Willebrand_disease ^xsd:string
      • url:http://ghr.nlm.nih.gov/condition/von-willebrand-disease ^xsd:string
• has exact synonym
  • vascular pseudohemophilia ^@en
  • von Willebrand's-Jurgens' disease ^@en
  • von Willebrand-Jrgens disease ^@en
  • vascular hemophilia ^@en
  • von Willebrand disorder ^@en
  • von Willebrand disease ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:12531 ^xsd:string
• in_subset
  • obo:doid#DO_rare_slim
  • obo:doid#NCIthesaurus
• oio:hasDbXref
  • ICD10CM:D68.0 ^xsd:string
  • MESH:D014842 ^xsd:string
  • UMLS_CUI:C0042974 ^xsd:string
  • NCI:C68677 ^xsd:string
  • GARD:7867 ^xsd:string
  • SNOMEDCT_US_2023_03_01:11093006 ^xsd:string
  • ICD9CM:286.4 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • blood coagulation disease