DOID:12134

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • hematopoietic system disease
              • blood coagulation disease
                • factor VIII deficiency
          • genetic disease
            • monogenic disease
              • X-linked monogenic disease
                • X-linked recessive disease
                  • factor VIII deficiency
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • factor VIII deficiency ^xsd:string
• comment
  • OMIM mapping confirmed by DO. [SN]. ^xsd:string
• definition
  • A blood coagulation disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. ^xsd:string
    • dce:type
      • obo:ECO_0007638
    • oio:hasDbXref
      • url:http://en.wikipedia.org/wiki/Hemophilia_A ^xsd:string
    • comment
      • sn:IEDB ^xsd:string
• has exact match
  • MESH:D006467 ^xsd:string
• has exact synonym
  • Congenital factor VIII disorder ^@en
  • Hemophilia A ^@en
  • Subhemophilia ^@en
  • classic hemophilia A ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:12134 ^xsd:string
• in_subset
  • obo:doid#NCIthesaurus
  • obo:doid#DO_rare_slim
• oio:hasDbXref
  • MESH:D006467 ^xsd:string
  • OMIM:306700 ^xsd:string
  • ORDO:98878 ^xsd:string
  • NCI:C27146 ^xsd:string
  • UMLS_CUI:C0019069 ^xsd:string
  • SNOMEDCT_US_2023_03_01:28293008 ^xsd:string
  • GARD:6591 ^xsd:string
  • ICD9CM:286.0 ^xsd:string
  • ICD10CM:D66 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • X-linked recessive disease
  • blood coagulation disease