DOID:9169

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • genetic disease
            • monogenic disease
              • X-linked monogenic disease
                • X-linked recessive disease
                  • Wiskott-Aldrich syndrome
          • syndrome
            • Wiskott-Aldrich syndrome
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • Wiskott-Aldrich syndrome ^xsd:string
• comment
  • OMIM mapping confirmed by DO. [SN]. ^xsd:string
• definition
  • A syndrome that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia). ^xsd:string
    • dce:type
      • obo:ECO_0007637
    • oio:hasDbXref
      • url:https://ghr.nlm.nih.gov/condition/wiskott-aldrich-syndrome ^xsd:string
• has exact synonym
  • Wiskott syndrome ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:9169 ^xsd:string
• in_subset
  • obo:doid#NCIthesaurus
• oio:hasDbXref
  • SNOMEDCT_US_2023_03_01:36070007 ^xsd:string
  • ICD9CM:279.12 ^xsd:string
  • MESH:D014923 ^xsd:string
  • NCI:C3448 ^xsd:string
  • OMIM:301000 ^xsd:string
  • ICD10CM:D82.0 ^xsd:string
  • UMLS_CUI:C0043194 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • syndrome
  • X-linked recessive disease