DOID:1826

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • nervous system disease
              • central nervous system disease
                • brain disease
                  • epilepsy
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • epilepsy ^xsd:string
• definition
  • A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. ^xsd:string
    • dce:type
      • obo:ECO_0007643
    • oio:hasDbXref
      • url:http://books.google.com/books?id=YXqX04Te9ioC&printsec=frontcover&source=gbs_ge_summary_r&cad=0#v=onepage&q&f=false ^xsd:string
      • url:http://www.merriam-webster.com/medlineplus/epilepsy ^xsd:string
• has exact match
  • ICD10CM:G40 ^xsd:string
• has exact synonym
  • epilepsy syndrome ^@en
  • epileptic syndrome ^@en
• has narrower match
  • ICD10CM:G40.909 ^xsd:string
  • ICD10CM:G40.9 ^xsd:string
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:1826 ^xsd:string
• in_subset
  • obo:doid#NCIthesaurus
  • obo:doid#DO_FlyBase_slim
• oio:hasDbXref
  • EFO:0000474 ^xsd:string
  • MESH:D004827 ^xsd:string
  • SNOMEDCT_US_2023_03_01:267698007 ^xsd:string
  • ICD9CM:345.9 ^xsd:string
  • NCI:C3020 ^xsd:string
  • UMLS_CUI:C0014544 ^xsd:string
  • ICD10CM:G40 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • brain disease