DOID:332

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • nervous system disease
              • central nervous system disease
                • neurodegenerative disease
                  • motor neuron disease
                    • amyotrophic lateral sclerosis
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • amyotrophic lateral sclerosis ^xsd:string
• definition
  • A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing. ^xsd:string
    • dce:type
      • obo:ECO_0007638
    • oio:hasDbXref
      • url:http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis ^xsd:string
      • url:http://www.ninds.nih.gov/disorders/amyotrophiclateralsclerosis/detail_ALS.htm ^xsd:string
• has exact match
  • MESH:D000690 ^xsd:string
• has exact synonym
  • Lou Gehrig's disease ^@en
  • ALS ^@en
  • motor neuron disease, bulbar ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:332 ^xsd:string
• in_subset
  • obo:doid#NCIthesaurus
  • obo:doid#DO_FlyBase_slim
  • obo:doid#DO_rare_slim
• oio:hasDbXref
  • ICD10CM:G12.21 ^xsd:string
  • NCI:C34373 ^xsd:string
  • ICD9CM:335.20 ^xsd:string
  • GARD:5786 ^xsd:string
  • KEGG:05014 ^xsd:string
  • OMIM:PS105400 ^xsd:string
  • SNOMEDCT_US_2023_03_01:86044005 ^xsd:string
  • ORDO:803 ^xsd:string
  • MESH:D000690 ^xsd:string
  • UMLS_CUI:C0002736 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • motor neuron disease