DOID:0050177

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • genetic disease
            • monogenic disease
              • X-linked monogenic disease (1)
              • autosomal genetic disease (2)
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • monogenic disease ^xsd:string
• definition
  • A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. ^xsd:string
    • dce:type
      • obo:ECO_0007637
    • oio:hasDbXref
      • url:https://www.genome.gov/For-Patients-and-Families/Genetic-Disorders ^xsd:string
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:0050177 ^xsd:string
• in_subset
  • obo:doid#DO_GXD_slim
  • obo:doid#DO_AGR_slim
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • genetic disease