ORDO

Orphanet Rare Disease Ontology
  • curator_inference0
  • has_annual_incidence_average_value0
  • has_birth_prevalence_average_value0
  • has_chromosomal_location0
  • has_lifetime_prevalence_average_value0
  • has_point_prevalence_average_value0
  • manual_assertion0
  • Candidate gene tested in0
  • Disease-causing germline mutation(s) in0
  • Disease-causing germline mutation(s) (loss of function) in0
  • Disease-causing germline mutation(s) (gain of function) in0
  • Disease-causing somatic mutation(s) in0
  • Major susceptibility factor in0
  • Modifying germline mutation in0
  • Modifying somatic mutation in0
  • Part of a fusion gene in0
  • Role in the phenotype of0
  • age of onset0
  • epidemiology0
  • genetic material0
  • geography0
  • has_AgeOfOnset0
  • has_annual_incidence_range0
  • has_cases/family0
  • has_inheritance0
  • has_lifetime_prevalence_range0
  • has_point_prevalence_range0
  • has_prevalence_at_birth_range0
  • inheritance0
  • obsolete_class20
  • part_of0
  • phenome0
  • present_in0
URI
http://purl.obolibrary.org/obo/ECO_0000205
Label
curator_inference