ORDO

OrphanetRareDiseaseOntology
  • age of onset0
  • biomarker tested in0
  • candidate gene tested in0
  • clinical entity0
  • curator_inference0
  • disease-causing germline mutation(s) in0
  • disease-causing germline mutation(s) (gain of function) in0
  • disease-causing germline mutation(s) (loss of function) in0
  • disease-causing somatic mutation(s) in0
  • epidemiology0
  • genetic material0
  • geography0
  • has_age_of_onset0
  • has_annual_incidence_average_value0
  • has_annual_incidence_range0
  • has_birth_prevalence_average_value0
  • has_birth_prevalence_range0
  • has_cases/families_value0
  • has_chromosomal location0
  • has_inheritance0
  • has_lifetime_prevalence_average_value0
  • has_lifetime_prevalence_range0
  • has_point_prevalence_average_value0
  • has_point_prevalence_range0
  • inheritance0
  • major susceptibility factor in0
  • manual_assertion0
  • modifying germline mutation in0
  • obsolete class0
  • part of a fusion gene in0
  • part_of0
  • part_of0
  • present_in0
  • role in the phenotype of0
  • CC BY 4.00
URI
http://www.orpha.net/ORDO/Orphanet_C023
Label
age of onset
http://www.ebi.ac.uk/efo/definition
Age of onset of clinical manifestations related to a clinical entity.