ch-elm-results-cjd-org
type: ValueSet
node role: treeRoot
resource.id:
  value: ch-elm-results-cjd-org
domain resource.text:
  narrative.status:
    value: generated
  narrative.div: Generated Narrative: ValueSet ch-elm-results-cjd-org Include these codes as defined in http://snomed.info/sct version Not Stated (use latest from terminology server) Code Display 715807002 Familial Creutzfeldt-Jakob (disorder) 715662009 Iatrogenic Jakob-Creutzfeldt disease (disorder) 304603007 Variant Creutzfeldt-Jakob disease (disorder) 713060000 Sporadic Creutzfeldt-Jakob disease (disorder) 84676004 Prion (organism) 721165001 Variably protease sensitive prionopathy (disorder)
value set.url:
  value: http://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org
value set.version:
  value: 1.15.0
value set.name:
  value: ChElmResultsCjdOrg
value set.title:
  value: CH ELM Results Cjd Org
value set.status:
  value: active
value set.experimental:
  value: false
value set.date:
  value: 2026-08-12T07:05:53+00:00
value set.publisher:
  value: Federal Office of Public Health FOPH
value set.contact:
  index: 0
  contact detail.name:
    value: Federal Office of Public Health FOPH
  contact detail.telecom:
    index: 0
    contact point.system:
      value: url
    contact point.value:
      value: https://www.bag.admin.ch/bag/en/home/das-bag/kontakt-standort.html
value set.description:
  value: The "CH ELM Results Cjd Org" organism group provides a curated set of codes representing specific organisms. Each code within this group has been selected to ensure precise representation and consistency in relation to the primary LOINC codes. Clients utilizing the "CH ELM Results Cjd Org" group should refer to the provided codes to accurately and uniformly capture and report organism-related information.
value set.jurisdiction:
  index: 0
  codeable concept.coding:
    index: 0
    coding.system:
      value: urn:iso:std:iso:3166
    coding.code:
      value: CH
value set.copyright:
  value: CC0-1.0
value set.compose:
  value set.compose.include:
    index: 0
    value set.compose.include.system:
      value: http://snomed.info/sct
    value set.compose.include.concept:
      index: 0
      value set.compose.include.concept.code:
        value: 715807002
      value set.compose.include.concept.display:
        value: Familial Creutzfeldt-Jakob (disorder)
    value set.compose.include.concept:
      index: 1
      value set.compose.include.concept.code:
        value: 715662009
      value set.compose.include.concept.display:
        value: Iatrogenic Jakob-Creutzfeldt disease (disorder)
    value set.compose.include.concept:
      index: 2
      value set.compose.include.concept.code:
        value: 304603007
      value set.compose.include.concept.display:
        value: Variant Creutzfeldt-Jakob disease (disorder)
    value set.compose.include.concept:
      index: 3
      value set.compose.include.concept.code:
        value: 713060000
      value set.compose.include.concept.display:
        value: Sporadic Creutzfeldt-Jakob disease (disorder)
    value set.compose.include.concept:
      index: 4
      value set.compose.include.concept.code:
        value: 84676004
      value set.compose.include.concept.display:
        value: Prion (organism)
    value set.compose.include.concept:
      index: 5
      value set.compose.include.concept.code:
        value: 721165001
      value set.compose.include.concept.display:
        value: Variably protease sensitive prionopathy (disorder)