ValueSet Comparison between http://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org vs http://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org

Messages

ErrorValueSet.versionValues for version differ: '1.6.0' vs '1.7.0'
InformationValueSet.dateValues for date differ: '2024-10-31T11:08:34+00:00' vs '2024-11-28T14:09:02+00:00'

Metadata

NameValueComments
.compose.inactive
    .compose.lockedDate
      .copyrightCC0-1.0
        .date2024-10-31T11:08:34+00:002024-11-28T14:09:02+00:00
        • Values Differ
        .descriptionThe "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.
          .experimentalfalse
            .immutable
              .jurisdiction
                ..jurisdiction[0]urn:iso:std:iso:3166#CHE
                  .nameChElmResultsCjdOrg
                    .publisherFederal Office of Public Health FOPH
                      .purpose
                        .statusactive
                          .titleCH ELM Results Cjd Org
                            .urlhttp://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org
                              .version1.6.01.7.0
                              • Values Differ

                              Definition

                              ItemPropertyValueComments
                              .includehttp://snomed.info/sct
                                ..Concept715807002Familial Creutzfeldt-Jakob (disorder)
                                  ..Concept715662009Iatrogenic Jakob-Creutzfeldt disease (disorder)
                                    ..Concept304603007Variant Creutzfeldt-Jakob disease (disorder)
                                      ..Concept84676004Prion (organism)
                                        ..Concept721165001Variably protease sensitive prionopathy (disorder)

                                          Expansion

                                          Unable to generate expansion - see errors