CH ELM (R4), published by Federal Office of Public Health FOPH. This guide is not an authorized publication; it is the continuous build for version 1.16.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/ahdis/ch-elm/ and changes regularly. See the Directory of published versions
| Official URL: http://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org | Version: 1.16.0 | ||||
| Active as of 2026-10-22 | Computable Name: ChElmResultsCjdOrg | ||||
Copyright/Legal: CC0-1.0 |
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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.
References
This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)
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) |
Expansion from tx.fhir.ch based on SNOMED CT Swiss Edition edition 07-Jun 2026
This value set contains 6 concepts
| System | Code | Display (en) | JSON | XML |
http://snomed.info/sct | 715807002 | Familial Creutzfeldt-Jakob | ||
http://snomed.info/sct | 715662009 | Iatrogenic Jakob-Creutzfeldt disease | ||
http://snomed.info/sct | 304603007 | Variant Creutzfeldt-Jakob disease | ||
http://snomed.info/sct | 713060000 | Sporadic Creutzfeldt-Jakob disease | ||
http://snomed.info/sct | 84676004 | Prion | ||
http://snomed.info/sct | 721165001 | Variably protease sensitive prionopathy |