CH ELM (R4)
1.7.0 - release
CH ELM (R4)
1.7.0 - release
This page is part of the Observations of notifiable communicable infectious diseases (v1.7.0: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
| Official URL: http://fhir.ch/ig/ch-elm/ValueSet/ch-elm-results-cjd-org | Version: 1.7.0 | |||
| Active as of 2024-11-28 | 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)
Generated Narrative: ValueSet ch-elm-results-cjd-org
http://snomed.info/sct| 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) |
Generated Narrative: ValueSet
Expansion based on SNOMED CT International edition 01-Aug 2024
This value set contains 6 concepts
| Code | System | Display |
| 715807002 | http://snomed.info/sct | Familial Creutzfeldt-Jakob (disorder) |
| 715662009 | http://snomed.info/sct | Iatrogenic Jakob-Creutzfeldt disease (disorder) |
| 304603007 | http://snomed.info/sct | Variant Creutzfeldt-Jakob disease (disorder) |
| 713060000 | http://snomed.info/sct | Sporadic Creutzfeldt-Jakob disease (disorder) |
| 84676004 | http://snomed.info/sct | Prion |
| 721165001 | http://snomed.info/sct | Variably protease sensitive prionopathy (disorder) |
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |