NHS North West Genomics
2.2.5 - ci-build
NHS North West Genomics - Local Development build (v2.2.5) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
| Draft as of 2026-11-04 |
<CodeSystem xmlns="http://hl7.org/fhir">
<id value="GenomicReportSection"/>
<language value="en"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: CodeSystem GenomicReportSection</b></p><a name="GenomicReportSection"> </a><a name="hcGenomicReportSection"> </a><p>This case-sensitive code system <code>https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicReportSection</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style="white-space:nowrap">interpretation<a name="GenomicReportSection-interpretation"> </a></td><td>Interpretation</td><td>The clinical scientist's interpretation of the results, including diagnostic and therapeutic implications</td></tr><tr><td style="white-space:nowrap">methodology<a name="GenomicReportSection-methodology"> </a></td><td>Methodology and limitations</td><td>The genes or regions studied, the technology used, coverage, and the limitations of the test</td></tr></table></div>
</text>
<url
value="https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicReportSection"/>
<version value="2.2.5"/>
<name value="GenomicReportSection"/>
<title value="Genomic Report Section"/>
<status value="draft"/>
<experimental value="true"/>
<date value="2026-11-04"/>
<publisher value="NHS North West Genomics"/>
<contact>
<telecom>
<system value="url"/>
<value value="https://www.nwgenomics.nhs.uk/contact-us"/>
</telecom>
</contact>
<description
value="Section codes for the [Composition Genomic Report](StructureDefinition-Composition-GenomicReport.html) where no LOINC document section code was found. Draft - see [Document Layout](StructureDefinition-Composition-GenomicReport.html#document-layout)."/>
<jurisdiction>
<coding>
<system value="urn:iso:std:iso:3166"/>
<code value="GB"/>
<display value="United Kingdom of Great Britain and Northern Ireland"/>
</coding>
</jurisdiction>
<caseSensitive value="true"/>
<content value="complete"/>
<count value="2"/>
<concept>
<code value="interpretation"/>
<display value="Interpretation"/>
<definition
value="The clinical scientist's interpretation of the results, including diagnostic and therapeutic implications"/>
</concept>
<concept>
<code value="methodology"/>
<display value="Methodology and limitations"/>
<definition
value="The genes or regions studied, the technology used, coverage, and the limitations of the test"/>
</concept>
</CodeSystem>