{
  "resourceType" : "CodeSystem",
  "id" : "GenomicReportSection",
  "language" : "en",
  "text" : {
    "status" : "generated",
    "div" : "<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>"
  },
  "url" : "https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicReportSection",
  "version" : "2.2.5",
  "name" : "GenomicReportSection",
  "title" : "Genomic Report Section",
  "status" : "draft",
  "experimental" : true,
  "date" : "2026-11-04",
  "publisher" : "NHS North West Genomics",
  "contact" : [{
    "telecom" : [{
      "system" : "url",
      "value" : "https://www.nwgenomics.nhs.uk/contact-us"
    }]
  }],
  "description" : "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" : "urn:iso:std:iso:3166",
      "code" : "GB",
      "display" : "United Kingdom of Great Britain and Northern Ireland"
    }]
  }],
  "caseSensitive" : true,
  "content" : "complete",
  "count" : 2,
  "concept" : [{
    "code" : "interpretation",
    "display" : "Interpretation",
    "definition" : "The clinical scientist's interpretation of the results, including diagnostic and therapeutic implications"
  },
  {
    "code" : "methodology",
    "display" : "Methodology and limitations",
    "definition" : "The genes or regions studied, the technology used, coverage, and the limitations of the test"
  }]
}