NHS North West Genomics, published by NHS North West Genomics. This guide is not an authorized publication; it is the continuous build for version 0.0.8 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/nw-gmsa/nw-gmsa.github.com/ and changes regularly. See the Directory of published versions

• Narrative Content
• XML
• JSON

: Genomic Study - Cystic Fibrosis - XML Representation

Raw xml | Download

<Procedure xmlns="http://hl7.org/fhir">
  <id value="7b362aa5-41a7-4168-94b4-f12dff0dfb2a"/>
  <meta>
    <profile
             value="https://fhir.nwgenomics.nhs.uk/StructureDefinition/Procedure-GenomicStudy"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: Procedure 7b362aa5-41a7-4168-94b4-f12dff0dfb2a</b></p><a name="7b362aa5-41a7-4168-94b4-f12dff0dfb2a"> </a><a name="hc7b362aa5-41a7-4168-94b4-f12dff0dfb2a"> </a><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px"/><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-Procedure-GenomicStudy.html">Procedure Genomic Study</a></p></div><p><b>identifier</b>: 7b362aa5-41a7-4168-94b4-f12dff0dfb2a</p><p><b>status</b>: Completed</p><p><b>category</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/observation-category laboratory}">Laboratory</span></p><p><b>subject</b>: <a href="Patient-Patient-Manchester.html">Liam MANCHESTER</a></p><p><b>performed</b>: 2025-10-23 10:37:26+0000</p><p><b>asserter</b>: <a href="PractitionerRole-59577028-8fcc-4554-8b43-988561d41d9c.html">PractitionerRole</a></p><p><b>reasonCode</b>: <span title="Codes:{https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicClinicalIndication R185}">Cystic fibrosis carrier testing</span></p><p><b>outcome</b>: <span title="Codes:{https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicTestOutcomeCode 321}">VARIANT DETECTED</span></p></div>
  </text>
  <identifier>
    <value value="7b362aa5-41a7-4168-94b4-f12dff0dfb2a"/>
  </identifier>
  <status value="completed"/>
  <category>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/observation-category"/>
      <code value="laboratory"/>
    </coding>
  </category>
  <subject>🔗 
    <reference value="Patient/Patient-Manchester"/>
    <display value="Liam MANCHESTER"/>
  </subject>
  <performedDateTime value="2025-10-23T10:37:26+00:00"/>
  <asserter>🔗 
    <reference value="PractitionerRole/59577028-8fcc-4554-8b43-988561d41d9c"/>
  </asserter>
  <reasonCode>
    <coding>
      <system
              value="https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicClinicalIndication"/>
      <code value="R185"/>
      <display value="Cystic fibrosis carrier testing"/>
    </coding>
  </reasonCode>
  <outcome>
    <coding>
      <system
              value="https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicTestOutcomeCode"/>
      <code value="321"/>
      <display value="VARIANT DETECTED"/>
    </coding>
  </outcome>
</Procedure>