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 - Lynch Syndrome - JSON Representation

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{
  "resourceType" : "Procedure",
  "id" : "f0036554-cd1a-463c-ac8a-d891ca409af9",
  "meta" : {
    "profile" : [
      🔗 "https://fhir.nwgenomics.nhs.uk/StructureDefinition/Procedure-GenomicStudy"
    ]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: Procedure f0036554-cd1a-463c-ac8a-d891ca409af9</b></p><a name=\"f0036554-cd1a-463c-ac8a-d891ca409af9\"> </a><a name=\"hcf0036554-cd1a-463c-ac8a-d891ca409af9\"> </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>: f0036554-cd1a-463c-ac8a-d891ca409af9</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-Liverpool.html\">Paul LIVERPOOL</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 R210}\">Inherited MMR deficiency (Lynch syndrome)</span></p><p><b>outcome</b>: <span title=\"Codes:{https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicTestOutcomeCode 321}\">VARIANT DETECTED</span></p></div>"
  },
  "identifier" : [
    {
      "value" : "f0036554-cd1a-463c-ac8a-d891ca409af9"
    }
  ],
  "status" : "completed",
  "category" : {
    "coding" : [
      {
        "system" : "http://terminology.hl7.org/CodeSystem/observation-category",
        "code" : "laboratory"
      }
    ]
  },
  "subject" : {
    🔗 "reference" : "Patient/Patient-Liverpool",
    "display" : "Paul LIVERPOOL"
  },
  "performedDateTime" : "2025-10-23T10:37:26+00:00",
  "asserter" : {
    🔗 "reference" : "PractitionerRole/59577028-8fcc-4554-8b43-988561d41d9c"
  },
  "reasonCode" : [
    {
      "coding" : [
        {
          "system" : "https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicClinicalIndication",
          "code" : "R210",
          "display" : "Inherited MMR deficiency (Lynch syndrome)"
        }
      ]
    }
  ],
  "outcome" : {
    "coding" : [
      {
        "system" : "https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicTestOutcomeCode",
        "code" : "321",
        "display" : "VARIANT DETECTED"
      }
    ]
  }
}