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Packageuk.nhsengland.genomics.r4
Resource TypeBundle
IdBundle-GenomicReportVisibility-JamesWilson-Example.json
FHIR VersionR4

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Source1

{
  "resourceType": "Bundle",
  "id": "Bundle-GenomicReportVisibility-JamesWilson-Example",
  "type": "collection",
  "entry": [
    {
      "resource": {
        "resourceType": "Patient",
        "id": "Patient-JamesWilson",
        "meta": {
          "security": [
            {
              "system": "http://terminology.hl7.org/CodeSystem/v3-ActCode",
              "code": "PROCESSINLINELABEL",
              "display": "Process Inline Security Labels"
            }
          ]
        },
        "gender": "male",
        "_gender": {
          "extension": [
            {
              "url": "http://hl7.org/fhir/uv/security-label-ds4p/StructureDefinition/extension-inline-sec-label",
              "valueCoding": {
                "system": "http://terminology.hl7.org/CodeSystem/v3-ActCode",
                "code": "NOPAT",
                "display": "No disclosure to patient"
              }
            }
          ]
        },
        "name": [
          {
            "given": [
              "James"
            ],
            "family": "Wilson"
          }
        ]
      }
    },
    {
      "resource": {
        "resourceType": "ServiceRequest",
        "id": "SR-JamesWilson",
        "status": "active",
        "intent": "order",
        "subject": {
          "reference": "Patient/Patient-JamesWilson"
        },
        "code": {
          "text": "Whole Genome Sequencing"
        },
        "authoredOn": "2026-06-15T09:00:00Z"
      }
    },
    {
      "resource": {
        "resourceType": "DiagnosticReport",
        "id": "DR-JamesWilson",
        "status": "final",
        "subject": {
          "reference": "Patient/Patient-JamesWilson"
        },
        "code": {
          "text": "Genomic Report"
        },
        "conclusion": "No clinically significant variants identified."
      }
    }
  ]
}