Merge pull request #235 from NHSDigital/Feature-IOPS-3702-Withheld-data-items

Feature iops 3702 withheld data items

Author: vickyjaiswal0308

Bundle/Bundle-GenomicReportVisibility-JamesWilson-Example.json

@@ -0,0 +1,72 @@
+{
+  "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."
+      }
+    }
+  ]
+}

package.json

@@ -14,6 +14,7 @@
     "fhir.r4.nhsengland.pars": "0.1.2-alpha",
     "fhir.r4.nhsengland.pathology": "0.2.4-alpha",
     "hl7.fhir.uv.tools.r4": "1.1.2",
+    "hl7.fhir.uv.security-label-ds4p": "1.0.0",
     "fhir.r4.nhsengland.nhse-identifiers": "0.1.1-alpha",
     "fhir.r4.ukcore.stu3.currentbuild": "0.29.0-pre-release"
   },