Bundle-GenomicReportVisibility-JamesWilson-Example

Example of marking data Items as withheld, where a data item is required for clinical interpretation but must not be disclosed to the patient (e.g. sex assigned at birth used for interpretation of results or genomic analysis).

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