NHS North West Genomics
2.2.0 - ci-build
NHS North West Genomics
2.2.0 - ci-build
NHS North West Genomics - Local Development build (v2.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
Language: en
Profile: Bundle - FHIR Messaging
Bundle dWGS-Singleton-r2026000201 of type message
Entry 1 - fullUrl = urn:uuid:7ae6e4d1-b8a6-4364-8c76-521ac72f8e6a
Resource MessageHeader:
Language: en
event: event: O21 (OML - Laboratory order)
Destinations
Receiver Identifier: ODS Organisation Code/699X0 sender: Identifier: ODS Organisation Code/699C0
Sources
Software NE&Y Genomics focus: ServiceRequest Acutely unwell children with a likely monogenic disorder (WGS)
Entry 2 - fullUrl = urn:uuid:63004dab-d363-4e39-acbb-88fb2c2b398d
Resource Patient:
Language: en
Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
Other Id: Patient internal identifier/p2026000101
Entry 3 - fullUrl = urn:uuid:69e1c0a7-0582-49b3-a8f3-8352c317de5c
Resource Specimen:
Language: en
identifier: Placer Identifier/RR8-P0001, Filler Identifier/YNE26-P0001, Shipment Tracking Number/NEY-CONSIGN-2026-100
type: Whole blood specimen (specimen)
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
receivedTime: 2026-08-20 00:00:00+0000
Collections
Collected[x] Quantity Method 2026-08-18 00:00:00+0000 120.0 uL (Details: UCUM codeuL = 'uL') Qiagen container
Entry 4 - fullUrl = urn:uuid:90544717-e678-4a50-b07a-90176ae2fd16
Resource Observation:
Language: en
status: Final
category: Exam
code: Family Structure
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
value: Singleton
Entry 5 - fullUrl = urn:uuid:92aea5db-001f-453e-b27d-1bab08980673
Resource Observation:
Language: en
status: Final
category: Exam
code: Participant Type
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
value: Proband
Entry 6 - fullUrl = urn:uuid:d48710fc-4e15-459c-9aa8-51790c5abbc8
Resource ServiceRequest:
Language: en
identifier: Filler Identifier/r2026000201-p2026000101
requisition: r2026000201
status: Active
intent: Filler Order
category: Molecular genetics procedure
code: No display for ServiceRequest.code (concept: Acutely unwell children with a likely monogenic disorder (WGS))
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
requester: The Leeds Genetics Laboratory (NE&Y Genomics) (Identifier: ODS Organisation Code/699C0)
supportingInfo:
- No display for ServiceRequest.supportingInfo (reference: ->Observation )
- No display for ServiceRequest.supportingInfo (reference: ->Observation )
note:
Suspected inherited neurodevelopmental condition.