Generated Narrative: MessageHeader
event: event: O21 (OML - Laboratory order)
| Endpoint | Receiver |
| https://fhir.nwgenomics.nhs.uk/Endpoint/RIE | Identifier: ODS Organisation Code/699X0 |
sender: Identifier: ODS Organisation Code/699C0
| Software | Endpoint |
| NE&Y Genomics | https://fhir.nwgenomics.nhs.uk/Endpoint/NEYGenomics |
focus: ServiceRequest Acutely unwell children with a likely monogenic disorder (WGS)
Generated Narrative: Specimen
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
| Collected[x] | Quantity | Method |
| 2026-08-18 00:00:00+0000 | 120.0 uL (Details: UCUM codeuL = 'uL') | Qiagen |
| Identifier |
| Container Identifier/FX000000001 |
Generated Narrative: Observation
status: Final
category: Exam
code: Family Structure
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
value: Singleton
Generated Narrative: Observation
status: Final
category: Exam
code: Participant Type
subject: Rob Leeds (no stated gender), DoB: 1978-01-17 ( National Health Plan Identifier)
value: Proband
Generated Narrative: ServiceRequest
identifier: Filler Identifier/r2026000201-p2026000101
requisition: r2026000201
status: Active
intent: Filler Order
category: Molecular genetics procedure
code: 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:
note:
Suspected inherited neurodevelopmental condition.