NHS North West Genomics
0.0.8 - ci-build United Kingdom flag

NHS North West Genomics, published by NHS North West Genomics. This guide is not an authorized publication; it is the continuous build for version 0.0.8 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/nw-gmsa/nw-gmsa.github.com/ and changes regularly. See the Directory of published versions

Example ServiceRequest: ServiceRequest Coded Entries Example

version: 1.0

Profile: ServiceRequest

identifier: Placer Identifier/1601737, Filler Identifier/1001166717

status: Active

intent: Order

category: Molecular genetics procedure, Cancer - WGS

code: Diagnostic testing for known variant(s)

subject: Octavia CHISLETT

encounter: Encounter: identifier = Visit number; status = finished; class = AMB (AMB); period = 2025-01-29 10:37:26+0000 --> (ongoing)

authoredOn: 2025-01-29

requester: PractitionerRole: specialty = General Surgery

reasonCode: Diagnostic testing for known mutation(s)

reasonReference: Condition Malignant tumour of stomach

supportingInfo: Observation GENETICS TEST PERFORMABLE

specimen: Specimen: identifier = Placer Identifier; accessionIdentifier = Accession ID; status = available; type = Whole blood specimen

note:

Referral lab PLEASE do following tests:

Test(s) required: WGS Sample type: Blood Transport used: Merlin Courier Tracking Number: ABC123 Sample sent to: LWH Genetics By: PDAY on: 02/04/25

Speciality Requesting Clinician: PAEDS Test Group: Neurology Ethnic Group: White British Patient is from consanguineous union? : Unknown Specimen Collection Status: Collect & send with order Infection Risk: No Specific Risk Clinical details:

TESTING Contact/Bleep No: 123