North West Genomic Medicine Service Alliance
0.0.1 - ci-build United Kingdom flag

DRAFT Implementation Guide

This is for collaboration and discussion purposes and is subject to change.

North West Genomic Medicine Service Alliance - Local Development build (v0.0.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

Questionnaire: North West Genomics Test Order

Official URL: https://nw-gmsa.github.io/Questionnaire/GenomicTestOrder Version: 0.0.1
Draft as of 2025-06-19 Computable Name:

THIS IS FOR ANALYSIS, and is not to be used for implementation at present.

The aim of this is to support conversion of multiple Genomic Order Forms HL7 v2 and FHIR.

Questionnaire Viewer

THIS IS FOR ANALYSIS PURPOSES ONLY, and is not to be used for implementation.

Structure
LinkIDTextCardinalityTypeDescription & Constraintsdoco
.. THIS IS FOR ANALYSIS, and is not to be used for implementation at present. The aim of this is to support conversion of multiple Genomic Order Forms HL7 v2 and FHIR.Questionnairehttps://nw-gmsa.github.io/Questionnaire/GenomicTestOrder#0.0.1
... PatientPatient0..1groupDefinition: Patient
.... LN/45394-4Patient surname1..1stringDefinition: Patient.name.family
.... LN/45392-8Patient first name1..1stringDefinition: Patient.name.given
.... LN/21112-8Date of birth1..1dateDefinition: Patient.birthDate
.... LN/81954-0Date of death0..1dateDefinition: Patient.deceasedDateTime
.... LN/56799-0Address0..1groupDefinition: Patient.address
..... HL7/PID-11-1Address Line0..*stringDefinition: Patient.address.line
..... HL7/PID-11-3City0..1stringDefinition: Patient.address.city
..... LN/45401-7Postcode0..1stringDefinition: Patient.address.postalCode
.... LN/46098-0Sex registered at birth0..1choiceDefinition: Patient.gender
Value Set: AdministrativeGender
.... LN/32624-9Ethnic Category0..1choiceDefinition: Patient.extension:ethnicCategory
Value Set: Ethnicity
.... LN/89061-6NHS Number0..1stringDefinition: Patient.identifier:nhsNumber
.... LN/76435-7Hospital Number (Medical Record Number)1..1stringDefinition: Patient.identifier:MedicalRecordNumber
.... LN/56797-4Account Number (Episode or Stay Number)0..1stringDefinition: ServiceRequest.encounter.identifier.value
..... LN/56797-4-designNotePV1-19 (also known as stay number)0..1display
.... ageAtCollectionAge at collection (ignore for FHIR)0..1decimal
.... LN/89009-5Location0..1stringDefinition: Encounter.location
.... HL7/PD1-3GP Surgery (ODS Code)0..1choiceDefinition: Patient.generalPractitioner
... HealthcareProfessionalHealthcare Professional0..1groupDefinition: PractitionerRole
.... LN/18705-4Referring Clinician Name1..1stringDefinition: PractitionerRole.practitioner.display
.... LN/18707-0Referring Clinician Current Speciality1..1choiceDefinition: PractitionerRole.specialty.coding.code
Value Set: UK Core Practice Setting Code
.... LN/46608-6Referring Clinician Professional Identifier1..1stringDefinition: PractitionerRole.practitioner.identifier.value
.... LN/89058-2Email0..*stringDefinition: PractitionerRole.telecom.value
.... LN/81230-5Phone0..1stringDefinition: PractitionerRole.telecom.value
.... HL7/ORC-21Referring Organisation ODS Code0..1stringDefinition: PractitionerRole.organization.identifier.value
... TestRequestTest Request0..1groupDefinition: ServiceRequest
.... SNM/15220000Test Category0..1choiceDefinition: ServiceRequest.category
Value Set: Order Category
Options: 5 options
.... HL7/OBR-4-rTest Code (Rare and inherited diseases)1..*choiceDefinition: ServiceRequest.code
Enable When: SNM/15220000 =
Value Set: Genomic Rare and Inherited Disease Test Directory
.... HL7/OBR-4-hTest Code (Haemoglobinopathy)1..*choiceDefinition: ServiceRequest.code
Enable When: SNM/15220000 =
Options: 5 options
.... HL7/OBR-4-cTest Code (Cancer)1..*choiceDefinition: ServiceRequest.code
Enable When: SNM/15220000 =
Value Set: Genomic Cancer Test Directory
.... pedigreeNumberG Number (Pedigree Number) - Order Group Number0..1stringDefinition: ServiceRequest.requisition
.... LN/106194-4Test request ID/Order ID0..1stringDefinition: ServiceRequest.identifier:placerOrderNumber
.... LN/82768-3Priority0..1choiceDefinition: ServiceRequest.priority
Value Set: Request Priority
.... NOS/GeneticistEmailClinical Geneticist email0..1stringDefinition: Observation.valueString
.... NOS/GeneticistDepartmentEmailClinical Geneticist department email0..1stringDefinition: Observation.valueString
.... ConsentConsent0..1group
..... LN/19826-7Has consent has been obtained for tests (Y/N)0..1choiceDefinition: Observation.valueCodeableConcept
Options: 2 options
..... LN/75520-7Has consent has been obtained for DNA storage (Y/N)0..1choiceDefinition: Observation.valueCodeableConcept
Options: 2 options
..... NOS/RODToFollowROD attached or to follow0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
.... PatientClinicalInformationPatient Clinical Information0..1group
..... LN/51967-8CITT code (Specific disease suspected/reason for testing)0..*choiceDefinition: ServiceRequest.reasonCode
Value Set: Genomic Condition Code
..... HL7/NTE-1Relevant clinical information and family history0..1stringDefinition: ServiceRequest.note
..... HL7/NTE-2Reason For Variant Re-Interpretation Request0..1stringDefinition: ServiceRequest.note
... SpecimenSpecimen/Biopsy0..1groupDefinition: Specimen
.... HL7/SPMSample collection status0..1stringDefinition: Specimen.status
Value Set: SpecimenStatus
.... LN/80398-1Specimen ID Number0..1stringDefinition: Specimen.identifier
..... LN/80398-1-designNoteORM v2.4 - OBX-3 = LOINC 80398-1 and OBX-2 = CE. OML v2.5.1 SPM-20..1display
.... Specimen/accessionIdentifierLab DNA Number (If Known)0..1stringDefinition: Specimen.accessionIdentifier
.... LN/80398-1-ODSPathology Laboratory Hospital/Trust ID (for Path Lab Sample/Stored DNA)0..1stringDefinition: Specimen.accessionIdentifier.assigner.identifier.value
.... LN/33882-2Specimen Collection Date0..1dateTimeDefinition: Specimen.collection.collectedDateTime
..... LN/33882-2-designNoteORM v2.4 - OBX-3 = LOINC 33882-2 and OBX-2 = TS . OML v2.5.1 SPM-170..1display
.... LN/66746-9Specimen Type0..1choiceDefinition: Specimen.type.coding.code
Value Set: Specimen Type
..... LN/66746-9-designNoteORM v2.4 - OBX-3 = LOINC 66746-9 and OBX-2 = CE. OML v2.5.1 SPM-40..1display
.... SNM/281269004High Infection Risk?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 2 options
.... NOS/InfectionRiskDetailsHigh infection Risk Details0..1stringDefinition: Observation.valueString
.... LN/74384-9Anticoagulant/preservative?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 2 options
.... LN/39111-0Tissue source/organ of origin0..1choiceDefinition: Specimen.collection.bodySite
.... LN/3169-0Specimen Volume/number of slides or scrolls0..1stringDefinition: Specimen.collection.quantity
.... OrderTrackingAudit (Specimen Tracking)0..1groupDefinition: Specimen.collection
..... NOS/SampleReceivedDate and time sample received in lab0..1dateDefinition: Specimen.receivedTime
..... NOS/SampleSentDate and time sample sent0..1dateDefinition: Observation.valueDateTime
..... NOS/TransportUsedTransport used0..1stringDefinition: Observation.valueString
..... LN/97209-1Tracking number0..1stringDefinition: Observation.valueString
..... NOS/SampleSentToSample sent to0..1stringDefinition: Observation.valueString
..... NOS/SampleSentToNameName of person who sent sample0..1stringDefinition: Observation.valueString
... AskAtOrderEntryAsk At Order Entry Questions0..1group
.... SNM/842009Patient is from consanguineous union?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
.... SNM/74996004-pathology-reportConfirm that a pathology report will be provided alongside the sample.0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
.... SNM/118185001Neonatal/Prenatal/Neither?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
..... pregnantPregnant0..1groupEnable When: SNM/118185001 =
...... SNM/370386005Does this test relate to a pregnancy with > 1 fetus?0..1stringDefinition: Observation.valueCodeableConcept
Options: 3 options
...... SNM/161714006Patient expected delivery date0..1dateDefinition: Observation.valueDateTime
...... SNM/598151000005105Patient gestation0..1integerDefinition: Observation.valueQuantity
.... SNM/17369002Is this test for a pregnancy loss?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
.... SNM/419099009Is this test for a deceased infant?0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
... PriorResultsPrior Results0..1group

doco Documentation for this format

Options Sets

Answer options for SNM/15220000

  • https://nw-gmsa.github.io/CodeSystem/nwgmsa#RareAndInheritedDiseasesGeneticTesting ("Rare and inherited diseases Genetic Testing (procedure)")
  • http://snomed.info/sct#1186936003 ("Storage of specimen (procedure)")
  • https://nw-gmsa.github.io/CodeSystem/nwgmsa#PreNatalGeneticTesting ("Pre Natal Genetic Testing (procedure)")
  • https://nw-gmsa.github.io/CodeSystem/nwgmsa#HaemoglobinopathyGeneticTesting ("Haemoglobinopathy Genetic Testing (procedure)")
  • https://nw-gmsa.github.io/CodeSystem/nwgmsa#CancerGeneticTesting ("Cancer Genetic Testing (procedure)")

Answer options for HL7/OBR-4-h

  • https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory#R361.1 ("R361.1 Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing")
  • https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory#R361.2 ("R361.2 Sickle cell, thalassaemia and other haemoglobinopathies trait or carrier testing")
  • https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory#R372.1 ("R372.1 Newborn screening for sickle cell disease in a transfused baby")
  • https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory#R93.1 ("R93.1 Sickle cell, thalassaemia and other haemoglobinopathies")
  • https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory#R93.2 ("R93.2 Sickle cell, thalassaemia and other haemoglobinopathies")

Answer options for LN/19826-7

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")

Answer options for LN/75520-7

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")

Answer options for NOS/RODToFollow

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")

Answer options for SNM/281269004

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")

Answer options for LN/74384-9

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")

Answer options for SNM/842009

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")

Answer options for SNM/74996004-pathology-report

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")

Answer options for SNM/118185001

  • http://snomed.info/sct#77386006 ("Pregnancy")
  • http://snomed.info/sct#255407002 ("Neonatal")
  • http://loinc.org#LA32-8 ("No")

Answer options for SNM/370386005

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")

Answer options for SNM/17369002

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")

Answer options for SNM/419099009

  • http://loinc.org#LA33-6 ("Yes")
  • http://loinc.org#LA32-8 ("No")
  • http://loinc.org#LA4489-6 ("Unknown")