CodeSystems

The CodeSystems created specifically for use in Genomics are listed below. Some of the CodeSystems listed may still be in draft and pending further changes once requirements for the GMS have been finalised.

Codes for requestable entities (Test Directory codes) are dependent upon the digitisation of the test directory. This is treated as a separate project.

By default, the central Genomic Order Management Broker will validate all CodeSystems included within the Genomics IG. It will also validate core HL7 CodeSystems, SNOMED CT codes and HPO codes (with the system http://human-phenotype-ontology.org) against the UK OntoServer. All other codes, from unknown CodeSystem, will not be validated against.

CodeSystem Additional Information Type Genomics

Usage

CodeSystem to specify reference to additional details of the input's use as part of the task execution or the output generated from task completion.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/additional-infotype-genomics defines the following codes:

CodeDisplayDefinition
ConsentConsentConsent for treatment record
ConsignmentNumberConsignment NumberThe specimen consignment number
DiagnosticReportDiagnosticReportThe DiagnosticReport generated upon the task completion
RackIdRack NumberThe specimen rack number
SpecimenSpecimenThe specimen provided for the task execution
WellIdWell Identification NumberThe specimen well identification number

Table View

CodeSystem.id[0]additional-infotype-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/additional-infotype-genomics
CodeSystem.version[0]0.1.0
CodeSystem.name[0]AdditionalInfoTypeGenomics
CodeSystem.title[0]Additional Information Type Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-05-31T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]CodeSystem to specify reference to additional details of the input's use as part of the task execution or the output generated from task completion.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]Consent
CodeSystem.concept[0].display[0]Consent
CodeSystem.concept[0].definition[0]Consent for treatment record
CodeSystem.concept[1].code[0]ConsignmentNumber
CodeSystem.concept[1].display[0]Consignment Number
CodeSystem.concept[1].definition[0]The specimen consignment number
CodeSystem.concept[2].code[0]DiagnosticReport
CodeSystem.concept[2].display[0]DiagnosticReport
CodeSystem.concept[2].definition[0]The DiagnosticReport generated upon the task completion
CodeSystem.concept[3].code[0]RackId
CodeSystem.concept[3].display[0]Rack Number
CodeSystem.concept[3].definition[0]The specimen rack number
CodeSystem.concept[4].code[0]Specimen
CodeSystem.concept[4].display[0]Specimen
CodeSystem.concept[4].definition[0]The specimen provided for the task execution
CodeSystem.concept[5].code[0]WellId
CodeSystem.concept[5].display[0]Well Identification Number
CodeSystem.concept[5].definition[0]The specimen well identification number

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="additional-infotype-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/additional-infotype-genomics" />
<version value="0.1.0" />
<name value="AdditionalInfoTypeGenomics" />
<title value="Additional Information Type Genomics" />
<status value="draft" />
<date value="2024-05-31T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="CodeSystem to specify reference to additional details of the input's use as part of the task execution or the output generated from task completion." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="Consent" />
<display value="Consent" />
<definition value="Consent for treatment record" />
</concept>
<code value="ConsignmentNumber" />
<display value="Consignment Number" />
<definition value="The specimen consignment number" />
</concept>
<code value="DiagnosticReport" />
<display value="DiagnosticReport" />
<definition value="The DiagnosticReport generated upon the task completion" />
</concept>
<code value="RackId" />
<display value="Rack Number" />
<definition value="The specimen rack number" />
</concept>
<code value="Specimen" />
<display value="Specimen" />
<definition value="The specimen provided for the task execution" />
</concept>
<code value="WellId" />
<display value="Well Identification Number" />
<definition value="The specimen well identification number" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "additional-infotype-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/additional-infotype-genomics",
"version": "0.1.0",
"name": "AdditionalInfoTypeGenomics",
"title": "Additional Information Type Genomics",
"status": "draft",
"date": "2024-05-31T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "CodeSystem to specify reference to additional details of the input's use as part of the task execution or the output generated from task completion.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "Consent",
"display": "Consent",
"definition": "Consent for treatment record"
},
{
"code": "ConsignmentNumber",
"display": "Consignment Number",
"definition": "The specimen consignment number"
},
{
"code": "DiagnosticReport",
"display": "DiagnosticReport",
"definition": "The DiagnosticReport generated upon the task completion"
},
{
"code": "RackId",
"display": "Rack Number",
"definition": "The specimen rack number"
},
{
"code": "Specimen",
"display": "Specimen",
"definition": "The specimen provided for the task execution"
},
{
"code": "WellId",
"display": "Well Identification Number",
"definition": "The specimen well identification number"
}
]
}


CodeSystem Business Status Genomics

Usage

Business status for test order Tasks in genomics

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/business-status-genomics defines the following codes:

CodeDisplay
determining-test-recoverabilityDetermining Test Recoverability
test-recoverableTest Recoverable
notifying-requester-of-failureNotifying Requester Of Failure
sample-requestedSample Requested (from external lab)
sample-availability-confirmedSample Availability Confirmed
sample-booked-into-labSample Booked Into Lab
variants-priorities-list-requiredVariants Priorities List Required
variants-priorities-list-retrievedVariants Priorities List Retrieved
previous-genomic-sequence-data-requiredPrevious Genomic Sequence Data Required
previous-genomic-sequence-data-retrievedPrevious Genomic Sequence Data Retrieved
remote-sample-prep-requiredRemote Sample Prep Required
sample-sentSample Sent
sample-receivedSample Received
sample-storedSample Stored
further-sample-prep-requiredFurther Sample Prep Required
remote-processing-requiredRemote Processing Required
remote-genomic-data-processing-requiredRemote Genomic Data Processing Required
remote-interpretation-requiredRemote Interpretation Required
further-clinical-details-requiredFurther Clinical Details Required
further-clinical-details-providedFurther Clinical Details Provided
reflex-confirmatory-test-requiredReflex/Confirmatory Test Required
reflex-confirmatory-test-completeReflex/Confirmatory Test Complete
otherother

Table View

CodeSystem.id[0]business-status-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/business-status-genomics
CodeSystem.version[0]0.4.1
CodeSystem.name[0]BusinessStatusGenomics
CodeSystem.title[0]Business Status Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-07-23
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]Business status for test order Tasks in genomics
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]determining-test-recoverability
CodeSystem.concept[0].display[0]Determining Test Recoverability
CodeSystem.concept[1].code[0]test-recoverable
CodeSystem.concept[1].display[0]Test Recoverable
CodeSystem.concept[2].code[0]notifying-requester-of-failure
CodeSystem.concept[2].display[0]Notifying Requester Of Failure
CodeSystem.concept[3].code[0]sample-requested
CodeSystem.concept[3].display[0]Sample Requested (from external lab)
CodeSystem.concept[4].code[0]sample-availability-confirmed
CodeSystem.concept[4].display[0]Sample Availability Confirmed
CodeSystem.concept[5].code[0]sample-booked-into-lab
CodeSystem.concept[5].display[0]Sample Booked Into Lab
CodeSystem.concept[6].code[0]variants-priorities-list-required
CodeSystem.concept[6].display[0]Variants Priorities List Required
CodeSystem.concept[7].code[0]variants-priorities-list-retrieved
CodeSystem.concept[7].display[0]Variants Priorities List Retrieved
CodeSystem.concept[8].code[0]previous-genomic-sequence-data-required
CodeSystem.concept[8].display[0]Previous Genomic Sequence Data Required
CodeSystem.concept[9].code[0]previous-genomic-sequence-data-retrieved
CodeSystem.concept[9].display[0]Previous Genomic Sequence Data Retrieved
CodeSystem.concept[10].code[0]remote-sample-prep-required
CodeSystem.concept[10].display[0]Remote Sample Prep Required
CodeSystem.concept[11].code[0]sample-sent
CodeSystem.concept[11].display[0]Sample Sent
CodeSystem.concept[12].code[0]sample-received
CodeSystem.concept[12].display[0]Sample Received
CodeSystem.concept[13].code[0]sample-stored
CodeSystem.concept[13].display[0]Sample Stored
CodeSystem.concept[14].code[0]further-sample-prep-required
CodeSystem.concept[14].display[0]Further Sample Prep Required
CodeSystem.concept[15].code[0]remote-processing-required
CodeSystem.concept[15].display[0]Remote Processing Required
CodeSystem.concept[16].code[0]remote-genomic-data-processing-required
CodeSystem.concept[16].display[0]Remote Genomic Data Processing Required
CodeSystem.concept[17].code[0]remote-interpretation-required
CodeSystem.concept[17].display[0]Remote Interpretation Required
CodeSystem.concept[18].code[0]further-clinical-details-required
CodeSystem.concept[18].display[0]Further Clinical Details Required
CodeSystem.concept[19].code[0]further-clinical-details-provided
CodeSystem.concept[19].display[0]Further Clinical Details Provided
CodeSystem.concept[20].code[0]reflex-confirmatory-test-required
CodeSystem.concept[20].display[0]Reflex/Confirmatory Test Required
CodeSystem.concept[21].code[0]reflex-confirmatory-test-complete
CodeSystem.concept[21].display[0]Reflex/Confirmatory Test Complete
CodeSystem.concept[22].code[0]other
CodeSystem.concept[22].display[0]other

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="business-status-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/business-status-genomics" />
<version value="0.4.1" />
<name value="BusinessStatusGenomics" />
<title value="Business Status Genomics" />
<status value="draft" />
<date value="2024-07-23" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="Business status for test order Tasks in genomics" />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="determining-test-recoverability" />
<display value="Determining Test Recoverability" />
</concept>
<code value="test-recoverable" />
<display value="Test Recoverable" />
</concept>
<code value="notifying-requester-of-failure" />
<display value="Notifying Requester Of Failure" />
</concept>
<code value="sample-requested" />
<display value="Sample Requested (from external lab)" />
</concept>
<code value="sample-availability-confirmed" />
<display value="Sample Availability Confirmed" />
</concept>
<code value="sample-booked-into-lab" />
<display value="Sample Booked Into Lab" />
</concept>
<code value="variants-priorities-list-required" />
<display value="Variants Priorities List Required" />
</concept>
<code value="variants-priorities-list-retrieved" />
<display value="Variants Priorities List Retrieved" />
</concept>
<code value="previous-genomic-sequence-data-required" />
<display value="Previous Genomic Sequence Data Required" />
</concept>
<code value="previous-genomic-sequence-data-retrieved" />
<display value="Previous Genomic Sequence Data Retrieved" />
</concept>
<code value="remote-sample-prep-required" />
<display value="Remote Sample Prep Required" />
</concept>
<code value="sample-sent" />
<display value="Sample Sent" />
</concept>
<code value="sample-received" />
<display value="Sample Received" />
</concept>
<code value="sample-stored" />
<display value="Sample Stored" />
</concept>
<code value="further-sample-prep-required" />
<display value="Further Sample Prep Required" />
</concept>
<code value="remote-processing-required" />
<display value="Remote Processing Required" />
</concept>
<code value="remote-genomic-data-processing-required" />
<display value="Remote Genomic Data Processing Required" />
</concept>
<code value="remote-interpretation-required" />
<display value="Remote Interpretation Required" />
</concept>
<code value="further-clinical-details-required" />
<display value="Further Clinical Details Required" />
</concept>
<code value="further-clinical-details-provided" />
<display value="Further Clinical Details Provided" />
</concept>
<code value="reflex-confirmatory-test-required" />
<display value="Reflex/Confirmatory Test Required" />
</concept>
<code value="reflex-confirmatory-test-complete" />
<display value="Reflex/Confirmatory Test Complete" />
</concept>
<code value="other" />
<display value="other" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "business-status-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/business-status-genomics",
"version": "0.4.1",
"name": "BusinessStatusGenomics",
"title": "Business Status Genomics",
"status": "draft",
"date": "2024-07-23",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "Business status for test order Tasks in genomics",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "determining-test-recoverability",
"display": "Determining Test Recoverability"
},
{
"code": "test-recoverable",
"display": "Test Recoverable"
},
{
"code": "notifying-requester-of-failure",
"display": "Notifying Requester Of Failure"
},
{
"code": "sample-requested",
"display": "Sample Requested (from external lab)"
},
{
"code": "sample-availability-confirmed",
"display": "Sample Availability Confirmed"
},
{
"code": "sample-booked-into-lab",
"display": "Sample Booked Into Lab"
},
{
"code": "variants-priorities-list-required",
"display": "Variants Priorities List Required"
},
{
"code": "variants-priorities-list-retrieved",
"display": "Variants Priorities List Retrieved"
},
{
"code": "previous-genomic-sequence-data-required",
"display": "Previous Genomic Sequence Data Required"
},
{
"code": "previous-genomic-sequence-data-retrieved",
"display": "Previous Genomic Sequence Data Retrieved"
},
{
"code": "remote-sample-prep-required",
"display": "Remote Sample Prep Required"
},
{
"code": "sample-sent",
"display": "Sample Sent"
},
{
"code": "sample-received",
"display": "Sample Received"
},
{
"code": "sample-stored",
"display": "Sample Stored"
},
{
"code": "further-sample-prep-required",
"display": "Further Sample Prep Required"
},
{
"code": "remote-processing-required",
"display": "Remote Processing Required"
},
{
"code": "remote-genomic-data-processing-required",
"display": "Remote Genomic Data Processing Required"
},
{
"code": "remote-interpretation-required",
"display": "Remote Interpretation Required"
},
{
"code": "further-clinical-details-required",
"display": "Further Clinical Details Required"
},
{
"code": "further-clinical-details-provided",
"display": "Further Clinical Details Provided"
},
{
"code": "reflex-confirmatory-test-required",
"display": "Reflex/Confirmatory Test Required"
},
{
"code": "reflex-confirmatory-test-complete",
"display": "Reflex/Confirmatory Test Complete"
},
{
"code": "other",
"display": "other"
}
]
}


CodeSystem MDS Question Tag Genomics

Usage

A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics defines the following codes:

LvlCodeDisplayDefinition
1datagroup-healthcare-professionalHealthcare ProfessionalData group - Healthcare professional
2  HCP-1HCP - Genomic test order roleHCP's function within the genomic test ordering process
2  HCP-2HCP - First nameHCP's first name.
2  HCP-13HCP - surnameHCP'surname
2  HCP-3HCP - Job titleHCP's job title.
2  HCP-4HCP - Current specialtyHCP's current specialty.
2  HCP-5HCP - Telephone numberHCP's telephone number.
2  HCP-6HCP - Email addressHCP's email address.
2  HCP-7HCP - Organisation nameHCP's requesting organisation name.
2  HCP-9HCP - Organisation ODS codeHCP's organisation ODS code
2  HCP-10HCP - Department nameHCP's department name.
2  HCP-11HCP - Professional registration numberHCP's professional registration number such as their GMC number.
2  HCP-12HCP - Professional registration number typeHCP's professional registration number type such as 'GMC'.
1datagroup-patientPatientData group - Patient
2  P-1Patient - TitlePatient's title.
2  P-2Patient - First namePatient's first name.
2  P-40Patient - MiddlenamePatient's middle name.
2  P-3Patient - SurnamePatient's last name.
2  P-41Patient - Name useLinks each patient name entry to confirm if current, previous or what the patient is known as.
2  P-4Patient - Date of birthPatient's date of birth.
2  P-6Patient - PostcodePatient's home postcode.
2  P-7Patient - Country of residencePatient's home country.
2  P-9Patient - EthnicityPatient's ethnicity.
2  P-10Patient - Sex defined at birthPatient's phenotypic sex classification as defined at birth based on physical characteristic.
2  P-12Patient - GP practice's ODS CodePatient's GP practice ODS code.
2  P-13Patient - Is from consanguineous unionThe fact of the patient's biological parents being descended from the same ancestor.
2  P-15Patient - NHS numberPatient's NHS number.
2  P-16Patient - Local identifierPatient's identification code other than NHS number.
2  P-42Patient - ODS code of organisation which assigned local identifierODS code of the organisation which assigned the local identifier P-16.
2  P-17Patient - Reason for unavailable NHS numberReason for an NHS number not being provided.
2  P-18Patient - Relationship to probandThis patient's relationship to the primary patient.
2  P-19Patient - Gender IdentityPatient's stated gender, determined by the patient.
2  P-20Patient - Deceased datePatient's date of death.
2  P-21Patient - Chromosomal sexPatient's genomic / karyotypic characteristic. Determined by genomic testing.
2  P-35Patient - Withheld identity reasonConfirmation why the patient is withholding identity details.
2  P-37Patient - Local Pedigree / Family identifierPatient's pedigree or family identifying id.
2  P-39Patient - Reason for inclusion in genomic test requestReason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting
1datagroup-fetusFetusData group - Fetus
2  F-1Fetus - Local identifierFetus' identification code other than NHS number.
2  F-7Fetus - ODS code of organisation which assigned local identifierODS code of the organisation which assigned the local identifier F-1.
2  F-2Fetus - Observed sexFetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM.
2  F-3Fetus - Chromosomal sexFetus' genomic / karyotypic characteristic. Determined by genomic testing.
2  F-6Fetus - Life status at time of requestFetus' alive or deceased status details at the point of test ordering.
2  F-8Fetus - Pregnancy idThe id of a given pregnancy which this fetus belongs to.
1datagroup-test-requestTest RequestData group - Test Request
2  TR-2Test Request - Payment statusHow the test request is funded
2  TR-4Test Request - Requesting reason rare diseaseThe reason for a rare disease genomic test.
2  TR-38Test Request - Requesting reason cancerThe reason for a cancer genomic test.
2  TR-5Test Request - High level test identifierLegacy high level ids which identify the requested test. Options provided by old Test Directory.
2  TR-6Test Request - High level test identifier descriptionLegacy high level name of the id requested
2  TR-7Test Request - Low level test identifierThe low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE).
2  TR-8Test Request - Low level test identifier descriptionThe low level CITT name of the considered test.
2  TR-9Test Request - Low level multipurpose test identifierThe low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION).
2  TR-10Test Request - Low level multipurpose test identifier descriptionThe low level name of the test to be actioned when the CITT code is multipurpose.
2  TR-21Test Request - Genomic package idId of the package requested.
2  TR-22Test Request - Genomic package nameName of the package requested.
2  TR-23Test Request - Genomic package versionVersion of the package requested.
2  TR-24Test Request - Genomic test idId of the test requested.
2  TR-25Test Request - Genomic test nameName of the test requested.
2  TR-26Test Request - Genomic test versionVersion of the test requested.
2  TR-27Test Request - Additional panelsAdditional panels to test.
2  TR-28Test request - Target typeType of target to test.
2  TR-29Test request - Target detailDetail of target to test.
2  TR-11Test Request - Count of patients to be testedCount of patients to be tested including the proband/primary patient.
2  TR-12Test Request - Urgency reasonThe test request urgency reason.
2  TR-13Test Request - Reanalysis reasonThe reason reanalysis has been requested.
2  TR-14Test Request - Detail of reason for requestFurther detail associated to the reason reanalysis has been requested.
2  TR-15Test Request - Type of reanalysisThe type of reanalysis which has been requested.
2  TR-17Test Request - Is urgentConfirmation if the test request is urgent.
2  TR-35Test Request - Purpose of linkingThe reason a given test request has been linked to another test request.
2  TR-36Test Request - Central email address for reportingCentral email address for contingency in the event of not being able to obtain a report via the requester.
2  TR-20Test Request - Genomic report delivery methodTest Request - Genomic report delivery method
2  TR-30Test Request - Add private genomic request and report to NHS recordConfirmation if the content of a private genomic test request should be added to an NHS record.
2  TR-31Test Request - Test request form versionVersion of the test order form completed and submitted.
2  TR-32Test Request - File / Link to fileUpload of a file or a link to a file for adding documents such as previous genomic reports to a test order.
2  TR-33Test Request - File detailDetail to provide context to an uploaded file or document link.
2  TR-34Test Request - Clinical utilityClinical benefit to patient of obtaining a requested genomic report.
2  TR-39Test Request - Linked test request referenceThe reference to any associated test requests
1datagroup-ngrl-consentNGRL-consentData group - NGRL consent
2  NGRL-1NGRL consent - Date of NGRL consentThe date NGRL consent was provided.
2  NGRL-2NGRL consent - Patient has made their own choice to consent to the NGRLConfirmation if the patient to be tested has provided NGRL consent themselves.
2  NGRL-3NGRL consent - Patient representative name (if patient cannot make their own choice)The name of the patient representative.
2  NGRL-4NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for researchThe outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL.
2  NGRL-5NGRL consent - NGRL consent document linkA URL where a copy of a completed NGRL consent form may be found.
1datagroup-primary-samplePrimary SampleData group - Primary Sample
2  PS-2Primary Sample - Local identifierLocal ids applied to a sample
2  PS-3Primary Sample - ODS code of organisation which assigned local idODS code of the organisation which assigned the local sample id.
2  PS-10Primary Sample - Obtained dateDate at which a specimen/biopsy was obtained from patient.
2  PS-11Primary Sample - Primary sampleThe primary sample material.
2  PS-12Primary Sample - Primary sample stateThe state of the primary sample.
2  PS-25Primary Sample - Preservative/ContainerHow the primary sample is preserved.
2  PS-30Primary Sample - Block identifierSample block identifier
2  PS-31Primary Sample - Fixative typeSample fixative type
2  PS-32Primary Sample - Hours to fixationSample hours to fixation
2  PS-33Primary Sample - Hours in fixativeSample hours in fixative
2  PS-34Primary Sample - Tumour enrichment methodMethod used for tumour enrichment.
2  PS-13Primary Sample - Necrosis% necrotic (dead) cells in primary sample.
2  PS-14Primary Sample - Nucleated cell countNucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc).
2  PS-15Primary Sample - Tumour nuclear content in whole sectionNeoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)
2  PS-26Primary Sample - Tumour nuclear content in marked areaNeoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)
2  PS-17Primary Sample - Solid tumour morphologyThe histology and likely course of development of a tumour.
2  PS-18Primary Sample - Solid tumour topographyThe tumour sample site. e.g. from colon, stomach etc.
2  PS-29Primary Sample - Is biopsyPrimary Sample - Is biopsy
2  PS-19Primary Sample - Biopsy siteDigital confirmation that the sample is a biopsy.
2  PS-21Primary Sample - Observed maternal cell contamination (MCC)An observed outcome which may indicate MCC
2  PS-27Primary Sample - Test confirmed maternal cell contamination (MCC)Analytically confirmed MCC levels
2  PS-22Primary Sample - Option for all products of conceptionPrimary Sample - Option for all products of conception
2  PS-23Primary Sample - Blasts %Future management for products of conception.
2  PS-24Primary Sample - High infection risk reasonThe high contamination risk reason for a primary sample.
2  PS-28Primary Sample - Patient life status at the time of collectionIf the patient was alive or deceased at the point of collecting a sample.
2  PS-35Primary Sample - Solid tumour typeThe origin or context of a tumour sample.
1datagroup-patient-clinical-informationPatient Clinical InformationData group - Patient Clinical Information
2  PCI-1Patient clinical information - Genomic EthnicityPatient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish
2  PCI-2Patient clinical information - Disease StatusIf the patient is affected, unaffected, or it is unknown.
2  PCI-4Patient clinical information - Age at disease onsetThe age when a change in patients' health was first noted in line with suspected diagnosis.
2  PCI-5Patient clinical information - Known/Suspected DiseaseDisease a patient is believed, known to have, or be at risk of developing.
2  PCI-6Patient clinical information - Phenotypic detailsThe HPO (or alternative ontology as appropriate) term names for the observable disease traits.
2  PCI-7Patient clinical information - SymptomsThe patient's symptoms
2  PCI-10Patient clinical information - Count of tumoursHow many tumours the patient has.
2  PCI-11Patient clinical information - Site of tumourLocation of the tumours on the body.
2  PCI-14Patient clinical information - Tumour sites - Body image diagramImage attachment of body with tumour sites highlighted.
2  PCI-15Patient clinical information - Pedigree details / Relevant family historyThe patient's pedigree/family history details (inc family history of cancer).
2  PCI-16Patient clinical information - Pedigree diagramImage attachment of pedigree details
2  PCI-17Patient clinical information - Laterality of hearing lossLaterality of the hearing loss i.e. bilateral or unilateral.
2  PCI-18Patient clinical information - Fetal haemoglobinopathy maternal screening genotypeMaternal screening genotype for haemoglobinopathy testing.
2  PCI-21Patient clinical information - Legal considerationsLegal considerations for a given request.
2  PCI-22Patient clinical information - Fetal haemoglobinopathy paternal screening genotypePaternal screening genotype for haemoglobinopathy testing
2  PCI-23Patient clinical information - Expected Maternity Unit - Organisation nameRequesting clinician's organisation name.
2  PCI-24Patient clinical information - Expected Maternity Unit - Organisation addressRequesting clinician's organisation address.
2  PCI-25Patient clinical information - Expected Maternity Unit - Organisation ODS codeRequesting clinician's organisation ODS code.
2  PCI-26Patient clinical information - Expected Maternity Unit - Department nameRequesting clinician's department name.
2  PCI-27Patient clinical information - Growth historySummary passage of text to highlight patient centile history e.g. head circumference, weight, etc.
2  PCI-28Patient clinical information - Severity of hearing lossFree text regarding hearing loss
2  PCI-29Patient clinical information - Retinal degenerationFree text regarding retinal degeneration
2  PCI-30Patient clinical information - Risk factorsToxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication.
2  PCI-31Patient clinical information - Suspected inborn error type(s)Suspected inborn error type(s)
2  PCI-32Patient clinical information - Abnormal infection history siteAbnormal infection history site organism
2  PCI-33Patient clinical information - Abnormal infection history site organismAbnormal infection history site organism
2  PCI-34Is on ig replacementIf the patient is on immunoglobin replacement treatment.
2  PCI-35Patient clinical information - Current and previous treatment detailDetail regarding relevant current and previous medical treatments.
2  PCI-36Patient clinical information - Pregnancy statusPatient`s pregnancy status
2  PCI-37Patient clinical information - Pregnancy typeType of conception
2  PCI-38Patient clinical information - Pregnancy gestation periodPatient's term of active pregnancy at point of test request.
2  PCI-39Patient clinical information - Fetal gestationStage during patient pregnancy at which it terminated.
2  PCI-40Patient clinical information - Estimated delivery date (EDD)Patient's estimated delivery date.
2  PCI-41Patient clinical information - IVF age of egg donorThe age of the patient who donated the egg at the time of donation.
2  PCI-42Patient clinical information - Had transplantHas the patient ever had a transplant.
2  PCI-43Patient clinical information - Type of transplantWhat type of transplant the patient had.
2  PCI-44Patient clinical information - Transplant dateWhen the patient had the transplant.
2  PCI-45Patient clinical information - Had transfusion in the last 6 weeksHas the patient had a transfusion in the last 6 weeks.
2  PCI-46Patient clinical information - Type of transfusionWhat type of transfusion the patient has had.
2  PCI-47Patient clinical information - Transfusion dateWhen the patient had the transfusion.
2  PCI-48Patient clinical information - Height (m)Patient's height.
1datagroup-miscellaneousMiscellaneousData group - Miscellaneous
2  MIS-1Further supporting informationSupporting information which has not been captured elsewhere.
1datagroup-hospital-encounterHospital encounterData group - Hospital encounter
2  HE-1Treatment function code (TFC)The identifier for the clinical specialty or service under which the patient is being treated.
2  HE-2Hospital provider spell identifierThe identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge.
2  HE-3Outpatient attendance identifierThe identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered.
2  HE-4Hospital point of delivery codeThe identifier that defines the type of care setting in which the genomic test was requested.

Table View

CodeSystem.id[0]mds-questiontag-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics
CodeSystem.version[0]0.1.1
CodeSystem.name[0]MDSQuestionTagGenomics
CodeSystem.title[0]MDS Question Tag Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2025-12-15T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.
CodeSystem.copyright[0]Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.hierarchyMeaning[0]grouped-by
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]datagroup-healthcare-professional
CodeSystem.concept[0].display[0]Healthcare Professional
CodeSystem.concept[0].definition[0]Data group - Healthcare professional
CodeSystem.concept[0].concept[0].code[0]HCP-1
CodeSystem.concept[0].concept[0].display[0]HCP - Genomic test order role
CodeSystem.concept[0].concept[0].definition[0]HCP's function within the genomic test ordering process
CodeSystem.concept[0].concept[1].code[0]HCP-2
CodeSystem.concept[0].concept[1].display[0]HCP - First name
CodeSystem.concept[0].concept[1].definition[0]HCP's first name.
CodeSystem.concept[0].concept[2].code[0]HCP-13
CodeSystem.concept[0].concept[2].display[0]HCP - surname
CodeSystem.concept[0].concept[2].definition[0]HCP'surname
CodeSystem.concept[0].concept[3].code[0]HCP-3
CodeSystem.concept[0].concept[3].display[0]HCP - Job title
CodeSystem.concept[0].concept[3].definition[0]HCP's job title.
CodeSystem.concept[0].concept[4].code[0]HCP-4
CodeSystem.concept[0].concept[4].display[0]HCP - Current specialty
CodeSystem.concept[0].concept[4].definition[0]HCP's current specialty.
CodeSystem.concept[0].concept[5].code[0]HCP-5
CodeSystem.concept[0].concept[5].display[0]HCP - Telephone number
CodeSystem.concept[0].concept[5].definition[0]HCP's telephone number.
CodeSystem.concept[0].concept[6].code[0]HCP-6
CodeSystem.concept[0].concept[6].display[0]HCP - Email address
CodeSystem.concept[0].concept[6].definition[0]HCP's email address.
CodeSystem.concept[0].concept[7].code[0]HCP-7
CodeSystem.concept[0].concept[7].display[0]HCP - Organisation name
CodeSystem.concept[0].concept[7].definition[0]HCP's requesting organisation name.
CodeSystem.concept[0].concept[8].code[0]HCP-9
CodeSystem.concept[0].concept[8].display[0]HCP - Organisation ODS code
CodeSystem.concept[0].concept[8].definition[0]HCP's organisation ODS code
CodeSystem.concept[0].concept[9].code[0]HCP-10
CodeSystem.concept[0].concept[9].display[0]HCP - Department name
CodeSystem.concept[0].concept[9].definition[0]HCP's department name.
CodeSystem.concept[0].concept[10].code[0]HCP-11
CodeSystem.concept[0].concept[10].display[0]HCP - Professional registration number
CodeSystem.concept[0].concept[10].definition[0]HCP's professional registration number such as their GMC number.
CodeSystem.concept[0].concept[11].code[0]HCP-12
CodeSystem.concept[0].concept[11].display[0]HCP - Professional registration number type
CodeSystem.concept[0].concept[11].definition[0]HCP's professional registration number type such as 'GMC'.
CodeSystem.concept[1].code[0]datagroup-patient
CodeSystem.concept[1].display[0]Patient
CodeSystem.concept[1].definition[0]Data group - Patient
CodeSystem.concept[1].concept[0].code[0]P-1
CodeSystem.concept[1].concept[0].display[0]Patient - Title
CodeSystem.concept[1].concept[0].definition[0]Patient's title.
CodeSystem.concept[1].concept[1].code[0]P-2
CodeSystem.concept[1].concept[1].display[0]Patient - First name
CodeSystem.concept[1].concept[1].definition[0]Patient's first name.
CodeSystem.concept[1].concept[2].code[0]P-40
CodeSystem.concept[1].concept[2].display[0]Patient - Middlename
CodeSystem.concept[1].concept[2].definition[0]Patient's middle name.
CodeSystem.concept[1].concept[3].code[0]P-3
CodeSystem.concept[1].concept[3].display[0]Patient - Surname
CodeSystem.concept[1].concept[3].definition[0]Patient's last name.
CodeSystem.concept[1].concept[4].code[0]P-41
CodeSystem.concept[1].concept[4].display[0]Patient - Name use
CodeSystem.concept[1].concept[4].definition[0]Links each patient name entry to confirm if current, previous or what the patient is known as.
CodeSystem.concept[1].concept[5].code[0]P-4
CodeSystem.concept[1].concept[5].display[0]Patient - Date of birth
CodeSystem.concept[1].concept[5].definition[0]Patient's date of birth.
CodeSystem.concept[1].concept[6].code[0]P-6
CodeSystem.concept[1].concept[6].display[0]Patient - Postcode
CodeSystem.concept[1].concept[6].definition[0]Patient's home postcode.
CodeSystem.concept[1].concept[7].code[0]P-7
CodeSystem.concept[1].concept[7].display[0]Patient - Country of residence
CodeSystem.concept[1].concept[7].definition[0]Patient's home country.
CodeSystem.concept[1].concept[8].code[0]P-9
CodeSystem.concept[1].concept[8].display[0]Patient - Ethnicity
CodeSystem.concept[1].concept[8].definition[0]Patient's ethnicity.
CodeSystem.concept[1].concept[9].code[0]P-10
CodeSystem.concept[1].concept[9].display[0]Patient - Sex defined at birth
CodeSystem.concept[1].concept[9].definition[0]Patient's phenotypic sex classification as defined at birth based on physical characteristic.
CodeSystem.concept[1].concept[10].code[0]P-12
CodeSystem.concept[1].concept[10].display[0]Patient - GP practice's ODS Code
CodeSystem.concept[1].concept[10].definition[0]Patient's GP practice ODS code.
CodeSystem.concept[1].concept[11].code[0]P-13
CodeSystem.concept[1].concept[11].display[0]Patient - Is from consanguineous union
CodeSystem.concept[1].concept[11].definition[0]The fact of the patient's biological parents being descended from the same ancestor.
CodeSystem.concept[1].concept[12].code[0]P-15
CodeSystem.concept[1].concept[12].display[0]Patient - NHS number
CodeSystem.concept[1].concept[12].definition[0]Patient's NHS number.
CodeSystem.concept[1].concept[13].code[0]P-16
CodeSystem.concept[1].concept[13].display[0]Patient - Local identifier
CodeSystem.concept[1].concept[13].definition[0]Patient's identification code other than NHS number.
CodeSystem.concept[1].concept[14].code[0]P-42
CodeSystem.concept[1].concept[14].display[0]Patient - ODS code of organisation which assigned local identifier
CodeSystem.concept[1].concept[14].definition[0]ODS code of the organisation which assigned the local identifier P-16.
CodeSystem.concept[1].concept[15].code[0]P-17
CodeSystem.concept[1].concept[15].display[0]Patient - Reason for unavailable NHS number
CodeSystem.concept[1].concept[15].definition[0]Reason for an NHS number not being provided.
CodeSystem.concept[1].concept[16].code[0]P-18
CodeSystem.concept[1].concept[16].display[0]Patient - Relationship to proband
CodeSystem.concept[1].concept[16].definition[0]This patient's relationship to the primary patient.
CodeSystem.concept[1].concept[17].code[0]P-19
CodeSystem.concept[1].concept[17].display[0]Patient - Gender Identity
CodeSystem.concept[1].concept[17].definition[0]Patient's stated gender, determined by the patient.
CodeSystem.concept[1].concept[18].code[0]P-20
CodeSystem.concept[1].concept[18].display[0]Patient - Deceased date
CodeSystem.concept[1].concept[18].definition[0]Patient's date of death.
CodeSystem.concept[1].concept[19].code[0]P-21
CodeSystem.concept[1].concept[19].display[0]Patient - Chromosomal sex
CodeSystem.concept[1].concept[19].definition[0]Patient's genomic / karyotypic characteristic. Determined by genomic testing.
CodeSystem.concept[1].concept[20].code[0]P-35
CodeSystem.concept[1].concept[20].display[0]Patient - Withheld identity reason
CodeSystem.concept[1].concept[20].definition[0]Confirmation why the patient is withholding identity details.
CodeSystem.concept[1].concept[21].code[0]P-37
CodeSystem.concept[1].concept[21].display[0]Patient - Local Pedigree / Family identifier
CodeSystem.concept[1].concept[21].definition[0]Patient's pedigree or family identifying id.
CodeSystem.concept[1].concept[22].code[0]P-39
CodeSystem.concept[1].concept[22].display[0]Patient - Reason for inclusion in genomic test request
CodeSystem.concept[1].concept[22].definition[0]Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting
CodeSystem.concept[2].code[0]datagroup-fetus
CodeSystem.concept[2].display[0]Fetus
CodeSystem.concept[2].definition[0]Data group - Fetus
CodeSystem.concept[2].concept[0].code[0]F-1
CodeSystem.concept[2].concept[0].display[0]Fetus - Local identifier
CodeSystem.concept[2].concept[0].definition[0]Fetus' identification code other than NHS number.
CodeSystem.concept[2].concept[1].code[0]F-7
CodeSystem.concept[2].concept[1].display[0]Fetus - ODS code of organisation which assigned local identifier
CodeSystem.concept[2].concept[1].definition[0]ODS code of the organisation which assigned the local identifier F-1.
CodeSystem.concept[2].concept[2].code[0]F-2
CodeSystem.concept[2].concept[2].display[0]Fetus - Observed sex
CodeSystem.concept[2].concept[2].definition[0]Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM.
CodeSystem.concept[2].concept[3].code[0]F-3
CodeSystem.concept[2].concept[3].display[0]Fetus - Chromosomal sex
CodeSystem.concept[2].concept[3].definition[0]Fetus' genomic / karyotypic characteristic. Determined by genomic testing.
CodeSystem.concept[2].concept[4].code[0]F-6
CodeSystem.concept[2].concept[4].display[0]Fetus - Life status at time of request
CodeSystem.concept[2].concept[4].definition[0]Fetus' alive or deceased status details at the point of test ordering.
CodeSystem.concept[2].concept[5].code[0]F-8
CodeSystem.concept[2].concept[5].display[0]Fetus - Pregnancy id
CodeSystem.concept[2].concept[5].definition[0]The id of a given pregnancy which this fetus belongs to.
CodeSystem.concept[3].code[0]datagroup-test-request
CodeSystem.concept[3].display[0]Test Request
CodeSystem.concept[3].definition[0]Data group - Test Request
CodeSystem.concept[3].concept[0].code[0]TR-2
CodeSystem.concept[3].concept[0].display[0]Test Request - Payment status
CodeSystem.concept[3].concept[0].definition[0]How the test request is funded
CodeSystem.concept[3].concept[1].code[0]TR-4
CodeSystem.concept[3].concept[1].display[0]Test Request - Requesting reason rare disease
CodeSystem.concept[3].concept[1].definition[0]The reason for a rare disease genomic test.
CodeSystem.concept[3].concept[2].code[0]TR-38
CodeSystem.concept[3].concept[2].display[0]Test Request - Requesting reason cancer
CodeSystem.concept[3].concept[2].definition[0]The reason for a cancer genomic test.
CodeSystem.concept[3].concept[3].code[0]TR-5
CodeSystem.concept[3].concept[3].display[0]Test Request - High level test identifier
CodeSystem.concept[3].concept[3].definition[0]Legacy high level ids which identify the requested test. Options provided by old Test Directory.
CodeSystem.concept[3].concept[4].code[0]TR-6
CodeSystem.concept[3].concept[4].display[0]Test Request - High level test identifier description
CodeSystem.concept[3].concept[4].definition[0]Legacy high level name of the id requested
CodeSystem.concept[3].concept[5].code[0]TR-7
CodeSystem.concept[3].concept[5].display[0]Test Request - Low level test identifier
CodeSystem.concept[3].concept[5].definition[0]The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE).
CodeSystem.concept[3].concept[6].code[0]TR-8
CodeSystem.concept[3].concept[6].display[0]Test Request - Low level test identifier description
CodeSystem.concept[3].concept[6].definition[0]The low level CITT name of the considered test.
CodeSystem.concept[3].concept[7].code[0]TR-9
CodeSystem.concept[3].concept[7].display[0]Test Request - Low level multipurpose test identifier
CodeSystem.concept[3].concept[7].definition[0]The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION).
CodeSystem.concept[3].concept[8].code[0]TR-10
CodeSystem.concept[3].concept[8].display[0]Test Request - Low level multipurpose test identifier description
CodeSystem.concept[3].concept[8].definition[0]The low level name of the test to be actioned when the CITT code is multipurpose.
CodeSystem.concept[3].concept[9].code[0]TR-21
CodeSystem.concept[3].concept[9].display[0]Test Request - Genomic package id
CodeSystem.concept[3].concept[9].definition[0]Id of the package requested.
CodeSystem.concept[3].concept[10].code[0]TR-22
CodeSystem.concept[3].concept[10].display[0]Test Request - Genomic package name
CodeSystem.concept[3].concept[10].definition[0]Name of the package requested.
CodeSystem.concept[3].concept[11].code[0]TR-23
CodeSystem.concept[3].concept[11].display[0]Test Request - Genomic package version
CodeSystem.concept[3].concept[11].definition[0]Version of the package requested.
CodeSystem.concept[3].concept[12].code[0]TR-24
CodeSystem.concept[3].concept[12].display[0]Test Request - Genomic test id
CodeSystem.concept[3].concept[12].definition[0]Id of the test requested.
CodeSystem.concept[3].concept[13].code[0]TR-25
CodeSystem.concept[3].concept[13].display[0]Test Request - Genomic test name
CodeSystem.concept[3].concept[13].definition[0]Name of the test requested.
CodeSystem.concept[3].concept[14].code[0]TR-26
CodeSystem.concept[3].concept[14].display[0]Test Request - Genomic test version
CodeSystem.concept[3].concept[14].definition[0]Version of the test requested.
CodeSystem.concept[3].concept[15].code[0]TR-27
CodeSystem.concept[3].concept[15].display[0]Test Request - Additional panels
CodeSystem.concept[3].concept[15].definition[0]Additional panels to test.
CodeSystem.concept[3].concept[16].code[0]TR-28
CodeSystem.concept[3].concept[16].display[0]Test request - Target type
CodeSystem.concept[3].concept[16].definition[0]Type of target to test.
CodeSystem.concept[3].concept[17].code[0]TR-29
CodeSystem.concept[3].concept[17].display[0]Test request - Target detail
CodeSystem.concept[3].concept[17].definition[0]Detail of target to test.
CodeSystem.concept[3].concept[18].code[0]TR-11
CodeSystem.concept[3].concept[18].display[0]Test Request - Count of patients to be tested
CodeSystem.concept[3].concept[18].definition[0]Count of patients to be tested including the proband/primary patient.
CodeSystem.concept[3].concept[19].code[0]TR-12
CodeSystem.concept[3].concept[19].display[0]Test Request - Urgency reason
CodeSystem.concept[3].concept[19].definition[0]The test request urgency reason.
CodeSystem.concept[3].concept[20].code[0]TR-13
CodeSystem.concept[3].concept[20].display[0]Test Request - Reanalysis reason
CodeSystem.concept[3].concept[20].definition[0]The reason reanalysis has been requested.
CodeSystem.concept[3].concept[21].code[0]TR-14
CodeSystem.concept[3].concept[21].display[0]Test Request - Detail of reason for request
CodeSystem.concept[3].concept[21].definition[0]Further detail associated to the reason reanalysis has been requested.
CodeSystem.concept[3].concept[22].code[0]TR-15
CodeSystem.concept[3].concept[22].display[0]Test Request - Type of reanalysis
CodeSystem.concept[3].concept[22].definition[0]The type of reanalysis which has been requested.
CodeSystem.concept[3].concept[23].code[0]TR-17
CodeSystem.concept[3].concept[23].display[0]Test Request - Is urgent
CodeSystem.concept[3].concept[23].definition[0]Confirmation if the test request is urgent.
CodeSystem.concept[3].concept[24].code[0]TR-35
CodeSystem.concept[3].concept[24].display[0]Test Request - Purpose of linking
CodeSystem.concept[3].concept[24].definition[0]The reason a given test request has been linked to another test request.
CodeSystem.concept[3].concept[25].code[0]TR-36
CodeSystem.concept[3].concept[25].display[0]Test Request - Central email address for reporting
CodeSystem.concept[3].concept[25].definition[0]Central email address for contingency in the event of not being able to obtain a report via the requester.
CodeSystem.concept[3].concept[26].code[0]TR-20
CodeSystem.concept[3].concept[26].display[0]Test Request - Genomic report delivery method
CodeSystem.concept[3].concept[26].definition[0]Test Request - Genomic report delivery method
CodeSystem.concept[3].concept[27].code[0]TR-30
CodeSystem.concept[3].concept[27].display[0]Test Request - Add private genomic request and report to NHS record
CodeSystem.concept[3].concept[27].definition[0]Confirmation if the content of a private genomic test request should be added to an NHS record.
CodeSystem.concept[3].concept[28].code[0]TR-31
CodeSystem.concept[3].concept[28].display[0]Test Request - Test request form version
CodeSystem.concept[3].concept[28].definition[0]Version of the test order form completed and submitted.
CodeSystem.concept[3].concept[29].code[0]TR-32
CodeSystem.concept[3].concept[29].display[0]Test Request - File / Link to file
CodeSystem.concept[3].concept[29].definition[0]Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order.
CodeSystem.concept[3].concept[30].code[0]TR-33
CodeSystem.concept[3].concept[30].display[0]Test Request - File detail
CodeSystem.concept[3].concept[30].definition[0]Detail to provide context to an uploaded file or document link.
CodeSystem.concept[3].concept[31].code[0]TR-34
CodeSystem.concept[3].concept[31].display[0]Test Request - Clinical utility
CodeSystem.concept[3].concept[31].definition[0]Clinical benefit to patient of obtaining a requested genomic report.
CodeSystem.concept[3].concept[32].code[0]TR-39
CodeSystem.concept[3].concept[32].display[0]Test Request - Linked test request reference
CodeSystem.concept[3].concept[32].definition[0]The reference to any associated test requests
CodeSystem.concept[4].code[0]datagroup-ngrl-consent
CodeSystem.concept[4].display[0]NGRL-consent
CodeSystem.concept[4].definition[0]Data group - NGRL consent
CodeSystem.concept[4].concept[0].code[0]NGRL-1
CodeSystem.concept[4].concept[0].display[0]NGRL consent - Date of NGRL consent
CodeSystem.concept[4].concept[0].definition[0]The date NGRL consent was provided.
CodeSystem.concept[4].concept[1].code[0]NGRL-2
CodeSystem.concept[4].concept[1].display[0]NGRL consent - Patient has made their own choice to consent to the NGRL
CodeSystem.concept[4].concept[1].definition[0]Confirmation if the patient to be tested has provided NGRL consent themselves.
CodeSystem.concept[4].concept[2].code[0]NGRL-3
CodeSystem.concept[4].concept[2].display[0]NGRL consent - Patient representative name (if patient cannot make their own choice)
CodeSystem.concept[4].concept[2].definition[0]The name of the patient representative.
CodeSystem.concept[4].concept[3].code[0]NGRL-4
CodeSystem.concept[4].concept[3].display[0]NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research
CodeSystem.concept[4].concept[3].definition[0]The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL.
CodeSystem.concept[4].concept[4].code[0]NGRL-5
CodeSystem.concept[4].concept[4].display[0]NGRL consent - NGRL consent document link
CodeSystem.concept[4].concept[4].definition[0]A URL where a copy of a completed NGRL consent form may be found.
CodeSystem.concept[5].code[0]datagroup-primary-sample
CodeSystem.concept[5].display[0]Primary Sample
CodeSystem.concept[5].definition[0]Data group - Primary Sample
CodeSystem.concept[5].concept[0].code[0]PS-2
CodeSystem.concept[5].concept[0].display[0]Primary Sample - Local identifier
CodeSystem.concept[5].concept[0].definition[0]Local ids applied to a sample
CodeSystem.concept[5].concept[1].code[0]PS-3
CodeSystem.concept[5].concept[1].display[0]Primary Sample - ODS code of organisation which assigned local id
CodeSystem.concept[5].concept[1].definition[0]ODS code of the organisation which assigned the local sample id.
CodeSystem.concept[5].concept[2].code[0]PS-10
CodeSystem.concept[5].concept[2].display[0]Primary Sample - Obtained date
CodeSystem.concept[5].concept[2].definition[0]Date at which a specimen/biopsy was obtained from patient.
CodeSystem.concept[5].concept[3].code[0]PS-11
CodeSystem.concept[5].concept[3].display[0]Primary Sample - Primary sample
CodeSystem.concept[5].concept[3].definition[0]The primary sample material.
CodeSystem.concept[5].concept[4].code[0]PS-12
CodeSystem.concept[5].concept[4].display[0]Primary Sample - Primary sample state
CodeSystem.concept[5].concept[4].definition[0]The state of the primary sample.
CodeSystem.concept[5].concept[5].code[0]PS-25
CodeSystem.concept[5].concept[5].display[0]Primary Sample - Preservative/Container
CodeSystem.concept[5].concept[5].definition[0]How the primary sample is preserved.
CodeSystem.concept[5].concept[6].code[0]PS-30
CodeSystem.concept[5].concept[6].display[0]Primary Sample - Block identifier
CodeSystem.concept[5].concept[6].definition[0]Sample block identifier
CodeSystem.concept[5].concept[7].code[0]PS-31
CodeSystem.concept[5].concept[7].display[0]Primary Sample - Fixative type
CodeSystem.concept[5].concept[7].definition[0]Sample fixative type
CodeSystem.concept[5].concept[8].code[0]PS-32
CodeSystem.concept[5].concept[8].display[0]Primary Sample - Hours to fixation
CodeSystem.concept[5].concept[8].definition[0]Sample hours to fixation
CodeSystem.concept[5].concept[9].code[0]PS-33
CodeSystem.concept[5].concept[9].display[0]Primary Sample - Hours in fixative
CodeSystem.concept[5].concept[9].definition[0]Sample hours in fixative
CodeSystem.concept[5].concept[10].code[0]PS-34
CodeSystem.concept[5].concept[10].display[0]Primary Sample - Tumour enrichment method
CodeSystem.concept[5].concept[10].definition[0]Method used for tumour enrichment.
CodeSystem.concept[5].concept[11].code[0]PS-13
CodeSystem.concept[5].concept[11].display[0]Primary Sample - Necrosis
CodeSystem.concept[5].concept[11].definition[0]% necrotic (dead) cells in primary sample.
CodeSystem.concept[5].concept[12].code[0]PS-14
CodeSystem.concept[5].concept[12].display[0]Primary Sample - Nucleated cell count
CodeSystem.concept[5].concept[12].definition[0]Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc).
CodeSystem.concept[5].concept[13].code[0]PS-15
CodeSystem.concept[5].concept[13].display[0]Primary Sample - Tumour nuclear content in whole section
CodeSystem.concept[5].concept[13].definition[0]Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)
CodeSystem.concept[5].concept[14].code[0]PS-26
CodeSystem.concept[5].concept[14].display[0]Primary Sample - Tumour nuclear content in marked area
CodeSystem.concept[5].concept[14].definition[0]Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)
CodeSystem.concept[5].concept[15].code[0]PS-17
CodeSystem.concept[5].concept[15].display[0]Primary Sample - Solid tumour morphology
CodeSystem.concept[5].concept[15].definition[0]The histology and likely course of development of a tumour.
CodeSystem.concept[5].concept[16].code[0]PS-18
CodeSystem.concept[5].concept[16].display[0]Primary Sample - Solid tumour topography
CodeSystem.concept[5].concept[16].definition[0]The tumour sample site. e.g. from colon, stomach etc.
CodeSystem.concept[5].concept[17].code[0]PS-29
CodeSystem.concept[5].concept[17].display[0]Primary Sample - Is biopsy
CodeSystem.concept[5].concept[17].definition[0]Primary Sample - Is biopsy
CodeSystem.concept[5].concept[18].code[0]PS-19
CodeSystem.concept[5].concept[18].display[0]Primary Sample - Biopsy site
CodeSystem.concept[5].concept[18].definition[0]Digital confirmation that the sample is a biopsy.
CodeSystem.concept[5].concept[19].code[0]PS-21
CodeSystem.concept[5].concept[19].display[0]Primary Sample - Observed maternal cell contamination (MCC)
CodeSystem.concept[5].concept[19].definition[0]An observed outcome which may indicate MCC
CodeSystem.concept[5].concept[20].code[0]PS-27
CodeSystem.concept[5].concept[20].display[0]Primary Sample - Test confirmed maternal cell contamination (MCC)
CodeSystem.concept[5].concept[20].definition[0]Analytically confirmed MCC levels
CodeSystem.concept[5].concept[21].code[0]PS-22
CodeSystem.concept[5].concept[21].display[0]Primary Sample - Option for all products of conception
CodeSystem.concept[5].concept[21].definition[0]Primary Sample - Option for all products of conception
CodeSystem.concept[5].concept[22].code[0]PS-23
CodeSystem.concept[5].concept[22].display[0]Primary Sample - Blasts %
CodeSystem.concept[5].concept[22].definition[0]Future management for products of conception.
CodeSystem.concept[5].concept[23].code[0]PS-24
CodeSystem.concept[5].concept[23].display[0]Primary Sample - High infection risk reason
CodeSystem.concept[5].concept[23].definition[0]The high contamination risk reason for a primary sample.
CodeSystem.concept[5].concept[24].code[0]PS-28
CodeSystem.concept[5].concept[24].display[0]Primary Sample - Patient life status at the time of collection
CodeSystem.concept[5].concept[24].definition[0]If the patient was alive or deceased at the point of collecting a sample.
CodeSystem.concept[5].concept[25].code[0]PS-35
CodeSystem.concept[5].concept[25].display[0]Primary Sample - Solid tumour type
CodeSystem.concept[5].concept[25].definition[0]The origin or context of a tumour sample.
CodeSystem.concept[6].code[0]datagroup-patient-clinical-information
CodeSystem.concept[6].display[0]Patient Clinical Information
CodeSystem.concept[6].definition[0]Data group - Patient Clinical Information
CodeSystem.concept[6].concept[0].code[0]PCI-1
CodeSystem.concept[6].concept[0].display[0]Patient clinical information - Genomic Ethnicity
CodeSystem.concept[6].concept[0].definition[0]Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish
CodeSystem.concept[6].concept[1].code[0]PCI-2
CodeSystem.concept[6].concept[1].display[0]Patient clinical information - Disease Status
CodeSystem.concept[6].concept[1].definition[0]If the patient is affected, unaffected, or it is unknown.
CodeSystem.concept[6].concept[2].code[0]PCI-4
CodeSystem.concept[6].concept[2].display[0]Patient clinical information - Age at disease onset
CodeSystem.concept[6].concept[2].definition[0]The age when a change in patients' health was first noted in line with suspected diagnosis.
CodeSystem.concept[6].concept[3].code[0]PCI-5
CodeSystem.concept[6].concept[3].display[0]Patient clinical information - Known/Suspected Disease
CodeSystem.concept[6].concept[3].definition[0]Disease a patient is believed, known to have, or be at risk of developing.
CodeSystem.concept[6].concept[4].code[0]PCI-6
CodeSystem.concept[6].concept[4].display[0]Patient clinical information - Phenotypic details
CodeSystem.concept[6].concept[4].definition[0]The HPO (or alternative ontology as appropriate) term names for the observable disease traits.
CodeSystem.concept[6].concept[5].code[0]PCI-7
CodeSystem.concept[6].concept[5].display[0]Patient clinical information - Symptoms
CodeSystem.concept[6].concept[5].definition[0]The patient's symptoms
CodeSystem.concept[6].concept[6].code[0]PCI-10
CodeSystem.concept[6].concept[6].display[0]Patient clinical information - Count of tumours
CodeSystem.concept[6].concept[6].definition[0]How many tumours the patient has.
CodeSystem.concept[6].concept[7].code[0]PCI-11
CodeSystem.concept[6].concept[7].display[0]Patient clinical information - Site of tumour
CodeSystem.concept[6].concept[7].definition[0]Location of the tumours on the body.
CodeSystem.concept[6].concept[8].code[0]PCI-14
CodeSystem.concept[6].concept[8].display[0]Patient clinical information - Tumour sites - Body image diagram
CodeSystem.concept[6].concept[8].definition[0]Image attachment of body with tumour sites highlighted.
CodeSystem.concept[6].concept[9].code[0]PCI-15
CodeSystem.concept[6].concept[9].display[0]Patient clinical information - Pedigree details / Relevant family history
CodeSystem.concept[6].concept[9].definition[0]The patient's pedigree/family history details (inc family history of cancer).
CodeSystem.concept[6].concept[10].code[0]PCI-16
CodeSystem.concept[6].concept[10].display[0]Patient clinical information - Pedigree diagram
CodeSystem.concept[6].concept[10].definition[0]Image attachment of pedigree details
CodeSystem.concept[6].concept[11].code[0]PCI-17
CodeSystem.concept[6].concept[11].display[0]Patient clinical information - Laterality of hearing loss
CodeSystem.concept[6].concept[11].definition[0]Laterality of the hearing loss i.e. bilateral or unilateral.
CodeSystem.concept[6].concept[12].code[0]PCI-18
CodeSystem.concept[6].concept[12].display[0]Patient clinical information - Fetal haemoglobinopathy maternal screening genotype
CodeSystem.concept[6].concept[12].definition[0]Maternal screening genotype for haemoglobinopathy testing.
CodeSystem.concept[6].concept[13].code[0]PCI-21
CodeSystem.concept[6].concept[13].display[0]Patient clinical information - Legal considerations
CodeSystem.concept[6].concept[13].definition[0]Legal considerations for a given request.
CodeSystem.concept[6].concept[14].code[0]PCI-22
CodeSystem.concept[6].concept[14].display[0]Patient clinical information - Fetal haemoglobinopathy paternal screening genotype
CodeSystem.concept[6].concept[14].definition[0]Paternal screening genotype for haemoglobinopathy testing
CodeSystem.concept[6].concept[15].code[0]PCI-23
CodeSystem.concept[6].concept[15].display[0]Patient clinical information - Expected Maternity Unit - Organisation name
CodeSystem.concept[6].concept[15].definition[0]Requesting clinician's organisation name.
CodeSystem.concept[6].concept[16].code[0]PCI-24
CodeSystem.concept[6].concept[16].display[0]Patient clinical information - Expected Maternity Unit - Organisation address
CodeSystem.concept[6].concept[16].definition[0]Requesting clinician's organisation address.
CodeSystem.concept[6].concept[17].code[0]PCI-25
CodeSystem.concept[6].concept[17].display[0]Patient clinical information - Expected Maternity Unit - Organisation ODS code
CodeSystem.concept[6].concept[17].definition[0]Requesting clinician's organisation ODS code.
CodeSystem.concept[6].concept[18].code[0]PCI-26
CodeSystem.concept[6].concept[18].display[0]Patient clinical information - Expected Maternity Unit - Department name
CodeSystem.concept[6].concept[18].definition[0]Requesting clinician's department name.
CodeSystem.concept[6].concept[19].code[0]PCI-27
CodeSystem.concept[6].concept[19].display[0]Patient clinical information - Growth history
CodeSystem.concept[6].concept[19].definition[0]Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc.
CodeSystem.concept[6].concept[20].code[0]PCI-28
CodeSystem.concept[6].concept[20].display[0]Patient clinical information - Severity of hearing loss
CodeSystem.concept[6].concept[20].definition[0]Free text regarding hearing loss
CodeSystem.concept[6].concept[21].code[0]PCI-29
CodeSystem.concept[6].concept[21].display[0]Patient clinical information - Retinal degeneration
CodeSystem.concept[6].concept[21].definition[0]Free text regarding retinal degeneration
CodeSystem.concept[6].concept[22].code[0]PCI-30
CodeSystem.concept[6].concept[22].display[0]Patient clinical information - Risk factors
CodeSystem.concept[6].concept[22].definition[0]Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication.
CodeSystem.concept[6].concept[23].code[0]PCI-31
CodeSystem.concept[6].concept[23].display[0]Patient clinical information - Suspected inborn error type(s)
CodeSystem.concept[6].concept[23].definition[0]Suspected inborn error type(s)
CodeSystem.concept[6].concept[24].code[0]PCI-32
CodeSystem.concept[6].concept[24].display[0]Patient clinical information - Abnormal infection history site
CodeSystem.concept[6].concept[24].definition[0]Abnormal infection history site organism
CodeSystem.concept[6].concept[25].code[0]PCI-33
CodeSystem.concept[6].concept[25].display[0]Patient clinical information - Abnormal infection history site organism
CodeSystem.concept[6].concept[25].definition[0]Abnormal infection history site organism
CodeSystem.concept[6].concept[26].code[0]PCI-34
CodeSystem.concept[6].concept[26].display[0]Is on ig replacement
CodeSystem.concept[6].concept[26].definition[0]If the patient is on immunoglobin replacement treatment.
CodeSystem.concept[6].concept[27].code[0]PCI-35
CodeSystem.concept[6].concept[27].display[0]Patient clinical information - Current and previous treatment detail
CodeSystem.concept[6].concept[27].definition[0]Detail regarding relevant current and previous medical treatments.
CodeSystem.concept[6].concept[28].code[0]PCI-36
CodeSystem.concept[6].concept[28].display[0]Patient clinical information - Pregnancy status
CodeSystem.concept[6].concept[28].definition[0]Patient`s pregnancy status
CodeSystem.concept[6].concept[29].code[0]PCI-37
CodeSystem.concept[6].concept[29].display[0]Patient clinical information - Pregnancy type
CodeSystem.concept[6].concept[29].definition[0]Type of conception
CodeSystem.concept[6].concept[30].code[0]PCI-38
CodeSystem.concept[6].concept[30].display[0]Patient clinical information - Pregnancy gestation period
CodeSystem.concept[6].concept[30].definition[0]Patient's term of active pregnancy at point of test request.
CodeSystem.concept[6].concept[31].code[0]PCI-39
CodeSystem.concept[6].concept[31].display[0]Patient clinical information - Fetal gestation
CodeSystem.concept[6].concept[31].definition[0]Stage during patient pregnancy at which it terminated.
CodeSystem.concept[6].concept[32].code[0]PCI-40
CodeSystem.concept[6].concept[32].display[0]Patient clinical information - Estimated delivery date (EDD)
CodeSystem.concept[6].concept[32].definition[0]Patient's estimated delivery date.
CodeSystem.concept[6].concept[33].code[0]PCI-41
CodeSystem.concept[6].concept[33].display[0]Patient clinical information - IVF age of egg donor
CodeSystem.concept[6].concept[33].definition[0]The age of the patient who donated the egg at the time of donation.
CodeSystem.concept[6].concept[34].code[0]PCI-42
CodeSystem.concept[6].concept[34].display[0]Patient clinical information - Had transplant
CodeSystem.concept[6].concept[34].definition[0]Has the patient ever had a transplant.
CodeSystem.concept[6].concept[35].code[0]PCI-43
CodeSystem.concept[6].concept[35].display[0]Patient clinical information - Type of transplant
CodeSystem.concept[6].concept[35].definition[0]What type of transplant the patient had.
CodeSystem.concept[6].concept[36].code[0]PCI-44
CodeSystem.concept[6].concept[36].display[0]Patient clinical information - Transplant date
CodeSystem.concept[6].concept[36].definition[0]When the patient had the transplant.
CodeSystem.concept[6].concept[37].code[0]PCI-45
CodeSystem.concept[6].concept[37].display[0]Patient clinical information - Had transfusion in the last 6 weeks
CodeSystem.concept[6].concept[37].definition[0]Has the patient had a transfusion in the last 6 weeks.
CodeSystem.concept[6].concept[38].code[0]PCI-46
CodeSystem.concept[6].concept[38].display[0]Patient clinical information - Type of transfusion
CodeSystem.concept[6].concept[38].definition[0]What type of transfusion the patient has had.
CodeSystem.concept[6].concept[39].code[0]PCI-47
CodeSystem.concept[6].concept[39].display[0]Patient clinical information - Transfusion date
CodeSystem.concept[6].concept[39].definition[0]When the patient had the transfusion.
CodeSystem.concept[6].concept[40].code[0]PCI-48
CodeSystem.concept[6].concept[40].display[0]Patient clinical information - Height (m)
CodeSystem.concept[6].concept[40].definition[0]Patient's height.
CodeSystem.concept[7].code[0]datagroup-miscellaneous
CodeSystem.concept[7].display[0]Miscellaneous
CodeSystem.concept[7].definition[0]Data group - Miscellaneous
CodeSystem.concept[7].concept[0].code[0]MIS-1
CodeSystem.concept[7].concept[0].display[0]Further supporting information
CodeSystem.concept[7].concept[0].definition[0]Supporting information which has not been captured elsewhere.
CodeSystem.concept[8].code[0]datagroup-hospital-encounter
CodeSystem.concept[8].display[0]Hospital encounter
CodeSystem.concept[8].definition[0]Data group - Hospital encounter
CodeSystem.concept[8].concept[0].code[0]HE-1
CodeSystem.concept[8].concept[0].display[0]Treatment function code (TFC)
CodeSystem.concept[8].concept[0].definition[0]The identifier for the clinical specialty or service under which the patient is being treated.
CodeSystem.concept[8].concept[1].code[0]HE-2
CodeSystem.concept[8].concept[1].display[0]Hospital provider spell identifier
CodeSystem.concept[8].concept[1].definition[0]The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge.
CodeSystem.concept[8].concept[2].code[0]HE-3
CodeSystem.concept[8].concept[2].display[0]Outpatient attendance identifier
CodeSystem.concept[8].concept[2].definition[0]The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered.
CodeSystem.concept[8].concept[3].code[0]HE-4
CodeSystem.concept[8].concept[3].display[0]Hospital point of delivery code
CodeSystem.concept[8].concept[3].definition[0]The identifier that defines the type of care setting in which the genomic test was requested.

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="mds-questiontag-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics" />
<version value="0.1.1" />
<name value="MDSQuestionTagGenomics" />
<title value="MDS Question Tag Genomics" />
<status value="draft" />
<date value="2025-12-15T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag." />
<copyright value="Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<hierarchyMeaning value="grouped-by" />
<content value="complete" />
<code value="datagroup-healthcare-professional" />
<display value="Healthcare Professional" />
<definition value="Data group - Healthcare professional" />
<code value="HCP-1" />
<display value="HCP - Genomic test order role" />
<definition value="HCP's function within the genomic test ordering process" />
</concept>
<code value="HCP-2" />
<display value="HCP - First name" />
<definition value="HCP's first name." />
</concept>
<code value="HCP-13" />
<display value="HCP - surname" />
<definition value="HCP'surname " />
</concept>
<code value="HCP-3" />
<display value="HCP - Job title" />
<definition value="HCP's job title." />
</concept>
<code value="HCP-4" />
<display value="HCP - Current specialty" />
<definition value="HCP's current specialty." />
</concept>
<code value="HCP-5" />
<display value="HCP - Telephone number" />
<definition value="HCP's telephone number." />
</concept>
<code value="HCP-6" />
<display value="HCP - Email address" />
<definition value="HCP's email address." />
</concept>
<code value="HCP-7" />
<display value="HCP - Organisation name" />
<definition value="HCP's requesting organisation name." />
</concept>
<code value="HCP-9" />
<display value="HCP - Organisation ODS code" />
<definition value="HCP's organisation ODS code" />
</concept>
<code value="HCP-10" />
<display value="HCP - Department name" />
<definition value="HCP's department name." />
</concept>
<code value="HCP-11" />
<display value="HCP - Professional registration number" />
<definition value="HCP's professional registration number such as their GMC number." />
</concept>
<code value="HCP-12" />
<display value="HCP - Professional registration number type" />
<definition value="HCP's professional registration number type such as 'GMC'." />
</concept>
</concept>
<code value="datagroup-patient" />
<display value="Patient" />
<definition value="Data group - Patient" />
<code value="P-1" />
<display value="Patient - Title" />
<definition value="Patient's title." />
</concept>
<code value="P-2" />
<display value="Patient - First name" />
<definition value="Patient's first name." />
</concept>
<code value="P-40" />
<display value="Patient - Middlename" />
<definition value="Patient's middle name." />
</concept>
<code value="P-3" />
<display value="Patient - Surname" />
<definition value="Patient's last name." />
</concept>
<code value="P-41" />
<display value="Patient - Name use" />
<definition value="Links each patient name entry to confirm if current, previous or what the patient is known as." />
</concept>
<code value="P-4" />
<display value="Patient - Date of birth" />
<definition value="Patient's date of birth." />
</concept>
<code value="P-6" />
<display value="Patient - Postcode" />
<definition value="Patient's home postcode." />
</concept>
<code value="P-7" />
<display value="Patient - Country of residence" />
<definition value="Patient's home country." />
</concept>
<code value="P-9" />
<display value="Patient - Ethnicity" />
<definition value="Patient's ethnicity." />
</concept>
<code value="P-10" />
<display value="Patient - Sex defined at birth" />
<definition value="Patient's phenotypic sex classification as defined at birth based on physical characteristic." />
</concept>
<code value="P-12" />
<display value="Patient - GP practice's ODS Code" />
<definition value="Patient's GP practice ODS code." />
</concept>
<code value="P-13" />
<display value="Patient - Is from consanguineous union" />
<definition value="The fact of the patient's biological parents being descended from the same ancestor." />
</concept>
<code value="P-15" />
<display value="Patient - NHS number" />
<definition value="Patient's NHS number." />
</concept>
<code value="P-16" />
<display value="Patient - Local identifier" />
<definition value="Patient's identification code other than NHS number." />
</concept>
<code value="P-42" />
<display value="Patient - ODS code of organisation which assigned local identifier" />
<definition value="ODS code of the organisation which assigned the local identifier P-16." />
</concept>
<code value="P-17" />
<display value="Patient - Reason for unavailable NHS number" />
<definition value="Reason for an NHS number not being provided." />
</concept>
<code value="P-18" />
<display value="Patient - Relationship to proband" />
<definition value="This patient's relationship to the primary patient." />
</concept>
<code value="P-19" />
<display value="Patient - Gender Identity" />
<definition value="Patient's stated gender, determined by the patient." />
</concept>
<code value="P-20" />
<display value="Patient - Deceased date" />
<definition value="Patient's date of death." />
</concept>
<code value="P-21" />
<display value="Patient - Chromosomal sex" />
<definition value="Patient's genomic / karyotypic characteristic. Determined by genomic testing." />
</concept>
<code value="P-35" />
<display value="Patient - Withheld identity reason" />
<definition value="Confirmation why the patient is withholding identity details." />
</concept>
<code value="P-37" />
<display value="Patient - Local Pedigree / Family identifier" />
<definition value="Patient's pedigree or family identifying id." />
</concept>
<code value="P-39" />
<display value="Patient - Reason for inclusion in genomic test request" />
<definition value="Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting" />
</concept>
</concept>
<code value="datagroup-fetus" />
<display value="Fetus" />
<definition value="Data group - Fetus" />
<code value="F-1" />
<display value="Fetus - Local identifier" />
<definition value="Fetus' identification code other than NHS number." />
</concept>
<code value="F-7" />
<display value="Fetus - ODS code of organisation which assigned local identifier" />
<definition value="ODS code of the organisation which assigned the local identifier F-1." />
</concept>
<code value="F-2" />
<display value="Fetus - Observed sex" />
<definition value="Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM." />
</concept>
<code value="F-3" />
<display value="Fetus - Chromosomal sex" />
<definition value="Fetus' genomic / karyotypic characteristic. Determined by genomic testing." />
</concept>
<code value="F-6" />
<display value="Fetus - Life status at time of request" />
<definition value="Fetus' alive or deceased status details at the point of test ordering." />
</concept>
<code value="F-8" />
<display value="Fetus - Pregnancy id" />
<definition value="The id of a given pregnancy which this fetus belongs to." />
</concept>
</concept>
<code value="datagroup-test-request" />
<display value="Test Request" />
<definition value="Data group - Test Request" />
<code value="TR-2" />
<display value="Test Request - Payment status" />
<definition value="How the test request is funded" />
</concept>
<code value="TR-4" />
<display value="Test Request - Requesting reason rare disease" />
<definition value="The reason for a rare disease genomic test." />
</concept>
<code value="TR-38" />
<display value="Test Request - Requesting reason cancer" />
<definition value="The reason for a cancer genomic test." />
</concept>
<code value="TR-5" />
<display value="Test Request - High level test identifier" />
<definition value="Legacy high level ids which identify the requested test. Options provided by old Test Directory." />
</concept>
<code value="TR-6" />
<display value="Test Request - High level test identifier description" />
<definition value="Legacy high level name of the id requested" />
</concept>
<code value="TR-7" />
<display value="Test Request - Low level test identifier" />
<definition value="The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE)." />
</concept>
<code value="TR-8" />
<display value="Test Request - Low level test identifier description" />
<definition value="The low level CITT name of the considered test." />
</concept>
<code value="TR-9" />
<display value="Test Request - Low level multipurpose test identifier" />
<definition value="The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION)." />
</concept>
<code value="TR-10" />
<display value="Test Request - Low level multipurpose test identifier description" />
<definition value="The low level name of the test to be actioned when the CITT code is multipurpose." />
</concept>
<code value="TR-21" />
<display value="Test Request - Genomic package id" />
<definition value="Id of the package requested." />
</concept>
<code value="TR-22" />
<display value="Test Request - Genomic package name" />
<definition value="Name of the package requested." />
</concept>
<code value="TR-23" />
<display value="Test Request - Genomic package version" />
<definition value="Version of the package requested." />
</concept>
<code value="TR-24" />
<display value="Test Request - Genomic test id" />
<definition value="Id of the test requested." />
</concept>
<code value="TR-25" />
<display value="Test Request - Genomic test name" />
<definition value="Name of the test requested." />
</concept>
<code value="TR-26" />
<display value="Test Request - Genomic test version" />
<definition value="Version of the test requested." />
</concept>
<code value="TR-27" />
<display value="Test Request - Additional panels" />
<definition value="Additional panels to test." />
</concept>
<code value="TR-28" />
<display value="Test request - Target type" />
<definition value="Type of target to test." />
</concept>
<code value="TR-29" />
<display value="Test request - Target detail" />
<definition value="Detail of target to test." />
</concept>
<code value="TR-11" />
<display value="Test Request - Count of patients to be tested" />
<definition value="Count of patients to be tested including the proband/primary patient." />
</concept>
<code value="TR-12" />
<display value="Test Request - Urgency reason" />
<definition value="The test request urgency reason." />
</concept>
<code value="TR-13" />
<display value="Test Request - Reanalysis reason" />
<definition value="The reason reanalysis has been requested." />
</concept>
<code value="TR-14" />
<display value="Test Request - Detail of reason for request" />
<definition value="Further detail associated to the reason reanalysis has been requested." />
</concept>
<code value="TR-15" />
<display value="Test Request - Type of reanalysis" />
<definition value="The type of reanalysis which has been requested." />
</concept>
<code value="TR-17" />
<display value="Test Request - Is urgent" />
<definition value="Confirmation if the test request is urgent." />
</concept>
<code value="TR-35" />
<display value="Test Request - Purpose of linking" />
<definition value="The reason a given test request has been linked to another test request." />
</concept>
<code value="TR-36" />
<display value="Test Request - Central email address for reporting" />
<definition value="Central email address for contingency in the event of not being able to obtain a report via the requester." />
</concept>
<code value="TR-20" />
<display value="Test Request - Genomic report delivery method" />
<definition value="Test Request - Genomic report delivery method" />
</concept>
<code value="TR-30" />
<display value="Test Request - Add private genomic request and report to NHS record" />
<definition value="Confirmation if the content of a private genomic test request should be added to an NHS record." />
</concept>
<code value="TR-31" />
<display value="Test Request - Test request form version" />
<definition value="Version of the test order form completed and submitted." />
</concept>
<code value="TR-32" />
<display value="Test Request - File / Link to file" />
<definition value="Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order." />
</concept>
<code value="TR-33" />
<display value="Test Request - File detail" />
<definition value="Detail to provide context to an uploaded file or document link." />
</concept>
<code value="TR-34" />
<display value="Test Request - Clinical utility" />
<definition value="Clinical benefit to patient of obtaining a requested genomic report." />
</concept>
<code value="TR-39" />
<display value="Test Request - Linked test request reference" />
<definition value="The reference to any associated test requests" />
</concept>
</concept>
<code value="datagroup-ngrl-consent" />
<display value="NGRL-consent" />
<definition value="Data group - NGRL consent" />
<code value="NGRL-1" />
<display value="NGRL consent - Date of NGRL consent" />
<definition value="The date NGRL consent was provided." />
</concept>
<code value="NGRL-2" />
<display value="NGRL consent - Patient has made their own choice to consent to the NGRL" />
<definition value="Confirmation if the patient to be tested has provided NGRL consent themselves." />
</concept>
<code value="NGRL-3" />
<display value="NGRL consent - Patient representative name (if patient cannot make their own choice)" />
<definition value="The name of the patient representative." />
</concept>
<code value="NGRL-4" />
<display value="NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research" />
<definition value="The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL." />
</concept>
<code value="NGRL-5" />
<display value="NGRL consent - NGRL consent document link" />
<definition value="A URL where a copy of a completed NGRL consent form may be found." />
</concept>
</concept>
<code value="datagroup-primary-sample" />
<display value="Primary Sample" />
<definition value="Data group - Primary Sample" />
<code value="PS-2" />
<display value="Primary Sample - Local identifier" />
<definition value="Local ids applied to a sample" />
</concept>
<code value="PS-3" />
<display value="Primary Sample - ODS code of organisation which assigned local id" />
<definition value="ODS code of the organisation which assigned the local sample id." />
</concept>
<code value="PS-10" />
<display value="Primary Sample - Obtained date" />
<definition value="Date at which a specimen/biopsy was obtained from patient." />
</concept>
<code value="PS-11" />
<display value="Primary Sample - Primary sample" />
<definition value="The primary sample material." />
</concept>
<code value="PS-12" />
<display value="Primary Sample - Primary sample state" />
<definition value="The state of the primary sample." />
</concept>
<code value="PS-25" />
<display value="Primary Sample - Preservative/Container" />
<definition value="How the primary sample is preserved." />
</concept>
<code value="PS-30" />
<display value="Primary Sample - Block identifier" />
<definition value="Sample block identifier" />
</concept>
<code value="PS-31" />
<display value="Primary Sample - Fixative type" />
<definition value="Sample fixative type" />
</concept>
<code value="PS-32" />
<display value="Primary Sample - Hours to fixation" />
<definition value="Sample hours to fixation" />
</concept>
<code value="PS-33" />
<display value="Primary Sample - Hours in fixative" />
<definition value="Sample hours in fixative" />
</concept>
<code value="PS-34" />
<display value="Primary Sample - Tumour enrichment method" />
<definition value="Method used for tumour enrichment." />
</concept>
<code value="PS-13" />
<display value="Primary Sample - Necrosis" />
<definition value="% necrotic (dead) cells in primary sample." />
</concept>
<code value="PS-14" />
<display value="Primary Sample - Nucleated cell count" />
<definition value="Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc)." />
</concept>
<code value="PS-15" />
<display value="Primary Sample - Tumour nuclear content in whole section" />
<definition value="Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)" />
</concept>
<code value="PS-26" />
<display value="Primary Sample - Tumour nuclear content in marked area" />
<definition value="Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)" />
</concept>
<code value="PS-17" />
<display value="Primary Sample - Solid tumour morphology" />
<definition value="The histology and likely course of development of a tumour." />
</concept>
<code value="PS-18" />
<display value="Primary Sample - Solid tumour topography" />
<definition value="The tumour sample site. e.g. from colon, stomach etc." />
</concept>
<code value="PS-29" />
<display value="Primary Sample - Is biopsy" />
<definition value="Primary Sample - Is biopsy" />
</concept>
<code value="PS-19" />
<display value="Primary Sample - Biopsy site" />
<definition value="Digital confirmation that the sample is a biopsy." />
</concept>
<code value="PS-21" />
<display value="Primary Sample - Observed maternal cell contamination (MCC)" />
<definition value="An observed outcome which may indicate MCC" />
</concept>
<code value="PS-27" />
<display value="Primary Sample - Test confirmed maternal cell contamination (MCC)" />
<definition value="Analytically confirmed MCC levels" />
</concept>
<code value="PS-22" />
<display value="Primary Sample - Option for all products of conception" />
<definition value="Primary Sample - Option for all products of conception" />
</concept>
<code value="PS-23" />
<display value="Primary Sample - Blasts %" />
<definition value="Future management for products of conception." />
</concept>
<code value="PS-24" />
<display value="Primary Sample - High infection risk reason" />
<definition value="The high contamination risk reason for a primary sample." />
</concept>
<code value="PS-28" />
<display value="Primary Sample - Patient life status at the time of collection" />
<definition value="If the patient was alive or deceased at the point of collecting a sample." />
</concept>
<code value="PS-35" />
<display value="Primary Sample - Solid tumour type" />
<definition value="The origin or context of a tumour sample." />
</concept>
</concept>
<code value="datagroup-patient-clinical-information" />
<display value="Patient Clinical Information" />
<definition value="Data group - Patient Clinical Information" />
<code value="PCI-1" />
<display value="Patient clinical information - Genomic Ethnicity" />
<definition value="Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish" />
</concept>
<code value="PCI-2" />
<display value="Patient clinical information - Disease Status" />
<definition value="If the patient is affected, unaffected, or it is unknown." />
</concept>
<code value="PCI-4" />
<display value="Patient clinical information - Age at disease onset" />
<definition value="The age when a change in patients' health was first noted in line with suspected diagnosis." />
</concept>
<code value="PCI-5" />
<display value="Patient clinical information - Known/Suspected Disease" />
<definition value="Disease a patient is believed, known to have, or be at risk of developing." />
</concept>
<code value="PCI-6" />
<display value="Patient clinical information - Phenotypic details" />
<definition value="The HPO (or alternative ontology as appropriate) term names for the observable disease traits." />
</concept>
<code value="PCI-7" />
<display value="Patient clinical information - Symptoms" />
<definition value="The patient's symptoms" />
</concept>
<code value="PCI-10" />
<display value="Patient clinical information - Count of tumours" />
<definition value="How many tumours the patient has." />
</concept>
<code value="PCI-11" />
<display value="Patient clinical information - Site of tumour" />
<definition value="Location of the tumours on the body." />
</concept>
<code value="PCI-14" />
<display value="Patient clinical information - Tumour sites - Body image diagram" />
<definition value="Image attachment of body with tumour sites highlighted." />
</concept>
<code value="PCI-15" />
<display value="Patient clinical information - Pedigree details / Relevant family history" />
<definition value="The patient's pedigree/family history details (inc family history of cancer)." />
</concept>
<code value="PCI-16" />
<display value="Patient clinical information - Pedigree diagram" />
<definition value="Image attachment of pedigree details" />
</concept>
<code value="PCI-17" />
<display value="Patient clinical information - Laterality of hearing loss" />
<definition value="Laterality of the hearing loss i.e. bilateral or unilateral." />
</concept>
<code value="PCI-18" />
<display value="Patient clinical information - Fetal haemoglobinopathy maternal screening genotype" />
<definition value="Maternal screening genotype for haemoglobinopathy testing." />
</concept>
<code value="PCI-21" />
<display value="Patient clinical information - Legal considerations" />
<definition value="Legal considerations for a given request." />
</concept>
<code value="PCI-22" />
<display value="Patient clinical information - Fetal haemoglobinopathy paternal screening genotype" />
<definition value="Paternal screening genotype for haemoglobinopathy testing" />
</concept>
<code value="PCI-23" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation name" />
<definition value="Requesting clinician's organisation name." />
</concept>
<code value="PCI-24" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation address" />
<definition value="Requesting clinician's organisation address." />
</concept>
<code value="PCI-25" />
<display value="Patient clinical information - Expected Maternity Unit - Organisation ODS code" />
<definition value="Requesting clinician's organisation ODS code." />
</concept>
<code value="PCI-26" />
<display value="Patient clinical information - Expected Maternity Unit - Department name" />
<definition value="Requesting clinician's department name." />
</concept>
<code value="PCI-27" />
<display value="Patient clinical information - Growth history" />
<definition value="Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc." />
</concept>
<code value="PCI-28" />
<display value="Patient clinical information - Severity of hearing loss" />
<definition value="Free text regarding hearing loss" />
</concept>
<code value="PCI-29" />
<display value="Patient clinical information - Retinal degeneration" />
<definition value="Free text regarding retinal degeneration" />
</concept>
<code value="PCI-30" />
<display value="Patient clinical information - Risk factors" />
<definition value="Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication." />
</concept>
<code value="PCI-31" />
<display value="Patient clinical information - Suspected inborn error type(s)" />
<definition value="Suspected inborn error type(s)" />
</concept>
<code value="PCI-32" />
<display value="Patient clinical information - Abnormal infection history site" />
<definition value="Abnormal infection history site organism" />
</concept>
<code value="PCI-33" />
<display value="Patient clinical information - Abnormal infection history site organism" />
<definition value="Abnormal infection history site organism" />
</concept>
<code value="PCI-34" />
<display value="Is on ig replacement" />
<definition value="If the patient is on immunoglobin replacement treatment." />
</concept>
<code value="PCI-35" />
<display value="Patient clinical information - Current and previous treatment detail" />
<definition value="Detail regarding relevant current and previous medical treatments." />
</concept>
<code value="PCI-36" />
<display value="Patient clinical information - Pregnancy status" />
<definition value="Patient`s pregnancy status" />
</concept>
<code value="PCI-37" />
<display value="Patient clinical information - Pregnancy type" />
<definition value="Type of conception" />
</concept>
<code value="PCI-38" />
<display value="Patient clinical information - Pregnancy gestation period" />
<definition value="Patient's term of active pregnancy at point of test request." />
</concept>
<code value="PCI-39" />
<display value="Patient clinical information - Fetal gestation" />
<definition value="Stage during patient pregnancy at which it terminated." />
</concept>
<code value="PCI-40" />
<display value="Patient clinical information - Estimated delivery date (EDD)" />
<definition value="Patient's estimated delivery date." />
</concept>
<code value="PCI-41" />
<display value="Patient clinical information - IVF age of egg donor" />
<definition value="The age of the patient who donated the egg at the time of donation." />
</concept>
<code value="PCI-42" />
<display value="Patient clinical information - Had transplant" />
<definition value="Has the patient ever had a transplant." />
</concept>
<code value="PCI-43" />
<display value="Patient clinical information - Type of transplant" />
<definition value="What type of transplant the patient had." />
</concept>
<code value="PCI-44" />
<display value="Patient clinical information - Transplant date" />
<definition value="When the patient had the transplant." />
</concept>
<code value="PCI-45" />
<display value="Patient clinical information - Had transfusion in the last 6 weeks" />
<definition value="Has the patient had a transfusion in the last 6 weeks." />
</concept>
<code value="PCI-46" />
<display value="Patient clinical information - Type of transfusion" />
<definition value="What type of transfusion the patient has had." />
</concept>
<code value="PCI-47" />
<display value="Patient clinical information - Transfusion date" />
<definition value="When the patient had the transfusion." />
</concept>
<code value="PCI-48" />
<display value="Patient clinical information - Height (m)" />
<definition value="Patient's height." />
</concept>
</concept>
<code value="datagroup-miscellaneous" />
<display value="Miscellaneous" />
<definition value="Data group - Miscellaneous" />
<code value="MIS-1" />
<display value="Further supporting information" />
<definition value="Supporting information which has not been captured elsewhere." />
</concept>
</concept>
<code value="datagroup-hospital-encounter" />
<display value="Hospital encounter" />
<definition value="Data group - Hospital encounter" />
<code value="HE-1" />
<display value="Treatment function code (TFC)" />
<definition value="The identifier for the clinical specialty or service under which the patient is being treated." />
</concept>
<code value="HE-2" />
<display value="Hospital provider spell identifier" />
<definition value="The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge." />
</concept>
<code value="HE-3" />
<display value="Outpatient attendance identifier" />
<definition value="The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered." />
</concept>
<code value="HE-4" />
<display value="Hospital point of delivery code" />
<definition value="The identifier that defines the type of care setting in which the genomic test was requested." />
</concept>
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "mds-questiontag-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/mds-questiontag-genomics",
"version": "0.1.1",
"name": "MDSQuestionTagGenomics",
"title": "MDS Question Tag Genomics",
"status": "draft",
"date": "2025-12-15T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A set of codes used to map MDS Dataset to FHIR Resources.This is intended to be used on Resource.meta.tag.",
"copyright": "Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"hierarchyMeaning": "grouped-by",
"content": "complete",
"concept": [
{
"code": "datagroup-healthcare-professional",
"display": "Healthcare Professional",
"definition": "Data group - Healthcare professional",
"concept": [
{
"code": "HCP-1",
"display": "HCP - Genomic test order role",
"definition": "HCP's function within the genomic test ordering process"
},
{
"code": "HCP-2",
"display": "HCP - First name",
"definition": "HCP's first name."
},
{
"code": "HCP-13",
"display": "HCP - surname",
"definition": "HCP'surname"
},
{
"code": "HCP-3",
"display": "HCP - Job title",
"definition": "HCP's job title."
},
{
"code": "HCP-4",
"display": "HCP - Current specialty",
"definition": "HCP's current specialty."
},
{
"code": "HCP-5",
"display": "HCP - Telephone number",
"definition": "HCP's telephone number."
},
{
"code": "HCP-6",
"display": "HCP - Email address",
"definition": "HCP's email address."
},
{
"code": "HCP-7",
"display": "HCP - Organisation name",
"definition": "HCP's requesting organisation name."
},
{
"code": "HCP-9",
"display": "HCP - Organisation ODS code",
"definition": "HCP's organisation ODS code"
},
{
"code": "HCP-10",
"display": "HCP - Department name",
"definition": "HCP's department name."
},
{
"code": "HCP-11",
"display": "HCP - Professional registration number",
"definition": "HCP's professional registration number such as their GMC number."
},
{
"code": "HCP-12",
"display": "HCP - Professional registration number type",
"definition": "HCP's professional registration number type such as 'GMC'."
}
]
},
{
"code": "datagroup-patient",
"display": "Patient",
"definition": "Data group - Patient",
"concept": [
{
"code": "P-1",
"display": "Patient - Title",
"definition": "Patient's title."
},
{
"code": "P-2",
"display": "Patient - First name",
"definition": "Patient's first name."
},
{
"code": "P-40",
"display": "Patient - Middlename",
"definition": "Patient's middle name."
},
{
"code": "P-3",
"display": "Patient - Surname",
"definition": "Patient's last name."
},
{
"code": "P-41",
"display": "Patient - Name use",
"definition": "Links each patient name entry to confirm if current, previous or what the patient is known as."
},
{
"code": "P-4",
"display": "Patient - Date of birth",
"definition": "Patient's date of birth."
},
{
"code": "P-6",
"display": "Patient - Postcode",
"definition": "Patient's home postcode."
},
{
"code": "P-7",
"display": "Patient - Country of residence",
"definition": "Patient's home country."
},
{
"code": "P-9",
"display": "Patient - Ethnicity",
"definition": "Patient's ethnicity."
},
{
"code": "P-10",
"display": "Patient - Sex defined at birth",
"definition": "Patient's phenotypic sex classification as defined at birth based on physical characteristic."
},
{
"code": "P-12",
"display": "Patient - GP practice's ODS Code",
"definition": "Patient's GP practice ODS code."
},
{
"code": "P-13",
"display": "Patient - Is from consanguineous union",
"definition": "The fact of the patient's biological parents being descended from the same ancestor."
},
{
"code": "P-15",
"display": "Patient - NHS number",
"definition": "Patient's NHS number."
},
{
"code": "P-16",
"display": "Patient - Local identifier",
"definition": "Patient's identification code other than NHS number."
},
{
"code": "P-42",
"display": "Patient - ODS code of organisation which assigned local identifier",
"definition": "ODS code of the organisation which assigned the local identifier P-16."
},
{
"code": "P-17",
"display": "Patient - Reason for unavailable NHS number",
"definition": "Reason for an NHS number not being provided."
},
{
"code": "P-18",
"display": "Patient - Relationship to proband",
"definition": "This patient's relationship to the primary patient."
},
{
"code": "P-19",
"display": "Patient - Gender Identity",
"definition": "Patient's stated gender, determined by the patient."
},
{
"code": "P-20",
"display": "Patient - Deceased date",
"definition": "Patient's date of death."
},
{
"code": "P-21",
"display": "Patient - Chromosomal sex",
"definition": "Patient's genomic / karyotypic characteristic. Determined by genomic testing."
},
{
"code": "P-35",
"display": "Patient - Withheld identity reason",
"definition": "Confirmation why the patient is withholding identity details."
},
{
"code": "P-37",
"display": "Patient - Local Pedigree / Family identifier",
"definition": "Patient's pedigree or family identifying id."
},
{
"code": "P-39",
"display": "Patient - Reason for inclusion in genomic test request",
"definition": "Reason patient has been included in genomic test request, such as to support proband testing or providing own genomic reporting"
}
]
},
{
"code": "datagroup-fetus",
"display": "Fetus",
"definition": "Data group - Fetus",
"concept": [
{
"code": "F-1",
"display": "Fetus - Local identifier",
"definition": "Fetus' identification code other than NHS number."
},
{
"code": "F-7",
"display": "Fetus - ODS code of organisation which assigned local identifier",
"definition": "ODS code of the organisation which assigned the local identifier F-1."
},
{
"code": "F-2",
"display": "Fetus - Observed sex",
"definition": "Fetus' phenotypic sex classification. Estimated physical characteristic. Currently determined by ultrasound. Gender for PLCM."
},
{
"code": "F-3",
"display": "Fetus - Chromosomal sex",
"definition": "Fetus' genomic / karyotypic characteristic. Determined by genomic testing."
},
{
"code": "F-6",
"display": "Fetus - Life status at time of request",
"definition": "Fetus' alive or deceased status details at the point of test ordering."
},
{
"code": "F-8",
"display": "Fetus - Pregnancy id",
"definition": "The id of a given pregnancy which this fetus belongs to."
}
]
},
{
"code": "datagroup-test-request",
"display": "Test Request",
"definition": "Data group - Test Request",
"concept": [
{
"code": "TR-2",
"display": "Test Request - Payment status",
"definition": "How the test request is funded"
},
{
"code": "TR-4",
"display": "Test Request - Requesting reason rare disease",
"definition": "The reason for a rare disease genomic test."
},
{
"code": "TR-38",
"display": "Test Request - Requesting reason cancer",
"definition": "The reason for a cancer genomic test."
},
{
"code": "TR-5",
"display": "Test Request - High level test identifier",
"definition": "Legacy high level ids which identify the requested test. Options provided by old Test Directory."
},
{
"code": "TR-6",
"display": "Test Request - High level test identifier description",
"definition": "Legacy high level name of the id requested"
},
{
"code": "TR-7",
"display": "Test Request - Low level test identifier",
"definition": "The low level CITT code which identifies the requested test. Options provided by Test Directory (TEST IDENTIFIER OR TEST CODE)."
},
{
"code": "TR-8",
"display": "Test Request - Low level test identifier description",
"definition": "The low level CITT name of the considered test."
},
{
"code": "TR-9",
"display": "Test Request - Low level multipurpose test identifier",
"definition": "The low level code which identifies the test to be actioned when the CITT code is multipurpose (CLINICAL INDICATION)."
},
{
"code": "TR-10",
"display": "Test Request - Low level multipurpose test identifier description",
"definition": "The low level name of the test to be actioned when the CITT code is multipurpose."
},
{
"code": "TR-21",
"display": "Test Request - Genomic package id",
"definition": "Id of the package requested."
},
{
"code": "TR-22",
"display": "Test Request - Genomic package name",
"definition": "Name of the package requested."
},
{
"code": "TR-23",
"display": "Test Request - Genomic package version",
"definition": "Version of the package requested."
},
{
"code": "TR-24",
"display": "Test Request - Genomic test id",
"definition": "Id of the test requested."
},
{
"code": "TR-25",
"display": "Test Request - Genomic test name",
"definition": "Name of the test requested."
},
{
"code": "TR-26",
"display": "Test Request - Genomic test version",
"definition": "Version of the test requested."
},
{
"code": "TR-27",
"display": "Test Request - Additional panels",
"definition": "Additional panels to test."
},
{
"code": "TR-28",
"display": "Test request - Target type",
"definition": "Type of target to test."
},
{
"code": "TR-29",
"display": "Test request - Target detail",
"definition": "Detail of target to test."
},
{
"code": "TR-11",
"display": "Test Request - Count of patients to be tested",
"definition": "Count of patients to be tested including the proband/primary patient."
},
{
"code": "TR-12",
"display": "Test Request - Urgency reason",
"definition": "The test request urgency reason."
},
{
"code": "TR-13",
"display": "Test Request - Reanalysis reason",
"definition": "The reason reanalysis has been requested."
},
{
"code": "TR-14",
"display": "Test Request - Detail of reason for request",
"definition": "Further detail associated to the reason reanalysis has been requested."
},
{
"code": "TR-15",
"display": "Test Request - Type of reanalysis",
"definition": "The type of reanalysis which has been requested."
},
{
"code": "TR-17",
"display": "Test Request - Is urgent",
"definition": "Confirmation if the test request is urgent."
},
{
"code": "TR-35",
"display": "Test Request - Purpose of linking",
"definition": "The reason a given test request has been linked to another test request."
},
{
"code": "TR-36",
"display": "Test Request - Central email address for reporting",
"definition": "Central email address for contingency in the event of not being able to obtain a report via the requester."
},
{
"code": "TR-20",
"display": "Test Request - Genomic report delivery method",
"definition": "Test Request - Genomic report delivery method"
},
{
"code": "TR-30",
"display": "Test Request - Add private genomic request and report to NHS record",
"definition": "Confirmation if the content of a private genomic test request should be added to an NHS record."
},
{
"code": "TR-31",
"display": "Test Request - Test request form version",
"definition": "Version of the test order form completed and submitted."
},
{
"code": "TR-32",
"display": "Test Request - File / Link to file",
"definition": "Upload of a file or a link to a file for adding documents such as previous genomic reports to a test order."
},
{
"code": "TR-33",
"display": "Test Request - File detail",
"definition": "Detail to provide context to an uploaded file or document link."
},
{
"code": "TR-34",
"display": "Test Request - Clinical utility",
"definition": "Clinical benefit to patient of obtaining a requested genomic report."
},
{
"code": "TR-39",
"display": "Test Request - Linked test request reference",
"definition": "The reference to any associated test requests"
}
]
},
{
"code": "datagroup-ngrl-consent",
"display": "NGRL-consent",
"definition": "Data group - NGRL consent",
"concept": [
{
"code": "NGRL-1",
"display": "NGRL consent - Date of NGRL consent",
"definition": "The date NGRL consent was provided."
},
{
"code": "NGRL-2",
"display": "NGRL consent - Patient has made their own choice to consent to the NGRL",
"definition": "Confirmation if the patient to be tested has provided NGRL consent themselves."
},
{
"code": "NGRL-3",
"display": "NGRL consent - Patient representative name (if patient cannot make their own choice)",
"definition": "The name of the patient representative."
},
{
"code": "NGRL-4",
"display": "NGRL consent - I confirm that the patient (or their representative) agree to have their genomic and healthcare data used for research",
"definition": "The outcome of the patient or their representative’s choice in consenting to including their data used for research in the NGRL."
},
{
"code": "NGRL-5",
"display": "NGRL consent - NGRL consent document link",
"definition": "A URL where a copy of a completed NGRL consent form may be found."
}
]
},
{
"code": "datagroup-primary-sample",
"display": "Primary Sample",
"definition": "Data group - Primary Sample",
"concept": [
{
"code": "PS-2",
"display": "Primary Sample - Local identifier",
"definition": "Local ids applied to a sample"
},
{
"code": "PS-3",
"display": "Primary Sample - ODS code of organisation which assigned local id",
"definition": "ODS code of the organisation which assigned the local sample id."
},
{
"code": "PS-10",
"display": "Primary Sample - Obtained date",
"definition": "Date at which a specimen/biopsy was obtained from patient."
},
{
"code": "PS-11",
"display": "Primary Sample - Primary sample",
"definition": "The primary sample material."
},
{
"code": "PS-12",
"display": "Primary Sample - Primary sample state",
"definition": "The state of the primary sample."
},
{
"code": "PS-25",
"display": "Primary Sample - Preservative/Container",
"definition": "How the primary sample is preserved."
},
{
"code": "PS-30",
"display": "Primary Sample - Block identifier",
"definition": "Sample block identifier"
},
{
"code": "PS-31",
"display": "Primary Sample - Fixative type",
"definition": "Sample fixative type"
},
{
"code": "PS-32",
"display": "Primary Sample - Hours to fixation",
"definition": "Sample hours to fixation"
},
{
"code": "PS-33",
"display": "Primary Sample - Hours in fixative",
"definition": "Sample hours in fixative"
},
{
"code": "PS-34",
"display": "Primary Sample - Tumour enrichment method",
"definition": "Method used for tumour enrichment."
},
{
"code": "PS-13",
"display": "Primary Sample - Necrosis",
"definition": "% necrotic (dead) cells in primary sample."
},
{
"code": "PS-14",
"display": "Primary Sample - Nucleated cell count",
"definition": "Nucleated (with nucleous) cell (non tumour and tumour) count in the primary sample (Solid Tumour and Haem-Onc)."
},
{
"code": "PS-15",
"display": "Primary Sample - Tumour nuclear content in whole section",
"definition": "Neoplastic (tumour) cell content in the primary sample whole section(Solid Tumour) - sourced at local lab. (%)"
},
{
"code": "PS-26",
"display": "Primary Sample - Tumour nuclear content in marked area",
"definition": "Neoplastic (tumour) cell content in the primary sample marked area(Solid Tumour) - sourced at local lab. (%)"
},
{
"code": "PS-17",
"display": "Primary Sample - Solid tumour morphology",
"definition": "The histology and likely course of development of a tumour."
},
{
"code": "PS-18",
"display": "Primary Sample - Solid tumour topography",
"definition": "The tumour sample site. e.g. from colon, stomach etc."
},
{
"code": "PS-29",
"display": "Primary Sample - Is biopsy",
"definition": "Primary Sample - Is biopsy"
},
{
"code": "PS-19",
"display": "Primary Sample - Biopsy site",
"definition": "Digital confirmation that the sample is a biopsy."
},
{
"code": "PS-21",
"display": "Primary Sample - Observed maternal cell contamination (MCC)",
"definition": "An observed outcome which may indicate MCC"
},
{
"code": "PS-27",
"display": "Primary Sample - Test confirmed maternal cell contamination (MCC)",
"definition": "Analytically confirmed MCC levels"
},
{
"code": "PS-22",
"display": "Primary Sample - Option for all products of conception",
"definition": "Primary Sample - Option for all products of conception"
},
{
"code": "PS-23",
"display": "Primary Sample - Blasts %",
"definition": "Future management for products of conception."
},
{
"code": "PS-24",
"display": "Primary Sample - High infection risk reason",
"definition": "The high contamination risk reason for a primary sample."
},
{
"code": "PS-28",
"display": "Primary Sample - Patient life status at the time of collection",
"definition": "If the patient was alive or deceased at the point of collecting a sample."
},
{
"code": "PS-35",
"display": "Primary Sample - Solid tumour type",
"definition": "The origin or context of a tumour sample."
}
]
},
{
"code": "datagroup-patient-clinical-information",
"display": "Patient Clinical Information",
"definition": "Data group - Patient Clinical Information",
"concept": [
{
"code": "PCI-1",
"display": "Patient clinical information - Genomic Ethnicity",
"definition": "Patient's ethnicity where 'Patient - Ethnicity field' doesn't provide an adequate description. E.g Ashkenazi Jewish"
},
{
"code": "PCI-2",
"display": "Patient clinical information - Disease Status",
"definition": "If the patient is affected, unaffected, or it is unknown."
},
{
"code": "PCI-4",
"display": "Patient clinical information - Age at disease onset",
"definition": "The age when a change in patients' health was first noted in line with suspected diagnosis."
},
{
"code": "PCI-5",
"display": "Patient clinical information - Known/Suspected Disease",
"definition": "Disease a patient is believed, known to have, or be at risk of developing."
},
{
"code": "PCI-6",
"display": "Patient clinical information - Phenotypic details",
"definition": "The HPO (or alternative ontology as appropriate) term names for the observable disease traits."
},
{
"code": "PCI-7",
"display": "Patient clinical information - Symptoms",
"definition": "The patient's symptoms"
},
{
"code": "PCI-10",
"display": "Patient clinical information - Count of tumours",
"definition": "How many tumours the patient has."
},
{
"code": "PCI-11",
"display": "Patient clinical information - Site of tumour",
"definition": "Location of the tumours on the body."
},
{
"code": "PCI-14",
"display": "Patient clinical information - Tumour sites - Body image diagram",
"definition": "Image attachment of body with tumour sites highlighted."
},
{
"code": "PCI-15",
"display": "Patient clinical information - Pedigree details / Relevant family history",
"definition": "The patient's pedigree/family history details (inc family history of cancer)."
},
{
"code": "PCI-16",
"display": "Patient clinical information - Pedigree diagram",
"definition": "Image attachment of pedigree details"
},
{
"code": "PCI-17",
"display": "Patient clinical information - Laterality of hearing loss",
"definition": "Laterality of the hearing loss i.e. bilateral or unilateral."
},
{
"code": "PCI-18",
"display": "Patient clinical information - Fetal haemoglobinopathy maternal screening genotype",
"definition": "Maternal screening genotype for haemoglobinopathy testing."
},
{
"code": "PCI-21",
"display": "Patient clinical information - Legal considerations",
"definition": "Legal considerations for a given request."
},
{
"code": "PCI-22",
"display": "Patient clinical information - Fetal haemoglobinopathy paternal screening genotype",
"definition": "Paternal screening genotype for haemoglobinopathy testing"
},
{
"code": "PCI-23",
"display": "Patient clinical information - Expected Maternity Unit - Organisation name",
"definition": "Requesting clinician's organisation name."
},
{
"code": "PCI-24",
"display": "Patient clinical information - Expected Maternity Unit - Organisation address",
"definition": "Requesting clinician's organisation address."
},
{
"code": "PCI-25",
"display": "Patient clinical information - Expected Maternity Unit - Organisation ODS code",
"definition": "Requesting clinician's organisation ODS code."
},
{
"code": "PCI-26",
"display": "Patient clinical information - Expected Maternity Unit - Department name",
"definition": "Requesting clinician's department name."
},
{
"code": "PCI-27",
"display": "Patient clinical information - Growth history",
"definition": "Summary passage of text to highlight patient centile history e.g. head circumference, weight, etc."
},
{
"code": "PCI-28",
"display": "Patient clinical information - Severity of hearing loss",
"definition": "Free text regarding hearing loss"
},
{
"code": "PCI-29",
"display": "Patient clinical information - Retinal degeneration",
"definition": "Free text regarding retinal degeneration"
},
{
"code": "PCI-30",
"display": "Patient clinical information - Risk factors",
"definition": "Toxic medication - Prematurity (risk factor for hearing loss) e.g. Baby early birth - Ototoxic medication."
},
{
"code": "PCI-31",
"display": "Patient clinical information - Suspected inborn error type(s)",
"definition": "Suspected inborn error type(s)"
},
{
"code": "PCI-32",
"display": "Patient clinical information - Abnormal infection history site",
"definition": "Abnormal infection history site organism"
},
{
"code": "PCI-33",
"display": "Patient clinical information - Abnormal infection history site organism",
"definition": "Abnormal infection history site organism"
},
{
"code": "PCI-34",
"display": "Is on ig replacement",
"definition": "If the patient is on immunoglobin replacement treatment."
},
{
"code": "PCI-35",
"display": "Patient clinical information - Current and previous treatment detail",
"definition": "Detail regarding relevant current and previous medical treatments."
},
{
"code": "PCI-36",
"display": "Patient clinical information - Pregnancy status",
"definition": "Patient`s pregnancy status"
},
{
"code": "PCI-37",
"display": "Patient clinical information - Pregnancy type",
"definition": "Type of conception"
},
{
"code": "PCI-38",
"display": "Patient clinical information - Pregnancy gestation period",
"definition": "Patient's term of active pregnancy at point of test request."
},
{
"code": "PCI-39",
"display": "Patient clinical information - Fetal gestation",
"definition": "Stage during patient pregnancy at which it terminated."
},
{
"code": "PCI-40",
"display": "Patient clinical information - Estimated delivery date (EDD)",
"definition": "Patient's estimated delivery date."
},
{
"code": "PCI-41",
"display": "Patient clinical information - IVF age of egg donor",
"definition": "The age of the patient who donated the egg at the time of donation."
},
{
"code": "PCI-42",
"display": "Patient clinical information - Had transplant",
"definition": "Has the patient ever had a transplant."
},
{
"code": "PCI-43",
"display": "Patient clinical information - Type of transplant",
"definition": "What type of transplant the patient had."
},
{
"code": "PCI-44",
"display": "Patient clinical information - Transplant date",
"definition": "When the patient had the transplant."
},
{
"code": "PCI-45",
"display": "Patient clinical information - Had transfusion in the last 6 weeks",
"definition": "Has the patient had a transfusion in the last 6 weeks."
},
{
"code": "PCI-46",
"display": "Patient clinical information - Type of transfusion",
"definition": "What type of transfusion the patient has had."
},
{
"code": "PCI-47",
"display": "Patient clinical information - Transfusion date",
"definition": "When the patient had the transfusion."
},
{
"code": "PCI-48",
"display": "Patient clinical information - Height (m)",
"definition": "Patient's height."
}
]
},
{
"code": "datagroup-miscellaneous",
"display": "Miscellaneous",
"definition": "Data group - Miscellaneous",
"concept": [
{
"code": "MIS-1",
"display": "Further supporting information",
"definition": "Supporting information which has not been captured elsewhere."
}
]
},
{
"code": "datagroup-hospital-encounter",
"display": "Hospital encounter",
"definition": "Data group - Hospital encounter",
"concept": [
{
"code": "HE-1",
"display": "Treatment function code (TFC)",
"definition": "The identifier for the clinical specialty or service under which the patient is being treated."
},
{
"code": "HE-2",
"display": "Hospital provider spell identifier",
"definition": "The identifier for the patient's continuous period of care in a hospital provider setting, from admission to discharge."
},
{
"code": "HE-3",
"display": "Outpatient attendance identifier",
"definition": "The identifier for the patient's specific outpatient appointment at which the genomic test may have been ordered."
},
{
"code": "HE-4",
"display": "Hospital point of delivery code",
"definition": "The identifier that defines the type of care setting in which the genomic test was requested."
}
]
}
]
}


CodeSystem Message Events Genomics

Usage

Common messaging events for Genomics Test Orders and Reports.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/message-events-genomics defines the following codes:

CodeDisplayDefinition
genomictestrequestGenomic Test RequestA Service Request bundle for ordering genomic tests
genomictestresponseGenomic Test ResponseA Diagnostic Report bundle for test results

Table View

CodeSystem.id[0]message-events-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/message-events-genomics
CodeSystem.version[0]0.2.0
CodeSystem.name[0]MessageEventsGenomics
CodeSystem.title[0]Message Events Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2022-11-25
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]Common messaging events for Genomics Test Orders and Reports.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]genomictestrequest
CodeSystem.concept[0].display[0]Genomic Test Request
CodeSystem.concept[0].definition[0]A Service Request bundle for ordering genomic tests
CodeSystem.concept[1].code[0]genomictestresponse
CodeSystem.concept[1].display[0]Genomic Test Response
CodeSystem.concept[1].definition[0]A Diagnostic Report bundle for test results

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="message-events-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/message-events-genomics" />
<version value="0.2.0" />
<name value="MessageEventsGenomics" />
<title value="Message Events Genomics" />
<status value="draft" />
<date value="2022-11-25" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="Common messaging events for Genomics Test Orders and Reports." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="genomictestrequest" />
<display value="Genomic Test Request" />
<definition value="A Service Request bundle for ordering genomic tests" />
</concept>
<code value="genomictestresponse" />
<display value="Genomic Test Response" />
<definition value="A Diagnostic Report bundle for test results" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "message-events-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/message-events-genomics",
"version": "0.2.0",
"name": "MessageEventsGenomics",
"title": "Message Events Genomics",
"status": "draft",
"date": "2022-11-25",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "Common messaging events for Genomics Test Orders and Reports.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "genomictestrequest",
"display": "Genomic Test Request",
"definition": "A Service Request bundle for ordering genomic tests"
},
{
"code": "genomictestresponse",
"display": "Genomic Test Response",
"definition": "A Diagnostic Report bundle for test results"
}
]
}


CodeSystem Patient Choice Category Genomics

Usage

A set of codes use to identify the categories of sources of obtaining the patient consent before undergoing Genomic test.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/patient-choice-category-genomics defines the following codes:

CodeDisplay
adult-own-choiceAdult (made their own choice)
adult-lack-capacityAdult lacking capacity (choices advised by consultee)
childChild (parent or guardian choices)
clinicianClinician has agreed to the test (in the patient`s best interest)
deceasedDeceased (choices made on behalf of deceased individual)

Table View

CodeSystem.id[0]patient-choice-category-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/patient-choice-category-genomics
CodeSystem.version[0]0.2.0
CodeSystem.name[0]PatientChoiceCategoryGenomics
CodeSystem.title[0]Patient Choice Category Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2022-12-21T11:27:52.3231281+00:00
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]A set of codes use to identify the categories of sources of obtaining the patient consent before undergoing Genomic test.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]adult-own-choice
CodeSystem.concept[0].display[0]Adult (made their own choice)
CodeSystem.concept[1].code[0]adult-lack-capacity
CodeSystem.concept[1].display[0]Adult lacking capacity (choices advised by consultee)
CodeSystem.concept[2].code[0]child
CodeSystem.concept[2].display[0]Child (parent or guardian choices)
CodeSystem.concept[3].code[0]clinician
CodeSystem.concept[3].display[0]Clinician has agreed to the test (in the patient`s best interest)
CodeSystem.concept[4].code[0]deceased
CodeSystem.concept[4].display[0]Deceased (choices made on behalf of deceased individual)

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="patient-choice-category-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/patient-choice-category-genomics" />
<version value="0.2.0" />
<name value="PatientChoiceCategoryGenomics" />
<title value="Patient Choice Category Genomics" />
<status value="draft" />
<date value="2022-12-21T11:27:52.3231281+00:00" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="A set of codes use to identify the categories of sources of obtaining the patient consent before undergoing Genomic test." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="adult-own-choice" />
<display value="Adult (made their own choice)" />
</concept>
<code value="adult-lack-capacity" />
<display value="Adult lacking capacity (choices advised by consultee)" />
</concept>
<code value="child" />
<display value="Child (parent or guardian choices)" />
</concept>
<code value="clinician" />
<display value="Clinician has agreed to the test (in the patient`s best interest)" />
</concept>
<code value="deceased" />
<display value="Deceased (choices made on behalf of deceased individual)" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "patient-choice-category-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/patient-choice-category-genomics",
"version": "0.2.0",
"name": "PatientChoiceCategoryGenomics",
"title": "Patient Choice Category Genomics",
"status": "draft",
"date": "2022-12-21T11:27:52.3231281+00:00",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "A set of codes use to identify the categories of sources of obtaining the patient consent before undergoing Genomic test.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "adult-own-choice",
"display": "Adult (made their own choice)"
},
{
"code": "adult-lack-capacity",
"display": "Adult lacking capacity (choices advised by consultee)"
},
{
"code": "child",
"display": "Child (parent or guardian choices)"
},
{
"code": "clinician",
"display": "Clinician has agreed to the test (in the patient`s best interest)"
},
{
"code": "deceased",
"display": "Deceased (choices made on behalf of deceased individual)"
}
]
}


CodeSystem Patient Consultee Genomics

Usage

A code to identify if patient guardian is a Consultee

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/patient-consultee-genomics defines the following codes:

CodeDisplay
consulteeConsultee

Table View

CodeSystem.id[0]patient-consultee-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/patient-consultee-genomics
CodeSystem.version[0]0.2.0
CodeSystem.name[0]PatientConsulteeGenomics
CodeSystem.title[0]Patient Consultee Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2022-12-28T16:41:15.0168724+00:00
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]A code to identify if patient guardian is a Consultee
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]consultee
CodeSystem.concept[0].display[0]Consultee

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="patient-consultee-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/patient-consultee-genomics" />
<version value="0.2.0" />
<name value="PatientConsulteeGenomics" />
<title value="Patient Consultee Genomics" />
<status value="draft" />
<date value="2022-12-28T16:41:15.0168724+00:00" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="A code to identify if patient guardian is a Consultee" />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="consultee" />
<display value="Consultee" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "patient-consultee-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/patient-consultee-genomics",
"version": "0.2.0",
"name": "PatientConsulteeGenomics",
"title": "Patient Consultee Genomics",
"status": "draft",
"date": "2022-12-28T16:41:15.0168724+00:00",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "A code to identify if patient guardian is a Consultee",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "consultee",
"display": "Consultee"
}
]
}


CodeSystem Patient Choice Research Participation

Usage

A set of codes use to identify the sources of obtaining the patient consent in participating in the National Genomic Research.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/patient-choice-researchparticipation defines the following codes:

CodeDisplay
like-to-discuss-laterPatient would like to discuss at a later date
patient-lack-capacityPatient lacks capacity and no consultee available
inappropriate-to-discussInappropriate to have discussion
otherOther

Table View

CodeSystem.id[0]patient-choice-researchparticipation
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/patient-choice-researchparticipation
CodeSystem.version[0]0.2.0
CodeSystem.name[0]PatientChoiceResearchParticipation
CodeSystem.title[0]Patient Choice Research Participation
CodeSystem.status[0]draft
CodeSystem.date[0]2022-12-21T11:27:52.3231281+00:00
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]A set of codes use to identify the sources of obtaining the patient consent in participating in the National Genomic Research.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]like-to-discuss-later
CodeSystem.concept[0].display[0]Patient would like to discuss at a later date
CodeSystem.concept[1].code[0]patient-lack-capacity
CodeSystem.concept[1].display[0]Patient lacks capacity and no consultee available
CodeSystem.concept[2].code[0]inappropriate-to-discuss
CodeSystem.concept[2].display[0]Inappropriate to have discussion
CodeSystem.concept[3].code[0]other
CodeSystem.concept[3].display[0]Other

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="patient-choice-researchparticipation" />
<url value="https://fhir.nhs.uk/CodeSystem/patient-choice-researchparticipation" />
<version value="0.2.0" />
<name value="PatientChoiceResearchParticipation" />
<title value="Patient Choice Research Participation" />
<status value="draft" />
<date value="2022-12-21T11:27:52.3231281+00:00" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="A set of codes use to identify the sources of obtaining the patient consent in participating in the National Genomic Research." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="like-to-discuss-later" />
<display value="Patient would like to discuss at a later date" />
</concept>
<code value="patient-lack-capacity" />
<display value="Patient lacks capacity and no consultee available" />
</concept>
<code value="inappropriate-to-discuss" />
<display value="Inappropriate to have discussion" />
</concept>
<code value="other" />
<display value="Other" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "patient-choice-researchparticipation",
"url": "https://fhir.nhs.uk/CodeSystem/patient-choice-researchparticipation",
"version": "0.2.0",
"name": "PatientChoiceResearchParticipation",
"title": "Patient Choice Research Participation",
"status": "draft",
"date": "2022-12-21T11:27:52.3231281+00:00",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "A set of codes use to identify the sources of obtaining the patient consent in participating in the National Genomic Research.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "like-to-discuss-later",
"display": "Patient would like to discuss at a later date"
},
{
"code": "patient-lack-capacity",
"display": "Patient lacks capacity and no consultee available"
},
{
"code": "inappropriate-to-discuss",
"display": "Inappropriate to have discussion"
},
{
"code": "other",
"display": "Other"
}
]
}


CodeSystem Genomic Patient Role

Usage

CodeSystem used to specify the role of the subject patient in the genomic test (proband vs consultand)

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/patient-role-genomics defines the following codes:

CodeDisplayDefinition
probandProbandThe primary subject for the genomic testing
consultandConsultandFamily member

Table View

CodeSystem.id[0]patient-role-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/patient-role-genomics
CodeSystem.version[0]0.1.0
CodeSystem.name[0]PatientRoleGenomics
CodeSystem.title[0]Patient Role Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2025-12-18T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]CodeSystem used to specify the role of the subject patient in the genomic test (proband vs consultand)
CodeSystem.copyright[0]Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]proband
CodeSystem.concept[0].display[0]Proband
CodeSystem.concept[0].definition[0]The primary subject for the genomic testing
CodeSystem.concept[1].code[0]consultand
CodeSystem.concept[1].display[0]Consultand
CodeSystem.concept[1].definition[0]Family member

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="patient-role-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/patient-role-genomics" />
<version value="0.1.0" />
<name value="PatientRoleGenomics" />
<title value="Patient Role Genomics" />
<status value="draft" />
<date value="2025-12-18T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="CodeSystem used to specify the role of the subject patient in the genomic test (proband vs consultand)" />
<copyright value="Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="proband" />
<display value="Proband" />
<definition value="The primary subject for the genomic testing" />
</concept>
<code value="consultand" />
<display value="Consultand" />
<definition value="Family member" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "patient-role-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/patient-role-genomics",
"version": "0.1.0",
"name": "PatientRoleGenomics",
"title": "Patient Role Genomics",
"status": "draft",
"date": "2025-12-18T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work",
"rank": 1
}
]
}
],
"description": "CodeSystem used to specify the role of the subject patient in the genomic test (proband vs consultand)",
"copyright": "Copyright © 2025+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "proband",
"display": "Proband",
"definition": "The primary subject for the genomic testing"
},
{
"code": "consultand",
"display": "Consultand",
"definition": "Family member"
}
]
}

CodeSystem Reason for Testing Genomics

Usage

A set of codes use to identify the reason for requesting a genomics test.This is intended to be used on ServiceRequest.category.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics defines the following codes:

LvlCodeDisplay
1primary-test-requestPrimary Test Request
2  carrierCarrier
2  diagnosticDiagnostic
2  disease-monitoring-mrdmechanismDisease Monitoring MRD CHIMERISM
2  dna-storageDNA Storage
2  follow-upFollow Up
2  predictivePredictive
2  relapseRelapse
2  staging-or-prognosisStaging or Prognosis
2  unknownUnknown
1reanalysis-test-requestReanalysis Test Request
2  change-in-presentationChange In Presentation
2  newly-affected-family-memberNewly Affected Family Member
2  new-pregnancyNew Pregnancy
2  new-treatment-clinical-managementNew Treatment/Clinical Management
2  recently-deceased-to-inform-familyRecently Deceased To Inform Family
1otherOther

Table View

CodeSystem.id[0]reasonfortesting-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics
CodeSystem.version[0]0.2.0
CodeSystem.name[0]ReasonforTestingGenomics
CodeSystem.title[0]Reason for Testing Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2025-09-09T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]A set of codes use to identify the reason for requesting a genomics test.This is intended to be used on ServiceRequest.category.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]primary-test-request
CodeSystem.concept[0].display[0]Primary Test Request
CodeSystem.concept[0].concept[0].code[0]carrier
CodeSystem.concept[0].concept[0].display[0]Carrier
CodeSystem.concept[0].concept[1].code[0]diagnostic
CodeSystem.concept[0].concept[1].display[0]Diagnostic
CodeSystem.concept[0].concept[2].code[0]disease-monitoring-mrdmechanism
CodeSystem.concept[0].concept[2].display[0]Disease Monitoring MRD CHIMERISM
CodeSystem.concept[0].concept[3].code[0]dna-storage
CodeSystem.concept[0].concept[3].display[0]DNA Storage
CodeSystem.concept[0].concept[4].code[0]follow-up
CodeSystem.concept[0].concept[4].display[0]Follow Up
CodeSystem.concept[0].concept[5].code[0]predictive
CodeSystem.concept[0].concept[5].display[0]Predictive
CodeSystem.concept[0].concept[6].code[0]relapse
CodeSystem.concept[0].concept[6].display[0]Relapse
CodeSystem.concept[0].concept[7].code[0]staging-or-prognosis
CodeSystem.concept[0].concept[7].display[0]Staging or Prognosis
CodeSystem.concept[0].concept[8].code[0]unknown
CodeSystem.concept[0].concept[8].display[0]Unknown
CodeSystem.concept[1].code[0]reanalysis-test-request
CodeSystem.concept[1].display[0]Reanalysis Test Request
CodeSystem.concept[1].concept[0].code[0]change-in-presentation
CodeSystem.concept[1].concept[0].display[0]Change In Presentation
CodeSystem.concept[1].concept[1].code[0]newly-affected-family-member
CodeSystem.concept[1].concept[1].display[0]Newly Affected Family Member
CodeSystem.concept[1].concept[2].code[0]new-pregnancy
CodeSystem.concept[1].concept[2].display[0]New Pregnancy
CodeSystem.concept[1].concept[3].code[0]new-treatment-clinical-management
CodeSystem.concept[1].concept[3].display[0]New Treatment/Clinical Management
CodeSystem.concept[1].concept[4].code[0]recently-deceased-to-inform-family
CodeSystem.concept[1].concept[4].display[0]Recently Deceased To Inform Family
CodeSystem.concept[2].code[0]other
CodeSystem.concept[2].display[0]Other

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="reasonfortesting-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" />
<version value="0.2.0" />
<name value="ReasonforTestingGenomics" />
<title value="Reason for Testing Genomics" />
<status value="draft" />
<date value="2025-09-09T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A set of codes use to identify the reason for requesting a genomics test.This is intended to be used on ServiceRequest.category." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="primary-test-request" />
<display value="Primary Test Request" />
<code value="carrier" />
<display value="Carrier" />
</concept>
<code value="diagnostic" />
<display value="Diagnostic" />
</concept>
<code value="disease-monitoring-mrdmechanism" />
<display value="Disease Monitoring MRD CHIMERISM" />
</concept>
<code value="dna-storage" />
<display value="DNA Storage" />
</concept>
<code value="follow-up" />
<display value="Follow Up" />
</concept>
<code value="predictive" />
<display value="Predictive" />
</concept>
<code value="relapse" />
<display value="Relapse" />
</concept>
<code value="staging-or-prognosis" />
<display value="Staging or Prognosis" />
</concept>
<code value="unknown" />
<display value="Unknown" />
</concept>
</concept>
<code value="reanalysis-test-request" />
<display value="Reanalysis Test Request" />
<code value="change-in-presentation" />
<display value="Change In Presentation" />
</concept>
<code value="newly-affected-family-member" />
<display value="Newly Affected Family Member" />
</concept>
<code value="new-pregnancy" />
<display value="New Pregnancy" />
</concept>
<code value="new-treatment-clinical-management" />
<display value="New Treatment/Clinical Management" />
</concept>
<code value="recently-deceased-to-inform-family" />
<display value="Recently Deceased To Inform Family" />
</concept>
</concept>
<code value="other" />
<display value="Other" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "reasonfortesting-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics",
"version": "0.2.0",
"name": "ReasonforTestingGenomics",
"title": "Reason for Testing Genomics",
"status": "draft",
"date": "2025-09-09T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A set of codes use to identify the reason for requesting a genomics test.This is intended to be used on ServiceRequest.category.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "primary-test-request",
"display": "Primary Test Request",
"concept": [
{
"code": "carrier",
"display": "Carrier"
},
{
"code": "diagnostic",
"display": "Diagnostic"
},
{
"code": "disease-monitoring-mrdmechanism",
"display": "Disease Monitoring MRD CHIMERISM"
},
{
"code": "dna-storage",
"display": "DNA Storage"
},
{
"code": "follow-up",
"display": "Follow Up"
},
{
"code": "predictive",
"display": "Predictive"
},
{
"code": "relapse",
"display": "Relapse"
},
{
"code": "staging-or-prognosis",
"display": "Staging or Prognosis"
},
{
"code": "unknown",
"display": "Unknown"
}
]
},
{
"code": "reanalysis-test-request",
"display": "Reanalysis Test Request",
"concept": [
{
"code": "change-in-presentation",
"display": "Change In Presentation"
},
{
"code": "newly-affected-family-member",
"display": "Newly Affected Family Member"
},
{
"code": "new-pregnancy",
"display": "New Pregnancy"
},
{
"code": "new-treatment-clinical-management",
"display": "New Treatment/Clinical Management"
},
{
"code": "recently-deceased-to-inform-family",
"display": "Recently Deceased To Inform Family"
}
]
},
{
"code": "other",
"display": "Other"
}
]
}


CodeSystem Genomic Sample Category

Usage

A CodeSystem to record the categorisation of a specimen, either sourced from a Tumour or Germline.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-SampleCategory defines the following codes:

LvlCodeDisplay
1tumourTumour
2  solid-tumourSolid Tumour
2  liquid-tumourLiquid Tumour
1germlineGermline
1otherOther
1not-knownNot Known

Table View

CodeSystem.id[0]UKCore-SampleCategory
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-SampleCategory
CodeSystem.version[0]2.0.0
CodeSystem.name[0]UKCoreSampleCategory
CodeSystem.title[0]UK Core Sample Category
CodeSystem.status[0]active
CodeSystem.date[0]2024-08-05
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A CodeSystem to record the categorisation of a specimen.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.hierarchyMeaning[0]is-a
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]tumour
CodeSystem.concept[0].display[0]Tumour
CodeSystem.concept[0].concept[0].code[0]solid-tumour
CodeSystem.concept[0].concept[0].display[0]Solid Tumour
CodeSystem.concept[0].concept[1].code[0]liquid-tumour
CodeSystem.concept[0].concept[1].display[0]Liquid Tumour
CodeSystem.concept[1].code[0]germline
CodeSystem.concept[1].display[0]Germline
CodeSystem.concept[2].code[0]other
CodeSystem.concept[2].display[0]Other
CodeSystem.concept[3].code[0]not-known
CodeSystem.concept[3].display[0]Not Known

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-SampleCategory" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-SampleCategory" />
<version value="2.0.0" />
<name value="UKCoreSampleCategory" />
<title value="UK Core Sample Category" />
<status value="active" />
<date value="2024-08-05" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A CodeSystem to record the categorisation of a specimen." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<hierarchyMeaning value="is-a" />
<content value="complete" />
<code value="tumour" />
<display value="Tumour" />
<code value="solid-tumour" />
<display value="Solid Tumour" />
</concept>
<code value="liquid-tumour" />
<display value="Liquid Tumour" />
</concept>
</concept>
<code value="germline" />
<display value="Germline" />
</concept>
<code value="other" />
<display value="Other" />
</concept>
<code value="not-known" />
<display value="Not Known" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-SampleCategory",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-SampleCategory",
"version": "2.0.0",
"name": "UKCoreSampleCategory",
"title": "UK Core Sample Category",
"status": "active",
"date": "2024-08-05",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A CodeSystem to record the categorisation of a specimen.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"hierarchyMeaning": "is-a",
"content": "complete",
"concept": [
{
"code": "tumour",
"display": "Tumour",
"concept": [
{
"code": "solid-tumour",
"display": "Solid Tumour"
},
{
"code": "liquid-tumour",
"display": "Liquid Tumour"
}
]
},
{
"code": "germline",
"display": "Germline"
},
{
"code": "other",
"display": "Other"
},
{
"code": "not-known",
"display": "Not Known"
}
]
}


CodeSystem Specimen Collection Special Handling Genomics

Usage

A set of codes use to identify the type of special collection process require to handle some specimen in genomics.This is intended to be used on Specimen.collection.extension:specialHandling element.

ription:description

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/specimen-collection-specialhandling-genomics defines the following codes:

CodeDisplay
sensitive-incinerationSensitive Incineration
cremationCremation
return-to-patientReturn To Patient

Table View

CodeSystem.id[0]specimen-collection-specialhandling-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/specimen-collection-specialhandling-genomics
CodeSystem.version[0]0.1.0
CodeSystem.name[0]SpecimenCollectionSpecialHandlingGenomics
CodeSystem.title[0]Specimen Collection Special Handling Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-08-05T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]A set of codes use to identify the type of special collection process require to handle some specimen in genomics.This is intended to be used on Specimen.collection.extension:specialHandling element.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]sensitive-incineration
CodeSystem.concept[0].display[0]Sensitive Incineration
CodeSystem.concept[1].code[0]cremation
CodeSystem.concept[1].display[0]Cremation
CodeSystem.concept[2].code[0]return-to-patient
CodeSystem.concept[2].display[0]Return To Patient

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="specimen-collection-specialhandling-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/specimen-collection-specialhandling-genomics" />
<version value="0.1.0" />
<name value="SpecimenCollectionSpecialHandlingGenomics" />
<title value="Specimen Collection Special Handling Genomics" />
<status value="draft" />
<date value="2024-08-05T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A set of codes use to identify the type of special collection process require to handle some specimen in genomics.This is intended to be used on Specimen.collection.extension:specialHandling element." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="sensitive-incineration" />
<display value="Sensitive Incineration" />
</concept>
<code value="cremation" />
<display value="Cremation" />
</concept>
<code value="return-to-patient" />
<display value="Return To Patient" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "specimen-collection-specialhandling-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/specimen-collection-specialhandling-genomics",
"version": "0.1.0",
"name": "SpecimenCollectionSpecialHandlingGenomics",
"title": "Specimen Collection Special Handling Genomics",
"status": "draft",
"date": "2024-08-05T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A set of codes use to identify the type of special collection process require to handle some specimen in genomics.This is intended to be used on Specimen.collection.extension:specialHandling element.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "sensitive-incineration",
"display": "Sensitive Incineration"
},
{
"code": "cremation",
"display": "Cremation"
},
{
"code": "return-to-patient",
"display": "Return To Patient"
}
]
}


CodeSystem Task Code Genomics

Usage

A set of codes use to identify the type of task for Genomic Order Management

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/task-code-genomics defines the following codes:

CodeDisplay
process-genomic-test-requestProcess Genomic Test Request
request-sample-alignmentRequest & Sample Alignment
sample-preparationSample Preparation
sample-processingSample Processing
genetic-genomic-data-processingGenetic/Genomic Data Processing
interpretationInterpretation
produce-interim-reportProduce Interim Report
genomic-mdtGenomic MDT
produce-final-reportProduce Final Report
distribute-reportDistribute Report

Table View

CodeSystem.id[0]task-code-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/task-code-genomics
CodeSystem.version[0]0.3.0
CodeSystem.name[0]TaskCodeGenomics
CodeSystem.title[0]Task Code Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-02-28T15:33:00+00:00
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]A set of codes use to identify the type of task for Genomic Order Management
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]process-genomic-test-request
CodeSystem.concept[0].display[0]Process Genomic Test Request
CodeSystem.concept[0].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[0].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[0].designation[0].use[0].display[0]Synonym
CodeSystem.concept[0].designation[0].value[0]50.00
CodeSystem.concept[1].code[0]request-sample-alignment
CodeSystem.concept[1].display[0]Request & Sample Alignment
CodeSystem.concept[1].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[1].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[1].designation[0].use[0].display[0]Synonym
CodeSystem.concept[1].designation[0].value[0]100.00
CodeSystem.concept[2].code[0]sample-preparation
CodeSystem.concept[2].display[0]Sample Preparation
CodeSystem.concept[2].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[2].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[2].designation[0].use[0].display[0]Synonym
CodeSystem.concept[2].designation[0].value[0]150.00
CodeSystem.concept[3].code[0]sample-processing
CodeSystem.concept[3].display[0]Sample Processing
CodeSystem.concept[3].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[3].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[3].designation[0].use[0].display[0]Synonym
CodeSystem.concept[3].designation[0].value[0]200.00
CodeSystem.concept[4].code[0]genetic-genomic-data-processing
CodeSystem.concept[4].display[0]Genetic/Genomic Data Processing
CodeSystem.concept[4].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[4].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[4].designation[0].use[0].display[0]Synonym
CodeSystem.concept[4].designation[0].value[0]250.00
CodeSystem.concept[5].code[0]interpretation
CodeSystem.concept[5].display[0]Interpretation
CodeSystem.concept[5].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[5].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[5].designation[0].use[0].display[0]Synonym
CodeSystem.concept[5].designation[0].value[0]300.00
CodeSystem.concept[6].code[0]produce-interim-report
CodeSystem.concept[6].display[0]Produce Interim Report
CodeSystem.concept[6].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[6].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[6].designation[0].use[0].display[0]Synonym
CodeSystem.concept[6].designation[0].value[0]350.00
CodeSystem.concept[7].code[0]genomic-mdt
CodeSystem.concept[7].display[0]Genomic MDT
CodeSystem.concept[7].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[7].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[7].designation[0].use[0].display[0]Synonym
CodeSystem.concept[7].designation[0].value[0]400.00
CodeSystem.concept[8].code[0]produce-final-report
CodeSystem.concept[8].display[0]Produce Final Report
CodeSystem.concept[8].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[8].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[8].designation[0].use[0].display[0]Synonym
CodeSystem.concept[8].designation[0].value[0]450.00
CodeSystem.concept[9].code[0]distribute-report
CodeSystem.concept[9].display[0]Distribute Report
CodeSystem.concept[9].designation[0].use[0].system[0]http://snomed.info/sct
CodeSystem.concept[9].designation[0].use[0].code[0]900000000000013009
CodeSystem.concept[9].designation[0].use[0].display[0]Synonym
CodeSystem.concept[9].designation[0].value[0]500.00

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="task-code-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/task-code-genomics" />
<version value="0.3.0" />
<name value="TaskCodeGenomics" />
<title value="Task Code Genomics" />
<status value="draft" />
<date value="2024-02-28T15:33:00+00:00" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="A set of codes use to identify the type of task for Genomic Order Management" />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="process-genomic-test-request" />
<display value="Process Genomic Test Request" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="50.00" />
</designation>
</concept>
<code value="request-sample-alignment" />
<display value="Request & Sample Alignment" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="100.00" />
</designation>
</concept>
<code value="sample-preparation" />
<display value="Sample Preparation" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="150.00" />
</designation>
</concept>
<code value="sample-processing" />
<display value="Sample Processing" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="200.00" />
</designation>
</concept>
<code value="genetic-genomic-data-processing" />
<display value="Genetic/Genomic Data Processing" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="250.00" />
</designation>
</concept>
<code value="interpretation" />
<display value="Interpretation" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="300.00" />
</designation>
</concept>
<code value="produce-interim-report" />
<display value="Produce Interim Report" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="350.00" />
</designation>
</concept>
<code value="genomic-mdt" />
<display value="Genomic MDT" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="400.00" />
</designation>
</concept>
<code value="produce-final-report" />
<display value="Produce Final Report" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="450.00" />
</designation>
</concept>
<code value="distribute-report" />
<display value="Distribute Report" />
<use>
<system value="http://snomed.info/sct" />
<code value="900000000000013009" />
<display value="Synonym" />
</use>
<value value="500.00" />
</designation>
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "task-code-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/task-code-genomics",
"version": "0.3.0",
"name": "TaskCodeGenomics",
"title": "Task Code Genomics",
"status": "draft",
"date": "2024-02-28T15:33:00+00:00",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "A set of codes use to identify the type of task for Genomic Order Management",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "process-genomic-test-request",
"display": "Process Genomic Test Request",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "50.00"
}
]
},
{
"code": "request-sample-alignment",
"display": "Request & Sample Alignment",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "100.00"
}
]
},
{
"code": "sample-preparation",
"display": "Sample Preparation",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "150.00"
}
]
},
{
"code": "sample-processing",
"display": "Sample Processing",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "200.00"
}
]
},
{
"code": "genetic-genomic-data-processing",
"display": "Genetic/Genomic Data Processing",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "250.00"
}
]
},
{
"code": "interpretation",
"display": "Interpretation",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "300.00"
}
]
},
{
"code": "produce-interim-report",
"display": "Produce Interim Report",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "350.00"
}
]
},
{
"code": "genomic-mdt",
"display": "Genomic MDT",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "400.00"
}
]
},
{
"code": "produce-final-report",
"display": "Produce Final Report",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "450.00"
}
]
},
{
"code": "distribute-report",
"display": "Distribute Report",
{
"use": {
"system": "http://snomed.info/sct",
"code": "900000000000013009",
"display": "Synonym"
},
"value": "500.00"
}
]
}
]
}


CodeSystem Task Status Reason Genomics

Usage

Status reasons for Tasks in genomics

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/task-statusReason-genomics defines the following codes:

CodeDisplay
further-information-neededFurther Information Needed
awaiting-sampleAwaiting Sample
awaiting-rod-and-or-sampleAwaiting Record of Discussion and/or Sample
invalid-requestInvalid Request
pipeline-errorPipeline Error
time-for-task-exceededTime For Task Exceeded
unable-to-interpretUnable To Interpret
sample-sub-optimalSample Sub-Optimal
task-no-longer-requiredTask No Longer Required
no-sample-providedNo Sample Provided
scheduled-delayScheduled Delay
awaiting-order-detailAwaiting Order Detail
otherother

Table View

CodeSystem.id[0]task-statusReason-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/task-statusReason-genomics
CodeSystem.version[0]0.3.1
CodeSystem.name[0]TaskStatusReasonGenomics
CodeSystem.title[0]Task StatusReason Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-07-23
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.description[0]Status reasons for Tasks in genomics
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]further-information-needed
CodeSystem.concept[0].display[0]Further Information Needed
CodeSystem.concept[1].code[0]awaiting-sample
CodeSystem.concept[1].display[0]Awaiting Sample
CodeSystem.concept[2].code[0]awaiting-rod-and-or-sample
CodeSystem.concept[2].display[0]Awaiting Record of Discussion and/or Sample
CodeSystem.concept[3].code[0]invalid-request
CodeSystem.concept[3].display[0]Invalid Request
CodeSystem.concept[4].code[0]pipeline-error
CodeSystem.concept[4].display[0]Pipeline Error
CodeSystem.concept[5].code[0]time-for-task-exceeded
CodeSystem.concept[5].display[0]Time For Task Exceeded
CodeSystem.concept[6].code[0]unable-to-interpret
CodeSystem.concept[6].display[0]Unable To Interpret
CodeSystem.concept[7].code[0]sample-sub-optimal
CodeSystem.concept[7].display[0]Sample Sub-Optimal
CodeSystem.concept[8].code[0]task-no-longer-required
CodeSystem.concept[8].display[0]Task No Longer Required
CodeSystem.concept[9].code[0]no-sample-provided
CodeSystem.concept[9].display[0]No Sample Provided
CodeSystem.concept[10].code[0]scheduled-delay
CodeSystem.concept[10].display[0]Scheduled Delay
CodeSystem.concept[11].code[0]awaiting-order-detail
CodeSystem.concept[11].display[0]Awaiting Order Detail
CodeSystem.concept[12].code[0]other
CodeSystem.concept[12].display[0]other

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="task-statusReason-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/task-statusReason-genomics" />
<version value="0.3.1" />
<name value="TaskStatusReasonGenomics" />
<title value="Task StatusReason Genomics" />
<status value="draft" />
<date value="2024-07-23" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
<use value="work" />
</telecom>
</contact>
<description value="Status reasons for Tasks in genomics" />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="further-information-needed" />
<display value="Further Information Needed" />
</concept>
<code value="awaiting-sample" />
<display value="Awaiting Sample" />
</concept>
<code value="awaiting-rod-and-or-sample" />
<display value="Awaiting Record of Discussion and/or Sample" />
</concept>
<code value="invalid-request" />
<display value="Invalid Request" />
</concept>
<code value="pipeline-error" />
<display value="Pipeline Error" />
</concept>
<code value="time-for-task-exceeded" />
<display value="Time For Task Exceeded" />
</concept>
<code value="unable-to-interpret" />
<display value="Unable To Interpret" />
</concept>
<code value="sample-sub-optimal" />
<display value="Sample Sub-Optimal" />
</concept>
<code value="task-no-longer-required" />
<display value="Task No Longer Required" />
</concept>
<code value="no-sample-provided" />
<display value="No Sample Provided" />
</concept>
<code value="scheduled-delay" />
<display value="Scheduled Delay" />
</concept>
<code value="awaiting-order-detail" />
<display value="Awaiting Order Detail" />
</concept>
<code value="other" />
<display value="other" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "task-statusReason-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/task-statusReason-genomics",
"version": "0.3.1",
"name": "TaskStatusReasonGenomics",
"title": "Task StatusReason Genomics",
"status": "draft",
"date": "2024-07-23",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net",
"use": "work"
}
]
}
],
"description": "Status reasons for Tasks in genomics",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "further-information-needed",
"display": "Further Information Needed"
},
{
"code": "awaiting-sample",
"display": "Awaiting Sample"
},
{
"code": "awaiting-rod-and-or-sample",
"display": "Awaiting Record of Discussion and/or Sample"
},
{
"code": "invalid-request",
"display": "Invalid Request"
},
{
"code": "pipeline-error",
"display": "Pipeline Error"
},
{
"code": "time-for-task-exceeded",
"display": "Time For Task Exceeded"
},
{
"code": "unable-to-interpret",
"display": "Unable To Interpret"
},
{
"code": "sample-sub-optimal",
"display": "Sample Sub-Optimal"
},
{
"code": "task-no-longer-required",
"display": "Task No Longer Required"
},
{
"code": "no-sample-provided",
"display": "No Sample Provided"
},
{
"code": "scheduled-delay",
"display": "Scheduled Delay"
},
{
"code": "awaiting-order-detail",
"display": "Awaiting Order Detail"
},
{
"code": "other",
"display": "other"
}
]
}


CodeSystem Genomic Coverage

Usage

A set of codes that define the funding category for a patient.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory defines the following codes:

LvlCodeDisplay
1publicPublic
2  nhs-englandNHS England
2  nhs-scotlandNHS Scotland
2  nhs-walesNHS Wales
2  hsc-northern-irelandHSC Northern Ireland
2  jerseyJersey
2  guernseyGuernsey
2  isle-of-manIsle of Man
2  overseas-visitorOverseas Visitor
1privatePrivate

Table View

CodeSystem.id[0]UKCore-FundingCategory
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory
CodeSystem.version[0]2.0.0
CodeSystem.name[0]UKCoreFundingCategory
CodeSystem.title[0]UK Core Funding Category
CodeSystem.status[0]active
CodeSystem.date[0]2024-06-14
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A set of codes that define the funding category for a patient.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.hierarchyMeaning[0]is-a
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]public
CodeSystem.concept[0].display[0]Public
CodeSystem.concept[0].concept[0].code[0]nhs-england
CodeSystem.concept[0].concept[0].display[0]NHS England
CodeSystem.concept[0].concept[1].code[0]nhs-scotland
CodeSystem.concept[0].concept[1].display[0]NHS Scotland
CodeSystem.concept[0].concept[2].code[0]nhs-wales
CodeSystem.concept[0].concept[2].display[0]NHS Wales
CodeSystem.concept[0].concept[3].code[0]hsc-northern-ireland
CodeSystem.concept[0].concept[3].display[0]HSC Northern Ireland
CodeSystem.concept[0].concept[4].code[0]jersey
CodeSystem.concept[0].concept[4].display[0]Jersey
CodeSystem.concept[0].concept[5].code[0]guernsey
CodeSystem.concept[0].concept[5].display[0]Guernsey
CodeSystem.concept[0].concept[6].code[0]isle-of-man
CodeSystem.concept[0].concept[6].display[0]Isle of Man
CodeSystem.concept[0].concept[7].code[0]overseas-visitor
CodeSystem.concept[0].concept[7].display[0]Overseas Visitor
CodeSystem.concept[1].code[0]private
CodeSystem.concept[1].display[0]Private

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-FundingCategory" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory" />
<version value="2.0.0" />
<name value="UKCoreFundingCategory" />
<title value="UK Core Funding Category" />
<status value="active" />
<date value="2024-06-14" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A set of codes that define the funding category for a patient." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<hierarchyMeaning value="is-a" />
<content value="complete" />
<code value="public" />
<display value="Public" />
<code value="nhs-england" />
<display value="NHS England" />
</concept>
<code value="nhs-scotland" />
<display value="NHS Scotland" />
</concept>
<code value="nhs-wales" />
<display value="NHS Wales" />
</concept>
<code value="hsc-northern-ireland" />
<display value="HSC Northern Ireland" />
</concept>
<code value="jersey" />
<display value="Jersey" />
</concept>
<code value="guernsey" />
<display value="Guernsey" />
</concept>
<code value="isle-of-man" />
<display value="Isle of Man" />
</concept>
<code value="overseas-visitor" />
<display value="Overseas Visitor" />
</concept>
</concept>
<code value="private" />
<display value="Private" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-FundingCategory",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory",
"version": "2.0.0",
"name": "UKCoreFundingCategory",
"title": "UK Core Funding Category",
"status": "active",
"date": "2024-06-14",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A set of codes that define the funding category for a patient.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"hierarchyMeaning": "is-a",
"content": "complete",
"concept": [
{
"code": "public",
"display": "Public",
"concept": [
{
"code": "nhs-england",
"display": "NHS England"
},
{
"code": "nhs-scotland",
"display": "NHS Scotland"
},
{
"code": "nhs-wales",
"display": "NHS Wales"
},
{
"code": "hsc-northern-ireland",
"display": "HSC Northern Ireland"
},
{
"code": "jersey",
"display": "Jersey"
},
{
"code": "guernsey",
"display": "Guernsey"
},
{
"code": "isle-of-man",
"display": "Isle of Man"
},
{
"code": "overseas-visitor",
"display": "Overseas Visitor"
}
]
},
{
"code": "private",
"display": "Private"
}
]
}


CodeSystem Genomic NHSNumber Unavailable Reason

Usage

A set of concepts that define the reason that an NHS number is not available for use as an identifier.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-NHSNumberUnavailableReason defines the following codes:

CodeDisplay
nhs-number-not-knownNHS number not known
overseas-patientOverseas patient
devolved-nationDevolved nation

Table View

CodeSystem.id[0]UKCore-NHSNumberUnavailableReason
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-NHSNumberUnavailableReason
CodeSystem.version[0]1.0.0
CodeSystem.name[0]UKCoreNHSNumberUnavailableReason
CodeSystem.title[0]UK Core NHS Number Unavailable Reason
CodeSystem.status[0]active
CodeSystem.date[0]2023-04-28
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A set of concepts that define the reason that an NHS number is not available for use as an identifier.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]nhs-number-not-known
CodeSystem.concept[0].display[0]NHS number not known
CodeSystem.concept[1].code[0]overseas-patient
CodeSystem.concept[1].display[0]Overseas patient
CodeSystem.concept[2].code[0]devolved-nation
CodeSystem.concept[2].display[0]Devolved nation

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-NHSNumberUnavailableReason" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-NHSNumberUnavailableReason" />
<version value="1.0.0" />
<name value="UKCoreNHSNumberUnavailableReason" />
<title value="UK Core NHS Number Unavailable Reason" />
<status value="active" />
<date value="2023-04-28" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A set of concepts that define the reason that an NHS number is not available for use as an identifier." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="nhs-number-not-known" />
<display value="NHS number not known" />
</concept>
<code value="overseas-patient" />
<display value="Overseas patient" />
</concept>
<code value="devolved-nation" />
<display value="Devolved nation" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-NHSNumberUnavailableReason",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-NHSNumberUnavailableReason",
"version": "1.0.0",
"name": "UKCoreNHSNumberUnavailableReason",
"title": "UK Core NHS Number Unavailable Reason",
"status": "active",
"date": "2023-04-28",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A set of concepts that define the reason that an NHS number is not available for use as an identifier.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "nhs-number-not-known",
"display": "NHS number not known"
},
{
"code": "overseas-patient",
"display": "Overseas patient"
},
{
"code": "devolved-nation",
"display": "Devolved nation"
}
]
}


CodeSystem Genomic Organization Type

Usage

A set of codes to define additional genomic lab concepts for an organisation type.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-OrganizationTypeGenomics defines the following codes:

CodeDisplay
GLHGenomic Lab Hub
GELGenomics England
LABOther Genomics Laboratory

Table View

CodeSystem.id[0]UKCore-OrganizationTypeGenomics
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-OrganizationTypeGenomics
CodeSystem.version[0]1.0.0
CodeSystem.name[0]UKCoreOrganizationTypeGenomics
CodeSystem.title[0]UK Core Organization Type Genomics
CodeSystem.status[0]active
CodeSystem.date[0]2023-04-28
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A set of codes to define additional genomic lab concepts for an organisation type.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]GLH
CodeSystem.concept[0].display[0]Genomic Lab Hub
CodeSystem.concept[1].code[0]GEL
CodeSystem.concept[1].display[0]Genomics England
CodeSystem.concept[2].code[0]LAB
CodeSystem.concept[2].display[0]Other Genomics Laboratory

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-OrganizationTypeGenomics" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-OrganizationTypeGenomics" />
<version value="1.0.0" />
<name value="UKCoreOrganizationTypeGenomics" />
<title value="UK Core Organization Type Genomics" />
<status value="active" />
<date value="2023-04-28" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A set of codes to define additional genomic lab concepts for an organisation type." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="GLH" />
<display value="Genomic Lab Hub" />
</concept>
<code value="GEL" />
<display value="Genomics England" />
</concept>
<code value="LAB" />
<display value="Other Genomics Laboratory" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-OrganizationTypeGenomics",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-OrganizationTypeGenomics",
"version": "1.0.0",
"name": "UKCoreOrganizationTypeGenomics",
"title": "UK Core Organization Type Genomics",
"status": "active",
"date": "2023-04-28",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A set of codes to define additional genomic lab concepts for an organisation type.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "GLH",
"display": "Genomic Lab Hub"
},
{
"code": "GEL",
"display": "Genomics England"
},
{
"code": "LAB",
"display": "Other Genomics Laboratory"
}
]
}


CodeSystem Genomic Primary Sample State

Usage

A CodeSystem to record the categorisation of a specimen, either sourced from a Tumour or Germline.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-PrimarySampleState defines the following codes:

CodeDisplayDefinition
blood-spotBlood spot
FFPEFormalin-fixed paraffin-embedded
freshFresh
otherOtherAny other suitable sample condition that is an alternative to concepts provided in this CodeSystem. This should be provided by free text.

Table View

CodeSystem.id[0]UKCore-PrimarySampleState
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-PrimarySampleState
CodeSystem.version[0]2.0.0
CodeSystem.name[0]UKCorePrimarySampleState
CodeSystem.title[0]UK Core Primary Sample State
CodeSystem.status[0]active
CodeSystem.date[0]2024-11-08
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A CodeSystem used to indicate the sample state/condition. The codes and their description are datasets definition from the Genomics Master Datasets.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]blood-spot
CodeSystem.concept[0].display[0]Blood spot
CodeSystem.concept[1].code[0]FFPE
CodeSystem.concept[1].display[0]Formalin-fixed paraffin-embedded
CodeSystem.concept[2].code[0]fresh
CodeSystem.concept[2].display[0]Fresh
CodeSystem.concept[3].code[0]other
CodeSystem.concept[3].display[0]Other
CodeSystem.concept[3].definition[0]Any other suitable sample condition that is an alternative to concepts provided in this CodeSystem. This should be provided by free text.

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-PrimarySampleState" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-PrimarySampleState" />
<version value="2.0.0" />
<name value="UKCorePrimarySampleState" />
<title value="UK Core Primary Sample State" />
<status value="active" />
<date value="2024-11-08" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A CodeSystem used to indicate the sample state/condition. The codes and their description are datasets definition from the Genomics Master Datasets." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="blood-spot" />
<display value="Blood spot" />
</concept>
<code value="FFPE" />
<display value="Formalin-fixed paraffin-embedded" />
</concept>
<code value="fresh" />
<display value="Fresh" />
</concept>
<code value="other" />
<display value="Other" />
<definition value="Any other suitable sample condition that is an alternative to concepts provided in this CodeSystem. This should be provided by free text." />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-PrimarySampleState",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PrimarySampleState",
"version": "2.0.0",
"name": "UKCorePrimarySampleState",
"title": "UK Core Primary Sample State",
"status": "active",
"date": "2024-11-08",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A CodeSystem used to indicate the sample state/condition. The codes and their description are datasets definition from the Genomics Master Datasets.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "blood-spot",
"display": "Blood spot"
},
{
"code": "FFPE",
"display": "Formalin-fixed paraffin-embedded"
},
{
"code": "fresh",
"display": "Fresh"
},
{
"code": "other",
"display": "Other",
"definition": "Any other suitable sample condition that is an alternative to concepts provided in this CodeSystem. This should be provided by free text."
}
]
}


CodeSystem Genomic Test Types

Usage

A CodeSystem to categorise if the service request is for Whole Genome Sequencing (WGS)/non-WGS Rare Disease/Cancer.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory defines the following codes:

CodeDisplay
rare-disease-wgsRare Disease - WGS
rare-disease-non-wgsRare Disease - Non-WGS
cancer-wgsCancer - WGS
cancer-non-wgsCancer - Non-WGS

Table View

CodeSystem.id[0]UKCore-GenomeSequencingCategory
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory
CodeSystem.version[0]1.0.0
CodeSystem.name[0]UKCoreGenomeSequencingCategory
CodeSystem.title[0]UK Core Genome Sequencing Category
CodeSystem.status[0]active
CodeSystem.date[0]2023-04-28
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A CodeSystem to categorise if the service request is for Whole Genome Sequencing (WGS)/non-WGS Rare Disease/Cancer.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]rare-disease-wgs
CodeSystem.concept[0].display[0]Rare Disease - WGS
CodeSystem.concept[1].code[0]rare-disease-non-wgs
CodeSystem.concept[1].display[0]Rare Disease - Non-WGS
CodeSystem.concept[2].code[0]cancer-wgs
CodeSystem.concept[2].display[0]Cancer - WGS
CodeSystem.concept[3].code[0]cancer-non-wgs
CodeSystem.concept[3].display[0]Cancer - Non-WGS

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-GenomeSequencingCategory" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" />
<version value="1.0.0" />
<name value="UKCoreGenomeSequencingCategory" />
<title value="UK Core Genome Sequencing Category" />
<status value="active" />
<date value="2023-04-28" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A CodeSystem to categorise if the service request is for Whole Genome Sequencing (WGS)/non-WGS Rare Disease/Cancer." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="rare-disease-wgs" />
<display value="Rare Disease - WGS" />
</concept>
<code value="rare-disease-non-wgs" />
<display value="Rare Disease - Non-WGS" />
</concept>
<code value="cancer-wgs" />
<display value="Cancer - WGS" />
</concept>
<code value="cancer-non-wgs" />
<display value="Cancer - Non-WGS" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-GenomeSequencingCategory",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory",
"version": "1.0.0",
"name": "UKCoreGenomeSequencingCategory",
"title": "UK Core Genome Sequencing Category",
"status": "active",
"date": "2023-04-28",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A CodeSystem to categorise if the service request is for Whole Genome Sequencing (WGS)/non-WGS Rare Disease/Cancer.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "rare-disease-wgs",
"display": "Rare Disease - WGS"
},
{
"code": "rare-disease-non-wgs",
"display": "Rare Disease - Non-WGS"
},
{
"code": "cancer-wgs",
"display": "Cancer - WGS"
},
{
"code": "cancer-non-wgs",
"display": "Cancer - Non-WGS"
}
]
}


CodeSystem Types of Re-Analysis Test Genomics

Usage

A set of codes use to identify the types of re-analysis test request in genomics.This is intended to be used on ServiceRequest.orderDetail element.

HTML View

Concepts

This code system https://fhir.nhs.uk/CodeSystem/types-of-reanalysistest-genomics defines the following codes:

CodeDisplay
original-gene-panelsOriginal Gene Panels
change-in-penetrance-settingChange in Penetrance Setting
new-gene panel-analysisNew Gene Panel Analysis
change-in-affection-status-of-family-memberChange in Affection Status of Family Member

Table View

CodeSystem.id[0]types-of-reanalysistest-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/types-of-reanalysistest-genomics
CodeSystem.version[0]0.1.0
CodeSystem.name[0]TypesofReAnalysisTestGenomics
CodeSystem.title[0]Types of Re-Analysis Test Genomics
CodeSystem.status[0]draft
CodeSystem.date[0]2024-07-09T00:00:00.000Z
CodeSystem.publisher[0]NHS England
CodeSystem.contact[0].name[0]NHS England
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]interoperabilityteam@nhs.net
CodeSystem.description[0]A set of codes use to identify the types of re-analysis test request in genomics.This is intended to be used on ServiceRequest.orderDetail element.
CodeSystem.copyright[0]Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.concept[0].code[0]original-gene-panels
CodeSystem.concept[0].display[0]Original Gene Panels
CodeSystem.concept[1].code[0]change-in-penetrance-setting
CodeSystem.concept[1].display[0]Change in Penetrance Setting
CodeSystem.concept[2].code[0]new-gene panel-analysis
CodeSystem.concept[2].display[0]New Gene Panel Analysis
CodeSystem.concept[3].code[0]change-in-affection-status-of-family-member
CodeSystem.concept[3].display[0]Change in Affection Status of Family Member

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="types-of-reanalysistest-genomics" />
<url value="https://fhir.nhs.uk/CodeSystem/types-of-reanalysistest-genomics" />
<version value="0.1.0" />
<name value="TypesofReAnalysisTestGenomics" />
<title value="Types of Re-Analysis Test Genomics" />
<status value="draft" />
<date value="2024-07-09T00:00:00.000Z" />
<publisher value="NHS England" />
<name value="NHS England" />
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A set of codes use to identify the types of re-analysis test request in genomics.This is intended to be used on ServiceRequest.orderDetail element." />
<copyright value="Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<code value="original-gene-panels" />
<display value="Original Gene Panels" />
</concept>
<code value="change-in-penetrance-setting" />
<display value="Change in Penetrance Setting" />
</concept>
<code value="new-gene panel-analysis" />
<display value="New Gene Panel Analysis" />
</concept>
<code value="change-in-affection-status-of-family-member" />
<display value="Change in Affection Status of Family Member" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "types-of-reanalysistest-genomics",
"url": "https://fhir.nhs.uk/CodeSystem/types-of-reanalysistest-genomics",
"version": "0.1.0",
"name": "TypesofReAnalysisTestGenomics",
"title": "Types of Re-Analysis Test Genomics",
"status": "draft",
"date": "2024-07-09T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A set of codes use to identify the types of re-analysis test request in genomics.This is intended to be used on ServiceRequest.orderDetail element.",
"copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"concept": [
{
"code": "original-gene-panels",
"display": "Original Gene Panels"
},
{
"code": "change-in-penetrance-setting",
"display": "Change in Penetrance Setting"
},
{
"code": "new-gene panel-analysis",
"display": "New Gene Panel Analysis"
},
{
"code": "change-in-affection-status-of-family-member",
"display": "Change in Affection Status of Family Member"
}
]
}


CodeSystem Genomic Withheld Identity Reason

Usage

A CodeSystem to record the categorisation of a specimen, either sourced from a Tumour or Germline.

HTML View

Concepts

This code system https://fhir.hl7.org.uk/CodeSystem/UKCore-WithheldIdentityReason defines the following codes:

CodeDisplay
01Record anonymised for legal/statutory reasons
02Record anonymised at request of Caldicott Guardian
03Record anonymised at request of Patient
97Record anonymised for other reason
99Identity withheld but reason not known

Table View

CodeSystem.id[0]UKCore-WithheldIdentityReason
CodeSystem.url[0]https://fhir.hl7.org.uk/CodeSystem/UKCore-WithheldIdentityReason
CodeSystem.version[0]0.0.1
CodeSystem.name[0]UKCoreWithheldIdentityReason
CodeSystem.title[0]UK Core Withheld Identity Reason
CodeSystem.status[0]draft
CodeSystem.date[0]2024-06-14
CodeSystem.publisher[0]HL7 UK
CodeSystem.contact[0].name[0]HL7 UK
CodeSystem.contact[0].telecom[0].system[0]email
CodeSystem.contact[0].telecom[0].value[0]ukcore@hl7.org.uk
CodeSystem.contact[0].telecom[0].use[0]work
CodeSystem.contact[0].telecom[0].rank[0]1
CodeSystem.description[0]A set of codes that define the valid reason for which a record has been purposely anonymised. These codes and their descriptions are copied from the content of the [NHS Data Model and Dictionary](https://www.datadictionary.nhs.uk/data_elements/withheld_identity_reason.html) web page on 2024-06-14.
CodeSystem.copyright[0]Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.
CodeSystem.caseSensitive[0]True
CodeSystem.content[0]complete
CodeSystem.count[0]5
CodeSystem.concept[0].code[0]01
CodeSystem.concept[0].display[0]Record anonymised for legal/statutory reasons
CodeSystem.concept[1].code[0]02
CodeSystem.concept[1].display[0]Record anonymised at request of Caldicott Guardian
CodeSystem.concept[2].code[0]03
CodeSystem.concept[2].display[0]Record anonymised at request of Patient
CodeSystem.concept[3].code[0]97
CodeSystem.concept[3].display[0]Record anonymised for other reason
CodeSystem.concept[4].code[0]99
CodeSystem.concept[4].display[0]Identity withheld but reason not known

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
<id value="UKCore-WithheldIdentityReason" />
<url value="https://fhir.hl7.org.uk/CodeSystem/UKCore-WithheldIdentityReason" />
<version value="0.0.1" />
<name value="UKCoreWithheldIdentityReason" />
<title value="UK Core Withheld Identity Reason" />
<status value="draft" />
<date value="2024-06-14" />
<publisher value="HL7 UK" />
<name value="HL7 UK" />
<system value="email" />
<value value="ukcore@hl7.org.uk" />
<use value="work" />
<rank value="1" />
</telecom>
</contact>
<description value="A set of codes that define the valid reason for which a record has been purposely anonymised. These codes and their descriptions are copied from the content of the [NHS Data Model and Dictionary](https://www.datadictionary.nhs.uk/data_elements/withheld_identity_reason.html) web page on 2024-06-14." />
<copyright value="Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html." />
<caseSensitive value="true" />
<content value="complete" />
<count value="5" />
<code value="01" />
<display value="Record anonymised for legal/statutory reasons" />
</concept>
<code value="02" />
<display value="Record anonymised at request of Caldicott Guardian" />
</concept>
<code value="03" />
<display value="Record anonymised at request of Patient" />
</concept>
<code value="97" />
<display value="Record anonymised for other reason" />
</concept>
<code value="99" />
<display value="Identity withheld but reason not known" />
</concept>
</CodeSystem>

JSON View

{
"resourceType": "CodeSystem",
"id": "UKCore-WithheldIdentityReason",
"url": "https://fhir.hl7.org.uk/CodeSystem/UKCore-WithheldIdentityReason",
"version": "0.0.1",
"name": "UKCoreWithheldIdentityReason",
"title": "UK Core Withheld Identity Reason",
"status": "draft",
"date": "2024-06-14",
"publisher": "HL7 UK",
"contact": [
{
"name": "HL7 UK",
"telecom": [
{
"system": "email",
"value": "ukcore@hl7.org.uk",
"use": "work",
"rank": 1
}
]
}
],
"description": "A set of codes that define the valid reason for which a record has been purposely anonymised. These codes and their descriptions are copied from the content of the [NHS Data Model and Dictionary](https://www.datadictionary.nhs.uk/data_elements/withheld_identity_reason.html) web page on 2024-06-14.",
"copyright": "Copyright © 2021+ HL7 UK Licensed under the Apache License, Version 2.0 (the \"License\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \"AS IS\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.",
"caseSensitive": true,
"content": "complete",
"count": 5,
"concept": [
{
"code": "01",
"display": "Record anonymised for legal/statutory reasons"
},
{
"code": "02",
"display": "Record anonymised at request of Caldicott Guardian"
},
{
"code": "03",
"display": "Record anonymised at request of Patient"
},
{
"code": "97",
"display": "Record anonymised for other reason"
},
{
"code": "99",
"display": "Identity withheld but reason not known"
}
]
}


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