FHIR Genomics Implementation Guide

Notice

Important: This guidance is under active development by NHS England and content may be added or updated on a regular basis.
This Implementation Guide is currently in Draft and SHOULD NOT be used for development or active implementation without express direction from the NHS England Genomics Unit.

ValueSet Genomic Reason for Testing

Usage
A Composite ValueSet of reasons for requesting or linking genomics test.

HTML View

This value set includes codes from the following code systems:

Import all codes from CodeSystem other
Import all codes from CodeSystem other
Import all codes from CodeSystem unaffected-relatives-seeking-predictive-testing
Import all codes from CodeSystem germline-later

Expansion

This expansion was generated on 2026-02-10T00:00:00Z

This value set contains 30 concepts

Code	System	Display
sample-storage	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Sample storage
diagnostic	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Diagnostic
carrier	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Carrier
predictive	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Predictive
prenatal-diagnosis	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Prenatal diagnosis
family-member-to-aid-interpretation	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Family member to aid interpretation of a relative's result/variant
reanalysis	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Reanalysis
pharmacogenomics	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Pharmacogenomics
other	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics	Other
sample-storage	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Sample storage
diagnostic	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Diagnostic
differential-diagnosis	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Differential diagnosis
prognostic	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Prognostic
treatment-determining	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Treatment determining
disease-monitoring	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Disease monitoring
relapse-recurrence	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Relapse or recurrence
remission	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Remission
transformation	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Transformation
research-trial-eligibility	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Research or trial eligibility
pharmacogenomics	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Pharmacogenomics
other	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics	Other
patient-management	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics	Patient management
reproductive-decision-making	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics	Reproductive decision making
unaffected-relatives-seeking-predictive-testing	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics	Unaffected relatives seeking predictive testing
reanalysis	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Re-analysis
reinterpretation	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Re-interpretation
retest	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Re-test
follow-on-test	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Follow on test
family-associated	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Family associated
germline-later	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics	Germline later

Table View

ValueSet.id[0]	genomics-reasonfortesting
ValueSet.url[0]	https://fhir.nhs.uk/ValueSet/genomics-reasonfortesting
ValueSet.version[0]	0.3.0
ValueSet.name[0]	GenomicsReasonforTesting
ValueSet.title[0]	Genomics Reason for Testing
ValueSet.status[0]	draft
ValueSet.date[0]	2026-02-09T00:00:00.000Z
ValueSet.publisher[0]	NHS England
ValueSet.contact[0].name[0]	NHS England
ValueSet.contact[0].telecom[0].system[0]	email
ValueSet.contact[0].telecom[0].value[0]	interoperabilityteam@nhs.net
ValueSet.description[0]	A Composite ValueSet of reasons for requesting or linking genomics test.
ValueSet.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.
ValueSet.compose[0].include[0].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.compose[0].include[0].version[0]	0.1.0
ValueSet.compose[0].include[1].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.compose[0].include[1].version[0]	0.1.0
ValueSet.compose[0].include[2].system[0]	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics
ValueSet.compose[0].include[2].version[0]	0.1.0
ValueSet.compose[0].include[3].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.compose[0].include[3].version[0]	0.1.0
ValueSet.expansion[0].identifier[0]	urn:uuid:3f2a1b9c-2d75-45cc-8ea3-2e747e4b61d4
ValueSet.expansion[0].timestamp[0]	2026-02-10T00:00:00Z
ValueSet.expansion[0].total[0]	30
ValueSet.expansion[0].contains[0].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[0].code[0]	sample-storage
ValueSet.expansion[0].contains[0].display[0]	Sample storage
ValueSet.expansion[0].contains[1].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[1].code[0]	diagnostic
ValueSet.expansion[0].contains[1].display[0]	Diagnostic
ValueSet.expansion[0].contains[2].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[2].code[0]	carrier
ValueSet.expansion[0].contains[2].display[0]	Carrier
ValueSet.expansion[0].contains[3].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[3].code[0]	predictive
ValueSet.expansion[0].contains[3].display[0]	Predictive
ValueSet.expansion[0].contains[4].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[4].code[0]	prenatal-diagnosis
ValueSet.expansion[0].contains[4].display[0]	Prenatal diagnosis
ValueSet.expansion[0].contains[5].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[5].code[0]	family-member-to-aid-interpretation
ValueSet.expansion[0].contains[5].display[0]	Family member to aid interpretation of a relative's result/variant
ValueSet.expansion[0].contains[6].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[6].code[0]	reanalysis
ValueSet.expansion[0].contains[6].display[0]	Reanalysis
ValueSet.expansion[0].contains[7].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[7].code[0]	pharmacogenomics
ValueSet.expansion[0].contains[7].display[0]	Pharmacogenomics
ValueSet.expansion[0].contains[8].system[0]	https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics
ValueSet.expansion[0].contains[8].code[0]	other
ValueSet.expansion[0].contains[8].display[0]	Other
ValueSet.expansion[0].contains[9].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[9].code[0]	sample-storage
ValueSet.expansion[0].contains[9].display[0]	Sample storage
ValueSet.expansion[0].contains[10].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[10].code[0]	diagnostic
ValueSet.expansion[0].contains[10].display[0]	Diagnostic
ValueSet.expansion[0].contains[11].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[11].code[0]	differential-diagnosis
ValueSet.expansion[0].contains[11].display[0]	Differential diagnosis
ValueSet.expansion[0].contains[12].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[12].code[0]	prognostic
ValueSet.expansion[0].contains[12].display[0]	Prognostic
ValueSet.expansion[0].contains[13].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[13].code[0]	treatment-determining
ValueSet.expansion[0].contains[13].display[0]	Treatment determining
ValueSet.expansion[0].contains[14].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[14].code[0]	disease-monitoring
ValueSet.expansion[0].contains[14].display[0]	Disease monitoring
ValueSet.expansion[0].contains[15].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[15].code[0]	relapse-recurrence
ValueSet.expansion[0].contains[15].display[0]	Relapse or recurrence
ValueSet.expansion[0].contains[16].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[16].code[0]	remission
ValueSet.expansion[0].contains[16].display[0]	Remission
ValueSet.expansion[0].contains[17].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[17].code[0]	transformation
ValueSet.expansion[0].contains[17].display[0]	Transformation
ValueSet.expansion[0].contains[18].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[18].code[0]	research-trial-eligibility
ValueSet.expansion[0].contains[18].display[0]	Research or trial eligibility
ValueSet.expansion[0].contains[19].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[19].code[0]	pharmacogenomics
ValueSet.expansion[0].contains[19].display[0]	Pharmacogenomics
ValueSet.expansion[0].contains[20].system[0]	https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics
ValueSet.expansion[0].contains[20].code[0]	other
ValueSet.expansion[0].contains[20].display[0]	Other
ValueSet.expansion[0].contains[21].system[0]	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics
ValueSet.expansion[0].contains[21].code[0]	patient-management
ValueSet.expansion[0].contains[21].display[0]	Patient management
ValueSet.expansion[0].contains[22].system[0]	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics
ValueSet.expansion[0].contains[22].code[0]	reproductive-decision-making
ValueSet.expansion[0].contains[22].display[0]	Reproductive decision making
ValueSet.expansion[0].contains[23].system[0]	https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics
ValueSet.expansion[0].contains[23].code[0]	unaffected-relatives-seeking-predictive-testing
ValueSet.expansion[0].contains[23].display[0]	Unaffected relatives seeking predictive testing
ValueSet.expansion[0].contains[24].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[24].code[0]	reanalysis
ValueSet.expansion[0].contains[24].display[0]	Re-analysis
ValueSet.expansion[0].contains[25].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[25].code[0]	reinterpretation
ValueSet.expansion[0].contains[25].display[0]	Re-interpretation
ValueSet.expansion[0].contains[26].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[26].code[0]	retest
ValueSet.expansion[0].contains[26].display[0]	Re-test
ValueSet.expansion[0].contains[27].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[27].code[0]	follow-on-test
ValueSet.expansion[0].contains[27].display[0]	Follow on test
ValueSet.expansion[0].contains[28].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[28].code[0]	family-associated
ValueSet.expansion[0].contains[28].display[0]	Family associated
ValueSet.expansion[0].contains[29].system[0]	https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics
ValueSet.expansion[0].contains[29].code[0]	germline-later
ValueSet.expansion[0].contains[29].display[0]	Germline later

XML View

<id value="genomics-reasonfortesting" />
<url value="https://fhir.nhs.uk/ValueSet/genomics-reasonfortesting" />
<version value="0.3.0" />
<name value="GenomicsReasonforTesting" />
<title value="Genomics Reason for Testing" />
<status value="draft" />
<date value="2026-02-09T00:00:00.000Z" />
<publisher value="NHS England" />
<contact>
<name value="NHS England" />
<telecom>
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="A Composite ValueSet of reasons for requesting or linking genomics 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." />
<compose>
<include>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<version value="0.1.0" />
</include>
<include>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<version value="0.1.0" />
</include>
<include>
<system value="https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics" />
<version value="0.1.0" />
</include>
<include>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<version value="0.1.0" />
</include>
</compose>
<expansion>
<identifier value="urn:uuid:3f2a1b9c-2d75-45cc-8ea3-2e747e4b61d4" />
<timestamp value="2026-02-10T00:00:00Z" />
<total value="30" />
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="sample-storage" />
<display value="Sample storage" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="diagnostic" />
<display value="Diagnostic" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="carrier" />
<display value="Carrier" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="predictive" />
<display value="Predictive" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="prenatal-diagnosis" />
<display value="Prenatal diagnosis" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="family-member-to-aid-interpretation" />
<display value="Family member to aid interpretation of a relative's result/variant" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="reanalysis" />
<display value="Reanalysis" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="pharmacogenomics" />
<display value="Pharmacogenomics" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics" />
<code value="other" />
<display value="Other" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="sample-storage" />
<display value="Sample storage" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="diagnostic" />
<display value="Diagnostic" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="differential-diagnosis" />
<display value="Differential diagnosis" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="prognostic" />
<display value="Prognostic" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="treatment-determining" />
<display value="Treatment determining" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="disease-monitoring" />
<display value="Disease monitoring" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="relapse-recurrence" />
<display value="Relapse or recurrence" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="remission" />
<display value="Remission" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="transformation" />
<display value="Transformation" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="research-trial-eligibility" />
<display value="Research or trial eligibility" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="pharmacogenomics" />
<display value="Pharmacogenomics" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics" />
<code value="other" />
<display value="Other" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics" />
<code value="patient-management" />
<display value="Patient management" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics" />
<code value="reproductive-decision-making" />
<display value="Reproductive decision making" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics" />
<code value="unaffected-relatives-seeking-predictive-testing" />
<display value="Unaffected relatives seeking predictive testing" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="reanalysis" />
<display value="Re-analysis" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="reinterpretation" />
<display value="Re-interpretation" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="retest" />
<display value="Re-test" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="follow-on-test" />
<display value="Follow on test" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="family-associated" />
<display value="Family associated" />
</contains>
<contains>
<system value="https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics" />
<code value="germline-later" />
<display value="Germline later" />
</contains>
</expansion>

</ValueSet>

JSON View

{

"resourceType": "ValueSet",
"id": "genomics-reasonfortesting",
"url": "https://fhir.nhs.uk/ValueSet/genomics-reasonfortesting",
"version": "0.3.0",
"name": "GenomicsReasonforTesting",
"title": "Genomics Reason for Testing",
"status": "draft",
"date": "2026-02-09T00:00:00.000Z",
"publisher": "NHS England",
"contact": [
{
"name": "NHS England",
"telecom": [
{
"system": "email",
"value": "interoperabilityteam@nhs.net"
}
]
}
],
"description": "A Composite ValueSet of reasons for requesting or linking genomics 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.",
"compose": {
"include": [
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"version": "0.1.0"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"version": "0.1.0"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics",
"version": "0.1.0"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"version": "0.1.0"
}
]
},
"expansion": {
"identifier": "urn:uuid:3f2a1b9c-2d75-45cc-8ea3-2e747e4b61d4",
"timestamp": "2026-02-10T00:00:00Z",
"total": 30,
"contains": [
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "sample-storage",
"display": "Sample storage"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "diagnostic",
"display": "Diagnostic"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "carrier",
"display": "Carrier"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "predictive",
"display": "Predictive"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "prenatal-diagnosis",
"display": "Prenatal diagnosis"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "family-member-to-aid-interpretation",
"display": "Family member to aid interpretation of a relative's result/variant"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "reanalysis",
"display": "Reanalysis"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "pharmacogenomics",
"display": "Pharmacogenomics"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
"code": "other",
"display": "Other"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "sample-storage",
"display": "Sample storage"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "diagnostic",
"display": "Diagnostic"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "differential-diagnosis",
"display": "Differential diagnosis"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "prognostic",
"display": "Prognostic"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "treatment-determining",
"display": "Treatment determining"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "disease-monitoring",
"display": "Disease monitoring"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "relapse-recurrence",
"display": "Relapse or recurrence"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "remission",
"display": "Remission"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "transformation",
"display": "Transformation"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "research-trial-eligibility",
"display": "Research or trial eligibility"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "pharmacogenomics",
"display": "Pharmacogenomics"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/cancer-testing-genomics",
"code": "other",
"display": "Other"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics",
"code": "patient-management",
"display": "Patient management"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics",
"code": "reproductive-decision-making",
"display": "Reproductive decision making"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/clinical-utility-genomics",
"code": "unaffected-relatives-seeking-predictive-testing",
"display": "Unaffected relatives seeking predictive testing"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "reanalysis",
"display": "Re-analysis"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "reinterpretation",
"display": "Re-interpretation"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "retest",
"display": "Re-test"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "follow-on-test",
"display": "Follow on test"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "family-associated",
"display": "Family associated"
},
{
"system": "https://fhir.nhs.uk/CodeSystem/test-associationReason-genomics",
"code": "germline-later",
"display": "Germline later"
}
]
}

}

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