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.reasonCode.

HTML View

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

Table View

CodeSystem.id[0]reasonfortesting-genomics
CodeSystem.url[0]https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics
CodeSystem.version[0]0.1.0
CodeSystem.name[0]ReasonforTestingGenomics
CodeSystem.title[0]Reason for Testing 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 reason for requesting a genomics test.This is intended to be used on ServiceRequest.reasonCode.
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

XML View

<CodeSystem xmlns="http://hl7.org/fhir">
    <id value="reasonfortesting-genomics" />
    <url value="https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" />
    <version value="0.1.0" />
    <name value="ReasonforTestingGenomics" />
    <title value="Reason for Testing Genomics" />
    <status value="draft" />
    <date value="2024-07-09T00:00:00.000Z" />
    <publisher value="NHS England" />
    <contact>
        <name value="NHS England" />
        <telecom>
            <system value="email" />
            <value value="interoperabilityteam@nhs.net" />
        </telecom>
    </contact>
    <description value="A set of codes use to identify the reason for requesting a genomics test.This is intended to be used on ServiceRequest.reasonCode." />
    <copyright value="Copyright &#169; 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \&quot;License\&quot;); 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 \&quot;AS IS\&quot; 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&#174; FHIR&#174; standard Copyright &#169; 2011+ HL7 The HL7&#174; FHIR&#174; 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" />
    <concept>
        <code value="primary-test-request" />
        <display value="Primary Test Request" />
        <concept>
            <code value="carrier" />
            <display value="Carrier" />
        </concept>
        <concept>
            <code value="diagnostic" />
            <display value="Diagnostic" />
        </concept>
        <concept>
            <code value="disease-monitoring-mrdmechanism" />
            <display value="Disease Monitoring MRD CHIMERISM" />
        </concept>
        <concept>
            <code value="dna-storage" />
            <display value="DNA Storage" />
        </concept>
        <concept>
            <code value="follow-up" />
            <display value="Follow Up" />
        </concept>
        <concept>
            <code value="predictive" />
            <display value="Predictive" />
        </concept>
        <concept>
            <code value="relapse" />
            <display value="Relapse" />
        </concept>
        <concept>
            <code value="staging-or-prognosis" />
            <display value="Staging or Prognosis" />
        </concept>
        <concept>
            <code value="unknown" />
            <display value="Unknown" />
        </concept>
    </concept>
    <concept>
        <code value="reanalysis-test-request" />
        <display value="Reanalysis Test Request" />
        <concept>
            <code value="change-in-presentation" />
            <display value="Change In Presentation" />
        </concept>
        <concept>
            <code value="newly-affected-family-member" />
            <display value="Newly Affected Family Member" />
        </concept>
        <concept>
            <code value="new-pregnancy" />
            <display value="New Pregnancy" />
        </concept>
        <concept>
            <code value="new-treatment-clinical-management" />
            <display value="New Treatment/Clinical Management" />
        </concept>
        <concept>
            <code value="recently-deceased-to-inform-family" />
            <display value="Recently Deceased To Inform Family" />
        </concept>
    </concept>
</CodeSystem>

JSON View

{
    "resourceType": "CodeSystem",
    "id": "reasonfortesting-genomics",
    "url": "https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics",
    "version": "0.1.0",
    "name": "ReasonforTestingGenomics",
    "title": "Reason for Testing 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 reason for requesting a genomics test.This is intended to be used on ServiceRequest.reasonCode.",
    "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"
                }
            ]
        }
    ]
}