Genomics Reporting Implementation Guide
2.0.0 - trial-use
Genomics Reporting Implementation Guide
2.0.0 - trial-use
This page is part of the Genetic Reporting Implementation Guide (v2.0.0: STU 2) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions 
<ValueSet xmlns="http://hl7.org/fhir">
<id value="genetic-therapeutic-implications-vs"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p>This value set includes codes based on the following rules:</p><ul><li>Include these codes as defined in <a href="http://loinc.org"><code>http://loinc.org</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA10315-2.html">LA10315-2</a></td><td>Ultrarapid metabolizer</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25391-6.html">LA25391-6</a></td><td>Normal metabolizer</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25390-8.html">LA25390-8</a></td><td>Rapid metabolizer</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA10317-8.html">LA10317-8</a></td><td>Intermediate metabolizer</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA9657-3.html">LA9657-3</a></td><td>Poor metabolizer</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA19542-2.html">LA19542-2</a></td><td>Low Risk</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA19541-4.html">LA19541-4</a></td><td>High Risk</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA6676-6.html">LA6676-6</a></td><td>Resistant</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA6677-4.html">LA6677-4</a></td><td>Responsive</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA9660-7.html">LA9660-7</a></td><td>Presumed resistant</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA9661-5.html">LA9661-5</a></td><td>Presumed responsive</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA6682-4.html">LA6682-4</a></td><td>Unknown Significance</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA6675-8.html">LA6675-8</a></td><td>Benign</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA6674-1.html">LA6674-1</a></td><td>Presumed Benign</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA9662-3.html">LA9662-3</a></td><td>Presumed non-responsive</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25392-4.html">LA25392-4</a></td><td>Increased function</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25393-2.html">LA25393-2</a></td><td>Normal function</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25395-7.html">LA25395-7</a></td><td>Decreased function</td></tr><tr><td><a href="http://details.loinc.org/LOINC/LA25394-0.html">LA25394-0</a></td><td>Poor function</td></tr></table></li><li>Include these codes as defined in <a href="http://www.snomed.org/"><code>http://snomed.info/sct</code></a><table class="none"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td><a href="http://snomed.info/id/444734003">444734003</a></td><td>Does not meet eligibility criteria for clinical trial (finding)</td></tr><tr><td><a href="http://snomed.info/id/399223003">399223003</a></td><td>Patient eligible for clinical trial (finding)</td></tr></table></li></ul></div>
</text>
<url
value="http://hl7.org/fhir/uv/genomics-reporting/ValueSet/genetic-therapeutic-implications-vs"/>
<version value="2.0.0"/>
<name value="GeneticTherapeuticImplicationsVS"/>
<title value="Genetic Therapeutic Implications"/>
<status value="active"/>
<date value="2022-05-09T16:53:07+00:00"/>
<publisher value="HL7 Clinical Genomics Working Group"/>
<contact>
<name value="HL7 Clinical Genomics Working Group"/>
<telecom>
<system value="url"/>
<value value="http://www.hl7.org/Special/committees/clingenomics"/>
</telecom>
<telecom>
<system value="email"/>
<value value="cg@lists.HL7.org"/>
</telecom>
</contact>
<description
value="Value Set for terms that describe a predicted ramification based on the presence of associated molecular finding(s)."/>
<jurisdiction>
<coding>
<system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
<code value="001"/>
<display value="World"/>
</coding>
</jurisdiction>
<copyright
value="This material contains content from LOINC (http://loinc.org). LOINC is copyright © 1995-2020, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license. LOINC® is a registered United States trademark of Regenstrief Institute, Inc.
This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement."/>
<compose>
<include>
<system value="http://loinc.org"/>
<concept>
<code value="LA10315-2"/>
<display value="Ultrarapid metabolizer"/>
</concept>
<concept>
<code value="LA25391-6"/>
<display value="Normal metabolizer"/>
</concept>
<concept>
<code value="LA25390-8"/>
<display value="Rapid metabolizer"/>
</concept>
<concept>
<code value="LA10317-8"/>
<display value="Intermediate metabolizer"/>
</concept>
<concept>
<code value="LA9657-3"/>
<display value="Poor metabolizer"/>
</concept>
<concept>
<code value="LA19542-2"/>
<display value="Low Risk"/>
</concept>
<concept>
<code value="LA19541-4"/>
<display value="High Risk"/>
</concept>
<concept>
<code value="LA6676-6"/>
<display value="Resistant"/>
</concept>
<concept>
<code value="LA6677-4"/>
<display value="Responsive"/>
</concept>
<concept>
<code value="LA9660-7"/>
<display value="Presumed resistant"/>
</concept>
<concept>
<code value="LA9661-5"/>
<display value="Presumed responsive"/>
</concept>
<concept>
<code value="LA6682-4"/>
<display value="Unknown Significance"/>
</concept>
<concept>
<code value="LA6675-8"/>
<display value="Benign"/>
</concept>
<concept>
<code value="LA6674-1"/>
<display value="Presumed Benign"/>
</concept>
<concept>
<code value="LA9662-3"/>
<display value="Presumed non-responsive"/>
</concept>
<concept>
<code value="LA25392-4"/>
<display value="Increased function"/>
</concept>
<concept>
<code value="LA25393-2"/>
<display value="Normal function"/>
</concept>
<concept>
<code value="LA25395-7"/>
<display value="Decreased function"/>
</concept>
<concept>
<code value="LA25394-0"/>
<display value="Poor function"/>
</concept>
</include>
<include>
<system value="http://snomed.info/sct"/>
<concept>
<code value="444734003"/>
<display
value="Does not meet eligibility criteria for clinical trial (finding)"/>
</concept>
<concept>
<code value="399223003"/>
<display value="Patient eligible for clinical trial (finding)"/>
</concept>
</include>
</compose>
</ValueSet>
IG © 2022+ HL7 Clinical Genomics Working Group. Package hl7.fhir.uv.genomics-reporting#2.0.0 based on FHIR 4.0.1. Generated 2022-05-09
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