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. For a full list of available versions, see the Directory of published versions 
{
"resourceType" : "ValueSet",
"id" : "genetic-therapeutic-implications-vs",
"text" : {
"status" : "generated",
"div" : "<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>"
},
"url" : "http://hl7.org/fhir/uv/genomics-reporting/ValueSet/genetic-therapeutic-implications-vs",
"version" : "2.0.0",
"name" : "GeneticTherapeuticImplicationsVS",
"title" : "Genetic Therapeutic Implications",
"status" : "active",
"date" : "2022-05-09T16:59:16+00:00",
"publisher" : "HL7 Clinical Genomics Working Group",
"contact" : [
{
"name" : "HL7 Clinical Genomics Working Group",
"telecom" : [
{
"system" : "url",
"value" : "http://www.hl7.org/Special/committees/clingenomics"
},
{
"system" : "email",
"value" : "cg@lists.HL7.org"
}
]
}
],
"description" : "Value Set for terms that describe a predicted ramification based on the presence of associated molecular finding(s).",
"jurisdiction" : [
{
"coding" : [
{
"system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
"code" : "001",
"display" : "World"
}
]
}
],
"copyright" : "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.\nThis 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" : "http://loinc.org",
"concept" : [
{
"code" : "LA10315-2",
"display" : "Ultrarapid metabolizer"
},
{
"code" : "LA25391-6",
"display" : "Normal metabolizer"
},
{
"code" : "LA25390-8",
"display" : "Rapid metabolizer"
},
{
"code" : "LA10317-8",
"display" : "Intermediate metabolizer"
},
{
"code" : "LA9657-3",
"display" : "Poor metabolizer"
},
{
"code" : "LA19542-2",
"display" : "Low Risk"
},
{
"code" : "LA19541-4",
"display" : "High Risk"
},
{
"code" : "LA6676-6",
"display" : "Resistant"
},
{
"code" : "LA6677-4",
"display" : "Responsive"
},
{
"code" : "LA9660-7",
"display" : "Presumed resistant"
},
{
"code" : "LA9661-5",
"display" : "Presumed responsive"
},
{
"code" : "LA6682-4",
"display" : "Unknown Significance"
},
{
"code" : "LA6675-8",
"display" : "Benign"
},
{
"code" : "LA6674-1",
"display" : "Presumed Benign"
},
{
"code" : "LA9662-3",
"display" : "Presumed non-responsive"
},
{
"code" : "LA25392-4",
"display" : "Increased function"
},
{
"code" : "LA25393-2",
"display" : "Normal function"
},
{
"code" : "LA25395-7",
"display" : "Decreased function"
},
{
"code" : "LA25394-0",
"display" : "Poor function"
}
]
},
{
"system" : "http://snomed.info/sct",
"concept" : [
{
"code" : "444734003",
"display" : "Does not meet eligibility criteria for clinical trial (finding)"
},
{
"code" : "399223003",
"display" : "Patient eligible for clinical trial (finding)"
}
]
}
]
}
}
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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