This page is part of the FHIR Specification (v1.6.0: STU 3 Ballot 4). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
Definition for Value SetLOINC 53037-8 answerlist
<ValueSet xmlns="http://hl7.org/fhir"> <id value="LOINC-53037-8-answerlist"/> <meta> <lastUpdated value="2016-08-11T17:02:54.322+10:00"/> <profile value="http://hl7.org/fhir/StructureDefinition/valueset-shareable-definition"/> </meta> <text> <status value="extensions"/> <div xmlns="http://www.w3.org/1999/xhtml"> <h2>LOINC 53037-8 answerlist</h2> <div> <p>LOINC answer list for Genetic disease sequence variation interpretation</p> </div> <p> <b>Copyright Statement:</b> This content LOINC® is copyright © 1995 Regenstrief Institute, Inc. and the LOINC Committee, and available at no cost under the license at http://loinc.org/terms-of-use </p> <p>This value set includes codes from the following code systems:</p> <ul> <li>Include these codes as defined in http://loinc.org <table> <tr> <td> <b>Code</b> </td> <td> <b>Display</b> </td> <td> <b>Definition</b> </td> </tr> <tr> <td>LA6668-3</td> <td>Pathogenic</td> <td>Pathogenic</td> </tr> <tr> <td>LA6669-1</td> <td>Presumed pathogenic</td> <td>Presumed pathogenic</td> </tr> <tr> <td>LA6682-4</td> <td>Unknown significance</td> <td>Unknown significance</td> </tr> <tr> <td>LA6675-8</td> <td>Benign</td> <td>Benign</td> </tr> <tr> <td>LA6674-1</td> <td>Presumed benign</td> <td>Presumed benign</td> </tr> </table> </li> </ul> </div> </text> <url value="http://hl7.org/fhir/ValueSet/LOINC-53037-8-answerlist"/> <identifier> <system value="urn:ietf:rfc:3986"/> <value value="urn:oid:2.16.840.1.113883.4.642.2.511"/> </identifier> <version value="1.6.0"/> <name value="LOINC 53037-8 answerlist"/> <status value="draft"/> <experimental value="false"/> <publisher value="HL7 (FHIR Project)"/> <contact> <telecom> <system value="other"/> <value value="http://hl7.org/fhir"/> </telecom> <telecom> <system value="email"/> <value value="fhir@lists.hl7.org"/> </telecom> </contact> <date value="2016-08-11T17:02:54+10:00"/> <description value="LOINC answer list for Genetic disease sequence variation interpretation"/> <copyright value="This content LOINC® is copyright © 1995 Regenstrief Institute, Inc. and the LOINC Committee, and available at no cost under the license at http://loinc.org/terms-of-use"/> <compose> <include> <system value="http://loinc.org"/> <concept> <extension url="http://hl7.org/fhir/StructureDefinition/valueset-definition"> <valueString value="Pathogenic"/> </extension> <code value="LA6668-3"/> <display value="Pathogenic"/> </concept> <concept> <extension url="http://hl7.org/fhir/StructureDefinition/valueset-definition"> <valueString value="Presumed pathogenic"/> </extension> <code value="LA6669-1"/> <display value="Presumed pathogenic"/> </concept> <concept> <extension url="http://hl7.org/fhir/StructureDefinition/valueset-definition"> <valueString value="Unknown significance"/> </extension> <code value="LA6682-4"/> <display value="Unknown significance"/> </concept> <concept> <extension url="http://hl7.org/fhir/StructureDefinition/valueset-definition"> <valueString value="Benign"/> </extension> <code value="LA6675-8"/> <display value="Benign"/> </concept> <concept> <extension url="http://hl7.org/fhir/StructureDefinition/valueset-definition"> <valueString value="Presumed benign"/> </extension> <code value="LA6674-1"/> <display value="Presumed benign"/> </concept> </include> </compose> </ValueSet>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.