MII Implementierungsleitfaden Kerndatensatz-Modul Molekulargenetischer Befundbericht
2027.0.0-ballot.1 - Germany

This page is part of the MII IG Kerndatensatz-Modul Molekulargenetischer Befundbericht (v2027.0.0-ballot.1: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: Anforderung Whole Exome Sequencing

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  <id value="mii-exa-molgen-anforderung-wes"/>
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    <profile
             value="https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/anforderung-genetischer-test|2027.0.0-ballot.1"/>
  </meta>
  <language value="de"/>
  <text>
    <status value="generated"/>
    <div xml:lang="de" lang="de"><hr/><p><b>German</b></p><hr/><p class="res-header-id"><b>Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-wes</b></p><a name="de-mii-exa-molgen-anforderung-wes"> </a><a name="de-hcmii-exa-molgen-anforderung-wes"> </a><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px"/><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-mii-pr-molgen-anforderung-genetischer-test.html">MII PR MolGen Anforderung genetischer Test</a> version: 2027.0.0-ballot.1</p></div><p><b>status</b>: Completed</p><p><b>intent</b>: Order</p><p><b>code</b>: <span title="Codes:{http://loinc.org 86205-2}">Whole exome sequence analysis in Blood or Tissue by Molecular genetics method</span></p><p><b>subject</b>: <a href="Patient-mii-exa-molgen-patient.html">Maja Julia Van-der-Dussen (official) Female, DoB: 1968-09-19 ( Krankenaktennummer (use: usual, ))</a></p><p><b>authoredOn</b>: 2024-01-10</p><p><b>requester</b>: <a href="Practitioner-mii-exa-molgen-practitioner-ordering.html">Practitioner Klaus Müller </a></p><p><b>reasonCode</b>: <span title="Codes:{http://snomed.info/sct 224958001}">Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH</span></p></div>
  </text>
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      <system value="http://loinc.org"/>
      <code value="86205-2"/>
      <display
               value="Whole exome sequence analysis in Blood or Tissue by Molecular genetics method"/>
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  </code>
  <subject>🔗 
    <reference value="Patient/mii-exa-molgen-patient"/>
  </subject>
  <authoredOn value="2024-01-10"/>
  <requester>🔗 
    <reference value="Practitioner/mii-exa-molgen-practitioner-ordering"/>
  </requester>
  <reasonCode>
    <coding>
      <system value="http://snomed.info/sct"/>
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      <display value="Global developmental delay"/>
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</ServiceRequest>