MII IG Kerndatensatz-Modul Molekulares Tumorboard, published by Medizininformatik-Initiative. This guide is not an authorized publication; it is the continuous build for version 2026.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/medizininformatik-initiative/kerndatensatzmodul-molekulares-tumorboard/ and changes regularly. See the Directory of published versions

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: MII CS Genomic Analysis Method Type - XML Representation

Active as of 2026-02-09

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="mii-cs-mtb-genomic-analysis-method-type"/>
  <language value="de-DE"/>
  <text>
    <status value="generated"/>
    <div xml:lang="de-DE" xmlns="http://www.w3.org/1999/xhtml" lang="de-DE"><p class="res-header-id"><b>Generated Narrative: CodeSystem mii-cs-mtb-genomic-analysis-method-type</b></p><a name="mii-cs-mtb-genomic-analysis-method-type"> </a><a name="hcmii-cs-mtb-genomic-analysis-method-type"> </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">Language: de-DE</p></div><p>This case-sensitive code system <code>https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomic-analysis-method-type</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style="white-space:nowrap">tngs<a name="mii-cs-mtb-genomic-analysis-method-type-tngs"> </a></td><td>Targeted NGS</td></tr><tr><td style="white-space:nowrap">gene-panel<a name="mii-cs-mtb-genomic-analysis-method-type-gene-panel"> </a></td><td>Genpanel</td></tr><tr><td style="white-space:nowrap">fusion-detection-panel<a name="mii-cs-mtb-genomic-analysis-method-type-fusion-detection-panel"> </a></td><td>Fusions-Detektions-Panel</td></tr><tr><td style="white-space:nowrap">whole-genom-sequencing<a name="mii-cs-mtb-genomic-analysis-method-type-whole-genom-sequencing"> </a></td><td>Whole Genom Sequencing (WGS)</td></tr><tr><td style="white-space:nowrap">whole-exom-sequencing<a name="mii-cs-mtb-genomic-analysis-method-type-whole-exom-sequencing"> </a></td><td>Whole Exom Sequencing (WES)</td></tr><tr><td style="white-space:nowrap">rnaseq-transcriptomics<a name="mii-cs-mtb-genomic-analysis-method-type-rnaseq-transcriptomics"> </a></td><td>RNA Sequencing (RNA-Seq)</td></tr></table></div>
  </text>
  <url
       value="https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomic-analysis-method-type"/>
  <version value="2026.0.0"/>
  <name value="MII_CS_MTB_Genomic_Analysis_Method_Type"/>
  <title value="MII CS Genomic Analysis Method Type"/>
  <status value="active"/>
  <experimental value="false"/>
  <date value="2026-02-09T10:07:17+00:00"/>
  <publisher value="Medizininformatik-Initiative"/>
  <contact>
    <name value="Medizininformatik-Initiative"/>
    <telecom>
      <system value="url"/>
      <value value="https://www.medizininformatik-initiative.de"/>
    </telecom>
  </contact>
  <description
               value="Codesystem, welches die verwendeten NGS-Methodiken gemäß dnpm-Kodierung high-level auflistet"/>
  <jurisdiction>
    <coding>
      <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/>
      <code value="276"/>
    </coding>
  </jurisdiction>
  <caseSensitive value="true"/>
  <content value="complete"/>
  <count value="6"/>
  <concept>
    <code value="tngs"/>
    <display value="Targeted NGS"/>
  </concept>
  <concept>
    <code value="gene-panel"/>
    <display value="Genpanel"/>
  </concept>
  <concept>
    <code value="fusion-detection-panel"/>
    <display value="Fusions-Detektions-Panel"/>
  </concept>
  <concept>
    <code value="whole-genom-sequencing"/>
    <display value="Whole Genom Sequencing (WGS)"/>
  </concept>
  <concept>
    <code value="whole-exom-sequencing"/>
    <display value="Whole Exom Sequencing (WES)"/>
  </concept>
  <concept>
    <code value="rnaseq-transcriptomics"/>
    <display value="RNA Sequencing (RNA-Seq)"/>
  </concept>
</CodeSystem>