KIP Infrastructure
2.12.0 - ci-build

KIP Infrastructure, published by Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S. This guide is not an authorized publication; it is the continuous build for version 2.12.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/KIP-infrastructure/implementation-guide/ and changes regularly. See the Directory of published versions

: Cytogenetic changes - XML Representation

Active as of 2022-07-13

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<CodeSystem xmlns="http://hl7.org/fhir">
  <id value="CytogeneticChanges"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: CodeSystem CytogeneticChanges</b></p><a name="CytogeneticChanges"> </a><a name="hcCytogeneticChanges"> </a><p>This case-insensitive code system <code>https://kip.rkkp.dk/fhir/CodeSystem/CytogeneticChanges</code> defines the following codes:</p><table class="codes"><tr><td style="white-space:nowrap"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style="white-space:nowrap">hyperdiploidy<a name="CytogeneticChanges-hyperdiploidy"> </a></td><td>Hyperdiploidy</td><td>hyperdiploidi / hyperdiploidi / SNOMED-CT: 55597007</td></tr><tr><td style="white-space:nowrap">hypodiploidy<a name="CytogeneticChanges-hypodiploidy"> </a></td><td>Hypoploidy</td><td>Hypoploidy / hypodiploidi / SNOMED-CT: 15486006</td></tr><tr><td style="white-space:nowrap">pseudodiploidy<a name="CytogeneticChanges-pseudodiploidy"> </a></td><td>Pseudodiploidy</td><td>Pseudodiploidy / Pseudodiploidi</td></tr></table></div>
  </text>
  <url value="https://kip.rkkp.dk/fhir/CodeSystem/CytogeneticChanges"/>
  <version value="2.12.0"/>
  <name value="CytogeneticChanges"/>
  <title value="Cytogenetic changes"/>
  <status value="active"/>
  <date value="2022-07-13T00:00:00+02:00"/>
  <publisher
             value="Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S"/>
  <contact>
    <name
          value="Sundhedsvæsenets Kvalitetsinstitut with Trifork Digital Health A/S"/>
    <telecom>
      <system value="url"/>
      <value value="https://trifork.com"/>
    </telecom>
    <telecom>
      <system value="email"/>
      <value value="rbk@trifork.com"/>
    </telecom>
  </contact>
  <description value="Cytogenetic changes"/>
  <caseSensitive value="false"/>
  <content value="complete"/>
  <count value="3"/>
  <concept>
    <code value="hyperdiploidy"/>
    <display value="Hyperdiploidy"/>
    <definition value="hyperdiploidi / hyperdiploidi / SNOMED-CT: 55597007"/>
  </concept>
  <concept>
    <code value="hypodiploidy"/>
    <display value="Hypoploidy"/>
    <definition value="Hypoploidy / hypodiploidi / SNOMED-CT: 15486006"/>
  </concept>
  <concept>
    <code value="pseudodiploidy"/>
    <display value="Pseudodiploidy"/>
    <definition value="Pseudodiploidy / Pseudodiploidi"/>
  </concept>
</CodeSystem>