MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot - Germany

MII IG Kerndatensatz-Modul Seltene Erkrankungen - Downloaded Version 2027.0.0-ballot See the Directory of published versions

: Marfan-Syndrom - Genetische Diagnose

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<Condition xmlns="http://hl7.org/fhir">
  <id value="mii-exa-seltene-condition-marfan-genetic"/>
  <meta>
    <profile
             value="https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/StructureDefinition/mii-pr-seltene-genetic-diagnosis|2027.0.0-ballot"/>
  </meta>
  <language value="de"/>
  <text>
    <status value="extensions"/>
    <div xml:lang="de" lang="de"><hr/><p><b>German</b></p><hr/><p class="res-header-id"><b>Generated Narrative: Condition mii-exa-seltene-condition-marfan-genetic</b></p><a name="de-mii-exa-seltene-condition-marfan-genetic"> </a><a name="de-hcmii-exa-seltene-condition-marfan-genetic"> </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-seltene-genetic-diagnosis.html">MII PR SE Genetic Diagnosis</a> version: 2027.0.0-ballot</p></div><p><b>Condition Asserted Date</b>: 2024-12-20</p><p><b>clinicalStatus</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}">Active</span></p><p><b>verificationStatus</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-ver-status confirmed}">Confirmed</span></p><p><b>category</b>: <span title="Codes:{http://snomed.info/sct 782964007}">Genetic disease</span></p><p><b>code</b>: <span title="Codes:{http://omim.org 154700}, {http://snomed.info/sct 19346006}, {http://www.orpha.net 558}">Marfan-Syndrom - genetisch bestätigt</span></p><p><b>subject</b>: <a href="Patient-mii-exa-seltene-patient-marfan-001.html">Anonymous Patient Male, DoB: 2005-01-01 ( https://www.medizininformatik-initiative.de/fhir/sid/patient-id#MRF-2024-001)</a></p><p><b>recordedDate</b>: 2024-12-20</p><h3>Evidences</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Code</b></td><td><b>Detail</b></td></tr><tr><td style="display: none">*</td><td><span title="Codes:{http://snomed.info/sct 106221001}">Genetic finding</span></td><td><a href="Observation-mii-exa-seltene-variant-fbn1-001.html">Observation Genetic analysis master panel</a></td></tr></table><p><b>note</b>: </p><blockquote><div><p>FBN1-Mutation c.3217G&gt;A (p.Gly1073Arg) nachgewiesen, krankheitsursächlich. Genetische Diagnose existiert parallel zur klinischen Diagnose.</p>
</div></blockquote></div>
  </text>
  <extension
             url="http://hl7.org/fhir/StructureDefinition/condition-assertedDate">
    <valueDateTime value="2024-12-20"/>
  </extension>
  <clinicalStatus>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-clinical"/>
      <code value="active"/>
    </coding>
  </clinicalStatus>
  <verificationStatus>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-ver-status"/>
      <code value="confirmed"/>
    </coding>
  </verificationStatus>
  <category>
    <coding>
      <system value="http://snomed.info/sct"/>
      <code value="782964007"/>
      <display value="Genetic disease"/>
    </coding>
  </category>
  <code>
    <coding>
      <system value="http://omim.org"/>
      <version value="2024"/>
      <code value="154700"/>
      <display value="Marfan syndrome"/>
    </coding>
    <coding>
      <system value="http://snomed.info/sct"/>
      <code value="19346006"/>
      <display value="Marfan syndrome"/>
    </coding>
    <coding>
      <system value="http://www.orpha.net"/>
      <code value="558"/>
      <display value="Marfan syndrome"/>
    </coding>
    <text value="Marfan-Syndrom - genetisch bestätigt"/>
  </code>
  <subject>🔗 
    <reference value="Patient/mii-exa-seltene-patient-marfan-001"/>
  </subject>
  <recordedDate value="2024-12-20"/>
  <evidence>
    <code>
      <coding>
        <system value="http://snomed.info/sct"/>
        <code value="106221001"/>
        <display value="Genetic finding"/>
      </coding>
    </code>
    <detail>🔗 
      <reference value="Observation/mii-exa-seltene-variant-fbn1-001"/>
    </detail>
  </evidence>
  <note>
    <text
          value="FBN1-Mutation c.3217G&gt;A (p.Gly1073Arg) nachgewiesen, krankheitsursächlich. Genetische Diagnose existiert parallel zur klinischen Diagnose."/>
  </note>
</Condition>