MII IG Kerndatensatz-Modul Molekulargenetischer Befundbericht - Downloaded Version 2027.0.0-ballot.1 See the Directory of published versions

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: Polygener Risiko Score BRCA1 Variante

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<RiskAssessment xmlns="http://hl7.org/fhir">
  <id value="mii-exa-molgen-prs-brca1"/>
  <meta>
    <profile
             value="https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/polygener-risiko-score|2027.0.0-ballot.1"/>
  </meta>
  <language value="en"/>
  <text>
    <status value="generated"/>
    <div xml:lang="en" lang="en"><hr/><p><b>English</b></p><hr/><p class="res-header-id"><b>Generated Narrative: RiskAssessment mii-exa-molgen-prs-brca1</b></p><a name="mii-exa-molgen-prs-brca1"> </a><a name="hcmii-exa-molgen-prs-brca1"> </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-polygener-risiko-score.html">MII PR MolGen Polygener Risiko Score</a> version: 2027.0.0-ballot.1</p></div><p><b>status</b>: Final</p><p><b>subject</b>: <a href="Patient-mii-exa-molgen-patient-2.html">Melanie Marie Müller (official) Female, DoB: 2021-09-19 ( Medical record number (use: usual, ))</a></p><p><b>occurrence</b>: 2022-11-01</p><p><b>basis</b>: <a href="Observation-mii-exa-molgen-variante-brca1.html">Observation Genetic variant assessment</a></p><h3>Predictions</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Extension</b></td><td><b>Outcome</b></td><td><b>QualitativeRisk</b></td></tr><tr><td style="display: none">*</td><td/><td><span title="Codes:{http://snomed.info/sct 718220008}">Hereditary breast and ovarian cancer syndrome (disorder)</span></td><td><span title="Codes:{http://terminology.hl7.org/CodeSystem/risk-probability high}">High likelihood</span></td></tr></table></div>
  </text>
  <status value="final"/>
  <subject>🔗 
    <reference value="Patient/mii-exa-molgen-patient-2"/>
  </subject>
  <occurrenceDateTime value="2022-11-01"/>
  <basis>🔗 
    <reference value="Observation/mii-exa-molgen-variante-brca1"/>
  </basis>
  <prediction>
    <extension
               url="https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/risk-assessment-einflussfaktor">
      <valueCodeableConcept>
        <coding>
          <system value="http://snomed.info/sct"/>
          <code value="414152003"/>
          <display value="European (ethnic group)"/>
        </coding>
        <text
              value="Der verwendete Polygene Risikoscore wurde bisher nur für die europäische Bevölkerung bei Brustkrebs validiert."/>
      </valueCodeableConcept>
    </extension>
    <outcome>
      <coding>
        <system value="http://snomed.info/sct"/>
        <code value="718220008"/>
        <display
                 value="Hereditary breast and ovarian cancer syndrome (disorder)"/>
      </coding>
    </outcome>
    <qualitativeRisk>
      <coding>
        <system
                value="http://terminology.hl7.org/CodeSystem/risk-probability"/>
        <code value="high"/>
        <display value="High likelihood"/>
      </coding>
    </qualitativeRisk>
  </prediction>
</RiskAssessment>