GenomeX Data Exchange FHIR IG, published by MITRE. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/CodeX-HL7-FHIR-Accelerator/GenomeX-DataExchange/ and changes regularly. See the Directory of published versions

• Narrative Content
• XML
• JSON

: PrenatalResidualRiskFactorXiDeficiencyPatientMale - XML Representation

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<RiskAssessment xmlns="http://hl7.org/fhir">
  <id value="PrenatalResidualRiskFactorXiDeficiencyPatientMale"/>
  <meta>
    <versionId value="1"/>
    <lastUpdated value="2024-09-25T00:02:13.030+00:00"/>
    <source value="#mzuK1EHcvMPipAda"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: RiskAssessment PrenatalResidualRiskFactorXiDeficiencyPatientMale</b></p><a name="PrenatalResidualRiskFactorXiDeficiencyPatientMale"> </a><a name="hcPrenatalResidualRiskFactorXiDeficiencyPatientMale"> </a><a name="PrenatalResidualRiskFactorXiDeficiencyPatientMale-en-US"> </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">version: 1; Last updated: 2024-09-25 00:02:13+0000; </p><p style="margin-bottom: 0px">Information Source: #mzuK1EHcvMPipAda</p></div><p><b>status</b>: Final</p><p><b>subject</b>: <a href="Patient-PatientMale.html">Higado Sobreviviente (official) Male, DoB: 1996-05-13 ( Patient ID: fec6172efdca41b4a13341e75cb62e0f (use: official, ))</a></p><p><b>occurrence</b>: 2024-06-26</p><p><b>basis</b>: <a href="Observation-PrenatalVariant1CNVFactorXiDeficiencyPatientMale.html">Observation Genetic variant assessment</a></p><h3>Predictions</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Outcome</b></td><td><b>Probability[x]</b></td></tr><tr><td style="display: none">*</td><td><span title="Codes:">Patient has a disease-causing mutation for factor XI deficiency</span></td><td>1</td></tr></table></div>
  </text>
  <status value="final"/>
  <subject>🔗 
    <reference value="Patient/PatientMale"/>
  </subject>
  <occurrenceDateTime value="2024-06-26"/>
  <basis>🔗 
    <reference
               value="Observation/PrenatalVariant1CNVFactorXiDeficiencyPatientMale"/>
  </basis>
  <prediction>
    <outcome>
      <text
            value="Patient has a disease-causing mutation for factor XI deficiency"/>
    </outcome>
    <probabilityDecimal value="1"/>
  </prediction>
</RiskAssessment>