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

: PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale - XML Representation

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<RiskAssessment xmlns="http://hl7.org/fhir">
  <id value="PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale"/>
  <meta>
    <versionId value="1"/>
    <lastUpdated value="2024-09-25T00:01:34.798+00:00"/>
    <source value="#hrQE3dHjuHuJ5zkf"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: RiskAssessment PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale</b></p><a name="PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale"> </a><a name="hcPrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale"> </a><a name="PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale-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 00:01:34+0000; </p><p style="margin-bottom: 0px">Information Source: #hrQE3dHjuHuJ5zkf</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>: 2024-07-09</p><p><b>basis</b>: <a href="Observation-PrenatalVariantAutosomalRecessiveSAoCSPatientMale.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 autosomal recessive spastic ataxia of Charlevoix-Saguenay</span></td><td>0.00002277238382929289</td></tr></table></div>
  </text>
  <status value="final"/>
  <subject>🔗 
    <reference value="Patient/PatientMale"/>
  </subject>
  <occurrenceDateTime value="2024-07-09"/>
  <basis>🔗 
    <reference
               value="Observation/PrenatalVariantAutosomalRecessiveSAoCSPatientMale"/>
  </basis>
  <prediction>
    <outcome>
      <text
            value="Patient has a disease-causing mutation for autosomal recessive spastic ataxia of Charlevoix-Saguenay"/>
    </outcome>
    <probabilityDecimal value="0.00002277238382929289"/>
  </prediction>
</RiskAssessment>