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: Condition - Congenital Anomaly of Newborn - Baby G Quinn - XML Representation

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<Condition xmlns="http://hl7.org/fhir">
  <id value="condition-congenital-anomaly-of-newborn-babyg-quinn-2"/>
  <meta>
    <versionId value="3"/>
    <lastUpdated value="2023-04-18T10:17:36.911Z"/>
    <profile
             value="http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative: Condition</b><a name="condition-congenital-anomaly-of-newborn-babyg-quinn-2"> </a></p><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">Resource Condition &quot;condition-congenital-anomaly-of-newborn-babyg-quinn-2&quot; Version &quot;3&quot; Updated &quot;2023-04-18 10:17:36+0000&quot; </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-Condition-congenital-anomaly-of-newborn.html">Condition - Congenital Anomaly of Newborn</a></p></div><p><b>clinicalStatus</b>: Active <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.0.0/CodeSystem-condition-clinical.html">Condition Clinical Status Codes</a>#active)</span></p><p><b>category</b>: Problem List Item <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.0.0/CodeSystem-condition-category.html">Condition Category Codes</a>#problem-list-item)</span>, Congenital anomalies of the newborn [US Standard Certificate of Live Birth] <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a>#73780-9)</span></p><p><b>code</b>: Anomaly of chromosome pair 21 (disorder) <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#70156005)</span></p><p><b>subject</b>: <a href="Patient-patient-child-babyg-quinn.html">Patient/patient-child-babyg-quinn: Patient - Child (Baby G Quinn)</a> &quot; QUINN&quot;</p><h3>Evidences</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Code</b></td></tr><tr><td style="display: none">*</td><td>Karyotype determination pending <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#312948004 &quot;Karyotype determination&quot;)</span></td></tr></table></div>
  </text>
  <clinicalStatus>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-clinical"/>
      <code value="active"/>
      <display value="Active"/>
    </coding>
    <text value="Active"/>
  </clinicalStatus>
  <category>
    <coding>
      <system
              value="http://terminology.hl7.org/CodeSystem/condition-category"/>
      <code value="problem-list-item"/>
      <display value="Problem List Item"/>
    </coding>
  </category>
  <category>
    <coding>
      <system value="http://loinc.org"/>
      <code value="73780-9"/>
      <display
               value="Congenital anomalies of the newborn [US Standard Certificate of Live Birth]"/>
    </coding>
  </category>
  <code>
    <coding>
      <system value="http://snomed.info/sct"/>
      <code value="70156005"/>
      <display value="Anomaly of chromosome pair 21 (disorder)"/>
    </coding>
    <text value="Anomaly of chromosome pair 21 (disorder)"/>
  </code>
  <subject>
    <reference value="Patient/patient-child-babyg-quinn"/>
    <display value="Patient - Child (Baby G Quinn)"/>
  </subject>
  <evidence>
    <code>
      <coding>
        <system value="http://snomed.info/sct"/>
        <code value="312948004"/>
        <display value="Karyotype determination"/>
      </coding>
      <text value="Karyotype determination pending"/>
    </code>
  </evidence>
</Condition>