UV_Vital Records Birth and Fetal Death Reporting, published by IHE International. This guide is not an authorized publication; it is the continuous build for version 1.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/IHE/fhir-bfdr/ and changes regularly. See the Directory of published versions

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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="https://profiles.ihe.net/QRPH/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn"/>
  </meta>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: Condition condition-congenital-anomaly-of-newborn-babyg-quinn-2</b></p><a name="condition-congenital-anomaly-of-newborn-babyg-quinn-2"> </a><a name="hccondition-congenital-anomaly-of-newborn-babyg-quinn-2"> </a><a name="hccondition-congenital-anomaly-of-newborn-babyg-quinn-2-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: versionId: id (PrimitiveType/Condition.meta.versionId): element = id -&gt; versionId=id[3]; Last updated: 2023-04-18 10:17:36+0000</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>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}">Active</span></p><p><b>category</b>: <span title="Codes:{http://terminology.hl7.org/CodeSystem/condition-category problem-list-item}">Problem List Item</span>, <span title="Codes:{http://loinc.org 73780-9}">Congenital anomalies of the newborn [US Standard Certificate of Live Birth]</span></p><p><b>code</b>: <span title="Codes:{http://snomed.info/sct 70156005}">Anomaly of chromosome pair 21 (disorder)</span></p><p><b>subject</b>: <a href="Patient-patient-child-babyg-quinn.html">Patient - Child (Baby G Quinn)</a></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><span title="Codes:{http://snomed.info/sct 312948004}">Karyotype determination pending</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>