Vital Records Birth and Fetal Death Reporting
0.1.0 - STU 1 Ballot

This page is part of the Vital Records Birth and Fetal Death Reporting (v0.1.0: STU 1 on FHIR R4 Ballot 1) based on FHIR R4. The current version which supercedes this version is 1.0.0. For a full list of available versions, see the Directory of published versions

: Condition - Congenital Anomaly of Newborn example [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="2"/>
    <lastUpdated value="2020-08-20T23:20:37.897+00:00"/>
    <source value="#8nHKxfsyONG1qyLw"/>
    <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</b></p><p><b>category</b>: <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). Generated Summary: Medical Record Number: 9932702 (USUAL); Baby G Quinn ; gender: female; birthDate: 2019-02-12; 1</a></p><h3>Evidences</h3><table class="grid"><tr><td>-</td><td><b>Code</b></td></tr><tr><td>*</td><td><span title="Codes: {http://snomed.info/sct 312948004}">Karyotype determination pending</span></td></tr></table></div>
  </text>
  <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>