Birth And Fetal Death (BFDR) FHIR Implementation Guide
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This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0: STU2) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

: 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>
    <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 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="condition-congenital-anomaly-of-newborn-babyg-quinn-2-en-US"> </a><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>