This page is part of the Vital Records Birth and Fetal Death Reporting (v1.0.0: STU 1 on FHIR R4) based on FHIR 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 xmlns="http://hl7.org/fhir">
<id value="condition-congenital-anomaly-of-newborn-babyg-quinn"/>
<meta>
<versionId value="1"/>
<lastUpdated value="2020-08-10T06:40:28.557+00:00"/>
<source value="#Yb3Kll5UAFaWEn6C"/>
<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 12770006}">Cyanotic congenital heart disease (disorder)</span></p><p><b>subject</b>: <a href="Patient-patient-child-babyg-quinn.html">BabyG Quinn. Generated Summary: Medical Record Number: 9932702 (USUAL); Baby G Quinn ; gender: female; birthDate: 2019-02-12; 1</a></p></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="12770006"/>
<display value="Cyanotic congenital heart disease (disorder)"/>
</coding>
<text value="Cyanotic congenital heart disease (disorder)"/>
</code>
<subject>
<reference value="Patient/patient-child-babyg-quinn"/>
<display value="BabyG Quinn"/>
</subject>
</Condition>