Birth And Fetal Death (BFDR) FHIR Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
<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"/>
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<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>