This page is part of the Vital Records Birth and Fetal Death Reporting (v2.0.0-ballot: STU 2 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 1.1.0. 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><b>Generated Narrative: Condition</b><a name="condition-congenital-anomaly-of-newborn-babyg-quinn-2"> </a></p><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">Resource Condition "condition-congenital-anomaly-of-newborn-babyg-quinn-2" </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>: Active <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.0.0/CodeSystem-condition-clinical.html">Condition Clinical Status Codes</a>#active)</span></p><p><b>category</b>: Problem List Item <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="http://terminology.hl7.org/5.0.0/CodeSystem-condition-category.html">Condition Category Codes</a>#problem-list-item)</span>, Congenital anomalies of the newborn [US Standard Certificate of Live Birth] <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://loinc.org/">LOINC</a>#73780-9)</span></p><p><b>code</b>: Anomaly of chromosome pair 21 (disorder) <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#70156005)</span></p><p><b>subject</b>: <a href="Patient-patient-child-babyg-quinn.html">Patient/patient-child-babyg-quinn: Patient - Child (Baby G Quinn)</a> " QUINN"</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>Karyotype determination pending <span style="background: LightGoldenRodYellow; margin: 4px; border: 1px solid khaki"> (<a href="https://browser.ihtsdotools.org/">SNOMED CT</a>#312948004 "Karyotype determination")</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>