Vital Records Birth and Fetal Death Reporting
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This page is part of the Vital Records Birth and Fetal Death Reporting (v1.1.0: STU 1) 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 - Congenital Anomaly of Newborn - Baby G Quinn - TTL Representation

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@prefix fhir: <http://hl7.org/fhir/> .
@prefix loinc: <https://loinc.org/rdf/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix sct: <http://snomed.info/id/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

# - resource -------------------------------------------------------------------

 a fhir:Condition ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "condition-congenital-anomaly-of-newborn-babyg-quinn-2"] ; # 
  fhir:meta [
fhir:versionId [ fhir:v "3" ] ;
fhir:lastUpdated [ fhir:v "2023-04-18T10:17:36.911Z"^^xsd:dateTime ] ;
    ( fhir:profile [
fhir:v "http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn"^^xsd:anyURI ;
fhir:link <http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn>     ] )
  ] ; # 
  fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<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 &quot;condition-congenital-anomaly-of-newborn-babyg-quinn-2&quot; Version &quot;3&quot; Updated &quot;2023-04-18 10:17:36+0000&quot; </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> &quot; QUINN&quot;</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 &quot;Karyotype determination&quot;)</span></td></tr></table></div>"
  ] ; # 
  fhir:clinicalStatus [
    ( fhir:coding [
fhir:system [ fhir:v "http://terminology.hl7.org/CodeSystem/condition-clinical"^^xsd:anyURI ] ;
fhir:code [ fhir:v "active" ] ;
fhir:display [ fhir:v "Active" ]     ] ) ;
fhir:text [ fhir:v "Active" ]
  ] ; # 
  fhir:category ( [
    ( fhir:coding [
fhir:system [ fhir:v "http://terminology.hl7.org/CodeSystem/condition-category"^^xsd:anyURI ] ;
fhir:code [ fhir:v "problem-list-item" ] ;
fhir:display [ fhir:v "Problem List Item" ]     ] )
  ] [
    ( fhir:coding [
a loinc:73780-9 ;
fhir:system [ fhir:v "http://loinc.org"^^xsd:anyURI ] ;
fhir:code [ fhir:v "73780-9" ] ;
fhir:display [ fhir:v "Congenital anomalies of the newborn [US Standard Certificate of Live Birth]" ]     ] )
  ] ) ; # 
  fhir:code [
    ( fhir:coding [
a sct:70156005 ;
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
fhir:code [ fhir:v "70156005" ] ;
fhir:display [ fhir:v "Anomaly of chromosome pair 21 (disorder)" ]     ] ) ;
fhir:text [ fhir:v "Anomaly of chromosome pair 21 (disorder)" ]
  ] ; # 
  fhir:subject [
fhir:reference [ fhir:v "Patient/patient-child-babyg-quinn" ] ;
fhir:display [ fhir:v "Patient - Child (Baby G Quinn)" ]
  ] ; # 
  fhir:evidence ( [
    ( fhir:code [
      ( fhir:coding [
a sct:312948004 ;
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
fhir:code [ fhir:v "312948004" ] ;
fhir:display [ fhir:v "Karyotype determination" ]       ] ) ;
fhir:text [ fhir:v "Karyotype determination pending" ]     ] )
  ] ) . #