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 - 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: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 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>"
] ; #
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" ] ] )
] ) . #
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