FHIR Cross-Version Extensions package for FHIR R4 from FHIR R4B - Version 0.0.1-snapshot-2. See the Directory of published versions
: Genetic Observation Secondary Findings - TTL Representation
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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:CodeSystem ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "secondary-finding"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\">\n <p>This code system http://hl7.org/fhir/secondary-finding defines the following codes:</p>\n <table class=\"codes\">\n <tr>\n <td style=\"white-space:nowrap\">\n <b>Code</b>\n </td>\n <td>\n <b>Display</b>\n </td>\n <td>\n <b>Definition</b>\n </td>\n </tr>\n <tr>\n <td style=\"white-space:nowrap\">acmg-version1\n <a name=\"secondary-finding-acmg-version1\"> </a>\n </td>\n <td>ACMG Version 1</td>\n <td>First release (2013): ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727274/</td>\n </tr>\n <tr>\n <td style=\"white-space:nowrap\">acmg-version2\n <a name=\"secondary-finding-acmg-version2\"> </a>\n </td>\n <td>ACMG Version 2</td>\n <td>Second release (2016): Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. https://www.ncbi.nlm.nih.gov/pubmed/27854360</td>\n </tr>\n </table>\n </div>"^^rdf:XMLLiteral
] ; #
fhir:extension ( [
( fhir:extension [
fhir:url [ fhir:v "packageId"^^xsd:anyURI ] ;
fhir:value [
a fhir:id ;
fhir:v "hl7.fhir.uv.xver-r4b.r4" ] ] [
fhir:url [ fhir:v "version"^^xsd:anyURI ] ;
fhir:value [
a fhir:string ;
fhir:v "0.0.1-snapshot-2" ] ] ) ;
fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/package-source"^^xsd:anyURI ]
] [
fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg"^^xsd:anyURI ] ;
fhir:value [
a fhir:code ;
fhir:v "oo" ]
] ) ; #
fhir:url [ fhir:v "http://hl7.org/fhir/secondary-finding"^^xsd:anyURI] ; #
fhir:version [ fhir:v "4.3.0"] ; #
fhir:name [ fhir:v "GeneticObservationSecondaryFindings"] ; #
fhir:title [ fhir:v "Genetic Observation Secondary Findings"] ; #
fhir:status [ fhir:v "draft"] ; #
fhir:experimental [ fhir:v false] ; #
fhir:date [ fhir:v "2025-09-13T16:38:45-04:00"^^xsd:dateTime] ; #
fhir:publisher [ fhir:v "Orders and Observations"] ; #
fhir:contact ( [
fhir:name [ fhir:v "Orders and Observations" ] ;
( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "http://www.hl7.org/Special/committees/orders" ] ] )
] ) ; #
fhir:description [ fhir:v "Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding."] ; #
fhir:jurisdiction ( [
( fhir:coding [
fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm"^^xsd:anyURI ] ;
fhir:code [ fhir:v "001" ] ;
fhir:display [ fhir:v "World" ] ] )
] ) ; #
fhir:caseSensitive [ fhir:v true] ; #
fhir:valueSet [
fhir:v "http://hl7.org/fhir/ValueSet/secondary-finding|5.2.0"^^xsd:anyURI ;
fhir:link <http://hl7.org/fhir/ValueSet/secondary-finding|5.2.0>
] ; #
fhir:content [ fhir:v "complete"] ; #
fhir:concept ( [
fhir:code [ fhir:v "acmg-version1" ] ;
fhir:display [ fhir:v "ACMG Version 1" ] ;
fhir:definition [ fhir:v "First release (2013): ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727274/" ]
] [
fhir:code [ fhir:v "acmg-version2" ] ;
fhir:display [ fhir:v "ACMG Version 2" ] ;
fhir:definition [ fhir:v "Second release (2016): Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. https://www.ncbi.nlm.nih.gov/pubmed/27854360" ]
] ) . #
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