Definition for Code SystemGeneticObservationSecondaryFindings

{
  "resourceType" : "CodeSystem",
  "id" : "secondary-finding",
  "meta" : {
    "lastUpdated" : "2022-09-10T04:52:37.223+10:00",
    "profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]
  },
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This code system <code>http://hl7.org/fhir/secondary-finding</code> defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style=\"white-space:nowrap\">acmg-version1<a name=\"secondary-finding-acmg-version1\"> </a></td><td>ACMG Version 1</td><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></tr><tr><td style=\"white-space:nowrap\">acmg-version2<a name=\"secondary-finding-acmg-version2\"> </a></td><td>ACMG Version 2</td><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></tr></table></div>"
  },
  "extension" : [{
    "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
    "valueCode" : "oo"
  }],
  "url" : "http://hl7.org/fhir/secondary-finding",
  "identifier" : [{
    "system" : "urn:ietf:rfc:3986",
    "value" : "urn:oid:2.16.840.1.113883.4.642.4.1286"
  }],
  "version" : "5.0.0-ballot",
  "name" : "GeneticObservationSecondaryFindings",
  "title" : "Genetic Observation Secondary Findings",
  "status" : "draft",
  "experimental" : false,
  "description" : "Codes to denote a guideline or policy statement when a genetic test result is being shared as a secondary finding.",
  "caseSensitive" : true,
  "valueSet" : "http://hl7.org/fhir/ValueSet/secondary-finding",
  "content" : "complete",
  "concept" : [{
    "code" : "acmg-version1",
    "display" : "ACMG Version 1",
    "definition" : "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/"
  },
  {
    "code" : "acmg-version2",
    "display" : "ACMG Version 2",
    "definition" : "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"
  }]
}