FHIR Cross-Version Extensions package for FHIR R4 from FHIR R4B - Version 0.0.1-snapshot-2. See the Directory of published versions

• Narrative Content
• XML
• JSON
• TTL

: Genetic Observation Secondary Findings - JSON Representation

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{
  "resourceType" : "CodeSystem",
  "id" : "secondary-finding",
  "text" : {
    "status" : "generated",
    "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>"
  },
  "extension" : [
    {
      "extension" : [
        {
          "url" : "packageId",
          "valueId" : "hl7.fhir.uv.xver-r4b.r4"
        },
        {
          "url" : "version",
          "valueString" : "0.0.1-snapshot-2"
        }
      ],
      "url" : "http://hl7.org/fhir/StructureDefinition/package-source"
    },
    {
      "url" : "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
      "valueCode" : "oo"
    }
  ],
  "url" : "http://hl7.org/fhir/secondary-finding",
  "version" : "4.3.0",
  "name" : "GeneticObservationSecondaryFindings",
  "title" : "Genetic Observation Secondary Findings",
  "status" : "draft",
  "experimental" : false,
  "date" : "2025-09-13T16:38:45-04:00",
  "publisher" : "Orders and Observations",
  "contact" : [
    {
      "name" : "Orders and Observations",
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://www.hl7.org/Special/committees/orders"
        }
      ]
    }
  ],
  "description" : "Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code" : "001",
          "display" : "World"
        }
      ]
    }
  ],
  "caseSensitive" : true,
  "valueSet" : "http://hl7.org/fhir/ValueSet/secondary-finding|5.2.0",
  "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"
    }
  ]
}