Observation Category Codes

{
  "description" : "Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.",
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    "lastUpdated" : "2019-11-01T09:29:23.356+11:00",
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  "name" : "ObservationCategoryCodes",
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  "resourceType" : "CodeSystem",
  "title" : "Observation Category Codes",
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  "valueSet" : "http://hl7.org/fhir/ValueSet/secondary-finding",
  "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"
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    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\">\n            <h2>Observation Category Codes</h2>\n            <div>\n              <p>Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.</p>\n\n            </div>\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>",
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