http://hl7.org/fhir/secondary-finding|4.0.1

{
  "description" : "Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.",
  "compose" : null,
  "package" : "hl7.fhir.r4.core@4.0.1",
  "date" : null,
  "meta" : {
    "profile" : [ "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ],
    "lastUpdated" : "2019-11-01T09:29:23.356+11:00"
  },
  "publisher" : "FHIR Project team",
  "content" : "complete",
  "name" : "ObservationCategoryCodes",
  "experimental" : false,
  "resourceType" : "CodeSystem",
  "title" : "Observation Category Codes",
  "supliment" : null,
  "status" : "draft",
  "id" : "7cc1e3aa-59f3-57ab-9008-2f3324dc107f",
  "valueSet" : "http://hl7.org/fhir/ValueSet/secondary-finding",
  "url" : "http://hl7.org/fhir/secondary-finding",
  "identifier" : [ {
    "value" : "urn:oid:2.16.840.1.113883.4.642.4.1286",
    "system" : "urn:ietf:rfc:3986"
  } ],
  "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"
  } ],
  "caseSensitive" : true,
  "version" : "4.0.1",
  "contact" : [ {
    "telecom" : [ {
      "value" : "http://hl7.org/fhir",
      "system" : "url"
    } ]
  } ]
}