{
  "description": "Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.",
  "_filename": "CodeSystem-secondary-finding.json",
  "package_name": "hl7.fhir.r4b.core",
  "date": null,
  "meta": {
    "profile": [ "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ],
    "lastUpdated": "2021-03-11T17:06:20.662+11:00"
  },
  "publisher": null,
  "content": "complete",
  "name": "GeneticObservationSecondaryFindings",
  "type": null,
  "experimental": "false",
  "resourceType": "CodeSystem",
  "title": "Genetic Observation Secondary Findings",
  "package_version": "4.1.0",
  "extension": [ {
    "url": "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg",
    "valueCode": "oo"
  } ],
  "status": "draft",
  "id": "6cb1f1a4-050a-4689-9839-edbceee1a848",
  "valueSet": "http://hl7.org/fhir/ValueSet/secondary-finding",
  "kind": null,
  "url": "http://hl7.org/fhir/secondary-finding",
  "identifier": [ {
    "value": "urn:oid:2.16.840.1.113883.4.642.1.1286",
    "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": "4.1.0"
}