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. Page versions: R4B R4
| Vocabulary Work Group | Maturity Level: N/A | Standards Status: Informative |
Raw JSON (canonical form + also see JSON Format Specification)
Definition for Code System ObservationCategoryCodes
{
"resourceType" : "CodeSystem",
"id" : "secondary-finding",
"meta" : {
"lastUpdated" : "2019-11-01T09:29:23.356+11:00",
"profile" : ["http://hl7.org/fhir/StructureDefinition/shareablecodesystem"]
},
"text" : {
"status" : "generated",
"div" : "<div>!-- Snipped for Brevity --></div>"
},
"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" : "4.0.1",
"name" : "ObservationCategoryCodes",
"title" : "Observation Category Codes",
"status" : "draft",
"experimental" : false,
"publisher" : "FHIR Project team",
"contact" : [{
"telecom" : [{
"system" : "url",
"value" : "http://hl7.org/fhir"
}]
}],
"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"
}]
}
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.