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Contents
{ "resourceType": "CodeSystem", "id": "secondary-finding", "meta": { "lastUpdated": "2019-11-01T09:29:23.356+11:00", "profile": [ "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ] }, "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" } ] }
Version data entries
7 entries across 7 versions & 1 rubygems