Release 4B 5 Ballot

This page is part of the FHIR Specification (v4.3.0: R4B (v5.0.0-ballot: R5 Ballot - STU see ballot notes ). The current version which supercedes this version is 5.0.0 . For a full list of available versions, see the Directory of published versions . Page versions: R4B R4

Using Codes Code Systems Value Sets Concept Maps Identifier Systems

4.4.1.558 4.4.1.325 Value Set ValueSet http://hl7.org/fhir/ValueSet/secondary-finding

Orders and Observations icon Work Group   Maturity Level : 0 Informative Use Context : Any

This is a value set defined by the FHIR project.

Summary

Defining URL: http://hl7.org/fhir/ValueSet/secondary-finding
Version: 4.3.0 5.0.0-ballot
Name: ObservationCategoryCodes GeneticObservationSecondaryFindings
Title: Genetic Observation Category Codes Secondary Findings
Status: draft
Definition:

Codes to denote a guideline or policy statement.when statement when a genetic test result is being shared as a secondary finding.

Committee: Orders and Observations icon Work Group
OID: 2.16.840.1.113883.4.642.3.1285 (for OID based terminology systems)
Source Resource Flags: XML / JSON

This value set is used in the following places:

4.4.1.558.1 4.4.1.325.1 Content Logical Definition

 

4.4.1.558.2 4.4.1.325.2 Expansion

This expansion generated 28 May 10 Sep 2022

This value set contains 2 concepts

Expansion based on Genetic Observation Secondary Findings v4.3.0 v5.0.0-ballot (CodeSystem)

All codes in this table are from the system http://hl7.org/fhir/secondary-finding
Code System Display Definition
   acmg-version1 http://hl7.org/fhir/secondary-finding ACMG Version 1

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/

   acmg-version2 http://hl7.org/fhir/secondary-finding ACMG Version 2

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

 

See the full registry of value sets defined as part of FHIR.

Explanation of the columns that may appear on this page:

Lvl A few code lists that FHIR defines are hierarchical - each code is assigned a level. For value sets, levels are mostly used to organize codes for user convenience, but may follow code system hierarchy - see Code System for further information
Source The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance). If the code is in italics, this indicates that the code is not selectable ('Abstract')
Display The display (used in the display element of a Coding ). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code