|Vocabulary Work Group||Maturity Level : 0||Informative||Use Context : Any|
This is a code system defined by the FHIR project.
|Title:||Observation Category Codes|
Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding.
|Source Resource||XML / JSON|
This Code system is used in the following value sets:
|acmg-version1||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||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 code systems defined as part of FHIR.
Explanation of the columns that may appear on this page:
|Level||A few code lists that FHIR defines are hierarchical - each code is assigned a level. 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|