ObservationCategoryCodes

Observation Category Codes

draftcomplete2 conceptsv4.0.1

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

Metadata

hl7.org/fhir
Canonical URL
http://hl7.org/fhir/secondary-finding
All-Codes Value Set
http://hl7.org/fhir/ValueSet/secondary-finding
ID
secondary-finding
Version
4.0.1
Publisher
FHIR Project team
Case Sensitive
Yes
In the unified registry

Concepts (2)

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