Profile Comparison between http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding vs http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding

Messages

Metadata

Name	Value		Comments
abstract	false
baseDefinition	http://hl7.org/fhir/StructureDefinition/Extension
copyright
description	Secondary findings are genetic test results that provide information about variants in a gene unrelated to the primary purpose for the testing, most often discovered when [Whole Exome Sequencing (WES)](https://en.wikipedia.org/wiki/Exome_sequencing) or [Whole Genome Sequencing (WGS)](https://en.wikipedia.org/wiki/Whole_genome_sequencing) is performed. This extension should be used to denote when a genetic finding is being shared as a secondary finding, and ideally refer to a corresponding guideline or policy statement. For more detail, please see: https://ghr.nlm.nih.gov/primer/testing/secondaryfindings.
experimental	false
fhirVersion	5.0.0
jurisdiction
jurisdiction[0]	http://unstats.un.org/unsd/methods/m49/m49.htm#001
kind	complex-type
name	ObsSecondaryFinding
publisher	HL7 International / Orders and Observations
purpose
status	active
title	Observation Secondary Finding
type	Extension
url	http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding

Structure

Name	L Flags	L Card.	L Type	L Description & Constraints	R Flags	R Card.	R Type	R Description & Constraints	Comments
Extension		0..1	Extension	Secondary findings are genetic test results that provide information about variants in a gene unrelated to the primary purpose for the testing, most often discovered when [Whole Exome Sequencing (WES)](https://en.wikipedia.org/wiki/Exome_sequencing) or [Whole Genome Sequencing (WGS)](https://en.wikipedia.org/wiki/Whole_genome_sequencing) is performed. This extension should be used to denote when a genetic finding is being shared as a secondary finding, and ideally refer to a corresponding guideline or policy statement. For more detail, please see: https://ghr.nlm.nih.gov/primer/testing/secondaryfindings		0..1	Extension	Secondary findings are genetic test results that provide information about variants in a gene unrelated to the primary purpose for the testing, most often discovered when [Whole Exome Sequencing (WES)](https://en.wikipedia.org/wiki/Exome_sequencing) or [Whole Genome Sequencing (WGS)](https://en.wikipedia.org/wiki/Whole_genome_sequencing) is performed. This extension should be used to denote when a genetic finding is being shared as a secondary finding, and ideally refer to a corresponding guideline or policy statement. For more detail, please see: https://ghr.nlm.nih.gov/primer/testing/secondaryfindings
id		0..1	id	Unique id for inter-element referencing		0..1	id	Unique id for inter-element referencing
Slices for extension		0..0		Extension Slice: Unordered, Open by value:url		0..0		Extension Slice: Unordered, Open by value:url
url		1..1	uri	"http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding"		1..1	uri	"http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding"
value[x]		1..1	CodeableConcept	Value of extension Binding: ?? (extensible): Codes to denote a guideline or policy statement when a genetic test result is being shared as a secondary finding.		1..1	CodeableConcept	Value of extension Binding: ?? (extensible): Codes to denote a guideline or policy statement when a genetic test result is being shared as a secondary finding.
Documentation for this format