| 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 / FHIR Infrastructure | HL7 International / Orders and Observations | |
| purpose | | |
| status | active | |
| title | Observation Secondary Finding | |
| type | Extension | |
| url | http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding | |
| 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 | | | | 0..0 | | | |
| 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 |