abstractbaseDefinitioncopyrightdescriptionexperimentalfhirVersionjurisdiction
jurisdiction[0]kindnamepublisher- Values Differ
purposestatustitletypeurl| Left: | Observation Secondary Finding (http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding) |
| Right: | Observation Secondary Finding (http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding) |
| Information | StructureDefinition.publisher | Values for publisher differ: 'HL7 International / FHIR Infrastructure' vs 'HL7 International / Orders and Observations' |
| Information | StructureDefinition.definition | Values for definition differ: 'Value of extension - must be one of a constrained set of the data types (see [Extensibility](http://hl7.org/fhir/5.0.0-snapshot3/extensibility.html) for a list).' vs 'Value of extension - must be one of a constrained set of the data types (see [Extensibility](http://hl7.org/fhir/R5/extensibility.html) for a list).' |
| 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 | |||||||||