This page is part of the FHIR Specification (v5.0.0-ballot: R5 Ballot - see ballot notes). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4
Orders and Observations Work Group | Maturity Level: 1 | Informative | Use Context: Any |
Detailed Descriptions for the elements in the extension.
Extension | |||||||||||||
Element Id | Extension | ||||||||||||
Definition | 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) or Whole Genome Sequencing (WGS) 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. | ||||||||||||
Short Display | 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 | ||||||||||||
Cardinality | 0..1 | ||||||||||||
Invariants |
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Extension.id | |||||||||||||
Element Id | Extension.id | ||||||||||||
Definition | Unique id for the element within a resource (for internal references). This may be any string value that does not contain spaces. | ||||||||||||
Short Display | Unique id for inter-element referencing | ||||||||||||
Cardinality | 0..1 | ||||||||||||
Type | id | ||||||||||||
Extension.extension | |||||||||||||
Element Id | Extension.extension | ||||||||||||
Definition | An Extension | ||||||||||||
Short Display | Extension | ||||||||||||
Cardinality | 0..0 | ||||||||||||
Type | Extension | ||||||||||||
Invariants |
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Slicing | This element introduces a set of slices. The slicing rules are:
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Extension.url | |||||||||||||
Element Id | Extension.url | ||||||||||||
Definition | Source of the definition for the extension code - a logical name or a URL. | ||||||||||||
Short Display | identifies the meaning of the extension | ||||||||||||
Cardinality | 1..1 | ||||||||||||
Type | uri | ||||||||||||
Comments | The definition may point directly to a computable or human-readable definition of the extensibility codes, or it may be a logical URI as declared in some other specification. The definition SHALL be a URI for the Structure Definition defining the extension. | ||||||||||||
Fixed Value | http://hl7.org/fhir/StructureDefinition/observation-secondaryFinding | ||||||||||||
Extension.value[x] | |||||||||||||
Element Id | Extension.value[x] | ||||||||||||
Definition | Value of extension - must be one of a constrained set of the data types (see Extensibility for a list). | ||||||||||||
Short Display | Value of extension | ||||||||||||
Cardinality | 1..1 | ||||||||||||
Terminology Binding | Codes to denote a guideline or policy statement when a genetic test result is being shared as a secondary finding. The codes SHALL be taken from Genetic Observation Secondary Findings; other codes may be used where these codes are not suitable | ||||||||||||
Type | CodeableConcept | ||||||||||||
[x] Note | See Choice of Datatypes for further information about how to use [x] | ||||||||||||
Invariants |
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