FHIRPath is a path based navigation and extraction language.
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Default
What is FHIRPath?
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FHIRPath Inspect resource
FHIRPath Playground
Try out the FHIRPath playground and navigate inside this resource.
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Documentation on FHIRPath
Documentation
Find out what FHIRPath is or learn how to write FHIRPath scripts.
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Project FHIR API
This is the location where you can find your resource using a FHIR client.
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Simplifier FHIR API
The global endpoint is where users can search for all resources in Simplifier. Resources have a globally unique guid Id here.
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Custom Example generation
Custom Example generation beta
Experiment with resource instance generation using YamlGen and based on this profile.
This feature is in beta. You can help us improve it by giving feedback with the feedback button at the top of the screen.
Secondary Finding
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.
- type Extension
- FHIR STU3
- status Draft
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version4.0.1
The canonical from this resource does not match any claim in this context and conflicts with a claim from another scope.
http://hl7.org/fhir
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