FQL is a query language that allows you to retrieve, filter and project data from any data source containing FHIR Resources. It brings the power of three existing languages together: SQL, JSON and FhirPath. It allows you to create tables and is useful for gaining insight and perform quality control.
Query
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Default
What is FQL?
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FQL Query resources
FQL Playground
Try Firely Query Language in our playground by using this scope as data source.
- FQL Documentation
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FQL Language
Syntax specification
To learn more about FQL syntax choose this menu item.
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YamlGen Generate resources
YamlGen Playground
Try YamlGen in our playground by using this scope as data source.
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YamlGen Language
YamlGen Syntax specification
To learn more about YamlGen syntax choose this.
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FHIRPath Inspect resource
FHIRPath Playground
Try out the FHIRPath playground and navigate inside this resource.
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FHIRPath Documentation
FHIRPath Documentation
Find out what FHIRPath is or learn how to write FHIRPath scripts.
API
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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.
Tools
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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.
Organization FHIR Core /
Project Core StructureDefinitions - STU3
AllelicState
The level of occurrence of a single DNA Sequence Variant within a set of chromosomes. Heterozygous indicates the DNA sequence variant is only present in one of the two genes contained in homologous chromosomes. Homozygous indicates the DNA Sequence Variant is present in both genes contained in homologous chromosomes. Hemizygous indicates the DNA Sequence Variant exists in the only single copy of a gene in a non-homologous chromosome (the male X and Y chromosome are non-homologous). Hemiplasmic indicates that the DNA Sequence Variant is present in some but not all of the copies of mitochondrial DNA. Homoplasmic indicates that the DNA Sequence Variant is present in all of the copies of mitochondrial DNA. LOINC Code: (53034-5).
- type Extension
- FHIR STU3
- status Maturity Level 0
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versionnone
Valid canonical
This resource matches a canonical claim from this project.
Claim: http://hl7.org/fhir
Canonical claims are used to verify ownership of your canonical URLs.
Canonical
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