FHIR Cross-Version Extensions package for FHIR R4 from FHIR R5
0.0.1-snapshot-2 - informative International flag

FHIR Cross-Version Extensions package for FHIR R4 from FHIR R5 - Version 0.0.1-snapshot-2. See the Directory of published versions

ValueSet: Cross-version VS for R5.ResourceType for use in FHIR R4

Official URL: http://hl7.org/fhir/5.0/ValueSet/R5-resource-types-for-R4 Version: 0.0.1-snapshot-2
Standards status: Informative Maturity Level: 5 Computable Name: R5_resource_types_for_R4

This cross-version ValueSet represents concepts from http://hl7.org/fhir/ValueSet/resource-types 5.0.0 for use in FHIR R4. Concepts not present here have direct equivalent mappings crossing all versions from R5 to R4.

References

Logical Definition (CLD)

  • Include these codes as defined in http://hl7.org/fhir/fhir-types version 5.0.0
    CodeDisplayDefinition
    ActorDefinitionActorDefinitionThe ActorDefinition resource is used to describe an actor - a human or an application that plays a role in data exchange, and that may have obligations associated with the role the actor plays.
    ArtifactAssessmentArtifactAssessmentThis Resource provides one or more comments, classifiers or ratings about a Resource and supports attribution and rights management metadata for the added content.
    BiologicallyDerivedProductDispenseBiologicallyDerivedProductDispenseA record of dispensation of a biologically derived product.
    ConditionDefinitionConditionDefinitionA definition of a condition and information relevant to managing it.
    DeviceAssociationDeviceAssociationA record of association of a device.
    DeviceDispenseDeviceDispenseIndicates that a device is to be or has been dispensed for a named person/patient. This includes a description of the product (supply) provided and the instructions for using the device.
    DeviceUsageDeviceUsageA record of a device being used by a patient where the record is the result of a report from the patient or a clinician.
    EncounterHistoryEncounterHistoryA record of significant events/milestones key data throughout the history of an Encounter
    FormularyItemFormularyItemThis resource describes a product or service that is available through a program and includes the conditions and constraints of availability. All of the information in this resource is specific to the inclusion of the item in the formulary and is not inherent to the item itself.
    GenomicStudyGenomicStudyA set of analyses performed to analyze and generate genomic data.
    ImagingSelectionImagingSelectionA selection of DICOM SOP instances and/or frames within a single Study and Series. This might include additional specifics such as an image region, an Observation UID or a Segmentation Number, allowing linkage to an Observation Resource or transferring this information along with the ImagingStudy Resource.
    InventoryItemInventoryItemfunctional description of an inventory item used in inventory and supply-related workflows.
    InventoryReportInventoryReportA report of inventory or stock items.
    NutritionIntakeNutritionIntakeA record of food or fluid that is being consumed by a patient. A NutritionIntake may indicate that the patient may be consuming the food or fluid now or has consumed the food or fluid in the past. The source of this information can be the patient, significant other (such as a family member or spouse), or a clinician. A common scenario where this information is captured is during the history taking process during a patient visit or stay or through an app that tracks food or fluids consumed. The consumption information may come from sources such as the patient's memory, from a nutrition label, or from a clinician documenting observed intake.
    PermissionPermissionPermission resource holds access rules for a given data and context.
    RequestOrchestrationRequestOrchestrationA set of related requests that can be used to capture intended activities that have inter-dependencies such as "give this medication after that one".
    RequirementsRequirementsThe Requirements resource is used to describe an actor - a human or an application that plays a role in data exchange, and that may have obligations associated with the role the actor plays.
    SubstanceNucleicAcidSubstanceNucleicAcidNucleic acids are defined by three distinct elements: the base, sugar and linkage. Individual substance/moiety IDs will be created for each of these elements. The nucleotide sequence will be always entered in the 5’-3’ direction.
    SubstancePolymerSubstancePolymerProperties of a substance specific to it being a polymer.
    SubstanceProteinSubstanceProteinA SubstanceProtein is defined as a single unit of a linear amino acid sequence, or a combination of subunits that are either covalently linked or have a defined invariant stoichiometric relationship. This includes all synthetic, recombinant and purified SubstanceProteins of defined sequence, whether the use is therapeutic or prophylactic. This set of elements will be used to describe albumins, coagulation factors, cytokines, growth factors, peptide/SubstanceProtein hormones, enzymes, toxins, toxoids, recombinant vaccines, and immunomodulators.
    SubstanceReferenceInformationSubstanceReferenceInformationTodo.
    SubstanceSourceMaterialSubstanceSourceMaterialSource material shall capture information on the taxonomic and anatomical origins as well as the fraction of a material that can result in or can be modified to form a substance. This set of data elements shall be used to define polymer substances isolated from biological matrices. Taxonomic and anatomical origins shall be described using a controlled vocabulary as required. This information is captured for naturally derived polymers ( . starch) and structurally diverse substances. For Organisms belonging to the Kingdom Plantae the Substance level defines the fresh material of a single species or infraspecies, the Herbal Drug and the Herbal preparation. For Herbal preparations, the fraction information will be captured at the Substance information level and additional information for herbal extracts will be captured at the Specified Substance Group 1 information level. See for further explanation the Substance Class: Structurally Diverse and the herbal annex.
    TestPlanTestPlanA plan for executing testing on an artifact or specifications
    TransportTransportRecord of transport.
    AdministrableProductDefinitionAdministrableProductDefinitionA medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed).
    CitationCitationThe Citation Resource enables reference to any knowledge artifact for purposes of identification and attribution. The Citation Resource supports existing reference structures and developing publication practices such as versioning, expressing complex contributorship roles, and referencing computable resources.
    ClinicalUseDefinitionClinicalUseDefinitionA single issue - either an indication, contraindication, interaction or an undesirable effect for a medicinal product, medication, device or procedure.
    EvidenceReportEvidenceReportThe EvidenceReport Resource is a specialized container for a collection of resources and codeable concepts, adapted to support compositions of Evidence, EvidenceVariable, and Citation resources and related concepts.
    IngredientIngredientAn ingredient of a manufactured item or pharmaceutical product.
    ManufacturedItemDefinitionManufacturedItemDefinitionThe definition and characteristics of a medicinal manufactured item, such as a tablet or capsule, as contained in a packaged medicinal product.
    MedicinalProductDefinitionMedicinalProductDefinitionDetailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use, drug catalogs, to support prescribing, adverse events management etc.).
    NutritionProductNutritionProductA food or supplement that is consumed by patients.
    PackagedProductDefinitionPackagedProductDefinitionA medically related item or items, in a container or package.
    RegulatedAuthorizationRegulatedAuthorizationRegulatory approval, clearance or licencing related to a regulated product, treatment, facility or activity that is cited in a guidance, regulation, rule or legislative act. An example is Market Authorization relating to a Medicinal Product.
    SubscriptionStatusSubscriptionStatusThe SubscriptionStatus resource describes the state of a Subscription during notifications. It is not persisted.
    SubscriptionTopicSubscriptionTopicDescribes a stream of resource state changes identified by trigger criteria and annotated with labels useful to filter projections from this topic.
    SubstanceDefinitionSubstanceDefinitionThe detailed description of a substance, typically at a level beyond what is used for prescribing.

 

Expansion

This value set expansion contains 37 concepts.

CodeSystemDisplayDefinition
  ActorDefinitionhttp://hl7.org/fhir/fhir-typesActorDefinition

The ActorDefinition resource is used to describe an actor - a human or an application that plays a role in data exchange, and that may have obligations associated with the role the actor plays.

  ArtifactAssessmenthttp://hl7.org/fhir/fhir-typesArtifactAssessment

This Resource provides one or more comments, classifiers or ratings about a Resource and supports attribution and rights management metadata for the added content.

  BiologicallyDerivedProductDispensehttp://hl7.org/fhir/fhir-typesBiologicallyDerivedProductDispense

A record of dispensation of a biologically derived product.

  ConditionDefinitionhttp://hl7.org/fhir/fhir-typesConditionDefinition

A definition of a condition and information relevant to managing it.

  DeviceAssociationhttp://hl7.org/fhir/fhir-typesDeviceAssociation

A record of association of a device.

  DeviceDispensehttp://hl7.org/fhir/fhir-typesDeviceDispense

Indicates that a device is to be or has been dispensed for a named person/patient. This includes a description of the product (supply) provided and the instructions for using the device.

  DeviceUsagehttp://hl7.org/fhir/fhir-typesDeviceUsage

A record of a device being used by a patient where the record is the result of a report from the patient or a clinician.

  EncounterHistoryhttp://hl7.org/fhir/fhir-typesEncounterHistory

A record of significant events/milestones key data throughout the history of an Encounter

  FormularyItemhttp://hl7.org/fhir/fhir-typesFormularyItem

This resource describes a product or service that is available through a program and includes the conditions and constraints of availability. All of the information in this resource is specific to the inclusion of the item in the formulary and is not inherent to the item itself.

  GenomicStudyhttp://hl7.org/fhir/fhir-typesGenomicStudy

A set of analyses performed to analyze and generate genomic data.

  ImagingSelectionhttp://hl7.org/fhir/fhir-typesImagingSelection

A selection of DICOM SOP instances and/or frames within a single Study and Series. This might include additional specifics such as an image region, an Observation UID or a Segmentation Number, allowing linkage to an Observation Resource or transferring this information along with the ImagingStudy Resource.

  InventoryItemhttp://hl7.org/fhir/fhir-typesInventoryItem

functional description of an inventory item used in inventory and supply-related workflows.

  InventoryReporthttp://hl7.org/fhir/fhir-typesInventoryReport

A report of inventory or stock items.

  NutritionIntakehttp://hl7.org/fhir/fhir-typesNutritionIntake

A record of food or fluid that is being consumed by a patient. A NutritionIntake may indicate that the patient may be consuming the food or fluid now or has consumed the food or fluid in the past. The source of this information can be the patient, significant other (such as a family member or spouse), or a clinician. A common scenario where this information is captured is during the history taking process during a patient visit or stay or through an app that tracks food or fluids consumed. The consumption information may come from sources such as the patient's memory, from a nutrition label, or from a clinician documenting observed intake.

  Permissionhttp://hl7.org/fhir/fhir-typesPermission

Permission resource holds access rules for a given data and context.

  RequestOrchestrationhttp://hl7.org/fhir/fhir-typesRequestOrchestration

A set of related requests that can be used to capture intended activities that have inter-dependencies such as "give this medication after that one".

  Requirementshttp://hl7.org/fhir/fhir-typesRequirements

The Requirements resource is used to describe an actor - a human or an application that plays a role in data exchange, and that may have obligations associated with the role the actor plays.

  SubstanceNucleicAcidhttp://hl7.org/fhir/fhir-typesSubstanceNucleicAcid

Nucleic acids are defined by three distinct elements: the base, sugar and linkage. Individual substance/moiety IDs will be created for each of these elements. The nucleotide sequence will be always entered in the 5’-3’ direction.

  SubstancePolymerhttp://hl7.org/fhir/fhir-typesSubstancePolymer

Properties of a substance specific to it being a polymer.

  SubstanceProteinhttp://hl7.org/fhir/fhir-typesSubstanceProtein

A SubstanceProtein is defined as a single unit of a linear amino acid sequence, or a combination of subunits that are either covalently linked or have a defined invariant stoichiometric relationship. This includes all synthetic, recombinant and purified SubstanceProteins of defined sequence, whether the use is therapeutic or prophylactic. This set of elements will be used to describe albumins, coagulation factors, cytokines, growth factors, peptide/SubstanceProtein hormones, enzymes, toxins, toxoids, recombinant vaccines, and immunomodulators.

  SubstanceReferenceInformationhttp://hl7.org/fhir/fhir-typesSubstanceReferenceInformation

Todo.

  SubstanceSourceMaterialhttp://hl7.org/fhir/fhir-typesSubstanceSourceMaterial

Source material shall capture information on the taxonomic and anatomical origins as well as the fraction of a material that can result in or can be modified to form a substance. This set of data elements shall be used to define polymer substances isolated from biological matrices. Taxonomic and anatomical origins shall be described using a controlled vocabulary as required. This information is captured for naturally derived polymers ( . starch) and structurally diverse substances. For Organisms belonging to the Kingdom Plantae the Substance level defines the fresh material of a single species or infraspecies, the Herbal Drug and the Herbal preparation. For Herbal preparations, the fraction information will be captured at the Substance information level and additional information for herbal extracts will be captured at the Specified Substance Group 1 information level. See for further explanation the Substance Class: Structurally Diverse and the herbal annex.

  TestPlanhttp://hl7.org/fhir/fhir-typesTestPlan

A plan for executing testing on an artifact or specifications

  Transporthttp://hl7.org/fhir/fhir-typesTransport

Record of transport.

  AdministrableProductDefinitionhttp://hl7.org/fhir/fhir-typesAdministrableProductDefinition

A medicinal product in the final form which is suitable for administering to a patient (after any mixing of multiple components, dissolution etc. has been performed).

  Citationhttp://hl7.org/fhir/fhir-typesCitation

The Citation Resource enables reference to any knowledge artifact for purposes of identification and attribution. The Citation Resource supports existing reference structures and developing publication practices such as versioning, expressing complex contributorship roles, and referencing computable resources.

  ClinicalUseDefinitionhttp://hl7.org/fhir/fhir-typesClinicalUseDefinition

A single issue - either an indication, contraindication, interaction or an undesirable effect for a medicinal product, medication, device or procedure.

  EvidenceReporthttp://hl7.org/fhir/fhir-typesEvidenceReport

The EvidenceReport Resource is a specialized container for a collection of resources and codeable concepts, adapted to support compositions of Evidence, EvidenceVariable, and Citation resources and related concepts.

  Ingredienthttp://hl7.org/fhir/fhir-typesIngredient

An ingredient of a manufactured item or pharmaceutical product.

  ManufacturedItemDefinitionhttp://hl7.org/fhir/fhir-typesManufacturedItemDefinition

The definition and characteristics of a medicinal manufactured item, such as a tablet or capsule, as contained in a packaged medicinal product.

  MedicinalProductDefinitionhttp://hl7.org/fhir/fhir-typesMedicinalProductDefinition

Detailed definition of a medicinal product, typically for uses other than direct patient care (e.g. regulatory use, drug catalogs, to support prescribing, adverse events management etc.).

  NutritionProducthttp://hl7.org/fhir/fhir-typesNutritionProduct

A food or supplement that is consumed by patients.

  PackagedProductDefinitionhttp://hl7.org/fhir/fhir-typesPackagedProductDefinition

A medically related item or items, in a container or package.

  RegulatedAuthorizationhttp://hl7.org/fhir/fhir-typesRegulatedAuthorization

Regulatory approval, clearance or licencing related to a regulated product, treatment, facility or activity that is cited in a guidance, regulation, rule or legislative act. An example is Market Authorization relating to a Medicinal Product.

  SubscriptionStatushttp://hl7.org/fhir/fhir-typesSubscriptionStatus

The SubscriptionStatus resource describes the state of a Subscription during notifications. It is not persisted.

  SubscriptionTopichttp://hl7.org/fhir/fhir-typesSubscriptionTopic

Describes a stream of resource state changes identified by trigger criteria and annotated with labels useful to filter projections from this topic.

  SubstanceDefinitionhttp://hl7.org/fhir/fhir-typesSubstanceDefinition

The detailed description of a substance, typically at a level beyond what is used for prescribing.


Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code