GenomeX Data Exchange FHIR IG
0.2.0 - draft

GenomeX Data Exchange FHIR IG, published by MITRE. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/CodeX-HL7-FHIR-Accelerator/GenomeX-DataExchange/ and changes regularly. See the Directory of published versions

Example Bundle: ct-xT-bundle

Generated Narrative: Bundle ct-xT-bundle

Bundle ct-xT-bundle of type transaction


Entry 1 - fullUrl = urn:uuid:2ddeec04-75de-441c-8767-18c884ece7h4

Resource Patient:

Generated Narrative: Patient ct-xT-Patient

Mela Mann Female, DoB: 1926-08-06 ( Medical Record Number: 993456789 (use: official, ))


Other Id:Patient external identifier/23ef1d1b-03a5-47d6-81e0-b9b4cbb15ccf (use: official, )

Request:

POST Patient

Entry 2 - fullUrl = urn:uuid:56eeebfb-9df4-4789-955b-76bcec2d77a4

Resource DiagnosticReport:

Generated Narrative: DiagnosticReport ct-xT-DiagnosticReport

Genetic analysis report (Genetics, DNA, Genetics)

SubjectNot done yet
When For2019-02-15 19:28:58+0500
Performer Bundle: type = transaction
Identifiers Accession ID/TL-22-D3MTCAU4 Pipeline Version/3.9.3 Placer Identifier/d6eeedd1-92d3-45b9-bf33-6401e804425f

Report Details

CodeValue

Request:

POST DiagnosticReport

Entry 3 - fullUrl = urn:uuid:28395cc2-c6e4-4006-84af-ebf40113656a

Resource ServiceRequest:

Generated Narrative: ServiceRequest ct-xT-ServiceRequest

identifier: Filler Identifier/23gcimeh

requisition: Accession ID/TL-23-5B8EHM49

status: Completed

intent: Order

code: xT - 648 gene panel

subject: Bundle: type = transaction

requester: Bundle: type = transaction

reasonCode: Malignant neoplasm of unspecified part of bronchus or lung

Request:

POST ServiceRequest

Entry 4 - fullUrl = urn:uuid:3b3363be-d153-40ae-952f-09d15df1d9bf

Resource Practitioner:

Generated Narrative: Practitioner ct-xT-practitioner

identifier: United States National Provider Identifier/9988776345

name: Test Physician

address: 600 Chicago Drive Everywhere TX 16789 US (work)

gender: Female

Qualifications

-Code
*Doctor of Medicine

Request:

POST Practitioner

Entry 5 - fullUrl = urn:uuid:60863097-6033-41af-9f6a-d7b012e276ae

Resource PractitionerRole:

Generated Narrative: PractitionerRole ct-xT-physicianRole

practitioner: Bundle: type = transaction

organization: Bundle: type = transaction

Request:

POST PractitionerRole

Entry 6 - fullUrl = urn:uuid:f55969f0-aad6-4d9d-8af8-ae73b0ca4e8e

Resource Organization:

Generated Narrative: Organization ct-xT-OrderingOrganization

identifier: Clinical Laboratory Improvement Amendments/14D2114007

active: true

name: Ordering Organization

Request:

POST Organization

Entry 7 - fullUrl = urn:uuid:9ebd0cb1-4733-4b8e-999c-a66bcbd939dd

Resource Practitioner:

Generated Narrative: Practitioner ct-xT-Pathologist

identifier: http://www.acme.com/identifiers/patient/123456

name: Test Pathologist

Request:

POST Practitioner

Entry 8 - fullUrl = urn:uuid:3970f176-e402-4eaf-989c-959e80d918ae

Resource Organization:

Generated Narrative: Organization ct-xT-Tempus-Organization

identifier: Clinical Laboratory Improvement Amendments/14D2114007

active: true

name: Tempus Labs, Inc

telecom: support@tempus.com

address: 600 W Chicago Avenue, Ste 510 Chicago IL 60654 USA

Contacts

-Name
*Nike Beaubier, M,FCAP,MGAP

Request:

POST Organization

Entry 9 - fullUrl = urn:uuid:f5418e88-295b-43f8-af03-76c8c4aa516e

Resource Specimen:

Generated Narrative: Specimen ct-xT-specimen-tumor

status: Available

type: Tumor

subject: Bundle: type = transaction

receivedTime: 2021-02-09 21:30:50+0500

collection

id

TestInstitutionPathologyLaboratoryS22123456

collected: 2021-02-06 17:15:00+0500

bodySite: Left lung structure (body structure)

Containers

-Identifier
*Specimen ID/A2

Request:

POST Specimen

Entry 10 - fullUrl = urn:uuid:1e6f171a-1dea-41b8-a51d-1f86130a43cc

Resource Specimen:

Generated Narrative: Specimen ct-xT-specimen-normal

status: Available

type: Whole Blood

subject: Bundle: type = transaction

receivedTime: 2021-02-09 21:30:50+0500

Collections

-Collected[x]
*2021-02-06 17:15:00+0500

Request:

POST Specimen

Entry 11 - fullUrl = urn:uuid:ccab39c5-49cf-4aa6-a1e7-2e0c9dd3a7d5

Resource Observation:

Generated Narrative: Observation ct-xT-Observation1

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: BAP1

component

code: Transcript reference sequence [ID]

value: NM_004656.4

component

code: DNA change (c.HGVS)

value: c.1768C>T

component

code: Amino acid change (pHGVS)

value: p.Q590*

component

code: Genomic source class [Type]

value: Somatic

component

code: Sample variant allelic frequency [NFr]

value: 57.4 % (Details: UCUM code% = '%')

component

code: Human reference sequence assembly version

value: GRCh37

Request:

POST Observation

Entry 12 - fullUrl = urn:uuid:fc637e0b-dced-4245-946e-3fa13ec128e3

Resource Observation:

Generated Narrative: Observation ct-xT-Observation2

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: CDKN2A

component

code: DNA change type

value: copy number loss

component

code: Genomic source class [Type]

value: Somatic

component

code: Human reference sequence assembly version

value: GRCh37

Request:

POST Observation

Entry 13 - fullUrl = urn:uuid:c7a1db28-0c8f-4667-a40a-79401833b26b

Resource Observation:

Generated Narrative: Observation ct-xT-Observation3

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: MTAP

component

code: Genomic source class [Type]

value: Somatic

component

code: DNA change type

value: copy number loss

component

code: Human reference sequence assembly version

value: GRCh37

Request:

POST Observation

Entry 14 - fullUrl = urn:uuid:6e333995-6a74-4dcd-ac7f-d7cf5ad20ac9

Resource Observation:

Generated Narrative: Observation ct-xT-Observation4

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: NTHL1 encodes an endonuclease III-like protein important in the base excision pathway usually through repair of oxidative pyrimidine lesions. Germline pathogenic variants in NTHL1 have been associated with autosomal recessive NTHL1-associated polyposis; heterozygotes are considered carriers, while homozygotes or compound heterozygotes are likely to be affected (PMID: 30753826). This is an adult onset hereditary cancer predisposition syndrome associated with development of colonic adenomas which can progress to colorectal cancer. Clinical correlation, including confirmation of this variant through a validated germline assay, and genetic counseling are recommended for this patient and any potentially at-risk family members.

component

code: Genomic source class [Type]

value: Germline

component

code: Transcript reference sequence [ID]

value: NM_002528.7

component

code: DNA change (c.HGVS)

value: c.268C>T

component

code: Amino acid change (pHGVS)

value: p.Q90*

component

code: Chromosome [Identifier] in Blood or Tissue by Molecular genetics method

value: Chromosome 16

component

code: Variant exact start-end

value: 2096239-?

component

code: Human reference sequence assembly version

value: GRCh37

Request:

POST Observation

Entry 15 - fullUrl = urn:uuid:d7318c30-3975-4f62-9840-3b8d7e7b56cd

Resource Observation:

Generated Narrative: Observation ct-xT-Observation5

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: APC encodes a multi-domain protein that interacts with factors involved in cellular proliferation, differentiation, maintenance, and structure including the microtubules and beta-catenin within the Wnt pathway. The APC p.I1307K variant has been associated with increased risk of developing colorectal cancer in the Ashkenazi Jewish population. For heterozygous patients, the increased risk if estimated as follows: odds ratio (OR) of 2.17 (95% confidence interval: 1.64-2.86) (PMID: 23576677) or adjusted OR of 1.75 (95% confidence interval: 1.26-2.45) (PMID: 23896379). The risk may be further increased in homozygous patients. The risk associated with the APC p.I1307K variant in other populations is still under study. Clinical correlation, including confirmation of this variant through a validated germline assay, and genetic counseling are recommended for this patient and any potentially at-risk family members.

component

code: Genomic source class

value: Germline

component

code: Transcript reference sequence [ID]

value: NM_000038.6

component

code: DNA change (c.HGVS)

value: c.3920T>A

component

code: Amino acid change (pHGVS)

value: p.I1307K

component

code: Chromosome [Identifier] in Blood or Tissue by Molecular genetics method

value: Chromosome 5

component

code: Variant exact start-end

value: 112175211-?

Request:

POST Observation

Entry 16 - fullUrl = urn:uuid:86ad3e6b-7ed8-4c7d-b99c-574ac5e2b4b9

Resource Observation:

Generated Narrative: Observation ct-xT-Observation6

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: POF1B

component

code: Genomic source class [Type]

value: Somatic

component

code: Transcript reference sequence [ID]

value: NM_004656

component

code: DNA change (c.HGVS)

value: c.430C>T

component

code: Amino acid change (pHGVS)

value: p.P144S

component

code: Sample variant allelic frequency [NFr]

value: 78.6 % (Details: UCUM code% = '%')

component

code: Human reference sequence assembly version

value: GRCh37

Request:

POST Observation

Entry 17 - fullUrl = urn:uuid:82a8b9db-a68e-4e06-897e-77ed3ea5aced

Resource Observation:

Generated Narrative: Observation ct-xT-variant-fusion-met-alk

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Genetic variant assessment

subject: Bundle: type = transaction

effective: 2019-04-01

value: Present

method: Sequencing

component

code: Gene studied [ID]

value: MET

component

code: Gene studied [ID]

value: ALK

component

code: DNA change type

value: complex_chromosomal_rearrangement

component

code: Genomic source class [Type]

value: Somatic

Request:

POST Observation

Entry 18 - fullUrl = urn:uuid:5dfa33cc-9038-44d0-9f71-f319b3cb4c9a

Resource Observation:

Generated Narrative: Observation ct-xT-molecular-consequence-observation-1

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Molecular Consequence

subject: Bundle: type = transaction

effective: 2019-08-23

performer: Bundle: type = transaction

derivedFrom: Bundle: type = transaction

component

code: Feature Consequence

value: Stop gain

component

code: Functional Effect

value: loss of function

Request:

POST Observation

Entry 19 - fullUrl = urn:uuid:3c30e177-2c41-4f13-b6c0-1adf5af4c71d

Resource Observation:

Generated Narrative: Observation ct-xT-molecular-consequence-observation-4

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Molecular Consequence

subject: Bundle: type = transaction

effective: 2019-08-23

performer: Bundle: type = transaction

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Feature ConsequenceStop gain

Request:

POST Observation

Entry 20 - fullUrl = urn:uuid:0c06b231-47e9-4a3b-88bd-2d8937d615a7

Resource Observation:

Generated Narrative: Observation ct-xT-molecular-consequence-observation-5

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Molecular Consequence

subject: Bundle: type = transaction

effective: 2019-08-23

performer: Bundle: type = transaction

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Feature ConsequenceMissense variant

Request:

POST Observation

Entry 21 - fullUrl = urn:uuid:00e47ced-f260-4baf-9da4-ee88224d3bc5

Resource Observation:

Generated Narrative: Observation ct-xT-molecular-consequence-observation-6

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Molecular Consequence

subject: Bundle: type = transaction

effective: 2019-08-23

performer: Bundle: type = transaction

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Feature ConsequenceMissense variant

Request:

POST Observation

Entry 22 - fullUrl = urn:uuid:dc69c7c9-031b-466f-bf63-8be56d658c50

Resource Observation:

Generated Narrative: Observation ct-xT-molecular-consequence-observation-fusion

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Molecular Consequence

subject: Bundle: type = transaction

effective: 2019-08-23

performer: Bundle: type = transaction

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Feature Consequencegene_fusion

Request:

POST Observation

Entry 23 - fullUrl = urn:uuid:kbe36a66-b7c9-4130-a181-81bb72e3f4zz

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-fusion

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Genetic variation clinical significance [Imp]Pathogenic

Request:

POST Observation

Entry 24 - fullUrl = urn:uuid:bbe36a66-b7c9-4130-a181-81bb72e3f4cc

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-1

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Genetic variation clinical significance [Imp]Pathogenic

Request:

POST Observation

Entry 25 - fullUrl = urn:uuid:7bb9b47d-2b77-47a6-ae2a-62f0b1d01d05

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-2

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Genetic variation clinical significance [Imp]Pathogenic

Request:

POST Observation

Entry 26 - fullUrl = urn:uuid:52554ca2-dcdd-4105-9cb7-059f0a863483

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-3

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Genetic variation clinical significance [Imp]Pathogenic

Request:

POST Observation

Entry 27 - fullUrl = urn:uuid:dddaac5f-e8ba-4c55-a70c-5c6d80903356

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-4

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

component

code: Genetic variation clinical significance [Imp]

value: Pathogenic

component

code: Associated phenotype

value: NTHL1 tumor syndrome, NTHL1-associated polyposis

Request:

POST Observation

Entry 28 - fullUrl = urn:uuid:69b54656-b1eb-4393-ac69-f25f32fde680

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-5

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

component

code: Genetic variation clinical significance [Imp]

value: Likely Pathogenic

component

code: Associated phenotype

value: APC-associated conditions

Request:

POST Observation

Entry 29 - fullUrl = urn:uuid:f845d26f-7308-45ab-9898-ebc86d6ae22c

Resource Observation:

Generated Narrative: Observation ct-xT-diagnostic-implication-6

status: Final

category: Laboratory, Genetics, Laboratory, Genetics

code: Diagnostic Implication

subject: Bundle: type = transaction

effective: 2019-04-01

derivedFrom: Bundle: type = transaction

Components

-CodeValue[x]
*Genetic variation clinical significance [Imp]Uncertain Significance

Request:

POST Observation

Entry 30 - fullUrl = urn:uuid:5fe0e4c4-fd4b-4e9d-af1e-b3b40c28a21a

Resource Procedure:

Generated Narrative: Procedure ct-xT-procedure1

Genomic Study Analysis Regions

  • description: Pertinent Negative
  • studied: NRAS
  • studied: KIT
  • studied: BRAF

status: Completed

category: Laboratory

subject: Bundle: type = transaction

performed: 2023-08-09 01:01:10-0600

Request:

POST Procedure

Entry 31 - fullUrl = urn:uuid:16f2715b-10ea-42ae-a3a2-185b14e6e21f

Resource Procedure:

Generated Narrative: Procedure ct-xT-genomicStudy

Genomic Study Analysis Extension: Bundle: type = transaction

basedOn: Bundle: type = transaction

status: Completed

category: Laboratory

code: xT panel

subject: Bundle: type = transaction

performed: 2023-08-09

Request:

POST Procedure

Entry 32 - fullUrl = urn:uuid:4be89099-d07b-4c94-a1ef-be16233a79d8

Resource Observation:

Generated Narrative: Observation gx-genomic-tmb

status: Final

category: Laboratory, A characterization of a given biomarker observation., Genetics

code: Mutations/Megabase [# Ratio] in Tumor

subject: Bundle: type = transaction

value: 5.2 1/1000000{Base} (Details: UCUM code1/1000000{Base} = '1/1000000{Base}')

Request:

POST Observation

Entry 33 - fullUrl = urn:uuid:68b6b4ac-47df-4b0b-857a-d9427d5e2538

Resource ResearchStudy:

Generated Narrative: ResearchStudy gx-genomic-research-study-implication-clinical-trial-NCT02693535

identifier: ClinicalTrials.gov/NCT02693535

title: TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer

status: Active

phase: Phase 2

RelatedArtifacts

-TypeUrl
*Citationhttps://clinicaltrials.gov/ct2/show/NCT02693535

site: Zion, Illinois (Identifier: https://www.usps.com//IL)

Request:

POST ResearchStudy

Entry 34 - fullUrl = urn:uuid:cd1ba6c7-553d-4b04-b5d6-07571129c52d

Resource Observation:

Generated Narrative: Observation ct-xT-clinicalTrial

status: Final

category: Laboratory, Genetics

code: Therapeutic Implication

derivedFrom: Bundle: type = transaction

Components

-ExtensionCodeValue[x]
*Associated TherapyNCT02693535

Request:

POST Observation

Entry 35 - fullUrl = urn:uuid:da3cfb61-7b73-429d-b933-36b41b5e4a66

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-A-haplotype1

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-A*03:01

Components

-CodeValue[x]
*Gene studied [ID]HLA-A

Request:

POST Observation

Entry 36 - fullUrl = urn:uuid:b745fef5-462d-4b6c-bddc-a7c573c614ef

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-A-haplotype2

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-A*31:01

Components

-CodeValue[x]
*Gene studied [ID]HLA-A

Request:

POST Observation

Entry 37 - fullUrl = urn:uuid:29d40ea4-2946-4a90-a259-7a6025b3b090

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-B-haplotype1

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-B*07:02

Components

-CodeValue[x]
*Gene studied [ID]HLA-B

Request:

POST Observation

Entry 38 - fullUrl = urn:uuid:9095423d-db5e-4c28-a876-53a3b19fb6de

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-B-haplotype2

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-B*35:01

Components

-CodeValue[x]
*Gene studied [ID]HLA-B

Request:

POST Observation

Entry 39 - fullUrl = urn:uuid:da9b5431-1b88-461d-ab57-49502fe20117

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-C-haplotype1

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-C*04:01

Components

-CodeValue[x]
*Gene studied [ID]HLA-C

Request:

POST Observation

Entry 40 - fullUrl = urn:uuid:148fddd2-ab27-4abe-b096-8cf905905bc0

Resource Observation:

Generated Narrative: Observation ct-xT-HLA-C-haplotype2

status: Final

category: Laboratory, Genetics

code: Haplotype Name

subject: Bundle: type = transaction

effective: 2019-02-01

issued: 2019-02-01 00:00:00-0500

performer: Bundle: type = transaction

value: HLA-C*07:02

Components

-CodeValue[x]
*Gene studied [ID]HLA-C

Request:

POST Observation

Entry 41 - fullUrl = urn:uuid:b3s0f176-e402-4eaf-989c-959e80d91n5f

Resource DocumentReference:

Generated Narrative: DocumentReference ct-xT-GeneList

identifier: https://www.tempus.com/11120

status: Current

docStatus: Preliminary

description: Gene List

content

Attachments

-UrlTitleCreation
*https://edge-api-demo.stagingtempus.com/fhir/R4/static/Gene_List_1.jsonGeneList2019-03-01 01:02:01+0100

Request:

POST DocumentReference

Entry 42 - fullUrl = urn:uuid:11163097-6033-41af-9f6a-d7b012e27aaa

Resource Procedure:

Generated Narrative: Procedure ct-xT-genomicStudyAnalysis

Genomic Study Analysis Regions

Genomic Study Analysis Specimen: Bundle: type = transaction

Genomic Study Analysis Focus: Bundle: type = transaction

status: Completed

category: Laboratory

subject: Bundle: type = transaction

performed: 2023-02-02 01:01:10-0600

Request:

POST Procedure

Entry 43 - fullUrl = urn:uuid:88f2715b-10ea-42ae-a3a2-185b14e6e666

Resource Procedure:

Generated Narrative: Procedure ct-xT-genomicStudy-2

Genomic Study Analysis Extension: Bundle: type = transaction

basedOn: Bundle: type = transaction

status: Completed

category: Laboratory

code: xT panel

subject: Bundle: type = transaction

performed: 2023-08-09

Request:

POST Procedure