From 95628a325266e07c28fdbc2b2d4796842c27ec6e Mon Sep 17 00:00:00 2001 From: Kazeem Hamzat Date: Thu, 9 Jul 2026 18:17:04 +0100 Subject: [PATCH] Delete-CodeSystem-test-type-genomics Delete-CodeSystem-test-type-genomics --- ...em-Genomics-DGTS-testpackage-modality.json | 2 +- .../CodeSystem-Genomics-test-types.json | 37 ------------------- ...gland-Composition-GenomicsEULabReport.json | 6 --- ...ngland-DiagnosticReport-GenomicReport.json | 18 --------- .../NHSEngland-Patient-Genomics.json | 3 -- .../NHSEngland-ServiceRequest-Genomics.json | 3 -- .../NHSEngland-Specimen-Genomics.json | 13 ------- ValueSet/ValueSet-Genomics-test-types.json | 32 ---------------- 8 files changed, 1 insertion(+), 113 deletions(-) delete mode 100644 CodeSystem/CodeSystem-Genomics-test-types.json delete mode 100644 ValueSet/ValueSet-Genomics-test-types.json diff --git a/CodeSystem/CodeSystem-Genomics-DGTS-testpackage-modality.json b/CodeSystem/CodeSystem-Genomics-DGTS-testpackage-modality.json index 75b16ca..30b67f4 100644 --- a/CodeSystem/CodeSystem-Genomics-DGTS-testpackage-modality.json +++ b/CodeSystem/CodeSystem-Genomics-DGTS-testpackage-modality.json @@ -26,7 +26,7 @@ "copyright": "Copyright © 2026+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.", "caseSensitive": true, "content": "complete", - "count": 7, + "count": 9, "concept": [ { "code": "solid-cancer", diff --git a/CodeSystem/CodeSystem-Genomics-test-types.json b/CodeSystem/CodeSystem-Genomics-test-types.json deleted file mode 100644 index af1a974..0000000 --- a/CodeSystem/CodeSystem-Genomics-test-types.json +++ /dev/null @@ -1,37 +0,0 @@ -{ - "resourceType": "CodeSystem", - "id": "test-type-genomics", - "url": "https://fhir.nhs.uk/CodeSystem/test-type-genomics", - "version": "0.2.0", - "name": "TestTypeGenomics", - "title": "Test Type Genomics", - "status": "draft", - "date": "2022-12-21T11:27:52.3231281+00:00", - "publisher": "NHS England", - "contact": [ - { - "name": "NHS England", - "telecom": [ - { - "system": "email", - "value": "interoperabilityteam@nhs.net", - "use": "work" - } - ] - } - ], - "description": "A set of codes use to identify the category of genomic test types", - "copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\"License\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\"AS IS\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.", - "caseSensitive": true, - "content": "complete", - "concept": [ - { - "code": "RID-WGS", - "display": "Rare and Inherited Diseases - WGS" - }, - { - "code": "C-WGS", - "display": "Cancer (paired tumour normal) - WGS" - } - ] -} \ No newline at end of file diff --git a/StructureDefinition/NHSEngland-Composition-GenomicsEULabReport.json b/StructureDefinition/NHSEngland-Composition-GenomicsEULabReport.json index c31e397..ca4fa03 100644 --- a/StructureDefinition/NHSEngland-Composition-GenomicsEULabReport.json +++ b/StructureDefinition/NHSEngland-Composition-GenomicsEULabReport.json @@ -174,9 +174,6 @@ { "id": "Composition.category", "path": "Composition.category", - "slicing": { - "rules": "open" - }, "definition": "Fixed codes for conformance to the EU Lab Composition profile (for cross border sharing of lab reports)." }, { @@ -268,9 +265,6 @@ { "id": "Composition.section", "path": "Composition.section", - "slicing": { - "rules": "open" - }, "definition": "To conform to EU Lab, SHOULD include references to the results that form part of the genomic report. For the UGR, will include sections that conform to the UGR folders, this work is currently in development." }, { diff --git a/StructureDefinition/NHSEngland-DiagnosticReport-GenomicReport.json b/StructureDefinition/NHSEngland-DiagnosticReport-GenomicReport.json index be3df23..8d9a8e7 100644 --- a/StructureDefinition/NHSEngland-DiagnosticReport-GenomicReport.json +++ b/StructureDefinition/NHSEngland-DiagnosticReport-GenomicReport.json @@ -61,21 +61,6 @@ "path": "DiagnosticReport.extension.value[x].type", "fixedCode": "citation" }, - { - "id": "DiagnosticReport.extension:diagnosticReportCompositionR5", - "path": "DiagnosticReport.extension", - "sliceName": "diagnosticReportCompositionR5", - "definition": "TBC. Only relevant for EU Lab aligned reports (included in HL7 EU Laboratory Report: DiagnosticReport Profile). A reference to the Composition which wraps this report for data sharing.", - "type": [ - { - "code": "Extension", - "profile": [ - "http://hl7.org/fhir/5.0/StructureDefinition/extension-DiagnosticReport.composition" - ] - } - ], - "isModifier": false - }, { "id": "DiagnosticReport.identifier", "path": "DiagnosticReport.identifier", @@ -191,9 +176,6 @@ { "id": "DiagnosticReport.category", "path": "DiagnosticReport.category", - "slicing": { - "rules": "open" - }, "definition": "Potentially multiple categories to specify the specialty the report is relevant for. Different codings are expected by the Genomic Report and EU Lab profiles." }, { diff --git a/StructureDefinition/NHSEngland-Patient-Genomics.json b/StructureDefinition/NHSEngland-Patient-Genomics.json index 5bee313..53a7a56 100644 --- a/StructureDefinition/NHSEngland-Patient-Genomics.json +++ b/StructureDefinition/NHSEngland-Patient-Genomics.json @@ -107,9 +107,6 @@ { "id": "Patient.identifier", "path": "Patient.identifier", - "slicing": { - "rules": "open" - }, "definition": "SHALL be present for Patients within the Genomic Order Management ecosystem. It is preferred that all patients with an NHS number have this included within the Patient resource upon submission of a test order. Patient who do not have an NHS number SHOULD have a temporary one registered/assigned with PDS.\r\nFor patient records where the NHS number has been traced from PDS, the trace status SHOULD be provided within the NHS Number identifier slice.\r\n\r\nAdditional identifiers SHOULD include an appropriate naming system scheme which clearly identifies the assigner (to disambiguate the identifier from other resources where these are not nationally unique). Alternatively, the OID for local identifier MAY be used, with the 'assigner' organization explicitly referenced.", "min": 1 }, diff --git a/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json b/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json index 30c3dfe..bcdd207 100644 --- a/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json +++ b/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json @@ -222,9 +222,6 @@ { "id": "ServiceRequest.category", "path": "ServiceRequest.category", - "slicing": { - "rules": "open" - }, "definition": "Category SHALL be populated with the reason for the request being ordered e.g. Diagnostic, Carrier, Predictive, Stored DNA etc. The final list of applicable codes which can be selected is still under review, the Genomic-ReasonforTesting ValueSet SHOULD be used for this categorisation.", "min": 1 }, diff --git a/StructureDefinition/NHSEngland-Specimen-Genomics.json b/StructureDefinition/NHSEngland-Specimen-Genomics.json index 9aadddf..54dfe10 100644 --- a/StructureDefinition/NHSEngland-Specimen-Genomics.json +++ b/StructureDefinition/NHSEngland-Specimen-Genomics.json @@ -302,19 +302,6 @@ "definition": "The UK Core STU3 version of Specimen backports the R5 changes to the container BackboneElement to support capturing of storage location for a sample (through `container.location`) and recursive capture of device identifiers (e.g. tube, well, rack, freezer through `container.device`).\r\nThe container.identifier should match the identifier associated with the barcode for the tube/collection device. This can be searched using the container-id SearchParameter.\r\n\r\nAdditional examples/guidance will be provided within this IG once use of the fields has been appropriately tested.\r\n\r\nSample tracking information SHOULD be added to Tasks acting on Specimen resources, e.g. Tasks marked SamplePreparation or SampleProcessing, on either the output or input elements. This information MAY include consignment number, destination, date sent etc.\r\n\r\nIf known, the container type SHOULD be populated, using the example bound ValueSet, in SNOMED CT. If an appropraite code cannot be found, the specimen container type should be populated using free text, in Specimen.container.type.text. Additional container elements, such as capacity or specimenQuantity MAY be populated if known.", "max": "1" }, - { - "id": "Specimen.container.extension:specimenContainerLocationR5", - "path": "Specimen.container.extension", - "sliceName": "specimenContainerLocationR5", - "type": [ - { - "code": "Extension", - "profile": [ - "http://hl7.org/fhir/5.0/StructureDefinition/extension-Specimen.container.location" - ] - } - ] - }, { "id": "Specimen.condition", "path": "Specimen.condition", diff --git a/ValueSet/ValueSet-Genomics-test-types.json b/ValueSet/ValueSet-Genomics-test-types.json deleted file mode 100644 index b885e6d..0000000 --- a/ValueSet/ValueSet-Genomics-test-types.json +++ /dev/null @@ -1,32 +0,0 @@ -{ - "resourceType": "ValueSet", - "id": "genomics-test-types", - "url": "https://fhir.nhs.uk/ValueSet/genomics-test-types", - "version": "0.1.1", - "name": "GenomicsTestTypes", - "title": "Genomics Test Types", - "status": "draft", - "date": "2024-09-10T10:17:52.3231281+00:00", - "publisher": "NHS England", - "contact": [ - { - "name": "NHS England", - "telecom": [ - { - "system": "email", - "value": "interoperabilityteam@nhs.net" - } - ] - } - ], - "description": "A ValueSet to identify the category of genomic test types", - "copyright": "Copyright © 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \\\\\\\"License\\\\\\\"); you may not use this file except in compliance with the License. You may obtain a copy of the License at http://www.apache.org/licenses/LICENSE-2.0 Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an \\\\\\\"AS IS\\\\\\\" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License. HL7® FHIR® standard Copyright © 2011+ HL7 The HL7® FHIR® standard is used under the FHIR license. You may obtain a copy of the FHIR license at https://www.hl7.org/fhir/license.html.", - "compose": { - "include": [ - { - "system": "https://fhir.nhs.uk/CodeSystem/test-type-genomics", - "version": "0.2.0" - } - ] - } -} \ No newline at end of file