From 77b0d8154370ebf90fc5d018cd7c3d4ed739bfa1 Mon Sep 17 00:00:00 2001 From: KazeemHamzat Date: Tue, 21 Oct 2025 09:16:35 +0100 Subject: [PATCH] Update ConceptMap-Genomics-fetal-maternal-screening-genotype Map code value 'other' to Snomed --- ...ics-fetal-maternal-screening-genotype.json | 188 +++++++++--------- 1 file changed, 94 insertions(+), 94 deletions(-) diff --git a/ConceptMap/ConceptMap-Genomics-fetal-maternal-screening-genotype.json b/ConceptMap/ConceptMap-Genomics-fetal-maternal-screening-genotype.json index 19578ce..d40484c 100644 --- a/ConceptMap/ConceptMap-Genomics-fetal-maternal-screening-genotype.json +++ b/ConceptMap/ConceptMap-Genomics-fetal-maternal-screening-genotype.json @@ -1,100 +1,100 @@ { - "resourceType": "ConceptMap", - "id": "genomics-fetal-maternal-screening-genotype", - "url": "https://fhir.nhs.uk/ConceptMap/genomics-fetal-maternal-screening-genotype", - "version": "0.2.0", - "name": "GenomicsFetalMaternalScreeningGenotype", - "title": "Genomics Fetal Maternal Screening Genotype", - "status": "draft", - "date": "2025-09-05T11:00:00.000Z", - "publisher": "NHS England", - "contact": [ + "resourceType": "ConceptMap", + "id": "genomics-fetal-maternal-screening-genotype", + "url": "https://fhir.nhs.uk/ConceptMap/genomics-fetal-maternal-screening-genotype", + "version": "0.3.0", + "name": "GenomicsFetalMaternalScreeningGenotype", + "title": "Genomics Fetal Maternal Screening Genotype", + "status": "draft", + "date": "2025-10-05T21:00:00.000Z", + "publisher": "NHS England", + "contact": [ + { + "name": "NHS England", + "telecom": [ { - "name": "NHS England", - "telecom": [ - { - "system": "email", - "value": "interoperabilityteam@nhs.net" - } - ] + "system": "email", + "value": "interoperabilityteam@nhs.net" } - ], - "description": "A ConceptMap used for the translation and recording of concepts from MDS source data(code-options) to equivalent Snomed CT codes, and FHIR spec.", - "purpose": "ConceptMap used for the translation and recording of concepts for fetal maternal screening genotype. This is intended for the element Condition.code. An appropriate SNOMED CT code or free text should be used to record the Genotype.", - "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.", - "targetUri": "http://snomed.info/sct", - "group": [ + ] + } + ], + "description": "A ConceptMap used for the translation and recording of concepts from MDS source data(code-options) to equivalent Snomed CT codes, and FHIR spec.", + "purpose": "ConceptMap used for the translation and recording of concepts for fetal maternal screening genotype. This is intended for the element Condition.code. An appropriate SNOMED CT code or free text should be used to record the Genotype.", + "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.", + "targetUri": "http://snomed.info/sct", + "group": [ + { + "source": "https://future.nhs.uk/NHSgenomics/view?objectId=222250117", + "target": "http://snomed.info/sct", + "element": [ { - "source": "https://future.nhs.uk/NHSgenomics/view?objectId=222250117", - "target": "http://snomed.info/sct", - "element": [ - { - "code": "alpha-beta-thalassaemia", - "display": "Alpha Beta Thalassaemia", - "target": [ - { - "code": "234389001", - "display": "Alpha-beta thalassemia", - "equivalence": "equivalent" - } - ] - }, - { - "code": "HbAC", - "display": "HbAC", - "target": [ - { - "code": "76050008", - "display": "Hemoglobin C trait", - "equivalence": "equivalent" - } - ] - }, - { - "code": "HbAS", - "display": "HbAS", - "target": [ - { - "code": "417357006", - "display": "Sickling disorder due to haemoglobin S", - "equivalence": "equivalent" - } - ] - }, - { - "code": "HbSC", - "display": "HbSC", - "target": [ - { - "code": "35434009", - "display": "Sickle cell-hemoglobin C disease", - "equivalence": "equivalent" - } - ] - }, - { - "code": "HbSS", - "display": "HbSS", - "target": [ - { - "code": "127040003", - "display": "Sickle cell-hemoglobin SS disease", - "equivalence": "equivalent" - } - ] - }, - { - "code": "other", - "display": "OTHER", - "target": [ - { - "code": "other", - "display": "Other", - "equivalence": "equivalent" - } - ] - } - ] + "code": "alpha-beta-thalassaemia", + "display": "Alpha Beta Thalassaemia", + "target": [ + { + "code": "234389001", + "display": "Alpha-beta thalassemia", + "equivalence": "equivalent" + } + ] + }, + { + "code": "HbAC", + "display": "HbAC", + "target": [ + { + "code": "76050008", + "display": "Hemoglobin C trait", + "equivalence": "equivalent" + } + ] + }, + { + "code": "HbAS", + "display": "HbAS", + "target": [ + { + "code": "417357006", + "display": "Sickling disorder due to haemoglobin S", + "equivalence": "equivalent" + } + ] + }, + { + "code": "HbSC", + "display": "HbSC", + "target": [ + { + "code": "35434009", + "display": "Sickle cell-hemoglobin C disease", + "equivalence": "equivalent" + } + ] + }, + { + "code": "HbSS", + "display": "HbSS", + "target": [ + { + "code": "127040003", + "display": "Sickle cell-hemoglobin SS disease", + "equivalence": "equivalent" + } + ] + }, + { + "code": "other", + "display": "OTHER", + "target": [ + { + "code": "427306008", + "display": "Hereditary hemoglobinopathy (disorder) ", + "equivalence": "wider" + } + ] } - ] + ] + } + ] } \ No newline at end of file