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FHIR IG Statistics: ConceptMap/genomics-fetal-maternal-screening-genotype

Packageuk.nhsengland.genomics.r4
Resource TypeConceptMap
Idgenomics-fetal-maternal-screening-genotype
FHIR VersionR4
Sourcehttps://simplifier.net/resolve?scope=uk.nhsengland.genomics.r4@0.4.4&canonical=https://fhir.nhs.uk/ConceptMap/genomics-fetal-maternal-screening-genotype
URLhttps://fhir.nhs.uk/ConceptMap/genomics-fetal-maternal-screening-genotype
Version0.1.0
Statusdraft
Date2024-08-08T18:15:00.000Z
NameGenomicsFetalMaternalScreeningGenotype
TitleGenomics Fetal Maternal Screening Genotype
DescriptionA ConceptMap used for the translation and recording of concepts from MDS source data(code-options) to equivalent Snomed CT codes, and FHIR spec.
PurposeConceptMap 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.
CopyrightCopyright © 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.

Resources that use this resource

No resources found


Resources that this resource uses

CodeSystem
sctSNOMED CT (all versions)

Narrative

No narrative content found in resource


Source

{
  "resourceType": "ConceptMap",
  "id": "genomics-fetal-maternal-screening-genotype",
  "url": "https://fhir.nhs.uk/ConceptMap/genomics-fetal-maternal-screening-genotype",
  "version": "0.1.0",
  "name": "GenomicsFetalMaternalScreeningGenotype",
  "title": "Genomics Fetal Maternal Screening Genotype",
  "status": "draft",
  "date": "2024-08-08T18:15:00.000Z",
  "publisher": "NHS England",
  "contact": [
    {
      "name": "NHS England",
      "telecom": [
        {
          "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": [
    {
      "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 (disorder)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "HbAC",
          "display": "HbAC",
          "target": [
            {
              "code": "76050008",
              "display": "Hemoglobin C trait (disorder)",
              "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 (disorder)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "HbSS",
          "display": "HbSS",
          "target": [
            {
              "code": "127040003",
              "display": "Sickle cell-hemoglobin SS disease (disorder)",
              "equivalence": "equivalent"
            }
          ]
        },
        {
          "code": "other",
          "display": "OTHER",
          "target": [
            {
              "code": "other",
              "display": "Other",
              "equivalence": "equivalent"
            }
          ]
        }
      ]
    }
  ]
}