XML View
<ConceptMap xmlns="http://hl7.org/fhir">
<id value="genomics-condition-pituitarytumourtype" />
<url value="https://fhir.nhs.uk/ConceptMap/genomics-condition-pituitarytumourtype" />
<version value="0.1.0" />
<name value="GenomicsConditionPituitaryTumourType" />
<title value="Genomics Condition Pituitary Tumour Type" />
<status value="draft" />
<date value="2024-06-11T00:00:00.000Z" />
<publisher value="NHS England" />
<contact>
<name value="NHS England" />
<telecom>
<system value="email" />
<value value="interoperabilityteam@nhs.net" />
</telecom>
</contact>
<description value="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 value="ConceptMap used for the translation and recording of concepts when Condition.code field = pituitary tumour type" />
<copyright value="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." />
<group>
<source value="https://future.nhs.uk/NHSgenomics/view?objectId=222250117" />
<target value="http://snomed.info/sct" />
<element>
<code value="gh-secreting" />
<display value="GH-SECRETING" />
<target>
<code value="254957009" />
<display value="Somatotroph adenoma (disorder)" />
<equivalence value="equivalent" />
</target>
</element>
<element>
<code value="prolactinoma" />
<display value="PROLACTINOMA" />
<target>
<code value="134209002" />
<display value="Prolactinoma (disorder)" />
<equivalence value="equivalent" />
</target>
</element>
<element>
<code value="non-functioning" />
<display value="NON-FUNCTIONING" />
<target>
<code value="254962005" />
<display value="Functionless pituitary adenoma (disorder)" />
<equivalence value="equivalent" />
</target>
</element>
<element>
<code value="cushing-disease" />
<display value="CUSHINGS DISEASE" />
<target>
<code value="190502001" />
<display value="Pituitary-dependent Cushing's disease (disorder)" />
<equivalence value="equivalent" />
</target>
</element>
</group>
</ConceptMap>
JSON View
{
"resourceType": "ConceptMap",
"id": "genomics-condition-pituitarytumourtype",
"url": "https://fhir.nhs.uk/ConceptMap/genomics-condition-pituitarytumourtype",
"version": "0.1.0",
"name": "GenomicsConditionPituitaryTumourType",
"title": "Genomics Condition Pituitary Tumour Type",
"status": "draft",
"date": "2024-06-11T00:00:00.000Z",
"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 when Condition.code field = pituitary tumour type",
"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.",
"group": [
{
"source": "https://future.nhs.uk/NHSgenomics/view?objectId=222250117",
"target": "http://snomed.info/sct",
"element": [
{
"code": "gh-secreting",
"display": "GH-SECRETING",
"target": [
{
"code": "254957009",
"display": "Somatotroph adenoma (disorder)",
"equivalence": "equivalent"
}
]
},
{
"code": "prolactinoma",
"display": "PROLACTINOMA",
"target": [
{
"code": "134209002",
"display": "Prolactinoma (disorder)",
"equivalence": "equivalent"
}
]
},
{
"code": "non-functioning",
"display": "NON-FUNCTIONING",
"target": [
{
"code": "254962005",
"display": "Functionless pituitary adenoma (disorder)",
"equivalence": "equivalent"
}
]
},
{
"code": "cushing-disease",
"display": "CUSHINGS DISEASE",
"target": [
{
"code": "190502001",
"display": "Pituitary-dependent Cushing's disease (disorder)",
"equivalence": "equivalent"
}
]
}
]
}
]
}
