HTML View

Table View

XML View

<ConceptMap xmlns="http://hl7.org/fhir">
    <id value="genomics-condition-pancreatictumourtype" />
    <url value="https://fhir.nhs.uk/ConceptMap/genomics-condition-pancreatictumourtype" />
    <version value="0.1.0" />
    <name value="GenomicsConditionPancreaticTumourType" />
    <title value="Genomics Condition Pancreatic 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 = pancreatic tumour type" />
    <copyright value="Copyright &#169; 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \&quot;License\&quot;); 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 \&quot;AS IS\&quot; 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&#174; FHIR&#174; standard Copyright &#169; 2011+ HL7 The HL7&#174; FHIR&#174; 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="insulinoma" />
            <display value="INSULINOMA" />
            <target>
                <code value="20955008" />
                <display value="Insulinoma, malignant (morphologic abnormality)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="gastrinoma" />
            <display value="GASTRINOMA" />
            <target>
                <code value="19756007" />
                <display value="Gastrinoma, malignant (morphologic abnormality)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="glucagonoma" />
            <display value="GLUCAGONOMA" />
            <target>
                <code value="66515009" />
                <display value="Glucagonoma, malignant (morphologic abnormality)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="vipoma" />
            <display value="VIPOMA" />
            <target>
                <code value="31131002" />
                <display value="Vipoma, malignant (morphologic abnormality)" />
                <equivalence value="equivalent" />
            </target>
        </element>
    </group>
</ConceptMap>

JSON View

{
    "resourceType": "ConceptMap",
    "id": "genomics-condition-pancreatictumourtype",
    "url": "https://fhir.nhs.uk/ConceptMap/genomics-condition-pancreatictumourtype",
    "version": "0.1.0",
    "name": "GenomicsConditionPancreaticTumourType",
    "title": "Genomics Condition Pancreatic 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 = pancreatic 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": "insulinoma",
                    "display": "INSULINOMA",
                    "target":  [
                        {
                            "code": "20955008",
                            "display": "Insulinoma, malignant (morphologic abnormality)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "gastrinoma",
                    "display": "GASTRINOMA",
                    "target":  [
                        {
                            "code": "19756007",
                            "display": "Gastrinoma, malignant (morphologic abnormality)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "glucagonoma",
                    "display": "GLUCAGONOMA",
                    "target":  [
                        {
                            "code": "66515009",
                            "display": "Glucagonoma, malignant (morphologic abnormality)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "vipoma",
                    "display": "VIPOMA",
                    "target":  [
                        {
                            "code": "31131002",
                            "display": "Vipoma, malignant (morphologic abnormality)",
                            "equivalence": "equivalent"
                        }
                    ]
                }
            ]
        }
    ]
}

Propose a change to ConceptMap Genomic Condition Pancreatic Tumour Type

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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 &#169; 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \&quot;License\&quot;); 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 \&quot;AS IS\&quot; 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&#174; FHIR&#174; standard Copyright &#169; 2011+ HL7 The HL7&#174; FHIR&#174; 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&#39;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"
                        }
                    ]
                }
            ]
        }
    ]
}

Propose a change to ConceptMap Genomic Condition Pituitary Tumour Type

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XML View

<ConceptMap xmlns="http://hl7.org/fhir">
    <id value="genomics-condition-solidtumourtype" />
    <url value="https://fhir.nhs.uk/ConceptMap/genomics-condition-solidtumourtype" />
    <version value="0.1.0" />
    <name value="GenomicsConditionSolidTumourType" />
    <title value="Genomics Condition Solid 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 for solid tumour types. This is intended for the element Condition.note" />
    <copyright value="Copyright &#169; 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \&quot;License\&quot;); 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 \&quot;AS IS\&quot; 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&#174; FHIR&#174; standard Copyright &#169; 2011+ HL7 The HL7&#174; FHIR&#174; 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="solid" />
            <display value="SOLID" />
            <target>
                <code value="35702001" />
                <display value="Solid (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="primary" />
            <display value="PRIMARY" />
            <target>
                <code value="63161005" />
                <display value="Principal (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="metastatic" />
            <display value="METASTATIC" />
            <target>
                <code value="1505291000004100" />
                <display value="Discontinuous metastatic spread (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="unknown" />
            <display value="UNKNOWN" />
            <target>
                <code value="261665006" />
                <display value="UNKNOWN" />
                <equivalence value="equivalent" />
            </target>
        </element>
    </group>
</ConceptMap>

JSON View

{
    "resourceType": "ConceptMap",
    "id": "genomics-condition-solidtumourtype",
    "url": "https://fhir.nhs.uk/ConceptMap/genomics-condition-solidtumourtype",
    "version": "0.1.0",
    "name": "GenomicsConditionSolidTumourType",
    "title": "Genomics Condition Solid 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 for solid tumour types. This is intended for the element Condition.note",
    "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": "solid",
                    "display": "SOLID",
                    "target":  [
                        {
                            "code": "35702001",
                            "display": "Solid (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "primary",
                    "display": "PRIMARY",
                    "target":  [
                        {
                            "code": "63161005",
                            "display": "Principal (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "metastatic",
                    "display": "METASTATIC",
                    "target":  [
                        {
                            "code": "1505291000004100",
                            "display": "Discontinuous metastatic spread (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "unknown",
                    "display": "UNKNOWN",
                    "target":  [
                        {
                            "code": "261665006",
                            "display": "UNKNOWN",
                            "equivalence": "equivalent"
                        }
                    ]
                }
            ]
        }
    ]
}

Propose a change to ConceptMap Genomic Condition Solid Tumour Type

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Table View

XML View

<ConceptMap xmlns="http://hl7.org/fhir">
    <id value="genomics-specimen-tumourcellularity" />
    <url value="https://fhir.nhs.uk/ConceptMap/genomics-specimen-tumourcellularity" />
    <version value="0.1.0" />
    <name value="GenomicsSpecimenTumourCellularity" />
    <title value="Genomics Specimen Tumour Cellularity" />
    <status value="draft" />
    <date value="2024-08-05T00:00:00.000Z" />
    <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 for the proportion of tumour cellularity. This is intended for the element Observation.valueCodeableConcept." />
    <copyright value="Copyright &#169; 2023+ NHS England Licensed under the Apache License, Version 2.0 (the \&quot;License\&quot;); 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 \&quot;AS IS\&quot; 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&#174; FHIR&#174; standard Copyright &#169; 2011+ HL7 The HL7&#174; FHIR&#174; 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 value="http://snomed.info/sct?fhir_vs=ecl/%3C!%20362981000%20" />
    <group>
        <source value="https://future.nhs.uk/NHSgenomics/view?objectId=222250117" />
        <target value="http://snomed.info/sct" />
        <element>
            <code value="high" />
            <display value="High" />
            <target>
                <code value="75540009" />
                <display value="High (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="low" />
            <display value="Low" />
            <target>
                <code value="62482003" />
                <display value="Low (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="medium" />
            <display value="Medium" />
            <target>
                <code value="255508009" />
                <display value="Medium (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="very-high" />
            <display value="Very High" />
            <target>
                <code value="260360000" />
                <display value="Very high (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
        <element>
            <code value="very-low" />
            <display value="Very Low" />
            <target>
                <code value="260360000" />
                <display value="Very low (qualifier value)" />
                <equivalence value="equivalent" />
            </target>
        </element>
    </group>
</ConceptMap>

JSON View

{
    "resourceType": "ConceptMap",
    "id": "genomics-specimen-tumourcellularity",
    "url": "https://fhir.nhs.uk/ConceptMap/genomics-specimen-tumourcellularity",
    "version": "0.1.0",
    "name": "GenomicsSpecimenTumourCellularity",
    "title": "Genomics Specimen Tumour Cellularity",
    "status": "draft",
    "date": "2024-08-05T00:00:00.000Z",
    "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 for the proportion of tumour cellularity. This is intended for the element Observation.valueCodeableConcept.",
    "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?fhir_vs=ecl/%3C!%20362981000%20",
    "group":  [
        {
            "source": "https://future.nhs.uk/NHSgenomics/view?objectId=222250117",
            "target": "http://snomed.info/sct",
            "element":  [
                {
                    "code": "high",
                    "display": "High",
                    "target":  [
                        {
                            "code": "75540009",
                            "display": "High (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "low",
                    "display": "Low",
                    "target":  [
                        {
                            "code": "62482003",
                            "display": "Low (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "medium",
                    "display": "Medium",
                    "target":  [
                        {
                            "code": "255508009",
                            "display": "Medium (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "very-high",
                    "display": "Very High",
                    "target":  [
                        {
                            "code": "260360000",
                            "display": "Very high (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                },
                {
                    "code": "very-low",
                    "display": "Very Low",
                    "target":  [
                        {
                            "code": "260360000",
                            "display": "Very low (qualifier value)",
                            "equivalence": "equivalent"
                        }
                    ]
                }
            ]
        }
    ]
}

Propose a change to ConceptMap Genomic Specimen Tumour Cellularity