Package | de.medizininformatikinitiative.kerndatensatz.onkologie |
Resource Type | ConceptMap |
Id | mii-cm-onko-genetische-variante-auspraegung-sct |
FHIR Version | R4 |
Source | https://simplifier.net/resolve?scope=de.medizininformatikinitiative.kerndatensatz.onkologie@2025.1.0&canonical=https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct |
URL | https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct |
Version | 2025.1.0 |
Status | active |
Date | 2024-04-10 |
Name | MII CM Onko Genetische Variante Auspraegung SCT Mapping |
Title | MII CM Onko Genetische Variante Auspraegung SNOMED Mapping |
Realm | de |
Description | Mapping Therapieabweichung Codes zu SNOMED-CT |
Purpose | Technical mapping to transform oBDS-Data into SNOMED |
No resources found
CodeSystem | |
mii-cs-onko-genetische-variante-auspraegung | MII CS Onkologie Genetische Variante Ausprägung |
No narrative content found in resource
{ "resourceType": "ConceptMap", "id": "mii-cm-onko-genetische-variante-auspraegung-sct", "url": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ConceptMap/mii-cm-onko-genetische-variante-auspraegung-sct", "version": "2025.1.0", "name": "MII CM Onko Genetische Variante Auspraegung SCT Mapping", "title": "MII CM Onko Genetische Variante Auspraegung SNOMED Mapping", "status": "active", "experimental": false, "date": "2024-04-10", "description": "Mapping Therapieabweichung Codes zu SNOMED-CT", "purpose": "Technical mapping to transform oBDS-Data into SNOMED", "sourceUri": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/", "targetUri": "http://snomed.info/sct/900000000000207008/version/20240401", "group": [ { "source": "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung", "target": "http://snomed.info/sct/900000000000207008/version/20240401", "element": [ { "code": "M", "display": "Mutation/positiv", "target": [ { "code": "55446002", "display": "Genetic mutation (finding)", "equivalence": "equivalent" } ] }, { "code": "W", "display": "Wildtyp/nicht mutiert/ negativ", "target": [ { "code": "412730000", "display": "Genetic finding not detected (finding)", "equivalence": "equivalent" } ] }, { "code": "P", "display": "Polymorphismus", "target": [ { "code": "50334000", "display": "Genetic polymorphism (finding)", "equivalence": "equivalent" } ] }, { "code": "S", "display": "Sonstiges", "target": [ { "code": "74964007", "display": "Other (qualifier value)", "equivalence": "equivalent" } ] }, { "code": "N", "display": "Nicht bestimmbar", "target": [ { "code": "1156316003", "display": "Cannot be determined (qualifier value)", "equivalence": "equivalent" } ] }, { "code": "U", "display": "Unbekannt", "target": [ { "code": "261665006", "display": "Unknown (qualifier value)", "equivalence": "equivalent" } ] } ] } ] }