| 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"
}
]
}
]
}
]
}