Package | de.medizininformatikinitiative.kerndatensatz.onkologie |
Type | ConceptMap |
Id | Id |
FHIR Version | R4 |
Source | https://simplifier.net/resolve?scope=de.medizininformatikinitiative.kerndatensatz.onkologie@2025.0.3&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 |
Status | active |
Date | 2024-04-10 |
Name | MII CM Onko Genetische Variante Auspraegung SCT Mapping |
Title | MII CM Onko Genetische Variante Auspraegung SNOMED Mapping |
Experimental | False |
Realm | de |
Description | Mapping Therapieabweichung Codes zu SNOMED-CT |
Purpose | Technical mapping to transform oBDS-Data into SNOMED |
No resources found
CodeSystem | |
http://snomed.info/sct ![]() | SNOMED CT (all versions) |
http://snomed.info/sct ![]() | SNOMED CT (all versions) |
http://snomed.info/sct ![]() | veri |
https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung ![]() | MII CS Onkologie Genetische Variante Ausprägung |
{
"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",
"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",
"group" : [
{
"source" : "https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/CodeSystem/mii-cs-onko-genetische-variante-auspraegung",
"target" : "http://snomed.info/sct",
"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"
}
]
}
]
}
],
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.