MII IG Kerndatensatz-Modul Onkologie
2027.0.0-ballot.1 -
Germany
MII IG Kerndatensatz-Modul Onkologie
2027.0.0-ballot.1 -
Germany
This page is part of the MII IG Kerndatensatz-Modul Onkologie (v2027.0.0-ballot.1: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
| Active as of 2024-04-10 |
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"div" : "<div xml:lang=\"en\" lang=\"en\"><hr/><p><b>English</b></p><hr/><p class=\"res-header-id\"><b>Generated Narrative: ConceptMap mii-cm-onko-genetische-variante-auspraegung-sct</b></p><a name=\"mii-cm-onko-genetische-variante-auspraegung-sct\"> </a><a name=\"hcmii-cm-onko-genetische-variante-auspraegung-sct\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\"/><p style=\"margin-bottom: 0px\">Profiles: <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-crmi-shareableconceptmap.html\">CRMI Shareable ConceptMap</a>, <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-crmi-publishableconceptmap.html\">CRMI Publishable ConceptMap</a></p></div><p>Mapping from https://www.medizininformatik-initiative.de/fhir/ext/modul-onko/ to http://snomed.info/sct/900000000000207008/version/20240401</p><br/><p>Mapping from <a href=\"CodeSystem-mii-cs-onko-genetische-variante-auspraegung.html\">MII CS Onkologie Genetische Variante Ausprägung</a> to <code>http://snomed.info/sct/900000000000207008/version/20240401</code></p><table class=\"grid\"><tr><td><b>Source Code</b></td><td><b>Relationship</b></td><td><b>Target Code</b></td></tr><tr><td>M (Mutation/positiv)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>55446002 (Genetic mutation (finding))</td></tr><tr><td>W (Wildtyp/nicht mutiert/ negativ)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>412730000 (Genetic finding not detected (finding))</td></tr><tr><td>P (Polymorphismus)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>50334000 (Genetic polymorphism (finding))</td></tr><tr><td>S (Sonstiges)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>74964007 (Other (qualifier value))</td></tr><tr><td>N (Nicht bestimmbar)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>1156316003 (Cannot be determined (qualifier value))</td></tr><tr><td>U (Unbekannt)</td><td><a href=\"http://hl7.org/fhir/R4/codesystem-concept-map-equivalence.html#concept-map-equivalence-equivalent\" title=\"equivalent\">is equivalent to</a></td><td>261665006 (Unknown (qualifier value))</td></tr></table></div>"
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"version" : "2027.0.0-ballot.1",
"name" : "MII CM Onko Genetische Variante Auspraegung SCT Mapping",
"title" : "MII CM Onko Genetische Variante Auspraegung SNOMED Mapping",
"status" : "active",
"experimental" : true,
"date" : "2024-04-10",
"publisher" : "Medizininformatik Initiative",
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"description" : "Mapping Therapieabweichung Codes zu SNOMED-CT STATUS DIESER ZUORDNUNG: 2024 erstellt, gegen SNOMED CT International 20240401. Sie ist WEDER OFFIZIELL ENDORSED NOCH FINAL QUALITAETSGESICHERT - es handelt sich um einen projektseitigen Arbeitsstand, nicht um eine abgestimmte Referenz. Die Zielcodes sind gegen neuere SNOMED-Releases nicht nachverifiziert; einzelne Konzepte koennen inzwischen inaktiviert oder ersetzt sein. Vor einer Nutzung in Produktivsystemen sind fachliche Pruefung und ein Abgleich gegen die eingesetzte SNOMED-Version erforderlich.",
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"purpose" : "Technical mapping to transform oBDS-Data into SNOMED",
"copyright" : "This material includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of SNOMED International. All rights reserved. SNOMED CT®, was originally created by The College of American Pathologists. SNOMED and SNOMED CT are registered trademarks of SNOMED International. Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license.",
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