minimal Common Oncology Data Elements (mCODE) Implementation Guide
2.0.0 - STU 2

This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.0.0: STU 2) based on FHIR 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

ValueSet: Genomic Molecular Consequence Value Set

Summary

Defining URL:http://hl7.org/fhir/us/mcode/ValueSet/mcode-genomic-molecular-consequence-vs
Version:2.0.0
Name:GenomicMolecularConsequenceVS
Title:Genomic Molecular Consequence Value Set
Status:Active as of 1/18/22 3:17 AM
Definition:

Changes in a structural features of a sequence due to the observed variant.

Publisher:HL7 International Clinical Interoperability Council
Source Resource:XML / JSON / Turtle

References

Logical Definition (CLD)

  • Include codes from http://www.sequenceontology.org/ where concept descends from SO:0001537

 

Expansion

No Expansion for this valueset (Unknown Code System)

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code