HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1
1.0.0 - STU1

This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.0.0: STU 1) based on FHIR R4. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions

Human Genome Variation Society Sequence Variant Nomenclature Value Set

Summary

Defining URL:http://hl7.org/fhir/us/mcode/ValueSet/mcode-hgvs-vs
Version:1.0.0
Name:HGVSVS
Status:Active
Title:Human Genome Variation Society Sequence Variant Nomenclature Value Set
Definition:

HGVS nomenclature is used to report and exchange information regarding variants found in DNA, RNA, and protein sequences.

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

References

Content Logical Definition

Definition

  • Include all codes defined in http://varnomen.hgvs.org

 

Expansion

No Expansion for this valueset (not supported by Publication Tooling)

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
Source 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