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

This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v0.9.1: STU 1 Ballot 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

GenomicSourceClassVS

GenomicSourceClassVS ValueSet

The genomic class of the specimen being analyzed, for example, germline for inherited genome, somatic for cancer genome, and prenatal for fetal genome.

Defining URL:http://hl7.org/fhir/us/mcode/ValueSet/onco-core-GenomicSourceClassVS
Version:0.9.1
Name:GenomicSourceClassVS
Definition:

The genomic class of the specimen being analyzed, for example, germline for inherited genome, somatic for cancer genome, and prenatal for fetal genome.

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

Expansion

This value set contains 8 concepts

All codes from system http://loinc.org

CodeDisplay
LA6683-2Germline
LA6684-0Somatic
LA10429-1Fetal
LA18194-3Likely germline
LA18195-0Likely somatic
LA18196-8Likely fetal
LA18197-6Unknown genomic origin
LA26807-0De novo

References

This value set is used by the following logical models, profiles and extensions: