Loading...

XML

Word

Printable

JSON

Specification:

US Minimal Common Oncology Data Elements (mCODE) (FHIR)
Raised in Version:

1.16.0 [deprecated]
Work Group:

Clinical Interoperability Council
Related URL:
http://hl7.org/fhir/us/mcode/2021May/StructureDefinition-mcode-cancer-genetic-variant.html
Related Artifact(s):

Cancer Genetic Variant [deprecated]
Grouping:
- Block-Vote-5
- Genetic
Resolution Description:
Hide

Interim approach until the HL7 CGWG has a more holistic approach to fusion genes:

create new component for variant-category (put CG Reporting IG) for the LOINC code and value set (SO)

document using gene-studied (which is 0..*) to include both genes for components. document in the IG that order matters in the mCODE Genomics Implementation page.
Show
Interim approach until the HL7 CGWG has a more holistic approach to fusion genes: create new component for variant-category (put CG Reporting IG) for the LOINC code and value set (SO) document using gene-studied (which is 0..*) to include both genes for components. document in the IG that order matters in the mCODE Genomics Implementation page.
Resolution Vote:
Sherita Alai / Mark Kramer /8-0-3
Change Category:
Enhancement
Change Impact:
Compatible, substantive
Pre Applied:
Yes

Multiple Genomics reports designate fusion events.

Creating two gene-studied components in CancerGeneticVariant does not adequately represent the fusion type or asserts that it is a fusion event.