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Specification:

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

1.16.0 [deprecated]
Work Group:

Clinical Interoperability Council
Related Artifact(s):

DNA Change Type Value Set [deprecated]
Genomic Region Studied Profile
Grouping:
- Block-Vote-6
Resolution Description:

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This issue has been split into a number of other issues, and these will be considered separately as part of Block Vote 6.

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This issue has been split into a number of other issues, and these will be considered separately as part of Block Vote 6.
Resolution Vote:
Saul Kravitz/Sherita Alai:4-0-0
Change Category:
Correction
Change Impact:
Non-compatible
Pre Applied:
Yes

1	mCODE CancerGeneticVariant missing genomic variant category	Change request	1.16.0
2	mCODE does not have an adequate way to support fusion events	Change request	1.16.0	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.
3	mCODE CancerGeneticVariant missing clinical significance	Change request	1.16.0
4	mCODE CancerGeneticVariant missing allelic frequency	Change request	1.16.0
5	mCODE CancerGeneticVariant missing Genomic Structural Variant Copy Number	Change request	1.16.0
6	Consider renaming CancerGeneticVariant to a more accurate name which covers both dna and amino acid changes	Change request