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Type:
Change Request
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Resolution: Persuasive with Modification
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Priority:
Medium
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US Minimal Common Oncology Data Elements (mCODE) (FHIR)
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STU3
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Clinical Interoperability Council
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STU
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Profiles
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May Terry/Richard Esmond: 11-0-0
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Enhancement
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Compatible, substantive
GeneticVariantFound should derive from something from the HL7 CG Genomics Reporting IG (e.g., http://build.fhir.org/ig/HL7/genomics-reporting/obs-haplotype.html) . If you have a use case that it doesn't satisfy, work with the Clinical Genomics WG to enhance their IG. Avoid creating new genomics standards where there's already work in HL7 that is addressing this. At least components should be consisnent with each other.
- is duplicated by
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FHIR-24000 Align GeneticVariantFound to CG's Variant profile
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- Duplicate
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- is voted on by
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BALLOT-10653 Negative - Bob Milius : 2019-Sep-FHIR IG MCODE R1
- Withdrawn
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BALLOT-10654 Negative - Bob Milius : 2019-Sep-FHIR IG MCODE R1
- Balloted