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Type:
Change Request
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Resolution: Persuasive
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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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(NA)
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Richard Esmond/May Terry: 12-0-1
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Enhancement
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Compatible, substantive
Comment:
The current IG lacks cytogenetics or structured genetic variant reporting. Suggest looking at ISCN and perhaps use as HGVS has been used for a ChromosomalStructueFindings component. Look at component:cytogenomic-nomenclature in the CG IG for an example http://build.fhir.org/ig/HL7/genomics-reporting/obs-variant.html. consider adopting the component (essentially copy/paste from the CG WG IG. If you like, mention the CG WG IG In the component definition to make the connection obvious to implementors?)
Summary:
Lacks cytogenetics or structured variant reporting, consider adopting component:cytogenomic-nomenclature in the CG IG
- is voted on by
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BALLOT-10698 Negative - Bret Heale : 2019-Sep-FHIR IG MCODE R1
- Balloted