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Type:
Change Request
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Resolution: Persuasive
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Priority:
Medium
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FHIR Core (FHIR)
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DSTU2
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Clinical Genomics
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(profiles)
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10.1.13.4
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David Kreda/Clem McDownload: 25-0-2
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Clarification
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Non-substantive
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DSTU2
Comment:
This section lists a set of variables that look like they were taken directly from the V2 genetics reporting specification, and that is good, but they do not show the associated LOINC codes. They are extensions to the observation, I think. They could all be component observations and then would line up closely with the HL7 V2 Coded Clinical Genomics lite. But not clear again how sequence connects to the observations or vice versa.
Summary:
LOINC codes for genetics reporting
- is voted on by
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BALLOT-3106 Affirmative - Clement McDonald : 2018-Sep-FHIR R1
- Closed