LOINC codes for genetics reporting - 2016-09 core #472

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    • Type: Change Request
    • Resolution: Persuasive
    • Priority: Medium
    • FHIR Core (FHIR)
    • DSTU2
    • Clinical Genomics
    • (profiles)
    • 10.1.13.4
    • Hide

      Persuasive – add LOINC code

      The function of component and extension is different, observation.component element will be used for knowledge-based interpretations of the sequence variant, and extension is used to provide genetics information.

      We will add missed LOINC code for the extensions.

      Some of the extensions don't have the LOINC code thus they would not include the LOINC code link in the description box.

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      Persuasive – add LOINC code The function of component and extension is different, observation.component element will be used for knowledge-based interpretations of the sequence variant, and extension is used to provide genetics information. We will add missed LOINC code for the extensions. Some of the extensions don't have the LOINC code thus they would not include the LOINC code link in the description box.
    • David Kreda/Clem McDownload: 25-0-2
    • Clarification
    • Non-substantive
    • 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

            Assignee:
            Unassigned
            Reporter:
            clemmcdonald
            clemmcdonald
            Watchers:
            2 Start watching this issue

              Created:
              Updated:
              Resolved: