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This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
88184-Flow cytometry, first marker
88185 x 2-Flow cytometry, each additional marker
|Test ID||Test Order Name||Order LOINC Code|
|CVID||CVID Confirmation Flow Panel||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|28113||CD19+ TACI+ % of CD19 B cells||In Process|
|28121||CD19+ BAFF-R+ % of CD19 B cells||In Process|