AutoICD API

73810-4

Laboratory

CD3-CD16+CD56+HLA-DR+ (activated Natural Killer) cells/Cells.CD3-CD16+CD56+ in Blood by Flow cytometry (FC)

Definition

The % activated natural killer (NK) cells can be determined by comparing the number of activated NK cells (CD3-CD16+CD56+HLA-DR+) out of 100 NK cells (CD3-CD16+CD56+). The submitter's lab uses HLA DR antibodies (HLA DR+) for late activation of NK cells within a subpopulation of NK cells that lack CD3 expression (CD3-) and express CD16 and CD56 (CD16+, CD56+).

LOINC 6-Axis Classification

Component

Cells.CD3-CD16+CD56+HLA-DR+/Cells.CD3-CD16+CD56+

Property

NFr

Time Aspect

Pt

System

Bld

Scale Type

Qn

Method Type

Flow cytometry

Details

Class

CELLMARK

Order/Observation

Both

Short Name

NK activated/NK NFr Bld FC

Display Name

CD3-CD16+CD56+HLA-DR+ (activated Natural Killer) cells/Cells.CD3-CD16+CD56+ FC (Bld)

Related Names

BloodCD3 CellsCD3+CD16+ CellsCD3+CD16+CD56+ CellsCD3-CD16+ CellsCD3-CD16+CD56+ CellsCellCELL MARKERSCellularityDynamicFCFCGR3AHuman Leukocyte AntigenI3Leu11Leu-11Leu11bLeu-11BLeu19Leu-19Leu4Leu-4Natural killer cellsNCAMNeural cell adhesion moleculeNKNK activatedNKH1Number fractionPercentPoint in timeQNTQuanQuantQuantitativeRandomT3WBWhole blood

Frequently Asked Questions

What is LOINC code 73810-4?

LOINC code 73810-4 identifies "CD3-CD16+CD56+HLA-DR+ (activated Natural Killer) cells/Cells.CD3-CD16+CD56+ in Blood by Flow cytometry (FC)". The % activated natural killer (NK) cells can be determined by comparing the number of activated NK cells (CD3-CD16+CD56+HLA-DR+) out of 100 NK cells (CD3-CD16+CD56+). The submitter's lab uses HLA DR antibodies (HLA DR+) for late activation of NK cells within a subpopulation of NK cells that lack CD3 expression (CD3-) and express CD16 and CD56 (CD16+, CD56+).

What does 73810-4 measure?

This code measures Cells.CD3-CD16+CD56+HLA-DR+/Cells.CD3-CD16+CD56+ in Bld. It belongs to the CELLMARK class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.