AutoICD API

70162-3

Laboratory

Chlamydia trachomatis and Neisseria gonorrhoeae rRNA panel - Urethra by NAA with probe detection

Definition

This panel was created based on Gen-Probe APTIMA COMBO 2 Assay. The test is used for detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis and/or Neisseria gonorrhoeae.

LOINC 6-Axis Classification

Component

Chlamydia trachomatis & Neisseria gonorrhoeae rRNA panel

Property

-

Time Aspect

Pt

System

Urethra

Scale Type

-

Method Type

Probe.amp.tar

Details

Class

PANEL.MICRO

Order/Observation

Order

Short Name

C trach+GC pnl Urth NAA+probe

Display Name

C. trachomatis and N. gonorrhoeae rRNA panel NAA+probe (Urethra)

Related Names

3 Self-Sustaining Sequence Replication3SR SRAmplifAmplificationAmplifiedC tracC trachC trach+GCC trach+GC pnlC trachoC trachomatisChlamChlam tracChlamidCTCT/GCDNA NUCLEIC ACID PROBEDNA probeGCGenital tractGen-ProbeGonoGonorrheaIDInfectious DiseaseInfectiousDiseaseLATLCRLGVLigase chain reactionLigation-activated transcriptionLymphogranuloma venereumMicrobiologyN gonorrhoeaN gonorrhoeaeNAA+probeNAATNASBANucleic acid sequence based analysisPanPANEL.MICROBIOLOGYPanlPCRPnlPoint in timePolymerase chain reactionProbe ampProbe with ampificationProbe with target amplificationQBRRandomribosomal RNASDAStrand Displacement AmplificationTMATrachomaTranscription mediated amplificationUrth

Frequently Asked Questions

What is LOINC code 70162-3?

LOINC code 70162-3 identifies "Chlamydia trachomatis and Neisseria gonorrhoeae rRNA panel - Urethra by NAA with probe detection". This panel was created based on Gen-Probe APTIMA COMBO 2 Assay. The test is used for detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis and/or Neisseria gonorrhoeae.

What does 70162-3 measure?

This code measures Chlamydia trachomatis & Neisseria gonorrhoeae rRNA panel in Urethra. It belongs to the PANEL.MICRO 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.