AutoICD API

94660-8

Laboratory

SARS-CoV-2 (COVID-19) RNA [Presence] in Serum or Plasma by NAA with probe detection

Definition

Qualitative detection of SARS coronavirus 2 (SARS-CoV-2) in serum or plasma specimens by nucleic acid amplification with probe-based detection. Results may be based on multiple assays to determine the presence of the virus in a specimen.

LOINC 6-Axis Classification

Component

SARS coronavirus 2 RNA

Property

PrThr

Time Aspect

Pt

System

Ser/Plas

Scale Type

Ord

Method Type

Probe.amp.tar

Details

Class

MICRO

Order/Observation

Both

Short Name

SARS-CoV-2 RNA SerPl Ql NAA+probe

Display Name

SARS-CoV-2 (COVID-19) RNA NAA+probe Ql

Related Names

2019 Novel Coronavirus2019-nCoV3 Self-Sustaining Sequence Replication3SR SRAmplifAmplificationAmplifiedCorona virusCOVID19COVID-19DNA NUCLEIC ACID PROBEDNA probeIDIIInfectious DiseaseInfectiousDiseaseLATLCRLigase chain reactionLigation-activated transcriptionMicrobiologyNAA+probeNAATNASBANucleic acid sequence based analysisOrdinalPCRPlPlasmaPlsmPoint in timePolymerase chain reactionPRProbe ampProbe with ampificationProbe with target amplificationQBRQLQualQualitativeRandomRibonucleic acidSARS Coronavirus 1SARS-CoVSARS-CoV-1SARS-CoV-2ScreenSDASerPSerPlSerPlasSerumSerum or plasmaSevere Acute Respiratory SyndromeSRStrand Displacement AmplificationTMATranscription mediated amplificationViral PneumoniasWuhan coronavirus

Frequently Asked Questions

What is LOINC code 94660-8?

LOINC code 94660-8 identifies "SARS-CoV-2 (COVID-19) RNA [Presence] in Serum or Plasma by NAA with probe detection". Qualitative detection of SARS coronavirus 2 (SARS-CoV-2) in serum or plasma specimens by nucleic acid amplification with probe-based detection. Results may be based on multiple assays to determine the presence of the virus in a specimen.

What does 94660-8 measure?

This code measures SARS coronavirus 2 RNA in Ser/Plas. It belongs to the 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.