AutoICD API

41066-2

Laboratory

PRX gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PRX gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PRX gene Mut Anl Bld/T

Display Name

PRX gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

1-CysaiPLA2AOP2BloodCMT4FGeneticsHEL-S-128mHeredityHeritableIdentity or presenceInheritedKIAA1620Molecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalNSGPxp29PCRPeriaxinperoxiredoxin 6Point in timePRXRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41066-2?

LOINC code 41066-2 identifies "PRX gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PRX gene targeted mutation analysis in Bld/Tiss.

What does 41066-2 measure?

This code measures PRX gene targeted mutation analysis in Bld/Tiss. It belongs to the MOLPATH.MUT 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.