AutoICD API

41068-8

Laboratory

PRF1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PRF1 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

PRF1 gene Mut Anl Bld/T

Display Name

PRF1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodFLH2GeneticsHeredityHeritableHPLH2Identity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalP1PCRPerforin 1perforin 1 (pore forming protein)PFN1PFPPoint in timePore forming protein genepreforming proteinRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 41068-8?

LOINC code 41068-8 identifies "PRF1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PRF1 gene targeted mutation analysis in Bld/Tiss.

What does 41068-8 measure?

This code measures PRF1 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.