AutoICD API

41067-0

Laboratory

PRF1 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PRF1 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Amnio fld

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PRF1 gene Mut Anl Amn

Display Name

PRF1 gene targeted mutation analysis Molgen Nom (Amn fld)

Related Names

AFAmnAmn flAmnioAmniotic fluAmniotic fluidFLH2GeneticsGynGynecologyHeredityHeritableHPLH2Identity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalOBObGynObstetricsP1PCRPerforin 1perforin 1 (pore forming protein)PFN1PFPPoint in timePore forming protein genepreforming proteinRandom

Frequently Asked Questions

What is LOINC code 41067-0?

LOINC code 41067-0 identifies "PRF1 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal". It measures PRF1 gene targeted mutation analysis in Amnio fld.

What does 41067-0 measure?

This code measures PRF1 gene targeted mutation analysis in Amnio fld. 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.