AutoICD API

21727-3

Laboratory

PMP22 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PMP22 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

PMP22 gene Mut Anl Bld/T

Display Name

PMP22 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodCharcot-Marie Tooth diseaseCMTCMT1ACMT1EDejerine-Sottas syndromeDSSGAS3GAS-3GeneticsGrowth arrest specific gene 3Hereditary neuropathy with liability to pressure palsiesHeredityHeritableHMSNIAHNPPIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPeripheral myelin protein 22PMP-22Point in timeRandomSp110TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 21727-3?

LOINC code 21727-3 identifies "PMP22 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PMP22 gene targeted mutation analysis in Bld/Tiss.

What does 21727-3 measure?

This code measures PMP22 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.