AutoICD API

21728-1

Laboratory

PMP22 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PMP22 gene mutations tested for

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Observation

Short Name

PMP22 gene Mut Tested Bld/T

Display Name

PMP22 gene mutations tested for Molgen Nom (Bld/Tiss)

Related Names

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

Frequently Asked Questions

What is LOINC code 21728-1?

LOINC code 21728-1 identifies "PMP22 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal". It measures PMP22 gene mutations tested for in Bld/Tiss.

What does 21728-1 measure?

This code measures PMP22 gene mutations tested for 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.