AutoICD API

39089-8

Laboratory

PLP1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PLP1 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

PLP1 gene Mut Anl Bld/T

Display Name

PLP1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BloodGeneticsGPM6CHeredityHeritableHLD1Identity or presenceInheritedLipophilinMajor myelin proteolipid protein geneMMPLMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalPCRPelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicatedPLPPLP/DM20PMDPoint in timeproteolipid protein 1RandomSPG2TissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 39089-8?

LOINC code 39089-8 identifies "PLP1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PLP1 gene targeted mutation analysis in Bld/Tiss.

What does 39089-8 measure?

This code measures PLP1 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.