AutoICD API

81877-3

Laboratory

SPG3A gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

SPG3A gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

SPG3A gene Fam Mut Anl Bld/T

Display Name

SPG3A gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

AD-FSPatlastinatlastin GTPase 1atlastin1BloodDocumentFam Mut AnlFindingFindingsFSP1GBP3GeneticsGuanylate-binding protein 3 geneHeredityHeritableHSN1DInheritedLMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsPCRPoint in timeRandomSpastic paraplegia 3ASPG3SPG3ATissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 81877-3?

LOINC code 81877-3 identifies "SPG3A gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures SPG3A gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 81877-3 measure?

This code measures SPG3A gene mutation analysis limited to known familial mutations 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.