AutoICD API

81872-4

Laboratory

SCN5A gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

SCN5A 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

SCN5A gene Fam Mut Anl Bld/T

Display Name

SCN5A gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

Bloodcardiac sodium channel alpha subunitCDCD2CMD1ECMPD2DocumentFam Mut AnlFindingFindingsGeneticsHB1HB2HBBHBBDHeredityHeritableHH1ICCDInheritedIVFLMTEDLQT3LTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsNav1.5PCRPFHB1Point in timeRandomSodium channel protein cardiac muscle subunit alphaSodium channel protein type V subunit alphasodium channel, voltage gated, type V alpha subunitSSS1TissueTissue, unspecifiedVF1Voltage-gated sodium channel subunit alpha Nav1.5WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 81872-4?

LOINC code 81872-4 identifies "SCN5A gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures SCN5A gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 81872-4 measure?

This code measures SCN5A 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.