AutoICD API

94236-7

Laboratory

F5 gene full mutation analysis in Blood or Tissue by Sequencing

Definition

Full gene sequence analysis of the F5 gene to identify a pathogenic mutation associated with Factor V deficiency. This test may also detect rare alterations in F5 that cause activated protein C (APC) resistance, resulting in thrombophilia.[GHR gene: F5]

LOINC 6-Axis Classification

Component

F5 gene full mutation analysis

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Sequencing

Details

Class

MOLPATH

Order/Observation

Both

Short Name

F5 gene Full Mut Anl Bld/T Seq

Display Name

F5 gene full mutation analysis Sequencing Doc (Bld/Tiss)

Related Names

Activated protein C cofactorAPCBloodCoagulation Factor V - Leiden genecoagulation factor V (proaccelerin, labile factor)DocumentFindingFindingsfull gene sequencingFull Mut AnlFVLGeneticsHeredityHeritablehigh-throughput sequencingHTSInheritedLabile factorMolecular pathologyMOLPATHMutMutationsNext generation sequencingNGSPCCFPoint in timeProaccelerin geneRandomRPRGL1sequencing of entire coding regionTHPH2ThrombophiliaTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 94236-7?

LOINC code 94236-7 identifies "F5 gene full mutation analysis in Blood or Tissue by Sequencing". Full gene sequence analysis of the F5 gene to identify a pathogenic mutation associated with Factor V deficiency. This test may also detect rare alterations in F5 that cause activated protein C (APC) resistance, resulting in thrombophilia.[GHR gene: F5]

What does 94236-7 measure?

This code measures F5 gene full mutation analysis in Bld/Tiss. It belongs to the MOLPATH 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.