92992-7

LOINC 2.82

FGA, FGB, and FGG gene full mutation analysis in Blood or Tissue by Sequencing

FGA + FGB + FGG Full Mut Anl Bld/T Seq

Definition

  • This test detects pathogenic alterations within the FGA, FGB, and FGG genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of congenital afibrinogenemia/hypofibrinogenemia or dysfibrinogenemia/hypodysfibrinogenemia.

Component

  • FGA gene & FGB gene & FGG gene full mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH

Property

  • Find

Scale

  • Doc

Method

  • Sequencing

Related names

  • Blood; Document; FGA + FGB + FGG; Fib2; fibrinogen alpha chain; fibrinogen beta chain; Finding; Findings; full gene sequencing; Full Mut Anl; HEL-S-78p; high-throughput sequencing; HTS; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • Document
  • FGA + FGB + FGG
  • FGA gene & FGB gene & FGG gene full mutation analysis
  • Fib2
  • fibrinogen alpha chain
  • fibrinogen beta chain
  • Finding
  • Findings
  • full gene sequencing
  • Full Mut Anl
  • HEL-S-78p
  • high-throughput sequencing
  • HTS
  • Molecular pathology
  • MOLPATH
  • Mut
  • Mutations
  • Next generation sequencing
  • NGS
  • Point in time
  • Random
  • sequencing of entire coding region
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue