92991-9

LOINC 2.82

F13A1 and F13B gene full mutation analysis in Blood or Tissue by Sequencing

F13A1 + F13B Full Mut Anl Bld/T Seq

Definition

  • This test detects pathogenic alterations within the F13A1 and F13B genes to delineate the underlying molecular defect in a patient with a laboratory diagnosis of factor XIII deficiency.

Component

  • F13A1 gene & F13B gene full mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH

Property

  • Find

Scale

  • Doc

Method

  • Sequencing

Related names

  • Blood; Coagulation factor XIII, A1 polypeptide gene; Coagulation factor XIIIa gene; Document; F13A; F13A1 + F13B; Factor XIIIa gene; Finding; Findings; full gene sequencing; Full Mut Anl; FXIIIA; 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
  • Coagulation factor XIII, A1 polypeptide gene
  • Coagulation factor XIIIa gene
  • Document
  • F13A
  • F13A1 + F13B
  • F13A1 gene & F13B gene full mutation analysis
  • Factor XIIIa gene
  • Finding
  • Findings
  • full gene sequencing
  • Full Mut Anl
  • FXIIIA
  • 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