77627-8

LOINC 2.82

HBB gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal

HBB gene Full Mut Anl Bld/T Seq

Component

  • HBB gene full mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Sequencing

Related names

  • Beta globulin gene; Beta thalessemia; beta-globin; Blood; CD113t-C; full gene sequencing; Full Mut Anl; Genetics; Hemoglobin beta chain; Hemoglobin S gene; hemoglobin, beta; Heredity; Heritable; high-throughput sequencing; HTS; Identity or presence; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; Nominal; Point in time; Random; sequencing of entire coding region; Sickle cell anemia; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Beta globulin gene
  • Beta thalessemia
  • beta-globin
  • Blood
  • CD113t-C
  • full gene sequencing
  • Full Mut Anl
  • Genetics
  • HBB gene full mutation analysis
  • Hemoglobin beta chain
  • Hemoglobin S gene
  • hemoglobin, beta
  • Heredity
  • Heritable
  • high-throughput sequencing
  • HTS
  • Identity or presence
  • Inherited
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutations
  • Next generation sequencing
  • NGS
  • Nominal
  • Point in time
  • Random
  • sequencing of entire coding region
  • Sickle cell anemia
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue