48033-5

LOINC 2.82

TTR gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

TTR gene Mut Anl Bld/T

Component

  • TTR gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; CTS; CTS1; Genetics; HEL111; Heredity; Heritable; HsT2651; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PALB; PCR; Point in time; Random; TBPA; Tissue; Tissue, unspecified; transthyretin; Transthyretin (prealbumin, amyloidosis type I) gene; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • CTS
  • CTS1
  • Genetics
  • HEL111
  • Heredity
  • Heritable
  • HsT2651
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • PALB
  • PCR
  • Point in time
  • Random
  • TBPA
  • Tissue
  • Tissue, unspecified
  • transthyretin
  • Transthyretin (prealbumin, amyloidosis type I) gene
  • TTR gene targeted mutation analysis
  • WB
  • Whole blood
  • Whole blood or Tissue