41084-5

LOINC 2.82

MSH2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

MSH2 gene Mut Anl Bld/T

Component

  • MSH2 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • BAT-26; Blood; COCA1; Colon cancer nonpolyposis type 1; FCC1; Genetics; Heredity; Heritable; HNPCC; HNPCC1; Identity or presence; Inherited; LCFS2; Lynch syndrome; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; mutS homolog 2; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • BAT-26
  • Blood
  • COCA1
  • Colon cancer nonpolyposis type 1
  • FCC1
  • Genetics
  • Heredity
  • Heritable
  • HNPCC
  • HNPCC1
  • Identity or presence
  • Inherited
  • LCFS2
  • Lynch syndrome
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MSH2 gene targeted mutation analysis
  • Mut
  • Mut Anl
  • Mutations
  • mutS homolog 2
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue