58010-0

LOINC 2.82

MSH2 gene+MLH1 gene+MSH6 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

MSH2+MLH1+MSH6 gene Mut Anl Bld/T

Component

  • MSH2 gene+MLH1 gene+MSH6 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • BAT-26; Blood; COCA1; COCA2; Colon cancer nonpolyposis type 1; FCC1; FCC2; G/T mismatch-binding protein gene; Genetics; GTBP; GTMBP; Hereditary Nonpolyposis Colorectal Cancer; Heredity; Heritable; hMLH1; HNPCC; HNPCC1; HNPCC2; HNPCC5; HSAP; Identity or presence; Inherited; LCFS2; Lynch syndrome; MGC5172; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MSH2+MLH1 gene; MSH2+MLH1+MSH6 gene; Mut; Mut Anl; Mutations; mutL homolog 1; MutL homolog 1, colon cancer, nonpolyposis type 2; mutS homolog 2; mutS homolog 6; Nominal; p160; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • BAT-26
  • Blood
  • COCA1
  • COCA2
  • Colon cancer nonpolyposis type 1
  • FCC1
  • FCC2
  • G/T mismatch-binding protein gene
  • Genetics
  • GTBP
  • GTMBP
  • Hereditary Nonpolyposis Colorectal Cancer
  • Heredity
  • Heritable
  • hMLH1
  • HNPCC
  • HNPCC1
  • HNPCC2
  • HNPCC5
  • HSAP
  • Identity or presence
  • Inherited
  • LCFS2
  • Lynch syndrome
  • MGC5172
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MSH2 gene+MLH1 gene+MSH6 gene targeted mutation analysis
  • MSH2+MLH1 gene
  • MSH2+MLH1+MSH6 gene
  • Mut
  • Mut Anl
  • Mutations
  • mutL homolog 1
  • MutL homolog 1, colon cancer, nonpolyposis type 2
  • mutS homolog 2
  • mutS homolog 6
  • Nominal

9 further terms