35379-7

LOINC 2.82

HNPCC genes mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

HNPCC genes Mut Anl Bld/T

Component

  • HNPCC genes targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; COCA2; FCC2; Genetics; Hereditary Nonpolyposis Colorectal Cancer; Heredity; Heritable; hMLH1; HNPCC; HNPCC2; Identity or presence; Inherited; Lynch syndrome; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; mutL homolog 1; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • COCA2
  • FCC2
  • Genetics
  • Hereditary Nonpolyposis Colorectal Cancer
  • Heredity
  • Heritable
  • hMLH1
  • HNPCC
  • HNPCC genes targeted mutation analysis
  • HNPCC2
  • Identity or presence
  • Inherited
  • Lynch syndrome
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • mutL homolog 1
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue