21247-2

LOINC 2.82

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

DMD gene Mut Anl Bld/T

Component

  • DMD gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; BMD; CMD3B; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; Dystrophin; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRX85; Muscular dystrophy, Duchenne and Becker types; Mut; Mut Anl; Mutations; Neuro; Neurology; Nominal; PCR; Point in time; Pseudohypertrophic progressive; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • BMD
  • CMD3B
  • DMD gene targeted mutation analysis
  • DXS142
  • DXS164
  • DXS206
  • DXS230
  • DXS239
  • DXS268
  • DXS269
  • DXS270
  • DXS272
  • Dystrophin
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MRX85
  • Muscular dystrophy, Duchenne and Becker types
  • Mut
  • Mut Anl
  • Mutations
  • Neuro
  • Neurology
  • Nominal
  • PCR
  • Point in time
  • Pseudohypertrophic progressive
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue