22069-9

LOINC 2.82

MT-ATP6 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

MT-ATP6 gene Mut Tested Bld/T

Component

  • MT-ATP6 gene mutations tested for

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • ATP synthase 6; ATP synthase A chain; ATP6; ATPASE 6; Blood; Gene mut tested; Genetics; Heredity; Heritable; Identity or presence; Inherited; Leigh syndrome; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MTATP6; Mut; Mut Tested; Mutation; Muts; NARP syndrome; Neurogenic muscle weakness, ataxia and retinitis pigmentosa; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • ATP synthase 6
  • ATP synthase A chain
  • ATP6
  • ATPASE 6
  • Blood
  • Gene mut tested
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Leigh syndrome
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MTATP6
  • Mut
  • Mut Tested
  • Mutation
  • Muts
  • NARP syndrome
  • Neurogenic muscle weakness, ataxia and retinitis pigmentosa
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue