41085-2

LOINC 2.82

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

MPZ gene Mut Anl Bld/T

Component

  • MPZ gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; Charcot-Marie-Tooth neuropathy 1B; CHM; CMT1; CMT1B; CMT2I; CMT2J; CMT4E; CMTDI3; CMTDID; DSS; Genetics; Heredity; Heritable; HMSNIB; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MPP; Mut; Mut Anl; Mutations; myelin protein zero; Nominal; P0; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • Charcot-Marie-Tooth neuropathy 1B
  • CHM
  • CMT1
  • CMT1B
  • CMT2I
  • CMT2J
  • CMT4E
  • CMTDI3
  • CMTDID
  • DSS
  • Genetics
  • Heredity
  • Heritable
  • HMSNIB
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MPP
  • MPZ gene targeted mutation analysis
  • Mut
  • Mut Anl
  • Mutations
  • myelin protein zero
  • Nominal
  • P0
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue