75382-2

LOINC 2.82

ATP7B gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

ATP7B gene Fam Mut Anl Bld/T

Component

  • ATP7B gene mutation analysis limited to known familial mutations

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • ATPase gene; ATPase, Cu++ transporting, beta polypeptide; Blood; CU(2+)- transporting beta polypeptide; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; PCR; Point in time; PWD; Random; Tissue; Tissue, unspecified; WB; WC1; WD; Whole blood; Whole blood or Tissue; Wilson disease; WND

Index terms

  • ATPase gene
  • ATPase, Cu++ transporting, beta polypeptide
  • Blood
  • CU(2+)- transporting beta polypeptide
  • Document
  • Fam Mut Anl
  • Finding
  • Findings
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • LMTED
  • LTD
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutation
  • Mutations
  • Muts
  • PCR
  • Point in time
  • PWD
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • WC1
  • WD
  • Whole blood
  • Whole blood or Tissue
  • Wilson disease
  • WND