21627-5

LOINC 2.82

ATP7B gene c.2010_2016del [Presence] in Blood or Tissue by Molecular genetics method

ATP7B c.2010_2016del Bld/T Ql

Component

  • ATP7B gene.c.2010_2016del

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • PrThr

Scale

  • Ord

Method

  • Molgen

Related names

  • 7 BP deletion; ATP7B c.2010_2016del; ATPase gene; ATPase, Cu++ transporting, beta polypeptide; Blood; CU(2+)- transporting beta polypeptide; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; NT2010; Ordinal; PCR; Point in time; PR; PWD; QL; Qual; Qualitative; Random; Screen; Tissue; Tissue, unspecified; WB; WC1; WD; Whole blood; Whole blood or Tissue; Wilson disease; WND

Index terms

  • 7 BP deletion
  • ATP7B c.2010_2016del
  • ATP7B gene.c.2010_2016del
  • ATPase gene
  • ATPase, Cu++ transporting, beta polypeptide
  • Blood
  • CU(2+)- transporting beta polypeptide
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • NT2010
  • Ordinal
  • PCR
  • Point in time
  • PR
  • PWD
  • QL
  • Qual
  • Qualitative
  • Random
  • Screen
  • Tissue
  • Tissue, unspecified
  • WB
  • WC1
  • WD
  • Whole blood
  • Whole blood or Tissue
  • Wilson disease
  • WND