77119-6

LOINC 2.82

RPGR gene full mutation analysis in Blood or Tissue by Sequencing

RPGR Full Mut Anl Bld/T Seq

Component

  • RPGR gene full mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Sequencing

Related names

  • Blood; COD1; CORDX1; CRD; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; orf15; PCDX; Point in time; Random; retinitis pigmentosa GTPase regulator; RP15; RP3; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; X-linked retinitis pigmentosa; XLRP3

Index terms

  • Blood
  • COD1
  • CORDX1
  • CRD
  • Document
  • Finding
  • Findings
  • full gene sequencing
  • Full Mut Anl
  • Genetics
  • Heredity
  • Heritable
  • high-throughput sequencing
  • HTS
  • Inherited
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutations
  • Next generation sequencing
  • NGS
  • orf15
  • PCDX
  • Point in time
  • Random
  • retinitis pigmentosa GTPase regulator
  • RP15
  • RP3
  • sequencing of entire coding region
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue
  • X-linked retinitis pigmentosa
  • XLRP3