77125-3

LOINC 2.82

PCDH15 gene full mutation analysis in Blood or Tissue by Sequencing

PCDH15 Full Mut Anl Bld/T Seq

Component

  • PCDH15 gene full mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Sequencing

Related names

  • Blood; CDHR15; DFNB23; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; hearing loss; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; Point in time; protocadherin-related 15; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; USH1F; Usher syndrome type 1F; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • CDHR15
  • DFNB23
  • Document
  • Finding
  • Findings
  • full gene sequencing
  • Full Mut Anl
  • Genetics
  • hearing loss
  • Heredity
  • Heritable
  • high-throughput sequencing
  • HTS
  • Inherited
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutations
  • Next generation sequencing
  • NGS
  • Point in time
  • protocadherin-related 15
  • Random
  • sequencing of entire coding region
  • Tissue
  • Tissue, unspecified
  • USH1F
  • Usher syndrome type 1F
  • WB
  • Whole blood
  • Whole blood or Tissue