99972-2

LOINC 2.82

Hearing loss multigene analysis in Blood or Tissue by Molecular genetics method

Hearing loss multigene analy Bld/T

Definition

  • Multigene analysis for both syndromic and non-syndromic forms of hearing loss. Genetic forms of hearing loss may be classified as autosomal dominant, recessive, X-linked or mitochondrial. Determining the cause of hearing loss, whether it is acquired or genetic, is useful for diagnosis, prognosis, and determining treatment options for the patient.[NCBI Books: NBK1434]

Component

  • Hearing loss multigene analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Blood; Deafness multi-Gene study; Document; Finding; Findings; Gene; Gene panel; Molecular genetics; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; Otogenetics Deafness Panel; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • Deafness multi-Gene study
  • Document
  • Finding
  • Findings
  • Gene
  • Gene panel
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • Multi-gene study
  • Multiple-gene panel test
  • Otogenetics Deafness Panel
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue