hearing loss genomic sequencing

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^[1]^[2]

Genetics

implicated genes:^[1]
- CDH23
- CLRN1
- GJB2
- GPR98
- MTRNR1
- MYO7A
- MYO15A
- PCDH15
- OTOF
- SLC26A4
- TMC1
- TMPRSS3
- USH1C
- USH1G
- USH2A
- WFS1^[1]

Indications

unexplained hearing loss in infant or child

More general terms

genome sequencing

Additional terms

hearing loss (hearing impairment, hard of hearing, HOH)

References

↑ ^1.0 ^1.1 ^1.2 CPT :accession 81430
↑ ARUP Consult: Hearing Loss https://arupconsult.com/ati/Hearing-Loss-Panel

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