Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel

Test Information

Title
Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
Lab
Category
Audiology
Test Name (CMS Title)
Common and Non-Syndromic Hearing Loss
Gene/Platform/Region List
ACTG1, ADGRV1, CDH23, CHD7, CLDN14, COCH, DFNA5, DFNB59, DIAPH1, ESPN, ESRRB, EYA1, EYA4, GIPC3, GJB2, GJB6, GPSM2, GRHL2, GRXCR1, HGF, ILDR1, KCNE1, KCNQ1, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, OTOG, OTOGL, PCDH15, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, SERPINB6, SIX1, SLC17A8, SLC26A4, SMPX, STRC, TECTA, TMC1, TMIE, TMPRSS3, TPRN, TRIOBP, USH2A, WFS1
Test type
Samples Accepted
Blood, DNA, DNA (Not Accepted for MLPA)
Indications
Diagnosis
Test Methodology
Sequencing
Methodology Notes
Exome; MLPA: STRC dosage
Disease/Condition
Common and Non-Syndromic Hearing Loss

Last Updated: November 14, 2025

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