Genetic Test Details
Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
Test Information
- Titre
- Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
- Catégorie
- Audiology
- Sub Category
- 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
- Gene Panel
- Samples Accepted
- DNA , Blood , DNA (Not Accepted for MLPA)
- Indications
- Diagnosis , Prenatal
- Test Methodology
- Sequencing , CNV
- Methodology Notes
- Exome; MLPA: STRC dosage
- Disease/Condition
- Common and Non-Syndromic Hearing Loss
Dernière Mise à Jour: 18 juin 2025