Deafness / hearing loss, autosomal recessive 2 (extended panel)

ABHD12, ADCY1, ADGRV1, ATP6V1B1, BDP1, BSND, CABP2, CACNA1D, CDC14A, CDH23, CEACAM16, CIB2, CLDN14, CLDN9, CLIC5, COL11A2, COL4A6, DCDC2, EDN3, EDNRB, ELMOD3, EPS8, EPS8L2, ERAL1, ESPN, ESRP1, ESRRB, FOXI1, GAB1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRAP, GRXCR1, GRXCR2, HGF, HSD17B4, ILDR1, KARS, KCNE1, KCNJ10, KCNQ1, LARS2, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MPZL2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, NARS2, OTOA, OTOF, OTOG, OTOGL, PAX3, PCDH15, PDZD7, PJVK, PNPT1, POU3F4, PPIP5K2, PRPS1, PTPRQ, RDX, RIPOR2, ROR1, S1PR2, SERPINB6, SLC22A4, SLC26A4, SLC26A5, SLITRK6, SMPX, SNAI2, SPNS2, STRC, SYNE4, TBC1D24, TECTA, TMC1, TMEM132E, TMIE, TMPRSS3, TPRN, TRIOBP, TSPEAR, TWNK, USH1C, WBP2, WHRN

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