Syndromale Schwerhörigkeit, umfassende Diagnostik : 147 Gene (376,5 kb)

ABHD12, ADGRV1, AFG2A, AFG2B, AIFM1, ALMS1, ANKH, AP1S1, ARSG, ATP1A3, ATP6V0A4, ATP6V1B1, ATP6V1B2, BCAP31, BCS1L, BRAF, BSND, BTD, CACNA1D, CATSPER2, CD151, CDH23, CEP78, CEP250, CHD7, CHSY1, CIB2, CISD2, CLPP, CLRN1, COL2A1, COL4A3, COL4A4, COL4A5, COL9A1, COL9A2, COL9A3, COL11A1, COL11A2, CRLS1, DAP3, DCAF17, DIAPH3, DLX5, DNAJC3, DNMT1, DSPP, EDN3, EDNRB, ERAL1, ESPN, EXOSC2, EYA1, FDXR, FGF3, FGFR3, FOXC1, FOXI1, GATA3, GGPS1, GJA1, GJB2, GPSM2, HAAO, HARS1, HARS2, HOXA2, HSD17B4, KCNE1, KCNJ10, KCNJ16, KCNQ1, KITLG, LARS2, LETM1, LHX3, LRP2, MAF, MANBA, MASP1, MITF, MPZ, MRPL49, MYH9, MYH14, MYO7A, NF2, NLRP3, OPA1, PAX3, PCDH15, PDZD7, PEX1, PEX2, PEX3, PEX5, PEX6, PEX7, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26, PHYH, PLOD3, PMP22, POLD1, POLR1C, POLR1D, PRDM5, PRPS1, PSMC3, PTPN11, RAF1, RNF220, RPGR, RPS6KA3, SALL1, SALL4, SEMA3E, SERAC1, SGPL1, SIX1, SIX5, SLC4A11, SLC19A2, SLC26A4, SLC52A2, SLC52A3, SLITRK6, SNAI2, SOX10, TCOF1, TFAP2A, TIMM8A, TUBB4B, TWNK, TYR, USH1C, USH1G, USH2A, WFS1, WHRN, ZNF469