Zugehörige Erkrankungen:
Kongenitale sensorineurale Taubheit
Autosomal-dominante Formen der Schwerhörigkeit
Autosomal-rezessive Formen der Schwerhörigkeit
X-Chromosomale Formen der Schwerhörigkeit
Syndromale Formen der Schwerhörigkeit
Schwerhörigkeit Gen-Panel (169 Gene)
ABHD12, ACTB, ACTG1, ALMS1, ANKH, AP1S1, ATP2B2, ATP6V1B1, BCS1L, BSND, CACNA1D, CATSPER2, CCDC50, CD151, CDH23, CDKN1C, CEACAM16, CHD7, CHSY1, CIB2, CLDN14, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL4A3, COL4A4, COL4A5, COL4A6, COL9A1, COL9A2, COL9A3, CRYM, DCDC2, DFNA5, DFNB31, DFNB59, DIABLO, DIAPH1, DIAPH3, DLX5, DNMT1, DSPP, ECE1, EDN3, EDNRA, EDNRB, ERCC2, ERCC3, ESPN, ESRRB, EYA1, EYA4, FAS, FGF3, FGFR3, FOXI1, GATA3, GIPC3, GJA1, GJB1, GJB2, GJB3, GJB4, GJB6, GPR98, GPSM2, GRHL2, GRXCR1, GSTP1, HAL, HARS, HARS2, HGF, HOMER2, HOXA1, HSD17B4, IGF1, ILDR1, JAG1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, KIAA1199, LHFPL5, LHX3, LOXHD1, LRTOMT, MANBA, MARVELD2, MET, MIR182, MIR96, MITF, MSRB3, MTAP, MYH14, MYH9, MYO15A, MYO1A, MYO1C, MYO1F, MYO3A, MYO6, MYO7A, NARS2, NDP, NLRP3, NR2F1, OTOA, OTOF, OTOR, PAX3, PCDH15, PDZD7, PMP22, POLD1, POLR1C, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, RPGR, SDHD, SEMA3E, SERPINB6, SIX1, SIX5, SLC12A1, SLC17A8, SLC19A2, SLC26A4, SLC26A5, SLC4A11, SLC52A3, SMPX, SNAI2, SOX10, SOX2, SPINK5, STRC, SUCLA2, TBC1D24, TBL1X, TCF21, TCOF1, TECTA, TFAP2A, TFCP2, TIMM8A, TJP2, TMC1, TMIE, TMPRSS3, TMPRSS5, TNC, TPRN, TRIOBP, TRMU, TYR, USH1C, USH1G, USH2A, WFS1
