Hipoacusias hereditarias
Catálogo: Catálogo genética médica con informe
Referencia: LV4924
GEN_000444
G16024
Especialidad: Otorrinolaringología
ABHD12, ACOX1, ACTG1, ADGRV1, AIFM1, ALMS1, ANKH, AP1S1, ARSG, ATOH1, ATP11A, ATP2B2, ATP6V1B1, ATP6V1B2, BCS1L, BSND, CABP2, CACNA1D, CCDC50, CDC14A, CDH23, CEACAM16, CEP250, CEP78, CHD7, CIB2, CISD2, CLDN14, CLDN9, CLIC5, CLPP, CLRN1, COCH, COG4, COL11A1, COL11A2, COL2A1, COL4A3, COL4A4, COL4A5, COL9A1, COL9A2, COL9A3, CRLS1, CRYM, DIABLO, DIAPH1, DIAPH3, DMXL2, DNAJC3, DNMT1, DSPP, EDN3, EDNRB, ELMOD3, EPS8, EPS8L2, ERAL1, ESPN, ESRP1, ESRRB, EYA1, EYA4, FDXR, FGF3, FOXI1, GATA3, GGPS1, GIPC3, GJB2, GJB6, GPSM2, GREB1L, GRHL2, GRXCR1, GSDME, HAAO, HARS2, HGF, HOMER2, HOXA2, HSD17B4, ILDR1, KARS1, KCNE1, KCNJ10, KCNJ16, KCNQ1, KCNQ4, KDM3B, KIT, KITLG, LARS2, LETM1, LHFPL5, LMX1A, LOXHD1, LRTOMT, MARVELD2, MASP1, MINAR2, MITF, MN1, MORC2, MPZL2, MSRB3, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NARS2, NDP, NF2, NLRP3, OGDHL, OPA1, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX1, PAX2, PAX3, PBX1, PCDH15, PDSS1, PDZD7, PEX7, PHYH, PJVK, PLS1, PMP22, PNPT1, POLR1B, POLR1C, POLR1D, POU3F4, POU4F3, PPIP5K2, PRPS1, PTPRQ, RDX, REST, RIPOR2, RNF220, RMND1, S1PR2, SALL1, SALL4, SERAC1, SERPINB6, SGPL1, SIX1, SLC12A2, SLC17A8, SLC26A4, SLC26A5, SLC4A11, SLC52A2, SLC52A3, SLITRK6, SMPX, SOX10, SOX2, SPATA5, SPATA5L1, SPNS2, SPTBN4, SYNE4, TBC1D24, TCOF1, TECTA, THOC1, TIMM8A, TJP2, TMC1, TMEM132E, TMIE, TMPRSS3, TNC, TPRN, TRIOBP, TWNK, USH1C, USH1G, USH2A, USP48, WBP2, WFS1, WHRN, YARS1, cribado de la deleción de genes contiguos que incluye el gen STRC y análisis del genoma mitocondrial
