Buscador de Patologías y Genes

Panel NGS

P00341

Patología

TRASTORNOS DEL ESPECTRO AUTISTA (AUTISMO, SÍNDROME DE ASPERGER

204

Genes

ADCY3, ADSL, AFF2, ALDH5A1, ALDH7A1, AMT, ANK2, ANK3, ANKRD11, AP1S2, ARHGEF6, ARID1B, ARX, ATP10A, ATRX, AUTS2, AVPR1A, BCKDK, BCL11A, BDNF, BRAF, BRSK2, C12orf57, CACNA1C, CACNA1H, CACNA2D3, CADM1, CASK, CC2D1A, CDC42BPB, CDKL5, CHD2, CHD7, CHD8, CIC, CNTN4, CNTNAP2, CREBBP, CSMD1, CTNNB1, CTNND2, CTTNBP2, CUL3, DDC, DEAF1, DHCR7, DIAPH3, DIP2C, DISC1, DMD, DOCK4, DPP6, DPYD, DSCAM, DYNC1H1, DYRK1A, EFR3A, EHMT1, EN2, FAAH2, FBXO11, FGD1, FMR1, FOLR1, FOXG1, FOXP1, FOXP2, FRMPD4, GABRB3, GABRG1, GAMT, GATM, GCH1, GRIA3, GRIK4, GRIN2A, GRIN2B, GRIP1, GRPR, GSPT2, HCN1, HDAC8, HOXA1, HPRT1, HUWE1, IL1RAPL1, IMMP2L, KATNAL2, KCNQ2, KCNQ3, KCTD13, KDM5C, KIRREL3, KLHL3, KMT5B, KRAS, L1CAM, LAMC3, MAGEL2, MAOA, MBD1, MBD3, MBD4, MBD5, MBOAT7, MECP2, MED12, MED13L, MEF2C, MET, MFRP, MID1, MYO5A, MYO9B, MYT1L, NBEA, NDP, NEGR1, NEXMIF, NF1, NFIX, NHS, NIPBL, NLGN1, NLGN3, NLGN4X, NR1I3, NRXN1, NRXN2, NSD1, NSDHL, NTNG1, OCRL, OPHN1, PACS1, PAFAH1B1, PAX5, PCBD1, PCDH19, PDE4D, PDE8B, PHF3, PHF6, PLP1, PNKP, PNPO, POGZ, POMGNT1, PON3, PQBP1, PTCHD1, PTEN, PTPN11, PTS, QDPR, RAB39B, RAD21, RAI1, RBFOX1, RELN, RIMS3, RORA, RPL10, RPS6KA3, SATB2, SCN1A, SCN2A, SETBP1, SETD2, SGSH, SHANK2, SHANK3, SLC16A2, SLC2A1, SLC6A1, SLC6A3, SLC6A4, SLC9A6, SLC9A9, SMAD4, SMARCB1, SMC1A, SMC3, SOX5, SPAST, SPR, STXBP1, SYN1, SYN2, TBL1XR1, TBX1, TCF4, TH, TMLHE, TRIP12, TSC1, TSC2, TSPAN7, UBE2A, UBE3A, UPF3B, VPS13B, WDFY3, ZEB2

Solicitud de turno

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