Buscador de Patologías y Genes

Panel NGS

P00248

Patología

MALFORMACIÓN CARDÍACA/CARDIOPATÍAS CONGÉNITAS

201

Genes

ABCC9, ABL1, ACTA1, ACTA2, ACTB, ACTC1, ACTG1, ACVR1, ACVR2B, ACVRL1, ADAMTS10, ADAMTS17, AKT3, ALMS1, AMER1, ANKRD1, ANKRD11, ARHGAP31, ARID1A, ARID1B, ARL6, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BMPR2, BRAF, C12orf57, CBL, CC2D2A, CCDC103, CCDC28B, CCDC39, CCDC40, CEP290, CFAP53, CHD7, CHRM2, CITED2, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, CPS1, CREBBP, CRELD1, CTC1, CYR61, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DOCK6, DTNA, EFEMP2, EFTUD2, EHMT1, ELN, ENG, EP300, EVC, EVC2, EYA4, FBN1, FBN2, FLNA, FOXC1, FOXF1, FOXH1, FOXP1, G6PC3, GAA, GATA4, GATA5, GATA6, GDF1, GJA1, GJA5, GPC3, HAND1, HAND2, HDAC8, HOXA1, HRAS, INVS, IRX4, ISL1, JAG1, KAT6B, KCNA5, KCNJ8, KCNK3, KDM6A, KIF7, KMT2D, KRAS, KYNU, MAP2K1, MAP2K2, MED12, MED13L, MID1, MKKS, MKS1, MYBPC3, MYCN, MYH11, MYH6, MYH7, MYLK, NEK8, NEXN, NF1, NIPBL, NKX2-5, NKX2-6, NME8, NODAL, NOTCH1, NOTCH2, NOTCH3, NPHP3, NPHP4, NR2F2, NRAS, NSD1, NSDHL, NTRK3, OFD1, PDGFRA, PIK3CA, PIK3R2, PITX2, PLOD1, PTPN11, RAB23, RAF1, RAI1, RASA1, RBM10, RPGRIP1L, SALL1, SALL4, SEMA3E, SHOC2, SKI, SLC2A10, SMAD1, SMAD2, SMAD3, SMAD4, SMAD6, SMAD9, SMARCB1, SMC1A, SMC3, SOS1, SOX9, SPECC1L, SPRED1, STRA6, TAB2, TBX1, TBX20, TBX5, TCTN2, TFAP2B, TGFB2, TGFB3, TGFBR1, TGFBR2, TLL1, TMEM216, TMEM231, TMEM67, TNNI3, TNNI3K, TRIM32, TTC8, TTN, UPF3B, WDPCP, ZDHHC9, ZEB2, ZFPM2, ZIC3

Solicitud de turno

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