Cardiomyopathy panel

Arrhythmogenic right ventricular cardiomyopathy, Dilated cardiomyopathy, Hereditary transthyretin-mediated amyloidosis, Hypertrophic cardiomyopathy, Left ventricular noncompaction, Rasopathy syndromes, Noonan spectrum disorders, Restrictive cardiomyopathy.

Description

Arrhythmogenic right ventricular cardiomyopathy, Dilated cardiomyopathy, Hereditary transthyretin-mediated amyloidosis, Hypertrophic cardiomyopathy, Left ventricular noncompaction, Rasopathy syndromes, Noonan spectrum disorders, Restrictive cardiomyopathy.

Areas of expertise

Cardiology, G-Cardio

Technique

NGS

Genes

A2ML1, ABCC9, ACADVL, ACTB, ACTC1, ACTG1, ACTN2, AGL, ALMS1, ALPK3, ANKRD1, BAG3, BRAF, CACNA1C, CALR3, CAV3, CBL, CDH2, CHRM2, CPT2, CRYAB, CSRP3, CTF1, CTNNA3, DES, DMD, DNAJC19, DOLK, DSC2, DSG2, DSP, DTNA, ELAC2, EMD, EYA4, FHL1, FHL2, FKRP, FKTN, FLNC, GAA, GATA4, GATA6, GATAD1, GLA, HAND1, HCN4, HRAS, ILK, JPH2, JUP, KAT6B, KLF10, KRAS, LAMA4, LAMP2, LDB3, LMNA, LRRC10, LZTR1, MAP2K1, MAP2K2, MED12, MRAS, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYLK3, MYOM1, MYOZ2, MYPN, NEBL, NEXN, NF1, NKX2-5, NPPA, NRAS, NSUN2, PCCA, PCCB, PDLIM3, PKP2, PLEKHM2, PLN, PPA2, PPCS, PPP1CB, PRDM16, PRKAG2, PTPN11, RAF1, RASA1, RASA2, RBM20, RIT1, RRAS, RRAS2, RYR2, SCN5A, SDHA, SGCD, SHOC2, SLC22A5, SOS1, SOS2, SPRED1, TAZ, TBX20, TCAP, TMEM43, TMEM70, TMPO, TNNC1, TNNI3, TNNI3K, TNNT2, TPM1, TTN, TTR, TXNRD2, VCL, YWHAZ