Heart and circulation
About this category
People with hereditary type of cardiovascular and heart diseases are burdened with disorders in genes, which result in: changes in the structure of the heart muscle, changes in the structure of the aortic walls, changes in the transmission of signals in the heart muscle, high blood cholesterol levels.
All genetic tests are performed using the next-generation sequencing method, using Illumina sequencers. Our tests are subject to internal and external control. The laboratory is subject to continuous external quality control.
Panels in this category
20 panels-
Aortic disorders
53 genesABCC6; ABL1; ACTA2; ADAMTS10; ADAMTS17; ADAMTS2; ADAMTSL4; ALDH18A1; ATP7A; B3GAT3; BGN; CBS; COL1A1; COL1A2; COL2A1; COL3A1; COL4A5; COL5A1; COL5A2; COLGALT1; EFEMP2; ELN; ENPP1; FBLN5; FBN1; FBN2; FKBP14; FLNA; GATA5; HCN4; LOX; MAATS1; MAT2A; MED12; MFAP5; MYH11; MYLK; NOTCH1; NPSR1-AS1; PLOD1; PRKG1; ROBO4; SKI; SLC2A10; SLC39A13; SMAD2; SMAD3; SMAD4; TGFB2; TGFB3; TGFBR1; TGFBR2; ZDHHC9
615 EURDetails -
Arrythmias - large panel
74 genesABCC9; AKAP9; ANK2; BAG3; BVES; CACNA1C; CACNA2D1; CACNB2; CALM1; CALM2; CALM3; CASQ2; CAV3; CDH2; CTNNA3; DBH; DES; DSC2; DSG2; DSP; FLNC; GATA6; GJA5; GNB5; GPD1L; HADHA; HCN4; JUP; KCNA5; KCND3; KCNE1; KCNE1L; KCNE2; KCNE3; KCNH2; KCNJ2; KCNJ5; KCNJ8; KCNQ1; LDB3; LEMD2; LMNA; MYH6; MYH7; MYL4; NKX2-5; NOS1AP; NPPA; NUP155; PKP2; PLN; PPA2; PRKAG2; RANGRF; RYR2; SALL4; SCN10A; SCN1B; SCN2B; SCN3B; SCN4B; SCN5A; SLMAP; SNTA1; TBX5; TECRL; TGFB3; TMEM43; TNNI3; TNNI3K; TNNT2; TRDN; TRPM4; TTN
615 EURDetails -
Arrythmogenic right ventricular dysplasia
25 genesABCC9; BAG3; CAV3; CDH2; CTNNA3; DES; DSC2; DSG2; DSP; FLNC; JUP; LDB3; LEMD2; LMNA; MYH7; MYLK2; NKX2-5; PKP2; PLN; RYR2; SCN5A; TGFB3; TMEM43; TP63; TTN
615 EURDetails -
Brugada syndrome
16 genesCACNA1C; CACNA2D1; CACNB2; GPD1L; HCN4; KCND3; KCNE3; KCNH2; KCNJ8; RANGRF; SCN1B; SCN2B; SCN3B; SCN5A; SLMAP; TRPM4
615 EURDetails -
Cardiomyopathies - large panel
188 genesAARS2; ABCC6; ABCC9; ACAD9; ACADVL; ACTA1; ACTC1; ACTN2; AGK; AGL; ALMS1; ALPK3; ANKRD1; ANO5; APOA1; BAG3; BRAF; CACNA1C; CALR3; CAPN3; CASQ2; CASZ1; CAV3; CBL; CDH2; CHRM2; COX15; CPT2; CRYAB; CSRP3; CTNNA3; DBH; DES; DMD; DNAJC19; DOLK; DPM3; DSC2; DSG2; DSP; DTNA; DYSF; EEF1A2; ELAC2; EMD; EPG5; ETFA; ETFB; ETFDH; EYA4; FBXL4; FBXO32; FHL1; FHOD3; FKRP; FKTN; FLNC; FOXD4; FOXRED1; FXN; GAA; GATA4; GATA6; GATAD1; GATC; GBE1; GFM1; GLA; GLB1; GMPPB; GTPBP3; GUSB; HADHA; HAND1; HCN4; HFE; HRAS; IDUA; ILK; ISPD; JPH2; JUP; KANK2; KLHL24; KRAS; LAMA2; LAMA4; LAMP2; LARGE; LDB3; LEMD2; LMNA; LMOD2; LRRC10; LZTR1; MAP2K1; MAP2K2; MAP3K8; MIPEP; MLYCD; MTO1; MYBPC3; MYBPHL; MYH6; MYH7; MYL2; MYL3; MYL4; MYLK2; MYOT; MYOZ2; MYPN; MYRF; NDUFAF2; NEBL; NEXN; NF1; NKX2-5; NONO; NRAP; NRAS; PCCA; PCCB; PKP2; PLEC; PLEKHM2; PLN; PNPLA2; PPA2; PPCS; PPP1CB; PRDM16; PRKAG2; PSEN1; PSEN2; PTPN11; QRSL1; RAF1; RASA2; RBCK1; RBM20; RIT1; RMND1; RRAS; RYR2; SCN5A; SCNN1B; SCNN1G; SCO1; SCO2; SDHA; SEPN1; SGCA; SGCB; SGCD; SGCG; SHOC2; SLC22A5; SLC25A20; SLC25A4; SMCHD1; SOS1; SOS2; SPEG; SPRED1; TAB2; TAZ; TBX20; TBX5; TCAP; TGFB3; TMEM43; TMEM70; TMPO; TNNC1; TNNI3; TNNI3K; TNNT2; TOR1AIP1; TPM1; TRIM32; TSFM; TTN; TTR; VCL; VCP; VPS13A; XK
615 EURDetails -
Catecholaminergic polymorphic ventricular tachycardia
10 genesANK2; CALM1; CALM2; CALM3; CASQ2; KCNJ2; LMNA; RYR2; TECRL; TRDN
615 EURDetails -
Cerebrovascular accident (stroke)
30 genesACTA2; ACVRL1; CBS; CCM2; CECR1; COL3A1; COL4A1; COL4A2; CST3; ENG; EPHB4; GDF2; GLA; GUCY1A3; HTRA1; KRIT1; NOTCH3; PDCD10; RASA1; RNF213; SLC2A10; SMAD2; SMAD3; SMAD4; TEK; TGFB2; TGFB3; TGFBR1; TGFBR2; TREX1
615 EURDetails -
Dilated cardiomyopathy
102 genesABCC6; ABCC9; ACTA1; ACTC1; ACTN2; ALMS1; ALPK3; ANKRD1; APOA1; BAG3; CASZ1; CHRM2; CRYAB; CSRP3; DES; DMD; DNAJC19; DOLK; DPM3; DSC2; DSG2; DSP; DYSF; EEF1A2; EMD; EPG5; ETFA; ETFB; ETFDH; EYA4; FBXO32; FHOD3; FKTN; FLNC; FOXD4; GATA4; GATA6; GATAD1; GATC; GBE1; GLB1; HAND1; HCN4; ILK; JPH2; JUP; KLHL24; LAMA4; LAMP2; LDB3; LEMD2; LMNA; LMOD2; LRRC10; MLYCD; MURC; MYBPC3; MYBPHL; MYH6; MYH7; MYL4; MYPN; NEBL; NEXN; NKX2-5; NRAP; PCCA; PCCB; PDLIM3; PKP2; PLEKHM2; PLN; PPCS; PRDM16; PSEN1; PSEN2; QRSL1; RAF1; RBCK1; RBM20; RMND1; SCN5A; SGCD; SPEG; TAB2; TAZ; TBX20; TBX5; TCAP; TMEM43; TMPO; TNNC1; TNNI3; TNNI3K; TNNT2; TOR1AIP1; TPM1; TTN; TTR; TXNRD2; VCL; VPS13A
615 EURDetails -
Dilated cardiomyopathy - small panel
6 genesFLNC; LMNA; MYH6; MYH7; TNNT2; TTN
615 EURDetails -
Familial hypercholesterolemia
14 genesABCG5; ABCG8; APOA2; APOB; APOE; CYP27A1; EPHX2; GHR; LDLR; LDLRAP1; LIPA; LPL; PCSK9; PPP1R17
615 EURDetails -
Familial hypercholesterolemia - basic panel
7 genesABCG5; ABCG8; APOB; LDLR; LDLRAP1; LIPA; PCSK9
530 EURDetails -
Hyperlipidemia - large panel
20 genesABCA1; ABCG5; ABCG8; ALMS1; APOA1; APOA5; APOB; APOC2; APOC3; APOE; CREB3L3; GPIHBP1; LDLR; LDLRAP1; LIPA; LIPC; LMF1; LPL; PCSK9; USF1
615 EURDetails -
Hypertrophic cardiomyopathy
65 genesABCC9; ACAD9; ACADVL; ACTA1; ACTC1; ACTN2; AGK; AGL; ALPK3; ANKRD1; APOA1; BAG3; BRAF; CALR3; CAV3; CBL; COX15; CRYAB; CSRP3; DES; ELAC2; EPG5; FBXL4; FHL1; FHL2; FHOD3; FLNC; FXN; GAA; GLA; GSK3B; HRAS; JPH2; KLHL24; LAMP2; LDB3; MAP2K1; MIPEP; MYBPC3; MYH6; MYH7; MYL2; MYL3; MYLK2; MYOZ2; MYPN; NDUFAF2; NEXN; PDLIM3; PLN; PRKAG2; PTPN11; RAF1; RIT1; SLC25A4; SOS1; TCAP; TNNC1; TNNI3; TNNT2; TPM1; TRIM63; TTN; TTR; VCL
615 EURDetails -
Hypertrophic cardiomyopathy - basic panel
4 genesMYBPC3; MYH7; TNNI3; TNNT2
530 EURDetails -
Long QT syndrome
20 genesAKAP9; ALG10B; ANK2; CACNA1C; CALM1; CALM2; CALM3; CAV3; KCNE1; KCNE2; KCNH2; KCNJ2; KCNJ5; KCNQ1; NOS1AP; SCN4B; SCN5A; SNTA1; TECRL; TRDN
615 EURDetails -
Marfan syndrome and related disorders
61 genesABL1; ACTA2; ADAMTS10; ADAMTS17; ADAMTS2; ADAMTSL4; ALDH18A1; ATP6V0A2; ATP7A; B3GAT3; B4GALT7; BGN; CBS; CHST14; COL11A1; COL11A2; COL12A1; COL1A1; COL1A2; COL2A1; COL3A1; COL5A1; COL5A2; DLG4; DSE; EFEMP2; ELN; FBLN5; FBN1; FBN2; FKBP14; FLCN; FLNA; GORAB; LOX; LTBP4; MAT2A; MED12; MFAP5; MYH11; MYLK; NOTCH1; PLOD1; PRDM5; PRKG1; PYCR1; RIN2; SKI; SLC2A10; SLC39A13; SMAD2; SMAD3; TGFB2; TGFB3; TGFBR1; TGFBR2; TNXB; UPF3B; VCAN; ZDHHC9; ZNF469
615 EURDetails -
Non-compaction cardiomyopathy
10 genesACTC1; DES; DSP; MYBPC3; MYH7; NONO; RYR2; TAZ; TPM1; TTN
615 EURDetails -
Noonan syndrome
41 genesA2ML1; ACTB; ACTG1; AKT1; BRAF; CBL; CCNK; CDC42; EPHB4; FGD1; GNAS; HRAS; KAT6B; KRAS; LZTR1; MAP2K1; MAP2K2; MAP3K8; MRAS; NF1; NF2; NRAS; NSUN2; PPP1CB; PTPN11; RAF1; RASA1; RASA2; RIT1; RRAS; RRAS2; SASH1; SHOC2; SMARCB1; SOS1; SOS2; SPRED1; STAMBP; SYNGAP1; TSC1; TSC2
615 EURDetails -
Pulmonary artery hypertension
24 genesABCC8; ACVRL1; AQP1; ATP13A3; BMPR1B; BMPR2; CAV1; CBLN2; CPS1; EIF2AK4; ENG; FOXF1; GDF2; KCNA5; KCNK3; NFU1; NOTCH3; RASA1; SARS2; SMAD4; SMAD9; SOX17; STRA6; TBX4
615 EURDetails -
Short QT syndrome
5 genesCACNA1C; CACNB2; KCNH2; KCNJ2; KCNQ1
530 EURDetails
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