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Cardiomyopathy and Arrhythmia Deletion/Duplication, 83 Genes

CPT Code(s): 81161; 81282; 81404 (SGCG); 81479
Specimen Required: Patient Preparation:
Collect:Lavender (EDTA) or yellow (ACD Solution A or B).
Specimen Preparation:Transport 3 mL whole blood. (Min: 1 mL)
Storage/Transport Temperature:Refrigerated.
Stability:Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable
New York DOH Approval Status: Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Aliases:
  • ABCC9, ACTC1, ACTN2, AKAP9, ANK2, ANKRD1, CACNA1C, CACNB2, CASQ2, CAV3, CORIN, COX15, CSRP3, CTF1Arrhythmogenic right vernticular cardiomyopathy (ARVC)Brugada syndrome (BrS)catecholaminergic polymorphic ventricular tachycardia (CPVT)DES, DMD, DSC2, DSG2, DSP, DTNA, EYA4, FKRP, FKTN, FXN, GAA, GLA, GPD1L, ILK, JPH2, JUP, KCNE1, KCNE2Dilated cardiomyopathy (DCM),Hypertrophic cardiomyopathy (HCM),KCNE3, KCNH2, KCNJ2, KCNQ1, KLHL3, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYH10, MYL2Left ventricular noncompaction (LVNC)Long QT syndrome (LQTS)MYL3, MYLK2, MYOT, MYOZ2, MYPN, NEXN, OBSCN, PKP2, PLN, PRKAG2, RBM20, RYR2, SCN1B, SCN2B, SCN3BRomano-WardSCN4B, SCN5A, SCO2, SGCA, SGCB, SGCD, SGCG, SLC25A4, SNTA1, SYNE1, TCAP, TGFB3, TMEM43, TMPO, TNNC1, Short QT syndrome (SQTS)TNNI3, TNNT2, TPM1, TRPM4, TTN, TTR, VCL
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