Timely detection and diagnosis of heart disorders can lead to enhanced treatment options, help to prevent sudden cardiac death, and improve prognosis. Having identified genetic variants associated with cardiology diseases in over 300 different genes, we can support you in providing your patients with a precise diagnosis of a cardiovascular disease. Testing can also identify asymptomatic and at-risk family members, facilitating precautions or interventions to prevent illness or sudden death.

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CentoCardio® includes the most relevant genes for arrhythmias, congenital heart disease, and cardiomyopathies. Syndromes included: Long and short QT, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, cardiomyopathies dilated and hypertrophic, and congenital heart defects. In addition, this panel includes vascular abnormalities, such as dolichoectasia and hereditary hemorragic telangiectasia. The panel does not include analysis of PKD1.

No. of genes: 327
TAT: 25 business days
Coverage: ≥99.00% ≥20x
NGS including CNV analysis

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Common syndromes and disorders covered
  • Arrhythmogenic right ventricular cardiomyopathy
  • Brugada syndrome
  • Catecholaminergic polymorphic ventricular tachycardia
  • Congenital heart defects
  • Dilated cardiomyopathy
  • Dolichoectasia
  • Hereditary arrhythmia syndromes
  • Hereditary hemorrhagic telangiectasia
  • Heterotaxy syndrome
  • Hypertrophic cardiomyopathy
  • Hypomagnesemia
  • Long QT syndrome
  • Short QT syndrome


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CentoPortal® is a user-friendly, online, web-based ordering portal designed to assist you at every step of processing your patients' samples.

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