Cardio Genetics

Find hidden heart risks before they show up

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What is Cardio Genetics?

Our cardiovascular genetic test identifies inherited variations affecting heart structure, rhythm, and function, enabling early detection and personalized management. In India, congenital heart disease affects ~8 per 1,000 live births, highlighting the importance of early genetic evaluation in at-risk families.

Which cardiological conditions can be diagnosed?

  • Cardiomyopathies (e.g., hypertrophic, dilated, arrhythmogenic)
  • Inherited arrhythmias (e.g., Long QT syndrome, Brugada syndrome)
  • Congenital heart defects
  • Aortopathies (e.g., Marfan syndrome, thoracic aortic aneurysm)
  • Familial hypercholesterolemia and other lipid disorders
  • Sudden cardiac death syndromes

Who can consider testing ?

  • Individuals with unexplained cardiac symptoms (e.g., fainting, palpitations, arrhythmias)
  • Patients diagnosed with cardiomyopathy or inherited heart conditions
  • Individuals with a family history of heart disease or sudden cardiac death
  • Children or adults with congenital heart defects
  • Individuals with early onset or unexplained high cholesterol
  • Family members of patients with known genetic cardiac conditions

Tests offered by OneDNA

Comprehensive Cardiology Panel

For conditions like: Brugada syndrome, Long QT syndrome, cardiomyopathies, ASD, Noonan syndrome, Marfan syndrome, etc.

  • Methodology: NGS
  • Sample Type: Blood (EDTA)
  • TAT: 4 weeks

Chromosomal microarray

For conditions like: Congenital heart defects, DiGeorge syndrome (22q11.2 deletion syndrome), Williams syndrome, Alagille syndrome, etc.

  • Methodology: Microarray
  • Sample Type: Blood (EDTA)
  • TAT: 3 weeks

FISH

For conditions like: DiGeorge syndrome (22q11.2 deletion syndrome), Williams syndrome, etc.

  • Methodology: FISH
  • Sample Type: Blood (Heparin tube)
  • TAT: 4 days

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Why choose OneDNA

Comprehensive Coverage

Comprehensive testing across both molecular and cytogenetic platforms

Accredited Laboratories

NABL & CAP accredited lab

Support & Care

End-to-end support including genetic counselling and report guidance.

Early & Accurate

High accuracy with advanced technologies and stringent quality controls

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Download our brochure to learn more about Non-Invasive Prenatal Testing

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Frequently Asked Questions

It can identify if there’s an inherited condition affecting your heart’s structure, rhythm, or function.

Yes, some cholesterol disorders are inherited, and this test can help identify them.

It supports better risk management, early intervention, and informed family planning.

It helps rule out many inherited cardiac conditions and guides what to do next.

Yes, early detection can help manage risks and reduce the chances of complications.

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