Cardiovacular Diseases Can Be
Caused By Genetics

CardioGxOneTM is a comprehensive 213-gene genetic test
that assists in the differential diagnosis of over 30 inherited
cardiovascular diseases and sudden cardiac death

Sample Report
Information Sheet
CardioGxOne__Healthincode_Logo2-e1537985488639 CardioGxOne™
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Reports written by cardiologists, not genetic counselors

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Rapid Turnaround Time

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Adheres to medical guidelines

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Early intervention leads to significant cost savings

Major Covered Conditions


  • Hypertropic [HCM]
  • Dilated [DCM]
  • Restrictive[RCM]
  • LV non-compaction [LVNC]
  • Arrythmogenic [ARVC/D]
  • Noonan, Leopard, Costello, RASopathy
CardiomyopathiesLarge CardioGxOne™
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Arrythmias & Channelopathies*

  • Long QT/ Short QT syndrome
  • Beugada/ Jwave syndrome
  • Atrial fibrillation
  • Catecholaminergic [CPVT]
  • Cardiac conduction diseases [CCD]
  • Idiopathic VF, SADS, SUDS

Aortic / Vascular Diseases*

  • Marfan syndrome
  • Loeys-Dietz syndrome
  • Ehlers-Danlos syndrome
  • Aneurysm-ostearthritis
  • Idiopathic TAAD
  • Pulmonary HT & other rare diseases
aortic-vascularLarge CardioGxOne™

Common Symptoms Covered

  • Blood clots
  • Chest pain
  • Confusion
  • Dizziness
  • Fainting
  • Family history
  • Fatigue
  • Irregular heartbeat
  • Seizures
  • Shortness of breath
  • Stroke
  • Swelling in the legs

Proprietary Database

35,000 papers on inherited  cardiovascular diseases (400  added monthly)

>153,000 individuals

Approximately 65,000 families

500,176 genetic variants

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Clear and Actionable Reports

Clinical interpretation created by team of leading cardiologists

View Sample Report
ADMERA_HEALTH_CardioGxOne_Sample_Report_Page_01-min-e1553278565905 CardioGxOne™

Complements Admera Health’s CardioGxOneTM

AtheroGxOne_Logo-e1536074182204 CardioGxOne™

A comprehensive 84-gene genetic test to aid in the risk assessment and diagnosis of early atherosclerosis/dyslipidemias

Learn more