Cardiovascular Diseases Can Be
Caused By Genetics
CardioGxOneTM is a comprehensive 213-gene test that
assists in the differential diagnosis of over 30 inherited
cardiovascular diseases and sudden cardiac death
Reports written by
cardiologists trained in
medical genetics
Fast
turnaround
time
Follows
guidelines
of societies
Save time
and money via
early intervention
Major Covered Conditions
Cardiomyopathies
- Hypertrophic [HCM]
- Dilated [DCM]
- Restrictive [RCM]
- LV non-compaction [LVNC]
- Arrythmogenic [ARVC/D]
- Noonan, Leopard, Costello, RASopathy
Arrythmias & Channelopathies*
- Long QT/ Short QT syndrome
- Brugada/ 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
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 with Kaplan-Meier Curves
35,000+ papers on inherited cardiovascular
diseases (400 added monthly)
>153,000 individuals
Approximately 65,000 families
500,176+ genetic variants
Clear and Actionable Reports
Clinical interpretation created by a team of leading cardiologists
Complements Admera Health’s Cardiovascular Test Portfolio
A comprehensive 84-gene genetic
test to aid in the risk assessment
and diagnosis of early atherosclerosis/dyslipidemias
Genetic testing for optimizing cardiovascular
drug therapy. Improve cardiovascular
treatment from diagnosis to outcome
Complements Admera Health’s Cardiovascular Test Portfolio
A comprehensive 84-gene
genetic test to aid in the risk assessment and diagnosis of early atherosclerosis/dyslipidemias
Genetic testing for optimizing cardiovascular
drug therapy. Improve cardiovascular
treatment from diagnosis to outcome