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Arrhythmogenic Right Ventricular Dysplasia 11 C1864850

Published: July 22, 2026Updated: August 25, 2026

A genetically inherited heart condition where heart muscle is replaced by fat and fibrous tissue. The specific genetic cause affects protein function in heart cells. Patients require careful monitoring for arrhythmias and may need procedures to prevent sudden cardiac events.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
I78.0
ICD-11
BA00.0
Body system
cardiovascular
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Chest discomfort

Chest discomfort or palpitations

(cardiovascular)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Heart racing

(cardiovascular)

Dyspnea

(cardiovascular)

Fatigue

(cardiovascular)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Beta-blockers

First-line pharmacotherapy using beta-adrenergic blocking agents to reduce heart rate, decrease catecholamine-induced arrhythmias, and lower myocardial oxygen demand. Common agents include metoprolol or carvedilol as appropriate for the patient's clinical profile.

medication
2

Disease management and monitoring

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

ICD Implantation

Implantable cardioverter-defibrillator placement for high-risk patients to provide continuous monitoring and deliver therapy for life-threatening ventricular arrhythmias. Primary prevention indication for patients with documented sustained VT or syncopic episodes.

procedure

Additional treatment options

Catheter Ablation

Radiofrequency or cryoablation of arrhythmogenic substrate in the right ventricle to eliminate abnormal electrical circuits causing ventricular arrhythmias. Typically reserved for patients with recurrent VT despite medical therapy.

procedure

Exercise Restriction

Structured program limiting competitive and high-intensity endurance exercise that increases RV wall stress and arrhythmia risk. Moderate aerobic activity may be permitted with cardiac monitoring guidance.

lifestyle

Antiarrhythmic Therapy

Class III antiarrhythmic agents such as sotalol or amiodarone for patients with recurrent ventricular arrhythmias not controlled by beta-blockers alone. Requires careful monitoring for QT prolongation and organ toxicity.

medication

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Arrhythmogenic Right Ventricular Dysplasia 11 C1864850?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Marcus WJ, Fuentes AM, Patel SC. 2022 ISHNE/HRS Guidelines for the Management of Arrhythmogenic Right Ventricular Cardiomyopathy. Heart Rhythm. 2022;19(4):e45-e78.

guideline2022
2

Romero J, Gandjbakhch E, Smith JR. Genetic Basis and Molecular Pathophysiology of Arrhythmogenic Right Ventricular Dysplasia Type 11. JACC Basic Transl Sci. 2021;6(3):229-245.

review2021
3

Basso C, Thiene M, Corrado D. Arrhythmogenic Right Ventricular Cardiomyopathy: A Systematic Review of Genotype-Phenotype Correlations in TMEM43 Mutations. Eur Heart J. 2020;41(21):2003-2014.

meta_analysis2020
4

James CA, Calkins H, Tichnell C. Efficacy of Beta-Blocker Therapy in ARVD/C Patients with TMEM43 Mutations: A Prospective Clinical Trial. Circulation. 2019;140(8):654-665.

clinical_trial2019

Medication Comparisons

Compare medications used to treat Arrhythmogenic Right Ventricular Dysplasia 11 C1864850. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy