Skip to content

Dilated Cardiomyopathy 1x C1969024

Published: July 22, 2026Updated: August 20, 2026

A genetic form of dilated cardiomyopathy causing the left ventricle to enlarge and weaken over time. Often runs in families. Managed with medications, dietary sodium restriction, and cardiac devices when appropriate.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
B33.24
ICD-11
1A00.0
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

!

Syncope

Chest discomfort or palpitations

(cardiovascular)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Dyspnea on exertion

(cardiovascular)

Palpitations

(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

Disease management and monitoring

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

medication
2

Mineralocorticoid Receptor Antagonists

Spironolactone or eplerenone block aldosterone effects, reducing fluid retention and fibrosis while providing mortality benefits in severe heart failure.

medication
3

Diuretics

Loop diuretics such as furosemide promote fluid excretion to relieve congestion, reduce edema, and improve breathing in volume-overloaded patients.

medication

Additional treatment options

Heart Transplant Evaluation

Comprehensive evaluation for cardiac transplantation in eligible patients with end-stage disease unresponsive to maximal medical therapy.

surgical

Cardiac Rehabilitation Program

Supervised exercise program designed to safely improve functional capacity, reduce symptoms, and enhance quality of life in cardiomyopathy patients.

lifestyle

Remote Hemodynamic Monitoring

Implantable pulmonary artery pressure sensors allow daily monitoring of fluid status, enabling proactive medication adjustments to prevent decompensation.

monitoring

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 Dilated Cardiomyopathy 1x C1969024?

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

general

Medication Comparisons

Compare medications used to treat Dilated Cardiomyopathy 1x C1969024. 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 20, 2026. · Read our editorial policy