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Dilated Cardiomyopathy 1d C1832243

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

This genetic type of dilated cardiomyopathy results from inherited mutations that cause the heart chamber to enlarge and lose pumping strength. It can develop in both adults and children. Medical therapy and lifestyle changes are central to management.

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.

Chest discomfort or palpitations

(cardiovascular)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Orthopnea with pillow stacking

(cardiovascular)

Peripheral pitting edema

(cardiovascular)

Tachycardia

(cardiovascular)

Nocturnal cough

(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

ARNI Combination Therapy

Sacubitril/valsartan combines neprilysin inhibition with angiotensin receptor blockade, providing superior heart failure benefits by reducing cardiac strain and remodeling.

medication
2

Disease management and monitoring

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

medication
3

SGLT2 Inhibitors

Dapagliflozin or empagliflozin provide cardiorenal benefits through glucose excretion and osmotic diuresis, reducing heart failure hospitalizations.

medication

Additional treatment options

Cardiac Rehabilitation Program

Structured exercise training under medical supervision improves cardiovascular fitness, muscle strength, and quality of life in stable heart failure patients.

physical_therapy

Heart Failure Coping Strategies

Psychological support and education help patients manage anxiety, depression, and the emotional burden of living with chronic cardiac disease.

psychological

BNP/NT-proBNP Testing

Serial measurement of brain natriuretic peptide levels helps assess disease progression, treatment response, and need for therapy adjustment.

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 1d C1832243?

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 1d C1832243. 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