What is Familial hypertrophic cardiomyopathy 3?

What is Familial hypertrophic cardiomyopathy 3?

• Familial hypertrophic cardiomyopathy 3: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 3 is caused by a defect in the alpha-tropomyosin gene on chromosome 15q22.1.

Familial hypertrophic cardiomyopathy 3: Introduction

Types of Familial hypertrophic cardiomyopathy 3:

Broader types of Familial hypertrophic cardiomyopathy 3:

• Circulatory system conditions
• Heart muscle conditions
• Heart conditions
• Chest conditions
• Genetic conditions
• Muscle conditions
• more types...»

How serious is Familial hypertrophic cardiomyopathy 3?

Complications of Familial hypertrophic cardiomyopathy 3: see complications of Familial hypertrophic cardiomyopathy 3

What causes Familial hypertrophic cardiomyopathy 3?

Causes of Familial hypertrophic cardiomyopathy 3: see causes of Familial hypertrophic cardiomyopathy 3

What are the symptoms of Familial hypertrophic cardiomyopathy 3?

Symptoms of Familial hypertrophic cardiomyopathy 3: see symptoms of Familial hypertrophic cardiomyopathy 3

Complications of Familial hypertrophic cardiomyopathy 3: see complications of Familial hypertrophic cardiomyopathy 3

Onset of Familial hypertrophic cardiomyopathy 3: The age of presentation may vary from birth to adulthood. Sometimes there are no symptoms until sudden death occurs.

Familial hypertrophic cardiomyopathy 3: Testing

Diagnostic testing: see tests for Familial hypertrophic cardiomyopathy 3.

Misdiagnosis: see misdiagnosis and Familial hypertrophic cardiomyopathy 3.

How is it treated?

Doctors and Medical Specialists for Familial hypertrophic cardiomyopathy 3: Medical Geneticist, Cardiologist ; see also doctors and medical specialists for Familial hypertrophic cardiomyopathy 3.
Treatments for Familial hypertrophic cardiomyopathy 3: see treatments for Familial hypertrophic cardiomyopathy 3

Name and Aliases of Familial hypertrophic cardiomyopathy 3

Main name of condition: Familial hypertrophic cardiomyopathy 3

CMH3, cardiomyopathy, familial hypertrophic, 3

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