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What is Familial hypertrophic cardiomyopathy 10?

What is Familial hypertrophic cardiomyopathy 10?

  • Familial hypertrophic cardiomyopathy 10: An inherited condition characterized by increased thickness of the wall of the heart ventricle which affects the hearts function. Type 10 is caused by a defect in the MYL2 gene on chromosome 12q23-q24.

Familial hypertrophic cardiomyopathy 10: Introduction

Types of Familial hypertrophic cardiomyopathy 10:

Broader types of Familial hypertrophic cardiomyopathy 10:

How serious is Familial hypertrophic cardiomyopathy 10?

Complications of Familial hypertrophic cardiomyopathy 10: see complications of Familial hypertrophic cardiomyopathy 10

What causes Familial hypertrophic cardiomyopathy 10?

Causes of Familial hypertrophic cardiomyopathy 10: see causes of Familial hypertrophic cardiomyopathy 10

What are the symptoms of Familial hypertrophic cardiomyopathy 10?

Symptoms of Familial hypertrophic cardiomyopathy 10: see symptoms of Familial hypertrophic cardiomyopathy 10

Complications of Familial hypertrophic cardiomyopathy 10: see complications of Familial hypertrophic cardiomyopathy 10

Onset of Familial hypertrophic cardiomyopathy 10: The age of presentation may vary from birth to adulthood. Sometimes there are no symptoms until sudden death occurs.

Familial hypertrophic cardiomyopathy 10: Testing

Diagnostic testing: see tests for Familial hypertrophic cardiomyopathy 10.

Misdiagnosis: see misdiagnosis and Familial hypertrophic cardiomyopathy 10.

How is it treated?

Doctors and Medical Specialists for Familial hypertrophic cardiomyopathy 10: Medical Geneticist, Cardiologist ; see also doctors and medical specialists for Familial hypertrophic cardiomyopathy 10.
Treatments for Familial hypertrophic cardiomyopathy 10: see treatments for Familial hypertrophic cardiomyopathy 10

Name and Aliases of Familial hypertrophic cardiomyopathy 10

Main name of condition: Familial hypertrophic cardiomyopathy 10

Other names or spellings for Familial hypertrophic cardiomyopathy 10:

CMH10, cardiomyopathy, familial hypertrophic, 10

 

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