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What is Waardenburg syndrome type 2?

What is Waardenburg syndrome type 2?

  • Waardenburg syndrome type 2: A hereditary, autosomal dominant disorder.

Waardenburg syndrome type 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Waardenburg syndrome type 2, or a subtype of Waardenburg syndrome type 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Waardenburg syndrome type 2: Introduction

Types of Waardenburg syndrome type 2:

Broader types of Waardenburg syndrome type 2:

What causes Waardenburg syndrome type 2?

Causes of Waardenburg syndrome type 2: see causes of Waardenburg syndrome type 2

What are the symptoms of Waardenburg syndrome type 2?

Symptoms of Waardenburg syndrome type 2: see symptoms of Waardenburg syndrome type 2

Can anyone else get Waardenburg syndrome type 2?

More information: see contagiousness of Waardenburg syndrome type 2
Inheritance: see inheritance of Waardenburg syndrome type 2

Waardenburg syndrome type 2: Testing

Diagnostic testing: see tests for Waardenburg syndrome type 2.

Misdiagnosis: see misdiagnosis and Waardenburg syndrome type 2.

How is it treated?

Doctors and Medical Specialists for Waardenburg syndrome type 2: Medical Geneticist ; see also doctors and medical specialists for Waardenburg syndrome type 2.
Treatments for Waardenburg syndrome type 2: see treatments for Waardenburg syndrome type 2
Research for Waardenburg syndrome type 2: see research for Waardenburg syndrome type 2

Name and Aliases of Waardenburg syndrome type 2

Main name of condition: Waardenburg syndrome type 2

Other names or spellings for Waardenburg syndrome type 2:

WS 2, WS type 2

WS 2, WS type 2
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Waardenburg syndrome type 2: Related Conditions

Research the causes of these diseases that are similar to, or related to, Waardenburg syndrome type 2:

 

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