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Hanhart Syndrome

Hanhart Syndrome: Introduction

Hanhart Syndrome: An autosomal recessive disorder due to a deficiency in the body of the tyrosine amino transferase enzyme. More detailed information about the symptoms, causes, and treatments of Hanhart Syndrome is available below.

Symptoms of Hanhart Syndrome

Wrongly Diagnosed with Hanhart Syndrome?

Hanhart Syndrome: Complications

Read more about complications of Hanhart Syndrome.

Causes of Hanhart Syndrome

Read more about causes of Hanhart Syndrome.

Disease Topics Related To Hanhart Syndrome

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Misdiagnosis and Hanhart Syndrome

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Hanhart Syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hanhart Syndrome: Animations

Statistics for Hanhart Syndrome

Hanhart Syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Hanhart Syndrome, or answer someone else's question, on our message boards:

Definitions of Hanhart Syndrome:

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Hanhart Syndrome as a "rare disease".
Source - Orphanet

Related Hanhart Syndrome Info

More information about Hanhart Syndrome

  1. Hanhart Syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications

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