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Atransferrinemia: Introduction

Atransferrinemia: A rare inherited condition characterized by the absence of a compound called transferring which results in a buildup of iron in the body's tissues as well as anemia. More detailed information about the symptoms, causes, and treatments of Atransferrinemia is available below.

Symptoms of Atransferrinemia

Home Diagnostic Testing

Home medical testing related to Atransferrinemia:

Wrongly Diagnosed with Atransferrinemia?

Atransferrinemia: Complications

Review possible medical complications related to Atransferrinemia:

Causes of Atransferrinemia

Read more about causes of Atransferrinemia.

Disease Topics Related To Atransferrinemia

Research the causes of these diseases that are similar to, or related to, Atransferrinemia:

Less Common Symptoms of Atransferrinemia

Misdiagnosis and Atransferrinemia

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Atransferrinemia: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Atransferrinemia: Animations

Statistics for Atransferrinemia

Atransferrinemia: Broader Related Topics

User Interactive Forums

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

Definitions of Atransferrinemia:

Atransferrinemia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Atransferrinemia, or a subtype of Atransferrinemia, 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 Atransferrinemia as a "rare disease".
Source - Orphanet

Related Atransferrinemia Info

More information about Atransferrinemia

  1. Atransferrinemia: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications

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