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
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symptoms of Atransferrinemia
Home Diagnostic Testing
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Wrongly Diagnosed with Atransferrinemia?
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Causes of Atransferrinemia
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Disease Topics Related To Atransferrinemia
Research the causes of these diseases that are similar to, or related to, Atransferrinemia:
Less Common Symptoms of Atransferrinemia
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occasional symptoms of Atransferrinemia
Misdiagnosis and Atransferrinemia
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Read more about Misdiagnosis and Atransferrinemia
Atransferrinemia: Research Doctors & Specialists
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Statistics for Atransferrinemia
Atransferrinemia: Broader Related Topics
Types of Atransferrinemia
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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
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