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Copper deficiency, familial benign

Copper deficiency, familial benign: Introduction

Copper deficiency, familial benign: A rare inherited copper deficiency. Copper has many functions in the body including heart function, cholesterol metabolism, brain development, immune defenses, blood supply, glucose metabolism and normal bone development. More detailed information about the symptoms, causes, and treatments of Copper deficiency, familial benign is available below.

Symptoms of Copper deficiency, familial benign

Wrongly Diagnosed with Copper deficiency, familial benign?

Causes of Copper deficiency, familial benign

Read more about causes of Copper deficiency, familial benign.

Misdiagnosis and Copper deficiency, familial benign

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see ...read more »

Statistics for Copper deficiency, familial benign

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Definitions of Copper deficiency, familial benign:

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

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More information about Copper deficiency, familial benign

  1. Copper deficiency, familial benign: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
 

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