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Dictionary » Familial benign hypocupremia
 

Familial benign hypocupremia

Introduction: Familial benign hypocupremia

Description of Familial benign hypocupremia

Familial benign hypocupremia (medical condition): A rare inherited copper deficiency. Copper has many functions in the body...more »

See also:

Copper deficiency, familial benign:
  »Introduction: Copper deficiency, familial benign
  »Symptoms of Copper deficiency, familial benign

Familial benign hypocupremia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial benign hypocupremia:

Familial benign hypocupremia: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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

Familial benign hypocupremia as a Disease

Familial benign hypocupremia: Another name for Copper deficiency, familial benign (or close medical condition association).
  »Introduction: Copper deficiency, familial benign
  »Symptoms of Copper deficiency, familial benign

Familial benign hypocupremia: Related Diseases

Familial benign hypocupremia: Familial benign hypocupremia is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial benign hypocupremia (Copper deficiency, familial benign)

Some of the symptoms of Familial benign hypocupremia incude:

Terms associated with Familial benign hypocupremia:

Terms Similar to Familial benign hypocupremia:

Source - NIH

Interesting Medical Articles:

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