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Dictionary » Polycythemia, primary familial and congenital
 

Polycythemia, primary familial and congenital

Introduction: Polycythemia, primary familial and congenital

Description of Polycythemia, primary familial and congenital

Polycythemia, primary familial and congenital (medical condition): A rare genetic blood disorder resulting in an increased red...more »

See also:

Familial erythrocytosis, 1:
  »Introduction: Familial erythrocytosis, 1
  »Symptoms of Familial erythrocytosis, 1

Polycythemia, primary familial and congenital: Related Topics

These medical condition or symptom topics may be relevant to medical information for Polycythemia, primary familial and congenital:

Polycythemia, primary familial and congenital as a Disease

Polycythemia, primary familial and congenital: Another name for Familial erythrocytosis, 1 (or close medical condition association).
  »Introduction: Familial erythrocytosis, 1
  »Symptoms of Familial erythrocytosis, 1

Polycythemia, primary familial and congenital: Related Diseases

Polycythemia, primary familial and congenital: Polycythemia, primary familial and congenital is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Polycythemia, primary familial and congenital (Familial erythrocytosis, 1)

Some of the symptoms of Polycythemia, primary familial and congenital incude:

  • Increased red blood cell count
  • Increased hemoglobin concentration
  • Low serum erythropoietin level
  • Headache

Interesting Medical Articles:

Medical dictionaries:

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