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Dictionary » Debrie’s familial haemolytic disease
 

Debrie’s familial haemolytic disease

Introduction: Debrie’s familial haemolytic disease

Description of Debrie’s familial haemolytic disease

Debrie’s familial haemolytic disease (medical condition): An inherited blood disorder where a metabolic defect causes defects in the...more »

See also:

Hereditary spherocytic hemolytic anemia:
  »Introduction: Hereditary spherocytic hemolytic anemia
  »Symptoms of Hereditary spherocytic hemolytic anemia

Debrie’s familial haemolytic disease: Related Topics

These medical condition or symptom topics may be relevant to medical information for Debrie’s familial haemolytic disease:

Debrie’s familial haemolytic disease: Rare Disease

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

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

Debrie’s familial haemolytic disease as a Disease

Debrie’s familial haemolytic disease: Another name for Hereditary spherocytic hemolytic anemia (or close medical condition association).
  »Introduction: Hereditary spherocytic hemolytic anemia
  »Symptoms of Hereditary spherocytic hemolytic anemia

Debrie’s familial haemolytic disease: Related Diseases

Debrie’s familial haemolytic disease: Debrie’s familial haemolytic disease is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Debrie’s familial haemolytic disease (Hereditary spherocytic hemolytic anemia)

Some of the symptoms of Debrie’s familial haemolytic disease incude:

Terms associated with Debrie’s familial haemolytic disease:

Terms Similar to Debrie’s familial haemolytic disease:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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