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Dictionary » Congenital hemolytic jaundice
 

Congenital hemolytic jaundice

Introduction: Congenital hemolytic jaundice

Description of Congenital hemolytic jaundice

Congenital hemolytic jaundice (medical condition): An inherited blood disorder where a metabolic defect causes...more »

See also:

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

Congenital hemolytic jaundice: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital hemolytic jaundice:

Congenital hemolytic jaundice: Rare Disease

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

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

Congenital hemolytic jaundice as a Disease

Congenital hemolytic jaundice: Another name for Hereditary spherocytic hemolytic anemia (or close medical condition association).
  »Introduction: Hereditary spherocytic hemolytic anemia
  »Symptoms of Hereditary spherocytic hemolytic anemia

Congenital hemolytic jaundice: Related Diseases

Congenital hemolytic jaundice: Congenital hemolytic jaundice is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Congenital hemolytic jaundice (Hereditary spherocytic hemolytic anemia)

Some of the symptoms of Congenital hemolytic jaundice incude:

Terms associated with Congenital hemolytic jaundice:

Terms Similar to Congenital hemolytic jaundice:

Source - NIH

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