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Dictionary » Familial, nonhemolytic, nonobstructive jaundice
 

Familial, nonhemolytic, nonobstructive jaundice

Introduction: Familial, nonhemolytic, nonobstructive jaundice

Description of Familial, nonhemolytic, nonobstructive jaundice

Familial, nonhemolytic, nonobstructive jaundice (medical condition): An inherited enzyme deficiency (UDP glucoronyl transferase) which causes periodic mild jaundice, abdominal pain, weakness and fatigue.

See also:

Gilbert's Syndrome:
  »Introduction: Gilbert's Syndrome
  »Symptoms of Gilbert's Syndrome
  »Treatments for Gilbert's Syndrome

Familial, nonhemolytic, nonobstructive jaundice: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial, nonhemolytic, nonobstructive jaundice:

Familial, nonhemolytic, nonobstructive jaundice as a Disease

Familial, nonhemolytic, nonobstructive jaundice: Another name for Gilbert's Syndrome (or close medical condition association).
  »Introduction: Gilbert's Syndrome
  »Symptoms of Gilbert's Syndrome
  »Treatments for Gilbert's Syndrome

Symptoms of Familial, nonhemolytic, nonobstructive jaundice (Gilbert's Syndrome)

Some of the symptoms of Familial, nonhemolytic, nonobstructive jaundice incude:

See full list of 10 symptoms of Familial, nonhemolytic, nonobstructive jaundice (Gilbert's Syndrome)

Treatments for Familial, nonhemolytic, nonobstructive jaundice (Gilbert's Syndrome)

Treatments for Familial, nonhemolytic, nonobstructive jaundice (Gilbert's Syndrome) include:

  • None required

Read more about treatments for Familial, nonhemolytic, nonobstructive jaundice

Treatment of Familial, nonhemolytic, nonobstructive jaundice: For more treatment information about Familial, nonhemolytic, nonobstructive jaundice, see treatment of Gilbert's Syndrome (Familial, nonhemolytic, nonobstructive jaundice)

Familial, nonhemolytic, nonobstructive jaundice: Related Disease Topics

These medical disease topics may be related to Familial, nonhemolytic, nonobstructive jaundice:

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