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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
These medical condition or symptom topics may be relevant to medical information for Familial, nonhemolytic, nonobstructive jaundice:
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
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) include:
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)
These medical disease topics may be related to Familial, nonhemolytic, nonobstructive jaundice:
Search to find out more about Familial, nonhemolytic, nonobstructive jaundice:
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