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Gilbert Disease (medical condition): An inherited enzyme deficiency (UDP glucoronyl...more »
Gilbert Disease: A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Gilbert Disease:
Gilbert Disease: Gilbert Disease is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Gilbert Disease incude:
Treatments for Gilbert Disease (Gilbert's Syndrome) include:
Treatment of Gilbert Disease: For more treatment information about Gilbert Disease, see treatment of Gilbert's Syndrome (Gilbert Disease)
These medical disease topics may be related to Gilbert Disease:
The following list attempts to classify Gilbert Disease into categories where each line is subset of the next.
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