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Gilbert's Syndrome

Gilbert's Syndrome: Introduction

Gilbert's Syndrome: An inherited enzyme deficiency (UDP glucoronyl transferase) which causes periodic mild jaundice, abdominal pain, weakness and fatigue. More detailed information about the symptoms, causes, and treatments of Gilbert's Syndrome is available below.

Symptoms of Gilbert's Syndrome

Treatments for Gilbert's Syndrome

Wrongly Diagnosed with Gilbert's Syndrome?

Gilbert's Syndrome: Related Patient Stories

Gilbert's Syndrome: Deaths

Read more about Deaths and Gilbert's Syndrome.

Gilbert's Syndrome: Complications

Read more about complications of Gilbert's Syndrome.

Causes of Gilbert's Syndrome

Read more about causes of Gilbert's Syndrome.

Disease Topics Related To Gilbert's Syndrome

Research the causes of these diseases that are similar to, or related to, Gilbert's Syndrome:

Evidence Based Medicine Research for Gilbert's Syndrome

Medical research articles related to Gilbert's Syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Research about Gilbert's Syndrome

Visit our research pages for current research about Gilbert's Syndrome treatments.

Clinical Trials for Gilbert's Syndrome

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Gilbert's Syndrome include:

Statistics for Gilbert's Syndrome

Gilbert's Syndrome: Broader Related Topics

Gilbert's Syndrome Message Boards

Related forums and medical stories:

User Interactive Forums

Read about other experiences, ask a question about Gilbert's Syndrome, or answer someone else's question, on our message boards:

Definitions of Gilbert's Syndrome:

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 - Diseases Database)

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Gilbert's Syndrome as a "rare disease".
Source - Orphanet

 

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