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
Gilbert's Syndrome: Introduction
Gender Ratio for Gilbert's Syndrome: male predominance
Complications of Gilbert's Syndrome:
see complications of Gilbert's Syndrome
Causes of Gilbert's Syndrome: see causes of Gilbert's Syndrome
Symptoms of Gilbert's Syndrome: see symptoms of Gilbert's Syndrome
Complications of Gilbert's Syndrome: see complications of Gilbert's Syndrome
Diagnostic testing: see tests for Gilbert's Syndrome.
Misdiagnosis: see misdiagnosis and Gilbert's Syndrome.
Treatments for Gilbert's Syndrome:
see treatments for Gilbert's Syndrome
Research for Gilbert's Syndrome:
see research for Gilbert's Syndrome
Main name of condition: Gilbert's Syndrome
Other names or spellings for Gilbert's Syndrome:Gilbert-Lereboullet syndrome, Meulengracht syndrome, unconjugated benign bilirubinemia, low-grade, chronic hyperbilirubinemia, icterus intermittens juvenilis, familial, nonhemolytic, nonobstructive jaundice, familial unconjugated hyperbilirubinemia, Cholemia, familial, Hyperbilirubinemia type 1, Hyperbilirubinemia 1, Hyperbilirubinemia, Arias type
Meulengracht syndrome
Source - Diseases Database
Gilberts disease, Hyperbilirubinemia 1, Hyperbilirubinemia, Arias type, Gilberts disease, Hyperbilirubinemia 1, Hyperbilirubinemia, Arias type, Hyperbilirubinemia 1, Hyperbilirubinemia, Arias type
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, Gilbert's Syndrome:
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