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often shortened to GS, also called Gilbert–Meulengracht syndrome, is a common genetic liver disorder found in 3-12% of the population
often shortened to [[Gilbert's syndrome|GS]], also called Gilbert–Meulengracht syndrome, is a common genetic liver disorder found in 3-12% of the population.


{{disease|E80.4|Gilbert's syndrome}}
{{disease|E80.4|Gilbert's syndrome}}
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[[nl:Syndroom van Gilbert]]
[[nl:Syndroom van Gilbert]]
[[Category:Medicine]]

Revision as of 22:45, 23 July 2015

often shortened to GS, also called Gilbert–Meulengracht syndrome, is a common genetic liver disorder found in 3-12% of the population.

Disease classification WHO
E80.4 Gilbert's syndrome

Links

[Molecular pathology of Crigler-Najjar type I and II and Gilbert’s syndromes]