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Gilbert's syndrome: Difference between revisions
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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}} | ||
==Links== | ==Links== | ||
http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=10091414 | [http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=10091414 Molecular pathology of Crigler-Najjar type I and II and Gilbert’s syndromes] | ||
{{Wikidata|Q752216}} | |||
nl:Syndroom van Gilbert | [[nl:Syndroom van Gilbert]] | ||
[[Category:Medicine]] | |||
Latest revision as of 23:05, 18 May 2019
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
