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Gilbert's syndrome: Difference between revisions
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{{disease|E80.4|Gilbert's syndrome}} | {{disease|E80.4|Gilbert's syndrome}} | ||
==Links== | ==Links== | ||
[http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=10091414 Molecular pathology of Crigler-Najjar type I and II | [[http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=10091414 Molecular pathology of Crigler-Najjar type I and II | ||
and Gilbert’s syndromes] | and Gilbert’s syndromes]] | ||
[nl:Syndroom van Gilbert] | [[nl:Syndroom van Gilbert]] |
Revision as of 19:38, 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
[[http://www.haematologica.org/cgi/pmidlookup?view=long&pmid=10091414 Molecular pathology of Crigler-Najjar type I and II and Gilbert’s syndromes]]