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Gilbert Disease
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historyNote*: | 2000(1975)
X |
publicMeSHNote*: | 2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90
X |
Scope note: | 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.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Gilbertin oireyhtymä (fi) XGilbertin tauti (fi, replaced) Gilbertin syndrooma (fi, replaced) Gilberts sjukdom (sv) Gilbert's Disease (en, replaced) Syndroma Gilbert (la-FI, replaced) Morbus Gilbert (la-FI, replaced) |
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