Gilbert Disease
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.
推出的年份: 2000(1975)
树号: C16.320.565.300.528, C18.452.648.300.528
MeSH 单一 ID: D005878
进入的组:
Disease, Gilbert
Gilbert's Disease
Disease, Gilbert's
Gilberts Disease
Gilbert's Syndrome
Gilberts Syndrome
Syndrome, Gilbert's
Hyperbilirubinemia 1
Hyperbilirubinemia 1s
Unconjugated Benign Bilirubinemia
Hyperbilirubinemia, Arias Type
Arias Type Hyperbilirubinemia
Arias Type Hyperbilirubinemias
Hyperbilirubinemias, Arias Type
Constitutional Liver Dysfunction
Familial Nonhemolytic Jaundice
Gilbert-Lereboullet Syndrome
Meulengracht Syndrome
Gilbert Syndrome
Syndrome, Gilbert
Hyperbilirubinemia I
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