Concept information
Término preferido
Gilbert Disease
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Constitutional Liver Dysfunction
- Familial Nonhemolytic Jaundice
- Gilbert Syndrome
- Gilbert-Lereboullet Syndrome
- Gilbert's Disease
- Gilbert's Syndrome
- Hyperbilirubinemia 1
- Hyperbilirubinemia, Arias Type
- Hyperbilirubinemia I
- Meulengracht Syndrome
- Unconjugated Benign Bilirubinemia
En otras lenguas
-
francés
-
Cholémie de Gilbert
-
Cholémie familiale
-
Hyperbilirubinémie de type 1
-
Ictère héréditaire de Gilbert
URI
http://data.loterre.fr/ark:/67375/JVR-LHHB0CTN-S
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