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Dubin-Johnson syndrome
What is Dubin-Johnson syndrome?
Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterized clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells.
Other condition names
Dubin-Sprinz disease
Hyperbilirubinemia type 2
Sprinz-Nelson syndrome
Inheritance type
Autosomal recessive
Age of Onset
Adolescent
Adult
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.