1. Diseases
  2. Dubin-Johnson syndrome

Dubin-Johnson syndrome

Disease Export to PDF
Name:
Dubin-Johnson syndrome
Description:
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.
ORPHAcode:
234
Synonyms:
Dubin-Sprinz disease
Hyperbilirubinemia type 2
Sprinz-Nelson syndrome
XREF(s):
Orphanet
MeSH
MedDRA
ICD-10
OMIM
Analyte(s):
ABCC2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14