- Concept UI
- M0011823
- Scope Note
- A benign, autosomally recessive inherited hyperbilirubinemia characterized by the presence of a dark pigment in the centrilobular region of the liver cells. There is a functional defect in biliary excretion of bilirubin, cholephilic dyes, and porphyrins. Affected persons may be asymptomatic or have vague constitutional or gastrointestinal symptoms. The liver may be slightly enlarged, and oral and intravenous cholangiography fails to visualize the biliary tract.
- Terms
-
Jaundice, Chronic Idiopathic
Preferred Term
Term UI
T022740
Date01/01/1999
LexicalTag
NON
ThesaurusID
-
Dubin-Johnson Syndrome
Term UI
T022739
Date03/30/1974
LexicalTag
EPO
ThesaurusID
-
Hyperbilirubinemia 2
Term UI
T745900
Date02/24/2009
LexicalTag
NON
ThesaurusID
-
Hyperbilirubinemia II
Term UI
T824575
Date06/22/2012
LexicalTag
NON
ThesaurusID