Structured Summary
Abstract
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.
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Synonyms
12 entry terms
- Dubin-Johnson Syndrome
- Hyperbilirubinemia 2
- Hyperbilirubinemia II
- Jaundice, Chronic Idiopathic
- Chronic Idiopathic Jaundices
- Dubin Johnson Syndrome
- Hyperbilirubinemia 2s
- Hyperbilirubinemia IIs
- Idiopathic Jaundice, Chronic
- Idiopathic Jaundices, Chronic
- Jaundices, Chronic Idiopathic
- Syndrome, Dubin-Johnson
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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NLM Classification
WI 703
AMA Style
References
- National Library of Medicine. Chronic Idiopathic Jaundice. Medical Subject Headings (MeSH). 2026. Unique ID D007566. http://id.nlm.nih.gov/mesh/2026/D007566
- Chronic Idiopathic Jaundice. In: Wikipedia. https://en.wikipedia.org/wiki/Dubin%E2%80%93Johnson_syndrome
- Chronic Idiopathic Jaundice. In: Wikidata. https://www.wikidata.org/wiki/Q1263039