| Descriptor English: | Jaundice, Chronic Idiopathic | ||||||
| Descriptor Spanish: |
Ictericia Idiopática Crónica
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| Descriptor Portuguese: | Icterícia Idiopática Crônica | ||||||
| Descriptor French: | Ictère chronique idiopathique | ||||||
| Entry term(s): |
Chronic Idiopathic Jaundice Chronic Idiopathic Jaundices Dubin Johnson Syndrome Dubin-Johnson Syndrome Hyperbilirubinemia 2 Hyperbilirubinemia 2s Hyperbilirubinemia II Hyperbilirubinemia IIs Idiopathic Jaundice, Chronic Idiopathic Jaundices, Chronic Jaundices, Chronic Idiopathic Syndrome, Dubin-Johnson |
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| Tree number(s): |
C16.320.565.300.764 C16.614.451.500.250 C18.452.648.300.764 C23.550.291.500.479 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D007566 | ||||||
| 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| DeCS ID: | 7735 | ||||||
| Unique ID: | D007566 | ||||||
| NLM Classification: | WI 703 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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Jaundice, Chronic Idiopathic
- Preferred
| 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. |
| Preferred term | Jaundice, Chronic Idiopathic |
| Entry term(s) |
Chronic Idiopathic Jaundice Chronic Idiopathic Jaundices Dubin Johnson Syndrome Dubin-Johnson Syndrome Hyperbilirubinemia 2 Hyperbilirubinemia 2s Hyperbilirubinemia II Hyperbilirubinemia IIs Idiopathic Jaundice, Chronic Idiopathic Jaundices, Chronic Jaundices, Chronic Idiopathic Syndrome, Dubin-Johnson |
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