Dubin-Johnson syndrome (Q40116): Difference between revisions
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Latest revision as of 05:48, 13 August 2026
Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterised clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C58.02 |
||
| English | Dubin-Johnson syndrome |
Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterised clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells. |
Statements
CID11:5C58.02
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dki-india-5C58.02
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Concluído
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13 August 2026
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