Dubin-Johnson syndrome (Q40116): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
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
0 references
dki-india-5C58.02
0 references
Concluído
0 references
