Dubin-Johnson syndrome (Q40116): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de Dubin-Johnson (SDJ) é uma doença hepática hereditária benigna caracterizada clinicamente por hiperbilirrubinemia crônica, predominantemente conjugada e histopatologicamente por deposição de pigmento marrom-escuro nas células parenquimatosas do fígado.
@@ description / en / description / en @@
+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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1691610999
@@ Property / Canonical URI: https://id.who.int/icd/entity/1691610999 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:5C58.02
@@ Property / CURIE: CID11:5C58.02 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-5C58.02
@@ Property / Canary Token: dki-india-5C58.02 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+E80.6
@@ Property / Linked ICD 10: E80.6 / rank @@
+Normal rank

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.