Usher syndrome (Q46732): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Síndrome de Usher é a causa mais comum de surdez-cegueira hereditária combinada e é caracterizada pela associação de surdez neurossensorial (geralmente congênita) com retinite pigmentosa e perda progressiva da visão.
@@ description / en / description / en @@
+Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1452641873
@@ Property / Canonical URI: https://id.who.int/icd/entity/1452641873 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD2H.4
@@ Property / CURIE: CID11:LD2H.4 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD2H.4
@@ Property / Canary Token: dki-india-LD2H.4 / 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 @@
+FLAVIA MARIA DOS SANTOS BERGAMI
@@ Property / Linked ICD 10: FLAVIA MARIA DOS SANTOS BERGAMI / rank @@
+Normal rank

Latest revision as of 15:32, 13 August 2026

Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.

Language	Label	Description	Also known as
default for all languages	LD2H.4
English	Usher syndrome	Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.