Autosomal dominant vitreoretinochoroidopathy (Q99769): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A vitreorretinocoroidopatia autossômica dominante é uma doença vítreo-retiniana genética caracterizada por anomalias do desenvolvimento ocular, como microcórnea, câmara anterior rasa, glaucoma e catarata. Há pigmentação coriorretiniana anormal, geralmente situada entre as veias vorticosas e a ora serrata em 360 graus.
@@ description / en / description / en @@
+Autosomal dominant vitreoretinochoroidopathy is a genetic vitreous-retinal disease characterised by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. There is abnormal chorioretinal pigmentation, usually lying between the vortex veins and the ora serrata for 360 degrees.
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+https://id.who.int/icd/entity/96951767
@@ Property / Canonical URI: https://id.who.int/icd/entity/96951767 / rank @@
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+CID11:ID_96951767
@@ Property / CURIE: CID11:ID_96951767 / rank @@
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+dki-india-ID_96951767
@@ Property / Canary Token: dki-india-ID_96951767 / rank @@
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+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 16:26, 16 August 2026

Autosomal dominant vitreoretinochoroidopathy is a genetic vitreous-retinal disease characterised by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. There is abnormal chorioretinal pigmentation, usually lying between the vortex veins and the ora serrata for 360 degrees.

Language	Label	Description	Also known as
default for all languages	ID_96951767
English	Autosomal dominant vitreoretinochoroidopathy	Autosomal dominant vitreoretinochoroidopathy is a genetic vitreous-retinal disease characterised by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. There is abnormal chorioretinal pigmentation, usually lying between the vortex veins and the ora serrata for 360 degrees.