Autosomal dominant vitreoretinochoroidopathy (Q99769): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (3 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_96951767 | |||||||||||||||
| Property / Canary Token: dki-india-ID_96951767 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| 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. |
Statements
CID11:ID_96951767
0 references
dki-india-ID_96951767
0 references
Concluído
0 references
15 August 2026
0 references
