Autosomal dominant vitreoretinochoroidopathy (Q99769): Difference between revisions
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| 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. | |||
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 |
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| 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. |
