Autosomal dominant vitreoretinochoroidopathy (Q99769): Difference between revisions
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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 |
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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. |
Statements
CID11:ID_96951767
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dki-india-ID_96951767
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Concluído
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15 August 2026
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