Leber congenital amaurosis (Q1811132)
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retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
- AMAUROSIS CONGENITA OF LEBER I
- LCA
- Leber congenital amaurosis type 13
- Leber congenital amaurosis type 14
- Leber's amaurosis (disorder)
- Leber's congenital amaurosis
- Leber's disease
- Leber's amaurosis
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis |
retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness |
|
Statements
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Leber's congenital amaurosis
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Identifiers
Leber Congenital Amaurosis
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Sitelinks
Wikipedia(16 entries)
- arwiki كمنة ليبر الخلقية
- bswiki Leberova kongenitalna amauroza
- cawiki Amaurosi congènita de Leber
- dewiki Lebersche Kongenitale Amaurose
- enwiki Leber congenital amaurosis
- eswiki Amaurosis congénita de Leber
- etwiki Leberi tüüpi pärilik amauroos
- fawiki لبر آموروزیس مادرزادی
- fiwiki Leberin synnynnäinen amauroosi
- frwiki Amaurose congénitale de Leber
- huwiki Leber-féle veleszületett vakság
- itwiki Amaurosi congenita di Leber
- plwiki Wrodzona ślepota Lebera
- ptwiki Amaurose Congênita de Leber
- ruwiki Амавроз Лебера
- ttwiki Тумыштагы Лебер амаврозы
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Multilingual sites(1 entry)
- commonswiki Category:Leber's congenital amaurosis