Autosomal dominant optic atrophy and cataract (Q94802): Difference between revisions
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Atrofia óptica autossômica dominante e catarata é uma doença ocular genética caracterizada por atrofia óptica e catarata que geralmente aparecem durante a infância. Sinais moderados extrapiramidais também podem estar presentes. | |||
| description / en | description / en | ||
Autosomal dominant optic atrophy and cataract is a genetic eye disease characterised by optic atrophy and cataract that generally appears during childhood. Moderate extrapyramidal signs may also be present. | |||
Revision as of 10:15, 16 August 2026
Autosomal dominant optic atrophy and cataract is a genetic eye disease characterised by optic atrophy and cataract that generally appears during childhood. Moderate extrapyramidal signs may also be present.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1789029893 |
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| English | Autosomal dominant optic atrophy and cataract |
Autosomal dominant optic atrophy and cataract is a genetic eye disease characterised by optic atrophy and cataract that generally appears during childhood. Moderate extrapyramidal signs may also be present. |
