Deafness - optic atrophy syndrome (Q55786): Difference between revisions
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Atrofia óptica autossômica dominante e surdez congênita é uma forma de atrofia óptica autossômica dominante, caracterizada por surdez severa congênita e insuficiência visual progressiva na meia-idade. | |||
| description / en | description / en | ||
Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure. | |||
Revision as of 03:27, 14 August 2026
Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_412176667 |
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| English | Deafness - optic atrophy syndrome |
Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure. |
