Usher syndrome (Q46732): Difference between revisions
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Revision as of 15:31, 13 August 2026
Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD2H.4 |
||
| English | Usher syndrome |
Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss. |
Statements
CID11:LD2H.4
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