Usher syndrome
MONDO:0019501Also known as: USH, Usher's syndrome, deafness-retinitis pigmentosa syndrome, retinitis pigmentosa-deafness syndrome, Graefe-Usher syndrome
- MONDO:
- MONDO:0019501
- Orphanet:
- 886 ↗
Rare disease109 associated genes
Description
A syndromic diseae characterized by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
Associated genes
+99 more genes — install the extension to see the full list inline on any page.