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Usher syndrome

MONDO:0019501

Also 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.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.