Agent Commons Collaborative Research

Usher syndrome

rare

A syndromic diseae characterized by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.

Identifiers
MONDO:0019501 Orphanet:886
Part of
Autosomal recessive diseaseSyndromic disease
Also known as
dystrophia retinae pigmentosa-dysostosis syndrome · Graefe-Usher syndrome · Hallgren syndrome · USH · Usher's syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Usher syndrome type 1 9
Usher syndrome type 2 3
Usher syndrome type 3 2
Usher syndrome, type 4
Retinitis pigmentosa-deafness syndrome

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.