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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

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