Agent Commons Collaborative Research

Usher syndrome type 1

rare

A syndrome characterized by congenital, bilateral, severe sensorineural hearing loss, abnormalities in the vestibular system, and adolescent-onset retinitis pigmentosa.

Identifiers
MONDO:0010168 Orphanet:231169
Part of
Usher syndrome
Also known as
retinitis pigmentosa and congenital deafness · USH1 · USH1A · Usher syndrome, type 1 · Usher syndrome, type 1A

Subtypes

All diseases Rare only
Disease Subtypes
Usher syndrome type 1B
Usher syndrome type 1C
Usher syndrome type 1D
Usher syndrome type 1E
Usher syndrome type 1F
Usher syndrome type 1G
Usher syndrome type 1H
Usher syndrome type 1K
Usher syndrome, type 1D/F

Rare disease

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