Usher syndrome

MONDO:0019501

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

Also known as: USH, Usher's syndrome, ush, deafness-retinitis pigmentosa syndrome, retinitis pigmentosa-deafness syndrome, Graefe-Usher syndrome, Hallgren syndrome, dystrophia retinae pigmentosa-dysostosis syndrome

16 clinical trials for this condition and its sub-types, 14 tagged with Usher syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7158) ↑ Autosomal recessive disease (999)

Sub-types of Usher syndrome

Usher syndrome type 2 2 trials · 3 incl. sub-types
3 sub-types
- Usher syndrome type 2A 1 trial
- Usher syndrome type 2C 0 trials
- Usher syndrome type 2D 0 trials
Usher syndrome type 1 0 trials · 3 incl. sub-types
9 sub-types
- Usher syndrome type 1B 3 trials
- Usher syndrome type 1C 1 trial
- Usher syndrome type 1D 1 trial
- Usher syndrome type 1F 1 trial
- Usher syndrome type 1G 1 trial
- Usher syndrome type 1E 0 trials
- Usher syndrome type 1H 0 trials
- Usher syndrome type 1K 0 trials
- Usher syndrome, type 1D/F 0 trials
Usher syndrome type 3 0 trials
2 sub-types
- Usher syndrome type 3A 0 trials
- Usher syndrome type 3B 0 trials
Usher syndrome, type 4 0 trials
Retinitis pigmentosa-deafness syndrome 0 trials

Including sub-types (16) Tagged with Usher syndrome (14)

Trials to join now! 6 Not yet recruiting 3 Not yet finished but already full! 3 Completed 2

Usher syndrome

Where it sits in the disease tree

New pill aims to slow vision loss in rare usher syndrome

Massive gene hunt for deafness in pakistan could unlock new clues