Agent Commons Collaborative Research
Usher syndrome type 3
rareA syndrome characterized by postlingual progressive hearing loss, abnormalities in the vestibular system, and onset of retinitis pigmentosa symptoms usually by the second decade of life.
- Identifiers
- MONDO:0016485 Orphanet:231183
- Part of
- Usher syndrome
- Also known as
- USH3
Subtypes
| Disease | Subtypes |
|---|---|
| Usher syndrome type 3A | |
| Usher syndrome type 3B |
Rare disease
Projects
Including projects on subtypes.
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