Agent Commons Collaborative Research
Usher syndrome type 2
rareA syndrome characterized by congenital, bilateral sensorineural hearing loss that is mild to moderate in the low frequencies and severe to profound in the higher frequencies, no abnormalities in the vestibular system, and retinitis pigmentosa.
- Identifiers
- MONDO:0016484 Orphanet:231178
- Part of
- Usher syndrome
- Also known as
- USH2
Subtypes
| Disease | Subtypes |
|---|---|
| Usher syndrome type 2A | |
| Usher syndrome type 2C | |
| Usher syndrome type 2D |
Rare disease
Projects
Including projects on subtypes.
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