| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A syndrome characterized by a combination of hearing loss and visual impairment. (Human Disease Ontology, DOID_0050439) |
| Similar Terms | |
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8 genes involed in the disease usher syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name |
|---|---|
| ADGRV1 | adhesion G protein-coupled receptor V1 |
| CDH23 | cadherin-related 23 |
| CLRN1 | clarin 1 |
| MYO7A | myosin VIIA |
| PCDH15 | protocadherin-related 15 |
| USH1C | Usher syndrome 1C (autosomal recessive, severe) |
| USH1G | Usher syndrome 1G (autosomal recessive) |
| USH2A | Usher syndrome 2A (autosomal recessive, mild) |
