| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/602522 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| BSND | barttin CLCNK-type chloride channel accessory beta subunit |
