| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/614482 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC33A1 | solute carrier family 33 (acetyl-CoA transporter), member 1 |
