| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the cataract 35, congenital nuclear phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CTRCT35 | cataract, congenital nuclear, autosomal recessive |
