| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/614707 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the brown-vialetto-van laere syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC52A2 | solute carrier family 52 (riboflavin transporter), member 2 |
