|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050694)|
|Downloads & Tools|
1 genes/proteins associated with the disease Brown-Vialetto-Van Laere syndrome from the curated CTD Gene-Disease Associations dataset.
|SLC52A3||solute carrier family 52 (riboflavin transporter), member 3||2.88009|