Brown-Vialetto-Van laere syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050694)
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1 genes associated with the Brown-Vialetto-Van laere syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3