brown-vialetto-van laere syndrome 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614707
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Genes

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