Brown-Vialetto-van Laere syndrome 2

MONDO:0013867

Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A2 gene.

Also known as: BVVLS2, Brown-Vialetto-Van Laere syndrome type 2, Brown-Vialetto-van Laere syndrome 2, Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A2, SLC52A2 Brown-Vialetto-van Laere syndrome

10 clinical trials for this condition and its sub-types, 0 tagged with Brown-Vialetto-van Laere syndrome 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Riboflavin transporter deficiency (6)

Including sub-types (10) Tagged with Brown-Vialetto-van Laere syndrome 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.