Brown-Vialetto-van Laere syndrome 1

MONDO:0024537

Any Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene.

Also known as: Brown-Vialetto-Van Laere syndrome 1, Brown-Vialetto-van Laere syndrome 1, Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3, RTD2, Riboflavin transporter deficiency 2, SLC52A3 Brown-Vialetto-van Laere syndrome, rfvt2-related riboflavin transporter deficiency, BVVLS1

23 clinical trials for this condition and its sub-types.

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