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Brown-Vialetto-van Laere syndrome 1
rareAny Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A3 gene.
- Identifiers
- MONDO:0024537 OMIM:211530Orphanet:572543
- Causal genes
- SLC52A3
- Also known as
- Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3 · BVVLS1 · rfvt2-related riboflavin transporter deficiency · Riboflavin transporter deficiency 2 · RTD2
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