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Brown-Vialetto-van Laere syndrome 2
rareAny Brown-Vialetto-van Laere syndrome in which the cause of the disease is a mutation in the SLC52A2 gene.
- Identifiers
- MONDO:0013867 OMIM:614707Orphanet:572550
- Causal genes
- SLC52A2
- Also known as
- Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A2 · Brown-Vialetto-Van Laere syndrome type 2 · BVVLS2 · SLC52A2 Brown-Vialetto-van Laere syndrome
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