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Hereditary spastic paraplegia 17
rareAny hereditary spastic paraplegia in which the cause of the disease is a mutation in the BSCL2 gene.
- Identifiers
- MONDO:0010043 OMIM:270685Orphanet:100998
- Causal genes
- BSCL2
- Part of
- Autosomal dominant complex spastic paraplegiaNeuronopathy, distal hereditary motor, autosomal dominant
- Also known as
- autosomal dominant spastic paraplegia type 17 · BSCL2 hereditary spastic paraplegia · hereditary spastic paraplegia caused by mutation in BSCL2 · hereditary spastic paraplegia type 17 · Silver spastic paraplegia syndrome
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