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Hereditary spastic paraplegia 3A
rareAny hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene.
- Identifiers
- MONDO:0008437 OMIM:182600Orphanet:100984
- Causal genes
- ATL1
- Part of
- Hereditary spastic paraplegia
- Also known as
- ATL1 hereditary spastic paraplegia · autosomal dominant spastic paraplegia type 3 · FSP1 · hereditary spastic paraplegia caused by mutation in ATL1 · hereditary spastic paraplegia type 3A
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