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Hereditary spastic paraplegia 13
rareAny hereditary spastic paraplegia in which the cause of the disease is a mutation in the HSPD1 gene.
- Identifiers
- MONDO:0011532 OMIM:605280Orphanet:100994
- Causal genes
- HSPD1
- Part of
- Hereditary spastic paraplegia
- Also known as
- hereditary spastic paraplegia caused by mutation in HSPD1 · hereditary spastic paraplegia type 13 · HSPD1 hereditary spastic paraplegia · spastic paraplegia 13 · spastic paraplegia 13, autosomal dominant
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