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Hereditary spastic paraplegia 56
rareAny hereditary spastic paraplegia in which the cause of the disease is a mutation in the CYP2U1 gene.
- Identifiers
- MONDO:0014015 OMIM:615030Orphanet:320411
- Causal genes
- CYP2U1
- Part of
- Hereditary spastic paraplegia
- Also known as
- autosomal recessive spastic paraplegia type 56 · CYP2U1 hereditary spastic paraplegia · hereditary spastic paraplegia caused by mutation in CYP2U1 · hereditary spastic paraplegia type 56 · spastic paraplegia 56, autosomal recessive
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