Hereditary spastic paraplegia 56

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the CYP2U1 gene.

Also known as: CYP2U1 hereditary spastic paraplegia, SPG56, autosomal recessive spastic paraplegia type 56, hereditary spastic paraplegia caused by mutation in CYP2U1, hereditary spastic paraplegia type 56, spastic paraplegia 56, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 56 itself.