Hereditary spastic paraplegia 11

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene.

Also known as: HSP-TCC, Nakamura-Osame syndrome, SPG11, SPG11 hereditary spastic paraplegia, autosomal recessive spastic paraplegia type 11, hereditary spastic paraplegia caused by mutation in SPG11, hereditary spastic paraplegia type 11, spastic paraplegia-intellectual disability-thin corpus callosum syndrome

1 clinical trial for this condition and its sub-types.