Autosomal recessive complex spastic paraplegia type 9B

Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.

Also known as: ALDH18A1 autosomal recessive complex spastic paraplegia, AR-SPG9B, SPG9B, autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1, hereditary spastic paraplegia type 9B, hereditary spastic paraplegia 9B, spastic paraplegia 9B, autosomal recessive

0 clinical trials for this condition and its sub-types.