Hereditary spastic paraplegia 38

MONDO:0012867

A hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15.

Also known as: SPG38, autosomal dominant spastic paraplegia type 38, hereditary spastic paraplegia type 38, spastic paraplegia 38, autosomal dominant

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

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