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Hereditary spastic paraplegia 8

MONDO:0011339

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the WASHC5 gene.

Also known as: SPG8, WASHC5 hereditary spastic paraplegia, autosomal dominant spastic paraplegia type 8, hereditary spastic paraplegia caused by mutation in WASHC5, hereditary spastic paraplegia type 8, spastic paraplegia 8, spastic paraplegia 8, autosomal dominant

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 8 itself.

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↑ Pure hereditary spastic paraplegia (0)

Including sub-types (2) Tagged with Hereditary spastic paraplegia 8 (0)

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