Hereditary spastic paraplegia 13

MONDO:0011532

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the HSPD1 gene.

Also known as: HSPD1 hereditary spastic paraplegia, SPG13, hereditary spastic paraplegia caused by mutation in HSPD1, hereditary spastic paraplegia type 13, autosomal dominant spastic paraplegia type 13, spastic paraplegia 13, spastic paraplegia 13, autosomal dominant

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 13 itself.

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↑ Hereditary spastic paraplegia (33)

Including sub-types (2) Tagged with Hereditary spastic paraplegia 13 (0)

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