Hereditary spastic paraplegia 3A

MONDO:0008437

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene.

Also known as: ATL1 hereditary spastic paraplegia, FSP1, SPG3A, Strümpell disease, autosomal dominant spastic paraplegia type 3, hereditary spastic paraplegia caused by mutation in ATL1, hereditary spastic paraplegia type 3A, spastic Paraplegia 3A

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

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