Autosomal recessive spastic paraplegia type 78

MONDO:0014975

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.

Also known as: ATP13A2 hereditary spastic paraplegia, SPG78, hereditary spastic paraplegia caused by mutation in ATP13A2, spastic paraplegia 78, autosomal recessive, spastic paraplegia 78, autosomal recessive; SPG78

2 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive spastic paraplegia type 78 itself.

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↑ Autosomal recessive disease (994) ↑ Complex hereditary spastic paraplegia (7)

Including sub-types (2) Tagged with Autosomal recessive spastic paraplegia type 78 (0)

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