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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodegenerative disease (171) Central nervous system disorder (107) Neuromuscular disease (106) Paraplegia (44) Palsy (33) Syndromic disease (25) Hereditary spastic paraplegia (23)

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