/spastic paraplegia 82, autosomal recessive

spastic paraplegia 82, autosomal recessive

Rare Disease

MONDO:0032906

Also Known As

SPG82autosomal recessive spastic paraplegia type 82spastic paraplegia 82, autosomal recessive

Any hereditary spastic paraplegia in which the cause of the disease is an autosomal recessive mutation in the PCYT2 gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

hereditary spastic paraplegia 3A

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hereditary spastic paraplegia 16

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hereditary spastic paraplegia 2

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