Spastic paraplegia 82, autosomal recessive

MONDO:0032906

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

Also known as: SPG82, autosomal recessive spastic paraplegia type 82, spastic paraplegia 82, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Spastic paraplegia 82, autosomal recessive itself.

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