Hereditary spastic paraplegia 56

MONDO:0014015

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the CYP2U1 gene.

Also known as: CYP2U1 hereditary spastic paraplegia, SPG56, autosomal recessive spastic paraplegia type 56, hereditary spastic paraplegia caused by mutation in CYP2U1, hereditary spastic paraplegia type 56, spastic paraplegia 56, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 56 itself.

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↑ Hereditary spastic paraplegia (33)

Including sub-types (2) Tagged with Hereditary spastic paraplegia 56 (0)

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