Hereditary spastic paraplegia 72

MONDO:0014282

Any pure hereditary spastic paraplegia in which the cause of the disease is a mutation in the REEP2 gene.

Also known as: REEP2 pure hereditary spastic paraplegia, SPG72, autosomal spastic paraplegia type 72, hereditary spastic paraplegia type 72, pure hereditary spastic paraplegia caused by mutation in REEP2, spastic paraplegia 72, autosomal dominant, spastic paraplegia 72, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 72 itself.

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↑ Pure hereditary spastic paraplegia (0)

Including sub-types (2) Tagged with Hereditary spastic paraplegia 72 (0)

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