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Autosomal recessive complex spastic paraplegia type 9B

MONDO:0014702

Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.

Also known as: ALDH18A1 autosomal recessive complex spastic paraplegia, AR-SPG9B, SPG9B, autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1, hereditary spastic paraplegia type 9B, hereditary spastic paraplegia 9B, spastic paraplegia 9B, autosomal recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive complex spastic paraplegia type 9B itself.

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↑ Complex hereditary spastic paraplegia (7) ↑ P5CS deficiency (0)

Including sub-types (2) Tagged with Autosomal recessive complex spastic paraplegia type 9B (0)

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