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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

37 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Hereditary disease (172) Neurodegenerative disease (155) Neuromuscular disease (98) Central nervous system disorder (97) Inborn errors of metabolism (42) Paraplegia (37) Palsy (29)

Trials to join now! 18 Not yet recruiting 5 Not yet finished but already full! 5 Completed 9