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Autosomal recessive complex spastic paraplegia type 9B

rare

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

Identifiers
MONDO:0014702 OMIM:616586Orphanet:447760
Part of
P5CS deficiencyComplex hereditary spastic paraplegia
Also known as
ALDH18A1 autosomal recessive complex spastic paraplegia · AR-SPG9B · autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1 · hereditary spastic paraplegia type 9B · spastic paraplegia 9B, autosomal recessive

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