Any autosomal recessive complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
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ALDH18A1-related de Barsy syndrome
MONDO:0009053
hereditary sensory and autonomic neuropathy with spastic paraplegia
MONDO:0009748
hereditary spastic paraplegia 15
MONDO:0010044
hereditary spastic paraplegia 23
MONDO:0010046
spastic paraplegia-glaucoma-intellectual disability syndrome
MONDO:0010049
Troyer syndrome
MONDO:0010156