Any autosomal dominant complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
spastic paraplegia-epilepsy-intellectual disability syndrome
MONDO:0008439
spastic paraplegia-nephritis-deafness syndrome
MONDO:0008440
spastic paraplegia-neuropathy-poikiloderma syndrome
MONDO:0008442
spastic paraplegia-precocious puberty syndrome
MONDO:0008443
ALDH18A1-related de Barsy syndrome
MONDO:0009053
hereditary spastic paraplegia 17
MONDO:0010043