Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the BSCL2 gene.
Comprehensive, easy-to-understand information about this condition
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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
neuronopathy, distal hereditary motor, autosomal dominant 1
MONDO:0008451
neuronopathy, distal hereditary motor, autosomal dominant 8
MONDO:0010839