Hereditary spastic paraplegia 47

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4B1 gene.

Also known as: AP4B1 hereditary spastic paraplegia, SPG47, Spastic Paraplegia 47, hereditary spastic paraplegia 47, hereditary spastic paraplegia caused by mutation in AP4B1, hereditary spastic paraplegia type 47, cerebral palsy, spastic quadriplegic, 5, cerebral palsy, spastic quadriplegic, 5, formerly

1 clinical trial for this condition and its sub-types.