Hereditary spastic paraplegia 47

MONDO:0013551

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

15 clinical trials for this condition and its sub-types.

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