Hereditary spastic paraplegia 50

MONDO:0013048

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4M1 gene.

Also known as: AP4M1 hereditary spastic paraplegia, SPG50, Spastic Paraplegia 50, hereditary spastic paraplegia caused by mutation in AP4M1, hereditary spastic paraplegia type 50, cerebral palsy, spastic quadriplegic, 3, cerebral palsy, spastic quadriplegic, 3, formerly, spastic paraplegia 50, autosomal recessive

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

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