hereditary spastic paraplegia

hereditary spastic paraplegia

Bahemuka-Brown syndrome, Bahemuka–Brown syndrome, Bruyn Scheltens syndrome, Diomedi Bernardi Placidi syndrome, Familial spastic paralysis, Familial spastic paraparesis, Familial spastic paraplegia, Fitzsimmons-Walson-Mellor syndrome, Fitzsimmons–Walson–Mellor syndrome, Hereditary Spastic Paraplegia, Kjellin syndrome, Lison Kornbrut Feinstein syndrome, Lison syndrome, Nakamura Osame syndrome, Paraparesis amyotrophy of hands and feet, Silver syndrome, spastic ataxia, spastic paraparesis, Spastic paraparesis, infantile, spastic paraplegia, Spastic paraplegia, familial, Spastic paraplegia, hereditary, Spastic paraplegia 15, Spastic paraplegia epilepsy mental retardation, Spastic paraplegia facial cutaneous lesions, Spastic paraplegia familial autosomal recessive form, Spastic paraplegia glaucoma precocious puberty, Spastic paraplegia mental retardation corpus callosum, Spastic paraplegia nephritis deafness, Spastic paraplegia neuropathy poikiloderma, Spastic paraplegia type 1, X-linked, Spastic paraplegia type 2, X-linked, Spastic paraplegia type 3, dominant, Spastic paraplegia type 4, dominant, Spastic paraplegia type 5A, recessive, Spastic paraplegia type 5B, recessive, Spastic paraplegia type 6, dominant, Spastic paresis glaucoma mental retardation, Spatic paraparesis vitiligo premature graying, SPG5B, Struempell-Lorrain disease, Strumpell-Lorrain disease, Strumpell disease, Strumpell–Lorrain disease, Strümpell-Lorrain disease, Troyer syndrome

Familial spastic paraparesis, familial spastic paraplegia, French settlement disease, FSP, hereditary spastic paraparesis, HSMN V, HSP, SPG, StrC, Strumpell-Lorrain disease, Strümpell-Lorrain disease