Autosomal dominant spastic paraplegia type 19 (Q100872)

Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy.

Language	Label	Description	Also known as
default for all languages	ID_1020508875
English	Autosomal dominant spastic paraplegia type 19	Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy.