Autosomal dominant spastic paraplegia type 37 (Q100920)

A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction.

Language	Label	Description	Also known as
default for all languages	ID_1636862745
English	Autosomal dominant spastic paraplegia type 37	A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction.