Monarch Disease Ontology identifier MONDO_0013132 (hereditary spastic paraplegia 36) can be described as follows. Autosomal dominant spastic paraplegia type 36 (SPG36) is a complex form of hereditary spastic paraplegia, characterized by an onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait, spasticity, lower limb weakness, pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy. Also known as: SPG36, autosomal dominant spastic paraplegia 36, autosomal dominant spastic paraplegia type 36, hereditary spastic paraplegia type 36.