hereditary spastic paraplegia 36 https://www.malacards.org/card/spastic_paraplegia_36_autosomal_dominant 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. MONDO:0013132 OMIM:613096 hereditary spastic paraplegia type 36 DOID:0110787 GARD:0017472 Orphanet:320365 MESH:C567930 MEDGEN:422457 SPG36 autosomal dominant spastic paraplegia type 36 spastic paraplegia 36, autosomal dominant SCTID:723819007 UMLS:C2936879 autosomal dominant complex spastic paraplegia