hereditary spastic paraplegia 37 https://github.com/monarch-initiative/mondo/issues/6752 https://www.malacards.org/card/spastic_paraplegia_37_autosomal_dominant OMIM:611945 Autosomal dominant spastic paraplegia type 37 is a pure 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 at ankles and urinary dysfunction. Ankle clonus is also reported in some patients. GARD:0017064 SPG37 autosomal dominant spastic paraplegia type 37 MEDGEN:422458 UMLS:C2936880 MESH:C567931 DOID:0110788 spastic paraplegia 37, autosomal dominant hereditary spastic paraplegia type 37 Orphanet:171612 SCTID:763369007 MONDO:0012766 pure hereditary spastic paraplegia