hereditary spastic paraplegia 19 https://github.com/monarch-initiative/mondo/issues/6752 https://www.malacards.org/card/spastic_paraplegia_19_autosomal_dominant SPG19 spastic paraplegia 19, autosomal dominant OMIM:607152 MEDGEN:335494 spastic paraplegia 19 MONDO:0011785 Autosomal dominant spastic paraplegia type 19 is a pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy. UMLS:C1846685 GARD:0009588 Orphanet:100999 MESH:C536856 hereditary spastic paraplegia type 19 DOID:0110772 autosomal dominant spastic paraplegia type 19 SCTID:763375003 pure hereditary spastic paraplegia