hereditary spastic paraplegia 90A (DOID:0070459)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 90A; SPG90A
Alt IDs: OMIM:620416
Definition: A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in heterozygous mutation in the SPTSSA gene on chromosome 14q13.1.