hereditary spastic paraplegia 80 (DOID:0112341)
Alliance: disease page
Synonyms: spastic paraplegia 80 autosomal dominant; SPG80
Alt IDs: OMIM:618418
Definition: A hereditary spastic paraplegia characterized by juvenile-onset of progressive spasticity and hyperreflexia affecting mainly the lower limbs that has_material_basis_in heterozygous mutation in the UBAP1 gene on chromosome 9p13.3.