Term Name:	hereditary spastic paraplegia 80
Synonyms:	spastic paraplegia 80 autosomal dominant, SPG80
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.
Ontology:	Human Disease [DOID:0112341]   ( DOID:0112341 )