Term Name:	hereditary spastic paraplegia 8
Synonyms:	autosomal dominant spastic paraplegia 8, autosomal dominant spastic paraplegia type 8, SPG8
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24.
Ontology:	Human Disease [DOID:0110823]   ( DOID:0110823 )