Term Name:	hereditary spastic paraplegia 10
Synonyms:	autosomal dominant spastic paraplegia 10, autosomal dominant spastic paraplegia type 10, SPG10
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13.
Ontology:	Human Disease [DOID:0110763]   ( DOID:0110763 )