Term Name:	hereditary spastic paraplegia 13
Synonyms:	autosomal dominant spastic paraplegia 13, SPG13
Definition:	A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33.
Ontology:	Human Disease [DOID:0110766]   ( DOID:0110766 )