Term Name:	hereditary spastic paraplegia 46
Synonyms:	autosomal recessive spastic paraplegia 46, autosomal recessive spastic paraplegia type 46, SPG46
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.
Ontology:	Human Disease [DOID:0110798]   ( DOID:0110798 )