Term Name:	hereditary spastic paraplegia 12
Synonyms:	autosomal dominant spastic paraplegia 12, autosomal dominant spastic paraplegia type 12, SPG12
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.
Ontology:	Human Disease [DOID:0110765]   ( DOID:0110765 )