Term Name:	hereditary spastic paraplegia 31
Synonyms:	autosomal dominant spastic paraplegia 31, autosomal dominant spastic paraplegia type 31, SPG31
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.
Ontology:	Human Disease [DOID:0110782]   ( DOID:0110782 )