Term Name:	hereditary spastic paraplegia 41
Synonyms:	autosomal dominant spastic paraplegia 41, autosomal dominant spastic paraplegia type 41, SPG41
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.
Ontology:	Human Disease [DOID:0110793]   ( DOID:0110793 )