Term Name:	hereditary spastic paraplegia 37
Synonyms:	autosomal dominant spastic paraplegia 37, autosomal dominant spastic paraplegia type 37, SPG37
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3.
Ontology:	Human Disease [DOID:0110788]   ( DOID:0110788 )