Term Name:	hereditary spastic paraplegia 38
Synonyms:	autosomal dominant spastic paraplegia 38, autosomal dominant spastic paraplegia type 38, SPG38
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.
Ontology:	Human Disease [DOID:0110789]   ( DOID:0110789 )