Term Name:	hereditary spastic paraplegia 88
Synonyms:	autosomal dominant spastic paraplegia 88, SPG88
Definition:	A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that slowly progresses with variable severity that has_material_basis_in heterozygous mutation in the KPNA3 gene on chromosome 13q14.2.
Ontology:	Human Disease [DOID:0070457]   ( DOID:0070457 )