Term Name:	hereditary spastic paraplegia 90A
Synonyms:	autosomal dominant spastic paraplegia 90A, SPG90A
Definition:	A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in heterozygous mutation in the SPTSSA gene on chromosome 14q13.1.
Ontology:	Human Disease [DOID:0070459]   ( DOID:0070459 )