Term Name:	hereditary spastic paraplegia 79A
Synonyms:	autosomal dominant spastic paraplegia 79A, SPG79A
Definition:	A hereditary spastic paraplegia characterized by slowly progressive cerebellar or sensory ataxia and spasticity of the lower limbs that has_material_basis_in heterozygous mutation in the UCHL1 gene on chromosome 4p13.
Ontology:	Human Disease [DOID:0070455]   ( DOID:0070455 )