hereditary spastic paraplegia 79A (DOID:0070455)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 79A; SPG79A
Alt IDs: OMIM:620221
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.