Term Name:	hereditary spastic paraplegia 3A
Synonyms:	autosomal dominant familial spastic paraplegia 1, autosomal dominant spastic paraplegia 3, autosomal dominant spastic paraplegia type 3, FSP1, SPG3A, strumpell disease
Definition:	A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22.
Ontology:	Human Disease [DOID:0110791]   ( DOID:0110791 )