Term Name:	hereditary spastic paraplegia 4
Synonyms:	autosomal dominant spastic paraplegia 4, autosomal dominant spastic paraplegia type 4, SPG4
Definition:	A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22.
Ontology:	Human Disease [DOID:0110792]   ( DOID:0110792 )