Human genes for hereditary spastic paraplegia 4
Hereditary spastic paraplegia 4 [DOID:0110792]
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.
Synonyms: hereditary spastic paraplegia 4, DOID:0110792, familial spastic paraplegia 4, autosomal dominant spastic paraplegia 4, autosomal dominant spastic paraplegia type 4