hereditary spastic paraplegia 4 (DOID:0110792)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 4; autosomal dominant spastic paraplegia type 4; SPG4
Alt IDs: OMIM:182601, ICD10CM:G11.4, ORDO:100985
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.