hereditary spastic paraplegia (DOID:2476)
Alliance: disease page
Synonyms: familial spastic paraplegia; French settlement disease; hereditary spastic paraparesis; Strumpell-Lorrain disease
Alt IDs: ICD10CM:G11.4, ICD9CM:334.1, MESH:D015419, NCI:C140267, OMIM:PS303350, UMLS_CUI:C0037773
Definition: A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.