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hereditary spastic paraplegia 41

Disease Summary
Associated Targets ()

Mondo Description Autosomal dominant spastic paraplegia type 41 is a pure form of hereditary spastic paraplegia characterized by onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise.
Mondo Term and Equivalent IDs
MONDO:0013239:  hereditary spastic paraplegia 41
Orphanet:320355: 
SCTID:763069002: 
UMLS:CN203988: