DOID:2476 - hereditary spastic paraplegia
Disease Ontology Definition:A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs.
Synonyms: French settlement disease, Strumpell-Lorrain disease, familial spastic paraplegia, hereditary spastic paraparesis,
Echinobase Genes : ampd2, LOC592559, vps37a, spart, washc5, ap5z1, nt5c2, hspd1, ddhd1, tecpr2, ap4m1, spast, LOC581885, ap4e1, ap4b1,
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): paraplegia (is_a)