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Summary Literature (0)
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)