hereditary spastic paraplegia

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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: familial spastic paraplegia, French settlement disease, hereditary spastic paraparesis, Strumpell-Lorrain disease

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ampd2, LOC592559, vps37a, spart, washc5, ap5z1, nt5c2, hspd1, ddhd1, tecpr2, ap4m1, spast, LOC581885, ap4e1, ap4b1, [+]

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): paraplegia (is_a)