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Summary Literature (0)
DOID:0050952 - spastic ataxia

Disease Ontology Definition:A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy.

Synonyms:

Xenbase Genes : afg3l2, mtpap, kif1c, mars2, vamp1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0017845 - spastic ataxia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary ataxia (is_a)