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Summary Literature (0)
DOID:0111830 - X-linked spinocerebellar ataxia 2

Disease Ontology Definition:An X-linked cerebellar ataxia characterized by infantile onset of ataxia, severe atrophy of the cerebellum, diffuse small cysts, pale inferior olives, and gliosis with X-linked inheritance.

Synonyms: SCAX2, cerebellar ataxia with extrapyramidal involvement early-onset,

Xenbase Genes :



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

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