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Summary Literature (0)
DOID:0111831 - X-linked spinocerebellar ataxia 3

Disease Ontology Definition:An X-linked cerebellar ataxia characterized by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy with X-linked inheritance.

Synonyms: SCAX3, X-linked ataxia-deafness syndrome, X-linked spinocerebellar ataxia type 3,

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)