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Summary Literature (0)
DOID:0111833 - X-linked spinocerebellar ataxia 5

Disease Ontology Definition:An X-linked cerebellar ataxia characterized by neonatal hypotonia, delayed motor development, nonprogressive ataxia, nystagmus, and dysarthria that has_material_basis_in hemizygous mutation in region of chromosome Xq25-q27.1.

Synonyms: SCAX5, Spinocerebellar Ataxia, X-Linked 5, X-linked non progressive cerebellar ataxia,

Xenbase Genes :



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

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