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DOID:0111832 - X-linked spinocerebellar ataxia 4
Disease Ontology Definition:An X-linked cerebellar ataxia characterized by ataxia, pyramidal tract signs and adult-onset dementia with X-linked inheritance.
Synonyms: SCAX4, X-linked ataxia-dementia syndrome, X-linked spinocerebellar ataxia type 4,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)