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Disease Ontology Browser
X-linked spinocerebellar ataxia 4 (DOID:0111832)
Alliance: disease page
Synonyms: SCAX4; X-linked ataxia-dementia syndrome; X-linked spinocerebellar ataxia type 4
Alt IDs: OMIM:301840, MESH:C537316, ORDO:85292
Definition: An X-linked cerebellar ataxia characterized by ataxia, pyramidal tract signs and adult-onset dementia with X-linked inheritance.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory