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Disease Ontology Browser
X-linked spinocerebellar ataxia 3 (DOID:0111831)
Alliance: disease page
Synonyms: SCAX3; X-linked ataxia-deafness syndrome; X-linked spinocerebellar ataxia type 3
Alt IDs: OMIM:301790, MESH:C537315, ORDO:85297
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.


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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
04/16/2024
MGI 6.23
The Jackson Laboratory