About   Help   FAQ
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory