About   Help   FAQ
Disease Ontology Browser
spinocerebellar ataxia with axonal neuropathy 1 (DOID:0090115)
Alliance: disease page
Synonyms: autosomal recessive spinocerebellar ataxia with axonal neuropathy 1; SCAN1; spinocerebellar ataxia with axonal neuropathy type 1
Alt IDs: OMIM:607250, ICD10CM:G60.2, ORDO:94124
Definition: A nervous system disease characterized by autosomal recessive inheritance of spinocerebellar ataxia and peripheral neuropathy that has_material_basis_in homozygosity for a mutation in the TDP1 gene on chromosome 14q32.11.

Disease References using Mouse Models (1)
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