About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Spinocerebellar Ataxia, Autosomal Recessive 2; SCAR2
OMIM ID: 213200

Synonyms Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital; Cerebellar Hypoplasia, Nonprogressive Norman Type; Cerebelloparenchymal Disorder III; CPD III; CPD3
Associated Genes
 There are currently no human or mouse genes associated with this disease in the MGI database.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory