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Human Disease and Mouse Model Detail
Human Disease 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; CPD3; Cpd III; Spinocerebellar Ataxia
Genes and
mouse models
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
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last database update
MGI 6.04
The Jackson Laboratory