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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia
OMIM ID: 271320
Human Phenotype Ontology associations
Synonyms Bedouin Spastic Ataxia Syndrome
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
Citing These Resources
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last database update
MGI 6.07
The Jackson Laboratory