cerebellar ataxia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cerebellar disease characterized by ataxia originating in the cerebellum. (Human Disease Ontology, DOID_0050753)
External Link http://www.omim.org/entry/604290
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1 genes associated with the cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CP ceruloplasmin (ferroxidase)