Cerebellar Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

4 genes associated with the Cerebellar Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
C9ORF72 chromosome 9 open reading frame 72
CC2D2A coiled-coil and C2 domain containing 2A
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
OPHN1 oligophrenin 1