cerebellar cortical atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy (wasting) of the cerebellar cortex. (Human Phenotype Ontology, HP_0008278)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008278
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1 genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SIL1 SIL1 nucleotide exchange factor