|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Atrophy (wasting) of the cerebellar cortex. (Human Phenotype Ontology, HP_0008278)|
|Downloads & Tools|
1 genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|SIL1||SIL1 nucleotide exchange factor|