| 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 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| SIL1 | SIL1 nucleotide exchange factor |
